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Hydrogen heterogeneous removal

Figure 2. Sodium hydroxide consumption in a standard oxidation of methyl a-D-glucopyranoside over Ti-MCM-41 with hydrogen peroxide ( ), removal of the heterogeneous catalyst after Ih and further reaction of the solution ( ) and upon re-use of the solid catalyst ( ). Figure 2. Sodium hydroxide consumption in a standard oxidation of methyl a-D-glucopyranoside over Ti-MCM-41 with hydrogen peroxide ( ), removal of the heterogeneous catalyst after Ih and further reaction of the solution ( ) and upon re-use of the solid catalyst ( ).
Neither of the two types of chain termination reactions mentioned above in the isotopic hydrogen example is a fast reaction by these standards. Heterogeneous removal of chain centres requires as a minimum their delivery to a phase boundary, and at typical molecular speeds near 10 cm sec quite small apparatus dimensions would be necessary to yield a 10 sec reaction rate even under high vacuum conditions. This argument can be extended to the general observation that heterogeneous steps play no direct part in the interior of the shortlived experiments in shock tubes. [Pg.89]

Catalytic hydrogenation is mostly used to convert C—C triple bonds into C C double bonds and alkenes into alkanes or to replace allylic or benzylic hetero atoms by hydrogen (H. Kropf, 1980). Simple theory postulates cis- or syn-addition of hydrogen to the C—C triple or double bond with heterogeneous (R. L. Augustine, 1965, 1968, 1976 P. N. Rylander, 1979) and homogeneous (A. J. Birch, 1976) catalysts. Sulfur functions can be removed with reducing metals, e. g. with Raney nickel (G. R. Pettit, 1962 A). Heteroaromatic systems may be reduced with the aid of ruthenium on carbon. [Pg.96]

A particularly interesting system for the epoxidation of propylene to propylene oxide, working under pseudo-heterogeneous conditions, was reported by Zuwei and coworkers [61]. The catalyst, which was based on the Venturello anion combined with long-chained alkylpyridinium cations, showed unique solubility properties. I11 the presence of hydrogen peroxide the catalyst was fully soluble in the solvent, a 4 3 mixture of toluene and tributyl phosphate, but when no more oxidant was left, the tungsten catalyst precipitated and could simply be removed from the... [Pg.200]

As an application of Pt nanowires in heterogeneous catalysis, we performed preferential oxidation (PROX) of CO as a test reaction [32]. The PROX reaction is useful for PEM fuel cells for the selective removal of contaminating CO from hydrogen gas, because CO works as a strong catalyst poison for Pt electrode catalysts (Figure 15.24). H2 produced in steam-reforming and the water-gas shift reaction needs further to be purified in the PROX reaction to selectively oxidize a few% CO towards inert CO2 in a H 2-rich atmosphere, to reduce the CO content to <10ppm. Under the PROX conditions, the facile oxidation of H2 to H2O may also occur, thus the catalyst selectivity for CO oxidation over H2 oxidation is an... [Pg.624]


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See also in sourсe #XX -- [ Pg.58 , Pg.408 , Pg.409 ]




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