Highly efficient Cu/CeO2-hollow nanospheres catalyst for the reverse water-gas shift reaction: Investigation on the role of oxygen vacancies through in situ UV-Raman and DRIFTS

2020 ◽  
Vol 516 ◽  
pp. 146035 ◽  
Author(s):  
Yudong Zhang ◽  
Long Liang ◽  
Ziyang Chen ◽  
Jinjun Wen ◽  
Wen Zhong ◽  
...  
2020 ◽  
Vol 266 ◽  
pp. 118669 ◽  
Author(s):  
Ali M. Bahmanpour ◽  
Florent Héroguel ◽  
Murat Kılıç ◽  
Christophe J. Baranowski ◽  
Pascal Schouwink ◽  
...  

2020 ◽  
Vol 390 ◽  
pp. 124629 ◽  
Author(s):  
Jose A. Hernandez Lalinde ◽  
Pakpong Roongruangsree ◽  
Jan Ilsemann ◽  
Marcus Bäumer ◽  
Jan Kopyscinski

2020 ◽  
Vol 269 ◽  
pp. 118826 ◽  
Author(s):  
Christopher Panaritis ◽  
Johnny Zgheib ◽  
Sayed A.H. Ebrahim ◽  
Martin Couillard ◽  
Elena A. Baranova

2015 ◽  
Vol 2015 ◽  
pp. 1-9
Author(s):  
Maxime Lortie ◽  
Rima J. Isaifan

Cu50Ni50 nanoparticles were synthesized using a modified polyol method and deposited on samarium-doped ceria, SDC, and yttria-stabilized zirconia, YSZ, supports to form reverse water-gas shift, RWGS, catalysts. The best CO yields, obtained with the Cu50Ni50/SDC catalyst, were about 90% of the equilibrium CO yields. In contrast CO yields using Pt/SDC catalysts were equal to equilibrium CO yields at 700°C. Catalyst selectivity to CO was 100% at hydrogen partial pressures equal to CO2 partial pressures, 1 kPa, and decreased as methane was formed when the hydrogen partial pressure was 2 kPa or greater. The reaction results were explained using a combination of Eley-Rideal and Langmuir-Hinshelwood mechanisms that involved adsorption on the metal surface and the concentration of oxygen vacancies in the support. Finally the Cu50Ni50/SDC catalyst was found to be thermally stable for 48 hours at 600/700°C.


2018 ◽  
Vol 26 ◽  
pp. 350-358 ◽  
Author(s):  
Christopher Panaritis ◽  
Mahesh Edake ◽  
Martin Couillard ◽  
Raha Einakchi ◽  
Elena A. Baranova

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