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3284 results about "Acetylacetone" patented technology

Acetylacetone is an organic compound with the formula CH₃COCH₂COCH₃. It is a colorless liquid, classified as a 1,3-diketone. It exists in equilibrium with a tautomer CH₃C(O)CH=C(OH)CH₃. These tautomers interconvert so rapidly under most conditions that they are treated as a single compound in most applications. It is a colorless liquid that is a precursor to acetylacetonate anion (commonly abbreviated acac⁻), a bidentate ligand. It is also a building block for the synthesis of heterocyclic compounds.

Organometallic compound and organic electroluminescence device employing the same

Organometallic compounds and organic electroluminescence devices employing the same are provided. The organometallic compound has a chemical structure represented below:wherein, X is C—H or N, Y is CH2 or NH; R1 is H, or C1-8 alkyl; and A1 is acetylacetone ligand, acetylacetone with phenyl group ligand, or derivatives thereof.
Owner:IND TECH RES INST

Organic electroluminescent display element, finder screen display device, finder and optical device

An organic electroluminescent display element has at least a positive electrode, an organic luminescent film, an electron injection layer and a negative electrode. Each of the positive and negative electrodes is formed of a transparent conductive film, the electron injection layer is formed of a thin transparent film made of a halogenide of an alkali metal or an alkaline earth metal, or an organic metal complex containing an alkali metal or an alkaline earth metal as a metal, and the organic metal complex is at least one complex selected from the group consisting of acetylacetonate complexes, alpha-nitroso-beta-naphthol complexes, salicylaldoxime complexes, cupferron complexes, benzoinoxime complexes, bipyridine complexes, phenanthroline complexes, crown complexes, proline complexes and benzoylacetone complexes.
Owner:KONICA MINOLTA INC

Catalyst composition of ethylene oligomerization and the application

The present invention relates to catalyst composition for oligomerizing ethylene and its application. The catalyst composition includes complex of acetylacetone chromium, tetrahydrofuran chromium chloride and / or chromium isooctanate; ligand containing P and N; activator of methyl aluminoxane, ethyl aluminoxane, propyl aluminoxane and / or butyl aluminoxane; and promoter of X1R6X2, where, each of X1 and X2 is F, Cl, Br, I or alkoxyl, and R6 is alkyl or aryl group; with the molar ratio of the complex, the ligand, the activator and the promoter being 1 to 0.5-10 to 50-3000 to 0.5-10. The catalyst composition is used in oligomerizing reaction of ethylene to prepare 1-octene, and has high catalytic activity and high 1-octene selectivity.
Owner:PETROCHINA CO LTD

Hydroxymethyl Furfural Oxidation Methods

A method of oxidizing hydroxymethylfurfural (HMF) includes providing a starting material which includes HMF in a solvent comprising water into a reactor. At least one of air and O2 is provided into the reactor. The starting material is contacted with the catalyst comprising Pt on a support material where the contacting is conducted at a reactor temperature of from about 50° C. to about 200° C. A method of producing an oxidation catalyst where ZrO2 is provided and is calcined. The ZrO2 is mixed with platinum (II) acetylacetonate to form a mixture. The mixture is subjected to rotary evaporation to form a product. The product is calcined and reduced under hydrogen to form an activated product. The activated product is passivated under a flow of 2% O2.
Owner:BATTELLE MEMORIAL INST

Preparation method of metal monatomic site catalyst

The invention provides a preparation method of a metal monatomic site catalyst. According to the synthetic strategy, a porous complex composite material coated with an acetylacetone metal salt is formed from a zinc compound and an imidazole organic ligand through coordination in a methanol solution of the acetylacetone metal salt, and then a porous carbon support doped with nonmetal heteroatomic nitrogen is formed from the imidazole organic ligand through a high-temperature pyrolytic reaction in an inert gas atmosphere, wherein metal atoms interact with surrounding nonmetal heteroatomic nitrogen and exist in the form of single atoms. The method is simple, safe, low in cost and applicable to synthesis of various noble metal and non-noble metal monatomic site catalysts, and the obtained metal monatomic site catalyst is high in metal concentration and good in heat stability, can be applied to the fields of energy, catalysis, medicine, biology and the like and has quite broad market prospect.
Owner:TSINGHUA UNIV

Olefine polymerization catalyst, synthesis method and its use

The invention is a styrene or alpha olefine polymerization catalyzer, the synthesizing method and the use. The catalyzer is a pyridyl di-imine back-transition metal suitable matter, synthesized by pyridyl di-imine and back-transition metal compound and can catalyze the polymerization of styrene or alpha-olefine. The product is mainly ruleless polystyrene.
Owner:SHANGHAI INST OF ORGANIC CHEM CHINESE ACAD OF SCI +1

Organosilicon pesticide booster and preparing method thereof

InactiveCN101011062ALower the surface tension of the liquidGood physiological safety performanceBiocideAnimal repellantsSodium bicarbonatePlatinum
The invention relates to an organic silicon pesticide booster with low surface tension, less side effect and high yield. The chemical formula of invention is as following one, wherein, Me=CH3, R1=CH3, R2=H, CH3, C4H9, -O(O)CCH3, x=0-10, y=1-20, a=5-25, b=0-15. And the preparation comprises that putting the hydrogen siloxane and polyalkenylethers into reaction kettle, protected by N2, to increase temperature and be mixed quickly; then adding some platinum-1.3-divinyl tetramethyl disilyloxy-acetylacetone as catalyst, naturally increasing temperature to 110Deg. C, making solution transparent, adding baking soda, compressing and filtering, to obtain needed organic silicon pesticide booster. The invention has wide application in variable pesticides.
Owner:ZHANGJIAGANG JUNBO NEW MATERIAL

Method and equipment of preparing high performance zirconium oxide continuous fiber

A process for preparing high-performance continuous fibre of zirconium oxide includes such steps as synthesizing acetylacetone-zirconium polymer as precursor from acetylacetone and zirconium oxychloride as main materials, dissolving in methanol to obtain the spinning solution, drying spinning to obtain continuous fibre of precursor, heat treating in a multifunctional sintering furnace by special atmosphere and high-temp. airflow spraying for stretching. Its advantages are high tensile strength (over 2.6 GPa) and long length up to several kilometers.
Owner:绍兴市圣诺超高温晶体纤维材料有限公司

Bidentate ligand and its iridium complex and electroluminescent device therewith

Bidentate ligand, iridium complex and electro-generated phosphorescent device of iridium complex are disclosed. The bidentate contains cavity transmission group carbazole, the chemical formula of the iridium complex is Ir(C^N)2 (acac), acac= acetyl acetone. The electro-luminescent device consists of conductive glass lining bottom, cavity injecting layer, luminescent layer and cathodic layer. The doping material of luminescent layer is iridium complex of bidentate ligand. Its advantages include to balance transmission ability of current carrier, and to improve brightness and efficiency of device for organic electro-luminescent domain.
Owner:WUHAN UNIV

Zirconium oxide fabrics prepared from organic polyzirconium fore spinning solution by silk process

The manufacture method of a kind of zirconia fibre cotton relates to the field of resistance of fire fibre material. We compose van-style acetamide acetone zirconium polymer according to chloridze zirconia, acetamide acetone and three-ethylamine. We use methanol as the dilute impregnant, we mix round them to let hloridize zirconia, acetamide acetone and three-ethylamine react at 40-20 deg.C, and we can receive poly-acetamide acetone zirconium van-substance. Four-hydrogen furan filtrate and remove the outgrowth hydrochloric three-ethylamine. The offspring dissolve in the filature liquid made of methanol. After centrifugal swing, we can receive van-substance fibre. After we do special hear treatment, the zirconia fibre cotton we receive has the characteristic of good filature ability, high content of zirconium, equality andclarity and jarles capability. It can be used as industrial stove, roomage fusion stove, atomic energy reactor and the high temperature heat insulation material used in aviation and military. The material of the invention cost low, the method is easy, the impregnant can be recycled, the preparation of fibre cost low.
Owner:绍兴市圣诺超高温晶体纤维材料有限公司

Preparation method for controllable duplex metal alloy nano particle

ActiveCN103192086AUniform and controllable sizeHas a face centered cubic structureNanotechnologyN-ButyllithiumHydrogenation reaction
The invention relates to a preparation method for a controllable duplex metal alloy nano particle. The metal alloy nano particles is a Pt / Pd-M alloy nano particle, wherein the M is selected from Ni, Fe, Co, Mn, Pd, Zn, Cu and Mo; during preparation, n-butyllithium is used as a strong reducing agent and oleylamine and tri-n-octylphosphine are used as protective agents to reduce acetylacetone, chlorate or acetate of the Pt / Pd-M (M= Ni, Fe, Co, Mn, Pd, Zn, Cu,Mo) at the same time so as to form the uniform and size-controllable Pt / Pd-M alloy nano particle without a concentration gradient. The preparation method is simple and controllable in preparation technology, and can solve the problem that when precursor reduction potentials of two metals are greatly different, one metal can be reduced in prior, so that the alloy nano particle can not be obtained easily, provides a better and universal synthetic method for the preparation of the duplex metal alloy nano particle, and provides a key precursor for the preparation of a new generation of metal-oxide nano hybridization body catalyst used for selective hydrogenation reaction.
Owner:NINGBO INST OF MATERIALS TECH & ENG CHINESE ACADEMY OF SCI

Plasma display panel and method for manufacturing the same

ActiveUS20090140652A1Large secondary electron emission coefficientLaunch evenlyTube/lamp screens manufactureAddress electrodesLow voltagePlasma display
Discharge delay” and “dependence of discharge delay on temperatures” are solved by improving a protective layer, thus a PDP can be driven at a low voltage. Furthermore, the PDP can display excellent images by suppressing “dependence of discharge delay on space charges.” Liquid-phase magnesium alkoxide (Mg (OR)2) or acetylacetone magnesium ate whose purity is 99.95% or more is prepared, and is hydrolyzed by adding a small amount of acids to the solution. Thus, a gel of magnesium hydroxide that is a magnesium oxide precursor is formed. Burning the gel in atmosphere at 700° C. or more produces powder containing MgO particles 16a-16d having the NaCl crystal structure with (100) and (111) crystal faces or with (100), (110) and (111) crystal faces. By pasting the powder on a dielectric layer 7 or a surface layer 8, the MgO powder 16 is formed so as to serve as the protective layer.
Owner:PANASONIC CORP

Carbon nitride-modified titanium dioxide super-hydrophilic porous film as well as preparation method and application thereof

ActiveCN104084229AImproving the conditions for realizing superhydrophilicityImprove photocatalytic activityOther chemical processesCatalyst activation/preparationAlcoholUltraviolet
The invention discloses a carbon nitride-modified titanium dioxide super-hydrophilic porous film as well as a preparation method and an application thereof. The method comprises the following steps: with dicyandiamide or tripolycyanamide as a precursor, calcining to prepare a carbon nitride nanosheet; dispersing the carbon nitride nanosheet in absolute ethanol so as to obtain a carbon nitride dispersion liquid, then adding a titanium dioxide precursor, diacetone and alcohol amine, uniformly stirring to obtain a uniform solution, dropwise adding the mixed liquid prepared from the absolute ethanol, water and acid into the uniform solution so as to obtain carbon nitride / titanium dioxide composite sol, aging for a period of time, coating the carbon nitride / titanium dioxide composite sol on a preprocessed substrate, carrying out drying and ultraviolet irradiation, so as to obtain the carbon nitride-modified titanium dioxide super-hydrophilic porous film. The carbon nitride-modified titanium dioxide super-hydrophilic porous film is prepared from the raw materials which are cheap and easily available, the preparation condition is easy to realize, and the film can be obtained without carrying out high-temperature calcining, so that the preparation coat of a super-hydrophilic film product is lowered, and the popularization and application of the technique is benefited.
Owner:SOUTH CHINA UNIV OF TECH

Solution for forming rare-earth superconductive film and production method thereof

Provided is a coating solution where, upon producing a rare-earth superconductive composite metal oxide film by means of a coating-pyrolysis method, cracks are not generated in the heat treatment process for eliminating organic components, even when the thickness of the rare-earth superconductive film produced in a single coating is 500 nm or more, and without having to repeat the coating and annealing process. A solution for producing a rare-earth superconductive film which is made into a homogeneous solution by dissolving, in a solvent formed by adding a polyhydric alcohol to a univalent linear alcohol having a carbon number of 1 to 8 and / or water, a metal complex coordinated, relative to metal ions of a metallic species containing rare-earth elements, barium and copper, with pyridine and / or at least one type of tertiary amine, at least one type of carboxylic acid having a carbon number of 1 to 8, and, as needed, an acetylacetonato group.
Owner:NAT INST OF ADVANCED IND SCI & TECH

Catalyst composition for ethylene oligomerization and the use thereof

The present invention relates to a catalyst composition for ethylene oligomerization and the use thereof. Such catalyst composition includes chromium compound, ligand containing P and N, activator and accelerator; wherein the chromium compound is selected from the group consisting of acetyl acetone chromium, THF-chromium chloride and Cr(2-ethylhecanoate)3; general formula of the ligand containing P and N is shown as:in which R1, R2, R3 and R4 are phenyl, benzyl, or naphthyl. R5 is isopropyl, butyl, cyclopropyl, cyclopentyl, cyclohexyl or fluorenyl; the activatior is methyl aluminoxane, ethyl aluminoxane, propyl aluminoxane and / or butyl aluminoxane; the accelerator is selected from the group consisting of 1,1,2,2,-tetrachloroethane, 1,1,2,2-tetrabromoethane, 1,1,2,2-tetrafluoroethane, and compounds having a formula of X1R6X2, in which X1 and X2 are F, Cl, Br, I or alkoxyl, R6 is alkylene or arylene group; the molar ratio of chromium compound, ligand containing P and N, activator and accelerator is 1:0.5˜10:50˜3000:0.5˜10. After mixing the four components mentioned previously under nitrogen atmosphere for 10 minutes, they are incorporated to the reactor, or these four components are incorporated directly into the reactor. Then ethylene is introduced for oligomerization. Such catalyst can be used in producing 1-octene through ethylene oligomerization. It is advantageous in high catalysing activity, high 1-octene selectivity, etc. The catalytic activity is more than 1.0×106 g product·ma−1 Cr·h−1, the fraction of C8 linear α-olefin is more than 70% by mass.
Owner:PETROCHINA CO LTD

Preparation of complete stable cubic phase zircite crystal fibre

The invention relates to a method of preparing full-stable and cubic-phase zirconia crystal fibers, which mainly comprises the following steps: using zirconium oxychloride, acetylacetone and triethylamine as main raw material and using ethanol as diluent solvent to directly react at a temperature of 0 DEG C to 50 DEG C under a stirring condition so as to generate an organic polymer solution comprising zirconium; evaporating the ethanol and using acetone as solvent to dissolve soluble substances and filter and remove an undissolved substance of triethylamine hydrochloride; recycling the acetone, dissolving the obtained products and yttrium salt to the ethanol to prepare a spinning solution which is centrifugally flung at a high speed to obtain organic polymer fibers comprising zirconium; and carrying out heat treatment in a special atmosphere and ultra-high temperature treatment of the organic polymer fibers comprising zirconium. The invention has simple preparation technology and can recycle the solvent, and the prepared crystal fibers have single ingredients, high purity and stable high-temperature performance and can be used in a range from 1700 DEG C to 2150 DEG C for a long time.
Owner:SHANDONG UNIV +1

Organometallic complexes as singlet oxygen sensitizers

A series of organometallic complexes and the singlet oxygen sensitization properties of these complexes are provided. Complexes with acetylacetonate ligands give singlet oxygen quantum yields near unity, whether exciting the ligand-based state or the lowest energy excited state (MLCT+3LC). The singlet oxygen quenching rates for these β-diketonate complexes are small, roughly three orders of magnitude slower than the corresponding phosphorescence quenching rate. Similar complexes were prepared with glycine or pyridine tethered to the Ir(III) center (i.e. (bsn)2Ir(gly) and (bt)2Ir(py)Cl, where gly=glycine, and py=pyridine). The glycine and pyridine derivatives give high singlet oxygen yields.
Owner:UNIV OF SOUTHERN CALIFORNIA

Method for preparing carbon nano-tube/nano-nickel composite film

A preparation method for carbon nanotube / nanonickel composite film material, relating to a method for preparing carbon nanotube / nanonickel composite film material on surface of metal foil, providing a method for preparing carbon nanotube film in acetylacetone by electrophoretic deposition, then electronically depositing nanoparticle of nickel on the carbon nanotube film by electrophoretic deposition, so as to prepare carbon nanotube / nanonickel composite film material with good catalytic and corrosion resisting property on surface of metal foil; depositing the metal foil processed by surface polishing and acetone oil removal in acetylacetone suspension having carbon nanotube by electrophoresis, undergoing electrophoretic deposition by direct current supply, then undergoing electrodeposit in nickel plating solution with constant current, after that, obtaining the carbon nanotube / nanonickel composite film material by drying process.
Owner:XIAMEN UNIV

Ferro-nickel oxyhydroxide-modified bismuth vanadate photoelectrode and preparation method and application thereof

The invention discloses a ferro-nickel oxyhydroxide-modified bismuth vanadate photoelectrode and a preparation method and application thereof. The preparation method comprises the following steps: firstly, depositing bismuth oxyiodide on the surface of conductive glass, then coating the surface with the deposited bismuth oxyiodide with a dimethyl sulfoxide solution of vanadyl acetylacetonate, annealing, performing alkali soaking and rinsing with water to remove excessive vanadium pentoxide, and then drying to obtain a bismuth vanadate photoelectrode, and modifying ferro-nickel oxyhydroxide on the surface of the bismuth vanadate photoelectrode by adopting a cyclic voltammetry method in a three-electrode system, thus obtaining the ferro-nickel oxyhydroxide-modified bismuth vanadate photoelectrode. The invention further discloses applications of the ferro-nickel oxyhydroxide-modified bismuth vanadate photoelectrode in photoelectrocatalytic decomposition water. The prepared photoelectrode is used for producing hydrogen from photoelectrocatalytic decomposition water, can inhibit the compounding of photon-generated carriers, the service life of carriers generated by a BiVO4 photoelectrode can be effectively prolonged, and the oxygen evolution reaction on the surface of the photoelectrode can be promoted, so that the solar optic hydrogen conversion efficiency of a semiconductor photoelectrode can be improved.
Owner:HUANGHE S & T COLLEGE

Preparing method for titanium dioxide fibre

The producing method of two-oxidation titanium fibre belongs to function fibre material technology scopes. Compose poly-acetamide acetone titanium to be the van-substance. Let chemic dosage of four-chloridize titanium, distilled water, acetamide acetone and three-ethylamine dilute in methanol respectively. Mix them and react when mixing round at 0-25 deg.C. Compose poly-acetyl acet, titanium. Remove hydrochloric three-ethylamine by using four-hydrogen furan. Dissolve poly-acetyl acet, titanium in methanol to make filature liquid. Obtain van-substance short fibre by using acentric swing method. Obtain van-substance long fibre by using dry filature method. And we can obtain two-oxidation titanium fibre by using high pressure or normal pressure vapor heat treatment technique agglomeration. The intension of extend of this invention is 100 MPa-1.2GPa. The diameter is 3um-20um. The one-thread series length is 1 cm-50 cm or higher than 1 m. The crystal diameter is 5 nm-100 nm. The appearance is two-oxide ation short fibre or consecutive fibre with titanium droff-titanium-mine posture or rutile posture or coexistence.
Owner:SHANDONG UNIV

Plasma display panel and method for manufacturing the same

InactiveUS20090146566A1Increase dependenceLarge secondary electron emission coefficientTube/lamp screens manufactureAddress electrodesLow voltageSpace charge
Discharge delay” and “dependence of discharge delay on temperatures” are solved by improving a protective layer, thus a PDP can be driven at a low voltage. Furthermore, the PDP can display excellent images by suppressing “dependence of discharge delay on space charges.” Liquid-phase magnesium alkoxide (Mg(OR)2) or acetylacetone magnesium ate whose purity is 99.95% or more is prepared, and is hydrolyzed by adding a small amount of acids to the solution. Thus, a gel of magnesium hydroxide that is a magnesium oxide precursor is formed. Burning the gel in atmosphere at 700° C. or more produces powder containing MgO particles 16a-16d having the NaCl crystal structure with (100) and (111) crystal faces or with (100), (110) and (111) crystal faces. By pasting the powder on a dielectric layer 7 or a surface layer 8, the MgO powder 16 is formed so as to serve as the protective layer.
Owner:PANASONIC CORP

Adhesive addition liquid silicone rubber

ActiveCN103589164AImprove adhesionConvenient sourcePolymer scienceMetal acetylacetonates
The invention provides an adhesive addition liquid silicone rubber. The adhesive addition liquid silicone rubber can be prepared via glue preparation from a prepared basic glue, an A component and a B component; or can be prepared by adding hydrogen-contained silicone oil, a platinum complex, tetravinyl tetramethylcyelo tetrasiloxane, silica powder of 3000 meshes, ZnO, a complex of aluminium and acetylacetone, polyborosiloxane, modified silane coupling agent, and a tackifier into dimethyl vinyl methylsiloxy-terminated polydimethylsiloxane, and full mixing. The adhesive addition liquid silicone rubber possesses advantages such as autoadhesion, low viscosity, high fluidity and excellent mechanical strength.
Owner:深圳市红叶杰科技有限公司

Method for reduction preparation of silver nanowire by composite solvent

The invention relates to a method for using compound solvent reduction method to prepae silver nanometer wire, belonging to the technique of metallic powder preparation, with lower cost, environment protection and the application for industrial production. The method comprises: dissolving polyvinyl pyrrolidon in compound solvent whose volume ration is 1:0.1-1:1 between glycerin, and water, ethanol, isopropanol, glycol, or acetylacetone, to be heated; adding silver nitrate into the solution of glycerin and ion-exchange water whose volume is 1:2, to attain the Ag+ solution in 0.5-2.0M; using said solution to spray compound solvent and react 1 / 4-4 hours in 90-160Deg. C; collecting products; the mol percentage between the polyvinyl pyrrolidon and the Ag+ is 0.5-10; and the Ag+ solution sprays the regurgitated compound solvent in the speed of 3g / m2.s-10g / m2.s while the reaction time is 1-4 hours and the reaction temperature is 120-160Deg. C. The shape and size of particles are controlled by the ration of react matters and react condition, and said invention can attain the silver nanometer wires whose length is 5 mum-200 mum, diameter is 70-90nm, and reduced silver rate is 99%.
Owner:YUNNAN UNIV

Sunlight responding nano hetero-structure photocatalyst and preparation method thereof

InactiveCN103706362ASolving the problem of difficult near-infrared photoresponseEfficient separationMetal/metal-oxides/metal-hydroxide catalystsFiberSolar photocatalysis
The invention provides a sunlight full-spectrum responding Ag2O / TiO2 / V2O5 nano hetero-structure photocatalyst and a preparation method thereof. The preparation method is characterized by comprising the following steps: mixing tetrabutyl titanate, polyvinylpyrrolidone, absolute ethanol, dimethyl acetamide and glacial acetic acid so as to obtain a solution A, mixing vanadium(IV) oxide acetylacetonate, polyvinylpyrrolidone and dimethyl acetamide so as to obtain a solution B, mixing the solution A and the solution B so as to obtain a polyvinylpyrrolidone / titanate / vanadium(IV) oxide acetylacetonate mixed solution, spinning the mixed solution by an electro-spinning method so as to obtain TiO2 / V2O5 nano fibers, then soaking AgNO3 and the TiO2 / V2O5 nano fibers in deionized water, injecting a NaOH solution into the deionized water, and drying so as to obtain the Ag2O / TiO2 / V2O5 nano hetero-structure photocatalyst. The Ag2O / TiO2 / V2O5 nano hetero-structure photocatalyst can well absorb lights in the ultraviolet zone, visible zone, and near infrared zone; at the same time, energy bands of the Ag2O, TiO2, and V2O5 are reasonably matched, thus the photo-produced electronic cavities can be effectively separated, so the Ag2O / TiO2 / V2O5 nano hetero-structure photocatalyst has a very high sunlight catalytic activity.
Owner:INST OF FLUID PHYSICS CHINA ACAD OF ENG PHYSICS

Method for preparing proton-exchange membrane fuel cell oxygen reduction catalyst based on PtNi (111) octahedral single crystal nanoparticles

The invention discloses a method for preparing a proton-exchange membrane fuel cell oxygen reduction catalyst based on PtNi (111) octahedral single crystal nanoparticles, which mainly solves the problem in the prior art that a conventional single-Pt catalyst or a Pt-based catalyst based on bimetallic spherical core-shell-structured nanoparticles is low in activity and poor in Pt atomic efficiency. Meanwhile, the influence factor and the synthesis optimization condition for morphology-controlled PtNi (111) octahedral single crystal nanoparticles are obtained. According to the technical scheme of the invention, platinum acetylacetonate and nickel acetylacetonate are adopted as metal salt precursors, and N, N-dimethylformamide (DMF) is adopted as a crystal face growth control agent. Through the heating reduction process, morphology-controlled PtNi (111) octahedral single crystal nanoparticles are obtained. The morphology-controlled PtNi (111) octahedral single crystal nanoparticles are subjected to ultrasonic dispersion in n-hexane, and then the well dispersed sol is slowly added onto the conductive carbon black of high specific surface area drop by drop through the residual titration process. Therefore, the electro-catalysis specific activity of the obtained oxygen reduction catalyst is high up to 1.5 A / mg Pt, and is improved by 9-10 times compared with that of conventional commercial Pt / C catalysts.
Owner:昆明贵研催化剂有限责任公司

Filament lamp for emission of yellow light

A filament lamp for an emission of yellow light, with a color film which is formed on the surface of the bulb, where the color film is essentially composed of a combined oxide of titanium, nickel and antimony. The color film may have a ratio of titanium, nickel and antimony to one another in a weight ratio of 5.6 to 8.6:3.6 to 6.6:1.0 to 1.8. Also, the color film may be a sintered coating formed by admixing a solution A produced by dissolving a nickel salt and an antimony salt in an organic solvent, addition of a titanium alkoxide and reaction of the reaction mixture; and addition of a stabilizer which forms a chelate with titanium with a solution B produced in substantially the same manner as solution A. The solutions A and B contain nickel nitrate-6-hydrate, antimony trioxide, tetraisopropoxy titanium, acetyl acetone, and / or water.
Owner:USHIO DENKI KK

Improved stability of polyurethane polyol blends containing halogenated olefin blowing agents

InactiveUS20140051776A1Extended shelf lifeEnhance foam characteristic of foamOther chemical processesPolymer sciencePtru catalyst
A polyol pre-mix composition includes a blowing agent having a halogenated hydroolefin, a polyol, a surfactant, a catalyst composition, and a metal salt. The metal salt may be, for example, a carboxylate, acetylacetonate, alcoholate of a metal selected from the group consisting of Zn, Co, Ca, and Mg. The metal salt may be, for example, a carboxylate and / or alcoholate of a C1-C21 straight chain or branched aliphatic monocarboxylic acid or monoalcohol, such as magnesium formate, zinc octoate, calcium octoate, cobalt octoate, and magnesium octoate, and mixtures thereof. The metal acetylacetonate may be, for example, zinc acetylacetonate, cobalt acetylacetonate, magnesium acetylacetonate, or calcium acetylacetonate. A two-part system for producing a thermosetting foam blend includes (a) a polyisocyanate and, optionally, one or more isocyanate compatible raw materials; and (b) the polyol pre-mix composition. A method for producing a thermosetting foam blend includes combining: (a) a polyisocyanate; and (b) the polyol pre-mix composition.
Owner:ARKEMA INC

Process for preparing metal coatings from liquid solutions utilizing cold plasma

A method for depositing metals, metal blends and alloys onto substrate surfaces, including microporous substrates utilizing a plasma operation undertaken at room temperature. In the process, a liquid solution of a monomer or comonomer precursor having a metallic component is utilized to wet the surface of the substrate, with the solvent portion thereafter being removed to leave the substrate surface coated with a dry deposit. The coated substrate is then introduced into a plasma reaction chamber with RF energy being applied across spaced electrodes to create a plasma glow along with the introduction of a plasma supporting gas. The substrate is exposed to the plasma glow for conversion of the precursor to dissociated form to create a deposit consisting essentially of the metallic component in elemental form as a cohesive film on the substrate surface. Preferred metals include such noble metals as platinum, gold and silver, as well as other metals. Preferred precursors include platinum hexafluoro-acetylacetonate, (trimethyl) methylcyclopentadienyl platinum, dimethyl(acetylacetonate) gold, and trimethyl phosphine (hexafluoroacetyl acetonate) silver.
Owner:AMT HLDG

Interlayer film for laminated glass and laminated glass

It is an object of the present invention to provide an interlayer film for a laminated glass which can prevent the formation of a colored spot in a metal coating on a glass surface due to remaining alkali metal, has excellent penetration resistance and hardly causes temporal changes in the interlayer film's adhesion to glass and buildup (colored streaks of an interlayer film for a laminated glass), and a laminated glass. The present invention is directed to an interlayer film for a laminated glass, which contains a matrix resin, a liquid plasticizer, acetyl acetone, alkali metal and at least one kind of metal selected from the group consisting of magnesium and alkaline earth metal, the content of the alkali metal being 20 to 120 ppm, the content of at least one kind of metal selected from the group consisting of magnesium and alkaline earth metal being 15 ppm or more and less than 60 ppm, and the content of the acetyl acetone being 0.008 parts by weight or more with respect to 100 parts by weight of the matrix resin.
Owner:SEKISUI CHEM CO LTD
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