4869 results about "Reaction product" patented technology

The invention discloses a carbon dioxide mineralization storage dynamic intelligent regulation and control and permeation enhancement optimization method and system. The optimization method comprises the following steps: collecting field monitoring injection parameters and related data of reaction products in a mineralization storage process in real time; according to injection parameters monitored on site and related data of reaction products, two optimization objective functions of mineralization rate and free CO2 volume are formed; constructing a mineralization sequestration multi-objective optimization model, and screening out an optimal injection parameter set value from the Pareto solution set to obtain an optimal condition parameter; optimal injection parameters in the Pareto optimal solution set are input into the constructed field enhancement regulation and control module, and control variables are adjusted in real time according to real-time changes of reservoir response, mineralization reaction process and injection working conditions; and fracturing transformation is conducted on the target storage rock mass, the seepage enhancement effect of the target storage rock mass is quantitatively evaluated, an injection scheme is dynamically updated based on the transformed reservoir parameters, and the mineralization regulation and control system is enhanced.

The invention discloses a deep eutectic solvent / bimetal organic framework co-catalyzed straw polyol as well as a preparation method and application thereof, the straw polyol is prepared by the following method: uniformly mixing straw powder, small molecular alcohol, an acid catalyst and a deep eutectic solvent in a nitrogen atmosphere, and reacting to obtain a reaction product; and adding a bimetal organic framework catalyst into the reaction product, and reacting to obtain the straw polyol. A green, natural and pollution-free eutectic solvent catalytic liquefaction technology is adopted, lignin and hemicellulose can be dissolved, the cross-linking effect between lignin and hemicellulose and cellulose is reduced, the crystalline structure of cellulose can be destroyed, the available surface area is increased, the contact with a liquefying agent is enhanced, the conversion efficiency is improved, and the residue rate is reduced; the bimetallic organic framework catalyst is added in the middle and later periods of the reaction, aldehydes, ketones and acid and ester substances can be reduced and upgraded into alcohols, the hydroxyl value of the liquefied polyol is greatly increased, and the film-forming crosslinking degree is improved.

The invention relates to a crown ether covalent organic framework material as well as a preparation method and application thereof. The preparation method comprises the following steps: dissolving a crown ether monomer and an amino monomer in an o-dichlorobenzene solvent, adding a catalyst acetic acid aqueous solution, and uniformly dispersing to form a reaction solution; the method comprises the following steps: freezing a reaction solution through a liquid nitrogen bath, vacuumizing, filling nitrogen, carrying out a heating reaction, and carrying out post-treatment operations such as washing and drying on a reaction product, so as to obtain the crown ether covalent organic framework material BADT-DB18C6-COF. The crown ether covalent organic framework material is formed by condensation of a crown ether aldehyde monomer and an amino monomer, the crown ether monomer is 4, 4 ', 4' ', 4 '''-(6, 7, 9, 10, 17, 18, 20, 21-octahydrodibenzo [B, K] [1, 4, 7, 10, 13, 16] hexaoxacyclo octadecene-2, 3, 13, 14-tetrayl) tetrabenzaldehyde, and the crown ether monomer is 4, 4 ', 4' ', 4'''-(6, 7, 9, 10, 17, 18, 20, 21-octahydrodibenzo [B, K] [1, 4, 7, 10, 13, 16] hexaoxacyclo octadecene-2, 3, 13, 14-tetrayl) tetrabenzaldehyde. The amino monomer is 4 ', 5'-bis (4-aminophenyl)-[1, 1 ': 2', 1 ''-terphenyl]-4, 4''-diamine. The crown ether covalent organic framework material BADT-DB18C6-COF prepared by the invention is mainly used as an adsorbent, is used for adsorbing and recovering uranium, thorium and americium ions from a solution, shows good adsorption capacity on radionuclides U-238, Th-232 and Am-243, and is particularly suitable for the field of spent fuel post-treatment in the nuclear industry.

The invention discloses a synthesis method of amphiphilic quantum dots and application of the amphiphilic quantum dots in nano oil displacement, and belongs to the field of nano oil displacement. The synthesis method comprises the following steps: heating a mixture containing a carbon source and a nitrogen source in an air atmosphere for reaction, and centrifuging, filtering and drying a reaction product to obtain the amphiphilic quantum dots, the carbon source is selected from at least one of glucose, mannose, citric acid, lignin, chitosan and starch; the nitrogen source is selected from at least one of alkylamine, and the carbon chain length of the alkylamine is C6 to C12. The synthesis method is simple, heating of a high-pressure reaction kettle is not needed, the technological process is simple, and the method is suitable for large-scale industrial production; the series of amphiphilic carbon quantum dots show better solubility and higher absolute fluorescence quantum yield in water and various organic solvents.

The invention relates to the technical field of preparation of iron phosphate materials, in particular to a method for doping iron phosphate with titanium, which comprises the following steps: 1, dissolving a titanium dioxide by-product ferrous sulfate powder in water to prepare a titanium-containing iron source solution; 2, adding water into the reaction kettle, and stirring; 3, adding the titanium-containing iron source solution, the phosphorus source solution, ammonia water and an oxidizing agent into a reaction kettle to prepare primary slurry; 4, carrying out filter pressing on the primary slurry, washing until the conductivity is less than or equal to 2000us / cm, and then adding water to prepare secondary slurry; 5, phosphoric acid is added into the reaction kettle for bottoming, and the temperature is increased to 60-70 DEG C; 6, adding the secondary slurry into the reaction kettle, and carrying out heat preservation reaction on the secondary slurry and phosphoric acid; and 7, filtering the reaction product obtained in the step 6, washing until the conductivity is less than or equal to 500us / cm, and then drying and sintering. According to the method, the titanium doping technological process is simplified, and meanwhile the titanium element utilization rate in the titanium dioxide by-product and the purity of the titanium-doped iron phosphate product are improved.

A photobase generator includes a compound including: first skeletons represented by the following formula (a); and a second skeleton including nitrogen atoms bonding to bonding positions of the first skeletons to form amide groups, wherein, in a molecule, a number of the first skeletons is two or more, a number of the nitrogen atoms, configuring the amide groups, in the second skeleton is the same as the number of the first skeletons, and at least one of the nitrogen atoms configuring the amide groups is converted into a nitrogen atom configuring a secondary amine or a tertiary amine by light irradiation. In the formula (a), G is a divalent aromatic group, and * represents the bonding position with the nitrogen atom.

Disclosed in the present invention is a method for co-producing 3,3,3-trifluoropropene and 2,3,3,3-tetrafluoropropene. The method comprises: introducing 1,1,1,3-tetrachloropropane, 1,1,1,2,3-pentachloropropane, and hydrogen fluoride into a first reactor, and reacting under the action of a first catalyst to obtain a first reactor reaction product; performing rectification on the first reactor reaction product to obtain a 3,3,3-trifluoropropene product and a tower kettle product, mixing the tower kettle product with hydrogen fluoride, and then introducing the mixture into a second reactor, and reacting under the action of a second catalyst to obtain a second reactor reaction product; and separating the second reactor reaction product from hydrogen chloride, water washing, alkaline washing, and drying to obtain a 2,3,3,3-tetrafluoropropene product. The present invention has the advantages of simple process, high efficiency, flexible operation, low investment, and low energy consumption.

The invention provides a platinum-carbon catalyst taking hollow carbon nanospheres as a carrier and a preparation method of the platinum-carbon catalyst. The method comprises the following steps: adding a polymer monomer into a nano template dispersion liquid with a uniform size; then adding a proper amount of platinum salt into the solution to obtain a mixed solution, and stirring to react for 0.5-30 hours to obtain a reaction product; and annealing the reaction product, and then removing the nano template to obtain the platinum-carbon catalyst. The obtained platinum-carbon catalyst takes the hollow carbon nanospheres as a carrier and has a larger specific surface area, the platinum catalyst is loaded on the surfaces of the carbon nanospheres and can be in better contact with an electrolyte, and the obtained catalyst has good electrochemical activity and shows excellent electro-catalytic hydrogen evolution performance and oxygen reduction performance; and the related preparation method is simple and reliable, is suitable for preparation of an electrocatalytic hydrogen evolution electrode and an oxygen reduction electrode, and has a good application prospect in the fields of proton exchange membrane electrolytic cells, hydrogen fuel cells and the like.

The invention discloses a high-temperature-resistant lignite resin and a preparation method thereof, and belongs to the field of drilling fluids, and the preparation method comprises the following steps: obtaining and preparing an extracting solution containing humic acid from lignite; adding hydrochloric acid into the extracting solution, separating, filtering and precipitating, dissolving the precipitating in a sodium hydroxide solution to obtain a humic acid solution, adding formaldehyde and sodium pyrosulfite into the humic acid solution, preheating to 80 DEG C, adding the extracting solution, heating to 110-130 DEG C, continuously stirring, reacting for 1-3 hours, and cooling to 60 DEG C or below to obtain a reaction product; transferring a reaction product to a neutralizing tank, dropwise adding a NaOH solution, adjusting the pH value to 10-11, and controlling the temperature below 55 DEG C; the mass ratio of the dry basis mass of sulfonated humic acid to ECH is 1: (0.05-0.15), the temperature is kept at 45-55 DEG C, the stirring speed is 400-600 rpm, and the reaction is performed for 2-4 hours; meanwhile, a NaOH solution is continuously added, and the pH is kept at 10-11. Adjusting the pH value of the reaction liquid to 7-8 by using dilute HCl, and terminating the reaction; and obtaining a resin product.

The invention discloses preparation of a high-uniformity cerium oxide abrasive material and application of the high-uniformity cerium oxide abrasive material in a chemical mechanical polishing solution. According to a method, cerium nitrate or cerium oxalate is used as a cerium source, a cationic or nonionic surfactant is used as a structure-directing agent, and the high-uniformity cerium oxide abrasive material is prepared in a mixed solvent system formed by water and isopropanol or water and diethylene glycol according to a specific volume ratio. The preparation method comprises the following steps: regulating the particle size and the morphology structure through a solvothermal reaction, carrying out cleaning, drying and high-temperature calcination treatment on a reaction product to obtain sphere-like cerium oxide nano-particles with high particle size concentration ratio, moderate surface roughness and good dispersity, adding cerium oxide powder into deionized water, and carrying out ultrasonic dispersion to obtain the spherical cerium oxide nano-particles. And sequentially adding a dispersing agent and amino acid while stirring, uniformly stirring, fixing the volume, and adding a pH regulator to enable the solution to be weakly acidic, thereby obtaining the chemical mechanical polishing solution. The cerium oxide submicron powder which is different in surface appearance, particle size and distribution uniformity is prepared by adjusting the solvent ratio and other reaction conditions.

The invention discloses a preparation method of a polymeric cyanamide low-toxicity gold leaching agent, and belongs to the field of hydrometallurgy. The preparation method comprises the following steps: uniformly mixing urea, sodium carbonate and ferrous chloride and finely grinding; then putting the fine grinding material into a high-temperature heating container, gradually raising the temperature, and preserving the heat; gradually cooling the reaction product to room temperature along with the furnace; and finally, a reaction product is crushed and ground into powder, and the polymeric cyanamide low-toxicity gold leaching agent is obtained. The synthetic raw materials of the gold leaching agent are simple, cheap and easy to obtain, the synthetic process is simple and easy to regulate and control, and the synthetic cost is low. The gold leaching agent obtained through the method is low in toxicity, the gold leaching speed is high, the gold leaching rate is high, and leaching tailings are common solid waste and are easier to treat.

The invention discloses a method for joint production of cyclohexylamine and dicyclohexylamine, which comprises the following steps: 1) feeding aniline tail gas of a nitrobenzene catalytic hydrogenation production device into a gas-liquid separator for gas-liquid separation to obtain aniline tail hydrogen and aniline condensate; 2) mixing aniline tail hydrogen and new hydrogen as a raw material A, and mixing defective aniline and fresh aniline in proportion as a raw material B; (3) feeding the vaporized raw material B and the vaporized raw material A into a fixed bed reactor according to a certain hydrogen-oil ratio, and carrying out hydrogenation reaction; a hydrogenation reaction product is subjected to heat exchange condensation and then enters a gas-liquid separator for gas-liquid separation, a gas phase serves as recycle hydrogen to be mixed with the raw material A, and a liquid phase is fed into a distillation device; and 4) carrying out primary distillation and rectification purification in sequence to obtain cyclohexylamine and dicyclohexylamine. According to the method, aniline tail gas resources and defective aniline are fully utilized, the three-waste treatment cost is reduced, product benefits can be improved, pollution to the environment can be reduced, and economic benefits and social benefits are remarkable.

The purpose of the present invention is to provide a curing catalyst that is highly stable and has a practical curing speed. The present invention provides a curing catalyst [B] used for curing a polymer [A] that has a reactive hydrolyzable silicon-containing group. The curing catalyst [B] contains the reaction products of a metal alkoxide [B1] and an ammonium hydroxide [B2]. The metal alkoxide [B1] includes one or both of a titanium compound [B1a] that is represented by chemical formula (1), and another metal alkoxide [B1b]. The other metal alkoxide [B1b] is an alkoxide of a metal other than titanium, and the ammonium hydroxide [B2] is represented by chemical formula (2).

The invention discloses a preparation method of a nano HZSM-5 molecular sieve, and belongs to the technical field of nano molecular sieve preparation, the preparation method comprises the following steps: 1, adding a silicon source, an aluminum source and a template agent into a supercritical crystallization reaction kettle, heating, stirring, and carrying out a melting reaction on the raw materials to obtain a seed crystal mixed material; introducing absolute ethyl alcohol into the seed crystal mixed material obtained by the melting reaction, heating, stirring, and carrying out crystallization reaction to obtain a reaction product; and cooling, washing, drying and roasting the obtained reaction product to obtain the nano HZSM-5 molecular sieve. According to the present invention, the melting reaction and the supercritical ethanol crystallization reaction technology are introduced into the preparation of the nanometer HZSM-5 molecular sieve for the first time, and the prepared nanometer HZSM-5 molecular sieve has advantages of small grain size, uniform distribution, large specific surface area and high yield.

A method of preparing an acrylate-functional branched organosilicon compound (“compound”) is provided, and comprises reacting (A) a branched organosilicon compound and (B) an acrylate compound in the presence of (C) a catalyst, wherein component (A) has the general formula X—Si(R1)3, where X comprises a halogen-functional moiety and each R1 is selected from R and —OSi(R4)3, with the proviso that at least one R1 is —OSi(R4)3; each R4 is selected from R, —OSi(R5)3, and —[OSiR2]mOSiR3; each R5 is selected from R, —OSi(R6)3, and —[OSiR2]mOSiR3; each R6 is selected from R and —[OSiR2]mOSiR3; each R is an independently selected hydrocarbyl group; and 0≤m≤100; with the proviso that at least one of R4, R5 and R6 is —[OSiR2]mOSiR3. The compound prepared by the method, a copolymer comprising the reaction product of the compound and a second compound, a method of forming the copolymer, and a composition comprising the copolymer are each also provided.

The invention provides phosphorus-doped hydrothermal synchronously-activated hierarchical pore green biochar, a preparation method thereof and application of the phosphorus-doped hydrothermal synchronously-activated hierarchical pore green biochar in formaldehyde adsorption, and belongs to the technical field of biomass resource high-value utilization and air pollution control. The preparation method comprises the following steps: mixing a biomass raw material with a phosphoric acid catalyst, carrying out hydrothermal carbonization reaction, carrying out solid-liquid separation on a reaction product after the reaction is finished, collecting a solid-phase material, drying, mixing with potassium hydroxide, activating, washing and drying the obtained product, and thus obtaining the phosphorus-doped hydrothermal synchronously-activated hierarchical porous green charcoal. Phosphoric acid is introduced in the hydrothermal stage to serve as a structure-directing agent and a doping source, uniform doping of phosphorus and coordinated regulation and control of a pore structure are achieved, a hierarchical pore channel system is formed in the subsequent activation process, and the physical adsorption and chemical fixation capacity of the biochar to formaldehyde molecules is greatly improved.

The invention discloses a method for preparing 12-mercaptan through solid organic acid catalysis, belongs to the technical field of 12-mercaptan preparation, and aims to solve the problems of low catalyst activity, harsh reaction conditions, serious pollution, high cost and dependence on import in the prior art. N-dodecanol and hydrogen sulfide are used as raw materials and are mixed according to the molar ratio of 1: 1.2-1: 1.3; the method comprises the following steps: gasifying n-dodecanol, mixing with purified hydrogen sulfide, preheating to 210-240 DEG C, introducing into a fixed bed reactor filled with a solid organic acid catalyst, and reacting at-0.08-3.0 MPa for 3.5-4 hours; and cooling and condensing the reaction product, carrying out gas-liquid separation, rectifying and purifying the liquid product to obtain 12-mercaptan with the purity of more than or equal to 99.5%, and recycling unreacted hydrogen sulfide. The solid organic acid can be a catalyst of p-toluenesulfonic acid and the like or mesoporous silica loaded nickel, cobalt and molybdenum metal oxides. The method has the advantages of high catalytic activity, mild reaction conditions, high product yield (the conversion rate of n-dodecanol is greater than or equal to 94.5%), environmental protection and low cost, can realize the domestic mass production of 12-mercaptan, and meets the market demand.

The instant disclosure is drawn to a cosmetic or personal care compositions in the form of oil-in-water dispersions, wherein the dispersion comprises oil droplets having a size from about 10 nm to about 1 μm. The compositions also include: (a) a hydrophobic polymer formed from a reaction product of a natural or food-derived oil and a methacrylate or acrylate polymer; (b) one or more solvents capable of solubilizing the hydrophobic polymer; (c) one or more biosurfactants, and optionally, one or more co-surfactants; and (d) water. Methods for making and using the compositions and methods for boosting foam are also disclosed.

A method for continuously producing m-xylylenediamine belongs to the technical field of organic synthesis and comprises the following steps: (1) mixing isophthalonitrile, toluene and liquid ammonia according to a mass ratio of 1: (3-5): (13-17) in a nitrogen atmosphere to form a reaction mixture; (2) heating the interior of a reaction bed containing a catalyst to 90-95 DEG C, continuously introducing hydrogen into the reaction bed, introducing the reaction mixture after the pressure intensity of the reaction bed is stable, and carrying out a catalytic hydrogenation reaction to generate a reaction product; and (3) carrying out gas-liquid separation on the reaction product, removing liquid ammonia from the liquid-phase product through an ammonia distillation process, and separating toluene and m-xylylenediamine through a rectification process to obtain m-xylylenediamine. According to the method, isophthalonitrile and hydrogen are used as raw materials, liquid ammonia and methylbenzene are used as reaction solvents, the raw materials and the reaction solvents are heated to 90-95 DEG C under the catalytic action of a catalyst for an exothermic reaction, m-xylylenediamine is generated through the reaction, and the reaction yield is larger than 99%.

The present invention discloses a method, device and application for producing aviation kerosene from methanol, and belongs to the field of petrochemical product processing technology. The method comprises: generating a methanol dehydration reaction product from a methanol raw material under the catalytic action of a first molecular sieve catalyst, separating and treating the methanol dehydration reaction product, and then mixing it with one or more of recycled fuel gas, recycled liquefied gas or recycled gasoline under the catalytic action of a second molecular sieve catalyst to generate a reaction oil gas, the reaction oil gas is fractionated to obtain a kerosene fraction, and the kerosene fraction is subjected to a hydrogenation and refining treatment to obtain aviation kerosene. The method for producing aviation kerosene using methanol as a raw material provided by the present invention has opened up a new way to produce aviation kerosene; the process flow is short and compact, and can effectively achieve energy conservation and emission reduction.

A self-stabilized glyoxalated polyacrylamide (gPAM) resin composition is disclosed. The gPAM resin composition consists essentially of an aqueous reaction product of a cationic polyacrylamide (cPAM) prepolymer and glyoxal carried out in an aqueous reaction mixture having a total solids of less than a critical concentration of the gPAM resin and a pH of at least about 7.5. The cPAM prepolymer comprises a weight average molecular weight (Mw) of at least about 5,000 Da and a cationic monomer content of at least about 4, alternatively at least about 10 mol %. The reaction product is prepared without addition of any acid. The gPAM resin composition maintains a substantially single phase for a stability period of at least about 1 day after preparation, without the addition of any acid or other stabilizing compounds. Methods of preparing and using the gPAM resin composition are also disclosed.

Disclosed are compositions comprising a first component, a second component, and thermally conductive filler. The first component comprises an isocyanate functional prepolymer formed as a reaction product of reactants comprising a first polyisocyanate and a polyester polyol or a polyether polyol, the polyol comprising more than two hydroxyl functional groups. The second component comprises a polyol. Also disclosed are methods of coating a substrate and substrates comprising a coating formed on a surface from a composition disclosed herein. Also disclosed are batteries comprising a battery cell and any of the compositions disclosed herein in an at least partially cured state. Also disclosed are uses of the compositions disclosed herein.

The invention belongs to the technical field of organic synthesis of ethers, and particularly relates to a method for continuously synthesizing ethylene glycol dimethyl ether. The method comprises the following steps that ethylene glycol, sodium hydroxide and methane chloride serve as raw materials, multi-stage continuous reaction is carried out in liquid membrane reactors to synthesize ethylene glycol dimethyl ether, ethylene glycol, sodium hydroxide and methane chloride are introduced into the first-stage liquid membrane reactor, sodium hydroxide and methane chloride are introduced into the subsequent stages of liquid membrane reactors, and the first-stage liquid membrane reactor and the second-stage liquid membrane reactor are connected with the second-stage liquid membrane reactor. A byproduct sodium chloride is separated from a reaction product in the previous-stage liquid membrane reactor and then enters the next-stage liquid membrane reactor, a byproduct sodium chloride is separated from a reaction product in the last-stage liquid membrane reactor and then clear liquid is obtained, and ethylene glycol dimethyl ether is obtained through rectification treatment. The invention develops a novel process mode for continuously synthesizing an ethylene glycol dimethyl ether product, and provides a new idea for large-scale continuous production of ethylene glycol dimethyl ether.

The invention belongs to the field of flexible piezoelectric polymer materials, and discloses a polyvinylidene fluoride based ferroelectric polymer and a preparation method thereof. The preparation method comprises the following steps: (1) adding an inorganic alkaline reagent into a polyvinylidene fluoride-trifluoroethylene ferroelectric polymer solution, carrying out dehydrofluorination and nucleophilic addition-elimination reaction to generate a polymer with an enol structure, and then washing, precipitating and purifying a reaction product; and (2) re-dissolving by using an organic solvent, then forming a film by using a tape casting method, and carrying out ketone-enol tautomerization reaction in the film forming process of the tape casting method to finally prepare the polyvinylidene fluoride based ferroelectric polymer film. According to the effective modification and preparation method disclosed by the invention, an enol structure is promoted to be converted into a more stable ketone structure through a ketone-enol tautomerization reaction by utilizing a high-temperature environment in a film forming process, so that C = O double bonds are introduced into a polymer chain, and the piezoelectric property of the polymer is remarkably enhanced.

The invention relates to a supergravity adiponitrile production system and method, the system comprises a supergravity nitrile reactor, a separation tower, a semi-nitrile evaporator and a refining device, the middle part of the supergravity nitrile reactor is communicated with the lower part of the separation tower through a main pipeline, and the top of the supergravity nitrile reactor is communicated with a main ammonia gas pipeline; the top of the separation tower is respectively communicated with an ammonia recovery pipeline and a water recovery pipeline, and the upper part of the separation tower is communicated with the refining device through a pipeline; and the top of the semi-nitrile evaporator is respectively communicated with the bottom of the separation tower, the main pipeline and the main ammonia gas pipeline through pipelines. The reactor has the beneficial effects that the characteristics of structure, technology and the like of the supergravity reactor are utilized, the reverse concentration gradient of ammonia gas and molten adipic acid is formed in the radial direction of the rotor from inside to outside, the gas-liquid contact specific area is increased, the mass transfer driving force is increased, the reaction rate is increased, reaction products are separated out in the reaction process, and the reaction is accelerated and pushed.

The invention discloses a mesoporous solid acid composite catalyst as well as preparation and application thereof, and particularly relates to a preparation method and application of an acid-functionalized COF polymer and Beta molecular sieve composite catalyst. The solid acid composite catalyst is prepared from an acid functionalized COF polymer and a molecular sieve material through mechanical grinding, and the preparation method is simple and convenient. The solid acid composite catalyst has the advantages of high crystallinity, large specific surface area, rich pore structure, good chemical stability and the like. The prepared composite catalyst is stable in performance and high in activity at low temperature, polyoxymethylene dialkyl ether can be selectively synthesized, and the effect that reaction products do not conform to Schulz-Flory distribution is achieved by adjusting the composition of the composite catalyst.

A method of forming a substituted or unsubstituted gamma-lactone includes forming a reaction mixture that includes a substituted or unsubstituted cyano(C4-C10)alkene and / or a hydrolysis reaction product thereof. The reaction mixture also includes an acid, a solid acid catalyst, or a combination thereof. The method includes allowing the reaction mixture to react to form the substituted or unsubstituted gamma-lactone.

The invention relates to the technical field of geotechnical engineering material modification and industrial solid waste resource utilization, in particular to an industrial solid waste curing agent formula screening method for salinized loess improvement, which comprises the following steps: constructing a curing system with different industrial solid waste (such as fly ash, slag and steel slag) composite proportions, identifying the salt type and salt concentration of salinized loess, and determining the salt concentration of the salinized loess. The method comprises the following steps: preparing, maintaining and curing a sample, carrying out unconfined compressive strength test and X-ray diffraction (XRD) analysis, extracting peak areas of main reaction products, and calculating a structure-performance coupling mechanism index Mi = S / f7 (S is the XRD peak area, and f7 is the compressive strength of 7 days). The Mi value and the 28-day strength are used as judgment criteria, and a preferable formula with good structural product master control and strength development is screened out. The screening method provided by the invention has the advantages of distinguishable mechanism, quantifiable index, generalizable process and the like, and is suitable for formula design and engineering application of the industrial solid waste-based curing agent under the conditions of different salt concentrations and ion types.

The invention discloses a fly ash-based geopolymer carbon sequestration adsorption material and a preparation method thereof, and belongs to the technical field of engineering materials. The material disclosed by the invention is modified by adding 13X zeolite with a specific particle size, and the carbon sequestration adsorption performance of the material is remarkably improved through an in-situ hydrothermal conversion process. The fly ash-based geopolymer material and the preparation method disclosed by the invention are simple and easy to implement, are easy to implement in industrial production, and can overcome the defects of low mineralization efficiency and unstable reaction products caused by direct reaction of solid waste with CO2 to generate a mineralized (carbonate) filling material at present. The geopolymer carbon sequestration adsorption material has a wide application prospect, provides a new method for synergistically solving the problems of carbon sequestration, solid waste disposal and waste underground space reutilization, and has important environmental protection, social and economic benefits.

The invention relates to the technical field of lithium ion battery materials, in particular to a preparation method of a manganese iron carbonate precursor and a lithium manganese iron phosphate positive electrode material, which comprises the following steps: preparing a mixed salt solution from a bivalent manganese salt and a bivalent iron salt; adding pure water and the mixed salt solution into a first-stage reaction kettle, preparing a reaction base solution, and adding a first precipitator into the first-stage reaction kettle to obtain a first reaction product; enabling the first reaction product to flow into a second reaction kettle through overflow, and adding a second precipitator to obtain a second reaction product; and enabling the second reaction product to flow into a slurry transfer tank through overflow, washing and drying the second reaction product to obtain a manganese iron carbonate precursor, mixing a lithium source, a phosphorus source, a carbon source and the manganese iron carbonate precursor, and sintering to prepare the carbon-coated lithium iron manganese phosphate positive electrode material. The primary particle size of the prepared manganese iron carbonate precursor can be less than or equal to 200nm, and the rate capability and the cycling stability of a positive electrode material lithium ion battery finally prepared by sintering are improved.