3678 results about "Sulfonic acid ester" patented technology

The invention relates to the technical field of fracturing fluids, and discloses a preparation method of a temperature-resistant and salt-resistant fracturing fluid, which comprises the following steps: carrying out polymerization reaction on acrylamide, acrylic acid and an acrylamide sulfonic acid monomer to obtain a polymer thickening agent, and compounding the polymer thickening agent with a cross-linking agent, a clay stabilizer and the like to obtain the temperature-resistant and salt-resistant fracturing fluid. The polymer thickening agent contains long-chain alkyl, a physical cross-linked spatial network structure can be formed through a hydrophobic association effect, the hydrodynamic volume is increased, a good tackifying effect is achieved, and after high-speed shearing, the long-chain alkyl can be cross-linked again to form a spatial network structure, so that a solution still keeps very high apparent viscosity, and the viscosity of the solution is improved. Good anti-shearing performance is realized. The acrylamide sulfonic acid monomer contains a sulfonate group and is used as a temperature-resistant and salt-resistant monomer, so that the polymer thickening agent has good temperature resistance and salt resistance, and the fracturing fluid still keeps relatively high apparent viscosity after being subjected to high-temperature heat treatment and in formation water with high salinity.

The invention relates to the technical field of oilfield chemistry, and discloses a graft modified cellulose filtrate reducer and a preparation method thereof.The preparation method comprises the following steps that modified hydroxyethyl cellulose, 2-acrylamide-2-methyl propane sulfonic acid, dimethyl diallyl ammonium chloride, alkenylated cardanol and N, N '-methylene bisacrylamide are added into deionized water, stirring is conducted, and a mixture is obtained; the preparation method comprises the following steps: adding cellulose into a reaction kettle, stirring for 10-15 minutes at the temperature of 40-60 DEG C at the speed of 300-400 rpm, dropwise adding ammonium persulfate and sodium hydrogen sulfite into a system, and continuously reacting for 4-6 hours to obtain the grafted modified cellulose filtrate reducer. The filtrate reducer disclosed by the invention has good high temperature resistance and salt resistance.

The invention discloses a preparation method of a degradable transparent conductive polymer film, and belongs to the technical field of film preparation. Preparing dispersion liquid I through graphene oxide quantum dots; preparing a dispersion liquid II from polyaniline nanofibers; dissolving pyrrole and toluenesulfonic acid in N, N-dimethylformamide to prepare a reaction solution, adding the dispersion liquid I and the dispersion liquid II, stirring, and adding ferric chloride hexahydrate to obtain a reaction solution; adjusting the pH value of the reaction solution to 1.5, and heating to obtain a polypyrrole solution; preparing cellulose acetate, polyvinyl alcohol and N, N-dimethylformamide to obtain a cellulose acetate solution; mixing the polypyrrole solution and the cellulose acetate solution, adding glutaraldehyde to obtain a mixed solution, and pouring the mixed solution into a mold to prepare a composite wet film; and putting the composite wet film into a hot-pressing forming machine for hot-pressing to generate the polymer film. The conductive polymer film prepared by the invention can be applied to the fields of supercapacitor electrode materials, electromagnetic shielding materials, flexible sensors and the like, and provides a new high-performance material choice for the development of related fields.

The invention relates to the technical field of lithium-sulfur batteries, and discloses a sulfonyl ZIF-8 metal organic framework material, a lithium-sulfur battery diaphragm and a preparation method of the lithium-sulfur battery diaphragm. The preparation method of the sulfonyl ZIF-8 metal organic framework material comprises the following steps: dissolving a metal precursor and a mixed ligand in an organic solvent, and carrying out a coordination reaction under the action of organic alkali; solid is collected, washed and dried, and the sulfonic group ZIF-8 metal organic framework material is obtained. The metal precursor is soluble zinc salt; the mixed ligand comprises 2-methylimidazole and an imidazole derivative containing a sulfonic acid group. The sulfo group ZIF-8 metal organic framework material is prepared through a ligand doping strategy and is used for functional modification of the lithium-sulfur battery diaphragm; the shuttle behavior of lithium polysulfide (LiPS) can be effectively inhibited through the electrostatic repulsion effect of sulfonic acid groups and the synergistic effect of high-polarity adsorption sites; and the migration of Li < + > and the conversion efficiency of LiPS are remarkably promoted by an efficient ion transmission network, so that the cycle performance of the lithium-sulfur battery is improved.

The invention discloses a single-ion conductor polymer, a ternary composite binder solution, high-solid-content sulfide electrolyte slurry and a wet film forming method and application thereof, and belongs to the technical field of all-solid-state lithium batteries. The key technical problems in the wet membrane preparation of the sulfide electrolyte are solved through an innovative solvent-binder synergistic system, and the method specifically comprises the steps that 1, through the synergistic effect of a non-polar solvent and a weak-polar solvent, low-viscosity coating of high-solid-content slurry is achieved while the chemical stability of the sulfide electrolyte is guaranteed; 2, a poly (lithium styrenesulfonate-butyl acrylate), styrene butadiene rubber and polyisobutene ternary composite binder is designed, a lithium ion transmission channel is provided through a lithium sulfonate group, a benzene ring structure in the styrene butadiene rubber enhances the mechanical strength, long-chain alkane in the polyisobutene improves the interface adhesive force, and the mechanical strength is improved; the three components cooperate to realize balance of mechanical and electrochemical properties of the electrolyte membrane, so that the prepared electrolyte membrane has low porosity, high ionic conductivity and mechanical strength.

The invention provides high-stability ceramic ink and a preparation method thereof. The high-stability ceramic ink is prepared from the following components in parts by mass: 30 parts of inorganic pigment, 2 to 8 parts of sulfonic block polymer, 1 to 3 parts of polyvinyl alcohol grafted glycidyl methacrylate and 50 to 70 parts of organic solvent, wherein the polyving akohol grafted glycidyl methacrylate contains a plurality of epoxy groups. According to the high-stability ceramic ink, by constructing a composite system containing a sulfonic block polymer dispersing agent and polyvinyl alcohol grafted glycidyl methacrylate, stable dispersion of an inorganic pigment, construction of a thermal anchoring structure of an ink-jet pattern area and optimization of glaze layer fusion compatibility are realized; the high-stability ceramic ink effectively solves the problems of fuzzy pattern boundary and glaze-ink separation in the high-temperature sintering process of the existing ceramic ink, so that the high-stability ceramic ink has good storage stability and glaze-ink separation resistance.

The invention discloses a sulfonate-based electrolyte and a preparation method and application thereof, and belongs to the technical field of electrolyte preparation, the electrolyte comprises a solute, a sulfonate-based compound and a cosolvent, the mass fraction of the solute is 1-90%, the mass fraction of the sulfonate-based compound is 0.1-99%, and the mass fraction of the cosolvent is 0-99%. According to the sulfonate-based electrolyte as well as the preparation method and the application thereof, the sulfonate-based solvent is used as a main solvent, a cosolvent, an additive and the like to develop a novel electrolyte, so that the balance between strong solvation and rapid charging capability of the electrolyte is promoted, and a high-voltage battery with high energy density is developed.

The invention provides a metal organic sulfonic acid-based solid acid catalyst applied to nylon 6 recovery and depolymerization and a preparation method thereof, and realizes upgrading and recovery of waste nylon 6. The main contents are as follows: (1) a structural design and a preparation method of the metal organic framework sulfonic acid-based solid acid catalyst; and (2) the solid acid is used for catalytic depolymerization of nylon 6. The problems that equipment corrosion is aggravated by inorganic acid in the nylon 6 recovery process and a liquid-phase catalyst is difficult to separate and recover are solved, and the application prospect is good.

The invention discloses an electrolyte, an electrochemical device comprising the electrolyte and a vehicle. The electrolyte comprises a solvent, a first additive and a second additive, the solvent comprises chain carboxylic ester, and the first additive comprises a sulfonate compound or / and a sulfate compound; the second additive comprises vinylene carbonate or / and fluoroethylene carbonate. According to the electrolyte disclosed by the invention, the chain carboxylic ester solvent, the first additive containing the sulfonate compound or / and the sulfate compound and the second additive containing the vinylene carbonate or / and the fluoroethylene carbonate are matched for use; the rapid charging capability and the high-temperature cycle performance of a lithium iron phosphate system battery with high safety performance can be improved, and the application of lithium iron phosphate in a power battery is further widened.

The invention discloses a polybenzimidazole modified ion exchange membrane as well as preparation and application thereof. The polybenzimidazole modified ion exchange membrane comprises a polybenzimidazole-containing porous base membrane, the surface of the porous base membrane is grafted with a sulfonic acid modified layer, and the outer surface of the sulfonic acid modified layer is coated with an aluminum fluoride layer. The preparation method of the membrane comprises the following steps: immersing a polybenzimidazole-based membrane into an ammonium acetate aqueous solution for reaction, taking out the base membrane after the reaction, and drying to obtain a pretreated base membrane; immersing the pretreated base membrane into a sulfonic acid group grafting solution, heating for reaction, cleaning the base membrane after the reaction, and drying to obtain a sulfonic acid modified base membrane; and immersing the sulfonic acid modified base membrane into an ethanol solution of aluminum fluoride for reaction, taking out the membrane after the reaction, cleaning and drying to obtain the membrane. The membrane can be used for assembling a flow battery. According to the invention, the problem that a sulfonic acid modified layer is incompatible with metal fluoride is overcome, and a proper combination of a sulfonating agent and metal fluoride is screened, so that the high-performance ion exchange membrane which can be used for a flow battery is successfully obtained.

The invention provides an amino acid frosted cleaning composition as well as a preparation method and application thereof. The amino acid frosted cleaning composition comprises a surfactant, an amino acid composition, a thickening agent, a humectant, an antioxidant, a pH regulator and water, the surfactant is a combination of cocoyl glycinate, cocamidopropyl hydroxy sulfobetaine, sodium cocoyl methyl taurine taurate, sulfonic acid hydroxypropyl ester lauryl glucoside cross-linked polymer sodium and glycolipid. According to the invention, a mild surfactant system with amino acid as a main component is adopted, so that the shampoo has rich and fine foam, quick foaming performance and easy washing performance, and the skin feeling is smooth and soft after washing. In addition, the system contains suspended crystal frosted particles formed by self-assembly of the amino acid composition, the appearance is novel, the better efficacy performance is achieved, and meanwhile the cleaning effect and the use comfort are improved.

The invention provides composite anionic cellulose ether as well as a preparation method and application thereof. The composite anionic cellulose ether is prepared by etherifying alkalized cellulose through an etherifying agent A and an etherifying agent B in sequence, the etherifying agent A is selected from water-soluble halogenated alkyl sulfonic acid and / or water-soluble halogenated alkyl sulfonate; the etherifying agent B is selected from water-soluble halogenated alkyl carboxylic acid and / or water-soluble halogenated alkyl carboxylate. According to the composite anionic cellulose ether, a sulfonic acid group and a carboxylic acid group are sequentially introduced, so that the composite anionic cellulose ether has relatively high temperature resistance and salt and calcium resistance; the compound can be used as a filtrate reducer for the drilling fluid, can effectively control the filter loss of the drilling fluid, and can improve the salt pollution resistance of the drilling fluid, especially the calcium and magnesium ion pollution resistance.

The invention discloses zwitter-ion supramolecular hydrogel based on anion-pi as well as a preparation method and application of the zwitter-ion supramolecular hydrogel. The hydrogel is formed by self-assembly of a zwitterionic copolymer and a p-styrenesulfonic acid copolymer. According to the supramolecular hydrogel disclosed by the invention, the supramolecular hydrogel can be rapidly formed only by simply mechanically mixing the zwitterionic polymer copolymer and the p-styrene sulfonate copolymer solution, and the supramolecular hydrogel is endowed with excellent injectability and self-repairing performance due to the dynamic cross-linking characteristic. The hydrogel is composed of zwitterions with excellent immunocompatibility and poly (p-styrene sulfonate) with heparin-imitating performance, so that the hydrogel has excellent immunocompatibility, can play a role in various in-vivo application scenes, and in addition, the hydrogel can be used for preparing an anti-inflammatory drug. The dynamic cross-linked network based on anion-pi interaction and the heparin-like structure are very beneficial to protein preservation, and have wide application prospects in the fields of protein delivery and cell encapsulation.

The invention relates to a phosphorus-free zinc-free seawater special-purpose scale and corrosion inhibitor, which comprises, by weight, 20-25% of sulfonic acid modified polyaspartic acid, 8-12% of quaternized chitosan, 5-10% of a sulfonate copolymer, 5-10% of polyepoxysuccinic acid, 1-3% of benzotriazole or methyl benzotriazole, 0.5-1% of sodium tungstate, and the balance of deionized water. According to the formula, traditional corrosion inhibitors such as phosphorus and zinc are completely abandoned, functions are achieved through natural polymer derivatives such as sulfonic acid modified polyaspartic acid and quaternized chitosan, and the scale and corrosion inhibitor has the following environmental protection advantages that the scale and corrosion inhibitor does not contain phosphorus and zinc elements at all, and water eutrophication and heavy metal accumulation caused by a traditional phosphorus and zinc formula are avoided.

The present invention provides a multifunctional silane coupling agent, which is prepared from commercially available 3-aminopropylsilane coupling agent, acryloxy polyetheramine, and one of an alkylating agent, polyether sulfonate, γ-propane sultone or γ-butyrolactone through Michael addition reaction and quaternization reaction. The multifunctional silane coupling agent is a new variety carrying zwitterions, quaternary ammonium cations and polyether chains, enriching the functions and application scope of silane coupling agents. It can endow some modified materials with surface hydrophilicity, conductivity, antibacterial, antifogging, antifouling, biocompatibility, anticoagulant and wet lubrication properties, etc. at the same time.

The invention discloses a bionic lignin-based saline-alkali soil improvement material and a preparation method thereof, and belongs to the technical field of high polymer materials and soil improvement. According to the saline-alkali soil improving material, lignin or a derivative thereof serves as a framework, glutenin charge distribution and a dynamic disulfide bond sodium ion response function are simulated, and the sequence and the proportion of chain segments of sulfonic acid groups and quaternary ammonium salt groups are accurately regulated and controlled through step-by-step activation and alternate copolymerization in an aqueous solution polymerization reaction system; positive and negative charges form more uniform sequence distribution, so that the amphipathy of the lignin compound is realized; then, sulfydryl is introduced through click chemistry, linear regulation and control of material viscosity and water solubility are achieved through the chain transfer characteristic of multi-sulfydryl functional groups, and the requirements of different saline-alkali soil application scenes are met. The limitation that a traditional lignin product is single in function is broken through, efficient utilization of lignin is achieved, and the intelligent saline-alkali soil improvement material integrating high stability and pH and Na < + > multi-environment response is developed.

The invention belongs to the technical field of analysis and detection, and discloses a method for detecting perfluorinated and polyfluoroalkyl substances in cosmetics, which comprises the following steps: (1) mixing a perfluorinated and polyfluoroalkyl substance standard solution and an isotope internal standard solution to obtain a mixed standard solution; detecting the mixed standard solution by adopting a liquid chromatograph-mass spectrometer, drawing a standard curve, and calculating to obtain a linear equation; (2) mixing a cosmetic sample with the isotope internal standard solution, adding an extracting solution, extracting, and filtering to obtain a mixed solution to be detected; detecting the mixed to-be-detected solution by adopting the liquid chromatograph-mass spectrometer to obtain a detection result, and substituting the detection result into the linear equation to obtain the content of the perfluoro and polyfluoroalkyl substances in the mixed to-be-detected solution, the perfluoro and polyfluoroalkyl substances comprise perfluorocarboxylic acid, perfluorosulfonic acid, a fluorine polymer, perfluoroalkyl ether sulfonic acid, saturated fluorine telomere acid and perfluoroether carboxylic acid.

The invention discloses a special grinding aid for gold ore and a preparation method thereof, and belongs to the technical field of mineral processing, the special grinding aid for gold ore comprises the following raw materials: a monomer, an initiator, a chain transfer agent and a solvent; the monomers are an unsaturated polyether monomer A and an unsaturated carboxylic acid monomer B; or a monomer C containing an ethylenically unsaturated sulfonic acid group. The preparation method comprises the following steps: putting the raw materials into a water bath kettle, and polymerizing in a separate dropwise adding manner to prepare the special grinding aid for the gold ore. The prepared grinding aid can improve the problems of particle agglomeration, low fine grinding efficiency, low gold dissociation efficiency and the like in the gold ore grinding process, the concentrated utilization of the grinding aid limited in the fields of cement, ceramics and the like is improved, the grinding energy consumption can be reduced, and the material quality can be improved.

The invention provides an electrochemical device and electronic equipment, the electrochemical device comprises a positive pole piece, a negative pole piece and an electrolyte, the negative pole piece comprises a negative current collector and a negative active material layer arranged on at least one surface of the negative current collector, the positive pole piece comprises a positive current collector and a positive active material layer arranged on at least one surface of the positive current collector, the negative pole piece and the positive pole piece are laminated, the negative active material layer comprises an extension region which is not overlapped with the positive active material layer, and the ratio of the area of the extension region to the area of the negative active material layer is a%; the electrolyte comprises a sulfonate-group-containing compound, and the mass percentage content of the sulfonate-group-containing compound in the electrolyte is b%; and 0.0003 < = b / a < = 5. The electrochemical device has good cycle performance.

The invention relates to the field of fuel cells, and discloses a preparation method of an MOF (at) COF core-shell heterostructure doped Nafion-based proton exchange membrane, and the preparation method comprises the following steps: step 1, preparing MOF-NH2 powder; step 2, preparing MOF-NH2 (at) COF-SO3H powder, and preparing a COF-SO3H powder; and step 3, dispersing the MOF-NH2 (at) COF-SO3H powder into a 5% Nafion dispersion liquid, and drying to form the film. The proton exchange membrane is based on Nafion, COF and MOF, the MOF and the COF form an MOF-coated COF core-shell heterostructure, pore channels of the COF are modified by sulfonic acid, so that water molecules can be effectively confined, the water retention rate is increased, and a rigid MOF framework provides enough strength to prevent the proton exchange membrane from swelling.

The rubber composition for a tire tread according to the embodiment contains a rubber component containing a diene rubber and vegetable granules having a surface treated with a sulfonic acid-type surfactant. The rubber composition for a tire tread has excellent on-ice performance, excellent wet performance, and excellent low heat generation property.

The present invention discloses a preparation method of yellow azoxy and azo stilbene dyes. Using 4-nitrotoluene-2-sulfonic acid as a raw material and water as a reaction solvent, in the presence of choline hydroxide, dye yellow 11 is obtained through a condensation reaction. The molecular structure of choline hydroxide contains a quaternary ammonium salt group and a hydroxyl group. The hydroxyl group provides additional hydrophilicity, which helps to improve the solubility and dispersibility of the dye in an aqueous medium and enhance the affinity between the dye and the fiber. Choline hydroxide can effectively provide the alkaline environment required for the reaction, promote the synthesis reaction of the dye, and better control the selectivity and yield of the reaction. Since the choline hydroxide molecule contains a hydroxyl group, it can form hydrogen bonds with the sulfonic acid groups in the dye molecule, enhance the stability between dye molecules, and improve the light fastness and acid and alkali resistance of the dye. Using choline hydroxide not only optimizes the reaction conditions, improves the purity and yield of the dye, but also significantly improves the performance of dye yellow 11.

The invention relates to an adsorbent and a preparation method and application thereof, the adsorbent comprises a polymer matrix and a nanofiller uniformly embedded in the polymer matrix, the polymer matrix comprises a calcium / boron cross-linked polyvinyl alcohol-sodium alginate blend, and the nanofiller is sulfonic acid / carboxylic acid functionalized graphene oxide; the mass fraction of the nano filler in the adsorbent is 0.05%-0.60%; wrinkles and irregular hole structures are distributed on the surface of the adsorbent. The adsorbent is used for removing tritium in water and is high in adsorption capacity, stable in structure and good in recycling performance. The removal rate of tritium in the single-stage adsorption process is greater than 8.5%, and the removal rate of tritium in the third-stage adsorption process is 19.4-57.7%.

The invention is applicable to the technical field of proton exchange membranes, and particularly relates to a perfluorosulfonic acid proton exchange composite membrane which is prepared by the following steps: preparing a perfluorosulfonic acid resin solution: dissolving the perfluorosulfonic acid resin solution in a mixed solvent to form a membrane casting solution; impregnating and filling: impregnating a porous base membrane in the obtained perfluorinated sulfonic acid resin solution, and keeping at 20-80 DEG C for 1-120 minutes; drying and forming: taking out the impregnated film, and drying to form a composite film; and protonation treatment: treating the composite membrane in an acid solution, and washing to be neutral to obtain the perfluorosulfonic acid proton exchange composite membrane. According to the invention, the problems of deformation and damage of the battery in operation are effectively avoided; meanwhile, the high proton conductivity is ensured, so that the ion transmission efficiency is maintained; the introduction of the ePTFE porous skeleton enhances the membrane body and reduces the use amount of the perfluorinated sulfonic acid resin at the same time, the composite membrane is compact in structure and balanced in performance, and the durability and reliability of the fuel cell are greatly improved.

The invention discloses a preparation method and application of self-crosslinking hydrogel containing a capsaicin functional structure, and belongs to the technical field of dye adsorption materials. The capsaicin functional structure monomer is introduced into an acrylic acid system, so that the self-crosslinking of the hydrogel is realized, and meanwhile, the adsorption performance of the hydrogel is remarkably improved; mono-substituted capsaicin functional structure monomers containing carboxyl and sulfonic acid groups are used as components, a disubstituted capsaicin functional structure monomer with polyhydroxy and carboxyl is used as a cross-linking agent, the self-crosslinking hydrogel with multiple adsorption sites is successfully constructed through free radical polymerization, and the adsorption capacity and efficiency of the hydrogel are greatly improved. The hydrogel-based carbon material is obtained by carbonizing the self-crosslinking hydrogel containing the capsaicin functional structure, the adsorption performance of the hydrogel material is further improved, the obtained hydrogel-based carbon material can be desorbed and recycled in ethyl alcohol, and the service life of the hydrogel-based carbon material is prolonged. And the problem of secondary pollution of the existing hydrogel material in the acid / alkali desorption process is effectively avoided.

Mobile or stationary air filter (L) or room fan (RL) according to Figure 1, comprising an outer wall (5), a (2) for generating an airflow (3) which is guided through an air filter material (1.1), an air inlet (2.1) and an air outlet (2.2), wherein the air filter material (1.1) contains poly(styrenesulfonic acid) (sulfonic acid biocide) (1.3) cross-linked with divinylbenzene and / or an acidic salt (1.3.1) (sulfonic acid biocide salt) of the sulfonic acid biocide (1.3) with biocidal cations, wherein the sulfonic acid biocide (1.3) and / or sulfonic acid biocide salt (1.3.1)(i) are positively and / or materially bonded to and / or in inert carriers and, in the fixed state, are in direct contact with carrier materials (1.1.7) on and / or in which biocidal Metal microparticles of a mean particle size d50 of 0.1 µm to <1,000 µm are fixed, and / or (ii) with carrier materials (1.1.7) on and / or in which biocidal metal microparticles of a mean particle size d50 of 0.1 µm to <1.000 µm are fixed, are mixed; its use and methods for the production and environmentally friendly disposal of air filter materials (1.1).

The invention relates to a compound, a preparation method, a hole transport layer material, a photovoltaic device and a photovoltaic module. R1 and R4 are respectively and independently selected from amino and derivatives thereof, hydroxyl and derivatives thereof, methoxyl and derivatives thereof, sulfydryl and derivatives thereof, methylthio and derivatives thereof, thiophene groups and derivatives thereof, phosphate groups and derivatives thereof, carboxylic acid groups and derivatives thereof, and sulfonic acid groups and derivatives thereof; r2 and R3 are independently selected from alkyl, a phosphate group and derivatives thereof, a carboxylic acid group and derivatives thereof, a sulfonic acid group and derivatives thereof, and trimethoxysilyl propyl and derivatives thereof. The material is beneficial to improving the photoelectric conversion efficiency of photovoltaic devices and photovoltaic modules.

The invention relates to the technical field of building materials, and discloses cement containing sulfonic acid cellulose and a preparation method thereof.The preparation method includes the steps that gypsum, coal gangue and Portland cement clinker are smashed and added into a concrete mixer to be stirred, then sulfonic acid cellulose, kieselguhr, calcium formate and quaternary ammonium salt modified polyurethane are added into the concrete mixer to be stirred, and the cement containing sulfonic acid cellulose is obtained; the cement containing the sulfonic acid cellulose is obtained. The cement containing sulfonic acid cellulose provided by the invention has better crack resistance, durability and good mechanical properties.

The invention discloses a preparation method of an optical OCA (Optical Clear Adhesive) and application of the optical OCA in a mobile phone folding screen, and relates to the technical field of optical cement, the optical OCA is prepared from the following raw materials in parts by weight: 50 parts of acrylate prepolymers, 2-4 parts of 3-allyl-2-mercapto-3H-quinazoline-4-ketone, 1-3 parts of diallyl disulfide, 1-3 parts of 3-[N, N-dimethyl formamide], 1-3 parts of 2, 3, 5-trimethyl-1, 3-pentanediol monoisobutyronitrile, 1-3 parts of 2, 3, 5-trimethyl-1, 3, 5-trimethyl-1, 3, 5-trimethyl-1, 3 The preparation method comprises the following steps: adding 3-5 parts of N, N-dimethyl-[2-(2-methylpropane-2-enoyloxy) ethyl] ammonium] propane-1-sulfonic acid inner salt, 1-3 parts of allyl succinimido carbonate, 2-4 parts of dicyclopentene methacrylate, 1-3 parts of 1, 3, 5-triacryloyl hexahydro-1, 3, 5-trimethyl-1, 3, 5-trimethyl-1, 3, 5-trimethyl-1, 3, 5-trimethyl-1, 3, 5-trimethyl-1, 3, 5-trimethyl-1, 3, 5-trimethyl-1, 3, 5- The invention relates to a graphene quantum dot photoinitiator which is prepared from the following components in parts by weight: 1-3 parts of 1, 3, 5-triazine, 0.8-1.2 parts of a photoinitiator, 1-3 parts of an aziridine cross-linking agent, 1-3 parts of graphene quantum dots, 0.8-1.2 parts of a coupling agent and 40-50 parts of a diluent. The optical OCA adhesive is high in light transmittance and bonding strength, good in weather resistance and excellent in folding resistance.

The invention relates to the technical field of oilfield chemistry, in particular to an aminoethanesulfonic acid type surfactant and a preparation method and application thereof.The preparation method of the aminoethanesulfonic acid type surfactant comprises the steps that firstly, fatty amine is dissolved in a first solvent, a sodium chloroethanesulfonate aqueous solution is added, and N-long-chain alkyl-2-sodium aminoethanesulfonate is obtained through a reaction; and 2, dissolving a required amount of N-long-chain alkyl-2-sodium aminoethanesulfonate in a second solvent, adding a required amount of methyl acrylate, and reacting to obtain the aminoethanesulfonic acid type surfactant. The aminoethanesulfonic acid type surfactant disclosed by the invention contains long-chain alkyl, amino, ester groups and sulfonic acid groups, so that the aminoethanesulfonic acid type surfactant has good surface activity and can meet the development requirements of oil and gas fields. The microemulsion cleanup additive prepared from the aminoethanesulfonic acid type surfactant can effectively reduce the surface tension and the interfacial tension of an aqueous solution, and the preparation method is easy and convenient to operate, mild in condition and suitable for industrial production.