714 results about "Ester bond" patented technology

The invention discloses a light-moisture dual-curing underwater epoxy coating with a self-repairing function as well as a preparation method and a construction method of the light-moisture dual-curing underwater epoxy coating. The epoxy coating comprises a component A and a component B, wherein the mass ratio of the component A to the component B is (1.5-3.5): 1; the component A is prepared from the following raw materials: bisphenol F type epoxy resin, dynamic disulfide bond modified polysulfide rubber, boron nitride nanosheet and silicon carbide nanowire hybrid filler, a photoinitiator and a silane coupling agent; the component B is prepared from the following raw materials: moisture-cured polyether amine, a boric acid ester bond cross-linking agent and hydrophobic modified graphene oxide. According to the invention, a light-moisture dual-curing mechanism is adopted, ultraviolet irradiation initiates rapid surface curing, and then environmental moisture permeates to complete deep curing. The material provided by the invention has the advantages of rapid curing, excellent self-repairing function, significantly improved underwater adhesion and good thermal conductivity, and provides a new solution for rapid repairing and long-acting protection of underwater structures.

The invention discloses a cellulose coated diaphragm and a preparation method thereof in the field of lithium ion batteries, the diaphragm comprises alpha-cellulose pulp, a cellulose grafted phenylboronic acid-co-oligomeric ethylene oxide copolymer, a thermal response star zwitterionic polymer and nano aluminum oxide, and an N-methylmorpholine-N-oxide aqueous solution is adopted as a solvent system. The preparation method comprises the following steps: firstly synthesizing a cellulose grafted copolymer with dynamic borate bonds through atom transfer radical polymerization, then preparing a star polymer with thermal response arms and zwitter-ion terminals by taking cyclodextrin as a core, and finally mixing all the components to prepare coating slurry. And the composite diaphragm is prepared through the processes of coating, phase conversion, ultraviolet curing and drying. The diaphragm combines the thermal stability and lyophilic property of cellulose, forms a dynamic self-adaptive interface layer through the synergistic effect of two functional compounds, has the advantages of active safety protection, dendritic crystal inhibition, long cycle life and the like, and remarkably improves the comprehensive performance of the lithium ion battery.

The invention discloses a dynamic borate bond-based self-healing polyacrylic acid binder and a preparation method thereof. The dynamic borate bond-based self-healing polyacrylic acid binder comprises a polymer main chain and a dynamic cross-linking agent, the dynamic cross-linking agent is a polyol compound containing at least two pairs of ortho-hydroxyl groups; the polymer main chain is formed by copolymerizing the following monomers: an acrylic structural monomer, the molar fraction of which accounts for 85-94% of the total monomer; a functional monomer containing a boric acid group, wherein the molar fraction of the functional monomer accounts for 3-8% of the total monomer; the mole fraction of the flexible monomer containing the acrylate group accounts for 3-8% of the total monomer. Various stresses generated by different negative electrode materials in circulation can be effectively adapted and buffered through a network formed by dynamic boric acid ester bonds and reversible fracture and combination of the boric acid ester bonds, so that the service life of the battery is generally prolonged, the working temperature range of the battery can be remarkably widened, the low-temperature discharge capacity can be remarkably increased, and the high-temperature cycle life can be prolonged.

The invention discloses a reprocessable solid-solid phase change material based on dynamic borate bonds and a preparation method of the reprocessable solid-solid phase change material. Based on the mechanism that boric acid ester is subjected to ester exchange during thermal stimulation, a dynamic cross-linking agent containing boric acid ester is adopted for cross-linking a polyurethane prepolymer, polyethylene glycol is cross-linked through chemical bonds, the tensile strength and the elongation at break of the phase change material are improved, and the problem that the phase change material is prone to leakage in the phase change process is solved; besides, borate bonds belong to associated dynamic covalent bonds and can keep the crosslinking density of the material unchanged when ester exchange occurs under thermal stimulation, so that the thermal stability of the material is relatively good; the solid-solid phase change material disclosed by the invention is excellent in mechanical property, has a relatively high enthalpy value, can be reprocessed, and has an application prospect in the fields of thermal management, energy storage, infrared stealth and the like.

The invention discloses resin composite liquid with dual self-repairing and high ethanol solvent wiping resistance as well as a preparation method and application of the resin composite liquid, and belongs to the technical field of polyurethane emulsion coatings. Aiming at the problems that an existing waterborne polyurethane coating is poor in ethanol resistance due to residual carboxyl / hydroxyl of a hydrophilic chain extender and the self-repairing efficiency of a single dynamic bond is low, a metal ion buffer solution is added into a hydroxyl-terminated polyurethane emulsion to coordinate with the carboxyl of the hydrophilic chain extender, so that a hydrophilic group is closed, and the crosslinking density is increased; meanwhile, a boric acid compound is introduced to form dynamic boric acid ester bonds with residual hydroxyl groups of the system, and hydrophilic groups in the system are consumed while a dual self-repairing network is constructed. The coating prepared by the invention has good self-repairing and ethanol wiping resistance.

The invention provides a preparation method of a shape-adaptive hydrogel material for tissue repair. The method comprises the following steps: S1, preparing HPC (Hydroxypropyl Chitosan); s2, preparation of phenylboronic acid functional chitosan PHPC (Polyhydroxyalkanoate); s3, preparing a PHPC solution; s4, preparing a polyvinyl alcohol (PVA) solution; and S5, preparing the dynamic covalent bond hydrogel. According to the invention, a dynamic covalent bond-boric acid ester bond with stimulation response capability is introduced on the basis of common dual-network CS-PVA hydrogel; on the premise of not changing the biocompatibility and biodegradability of the original dual-network hydrogel, the hydrogel is endowed with response capability under physical and chemical stimulation, and the diversity of application scenes is expanded; the dynamic mechanical behavior changes of the PCA hydrogel at four different strain rates of 0.05 mm / s, 0.5 mm / s, 5 mm / s and 50 mm / s are explored, and the passive shape adaptability of the PCA hydrogel along with tissue growth is studied; meanwhile, changes of hydrogel creep deformation and stress relaxation caused by addition of dynamic covalent bonds are researched.

The invention discloses an anti-corrosion self-repairing super-amphiphobic coating film and a preparation method thereof, and belongs to the technical field of polymer coating materials. The coating film sequentially comprises a nano particle skeleton layer, a dynamic borate bond layer and a super-amphiphobic functional layer from inside to outside, and the three-layer gradient design synergistically realizes micro / nano structure stability, self-repairing and super-amphiphobic functions. The framework layer takes SiO2-TiO2 composite nanoparticles as a substrate and provides support; the dynamic boric acid ester bond layer forms a dynamic network through polycondensation of an organic boron compound, endows the self-repairing capability and enhances interface bonding; the super-amphiphobic functional layer is formed by grafting a fluorine-containing organosilicon compound and has hydrophobic and oleophobic properties. A multi-layer structure is constructed step by step, the reaction condition is mild, the operation is simple, the cost is low, the method is suitable for large-scale industrial preparation, the coating film has excellent super-amphiphobic performance and interface adhesion performance, the super-amphiphobic performance of the coating film can still be kept stable in long-term use or a complex environment, and the problem that an existing super-amphiphobic material is prone to damage is effectively solved.

The invention provides a polyurethane composite material and application thereof, and relates to the technical field of polyurethane materials. The polyurethane composite material consists of a component A and a component B, the component A comprises the following raw material components in parts by weight: 100 parts of polymer dihydric alcohol, 1-8 parts of a chain extender, 1-3 parts of a catalyst, 0-5 parts of a cross-linking agent, 0.1-2 parts of a carbon-based material, 1-10 parts of an anthraquinone compound and 0.5-2 parts of water; and the component B is an isocyanate curing agent and comprises a prepolymer with a plurality of ester bonds and urea bonds. The polyurethane composite material disclosed by the invention has relatively high mechanical strength, wear resistance and the like, and is suitable for treating nitrogen-containing sewage.

The invention relates to the technical field of rice bran processing, and discloses a rice bran degreasing and nutrition retention edible process synergistic treatment method which comprises the following steps: (a) in an NADES-aqueous solution medium, adding an immobilized catalyst A, and hydrolyzing ferulate bonds and phospholipids in rice bran at low temperature; (b) carrying out intermediate dehydration on the slurry obtained in the step (a) to reduce the water activity; (c) adding an immobilized catalyst B into the dehydrated slurry in the step (b), carrying out esterification reaction, and grafting free ferulic acid generated by hydrolysis to glyceride in situ; and (d) carrying out solid-liquid separation on the slurry obtained in the step (c) to obtain finished oil and finished powder. According to the method, an NADES medium is adopted to replace an organic solvent, the whole process is carried out at low temperature, degradation of heat-sensitive nutrient substances is avoided, and resource utilization of ferulic acid is achieved. The prepared functional rice bran oil is rich in feruloyl glyceride, total tocopherol and oryzanol, and is low in acid value and peroxide value.

The invention discloses an optical monomer and a preparation method thereof, a composition, a resin material and a preparation method thereof. The optical monomer provided by the invention comprises a quaternary carbon structure and a side chain connected with the quaternary carbon structure through an ester bond. The side chain comprises a thioether chain segment connected with an ester bond, an aromatic group connected with the thioether chain segment and an epoxy group connected with the thioether chain segment. The optical monomer provided by the embodiment of the invention takes a quaternary carbon structure as a core skeleton, and a side chain sequentially comprises an aromatic group, a thioether chain segment and a terminal epoxy group. A thioether structure with high polarizability and an aromatic group are introduced into the molecular design of the optical monomer, so that the refractive index and the optical transparency of a resin material are remarkably improved. And the rigidity of the epoxy aromatic ring is beneficial to improving the thermal stability and mechanical strength of the resin material. The epoxy group at the tail end can react with conventional epoxy resin to form a compact network structure, so that the stability of the resin material is improved, and the yellowing tendency is reduced.

The invention discloses a hydrogel-based helicobacter pylori killing medicine and a preparation method thereof in the technical field of biomedical materials, and the hydrogel medicine adopts a shell-core layered structure and comprises an outer layer and an inner layer; the outer layer is a high-density cross-linked polyethylene glycol diacrylate network, and cellulose nanocrystals modified by silane are dispersed in the polyethylene glycol diacrylate network; pH-sensitive Schiff base bonds and / or boric acid ester bonds are embedded in the inner layer, and an antibacterial agent is loaded on the inner layer. Structural expansion and breaking of the hydrogel are controlled through a multi-layer structure, multiple loaded antibacterial agents are released according to pH response, the influence of drug resistance is avoided through sterilization of multiple mechanisms, the preparation process and device of the hydrogel drug are integrated, the production cost is reduced, and the clinical conversion efficiency is guaranteed.

The invention discloses HA-PAS hydrogel for enhancing cartilage repair of early osteoarthritis and a preparation method of the HA-PAS hydrogel. According to the hydrogel, formylated hyaluronic acid, hydrazide modified low-methoxyl pectin and phenylboronic acid modified alginate form a ternary polysaccharide skeleton, a double-dynamic cross-linked network is formed through acylhydrazone bonds and boric acid ester bonds, and a triple network structure is formed by combining permanent cross-linking catalyzed by horse radish peroxidase. The hydrogel integrates functional components such as nano-selenium, a pulullan-strontium chelate and a mesenchymal stem cell source exosome, so that multiple effects of resisting oxidation, resisting inflammation, promoting cartilage differentiation and repairing subchondral bones are achieved. The compression modulus of the hydrogel is 0.8-1.5 MPa, and the hydrogel can be injected for in-situ gelling and MMP responsive degradation, shows an excellent cartilage repair effect in animal experiments, and provides a new solution for treatment of early osteoarthritis.

The application belongs to the technical field of deep eutectic solvents, and particularly relates to a ternary deep eutectic solvent and preparation and application thereof. The ternary deep eutectic solvent is composed of choline chloride, 5-sulfosalicylic acid and gamma valerolactone according to a molar ratio of 1:4:(3-25). The strong hydrogen bond network structure between the green solvent system first destroys the ester bond between lignin and hemicellulose, then cuts off the beta-O-4 bond between lignin molecules, so as to separate lignin. Meanwhile, the deep eutectic solvent can improve the stability of carbon cations due to the conjugation effect between the lone pair electrons on the heteroatom oxygen and the central carbon in the molecular structure of gamma valerolactone, so as to inhibit the condensation reaction of lignin.

The invention discloses a bio-based recoverable high-thermal-conductivity dynamic ordered network composite material and a preparation method thereof, and is characterized in that the material takes a bio-based multifunctional epoxy system and a carboxylic acid compound containing disulfide bonds as reaction monomers, and the reaction monomers are reacted under the conditions of high temperature and metal salt catalyzed epoxy-carboxylic acid esterification reaction to obtain the bio-based recoverable high-thermal-conductivity dynamic ordered network composite material. A dynamic ordered network structure simultaneously containing disulfide bonds and beta-hydroxyl ester bonds is constructed, and the dynamic ordered network can be used as a springboard for phonon transmission, serves as an efficient'thermal bridge ', and plays a role similar to an ordered'crystal domain', so that higher heat-conducting property is shown when heat-conducting filler is not introduced, high flexibility and intrinsic heat conduction are realized, and the service life of the material is prolonged. And the material is endowed with reprocessing and recycling characteristics. Due to the synergistic existence of carboxyl, hydroxyl generated by epoxy ring opening and metal coordination in the system, and in combination with electrostatic interaction, Van der Waals force and hydrophobic interaction, the material has the adhesion characteristic suitable for a thermal interface at the same time.

The invention discloses a photosensitive polyimide, a negative photoresist and an application of the photosensitive polyimide in preparation of a film, the structure of the photosensitive polyimide is shown in the specification, X is a tetravalent organic group and is a residue X of a polyimide polymerization monomer tetracarboxylic dianhydride; y is a divalent organic group and is a residue Y of a polyimide polymerization monomer diamine; r1 and R2 are monovalent organic groups and are residues of primary alcohol forming side chain ester bonds of side chain polyamic acid ester; side chains R1 and R2 at least contain tertiary amine structures, and at least one of the side chains R1 and R2 containing the tertiary amine structures can form ammonium salt with phosphate containing an allyl structure; and n is an integer from 2 to 150. The invention provides a photosensitive polyimide which can be developed by adopting an alkaline aqueous solution, can be cured at low temperature and can form a negative pattern, a preparation method of a photoresist composition of the photosensitive polyimide, and a photoetching curing film, which can be applied to display industry or semiconductor industry as an insulating layer, a passivation layer or an interlayer dielectric layer and the like.

The invention discloses a degradable solid insulating material for a transformer. The degradable solid insulating material comprises the following raw materials in percentage by mass: 43-58% of bio-based epoxy resin; 3%-6% of polyethylene glycol; 25%-35% of a functional filler; 5%-10% of degradable reinforced fibers; 3%-8% of a degradation triggering auxiliary agent; 1%-3% of a degradation agent; the invention relates to the technical field of electrical insulation. According to the degradable solid insulating material for the transformer, natural degradation is achieved through hydrolyzable ester bonds of the bio-based epoxy resin in cooperation with the polylactic acid microspheres, the solid waste amount is reduced, meanwhile, degradation products are fatty acid and polysaccharide substances, the environmental safety standard is guaranteed, and through the synergistic effect of the modified calcined kaolin and the boron nitride nanosheets, the breakdown strength is improved; the insulation requirement is met, meanwhile, the heat conduction efficiency can be improved, the dielectric loss is reduced by filling micropores with nano silicon micro powder, and the density of the material is effectively reduced while the bending strength of the material is improved through alkali treatment of linen fibers.

The invention relates to a preparation method and application of dynamic borate bond hydrogel loaded with adriamycin and an alphaOX40 antibody, and belongs to the technical field of tumors. According to the invention, the dynamic borate bond hydrogel loaded with adriamycin and an alphaOX40 antibody is prepared, and the hydrogel is constructed on the basis of dynamic crosslinking of phenylboronic acid modified hyaluronic acid (HA-PBA) and tannic acid (TA) through a borate bond, and has excellent tissue adhesion and programmed drug release characteristics.

The invention discloses a gallium-based liquid metal conductive hydrogel and a preparation method and application thereof.The method includes the steps that firstly, liquid metal gallium is modified through an amphiphilic block copolymer, so that the liquid metal gallium can be stably dispersed in a hydrogel precursor solution, hydroxyl radicals are generated through the liquid metal gallium, and the hydrogel precursor solution is formed; in-situ polymerization of an ionic liquid monomer and an acrylic acid monomer is further initiated to form a second network in the dual-network hydrogel, and the second network cooperates with a borate bond cross-linked polyvinyl alcohol first network to prepare the liquid metal-based conductive hydrogel with excellent conductivity, good mechanical properties and relatively strong interface adhesion. The problems that existing conductive hydrogel is poor in conductive filler compatibility, poor in liquid metal interface stability and the like are solved.

The invention discloses a cationic lipid capable of being ionized and application of the cationic lipid. According to the ionizable cationic grease, adsorption is formed by the structural design of the head and biological drugs such as nucleic acid, and the encapsulation efficiency is improved; the tail part adopts a saturated or unsaturated aliphatic chain to form a branch structure, and the head part and the tail part are connected by an ester bond, so that in-vivo degradation is facilitated to reduce toxicity; due to the design of the unsaturated aliphatic chain, the membrane flowability during release of the endosome is improved, and the release efficiency of the biological medicine is effectively improved; moreover, the ionizable cationic grease provided by the invention has good temperature stability, not only can the product quality be improved, but also the accessibility of the product is expanded. In a word, the ionizable cationic lipid disclosed by the invention has the advantages of high encapsulation efficiency, low toxicity, high endosome release efficiency, good temperature stability and the like, the quality and the treatment effect of lipid nanoparticle drugs can be improved, and a new scheme and a new choice are provided for biological drug delivery.

The invention discloses modified cellulose nanofiber reinforced bi-crosslinking immunoregulation hydrogel as well as a preparation method and application thereof, and belongs to the technical field of biological materials and biomedical engineering. Oxidized sodium alginate and dopamine grafted gelatin are adopted to prepare a main body of the composite hydrogel, aldehyde groups on the oxidized sodium alginate and amino groups on the gelatin can form Schiff base bonds, and borax, the oxidized sodium alginate and vicinal diol structures on modified cellulose nanofibers can form boric acid ester bonds. The double-crosslinking structure enhances the mechanical property of the hydrogel. The borate bond and the Schiff base bond are both dynamic chemical bonds and can respond to pH change, so that the hydrogel is endowed with self-healing performance and pH-responsive drug release ability, the hydrogel can quickly release liposome with an anti-inflammatory function in an acidic inflammatory environment in the early stage of cartilage injury, and the hydrogel recovers to an original state after fracture caused by joint movement. And the overall stability of the hydrogel is ensured by the double-crosslinking structure.

The invention relates to the technical field of surface treatment, in particular to a bio-based degradable cable material and a preparation method thereof. The bio-based degradable cable material is prepared from 55 to 65 parts of matrix resin mixed by poly L-lactic acid and poly-3-hydroxybutyrate-3-hydroxyhexanoate, 4 to 6 parts of dianhydride modified castor oil polyol, 10 to 15 parts of polypentamethylene diamine adipate, 5 to 8 parts of nano reinforcing filler, 6 to 10 parts of bio-based plasticizer, 0.5 to 1.0 part of antioxidant and 8 to 12 parts of environment-friendly flame retardant. A dynamic ester bond cross-linked network formed by the reaction of a dynamic ester bond cross-linking agent dianhydride modified castor oil polyol only undergoes ester bond breakage at a high temperature exceeding a normal working range to release stress, and the temperature returns to normal and can be recombined; the semi-interpenetrating network reinforced phase poly (pentamethylene diamine adipate) and the matrix resin form an interpenetrating structure in a molecular chain interpenetrating manner, a stable heat-resistant skeleton is constructed, high-temperature deformation is effectively inhibited, the overall degradability of the material is ensured by the bio-based structure, and the balance of heat resistance and degradability is realized.

The invention provides a high-elasticity tear-resistant silicone rubber material and a preparation method thereof.The high-elasticity tear-resistant silicone rubber material is characterized by being prepared from, by mass, 100 parts of vinyl polysiloxane, 5-15 parts of phenylboronic acid end group modified polydimethylsiloxane and 1-5 parts of 2, 3-dihydroxypropyl disulfide, the adhesive comprises the following components in parts by mass: 10-30 parts of fumed silica, 1-5 parts of a cross-linking agent, 1-2 parts of a plasticizer and 0.001-0.005 part of a catalyst. By introducing the combination of phenylboronic acid end group modified polydimethylsiloxane and 2, 3-dihydroxypropyl disulfide, a dual dynamic covalent bond network with a stress triggering characteristic is constructed in a silicone rubber system, and when the material is subjected to external force, a disulfide bond is used as a sacrificial unit to preferentially break to dissipate energy and generate micro-voids, so that the stress triggering performance of the material is improved. And then stress-triggered boric acid ester bond dynamic recombination further disperses stress and stabilizes a micro-cavity structure, so that graded dissipation of energy is realized, crack propagation is reduced, and the elasticity and tear resistance of the material are improved.

The invention discloses a preparation process of polyether-ether-ketone, and relates to the technical field of preparation of inorganic compounds. The preparation process comprises the following steps: reacting 4, 4 '-difluorobenzophenone, sodium carbonate and hydroquinone to generate polyether-ether-ketone, taking a polyaryletherketone block oligomer as an end-capping reagent, reacting 4, 4'-difluorobenzophenone with 4, 4 '-dimercaptodiphenyl sulfone, and then reacting with pentaerythritol phosphate to obtain the polyaryletherketone block oligomer. The thioester bond reversibly breaks at the polymerization temperature, exposed active sulfenyl reacts with hydroxyl at the tail end of the polyether-ether-ketone to form a more stable covalent bond, volatilization of the end-capping reagent is avoided, meanwhile, the initial decomposition temperature of the end-capped polyether-ether-ketone is increased, and the stability of the end-capping reagent is improved. The polyether-ether-ketone generated in the polyether-ether-ketone resin product is subjected to treatment procedures of crushing, organic solvent extraction, water washing, filtering, drying and the like, so that the product polyether-ether-ketone is obtained, less three wastes are generated, the solvent can be recycled, the atom economy is relatively high, and the preparation process of comprehensive utilization of resources is realized.

The invention belongs to the technical field of polyurethane, and particularly relates to bio-based flame-retardant polyurethane polystyrene foam. The bio-based flame-retardant polyurethane polystyrene foam is prepared from the following raw materials in parts by weight: 60 to 75 parts of amino acid-based modified polyether polyol; 25-40 parts of a nitrogen and phosphorus-containing hydroxyl-terminated modified polymer; 380 to 440 parts of modified isocyanate; 100 to 130 parts of chlorinated paraffin; 40 to 60 parts of filler; 8-10 parts of silicone oil; 80 to 100 parts of a propellant; and 3-5 parts of a catalyst. Bio-based raw materials such as castor oil and amino acid are introduced into the molecular structure of the polyurethane polystyrene foam through chemical modification, so that the biodegradability of the material is improved; a proper polymeric monomer is screened, and a flame-retardant element chlorine is introduced into a polyether molecular structure through chemical polymerization and forms multi-element synergy with nitrogen and phosphorus elements bridged through ester bonds, so that the content of the flame-retardant element in the polystyrene foam material is effectively increased, and the flame retardance is improved.

The invention discloses a preparation method of a self-crosslinking hyaluronic acid microsphere without an exogenous crosslinking agent, which comprises the following steps: activating carboxyl on hyaluronic acid only by using an activator with good biocompatibility, carrying out esterification reaction on the activated carboxyl and hydroxyl on the hyaluronic acid, and curing and crosslinking water-in-oil emulsion at room temperature by continuously stirring to obtain the self-crosslinking hyaluronic acid microsphere without the exogenous crosslinking agent. The self-crosslinking hyaluronic acid microspheres are formed. As an exogenous cross-linking agent is not introduced, hyaluronic acid forms an ester bond through self-crosslinking after being activated instead of forming an amido bond with the exogenous cross-linking agent, and the formation of the ester bond can effectively improve the storage modulus of the hyaluronic acid microspheres. Compared with a commercially available sieved gel product, the self-crosslinked hyaluronic acid microsphere disclosed by the invention has the advantages that the crosslinking degree is higher, the immunogenicity risk of free HA is reduced, the self-crosslinked hyaluronic acid microsphere is suitable for deep or subcutaneous injection of dermis, and a more uniform three-dimensional support is provided.

The invention discloses a temperature-sensitive self-repairing expandable epoxy resin material and a preparation method thereof. The temperature-sensitive self-repairing expandable epoxy resin material is prepared from the following components: 1) epoxy resin; 2) a curing agent containing a dynamic covalent bond, wherein the dynamic covalent bond is selected from a disulfide bond and an ester bond; 3) a catalyst; the porous material is used for regulating and controlling the expansion performance; the epoxy resin and the curing agent are subjected to cross-linking reaction under the action of the catalyst to form a three-dimensional network structure, so that the epoxy resin material has self-repairing performance, and meanwhile, the epoxy resin material has expansion performance through a solid-state composite foaming method and a hot compression mode. According to the invention, the dynamic covalent bond is added, so that the cured epoxy resin material can be self-repaired at 40-100 DEG C, the repair efficiency is 90% or more, meanwhile, a micromolecule ethylene glycol solution is added at high temperature, the epoxy resin material can be degraded and recycled, the utilization rate of the material is greatly improved, and after the porous material is added, the expansion rate can reach 0-80% through a solid composite foaming method.

The invention discloses foamed 3D printing elastomer photosensitive resin and a preparation method, and relates to the technical field of additive manufacturing materials. The thermal-expansion polyurethane acrylate composite material is prepared from the following materials in parts: 400 to 700 parts of a polyurethane acrylate oligomer containing dynamic oxime ester bonds and acrylate groups, 200 to 500 parts of a reactive diluent, 50 to 200 parts of thermal-expansion microspheres, 10 to 50 parts of a photoinitiator and 1 to 50 parts of a stability auxiliary agent, the polyurethane acrylate oligomer containing the dynamic oxime ester bond and the acrylate group is prepared by reacting isocyanate, polyol, a compound containing oxime hydroxyl and an acrylate end-capping reagent. According to the 3D printing elastomer photosensitive resin and the preparation method thereof, by introducing dynamic oxime ester bonds, controllable foaming of the material in the heat treatment process is achieved, the technical bottleneck that traditional light-cured resin is large in foaming difficulty is broken through, the material is endowed with the excellent lightweight characteristic through design, good mechanical performance and heat stability are kept, and the 3D printing elastomer photosensitive resin is suitable for 3D printing. The high requirement on the material performance is met.

The present disclosure relates to an adhesive containing a polyester (A) satisfying the following requirements (1) to (4): (1) the polyester (A) has a structural site derived from a polyvalent carboxylic acid (a1) and a structural site derived from a polyhydric alcohol (a2); (2) the polyester (A) has an ester bond concentration of 10.00 mmol / g or less; (3) the polyester (A) has a melting point of 30° C. or higher; and (4) the polyester (A) has a mass-average molecular weight of 25000 or more.

The object of the present invention is to provide a novel ascorbic acid derivative with excellent stability, and its applications. [Solution] A compound (compound of general formula (1) below) is used, in which a phosphocholine group is introduced to the hydroxyl group at the 2 position of ascorbic acid via a phosphate ester bond. The ascorbic acid derivative of the present invention has excellent whitening and antioxidant properties, and is also highly stable. Therefore, the ascorbic acid derivative of the present invention can be preferably used as an active ingredient in cosmetics and topical skin preparations. TIFF2026055124000012.tif39101

The invention discloses a high specific surface area polyester fiber and a preparation method thereof, polybutylene terephthalate, polyethylene glycol and an antioxidant are put into a twin-screw extruder in proportion to obtain modified polyethylene glycol, the modified polyethylene glycol is used as a sea phase, the modified polyethylene glycol and PET are used as an island phase to carry out melt blending spinning, and after heat setting, drafting is carried out to obtain a sea-island fiber with PET as the island phase. An alkali dissolution-alcohol dissolution synergistic effect system is constructed by utilizing the alkali dissolution characteristic of low-molecular-weight polybutylene terephthalate and the alcohol dissolution characteristic of polyethylene glycol in the marine phase component, under the condition of 50-60 DEG C, an alkali agent directionally breaks ester bonds of polybutylene terephthalate, an alcohol solvent synchronously dissolves polyethylene glycol, efficient marine phase stripping is achieved, and the service life of the marine phase component is prolonged. And finally, the high-specific-surface-area polyester fiber with a complete structure and an excellent specific surface area is prepared.