2615 results about "Ethylic acid" patented technology

The invention provides a preparation method of medicinal liquor and application of the medicinal liquor in preparation of analgesic and anti-inflammatory products, and relates to the technical field of medicines. The preparation method comprises the following steps: (1) crushing; (2) extracting; (3) standing and separating; and (4) freezing and filtering to obtain the medicinal liquor. In the preparation process, traditional Chinese medicine components are extracted through the steps of batch crushing, mixed extraction, standing, freezing and separation of supernate and suspension in different separation modes to obtain the medicinal liquor, and the medicinal liquor can better inhibit pain caused by thermal stimulation and chemical substances and has a better analgesic effect; the traditional Chinese medicine composition can inhibit capillary permeability increase caused by acetic acid, has a better effect of inhibiting inflammation exudation, and has remarkable analgesic and anti-inflammatory effects.

The invention discloses a method for preparing nano barium titanate based on sol-gel synergistic hydrothermal reaction, which comprises the following steps: (1) dissolving barium acetate in an acetic acid aqueous solution to obtain a barium source solution; weighing tetrabutyl titanate according to the molar ratio of barium to titanium being greater than 1.25, and dissolving the tetrabutyl titanate in alcohol to obtain a titanium source solution; (2) uniformly mixing the barium source solution and the titanium source solution, preserving heat at 20-80 DEG C to obtain gel, drying and grinding to obtain white powder of the barium titanate precursor: (3) preparing a 2-4mol / L inorganic strong alkali aqueous solution, adding the white powder and a dispersing agent into the inorganic strong alkali aqueous solution, and fully stirring to obtain a barium titanate precursor suspension; and (4) transferring the barium titanate precursor suspension into a reaction kettle for hydrothermal reaction, and after the reaction is completed, washing, drying and grinding to obtain the nano barium titanate powder. The preparation method is low in cost, and the prepared nano barium titanate powder is uniform in distribution, spherical or sphere-like in morphology, small in particle size, 80-150nm in average particle size and good in particle crystallinity.

The invention relates to a starch-based soft capsule shell and a preparation method thereof. The starch-based soft capsule shell is prepared from the following raw materials in parts by mass: 60 to 70 parts of hydroxypropyl starch, 9 to 20 parts of carrageenan, 5 to 15 parts of diquat, 5 to 15 parts of polylysine, 5 to 10 parts of hydroxypropyl methyl cellulose acetate succinate, 15 to 20 parts of glycerol and 30 to 40 parts of pure water. According to the soft capsule shell, hydroxypropyl starch serves as a base material, gelatin is not added, the conditions of poor weather resistance and fishy smell caused by use of gelatin are avoided, through the synergistic effect of all the components, the defects that a starch-based material is poor in plasticity, fragile and insufficient in mechanical strength are overcome, the structural stability is enhanced through chemical crosslinking, and the mechanical strength is improved; and the mechanical property is improved by virtue of physical compounding, so that the low-temperature resistance, high-temperature resistance and mechanical strength of the capsule skin are improved.

The invention is applicable to the technical field of intelligent response materials, and provides a three-dimensional azobenzene functionalized covalent organic framework intelligent response material and a preparation method thereof. The three-dimensional azobenzene functionalized covalent organic framework intelligent response material is prepared by uniformly grinding 3, 3 ', 5'-tetra [(3 ', 5'-diformylphenyl)]-hexamethyl biphenyl and azobenzene-4, 4 '-diaminotriphenylamine, adding an organic solvent, adding a catalyst acetic acid aqueous solution, quickly freezing, emptying air, sealing with flame, heating after recovering to room temperature, and obtaining the three-dimensional azobenzene functionalized covalent organic framework intelligent response material. According to the invention, the azobenzene functionalized covalent organic framework material with a bcu topological structure is synthesized; the material has excellent photostimulation response CO2 adsorption performance; reversible control of CO2 adsorption capacity can be realized through ultraviolet light and heating conditions, at least five times of circulation can be maintained, and good circulation stability is achieved.

The invention relates to the technical field of purification of organic chemicals, in particular to an aroma purification method of leaf alcohol. Comprising the following steps: preparing a methanesulfonic acid magnetic catalyst; esterification of leaf alcohol; and alcoholysis and fractionation of the esterification solution. According to the method, acetic acid is used for esterification of leaf alcohol, then clear water and a sodium carbonate solution are used for washing, the clear water can effectively remove some water-soluble impurities and acidic byproducts, and the sodium carbonate solution not only can neutralize residual acidic substances, but also can promote siloxane impurities in initial leaf alcohol to be hydrolyzed and then taken away by a water phase, so that the content of the siloxane impurities in the leaf alcohol is reduced; in the subsequent process of producing leaf alcohol through alcoholysis of the organic phase I, pure water and ethanol, silyl ether impurities are hydrolyzed in a high-temperature and strong-alkali environment, products are dissolved in waste liquid to be removed, olefine aldehyde impurities with the boiling point lower than that of leaf alcohol are removed through azeotropic fractionation with ethanol, in conclusion, the impurities in the finished product leaf alcohol can be effectively reduced, and the yield of the finished product leaf alcohol is increased. And the prepared finished product leaf alcohol is high in purity and pure in fragrance.

The invention belongs to the technical field of pharmaceutic adjuvants, and particularly relates to a plant polysaccharide extract as well as a preparation method and application thereof. According to the method, pretreatment is carried out through the composite acid liquor composed of acetic acid and oxalic acid, meanwhile, efficient extraction is carried out through the deep-eutectic solvent, and impurity removal treatment is carried out in cooperation with modified activated carbon, so that the plant polysaccharide extract is efficiently obtained, and the extraction rate and purity of the extract are improved.

The invention discloses a preparation method of a bionic cornea stroma lens for refractive correction, which comprises the following steps: solution preparation: dissolving type I collagen in an acetic acid solution, adding a film aid, fully stirring, and centrifugally defoaming to obtain a type I collagen composite solution; the I-type collagen composite solution is poured into an assembling groove, the curvature radius of titanium metal is set to be 6.8-8.0 mm, the titanium metal serves as a working electrode material, platinum metal serves as a counter electrode material, current parameters are set according to the needed thickness of the lens blank, the density is 3.50-6.50 mA / cm < 2 >, and the thickness of the lens blank is set to be 3.50-6.50 mA / cm < 2 >; a high-transparency cornea embryo material which is uniform in curvature in all directions and similar to human cornea fiber structure arrangement is formed after electrochemical assembly and cross-linking curing, accurate cutting machining is carried out through excimer laser, a concave / convex matrix lens with the needed correction degree is obtained, the correction precision is high after cornea interlayer implantation, and the correction precision is high. And meanwhile, the compound has excellent performance in the aspects of in-vivo stability and biological safety.

The invention provides weather-resistant anti-freezing road concrete and a preparation method thereof, and belongs to the technical field of concrete. The concrete comprises the following components: sulphoaluminate cement, Portland cement, silica fume, fly ash, modified granite gravel coarse aggregate, medium sand fine aggregate, silica fume blended fiber, silica fume blended polyacrylonitrile fiber, a composite air entraining agent, a functional modifier, a composite antifreeze agent, pre-absorbent zeolite powder and the like. The preparation method comprises the following steps: modifying granite macadam with Al (H2PO4) 3, SiO2 and methoxypolyethylene glycol triethoxysilane, and modifying with a lithium silicate aqueous solution to obtain the modified granite macadam coarse aggregate. The composite air entraining agent comprises a JRY-Q air entraining agent and sodium alpha-olefin sulfonate. The functional modifier is prepared from gas phase method spherical nano silicon dioxide and nano alpha-Al2O3. The composite antifreeze agent comprises ethylene glycol butyl ether acetate and modified calcium carbonate. The modified calcium carbonate is obtained by sequentially modifying nano calcium carbonate with calcium chloride, a KH-550 silane coupling agent and stearic acid.

The invention provides a modified chitosan flocculant for slime water treatment. The modified chitosan flocculant is prepared from the following raw materials: chitosan, dimethyl diallyl ammonium chloride, acrylamide, acetic acid and potassium persulfate. The invention also provides a preparation method of the modified chitosan flocculant for slime water treatment. The preparation method comprises the following steps: dissolving chitosan in a dilute acetic acid solution with the mass concentration of 60%, and stirring; adding acrylamide and dimethyl propyl chloride cyclic amine into the mixed solution, uniformly stirring, adding a potassium persulfate solution with the mass concentration of 4%, and introducing nitrogen for 20 minutes; then carrying out microwave reaction, and cooling to room temperature after the reaction is completed; adding absolute ethyl alcohol, centrifuging for 10 minutes, taking out, and continuously soaking in absolute ethyl alcohol for 12 hours, so as to obtain a final insoluble substance which is a graft polymer CS-g-ADM; and drying the polymer in a drying box at 105 DEG C until no weight loss occurs, and then grinding and storing. The flocculating agent disclosed by the invention has relatively good flocculability.

The invention provides a preparation method and application of an adsorption material, and belongs to the field of adsorption. The preparation method provided by the invention comprises the following steps: (1) preparing a coconut shell biomass material from a coconut shell waste raw material; (2) calcining and grinding the biomass material obtained in the step (1) to obtain coconut shell derived charcoal; (3) adding the coconut shell derived biochar obtained in the step (2) into a citric acid solution, fully mixing, adding into hydrosol generated by acetic acid and chitosan, and dropwise adding the fully mixed hydrosol into a NaOH solution to form microspheres; and (4) hardening the microspheres obtained in the step (3), fully immersing the microspheres in a mixed solution of methanol and pentanediol, washing, and drying to obtain the chitosan-coated citric acid modified coconut shell charcoal spherical adsorbent. The adsorbent provided by the invention is low in cost, high in silver ion adsorption efficiency and good in adsorption effect.

The invention discloses a 3-ketosteroid-delta1-dehydrogenase mutant and application thereof in synthesis of prednisone acetate, the mutant with high catalytic activity on cortisone acetate is obtained through screening, and a methanol-water phase (Tris-HCl buffer solution) system is adopted to increase the solubility of a substrate so as to improve the biological catalytic efficiency. In a single water phase system (Tris-HCl buffer solution) without methanol, the conversion efficiency is only 64.8% for 60g / L of cortisone acetate, and under the condition that other conditions are the same, the conversion rate in the Tris-HCl buffer solution system with methanol is increased to 92.1%, and the conversion rate is increased by 1.42 times.

The invention discloses a silane modified polyether flame-retardant adhesive and a preparation process thereof, and relates to the technical field of sealants, a phosphate plasticizer is selected as a plasticizer, a flame-retardant filler is selected from any one or two of aluminum hydroxide and magnesium hydroxide, and silane modified polyether resin is added as flame-retardant resin. All the components are compounded and mixed to obtain the modified flame-retardant adhesive, and the flame-retardant resin, the flame-retardant filler and the plasticizer have a good synergistic flame-retardant effect, so that the flame-retardant adhesive achieves a good flame-retardant effect. According to the invention, mercaptoacetic acid modified silicon resin microspheres are prepared, then the mercaptoacetic acid modified silicon resin microspheres react with lead acetate and zinc acetate by utilizing the adsorbability of sulfydryl to prepare modified silicon resin, and the silicon resin is an anti-dripping flame retardant and can form a stable and compact carbon layer structure after combustion; lead acetate and zinc acetate are beneficial to dehydrogenation and charring in the combustion process, so that the flame retardant property is further improved.

The invention relates to the technical field of gas detection, in particular to response type aerogel and application thereof. The response type aerogel is prepared according to the following steps: mixing and dissolving a metal organic framework material and lead acetate to obtain an adsorption and response integrated probe; mixing silk fibroin, polyethylene glycol diacrylate and the adsorption-response integrated probe, and performing light curing reaction under the action of a photo-crosslinking agent to obtain the adsorption-response integrated probe. Wherein a double-grid aerogel substrate generated by reaction of silk fibroin and polyethylene glycol diacrylate can adsorb water molecules in environments with different humidity to wet the substrate, and a saturated microscopic water environment is provided for colorimetric reaction on the surface of a pore wall, so that interference of environmental humidity on response is effectively relieved. The quantitative method established by using the response type aerogel can be used for high-sensitivity quantitative detection of hydrogen sulfide in livestock and poultry farms.

The invention discloses a photocatalytic material with a baseball-shaped structure as well as a preparation method and application of the photocatalytic material, and belongs to the technical field of photocatalytic synthesis of ammonia. The invention discloses a photocatalytic material with a baseball-shaped structure. The photocatalytic material comprises FeMOF with a rod-shaped structure and MnMOF with a spherical structure, the photocatalytic material with the baseball-shaped structure takes FeMOF with a rod-shaped structure as a substrate, and MnMOF with a spherical structure grows on the FeMOF with the rod-shaped structure; and the MnMOF with the spherical structure contains acetate ions. The preparation method comprises the following steps: dissolving an iron source and a manganese source in a solvent, adding an organic ligand, carrying out ultrasonic treatment, and carrying out a hydrothermal reaction; the manganese source is manganese acetate tetrahydrate. According to the photocatalytic material with the baseball-shaped structure, MnMOF with the spherical structure uniformly grows on FeMOF with the rod-shaped structure to form an electron and hole conversion channel, so that the electron and hole transmission rate is enhanced, the photocatalytic performance of the bimetal organic framework structure is enhanced, and the yield of photocatalytic synthesis ammonia is remarkably improved.

The invention discloses a preparation method of antibacterial and hemostatic medical sponge, and relates to the technical field of preparation of medical sponge. The preparation method of the antibacterial hemostatic medical sponge comprises the following steps: cleaning silkworm cocoons after removing impurities, and immersing the cleaned silkworm cocoons in a neutral protease solution to complete degumming so as to obtain fibroin fibers; the preparation method comprises the following steps: dissolving chitosan in an acetic acid solution, dissolving polyvinyl alcohol in deionized water, adding sodium alginate, adding a silk fibroin solution to form a composite solution, dropwise adding an AgNO3 solution, introducing CO2, maintaining the pressure, quickly releasing the pressure, foaming, injecting into a mold, carrying out gradient freezing to form a multistage-aperture sponge matrix, immersing in a genipin ethanol solution, and transferring into a 5% CaC 12 solution for soaking. The silk fibroin provides a biocompatible substrate and promotes cell adhesion, the sponge is constructed into a hierarchical pore structure with a compact surface and a loose interior, and liquid absorption and blood coagulation factor enrichment are accelerated.

The invention relates to a degradable composition and flame-retardant degradable plastic. The degradable composition comprises PLA particles, modified lignin and a bio-based flame retardant, wherein the modified lignin is obtained by grafting polycaprolactone on lignin and then forming a core-shell structure on the surface of silane coupling modified calcium carbonate; the preparation method of the bio-based flame retardant comprises the following steps: heating and dissolving chitosan in an acetic acid solution, introducing nitrogen, adding an initiator, then adding a DOPO derivative with double bonds at the tail end, MDO and AA, and carrying out a polymerization reaction to prepare the flame retardant. According to the scheme, the lignin-PCL / calcium carbonate core-shell toughening agent and the P-N synergistic chitosan flame retardant are prepared and are jointly added into the PLA, the compatibility with the PLA is good, the problem of high brittleness of the PLA can be effectively solved, the elongation at break is improved, meanwhile, the material is endowed with flame retardance, and the biodegradability of the PLA material can be well kept.

The invention discloses a process for treating nickel wastewater containing nickel acetate cleaning water and nickel acetate concentrated water, which comprises the following steps: S1, filtering nickel wastewater, S2, carrying out primary concentration treatment, S3, carrying out secondary concentration treatment, S4, treating by a sodium metaaluminate method, S5, carrying out collaborative filtration treatment, and S6, discharging RO (Reverse Osmosis) produced water up to the standard. The method comprises the following steps: primarily enriching nickel ions by adopting primary nickel concentration treatment and secondary nickel concentration treatment, adding a sodium metaaluminate solution into a mixed solution, enabling the pH value of the mixed solution to be 8-12, enabling the nickel ions to react with hydroxyl ions to generate a nickel hydroxide precipitate, adding a sulfuric acid solution to adjust the pH value of the mixed solution back to 6.5-7.5, hydrolyzing sodium metaaluminate to generate an aluminum hydroxide precipitate, and carrying out secondary nickel concentration treatment on the aluminum hydroxide precipitate; aluminum hydroxide adsorbs nickel hydroxide to form a composite precipitate, aluminum ions and nickel ions are subjected to a competitive complexation reaction, and a flocculating agent is added into a mixed solution to form a flocculent precipitate, so that the reaction time is short, the nickel content in the nickel sludge can be greatly increased, the treatment period can be shortened, and the operation cost can be reduced.

The invention relates to the technical field of electro-catalysis, in particular to a modified iron monatomic catalyst based on biomass carbon as well as a preparation method and application of the modified iron monatomic catalyst. The preparation method comprises the following steps: mixing and stirring chitosan, an acetic acid solution, thiourea and ferric chloride, adjusting the pH value to 7.5-8.5, and freeze-drying to obtain an aerogel precursor; pre-carbonizing the aerogel precursor to obtain a pre-carbonized product; mixing the pre-carbonized product with an alkali reagent, and calcining to obtain a metal nanoparticle doped monatomic catalyst; and carrying out ultrasonic treatment on the metal nanoparticle doped monatomic catalyst by using a mixed acid solution, washing to be neutral, and drying to obtain the modified iron monatomic catalyst. By adopting the modified iron monatomic catalyst provided by the invention, non-polar CO2 molecules and NO3 <-> are efficiently converted into urea under mild conditions, the yield of the urea is up to 2978.6 mu g h <-1 > mgcat <-1 >, and the maximum Faraday efficiency is up to 30.4%.

The invention provides a method for rapidly determining the content of 4, 4-dichlorodihydroxydiphenyl ether in a laundry detergent, and belongs to the technical field of detergent component content detection. According to the method, the content of 4, 4-dichlorodihydroxydiphenyl ether in the laundry detergent is measured by adopting a high performance liquid chromatography. In the determination process, an acetonitrile-water-sodium chloride three-phase mixture is used for removing impurities, and a mixed solution of acetonitrile and toluene is used as an extracting agent for solid-phase elution; a flowing phase A is an acetic acid aqueous solution with the pH value of 3.5-4, and a flowing phase B is acetonitrile. According to the method, the high performance liquid chromatography is combined with the solid phase extraction technology, high-sensitivity and high-accuracy determination can be achieved, a standard curve is established, and the reliability and accuracy of a result are further guaranteed. The method disclosed by the invention is simple to operate, good in stability and repeatability, and capable of accurately and rapidly measuring the content of 4, 4-dichlorodihydroxydiphenyl ether.

The invention discloses a high-performance polyurethane paint and a preparation method thereof, and particularly relates to the technical field of coatings. The high-performance polyurethane paint is prepared from the following components in parts by weight: 45 to 60 parts of functional polyurethane prepolymer, 4 to 7 parts of modified kaolin, 1 to 3 parts of propylene glycol methyl ether acetate, 0.1 to 0.5 part of defoaming agent, 0.2 to 0.6 part of flatting agent, 10 to 15 parts of titanium dioxide and 0.5 to 1 part of dispersing agent, the preparation method of the functional polyurethane prepolymer comprises the following steps: mixing polytetrahydrofuran glycol, diisocyanate and dibutyltin dilaurate to carry out a first reaction, and then adding a functional diol monomer to carry out a second reaction, thereby obtaining the functional polyurethane prepolymer. The coating is mildew-proof and antibacterial, and has good waterproof self-cleaning performance, mechanical property and storage stability.

The invention provides a method for alcoholysis of polyethylene glycol terephthalate, and relates to the technical field of PET degradation. The PET alcoholysis method provided by the invention comprises the following steps: mixing PET, ethylene glycol, a cosolvent and a composite catalyst, and carrying out alcoholysis reaction to obtain bis (hydroxyethyl) terephthalate (BHET). According to the invention, dimethyl sulfoxide is taken as a cosolvent, zinc acetate and 1, 8-diazabicyclo [5.4. 0] undec-7-ene are taken as a composite catalyst, catalysis and solvent effect driving are combined, and ethylene glycol alcoholysis of PET is carried out under the synergistic effect of the composite catalyst and the cosolvent. According to the method, effective decomposition of PET can be achieved at the low temperature (140-155 DEG C) and within the short reaction time (60-100 min), and the yield of BHET is high (66% or above and can reach 80% or above). The method provided by the invention can realize high-efficiency alcoholysis of PET with ethylene glycol.

The invention discloses a protective coating for an aluminum alloy heat exchange tube and a preparation method of the protective coating, and relates to the technical field of coating materials. The protective coating for the aluminum alloy heat exchange tube at least comprises the following raw materials in parts by mass: 100 parts of bisphenol A epoxy resin; 28 to 32 parts of polyether amine D230; 8 to 12 parts of a modified MgAlCe-BTC-LDH filling material; 4 to 6 parts of polydopamine modified hexagonal boron nitride; 35 to 45 parts of propylene glycol methyl ether acetate; and 1-2 parts of a dispersant. The modified MgAlCe-BTC-LDH filler prepared by the invention realizes triple functions of Ce element oxidation resistance, BTC corrosion inhibition and layered barrier, and the polydopamine modified hexagonal boron nitride prepared by the invention effectively improves the heat-conducting property, solves the contradiction between insulation and heat conduction, and adapts to the protection requirement of an aluminum alloy heat exchange tube.

This invention belongs to the field of coating technology, specifically relating to a moisture-proof and stain-resistant acrylic resin coating and its preparation process. The moisture-proof and stain-resistant acrylic resin coating comprises 100 parts by weight of a main agent and 20-25 parts by weight of a curing agent. The main agent comprises the following raw materials in weight percentages: dispersant 1.5-3%, butyl acetate 10-15%, xylene 5-10%, filler 10-20%, titanium dioxide 10-20%, carbon black 1-5%, cellulose acetate butyrate 1-2%, anti-settling agent 1-1.5%, leveling agent 0.5-1%, defoamer 0.1-0.5%, with the balance being acrylic resin. The moisture-proof and stain-resistant acrylic resin coating of this invention exhibits excellent comprehensive performance, high filling and sealing properties, strong adhesion to alloys, and good stain resistance, water resistance, and gloss retention.

The invention relates to the technical field of polypeptide synthesis, in particular to a synthetic method of desmopressin acetate. The synthesis method of the desmopressin acetate comprises the following steps that Fmoc-protected amino acids are coupled on amino resin one by one according to the sequence of the desmopressin acetate to obtain peptide resin, and the Fmoc-protected amino acids comprise Fmoc-Gly-OH, Fmoc-D-Arg (Pbf)-OH, Fmoc-Pro-OH, Fmoc-Cys (Trt)-OH, Fmoc-Asn (Trt)-OH, Fmoc-Gln (Trt)-OH, Fmoc-Phe-OH, Fmoc-Tyr-OH and Mpa (Trt)-OH; and carrying out cracking, oxidation, purification and salt conversion on the peptide resin to obtain desmopressin acetate. According to the synthesis method disclosed by the invention, Fmoc-protected amino acid without side chain protection is adopted, so that the generation of a specific impurity Mpa (tBu)-Tyr-Ph-Gln-Asn-Cys-Pro-D-Arg-Gly-NH2 can be effectively prevented, and the purity and the yield of the product are effectively improved.

The invention discloses a mineral cemented filling mortar material for mineralizing and sealing CO2 and a preparation method thereof, and relates to the technical field of low-carbon environment-friendly mortar materials, the raw materials comprise carbonic anhydrase-producing microorganisms, aggregate, a calcium source solution and nano zinc oxide; wherein the calcium source solution is an aqueous solution of calcium chloride, calcium nitrate or calcium acetate, the calcium source solution comprises a premixed calcium source solution and a gradient calcium source solution, the concentration of Ca < 2 + > in the premixed calcium source solution is 0.5 mol / L, the concentration of the gradient calcium source solution is 2 mol / L, and the premixed calcium source solution is used after being premixed with the aggregate; the particle size of the nano zinc oxide is 50-100 nm; according to the present invention, the storage amount of carbon dioxide can be increased so as to achieve the requirements of low carbon and carbon reduction, the reaction rate of CO2 hydration to generate HCO3 <-> / CO3 < 2-> can be significantly increased, the generation of HCO3 <-> / CO3 < 2-> can be accelerated, the CO2 hydration reaction and the subsequent gelling effect can be further accelerated, and the environmental protection and low carbon performance can be improved.

The invention belongs to the technical field of floor support plates, and particularly relates to a material for a concrete floor support plate, which is prepared from 150 to 170 parts of cement, 30 to 35 parts of mineral admixture, 200 to 250 parts of sand, 100 to 120 parts of gravel, 40 to 45 parts of fiber, 5 to 10 parts of early strength agent and 140 to 150 parts of water. The early strength agent comprises the following components in parts by weight: 20-30 parts of a polycarboxylate superplasticizer, 5-10 parts of modified nano zeolite powder, 5-9 parts of lithium acetate, 3-5 parts of a complexing agent, 5-10 parts of calcium sulfate and 1-4 parts of diisopropanolamine. The fibers, the mineral admixture and the early strength agent are added into the formula, early hydration of cement is promoted, dry shrinkage and cracking caused by too fast later hydration of cement are avoided, the compressive strength and breaking strength of the concrete floor support plate are effectively improved, the maintenance period of the concrete floor support plate is shortened, and the production cost is reduced.

The invention relates to the technical field of medical dressings, in particular to a liquid adhesive bandage and a preparation method thereof.The preparation method comprises the following steps that according to the formula amount, sodium chloride and sodium citrate are added into water, and a mixture A is obtained; adding copper gluconate into the mixture A to form a mixture B; mixing Tween 20 with glycerin, adding L-menthol, and stirring to form a mixture C; adding the mixture C into the mixture B to form a mixture D; the preparation method comprises the following steps: adding acetic acid into water, uniformly mixing, adding chitosan, and dissolving to obtain a chitosan-acetic acid solution; adding a chitosan-acetic acid solution into the mixture D, and dissolving to form a mixture E; adjusting the pH value of the mixture E to 4.5-6.5, filtering, filling and sterilizing to obtain the liquid adhesive bandage. The prepared liquid adhesive bandage can quickly form a layer of protective film on the surface of a wound, effectively inhibits growth of bacteria and promotes wound healing, and meanwhile, the liquid adhesive bandage has good flexibility and comfort and small irritation.

The invention discloses a monatomic-cluster double-active-site efficient ammonia cracking hydrogen production catalyst and a preparation method thereof, and belongs to the field of new energy catalytic materials. The catalyst comprises a 2-methylimidazole zinc derived nitrogen-doped carbon-loaded cobalt monatomic carrier, a molybdenum disulfide nanosheet-loaded iron cluster carrier, monatomic active metal, cluster active metal and an auxiliary agent. Wherein the 2-methylimidazole zinc derived nitrogen-doped carbon-loaded cobalt monatomic carrier is prepared by the following steps: stirring 2-methylimidazole, zinc acetate and cobalt nitrate hexahydrate in methanol to generate a ZIF-8 precursor, washing, drying, and calcining in an H2 / Ar mixed atmosphere, thereby obtaining the 2-methylimidazole zinc derived nitrogen-doped carbon-loaded cobalt monatomic carrier; the molybdenum disulfide nanosheet loaded iron cluster carrier is prepared by carrying out hydrothermal reaction on ammonium molybdate and thiourea to generate MoS2 nanosheets and then loading iron clusters. The catalyst prepared by the invention has high activity, long service life and industrial applicability.

The invention provides a new energy automobile battery flexible disassembling adhesive and a preparation method thereof, and belongs to the technical field of new energy automobile batteries, the flexible disassembling adhesive comprises the following components by weight: 45-50 parts of deionized water; 8 to 10 parts of gamma-butyrolactone; 5 to 8 parts of propylene glycol methyl ether acetate; 2 to 3 parts of microencapsulated lipase; 2 to 3 parts of nano cellulose immobilized protease; 6 to 8 parts of urea peroxide; 0.5 to 1 part of nano manganese dioxide; 0.7 to 1.1 parts of a sodium citrate / sodium lactate buffer solution; 1.5 to 2.5 parts of polyvinylpyrrolidone K30; 0.8 to 1.2 parts of hydroxypropyl methyl cellulose; 0.05 to 0.1 part of a graphene oxide nanosheet; 0.5 to 0.8 part of a benzotriazole derivative; 0.1 to 0.3 part of sodium molybdate; 6 to 8 parts of sorbitol; and 5-7 parts of ascorbic acid. The flexible disassembly adhesive solves the problems of low efficiency, serious environmental pollution, high safety risk and low material recovery rate in traditional battery disassembly.

The invention discloses a corrugated carton with waterproof and antibacterial properties, and belongs to the technical field of logistics packaging materials. The corrugated carton is formed by bonding surface paper, inner paper and corrugated paper. The surface paper, the inner paper and the corrugated paper are coated with a layer of composite waterproof antibacterial emulsion before being bonded, and a layer of waterproof antibacterial film is obtained; the composite waterproof antibacterial emulsion is prepared from the following components in parts by weight: 40 to 50 parts of waterborne polyurethane, 30 to 35 parts of acrylic resin emulsion, 20 to 25 parts of modified palm wax emulsion, 8 to 10 parts of composite waterproof antibacterial material dispersion liquid, 4 to 6 parts of organic silicon waterproof agent, 3 to 5 parts of nano zinc oxide, 2 to 4 parts of propylene glycol methyl ether acetate, 0.5 to 2 parts of hydroxyethyl cellulose and 0.1 to 0.5 part of defoaming agent. The corrugated carton prepared by the invention has good adhesion, waterproofness and antibacterial property.