Authors (11): K. Morgan, J. Touitou, J. -S. Choi, C. Coney, C. Hardacre, J. A. Pihl, C. E. Stere, M. -Y. Kim, C. Stewart, A. Goguet, W. P. Partridge
Themes: Energy (2016)
DOI: 10.1021/acscatal.5b02602
Citations: 72
Pub type: article-journal
Publisher: American Chemical Society (ACS)
Issue: 2
License: http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html
Publication date(s): 2016/02/05 (print) 2016/01/28 (online)
Pages: 1356-1381
Volume: 6 Issue: 2
Journal: ACS Catalysis
Link: https://pubs.acs.org/doi/pdf/10.1021/acscatal.5b02602
URL: http://dx.doi.org/10.1021/acscatal.5b02602The development and optimization of catalysts and catalytic processes requires knowledge of reaction kinetics and mechanisms. In traditional catalyst kinetic characterization, the gas composition is known at the inlet, and the exit flow is measured to determine changes in concentration. As such, the progression of the chemistry within the catalyst is not known. Technological advances in electromagnetic and physical probes have made visualizing the evolution of the chemistry within catalyst samples a reality, as part of a methodology commonly known as spatial resolution. Herein, we discuss and evaluate the development of spatially resolved techniques, including the evolutions and achievements of this growing area of catalytic research. The impact of such techniques is discussed in terms of the invasiveness of physical probes on catalytic systems, as well as how experimentally obtained spatial profiles can be used in conjunction with kinetic modeling. Furthermore, some aims and aspirations for further evolution of spatially resolved techniques are considered.
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