3500 results about "Nitrile" patented technology

A process for preparing a hydrocyanation catalyst comprising contacting a bidentate phosphorous-containing ligand with a molar excess of nickel chloride in the presence of a nitrile solvent and a reducing metal which is more electropositive than nickel. Preferably, the nickel chloride is dried before use.

PCT No. PCT / JP97 / 00578 Sec. 371 Date Aug. 11, 1998 Sec. 102(e) Date Aug. 11, 1998 PCT Filed Feb. 27, 1997 PCT Pub. No. WO97 / 32030 PCT Pub. Date Sep. 4, 1997A process for preparing alpha -hydroxy acids represented by the general formula (II): RCH(OH)COOH (wherein R represents a hydrogen atom, an optionally substituted C1-C6 alkyl group, an optionally substituted C2-C6 alkenyl group, an optionally substituted C1-C6 alkoxy group, an optionally substituted aryl group, an optionally substituted aryloxy group, or an optionally substituted heterocyclic group) by allowing a microorganism to act on alpha -hydroxy nitriles (I): RCH(OH)CN (wherein R is as defined above) to hydrolyze and convert the alpha -hydroxy nitrites to alpha -hydroxy acids (II), wherein the alpha -hydroxy acids (II) are produced and accumulated in an aqueous solvent by a microorganism having the concentration resistance to the alpha -hydroxy nitrites (I) and / or alpha -hydroxy acids (II) and durability preferably in the presence of a cyanide, and harvested. According to this process, the use of the microorganism having the concentration resistance to the alpha -hydroxy nitriles (I) and / or alpha -hydroxy acids (II) and durability high enough to permit the activity to persist for a long period of time enables alpha -hydroxy acids (II) to be accumulated in high concentrations and cell bodies to be repeatedly used, and hence enables alpha -hydroxy acids (II) to be efficiently prepared. The addition of a cyanide to the reaction system results in more efficient preparation of alpha -hydroxy acids (II).

In the preparation of an improved adhesive composition, an epoxy-based prepolymer is obtained by the reaction of one or more epoxy resins with amino-terminated polyethers and / or carboxyl-terminated butadiene-nitrile rubbers. In one embodiment of the invention, both a solid epoxy resin and a liquid epoxy resin, each of which is a diglycidyl ether of a polyphenol such as bisphenol A, are used. The epoxy-based prepolymer is mixed with an acrylate-terminated urethane resin (preferably, one based on a polyol having a number average molecular weight of at least about 400) and a heat-activated latent curing agent to make an adhesive composition which can be pumpable at room temperature. Curable adhesives capable of expansion to about 100% with high impact resistance after curing may be obtained by inclusion of expanding agents such as expandable microspheres.

The rechargeable lithium battery of the present invention includes a positive electrode including a positive active material, a negative electrode including a negative active material, and a non-aqueous electrolyte. The positive active material includes a core and a coating layer formed on the core. The core is made of a material such as LiCo0.98M′0.02O2, and the coating layer is made of a material such as MxPyOz. The electrolyte solution includes a nitrile-based additive. The rechargeable lithium battery of the present invention shows higher cycle-life characteristics and longer continuous charging time at high temperature.

Processes are provided for the storage and release of hydrogen by means of a substantially reversible catalytic hydrogenation of extended pi-conjugated substrates which include large polycyclic aromatic hydrocarbons, polycyclic aromatic hydrocarbons with nitrogen heteroatoms, polycyclic aromatic hydrocarbons with oxygen heteroatoms, polycyclic aromatic hydrocarbons with alkyl, alkoxy, nitrile, ketone, ether or polyether substituents, pi-conjugated molecules comprising 5 membered rings, pi-conjugated molecules comprising six and five membered rings with nitrogen or oxygen hetero atoms, and extended pi-conjugated organic polymers. The hydrogen, contained in the at least partially hydrogenated form of the extended pi-conjugated system, can be facilely released for use by a catalytic dehydrogenation of the latter in the presence of a dehydrogenation catalyst which can be effected by lowering the hydrogen gas pressure, generally to pressures greater than 0.1 bar or raising the temperature to less than 250° C. or less, or by a combination of these two process parameters.

Metal source containing precursor liquid solutions for chemical vapor deposition processes, including atomic layer deposition, for fabricating conformal metal-containing films on substrates are described. More specifically, the metal source precursor liquid solutions are comprised of (i) at least one metal complex selected from β-diketonates, β-ketoiminates, β-diiminates, alkyl metal, metal carbonyl, alkyl metal carbonyl, aryl metal, aryl metal carbonyl, cyclopentadienyl metal, cyclopentadienyl metal isonitrile, cyclopentadienyl metal nitrile, cyclopentadienyl metal carbonyl, metal alkoxide, metal ether alkoxide, and metal amides wherein the ligand can be monodentate, bidentate and multidentate coordinating to the metal atom and the metal is selected from group 2 to 14 elements, and (ii) a solvent selected from organic amides including linear amides and cyclic amides for such metal source containing precursors.

A carboxylic acid-modified nitrile copolymer latex is provided. The copolymer latex comprises a carboxylic acid-modified nitrile copolymer of an unsaturated monomer having at least one crosslinkable functional group selected from vinyl and epoxy groups. The use of the copolymer latex enables the production of a molded article that does not undergo long stirring and maturation, causes no allergic reactions due to the absence of sulfur and a vulcanization accelerator, has good oil resistance and high mechanical strength, and produces a soft feeling. Further provided is a latex composition for dip forming comprising the copolymer latex, and an article produced from the latex composition by dip forming.

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.

Disclosed in an electrolyte for a rechargeable lithium battery, including a mixture of organic solvents including a cyclic solvent and a nitrile-based solvent represented by formula 1 and a lithium salt.

The invention relates to a phosphorus-containing fire retardant, a preparation method of the phosphorus-containing fire retardant and a flame-retardant epoxy resin prepared from the phosphorus-containing fire retardant, and especially relates to a phosphorus-containing nitrile / DOPO double-base structure phosphorus-containing fire retardant, a preparation method of the phosphorus-containing nitrile / DOPO double-base structure phosphorus-containing fire retardant, and flame-retardant epoxy resin prepared from the phosphorus-containing nitrile / DOPO double-base structure phosphorus-containing fire retardant. The flame-retardant epoxy resin solves the problem that the existing epoxy resin has low flame retardation efficiency and poor compatibility between a polymer matrix and a fire retardant. The preparation method comprises the following steps of 1, dissolving p-hydroxybenzaldehyde and tetrahydrofuran, adding triethylamine into the solution and carrying out stirring, 2, dissolving phosphonitrilic chloride trimer in tetrahydrofuran, dropwisely adding the solution into the reaction system, and carrying out heating and stirring, 3, cooling the reaction system, concentrating the filtrate, pouring the filtrate into water for precipitate separation, carrying out pumping filtration, carrying out recrystallization on the precipitates and carrying out drying to obtain intermediates, and 4, dissolving the intermediates by a solvent, adding p-aminophenol into the solution, carrying out heating reflux, adding DOPO into the reflux product, carrying out condensation, pouring the concentrate into cold ethanol for solid precipitation, and washing and drying the solids to obtain the phosphorus-containing nitrile / DOPO double-base structure phosphorus-containing fire retardant. The flame-retardant epoxy resin comprises epoxy resin, a curing agent and the phosphorus-containing nitrile / DOPO double-base structure phosphorus-containing fire retardant. The preparation method is used for preparing the phosphorus-containing nitrile / DOPO double-base structure phosphorus-containing fire retardant.

The invention discloses a dark blue organic light-emitting material and a preparation method and application thereof. The dark blue organic light-emitting material contains a structural unit disclosedin the invention, wherein, M is B or Bi; X is O, S or NR4; R1-R4 are independently selected from connecting bonds or groups obtained from H-H, H-F, H-O-H, H-S-H, H-CN, saturated hydrocarbons, unsaturated hydrocarbons, fluorinated hydrocarbons, heterocyclic compounds, organoboron, organosilicone, alcohols, mercaptans, ethers, thioethers, phenols, thiophenol, aldehydes, ketones, amines, amides, nitriles or sulfones losing one or more H; R1-R3 are located at any substitution position on rings of the structural unit where R1-R3 are located, and the bond energy between the ring where R3 is locatedand M is greater than or equal to the bond energy between the ring where R2 is located and M. The dark blue organic light-emitting material containing the B / Bi-N main body structure has very narrow light-emitting spectrum and TADF properties; the color purity is high, and the stability is good.

The present invention relates to the preparing technology of composite rubber material. Carbon nanotube via surface treatment and liquid rubber are ultrasonically mixed and added into partial hydrogenated nitrile-butadiene rubber to prepare mother rubber; the mother rubber is mixed with the rest hydrogenated nitrile-butadiene rubber, carbon black, zinc oxide and sulfurizing agent, and the mixture is mixed in a rolling mixer or a Banbury mixer and sulfurized to obtain the carbon nanotube modified hydrogenated nitrile-butadiene rubber. The present invention has the beneficial effects of raised heat performance, antiwear performance, mechanical strength, antiageing performance, etc. raised use performance and expanded application range.

The invention discloses a preparation method of Ibrutinib (I). The preparation method comprises the following steps: performing condensation and methyl oxidization reaction on 4-phenoxyl benzoyl chloride (II) serving as a raw material and methylene cyanide and dimethyl sulfate to generate 4-phenoxyl phenyl (methoxyl) ethenylidene dicyan methane (III); performing pyrazol cyclization reaction between the intermediate (III) and 1-(3R-diazanyl-1-piperidyl)-2-propylene-1-ketone(IV) to obtain 1-[(3R)-[3-(4-phenoxyl phenyl)-4-nitrile-5-amino-1H-pyrazolyl]-1-piperidyl]-2-propylene-1-ketone(V). The pyrimidine cyclization reaction between the intermediate (V) and a cyclization agent is performed to prepare the Ibrutinib (I). The preparation method has easily-available raw materials, and is simple in process, economical and environment-friendly, and suitable for industrial production.

This invention relates to a process for converting a hydrocarbon reactant to a product comprising an oxygenate or a nitrile, the process comprising: (A) flowing a reactant composition comprising the hydrocarbon reactant, and oxygen or a source of oxygen, and optionally ammonia, through a microchannel reactor in contact with a catalyst to convert the hydrocarbon reactant to the product, the hydrocarbon reactant undergoing an exothermic reaction in the microchannel reactor; (B) transferring heat from the microchannel reactor to a heat exchanger during step (A); and (C) quenching the product from step (A).

The invention discloses a lithium ion power battery electrolyte and a lithium ion secondary battery. The electrolyte comprises the following components in percentages by weight: 10% to 20% of a lithium salt mixture, 73% to 88.5% of a high voltage resistant organic solvent, 0.5% to 3% of a stabilizer and 1% to 4% of an auxiliary additive. The lithium salt of the electrolyte in the invention is composed of various lithium salts, and due to the synergistic effect of the various lithium salts, the stability of lithium hexafluorophate is improved; a nitriles solvent, a sulfones solvent and a fluorinated solvent with higher heat stability and higher oxidation potential are contained in the organic solvent, so that the electrolyte can work at relatively high temperature and voltage; the stabilizer is added into the electrolyte, water in the electrolyte can be absorbed, the generation of HF in the electrolyte is reduced, and an SEI film of the battery can be compacter and stabler through the introduction of a film-forming additive, so that the battery has preferable cycle performance.

Perfluoroelastomer compositions comprising perfluoroelastomers having copolymerized units of tetrafluoroethylene, a perfluoro(vinyl ether), and a nitrile-containing cure site monomer are cured with certain nitrogen-containing nucleophilic compounds. The nucleophilic compounds also act as dual curatives in perfluoroelastomer compositions which incorporate other curing agents.

An electrolyte for a rechargeable lithium battery includes a non-aqueous organic solvent; a lithium salt; and an additive including vinylene carbonate, fluoroethylene carbonate, and a nitrile-based compound represented by Formula 1:wherein n ranges from 1 to 12 and R1 and R2 are independently a halogen, a hydrogen, or an alkyl group. Further, the alkyl group can be CmH(2m+1), in which m ranges from 1 to 10. The electrolyte for a rechargeable lithium battery improves storage stability of the rechargeable lithium battery at a high temperature. And, a rechargeable lithium battery including the electrolyte has improved storage stability.

The present invention realtes to a low temperature scouring and bleaching agent belonging to the pretreatment process technology field of the textile printing and dyeing industry, a manufacturing method thereof and a pretreatment process. Said low temperature scouring and bleaching agent consists of promoter QR2010 consisting of carbon tetrachloride, acetic acid esters, alkyl benzenes, emulsifying agents and scouring agents; promoter QR2011 consisting of potassium hydroxide, carbonates and penetrating agents; and promoter QR2020 consisting of acyls and nitriles activating agents and builders. Said three promoters are prepared using routine methods and are deposited solely. When used, the three promoters, together with hydrogen peroxide, are mixed according to different proportions to prepare solutions. Said low temperature scouring and bleaching agent is capable of annealing, boiling and bleaching a variety of cotton as well as cotton blending textiles at any temperature ranging from 40 DEG C to 80 DEG C, and being processed at different scouring and bleaching equipments, with a whiteness of higher than 80% and a capillary effect of 10-20 cm. Compared with the process in existing, the amount used of hydrogen peroxide activating agent is 1 / 7 to 1 / 5 of that originally used, the total energy consumption is reduced, the tonnage of used water is decreased, and billet flaws such as holes bleached by oxygen and lycra folded crepes sourced and bleached are avoided.

A rechargeable lithium battery includes a binder for a rechargeable lithium battery, and a positive active material composition. The binder for the rechargeable lithium battery includes a nitrile-based polymer nanoparticle and a fluorine-containing polymer nanoparticle.

The present invention relates to a block copolymer comprising at least one PA block and at least one PB block. The PA block represents a polymer block comprising one or more units of monomer A, and the PB block represents a polymer block comprising one or more units of monomer B. Monomer A is a vinyl, acrylic, diolefin, nitrile, dinitrile, or acrylonitrile monomer. Monomer B is a radically polymerizable plant oil monomer containing one or more triglycerides. The present invention also relates to a method of preparing a thermoplastic block copolymer by radical polymerizing a radically polymerizable monomer with a radically polymerizable plant oil monomer containing one or more triglycerides, in the presence of an initiator and a transition-metal catalyst system to form the thermoplastic block copolymer. The polymerized plant oil-based block copolymers are useful in a variety of applications, such as asphalt modifiers, rubber compositions, adhesives, tires, in the automobile industry, footwear, packaging, etc.

A polymerizable polymeric photoinitiator according to Formula (I):wherein:PL represents an n+m+p-functional polymeric core;n and m independently represent an integer from 1 to 30;p represents an integer from 0 to 10;o is 0 or 1;INI represents a group selected from the group consisting of a benzophenone, a thioxanthone, a carbazole, a anthraquinone, a camphor quinone, an α-hydroxyalkylphenone, an α-aminoalkylphenone, an acylphosphine oxide, a bisacyl phosphine oxide, an acylphosphine sulfide, a phenyl glyoxalate, a benzoin ether, a benzyl ketal, an α-dialkoxyacetophenone, a carbazolyl-O-acyl-oxime, an α-haloarylketone and an α-haloaryl sulfone;L3 and L4 represent a substituted or unsubstituted divalent linking group comprising 1 to 14 carbon atoms;A represents a radically polymerizable functional group selected from the group consisting of an acrylate, a methacrylate, a styrene, an acryl amide, a methacryl amide, a maleate, a fumarate, an itaconate, an vinyl ether, an allyl ether, an allyl ester, a maleimide, a vinyl nitrile and a vinyl ester; andR4 represents a substituted or unsubstituted alkyl group.Radiation curable compositions containing the polymerizable polymeric photoinitiator and methods for preparing the polymerizable polymeric photoinitiator are also disclosed.

An improved polymerization and work-up process makes it possible to produce specific nitrile rubbers which have a specific calcium and chloride content and have a particularly high storage stability.

An organically complexed nanocatalyst composition is applied to or mixed with coal prior to or upon introducing the coal into a coal burner in order to catalyze the removal of coal nitrogen from the coal and its conversion into nitrogen gas prior to combustion of the coal. This leads to reduced NOx production during coal combustion. The nanocatalyst compositions include a nanoparticle catalyst that is made using a dispersing agent. The dispersing agent includes at least one functional group such as a hydroxyl, a carboxyl, a carbonyl, an amine, an amide, a nitrile, a nitrogen having a free lone pair of electrons, an amino acid, a thiol, a sulfonic acid, a sulfonyl halide, and an. acyl halide. The dispersing agent forms stable, dispersed, nano-sized catalyst particles. The catalyst composition can be formed as a stable suspension to facilitate storage, transportation and application of the catalyst nanoparticles to a coal material. The catalyst composition can be applied before or after pulverizing the coal material or it may be injected directly into the coal burner together with pulverized coal.

The present invention provides a process for producing polyurethane foams from (A1) compounds with a molecular weight of 400-15,000 exhibiting hydrogen atoms that are reactive towards isocyanates, (A2) optionally, compounds with a molecular weight of 62-399 exhibiting hydrogen atoms that are reactive towards isocyanates, (A3) water and / or physical blowing agents, (A4) optionally, auxiliary substances and additives, (A5) compounds with at least one carbonamide group and one nitrile group, and (B) diisocyanates or polyisocyanates, which results in polyurethane foams with lowered emission of formaldehyde and wherein the activity of the raw-material mixture is not significantly influenced and wherein the mechanical properties of the resulting foam (in particular, compression set and ageing behaviour under humid conditions) are not influenced negatively.