A high pressure in situ x-ray absorption spectroscopy cell with two different path lengths and path positions is presented for studying element-specifically both the liquid phase and the solid/liquid interface at pressures up to 250 bar and temperatures up to 220 °C. For this purpose, one x-ray path probes the bottom, while the other x-ray path penetrates through the middle of the in situ cell. The basic design of the cell resembles a 10 ml volume batch reactor, which is equipped with in- and outlet lines to dose compressed gases and liquids as well as a stirrer for good mixing. Due to the use of a polyetheretherketone inset it is also suitable for measurements under corrosive conditions. The characteristic features of the cell are illustrated using case studies from catalysis and solid state chemistry: (a) the ruthenium-catalyzed formylation of an amine in “supercritical” carbon dioxide in the presence of hydrogen; (b) the cycloaddition of carbon dioxide to propylene oxide in the presence of a solid Zn-based catalyst, and (c) the solvothermal synthesis of MoO3 nanorods from MoO3∙2H2O.
Structural information has been gained during aerobic benzyl alcohol oxidation in ''supercritical'' carbon dioxide at 150 bar on alumina-supported palladium by X-ray absorption spectroscopy while monitoring simultaneously the performance of the catalyst. The reduction of the catalyst by benzyl alcohol could be monitored by the analysis of the near-edge region of the Pd K-edge. The palladium constituent was mainly in metallic state under operating conditions. Partial reoxidation was observed when only oxygen in ''supercritical'' carbon dioxide in the absence of alcohol was fed. The catalytic activity of the PdO x =Al 2 O 3 catalyst during benzyl alcohol oxidation was comparable to that in a conventional continuous fixed-bed reactor and depended on the oxygen concentration in the feed. The rate of alcohol conversion went through a maximum when the oxygen concentration was increased. At maximum rate, part of the palladium was in the oxidized state. Upon further increase of the oxygen concentration, the activity decreased because of the formation of surface palladium oxide. The reaction rate in ''supercritical'' carbon dioxide was strikingly higher than that observed for the corresponding liquid-phase oxidation.
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