387 results about "Keatite" patented technology

The invention relates to a low-temperature smoke denitration SCR (silicon controlled rectifier) catalyst, which comprises a carrier, a manganese oxide, and composite oxide of one or more of Ce, Zr, Ti, Co, Fe and Cu, the mass content of manganese is 0.1-66 percent, and the total mass content of the Ce, Zr, Ti, Co, Fe or/and Cu is 0-50 percent; and glass fiber and/or kieselguhr is used as the carrier, wherein the glass fiber of the carrier is calcined for 2-4 hours at temperature of 400-600 DEG C, then placed in a nitric acid, sulfuric acid or hydrochloric acid solution with mass concentration of 5-40 percent for acidizing for 1-8 hours, washed by distilled water to be neutered, dried at temperature of 80-120 DEG C, and crushed to have the fineness of 20-325 meshes. The catalyst uses the glass fiber and the kieselguhr as the carriers, so that the dispersion effect of nanoparticles and specific surface area of the catalyst are increased, the high adsorptive capacity and strong heat resistance and corrosion resistance capacity are achieved, stronger toxic resistance capacity to sulfur dioxide and stream contained in the smoke is realized, the invention can be used for 10-200 DEG C of low temperature smoke denitration, and has strong water resisting and sulphur toxic resisting capacities.

The invention provides a method for preparing a porous silicon/carbon composite material by using diatomite as the raw material, which is characterized by comprising the following steps of: with the diatomite as the raw material, performing simple refinement and purification processing to obtain silicon with a porous structure by means of metallothermic reduction; performing mechanical ball-milling with the carbon materials and/or precursors of carbon, hydro-thermal carbonization, pyrolytic carbonization or chemical vapor deposition to prepare the porous silicon/carbon composite material. Thecomposite material can be directly used as the cathode of the lithium ion battery, or can be mixed with other cathode materials to be used as the cathode materials of the lithium ion battery. Compared with a pure silicon material as the cathode material of the lithium ion battery, the porous silicon/carbon composite material has the advantages that the first reversible capacity and the circulation stability of the material are greatly improved. In the method, the inexpensive and accessible natural minerals are used as the raw materials, thus the cost is low and the preparation method is simple.

The invention relates to a composite ceramic filter core and a preparation method thereof, in particular to a low-temperature sintering and high-strength diatomaceous earth composite ceramic filter core containing multi-walled carbon nanotubes and a preparation method thereof. The composite ceramic filter core comprises, by mass, 60-80% of refined diatomaceous earth, 12-20 parts of activated carbon, 4.5-9 parts of dispersing agent, 2-6 parts of sintering additives, 1-3 parts of antibacterial agents and 0.5-2 parts of carbon nanotubes. According to the low-temperature sintering and high-strength diatomaceous earth composite ceramic filter core containing the carbon nanotubes, due to the fact that the multi-walled carbon nanotubes are evenly distributed in the composite ceramic filter core, mechanical performance of the ceramic filter core can be improved, and the multi-walled carbon nanotubes are of mesoporous structures simultaneously and can perform effective adsorption on remove heavy metal ions in water. In addition, the sintering temperature is reduced to be below 950 DEG C by adding micron-sized metal aluminum powder, natural nano micropores of the diatomaceous earth are reserved, the mechanical strength of the ceramic filter core is further improved, and the compression strength is above 0.5GPa.

The invention provides a lithium aluminosilicate flat float glass with a high thermal stability which can be chemically and thermally tempered and is suitable for economical and environmentally friendly production. The lithium aluminosilicate flat float glass which can be chemically and thermally tempered, is refined without using a standard refining agent such as arsenic oxide and/or antimony oxide and has excellent thermal stability is constituted so as to contain 2.5-6.0 wt.% Li2O, 0<4 wt.% in total of Na2O+K2O, 0-4 wt.% B2O3, 15-30 wt.% Al2O3, 55-75 wt.% SiO2and <2 wt.% in total of TiO2+ZrO2(the undesirable crystallization of [beta]-quartz and/or keatite solid solution is prevented) as main components per the weight of the total compositions.

The invention provides a process for synthesizing ZSM-5, characterized in that, diatomaceous soil is used as a silicon source, and total or part of aluminum source to be mixed with other aluminum source, NaOH and water, 0-10 wt.% molecular sieve is added in as seed crystal to prepare slurry of reaction mixture, performing water thermal crystallization in normal condition. The process can reduce gelatification, increase solid content and reduce the cost.

The invention discloses a Ti-Si molecular sieve/diatomite composite catalyst and a preparation method thereof, which is characterized in that: the catalyst is formed by compounding Ti-Si molecular sieve (such as TS-1 and TS-2) and diatomite with particular chemical property which is treated in a particular way, and is modified chemically by transition metal oxide after molding; the preparation method comprises the following steps: (1) after being treated with acid solution and alkaline solution, the diatomite needs heat treatment in high temperature to obtain particular chemical property; (2) the molding Ti-Si molecular sieve/diatomite composite catalyst is modified chemically by transition metal oxide (such as lanthanum and nickel). The composite catalyst can be used as the catalyst of selective oxidation reaction of the organic compound (such as the catalytic hydroxylation reaction of phenol) on fixed bed liquidoid, which uses hydrogen peroxide as the oxidant. The Ti-Si molecular sieve/diatomite composite catalyst has the advantages of high catalytic activity, high stability, long service life and easy separation, recovery and regeneration of the catalyst. When using the catalyst in the hydroxylation reaction of phenol of fixed bed liquidoid, under the reaction conditions of 84 DEG C, atmospheric pressure and 8.46h<-1> space velocity, the conversion rate of phenol is greater than 33%, the selectivity of diphenol reaches 99.9%, and the effective use rate of hydrogen peroxide is greater than 85%.

The invention relates to a magnesium-alloy metal-type casting coating and a preparation method thereof. Magnesia and forsterite are used as refractory aggregates; titania, asbestos powder or talcum powder or diatomite, and the like are added as heat-insulation aggregates; a mixed caking agent with favorable high-temperature caking property and a compound suspending agent are selected; and boric acid is added as a flame retardant. The preparation method comprises the following steps: mixing the magnesia, the forsterite, the titania, and the asbestos powder or talcum powder or diatomite, and preparing A after ball milling; mixing the caking agent and bentonite, and adding water to activate so as to obtain B; mixing the boric acid, sodium carboxymethyl cellulose and polyacrylamide, and addingwater to activate so as to obtain C; and finally, mixing A, B and C, and carrying out ball milling or colloid milling for more than 30 minutes to obtain the magnesium-alloy metal-type casting coating. The coating has the advantages of favorable heat insulation, caking property, coating property, flame retardance, stability and durability, is beneficial to continuous production and convenient forobtaining magnesium-alloy metal-type castings with favorable surface quality and superior performance, and prolongs the service life of moulds.

The invention belongs to the technical field of petrochemical industry, and relates to a NaY molecular sieve/natural mineral composite material having a multistage pore structure and a preparation method thereof. The composite material is a crystal product formed through in-situ crystallization by taking a natural kaolin mineral and a natural kieselguhr mineral as entire silicon sources and aluminum sources for molecular sieve synthesis and using the minerals as substrates for molecular sieve growth. In the composite material, the mass percent of the NaY molecular sieve is 25-50%, and the silicon-aluminum ratio of the NaY molecular sieve is 3-5.5. The invention widens the raw material sources in the preparation of the molecular sieve/natural mineral composite material through an in-situ synthesis method, and can simultaneously greatly lower the production cost of the molecular sieve/natural mineral composite material.

The invention discloses a method for producing bentonite cat litter by calcium-based bentonite. The method comprises the following steps of: grinding, acidification, sodium-modification, forming, drying and the like. In method, the calcium-based bentonite crude ores are used as a starting point, the bentonite slices are acidified and corroded by an acidifier so as to greatly increase a specific surface area of the bentonite, a sodium-modification agent is used for sodium-modification of the acidified calcium-based bentonite so as to improve a water absorption rate and bonding property of the bentonite, other additives such as wood flour and diatomite are added so as to adjust indexes, such as density and whiteness, of the cat litter, and finally the bentonite undergoes granulation, drying, screening and the like to form the bentonite cat litter having the advantages of quick water absorption, large amount of water absorption, high whiteness and high strength. The method has the advantages of good quality of the bentonite cat litter prepared by the method, simple process and low cost.

A process material with compound artery is prepared from the Si source chosen from amorphous SiO2, si sol, silicon oxide solid, silicon gel, diatomite and water glass, the Al source chosen from sodium aluminate, sodium metaaluminate, aluminium sulfate, aluminium nitrate, etc, at least one of lithium hydroxide, sodium hydroxide, potassium hydroxide, rubidium hydroxide and cesium hydroxide, and template agent through proportional mixing, reaction, ageing and crystallizing.

The invention discloses a decorative brick with diatomite as a main component. The decorative brick with the diatomite as the main component comprises the following components: 20-40 percent of refined diatomite, 50-70 percent of gypsum powder, 1-3 percent of plant fiber, 3-8 percent of titanium white powder, 0.5-2 percent of nano titanium dioxide and 1-3 percent of negative ion material. The decorative brick with the diatomite as the main component is made by adding a proper amount of plant pigment and water, uniformly stirring the mixture into paste, pouring the paste into a mould, solidifying and demoulding, putting into a drying box, and drying for 11-13 hours at the temperature of 70-90 DEG C. The diatomite brick has the characteristics that: the diatomite material with an air purifying function does not contain any harmful substance, has the functions of adsorbing and decomposing harmful gas, has a strong air humidity regulating function, and can be made into decorative bricks and mosaic tiles with different shapes; the transportation and the construction are simple; and the decorative bricks can be bonded onto a wall surface on site by using a special bonding agent.

The invention provides an additive which can accelerate ion exchange, purify a molten salt and prolong the service life of the molten salt aiming at the KNO3 molten salt in low-temperature ion exchange. The additive comprises the following components in percentage by weight: 2 to 10 percent of potassium hydroxide, 4 to 12 percent of potassium carbonate and 78 to 94 percent of kieselguhr. The chemical tempering process for glass comprises the following steps of: (1) adding the additive into the KNO3 molten salt in a weight ratio of the additive to the KNO3 molten salt of (1:15)-(1:25), heating to the temperature of between 400 and 440 DEG C, and keeping constant temperature for 24 to 72 hours; (2) heating the glass to the temperature of between 300 and 380 DEG C, and keeping the temperature for 30 to 90 minutes; and (3) putting the glass into the molten salt, and processing for 4 to 24 hours to obtain chemical tempered glass. According to the chemical tempering process, the additive is added into the KNO3 molten salt, so impurities in the molten salt can be adsorbed, the molten salt is purified, the quality of the ion exchange is stabilized, the replacement frequency of the molten salt is reduced, the service life of the molten salt is prolonged, and the production cost is reduced.

The invention discloses a multifunctional filter material for circulating water treatment, which is prepared from 1 to 10 weight percent of nano tourmaline powder, 55 to 80 weight percent of coarse tourmaline powder, 1 to 15 weight percent of kieselguhr, 1 to 15 weight percent of sepiolite powder, 1 to 15 weight percent of scallop powder, 1 to 10 weight percent of sodium bicarbonate and 0.5 to 1 weight percent of silver-carried zeolite powder. A preparation method comprises the following steps of: stirring and mixing raw materials uniformly, injecting the uniformly mixed powder into a turntable machine, and rotating the powder for 15 to 30 minutes with controlled humidity of 15 to 50 percent and rotational speed of 20 to 200 revolutions per minute by using attapulgite of 0.1 to 1 millimeter as a core; and finally sintering the powder for 4 to 8 hours at the temperature of between 400 and 600 DEG C in a muffle furnace to form a ceramic filter material with the diameter of 1 to 10 millimeters. The filter material can effectively remove Ca2+ and Mg2+ from the water and achieve the effects of inhibiting scales, preventing corrosion and removing biological sludge.

A method of producing a range of diatomaceous earth filter aids having selectable permeabilities and less than about 1 percent by weight total crystalline silica. The method includes milling diatomaceous earth ore to a size range of between about 100 micrometers and about 1400 micrometers; calcining the milled diatomaceous earth in a calciner; and milling the calcined diatomaceous earth in an adjustable milling and classification system to produce diatomaceous earth filter aids. Systems to implement such methods and compositions produced by such methods are also described.

The invention provides a method for preparing a mesoporous silica material, which comprises: grinding raw materials, which comprises one or more of rice hull ash from biomass power plants, silicon dioxide(SiO2)-containing smoke dust from metallurgical enterprises, micro silicon powder from metallurgical silicon plants and natural kieselguhr minerals, into fine powder, stirring and mixing the fine powder with 0.5 to 4 mol/L solution of hydrochloric acid, processing for 2 to 4 hours at 40 to 60 DEG C and separating out an intermediate raw material; mixing the intermediate raw material, NaOH, structure director and H2O in a molar ratio of 1:0.2-0.5:0.05-0.2:150-200 and stirring for 8 to 24 hours; performing hydrothermal synthesis or microwave synthesis and regulating the pH value of the synthesis solution to 10 to 12; and drying the synthesis solution, roasting for 2 to 5 hours at 400 to 800 DEG C, and cooling to obtain the mesoporous silica material. In the invention, the provided process flow is short; the operation is simple; the application range is wide; the product performance is high; the environmental load is small; the energy consumption is low; the cost is low; the added value of the product is high; and the problem of the shortage of a mesoporous silica raw material is solved.

A catalyst for lightening heavy arylhydrocarbon and transferring alkyl with high transform rate and low cost is prepared from the beta-zeolite and mordenite symbiotic molecular sieve (10-80 Wt%) and at least one inorganic adhesive chosen from gamma- Al2O3, alpha-AlO(OH), SiO3, silicon aluminum oxide, bentone, kaolinite, diatomite and montmorillonite through ammonium salt exchange to said symbiotic molecular sieve, calcining to become hydrogen-type symbiotic molecular sieve, mixing it with said adhesive, shaping, drying, and calcining.

A high-activity deoxidant for the deep deoxidization of N2, H2, CO, CH4, C2H4, C3H6, etc is composed of active component (the low-valence oxide of Mn and Fe) and the carrier chosen from cement, gypsum, kaolinite, alumina, diatomite, etc. Its preparing process is also disclosed.

A diatomaceous earth product with low crystalline silica content after at least one calcination step of between about 927° C. (1700° F.) and about 1149° C. (2100° F.) is disclosed. The product comprises natural diatomaceous earth and at least one binding agent comprising potassium silicate. Further the product comprises no more than about 4.0 wt % of crystalline silica and has a permeability in the range of about 0.3 darcy to greater than about 20 darcy. A process for making such diatomaceous earth product with a low crystalline silica content is disclosed. Moreover, a diatomaceous earth filter aid comprising such a diatomaceous earth product is disclosed.

The invention relates to a spherical diatomite mesoporous composite, a preparation method of the spherical diatomite mesoporous composite, the spherical diatomite mesoporous composite prepared by the method, a supported catalyst containing the spherical diatomite mesoporous composite, a preparation method of the supported catalyst, the supported catalyst prepared by the method, an application of the supported catalyst in an esterification reaction, and a method for preparing ethyl acetate by using the supported catalyst. The spherical diatomite mesoporous composite contains diatomite and a mesoporous molecular sieve material having a three dimensional cube tunnel structure. The spherical diatomite mesoporous composite can be used as a carrier to prepare the supported catalyst for obviously increasing the conversion rate of the raw materials in the esterification reaction process.

The invention relates to a preparation method of a diatomite-loaded N-doped nanometer TiO2 photocatalysis material, which belongs to the technical fields of mineral materials and photocatalysis. The method comprises the following steps of: adding water and concentrated hydrochloric acid into diatomite mineral powder, stirring, pulping, and adding a TiCl4 aqueous solution and an NH4Cl aqueous solution, adding an ammonia aqueous solution for adjusting the pH value of a reaction liquid, and performing a hydrolytic precipitation loading and liquid phase N doping reaction on NH<4+> serving as a nitrogen source; and filtering a reaction product, washing, drying, and calcining and crystalizing in a nitrogen atmosphere to obtain the diatomite-loaded N-doped nanometer TiO2 photocatalysis material. According to the diatomite-loaded N-doped nanometer TiO2 photocatalysis material prepared with the method disclosed by the invention, the photocatalysis performance of nanometer TiO2 under visible light can be improved remarkably, a continuous degradation function on formaldehyde is realized, and the degradation rate of formaldehyde is over 86 percent within 24 hours under the condition of visible light.

The invention discloses a glazing glass mineral desiccant, the technique highlight of which is that, the glazing glass mineral desiccant comprises warp clay, sodium-hydroxide, calcium oxide, diatom earth, and high-alumina earth, and the product is prepared after milling, granulating, drying, sifting, and packing. It has a good stability, a high wet absorption ratio, and a strong intensity. And it can apply to glazing glass devices and other location needing to keep dry.

The invention relates to a preparation method and application method of a hydrated calcium silicate seed crystal. The materials for preparing the hydrated calcium silicate seed crystal comprise a calcium material, a silicon material, deionized water, a dispersant, anhydrous ethanol and sodium hydroxide. The adopted calcium material is calcium oxide, the adopted silicon material is one of sodium silicate and diatomite, and the adopted dispersant is a poly-carboxylic acid high molecular polymer. The controlled factors comprise the ratio of calcium to silicon, the ratio of water to solid, the dosage of the dispersant, the reaction temperature, the reaction pressure and the reaction time. The product prepared by the method provided by the invention is suitable for a construction engineering adopting mixed material cement as a cementitious system, and has an obvious effect of promoting the development of the early strength of a mixed material cement base material, so that the application scope of the mixed material cement is expanded, the dilemma of solid waste emission is relieved, the cement production cost is reduced, the emissions of wastes during cement production are reduced, and the product is beneficial to low-carbonization and greening development of cement, and has good environmental protection benefits and social and economic benefits.

The invention relates to a calcium silicate material prepared from waste ceramic powder. The material comprises the following raw materials in part by weight: 35 to 70 parts of waste ceramic powder, 0 to 35 parts of other siliceous raw materials, 35 to 55 parts of calcareous raw material, 0 to 15 parts of reinforcing fiber and 0 to 10 parts of Portland cement, wherein the other siliceous raw materials are one or more of quartz powder, diatomite and mica. The calcium silicate material has the following advantages that: the waste ceramic powder is used for gradually replacing the primary siliceous raw material in the raw materials for producing the calcium silicate material; the cost is saved and environmental protection and quality stability are ensured; and the produced calcium silicate material can be used as gas filling blocks, calcium silicate boards or exterior wall bricks or as a porous carrier material.

The invention belongs to the technical field of molecular sieves and preparation methods thereof, and particularly relates to a technique for preparing an Fe-ZSM-5 molecular sieve. According to the method, natural mineral diatomite is used as the raw material to provide all of the silicon source, aluminum source and iron source required by synthesis of Fe-ZSM-5, and conventional hydrothermal crystallization is carried out under the condition of not adding any organic template. The natural mineral diatomite is used as the raw material to provide all the silicon and aluminum sources required by the synthesis of the molecular sieve, the Fe2O3 impurity contained in the diatomite raw material is fully utilized as the iron source, and a conventional hydrothermal process is carried out under the condition of not adding any organic template, thereby preparing the framework-iron-containing ZSM-5 molecular sieve (Fe-ZSM-5 molecular sieve). The method has obvious advantages in the aspects of widening the molecular sieve synthesis raw material range, enhancing the added value of the natural mineral product, lowering the molecular sieve production cost, reducing the environmental pollution and the like.

This invention discloses a method for preparing calcium sulfate whiskers and phosphoric acid. The method comprises: phosphate ore decomposition, slurry filtration and separation, calcium sulfate whisker crystallization, separating, washing and drying. The method adds composite additive A during the during phosphate ore decomposition process, and adds composite additive B during calcium sulfate whisker crystallization process to form calcium sulfate whiskers and phosphoric acid. Composite additive A is composed of humic acid and diatomite at a ratio of 1:(2-10). Composite additive B is composed of sodium dodecyl sulfonate and sulfate or phosphate of magnesium and aluminum at a ratio of (2-5):1. The addition amount of composite additive A is 0.5-5.0% of phosphate ore. The addition amount of composite additive B is 0.1-2.0% of theoretical formation amount of calcium sulfate whiskers. The method has such advantages as adequate utilization of raw materials, low solid waste discharge amount, and low production cost.