3284 results about "Acetylacetone" patented technology

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.

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.

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.

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.

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.

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.