Uranium oxide-supported gold catalyst for water–gas shift reaction

2015 ◽  
Vol 137 ◽  
pp. 164-169 ◽  
Author(s):  
Yuan-Yuan Dong ◽  
Wei-Ping Liao ◽  
Zhang-Huai Suo
RSC Advances ◽  
2015 ◽  
Vol 5 (96) ◽  
pp. 78864-78873 ◽  
Author(s):  
Subhi Baishya ◽  
Ramesh Ch. Deka

Neutral gold monomer supported on faujasite (Au0/FAU) exhibits superior catalytic activity towards water gas shift reaction compared to cationic monomer.


Catalysts ◽  
2018 ◽  
Vol 8 (12) ◽  
pp. 627 ◽  
Author(s):  
James H. Carter ◽  
Graham J. Hutchings

The low-temperature water–gas shift reaction (LTS: CO + H2O ⇌ CO2 + H2) is a key step in the purification of H2 reformate streams that feed H2 fuel cells. Supported gold catalysts were originally identified as being active for this reaction twenty years ago, and since then, considerable advances have been made in the synthesis and characterisation of these catalysts. In this review, we identify and evaluate the progress towards solving the most important challenge in this research area: the development of robust, highly active catalysts that do not deactivate on-stream under realistic reaction conditions.


2020 ◽  
Vol 10 (24) ◽  
pp. 8219-8229
Author(s):  
Zhongling Lang ◽  
Yangguang Li ◽  
Anna Clotet ◽  
Josep M. Poblet

We computationally investigated the WGSR mechanism on POM supported gold and revealed the role of POMs. A direct pathway by formation of COOHads from the co-adsorbed H2O and CO is proposed.


2020 ◽  
Author(s):  
Nore Stolte ◽  
Junting Yu ◽  
Zixin Chen ◽  
Dimitri A. Sverjensky ◽  
Ding Pan

The water-gas shift reaction is a key reaction in Fischer-Tropsch-type synthesis, which is widely believed to generate hydrocarbons in the deep carbon cycle, but is little known at extreme pressure-temperature conditions found in Earth’s upper mantle. Here, we performed extensive ab initio molecular dynamics simulations and free energy calculations to study the water-gas shift reaction. We found the direct formation of formic acid out of CO and supercritical water at 10∼13 GPa and 1400 K without any catalyst. Contrary to the common assumption that formic acid or formate is an intermediate product, we found that HCOOH is thermodynamically more stable than the products of the water-gas shift reaction above 3 GPa and at 1000∼1400 K. Our study suggests that the water-gas shift reaction may not happen in Earth’s upper mantle, and formic acid or formate may be an important carbon carrier, participating in many geochemical processes in deep Earth.<br>


2013 ◽  
Vol 33 (9) ◽  
pp. 1572-1577 ◽  
Author(s):  
Yuanzhuo ZHANG ◽  
Ziying YU ◽  
Fumin ZHANG ◽  
Qiang XIAO ◽  
Yijun ZHONG ◽  
...  

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