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Experimental methods in chemical engineering: Temperature programmed surface reaction spectroscopy— TPSR
Author(s) -
Jehng JihMirn,
Wachs Israel E.,
Patience Gregory S.,
Dai YongMing
Publication year - 2021
Publication title -
the canadian journal of chemical engineering
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.404
H-Index - 67
eISSN - 1939-019X
pISSN - 0008-4034
DOI - 10.1002/cjce.23913
Subject(s) - catalysis , chemistry , oxide , molecule , metal , redox , ruthenium , chemical reaction , inorganic chemistry , organic chemistry
Temperature programmed surface reaction spectroscopy (TPSR) is a powerful technique to determine the surface chemistry of bulk metal, supported metal, bulk metal oxide, supported metal oxide, zeolite, and molecular sieve catalysts. It can provide both qualitative and quantitative analysis of the surface active sites present on the catalyst surface, the reaction mechanisms, and kinetics occurring on the catalyst surface by using chemical probe molecules such as alcohols, carboxylates, and specific acidic‐basic reacting gases. In this tutorial review, the highly informative CH 3 OH chemical probe molecule was used to highlight the information that can be obtained from CH 3 OH ‐TPSR experiments. The CH 3 OH molecule readily interacts with the catalyst surface to form surface CH 3 O · and HCOO · intermediates that react to produce HCHO/ HCOOCH 3 / (CH 3 O) 2 CH 2 , CH 3 OCH 3 , and CO/CO 2 products related to the surface redox, acid and basic nature, respectively. Integration of the CH 3 OH ‐TPSR spectra peaks provide the number of surface active sites. The surface kinetic information provided by CH 3 OH ‐TPSR allows to discriminate between different reaction mechanisms (first‐order, second‐order, Langmuir‐Hinshelwood, and Mars‐van Krevelen). We discuss the uncertainty inherent in CH 3 OH ‐TPSR experiments and address source of errors and detection limits. Web of Science indexed over 800 articles citing TPSR since 1990. A bibliometric analysis identified four clusters of reactions and catalysts: the dominant catalysts for partial oxidation and water gas shift were Ni, Ru, and Pt; CeO 2 , Co, Cu, Rh, Pd, and perovskites were the main catalysts for combustion and hydrogenation; Ag and zeolites were grouped with reduction; and, Al 2 O 3 , ZrO 2 , SiO 2 , and V 2 O 5 were applied for dehydrogenation.