1879 results about "Propanoic acid" patented technology

The invention belongs to the technical field of flame-retardant macromolecules, and particularly relates to intrinsic heat-conducting flame-retardant recycled epoxy resin and a preparation method thereof. The preparation method comprises the following steps: (1) carrying out a reaction on diethanol amine and 9, 10-dihydro-9-oxa-10-phosphaphenanthrene 10-oxide (DOPO) to obtain an intermediate A; and (2) carrying out condensation polymerization on the intermediate A and phenylphosphonic acid to prepare the phosphate-terminated polyester flame retardant (PEF). And (3) carrying out epoxidation on 4, 4 '-biphenol to prepare the liquid crystal epoxy precursor LEP. And (4) mixing PEF, LEP and 3, 3 '-dithiodipropionic acid, and heating and curing to prepare the epoxy resin. The prepared epoxy resin has intrinsic heat conduction, flame retardance and efficient recoverability, and is a high polymer material with great potential.

The invention relates to the technical field of microorganisms, in particular to a culture medium and a method for culturing Ackermania muciniphila for activating Amuc-1260 by using lambda-carrageenan as a carbon source, according to the culture method, the lambda-carrageenan is used for replacing a traditional carbon source, thallus growth and proliferation can be remarkably promoted, the effect is optimal under the condition of 2.00 g / L, and the culture cost is low. Compared with the conventional carbon source (glucose), the carbon source is improved by 92.91%. Further research finds that the lambda-carrageenan can induce the Akk bacteria to up-regulate the expression of glycoside hydrolase such as Amuc-1260 and enhance the activity of pathways such as glycosaminoglycan degradation, amino acid metabolism and insulin signals, so that the metabolic adaptability and energy utilization efficiency of the bacteria are improved. Meanwhile, the Akk bacteria secrete more functional short-chain fatty acids such as acetic acid, propionic acid and the like under the condition, and have the effects of regulating intestinal health and maintaining metabolic homeostasis. The invention provides a new theoretical basis and technical support for large-scale culture of Akk bacteria and development of a metabiotic product.

The present invention relates to a preparation method of an intelligent self-repairing, flame-retardant and light-resistant water-based polyurethane coating. The method comprises the following steps: preparing a self-made hyperbranched flame retardant and using it in the synthesis of a polyurethane prepolymer; cooling the mixture to 58° C., adding 2,2-dimethylolpropionic acid, reacting the mixture for 1 to 2 hours, adding 1 to 2 parts of a disulfide compound, reacting the mixture for 1 to 2 hours at 60 to 80° C., adding 1 to 2 parts of a hydrogen bonding agent, reacting the mixture for 1 hour at 60 to 80° C., adding 0.5 to 1.5 parts of a coumarin derivative, and reacting the mixture for 60 to 90° C. The mixture was stirred for 1-2 hours, and then spiropyran, diethanol monoisopropanolamine, and 0.01 parts of p-toluenesulfonamide were added, and the mixture was reacted at 50°C for 30 minutes. The temperature was lowered to 40-45°C, and 1-2 parts of triethylamine were added, and the mixture was reacted for 1-2 hours. The mixture was cooled to room temperature, and 60-65 parts of water were added. The mixture was stirred at a speed of 1800-2000 r / min for 0.5-1 hour to obtain an intelligent self-healing, flame-retardant, and light-resistant water-based polyurethane coating. The flame retardancy and self-healing properties of the obtained water-based polyurethane were significantly improved.

The invention relates to the technical field of compound fertilizers, and discloses a boron-zinc-molybdenum synergistic compound fertilizer, which is prepared from the following raw materials in parts by weight: calcium nitrate, ammonium polyphosphate, potassium sulfate, magnesium sulfate, disodium octoborate tetrahydrate, sugar alcohol chelated zinc, sodium molybdate and a synergistic auxiliary agent, the feed additive is prepared from a feed additive, an activator, 5-alginic acid oligosaccharide, aminolevulinic acid, sugar alcohol chelated magnesium, an antagonist, a stress-resistant enhancer and a coating material. According to the boron-zinc-molybdenum synergistic interaction compound fertilizer and the preparation process thereof, the disodium octoborate tetrahydrate, the sugar alcohol chelated zinc and the sodium molybdate are compounded according to a specific proportion, antagonism is avoided through proportion limitation, the synergistic effect of the three elements is remarkably enhanced, and the problem that a single element is insufficient or excessive is solved; chelated elements such as sugar alcohol chelated zinc and sugar alcohol chelated magnesium are combined with an activating agent (humic acid chelated calcium and silica sol) to form a gel-state chelate, so that the trace elements can be prevented from being fixed by soil, and the transfer efficiency of the trace elements in crops is improved.

The invention discloses a method for preparing dimethyl carbonate through reaction of CO and methyl nitrite, belongs to the technical field of preparation of dimethyl carbonate, and aims to solve the problem that in the prior art, in the process of preparing dimethyl carbonate through catalysis of reaction of CO and methyl nitrite, the reaction time is short. The preparation method specifically comprises the following steps: in an inert gas atmosphere, mixing and stirring isocyanatopropyltriethoxysilane and N, N-dimethylformamide, raising the temperature of a reaction system to 50-60 DEG C, carrying out a reaction for 1-2 hours, and carrying out a reaction for 1-2 hours, so as to obtain a reaction solution; and 3-aminopropionic acid is added into the reaction system. According to the method, silicon-aluminum coating, potassium modification and 18-crown-6-ether modification are sequentially performed after a halogen-free palladium-copper catalytic system is prepared, so that the conversion rate of impurities and the chromatic value of a product are reduced, the conversion rate of methyl nitrite is effectively increased, and the service life of the catalyst is effectively prolonged.

The invention belongs to the field of detection and analysis, and relates to a method for separating and detecting enantiomers in (S)-2-amino-3-[2-(tert-butoxy)-2-oxoacetamido] tert-butyl propionate hydrochloride. According to the method, HPLC is adopted for separation and detection, a polysaccharide derivative chiral chromatographic column is selected as a chromatographic column, a mobile phase A is a weak base aqueous solution, and a mobile phase B is acetonitrile and / or methanol. The method is strong in specificity, high in separation degree, high in accuracy, stable, reliable and high in sensitivity, and a simple, accurate, rapid and reliable detection method is provided for control of impurities in a starting material of (S)-2-amino-3-[2-(tert-butoxy)-2-oxoacetamido] tert-butyl propionate hydrochloride.

The invention discloses a recombinant halomonas for producing polyhydroxyalkanoate as well as a construction method and application of the recombinant halomonas. The recombinant halomonas comprises an exogenous gene, the exogenous gene comprises a combination of an aldD gene, a dhaT gene and an orfz gene, and the recombinant halomonas weakens the expression of an endogenous prpc gene. According to the invention, a P34HB synthesis route is successfully constructed through a synthesis route of exogenous introduction from 1, 4-butanediol (BDO) to 4-hydroxybutyryl coenzyme A, the proportion of each monomer in the copolymer can be effectively regulated and controlled, especially after exogenous addition of short-chain fatty acids (such as formic acid, acetic acid, propionic acid, butyric acid and the like), the synthesis of copolymers such as PHB, PHBV, P34HB, P34HB3HV and the like can be further improved, and the synthesis efficiency of the copolymer is improved. And the proportion of different monomers is adjusted, so that the diversity and yield of the copolymer are enhanced.

The invention discloses a composition for improving the stability of oleuropein in a solution as well as a preparation method and application of the composition. The composition comprises oleuropein and at least one stabilizer, and the stabilizer is selected from the group consisting of anisic acid, lactobionic acid, glycyrrhizic acid, 3, 3-thiodipropionic acid, N-acetyl-L-glutamine, propyl-cysteine and lauramidopropyl betaine; and the pH value of the aqueous solution of the composition is 4.0-8.0. The preparation method comprises the following steps: dissolving oleuropein in water, adding the stabilizer, and uniformly mixing. Through simple physical mixing, by utilizing the synergistic effect of the specific stabilizer and the oleuropein, the degradation and discoloration of the oleuropein in the storage process are remarkably inhibited. Experiments show that after the preferable composition is preserved for 30 days in an open manner, the retention rate of the oleuropein still reaches up to 80% or above, and is far superior to that of blank control and a traditional liposome wrapping method. The composition is simple and convenient in preparation process and low in cost, and provides reliable technical support for wide application of oleuropein in liquid products such as food, medicine and cosmetics.

The invention relates to the field of polyester fibers, and discloses a composite enhanced polyester fiber for bags and suitcases and a preparation method thereof.The composite enhanced polyester fiber is prepared from polyethylene glycol terephthalate slices, polyethylene glycol, tris (2, 4-di-tert-butylbenzene) phosphite, tetra [beta-(3, 4-ditert-butylbenzene)] tetrakis [beta]-(2, 4-ditert-butylbenzene)] tetrakis [beta-(3, 4-ditert The composite material is prepared from 1, 3, 5-di-tert-butyl-4-hydroxyphenyl) propionic acid] pentaerythritol ester, modified nano-zinc oxide, tetrabutyl titanate, a chitosan aqueous solution and acetic acid. The modified nano zinc oxide is prepared from gamma-aminopropyltriethoxysilane, an ethanol water solution, acetic acid and nano zinc oxide. The composite enhanced polyester fiber disclosed by the invention has relatively good antibacterial property, hygroscopicity and mechanical property.

The present invention discloses an infrared-shielding polyurethane glass film and a preparation method thereof, relating to the field of polymer materials technology. When preparing the infrared-shielding polyurethane glass film, the present invention comprises reacting an organic nickel complex and 3-imidazole-1-propionic acid to produce a functionalized crosslinker; sequentially reacting 4-aminophenylacetonitrile with 3-hydroxypropyl acrylate and quinoline-4-carboxaldehyde to produce a UV-absorbing monomer; reacting polypropylene glycol, a UV-absorbing monomer, 1,4-butanediol, and 4-chloromethyl-1,3-phenylenediisocyanate to polymerize to produce polyurethane; reacting tungsten-doped titanium dioxide and chloropropyltriethoxysilane to produce modified titanium dioxide; and uniformly mixing the polyurethane, modified titanium dioxide, the functionalized crosslinker, and acetone, followed by coating and curing to produce the infrared-shielding polyurethane glass film. The infrared-shielding polyurethane glass film prepared by the present invention has excellent infrared shielding, anti-aging, antibacterial, and mechanical properties.

The invention relates to the technical field of vacuum bag films for aeronautical manufacturing, and discloses an eleven-layer co-extruded film for aeronautical use and a preparation process thereof, and the preparation process specifically comprises the following steps: carrying out grafting modification treatment on polyamide acid by using a monoalkenyl diepoxy composite flexible compound through a carboxyl-epoxy ring-opening reaction to prepare alkenyl functionalized processable polyimide; the preparation method comprises the following steps: carrying out modification treatment on nylon 6 resin by using 3-mercaptopropionic acid through an amino-carboxyl condensation reaction to prepare mercapto functionalized nylon; under the hot melting condition, alkenyl functionalized processable polyimide and sulfydryl functionalized nylon are induced to be subjected to reactive compounding through a free radical initiator, PA-PI alloy master batch is prepared, the master batch serves as a functional modification component of copolymerized polyamide 6 / 66 resin, an eleven-layer co-extrusion film is prepared through an eleven-layer co-extrusion blow molding process, and the eleven-layer co-extrusion film is used as a functional modification component of the copolymerized polyamide 6 / 66 resin. The film product has excellent comprehensive performance and can be used as a high-temperature-resistant vacuum bag film for curing aviation composite materials.

The invention belongs to the technical field of mineral flotation, and particularly discloses a method for recovering whole-fraction iron lepidolite through combination of multi-stage magnetic separation and synergistic flotation. Comprising a matched compound collecting agent which is composed of sodium dodecenesulfonate, amino acid methyl thiohydracrylate, an amphoteric polyacrylamide polymer, carboxyethylidene diphosphonic acid and polyethylene glycol, and efficient recovery of whole-size-fraction iron lepidolite is achieved by matching with a corresponding magnetic separation-flotation combined process. The compound collecting agent generates static electricity and physical and chemical adsorption on the iron lepidolite through specific groups such as sulfonic acid groups, carboxyl groups, amino groups, acylamino groups and phosphate groups, exerts excellent selectivity and collecting functions, generates a dispersion effect and a chelating flocculation effect on micro-fine-particle iron lepidolite, and well cooperates with multi-stage magnetic separation to recover whole-particle-size iron lepidolite, so that the recovery rate of the whole-particle-size iron lepidolite is increased, and the recovery rate of the whole-particle-size iron lepidolite is increased. And the existing combined beneficiation process of the iron lepidolite is optimized, the cost and the environmental influence are reduced, and technical support is provided for sustainable development of lithium resources.

The invention discloses a super-retarding type polycarboxylic acid water reducing agent and a preparation method and application thereof, and belongs to the field of concrete water reducing agents. The preparation method comprises the following steps: taking acrylic acid AA, isobutenol polyoxyethylene ether HPEG and hydroxyethyl acrylate HEA as monomers, taking mercaptopropionic acid MPA as a chain transfer agent, taking hydrogen peroxide H2O2 and L-ascorbic acid Vc, and mixing in proportion to serve as an initiator; preparing a first and second monomer mixed solution; adding bottom water into the reaction kettle, and carrying out stepwise polymerization reaction; and cooling the reaction liquid, adjusting the pH value, filtering, and discharging to obtain the product. According to the invention, an ester functional monomer hydroxyethyl acrylate HEA is introduced, and a step-by-step polymerization technology is adopted to control the dispersion process of water reducing agent molecules on cement particles, so that the water reducing agent molecules continuously disperse the cement particles within a certain period of time; the problem that the slump loss is too fast due to long-time and long-distance transportation of concrete or transportation in high-temperature weather is effectively relieved.

The invention relates to the technical field of building, chemical engineering and energy heat preservation, and discloses a silicon-based aerogel composite material and a preparation method and application thereof. The invention relates to a light-emitting diode (LED) photo-curing agent, which is prepared from tetraethyl orthosilicate, methyltrimethoxysilane, allyltriethoxysilane, pentaerythritol tetra (3-mercaptopropionate), N-(3-(triethoxysilyl) propyl) furfuryl amine, N-(3-(triethoxysilyl) propyl) maleimide, a photoacid generator and a photoinitiator. The composite material has a three-dimensional porous silicon dioxide network skeleton and a polymer interpenetrating network, the three-dimensional porous silicon dioxide network skeleton is formed by copolymerization of tetraethyl orthosilicate and methyltrimethoxysilane, and the polymer interpenetrating network is formed by reaction of pentaerythritol tetra (3-mercaptopropionate) and allyltriethoxysilane. The preparation method comprises the steps of sol preparation, light curing, solvent replacement, surface hydrophobic modification and normal-pressure drying. The material shows excellent thermal insulation and mechanical properties in the fields of building heat insulation, pipeline heat preservation and cryogenic heat insulation.

The invention relates to the technical field of anti-yellowing, in particular to anti-yellowing lining cloth with a hot melt coating and a preparation method of the anti-yellowing lining cloth. Composite carbon dots, an anti-yellowing agent and a composite chitosan solution are adopted to prepare finishing liquid for finishing the lining cloth; the preparation method comprises the following steps: selecting furfural and urea as a carbon source and a nitrogen source, performing one-step hydrothermal synthesis to obtain a nitrogen-doped furfural-based carbon dot, and grafting an amino-terminated polyimidazolium salt antibacterial compound to obtain a composite carbon dot; wherein the amino-terminated polyimidazolium salt antibacterial compound is an amino-terminated halogen-free polyimidazolium salt antibacterial compound which is prepared by taking ethylenediamine, butyric acid, glyoxal and formaldehyde as raw materials based on amine-aldehyde polycondensation and has good biocompatibility; the preparation method comprises the following steps: by taking polybutylene adipate, toluene diisocynate and isophorone diisocyanate as main monomers, polypropylene oxide triol as a crosslinking monomer, 2, 2-dimethylolpropionic acid and 4, 4 '-diaminodiphenyl disulfide as chain extenders and composite carbon dots as an end-capping reagent, adding water and emulsifying to obtain the waterborne polyurethane hot melt adhesive.

The present invention relates to a method for treating a bacterial infection by using Paracoccus wg1 T The invention relates to a method for treating wastewater containing high concentration of inorganic nitrogen, which belongs to the technical field of waste resource utilization and water environment treatment. T The seed liquid after culture is used to treat nitrogen-containing wastewater, and the Paracoccus wg1 of the present invention T , has a very high tolerance to high concentrations of inorganic nitrogen, and has excellent denitrification capabilities under conditions of high concentrations of inorganic nitrogen. Specifically, sodium nitrate is used as the nitrogen source, sodium propionate is used as the carbon source, NO3 ‑ When the ‑N concentration is 6258.85 mg / L‑N, 97.68 mg / L‑N of NO3 can be degraded in 48 hours ‑ -N; ammonium sulfate as nitrogen source, sodium propionate as carbon source, NH4 + When the ‑N concentration is 9326.28 mg / L‑N, 92.28 mg / L‑N of NH4 can be degraded in 48 hours + ‑N. paracoccus wg1 T Biological denitrification treatment of high-concentration inorganic nitrogen wastewater has great application prospects.

The application discloses a bacteriostatic and acne-removing microemulsion containing plant extracts and a preparation method thereof. The bacteriostatic and acne-removing microemulsion contains a microemulsion loaded with quercetin alone, a microemulsion loaded with sasanquasapernin alone, and a microemulsion loaded with quercetin and sasanquasapernin simultaneously. The bacteriostatic and acne-removing microemulsion containing plant extracts prepared by the application not only solves the problems of stickiness of camellia oil and poor solubility of quercetin, but also has a synergistic inhibitory effect on propionibacterium acnes, achieves the same high-efficiency bacteriostatic effect with a lower drug concentration, saves drug cost, reduces drug irritation, and expands the application of quercetin and sasanquasapernin in the cosmetic and pharmaceutical fields due to the rich pharmacological effect of the plant extracts, low side effect and safety. The microemulsion system prepared by the application is clear, transparent, uniform and stable, the preparation process is simple, the required energy is low, the cost is low, and the system is beneficial to commercial production.

The invention belongs to the technical field of fertilizers, and particularly discloses coated 5-aminolevulinic acid as well as a preparation method and application thereof. The preparation method of the coated 5-aminolevulinic acid comprises the following steps: (1) melting: melting urea phosphate to obtain a coating agent; and (2) mixing: uniformly mixing the coating agent and 5-aminolevulinic acid powder in a high-tower granulator, carrying out spray granulation, and cooling and curing to obtain the coated 5-aminolevulinic acid. The preparation method disclosed by the invention is simple in process, and the prepared coated 5-aminolevulinic acid is good in stability and can promote the growth of chilies.

The invention relates to equipment for preparing clobetasol propionate liniment and a preparation method of the clobetasol propionate liniment. The equipment comprises a material mixing mechanism, a barrel, a stirring shaft rotationally arranged on the barrel, stirring blades for stirring substances, a partition plate for separating the interior of the barrel, a crystallization rod for cooling materials and a drying mechanism for drying the substances. Wherein the stirring blades are fixedly arranged around the stirring shaft, and the stirring blades at the bottom are arranged around the stirring shaft in a swinging manner; the partition plate is movably arranged in the barrel around the stirring shaft; the crystallization rod is movably arranged at the bottom of the barrel; the drying mechanism communicates with the bottom of the barrel; the drying mechanism is communicated with the mixing mechanism; the partition plate is arranged between the fixed first ring frame and the rotary second ring frame; the partition plate is connected with the first ring frame and the second ring frame. The second ring frame rotates to drive the partition plate to open or separate the cylinder. The preparation method solves the problem that the preparation efficiency of clobetasol propionate is affected due to more preparation equipment caused by complex process steps in the clobetasol propionate liniment preparation process in the existing scheme.

The invention belongs to the technical field of rubber sealing rings, and particularly discloses a wading rubber sealing ring and a preparation method thereof, the wading rubber sealing ring comprises the following components by weight: 60-70 parts of modified ethylene propylene diene monomer, 35-50 parts of modified white carbon black, 20-30 parts of hydrogenated nitrile rubber, 0-10 parts of fluororubber, 2-5 parts of polyester fiber, 0.5-3 parts of an anti-hydrolysis agent, and 1-3 parts of a hydrophobic agent. 2-4 parts of an antimicrobial agent, 3-5 parts of an anti-aging agent and 1-7 parts of sulfur; the anti-hydrolysis agent is a mixture of tetrakis [beta-(3, 5-di-tert-butyl-4-hydroxyphenyl) propionic acid] pentaerythritol ester and a carbodiimide anti-hydrolysis agent; the hydrophobic agent is a mixture of polydimethylsiloxane and perfluorooctyltriethoxysilane, and the hydrophobic agent is a mixture of polydimethylsiloxane and perfluorooctyltriethoxysilane. The wading rubber sealing rubber ring and the preparation method thereof are suitable for fresh water and warm water scenes, and have wide application prospects in ship sealing and sewage treatment equipment in seawater and industrial wastewater scenes.

The invention relates to the field of inorganic material preparation, and particularly discloses pseudo-boehmite and a preparation method thereof. A preparation method of pseudo-boehmite comprises the following steps: (1) mixing an aluminum salt solution and an aluminate solution, adding a crystal form regulating agent, and stirring for reaction to obtain a sol system; the crystal form regulating agent is ZnS quantum dots modified by thiohydracrylic acid; (2) adding a pore diameter guiding agent into the sol system, and aging for 6-8 hours; the pore diameter guiding agent is a compound of a polyethylene glycol-polypropylene glycol-polyethylene glycol triblock copolymer and sodium citrate; and (3) carrying out solid-liquid separation on the aged sol system, and washing and drying the obtained solid to obtain the pseudo-boehmite. The proportion of 5-10nm pores of the pseudo-boehmite prepared by the preparation method disclosed by the invention reaches 90% or above, so that the pore distribution requirement of a fine catalytic reaction on the pseudo-boehmite can be met, and the efficient catalytic reaction is favorably realized.

The invention belongs to the technical field of 3D printing photocuring, and particularly relates to photocuring organic silicon modified polyurethane acrylate resin as well as preparation and application thereof. According to the invention, isophorone diisocyanate is used as a hard segment, polypropylene glycol-1000, dimethylolpropionic acid and dihydroxy-terminated silicone oil are used as soft segments, and the light-cured organic silicon modified polyurethane acrylic resin is synthesized with pentaerythritol triacrylate. By controlling the hydroxyl content in the double-terminal hydroxyl silicone oil and the proportion of the double-terminal hydroxyl silicone oil in a soft segment, the prepared organic silicon modified polyurethane acrylic resin has better flowability and light transmittance and higher double bond content; the organic silicon modified polyurethane acrylic resin, the acryloyl morpholine and the photoinitiator are cured according to a specific proportion, and the obtained elastomer has good mechanical properties and thermal stability and has high printing precision. The synthesized organic silicon modified polyurethane acrylate resin has the potential of replacing a traditional polyurethane acrylate material.

The invention discloses a self-repairing composite floor for a clean room and a preparation method of the self-repairing composite floor, and the preparation method comprises the following steps: carrying out amination treatment on nano silicon dioxide and carbon quantum dots by using a silane coupling agent, and sulfonating polyethersulfone ketone by using concentrated sulfuric acid; the preparation method comprises the following steps: carrying out curing treatment on epoxy resin, an amine curing agent, N-hydroxyethyl maleimide and tetrakis (3-mercaptopropionic acid) pentaerythritol ester to obtain epoxy-mercaptan resin; the preparation method comprises the following steps: carrying out prepolymerization reaction on vacuum dehydrated polyester polyol, tetrahydroxyethyl ethylenediamine, furanpropanol, diisocyanate, a catalyst, 2, 2 '-thiodiethanol and hydroxyl silicone oil to obtain a star-shaped polyurethane prepolymer, adding epoxy-thiol resin, glyceryl borate, sulfonated polyethersulfone ketone, aminated silicon dioxide, aminated carbon quantum dots and an auxiliary agent, carrying out ultrasonic treatment, and carrying out drying to obtain the star-shaped polyurethane resin. The self-repairing coating material is obtained; and coating the self-repairing coating material on the surface of a base plate, and performing hot-pressing curing molding to obtain the self-repairing composite floor for the clean room.

The invention discloses self-repairing waterborne polyurethane based on double dynamic bond synergy and a preparation method thereof.The method comprises the following steps that 1, in the nitrogen atmosphere, after isophorone diisocyanate, polytetrahydrofuran diol and dimethylolpropionic acid react for a period of time, a catalyst is added for continuous reaction, and a prepolymer is synthesized; (2) adding N, N-di-tert-butyl ethylenediamine into the prepolymer, and carrying out chain extension reaction; (3) adding dithiothreitol into the solution after the reaction in the step (2) to carry out cross-linking reaction; and (4) adding triethylamine into the solution obtained after the reaction in the step (3), and carrying out a salt forming reaction to obtain the self-repairing waterborne polyurethane emulsion based on double dynamic bond synergy. High self-healing efficiency and mechanical performance are achieved by introducing dynamic covalent bonds with double thermal responses, and reprocessing and recycling are achieved at the same time.

The invention relates to the technical field of chemical fiber manufacturing, in particular to a preparation process of graphene reinforced porous hollow polyester fibers. The problems that existing polyester fibers are insufficient in mechanical property and poor in moisture absorption and air permeability are solved. The preparation method comprises the following steps: modifying a PET sheet by using 2, 2-dimethylolpropionic acid and hydroxyl-terminated polydimethylsiloxane to obtain modified PET; the preparation method comprises the following steps: taking chitosan modified graphene as a carrier, and loading metal ions to obtain loaded graphene; polyethylene glycol and sodium bicarbonate are used as pore-foaming agents; modifying octadecyl dimethyl allyl ammonium chloride to obtain an antibacterial toughening agent; all the components are mixed, and the polyester fiber is prepared through melt spinning, stretching, heat treatment and alkali treatment. The mechanical property of the fiber is improved through the introduction of graphene and the modification treatment of the PET sheet; by utilizing the composite pore-foaming agent and adjusting the process, the moisture absorption and air permeability of the fiber are improved, and the service life of the fiber is prolonged.

The invention provides an anti-aging composition and application thereof, the composition at least contains pyrroloquinoline quinone disodium salt, ergothioneine and 5-aminolevulinic acid or salt thereof in physiologically acceptable media, the composition contains PQQ, ergothioneine and 5-aminolevulinic acid (5-ALA) or salt thereof, the three components are compounded to achieve a synergistic effect, and the anti-aging effect is achieved. The dyeing intensity of beta-galactosidase is reduced, and the anti-aging effect is achieved.

This invention discloses a strain of *Lactobacillus plantarum* Grx402 with the ability to promote intestinal absorption of short-chain fatty acids. *Lactobacillus plantarum* Grx402 was isolated from the intestines of long-lived individuals in Bama, Guangxi (CGMCC No. 28585). Using a Caco-2 cell model to construct an intestinal absorption model of short-chain fatty acids (SCFAs), it was found that *Lactobacillus plantarum* Grx402 can promote the absorption and transport of acetic acid, propionic acid, and butyric acid by intestinal epithelial cells, exhibiting excellent ability to promote intestinal absorption of short-chain fatty acids. It can be used to prepare dairy products or beverages that promote the intestinal absorption of short-chain fatty acids.

The invention discloses radix notoginseng stem and leaf rare ginsenoside as well as a preparation method and application thereof, and belongs to the technical field of ginsenoside. The radix notoginseng stem and leaf rare ginsenoside comprises Rk3, Rh4, S-Rg3, R-Rg3, Rk1 and Rg5. The radix notoginseng stem and leaf rare ginsenoside can be used for preparing radix notoginseng stem and leaf rare ginsenoside. The preparation method comprises the following steps: mixing the pseudo-ginseng stem and leaf extract with an acetic acid aqueous solution, reacting at 105-120 DEG C for 10-40 minutes, and drying; in the preparation process, macroporous resin purification is not carried out. According to the scheme, part of chemical substances in the panax notoginseng stem and leaf extract can be rapidly converted at a low temperature, new active substances Rh4, S-Rg3, R-Rg3, Rk1 and Rg5 with high purity are obtained at the same time, and the obtained panax notoginseng stem and leaf rare ginsenoside can effectively inhibit propionibacterium acnes, burkholderia cepacia and malassezia furfur.

The invention relates to the technical field of polyurethane materials, in particular to a non-MOCA type fitness equipment rubber coating material and a preparation method thereof. The preparation method comprises the following steps: adding polytetrahydrofuran, isophorone diisocyanate, 1, 4-butanediol, a 2, 2-dimethylolpropionic acid solution, a hydroxyl chain extender, triethylamine, deionized water and a flame-retardant filler to obtain a polyurethane emulsion; and coating the polyurethane emulsion to form a film, and drying to obtain the polyurethane adhesive film. Adding the flame-retardant filler into ethanol, and ultrasonically dispersing uniformly to obtain dispersion liquid; spraying the dispersion liquid onto the surface of a polyurethane adhesive film to obtain a pretreated polyurethane adhesive film; and carrying out layer-by-layer self-assembly on the surface of the pretreated polyurethane adhesive film for 5-6 times to obtain a finished product. The finished product prepared by the invention has excellent flame retardant property, antibacterial property and mechanical property, thereby having wide application prospect in the technical field of polyurethane materials.