44 results about "Alkyl sulfonate" patented technology

The invention relates to the technical field of daily chemical industry, and discloses a moisturizing and soothing composition and application thereof.The moisturizing and soothing composition comprises, by weight, 20-25% of C14-16 sodium olefin sulfonate, 20-25% of C14-16 sodium alkyl sulfonate, 20-25% of C14-16 sodium alkyl sulfonate, 10-20% of C14-16 0.3%-0.7% of a cationic polymer; a litchi pericarp extract; an aloe extract; and a rosemary extract; wherein the total weight percentage of the litchi peel extract, the aloe extract and the rosemary extract is 1.9%-3.3%. The components are compounded, the cationic polymer and the anionic surfactant are utilized to construct a deposition system, and the three plant extracts with specific total content are cooperated, so that the retention rate of active ingredients in scalp is effectively increased, and the problem that moisturizing and soothing ingredients are easy to wash away is solved. The invention also provides a preparation method combining hot preparation and cold preparation, and the stability of the system and the activity of the extract are ensured by homogenizing the phase A at high temperature and adding the phase E at low temperature. The composition can be used for preparing shampoo products for moisturizing or relieving scalp.

The invention discloses an electrolytic solution of a platinum-rhodium alloy, a preparation method and a preparation method of a plating layer of the platinum-rhodium alloy, and belongs to the technical field of precise electroplating. The electrolytic solution comprises a platinum salt, a rhodium salt, a first additive, a second additive, a first complexing agent, a second complexing agent, a first stabilizer and a second stabilizer, the first additive is a sulfamic acid compound containing 3-4 hydroxyalkyl groups, the second additive is sulfamic acid salt containing 3-4 hydroxyalkyl groups, and the first complexing agent and the second complexing agent are a platinum salt and a rhodium salt. The first complexing agent is a mixture of dicarboxylic acid and dicarboxylic acid containing amino or hydroxyl, the second complexing agent is a salt corresponding to the dicarboxylic acid, and the first stabilizer is a mixture of alkyl sulfonic acid and alkyl sulfonate. Through the synergistic effect of the additive, the complexing agent and the stabilizer, the additive, the complexing agent and the stabilizer form a five-membered to seven-membered heterocyclic coupling structure with platinum ions and rhodium ions, and the stability of the electrolytic solution is remarkably improved. And the obtained platinum-rhodium alloy coating is compact and uniform, and has excellent nitric acid steam and mixed gas corrosion resistance.

This invention discloses a pretreatment method for detecting trace perfluorinated and polyfluoroalkyl substances (PFAS) in complex matrix textiles, belonging to the field of materials analysis technology. The method involves placing the textile in an alkaline solvent containing an alkyl sulfonate displacing agent. Under heating conditions, the displacing agent utilizes its competitive adsorption mechanism to forcibly occupy matrix adsorption sites and displace the target analytes into the solvent. Subsequently, the temperature is rapidly lowered to the phase separation induction temperature, inducing supersaturation precipitation of the displacing agent, which then encapsulates impurities in situ and co-precipitates, forming a solid-liquid stratified system. Finally, the supernatant is collected for analysis. This invention utilizes the dual properties of the displacing agent—high-temperature solubilization and low-temperature phase change removal—to effectively break the strong adsorption equilibrium of aged textiles without using a solid-phase extraction column. This solves the contradiction between low extraction rate and significant matrix interference, significantly improving the recovery rate of PFAS. It offers advantages such as low cost, simple operation, and high accuracy.

The invention provides a self-assembled surfactant as well as preparation and application thereof. The preparation method comprises the following steps: adding an anionic surfactant and a nonionic surfactant into a buffer solution, uniformly mixing, and heating until the anionic surfactant and the nonionic surfactant are completely molten, so as to obtain the self-assembled surfactant. Wherein the anionic surfactant is one or more of lignosulfonate, secondary alkyl sulfonate and alpha-olefin sulfonate; the nonionic surfactant is one or more of polyethylene glycol, fatty alcohol-polyoxyethylene ether, polyoxyethylene alkyl ether and polyoxyethylene nonyl phenyl ether. The specific anionic surfactant and the nonionic surfactant are compounded, self-assembly is completed through heating, and the obtained self-assembly surfactant can remarkably improve the enzymolysis efficiency of lignocellulose.

The application discloses a magnesium alloy component processing method, a magnesium alloy component and an electronic device, and relates to the field of metal surface treatment.The processing method of the magnesium alloy comprises the following steps: providing a magnesium alloy workpiece; performing CNC high light processing on a first region of the magnesium alloy workpiece to form a high light surface; and forming a first transparent protective layer on the outer side of the high light surface by using a cutting fluid during the CNC high light processing, wherein the cutting fluid at least comprises alkyl sulfonate and a surfactant.The magnesium alloy component processing method provided by the embodiment of the application provides the cutting fluid capable of forming the first transparent protective layer, forms the protection of the high light surface at the same time when cutting is completed, avoids the case that the high light surface is easily corroded and loses luster by contacting oxygen and water, and does not need to additionally polish the high light surface, so that the magnesium alloy component with better metal high light quality is prepared.

The invention discloses a binuclear piperidine ionic liquid and a preparation method thereof. The dinuclear piperidine ionic liquid is prepared by taking glycol, phosphorus tribromide, piperidine, alkyl sultone and a sulfonic acid derivative as raw materials. The method comprises the following steps: preparing dibromoglycol by taking glycol and phosphorus tribromide as raw materials; piperidine and dibromoethylene glycol react to prepare a binuclear piperidine intermediate; reacting the binuclear piperidine intermediate with alkyl sultone to prepare binuclear piperidine sulfonic acid inner salt; the binuclear piperidine ionic liquid is prepared by taking binuclear piperidine sulfonic acid inner salt and a sulfonic acid derivative as raw materials. The invention provides a new scheme for preparing the polyfunctional group piperidine ionic liquid.

The objective is to provide a lubricating oil composition that has low volatility and excellent anti-foaming properties under reduced pressure. [Solution] The present invention relates to a lubricating oil composition comprising an ionic liquid (X) consisting of an anion (A) and a cation (B), wherein the anion (A) is at least one anion selected from the group consisting of alkyl carboxylate anions, alkyl sulfonate anions, dialkyl phosphate anions, dicyanamide anions, and thiocyanate anions, the water content in the lubricating oil composition is 50 ppm or less, and the viscosity of the lubricating oil composition at 25°C is 15 to 370 mPa·s.

The application discloses an aldehyde-containing photochromic merocyanine compound and a preparation method and application thereof, and the preparation method comprises the following steps: dissolving 2-hydroxy-5-methyl-m-xylylformaldehyde in an organic solvent, adding drop by drop an organic solvent containing an indolium alkyl sulfonate compound in an inert atmosphere, refluxing reaction, and purifying the reaction solution through post-treatment to obtain the aldehyde-containing photochromic merocyanine compound; through protection of the inert atmosphere and control of the dropping sequence of the reactants, generation of reaction by-products is reduced, and the aldehyde-containing photochromic merocyanine compound with fat solubility and water solubility is synthesized.

The application provides a low-smoke halogen-free cable sheath material and a preparation method thereof, and belongs to the technical field of high polymer materials. The terminal aluminum-based polyethylene is prepared through coordination chain transfer polymerization, is converted into terminal hydroxyl polyethylene through oxidation hydrolysis, is reacted with sodium hydride to obtain active polyethylene glycol sodium, alkyl sulfonate is used to initiate N -vinyl pyrrolidone cationic addition polymerization to prepare active polyvinyl pyrrolidone cation, and the two are connected through nucleophilic-electrophilic coupling reaction to form an ether bond connected PE-b-PVP block copolymer, and are used as an anchor agent to be blended and melt-extruded with polyolefin resin and phosphazene flame retardant, dipole-dipole interaction between the PVP segment and the phosphazene is utilized to realize in-situ physical enrichment of the flame retardant in the cable sheath. The sheath material has the characteristics of efficient flame retardation, excellent insulation, low smoke density and the like, and can be applied to the fields of medium and high voltage power cables, communication cables, special cables for rail transit and the like.

The application relates to the field of antistatic materials and discloses an antistatic agent, an antistatic resin composition and application thereof. Based on the total mass of the antistatic agent, the antistatic agent contains 93-99 wt% of a block copolymer and 1-7 wt% of component A; the block copolymer is obtained by reacting caprolactam, a dicarboxylic compound, a diamine compound and an antioxidant in the presence of an acidic catalyst; the diamine compound is selected from the combination of at least one of a polyether diamine and a C6-C15 linear alkyl diamine; component A contains sulfonate and stannate; the sulfonate is a halogen-substituted C1-C12 alkyl sulfonate. The antistatic agent has low surface resistivity, high heat resistance and excellent flame retardant performance.

This invention provides a high-temperature stabilizer for sulfonated drilling fluids, its preparation method, and its application. The stabilizer comprises low-valent sulfur oxyacid salts and hydroxyalkyl sulfonates. The high-temperature stabilizer for sulfonated drilling fluids is prepared according to the following steps: mixing low-valent sulfur oxyacid salts and carbonyl compounds in water, adding an inorganic alkali to adjust the pH to 8-10, and reacting under high-temperature sealed conditions to obtain the high-temperature stabilizer for sulfonated drilling fluids. The low-valent sulfur oxyacid salts include divalent sulfur oxyacid salts and / or tetravalent sulfur oxyacid salts; the carbonyl compounds include aldehydes and / or ketones; the molar ratio of sulfur in the low-valent sulfur oxyacid salts to the carbonyl groups in the carbonyl compounds is (1.2-2.0):1. The high-temperature stabilizer in this invention is a composition formed by low-valent sulfates and hydroxyalkyl sulfonates. This composition can simultaneously eliminate the active hydroxymethyl and hydrogen atoms on the phenolic ring structure of the sulfonated material and can also inhibit the desulfonation reaction of the treatment agent.

The present application relates to a kind of aerial prevention adjuvants and its preparation method and application, aerial prevention adjuvant includes adhesion promoter, synergist, compatible agent and dispersion medium, adhesion promoter includes oleyl ether and fatty alcohol random polyether;Synergist includes polyoxyethylene ether compound, fatty acid amide and polyethylene glycol fatty acid ester;Compatible agent includes first compatible agent, second compatible agent and third compatible agent, first compatible agent is selected from one or more of alkyl benzene sulfonate, alkyl sulfonate, alkyl sulfonate, alkyl sulfate, second compatible agent is selected from one or more of fatty alcohol polyoxyethylene ether sulfate, fatty alcohol polyoxyethylene ether phosphate, and third compatible agent is polyethylene glycol-5 coconut oil base methyl ammonium sulfate.The aerial prevention synergist provided by the present application has good applicability, can effectively improve the performance of pesticide solution, increase the rainwater scouring resistance of pesticide on target, weaken the adverse effects of rainfall on disease and pest control efficiency while improving the stability of various pesticide formulations and fertilizer mix.

A process for inhibiting microbial growth comprising administering a formulation comprising a pyridinium chloride compound of Formula (I), described herein, wherein R1-R6, independently comprise hydrogen, substituted or unsubstituted C1 to C24 alkyl, substituted or unsubstituted alkylaryl, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, sulfonate, aryl sulfonate, C1 to C24 alkyl sulfonate, taurine, carboxylate, amine, alkylamine, arylamine, alkylammonium, arylammonium, sulfonamide, halogen, hydroxy, amide, nitro, cyano, azide, O-alkyl, S-alkyl, silyl, trialkylsilyl, O-silyl, haloalkyl, alkylsulfhydryl, trifluoromethyl, hydrazide, substituted or unsubstituted aryl, heteroaryl, or heterocyclic alkynyl, carboxyalkyl, aminoalkyl, haloalkyl, azidoalkyl, amide, amino acid, or peptide; and X and Y independently comprise a heteroatom selected from oxygen, nitrogen, or sulfur, or a heterocarbyl comprising one or heteroatoms selected from oxygen, nitrogen, or sulfur.

The application provides a durable solid waste-based foam light soil and a preparation method thereof, and comprises the following raw materials in parts by weight: 25-30 parts of alkaline solid waste, 30-40 parts of silico-aluminous solid waste, 5-10 parts of sulfate solid waste, 0.1-0.3 parts of water reducing agent, 0.3-0.5 parts of composite foaming agent, 0.5-1.5 parts of expanding agent, 0.5-1.5 parts of anti-cracking fiber, 2-3 parts of anti-freezing agent, and 35-60 parts of water. The composite foaming agent is a compound of alkyl sulfonate and polymeric sulfonate at a mass ratio of 1:0.3-0.5. The polymeric sulfonate is prepared by copolymerization of an olefin sulfonate monomer and an unsaturated benzyl tertiary amine monomer at a mass ratio of 5-8:3. The polymeric sulfonate can not only form a tough and unbreakable bubble liquid film, but also help to complex calcium ions due to the tertiary amine group on the side group, so as to improve the calcium ion concentration around the foam, form a dense and solid pore wall, and improve the bearing capacity of the pore wall to the frost heaving pressure.

The application belongs to the field of organic synthesis, and relates to a bifunctional compound containing an alkenyl group and a sulfonyl fluoride which can be used as a switchable active linker, and a novel method for orderly linking of different nucleophiles. The method constructs intramolecular non-covalent interaction through Michael addition reaction of N-nucleophiles and the alkenyl end of the switchable active linker, thereby changing the reaction activity of the sulfonyl fluoride end of the linker, so that it can further react with various O- / N-nucleophiles to realize orderly linking between different nucleophiles. Compared with the traditional method of ensuring the orderly reaction by introducing and removing a protecting group, the method for orderly linking of the compound disclosed by the application reduces the operation and time cost of the synthesis process, and the reaction condition is mild and simple, and the reaction reagent is cheap and easy to obtain. In addition, the application also discloses a class of alkyl sulfonate and / or sulfonamide compounds synthesized by the method and the application of the alkyl sulfonate and / or sulfonamide compounds in medicine, materials and the like.

Provided is an electrolyte additive for a lithium-ion battery. The additive includes a sulfonic ester compound, and the sulfonic ester group of the sulfonic ester compound in the additive may form lithium alkyl sulfonate on an anode active material of the lithium-ion battery during a formation process, which helps to form a dense sulfur-rich interface film with high ionic conductivity. In addition, the additive includes the ring structure and unsaturated bond, such that the additive may preferentially perform ring-opening polymerization and / or addition polymerization on the surfaces of the cathode active material and the anode active material of the lithium-ion battery to form a polymer film, and the polymer film may isolate the contact between the surfaces of electrode material and the electrolyte, inhibit side reactions, and reduce a consumption of electrolyte and active lithium ion.

This invention discloses a filling material and method for the gap between tunnel segments and precast track bed structures, belonging to the field of rail transit technology. It comprises the following components in parts by weight: 15-20 parts of calcined magnesium oxide, 10-20 parts of potassium dihydrogen phosphate, 0-20 parts of fly ash, 20-25 parts of water, 3-5 parts of borax, 0.1-0.3 parts of polyvinyl alcohol, 0.1-0.5 parts of alkyl sulfonate, 0.1-0.15 parts of polypropylene fiber, and 30-40 parts of fine sand. This filling material, under its own weight or pressure, can densely fill the gaps between precast components, forming a high-strength structural filler with good interfacial curing and rigid connection. It can provide an effective protective layer for the connectors between precast components, thus protecting the precast components and their connectors.

The application relates to the fine chemical technology field and discloses a supported esterification catalyst, a preparation method thereof and application of the supported esterification catalyst in a methyl methacrylate synthesis reaction. The supported esterification catalyst comprises a spherical composite carrier and an alkyl sulfonate supported on the spherical composite carrier; the spherical composite carrier is an alumina-MCM-41 composite material, and the content of the spherical composite carrier is 45-75% by weight and the content of the alkyl sulfonate is 25-55% by weight based on the total weight of the supported esterification catalyst. The catalyst is used in a methyl methacrylate esterification reaction, and higher methyl methacrylate conversion rate and methyl methacrylate selectivity can be obtained.

The invention relates to the technical field of biological detection and fluorescence labeling, and particularly discloses an alkynyl-substituted azaindole polymethine cyanine dye and a synthesis method and application thereof, the alkynyl-substituted azaindole polymethine cyanine dye has a structure as shown in the following general formula I: in the general formula I, X is selected from H, F, Cl, Br or I; y is a C or N atom; n is an integer of 0, 1 or 2; r1, R3, R5 and R6 are respectively and independently selected from hydrogen, C-Calkyl, C-Ccarboxy alkyl, aryl, aryl carboxylic ester, C-Calkyl sulfonate, aryl sulfonate, C-Calkyl sulfonamide or aryl sulfonamide; r2 and R4 are respectively and independently selected from hydrogen, halogen,-COOH,-NHH,-SOH,-SONHH, C-Calkyl carboxylic ester, C-Camino alkyl, aryl, aryl carboxylic ester, C-Calkyl sulfonate, aryl sulfonate, C-Calkyl sulfonamide or aryl sulfonamide.

The invention discloses an adhesive for automotive trim and a preparation method of the adhesive. On one hand, the invention provides the adhesive for the automotive trim, and the adhesive is prepared from the following components in parts by weight: 18 to 28 parts of SBS (Styrene Butadiene Styrene) thermoplastic elastomer, 8 to 14 parts of SIS (Styrene Isoprene Styrene) thermoplastic elastomer, 48 to 56 parts of high-crystallinity polyester type polyurethane prepolymer, 6 to 12 parts of phenyl alkyl sulfonate, 12 to 24 parts of tackifying resin, 8 to 16 parts of polyurethane acrylic resin and 12 to 18 parts of bifunctional acrylate monomer resin. The light-cured acrylic resin is prepared from the following components in parts by weight: 6-10 parts of a light-cured acrylic monomer, 2-6 parts of an organophosphorus photoinitiator, 1-4 parts of a hindered phenol antioxidant and 4-8 parts of nano titanium dioxide. On the other hand, the invention further provides a preparation method of the adhesive for the automotive trim. According to the present invention, the cost is relatively low, the moisture permeation and water resistance are excellent, the grease solvent resistance is excellent, and the photo-thermal aging resistance is excellent.

This invention relates to a method for preparing a copolymer dispersant and its application. The method for preparing the copolymer dispersant includes the following steps: (1) imidizing an alkyl anhydride containing a carbon-carbon double bond with an amino alcohol to obtain an alcohol containing an imide group and a carbon-carbon double bond; (2) modifying the alcohol containing an imide group and a carbon-carbon double bond obtained in step (1) with an alkyl sulfonate lactone to prepare a polymer unit B; (3) subjecting polymer unit A and polymer unit B obtained in step (2) to free radical polymerization to obtain the copolymer dispersant; wherein polymer unit A is a compound containing an alkenyl group and a phenyl group. The copolymer dispersant provided by this invention exhibits excellent dispersion stability for organic pigments when used in the preparation of aqueous color pastes.

The invention relates to an FER / MFI mixed crystal molecular sieve and a preparation method and application thereof.The preparation method comprises the following steps that S1, an aluminum source, water, hydroxide of alkali metal, an organic template agent, a silicon source and a surfactant are mixed to obtain a raw material mixture, the ratio of silicon to aluminum in the raw material mixture is (10-1000): 1, the ratio of water to silicon is (5-300): 1 in terms of oxide and mole, and the raw material mixture is stirred to be uniform; the ratio of the hydroxide of the alkali metal to the silicon source is (0.01-0.5): 1, the ratio of the organic template to the silicon source is (0.01-1): 1, and the ratio of the surfactant to silicon is (0.01-1): 1; the organic template agent is selected from one or more of nitrogen-containing heterocyclic compounds, and the surfactant is selected from one or more of quaternary ammonium salt, alkyl sulfonate and alkyl sulfate; and S2, carrying out crystallization treatment and roasting treatment on the raw material mixture. The method provided by the invention can further improve the catalytic activity and catalytic stability of the mixed crystal molecular sieve.

The application discloses a kind of blueberry special biological organic fertilizer and preparation method thereof, belong to biological organic fertilizer technical field.The biological organic fertilizer of the application is prepared from grass carbon soil, synergist, pyroligneous liquid, furfural residue, corn straw, phosphoric acid, modifier, microbial inoculant, ferrous sulfate, pine needle, pig manure, EM bacteria liquid.The application is composed of two parts of blueberry special biological organic fertilizer granules and solution.Blueberry special biological organic fertilizer solution is synergized by sodium lignosulfonate and potassium humate in a mass ratio of 1:1 to improve the acidic soil environment around the roots;Activated biochar in blueberry special biological organic fertilizer granules is modified by tea polyphenol and sodium alpha-alkyl sulfonate in a mass ratio of 1:1 to graft strong acidic phosphate functional groups, while the water retention capacity is increased, and various substances such as microbial inoculant, fermented organic nutrients, grass carbon soil and ferrous ion work together to improve blueberry planting soil.

The present invention provides a fluorescent whitening agent or optical brightener of formula (I) or (II) formulated as a surfactant for use in a personal care product, wherein the fluorescent whitening agent or optical brightener of formula (I) or (II) has the structure, wherein: A is CR1R2(CH2)n wherein R1 is H, CH2OH or COY, R2 is H or CH2OH and wherein n is 1 or 2, or wherein A is an optionally substituted aromatic or heteroaromatic ring fused with N and X wherein N and X are respectively bound to adjacent carbon atoms on the ring; X is O, S or NR3; the or each Y is independently OM, OR3, O(CH2)qSO3M, NHOH, NHR3, NR3 2, or X'L, wherein, M is selected from an alkali metal or an alkaline earth metal; the or each R3 is independently hydrogen, a linear or branched alkyl, a linear or branched alkenyl, an aryl, an alkaryl, an aralkyl, a linear or branched alkyl alcohol, a linear or branched alkyl alcohol polyol, a hydroxyalkylamine, a linear or branched alkylamine, a polyhydric alcohol, a sugar, a linear or branched alkyl ether, a polyester having from 2 to 1000 repeat units, or a polyoxyalkylene chain having from 2 to 1000 repeating units; and q is 1 to 5; alternatively, NR3 2 represents a heterocyclic ring; when Y is X'L, X' is O, S or NR3, and L is a linker moiety connected to least one repeating unit of formula (I) or (II) having X' in place of Y; R is H, CHR5R6, R5, R6, an alkylsulphonate, a polyether, an optionally substituted aromatic or heteroaromatic ring, CH2COY or CH(COY)((CH)nCOY) in which each Y may be the same or different, R5 and R6 independently represent hydrogen, alkyl, alkenyl, vinyl, phenyl, hydroxymethyl, 1-hydroxyethyl, 2-hydroxyethyl, 1,2- dihydroxyethyl, aminomethyl, 1-(dimethylamino)methyl, 5-aminopentyl, or cyano, optionally wherein R5 and R6 are the same or different, and n is 1 or 2. Compositions and uses thereof in a personal care product are also provided.

The invention discloses polyfunctional group pyrrole acidic ionic liquid and a preparation method thereof. The polyfunctional group pyrrole acidic ionic liquid is prepared by taking glycol, phosphorus trichloride or phosphorus tribromide, pyrrole, alkyl sultone and a sulfonic acid derivative as raw materials. The method comprises the following steps: preparing dibromo (chloro) glycol by taking glycol, phosphorus trichloride or phosphorus tribromide as a raw material; the preparation method comprises the following steps: reacting pyrrole with dibromo (chloro) glycol to prepare a dinuclear pyrrole intermediate; reacting the dinuclear pyrrole intermediate with alkyl sultone to prepare dinuclear pyrrole sulfonic acid inner salt; the polyfunctional group pyrrole acidic ionic liquid is prepared by taking dinuclear pyrrole sulfonic acid inner salt and a sulfonic acid derivative as raw materials. The invention provides a new scheme for preparing the polyfunctional group acidic ionic liquid.

This invention relates to the field of oilfield oil recovery technology, providing an oil displacement composition and its application, an oil displacement agent and its preparation method and application. The oil displacement composition comprises an alkyl glycoside hydroxyalkyl sulfonate and a betaine-type surfactant. The oil displacement agent comprises an alkyl glycoside hydroxyalkyl sulfonate, a betaine-type surfactant, and water. The oil displacement agent provided by this invention has advantages such as high interfacial activity, strong emulsifying ability, good emulsification effect, and strong stability. It has a large adsorption capacity at the oil-water interface, effectively reduces interfacial tension, and can reduce injection pressure, exhibiting good enhanced oil recovery performance. When applied to enhanced oil recovery, it can significantly improve crude oil recovery. The preparation method is simple, it is convenient to use in oilfields, and it has biodegradability.

This invention discloses a method for preparing and applying anionic waterborne polyaspartic acid ester resin. The preparation method is as follows: (1) reacting an aliphatic polyamine with dialkyl maleate to obtain polyaspartic acid ester; (2) performing an ester exchange reaction between the obtained polyaspartic acid ester and hydroxyalkyl sulfonate to obtain the anionic waterborne polyaspartic acid ester resin. This invention uses hydroxysulfonate to modify polyaspartic acid ester to obtain anionic waterborne polyaspartic acid ester resin with a dendritic macromolecular structure in which anionic sulfonic acid groups extend outward. It can achieve self-emulsification by using water as a solvent, and has better emulsification properties when combined with sulfonate-modified isocyanate curing agents. When applied to coatings, it can produce waterborne PAE polyurea coatings with high strength, high adhesion, and good wear resistance and corrosion resistance.

The invention discloses a branched alkyl sulfonate surfactant as well as a preparation method and application thereof. The structural formula of the branched alkyl sulfonate surfactant is shown in the specification, n is an integer selected from 0-21, m is an integer selected from 1-21, and n + m is 9-21. In the structure of the surfactant, a sulfonic group is located between long-chain alkyl chains, and the surfactant has a unique double-alkyl branched chain structure and a specific chain length, so that the surfactant has better water solubility, salt resistance, calcium and magnesium resistance, wettability and other properties compared with a same carbon chain end group sulfonate surfactant, and can be well used in oil and gas exploitation.

The present invention relates to a pesticide composition comprising at least: a) an effective amount of a pesticide; b) one anionic surfactant selected from alkyl sulfates, alkyl ether sulfates, alkyl sulfonates, alkyl ether sulfonates, alpha olefin sulfonate, alkyl carboxylates, alkyl ether carboxylates, alkyl sulfosuccinates, alkyl ether sulfosuccinates, glutamates, isethionates, taurates, and sarcosinates; and c) one iminodipropionate.

A fire extinguishing agent comprises the following components in percentage by mass: 20-60% of a polar organic solvent, 1-15% of a phosphate inhibitor, 0.1-3% of an anionic surfactant and the balance of water, and the polar organic solvent is ethylene glycol, propylene glycol, glycerol or a combination thereof. The phosphate inhibitor is selected from one or more of dipotassium phosphate, monopotassium phosphate and disodium hydrogen phosphate, the anionic surfactant comprises secondary alkyl sulfonate and alpha-alkenyl sulfonate, the fire extinguishing agent improves the wetting and infiltration capacity by reducing the surface tension, and the fire extinguishing agent improves the wetting and infiltration capacity by combining the heat absorption and cooling effects of a water base and the residual covering effect of phosphate. The fire extinguishing agent can be used as a concentrated solution for storage and transportation, is sprayed or sprayed after being diluted during use, and is suitable for emergency disposal of fire disasters of single batteries, battery modules and electrochemical energy storage systems.