Oxidative carbonylation of aniline over a polymer-supported palladium-copper catalyst

The polymer-supported bimetallic catalyst FVP-PdCl2-2CuCl(2) (PVP, poly(N-vinyl-2-pyrrolidone), obtained in situ by the addition of CuCl2 to an alcoholic solution of PVP-PdCl2, exhibits high selectivity and activity for the oxidative carbonylation of aniline with carbon monoxide and oxygen to ethyl N-phenylcarbamate in the presence of a base (NaOAc) under atmospheric pressure. The strong synergic effect of Pd-Cu gives rise to a clear increase in the selectivity and activity. (C) 2000 Elsevier Science B.V. All rights reserved.

NO reduction and CO oxidation over Cu/Ce/Mg/Al mixed oxide catalyst in FCC operation

Simultaneous NO reduction and CO oxidation in the presence of O-2,H2O and SO2 over Cu/Mg/AUO (Cu-cat), Ce/Mg/Al/O (Ce-cat) and Cu/Ce/Mg/Al/O (CuCe-cat) were studied. At low temperatures (<340 degreesC), the presence of O-2 or H2O enhanced the activity of CuCe-cat for NO and CO conversions, but significantly suppressed the activity of Cu-cat and Ce-cat, At high temperature (720 degreesC), the presence of O-2 or H2O had no adverse effect on the NO and CO conversions over these catalysts. The addition of SO2 to NO + CO + O-2 + H2O system had no effect on the, reaction of CO + O-2 over Cu-cat, but deactivated this catalyst for NO + CO and CO + H2O reactions; over Ce-cat, all of these reactions of NO + CO, CO + O-2 and CO + H2O were suppressed significantly; over CuCe-cat, NO + CO and CO + O-2 reactions were not affected while the reaction of CO + H2O was slightly inhibited. (C) 2002 Elsevier Science B.V. All rights reserved.

FT-IR spectroscopic study of the oxidation of chlorobenzene over Mn-based catalyst

Adsorption and oxidation of chlorobenzene on Al(2)O(3), TiO(2)-Al(2)O(3), and MnO(x)/TiO(2)-Al(2)O(3) have been studied by in situ Fourier transform infrared (FT-IR) spectroscopy. At room temperature, chlorobenzene is only physisorbed on Al(2)O(3), TiO(2)-Al(2)O(3), and MnO(x)/TiO(2)-Al(2)O(3), and gives the same IR spectrum as that for liquid-phase chlorobenzene. On Al(2)O(3) no further interaction and reaction take place with treatment, at higher temperatures (up to 773 K), while phenolates are observed for TiO(2)-Al(2)O(3) and MnO(x)/TiO(2)-Al(2)O(3) at 773 K. When the adsorbed chlorobenzene coexists with oxygen, formates are detected for Al(2)O(3), while acetates are additionally observed for TiO(2-)Al(2)O(3) above 573 K. For MnO(x)/TiO(2-)Al(2)O(3), maleates are present at 573 And 673 K, while formates and acetates develop at 473 and 573 K. Almost all IR bands due to formates, acetates, and maleates disappear at 773 K, indicating that these oxygen-containing species are potential intermediates for the total oxidation of chlorobenzene.

A high coking-resistance catalyst for methane aromatization

Steaming-dealuminated HZSM-5-supported molybdenum catalysts have been found to be high coking-resistance catalysts for methane aromatization reactions; compared with conventional catalysts, they give a much higher selectivity towards aromatics.

Heterogeneous asymmetric hydrogenation of ethyl pyruvate on chirally modified Pt/Al2O3 catalyst with fixed-bed reactor

The enantioselective hydrogenation of ethyl pyruvate on the cinchonidine modified Pt/Al2O3 catalyst was investigated using a high-pressure reaction system with a fixed-bed reactor for the purpose to produce the,chiral product without separating the catalyst from the reaction system. The reaction was also investigated in a batch reactor for comparison. About 60% e. e. and 90% e. e. were obtained with the fixed-bed reactor and the batch reactor respectively, demonstrating the possibility for the heterogeneous asymmetric hydrogenation in the fixed-bed reactor. Some adsorbed chiral modifier, cinchonidine, can be slowly removed from the surface of Pt/Al2O3 under the continuous flow reaction, as a result, the e, e, values drops with the reaction time in the fixed-bed reactor. The enantio-selectivity is higher in the fixed-bed reactor, but lower in the batch reactor when ethanol was used as solvent than that when acetic acid as solvent. CO was used as molecular probe to characterize the adsorption of cinchonidine an the catalyst surface by IR spectroscopy, A red shift observed in IR spectra of coadsorbed CO with cinchonidine suggests that the cinchonidine adsorption is mainly through the pi -interaction with platinum surface and donating electron to the platinum surface.

In situ study of carbon nanotube formation by C2H2 decomposition on an iron-based catalyst

The properties and formation of nanotubes have been extensively studied, but very few deal with the catalytic production mechanism of nanotubes. Two different techniques, thermogravimetric analysis and UV-Raman, have been applied to analyse the carbon deposition by catalysed decomposition of acetylene over an iron-based catalyst. The nature of the produced carbon materials depends on reaction temperature. Also, TEM allows identification of carbon nanotubes, encapsulated particles, and other nanostructures, while UV-Raman confirms its graphitic and graphite-like nature. (C) 2000 Elsevier Science Ltd. All rights reserved.