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Hydrogen peroxide hydrocarbon oxidation

Hydrogen cyanide reactions catalysts, 6,296 Hydrogen ligands, 2, 689-711 Hydrogenolysis platinum hydride complexes synthesis, 5, 359 Hydrogen peroxide catalytic oxidation, 6, 332, 334 hydrocarbon oxidation iron catalysts, 6, 379 reduction... [Pg.141]

Titanium siliealites TS-1 and TS-2 catalyze hydroxylation in the aromatic ring of the monoalkylbenzenes studied to corresponding alkylphenols, using hydrogen peroxide as oxidant. Para-isomers are mainly formed in methanol or ethanol as solvents. In the case of ethyl- and 1-propylbenzenes, the first carbon atom of the aliphatic chain is also oxidised both to alcohols and ketones. As expected, the terminal methyl groups in all hydrocarbons are not oxidised. The probable reasons for this behaviour of titanium silicalites are discussed. [Pg.917]

Urea-hydrogen peroxide-trl Oxidations. This sysicn this regard, it is more effecu e Saturated hydrocarbons ait clohexane gives cyclohexyl tn... [Pg.482]

Mercury(II) oxide Chlorine, hydrazine hydrate, hydrogen peroxide, hypophosphorous acid, magnesium, phosphorus, sulfur, butadiene, hydrocarbons, methanethiol... [Pg.1209]

Organic hydroperoxides can be prepared by Hquid-phase oxidation of selected hydrocarbons in relatively high yield. Several cycHc processes for hydrogen peroxide manufacture from hydroperoxides have been patented (84,85), and others (86—88) describe the reaction of tert-huty hydroperoxide with sulfuric acid to obtain hydrogen peroxide and coproduct tert-huty alcohol or tert-huty peroxide. [Pg.477]

PoUowing further development (38), a two-cycle process has been adopted by industry. In the first concentration cycle, the clarified feed acid containing 100—200 mg/L U Og [1334-59-8] is oxidized, for example, with hydrogen peroxide or sodium chlorate [7775-09-9] to ensure that uranium is in its 6+ valence state is not extracted. Uranium is extracted with a solvent composed of 0.5 Af D2EHPA and 0.125 Af TOPO dissolved in an aUphatic hydrocarbon diluent. [Pg.320]

Tetracyanoethylene oxide [3189-43-3] (8), oxiranetetracarbonitnle, is the most notable member of the class of oxacyanocarbons (57). It is made by treating TCNE with hydrogen peroxide in acetonitrile. In reactions unprecedented for olefin oxides, it adds to olefins to form 2,2,5,5-tetracyanotetrahydrofuran [3041-31-4] in the case of ethylene, acetylenes, and aromatic hydrocarbons via cleavage of the ring C—C bond. The benzene adduct (9) is 3t ,7t -dihydro-l,l,3,3-phthalantetracarbonitrile [3041-36-9], C22HgN O. [Pg.405]

Since aluminum is not attacked by hydrogen sulfide (HjS) solutions, it is used widely as a material in refineries for the handling of hydrocarbons made from sour crudes. In the strongly oxidizing conditions of manufacturing hydrogen peroxide, aluminum is one of the few materials that does not undergo decomposition. [Pg.93]

Interesting hydrocarbon oxidations have been observed using Fe(II) catalysts with oxygen or hydrogen peroxide as the oxidant. These catalytic systems have become known as Gif chemistry after the location of their discovery in France.287 An Oxidations improved system involving Fe(III), picolinic acid, and H202 has been developed. The... [Pg.1150]

Chlorine dioxide Copper Fluorine Hydrazine Hydrocarbons (benzene, butane, propane, gasoline, turpentine, etc) Hydrocyanic acid Hydrofluoric acid, anhydrous (hydrogen fluoride) Hydrogen peroxide Ammonia, methane, phosphine or hydrogen sulphide Acetylene, hydrogen peroxide Isolate from everything Hydrogen peroxide, nitric acid, or any other oxidant Fluorine, chlorine, bromine, chromic acid, peroxide Nitric acid, alkalis Ammonia, aqueous or anhydrous Copper, chromium, iron, most metals or their salts, any flammable liquid, combustible materials, aniline, nitromethane... [Pg.165]

Emission from dimols of singlet oxygen may be detected by photomultipliers used for measurement of chemiluminescence from hydrocarbon polymers with a maximum spectral sensitivity at 460 nm. The above scheme, however, requires the presence of at least one molecule of hydrogen peroxide in close vicinity to the two recombining peroxyl radicals and assumes a large heterogeneity of the oxidation process. [Pg.465]

Ortiz Leon, M. Velasco, L., and Vazquez-Duhalt, R., Biocatalytic Oxidation of Polycyclic Aromatic-Hydrocarbons by Hemoglobin and Hydrogen-Peroxide. Biochemical and Biophysical Research Communications, 1995. 215(3) pp. 968-973. [Pg.225]


See other pages where Hydrogen peroxide hydrocarbon oxidation is mentioned: [Pg.102]    [Pg.407]    [Pg.91]    [Pg.187]    [Pg.66]    [Pg.7197]    [Pg.563]    [Pg.847]    [Pg.812]    [Pg.192]    [Pg.111]    [Pg.102]    [Pg.168]    [Pg.1286]    [Pg.336]    [Pg.477]    [Pg.294]    [Pg.257]    [Pg.516]    [Pg.981]    [Pg.76]    [Pg.9]    [Pg.108]    [Pg.729]    [Pg.1024]    [Pg.570]    [Pg.275]    [Pg.1642]    [Pg.196]    [Pg.199]    [Pg.495]    [Pg.491]    [Pg.8]   


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Hydrogenation hydrocarbons

Oxidants peroxides

Oxidation hydrogen peroxide

Oxidation peroxidation

Oxides peroxides

Oxidizers hydrogen peroxide

Peroxidative oxidation

Peroxidative oxidation hydrogen peroxide)

Peroxides oxidation

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