Grunwaldt Jan-Dierk, Baiker Alfons
Department of Chemistry and Applied Biosciences, Swiss Federal Institute of Technology, ETH Hönggerberg HCI, CH-8093 Zürich, Switzerland.
Phys Chem Chem Phys. 2005 Oct 21;7(20):3526-39. doi: 10.1039/b509667g. Epub 2005 Aug 11.
In situ characterization of catalysts by means of complementary spectroscopic techniques can be regarded as the first step towards rational catalyst design. Spurred by the growing interest of catalytic reactions in supercritical fluids and by several industrial reactions traditionally performed at high pressure (>10 bar), new demands and challenges are put to in situ spectroscopic characterization of heterogeneous catalytic reactions. In this article, we discuss the development and the use of spectroscopic and related techniques suitable for elucidating such high-pressure reactions. Selected examples from phase behaviour studies with a view cell, investigations with transmission and attenuated total reflection (ATR) infrared spectroscopy as well as X-ray absorption spectroscopy (EXAFS, XANES), are presented to show the strategies, opportunities and limitations of such high pressure in situ studies. Different facets appear to be important to gain insight into catalytic reactions in supercritical fluids: the identification of the phase behaviour of the reaction mixture, the behaviour of the fluid inside the porous catalyst, the processes occurring at the solid-fluid interface, the possible dissolution of active species and, similar as in gas-solid reactions, the establishment of structure-activity relationships.
通过互补光谱技术对催化剂进行原位表征可被视为迈向合理催化剂设计的第一步。受超临界流体中催化反应日益增长的兴趣以及传统上在高压(>10巴)下进行的若干工业反应的推动,多相催化反应的原位光谱表征面临着新的要求和挑战。在本文中,我们讨论了适用于阐明此类高压反应的光谱及相关技术的发展与应用。给出了从视窗池相行为研究、透射和衰减全反射(ATR)红外光谱以及X射线吸收光谱(EXAFS、XANES)研究中选取的示例,以展示此类高压原位研究的策略、机遇和局限性。要深入了解超临界流体中的催化反应,不同方面似乎都很重要:反应混合物相行为的识别、多孔催化剂内部流体的行为、固 - 液界面发生的过程、活性物种的可能溶解,以及与气 - 固反应类似的结构 - 活性关系的建立。