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Organic oxides

A large variety of organic oxidations, reductions, and rearrangements show photocatalysis at interfaces, usually of a semiconductor. The subject has been reviewed [326,327] some specific examples are the photo-Kolbe reaction (decarboxylation of acetic acid) using Pt supported on anatase [328], the pho-... [Pg.738]

Very large quantities of oxygen are used in steel manufacture (p. 392). Other important uses include organic oxidation reactions the oxidation of ethene CH2=CH2 to epoxyethane, CH2—CHj, is of... [Pg.268]

In addition to CuCfi, some other compounds such as Cu(OAc)2, Cu(N03)2-FeCl.i, dichromate, HNO3, potassium peroxodisulfate, and Mn02 are used as oxidants of Pd(0). Also heteropoly acid salts comtaining P, Mo, V, Si, and Ge are used with PdS04 as the redox system[2]. Organic oxidants such as benzo-quinone (BQ), hydrogen peroxide and some organic peroxides are used for oxidation. Alkyl nitrites are unique oxidants which are used in some industrial... [Pg.19]

The 70% H2O2 concentration is used in chemical processing and for certain organic oxidations. Dilution-grade 70% H2O2 is stabilized to allow for later dilution to 35—50% storage concentration. [Pg.479]

Iron(III) acetate [1834-30-6], Ee(C2H202)3, is prepared industrially by treatment of scrap iron with acetic acid followed by air oxidation. Iron(III) acetate is used as a catalyst in organic oxidation reactions, as a mordant, and as a starting material for the preparation of other iron-containing compounds. [Pg.433]

Winthrop Laboratories New York, N.Y. activated Mn02 organic oxidations ... [Pg.523]

AH of the commercial inorganic peroxo compounds except hydrogen peroxide are described herein, as are those commercial organic oxidation reactions that are beheved to proceed via inorganic peroxo intermediates. Ozonides and superoxides are also included, but not the dioxygen complexes of the transition metals. [Pg.90]

Transition-metal-catalyzed oxidations may or may not proceed via peroxocomplexes. Twelve important industrial organic oxidation processes catalyzed by transition metals, many of which probably involve peroxo intermediates, have been tabulated (88). Even when peroxo intermediates can be isolated from such systems, it does not necessarily foUow that these are tme intermediates in the main reaction. [Pg.96]

Other important uses of stannic oxide are as a putty powder for polishing marble, granite, glass, and plastic lenses and as a catalyst. The most widely used heterogeneous tin catalysts are those based on binary oxide systems with stannic oxide for use in organic oxidation reactions. The tin—antimony oxide system is particularly selective in the oxidation and ammoxidation of propylene to acrolein, acryHc acid, and acrylonitrile. Research has been conducted for many years on the catalytic properties of stannic oxide and its effectiveness in catalyzing the oxidation of carbon monoxide at below 150°C has been described (25). [Pg.65]

Minor uses of vanadium chemicals are preparation of vanadium metal from refined pentoxide or vanadium tetrachloride Hquid-phase organic oxidation reactions, eg, production of aniline black dyes for textile use and printing inks color modifiers in mercury-vapor lamps vanadyl fatty acids as driers in paints and varnish and ammonium or sodium vanadates as corrosion inhibitors in flue-gas scmbbers. [Pg.394]

Oxidation of butyraldehyde to butyric acid [107-92-6]is most commonly carried out employing air or oxygen as the oxidant. Alternatively, organic oxidants, eg, cumene hydroperoxide, can also be employed effectively to give high yields of butyric acid, (4). [Pg.378]

Chromic acid and its salts normally are prepared in lead. Lead is especially suitable for organic oxidations because its inertness avoids any interference from reactions. [Pg.86]

Ruthenium nowadays finds many uses in the electronics industry, particularly for making resistor tracks. It is used as an ingredient in various catalysts and, importantly, in electrode materials, e.g. Ru02-coated titanium elements in the chloralkali industry. Osmium tetroxide is a very useful organic oxidant and, classically, is used as a tissue stain. Both elements are employed in making certain platinum alloys. [Pg.417]

Oxonium Compounds. An addition or double compd of an organic oxide with strong acids or their salts, as, R20.HX (Refs 5 7)... [Pg.457]

Toxicity. The peroxy acid is highly toxic and may cause death or permanent injury after very short exposure to small quants (Ref 12) Uses. Peroxyacetic acid is the most important epoxidation reagent used today because of its economical availability and ease of use with a wide variety of reactants (Ref 10). It also finds wide usage as an organic oxidizing agent (Ref 11) Refs 1) Beil 2, 169, (78), [174] [379 ... [Pg.689]

It has been pointed out (S2) that this type of operation might be widely applicable for organic oxidation processes, provided suitable inert carrier liquids can be found. It may be noted in this connection that the liquid must be reasonably resistant against oxidation and that it must not cause catalyst deactivation—for example, by chemisorption. [Pg.78]

Aromatic nitro and nitroso compounds are easily reduced at carbon and mercury electrodes. Other nitro compounds such as nitrate esters, nitramines, and nitrosamines are also typically easily reduced. The complete reduction of a nitro compound consists of three two-electron steps (nitro-nitroso-hydroxylamine-amine). Since most organic oxidations are only two-electron processes, higher sensitivity is typically found for nitro compounds. Several LCEC based determination of nitro compounds have been reported... [Pg.26]

It is very well known that Pt is one of the best metal catalysts for hydrogen as well as for organic oxidations. Nevertheless, a comparison of the electrochemical behavior of hydrogen and any of these organic substances shows large differences. While hydrogen establishes its reversible thermodynamic potential with platinum in an aqueous acidic solution very quickly, the reversible potential of the other fuels could never be experimentally observed. [Pg.138]

Although no instability was noted, and a small sample was insensitive to a hammer blow, it should be treated as potentially unstable as an organic oxidant. [Pg.1239]

Peroxidase (HRP) horseradish redox/H202 amine, phenol, organics oxidation... [Pg.446]

Varies depending on the specific agent but may include HC1 and HCN. Several produce diphenylarsenious oxide. Other organic oxides of arsenic, antimony, or lead may also be present. [Pg.430]

Naumann, K., Zon, G., and Mislow, K., Perchloropolysilanes novel reducing agents for phosphine oxides and other organic oxides, /. Am. Chem. Soc., 91, 2788, 1969. [Pg.40]


See other pages where Organic oxides is mentioned: [Pg.480]    [Pg.250]    [Pg.92]    [Pg.228]    [Pg.187]    [Pg.1050]    [Pg.1130]    [Pg.13]    [Pg.733]    [Pg.348]    [Pg.187]    [Pg.191]    [Pg.196]    [Pg.94]    [Pg.99]    [Pg.1506]    [Pg.3]    [Pg.556]    [Pg.604]    [Pg.356]    [Pg.167]    [Pg.493]    [Pg.541]   


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Organic oxidant

Organic oxidation

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