1365 results about "Imine" patented technology

The invention relates to the technical field of biochemical engineering, in particular to a method for preparing chiral alpha-trifluoromethyl alcohol by using imine reductase AtRedAm, trifluoromethyl ketone is reduced into corresponding chiral trifluoromethyl alcohol at an excellent conversion rate by using the imine reductase AtRedAm, and enantioselectivity is high. The reaction depends on an NADPH (Nicotinamide Adenine Dinucleotide Phosphate) coenzyme circulation system, 10% dimethyl sulfoxide is used as a reaction cosolvent, the reaction is carried out in a 100mM (pH = 7.5) phosphate buffer solution for 16 hours, the highest molar conversion rate reaches 99%, and the highest optical purity reaches 95%.

The invention discloses a preparation method of a 3-micron ultrathin lithium battery copper foil. The preparation method comprises the following steps: preparing a copper sulfate electrolyte; a wetting agent, a brightening agent and a high resistance agent are added into the copper sulfate electrolyte, the high resistance agent is at least one of thiazolidinethione, polyethyleneimine, 2-mercaptobenzimidazole and ethylene thiourea, and a mixed additive is formed; polishing and grinding a cathode roller by adopting a flying wing wheel, and carrying out electrolytic treatment on the mixed additive through the polished and ground cathode roller to obtain a first-stage copper foil; and the first-stage copper foil is placed in a nitrogen furnace to be subjected to annealing treatment, and the 3-micron ultrathin lithium battery copper foil is obtained. The invention aims to solve the technical problems that in the prior art, edge tearing, foil breaking, warping, dark appearance oxidation and the like are prone to occurring in the production process of the ultrathin copper foil, the tensile strength and the ductility are difficult to consider at the same time, and stable mass production of the 3-micron copper foil is still difficult.

The invention discloses an omariglitazone intermediate as well as a synthesis method and application thereof, and belongs to the technical field of pharmaceutical chemistry synthesis. The invention provides a synthesis method of an omarigliflozin intermediate and application of the intermediate in synthesis of omarigliflozin. The key of the synthesis method provided by the invention lies in the deprotection process of polycyclic indole amide, nitrile groups are not hydrolyzed, indole carboxylic acid is generated with high selectivity, molecular lactamization is avoided in the condensation process with polycyclic imine B, and expensive amidation reagents such as HATU are not needed in the process, so that the synthesis method is simple and easy to implement. And the purpose of preparing omariglitazone with low cost and high yield is achieved. The synthesis method has the advantages of easily available raw materials, mild reaction conditions, small side reaction influence, simplicity and convenience in operation and high yield, improves the yield, is easy to purify, and is suitable for industrial production of omariglitazone.

The invention relates to a particulate composition comprising, or substantially consisting of, urea, an inhibitor, preferably a urease inhibitor and / or a nitrification inhibitor, and an additive, wherein the additive comprises components (i), (ii), and optionally (iii): (i) one or more polyhydric alcohols; preferably one or more carbohydrates, preferably selected from monosaccharides, disaccharides, and oligosaccharides; (ii) a first polymer, preferably an amine-containing polymer; more preferably a polyvinylamine or a polyalkyleneimine; and (ii) optionally, a second polymer, preferably a polar polymer; more preferably a water-soluble polar polymer. The invention further relates to a process for producing the particulate composition, an additive for a particulate composition, and the use of the particulate composition as a fertilizer.

The present invention relates to a process for producing a chiral aromatic amine, said process comprising the steps of: a) providing an aromatic imine, and b) contacting said aromatic imine from step a) with an imine reductase, thereby stereoselectively reducing said aromatic imine to a chiral aromatic amine with said imine reductase; and to novel imine reductases capable of catalytic reactions.

The invention belongs to the technical field of membrane separation, and particularly relates to a method for preparing a high-flux hollow fiber nanofiltration membrane based on interfacial polymerization, the obtained membrane and application. The method comprises the following steps: firstly, carrying out pre-adsorption treatment on a polyethersulfone hollow fiber ultrafiltration base membrane through a polyethyleneimine aqueous solution to form a reactive anchoring layer; then sequentially dipping in an aqueous phase solution containing piperazine, sodium phytate and nanoscale cellulose whiskers and an organic phase solution containing trimesoyl chloride and 5-isocyanate isopeptide acyl chloride for interfacial polymerization; and finally, carrying out heat treatment on the obtained primary composite membrane, and completing a gas-phase cross-linking reaction in a glutaraldehyde steam atmosphere. According to the method, the hollow fiber nanofiltration membrane with high flux, high selectivity, excellent chlorine resistance and pollution resistance is successfully prepared through a multi-stage strengthening process, and the hollow fiber nanofiltration membrane is suitable for the fields of drinking water purification, industrial wastewater reuse, material separation and the like.

The invention discloses application of sulfur quantum dot nanoparticles to improvement of plant waterlogging resistance. The invention provides sulfur quantum dot nanoparticles PEI-SQDs prepared from sulfur, sodium hydroxide, polyethylene glycol and polyethyleneimine. The sulfur quantum dot nanoparticles PEI-SQDs are simple in synthesis method, small in particle size, low in toxicity, low in price, simple to prepare, suitable for large-scale production, good in water solubility and good in biocompatibility; the compound has the capacity of removing active oxygen and ethylene in vitro, and can remove excessive active oxygen and ethylene in plants with waterlogging stress, relieve short-term waterlogging stress suffered by crops and recover growth and development of the crops when being applied to the plants with waterlogging stress; further, long-term waterflooding stress on the crops can be relieved, and the yield of the crops is increased; and the sulfur quantum dot nanoparticles are simple and convenient in use method and obvious in action effect.

The application relates to the technical field of packaging films, and discloses an antistatic plastic packaging film and a preparation process.The antistatic plastic packaging film comprises 100 parts by weight of polyethylene, 1-6 parts by weight of phenolic resin polyaniline antistatic agent and 0.2-0.3 parts by weight of an antioxidant.The dodecyl succinic anhydride esterified phenolic resin contains carboxyl groups, can be used as a protonic acid, is doped into polyaniline through an in-situ polymerization reaction, makes imine nitrogen atoms of the polyaniline protonate, forms a charged excited state polaron, and thus the conductivity of the polyaniline is improved, the resistance of the polyethylene is reduced, and the antistatic performance of the packaging film is improved.The dodecyl succinic anhydride esterified phenolic resin and the doped polyaniline have good compatibility with the polyethylene, have a certain reinforcing effect on the polyethylene, and make the film material have higher tensile strength and elongation at break.

The invention belongs to the technical field of high polymer materials, and particularly discloses a lignin-based charring agent containing silicon and nitrogen flame-retardant elements and an imine structure for flame-retardant polylactic acid and a preparation method of the lignin-based charring agent. The flame-retardant polylactic acid is prepared from the following components in parts by weight: 90 to 97 parts of polylactic acid, 1 to 3.33 parts of lignin-based charring agent and 2 to 6.67 parts of ammonium polyphosphate. The bio-based charring agent disclosed by the invention contains silicon and nitrogen flame-retardant elements and an imine structure, has remarkable charring and flame-retardant effects, is high in charring capacity, and can endow the PLA with relatively good flame-retardant property by compounding with ammonium polyphosphate and adding 1% of the lignin-based charring agent; the lignin and vanillin which are used as main raw materials for synthesizing the charring agent are bio-based sources and are easy to obtain, the production process is simple, industrial production is easy, the preparation process is non-toxic and environment-friendly, the dependence of charring agent synthesis on petroleum-based raw materials can be effectively relieved, and the sustainable development trend of materials is met.

The invention discloses a modified microfiltration membrane for enriching biological particles and a preparation method and application thereof, and belongs to the technical field of biological separation.The preparation method of the modified microfiltration membrane comprises the following steps that a mixed cellulose ester microfiltration membrane is provided and subjected to alkali liquor activating treatment; placing the activated membrane in a weakly alkaline buffer solution for balancing; the preparation method comprises the following steps: in a weakly alkaline buffer solution, firstly contacting the surface of the membrane with a tannic acid solution to carry out a first reaction, and then directly adding a polyethyleneimine solution to carry out a second reaction under the condition of not replacing a system, so as to form a phenol-amine cross-linked network on the surface of the membrane in situ; sodium cyanoborohydride is continuously added for reduction stabilization treatment, and the modified microporous filter membrane is obtained. The modified microporous filter membrane prepared by modifying the microporous filter membrane with tannic acid and polyethyleneimine can realize one-step synchronous enrichment of all negatively charged targets, and the problems of target loss, efficiency loss and the like caused by a multi-step process are avoided from the source.

The invention relates to a selective nanofiltration membrane as well as a preparation method and application thereof. The selective nanofiltration membrane comprises a support layer and a separation layer, the separation layer is obtained through interfacial polymerization of an oil-phase reactant and a water-phase reactant; the water-phase reactant comprises a negatively charged monomer and a positively charged monomer; the positively charged monomer comprises any one or a combination of at least two of polyvinylamine, polyethyleneimine, diethylenetriamine, water-soluble chitosan, quaternized polyethyleneimine, polyallylamine or triethylene tetramine. According to the method, monomers with different charges are added into a water phase, so that the nanofiltration membrane is wholly charged and neutral, the interception of sodium sulfate can be effectively reduced, the interception of antibiotics is increased, and the separation of the antibiotics and inorganic salts can be efficiently promoted.

The invention belongs to the technical field of organic light-emitting materials, and particularly relates to a carborane derivative as well as a preparation method and application thereof. According to the invention, carborane with great application potential is combined with an imine structure which is widely applied to obtain a series of novel carborane imine compounds, so that the blank of carborane ketimine is filled, and the preparation method of the carborane imine compounds is obtained by research; nested carborane formed after boron removal of the compound has a good fluorescent effect and is expected to be used in the technical field of organic light-emitting materials.

The application discloses a kind of corrosion and scale integrated fracturing fluid, and relates to fracturing fluid technical field.The fracturing fluid includes thickening agent, crosslinking agent, composite corrosion and scale inhibitor and water;The composite corrosion and scale inhibitor includes the first component and the second component with mass ratio of 3:0.5~1, wherein the first component is prepared by the reaction of polyethyleneimine, long-chain acrylate monomer, acrylic acid monomer and hydroxyethyl acrylate monomer, and the second component is prepared by imidazole compound containing a primary amine and glyoxylic acid.The corrosion and scale integrated fracturing fluid of the application has good compatibility between components, and at the same time, it has good corrosion and scale inhibition and anti-sloughing performance.

The invention relates to the technical field of enzyme engineering, and particularly discloses a preparation method of immobilized sucrose phosphorylase (SPase) with low cost and high stability. According to the method, epoxy resin is synergistically modified through gallic acid (GA) and a polyethyleneimine-chitosan copolymer (PEI-CS), a covalent bond-hydrogen bond-ionic bond ternary cross-linked network is formed, and efficient immobilization of SPase is achieved. The preparation method comprises the following steps: preparation of a PEI-CS copolymer, preparation of a GA-PEI-CS modification liquid, modification treatment of epoxy resin, immobilization of SPase and determination of enzyme activity. The prepared immobilized enzyme has high enzyme activity retention rate (96.5%), wide temperature and wide pH stability (high activity is kept at 60 DEG C and pH 4.0-10.0), long reuse life (82.1% of enzyme activity is kept after 50 times of reuse) and low cost (26.7 yuan / kg), and can be widely applied to the fields of food industry, cosmetic industry and biological pharmacy.

The invention provides a visible light photocatalytic hydrogen production material based on a D-pi-A type PTA-TFPTA imine bond COF as well as a preparation method and application of the visible light photocatalytic hydrogen production material, belongs to the technical field of functional material technologies and photocatalytic hydrogen production, and is used for solving the problem that a covalent organic framework material is generally insufficient in catalytic activity in the photocatalytic hydrogen production process. The material is prepared by mixing and reacting 2, 5, 8, 11-tetra (4-aminophenyl) perylene and an electron-deficient monomer; during application, the material is mixed with a sacrificial agent and a cocatalyst, and photocatalytic hydrogen production can be realized under visible light irradiation. The preparation process is simple and convenient, does not need complex equipment and harsh conditions, and is easy for large-scale production; the obtained material is good in crystallinity, excellent in visible light absorption performance and outstanding in photocatalytic hydrogen production activity.

The invention relates to fluorine-free polyimide containing hydrophobic groups and a preparation method thereof, and belongs to the field of novel high-performance polyimide materials. The fluorine-free polyimide containing the hydrophobic group has a repeating unit structure shown in a general formula (I) and is obtained by polymerizing a fluorine-free diamine monomer containing the hydrophobic group and having a structure shown in a general formula (II) with specific diamine and dianhydride monomers. The fluorine-free polyimide containing the hydrophobic group has relatively low water absorption rate, has a low dielectric constant and a low loss factor at high frequency, has excellent solubility and thermal stability, can meet the performance requirements of a high-frequency and high-speed circuit on a substrate material, and has a wide application prospect. The material can be used as an excellent fluoride-free insulating base material in the fields of super-large-scale integrated circuits, photosensitive polyamideimide and the like.

The invention relates to degradable self-repairing epoxy resin based on adjustable performance of dual dynamic covalent bonds and preparation and application of the degradable self-repairing epoxy resin. Firstly, two dynamic bond curing agents (a hindered urea bond and an imine bond) are prepared respectively, and an epoxy monomer bisphenol A diglycidyl ether, the two curing agents and a cross-linking agent 4, 4 '-diphenyl-1, 3-pentanediol diglycidyl ether are mixed to prepare a mixture; the preparation method comprises the following steps: mixing 4, 4 '-diaminodiphenylmethane according to the proportion of each dynamic bond, stirring and reacting at 70-80 DEG C for 30-60 minutes, and carrying out vacuum defoaming; and finally, pouring the mixture into a mold, and molding through a gradient curing process. Compared with the prior art, two different dynamic bond curing agents are utilized to construct a double-dynamic epoxy cross-linked network, so that the obtained material has excellent performance and degradable self-repairing capability, and a high-performance solution capable of repairing, degrading and prolonging the service cycle is provided for the field of electrical insulation.

The invention provides an intrinsic flame-retardant epoxy resin composition containing nitrogen and phosphorus elements and a preparation method of the intrinsic flame-retardant epoxy resin composition, and belongs to the technical field of high polymer materials. The intrinsic flame-retardant epoxy resin composition containing nitrogen and phosphorus elements comprises the following components in parts by weight: 1-2 parts of a mixed component C which is obtained by mixing a polyethyleneimine aqueous solution and a phytic acid aqueous solution; 1-16 parts by weight of bisphenol A type epoxy resin; and 0.01-1 part by weight of an anhydride curing agent. According to the composition, two flame-retardant elements, namely nitrogen and phosphorus, are simultaneously introduced into the epoxy resin, so that the mechanical property and the processing adaptability of the material can be considered while efficient flame retardance is realized.

The invention belongs to the field of electronic device protective coatings, and particularly relates to a water-based polyimide / POSS-GO composite coating and a preparation method and application thereof.The method comprises the steps that firstly, dianhydride and diamine monomers react to prepare polyamic acid, then tertiary amine is made into a salt agent to prepare water-soluble polyamic acid salt, and then the water-soluble polyamic acid salt is prepared into a water-soluble polyimide / POSS-GO composite coating; the preparation method comprises the following steps: modifying graphene oxide with aminated polyhedral oligomeric silsesquioxane to prepare a POSS-GO filler, uniformly dispersing the filler and water-based polyamic acid salt, spraying on the surface of a base material, and then carrying out thermal imidization treatment to prepare the water-based polyimide / POSS-GO composite coating. The composite coating prepared by the method is a novel coating material with excellent corrosion resistance and low dielectric property, not only provides a new thought for the design of a high-performance anticorrosive coating, but also provides a potential material strategy for a multifunctional protective coating of an electronic device.

A resin for grayscale digital light processing 3D printing includes a donor moiety, an acceptor moiety, a rigid moiety, a photoinitiator, and a photoabsorber. The donor moiety is an acrylate monomer with a side group of a free carbonyl, a primary amine on an acrylate, a secondary amine on an acrylate, and / or a tertiary amine on an acrylate. The acceptor moiety is different than the donor moiety and is an acrylate monomer with a side group of a free hydroxy, a primary amine, secondary amine, and / or an imine. And the rigid moiety is acrylate monomer with a side group of a cyclohexyl, a substituted cyclohexyl, or a bicyclic structure. A monolithic structure formed from the resin using grayscale digital light processing 3D printing can have a Young's modulus ranging from 0.1 MPa to 100 MPa.

The invention discloses a low dimer modified isocyanate composition and a preparation method thereof. The content of dimers in the modified isocyanate is reduced to 0.9 wt% or below mainly by controlling the reaction temperature of carbodiimide, the cooling rate after the reaction and the curing temperature. Through the method, the storage time of the modified isocyanate can be prolonged, and the stability of the modified isocyanate product is improved.

The invention relates to a polyimide composite film for realizing high-dispersion carbon nanotubes through chemical anchoring and a preparation method of the polyimide composite film, which are used for solving the problems that carbon nanotubes in the existing carbon nanotube / polyimide composite material are easy to agglomerate, poor in interfacial compatibility and low in grafting efficiency. The preparation method comprises the following steps: S1, ultrasonically dispersing aminated carbon nanotubes in anhydrous dimethylacetamide to obtain a stable dispersion liquid; s2, slowly dropwise adding pyromellitic dianhydride into the stable dispersion liquid under an ice bath condition, and enabling the pyromellitic dianhydride to react with the aminated carbon nanotubes under the assistance of triethylamine to form anchor points; s3, adding a diamine monomer 4, 4 '-diaminodiphenyl ether, and gradually adding the residual pyromellitic dianhydride to carry out in-situ polymerization; and S4, preparing a wet film by adopting a curtain coating or spin coating method, and carrying out step-by-step thermal imidization at 80-300 DEG C to obtain the covalent composite film. Controllable covalent connection of the carbon nanotubes and pure polyimide chain segments can be achieved on the molecular level, and therefore the composite film with excellent heat conductivity, electromagnetic shielding performance and mechanical performance is obtained.

The invention relates to the technical field of membrane material preparation, and particularly discloses an oil-water separation membrane and a preparation method thereof.The oil-water separation membrane is characterized in that polyethyleneimine is grafted to zeolite powder under the action of a cross-linking agent epichlorohydrin, and a large number of amido groups on a polyethyleneimine chain can serve as effective chelating coordination sites of metal ions in subsequent steps; meanwhile, polyethyleneimine has excellent hydrophilic performance and is grafted on the zeolite powder, so that the hydrophilic performance of the zeolite powder is improved; then, three metal salts of magnesium, aluminum and cerium are compounded with urea on the surface of the PEI grafted zeolite through a hydrothermal reaction to generate a composite metal hydroxide structure, Mg and Al form a basic framework of a layered double-metal hydroxide structure, oxygen vacancy defects can be easily formed by doping Ce, and the defects can adsorb water molecules, so that a stable hydration layer is formed on the surface of the material, and the surface of the material is protected; the excellent super-hydrophilicity is shown.

The invention discloses a bimetallic asymmetric reduction Schiff base catalyst for synthesizing ethylene carbonate and a preparation method of the bimetallic asymmetric reduction Schiff base catalyst. According to the catalyst, a diamine compound is subjected to selective single-side protection, the imine reduction position is controlled, and a bimetallic active center is introduced; the controllable synthesis of a product for reducing the outer side imine and a product for reducing the inner side imine is realized; the obtained product is recrystallized to obtain a monoimine-monoamine type ligand with a clear asymmetric structure, the monoimine-monoamine type ligand and metal salt form a bimetallic catalyst, and the catalyst generates a synergistic effect through double active sites and shows high catalytic activity and excellent product selectivity.

This invention discloses an MPP pipe for power cables and its preparation method, relating to the field of polymer materials technology. The invention comprises, by weight, 80-90 parts of a toughening nucleating agent; 40-45 parts of an insulating nucleating agent obtained by in-situ composite and gradient temperature imidization treatment of a polyamic acid prepolymer prepared from hexagonal boron nitride nanosheets (prepared by surface modification with dopamine hydrochloride, followed by modification with octyltriethoxysilane) to obtain a silanized boron nitride suspension; 40-45 parts of melamine cyanurate; 2.1-2.4 parts of an antioxidant; 2.6-3 parts of a light stabilizer; 8-9 parts of a lubricant; and 1340-1500 parts of polypropylene. The introduction of the toughening nucleating agent and insulating nucleating agent in this invention effectively improves the flame retardancy, low-temperature rigidity-toughness balance, and aging resistance of the MPP pipe.

This invention discloses a method and sensor for adiponectin detection using a polyaniline and polyacrylic acid-modified wire mesh carbon electrode, relating to the field of adiponectin detection technology. The method involves electrochemically activating the wire mesh carbon electrode, electropolymerizing it to form a polyaniline-polyacrylic acid composite modification layer, immobilizing adiponectin monoclonal antibody after activation with N-hydroxysuccinimide and 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide, blocking the antibody with bovine serum albumin, and reacting it with a serum sample. The adiponectin concentration is determined based on the peak potential shift and peak current change. This invention simultaneously achieves both conductive transport and antibody immobilization, reduces non-specific adsorption and serum interference, and improves detection sensitivity, repeatability, and quantitative accuracy.

The invention provides a 1, 4-diaza-butanetriene compound as well as a synthesis method and application thereof, and belongs to the technical field of organic synthesis. The preparation method comprises the following steps: carrying out a first reaction on a compound 1 and a compound 2 in a solvent A, removing the solvent A after the reaction is finished, extracting with benzene or toluene, filtering, mixing with 12-crown ether-4, and stirring to obtain a compound 3; the synthesis method of the compound 3 provided by the invention is high in yield, simple to operate, mild in reaction, simple in required reaction condition control and high in speed. The obtained compound 3 has excellent stability and can be used for key intermediates in various organic reactions, such as preparation of alpha-diimine ligands.

The invention discloses a preparation method of surface-modified degradable polymer microspheres, which comprises the following steps: (1) preparing dry microsphere powder: putting an oil-phase solution and a water-phase solution into emulsifying equipment for mixing and emulsifying to obtain emulsion; carrying out temperature rise and pressure reduction curing on the emulsion to obtain biodegradable microsphere dry powder; (2) dissolving the modification material: dissolving the modification material containing the amino group to obtain a solution containing the modification material; (3) swelling: dispersing the biodegradable microsphere dry powder in a third solvent and stirring to swell the surface structure of the biodegradable microsphere; (4) activation: adding a carbodiimide compound and an N-hydroxyl activator into the swollen biodegradable microsphere solution for activation, so that an O-acyl isourea intermediate is formed on the surface of the microsphere, and a surface-activated microsphere precipitate is obtained; and (5) modification: mixing the microsphere precipitate with a solution containing a modification material, and stirring to obtain the surface-modified degradable polymer microsphere. Compared with the prior art, the hydrogel has good hydrophilicity and biocompatibility.

This invention provides a method for preparing dibenzoyl-p-benzoquinone dioxime using a microchannel reactor. The method includes the following steps: 1,3-dicyclohexylcarbodiimide and a catalyst are mixed uniformly and preheated to obtain a premix; a chloroform solution of p-benzoquinone dioxime, a chloroform solution of benzoic acid, and the premix are simultaneously introduced into the microchannel reactor for reaction; the resulting reaction solution is subjected to vacuum distillation, washing, filtration, and drying to obtain dibenzoyl-p-benzoquinone dioxime. The synthesis method of this invention features high reaction conversion rate, high production efficiency, few side reactions, and high safety. The obtained dibenzoyl-p-benzoquinone dioxime product has stable quality. Furthermore, the organic solvent used can be recovered and reused after vacuum distillation, overcoming the problems of inaccurate temperature control, poor safety, numerous side reactions, and difficult waste treatment in traditional processes. This provides a new approach for the synthesis of dibenzoyl-p-benzoquinone dioxime.

This invention discloses a composite hydrogel based on a polysaccharide-based hybrid dual network, its preparation method, and its applications, belonging to the field of marine polysaccharide technology. Based on the important role of amorphous calcium phosphate, a precursor in biomineral formation, in mineralization, this invention prepares a multifunctional composite hydrogel with wet bonding, antibacterial, and remineralization functions. This composite hydrogel can achieve rapid and convenient repair of enamel demineralization. This invention prepares oxidized sodium alginate via an alcohol-aqueous phase using the sodium periodate method. Sodium alginate reacts with carboxymethyl chitosan and dopamine through a Schiff base reaction to form dynamic imine bonds, thus preparing an in-situ self-crosslinking hydrogel. Simultaneously, amorphous calcium phosphate is introduced for secondary crosslinking, preparing a dense dual-network composite hydrogel. The composite hydrogel prepared by this invention has an interconnected three-dimensional porous structure, stable mechanical properties, and uniformly dispersed amorphous calcium phosphate in the form of nanospheres. The composite hydrogel prepared by this invention provides an integrated strategy with clinical translational potential for orthodontic enamel demineralization, with broad market prospects.