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Reaction with Oxygen and Hydrogen

As mentioned in Sec. 7.1 above, the reaction rate is site preferential and oxidation is much higher along the zig-zag face of the crystal than it is along the armchair face (Fig. Oxidation can be hindered by [Pg.64]

Mineral, non-oxidizing (hydroxides, NaOH, hydrazine, molten Mg, KOH) [Pg.65]

Acids and Acid Solutions Mineral, non-oxidizing (HCI, HCN, H3PO4, HF) Boiling H2SO4 [Pg.65]

Organic, strong (pH 3) (acetic, carbolic, formic, maleic, oxalic, phenol, picric, salicic) [Pg.65]

Organic, weak (pH 3 - 7) (abietic, benzoic, citric, cresol, lactic, palmitic) [Pg.65]


Oxychlorination of Ethylene to Dichloroethane. Ethylene (qv) is converted to dichloroethane in very high yield in fixed-bed, multitubular reactors and fluid-bed reactors by reaction with oxygen and hydrogen chloride over potassium-promoted copper(II) chloride supported on high surface area, porous alumina (84) ... [Pg.203]

The HCN and N are converted rapidly to NO by reaction with oxygen and hydrogen atoms in the flame. [Pg.396]

In alkaline solutions D-glucose forms 3-deoxy-D-en/f/iro-hexosulose and 4-deoxy-D-gft/cero-2,3-hexodiulose which yield saccharinic acids. Machell and Richards (57) have shown that 3-deoxy-D-en/fhro-hexosulose (14) is oxidized by 30% hydrogen peroxide to formic acid and 2-deoxy-D-erythro-pentonic acid (15). Recently Rowell and Green (58) found that 14 in the presence of oxygen also forms 15 in addition to the saccharinic acids. They inferred that the reactions with oxygen and hydrogen peroxide are very similar, but they did not present reaction mechanisms. [Pg.90]

Referring to reaction Schemes V and VIII, one would expect the reactions with oxygen and hydrogen peroxide to be quite different. As outlined in Schemes X and XI, the reaction with oxygen should give 15 and carbon dioxide, whereas the reaction with hydrogen peroxide should give... [Pg.91]

Luminol derivatives produce emission of light by oxidation with oxygen and hydrogen peroxide under alkaline conditions. By utilizing this reaction, peroxides such as hydrogen peroxide and lipid hydroperoxides can be determined after HPLC separation. Metal ions [e.g., iron(II), cobalt(II), etc.] catalyzing the luminol CL reaction can also be determined. [Pg.396]

Reduction reactions of metal oxides by hydrogen start with the dissociative adsorption of H2, which is a much more difficult process on oxides than on metals. Atomic hydrogen takes care of the actual reduction. Depending on how fast or how slow the dissociative adsorption is in comparison to the subsequent reduction reactions which comprise diffusion of atomic hydrogen into the lattice, reaction with oxygen and removal of the hydroxyl species formed, two limiting cases are distinguished [1,7]. [Pg.28]

Riboflavin is the redox component of flavin adenine dinucleotide FAD. It is derived from FAD by hydrolysis of a phosphate ester link. The fully oxidised form of FAD is involved in many dehydrogenaze reactions during which it is converted to the fully reduced form. The fully oxidised state is restored either by another redox enzyme or by interaction with oxygen and hydrogen peroxide is liberated. The one-electron reduced, semiquinone form of FAD, is involved in some electron transfer steps. [Pg.253]

Fig. 17.8 Energy levels for a water splitting system with a combination of two photocatalytic reactions for oxygen and hydrogen production. Fig. 17.8 Energy levels for a water splitting system with a combination of two photocatalytic reactions for oxygen and hydrogen production.
How the reaction mechanism is reflected in the detonation velocity may be seen from the following comparison of two reactions hydrogen with oxygen and hydrogen with chlorine. The detonation velocity, calculated under the assumption that complete chemical equilibrium is achieved, depends equally in both cases on the pressure. In the case of hydrogen with oxygen, the dissociation of H20 in either direction of the reaction... [Pg.210]

Gierer, J., and Imsgard, F. (1977). The reactions of lignins with oxygen and hydrogen peroxide in alkaline media. Sven. Papperstidn. 80, 510-518. [Pg.167]

Reaction of propylene with oxygen and hydrogen over Au/, Pd/, Pt/Ti02 catalysts... [Pg.128]


See other pages where Reaction with Oxygen and Hydrogen is mentioned: [Pg.103]    [Pg.484]    [Pg.205]    [Pg.64]    [Pg.103]    [Pg.484]    [Pg.205]    [Pg.64]    [Pg.54]    [Pg.994]    [Pg.249]    [Pg.258]    [Pg.337]    [Pg.59]    [Pg.46]    [Pg.351]    [Pg.189]    [Pg.59]    [Pg.226]    [Pg.7]    [Pg.46]    [Pg.243]    [Pg.184]    [Pg.343]    [Pg.158]    [Pg.299]    [Pg.353]    [Pg.223]    [Pg.409]    [Pg.2297]    [Pg.1034]    [Pg.432]    [Pg.439]    [Pg.57]    [Pg.250]    [Pg.227]    [Pg.132]   


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Hydrogen with oxygen

Hydrogen/oxygen reaction

Hydrogenation reaction with

OXYGEN hydrogen

Oxygen and hydrogen

Reaction with hydrogen

Reaction with oxygen

Reactions hydrogen and

Reactions hydrogen-oxygen reaction

Reactions with oxygen and hydrogen peroxide

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