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107 results about "Nonene" patented technology

Nonene is an alkene with the molecular formula C₉H₁₈. Many structural isomers are possible, depending on the location of the C=C double bond and the branching of the other parts of the molecule. Industrially, the most important nonenes are trimers of propene. This mixture of branched nonenes is used in the alkylation of phenol to produce nonylphenol, a precursor to detergents, which are also controversial pollutants.

Catalytic conversion of cellulose to liquid hydrocarbon fuels by progressive removal of oxygen to facilitate separation processes and achieve high selectivities

Described is a method to make liquid chemicals, such as functional intermediates, solvents, and liquid fuels from biomass-derived cellulose. The method is cascading; the product stream from an upstream reaction can be used as the feedstock in the next downstream reaction. The method includes the steps of deconstructing cellulose to yield a product mixture comprising levulinic acid and formic acid, converting the levulinic acid to γ-valerolactone, and converting the γ-valerolactone to pentanoic acid. Alternatively, the γ-valerolactone can be converted to a mixture of n-butenes. The pentanoic acid so formed can be further reacted to yield a host of valuable products. For example, the pentanoic acid can be decarboxylated yield 1-butene or ketonized to yield 5-nonanone. The 5-nonanone can be hydrodeoxygenated to yield nonane, or 5-nonanone can be reduced to yield 5-nonanol. The 5-nonanol can be dehydrated to yield nonene, which can be dimerized to yield a mixture of C9 and C18 olefins, which can be hydrogenated to yield a mixture of alkanes. Alternatively, the nonene may be isomerized to yield a mixture of branched olefins, which can be hydrogenated to yield a mixture of branched alkanes. The mixture of n-butenes formed from γ-valerolactone can also be subjected to isomerization and oligomerization to yield olefins in the gasoline, jet and Diesel fuel ranges.
Owner:WISCONSIN ALUMNI RES FOUND

Mixed decyl mercaptans compositions and use thereof as mining chemical collectors

Disclosed herein is a process for the recovery of a metal from an ore using a collector composition. The process includes contacting the ore with the collector composition. The collector composition can include sulfur-containing compounds comprising (i) mercaptans comprising branched C10 mercaptans compounds selected from the group consisting of 5-methyl-1-mercapto-nonane, 3-propyl-1-mercapto-heptane, 4-ethyl-1-mercapto-octane, 2-butyl-1-mercapto-hexane, 5-methyl-2-mercapto-nonane, 3-propyl-2-mercapto-heptane, 4-ethyl-2-mercapto-octane, 5-methyl-5-mercapto-nonane, and combinations thereof; and (ii) sulfides comprising branched C20 sulfides represented by the structure R1—S—R2, wherein R1 and R2 are each independently a functional group derived from an olefin, wherein the olefin comprises 5-methyl-1-nonene, 3-propyl-1-heptene, 4-ethyl-1-octene, 2-butyl-1-hexene, or combinations thereof.
Owner:CHEVRON PHILLIPS CHEMICAL CO LP

Cationic type gemini fluorinated surfactant based on perfluorinated nonene and perfluorinated hexene and preparation method of cationic type gemini fluorinated surfactant

The invention discloses a cationic type gemini fluorinated surfactant based on perfluorinated nonene and perfluorinated hexene and a preparation method of the cationic type gemini fluorinated surfactant. The preparation method comprises the following steps of: with the perfluorinated nonene or perfluorinated hexene as a raw material, condensing the perfluorinated nonene or perfluorinated hexene with p-hydroxybenzoic acid, and carrying out chlorination on a matter obtained after condensation and thionyl chloride to prepare perfluorinated alkene oxyl benzoyl chloride; condensing the perfluorinated alkene oxyl benzoyl chloride without separation with 2-dimethylamino ethanol, 3-dimethylamino propanol, 2-dimethylamino ethylamine and 3-dimethylamino propylamine to obtain perfluorinated alkene oxyl benzoate or perfluorinated alkene oxyl benzamide with tertiary amine at an alkanol part or amine part; and finally, condensing the perfluorinated alkene oxyl benzoate or perfluorinated alkene oxyl benzamide with 1,2-dihaloethane, 1,3-dihalopropane, 1,4-dichlorobutane, 1,5-dichloropentane or 3-oxa-1,5-dichloropentane to prepare a quaternary ammonium gemini fluorinated surfactant. The synthesized compound is high in surface activity and is low in critical micelle concentration, has the characteristics of simpleness in synthesization, low cost and the like and has good application prospect.
Owner:江苏超至和新材料有限公司

Catalyst for preparation of nonene and dodecene from sthylenediamine and preparation method thereof

The invention belongs to the field of chemical industry, and specifically relates to a catalyst for preparation of nonene and dodecene from sthylenediamine and a preparation method thereof. Accordingto the catalyst for the preparation of the nonene and the dodecene by the sthylenediamine and the preparation method thereof, a core-shell structure with an aluminium oxide wrapped by molecular sievesis formed by loading the molecular sieves on the periphery of an aluminium oxide carrier after active ingredients are loaded on the aluminium oxide carrier. On the premise of fully playing the catalytic performance of the molecular sieves, the strength of the catalyst is effectively improved and the pulverization of simple molecular sieves is avoided by adding internal support of the aluminium oxide carrier; the active ingredients are positioned in the molecular sieves, so that the loss of the active ingredients is not caused easily, the stability of the catalyst is improved, and the servicelife of the catalyst is prolonged; the molecular sieves and aluminium oxide spheres form a core-shell shape, and both the molecular sieves and the aluminium oxide which is loaded with the active ingredients have catalytic activity, so that a stepped catalytic action is achieved; the raw materials which do not react on the peripheries of the molecular sieves enter aluminium oxide molecular sieves for further reaction; the catalytic actions of the molecular sieves and the aluminium oxide which is loaded with the active ingredients are added, so that the activity and the selectivity are further improved.
Owner:SOUTHWEST RES & DESIGN INST OF CHEM IND

Catalyst composition for production of polyurethane resin and method for producing polyurethane resin

To provide a catalyst composition which is a catalyst composition not impairing the physical properties of a polyurethane resin and the storage stability of the starting material blend liquid and which is capable of producing a polyurethane resin excellent in curability and also excellent in moldability by suppressing the initial reactivity, with good productivity.A catalyst composition for production of a polyurethane resin, which comprises (A) triethylenediamine, and (B) a polyisocyanurating catalyst and / or (C) a highly temperature sensitive catalyst, wherein the polyisocyanurating catalyst (B) is one or more compounds selected from the group consisting of an alkali metal salt of a carboxylic acid, a quaternary ammonium salt compound of the following formula (1):wherein each of R1 to R3 is a C1-12 linear or branched, saturated or unsaturated hydrocarbon group, provided that any two among R1 to R3 may form a hetero ring via an oxygen atom or a nitrogen atom, R4 is a C1-18 alkyl group or an aromatic hydrocarbon group, and X is an organic acid group having an acid dissociation constant (pKa) of at most 4.8, N,N,N′-trimethylaminoethylethanolamine and 2,4,6-tris(dimethylaminomethyl)phenol; the highly temperature sensitive catalyst (C) is one or more compounds selected from the group consisting of a triazole salt of 1,8-diazabicyclo[5.4.0]undecene-7, a benzotriazole salt of 1,8-diazabicyclo[5.4.0]undecene-7, a triazole salt of 1,5-diazabicyclo[4.3.0]nonene-5, a benzotriazole salt of 1,5-diazabicyclo[4.3.0]nonene-5, a triazole salt of 1,8-diazabicyclo[5.3.0]decene-7 and a benzotriazole salt of 1,8-diazabicyclo[5.3.0]decene-7; and the blend ratio of the polyisocyanurating catalyst (B) and / or the highly temperature sensitive catalyst (C) to the triethylenediamine (A) is from 2 wt % to 60 wt %.
Owner:TOSOH CORP
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