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Coke Formation during Propane Dehydrogenation over Ga−Rh Supported Catalytically Active Liquid Metal Solutions.

Authors :
Wolf, Moritz
Raman, Narayanan
Taccardi, Nicola
Haumann, Marco
Wasserscheid, Peter
Source :
ChemCatChem; 2/20/2020, Vol. 12 Issue 4, p1085-1094, 10p
Publication Year :
2020

Abstract

Supported Catalytically Active Liquid Metal Solutions (SCALMS) were recently described as a new class of heterogeneous catalysts, where the catalytic transformation takes place at the highly dynamic interface of a liquid alloy. Their application in alkane dehydrogenation has been claimed to be superior to classical heterogeneous catalysts, because the single atom nature of Rh dissolved in liquid Ga hinders the formation of significant amounts of coke, e. g. by oligomerisation of carbon fragments and excessive dehydrogenation. In the present study, we investigate the coking behaviour of Ga−Rh SCALMS during dehydrogenation of propane in detail by means of high‐resolution thermogravimetry. We report that the application of Ga−Rh SCALMS indeed limits the formation of coke when compared to the Ga‐free Rh catalyst, in particular when relating coke formation to the catalytic performance. Furthermore, the formed coke has been shown to be highly reactive during temperature programmed oxidation in 21 % O2/He with onset temperatures of approx. 150 °C enabling a regeneration of the Ga−Rh SCALMS system under mild conditions. The activation energy of the oxidation lies in the lower range of values reported for spent cracking catalysts. Monitoring the formation of coke and performance of SCALMS in situ via thermogravimetry coupled with mass spectrometry revealed the continuous formation of coke, which becomes the only process affecting the net weight change after a certain time on stream. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
18673880
Volume :
12
Issue :
4
Database :
Complementary Index
Journal :
ChemCatChem
Publication Type :
Academic Journal
Accession number :
141866795
Full Text :
https://doi.org/10.1002/cctc.201901922