1712 results about "Itaconic acid" patented technology

The present invention relates to the preparation of high-performance polyacrylonitrile-based carbon fiber. Acrylonitrile, itaconic acid and methyl methacrylate in a certain weight proportion are reacted to obtain spinning dope, and the spinning dope is made into greign fiber of high-performance carbon fiber through filtering, solidification, water washing, drafting in hot water, oiling, drying and densifying, re-oiling, drying and densifying for the second time, steam drafting and drying setting. The present invention has the advantages of high drafting rate, homogeneous fibre structure, and small mechanical performance variation coefficient.

The invention discloses a carbon nano tube-containing sulfur-based composite cathode material and a preparation method thereof. The sulfur-based composite cathode material is a ternary composite material AxByCz, wherein A is a dehydrocyclization product of an acrylonitrile-itaconic acid copolymer; B is elemental sulfur; C is a carbon nano tube; x is more than or equal to 30 weight percent and less than or equal to 60 weight percent; y is more than or equal to 30 weight percent and less than or equal to 60 weight percent; and z is more than or equal to 1 weight percent and less than or equal to 20 weight percent. The preparation method comprises the following steps of: in-situ polymerizing an acrylonitrile-itaconic acid monomer on the surface of the multi-wall carbon nano tube, and performing thermal treatment on both of the acrylonitrile-itaconic acid copolymer and the elemental sulfur, so that the sulfur is uniformly dispersed in a substrate formed by the dehydrocyclization of the acrylonitrile-itaconic acid copolymer. The carbon nano tube-containing sulfur-based composite cathode material and a lithium cathode form a secondary lithium-sulfur battery which is charged and discharged at the room temperature. The carbon nano tube-containing sulfur-based composite cathode material has the reversible specific capacity of 697 mAh/g and high cyclical stability.

The invention relates to a synthesis method of drilling fluid filtrate reducer. The method comprises: a, nonionic compound emulsifying agent is dissolved in oil and oil phase is made up; a first monomer chosen from fumaric acid, maleic acid, itaconic acid or crylic acid, a second monomer chosen from N, N- dimethylacrylamide, N, N-diethylacrylamide or acrylamide and a third monomer chosen from 4-vinylbenzenesulfonic acid sodium salt, sodium allylsulfonate, 3-allyloxy-2-dydroxy-1-sodium allylsulfonate, 2- methacryloxypropyl-2-methyl propanesulfonic acid, 2-acrylamido-2-methyl propanesulfonic acid or SMAS are dissolved in water with the molar ratio of 1:1 to 5:1 to 5, the pH value of the solution is adjusted to be between 8 and 11, evocating agent is added and water phase solution is made up; and b, the water solution is added to the oil phase solution and the temperature rises to 40 to 70 DEG C for polymerization. The method of the invention has the advantages of fast polymerization speed, high outcome molecular weight and high outcome stability, good filtrate reducing performance, high temperature resistance and high salt resistant performance.

The invention relates to a methyl acrylate pressure-sensitive adhesive for an LCD polarizer and a preparation method thereof, which belong to the technical field of tackiness agent. The pressure-sensitive adhesive comprises the following three materials with the quality shares: a. weight average molecular weight Mw is 100000-2000000, dispersion degree Mw/Mn is 4-20 acrylate copolymer 100 shares, b. coupling agent, c. cross linker 0-15 shares, the comonomer of prepared acrylate copolymer comprises two parts: 1. (methyl) acrylate monomer : 90%-99.5%, 2. functional monomer: 0.5%-10%, wherein the functional monomer is one or several of (methyl) acroleic acid and (methyl) acroleic acid hydroxy ethyl, (methyl) acroleic acid hydroxypropyl acrylate, itaconic acid, acrylamide, N-hydroxymethyl acrylamide and maleic anhydride. The methyl acrylate pressure-sensitive adhesive does not contain elasticizer or low-molecular-weight acrylate copolymer and the like, can reach the use requirement without cross linker under the condition that the requirement to sticking property is low, and the glue layer has better stress relaxation property, and pressure-sensitive adhesive initial adhesion and stripping strength are both extremely ideal.

The invention relates to a cationic acrylamide copolymer aqueous emulsion-water and the method for preparing the same. The compound comprises 5-25 wt% of cationic polymer, 1.0-15 wt% of polymer stabilizer and 15-32 wt% inorganic salt. Said active cationic polymer comprises 72.8-90 mol% of at least one water-soluble monomer (A), 10-26 mol% of at least one cationic monomer (B), and 0.2-1.0 mol% of at least one hydrophobic monomer (C), and said polymer is prepared through free radical polymerization with pH being 3-8. The monomer (A) (B) possesses general formula respectively, monomer (c) is C1-C8 dialkyl ester of itaconic acid or C1-C32 alkyl ester of acroleic acid or C1-C32 alkyl ester or diene monomer of methacrylic acid. The method is multi-stage, and it can reduce polymerization system viscosity, increase active material content and stability of aqueous emulsion-in-water, which is characterized by high concentration, low cost, good fluidity and easiness for treatment.

A method for preparing polymer for PAN precursor, by copolymerizing the water phase suspend using ammonium persulphate-ammonium sulfite or ammonium bisulfite as a primosome, is disclosed. The polyacrylonitrile powder material is obtained by adding the first monomer acrylonitrile, the second monomer crylic acid, methyl acrylate or acrylamide, and the third itaconic acid, or the first monomer crylic acid, the second monomer methyl acrylate or itaconic acid, and inorganic oxidation-reduction primosome without any metallic ion which comprises ammonium persulphate, ammonium sulfite or ammonium bisulfite and acidified deionized water into the polymerization kettle in defined proportions, controlling the temperature and stirring to react for a time, and discharging by removing the residual monomer, washing and drying. The average molecular weight is from 17.5 myriads to 26.1 myriads, and the distribution index of molecular weight is from 2.70 to 2.91; the intension of polyacrylonitrile precursor tested by spinning sample is from 4.58 to 6.61 CN/dtex; and the carbon fiber strength is 3.61-5.06MPa.

The invention relates to an early-strength polycarboxylic acid water reducing agent and a preparation method thereof. The early-strength polycarboxylic acid water reducing agent is in a liquid state, and the solid content is 40%. The preparation method comprises the following steps: polymerizing modified polyoxyethylene ether or polyoxypropylene ether, (methyl)acrylic acid or itaconic acid, acrylamide, sodium methyl propenyl sulfonate and other monomers under the actions of a molecular weight chain initiator and a chain transfer agent; and neutralizing to obtain the water reducing agent containing carboxy, amino, sulfonic and polyethenoxy side chains. The early-strength polycarboxylic acid water reducing agent provided by the invention has the advantages of low alkali content and high water reducing rate; and when the early-strength polycarboxylic acid water reducing agent, which accounts for 0.6-1.4 wt of the cementing material, is added to the cementing material, the concrete is labor-saving for operation, and the cement mixture has high flowability and good workability. The early-strength polycarboxylic acid water reducing agent can effectively shorten the setting time and enhance the early strength. The invention has the advantages of simple production technique, easily controlled reaction conditions and no environmental pollution.

A multilayer structure comprises a surface layer, a substrate, and optionally additional layers wherein the surface layer comprises or is produced from a blend comprising an ionomer and a polyamide; the ionomer is or must be derived from at least three repeat units derived from ethylene, an α,β-unsaturated C₃-C₈ carboxylic acid, and a dicarboxylic acid or its derivative; and the dicarboxylic acid or its derivative is maleic acid, fumaric acid, itaconic acid, maleic anhydride, fumaric anhydride, itaconic anhydride, maleic acid monoester, fumaric acid monoester, itaconic acid monoester, or combinations of two or more thereof.

Provided is carboxyl modified polyvinyl alcohol, which is prepared with raw materials of a monomer, an initiator and a solvent. The monomer comprises vinyl acetate and a second comonomer, the second comonomer is one solvent or a combination of any solvents selected from maleic acid, itaconic acid, glutaconic acid and itaconic acid anhydride. The preparation method comprises that the continuous polymerization in three kettles is adopted; the vinyl acetate monomer, the second comonomer prepared with the above solvents and the initiator solution are added into three serial polymerization kettles to react; the residence time of the reaction in each polymerization kettle is 60-180 min; and the carboxyl modified polyvinyl alcohol is then prepared through alcoholysis. The method has advantages of high polymerization efficiency, high production efficiency and simple operation. The carboxyl modified polyvinyl alcohol is characterized by excellent cross linking reaction performance, water solubility performance, dispersing performance, rheological performance, anti-skinning performance and anti-foaming performance.

The invention relates to a polyacrylonitrile-based hollow carbon fiber precursor and a preparation method thereof. The polyacrylonitrile-based hollow carbon fiber precursor of the invention can be used for preparing polyacrylonitrile-based hollow carbon fibers. An acrylonitrile binary copolymerization system containing itaconic acid or an acrylonitrile ternary polymerization system containing itaconic acid and methyl acrylate is adopted for spinning by a wet spinning process matched with a circular arc slit spinneret plate, and multiple filament bundles of the hollow carbon fiber precursor can be obtained, wherein the dimension of the outer diameter and the structure of the precursor meet the requirement of a conventional preoxidation carburizing process for precursor fibers, and the groove structure on the surface of the fiber is favorable for improving the interface performance of composite materials.

A process for recovering a desired organic acid from a solution includes the steps of: providing an aqueous solution including at least one desired organic acid or its acid anion; adjusting the proton concentration in the aqueous solution to a desired level, with the desired proton concentration being selected, at least in part, by the amount of available protons needed to associate with the acid anions of the desired organic acid(s) to be recovered and/or acid anions that are weaker than the desired organic acids; and recovering at least a portion of the at least one desired organic acid from the aqueous phase. The desired proton concentration can be based on the amount of available protons being greater than, less than or substantially equal, to the amount of protons needed to associate with the anion of the desired organic acid(s) and acid anions that are weaker than the desired organic acid(s).Specific examples of suitable organic acids include, but are not limited to, ascorbic, succinic, tartaric, glyconic, gulonic, citric, lactic, hialic, maleic, acetic, formic, gluconic pyruvic, propionic, butyric, itaconic acids and mixtures thereof. One embodiment of the present invention relates to the recovery of 2-keto-L-gulonic acid (KLG) from aqueous solutions such as fermentation baths.

The invention relates to a low-temperature heat-sealing high-barrier food packaging film coating latex. The composition points of the mixed monomer of the latex is that vinylidene chloride accounts for 80 to 93 percent of the total amount of the mixed monomer; methyl acrylate, methyl ethyl oxalate, methyl methacrylate, butyl ester, acrylonitrile or methacrylonitrile account for 2 to 10 percent of the total amount of the mixed monomer; itaconic acid, acrylic acid, methacrylic acid account for 0.5 to 5 percent of the total amount of the mixed monomer; the surfactants added are 0.7 portion of SAS and 0.3 portion of sodium dodecyl sulfate; the additive 3 is 0.01 portion of metallic salt. The preparation method includes the following steps: deionized water, surfactant and additive are added in a reactor; the reactor is vacuumized and the gas is replaced by nitrogen gas; the mixed monomer is added. The product of the invention has the advantages of low temperature heat sealing and high barrier performance, and the food using the product has longer shelf life.

The invention discloses an itaconic acid glycidyl ester, which is a compound having a structure shown as a formula I, wherein n represents an average degree of polymerization and satisfies a relation of: 0<n<=10. The epoxy resin has low viscosity and high epoxy value and can be used as an active epoxy resin diluent, when mixed with a market sale common epoxy resin, to reduce viscosity of the market sale common epoxy resin, so as to facilitate curing molding of the epoxy resin. The invention also discloses a preparation method of the itaconic acid glycidyl ester. The method comprises the stepsof: mixing well 100 weight parts of itaconic acid, 200-800 weight parts of epoxy halogenated propane and a catalyst under protection of nitrogen; reacting at 90-140 DEG C for 1-5h; cooling to 60-75 DEG C; adding alkaline compound and water; continuing to react for 2-5 h; washing, depriving solvent and drying to obtain the itaconic acid glycidyl ester. The preparation technology is simple, has strong maneuverability and good process controllability and is easy for industrialized practice.

The invention discloses a novel cement high temperature retarder used for cementing an oil (gas) well as well as a preparing method thereof. The invention relates to a macromolecular polymer which has high temperature resistance and is prepared by using an acetone liquid to deposit and wash an itaconic acid, 2-acrylamide-2-methyl propane sulfonic acid (AMPS), benzoperoxide and the like which are taken as materials. The novel cement high temperature retarder added into a cement pulp has the characteristics of good retardation effect, good fluidity as well as salt and calcium resistance under high temperature and the like. The invention can meet the demands of safe construction on cementing depth wells and ultra-deep wells.

The invention relates to a reinforcing agent for papermaking and a preparation method thereof. The reinforcing agent provided by the invention comprises the following raw materials expressed in mass parts: 15 to 16 parts of acrylamide monomers, 1.4 to 2 parts of N-methylolacrylamide, 1.4 to 2.4 parts of acrylic acid, itaconic acid and acrylate monomers, 1.6 to 2.6 parts of cationic monomers, 75 to 80 parts of water and a redox initiation system accounting for 0.1 to 0.5% of the total amount of the monomers. According to the invention, since N-methylolacrylamide, acrylic acid, itaconic acid and the acrylate monomers are added into the reinforcing agent for papermaking, the reinforcing agent is capable of carrying out self-crosslinking to form a net structure, acting forces among the reinforcing agent and between the reinforcing agent and cellulose are improved, and finally, action effects of the reinforcing agent are enhanced; meanwhile, introduction of the cationic monomers into polymer chains enables the reinforcing agent to have good resistance to interference by hetero-ions and improved adaptability.

The invention relates to a catalyst which uses the phosphor-phosphamide as ligand, which is the phosphor-phosphamide ligand metallic complex of chiral ferrocenyl bone, wherein, the metal is rhodium, ruthenium, iridium, platinum or palladium; and the mol rate between the ligand and the metal precursor is 1.1:1-2.2:1. The ligand is compounded from chiral ferrocenyl to intermediate compound via several reaction steps, to be processed condensation with phosphite ester chloridate to attain the phosphor-phosphamide ligand with different chiral centers. Said ligand has new structure, stable property, simple compounding method, and wider application to the catalyst, which has higher catalysis activity (TON reaches 10000) and higher spatial selectivity (ee reaches more than 99%) in catalyzing asymmetry hydrogenization of itaconic acid, etc.

The invention provides a super slump type polycarboxylate water reducing agent for bored pile concrete. The water reducing agent is in a liquid state and comprises the following ingredients: sodium oleate, water reducing type polycarboxylate plasticizer, slump type polycarboxylate plasticizer, hydroxyethylidene diphosphonic acid, 2-acrylamide-2-methylpropanesulfonic acid/itaconic acid/acrylic acid terpolymer, hydroxypropyl methyl cellulose or hydroxyethyl methyl cellulose, air entraining agent and triisopropanolamine. The super slump type polycarboxylate water reducing agent for bored pile concrete provided by the invention has the following beneficial effects that by using the super slump type polycarboxylate water reducing agent, the bored pile concrete is good in homogeneity, the static bleeding rate of the bored pile concrete can be generally less than 1%, stable working performance can be maintained within a long time span, meeting the working property of concrete after 0.5-5.0h can be met by adjusting the formulation and dosage and improving the compressive strength ratio of the concrete, and the 28 d strength can be more than 130% of that of benchmark concrete. The invention further provides a preparation method of the super slump type polycarboxylate water reducing agent for bored pile concrete.

The invention relates to binary acrylonitrile copolymer spinning solution and a corresponding production method. The spinning solution comprises main monomer acrylonitrile and dimethyl sulfoxide solution with copolymer of itaconic acid Beta- monoester; the weight of the main monomer accounts for 90% to 99.5% of that of monomer, while the weight of the comonomer accounts for 0.5% to 10% thereof. The monomer is composed of the main monomer and the comonomer and the weight percentage concentration of the monomer is from15% to 25%. The dimethyl sulfoxide solution, the main monomer acrylonitrile, the comonomer, free radical initiator of azobisisobutyronitrile are added to a reactor by proportion and then mixed at room temperature and reacted for six to thirty six hours at a constant temperature of 50 DEG C to 70 DEG C to remove bubble of residual monomer and obtain the solution with protection from nitrogen which has bubbled for twenty minutes. The solution has a uniform chain structure and itaconic acid Beta-monoester contains two functional groups of carboxy and ester, thus being able to improve spinnability of polyacrylonitrile resin as well as regulate an oxidation-carbonization process of carbon fiber precursor. Due to introduction of a bifunctional group of monomer itaconic acid Beta-monoester, the amount of acrylonitrile comonomer is greatly reduced to improve performance of carbon fiber.

The invention discloses a mud-resistant polycarboxylic acid water reducer which is prepared from the following components: allyl polyoxyethylene polyoxypropylene ether, components R, R1 and R2, a chain transfer agent, an initiating agent R3 and water, wherein the component R is one or more of maleic anhydride, sodium methallyl sulfonate, vinyl acetate, itaconic acid, itaconic anhydride and fumaric acid; R1 is one or a mixture of two of acrylic acid and methylacrylic acid; R2 is one or more of ascorbic acid, sodium formaldehyde sulfoxylate, ferrous sulfate, tin sulfate, sodium hypophosphite, sodium hydrogen sulfite and oxalic acid. The invention further discloses a preparation method for the mud-resistant polycarboxylic acid water reducer. The mud-resistant polycarboxylic acid water reducer has the following benefits: the water solubility and the steric hindrance of polycarboxylic acid are effectively kept; a large amount of non-hydrophilic structures on branch chains can be used for effectively preventing soil interlayer adsorption, so that the adsorption speed and effect are greatly reduced and the mud-resistant purpose is achieved.

The invention provides a high-performance binder for silicon materials for lithium ion batteries, which is a polyacrylonitrile copolymer, a polymeric monomer of the copolymer comprises acrylonitrile, also comprises a second monomer and/or a third monomer; and the second monomer is a monobutyl itaconate monomer, and the third monomer is selected from a mixture of one or more of an itaconic acid, sodium allylsulfonate, acrylamide, amino, a pyridyl or acylamino monomer, n-butyl acrylate or methyl acrylate. The invention also provides a preparation method of the binder. Compared with existing binders, the binder disclosed by the invention has better binding power, can effectively improve the expansion of silicon materials in the processes of charging and discharging, and can improve the performance of a silicon electrode in the process of cycling. Meanwhile, the binder is simple in preparation method, low in cost and good in repeatability, and can achieve the practical need of mass production.