856 results about "Azo compound" patented technology

An electronic device module comprising:A. At least one electronic device, e.g., a solar cell, andB. A polymeric material in intimate contact with at least one surface of the electronic device, the polymeric material comprising (1) an ethylene-based polymer composition characterized by a Comonomer Distribution Constant greater than about 45, more preferably greater than 50, most preferably greater than 95, and as high as 400, preferably as high as 200, wherein the composition has less than 120 total unsaturation unit / 1,000,000C, preferably the ethylene-based polymer compositions comprise up to about 3 long chain branches / 1000 carbons, more preferably from about 0.01 to about 3 long chain branches / 1000 carbons; the ethylene-based polymer composition can have a ZSVR of at least 2; the ethylene-based polymer compositions can be further characterized by comprising less than 20 vinylidene unsaturation unit / 1,000,000C; the ethylene-based polymer compositions can have a bimodal molecular weight distribution (MWD) or a multi-modal MWD; the ethylene-based polymer compositions can have a comonomer distribution profile comprising a mono or bimodal distribution from 35° C. to 120° C., excluding purge; the ethylene-based polymer compositions can comprise a single DSC melting peak; the ethylene-based polymer compositions can comprise a weight average molecular weight (Mw) from about 17,000 to about 220,000, (2) optionally, a vinyl silane, (3) optionally, a free radical initiator, e.g., a peroxide or azo compound, or a photoinitiator, e.g., benzophenone, and (4) optionally, a co-agent.

An ink containing at least one dye represented by formula (1): wherein R1, R2 and R3 are each independently a hydrogen atom or a monovalent group; Z is a nitrogen atom, or a carbon atom to which a hydrogen atom or a monovalent group is bonded; and at least one of R1, R2, R3, and the monovalent group that Z has is a substituent having a heterocyclic group substituted with an azo group.

An electronic device module comprising: A. At least one electronic device, e.g., a solar cell, and B. A polymeric material in intimate contact with at least one surface of the electronic device, the polymeric material comprising (1) a polyolefin copolymer with at least one of (a) a density of less than about 0.90 g / cc, (b) a 2% secant modulus of less than about 150 megaPascal (mPa) as measured by ASTM D-882-02), (c) a melt point of less than about 95 C, (d) an α-olefin content of at least about 15 and less than about 50 wt % based on the weight of the polymer, (e) a Tg of less than about −35 C, and (f) a SCBDI of at least about 50, (2) optionally, free radical initiator, e.g., a peroxide or azo compound, or a photoinitiator, e.g., benzophenone, and (3) optionally, a co-agent. Typically, the polyolefin copolymer is an ethylene / α-olefin copolymer. Optionally, the polymeric material can further comprise a vinyl silane and / or a scorch inhibitor, and the copolymer can remain uncrosslinked or be crosslinked.

The invention discloses a PVC foam wood / plastic composite material and relates to the technical field of composite materials. The PVC foam wood / plastic composite material is made from the following raw materials in parts by weight: 20-70 parts of PVC resin powder, 0-55 parts of wood flour, 5-40 parts of calcium carbonate powder, 0.1-0.5 part of sodium bicarbonate, 0.3-0.6 part of an azo-compound or hydrazine derivative, semicarbazide compound or nitroso-compound, 2-10 parts of a foaming regulator, 1.5-6 parts of a composite stabilizer, 0.7-2.1 parts of a lubricant, 0.5-1.2 part of soybean oil, 2.5-5.5 parts of an impact modifier, and 0.5-3 parts of a processing agent. The PVC foam wood / plastic composite material provided by the invention has the advantages of strong chemical stability, high strength, resistance to acid / alkaline corrosion, resistance to water seepage, flame retardancy and low cost.

This invention is to provide a method for surface-treatment of a water absorbent resin excelling in water absorption properties. This invention relates to a method for the surface-treatment of a water absorbent resin, which comprises: a) mixing 100 parts by weight of a water absorbent resin, 0.01-20 parts by weight of at least one radical polymerization initiator selected from the group-consisting of persulfates, hydrogen peroxide, and azo compounds, and a radically polymerizing compound and b) irradiating the resultant mixture with active energy rays. The treatment particularly exalts the absorption ratio against pressure and the saline flow conductivity.

Aqueous, colloidal gas black suspension containing:(a) a gas black, (b) an azo compound of the formula 1(c) and water. The aqueous, colloidal gas black suspension is produced by dispersing the gas black and the azo compound of the formula 1 in water. It can be used in the production of inks, ink-jet inks, surface coatings and colored printing inks.

A coloring composition for image formation comprising an azo dye having an aromatic nitrogen-containing 6-membered heterocyclic ring as a coupling component, a coloring composition which comprises an azo compound having an oxidation potential nobler than 1.0 V vs. SCE and comprising at least two substituents having a pKa value of −10 to 5 in water, and a method for improving ozone resistance of a color image, the method comprising using a compound having an oxidation potential nobler than 1.0 V vs. SCE and showing a maximum absorption at a wavelength between 500 nm and 580 nm with a half-value width of 150 nm or narrower.

According to the present invention there is provided a method for making lithographic printing plates including the following steps a) preparing a heat mode imaging element consisting of a lithographic base with a hydrophilic surface and a top layer which top layer is sensitive to IR-radiation, comprises a polymer, soluble in an aqueous alkaline solution and is unpenetrable for an alkaline developer containing SiO2 as silicates; b) exposing imagewise said heat mode imaging element to IR-radiation; c) developing said imagewise exposed heat mode imaging element with said alkaline developer so that the exposed areas of the top layer are dissolved and the unexposed areas of the top layer remain undissolved characterized in that said top layer includes an IR-dye selected from the group consisting of indoaniline dyes, cyanine dyes, merocyanine dyes, oxonol dyes, porphine derivatives, anthraquinone dyes, merostyryl dyes, pyrylium compounds, diphenyl and triphenyl azo compounds and squarylium derivatives.

A cross linking maleic anhydride-vinyl acetate copolymer preparation method belongs to the field of copolymers. At present, the research on maleic anhydride-vinyl acetate copolymers mostly focuses on the polymerization research of linear polymers. The invention introduces a monomer, cross linking agents and initiators into medium to dissolve under the condition of nitrogen protection, and reacts for 2 to 24 hours under the temperature of 60 DEG C to 90 DEG C; the monomer is maleic anhydride Man and styrene St, the mol ratio is 1:1, and the mass concentration in the polymerization system is 5 percent to 45 percent; the initiators are organic peroxides or azo compounds, and are 0.05 percent to 1 percent of the total mass of the monomers; the cross linking agents are polyfunctionality alkene organic compounds, and are 0.08 percent to 8.8 percent of the total mass of the reactions system, and the rest is the alkyl ester of medium organic acid. The invention does not use surface active agents or stabilizers, can realize the adjustment and control of crosslinking polymer particle size, appearance and chemical physical properties through the adjustment of the addition amount of the cross linking agents.

The present invention provides an ink jet ink having a magenta color which gives an image excellent in magenta color tone and also excellent in image fastness (lightfastness and gas resistance). The ink jet ink includes a first coloring material that is an anthrapyridone compound having a structure represented by general formula (I) and / or general formula (II) and a second coloring material that is an azo compound having a structure represented by general formula (III), wherein the mass ratio of the content of the first coloring material to the content of the second coloring material is from 2.5 or more to 10.0 or less.

There is provided a colorant compound improved in the dispersibility of an azo pigment into a water-insoluble solvent. The colorant compound is represented by the following general formula (1). R1 denotes an alkyl group having 1 to 6 carbon atoms, or a phenyl group; R2 to R6 each denote a hydrogen atom, or a substituent represented by the following general formula (2); R7 to R11 each denote a hydrogen atom, a COOR12 group, or a CONR13R14 group; and R12 to R14 each denote a hydrogen atom, or an alkyl group having 1 to 3 carbon atoms; and P1 denotes a polymeric component; L1 denotes an alkylene group having 1 to 3 carbon atoms or an arylene group having 6 to 10 carbon atoms; and * denotes a binding site.

A supported non-noble metal catalyst used for preparation of an azo compound from an aromatic nitro compound by hydrogenation coupling is disclosed, an active component of the supported non-noble metal catalyst is any one or more than two of Co, Mn, Fe, Ni and Cu, a carrier is a nitrogen-doped carbon-inorganic oxide composite, the content of the active component in the catalyst is 0.1-15wt%, and an inorganic oxide is any one of alumina, aluminum hydroxide, magnesium oxide, magnesium hydroxide, silica, SBA-15, magnesium aluminum hydrotalcite, titanium oxide and cerium oxide. A preparation process is as follows: the active component and a nitrogen-containing complex are together impregnated on the inorganic oxide, and then calcined at certain temperature. The catalyst has excellent catalytic performance in the preparation of the azo compound from a nitro compound by selective hydrogenation coupling one-step method. The catalyst is simple in preparation, and has high catalytic activity and stability.

Azo compounds represented by formula (1) or (2) (In the formulas, A represents a phenyl group or naphthyl group that has at least 1 substituent. R1-R4 represent a hydrogen atom, lower alkyl group or lower alkoxy group, with at least one of R1-R4 being a lower alkoxy group that has a sulfone group. X represents an optionally substituted amino group, optionally substituted benzoylamino group, optionally substituted phenylamino group, optionally substituted phenyl azo group or optionally substituted naphthotriazole group) and salts thereof.

A diagnostic test kit for detecting the presence or absence of nitrites within a test sample is provided. The test kit comprises an aromatic primary amine that is capable of reacting with a nitrite to form a diazonium ion. The test kit also comprises a lateral flow device that comprises a chromatographic medium and an absorbent material that receives the test sample after flowing through the chromatographic medium. The chromatographic medium defines a detection zone within which is contained a detection reagent (e.g., nucleophilic aromatic amine) that is capable of reacting with the diazonium ion to form an indicator (e.g., azo compound). The indicator exhibits a color that is different than the color of the detection reagent.

There is provided an azo compound for improvement in the dispersibility of an azo pigment into a water-insoluble solvent. The azo compound is represented by the following general formula (1):

Use of at least one type of water-dispersible carotenoid nanoparticles as taste modulators in compositions of matter; process for taste modulation of compositions of matter in which at least one type of water-dispersible carotenoid nanoparticles is added to compositions of matter; and also taste modulators for compositions of matter comprising(A) at least one type of water-dispersible carotenoid nanoparticles and(B) at least one azo compound, comprising at least one azo group.

A process for synthesizing the inorganic phase-change energy-accumulating microcapsules by solution deposition polymerizing method features that the water-soluble organic polyoxyvinylether as phase-change material, the vinyl or bivinyl monomers as the source of shell polymer, the organic solvent as medium, non-ionic surfactant as dispersing-protecting agent and the peroxide or azo compound as trigger take part in deposition polymerizing reaction at 20-100 deg.C to obtain said microcapsules.

A toner is provided that, even in a small amount thereof, gives a satisfactory image density and that is free of image problems, e.g., fogging and offset resistance, even during long-term use and in a high-temperature, high-humidity environment. The toner contains a binder resin, a pigment, and a prescribed azo compound wherein, designating as (A) the solubility of the azo compound in a toluene-hexane solubility test and as (B) the solubility of the binder resin constituting the toner in the toluene-hexane solubility test, the (A) and the (B) satisfy the relationship |(B)−(A)|≦60.

There is provided a metal-containing azo compound suitably used for an recording layer of an optical medium, which is represented by at least one of the following general formulae:wherein M(II) is a bivalent metal, X1 and X2 are each a residue that forms a monocyclic or polycyclic aromatic ring, Y1 and Y2 are each a residue that forms a nitrogen-containing aromatic heterocycle, and one residue is different from the other in at least one of a combination of X1 and X2, and a combination of Y1 and Y2; and there is also provided an optical recording medium of which recording layer comprises said metal-containing azo compound.

The invention provides negative electrode slurry of a lithium ion battery, a positive electrode of the lithium ion battery prepared by using the slurry, and the battery. The negative electrode slurry comprises a negative-electrode active material, a bonding agent, a solvent and a pore-forming agent, wherein the pore-forming agent is selected from one or more in azo-compound and / or sulfonylhydrazine compound. The slurry, the positive electrode and the battery have the advantages that under the condition of guaranteeing no reduction of the compaction density of a negative electrode piece, the porosity of the electrode piece can be increased, the uniformity of pore distribution is increased, the effective area of a liquid phase for conducting lithium ions is improved, the high energy density of the battery is guaranteed, simultaneously the rate capability and the low-temperature performance of the battery are improved and simultaneously the capacity is also improved.

Azo compounds whose free acid forms are represented by the general formula (1) are extremely useful as the dichroic dye to be used in polarizing plates which are excellent in polarization performance and endurance and reduced in the color cross-talk within the visible light region or in polarizers for liquid crystal projectors made by using them; (1) wherein R1 is sulfo, carboxy, or lower alkoxy and R2 is sulfo, carboxy, lower alkyl, or lower alkoxy, with the proviso that a case wherein both R1 and R2 are each sulfo is excepted; R3 to R6 are each independently hydrogen, lower alkyl, or lower alkoxy; and R7 and R8 are each independently hydrogen, amino, hydroxy, sulfo, or carboxy.

A diagnostic test kit for detecting the presence or absence of an enzyme (e.g., leukocyte esterase) within a test sample is provided. The test kit comprises a substrate that is capable of being cleaved in the presence of the enzyme to release a nucleophilic aromatic compound. The kit also comprises a lateral flow device that comprises a chromatographic medium. The chromatographic medium defines a detection zone within which is contained a first reagent (e.g., diazonium ion) that is capable of reacting with the nucleophilic aromatic compound to form a second reagent (e.g., aromatic azo compound). The second reagent exhibits a color that is different than the color of the first reagent. The lateral flow device also includes an absorbent material located adjacent to the chromatographic medium, the absorbent material receiving the test sample after flowing through the chromatographic medium.

A synthetic method of a styrene / maleic anhydride alternating copolymer with low molecular weight belongs to the field of macromolecular precipitation polymerization. Media and chain transfer agents used in the existing methods for preparing styrene / maleic anhydride copolymers by precipitation polymerization have disadvantages. In the synthetic method, the styrene / maleic anhydride alternating copolymer is prepared by taking a mixed solvent of organic acid alkyl ester and alkane as a reaction medium for the precipitation polymerization, alpha-methylstyrene or vinyl acetate as a molecular weight regulator and organic peroxide or an azo compound as an initiator for initiating a copolymerization reaction between styrene monomers and styrene. The synthetic method has simple process, the synthesized copolymer has good properties, and the method has the advantages of being economical, environment-friendly and the like.

A method of making carbon nanotubes doped with iron, nitrogen and sulphur for an oxygen reduction reaction catalyst includes the steps of mixing an iron containing oxidising agent with a sulphur-containing dye to form a fibrous fluctuate of reactive templates and using these for in-situ polymerisation of an azo compound to form polymer-dye nanotubes, adding an alkali to precipitate magnetite, and subjecting the nanotubes to pyrolysis, acid leaching, and heat treatment.

The invention relates to a preparation method of instant ultra-high molecular weight polyacrylamide dry powder. The method comprises the following steps of: taking acrylic amide AM as a monomer, adopting a low-temperature composite initiation system taking NTP and K2S2O8 as main initiators, and an azo compound as an auxiliary initiator; adopting ammonia water and urea as cosolvents; and adding the initiator in batches and controlling the concentration of the cosolvent and the pH value of the medium, so as to obtain the instant ultra-high molecular weight polyacrylamide dry powder. The relative molecular weight range of the ultra-high molecular weight polyacrylamide PAM is that Mw is smaller than or equal to 25000000 and greater than or equal to 5000000. The optimal production technology is determined by discussing the influence factors such as the initiation system, the cosolvent concentration, and the pH value of the medium; the obtained polyacrylamide is rapidly dissolved, and is high in relative molecular weight, high in percent conversion, low in monomer content, high in production efficiency, low in cost and suitable for industrial production.

The present invention relates to an azo compound represented by the following formula (1): wherein A denotes a phenyl group having 1 to 3 substituents such as sulfonic acid group, amino group, lower alkyl groups and lower alkoxyl groups, or a naphthyl group, B denotes hydrogen atom, sulfonic acid group, a lower alkyl group, a lower alkoxyl group or the like, each of R1 to R4 independently denotes hydrogen atom, a halogen atom, a lower alkyl group, a lower alkoxyl group or the like, D denotes —NHCO—, —N═N— or —NH—, E denotes hydrogen atom, a lower alkyl group or a phenyl group having 1 to 3 substituents such as hydroxyl group and amino group, n denotes 0 or 1, and m denotes 0 or 1, or a salt thereof, or a copper complex compound of either of them, which is used for a polarizing plate having excellent polarization performance and durability and furthermore little color leakage in visible light range.