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F oxidation

Silver f) oxide, Ag20, is obtained as a brown amorphous precipitate by the action of alkali on AgN03 solution. It cannot be obtained pure and is soluble in ammonia solution. [Pg.360]

These enable temperature control with built-in exchangers between the beds or with pumparound exchangers. Converters for ammonia, 80.3, cumene, and other processes may employ as many as five or six beds in series. The Sohio process for vapor-phase oxidation of propylene to acrylic acid uses hvo beds of bismuth molybdate at 20 to 30 atm (294 to 441 psi) and 290 to 400°C (554 to 752°F). Oxidation of ethylene to ethylene oxide also is done in two stages with supported... [Pg.2102]

Kofsted, P., High Temperature Oxidation of Metals, John Wiley, New York 0965) Kubaschewski, O. and Hopkins, B. F., Oxidation of Metals and Alloys, Butterworths, London... [Pg.115]

Adipose t Fatty acid transport and oxidation f Oxidative disposal of fatty acids... [Pg.944]

Similar studies have been performed with alcohol ether sulfates [343,344], The behavior of these substances is parallel to those of alcohol sulfates with only minor differences, f)-oxidation seems to be more complete in alcohol ether sulfates than with alcohol sulfates. [Pg.287]

C04-0045. Define each of these terms (a) percent yield (b) limiting reactant (c) spectator ion (d) precipitate (e) titration and (f) oxidation. [Pg.261]

In 1977, Fahey and Mahan described the first C-F oxidative addition of hexafluo-robenzene (C ) to the zerovalent nickel complex [Ni(cod)(PEt3)j] [11], The reaction was very slow and led, after several days at 30-35°C, to the formation of trani-[Ni(CgF3)(F)(PEt3)2] in very poor yield (7%). The use of [NiCPEtj) ] for the same reaction by Perutz and co-workers 20 years later allowed for a better conversion but the reaction rate remained slow (4 weeks were necessary to obtain 48% of the desired product) [12],... [Pg.192]

Ros Barcelo, A. Pomar, F. Oxidation of cinnamyl alcohols and aldehydes by a basic peroxidase from lignifying Zinnia elegans hypocotyls. Phytochemistry 2001, 57, 1105-1113. [Pg.418]

Oxidant Remaining After Storage 77°F % Oxidant Remaining After Storage 131°F ... [Pg.57]

Razina N.F. Oxide Electrodes in Aqueous Solutions (in Russian). Alma-Ata Nauka, 1982, 160 p. [Pg.355]

The major hormone-sensitive control point for the mobilization of fat and the (f-oxidation pathway is the effect of phosphorylation on the activity of the hormone-sensitive lipase of the adipose tissue. The major direct control point for (f oxidation is the inhibition of carnitine acyl-... [Pg.178]

Consider a planar combustion region in an adiabatic duct that is fixed in space and is steadily supplied with a mixture of fuel (F), oxidizer (O) and diluent (D) at the velocity Su. This condition defines Su and is depicted in Figure 4.10. The process is divided into two stages ... [Pg.90]

Colonna, S., Pironti, V., Carrea, G., Pasta, P. and Zambianchi, F., Oxidation of secondary amines by molecular oxygen and cyclohexanone monooxygenase. Tetrahedron, 2004,60, 569. [Pg.336]

Ferrero, F. Oxidative degradation of dyes and surfactant in the Fenton and photo-Fenton treatment of... [Pg.397]

F. Oxidation of very long-chain fatty acids (VLCFAs), ie, fatty acids having >22 carbons, requires special enzymes located in the peroxisome. [Pg.112]

Simpson, R.F., Oxidative pinking in white wines. Vitis 16, 286, 1977. [Pg.316]

Active low coordination, metastable state of the metal leads to anomalous electrochemical response in which hydrous f) oxide species (Au203 n H2O) are produced in a premonolayer oxidation. In contrast, conventional response yields a monolayer (a) oxide species (AU2O3). Since the activity of the active Au state is variable, the nature of the f oxide is also variable. Burke and Nugent [374] write about at least three forms of that oxide. [Pg.882]

Oxidation of water to evolve 02 is an important reaction for water photolysis as described in Sect. 2. Oxygen evolution from water by Ru(bpy)f+ oxidation with Ru02 catalyst was studied 41). The authors established an electron relay system for water oxidation (Scheme 3) by the polymer Ru(bpy) + complex and Ru02 catalyst with Pb02 as an oxidant40). [Pg.21]


See other pages where F oxidation is mentioned: [Pg.2123]    [Pg.209]    [Pg.426]    [Pg.201]    [Pg.34]    [Pg.34]    [Pg.358]    [Pg.323]    [Pg.613]    [Pg.613]    [Pg.944]    [Pg.944]    [Pg.898]    [Pg.137]    [Pg.438]    [Pg.61]    [Pg.24]    [Pg.115]    [Pg.360]    [Pg.274]    [Pg.1054]    [Pg.1114]    [Pg.804]    [Pg.252]    [Pg.882]    [Pg.1328]    [Pg.200]   
See also in sourсe #XX -- [ Pg.139 , Pg.142 , Pg.144 , Pg.152 ]




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F 2-Iminohexafluoropropane Iodine oxide

F 4-Octyne Osmium oxide

F Bicyclo hepta-2,5-diene Bis oxide

F Chlorotrimethylsilane Chromium oxide

F Chlorotrimethylsilane Cobalt oxide

F Chlorotrimethylsilane Copper oxide

F Ethylene oxide

F Induced Oxidative Cleavage of Phenyldimethylsilyl Groups

F Iodotrimethylsilane Iron oxide

F Isoxazole Lead oxide

F Malononitrile Manganese oxide

F Malononitrile Mercury oxide

F Neopentylamine Nickel oxide

F Oxybismethane Palladium oxide

F Propylene oxide

F Pyrrolidine Silver oxide

F Thiophene Tin oxide

F Trisilane Tungsten oxide

F Trisilane Vanadium oxide

F and oxidation

F+ oxidants

F+ oxidants

F-Butyl hydroperoxide oxidation

Organic Peroxide and F Oxidants

Oxidation State Ambiguity in the f Block Metallocenes

Oxidation States of the f-Block Elements

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