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319 results about "2-Methyl propane" patented technology

Firstly it is 2-methyl propane and not 2,2 dimethyl ethane. Secondly, yes the two are structural isomers since both have the formula C4H10 and different in structure and properties.

Method for preparing high-temperature resistant and salt resistant tackifier for drilling fluid

ActiveCN101955564ASolve the problem of viscosity reductionInhibition of hydration dispersionDrilling compositionGramTackifier
The invention relates to a method for preparing high-temperature resistant and salt resistant tackifier for drilling fluid, which comprises the following: (1) a step of preparing raw materials, in which 56 to 60 grams of 2-acrylamido-2-methyl propane sulfonic acid, 20 to 30 grams of acrylamide, 15 to 25 grams of acrylic acid and 0.1 to 0.2 grams of initiator are prepared according to the additionamount in each 100 milliliters of water; (2) a step of preparing mother solution, in which the 2-acrylamido-2-methyl propane sulfonic acid, the acrylamide and the acrylic acid are added into water toprepare initial mother solution, the pH value of the initial solution is regulated to 6 to 7 with sodium hydroxide solution at a mass percentage concentration of 20 to 30 percent to prepare the mother solution; (3) a step of polymerization, in which the mother solution obtained by the step (2) to 60 to 80 DEG C, the initiator is added, and a reaction is performed for 2 to 4 hours; and (4) a step of drying, in which the mixture formed after the reaction in the step (3) is dried at 95 to 105 DEG C and crushed, and thus the high-temperature resistant and salt resistant tackifier for drilling fluid is prepared. When added in high-temperature and high-salt drilling fluid, the high-temperature resistant and salt resistant tackifier for drilling fluid can regulate flow type, flocculate and coat drillings and inhibit shale hydrous disintegration.
Owner:北京奥凯立科技发展股份有限公司

Vinyl alcohol copolymers for use in aqueous dispersions and melt extruded articles

In a method of preparing an aqueous dispersion selected from drilling fluids, hydraulic cement compositions, mineral pigment containing coatings, and papermaking furnishes or in a method of preparing a melt extrudate, the improvement comprising: a) producing a copolymer of vinyl alcohol (VOH) and 2-acrylamido-2-methyl propane sulfonic acid or a salt of such acid (AMPS) by steps including continuously feeding with agitation, vinyl acetate (VAM) and AMPS as comonomers, a free radical yielding polymerization initiator, and a solvent for said comonomers, initiator, and copolymer resulting from the copolymerization of said comonomers, maintaining the resulting reaction mass in said first reaction zone under polymerization conditions for a residence time sufficient for a major proportion of AMPS fed to said first reaction zone to polymerize, continuously feeding reaction mass from said first reaction zone with an additional supply of AMPS to a second reaction zone, maintaining the reaction mass in the second reaction zone for a residence time sufficient to polymerize a major proportion of the AMPS added to the second reaction zone, continuously withdrawing reaction mass from the second reaction zone, separating copolymer of VAM and AMPS from the latter reaction mass, and saponifying by hydrolysis and/or alcoholysis a major proportion of the acetate groups in said copolymer to form a copolymer of VOH and AMPS; and b) incorporating the saponified copolymer into the aqueous dispersion or melt extrudate.
Owner:SEKISUI SPECIALTY CHEM AMERICA

Amphoteric ionic polymer water base fracturing fluid thickening agent and preparation method thereof

ActiveCN103131404AWith hydrophobic associationStrong shear stabilityDrilling compositionWater basedPolymer science
The invention relates to an amphoteric ionic polymer water base fracturing fluid thickening agent and a preparation method of the amphoteric ionic polymer water base fracturing fluid thickening agent, and belongs to the technical field of propping agent fracturing fluid used for oil and gas reservoir volume increase and injection increasing measures. The amphoteric ionic polymer water base fracturing fluid thickening agent is prepared through copolymerization of alkyl group acrylic amide, acrylic amide, 2-acrylic amide group-2-methyl propane sulfonic acid sodium aqueous solution, cationic monomers, vinyl monomers and polymerizable surface active agent monomers. The amphoteric ionic polymer water base fracturing fluid thickening agent and the preparation method of the amphoteric ionic polymer water base fracturing fluid thickening agent have the advantages that raw materials used for the amphoteric ionic polymer water base fracturing fluid thickening agent are all industrial products, purification treatment is not needed before a reaction, a complexing agent is added so that polymerization of the complexing agent and an initiating agent can be initiated at an appropriate temperature, and the preparation technology is simple; due to the fact that the surface active agent monomers are added, an obtained polymer has a hydrophobic association function and is higher in shearing stability, easy to dissolve, free of pollution and harm and good in sand carrying performance; and the amphoteric ionic polymer water base fracturing fluid thickening agent can be resistant to the high temperature of 180 DEG C, is suitable for fracturing of high temperature strata, has high shearing-resistant performance to meet the requirement of high-flow fracturing construction, has high sand carrying performance and no-residue performance, and causes no harm to reservoir strata.
Owner:CHINA PETROLEUM & CHEM CORP +3

Oil field compound type anti-scale corrosion inhibitor and preparation method thereof

The invention relates to an oil field compound type anti-scale corrosion inhibitor and a preparation method thereof, belonging to the technical field of corrosion inhibitor. The oil field compound type anti-scale corrosion inhibitor is characterized by comprising the components by mass percent: 5-10% of sodium molybdate, 10-20% of sodium phosphate, 0.5-1% of acrylic acid-2-acrylamido-2-methyl propane sulfonic acid (AA-AMPS) copolymer, 1-2% of amino trimethylene phosphonic acid and 1-2% of hydroxyl ethylidene diphosphonic acid (HEDP). The preparation method comprises the steps of: firstly, completely dissolving sodium molybdate and sodium phosphate by using water; then, adding the AA-AMPS copolymer under the condition of stirring until the copolymer is completely dissolved; subsequently, adding ATMP and the HEDP, and further stirring for dissolving; and finally, adding water until the concentration of the mixed solution is in accordance with the requirement, so as to obtain the oil field compound type anti-scale corrosion inhibitor. The inhibitor disclosed by the invention has the advantages of simple components, available raw materials, simple technology, high efficiency, low cost, low dosage, good scale inhibition, descaling and corrosion inhibition effects and the like, and is convenient to prepare, rapid.
Owner:E TECH ENERGY TECH DEV CORP

Slow-release slump-retaining type polycarboxylic acid high-performance water reducing agent and preparation method thereof

The invention relates to a slow-release slump-retaining type polycarboxylic acid high-performance water reducing agent and a preparation method of the slow-release slump-retaining type polycarboxylic acid high-performance water reducing agent, and belongs to the technical field of concrete admixtures. The reducing agent is characterized in that a polycarboxylate-type water reducing agent is provided and the polycarboxylate-type water reducing agent comprises the following components in parts by weight: 300 parts of isoamyl alkenyl polyoxyethylene ether, 1.5-3 parts of initiating agents, 93-164 parts of liquid A, and 64-137 parts of liquid B, wherein the liquid A is prepared from acrylic acid, hydroxyethyl acrylate, hydroxy-propyl acrylate, 2-acrylamido-2-methyl propane sulfonic acid (AMPS) and water; and the liquid B is prepared from a chain transfer agent and water. The water reducing agent is the slow-release slump-retaining type polycarboxylic acid high-performance water reducing agent; the slow-release slump-retaining type polycarboxylic acid high-performance water reducing agent is high in adaptability, and high in slump-retaining performance; moreover, the production process is a constant-temperature process, the heating is not needed so that the energy sources are saved; and compared with the prior art, the slow-release slump-retaining type polycarboxylic acid high-performance water reducing agent has the advantages that the production period is greatly shortened, and the production efficiency is improved.
Owner:四川恒泽建材有限公司

High-early-strength polycarboxylate water reducer as well as synthesis method and application method of polycarboxylate water reducer

InactiveCN103965414AVitamin CSynthesis methods
The invention belongs to the technical field of building materials, and in particular relates to a polycarboxylate water reducer with high water-reducing rate and good early-strength effect as well as a synthesis method and an application method of the polycarboxylate water reducer. The synthetic raw materials for the water reducer comprise isobutylene alcohol polyoxyethylene ether (HPEG), acrylic acid (AA), 2-acrylamide-2-methyl propane sulfonic acid (AMPS), hydrogen peroxide (H2O2), vitamin C (VC), thioglycollic acid (TGA), a base and water. The synthesis method comprises the following steps of mixing AA and AMPS with water to prepare a 45%-65% of solution compound A; then, mixing TGA and VC with water to prepare a 2%-5% of solution B material; mixing HPEG with water to prepare a 45%-65% of HPEG aqueous solution, adding the HPEG aqueous solution to a reaction kettle and heating under stirring so that complete dissolution is achieved, adding H2O2 when the temperature is raised to (40-45) DEG C, and dropwise adding the solution A material and the solution B material, wherein the adding time of the solution A material is controlled at 2-3 hours and the adding time of the solution B material A is controlled at 2-3 hours; after the dropwise addition is completed, maintaining the temperature for 1-2 hours and adjusting pH to be 6-8 after the reactant is cooled to obtain the desired product. According to the invention, the process is simple, the product has stable performance and good market prospects.
Owner:TONGJI UNIV
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