Spatially resolved mass spectrometry as a fast semi-quantitative tool for testing heterogeneous catalyst libraries under reducing stagnant-point flow conditions

被引:7
作者
Eckhard, K
Schlüter, O
Hagen, V
Wehner, B
Erichsen, T
Schuhmann, W
Muhler, M [1 ]
机构
[1] Ruhr Univ Bochum, Lehrstuhl Tech Chem, D-44780 Bochum, Germany
[2] Ruhr Univ Bochum, Lehrtuhl Analyt Chem, Arbeitsgrp Elektroanalyt & Sensor, D-44780 Bochum, Germany
关键词
spatially resolved mass spectrometry; palladium; ethene hydrogenation; high throughput experimentation; primary screening; semi-quantitative; Pd area determination;
D O I
10.1016/j.apcata.2004.11.027
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A calibrated quadrupole mass spectrometer (QMS) is combined with a home-made positioning unit deriving from scanning electrochemical microscopy (SECM) to sequentially address 25 catalysts, which are placed in wells. Highly reproducible catalytic data are obtained under stagnant-point flow conditions by means of coupled gas feed and QMS capillaries. The reaction array can be heated and is fully seated from the atmosphere by a covering glass lid. Additionally, the reaction chamber is flushed with argon making it possible to study the structure-insensitive hydrogenation of ethene over SiO2-supported palladium catalysts unimpaired by oxygen poisoning. Since the derived semi-quantitative degree of conversion is proportional to the Pd metal area under fixed reaction conditions, spatially resolved mass spectrometry provides a novel method for rapidly estimating the metal surface areas of a Pd catalyst library. (c) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:115 / 120
页数:6
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