1568 results about "Isopropyl" patented technology

The invention belongs to the technical field of biology, and relates to an escherichia coli engineering strain for producing L-isoleucine through a methyl malic acid way as well as a construction method and application of the escherichia coli engineering strain. According to the invention, Escherichia coli BW25113 is used as a chassis strain, and a methyl malic acid synthase high-activity mutant gene cimA3.7, an isopropyl malic acid isomerase gene GsleuCD, a 3-isopropyl malic acid dehydrogenase gene AfleuB and a leucine dehydrogenase gene Lsleudh are over-expressed; a methyl malic acid absorption protein gene is over-expressed, and a branched chain amino acid transport system is modified to improve the exosome of the L-isoleucine; all methyl malic acid pathway related genes are integrated to a genome of a chassis strain, and a plasmid-free L-isoleucine production strain is constructed; the copy number of a key gene on a genome is optimized, and the yield of the engineering strain L-isoleucine is increased by introducing a non-oxidative glycolysis approach. The yield of the L-isoleucine after the engineering strain is fermented for 34 hours in a fermentation tank is 56.6 g / L.

The present disclosure provides a method of treating a fatty liver disease (e.g., non-alcoholic steatohepatitis (NASH)) in a human subject (e.g., an adult human subject) in need of such treatment (e.g., NASH / improving liver fibrosis) with 2-(3,5-dichloro-4-((5-isopropyl-6-oxo-1,6-dihydropyridazin-3-yl)oxy)phenyl)-3,5-dioxo-2,3,4,5-tetrahydro-1,2,4-triazine-6-carbonitrile (resmetirom) or a pharmaceutically acceptable salt thereof. The present disclosure also provides a method of improving liver fibrosis in a human subject (e.g., an adult human subject) in need of such treatment (e.g., NASH / improving liver fibrosis) with 2-(3,5-dichloro-4-((5-isopropyl-6-oxo-1,6-dihydropyridazin-3-yl)oxy)phenyl)-3,5-dioxo-2,3,4,5-tetrahydro-1,2,4-triazine-6-carbonitrile (resmetirom) or a pharmaceutically acceptable salt thereof.

The invention relates to an anion exchange membrane based on isopropyl piperidone and biphenyl and a preparation method of a membrane electrode, the preparation method comprises the following steps: respectively dissolving an aromatic monomer and IPD in a first solvent, and mixing to obtain a mixed solution, the aromatic monomer being BP or TP; dropwise adding an acidic initiator into the mixed solution for reaction at the reaction temperature of-5 DEG C to 0 DEG C to obtain a nitrogen heterocyclic ring polymer intermediate; adding a quaternization reagent into the nitrogen-containing heterocyclic ring polymer intermediate to realize quaternization modification of nitrogen atoms to obtain a quaternization ionomer; and forming a film to obtain the AEM film. The preparation method of the membrane electrode comprises the following steps: respectively forming a cathode catalyst layer and an anode catalyst layer on two opposite sides of an AEM membrane through ultrasonic spraying to obtain the MEA. The AEM membrane and the MEA obtained according to the invention have the characteristics of excellent stability and high water electrolysis performance, can significantly improve the efficiency and durability of AEMWE, and are suitable for the fields of hydrogen production by water electrolysis and the like.

Provided herein is a process comprising heating a composition comprising (P)-compound A or a salt thereof and a solvent to a temperature of 250° C. to 350° C. to form racemized compound A. Also provided is a process for isolating (P)-compound A from a composition comprising (P)-compound A and a tartrate, as described herein. Further provided herein, is a process for isolating a free acid of a tartrate or a hydrate thereof from a composition comprising a tartrate, (P)-compound A, and an organic solvent.

The invention provides a temperature-sensitive nano-material and a preparation method thereof as well as an oil-displacing agent and application thereof, the temperature-sensitive nano-fluid comprises nano-silica and a polymer grafted on the surface of the nano-silica, and the polymer is formed by polymerizing a temperature-sensitive monomer and a vinyl hydrophilic monomer, the temperature-sensitive type monomer comprises isopropyl acrylamide and / or dimethylamino ethyl methacrylate. The temperature-sensitive nano material has excellent dispersity, thermal stability and temperature response characteristics, has good adaptability at the environment temperature of the low-permeability oil reservoir, and can improve the recovery rate of the low-permeability oil reservoir.

The present application relates to a various novel crystalline forms of 2- [3,5-dichloro -4-(5-isopropyl-6-oxo-1,6-dihydropyridazin-3-yloxy) phenyl]-3,5- dioxo- 2,3,4,5-tetrahydro [1,2,4] triazine-6-carbonitrile represented by the following structural formula-1, which is referred to as Resmetirom. The present application also relates to process for the preparation of various novel crystalline polymorphic forms of compound of formula-1.

The invention discloses a preparation method of a cell inflammatory factor adsorbent, which comprises the following steps: mixing styrene, divinyl benzene and hydroxyethyl acrylate, and adding a pore-foaming agent and mesoporous SiO2 nano powder to prepare a porous microsphere carrier; the preparation method comprises the following steps: mixing chitosan and poly (N-isopropylacrylamide) in an acetic acid solution to obtain a temperature-sensitive chitosan hydrogel precursor solution; the preparation method comprises the following steps: activating the surface of a porous microsphere carrier by using 1-ethyl-(3-dimethylaminopropyl) carbodiimide and N-hydroxysuccinimide, mixing the activated porous microsphere carrier and a temperature-sensitive chitosan hydrogel precursor solution to obtain a water phase, and assembling, washing and drying in an oil phase to obtain the cell inflammatory factor adsorbent. Through the design of the core-shell structure and the addition of the mesoporous SiO2 nano powder, the temperature response characteristic and the recyclable characteristic are given to the cell inflammatory factor adsorbent, the adsorption capacity of cell factors is also improved, and a new solution is provided for physical adsorption of the cell inflammatory factors.

The invention discloses a concrete polycarboxylic acid water reducing agent with high slump loss resistance and flocculation resistance and a preparation method of the concrete polycarboxylic acid water reducing agent, and belongs to the technical field of concrete admixtures. The water reducing agent is prepared from the following raw materials in parts by weight: 45 to 55 parts of isopentenyl polyoxyethylene ether, 3 to 8 parts of methacrylic acid phosphate, 8 to 12 parts of hydroxyethyl acrylate, 4 to 7 parts of N-isopropylacrylamide, 10 to 15 parts of auxiliary monomer, 8 to 12 parts of initiator and 0.3 to 0.6 part of chain transfer agent. And the technical problems that the fluidity of the concrete is reduced and the slump retaining effect is poor due to the fact that the temperature of the concrete is increased in the stirring process are solved.

Provided herein is a process for preparing compound A comprising (a) admixing 2-isopropyl-4-methylpyridin-3-amine (Compound B), or a salt thereof, a first base, and a reactive compound comprising phosgene or a phosgene equivalent in an organic solvent to form 3-isocyanato-2-isopropyl-4-methylpyridine (Compound C); (b) admixing Compound C and 2,6-dichloro-5-fluoronicotinamide (Compound D) to form 2,6-dichloro-5-fluoro-N-((2-isopropyl-4-methylpyridin-3-yl)carbamoyl)nicotinamide (Compound E); and (c) admixing Compound E and a second base to form a product mixture comprising Compound A and the second base. Also provided herein is a process for synthesizing AMG 510 comprising using Compound A prepared according to the disclosed processes

The invention relates to the field of medicine synthesis, and particularly discloses a preparation method of abesilib and an intermediate thereof. The invention relates to an abesiril intermediate, which is 4-chloro-5-fluoro-2-(methylsulfonyl) pyrimidine (IV) and 4-fluoro-6-(5-fluoro-2-(methylsulfonyl) pyrimidine-4-yl)-1-isopropyl-2-methyl-1H-benzo [d] imidazole (V). The invention further provides a preparation method of the abesiril intermediate. And carrying out nucleophilic substitution reaction on the abesilib intermediate V and 5-[(4-ethyl piperazine-1-yl) methyl] pyridine-2-amine to prepare the abesilib. According to the preparation method, the raw materials are cheap and easy to obtain, the reaction selectivity of functional groups is high, ectopic impurities generated by a halogen atom competition reaction are effectively avoided, meanwhile, introduction of heavy metal palladium can be reduced, and therefore the cost is reduced. The synthetic route is simple, the atom economy is high, the controllability in production is high, and the method is suitable for industrial production.

The invention discloses a composite thermochromic window with a dual-band dynamic regulation and control function. The composite thermochromic window comprises a first transparent substrate, a tungsten-doped vanadium dioxide film, a second transparent substrate and a hydrogel layer. The tungsten-doped vanadium dioxide film is deposited on the upper surface of the first transparent substrate, and the phase transition temperature is 25-32 DEG C; the hydrogel layer is thermo-sensitive poly (N-isopropylacrylamide) and is encapsulated between the two transparent substrates, and the low critical phase transition temperature is 32 + / -2 DEG C. When the temperature is lower than 25 DEG C, the infrared transmittance of the tungsten-doped vanadium dioxide film is larger than or equal to 75%, and the visible light scattering rate of the hydrogel layer is smaller than or equal to 10%; when the temperature is higher than 32 DEG C, the near-infrared transmittance of the tungsten-doped vanadium dioxide film is reduced to the minimum value, and the visible light scattering rate of the hydrogel layer is increased to 35% or above. Compared with the prior art, the system and the method have the advantages that dual-band dynamic regulation and control of visible light and near-infrared light are achieved, the indoor photo-thermal environment can be automatically regulated according to the environment temperature, and the building energy utilization efficiency is improved.

The present disclosure provides a method of treating a fatty liver disease (e.g., non-alcoholic steatohepatitis (NASH)) in a human subject (e.g., an adult human subject) in need of such treatment (e.g., NASH / improving liver fibrosis) with 2-(3,5-dichloro-4-((5-isopropyl-6-oxo-1,6-dihydropyridazin-3-yl)oxy)phenyl)-3,5-dioxo-2,3,4,5-tetrahydro-1,2,4-triazine-6-carbonitrile (resmetirom) or a pharmaceutically acceptable salt thereof. The present disclosure also provides a method of improving liver fibrosis in a human subject (e.g., an adult human subject) in need of such treatment (e.g., NASH / improving liver fibrosis) with 2-(3,5-dichloro-4-((5-isopropyl-6-oxo-1,6-dihydropyridazin-3-yl)oxy)phenyl)-3,5-dioxo-2,3,4,5-tetrahydro-1,2,4-triazine-6-carbonitrile (resmetirom) or a pharmaceutically acceptable salt thereof.

The invention discloses a hydrogel wound dressing with a synergistic healing promoting function as well as a preparation method and application thereof. The preparation method comprises the following steps: 1, dissolving oxidized methacrylated hyaluronic acid and dopamine in deionized water to obtain a solution A; the preparation method comprises the following steps: dissolving N-isopropylacrylamide, a photoinitiator 2-hydroxy-2-methyl-1-(4-(2-hydroxyethoxy) phenyl)-1-acetone and a cross-linking agent N, N '-methylene bisacrylamide in deionized water to obtain a solution B; 2, mixing the solution A and the solution B to obtain a pre-gel solution; or dissolving polyphenylboronic acid ester nanoparticles or polyphenylboronic acid ester-kaempferol with deionized water to obtain a solution C, and mixing the solution C with the solution A and the solution B to obtain a pre-gel solution; and 3, injecting the pre-gel liquid into a mold, and illuminating to obtain the hydrogel wound dressing loaded with the nanoparticles. The hydrogel disclosed by the invention can be used for effectively solving various problems in a wound healing process and promoting rapid and high-quality healing of a wound.

The present disclosure relates to an improved, efficient, scalable process to prepare intermediate compounds, such as 2-isopropyl-4-methylpyridin-3-amine, useful for the synthesis of compounds, such as Compound 9, for the treatment of KRAS G12C mutated cancers.

The invention relates to the technical field of fertilizer slow release, and discloses a temperature-responsive starch-based gel coated slow-release fertilizer, which comprises the following raw materials: amorphous starch: a starting material is common corn starch; the cross-linking agent is N, N '-methylene bisacrylamide (MBA); n-isopropylacrylamide (NIPAM) is used for endowing the gel with temperature responsiveness; acrylamide (AM): as a comonomer to improve gel performance; the urea is used as a core component of the slow-release fertilizer; the absolute ethyl alcohol is used for wetting the surface of urea and promoting uniform coating of the SNA powder. According to the invention, the gel can automatically adjust the internal microporous structure according to different soil temperatures, so as to accurately control the release rate of nutrients, effectively solve the problem that the traditional slow release fertilizer cannot dynamically adjust the nutrient release according to the environmental change, and meet the differentiated demands of plants for nutrients in different growth stages.

The invention discloses anti-attrition lubricating oil suitable for minimal quantity lubrication and a preparation method thereof, and belongs to the technical field of lubricating oil, molybdenum disulfide is nucleated and grows on the surface of porous cerium oxide nanosphere powder to form a cerium oxide and molybdenum disulfide compound, then modified silicon dioxide and tannic acid are pre-polymerized to form silicon dioxide prepolymer powder, and the silicon dioxide prepolymer powder is subjected to ball milling to obtain the anti-attrition lubricating oil suitable for minimal quantity lubrication. The preparation method comprises the following steps: taking a cerium oxide molybdenum disulfide compound as a core material, taking silicon dioxide prepolymer powder and an N-isopropylacrylamide polymer as a shell to obtain a composite temperature-sensitive microcapsule, and mixing the composite temperature-sensitive microcapsule with other raw materials to prepare the composite temperature-sensitive microcapsule. The outer-layer shell polymer chain of the composite temperature-sensitive microcapsule in the anti-attrition lubricating oil shrinks, the cerium oxide molybdenum disulfide compound inside is released, and controllable release of the inner core material is realized by using the temperature sensitivity of the shell polymer of the composite temperature-sensitive microcapsule and the external temperature change during operation.

The invention discloses a supported ozone catalyst for printing and dyeing wastewater treatment and a treatment process, and relates to the technical field of wastewater treatment, the supported ozone catalyst comprises an environmental response type porous medium, an active center and a biological enzyme modification layer; the environment-responsive porous medium is based on poly (N-isopropylacrylamide) grafted and modified mesoporous alumina, the initial aperture of the mesoporous alumina is 10-15nm, the grafting rate of poly (N-isopropylacrylamide) is 12-20%, and an active center is composed of a transition metal active center and quantum dots modified on the transition metal active center. The biological enzyme modified layer is obtained by carrying out deep biological modification on the surface of the catalyst by using laccase with oxidation-reduction activity. According to the invention, an environment-responsive porous medium is constructed by grafting mesoporous alumina with poly (N-isopropylacrylamide), so that the problems that a traditional fixed-aperture catalyst is low in mass transfer efficiency and poor in adaptability to working conditions, and the pollutant release efficiency is difficult to effectively improve under different temperature and pH conditions are solved.

The invention relates to the technical field of biomedical dressings, in particular to a dressing for a diabetic foot wound surface and a preparation method of the dressing. 0.2 to 0.8 part of reduced graphene oxide; 2 to 5 parts of beta-1, 3-glucan modified by chondroitin sulfate; 0.08 to 0.3 part of silver nitrate; 3 to 7 parts of N-isopropyl acrylamide-co-acrylic acid; 0.15 to 0.4 part of N, N '-methylene bisacrylamide; 2 to 5 parts of sulfhydrylated hyaluronic acid; 0.3 to 0.8 part of D-alpha-vitamin E polyethylene glycol succinate; 2 to 5 parts of amino-functionalized mesoporous silica; 1 to 3 parts of L-arginine-L-glutamate; 0.1 to 0.4 part of genipin; the super-strong mechanical property and the super-strong flexibility are realized, so that the dressing can better adapt to the irregular shape of a wound surface, and continuous protection is provided.

The invention provides an intelligent antibacterial konjac glucomannan composite film and a preparation method thereof. The intelligent antibacterial konjac glucomannan composite film is prepared by carrying out graft copolymerization on oxidized konjac glucomannan OKGM and amino-functionalized poly (N-isopropylacrylamide) PNIPAM-NH2 and then crosslinking with an antibacterial agent, the tail end of a molecular chain of the amino-functionalized poly (N-isopropylacrylamide) is provided with an amino group. The intelligent antibacterial konjac glucomannan composite film disclosed by the invention has temperature responsiveness, can control the release of an antibacterial agent according to environmental changes, ensures that the antibacterial agent is accurately released as required, and effectively prolongs the food preservation time and the food shelf life. The film is good in biocompatibility, has no obvious toxic reaction on human tissues and cells, and provides possibility for application in the field of biomedicine. Besides, the film has degradability, and the OKGM and the chitosan are natural high polymer materials and can be decomposed into harmless substances by microorganisms in the natural environment, so that the film meets the requirements of environmental protection and is beneficial to reducing environmental pollution.

The invention discloses a preparation method and application of a photo-thermal dual-response membrane material, and relates to the field of membrane materials. When the photo-thermal double-response membrane material is prepared, a photo-thermal material firstly reacts with 4-(triethoxysilyl) aniline and then reacts with 2, 4, 6-trihydroxy-1, 3, 5-benzenetricarboxaldehyde and p-phenylenediamine, and a modified photo-thermal material is prepared; the preparation method comprises the following steps: sequentially reacting benzaldehyde with 2-hydroxyacetophenone and 3-N, N-dimethylamino methacryloyl chloride to prepare a photo-initiation monomer; the preparation method comprises the following steps: mixing N-isopropylacrylamide, a photo-initiation monomer, N, N '-methylene bisacrylamide and a modified photo-thermal material, combining with a hydrophobic substrate membrane, preparing a membrane, and finishing the surface by using 2-bromo-1-[3, 5-di (tert-butyl)-4-hydroxyphenyl] ethanone, thereby obtaining the photo-thermal dual-response membrane material. The photo-thermal dual-response membrane material prepared by the invention has the characteristics of pollution resistance, easiness in cleaning, durability, antibacterial property, metal ion recovery and low energy consumption.

Provided herein are processes for preparing Compound A or a salt thereof, comprising admixing Compound B or a salt thereof and crotonaldehyde in the presence of an acid catalyst and a solvent to form Compound A

The invention relates to a nitrogen-containing heterocyclic compound as well as a preparation method and application thereof, belongs to the technical field of heterocyclic compound synthesis, and solves the problems of low reaction efficiency and high energy consumption caused by the fact that an existing method for synthesizing an indole maleimide derivative needs to be carried out step by step. The preparation method comprises the following steps: step 1, adding indoleacetamide and a nucleophilic reagent into a mixed solution, and reacting; 2, performing post-treatment to obtain a nitrogen-containing heterocyclic compound; the mixed solution comprises alkali, an additive and an organic solvent; the alkali comprises one of triethylamine (Et3N), N, N-diisopropylethylamine, pyridine and 1, 8-diazabicyclo [5.4. 0] undec-7-ene, and the alkali comprises one of 1, 8-diazabicyclo [5.4. 0] undec-7-ene.

The invention discloses a triisopropyl silane automatic rectification system and a control method thereof, and particularly relates to the technical field of triisopropyl silane extraction, the system comprises a crude product storage tank, a rectification kettle, a rectification tower, a condensation unit, a reflux ratio regulator, a front fraction receiving tank, a solvent receiving tank, a transition fraction tank, a product receiving tank and a vacuum unit; the method comprises the following steps: (1) feeding; (2) receiving a front fraction; (3) solvent receiving; (4) receiving a transition fraction; and (5) receiving the product. The triisopropyl silane automatic rectification system and the control method thereof provided by the invention have the beneficial effects that one-key start of the system is realized, the on-site operation state does not need to be operated by personnel, the triisopropyl silane rectification frequency operated by personnel is reduced, and the production cost is reduced; the process operation automation is realized, the continuous and stable execution can be realized, and the qualified triisopropyl silane product is produced.

The invention relates to the technical field of crude oil decalcification, in particular to a low-corrosivity crude oil decalcification agent and a preparation method thereof. The low-corrosivity crude oil decalcifying agent is prepared from the following raw materials: acetic acid, citric acid, modified chitosan, ethanol and deionized water, wherein the modified chitosan is prepared by synthesizing N-hydroxyacrylamide, performing sulfonation treatment, and grafting poly (N-isopropylacrylamide) with carboxymethyl chitosan. The preparation method comprises the following steps: adding deionized water and modified chitosan into a blending kettle, heating to 65-75 DEG C, stirring, sequentially adding acetic acid and citric acid, continuously stirring, finally adding ethanol, stirring, and cooling to obtain the decalcifying agent. The decalcifying agent can efficiently remove organic calcium, equipment corrosion is reduced through temperature-sensitive film forming, chelate is stable at high temperature, sewage COD is low, the decalcifying agent adapts to an existing electro-desalting process, and industrial application is easy.

The invention discloses a copper-titanium etching solution and a preparation method thereof, and belongs to the technical field of etching solution preparation. The etching solution is prepared from the following components in percentage by mass: 4.5-7.5% of potassium peroxymonosulfate composite salt, 1.2-2.8% of sodium percarbonate, 1.2-2.8% of benzotriazole-2, 3, 4-triazole-2, 3, 4-triazole-2, 3, 4-triazole-2, 3, 4-triazole-2, 3- The cleaning agent is prepared from the following components in percentage by weight: 1.2%-1.8% of 1, 3-dicarboxylic acid, 0.3%-0.8% of 5-aminotetrazole, 0.15%-0.45% of ethylenediamine tetraacetic acid tetrasodium salt, 0.15%-0.45% of hydroxyethylidene diphosphonic acid, 0.15%-0.45% of cocamidopropyl betaine, 0.3%-0.8% of benzotriazole, 0.15%-0.45% of 2-mercaptobenzothiazole, 0.02%-0.08% of poly-N-isopropylacrylamide, 0.7%-1.8% of potassium perchlorate and the balance of ultrapure water. According to the etching solution, the copper-titanium etching rate can be accurately regulated and controlled, back cutting and titanium residues are effectively inhibited, the stability of the etching solution is improved, and the service life of the etching solution is prolonged.

The invention discloses 5-chloro-5-phenyl-4, 5-dihydroisoxazole-3-carboxylic acid and a derivative thereof (formula I): # imgabs0 #, and in the formula I, R is selected from H, C1-C6 alkyl and C3-C8 cycloalkyl, preferably H, methyl, ethyl, propyl, isopropyl, cyclopropyl, cyclobutyl, cyclopentyl and cyclohexyl. When the compound shown in the formula I is used for synthesizing related active compounds, the synthesis route can be greatly shortened, the yield is increased, and the application prospect is wide.

The invention relates to a 4D printing hydrogel material and a preparation method and application thereof, and belongs to the technical field of hydrogel materials.The preparation method of the 4D printing hydrogel material comprises the steps that S1, N-isopropylacrylamide is subjected to a prepolymerization reaction under the action of a photoinitiator, and a prepolymer is obtained; s2, the prepolymer, [2-(methylacryloyloxy) ethyl] dimethyl-(3-sulfopropyl) ammonium hydroxide and a cross-linking agent are mixed, and printing slurry is obtained; s3, carrying out 3D photocuring printing by adopting the printing slurry to obtain a hydrogel matrix with a porous structure; and S4, soaking the hydrogel matrix in a lithium salt solution to obtain the 4D printing hydrogel material. The 4D printing hydrogel material provided by the invention can generate a volume swelling phenomenon in a moisture absorption process, has rapid moisture absorption dynamics and ultrahigh moisture absorption capacity, and has excellent moisture storage and water collection capacities.

The invention relates to the technical field of organic synthesis, in particular to 1-chloro-8-fluorine-7-isopropyl benzofuro [2, 3-c] pyridine as well as a synthesis method and an application of the 1-chloro-8-fluorine-7-isopropyl benzofuro [2, 3-c] pyridine. According to the invention, 1-chloro-8-fluoro-7-isopropyl benzofuro [2, 3-c] pyridine and nanogold are cooperated to cover the surface of a glassy carbon electrode (GCE), and a novel electrochemical modified electrode AuNPs / 1 / GCE is developed. The modified glassy carbon electrode shows good selectivity, high stability and sensitivity and wide detection range on the detection of the antibiotic furacilin.

The invention belongs to the technical field of thermoelectric materials and functional polymer materials, and particularly relates to thermoelectric hydrogel based on synergistic enhancement of zwitterions and a polar solvent as well as a method and application of the thermoelectric hydrogel. The thermoelectric hydrogel is obtained through the steps that a precursor solution is subjected to a polymerization reaction to form a gel matrix, then the gel matrix is soaked in a soaking solution, potassium ferricyanide / potassium ferrocyanide redox couple is introduced, and the thermoelectric hydrogel is obtained, and the precursor solution is prepared from acrylamide, N-isopropylacrylamide, dimethyl sulfoxide, N, N-dimethylformamide, N, N-dimethylformamide, N, N-dimethylformamide, N, N-dimethylformamide, N, N-dimethylformamide and N, N-dimethylformamide. The photoinitiator is prepared by mixing N, N-dimethylformamide, 1-ethyl-3-methylimidazolium tetrafluoroborate, a zwitterionic monomer [2-(methylacryloyloxy) ethyl] dimethyl-(3-sulfopropyl) ammonium hydroxide, a cross-linking agent N, N '-methylene bisacrylamide, a photoinitiator and deionized water. The thermoelectric hydrogel prepared by the invention has high mechanical strength, high ductility and high Seebeck coefficient, and has better temperature resistance.

This invention discloses a gypsum-based lightweight flame-retardant board and its preparation method, relating to the field of building materials technology. The gypsum-based lightweight flame-retardant board prepared by this invention is made by foaming a gypsum substrate with a foaming agent and a composite stabilizer, then introducing a self-made flame retardant and other raw materials, casting it between two layers of facing paper, and drying it. The composite stabilizer includes a modified acrylamide copolymer and acrylamide hydrogel. The modified acrylamide copolymer is obtained by copolymerizing N-isopropylacrylamide with silane acrylic acid and then reacting it with hyperbranched polyphosphate. The acrylamide hydrogel is obtained by polymerizing acrylic acid and acrylamide through an aqueous solution. The self-made flame retardant is obtained by reacting ammonium polyphosphate with a hydroxy heterocyclic amino alcohol. The hydroxy heterocyclic amino alcohol is obtained by reacting a heterocyclic amino alcohol with a double-terminated hydroxyl polyphenylene ether. This process gives the gypsum-based lightweight flame-retardant board excellent flame retardancy, mechanical properties, and flame-retardant stability.