Fabrication of CeO2 nanotube supported Pt catalyst encapsulated with silica for high and stable performance

2015 ◽  
Vol 51 (48) ◽  
pp. 9785-9788 ◽  
Author(s):  
Chao Wan ◽  
Dang-guo Cheng ◽  
Fengqiu Chen ◽  
Xiaoli Zhan
Keyword(s):  
High Activity ◽  
Water Gas Shift ◽  
Pt Catalyst ◽  
Water Gas Shift Reaction ◽  
Stable Performance ◽  
Shift Reaction ◽  
Water Gas ◽  
Supported Pt Catalyst

Pt/CeO2 nanotubes encapsulated with silica exhibit high activity and stability for the water–gas-shift reaction.

An investigation of possible mechanisms for the water–gas shift reaction over a ZrO2-supported Pt catalyst

2006 ◽  
Vol 244 (2) ◽  
pp. 183-191 ◽  
Author(s):  
D TIBILETTI ◽  
F MEUNIER ◽  
A GOGUET ◽  
D REID ◽  
R BURCH ◽  
...  
Keyword(s):  
Water Gas Shift ◽  
Pt Catalyst ◽  
Water Gas Shift Reaction ◽  
Shift Reaction ◽  
Water Gas ◽  
Supported Pt Catalyst

scholarly journals TEM Characterization of Ceria supported Pt Catalyst for Water-Gas Shift Reaction Produced by Reactive Spray Deposition Technique

2013 ◽  
Vol 19 (S2) ◽  
pp. 1722-1723
Author(s):  
R. Jain ◽  
C.-H. Kuo ◽  
J. Roller ◽  
S.L. Suib ◽  
C.B. Carter ◽  
...  
Keyword(s):  
Spray Deposition ◽  
Water Gas Shift ◽  
Pt Catalyst ◽  
Water Gas Shift Reaction ◽  
Deposition Technique ◽  
Tem Characterization ◽  
Shift Reaction ◽  
Water Gas ◽  
Supported Pt Catalyst

Extended abstract of a paper presented at Microscopy and Microanalysis 2013 in Indianapolis, Indiana, USA, August 4 – August 8, 2013.

Enhanced CeO2-supported Pt catalyst for water–gas shift reaction

2010 ◽  
Vol 91 (7) ◽  
pp. 729-736 ◽  
Author(s):  
Kyung-ran Hwang ◽  
Son-ki Ihm ◽  
Jong-soo Park
Keyword(s):  
Water Gas Shift ◽  
Pt Catalyst ◽  
Water Gas Shift Reaction ◽  
Shift Reaction ◽  
Water Gas ◽  
Supported Pt Catalyst

scholarly journals Activity of La0.75Sr0.25Cr0.5Mn0.5O3−δ, Ni3Sn2 and Gd-doped CeO2 towards the reverse water-gas shift reaction and carburisation for a high-temperature H2O/CO2 co-electrolysis

RSC Advances ◽  
2020 ◽  
Vol 10 (17) ◽  
pp. 10285-10296
Author(s):  
Nicky Bogolowski ◽  
Beatriz Sánchez Batalla ◽  
Baekkyoung Shin ◽  
Jean-Francois Drillet
Keyword(s):  
High Temperature ◽  
High Activity ◽  
Water Gas Shift ◽  
Water Gas Shift Reaction ◽  
Reverse Water Gas Shift ◽  
Rwgs Reaction ◽  
Doped Ceo2 ◽  
Shift Reaction ◽  
Water Gas

LSCrM, Ni3Sn2 and GDC20 powders show high activity and selectivity for the RWGS reaction.

Praseodymium hydroxide/gold-supported precursor: a new strategy for preparing stable and active catalyst for the water-gas shift reaction

2020 ◽  
Vol 10 (21) ◽  
pp. 7291-7301
Author(s):  
Junjie Shi ◽  
Hailian Li ◽  
Weixuan Zhao ◽  
Pengfei Qi ◽  
Hongxin Wang
Keyword(s):  
Heterogeneous Catalysis ◽  
High Activity ◽  
Active Catalyst ◽  
Water Gas Shift ◽  
Great Promise ◽  
Water Gas Shift Reaction ◽  
New Strategy ◽  
O Vacancy ◽  
Shift Reaction ◽  
Water Gas

Rod-shaped praseodymium hydroxide (Pr(OH)x) as a hydroxyl- and O vacancy-rich support can promote the dispersion and stabilization of Au species show high activity and stability for water gas shift reaction, and holds great promise in the field of heterogeneous catalysis.

A rationally designed CuFe2O4–mesoporous Al2O3 composite towards stable performance of high temperature water–gas shift reaction

2013 ◽  
Vol 49 (96) ◽  
pp. 11257 ◽  
Author(s):  
Vijayanand Subramanian ◽  
Edwin S. Gnanakumar ◽  
Dae-Woon Jeong ◽  
Won-Bi Han ◽  
Chinnakonda S. Gopinath ◽  
...  
Keyword(s):  
High Temperature ◽  
Water Gas Shift ◽  
Water Gas Shift Reaction ◽  
High Temperature Water ◽  
Al2o3 Composite ◽  
Stable Performance ◽  
Shift Reaction ◽  
Water Gas ◽  
Temperature Water

Methanation of Carbon Monoxide with Water over Supported Rhodium Catalysts.

1985 ◽  
Vol 38 (2) ◽  
pp. 293 ◽  
Author(s):  
Y Tanaka ◽  
T Iizuka
Keyword(s):  
Carbon Monoxide ◽  
Low Temperature ◽  
High Activity ◽  
Water Gas Shift ◽  
Rhodium Catalysts ◽  
Water Gas Shift Reaction ◽  
Carbonaceous Species ◽  
Co Dissociation ◽  
Shift Reaction ◽  
Water Gas

The formation of methane in the reaction of CO and H2O over Rh supported on ZrO2, Al2O3, TiO2, SiO2 and MgO was examined. The high activity was achieved over Rh/ZrO2 and Rh/TiO2 at 300°C and CO dissociation ability of the catalyst was concluded to be an important factor to obtain high activity. At low temperature (c. 200°C), CO was not hydrogenated effectively but CO2 formed by the water gas shift reaction was hydrogenated after the conversion of CO into CO2 was completed. The formation of CH4 appears to occur through the water gas shift reaction, followed by the hydrogenation of carbonaceous species formed by the dissociation of CO or CO2.

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