Cementitious reagents, their preparation and use

Abstract

The present invention provides a cementitious reagent material produced from globally abundant inorganic feedstocks, methods for the manufacture of such cementitious reagent material and for forming the reagent material as microspherical glassy particles, and also provides an apparatus, system, and method for the thermochemical production of glassy cementitious reagent having a spherical morphology. [Solution] A cementitious reagent is provided, which includes particles containing atoms of Si, Al, Fe, Ca, Mg, Na, and K, said particles having a spherical morphology with an average circularity (R) of >0.8, and said particles being at least 80% X-ray amorphous.

Description

[Technical Field]

[0001] CROSS-REFERENCE TO RELATED APPLICATIONS

[0001] This application claims the benefit under 35 U.S.C. §119(e) of U.S. Provisional Patent Application No. 62 / 867,480, filed June 27, 2019, and U.S. Provisional Patent Application No. 63 / 004,673, filed April 3, 2020, and U.S. Provisional Patent Application No. 63 / 025,148, filed May 14, 2020, the disclosures of which are incorporated herein by reference in their entireties. [Background technology]

[0002] FIELD OF THE DISCLOSURE

[0002] The field of this disclosure relates to cementitious reagents, and more particularly to the creation of relatively homogeneous cementitious materials and cementitious materials from abundant heterogeneous raw materials.

[0003] Concrete has played an important role in civilization for thousands of years and remains the most commonly used building material. Cement is the essential binding component of concrete, allowing the fluid concrete slurry to harden into a useful composite at ambient temperatures. While many binder chemistries have been successfully used to make concrete, Portland cement and its variants have been the primary concrete binder for nearly 200 years. Despite advances in production efficiency and material performance, there are significant and fundamental problems related to the chemistry of Portland cement that cannot be solved at a reasonable cost using current methods.

[0003]

[0004] Portland cement production is a CO2-intensive process that causes approximately 8% of global anthropogenic CO2 emissions. Some estimates predict that cement demand will increase by 12-23% by 2050. However, this growth in absolute demand for cement is at odds with the need for a complete decarbonization of the economy, which is also required by 2050 to avoid the catastrophic effects of global warming, in accordance with the UN IPCC Climate Report 2018. Therefore, there is an urgent need to significantly lower cement's specific CO2 emissions, especially as absolute production volumes increase.

[0004]

[0005] One way the industry has attempted to reduce cement's CO2 emissions is through the development of geopolymer cements, which are typically aluminosilicate inorganic polymers that harden through a geopolymerization process. Commercially viable geopolymer cements currently in use require access to several specific solids reagents, typically metakaolin (MK-750), ground granulated blast furnace slag (GGBFS), and coal fly ash. However, these reagents cannot meet the global transition to low CO2 emissions because their supply is geographically and quantitatively limited compared to the enormous demand for cement. Additionally, the cost of transporting these products from their manufacturing sites is also quite high compared to their market value.

[0005]

[0006] Cementitious agents are useful in both hydraulic cements and geopolymer cements. Geopolymer agents and supplemental cementitious materials (SCMs) are typically selected from several common cementitious materials: by-product ash from combustion (e.g., coal fly ash), slag by-products (e.g., ground granulated blast furnace slag), calcined clays (e.g., metakaolin), and natural pozzolans (e.g., volcanic ash). These materials are generally substantially amorphous and may be reactive in cementitious systems, such as geopolymer systems.

[0006]

[0007] Because most SCMs used in blended hydraulic cements are industrial by-products (e.g., coal combustion or high-quality iron production), their material properties are the result of industrial by-products and are not specifically tailored for high-quality cementitious reagents. Therefore, these materials lack any guarantee of ideal or even consistent composition and quality, and their suitability as cementitious reagents varies between plants and over time. Furthermore, with no control over production locations, the concrete industry lacks control over the future availability of these critical cementitious materials. It would be far more advantageous to be able to select production locations based on market needs, especially since transportation of cementitious materials is very expensive.

[0007]

[0008] Fly ash is a particularly glassy aluminosilicate by-product of coal combustion. It is frequently used as an admixture in hydraulic cement mixes to improve fluidity and create a pozzolanic reaction to improve concrete properties, including strength and resistance to alkali-silica reactivity. Unfortunately, only certain coals and combustion processes produce a consistent supply of fly ash of acceptable quality for use in concrete (e.g., ASTM Type C and F ash, or CSA Type C, CI, and F ash). Ash is not produced as an optimal SCM; rather, combustion is optimized for power generation and pollution prevention, and the consistency of the by-product ash is not guaranteed. Further issues regarding the future of fly ash in concrete include a significant decline in regional availability due to the transition from coal-fired energy to natural gas in many markets; carbon introduced after combustion can adversely affect air entrainment in concrete; ash recovery from temporary storage increases costs; and quality must be verified through testing on a case-by-case basis.

[0008]

[0009] Ground granulated blast furnace slag (GGBFS) is a glassy CaO-SiO2 by-product of iron production in blast furnaces. Concrete incorporating GGBFS has many advantageous properties, including improved chemical durability, whiteness, reduced heat of hydration, reduced CO2 emissions, and other beneficial properties. Unfortunately, due to the small number of blast furnaces operating in most markets, the supply of blast furnace slag is quite limited. Consequently, GGBFS is sought after as a high-quality SCM, and the price of this by-product is now similar to that of cement itself. Furthermore, limited geographic supply has led to shortages or at least high transportation costs in many local concrete markets. Finally, iron production and the resulting blast furnace slag supply are not directly tied to concrete demand, leaving the supply, local availability, and market price of these important admixtures largely at the mercy of chance.

[0009]

[0010] Natural pozzolans are siliceous or aluminosilicate materials that can precipitate in a pozzolanic reaction with Ca(OH)2. These include as-mined or calcined volcanic ash, diatomaceous earth, kaolinite and other clays, MK-750 and other natural minerals, and rocks that react with lime to produce hydrated calcium silicate compounds. While natural pozzolans can be very effective SCMs in concrete, they require the mining of nonrenewable resources, and pozzolans often require significant shipping distances because deposits are not very common. Natural materials also often require significant processing, such as calcination, to improve the reactivity of the natural pozzolans.

[0010]

[0011] Fly ash (usually with a low CaO content such as Type F), GGBFS, and certain natural and processed "pozzolans" (e.g., volcanic ash, zeolite, and MK-750) are also common geopolymer reagents, and the same adverse limitations on supply, geographic availability, price, quality, and consistency apply to their use in geopolymer binders and cements.

[0011]

[0012] To overcome certain limitations of these existing SCMs and geopolymer reagent supplies, several attempts have been made to improve aspects of traditional methods. Despite some improvements, these man-made products or compositions still have many deficiencies, for example, with regard to the reactivity and chemical properties of the reagents for use in geopolymer chemistry (e.g., optimizing the reagents for subsequent production of highly coordinated, branched, three-dimensional alkali / alkaline earth aluminosilicate polymers). They also require expensive laboratory-grade reagents and cannot simply use globally abundant raw materials.

[0012]

[0013] Also, previously produced glassy cementitious reagents have angular or fibrous particle morphology, and therefore cement pastes made from such reagents require large amounts of water and have relatively poor processability (e.g., excessive yield stress or higher than optimal plastic viscosity), which are obstacles to their use in practical concrete applications.

[0013]

[0014] Combustion ash and silica fume typically do not have angular particle morphology, however, they are not available in sufficient quantities, do not have suitable chemistry, and / or are too expensive to support a large-scale transition to high SCM blended hydraulic cements or geopolymer cements.

[0014]

[0015] Therefore, there is a need for cementitious reagents that solve existing processability problems while providing effectiveness comparable to superplasticizers and water reducers in equivalent Portland cement mix designs. There is also a need for methods to reduce CO2 emissions in the production of Portland cement, and in particular for engineered cementitious reagents with low or no process CO2 emissions that can be used as auxiliary cementitious materials in hydraulic cements and / or as solid geopolymer reagents.

[0015]

[0016] There is also a need for cementitious reagents that can be widely produced from globally abundant raw materials and that provide cementitious, reactive, and processable low yield stress cement mixes.

[0016]

[0017] Additionally, there is a need for the production of cementitious reagents where production locations can be selected based on market needs. In particular, there is a need for non-angular particles or microspheroidal glassy particles useful in cementitious reagents, geopolymer reagents, supplemental cementitious materials (SCMs), cement mixes, and concrete.

[0017]

[0018] There is also a need for economical production of such microspherical glassy particles, for example, by using globally abundant raw materials. There is also a need for apparatus, systems, and methods that use an in-air melting / quenching process in which solid particles are flowed as a suspension, melted as a suspension, and then quenched as a suspension.

[0018]

[0019] The present invention addresses these and other needs as will become apparent from a consideration of this disclosure and the following description of the features of the invention.

[0020] The primary cement used in concrete today is a hydrated, hardened form of calcium silicate known as Portland cement. Unfortunately, the production of Portland cement clinker generates significant global CO2 process emissions (from the heating of limestone) (approximately 3-5%, excluding fuel-related GHG emissions). The process is carried out in a rotary kiln with raw meal flowing countercurrently to the kiln burner. The process is very energy intensive, consuming approximately 3-5 GJ / tonne, of which approximately 1.5 GJ / tonne is used simply to calcine the limestone. Among the few processable strategies for reducing the environmental impact of cement, geopolymer chemistry offers a globally processable cement alternative with improved environmental and material performance. The inconsistent supply and limited geographic availability of traditional geopolymer reagents, such as fly ash and slag, have limited the standardization and adoption of geopolymer concrete. Meanwhile, the increasing demand for supplementary cementitious materials (SCMs) in hydraulic cements (to improve material and environmental performance) is further straining the demand for these materials.

[0019]

[0021] As mentioned above, various attempts have been made to prepare cementitious reagents, however, these methods suffer from significant deficiencies that have prevented an economical manufacturing process for glassy cementitious reagents.

[0020]

[0022] For example, existing academic research on cementitious reagents uses high-temperature refractory-lined furnaces and crucibles to directly contain the glass melt (a natural evolution of traditional glassmaking techniques). However, the crucibles and the solid refractory surrounding them in conventional furnaces require low heating and cooling rates (on the order of 10–50 °C / min) to avoid damage from thermal shock. Conventional melting furnaces have high thermal mass, which makes maintenance difficult and costly as a result of long startup and shutdown cycles. It would be preferable to eliminate the need for refractory material in direct contact with the melt, thereby eliminating complexity, abrasion, and significant startup and shutdown times.

[0021]

[0023] Quenching molten glass for cementitious reagents (e.g., blast furnace slag) previously required water, which is costly, inhibits heat recovery, can be environmentally harmful, and can require the added complexity of solid-liquid separation. Melt quenching methods are therefore either wasteful, slow, or reduce reactivity. Air quenching methods of cooling the melt require pressures of about 1 Pa, which is too slow or unfeasible for the most desirable feedstocks. * Either they require very specific chemistries to ensure low melt viscosities below 500 s.

[0022]

[0024] Previous glass manufacturing methods required costly particle size reduction (milling) of the vitreous product (typically before or after thermal processing). Summary of the Invention [Problem to be solved by the invention]

[0023]

[0025] Therefore, there remains a need for a convenient and economical method for producing glassy cementitious reagents from globally abundant feedstocks.

[0026] There is also a need to minimize energy consumption and handle very high and variable melt viscosities without the need for fluxes.

[0024]

[0027] There is also a need for methods for producing microspherical glass particles and for devices and systems useful for producing such microspherical glass particles.

[0028] The present invention addresses these and other needs as will become apparent from a consideration of this disclosure and the following description of the features of the invention. [Means for solving the problem]

[0025]

[0029] Embodiments relate, inter alia, to alternative cementitious materials (ACMs), which in some embodiments comprise solid microspherical glassy particles comprising one or more of the following properties: an average circularity (R) of >0.8; and particles having less than about 40% angular morphology.

[0026]

[0030] In some embodiments, the particles comprise an average circularity (R) of at least 0.9. In embodiments, less than about 30% of the particles, or less than about 25% of the particles, or less than about 20% of the particles, or less than about 15% of the particles, or less than about 10% of the particles have an angular morphology (R<0.7).

[0027]

[0031] In some embodiments, the particles have an average oxide formula (CaO,MgO)a·(NaO,KO)b·(AlO,FeO)c·(SiO) d It includes [Formula 1], in which a is about 0 to about 4, b is about 0.1 to about 1, c is 1, and d is about 1 to about 20.

[0028]

[0032] In some embodiments, the particles further comprise one or more of the following characteristics: (i) a content of 45%-100%, preferably 90-100%, of an X-ray amorphous solid; and (ii) a molar composition ratio of (CaO,MgO)0-12·(Na,K)0.05-1·(Al,Fe3+)·Si1-20.

[0029]

[0033] According to another aspect, some embodiments relate to a cementitious reagent comprising a mixture of microspherical glass particles as defined herein.

[0034] According to another specific aspect, the present invention in some embodiments relates to a cementitious reagent comprising a mixture of microspherical glassy particles, the particles having (i) an average circularity (R) of >0.8, (ii) less than about 20% of the particles having an angular morphology (R<0.7), (iii) oxide Formula 1 as defined previously, (iv) a content of X-ray amorphous solids of 45% to 100%, preferably 90 to 100%, and (v) (CaO, MgO) 0~12 (Na,K) 0.05~1 (Al,Fe3+ )·Si 1~20 and (vi) one or more of a low calcium content of about <10 wt.% CaO, or a medium calcium content of about 10 to about 20 wt.% CaO, or a high calcium content of >30 wt.% CaO.

[0030]

[0035] In some embodiments, the cementitious reagent is in the form of an amorphous solid. In some embodiments, the cementitious reagent is in the form of a powder. In embodiments, the particle size distribution has a D[3,2] (i.e., surface area average, or Sauter Mean Diameter) of about 20 μm or less, more preferably 10 μm or less, or most preferably 5 μm or less. In one embodiment, the mixture of microspherical glassy particles of the cementitious reagent comprises oxide Formula 1, defined above. In some embodiments, the cementitious reagent comprises less than about 10 wt% CaO. In some embodiments, the cementitious reagent comprises more than about 30 wt% CaO. In some embodiments, the cementitious reagent is about 40-100%, and preferably about 80% x-ray amorphous, 90% x-ray amorphous, and up to about 100% x-ray amorphous, and in some embodiments, 100% amorphous.

[0031]

[0036] According to some embodiments, the geopolymer binder comprises a cementitious agent as defined herein. According to another particular aspect, some embodiments of the present invention relate to a supplemental cementitious material (SCM) comprising a cementitious agent as defined herein, for example, the SCM comprises at least 20 wt.% of the cementitious agent.

[0032]

[0037] According to another particular aspect, some embodiments relate to solid concrete comprising a cementitious agent as defined herein.

[0038] According to another particular aspect, some embodiments relate to the use of the microspherical glass particles as defined herein and the cementitious reagents as defined to produce geopolymer binders or cements, hydraulic cements, supplemental cementitious materials (SCMs) and / or solid concrete.

[0033]

[0039] According to another particular aspect, some embodiments include a method for producing a crystalline aluminosilicate material by (i) providing a solid aluminosilicate material; (ii) in-flight melting / quenching the solid aluminosilicate material to melt the material into a liquid, and then quenching the liquid. and quenching the aluminosilicate material to obtain a melted / quenched powder comprising said microspherical glassy particles, thereby obtaining a cementitious reagent comprising said powder of microspherical glassy particles.

[0034]

[0040] In some embodiments, the method further comprises (iii) grinding the powder of microspherical glassy particles to a fine powder. In one embodiment, the powder comprises a particle size distribution with a D[3,2] of about 20 μm or less, more preferably 10 μm or less, or most preferably 5 μm or less.

[0035]

[0041] In some embodiments, the cementitious reagent obtained by this method comprises one or more of the following properties: reactive in cementitious and / or geopolymer systems; providing a workable geopolymer cement mix with a low yield stress of less than 25 Pa when the cement paste has an oxide molar ratio of HO / (Na2O, KO)<20; requiring a water content in the cement paste such that the oxide molar ratio HO / (Na2O, KO)<20; and providing a cement paste with higher workability than an equivalent paste with a substantially angular morphology, given the same water content.

[0036]

[0042] In some embodiments, the method further comprises adjusting the composition of the non-ideal solid aluminosilicate material to a desired content of the elements Ca, Na, K, Al, Fe, and Si. In one embodiment, the adjusting step comprises blending the non-ideal aluminosilicate material with a composition adjusting material to arrive at a desired ratio of one or more of the elements Ca, Na, K, Al, Fe, and Si.

[0037]

[0043] In some embodiments, the method further comprises fractionating the solid aluminosilicate material to obtain a powder of aluminosilicate material of a desired size, hi some embodiments, the method further comprises discarding unwanted waste material from the aluminosilicate material.

[0038]

[0044] In some embodiments, the method comprises in-flight melting at a liquidus temperature. In some embodiments, the temperature is about 1000-1600°C, or about 1300-1550°C.

[0039]

[0045] In some embodiments, the method further comprises adding a fluxing material to the solid aluminosilicate material to lower its melting point and / or induce a greater enthalpy, volume, or depolymerization of the liquid. In some embodiments, the fluxing material is mixed with the solid aluminosilicate material prior to or during melting.

[0040]

[0046] In some embodiments, the in-air melting / quenching process involves lowering the temperature of the liquid below the glass transition temperature to obtain a solid. In some embodiments, the in-air melting / quenching process involves lowering the temperature of the liquid below about 500°C, or preferably below about 200°C or less. In some embodiments, lowering the temperature of the liquid is performed by about 10 2 ks -1 ~about 10 6 Ks -1at a rate of preferably >10 3.5 Ks -1 In some embodiments, the quenching comprises a stream of cold air, steam, or water. In one embodiment, the method further comprises separating the quenched solid particles from the hot gas in a cyclone separator.

[0041]

[0047] In some embodiments, the method for producing a cementitious reagent from an aluminosilicate material further comprises reducing the particle size of the powder of solid microspherical glassy particles. In some embodiments, reducing the particle size comprises crushing and / or grinding the powder in a ball mill, roller mill, vertical roller mill, or the like.

[0042]

[0048] According to another aspect, some embodiments relate to an apparatus for producing microspherical glass particles, the apparatus comprising a burner, a melting chamber, and a quenching chamber, wherein the melting chamber and the quenching chamber may be completely separate or may be first and second sections, respectively, of the same chamber.

[0043]

[0049] The apparatus may be configured such that the solid particles are flowed as a suspension within the apparatus, melted as a suspension, and then quenched as a suspension.

[0050] In some embodiments, the burner provides a flame that heats the solid particles in suspension to a temperature sufficient to substantially melt the solid particles into a liquid. In some embodiments, the burner comprises a gas-fueled flame that entrains the aluminosilicate feedstock particles toward the melting / quenching chamber. The gas may include an oxidizer gas and a combustible fuel. In some embodiments, the burner comprises at least one of a plasma torch, an oxy-fuel burner, an air-fuel burner, a biomass burner, and a solar concentrating furnace.

[0044]

[0051] In some embodiments, the quenching chamber of the apparatus comprises a cooling system for providing cold air within the quenching chamber, where the cold air quenches the molten particles into solid microspherical glass particles, hi some embodiments, the cooling system comprises a liquid cooling loop positioned around the periphery of the cooling chamber.

[0045]

[0052] In some embodiments, the apparatus further comprises a cyclone separator for collecting the microspherical glassy particles. According to some embodiments, a method for producing a cementitious reagent from an aluminosilicate material comprises the steps of: (i) providing a solid aluminosilicate material; and (ii) in-air melting / quenching the solid aluminosilicate material to melt the material into a liquid, and then quenching the liquid to obtain a melted / quenched powder comprising the microspherical glassy particles, thereby obtaining a cementitious reagent comprising the powder of microspherical glassy particles.

[0046]

[0053] According to some embodiments, a method for producing microspherical glassy particles includes: (i) providing an in-air melting / quenching apparatus comprising a burner, a melting chamber, and a quenching chamber; providing solid particles; flowing the solid particles as a suspension in a gas combusted by the burner; heating the solid particles in the melting chamber to a heating temperature above the liquid phase to obtain liquid particles as a suspension; and quenching the liquid particles as a suspension to a cooling temperature below the liquid phase to obtain a powder comprising the microspherical glassy particles.

[0047]

[0054] In some embodiments of these methods, the solid particles comprise an aluminosilicate material. In some embodiments of these methods, the heating temperature is between about 1000-1600°C, or between about 1300-1550°C. In some embodiments of these methods, the cooling (quenching) temperature is less than about 500°C, or less than about 200°C.

[0048]

[0055] In some embodiments of these methods, the quenching comprises providing cold air into the quenching chamber. , further comprising collecting the powder in a cyclone separator.

[0049]

[0056] An additional aspect of some embodiments of the present invention relates to the use of an apparatus as defined herein, in particular an apparatus comprising at least one of a plasma torch, an oxy-fuel burner, an air-fuel burner, a biomass burner, and a solar concentrating furnace, for producing microspherical glass particles using an air melting / quenching process.

[0050]

[0057] An additional aspect of some embodiments of the present invention relates to the use of an apparatus as defined herein, in particular an apparatus comprising at least one of a plasma torch, an oxy-fuel burner, an air-fuel burner, a biomass burner, and a solar concentrating furnace, for producing a cementitious reagent from an aluminosilicate material using an air melting / quenching process.

[0051]

[0058] Additional aspects, advantages and features of the present invention will become more apparent upon reading the following non-limiting description of preferred embodiments, which are illustrative and should not be construed as limiting the scope of the invention.

[0052]

[0059] A better understanding of the features, advantages, and principles of the present disclosure may be obtained by reference to the detailed description that sets forth exemplary embodiments and the accompanying drawings. [Brief explanation of the drawings]

[0053] [Figure 1]

[0060] FIG. 1 is a flow diagram illustrating the production of a cementitious reagent starting from a solid aluminosilicate material, according to some embodiments. [Figure 2]

[0061] 1 is a set of four ternary CaO,MgO—SiO 2 —(Na 2 O,K 2 O)—(Al 2 O 3 ,Fe 2 O 3 ) composition diagrams, according to some embodiments. [Figure 3]

[0062] FIG. 3 is a three-dimensional quaternary diagram in (CaO, MgO)-(AlO, FeO)-(NaO, KO)-(SiO) space using the same material composition data plotted in FIG. 2, in accordance with some embodiments. [Figure 4]

[0063] 1 is a particle size distribution graph comparing the angular and spherical particle size distributions for commercially available natural volcanic glass powder (angular morphology) and particles produced according to Example 1 (spherical morphology). The volume percent of particles below a given diameter (y-axis) is provided as a function of particle diameter in micrometers (x-axis). Electron micrographs reveal the particle morphology of the samples. [Figure 5]

[0064] 5 is a graph providing a comparison of particle circularity (R) distributions of various powders (211-218, 519, 520, defined below), according to some embodiments, before (501) and after (502) processing, according to Examples 1-8. Image analysis was used to determine the R values ​​from micrographs of the same powders shown in Figures 6 and 7 according to the method of Takashimizu & Liyoshi (Takashimizu, Y., Iiyoshi, M. (2016). New parameter of roundness R: circularity corrected by aspect ratio. Progress in Earth and Planetary Sciences 3, 2. http: / / doi.org / 10.1186 / s40645-015-0078-x). For more precise data, see Table 17. For convenience, two Type F fly ash samples are also included: 519 (B-FA), a commercially available beneficiated fly ash, and 520 (LFA), an unbeneficiated fly ash directly from a coal-fired power plant. [Figure 6]

[0065] 5A-5C are panels showing a collection of electron micrograph pairs comparing raw particles (501) and processed particles (502) from various materials (211-218, as defined below) described in Examples 1-8. The field of view for each panel is 140 μm. [Figure 7]

[0066] Panels show photographs of two Type F fly ashes: one obtained directly from a coal-fired power plant in Nova Scotia (L-FA; 520), and one commercially available fly ash (B-FA; 519) that had been beneficiated to remove activated carbon and other contaminants. The field of view for each panel is 140 μm. [Figure 8]

[0067] FIG. 1 is a schematic process flow diagram of a system for producing a glass microsphere cementitious reagent, according to one embodiment of the present invention. [Figure 9A]

[0068] 1A-1C are photographs and corresponding diagrams of a burner flame (bottom) entering a melting-quenching processing chamber (top) containing entrained aluminosilicate feedstock particles, respectively, according to one embodiment of the present invention. [Figure 9B]

[0068] Figures 1A and 1B are photographs and corresponding diagrams of a burner flame (bottom) entering a melting-quenching processing chamber (top) containing entrained aluminosilicate feedstock particles, according to one embodiment of the present invention. [Figure 10]

[0069] FIG. 1 is a schematic diagram of an improved in-flight melting apparatus including a heat recovery loop to minimize energy input and CO2 emissions, according to one embodiment of the present invention. [Figure 11]

[0070] 1 is a complete set of ternary representations of novel compositions near Si, Al, Fe, Ca+Mg, and Na+K, according to some embodiments. [Figure 12]

[0071] 1 shows a ternary diagram for novel compositions from the Si perspective, according to some embodiments. [Figure 13]

[0072] 1 shows a ternary diagram for novel compositions from an Al perspective, according to some embodiments. [Figure 14]

[0073] FIG. 1 shows a ternary diagram for novel compositions from the Fe perspective, according to some embodiments. [Figure 15]

[0074] FIG. 1 shows a ternary diagram for novel compositions from a Ca+Mg perspective, according to some embodiments. [Figure 16]

[0075] FIG. 1 is a schematic flow diagram illustrating a process for producing alternative cement concrete using a relatively small, decentralized, airborne mini-kiln, according to some embodiments. [Figure 17]

[0076] FIG. 1 is a schematic diagram illustrating conventional cement and aggregate distribution in a modern centralized Portland cement kiln supply chain, according to some embodiments. [Figure 18]

[0077] FIG. 1 is a schematic diagram illustrating the transportation benefits of co-locating an alternative cementitious material (ACM) minikiln at an aggregate quarry in a novel distributed method, according to some embodiments. [Figure 19]

[0078] FIG. 1 is a schematic diagram illustrating the transportation benefits of co-locating an alternative cementitious material (ACM) mini-kiln with a concrete batch plant in a novel decentralized manner, according to some embodiments. [Figure 20]

[0079] FIG. 1 is a schematic diagram illustrating the transportation advantages of locating alternative cementitious material (ACM) mini-kilns in a novel, decentralized manner at independent locations near aggregate quarries and concrete batch plants, according to some embodiments. DETAILED DESCRIPTION OF THE INVENTION

[0054]

[0080] Further details of the invention and its advantages will become apparent from the following detailed description, in accordance with several embodiments.

[0081] The following detailed description provides a better understanding of the features and advantages of the invention described in this disclosure, in accordance with the embodiments disclosed herein. Although the detailed description includes many specific embodiments, these are provided by way of example only and should not be construed as limiting the scope of the invention disclosed herein.

[0055]

[0082] In the following description of the embodiments, references are made to the accompanying drawings, which show by way of illustration only certain examples in which the embodiments of the invention may be practiced. Other embodiments may be construed without departing from the scope of the disclosed invention. It will be appreciated that this can be easily done.

[0056]

[0083] Microspherical glass particles

[0084] Some embodiments relate to the production and use of solid microspherical glass particles. As explained in more detail below, a related aspect relates to cementitious reagents comprising a mixture of such microspherical glass particles or a plurality of such microspherical glass particles.

[0057]

[0085] In accordance with the present invention, the solid microspherical glassy particles are clearly round particles with high sphericity.

[0086] As used herein, the term "roundness" and the corresponding unit "R" refer to the circularity defined by Takashimizu & Ilyoshi (2016). The value required to calculate R can be determined by performing image analysis on appropriate micrographs of the powder. R (roundness) provides a convenient quantitative measure of roundness that is highly correlated with Krumbein's "roundness" (Krumbein, W.C. (1941) Measurement and geological significance of shape and roundness of sedimentary particles. Jounal of Sedimentary Petrology 11:64-72. http: / / doi.org / 10.1306 / D42690F3-2B26-11D7-8648000102C1865D).

[0058]

[0087] In some embodiments, the microspherical glass particles have an average circularity (R) of at least 0.9 (standard deviation <0.15).

[0088] In some embodiments, the microspherical glass particles have a bulk circularity (R) of at least 0.8 (standard deviation <0.15).

[0059]

[0089] In some embodiments, the microspherical glass particles have a bulk circularity (R) of at least 0.7, or 0.6, or 0.5 (standard deviation <0.15).

[0090] In some embodiments, the mixture of microspherical glass particles comprises less than about 50% of the particles, or less than about 40% of the particles, or less than about 30% of the particles, or less than about 25% of the particles, or less than about 20% of the particles, or less than 15% of the particles, or less than 10% of the particles having an angular morphology (e.g., R<0.7).

[0060]

[0091] In some embodiments, the mixture of microspherical glass particles, or a plurality of microspherical glass particles, is provided in powder form comprising a particle size distribution with a D[3,2] of about 20 μm or less, more preferably about 10 μm or less, or most preferably 5 μm or less.

[0061]

[0092] In some embodiments, the microspherical glassy particles are amorphous solids.

[0093] In some embodiments, the microspherical glassy particles have the oxide formula 1 (CaO,MgO)a·(NaO,KO)b·(AlO,FeO)c·(SiO) d It includes [Formula 1], in which a is about 0 to about 4, b is about 0.1 to about 1, c is 1, and d is about 1 to about 20.

[0062]

[0094] In some embodiments, the microspherical glassy particles have (i) an X-ray amorphous solid content of 45% to 100%, preferably 90 to 100%, and (ii) (CaO, MgO) 0~12 (Na,K)0.05~1 (Al,Fe 3+ )1·Si 1~20 The molar composition ratios include one or more of the following:

[0063]

[0095] In some embodiments, the microspherical glass particles are 40 to 100% x-ray amorphous, more preferably about 80 to about 100% x-ray amorphous, and in some embodiments So it is 100% amorphous.

[0064]

[0096] In some embodiments, the particles comprise less than about 10% by weight CaO.

[0097] In some embodiments, the particles comprise greater than about 30% by weight CaO.

[0098] In some embodiments, the particles have a Si / (Fe 3+ , Al) and a high calcium content with a CaO content of about 10 to about 50 wt %, preferably about 20 to 45 wt %.

[0065]

[0099] In some embodiments, the particles have a Si / (Fe 3+ , Al) and an intermediate calcium content with a CaO content of about 10 to about 20 wt. %.

[0066]

[0100] As described below, microspherical glassy particles can be advantageously produced from globally abundant inorganic feedstocks, such as aluminosilicate materials. As used herein, the term "aluminosilicate material" refers to a material containing aluminum or aluminum and iron, and silicon dioxide, selected from natural rocks and minerals, dredged material, mining waste containing rocks and minerals, waste glass, contaminated materials bearing aluminosilicates, and by-products of the aluminosilicate industry. The aluminosilicate material according to the present invention is preferably in the form of a crystalline solid (e.g., at least 50% by weight, or at least 60% by weight, or at least 70% by weight, or at least 80% by weight, or at least 90% by weight, or 100% by weight crystalline solid). In some embodiments, the aluminosilicate material comprises at least 2% by weight (NaO,K2O), or at least 3% by weight (NaO,K2O), or at least 4% by weight (NaO,K2O), or at least 5% by weight (NaO,K2O), or at least 6% by weight (NaO,K2O), or at least 7% by weight (NaO,K2O), or at least 8% by weight (NaO,K2O), or at least 10% by weight (NaO,K2O), or at least 12% by weight (NaO,K2O), or at least 15% by weight (NaO,K2O), or at least 20% by weight (NaO,K2O). In some cases, the inorganic feedstock is heterogeneous and the glassy particles produced are more homogeneous than the feedstock as demonstrated during partial homogenization during melting, i.e., more than 10% of the particles produced fall within the new intermediate formulation range.

[0067]

[0101] In some embodiments, the aluminosilicate material is selected from dredged sediments, demolition concrete, mining waste, glacial clays, glacial sediments, river sediments, rock and mineral mixtures, such as rock and mineral mixtures composed of some or all of the elements Ca, Mg, Na, K, Fe, Al, and Si. These aluminosilicate materials are widely abundant in many different geographic regions.

[0068]

[0102] As described below, the elemental composition of the feedstock can be analyzed and optimized for the desired application. The feedstock can be analyzed by quantitative or semi-quantitative methods such as XRF, XRD, LIBS, EDS, wet chemical analysis, and various other existing methods for determining feedstock elemental composition.

[0069]

[0103] As described below, microspherical glassy particles can be produced using processes or methods such as air-melting / quenching and / or suspension melting to melt the starting inorganic materials into a liquid, and then quenching the liquid into solid particles. As used herein, the terms "air-melting / quenching" or "suspension melting" refer to processes in which particles are flowed as a suspension, melted as a suspension, and then quenched as a suspension to obtain a powder.

[0070]

[0104] In some embodiments, the term "microspherical glassy particles" encompasses particles as defined above found in the powder obtained directly from the air-melting / quenching process. In embodiments, the term "microspherical glassy particles" encompasses particles obtained by grinding or milling (e.g., jaw crushers, ink jet printers, etc.) the powder obtained after the air-melting / quenching process. This refers to the particles obtained after processing (such as with a pact mill).

[0071]

[0105] As described below, the microspherical glass particles find many uses, including, but not limited to, such as or in the preparation of cementitious reagents, such as or in the preparation of geopolymer binders or cements, such as or in the preparation of hydraulic cements, such as or in the preparation of supplemental cementitious materials (SCMs), and in the production of solid concrete.

[0072]

[0106] One additional use could be as a fertilizer or soil conditioner, for example as a substitute for "rock dust".

[0073]

[0107] cement-based materials

[0108] Some embodiments described herein relate to cementitious reagent powders comprising microspherical glass particles as defined herein.

[0074]

[0109] Some embodiments also relate to a geopolymer binder or cement, a hydraulic cement, a supplemental cementitious material (SCM), a hydraulic concrete mix, and a solid concrete powder comprising the microspherical glass particles defined herein.

[0075]

[0110] Particle morphology has a significant impact on the physical properties and handling of cement slurries. Thus, the highly circular morphology of particles according to the present invention advantageously provides geopolymer cement mixes with increased processability, flowability, and / or reduced water demand. In particular, having high circularity reduces the yield stress and viscosity of the cement mix by reducing interparticle friction. Furthermore, a spherical morphology reduces water demand by improving packing for a given particle size distribution.

[0076]

[0111] As shown in Figures 2 and 3, the composition of cementitious reagents according to embodiments of the present invention differs from existing cementitious materials. Indeed, considering the combination of the ternary composition of the elemental groups (CaO, MgO), (AlO, FeO), (NaO, KO), and (SiO), an embodiment of cementitious reagent 201 occupies a position in these figures that is distinct and separate from fly ash (C and F) 202, ground granulated blast furnace slag (GGBS or GGBFS) 203, metakaolin 204, and Portland cement 205. Examples of specific feedstock compositions are shown in Figure 2. Volcanic pumice 211 (Example 1), basalt 212 (Example 2), secondary basalt 213 (Example 3), coal tailings sample 214 (Example 4), dredged sediment 215 (Example 5), porphyry copper flotation tailings 216 (Example 6), demolition concrete 217 (Example 7), diorite aggregate crusher dust 218 (Example 8).

[0077]

[0112] Advantageously, cementitious reagents are formulated from globally abundant rocks, minerals, and compounds of known composition. In this way, abundant feedstocks do not have to be transported from great distances to processing facilities, or cement plants. In some cases, cement plants are built at the source of the raw materials.

[0078]

[0113] In some embodiments, the cementitious reagent comprises a mixture of microspherical glassy particles as defined herein, (i) in the form of an amorphous solid, (ii) in the form of a powder, (iii) comprising a particle size distribution with a D[3,2] of about 20 μm or less, more preferably 10 μm or less, or most preferably 5 μm or less, (iv) having a particle size distribution as defined above. (v) a content of X-ray amorphous solids of 45% to 100%, and preferably 90 to 100%; (vi) (Ca, Mg) 0~12 (Na,K) 0.05~1 (Al,Fe 3+ )1·Si 1~20 (vii) containing less than about 10 wt. % CaO; (viii) containing more than about 30 wt. % CaO; (ix) a molar composition ratio of Si / (Fe 3+ , Al) molar composition, and a CaO content of about 10 to about 50 wt. %, preferably about 20 to about 45 wt. %, (x) Si / (Fe 3+ ,Al) and a CaO content of about 10 to about 20 wt. %, (xi) 40 to 100 wt. % X-ray amorphous, more preferably greater than 80%, greater than 90%, and in some cases up to 100% X-ray amorphous, and in some cases 100% amorphous; and (xii) a particle size distribution with a D[3,2] of about 20 μm or less, more preferably about 10 μm or less, or most preferably about 5 μm or less.

[0079]

[0114] In some cases, the CaO content is below about 30 wt. % to reduce the impact of CO2 on the cement by avoiding the need for decomposition of calcium from the carbonate source.

[0080]

[0115] In some embodiments, the cementitious reagent contains less than about 10% by weight CaO. In some embodiments, the cementitious reagent contains more than about 30% by weight CaO. In some examples, the composition of the cementitious reagent in terms of the molar ratio of (Na,K) and Ca may be varied to obtain certain advantages depending on the binder requirements. For example, a cementitious reagent containing less than about 10% by weight CaO is suitable for use in heat-setting geopolymers and as a fly ash substitute. Alternatively, a cementitious reagent containing more than about 30% by weight CaO is hydraulic and can be added to geopolymer resins to enable ambient temperature curing of geopolymer cements, directly replacing blast furnace slag in blended Portland cement.

[0081]

[0116] In some embodiments, the cementitious reagent has a Si / (Fe 3+ A low-calcium-containing cementitious reagent has a molar composition of (Ca, Al) and a CaO content of about 10% by weight or less. Preferably, such cementitious reagent is 40 to 100% X-ray amorphous, more preferably about 80% to about 100% X-ray amorphous, and in some embodiments, 100% amorphous. Such low-calcium-containing cementitious reagents may find numerous commercial applications, for example, as pozzolanic admixtures in hydraulic cements and / or as agents in geopolymer binders and cements.

[0082]

[0117] In some embodiments, the cementitious reagent has a Si / (Fe 3+,Al) and a CaO content of about 10 to about 50% by weight, preferably about 20 to about 45% by weight. Preferably, such cementitious reagents are 40 to 100% X-ray amorphous, more preferably about 80 to about 100% X-ray amorphous, and even more preferably 100% amorphous. Such high calcium-containing cementitious reagents can find numerous commercial applications, for example, as hydraulic admixtures in blended hydraulic cements and / or as reagents in geopolymer binders and cements.

[0083]

[0118] In some embodiments, the cementitious reagent has a Si / (Fe 3+ , Al) and a CaO content of about 10 to about 20% by weight. Preferably, such cementitious reagent is about 40 to 100%, and preferably about 80% to about 100% X-ray amorphous, and even more preferably 100% amorphous. Such intermediate calcium-containing cementitious reagents are useful, for example, as cementitious reagents with desired intermediate hydraulic and solubility properties, particularly in ambient setting geopolymers. Many commercial applications can be found in polymer applications.

[0084]

[0119] In some embodiments, the Na and K content in the cementitious reagent is optimized. This can be advantageous for SCM applications, where free lime in the hydraulic cement is exchanged with soluble alkali, which coordinates with sialic acid salt molecules from the cementitious reagent to create a relatively stable alkali aluminosilicate polymer, to a degree that significantly improves the chemical properties of traditional hydraulic cements. In embodiments, the Na and K content is optimized due to the fact that geopolymeric reagents with significant Na and K content require less soluble silicate hardener than would otherwise be needed, thus reducing the soluble silicate requirement (and cost) of the geopolymer mix design.

[0085]

[0120] Method of preparation

[0121] The microspherical glass particles defined herein and compositions containing same, such as cementitious reagents, geopolymer binders or cements, hydraulic cements, supplemental cementitious materials (SCMs), and concretes, can be prepared using any suitable method or process.

[0086]

[0122] 1 shows exemplary steps required to produce a cementitious reagent from an aluminosilicate material, according to some embodiments. Briefly, a finely divided aluminosilicate material powder is selected 101 and its chemical composition is analyzed 102 and evaluated. The feedstock can be analyzed by quantitative or semi-quantitative methods such as XRF, XRD, LIBS, EDS, wet chemical analysis, and various other existing methods for determining feedstock elemental composition.

[0087]

[0123] If the selected composition is not acceptable, the material may be modified as necessary, blended (e.g., in the vessel prior to thermochemical processing), for example through the addition of composition adjusting materials 104 (see below), or sorted 103, and any undesirable waste material discarded.

[0088]

[0124] The resulting solid aluminosilicate material, comprising a powder of the desired composition, is then heated 106, and individual particles or particle agglomerates are dissolved into a liquid as a suspension. The liquid particles are then quenched 107, resulting in a powder comprising solid microspherical glassy particles. The powder is then crushed and / or ground (partially or wholly) 108 as needed to reduce particle size and / or optimize reactivity, if desired, to obtain the cementitious reagent 109.

[0089]

[0125] With respect to the addition of composition-adjusting material 104, as used herein, the term "composition-adjusting material" refers to any solid or liquid material having a suitable composition to preferentially modify the bulk or surface composition of the aluminosilicate material toward one or more of the elements Ca, Na, K, Al, Fe, and Si.

[0090]

[0126] Composition-adjusting materials that introduce calcium (Ca) can consist of calcium salts including CaCO3, Ca(OH)2, CaO, CaCl, CaF2, calcium silicate minerals and compounds, calcium aluminum silicate minerals and compounds, waste Portland cement products, waste hydraulic cement products, wollastonite, gehlenite, and melilite group mineral compositions.

[0091]

[0127] Composition-modifying materials that introduce aluminum (Al) include aluminum rocks, minerals, soils, sediments, by-products, and compounds containing one or more of kaolinite, halloysite, and other aluminum-rich / poorly alkaline clay minerals, Al2SiO5 polyhydrates, and other aluminum-rich / poorly alkaline clay minerals. It may be composed of feldspars, chloritoid, staurolite, garnet, corundum, mullite, gehlenite, diaspore, boehmalite, gibbsite, and nepheline, as well as other feldspars. Other minerals that may be used include aluminum metal, bauxite, alumina, and red mud (alumina refinery residue).

[0092]

[0128] Iron (Fe)-introducing compositional modifiers can consist of iron-rich rocks, soils, sediments, by-products, and compounds such as olivine, chlorite ores (chamosite, clinochlore), pyroxene, amphibole, goethite, hematite, magnetite, ferrihydrite, lepidocrocite, and other iron oxyhydroxide compositions, iron-rich clays and phyllosilicate minerals, iron ore tailings, and elemental iron.

[0093]

[0129] Heating 106 is performed until a temperature higher than the liquidus temperature is reached, for example, about 1000-1600°C, or about 1300-1550°C, to obtain a liquid. Any suitable method or apparatus may be used for heating and obtaining a liquid, including, but not limited to, air melting (i.e., float melting). This can be achieved, for example, by using an air melting apparatus equipped with one or more plasma torches, oxygen-fuel burners, air-fuel burners, biomass burners, or solar concentrating furnaces. Typically, a furnace temperature of 1000-1600°C is required, and most typically, 1300-1550°C is required to rapidly obtain the desired liquid-phase particles as a suspension. In embodiments, the device is selected to ensure as fast melting as possible. Examples of suitable air melting apparatus and methods are described below.

[0094]

[0130] Regarding quenching 107, in some embodiments, the quenching step involves lowering the temperature of the liquid below the glass transition, for example, to about 500° C. or less, or preferably to about 200° C. or less. In embodiments, the quenching is rapid, i.e., the temperature is reduced to about 10° C. 2 Ks -1 ~10 6 Ks -1 (preferably >10 3.5 Ks -1 Any suitable method may be used for the quenching process, including but not limited to contacting the molten material with a sufficient flow of cold air, steam, or water to produce an amorphous solid.

[0095]

[0131] If desired, a solvent may be added to the solid aluminosilicate material to lower its melting point and / or induce depolymerization of the liquid. The solvent may be mixed with the solid aluminosilicate material before or during heating / melting. Common solvents that can induce depolymerization and / or lower the melting temperature of the melt include CaF, CaCO, waste glass, scrap glass, glass frit, alkali-containing minerals (e.g., feldspar, zeolite, clay, and feldspathoid minerals), borates, halides (fluoride- and chloride-containing salts), and calcium salts.

[0096]

[0132] Regarding the optional crushing and / or grinding step 108, this can be performed using any suitable method or apparatus, including, but not limited to, ball mills, roller mills, and vertical roller mills. Preferably, the particle size is reduced to obtain a fine powder useful for cement applications. As described, for example, in Example 9, obtaining a finer powder can be useful to increase surface area and provide faster reaction rates. Those skilled in the art will be able to determine the particle size desired for their particular needs and consider the economic tradeoffs between loss of spherical morphology / manufacturability, grinding costs, and final performance requirements. In embodiments, the powder comprises a particle size distribution with a D[3,2] of approximately 10 μm or less, or preferably 5 μm or less. Such particle sizes are generally desirable to ensure sufficient reactivity and consistent material properties.

[0097]

[0133] Use of aluminosilicate materials

[0134] As described herein, some embodiments relate to the use of aluminosilicate materials to produce solid microspherical glassy particles and amorphous cementitious agents as defined herein.

[0098]

[0135] Another aspect is the use of in-air thermochemical processing of aluminosilicate materials to produce solid microspherical glassy particles and / or solid cementitious reagents. The glassy particles and cementitious reagents described herein can be advantageously used as replacement supplemental cementitious materials (SCMs) in blended hydraulic cements and / or as geopolymer solid reagents in geopolymer binders (thus eliminating the need for some or all of the MK-750, fly ash, GGBFS, and other common solid reagents).

[0099]

[0136] Another related aspect is the use of an aluminosilicate material to produce at least one of a supplemental cementitious material (SCM) as defined herein and a geopolymeric reagent and / or an amorphous cementitious reagent comprising solid microspherical glass particles.

[0100]

[0137] Use of microspherical particles and cement-based reagents

[0138] One aspect of the described embodiments relates to the broad relevance of the solid microspherical glass particles and cementitious reagents described herein: The appropriate composition of engineered cementitious reagents can be used interchangeably in significant proportions in both geopolymer cements and hydraulic cements (i.e., cements that react with water).

[0101]

[0139] Thus, some embodiments encompass geopolymer cements or hydraulic cements that comprise at least 5% by weight, or at least 10% by weight, or at least 15% by weight, or at least 20% by weight, or at least 25% by weight, or at least 30% by weight, or at least 40% by weight, or at least 50% by weight, or at least 60% by weight, or at least 70% by weight, or at least 80% by weight, or at least 90% by weight or more of the solid microspherical glass particles and / or cementitious agents defined herein.

[0102]

[0140] According to some aspects, some embodiments described herein relate to a supplemental cementitious material (SCM) comprising a cementitious agent as defined herein. In some embodiments, the SCM comprises about 5% to about 50% by weight (preferably 20% by weight) of solid microspherical glass particles and / or cementitious agent as defined herein.

[0103]

[0141] According to another aspect, some embodiments described herein relate to a supplemental cementitious material (SCM) that includes one or more of the following characteristics: it contains less than about 35 wt.% CaO, and is in the form of an amorphous solid, with an acceptable content of Na+K (e.g., at least 2 wt.%, preferably at least 5 wt.%) and Al (e.g., at least 5 wt.%).

[0104]

[0142] According to another aspect, some embodiments relate to solid concrete comprising solid microspherical vitreous particles and / or cementitious agents as defined herein, i.e., comprising from about 5% to about 50% by weight (preferably at least 10% by weight, or at least 20% by weight, at least 30% by weight, or at least 40% by weight) of solid microspherical vitreous particles and / or cementitious agents as defined herein.

[0105]

[0143] According to another aspect, some embodiments comprise from about 5% to about 50% by weight (preferably at least 10%, or at least 20%, at least 30%, or at least 40% by weight) of solid microspherical glassy particles and / or vitreous particles as defined herein. or cementitious agents.

[0106]

[0144] Those skilled in the art will appreciate that embodiments of the present invention advantageously provide a means for producing versatile, low CO2-emitting reagents from abundant, inexpensive, naturally occurring materials. Another significant advantage is the creation of a single reagent that meets current specification standards for alternative SCMs while also meeting the needs of the growing geopolymer market. Furthermore, cementitious reagents can be formed from a variety of heterogeneous feedstocks, resulting in a more homogeneous and suitable reagent material for cementitious reagents through the described process.

[0107]

[0145] As will be appreciated, one advantage of the systems and methods described herein is that they provide control over the final composition of cementitious reagents, thereby producing reagents with predictable compositions, which is of great importance to the industry. Such tailored compositions are not available for other existing cementitious reagents because they are typically obtained from industrial by-products. According to the embodiments described herein, local feedstocks can be modified, if necessary, to standardize performance for a given application. For example, in an SCM for Portland cement, it may be desirable to limit alkali content, while in a geopolymer system, it may be desirable to have a high alkali content and require less alkali silicate hardener. In both scenarios, compositional modifications may be desirable to limit variability in the feedstock's composition.

[0108]

[0146] Another notable concern regarding the chemistry of geopolymeric reagents is their unstable calcium content. Both calcium content and calcium-containing phases are important variables for controlling the rate of strength development and the final material properties of geopolymer cements under different temperature conditions. The methods described herein allow for the design and fabrication of specific advantageous compositions of microsphere cementitious reagents that are currently not possible with by-product-based cementitious reagents.

[0109]

[0147] Air melting apparatus, method and system

[0148] Embodiments also relate to devices, systems, and associated methods for the thermochemical production of glassy cementitious reagents having spherical morphology.

[0110]

[0149] According to some embodiments, the apparatus is configured for in-air melting / quenching. According to some embodiments, such as that shown in Figures 9A and 9B, the apparatus 900 includes a melting chamber combined with a burner 809 and a quenching chamber 902. In some embodiments, the melting chamber and the quenching chamber may be first and second sections, respectively, of the same chamber 902. In some embodiments, the melting chamber and the quenching chamber are separate, continuous chambers.

[0111]

[0150] As shown, the apparatus 900 is configured for in-flight melting / quenching. Aluminosilicate feed particles 903 enter the melting / quenching chamber (top, 902) suspended within a flame 901 combusting an oxidizer gas 807 with a combustible fuel 808. As the aluminosilicate feed particles 903 heat above the liquid-liquid phase transition and eventually melt, they are entrained in the oxidizer gas by a venturi eductor and flow in suspension toward the melting / quenching chamber 902 during combustion. The gas may include an oxidizer gas, including but not limited to oxygen, and air mixed with a combustible fuel, including but not limited to propane, methane, liquid hydrocarbon fuels, coal, syngas, biomass, coal-water slurries, and mixtures thereof. Preferably, the flame 901 is stabilized by an annular flow of quench air 904 that protects the melting / quenching chamber 902 and prevents particles from sticking to the interior walls 905 of the melting / quenching chamber 902 .

[0112]

[0151] In the apparatus 900, the molten particles are then quenched by cooling in air once they have become turbulent from suspension at the end of the melting / quenching chamber 902. Cooling / quenching of the molten particles may be provided by cold quench air introduced directly into the melting / quenching chamber 902 and / or by an optional cooling system, such as a liquid cooling loop (not shown) around the quenching section of the melting / quenching chamber 902. The molten particles may be quenched or cooled into an amorphous solid powder, resulting in a powder containing microspherical glass particles. The apparatus may further include an optional cyclone separator operating under suction from a centrifugal blower (not shown) to collect the powder containing the microspherical glass particles.

[0113]

[0152] Apparatus 900, or the like, can be used in a variety of systems to produce glass microsphere cementitious reagents. Figure 8 shows one embodiment of a schematic process flow diagram of an exemplary system 800 for producing glass microsphere cementitious reagents, and in some cases, for producing microsphere glass reagent powder 109.

[0114]

[0153] In the embodiment of Figure 8, system 800 includes a milling circuit 801 to obtain aluminosilicate feed powder 101. Coarse aluminosilicate feed 802 is fed into a jaw crusher or impact mill 803 to produce a suitably sized feed 804 that allows for fine grinding in a ball mill 805. The resulting product is finely divided aluminosilicate feed powder 101.

[0115]

[0154] The finely divided aluminosilicate feed powder 101 is then entrained in an oxidizer gas (e.g., oxygen) 807 and mixed with a combustible fuel (e.g., propane) 808 in a burner 809, to which a liquid cooling loop 810 is attached for long torch life. Ambient temperature quench air 811 is preferably introduced near the burner 809 and flows around the outside of the walls of the melting / quenching chamber 812 to prevent the molten particles from sticking to the walls of the burner 809. Wall cooling may be provided by the quench air and / or by an optional liquid cooling loop 813. The molten particles are quenched by the cooled quench air as they transition from a suspended state to a turbulent flow at the end of the melting / quenching chamber. A cyclone separator 814 operating under suction from a centrifugal blower 815 can be used to collect the microspherical vitreous reagent powder 109.

[0116]

[0155] The apparatus of FIG. 9 and the system of FIG. 8 were successfully used to produce solid microspherical glassy particles, and cementitious reagents containing same, as defined herein and described in the Examples below. Operating parameters involved approximately stoichiometric combustion of propane and oxygen gas (actual mass ratios were not measured). Powdered feedstock 101 entered the burner from a pneumatic disperser and was delivered by a vibratory feeder. The feedstock and combustion air suspension consisted of approximately equal masses of oxygen and powdered feedstock, e.g., 1 gram of aluminosilicate feedstock suspended in 1 gram of oxygen.

[0117]

[0156] Those skilled in the art will recognize that the illustrated apparatus, system, and parameters are one of many potentially useful apparatus and systems encompassed by the present invention. For example, in an alternative embodiment, solid particles travel as a suspension in a carrier gas and are heated by one or more energy sources. Energy for melting can be provided by one or a combination of suitable high-temperature heat sources, such as plasma (arc discharge or inductively coupled), electrical induction heating, electrical resistance heating, microwave heating, solar radiation, or heat from a chemical reaction (e.g., combustion). Some of these energy sources can lower the CO2 footprint of the process, but the cost of CO2 emissions must be weighted against the unique cost of each energy source. Currently, in many jurisdictions, the cheapest energy source is the preferred energy source. The energy source is based on combustible hydrocarbon fuels. Therefore, the choice of energy source is largely driven by the price and cost of CO2 emissions in a given jurisdiction. Current economic and political factors dictate that solid particles preferably fly as a suspension in a gas, so that combustion heats them to a temperature above the liquid phase transition.

[0118]

[0157] Although an oxy-fuel burner was used in the example provided, one skilled in the art will understand that the choice of burner fuel is of only secondary importance as long as adequate heating occurs. Any heat source is possible, including from combustion, plasma, concentrated solar power, nuclear power, etc.

[0119]

[0158] In some embodiments, air-fired burners are preferred to avoid the cost of oxygen enrichment. When air consisting only of about 23 weight percent oxygen is burned with a fuel (e.g., propane or methane), the air-to-fuel ratio is highest (about 4-5 times) to maintain approximately stoichiometric combustion. Higher air-to-fuel ratios result in lower flame temperatures. Therefore, it is preferable to adjust the feedstock powder mass flow rate accordingly to ensure that the particles are heated above their solidus temperature, and preferably near or above their liquidus temperature (1000-1600°C, and typically above 1200°C).

[0120]

[0159] FIG. 10 illustrates another embodiment of an apparatus and system for in-flight melting / quenching according to embodiments described herein. Feedstock 101 passes through valve 1002 and enters cyclone 1003, where the feedstock is preheated by exchanging heat with hot gas. Valve 1004 meters the feedstock powder into hot gas (e.g., combustion air) flowing through pipe 1025. The combustion air and feedstock suspension are conveyed to burner 1005, where combustible gas is introduced through pipe 1006. A cylindrical melting chamber 1007 is configured to receive the gaseous heat stream (e.g., combustion gas) entraining aluminosilicate particles at various stages of melting 1008. Melting chamber 1007 comprises a cylindrical shell 1009 of a suitable material, such as steel, and a lining 1010 of a suitable refractory material. The melting chamber 1007 is also protected internally by a stream of cold air (primarily quench air) 1011 injected through an upper distribution ring 1012. The cooled air flows inside the melting chamber 1007 around the inner chamber walls in a laminar or swirling flow 1013 without significantly mixing with the central flow of molten suspended particles 1008. This air flow also protects the refractory lining 1010 and limits heat loss.

[0121]

[0160] The molten particles 1008 then enter a cooling chamber or quench zone 1014 where the particles interact with primary quench air 1013 and optionally pass through a distributor 1016 to interact with secondary cooling quench air 1015 injected 1017 into the cooling chamber 1014.

[0122]

[0161] The quenched hot solid particles 1018 flow as a suspension through pipe 1019 and are separated from the hot gases in cyclone separator 1020. The hot solid glassy particles pass through valve 1021, exchange heat with cooled combustion air 1024, and are separated in combustion air preheat cyclone 1022. Valve 1023 regulates pressure and allows for collection of the microspherical glassy product 109. The cyclone separators 1003, 1020, and 1022 also function as solid / gas heat exchangers for an important heat recovery loop that increases the energy efficiency of the process. In cyclone 1020, the hot gases from the melting chamber 1007 are separated from the solids, and these gases preheat the cooler feed powder 101 prior to separation in cyclone 1003. The heat-exchanged exhaust gas 1027 is directed to a suitable exhaust system (e.g., baghouse and blower) or passes through a further stage of heat-exchange cyclones. In the cyclones 1022, the heat-quenched particles 1018 transfer their heat to cold combustion air. 1024, preheated combustion air is used to convey the preheated feed powder to the melting chamber 1007, thereby significantly reducing the amount of energy that must be added to achieve melting of the suspended particles. [Example]

[0123]

[0162] Example 1: Reduction of yield stress with synthetic spherical particles

[0163] To demonstrate the improvement to the viscosity of geopolymer cement mixes, the following procedure was employed. Commercially available crushed volcanic glass powder was purchased with the oxide composition SiO2 - 73.77%; Al2O3 - 11.82%; Fe2O3 - 1.42%; MgO - 0.1%; CaO - 0.28%; Na2O - 4.22%; and KO - 4.09% with a D[3,2] average particle diameter of 10 micrometers and an angular morphology typical of finely crushed powders. Volcanic glass powder sample 402 (Figure 4) was processed by the disclosed method of air melting to produce an optimally melted / quenched powder 403 with a substantially spherical morphology characterized by a D[3,2] average particle size of 11 micrometers and a circularity R > 8 (see Figure 4). More specifically, natural volcanic glass powder (angular morphology) was processed using the apparatus shown in Figures 8 and 9. The burner was a commercially available Shanghai Welding & Cutting Tool Works oxygen-propane burner model QHT-7 / hA with a modified powder inlet. The burner fired into a steel melting chamber with water-cooled walls, and the particle temperature exceeded the average liquidus temperature of the material, approximately 1300 °C, as inferred from compositional data. The liquidus temperature was interpreted as having been exceeded based on i) the microspherical morphology resulting from surface tension in the liquid phase, ii) the homogeneous composition (under backscattered electron imaging), and iii) the absence of unmelted or partially melted particles in the final reagent. In this experiment, the burner was not tightly sealed to the melting chamber, allowing the cold quench air to surge along the walls of the melting chamber and quench only the entrained powder that melted after a sufficient residence time to allow melting. The quenched hot powder was separated from the hot combustion gases in a cyclone as shown in Figure 8, and the glass powder was collected for testing. The resulting product in this example is a highly spherical synthetic glass (D[3,2] = 11 micrometers) of identical composition and nearly identical particle size distribution (Figure 4) to the raw materials.

[0124]

[0164] The microspherical mineral glass powder has a molar Si / (Al,Fe 3+ ), and (Ca, Mg) 0.12 (Na,K)0.89 (Al,Fe 3+ )1·Si 19.68 and 0.28% by weight of CaO (0.38% of CaO, MgO).

[0125]

[0165] This experiment compares two geopolymer reagents with equal composition and nearly equal particle size distribution (confirmed by laser diffraction particle size analysis, Figure 4). The only significantly altered variable is particle morphology.

[0126]

[0166] The powders were mixed separately as a geopolymer binder paste using a mix design ("Mix A") optimized for minimal water usage for the following angular volcanic glass:

[0127]

[0167] A 99.5 g mixture is made containing 1.77 moles of water, 0.12 moles of Na2O + K2O, 0.82 moles of SiO2, and 0.08 moles of Al2O3 + Fe2O3. The source of Al2O3 + Fe2O3 is cementitious reagent glass or volcanic glass. The source of SiO2 is also cementitious reagent or volcanic glass and potassium silicate. The source of potassium oxide is potassium silicate and potassium hydroxide. The oxide molar ratios for each mix are provided in Table 1 below.

[0128]

[0168] When spherical mix A is mixed with angular mix A in the same mass ratio, Sphere Mix B, which contained only 15 wt. % HO, was more fluid than sphere Mix B and had very poor processability, even at a very high water content of 40 wt. % HO. Surprisingly, sphere Mix B, which contained only 15 wt. % HO, had excellent processability, as indicated by a low yield stress of about 6 Pa.

[0129]

[0169] The glass sphere powder was mixed again with equal amounts of solid reagents but with a lower proportion of silicate hardener and water ("Mix B").

[0170] A 79g mixture was made containing 0.73 moles of water, 0.11 moles of Na2O + K2O, 0.8 moles of SiO2, and 0.08 moles of Al2O3 + Fe2O3. The source of Al2O3 + Fe2O3 is spherical cementitious reagent. The SiO2 is also spherical cementitious reagent and calcium silicate. The source of potassium oxide is potassium silicate and potassium hydroxide. The oxide molar ratios for each mix are provided in Table 1, shown below.

[0130]

[0171] A mini-cone slump test (described by Tan et al., 2017) was employed to determine the approximate yield stress of the angular powder mix A (spreading radius 24 mm) and the spherical powder mix B (spreading radius 60 mm). The angular powder produced a non-shear flowable mass with an approximate yield stress of 425 Pa or greater (calculated by the slump flow equation 10 detailed in Pierre et al., 2013 (Pierre, A., Lanos, C., & Estelle, P. (2013). Extension of spread-slump formulae for yield stress evaluation. Applied Rheology, 23(6), 36-44)). Surprisingly, the spherical mix had only 41% of the molecular water content of the angular mix (containing water in a soluble silicate hardener), which still produced an easily pourable resinous fluid with a yield stress of only about 6.5 Pa (Tan et al. 2017). (Tan, Z., Bernal, SA, & Provis, JL (2017). Reproducible mini-slump test procedure for measuring the yield stress of cementitious pastes.Materials and Structures, 50(6), 235) using the diffusion flow equation.

[0131]

[0172]

[0132] [Table 1]

[0133]

[0173] The angular mix A and spherical mix B were heated and hardened in a sealed container at 80°C for 6 hours. The angular paste hardened poorly, probably due to its high water content, while the spherical paste hardened to a ceramic-like consistency with a fine glassy surface. It hardened to a solid.

[0134]

[0174] Example 2: Basalt "FC"

[0175] Cenozoic basaltic rocks were sampled in Vancouver, British Columbia. The mineralogy of the rocks is dominated by plagioclase, diopside, and clay-like phases, likely weathering products (Table 2, determined by XRD with Rietveld refinement). The oxide compositions of the major elements are provided in Table 3.

[0135]

[0176]

[0136] [Table 2]

[0137]

[0177]

[0138] [Table 3]

[0139]

[0178] The basalt was crushed in a jaw crusher, then crushed in a disc mill and further reduced in a ring mill to a powder with an average particle size of approximately 10 μm. The powder was fed into a vitrification apparatus where the mineral was heated to approximately 1450°C by liquid transition, followed by a rapid quenching step. The resulting glass was 96.7% X-ray amorphous (Table 4).

[0140]

[0179]

[0141] [Table 4]

[0142]

[0180] The microspherical basalt glass powder has a molar Si / (Al,Fe 3+ ), and (Ca, Mg) 3.15 (Na,K) 0.21 (Al,Fe 3+ )1·Si 6.93 The molar cementitious reagent formula was 9.51 wt% CaO (17.3% CaO, MgO).

[0143]

[0181] The individual particles were observed to be highly spherical, with an average circularity R >0.8 (as defined previously) and D[3,2] of 10.5 μm.

[0182] A 131 g mixture was prepared containing 1.31 moles of water, 0.1 moles of Na2O + K2O, 0.88 moles of SiO2, and 0.24 moles of Al2O3 + Fe2O3. The source of Al2O3 + Fe2O3 was the microspherical basalt powder prepared above. The source of SiO2 was also basalt powder and potassium silicate. The source of potassium oxide was potassium silicate and potassium hydroxide. The oxide molar ratios are provided in Table 5 below.

[0144]

[0183]

[0145] [Table 5]

[0146]

[0184] A mini-slump cone test was performed on the geopolymer cement paste, resulting in a flow diameter of 98.4 mm and a calculated yield stress of 21.7 Pa. 110 g of sand was added to the paste, followed by 6 hours of sealed curing at 80 degrees Celsius. The compressive strength of the mortar specimen cube was determined to be 19 MPa.

[0147]

[0185] Example 3: Basalt "BD"

[0186] Commercially available powdered basalt "BD" has the oxide composition provided in Table 6 below.

[0148]

[0187]

[0149] [Table 6]

[0150]

[0188] The powder was fed into a vitrification apparatus which heated the material to approximately 1450°C via a liquid phase change, followed by a rapid quenching step. Highly spherical bulk particle morphology indicated successful melting via the liquid phase for the majority of the particles.

[0151]

[0189] Microspherical basalt reagent powder "BD" has a molar Si / (Al,Fe ratio of 7.84 3+ ), and (Ca, Mg) 2.66 (Na,K) 0.23 (Al,Fe 3+ )1·Si 7.84 The molar cementitious reagent formula was 0.0100 and had 9.66 wt.% CaO (14.04% CaO,MgO). Individual particles were observed to be highly spherical, with a circularity R of >0.8 and a D[3,2] of 8.0 μm as measured by laser diffraction.

[0152]

[0190] A 116 g mixture was prepared containing 1.53 moles of water, 0.09 moles of Na2O + K2O, 0.75 moles of SiO2, and 0.17 moles of Al2O3 + Fe2O3. The source of Al2O3 + Fe2O3 was the microspherical basalt powder prepared above. The source of SiO2 was also basalt powder and potassium silicate. The source of potassium oxide was potassium silicate and potassium hydroxide. The oxide molar ratios are provided in Table 7.

[0153]

[0191]

[0154] [Table 7]

[0155]

[0192] 110 g of sand was added to the mixture followed by 6 hours of sealed curing at 80 degrees Celsius. From the three samples, the average compressive strength of the mortar was determined to be 27.4 MPa with a standard deviation of 2.22 MPa.

[0156]

[0193] Example 4: Coal Tailings

[0194] Coal tailings obtained from Cape Briton, Nova Scotia consisted of approximately 60% residual coal and 40% mineral material. The inorganic portion had the oxide composition provided in Table 8 below.

[0157]

[0195]

[0158] [Table 8]

[0159]

[0196] Dry coal tailings, with a measured D[3,2] of 9.9 μm, were fed into a vitrification unit that combusted excess coal to heat the inorganic material to approximately 1450°C through a liquid-liquid phase change, followed by a rapid quenching step. The coal fraction in the feedstock added significant energy to the process, and the flame power increased coal tailing processing by at least 46% compared to "inert" basalt processed at the same mass flow rate.

[0160]

[0197] Successful melting through the liquid phase for the inorganic particles was indicated by highly spherical bulk particle morphology with an average circularity (R) > 0.8 and D[3,2] of 11.2 μm.

[0161]

[0198] Microspherical Coal Note: The reagent powder has a molar Si / (Al,Fe ratio of 5.66 3+ ), and (Ca, Mg) 0.38 (Na,K) 0.10 (Al,Fe 3+ )1·Si 5.66 and 1.7% by weight of CaO (2.56% of CaO, MgO).

[0162]

[0199] A 45g mixture was prepared containing 0.57 moles of water, 0.04 moles of Na2O + K2O, 0.42 moles of SiO2, and 0.12 moles of Al2O3 + Fe2O3. The source of Al2O3 + Fe2O3 was the coal tailings microsphere powder prepared above. The source of SiO2 was also coal tailings powder and sodium silicate. The source of sodium oxide was sodium silicate and sodium hydroxide. The oxide molar ratios are provided in Table 9 below.

[0163]

[0200]

[0164] [Table 9]

[0165]

[0201] The mixture was cast into cube molds followed by sealed curing for 6 hours at 80 degrees C. The samples were demolded and found to have a compressive strength of 21 MPa and a glassy ceramic-like surface.

[0166]

[0202] Example 5: Dredged Sediment

[0203] The sediment sample was obtained from the central Vancouver Harbour in British Columbia and is shown as an example of dredged sediment. The sample has the oxide composition provided in Table 10 below.

[0167]

[0204]

[0168] [Table 10]

[0169]

[0205] The sample was dried and found to have a mass median diameter D50 of 47 μm. The sample was then sieved to remove particles that did not pass through 75 μm.

[0206] This powder was fed into a vitrification apparatus which heated the material to approximately 1450°C via a liquid phase change, followed by a rapid quenching step.

[0170]

[0207] Highly spherical bulk particle morphology indicated successful dissolution through the liquid phase for the majority of particles. The microsphere precipitation reagent powder had a molar Si / (Al,Fe) ratio of 11.49. 3+ ), and (Ca, Mg) 1.55 (Na,K) 0.51 (Al,Fe 3+ )1·Si 11.49 and 4.42% by weight of CaO (7.14% of CaO, MgO).

[0171]

[0208] The individual particles are highly spherical and smooth, with an average circularity (R) > 0.8 and a D[3,2] of 11.8 μm.

[0209] A 98 g mixture containing 0.89 moles of water, 0.09 moles of Na2O + K2O, 0.8 moles of SiO2, and 0.13 moles of Al2O3 + Fe2O3 is prepared. The source of Al2O3 + Fe2O3 is the microspherical precipitate powder prepared above. The source of SiO2 is also precipitate ore powder and calcium silicate. The source of potassium oxide is potassium silicate and potassium hydroxide. The oxide molar ratios are provided in Table 11.

[0172]

[0210]

[0173] [Table 11]

[0174]

[0211] 110 g of sand was added to the mixture and the samples were cast into cubes followed by sealed curing for 6 hours at 80 degrees Celsius. The compressive strength of the mortar cubes was determined to be 25 MPa.

[0175]

[0212] Example 6: Copper Tailings

[0213] A sample of porphyry copper flotation tailings was obtained from Argentina and is an example of a globally abundant aluminosilicate waste material. The sample has the oxide composition provided in Table 12 below.

[0176]

[0214]

[0177] [Table 12]

[0178]

[0215] The sample was sieved to remove particles that did not pass through 75 μm. The powder was fed into a vitrification apparatus, which heated the material to approximately 1450 °C via a liquid phase change, followed by a rapid quenching step. Highly spherical bulk particle morphology indicated successful melting via the liquid phase for the majority of the particles.

[0179]

[0216] The microsphere tailings reagent powder has a molar Si / (Al,Fe) ratio of 14.2. 3+ ), and (Ca, Mg) 0.6 (Na,K) 0.5 (Al,Fe 3+ )1·Si 14.2 and 1.94% by weight of CaO (4.87% of CaO, MgO).

[0180]

[0217] The individual particles are highly spherical and smooth, with an average circularity (R) of greater than 0.8 and a D[3,2] of 11.4 μm.

[0218] A 103.6 g mixture is made containing 0.76 moles of water, 0.11 moles of Na2O+K2O, 1.04 moles of SiO2, and 0.13 moles of Al2O3+Fe2O3. The source of Al2O3+Fe2O3 is the microspherical tailings powder prepared above. Si The sources of O2 are also tailings powder and potassium silicate. The sources of potassium oxide are potassium silicate and potassium hydroxide. The oxide molar ratios are provided in Table 13 below.

[0181]

[0219]

[0182] [Table 13]

[0183]

[0220] 110 g of sand was added to the mixture and the samples were cast into cubes followed by sealed curing for 6 hours at 80 degrees Celsius. The compressive strength of the mortar cubes was determined to be 18 MPa.

[0184]

[0221] Example 7: Waste concrete

[0222] Structural concrete cores were sampled from a mid-rise apartment building construction site in Vancouver, British Columbia. The material had the oxide composition provided in Table 14 below.

[0185]

[0223]

[0186] [Table 14]

[0187]

[0224] The sample was sieved to remove particles that did not pass through 75 μm, and the powder was fed into a vitrification apparatus that heated the material to approximately 1450 °C via a liquid phase change, followed by a rapid quenching step.

[0188]

[0225] Highly spherical bulk particle morphology indicated successful melting through the liquid phase for the majority of the particles.

[0226] The microsphere concrete reagent powder has a molar Si / (Al,Fe ratio of 12.3 3+ ), and (Ca, Mg) 3.06 (Na,K) 0.7 (Al,Fe 3+ )1·Si 12.3 and 12.55% by weight of CaO (13.97% of CaO, MgO).

[0189]

[0227] The individual particles are highly spherical and smooth, with an average circularity (R) of greater than 0.8 and a D[3,2] of 10.0 μm.

[0228] A 100g mixture containing 1.27 moles of water, 0.08 moles of Na2O + K2O, 0.73 moles of SiO2, and 0.13 moles of Al2O3 + Fe2O3 is prepared. The source of Al2O3 + Fe2O3 is the microspherical concrete powder prepared above. The source of SiO2 is also concrete powder and potassium silicate. The source of potassium oxide is potassium silicate and potassium hydroxide. The oxide molar ratios are provided in Table 15 below.

[0190]

[0229]

[0191] [Table 15]

[0192]

[0230] 100 g of sand was added to the mixture and the samples were cast into cubes followed by sealed curing for 6 hours at 80 degrees Celsius. The compressive strength of the mortar cubes was determined to be 27 MPa.

[0193]

[0231] Example 8: Quarried aggregate

[0232] Granodiorite crusher dust from an aggregate quarry near Vancouver, Canada, was sampled for the following experiments. The sample had an oxide composition (SEM-EDX) of approximately 73% SiO2, 15% Al2O3, 3% Fe2O3, 0% MgO, 2% CaO, 3% Na2O, and 4% K2O. The rock was further crushed and milled to a fine powder that completely passed through a 75 μm filter.

[0194]

[0233] The resulting powder was processed in an air vitrifier which heated the material to approximately 1450°C via a liquid phase change, followed by a rapid quenching step.

[0234] Highly smooth and spherical bulk particle morphology indicated successful melting through the liquid phase for the majority of the particles.

[0195]

[0235] The individual particles are highly spherical and smooth, with an average circularity (R) of >0.8 and a D[3,2] of 9.3 μm. The microspherical granodiorite glass reagent powder has a molar Si / (Al,Fe) ratio of 16.0. 3+ ), and (Ca, Mg) 2.5 (Na,K) 4.4 (Al,Fe 3+ )1·Si 16.0 and 2% by weight of CaO (2% of CaO, MgO).

[0196]

[0236] A 105 g mixture is prepared containing 1.53 moles of water, 0.1 moles of Na2O + K2O, 0.93 moles of SiO2, and 0.12 moles of Al2O3 + Fe2O3. The source of Al2O3 + Fe2O3 is the microspherical aggregate powder prepared above. The source of SiO2 is also the aggregate powder and potassium silicate. The source of potassium oxide is potassium silicate and potassium hydroxide. The oxide molar ratios are provided in Table 16.

[0197]

[0237]

[0198] [Table 16]

[0199]

[0238] The mixture was cast into cubes as a paste, followed by 24 hours of sealed curing at 80°C. The compressive strength of the paste cubes was determined to be 11 MPa, indicating that the material gains strength with heat curing, as expected. The lower relative strength can be explained by the omission of sand (as in mortar) and the higher unmelted quartz mineral content compared to the other examples (quartz melts at >1600°C), which acts as a relatively inert filler.

[0200]

[0239] Summary of Examples 1 to 8

[0240] Table 17 below summarizes the main results of Examples 1-8 and also provides a comparison of the performance of two fly ashes: one processed commercial Type F fly ash (B-FA), and one fly ash of synthetic cement-type composition sampled directly from a coal-fired power plant in Nova Scotia, Canada. A visual representation of the distribution of circularity R is provided in Figure 5.

[0201]

[0241]

[0202] [Table 17]

[0203]

[0242] Example 9: Use of synthetic cementitious reagents as alternative SCMs

[0243] The microspherical basalt sample "BD" from Example 3 above was further processed by crushing the powder in a ring mill for 5 minutes to break down the coarsest particles, thereby increasing the reactive surface area. The D[3,2] particle size was determined to be 3.6 μm by laser diffraction analysis. Interestingly, spheres <10 μm tend to act as ball bearings in the mill, resisting breakage. The strength activity index of the reagent was compared to that of a commercially available, high-quality Type F fly ash with an oxide composition of SiO2-52.09%; Al2O3-18.58%; Fe2O3-4.25%; MgO-2.98%; CaO-10.25%; Na2O-6.03%; and KO-1.72%.

[0204]

[0244] 50 mm cubes of Portland cement control mix, Portland cement with fly ash (20% and 40% substitution), and Portland cement with cementitious reagent BD powder (also 20% and 40% substitution) were cast in accordance with ASTM C618. Table 18 provides compressive strength results at 7 and 28 days. Performance was compared to commercial Type F fly ash at the 20% substitution of the BD mix, and the strength activity index was acceptable. The BD mix was easily workable and showed no significant changes in strength. Notably, both BD reagent and fly ash produced very useful mortar strengths of over 40 MPa after 28 days at a 40% replacement of Portland cement. Therefore, the BD cementitious reagent can be considered a suitable fly ash substitute in terms of compressive strength.

[0205]

[0245]

[0206] [Table 18]

[0207]

[0246] cement-based materials

[0247] According to some embodiments, novel methods of producing and using cementitious reagents, geopolymeric reagents and supplemental cementitious materials (SCMs) offer significant advantages over known methods and processes.

[0208]

[0248] According to some embodiments, the cementitious reagent comprises an oxide of Formula 1: (CaO,MgO)a·(NaO,KO)b·(AlO,FeO)c·(SiO) d [Formula 1] In the formula, a is from about 0 to about 4; b is about 0.1 to about 1, c is 1, d is about 1 to about 15.

[0209]

[0249] Advantageously, the cementitious reagent according to the present invention is formulated from abundant rocks, minerals and compounds of suitable composition. Preferably, the CaO content is less than about 30% by weight to reduce the impact of CO2 on the cement.

[0210]

[0250] In some embodiments, the cementitious reagent is in the form of an amorphous solid. In embodiments, the cementitious reagent is in the form of a powder comprising a particle size distribution having a D50 (median diameter) of approximately 20 μm or less, or preferably 10 μm or less.

[0211]

[0251] In an embodiment, the cementitious agent comprises an X-ray amorphous solid with a content of 45% to 100%, and preferably 90 to 100%, and (Ca, Mg) 0~12 (Na,K) 0.05~1 (Al,Fe 3+ )1·Si 1~20 The molar composition ratio of the fluorine-containing compound is at least one of the following:

[0212]

[0252] In some embodiments, the cementitious reagent comprises less than about 10% by weight of CaO. In other embodiments, the cementitious reagent comprises more than about 30% by weight of CaO. (Na,K The composition of the cementitious reagent with respect to the molar ratio of CaO and Ca may be varied to obtain certain advantages depending on the binder requirements. For example, cementitious reagents with less than 10 wt% CaO are suitable as fly ash substitutes for use in heat-setting geopolymers. Alternatively, cementitious reagents containing more than about 30 wt% CaO are hydraulic and can be added to geopolymer resins to enable ambient temperature curing of geopolymer cements, directly replacing blast furnace slag in blended Portland cement.

[0213]

[0253] In some embodiments, the cementitious reagent has a Si / (Fe 3+ A low-calcium-containing cementitious reagent has a molar composition of 0.05% CaO (0.05%, 0.05% CaO, 0.05% Al), and a CaO content of about 10% by weight or less. Preferably, such cementitious reagent is 40 to 100% X-ray amorphous, more preferably about 80% to about 100% X-ray amorphous, and even more preferably 100% amorphous. Such low-calcium-containing cementitious reagents may find numerous commercial applications, for example, as pozzolanic admixtures in hydraulic cements and / or as agents in geopolymer binders and cements.

[0214]

[0254] In another embodiment, the cementitious reagent has a Si / (Fe 3+,Al) and a CaO content of about 10 to about 50% by weight, preferably about 20 to about 45% by weight. Preferably, such cementitious reagents are 40 to 100% X-ray amorphous, more preferably about 80 to about 100% X-ray amorphous, and even more preferably 100% amorphous. Such high calcium-containing cementitious reagents can find numerous commercial applications, for example, as hydraulic admixtures in blended hydraulic cements and / or as reagents in geopolymer binders and cements.

[0215]

[0255] In another embodiment, the cementitious reagent has a Si / (Fe 3+ ,Al) and a CaO content of about 10 to about 20 wt. %. Preferably, such cementitious reagent is about 40 to 100% X-ray amorphous, and preferably about 80% to about 100% X-ray amorphous, and even more preferably 100% amorphous. Such intermediate calcium-containing cementitious reagents can find numerous commercial applications, for example, as cementitious reagents with desirable intermediate hydraulic and fossilane properties.

[0216]

[0256] One important advantage of optimizing Na / K in the cementitious reagent according to the present invention lies in the fact that 1) free lime in the hydraulic cement is exchanged with soluble alkali and coordinates with sialate molecules from the cementitious reagent to create a relatively stable alkali aluminosilicate polymer to some extent, which greatly improves the chemical properties of traditional hydraulic cements in SCM applications, and 2) geopolymer reagents with significant Na / K content require less soluble silicate hardener than would otherwise be needed, thus reducing the soluble silicate requirement (and cost) of the geopolymer mix design.

[0217]

[0257] Method of preparation

[0258] In some embodiments, an aluminosilicate material is selected as a feedstock for producing a cementitious reagent. Figure 1 shows exemplary steps required to produce a cementitious reagent from an aluminosilicate material, according to an embodiment of the present invention.

[0218]

[0259] Briefly, an aluminosilicate material 101 is selected and its chemical composition is analyzed 102 and evaluated. The feedstock may be analyzed by any suitable quantitative or semi-quantitative method, such as XRF, XRD using the Rietveld refinement, LIBS, EDS, wet chemical analysis, and various other known methods for determining the elemental composition of a feedstock.

[0219]

[0260] If the selected composition is not acceptable, the material is modified, blended (e.g., in a vessel prior to thermochemical treatment), or screened 103, for example, through the addition of a composition-adjusting material 104. As used herein, the term "composition-adjusting material" refers to any solid or liquid material having a suitable composition to preferentially alter the bulk composition of the aluminosilicate material toward one or more of the elements Ca, Na, K, Al, Fe, and Si.

[0220]

[0261] As mentioned above, calcium (Ca)-introducing compositional modifying materials can be composed of CaCO3, Ca(OH)2, CaO, CaCl, calcium silicate minerals and compounds, calcium aluminum silicate minerals and compounds, waste Portland cement products, wollastonite, gehlenite, and other melilite group mineral compositions.

[0221]

[0262] As mentioned above, aluminum (Al)-introducing composition-modifying materials can be composed of aluminum rocks, minerals, soils, sediments, by-products, and compounds, including one or more of kaolinite, halloysite, and other aluminum-rich / poorly alkaline clay minerals, Al2SiO5 polymorphs, chloritoid, staurolite, garnet, corundum, mullite, gehlenite, diaspore, boehmalite, gibbsite, and nepheline, as well as other feldspars. Other materials that can be used include aluminum metal, bauxite, alumina, and red mud (alumina refinery residue).

[0222]

[0263] As discussed above, compositional adjustment materials that introduce iron (Fe) can consist of iron-rich rocks, soils, sediments, by-products, and compounds such as olivine, chlorite ores (e.g., chamosite, clinochlore), pyroxene, amphibole, goethite, hematite, magnetite, ferrihydrite, lepidocrocite, and other iron oxyhydroxide compositions, iron-rich clays and phyllosilicate minerals, and elemental iron.

[0223]

[0264] Sorting 105 may also be used as a composition adjustment method 103, and any unwanted waste material may be disposed of.

[0265] The resulting solid aluminosilicate material containing the desired composition is then heated 106. Heating is performed to reach a temperature above the liquidus temperature to obtain a liquid, for example, at about 1000-1600°C or about 1300-1550°C. Any suitable method or apparatus can be used for heating and obtaining a liquid, including, but not limited to, air melting and / or batch melting. This can be achieved, for example, by using a plasma furnace, an oxygen-fuel furnace, an arc furnace, a reverberatory furnace, a rotary kiln, or a solar furnace. Typically, furnace temperatures of 1000-1600°C, and most typically, 1300-1550°C, are required to obtain the desired liquidus phase.

[0224]

[0266] If desired, a solvent may be added to the solid aluminosilicate material to lower its melting point and / or induce depolymerization of the liquid. The solvent may be mixed with the solid aluminosilicate material before (e.g., in a container) or during heating. Common solvents that can induce depolymerization and / or lower the melting temperature of the melt include CaF, CaCO, waste glass, scrap glass, glass frit, alkali-containing minerals (e.g., feldspar, zeolite, clay, and feldspathoid minerals), borates, halides (fluoride- and chloride-containing salts), and calcium salts.

[0225]

[0267] The aluminosilicate liquid is then quenched 107 to obtain a solid. In embodiments, the quenching step involves lowering the temperature of the liquid below the glass transition, for example, to about 500° C. or less, or preferably to about 200° C. or less. In embodiments, the quenching is rapid, i.e., the temperature is reduced to about 10° C. 2 Ks -1 ~10 6 Ks -1 (preferably >10 3.5 Ks -1 Any suitable method may be used for the quenching process. Methods that may be used include, but are not limited to, appropriately contacting the molten material with a sufficient flow of cold air, steam, or water to produce an amorphous solid.

[0226]

[0268] The solids are then crushed and / or ground to reduce particle size 108 and obtain the cementitious reagent 109. This can be done using any suitable method or apparatus, including, but not limited to, ball mills, roller mills, and vertical roller mills. Preferably, the particle size is reduced to obtain a fine powder useful for cement applications. In embodiments, the powder comprises a particle size distribution having a D50 (median diameter) of approximately 20 μm or less, or preferably 10 μm or less. Such particle sizes are generally desirable to ensure sufficient reactivity and consistent material properties.

[0227]

[0269] Use of cement-based reagents

[0270] A related aspect relates to the broad relevance of the cementitious reagents described herein: appropriate compositions of engineered cementitious reagents can be used interchangeably in significant proportions in both geopolymer cements and hydraulic cements (i.e., cements that react with water).

[0228]

[0271] Thus, embodiments described herein include geopolymer cements or hydraulic cements that include at least 5% by weight, or at least 10% by weight, or at least 15% by weight, or at least 20% by weight, or at least 25% by weight, or at least 30% by weight, or at least 40% by weight, or at least 50% by weight, or at least 60% by weight, or at least 70% by weight, or at least 80% by weight, or at least 90% by weight, or more, of the cementitious reagents described herein.

[0229]

[0272] According to another aspect, some embodiments relate to a supplemental cementitious material (SCM) comprising a cementitious reagent as defined herein. In embodiments, the SCM comprises about 5% to about 50% by weight (preferably at least 20% by weight) of a cementitious reagent as defined herein.

[0230]

[0273] According to another aspect, some embodiments relate to a supplemental cementitious material (SCM) that includes one or more of the following characteristics: it has an acceptable content of Na / K (e.g., at least 2 wt.%, preferably at least 5 wt.%) and Al content (e.g., at least 5 wt.%), contains less than about 35 wt.% CaO, and is in the form of an amorphous solid.

[0231]

[0274] According to another aspect, some embodiments relate to solid concrete comprising a cementitious agent as described herein, i.e., comprising about 5% to about 50% by weight (preferably at least 20% by weight) of a cementitious agent as defined herein.

[0232]

[0275] According to another aspect, some embodiments relate to blended hydraulic cements that are distinct from Portland cement. For example, solid-state Si NMR spectroscopy distinguishes blended hydraulic cements with low iron content (<5 wt%) according to the present invention from Portland cement (which has a major CSH binder component) by the amount and type of silica tetrahedral connectivity in the set cement. In fact, the set Portland cement binder phase is characterized by low coordination and hydration sites (Q1, Q1(OH), Q2, and Q2(OH)), little tetrahedral Al substitution, and an absence of high coordination (i.e., an absence of Q3 and Q4 sites). Blended hydraulic cements containing cementitious reagents according to the present invention, in addition to unique features such as aluminum substitution (e.g., Q2(1Al)), also exhibit the typical CSH-related sites described above and a "higher" level of coordination (i.e., branching) than Portland cement. For example, blended hydraulic cements according to the present invention include at least the Q3 level of coordination (e.g., Q3(2Al), Q3(1Al), Q3(0Al)). In embodiments, blended hydraulic cements according to the present invention contain a measurable proportion (>1 wt%) of three-dimensional crosslinks (Q4 sites), which are not known in conventional hydraulic cements. In another aspect, the present invention relates to a geopolymer binder comprising a cementitious reagent as defined herein, i.e., from about 5 wt% to about 90 wt% (preferably, at least 20 wt%, at least 30 wt%, at least 50 wt%, at least 75 wt%) of the cementitious reagent as defined herein.

[0233]

[0276] According to another aspect, some embodiments relate to solid geopolymer concrete comprising about 5% to about 50% by weight (preferably at least 20% by weight) of a cementitious agent as defined herein.

[0234]

[0277] Those skilled in the art will appreciate that the present invention advantageously provides a means for producing versatile, low CO2-emitting reagents from abundant, inexpensive, natural materials. Another significant advantage is the creation of a single reagent that meets current specification standards for alternative SCMs while also meeting the needs of the ever-expanding geopolymer market.

[0235]

[0278] Aluminosilicate Materials

[0279] As described herein, some embodiments provide methods for the thermochemical processing of aluminosilicate materials to produce solid cementitious reagents that can be advantageously used as alternative supplemental cementitious materials (SCMs) in blended hydraulic cements and / or as geopolymer solid reagents in geopolymer binders (thus eliminating the need for some or all of MK-750, fly ash, GGBFS, and other common solid reagents).

[0236]

[0280] In some cases, the aluminosilicate material is used to produce an amorphous cementitious reagent. In some embodiments, the aluminosilicate material is used to produce at least one of a supplemental cementitious material (SCM) and a geopolymer reagent.

[0237]

[0281] As used herein, the term "aluminosilicate material" refers to a material containing aluminum and / or Fe and silicon dioxide selected from natural rocks and minerals, dredged material, mining waste containing rocks and minerals, waste glass, contaminated materials bearing aluminosilicates, and by-products of the aluminosilicate industry. The aluminosilicate material according to the present invention is preferably in the form of a crystalline solid (e.g., at least 50% by weight, or at least 60% by weight, or at least 70% by weight, or at least 80% by weight, or at least 90% by weight, or 100% by weight crystalline solid). In some embodiments, the aluminosilicate material comprises at least 2 wt.% (NaO,K2O), or at least 3 wt.% (NaO,K2O), or at least 4 wt.% (NaO,K2O), or at least 5 wt.% (NaO,K2O), or at least 6 wt.% (NaO,K2O), or at least 7 wt.% (NaO,K2O), or at least 8 wt.% (NaO,K2O), or at least 10 wt.% (NaO,K2O), or at least 12 wt.% (NaO,K2O), or at least 15 wt.% (NaO,K2O), or at least 20 wt.% (NaO,K2O).

[0238]

[0282] In some embodiments, the aluminosilicate material is selected from the group consisting of dredged sediments, demolition concrete, mining waste, glacial clays, glacial sediments, river sediments, and mixtures of rocks and minerals, such as rocks composed of some or all of the elements Ca, Mg, Na, K, Fe, Al, and Si. Selected from a mixture of stones and minerals.

[0239]

[0283] In some embodiments, aluminosilicate materials are selected as feedstocks for producing cementitious reagents. The feedstocks can be analyzed by quantitative or semi-quantitative methods such as XRF, XRD using the Rietveld refinement, LIBS, EDS, wet chemical analysis, and various other existing methods for determining the elemental composition of the feedstocks.

[0240]

[0284] Example 10: Use of Dredged Sediment

[0285] Sediment samples were collected from the tidal reaches of the Fraser River downstream of Vancouver, British Columbia. The samples consisted of fine sand, silt, and clay fractions. The mineralogy of the samples is provided in Table 19 (determined by XRD using the Lieberth method), and the oxide composition of major elements was estimated from the mineralogy (Table 20).

[0241]

[0286]

[0242] [Table 19]

[0243]

[0287]

[0244] [Table 20]

[0245]

[0288] Fraser River Sediment (FRS) was dried and classified, and the fraction passing 120 μm was fed into a vitrification unit where the material was heated from its melting point to approximately 1450°C, followed by a quenching step to cool the powder. The resulting FRS glass powder was ground in a ball mill to a D50 of <20 μm. The X-ray amorphous content of the resulting powder was 52%. Mineral characterization results gave an estimated molar Si / (Al,Fe) of 11.46. 3+ ), and (Ca, Mg) 1.25 (Na,K) 0.34 (Al,Fe 3+ )1·Si 11.46 and 3.3 wt. % CaO, which satisfies the requirement of a "low Ca cementitious reagent."

[0246]

[0289] Heat-curing geopolymer binder: 5 parts of low-Ca cementitious reagent were mixed with 1 part of potassium silicate solution (molar ratio SiO2:K2O = 1.45). The paste was thoroughly mixed, placed in a sealed mold, and cured at 80°C for 4 hours. The resulting hardened paste achieved a compressive strength of at least 20 MPa in a cylinder compression test.

[0247]

[0290] Ambient setting geopolymer binder: Five parts of a low-Ca cementitious reagent were mixed with one part potassium silicate solution (molar ratio SiO2:K2O = 1.45), one part water, and 1.5 parts finely crushed CaSiO3. The silicate solution was mixed with CaSiO3 powder and allowed to react for 15 minutes. The resulting paste was thoroughly mixed with FRS glass powder and water, placed in a sealed mold, and allowed to harden at 20°C for seven days. The resulting hardened paste achieved a compressive strength of at least 20 MPa in a cylinder compression test.

[0248]

[0291] Ambient-Set SCM Applications in Portland Cement: A series of Portland cement mortar cubes were cast from a 50:50 mix of cement and sand. A low-Ca cementitious reagent was substituted for Portland cement in the mortar mix at 0%, 20%, 40%, 60%, and 80%. The cubes were cured at 100% humidity for 7 days, and the compressive strengths of the cubes are presented in Table 21. Substitution of up to 60% of Ordinary Portland Cement ("OPC") provides compressive strength useful for many applications while proportionally reducing the mortar's CO2 footprint.

[0249]

[0292]

[0250] [Table 21]

[0251]

[0293] Example 11: Use of demolished concrete

[0294] Structural concrete cores were sampled from a 2019 mid-rise housing development in Vancouver, British Columbia. The mineralogical composition of the concrete (including fine and coarse aggregates) is provided in Table 22 (XRD using the Rietveld method), and the bulk elemental composition is calculated from the mineralogical properties in Table 23.

[0252]

[0295]

[0253] [Table 22]

[0254]

[0296]

[0255] [Table 23]

[0256]

[0297] The concrete was crushed and ground into a powder with a D50 of approximately 20 μm. The powder was fed into a vitrification apparatus, which heated the material from its melting point to 1450°C, followed by a quenching step. The resulting glassy particles were finely ground into a powder with a D50 of approximately 5-15 μm.

[0257]

[0298] The mineral characterization results for this powder showed an estimated molar Si / (Al,Fe) ratio of 9.88. 3+ ), and (Ca, Mg) 2.79 (Na,K) 0.55 (Al,Fe 3+ )1·Si 19.88 This results in a molar cementitious reagent composition with 11 wt. % CaO. This can be considered an "intermediate Ca cementitious reagent."

[0258]

[0299] Ambient setting geopolymer cement: A cement paste was thoroughly mixed using powdered concrete glass (2.5 parts by weight), a potassium silicate solution (0.74 parts by weight) with a molar ratio of SiO2:KO2 = 1.45, and water (0.08 parts by weight). The paste was then placed in a cylindrical mold and allowed to harden at 20°C. Setting time was estimated by Vicat needle penetration testing. Initial setting occurred in 51 minutes, and the final setting time was 195 minutes.

[0259]

[0300] The compressive strength of a 50:50 ambient-hardened geopolymer cement and sand mortar mix was measured by compressively breaking a cylinder. After 3 days, the compressive strength reached approximately 25 MPa, and the tensile strength was approximately 2 MPa (by the split cylinder method).

[0260]

[0301] To test high-temperature performance, samples of the original structural concrete and 1-cm-diameter cast cylinders of geopolymer were exposed to 750°C in air for 2 hours. The Portland cement concrete cracked and turned powdery when handled, while the geopolymer mortar cylinders remained intact with no visible cracks or defects.

[0261]

[0302] The novel methods, systems, devices, and formulations presented herein offer many advantages, as detailed throughout. In some instances, the novel formulations and processes result in particles, powders, or reagents that are particularly useful as replacements for traditional cementitious additives in hydraulic cement or geopolymer cement compositions. The novel formulations can comprise the following molar compositions:

[0262]

[0303]

[0263]

number

[0264]

[0304]

[0265]

number

[0266]

[0305]

[0267]

number

[0268]

[0306]

[0269]

number

[0270]

[0307]

[0271]

number

[0272]

[0308] While the novel formulations presented herein result in unique materials that are particularly suited for the purposes described throughout, it can be difficult to distinguish materials solely by their individual elemental ranges or regions on the ternary diagram due to the limitations of the ternary diagram in accurately visualizing the three compositional parts and the fact that all elemental parts of the total composition have interdependencies.

[0273]

[0309] Geochemical compositions were classified as “compositional data” and a single-space to Euclidean space transformation (centered log ratio transformation - CLR) was applied to the seven-component compositions to preserve the information encoded in the molar composition in a manner that can be handled by standard statistical methods.

[0274]

[0310] For the CLR representation of the chemical data, a random forest classification was completed and an 8-rule classification set (presented below) was extracted from this predictive model. This rule set was used to determine whether fly ash and the listed feedstock compositions correspond to these ternary diagrams. The separation is achieved despite the fact that there may be compositional overlap between the materials. Such classification models are useful for accurately representing or classifying compositions beyond three-dimensional data.

[0275]

[0311] Modeling novel formulations and materials

[0312] The described glassy reagent ("new feedstock," or alternative cementitious material, "ACM") is distinguishable from fly ash in several important characteristics, including its time-temperature history, its ability to be produced in almost any location, and its relatively low levels of heavy metal contaminants of interest. The major elemental chemical compositions described herein are also readily distinguishable from fly ash to a satisfactory degree using compositional rules. As an example, a statistical model was constructed using fly ash compositional data from the literature and the predicted preferred feedstock compositions described herein. Classification rules were generated from a subsample as training data and tested on the remaining compositions (fly ash and the new compositions described herein) to evaluate the accuracy and predictive power of the classification rules. The following model predicted 94% of fly ash to be fly ash from 331 broad compositions from the literature, while the other 6% were classified as "outside the rule set." None of the fly ash samples were misclassified as the new feedstock geological materials described herein. When the model was applied to over 70,000 compositions of natural geomaterials that fit the disclosed molar composition range, the model predicts the novel feedstocks described herein with 99% success. Less than 1% of the compositions fell into the "outside the rule set" category. Clearly, significant and predictable differences exist between the novel feedstocks described herein and other by-product reagents, such as fly ash. The composition expressed in centered log ratio coordinates (CLR) alone is highly accurate in distinguishing the chemistry of the described glassy particles from fly ash.

[0276]

[0313] Applying the Model

[0314] To provide the following models: 1 Determine the bulk chemical composition of a given glassy sample by any suitable analytical method to provide the mole % of Si, Al, Fe, Ca, Mg, Na, and K. 2 Convert the molar data for the seven elements to CLR coordinates. 3 Apply the following conditions in order to predict whether the sample is fly ash or Terra reagent.

[0277]

[0315] Note: If the condition is not met, then the next condition applies. If no condition applies for a given composition, then ELSE predicts that the sample is outside the rule set of the model and cannot be predicted with confidence.

[0278]

[0316] rule 1. For glassy materials having a weight percent of bulk CaO oxide equal to <35%, and 2. Bulk mole % ratio Si / Al >2.

[0279]

[0317] Specifically, Rule 1 above can be used to rule out slag as a feedstock, and Rule 2 can be used to rule out metakaolin, kaolinite, and other 1:1 clay-rich feedstocks. The following conditions are applied to the undisclosed CLR converted molar sample composition using the logic IF (condition = TRUE), THEN (predict), ELSE (move to next condition) shown in Table 24 below.

[0280]

[0318]

[0281] [Table 24]

[0282]

[0319] Figure 11 shows the region of novel 7-part molar composition in the complete set of ternary diagrams. The circled areas highlight the differences between the novel feedstock and a wide range of fly ash samples from the literature. In the illustrated example, the top row of four ternary diagrams represents the Si perspective, shown in more detail in Figure 12. Referring to Figures 11-15, the black outlines of the samples indicate the alternative cementitious materials ("ACMs") described herein, which may also be referred to as novel feedstocks. The ACM compositions of Examples 1-8 are shown as black dots labeled with numbers corresponding to the composition of the example (numbers and compositions are summarized in Table 17). The gray outlines shown in the figures represent the 90% confidence intervals of the fly ash samples (as classified using the statistical model described above) based on 331 unique samples.

[0283]

[0320] The second row of FIG. 11 represents the ternary diagram from the perspective of Al, which is shown in more detail in FIG.

[0321] The third row of FIG. 11 represents the ternary diagram from the Fe perspective, which is shown in more detail in FIG.

[0284]

[0322] Finally, the last row of Figure 11 represents the ternary diagram from the Ca+Mg perspective, which is shown in greater detail in Figure 15 .

[0323] Figures 11-15 show the novel feedstock as it relates to a wide range of fly ash compositions, clearly demonstrating that the two material populations are highly distinguishable from one another even in the elemental mole ternary diagram. The apparent overlap area between the novel feedstock and fly ash is shown to be differentiated in the higher-order classification model provided herein. The novel feedstocks or ACMs described herein are not particularly alkali-tolerant and precipitate upon reaction with alkali hydroxides or lime as reagents.

[0285]

[0324] 16 shows a schematic flow diagram of a process 1600 for making alternative cement concrete using a relatively small, decentralized, aerial mini-kiln. The mini-kiln can be located in any suitable location, and due to its size and characteristics, is particularly suited for installation at an aggregate quarry, at a concrete batching plant, between a quarry and a concrete batching plant, or co-located at any suitable location, minimizing transportation times and distances typically required for concrete batching plants that rely on Portland cement. Minimize or at least reduce.

[0286]

[0325] At 1602, an aluminosilicate aggregate is provided as described herein. The aggregate may be any suitable aluminosilicate material, may be specially mined for the intended purpose, or may be waste material such as tailings, ground concrete, or some other type of aggregate. At block 1604, the aluminosilicate material is milled into a powder as described herein.

[0287]

[0326] At block 1606, the milled aluminosilicate material may be stored, transported, or provided as input to a mini-kiln described herein. At block 1608, energy is added to the milled aluminosilicate aggregate, such as combustion of an air / fuel mixture, a torch, industrial heat, or some other form of energy to raise the temperature of the aggregate. In some embodiments, the aluminosilicate particles are modified and blended as needed (e.g., in a vessel prior to thermochemical processing) through the addition of composition-adjusting materials to achieve a desired ratio(s), for example, for one or more of the elements Ca, Mg, Na, K, Al, Fe, and Si.

[0288]

[0327] In block 1608, the energy melts the aluminosilicate aggregate, which in some cases creates an aerated state where the aggregate is entrained in a column of air and / or air / fuel in the melting chamber.

[0289]

[0328] At block 1612, after the aggregate is melted and quenched, the feedstock becomes glassy aluminosilicate particles. In some cases, the particles are substantially spherical with a circularity R>0.8.

[0290]

[0329] At block 1614, the particles are combined with other ingredients in a concrete batch mix plant, which may optionally be coupled to a mini-kiln. At block 1616, additives such as hardeners, ambient hardening agents, admixtures, plasticizers, reinforcing materials, etc. may be added to the concrete. At block 1618, sand and coarse aggregate may be added to the cement, as known in the art.

[0291]

[0330] At block 1620, the final concrete mix is ​​formed and ready for use.

[0331] According to some embodiments, methods of cement production reduce cement transport distances (and therefore costs) compared to conventional methods. Some embodiments enable decentralized production of alternative cementitious materials (ACMs) in close proximity to aluminosilicate aggregate quarries and concrete batch plants. This ACM can be advantageously used as a key ingredient in suitable alternative cement formulations that can be used to make cost-effective and reduced CO2 concrete.

[0292]

[0332] Alternatively, ACM may be used as an alternative supplemental cementitious material (ASCM) to replace a proportion of Portland cement in conventional concrete, thereby reducing the cost and environmental impact of the resulting concrete.

[0293]

[0333] 17 shows a typical Portland cement plant 1702 where cement is typically transported long distances to arrive at a concrete batching plant 1704. Similarly, aggregates from a quarry 1706 may also be transported long distances to reach their destination at a concrete batching plant 1704. The time and energy required to transport these dense, voluminous products dramatically increases the costs associated with making concrete, as well as contributing to the overall CO2 emissions associated with concrete production.

[0294]

[0334] 18 shows an alternative arrangement 1800 utilizing the ACM described herein. In some cases, the ACM mini-kiln 1802 can be located at the aggregate quarry 1706 site. In this way, aluminosilicate material mined at the aggregate quarry 1706 can be processed on-site at the ACM mini-kiln 1802 without having to transport the aggregate to a remote location. The ACM and sufficient aggregate can then be sent to a concrete batching plant 1704, which may be in close proximity.

[0295]

[0335] 19 shows an alternative arrangement 1900 utilizing the ACM described herein. In the illustrated embodiment, an ACM mini-kiln 1802 may be collocated with a concrete batching plant 1704. Thus, aggregate from an aggregate quarry 1706 can be delivered to the concrete batching plant 1802, where it can be used by the ACM mini-kiln 1802 described herein and also used as coarse aggregate in the concrete mix.

[0296]

[0336] 20 shows an alternative arrangement 2000 utilizing the ACM described herein. In the illustrated embodiment, an ACM mini-kiln 1802 is located between an aggregate quarry 1706 and a concrete batching plant 1704. In this arrangement, aggregate can be delivered to the ACM mini-kiln, which utilizes the aggregate to compound the AXM as described herein, and the ACM and additional aggregate can be transported to the concrete batching plant.

[0297]

[0337] The mini-kiln design allows for a decentralized system that takes advantage of the smaller, even portable, characteristics of the ACM mini-kiln. Rather than relying on a single centralized Portland cement plant that requires transporting cement long distances, multiple ACM mini-kilns can replace the Portland cement plant, dramatically reducing transportation time and costs. The illustrated embodiment of Figures 17-20 provides a mobile, efficient, and waste-reducing design by locating the ACM mini-kiln in close proximity to the aggregate quarry, the concrete batch plant, or both.

[0298]

[0338] Suitable feedstocks and processes for converting the feedstocks into microspherical glass particles are disclosed in Applicant's co-pending applications having Serial No. 62 / 867,480, filed June 27, 2019, and Serial No. 63 / 004,673, filed April 3, 2020, the entire disclosures of which are incorporated herein by reference in their entirety. Suitable feedstocks are generally rocks and minerals that possess a proportion of both aluminum and silicon oxide. Conventional construction aggregates used in concrete are suitable, economical, and conveniently located for use as ideal cement feedstocks. Previously, it was not possible to produce cementitious materials from such normally crystalline aluminosilicate materials.

[0299]

[0339] One particular advantage of using aluminosilicate aggregate as an ACM is that the material is inexpensive and abundantly available.

[0340] Another particular advantage is that aluminosilicate aggregates are widely available and, in most markets, it is generally not necessary to license new quarries to produce ACM by this method.

[0300]

[0341] Another particular advantage of using aluminosilicate aggregates as ACMs is that mini-kilns (e.g., as described in applicant's co-pending application having Serial No. 63 / 004,673) can be installed at or very close to aggregate quarries, or concrete batch plants, or both, thus facilitating the transport of cement. Costs can be kept to a minimum. This is a major advantage because cement from large centralized kilns travels on average 5-10 times farther than aggregates (which have a decentralized supply), and is a natural consequence of the wide range of aggregate availability, low aggregate prices, and aggregate transportation.

[0301]

[0342] Another particular advantage of using aluminosilicate aggregate as an ACM is that quarries frequently have an abundance of by-product material that is "off-specification," meaning that there is no common use for a particular grade, even though such material generally shares the same composition as the main quarry product. Such by-product material is very cheaply available in both crushed aggregate quarries and sand and gravel quarries.

[0302]

[0343] Another particular advantage of decentralized ACM mini-kilns is that the capital costs per unit of throughput are expected to be similar to those of conventional rotary cement kilns, even though the absolute scale of the capital requirements is on the order of one-tenth of that required for Portland cement production.

[0303]

[0344] Another particular advantage of decentralized ACM mini-kilns is that operating expenditures per unit of throughput are not expected to exceed the corresponding costs in the manufacture of Portland cement, making ACM production cost-competitive with Portland cement at smaller scales, yet requiring 5 to 10 times less transportation costs.

[0304]

[0345] This disclosure includes the following numbered sections:

[0346] Item 1 Solid microspherical glassy particles comprising one or more of the following properties: an average circularity (R) of >0.8; and less than about 40% of the particles having an angular morphology (R<0.7).

[0305]

[0347] Item 2. The particles of item 1, wherein the particles have an average circularity (R) of at least 0.9.

[0348] Item 3. The particles of item 1 or 2, wherein less than about 30% of the particles, or less than about 25% of the particles, or less than about 20% of the particles, or less than about 15% of the particles, or less than about 10% of the particles have an angular morphology (R<0.7).

[0306]

[0349] Item 4: The particles of any one of items 1 to 3, wherein the particles comprise an average oxide formula 1: (CaO, MgO)a·(Na2O, KO)b·(Al2O3, Fe2O3)c·(SiO2)d [Formula 1]: where a is from about 0 to about 4, b is from about 0.1 to about 1, c is 1, and d is from about 1 to about 20.

[0307]

[0350] Item 5 The particles are characterized in that (i) 45% to 100%, preferably 90 to 100%, of the content is an X-ray amorphous solid; and (ii) (Ca, Mg) 0~12 (Na,K) 0.05~1 (Al,Fe 3+ )1·Si 1~20 5. The particles of any one of items 1 to 4, including one or more properties of having a molar composition ratio of:

[0308]

[0351] Item 6. The particles of any one of items 1 to 5, wherein the particles are 40 to 100% X-ray amorphous, more preferably about 80 to about 100% X-ray amorphous, and even more preferably 100% amorphous.

[0309]

[0352] Item 7. The particles of any one of items 1 to 6, wherein the particles contain less than about 10% by weight of CaO.

[0353] Item 8. The particles of any one of items 1 to 6, wherein the particles comprise greater than about 30% by weight of CaO.

[0310]

[0354] Item 9. The particles of any one of items 1 to 6, wherein the particles comprise a Si / (Fe3+,Al) ratio between 1 and 20 and a high calcium content of about 10 to about 50 wt. %, preferably about 20 to 45 wt. % CaO content.

[0311]

[0355] Item 10. The particles of any one of items 1 to 6, wherein the particles have a molar composition of Si / (Fe3+,Al) between 1 and 20, and an intermediate calcium content of about 10 to about 20 wt. % CaO content.

[0312]

[0356] Item 11. A cementitious reagent comprising a mixture of microspherical glass particles as defined in any one of items 1 to 10.

[0357] Item 12: A mixture of microspherical glassy particles, the particles comprising: (i) an average circularity (R) of >0.8; (ii) less than about 20% of the particles having an angular morphology (R<0.7); (iii) an oxide of Formula 1 as defined in claim 4; (iv) 45% to 100%, preferably 90% to 100%, of the content being an X-ray amorphous solid; and (v) (Ca, Mg) 0~12 (Na,K) 0.05~1 (Al,Fe 3+ )1·Si 1~20 and (vi) a low calcium content of about <10 wt.% CaO, or a medium calcium content of about 10 to about 20 wt.% CaO, or a high calcium content of >30 wt.% CaO.

[0313]

[0358] Item 13. The cementitious reagent of item 12, wherein the cementitious reagent is in the form of an amorphous solid.

[0359] Item 14. The cementitious reagent of Item 12 or 13, wherein the cementitious reagent is in the form of a powder.

[0314]

[0360] Item 15. The cementitious reagent of any one of items 12 to 14, wherein the cementitious reagent comprises a particle size distribution of about 20 μm or less, more preferably 10 μm or less, or most preferably 5 μm or less in D[3,2].

[0315]

[0361] Item 16: The cementitious reagent of any one of items 12 to 15, wherein the mixture of particles comprises an oxide of the formula (CaO, MgO)a·(Na2O, KO)b·(Al2O3, Fe2O3)c·(SiO2)d [Formula 1], where a is from about 0 to about 4, b is from about 0.1 to about 1, c is 1, and d is from about 1 to about 20.

[0316]

[0362] Item 17. The cementitious reagent of any one of items 12 to 16, wherein the cementitious reagent contains less than about 10% by weight of CaO.

[0363] Item 18. The cementitious reagent of any one of items 12 to 16, wherein the cementitious reagent comprises greater than about 30% by weight of CaO.

[0317]

[0364] Item 19 The cementitious reagent has a Si / (Fe ratio between 1 and 20. 3+ 17. The cementitious reagent of any one of items 12 to 16, which is a high calcium-containing cementitious reagent having a molar composition of (CuO, Al), and a CaO content of about 10 to about 50 wt. %, preferably about 20 to 45 wt. %.

[0318]

[0365] Item 20 The cementitious reagent has a Si / (Fe 3+ 17. The cementitious reagent of any one of items 12 to 16, which is an intermediate calcium-containing cementitious reagent having a molar composition of (CaO, Al), and a CaO content of about 10 to about 20 wt.%.

[0319]

[0366] Item 21: The cementitious reagent of any one of Items 12 to 20, wherein the cementitious reagent is about 40 to 100%, preferably about 80 to about 100%, X-ray amorphous, and even more preferably 100% amorphous.

[0320]

[0367] Item 22. A geopolymer binder containing a cementitious agent as defined in any one of items 11 to 21.

[0368] Item 23. A supplementary cementitious material (SCM) containing a cementitious reagent as defined in any one of items 11 to 21.

[0321]

[0369] Item 24. The SCM of Item 23, comprising at least 20% by weight of the cementitious agent.

[0370] Item 25 Solid concrete containing cementitious reagents as defined in any one of items 11 to 20.

[0322]

[0371] Item 26. Use of microspherical glass particles as defined in any one of items 1 to 10 and / or any one of cementitious reagents of items 11 to 20 to produce geopolymer binders or cements, underwater cements, supplementary cementitious materials (SCMs) and / or solid concrete.

[0323]

[0372] Item 27. A method for producing a cementitious reagent from an aluminosilicate material, comprising: (i) providing a solid aluminosilicate material; (ii) in-air melting / quenching the solid aluminosilicate material to melt the material into a liquid, and then quenching the liquid to obtain a melted / quenched powder comprising solid microspherical glassy particles; thereby obtaining a cementitious reagent comprising a powder of the microspherical glassy particles.

[0324]

[0373] Item 28. The method of item 27, further comprising the step (iii) of grinding the powder of microspherical glass particles into a finer powder.

[0374] Item 29. The method of items 27 or 28, wherein the powder comprises a particle size distribution of about 20 μm or less, more preferably 10 μm or less, or most preferably 5 μm or less in D[3,2].

[0325]

[0375] Item 30: The particles have an average circularity (R) of at least 0.7; an angular morphology of less than about 20% of the particles; an oxide of formula 1 as defined in claim 4; an X-ray amorphous solid with a content of 45% to 100%, preferably 90 to 100%; (Ca, Mg) 0~12 (Na,K) 0.05~1 (Al,Fe 3+ )1·Si 1~20 and a calcium content that is less than about 10 wt. % CaO.

[0326]

[0376] Item 31. The method of any one of items 27 to 30, comprising one or more of the following properties: the cementitious reagent is reactive in cementitious and / or geopolymer systems; delivers a low yield stress geopolymer cement mixture that is workable below 25 Pa when the cement paste has an oxide molar ratio of HO / (Na2O, KO)<20; requires a water content in the cement paste such that the oxide molar ratio is HO / (Na2O, KO)<20; and delivers a cement paste that has greater workability than an equivalent paste with a substantially angular morphology given the same water content.

[0327]

[0377] Item 32. The method of any one of items 27 to 31, further comprising adjusting the composition of the non-ideal solid aluminosilicate material to a desired content of the elements Ca, Mg, Na, K, Al, Fe, and Si.

[0328]

[0378] Item 33. The method of item 32, wherein the adjusting step includes blending the non-ideal aluminosilicate material with a composition adjusting material to reach a desired ratio(s) of one or more of the elements Ca, Mg, Na, K, Al, Fe, and Si.

[0329]

[0379] Item 34. The method of any one of items 27 to 33, further comprising the step of screening the solid aluminosilicate material to obtain a powder of aluminosilicate particles of a desired size.

[0330]

[0380] Item 35. The method of any one of items 27 to 34, further comprising the step of discarding undesirable waste material from the solid aluminosilicate material.

[0381] Item 36. The method of any one of Items 27 to 35, wherein the step of melting in air includes a step of heating at a temperature higher than the liquidus temperature to obtain a liquid.

[0331]

[0382] Item 37. The method according to Item 36, wherein the temperature is about 1000 to 1600°C or about 1300 to 1550°C.

[0383] Item 38. The method of any one of items 27 to 37, further comprising adding a flux material to the solid aluminosilicate material to lower its melting point and / or induce greater enthalpy, volume, or depolymerization of the liquid.

[0332]

[0384] Item 39. The method of item 38, wherein a flux material is mixed with the solid aluminosilicate material before or during the melting.

[0385] Item 40. The method of any one of items 27 to 39, wherein the in-air melting / quenching step comprises reducing the temperature of the liquid below the glass transition temperature to achieve a solid.

[0333]

[0386] Item 41. The method of item 40, wherein the step of in-air melting / quenching comprises reducing the temperature of the liquid to below about 500°C, or preferably to about 200°C or less.

[0334]

[0387] Item 42 The step of lowering the temperature of the liquid is 2 K s-1 from about 10 6 K s-1 at a rate of preferably >10 3.5 Ks -1 42. The method of claim 41, comprising quenching at a rate of

[0335]

[0388] Item 43. The method of item 41, wherein the quenching step includes a stream of cold air, steam, or water.

[0389] Item 44. The method of any one of items 27 to 43, further comprising reducing the particle size of the powder of solid microspherical glassy particles.

[0336]

[0390] Item 45. The method of item 44, wherein reducing particle size comprises crushing and / or grinding the powder in one of a ball mill, a roller mill, or a vertical roller mill.

[0337]

[0391] Item 46. The method of any one of items 27 to 45, further comprising separating the quenched solid particles from the hot gas in a cyclone separator.

[0392] Item 47. An apparatus for producing microspherical glass particles, comprising: a burner; a melting chamber; and a quenching chamber.

[0338]

[0393] Item 48. The apparatus of item 47, wherein the melting chamber and the quenching chamber are first and second sections, respectively, of the same chamber.

[0394] Item 49. The apparatus of items 47 or 48, wherein the apparatus is configured so that the solid particles flow as a suspension within the apparatus, melt as a suspension, and are then quenched as a suspension.

[0339]

[0395] Item 50. The apparatus of any one of items 47 to 49, wherein the burner provides sufficient heating temperature to flame-heat solid particles in suspension to substantially melt the solid particles into a liquid.

[0340]

[0396] Item 51. The apparatus of any one of items 47 to 50, wherein the burner includes a gas-fired flame that entrains the aluminosilicate feed material particles toward the melting / quenching chamber.

[0341]

[0397] Item 52. The apparatus of item 51, wherein the gas comprises an oxidizer gas and a combustible fuel.

[0398] Item 53. The apparatus of any one of items 47 to 52, wherein the quenching chamber includes a cooling system for providing cold air within the quenching chamber, the cold air quenching the molten particles into solid microspherical glass particles.

[0342]

[0399] Item 54. The apparatus of item 53, wherein the cooling system includes a liquid cooling loop positioned around the quenching chamber.

[0400] Item 55. The apparatus of any one of items 47 to 54, wherein the apparatus further comprises a cyclone separator that collects the microspherical glassy particles.

[0343]

[0401] Item 56. The apparatus of any one of items 47 to 55, wherein the burner includes at least one of a plasma torch, an oxygen-fuel burner, an air-fuel burner, a biomass burner, and a solar concentrating furnace.

[0344]

[0402] Item 57. A method for producing a cementitious reagent from an aluminosilicate material, comprising: (i) providing a solid aluminosilicate material; (ii) in-air melting / quenching the solid aluminosilicate material to melt the material into a liquid, and then quenching the liquid to obtain a melted / quenched powder comprising solid microspherical glassy particles; thereby obtaining a cementitious reagent comprising a powder of the microspherical glassy particles.

[0345]

[0403] Item 58. A method for producing microspherical glassy particles, comprising the steps of: providing an in-air melting / quenching apparatus comprising a burner, a melting chamber, and a quenching chamber; providing solid particles; flowing the solid particles in suspension through a gas to be combusted by the burner; heating the solid particles in the melting chamber to a heating temperature above the liquid phase to obtain liquid particles in suspension; and quenching the liquid particles in suspension to a cooling temperature below the liquid phase to obtain a powder comprising solid microspherical glassy particles.

[0346]

[0404] Item 59. The method of item 58, wherein the melting chamber and the quenching chamber are first and second sections, respectively, of the same chamber.

[0405] Item 60. The method according to Item 58 or 59, wherein the heating temperature is about 1000 to 1600°C or about 1300 to 1550°C.

[0347]

[0406] Item 61. The method of any one of items 58 to 60, wherein the cooling temperature is lower than 500°C or lower than 200°C.

[0407] Item 62. The method of any one of items 58 to 61, wherein the solid particles comprise an aluminosilicate material.

[0348]

[0408] Item 63. The method of any one of items 58 to 62, wherein the burner includes a flame burning with a gas that entrains solid particles toward the melting chamber.

[0409] Item 64. The method of item 63, wherein the gas comprises an oxidizer gas and a combustible fuel.

[0349]

[0410] Item 65. The method of any one of items 58 to 64, wherein the quenching step includes providing cold air into the quenching chamber.

[0411] Item 66. The method of any one of items 58 to 65, further comprising collecting the powder in a cyclone separator.

[0350]

[0412] Item 67. Use of an apparatus including at least one of a plasma torch, an oxygen-fuel burner, an air-fuel burner, a biomass burner, and a solar concentrating furnace for producing microspherical glass particles.

[0351]

[0413] Item 68. Use of an apparatus including at least one of a plasma torch, an oxygen-fuel burner, an air-fuel burner, a biomass burner, and a solar concentrating furnace for producing a cementitious reagent from an aluminosilicate material.

[0352]

[0414] Item 67. All novel compounds, compositions, processes, apparatus, systems, methods, and uses substantially as hereinbefore described with particular reference to the examples and drawings.

[0415] Headings are included herein for reference and to aid in locating particular sections. These headings are not intended to limit the scope of the concepts described herein, and these concepts may have applicability in other sections throughout the entire specification. Thus, the present invention is not intended to be limited to the embodiments shown herein, but is to be accorded the widest scope consistent with the principles and novel features disclosed herein.

[0353]

[0416] The singular forms "a," "an," and "the" include the corresponding plural referents unless the context clearly dictates otherwise. Thus, reference to "a solid microspheroidal glassy particle" includes one or more of such particles, and reference to "the method" includes reference to equivalent steps and methods known to those skilled in the art that may modify or substitute for the methods described herein.

[0354]

[0417] Unless otherwise indicated, all numbers expressing quantities of ingredients, reaction conditions, concentrations, properties, and the like used in the specification and claims are to be understood as being modified in all instances by the term "about." At the very least, each numerical parameter should be construed in light of the number of reported significant digits and by applying ordinary rounding techniques. Accordingly, unless otherwise indicated, the numerical parameters set forth in the specification and appended claims are approximations that may vary depending upon the properties sought to be obtained. Notwithstanding that the numerical ranges and parameters setting forth the broad scope of the embodiments are approximations, the numerical values ​​set forth in the specific examples are reported as precisely as possible. Any numerical value, however, inherently contains certain errors resulting from variations in experiments, testing measurements, statistical analyses, and the like.

[0355]

[0418] It is understood that the examples and embodiments described herein are for illustrative purposes only and that in light thereof, various modifications or changes will be suggested to those skilled in the art and are to be included within the scope of the present invention and the appended claims. Those skilled in the art will recognize that any process or method disclosed herein can be modified in many ways. The process parameters and sequence of steps described and / or illustrated herein are intended to be illustrative only. For example, although the steps illustrated and / or described herein may be shown or discussed in a particular order, these steps do not necessarily have to be performed in the order shown or discussed.

[0356]

[0419] The various exemplary methods described and / or illustrated herein may also omit one or more of the steps described or illustrated herein or may include additional steps in addition to those disclosed. Furthermore, the steps of any method disclosed herein may be combined with any one or more steps of any other method disclosed herein.

[0357]

[0420] Unless otherwise noted, the terms "connected to" and "coupled to" (and their derivatives) used in this specification and claims should be interpreted as allowing both direct and indirect (i.e., via other elements or components) connections. Additionally, the terms "a" or "an" used in this specification and claims should be interpreted as meaning "at least one of." Finally, for ease of use, the terms "including" and "having" (and their derivatives) used in this specification and claims are intended to be interchangeable with and have the same meaning as the word "comprising."

[0358]

[0421] The processors disclosed herein may be configured with instructions to perform any one or more steps of any of the methods disclosed herein.

[0422] As used herein, the term "or" is used inclusively to refer to items alternatively and in combination.

[0359]

[0423] As used herein, letters, such as numbers, refer to like elements.

[0424] While embodiments of the present disclosure have been described herein as set forth, they are provided by way of example only. Those skilled in the art will recognize numerous adaptations, modifications, variations, and substitutions without departing from the scope of the present disclosure. Several substitutions and combinations of the embodiments disclosed herein may be utilized without departing from the scope of the disclosure and invention(s) disclosed herein. Accordingly, the scope of the presently disclosed invention(s) is / are to be defined solely by the appended claims and their equivalents.

Claims

1. particles containing atoms of Si, Al, Fe, Ca, Mg, Na, and K; [Equation 1] and the particles have a spherical morphology with an average circularity (R) > 0.8; the particles are at least 80% x-ray amorphous; Cementitious reagents.

2. 2. The cementitious reagent of claim 1, wherein the particles are in the form of an amorphous solid.

3. 2. The cementitious reagent of claim 1, wherein the particles are in powder form having a particle size distribution of 20 μm or less in D[3,2].

4. 2. The cementitious reagent of claim 1, wherein the particles are solid microspherical glass particles.

5. 2. The cementitious reagent of claim 1, wherein less than 40% of the particles have an angular morphology with (R)<0.

7.

6. 2. The cementitious reagent of claim 1, wherein the particles comprise an average circularity (R) of at least 0.

9.

7. Average oxide formula 1, (CaO, MgO) ａ ・(Na ２ O, K ２ O) ｂ ・(Al ２ O ３ , Fe ２ O ３ ) ｃ ・(SiO ２ ) ｄ [Formula 1] wherein a is from about 0 to about 4; b is from about 0.1 to about 1; c is 1, d is about 1 to about 20. The cementitious reagent of claim 1, comprising:

8. 8. The cementitious reagent of claim 7, wherein the particles contain less than about 10% by weight CaO.

9. 2. The cementitious reagent of claim 1, wherein the particles have a size distribution in D[3,2] of about 20 μm or less.

10. 2. The cementitious reagent of claim 1, wherein the particles have a size distribution in D[3,2] of about 10 μm or less.

11. 2. The cementitious reagent of claim 1, wherein the particles are 100% amorphous.

12. a cementitious agent comprising non-fly ash microspherical glassy particles containing Si, Al, Fe, Ca, Mg, Na, and K; [Equation 2] and the particles have a spherical morphology with an average circularity (R) > 0.8; the particles are at least 90% x-ray amorphous; Supplementary cementitious materials.

13. 13. The supplemental cementitious material of claim 12, wherein the cementitious reagent comprises at least 20% by weight of the supplemental cementitious material.

14. providing a solid aluminosilicate material; milling the solid aluminosilicate material to have a particle size distribution in D[3,2] of less than 20 μm; melting the aluminosilicate material in a kiln by air melting; and quenching the aluminosilicate material by air quenching to produce solid microspherical glassy particles.

1. A method for producing a cementitious reagent from an aluminosilicate material, comprising:

15. 15. The method of claim 14, wherein said solid microspherical glassy particles have an average circularity (R) of at least 0.

8.

16. The cementitious reagent is (Ca, Mg) ０～１２ (Na, K) ０．０５～１ (Al, Fe ３＋ ) １ ・Si １～２０ The method of claim 14 having a molar composition ratio of

17. 15. The method of claim 14, further comprising controlling the air quenching profile to produce solid microspherical glassy particles that are greater than 80% x-ray amorphous.

18. 15. The method of claim 14, further comprising the step of: composition of the non-ideal solid aluminosilicate material to a desired content of the elements Ca, Na, K, Al, Fe, and Si.

19. The method of claim 14 further comprising locating the kiln in an aggregate quarry.

20. The method of claim 14 further comprising locating the kiln in a concrete batch plant.

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