3399 results about "Glyceride" patented technology

The invention relates to the technical field of folding screen supporting films, and particularly discloses a double-layer buffering supporting film for a flexible folding display screen and a preparation method of the double-layer buffering supporting film. The double-layer buffer supporting film for the flexible folding display screen sequentially comprises a release film layer, a first adhesive layer, a first stainless steel layer, a second adhesive layer, a second stainless steel layer and a protective film layer from top to bottom, the first adhesive layer and the second adhesive layer are prepared by curing the same pressure-sensitive adhesive composition; the pressure-sensitive adhesive composition is prepared from the following raw materials: acrylate copolymer, hydrogenated rosin glyceride, hyperbranched polyesteramide-dopamine conjugate, acylhydrazone bond modified siloxane, a curing agent and a silane coupling agent; the protective film layer comprises the following raw materials: PET particles, nano silicon dioxide, an ethylene-vinyl acetate copolymer and an antioxidant. The double-layer buffer supporting film has the advantages of being high in supporting rigidity and interlayer peel strength, and serious folds caused by long-term repeated folding of the folding screen can be relieved.

The invention belongs to the technical field of grease chemistry, and particularly relates to diglyceride prepared through enzymolysis and used for reducing blood fat, a preparation method and application of the diglyceride. The preparation method comprises the following steps: (1) mixing edible oil, lipase and water, hydrolyzing and dehydrating to obtain a hydrolysate; and (2) mixing the hydrolysate, glycerol and partial glyceride lipase, reacting, and distilling to obtain the diglyceride, the partial glyceride lipase in the step (2) is a mixture of lipase Lipase G50 and lipase Novozyme 435. The diglyceride prepared by the method disclosed by the invention has an excellent effect of reducing blood fat; and the obtained diglyceride is high in yield and low in acid value, and the finished product does not need deacidification treatment, so that the method is suitable for large-scale industrial production.

The invention relates to the technical field of textiles, and discloses a cool and washable bio-based nylon 56 fabric and a preparation method thereof. The preparation method of the cool and washable bio-based nylon 56 fabric comprises the following steps: loading modified nano aluminum oxide on modified aluminum nitride microchips to obtain a composite cool material; nylon 56, an ethylene-methyl acrylate-glycidyl methacrylate terpolymer, polypentamethylene guanidine hydrochloride and a composite cool feeling material are subjected to blending extrusion and melt spinning, and then the bio-based nylon 56 fabric is woven. Mixing the composite modified boron nitride and ethanol to obtain finishing liquid; spraying the finishing liquid on one side of the bio-based nylon 56 fabric, and drying to obtain the cool washable bio-based nylon 56 fabric. The cool and washable bio-based nylon 56 fabric disclosed by the invention has excellent cool feeling, antibacterial property, washable property, moisture absorption property and unidirectional perspiration property.

The invention relates to the technical field of degradable plastics, and provides biodegradable plastic particles as well as a preparation method and application thereof. The biodegradable plastic particles comprise the following components in parts by weight: 50-80 parts of PLA, 20-50 parts of PBAT, 5-20 parts of a filler, 1-8 parts of a flexibilizer, 1-5 parts of a lubricant and 5-10 parts of a modifier. The modifier comprises a polylactic acid-polyethylene glycol block copolymer and a polycaprolactone-polyglycidyl methacrylate block copolymer in a mass ratio of (1: 19)-(19: 1). According to the technical scheme, the problems of poor flexibility and strength of plastic particles in related technologies are solved.

A biodegradable polymer composite, a method of making the same and use for same are provided. The biodegradable polymer composite has about 30 to 99.5% by weight of a polymer selected from a group consisting of polybutylene adipate terephthalate (PBAT), polybutylene succinate (PBS), polyhydroxyalkanoates (PHA), and polycaprolactone (PCL) grafted with a compatibilizer selected from a group consisting of maleic anhydride, glycidyl methacrylate, pyromellitic anhydride, acrylic acid, polyacrylic acid, methylene diphenyl diisocyanate, poly(glycidyl methacrylate, copolymer(s) of glycidyl methacrylate; and about 0.5 to 50 % by weight a nano-filler or a micro-filler. The biodegradable polymer composite does not contain polylactic acid. Surfaces of the nano-filler or the micro-filler may be modified using a grafting agent so that the biodegradable polymer composite has enhanced mechanical properties, increased heat resistance, compostablity and / or improved processability. The biodegradable polymer composite may be used to make flexible articles, such as a freezer wrap and a farming sheet.

The invention belongs to the technical field of grease modification and lipid deep processing, and particularly relates to a method for enriching n-3 polyunsaturated fatty glyceride by an enzymic method. According to the method, alkyl-modified hollow mesoporous silica spheres are used as an immobilized enzyme carrier and an emulsifier, grease rich in n-3 polyunsaturated fatty acid is used as a raw material in a stable Pickering emulsion system, saturated fatty acid and monounsaturated fatty acid are selectively hydrolyzed by lipase, and polyunsaturated fatty glyceride is enriched. The method has the characteristics of fast reaction, high yield, wide substrate application range and reusability of the immobilized enzyme, and the content of polyunsaturated fatty acid in the polyunsaturated fatty glyceride reaches 58.05-90.53%.

The invention discloses a polytetrafluoroethylene film with high tensile strength and a preparation process thereof, and relates to the technical field of polytetrafluoroethylene films. The preparation method comprises the following steps: step 1, preparing a composite raw material: S1-1, sequentially putting a tetrafluoroethylene copolymer into acetone and methanol to be soaked, washed and dried; dispersing in a glycidyl methacrylate-methanol solution, and carrying out irradiation grafting in a nitrogen atmosphere; filtering, washing and drying to obtain an epoxy tetrafluoroethylene copolymer; s1-2, sequentially putting an epoxy tetrafluoroethylene copolymer and a composite filler into tetrahydrofuran, stirring for 24-48 hours at the temperature of 70-75 DEG C in a nitrogen atmosphere, filtering, washing and drying to obtain a composite raw material; 2, mixing polytetrafluoroethylene, the composite raw material and carboxylated polyphenylene sulfide to obtain a mixture; performing cold press molding and temperature-controlled sintering to obtain a basic film; 3, the basic film is subjected to turning forming and continuous rolling, and the polytetrafluoroethylene film is obtained.

The preparation method comprises the following steps: S1, crushing cordate houttuynia rhizomes, adding the crushed cordate houttuynia rhizomes into a mixed acid aqueous solution, and carrying out immersion treatment to obtain a cordate houttuynia mixed solution; s2, adjusting the pH value of the herba houttuyniae mixed solution to 4-5, adding pectinase, carrying out primary enzymolysis and enzyme deactivation, adjusting the pH value to 6-7, adding compound enzyme, carrying out secondary enzymolysis and enzyme deactivation, so as to obtain an enzymatic hydrolysate; s3, menthol is added into the enzymatic hydrolysate, water extraction is conducted, and water extract and filter residues are obtained; s4, the filter residues are added into ethyl alcohol, then salicylic acid and diacetyl tartaric acid ester of mono (di) glycerides are added, alcohol extraction and filtering are conducted, and an alcohol extraction solution is obtained; s5, mixing the water extract with the alcohol extract, and performing reduced pressure distillation to obtain the herba houttuyniae extract. According to the method, the extraction rate of polysaccharide and flavone in houttuynia cordata can be effectively increased, and meanwhile, the prepared houttuynia cordata extract has better oxidation resistance and has a good application prospect.

The invention provides a melogabalin besylate tablet and a preparation method thereof, the melogabalin besylate tablet comprises a plain tablet and a coating, the plain tablet comprises, by mass, 4.39% of melogabalin besylate, 75-85% of mannitol 150SD, 3-10% of a disintegrating agent, 0.5-3% of a lubricant, 0.1-0.5% of an adsorbent, 1-10% of a filler, 0.5-3% of an antioxidant A and 0.1-3% of an antioxidant B; and the coating comprises the following components in percentage by mass: 30-45% of talcum powder, 2-10% of lauryl sodium sulfate, 30-45% of glycerol monocaprylate / dicaprylate, 2-10% of titanium dioxide, 30-45% of polyvinyl alcohol, 0.5-2% of iron oxide yellow and 0.5-2% of iron oxide red. The melogabalin besylate tablet prepared by the invention uses specific coating composition and specific coating parameters, so that the melogabalin besylate tablet can be stably stored without a drying agent and a composite aluminum bag for medicine packaging, the stability of the tablet is greatly improved, the complexity of equipment required by production is simplified, and the production cost is greatly saved.

The invention discloses a self-healing injectable photo-crosslinking dual-network hydrogel and a preparation method thereof.The preparation method comprises the steps that silk fibroin is subjected to methacrylation modification through a glycidyl methacrylate solution, then dextran of the silk fibroin is subjected to an oxidation reaction through a sodium periodate solution, oxidized dextran is generated, and the self-healing injectable photo-crosslinking dual-network hydrogel is obtained; the amino group in the modified silk fibroin and the aldehyde group of the oxidized dextran are subjected to a Schiff base cross-linking reaction to form the double-network hydrogel. The hydrogel with the double-network structure prepared by the invention is more compact in structure, so that the hydrogel has a series of excellent performances such as injectability, relatively good adhesion, good mechanical property, self-healing property and slow release property after drug loading while having safety.

The invention discloses a carbon fiber reinforced polyamide composition as well as a preparation method and application thereof. The carbon fiber reinforced polyamide composition comprises the following components in parts by weight: 25-60 parts of polyamide resin; 30 to 65 parts of carbon fiber; 2-8 parts of a toughening agent; 0.5 to 6 parts of compatilizer; wherein the compatilizer is ethylene-acrylic ester grafted methacrylic ester glycidyl ester. Ethylene-acrylate grafted glycidyl methacrylate is added into the carbon fiber reinforced polyamide composition to serve as a compatilizer, ethylene-acrylate and carbon fibers have good compatibility, and GMA and polyamide resin end group reaction have good compatibility. And the toughening agent is cooperated, so that the prepared material has relatively good mechanical properties and good appearance.

The invention relates to a degradable epoxy resin composite material with an adjustable curing speed, and a preparation method and a mild total recycling method thereof. Existing degradable epoxy resin has the problems of high cost, harsh degradation conditions and the like, and is difficult to meet the requirements of different application scenes on curing speed and temperature at the same time. The invention provides an epoxy resin composite material which comprises curing agent components (an epoxy resin amine curing agent and an ester-containing polythiol curing agent) and epoxy resin components (glycidyl ether epoxy resin, glycidyl amine epoxy resin and glycidyl ester epoxy resin). The cured composite material can be fully recycled through catalytic degradation under mild conditions by using a lewis acid and an amino group breaking ester bond mechanism, and the degradation product can be directly used as a curing agent, a toughening agent and a chain extender. The epoxy resin composite material disclosed by the invention not only has adjustable curing speed and high use performance, but also realizes environmental friendliness and resource recycling, and provides a new solution for sustainable development of epoxy resin.

The invention discloses an atorvaquone enteric-coated tablet, the preparation comprises atorvaquone, glyceryl behenate, teloxpol, a filler, an adhesive, a disintegrating agent and an enteric coating, and the particle size D90 of the atorvaquone is 30-50 [mu] m. The atorvaquone enteric-coated tablet disclosed by the invention is stable and continuous in release and high in bioavailability, can be positioned and released in intestinal tracts and reduce liver circulation, so that the occurrence of phenomena such as liver injury is reduced, the phenomena such as sticking and cracking are avoided in a tabletting process, the quality is qualified and stable, and the dissolution performance and the stability of the atorvaquone enteric-coated tablet are also ensured.

The invention provides transparent high-impact-resistance heat-resistant MBS (methyl methacrylate-butadiene-styrene) resin and a preparation method thereof, and relates to the field of high polymer material preparation methods, the transparent high-impact-resistance heat-resistant MBS resin is prepared from the following raw materials: water, ethanol, maleic anhydride, an emulsifier, MBS resin grafted latex, potassium persulfate and an antioxidant; the MBS resin grafted latex is prepared from the following raw materials: water, modified styrene-butadiene latex, sodium hydrogen sulfite, potassium persulfate, methyl methacrylate and styrene, the modified styrene-butadiene latex is prepared from the following raw materials: a pre-emulsion, glycidyl methacrylate, ammonium persulfate, divinyl benzene and potassium persulfate; the pre-emulsion is prepared from the following raw materials: water, an emulsifier, butadiene and styrene. The product is good in heat resistance and good in PVC modification effect, and the modified PVC composite material is high in light transmittance, high in cantilever beam impact strength and resistant to aging.

The invention relates to a poly-(2-oxazoline) epoxy derivative and application thereof, and belongs to the technical field of crosslinking. The invention provides a poly-(2-oxazoline) epoxy derivative, which is completely different from existing cross-linking agents such as 1, 4-butanediol diglycidyl ether (BDDE), divinyl sulfone, glycidyl methacrylate and the like in structure, and has the advantages that the structure is simple; the polymer can be used as a cross-linking agent for cross-linking natural high-molecular polymers such as polysaccharide (such as hyaluronic acid) and protein and synthetic high-molecular polymers such as polyethylene glycol and polyvinyl alcohol. Compared with an existing cross-linking agent, the poly-(2-oxazoline) epoxy derivative has the advantages that the poly-(2-oxazoline) epoxy derivative can be easily subjected to a cross-linking reaction with high-molecular polymers such as hyaluronic acid, the prepared cross-linked substances such as sodium hyaluronate gel are more stable and uniform, the performance of the prepared cross-linked substances is easier to regulate and control and the like, and the poly-(2-oxazoline) epoxy derivative has a great application prospect.

The invention discloses an interface covalently bonded core-shell structure boron nitride polypropylene composite dielectric material and a method. The interface covalently bonded core-shell structure boron nitride polypropylene composite dielectric material comprises a maleic anhydride grafted polypropylene matrix and a core-shell structure filler dispersed in the maleic anhydride grafted polypropylene matrix, the core-shell structure filler comprises hydroxylated boron nitride nanoparticles covalently grafted on a polymer shell layer on the surface of the core-shell structure filler; the polymer shell layer is polyglycidyl methacrylate; the epoxy group of the polymer shell layer reacts with the anhydride group of the maleic anhydride grafted polypropylene matrix to form a covalent bond. The invention has the characteristics of strong interface bonding force, uniform filler dispersion, and excellent comprehensive electrical properties and processability.

The invention provides a modified amine curing agent, a preparation method, epoxy resin anticorrosive paint and application, and belongs to the technical field of paint. The modified amine curing agent provided by the invention is prepared from preparation raw materials including alicyclic diamine, m-xylylenediamine, a first glycidyl ether reagent, a second glycidyl ether reagent and a glycidyl ester reagent through amination reaction, the alicyclic diamine contains at least one primary amine group; the first glycidyl ether reagent is ethylene glycol diglycidyl ether and / or bisphenol A type diglycidyl ether; and the second glycidyl ether reagent is 1, 4-butanediol diglycidyl ether and / or C12-14 glycidyl ether. The modified amine curing agent is combined with the curing characteristics of amide and phenolic aldehyde amine, the epoxy resin anticorrosive paint prepared from the modified amine curing agent has a proper curing speed, the adhesive force of a cured coating is high, the anticorrosive effect is good, and the epoxy resin anticorrosive paint is particularly suitable for a high-humidity environment and an underwater environment.

The invention discloses a magnetic ion exchange resin and a preparation method thereof, and the preparation method comprises the following steps: preparing a reaction solution which comprises magnetic particles, glycidyl methacrylate, divinylbenzene and a photoinitiator; the mass ratio of the glycidyl methacrylate to the divinyl benzene is (4.5-10): 1; an ultraviolet-initiated polymerization step: irradiating the reaction solution by ultraviolet light to initiate a polymerization reaction to obtain magnetic microspheres; a functional modification step: mixing the magnetic microspheres with an ammoniation reagent for ammoniation reaction to prepare ammoniated magnetic microspheres; and mixing the ammoniated magnetic microspheres with an alkylation reagent, and carrying out an alkylation reaction to prepare the magnetic ion exchange resin. According to the method, the production time is remarkably shortened, the extra energy consumption is reduced, and the process production flow is effectively simplified.

The invention discloses a harmonica-shaped tube and a preparation method thereof, a liquid cooling plate, a battery and electric equipment. The harmonica-shaped tube is made of a polyphenylene sulfide composition, and the polyphenylene sulfide composition comprises polyphenylene sulfide resin and a toughening agent; the flexibilizer includes a copolymer of an olefin and a glycidyl ester. According to the application, the polyphenylene sulfide composition is used as the material of the harmonica-shaped tube, so that the occurrence of the conditions that the extruded material is easily broken, the extrusion process is not smooth and the like in the extrusion molding process of the harmonica-shaped tube is reduced; the harmonica-shaped tube has good mechanical strength, deformation resistance, corrosion resistance, heat resistance, heat dissipation performance, creep resistance and the like, the risk that cracking occurs when the harmonica-shaped tube is extruded in the working condition using process is reduced, and the production capacity and the product quality are improved.

The invention relates to an epoxy core-shell polymer particle and resin, a preparation method of the epoxy core-shell polymer particle and resin and application of the epoxy core-shell polymer particle and resin to epoxy resin. The preparation method of the epoxy core-shell polymer particle comprises the following steps: heating and mixing a polybutadiene seed emulsion, a reducing agent, an emulsifier and the like; adding methyl methacrylate and an initiator, and glycidyl methacrylate and an initiator, and heating to react; compared with the prior art, the core-shell particle with the outer layer of the synthesized shell containing the epoxy group can be used for toughening the epoxy resin, so that the toughness of the epoxy resin is effectively improved while the excellent heat resistance and mechanical properties of the epoxy resin are maintained.

The invention relates to a biodegradable composite material as well as a preparation method and application thereof, and belongs to the technical field of compositions of high-molecular compounds. The biodegradable composite material is prepared from the following components in parts by weight: 46 to 87 parts of PBAT resin, 2 to 10 parts of PLA resin, 10 to 40 parts of calcium carbonate, 0.5 to 2 parts of a slipping aid and 0.5 to 2 parts of an edge sealing aid, the molar content of D-lactic acid in the PLA resin is greater than or equal to 2%; the particle size D50 of the calcium carbonate is less than 1.8 microns; the edge sealing auxiliary agent is an ethylene-acrylic acid copolymer, an ethylene-vinyl acetate copolymer, an ethylene-methyl acrylate copolymer, an ethylene-methyl acrylate-glycidyl methacrylate terpolymer, an ethylene-butyl acrylate copolymer, an ethylene-butyl acrylate-glycidyl methacrylate terpolymer, an ethylene-vinyl acetate copolymer, an ethylene-vinyl acetate copolymer, an ethylene-vinyl acetate copolymer, an ethylene-vinyl acetate copolymer, an ethylene-vinyl acetate copolymer, an ethylene-vinyl acetate copolymer, an ethylene-vinyl acetate copolymer and an ethylene-vinyl acetate copolymer. And at least one of epoxy resin. The biodegradable composite material has excellent long-acting edge sealing performance.

The invention relates to the technical field of gel materials, and discloses whitening gel based on biological polysaccharide and a preparation method thereof, the whitening gel comprises the following raw materials: hyaluronic acid, deionized water and thunberg fritillary bulb polysaccharide microcapsules; wherein the bulbus fritillariae thunbergii polysaccharide microcapsule is prepared by taking konjac glucomannan, chitosan and perillaldehyde modified hyaluronic acid as a shell layer and embedding bulbus fritillariae thunbergii polysaccharide and glabridin as a core material; the perillaldehyde modified hyaluronic acid is prepared by reacting alkenyl hyaluronic acid with perillaldehyde under the action of an initiator; the alkenyl hyaluronic acid is prepared by reacting hyaluronic acid with glycidyl methacrylate under the action of a catalyst. The prepared whitening gel has excellent whitening, moisturizing, anti-oxidation and anti-aging effects, effective components are not prone to loss, and the whitening gel can be applied to the skin surface for a long time, plays a whitening role and delays the aging process of the skin.

The invention relates to the field of foaming materials, in particular to a low-solvent-residue expandable polystyrene material and a preparation method thereof. The expandable polystyrene material with low solvent residue comprises the following raw materials in percentage by weight: 0.35-0.45% of a free radical initiation system, 0.35-0.45% of S, S, S, S, S, S, S, S, S, S, S, S, S, S, S According to the present invention, the material comprises, by weight, 0.1-0.15% of S, S '-bis (alpha, alpha'-dimethyl-alpha ''-acetoxy) trithiocarbonate, 0.15-0.2% of ascorbic acid, 0.1-0.2% of a nucleating agent, 0.2-0.3% of a suspending agent, 0.001-0.003% of an emulsifier, 5-6% of a foaming agent, 0.15-0.25% of a plasticizer, 0.001-0.002% of hydroxyethyl cellulose, 0.05% of sodium phosphate, 0.1-0.2% of zinc stearate, and 0.1-0.2% of glyceryl stearate, the obtained material has low solvent residue, meets food safety requirements, and is suitable for food packaging.

The invention belongs to the technical field of 3PE corrosion prevention, and particularly relates to a high-temperature-resistant and cathodic disbonding-resistant 3PE corrosion-resistant pipeline and a preparation method thereof. A pipeline epoxy bottom layer, a middle adhesive layer and a polyethylene surface layer are subjected to systematic chemical synergistic modification, specifically, the epoxy bottom layer is modified with phenolic resin and amino silane, and a heat-resistant compact barrier is formed; the middle layer reacts with maleic anhydride grafted polyethylene through amino silane to construct a chemical bridge for simultaneously connecting the upper layer and the lower layer; the surface layer is grafted with high-density polyethylene through fluoroprimary amine modified glycidyl methacrylate, and a hydrophobic and oleophobic chain and a reactive functional group are introduced; according to the structure, through the synergistic effect of the high-temperature stability of the bottom layer, the two-way chemical bridging capacity of the middle layer and the inert hydrophobic characteristic of the surface layer, the long-term use temperature upper limit, the stripping resistance and the medium infiltration resistance of the pipeline are improved, and a solution is provided for long-term protection of the pipeline in the severe environment.

The invention belongs to the technical field of high polymer materials, and particularly relates to a high-strength papermaking forming net fiber. Comprising the following raw materials in parts by weight: 75-90 parts of polyethylene glycol terephthalate, 5-15 parts of polybutylene terephthalate, 3-10 parts of a modified fiber filler, 2-5 parts of modified graphene, 2-8 parts of silicon dioxide, 0.5-2 parts of a silane coupling agent KH-560, 1-3 parts of an anti-hydrolysis agent, 0.5-1.5 parts of an antioxidant and 0.3-1 part of a lubricant. Wherein the modified fiber filler is prepared by sequentially carrying out modification processes such as silane coupling agent, citric acid-glycerol esterification, iron bismuth oxide loading and the like on glass fibers; the modified graphene is prepared by introducing dopamine, cerium ions and glycidyl methacrylate for modification. The mechanical strength, the hydrolysis resistance and the wear resistance of the fiber are remarkably improved through the synergistic effect of all the components and the melt spinning-multi-stage stretching process, and the fiber is particularly suitable for a forming net of a high-speed paper machine.

The invention relates to the technical field of coating liquid, and particularly discloses anti-reflection self-cleaning type coating liquid as well as a preparation method and application thereof. The invention provides anti-reflection self-cleaning type coating liquid. The anti-reflection self-cleaning type coating liquid is specifically prepared from, by weight, 12-18 parts of polymethyl methacrylate, 5-8 parts of composite sol, 3-6 parts of silane, 2-4 parts of inorganic materials, 1-3 parts of an anti-reflection agent and 30-40 parts of a solvent. The composite sol is obtained by carrying out water bath heat preservation reaction treatment on a natural polymer colloid and a styrene-acrylonitrile-glycidyl methacrylate copolymer through a dopamine hydrochloride aqueous solution; the inorganic material is formed by mixing silicon dioxide with the particle size of 10-30 nm and silicon dioxide with the particle size of 40-70 nm according to the weight ratio of (0.5-1.5): (5-8). The anti-reflection self-cleaning coating liquid prepared by the invention can obviously improve the light transmittance and self-cleaning property of photovoltaic glass; and the durability and the stability of the coating layer are excellent.

The invention discloses a near-infrared responsive injectable MXene / fibroin / carboxymethyl chitosan / oxidized hyaluronic acid nano composite hydrogel SCO (at) M, and relates to the technical field of biomedical materials. The method disclosed by the invention comprises the following steps: 1) preparing an MXene single-layer nanosheet by adopting LiF-HCl in-situ HF etching; (2) modifying the fibroin through glycidyl methacrylate to obtain SF-MA; 3) oxidizing hyaluronic acid with sodium periodate to obtain oxidized hyaluronic acid OHA; (4) uniformly dispersing MXene in the SF-MA solution, and sequentially adding carboxymethyl chitosan CMCS and OHA, so as to prepare the injectable nano composite soft hydrogel with the shear thinning characteristic; and 5) through ultraviolet irradiation crosslinking, rapid in-situ curing of the hydrogel is realized, and the mechanical strength of the hydrogel is improved. The hydrogel provided by the invention has excellent injectability and mechanical property, has good photo-thermal antibacterial property, oxidation resistance and cell compatibility, can be used as a carrier of cells, medicines and bioactive substances in the field of biological medicines, and has a wide application prospect.

The invention relates to the field of automobile part manufacturing, and particularly discloses a barrier layer direct bonding type TPE material for an automobile air conditioner pipeline system and a preparation method and application of the barrier layer direct bonding type TPE material. The TPE material is prepared from the following raw materials: a thermoplastic elastomer TPE, PA, EVOH, polyether block amide, a glycidyl methacrylate grafted olefin copolymer elastomer, a toughening compatilizer, composite modified montmorillonite, a cold-resistant additive, an antioxidant and paraffin oil. Wherein the composite silane coupling agent, lauric acid and N, N '-carbonyldiimidazole are adopted to modify the nano-montmorillonite, so that the dispersity of nano-montmorillonite particles is improved, the formation of aggregates is effectively reduced, and the mechanical property of the material is enhanced; the polyether block amide, the glycidyl methacrylate grafted olefin copolymer elastomer and the toughening compatilizer have a synergistic effect, so that good adhesiveness of the TPE material and the barrier layer is realized.

The invention relates to the technical field of biological nano materials, in particular to a superparamagnetic strong anion exchange magnetic bead for virus enrichment and a preparation method and application thereof. The invention discloses a superparamagnetic strong anion exchange magnetic bead for virus enrichment and a preparation method of the superparamagnetic strong anion exchange magnetic bead. According to the superparamagnetic strong anion exchange magnetic bead, polyglycidyl methacrylate magnetic microspheres serve as raw materials, firstly, a large number of amino groups are introduced through reaction of active epoxy groups and a multi-amino compound, and then abundant quaternary ammonium salt groups are introduced through reaction of amino groups and epoxy quaternary ammonium salt under the alkaline condition. Through two times of epoxy ring-opening reactions, while enough quaternary ammonium salt groups are introduced, a large number of hydrophilic hydroxyl groups are introduced to the surfaces of the magnetic microspheres, so that the hydrophilicity of the anion exchange magnetic beads is improved, and the anion exchange magnetic beads are high in enrichment efficiency and elution efficiency and good in application prospect when being applied to enrichment of viruses.

The invention relates to a plasma metabolite composition for auxiliary diagnosis of sub-clinical mastitis of dairy cows and application of the plasma metabolite composition. The plasma metabolite combination is a first combination and / or a second combination, and the first combination is composed of glyceryl monolinoleate, 2-methylthiophene, L-cystine, (S)-(+)-citramalic acid, 9-hydroxy-10, 12-octadecadienoic acid, 16-hydroxyhexadecanoic acid, tyrosine hydroxyproline, stearoyl serotonin and histamine; the first composition is composed of 4, 5-dimethyl-2, 4, 5-trimethyloxazole, 12, 13-epoxy octadecadienoic acid, 2-cyclotetradecene-1-ketone, 4 [alpha]-carboxyl-5 [alpha]-cholest-8-ene-3 [beta]-alcohol, N-arachidonyl dopamine d8, 9 (Z) and 11 (E)-conjugated linoleic acid, and the second composition is composed of 2, 5-dihydro-2, 4, 5-trimethyloxazole, 12, 13-epoxy octadecadienoic acid, 2-cyclotetradecene-1-ketone, 4 [alpha]-carboxyl-5 [alpha]-cholest-8-ene-3 [beta]-alcohol, N-arachidonyl dopamine A product prepared based on the plasma metabolite composition and used for auxiliary diagnosis of cow subclinical mastitis is simple in use method and high in accuracy, can be used for assisting a milk somatic cell number method to diagnose cow subclinical mastitis, and reduces the probability of false negative and false positive.