2350 results about "Carboxylic salt" patented technology

A high early-strength cementitious composition comprising a hydraulic cement; and a combination admixture system wherein the combination admixture system comprises a polycarboxylate high range water reducing dispersant in combination with an accelerator and a retarder. The admixture allows for acceptable workability and development of high early-strength in cementitious compositions without the use of an external heat source.

A method of forming a film on a substrate using chemical vapor deposition techniques and carboxylate complexes. The complexes and method are particularly suitable for the preparation of semiconductor structures.

Nanoparticle compositions of noble metals, and methods of making them, are described. The nanoparticle compositions are made by reacting a salt or complex of a noble metal, such as Au, Ag, Cu or Pt, with a weak ligand, and a reducing agent, in a single liquid phase. The noble metal is typically provided as a halide or carboxylate. The ligand is preferably a fatty acid or aliphatic amine. The reducing agent is preferably a borohydride reagent, hydrazine, or a mixture thereof. Nanocrystals in the size range of 1 nm to 20 nm are produced, and can be made in substantially monodisperse form.

Nucleoside phosphinoamidite carboxylates and analogs are provided that have the structure of formula (III)wherein A is hydrogen, hydroxyl, lower alkoxy, lower alkoxy-substituted lower alkoxy, halogen, SH, NH2, azide or DL wherein D is O, S or NH and L is a heteroatom-protecting group, unsubstituted hydrocarbyl, substituted hydrocarbyl, heteroatom-containing hydrocarbyl, or substituted heteroatom-containing hydrocarbyl; B is a nucleobase; and one of R11 and R12 is a blocking group and the other is (IV) or (VI)in which W, X, Y, Z, R1 and n are as defined herein.

The present invention provides a method of producing a fluoropolymer, wherein polymerization using a carboxylate ester bond-containing carboxylic acid derivative as a surfactant in an aqueous medium to give the fluoropolymer is conducted, the above carboxylate ester bond-containing carboxylic acid derivative has a carboxylate ester bond and —COOM (M representing H, NH4, Li, Na or K), the above carboxylate ester bond may optionally be substituted by fluorine atom.

An apparatus and method are provided for developing photoresist patterns on electronic component substrates such as semiconductor wafers. The method and apparatus use a specially defined developer composition in sequence with a specially defined rinse composition to develop an exposed photoresist pattern and then to rinse the developed pattern. Both the developer composition and rinse composition contain an anionic surfactant and, when the solutions are used in sequence, have been found to provide a resist pattern which avoids pattern collapse even when small features such as line widths less than 150 nm with aspect ratios of greater than about 3 are formed. It is preferred to use a puddle developing and puddle rinsing process to develop and rinse the exposed wafer. Preferred anionic surfactants are ammonium perfluoroalkyl sulfonate and ammonium perfluoroalkyl carboxylate.

It is an object of this invention to provide a bonding material capable of realizing bonding by metallic bonding at a bonding interface at a lower temperature compared to a bonding material using a metal particle having an average particle diameter of not more than 100 nm and a bonding method. There is provided a bonding material including a metal particle precursor being at least one selected from the group consisting of a particle of a metal oxide, a particle of a metal carbonate, and a particle of a metal carboxylate and having an average particle diameter of 1 nm to 50 μm and a reducing agent composed of an organic substance, wherein the content of the metal particle precursor is more than 50 parts by mass and not more than 99 parts by mass per 100 parts by mass of the bonding material.

The invention relates to a preparation method of a slow-setting polycarboxylic acid water reducing agent, which is implemented by carrying out free radical copolymerization reaction on allylsulfonate monomers, acrylic monomers, polyethylene glycol nono-methyl ether methacrylate macromonomers and maleic anhydride grafted beta-cyclodextrin macromonomers. The invention is characterized in that a beta-cyclodextrin side chain is introduced into a polycarboxylic acid main chain, so that the polycarboxylate water reducing agent has favorable slow setting property, micro air-entraining property and better fluidity. The obtained polycarboxylic acid water reducing agent has the advantages of stable product performance, strong adaptability to cement and favorable compatibility; and the cement paste fluidity is up to higher than 290mm (W / C=0.29), the water reducing rate of concrete is up to 30-40%, and the slump protection time is 3-5 hours. The preparation method provided by the invention has the characteristics of unique technique, excellent product performance and the like.

The present invention discloses a process for preparing a nitrile compound, a carboxylic acid compound or a carboxylic acid ester compound represented by the formula (2): wherein R represents a cyano group, a carboxyl group or an ester group, R1 and R2 each represent a group which does not participate in the reaction, which may have a substituent, and R1 and R2 may be combined to each other to form a ring, which comprises subjecting an acetic acid compound represented by the formula (1): wherein R, R1 and R2 have the same meanings as defined above, to decarboxylation in the presence of a metal catalyst.

A self-leveling cementitious mixture with excellent flow properties and which hardens with a controlled rate of strength development to an ultra-high compressive strength composite composition for use in making articles such as cementitious armor panel with ballistic and blast resistant properties including: a continuous phase resulting from the curing of an aqueous mixture, in the absence of silica flour, of inorganic cement binder, inorganic mineral filler having a particle size of about 150-450 microns, pozzolanic mineral filler, polycarboxylate based self-leveling agent and water. The cementitious mixture may include alkanolamine, such as triethanolamine, and acid or acid salt, such as tartaric acid. The cementitious composition may be reinforced with reinforcing fibers, e.g. glass fibers, in an amount of about 0.5-6.0% by volume of the overall cementitious composition. The fibers are uniformly dispersed in the cementitious composition before it is cured to form a final cementitious armor panel.

A process comprising polymerizing at least one fluorinated monomer in an aqueous medium containing initiator and polymerization agent to form an aqueous dispersion of particles of fluoropolymer, the polymerization agent comprising: fluoropolyether acid or salt thereof having a number average molecular weight of at least about 800 g / mol; and fluorosurfactant having the formula: [R1—On-L-A−]Y+wherein: R1 is a linear or branched partially or fully fluorinated aliphatic group which may contain ether linkages; n is 0 or 1; L is a linear or branched alkylene group which may be nonfluorinated, partially fluorinated or fully fluorinated and which may contain ether linkages; A− is an anionic group selected from the group consisting of carboxylate, sulfonate, sulfonamide anion, and phosphonate; and Y+ is hydrogen, ammonium or alkali metal cation; with the proviso that the chain length of R1—On-L- is not greater than 6 atoms.

There is provided a topical composition that comprises (a) a substantially anhydrous insect repellent selected from the group consisting of ethyl 3-(N-butylacetylamino) propionate or a derivative thereof, p-menthane-3,8-diol, hydroxyethyl isobutyl piperidine carboxylate (1-piperidine carboxylic acid), and mixtures thereof, and (b) a non-volatile solvent. A second embodiment of the present composition includes the same insect repellent, and a volatile solvent, and, optionally, a film former. A third embodiment includes the same insect repellent, a non-volatile solvent, a volatile solvent, and, optionally, a film former.

A degradable disposable diaper includes one or more sheets made of polyolefin with the polyolefin including a prodegradant causing the sheet to degrade. The prodegradant includes a metal compound such as a metal selected from the group consisting of cobalt, cerium, and iron. The preferred metal compound is a metal carboxylate. The polyolefin is preferably polyethylene or polypropylene. A secondary polyolefin may be used to aid the incorporation of the prodegradant into the primary polyolefin. A filler may also be used with the polyolefin and prodegradant. The filler preferably has a particle size less than 150 mesh and is free of water. The filler is preferably calcium carbonate having a 1 to 10 micron particle size. The sheet contains between about 0.001 and about 15 weight % prodegradant and most preferably between about 0.01 and about 3 weight % prodegradant. The sheet also includes up to about 15 weight % filler. The diaper also includes a degradable absorbent core.

The invention discloses a preparation method and an application of an acrylate heterozygotic emulsion. In the invention, the acrylate heterozygotic emulsion is synthesized by adopting a seed emulsion polymerization process and combining a process of instantly neutralizing and segmentally adding polar monomers. The acrylate heterozygotic emulsion comprises macroparticles consisting of polymers P2 rich in hydroxyl groups on a surface layer and microparticles consisting of polymers P1 rich in carboxylate on the surface layer. Compared with a conventional hydroxy acrylate emulsion, the acrylate heterozygotic emulsion has smaller mean grain size and wider grain size distribution on emulsion particles. The acrylate heterozygotic emulsion can be adopted to prepare aqueous bi-component polyurethane wood coatings, and a coating layer of the coating has excellent property of resisting water and solvents, high crosslinking density and hardness, good mechanical property, scratching resistance and wear resistance. The acrylate heterozygotic emulsion has compact coating structure, high glossiness and better combination property, and not only can be applied to high-grade wood coatings, but also can be applied to automotive refinish paint, metallic anti-corrosion paint, other industrial protective paint, and the like.

The invention belongs to the technical field of preparation of semiconductor nanomaterials and discloses a single-size CsPbX3 perovskite nanocrystalline preparation method. The method includes: adding cesium carboxylate solution into N2 protected lead bromide solution to realize reaction for obtaining single-size CsPbBr3 perovskite nanocrystalline; scattering the single-size CsPbX3 perovskite nanocrystalline into normal hexane, and gradually adding lead chloride solution or lead iodide solution drop by drop to realize reaction for obtaining single-size CsPbBr3 perovskite nanocrystalline. The single-size CsPbX3 perovskite nanocrystalline preparation method has the advantages of simplicity in operation, easiness in size adjustment of products, component controllability and the like.

A process comprising polymerizing at least one fluorinated monomer in an aqueous medium containing initiator and polymerization agent to form an aqueous dispersion of particles of fluoropolymer, the polymerization agent comprising: fluoropolyether acid or salt thereof having a number average molecular weight of at least about 800 g / mol; and fluorosurfactant having the formula:[R1—On-L-A−] Y+wherein: R1 is a linear or branched partially or fully fluorinated aliphatic group which may contain ether linkages; n is 0 or 1; L is a linear or branched alkylene group which may be nonfluorinated, partially fluorinated or fully fluorinated and which may contain ether linkages; A− is an anionic group selected from the group consisting of carboxylate, sulfonate, sulfonamide anion, and phosphonate; and Y+ is hydrogen, ammonium or alkali metal cation; with the proviso that the chain length of R1—On-L- is not greater than 6 atoms.

Alicyclic carboxylates, such as alicyclic norbonane sodium dicarboxylate, may be used in relatively small amounts as crystallization nucleating agents for foamed polypropylene. The alicyclic carboxylates give improved cell structures at lower proportions than conventional crystallization nucleating agents. The use of alicyclic carboxylate crystallization nucleating agents together with conventional nucleating agents may help give lower density polypropylene foams across a broader melt temperature range.

Processes for preparing 10-amino-3-hydroxy-4-oxo-4,6,7,8,9,10-hexahydropyrimido[1,2-a]azepine-2-carboxylates and related compounds are disclosed. The preparation of carboxamide derivatives from these carboxylates is also disclosed. The carboxamides are HIV integrase inhibitors and are useful for treating HIV infection and AIDS.

The invention relates to a composite oil displacement agent containing a polymer and a cationic / anionic surfactant, and an oil displacement method, and mainly solves a problem of bad oil displacement efficiency of composite oil displacement agents used in the prior art. The composite oil displacement agent containing a polymer and a cationic / anionic surfactant includes the cationic / anionic surfactant, the polymer and water; the cationic / anionic surfactant comprises an anionic surfactant and a cationic surfactant according to a molar ratio of (1-100):1; the anionic surfactant is anyone of sulfonate, carboxylate and phosphate; the cationic surfactant is a quaternary ammonium salt or quaternary ammonium alkali; the polymer is modified polyacrylamide obtained by copolymerizing two monomers of acrylamide, 2-acrylamide-2-methylpropanesulfonic acid, and a molar ratio of the two monomers in the modified polyacrylamide is (1-4):1. The composite oil displacement agent solves the problem and can be used for enhanced oil displacement production of high temperature and low salinity oil reservoirs.

To provide a defoaming agent causing less cissing. The defoaming agent contains an aluminum carboxylate (A) and hydrocarbon oil (B), but contains no alkaline earth metals, wherein (A) is an aluminum di-carboxylate (A2) or a mixture of an aluminum mono-carboxylate (A1) and an aluminum di-carboxylate (A2), the content, by weight, of (A) is 0.1-60% and the content of (B) is 40-99.9% based on the weight of (A) and (B), and the content of A(1) is <=40% based on the total weight of (A1) and (A2). In addition, the defoaming agent contains free fatty acid (FA) and the content of (FA) is preferably 1-30% based on the weight of (A1) and (A2). In addition, the defoaming agent contains hydrocarbon oil (B) containing aromatic carbon (BA), and the content of (BA) is preferably 1-30% by number based on the total number of carbons of (B).

Methods are provided for removing filter cake containing a bridging agent soluble in a carboxylic acid salt from a formation fluids producing zone penetrated by a well bore. The methods basically comprise the steps of introducing in an aqueous carrier liquid a carboxylic acid ester and a base for slowly catalyzing the hydrolysis of the ester and forming a carboxylic acid salt therewith into the producing zone, and allowing the base to catalyze the hydrolysis of the carboxylic acid ester to form the carboxylic acid salt so that the carboxylic acid salt dissolves the bridging agent and the filter cake is removed.

Improvements in increasing the amount of available silver in thermoplastic articles comprising certain silver-containing antimicrobial agents are provided. Such an invention requires the incorporation of a sufficient amount of a carboxylic acid salt within the thermoplastic article simultaneously with the necessary silver-containing antimicrobial agent. Certain carboxylic acid salts are standard acid scavengers for thermoplastic applications; however, the amounts required within this inventive thermoplastic article is well in excess of that commonly added within such articles. Surprisingly, such an excess amount of such standard salts, as well as other non-standard salts, present within the target thermoplastic causes the release of greater amounts of silver to the target article's surface, thereby permitting a greater degree of antimicrobial activity, among other potential benefits for such an increase in surface-available silver. Methods of forming such inventive thermoplastics are also encompassed within this invention.

The invention discloses a formula of a ceramic aggregate aerated concrete brick and a method for making the concrete brick. The compositions in portion by weight of the concrete brick are: 12 to 26 portions of cement, 26 to 46 portions of fly ash, 16 to 28 portions of ceramic aggregate, 2 to 6 portions of slag, 2 to 6 portions of cinder, 16 to 26 portions of water and 2 portions of addition agent, wherein the concrete matters in percentage by weight of the addition agent are: 10 to 18 percent of aluminum powder (a foaming agent), 20 to 45 percent of polycarboxylate (a water reducing agent), 15 to 35 percent of 1122 fly ash excitant and 20 to 50 percent of coagulant hardening accelerator in which calcium chloride and sodium sulfate compounds respectively occupies 50 percent. The concrete steps for making the ceramic aggregate aerated concrete brick are as follows: raw materials are weighed; the weighed raw materials are placed in a stirring machine to carry out stirring and mixing in advance; an addition agent is added in the stirring machine to carry out full stirring; a brick die is prepared, and stirred raw materials are cast in the brick die; initial set and forming are carried out; stripping is carried out; a water-proofing agent is sprinkled on a stripped brick; and natural curing is carried out. Moreover, the obtained brick has light dead weight, low density, high strength, low water absorption rate and excellent sound insulation performance and heat-shielding performance.

The invention relates to a preparation method of azilsartan, comprising the following steps of: (1) preparing ethoxybenzimidazole-7-methyl carboxylate; (2) preparing 2-cyan-4'-bromomethyl biphenyl; (3) dissolving the ethoxybenzimidazole-7-methyl carboxylate and the 2-cyan-4'-bromomethyl biphenyl into ethanol; adding potassium carbonate to react to obtain 1-[(2'-cyan diphenyl-4-yl)methyl]-2-ethoxybenzimidazole-7-methyl carboxylate; (4) suspending the 1-[(2'-cyan diphenyl-4-yl)methyl]-2-ethoxybenzimidazole-7-methyl carboxylate in water; adding hydroxylamine hydrochloride, sodium hydroxide and tetrabutylammonium fluoride; heating and reflowing, and then cooling; adding the sodium hydroxide and ethyl chloroformate, heating and reflowing to obtain azilsartan methyl ester; and (5) hydrolyzing the azilsartan methyl ester to obtain a product. The preparation method of the azilsartan, disclosed by the invention, has the advantages of being short in process route, high in yield, and safe and reliable; and the purity of the azilsartan obtained by using the method is high.

This invention relates to a method of absorbing SO2 gas by the hydramine carboxylate ion liquid, which belongs to the chemical field. In the normal temperature, the aminoethyl alcohol, diethylehthanolamine, triethanolamine, and the diglycol have neutralization reaction with the acetic acid, lactic acid or the acid with similar structure, and then create a series of corresponding alkaline ion liquor. It cost small balancing time through using that ion liquor or loaded in the carrier to absorb the acid gas SO2.

The present invention provides a processes, having practical utility, for preparing 2-oxindoles, N-hydroxy-2-oxindoles, or mixtures thereof comprising: catalytically hydrogenating a 2-nitroarylmalonate diester to produce a 2-(N-hydroxyamino)arylmalonate diester, a 2-aminoarylmalonate diester, or mixtures thereof as a first reaction intermediate; cyclizing, by intramolecular aminolysis of one ester group, the first reaction intermediate to produce a N-hydroxy-2-oxindole-3-carboxylate ester, 2-oxindole-3-carboxylate ester, or mixtures thereof as a second reaction intermediate; and hydrolyzing and decarboxylating the remaining ester group of the second reaction intermediate to produce the N-hydroxy-2-oxindole, the 2-oxindole, or mixtures thereof, wherein the cyclization reaction and the hydrolysis and decarboxylation reaction are conducted in situ with the catalytic hydrogenation reaction without isolation of said reaction intermediates.

The invention discloses technology of preparing aluminium oxide based continuous fibers by a sol-gel process, which is characterized by adding one or more organic acid containing 1-8 carbon atoms into distilled water, adding aluminum powder and a catalyst after the mixture is evenly mixed and ensuring the mixture to react under the conditions of continuous stirring and reflux condensation under certain temperature to obtain transparent aluminum carboxylate solution; evaporating redundant organic acid in the aluminum carboxylate solution and then adding a solvent, a silicon-containing additive and a given quantity of spinning assistants to obtain precursor solution of aluminium oxide based fibers; concentrating the solution to obtain precursor sol of spinnable aluminium oxide based fibers; spinning by a dry or wet method to obtain aluminium oxide based continuous precursor fibers containing organics; and drying and sintering the precursor fibers to obtain the aluminium oxide based fibers. The aluminium oxide based continuous fibers prepared by the technology can be used in reinforcement in the composite, further improve the strength, ductility and heat resistance of the material and are widely applied in the fields of aerospace, automobile and the like.