Water–Gas Shift Reaction on Metal Nanoclusters Encapsulated in Mesoporous Ceria Studied with Ambient-Pressure X-ray Photoelectron Spectroscopy

ACS Nano ◽  
2012 ◽  
Vol 6 (10) ◽  
pp. 9305-9313 ◽  
Author(s):  
Cun Wen ◽  
Yuan Zhu ◽  
Yingchun Ye ◽  
Shiran Zhang ◽  
Fang Cheng ◽  
...  
2013 ◽  
Vol 125 (19) ◽  
pp. 5205-5209 ◽  
Author(s):  
Kumudu Mudiyanselage ◽  
Sanjaya D. Senanayake ◽  
Leticia Feria ◽  
Shankhamala Kundu ◽  
Ashleigh E. Baber ◽  
...  

2013 ◽  
Vol 52 (19) ◽  
pp. 5101-5105 ◽  
Author(s):  
Kumudu Mudiyanselage ◽  
Sanjaya D. Senanayake ◽  
Leticia Feria ◽  
Shankhamala Kundu ◽  
Ashleigh E. Baber ◽  
...  

2009 ◽  
Author(s):  
Daniela Zanchet ◽  
Cristiane B. Rodella ◽  
Laura J. S. Lopes ◽  
Marco A. Logli ◽  
Valéria P. Vicentini ◽  
...  

2015 ◽  
Vol 2015 ◽  
pp. 1-9 ◽  
Author(s):  
Maxime Lortie ◽  
Rima Isaifan ◽  
Yun Liu ◽  
Sander Mommers

A new polyol synthesis method is described in which CuNi nanoparticles of different Cu/Ni atomic ratios were supported on both carbon and gamma-alumina and compared with Pt catalysts using the reverse water gas shift, RWGS, reaction. All catalysts were highly selective for CO formation. The concentration of CH4was less than the detection limit. Cu was the most abundant metal on the CuNi alloy surfaces, as determined by X-ray photoelectron spectroscopy, XPS, measurements. Only one CuNi alloy catalyst, Cu50Ni50/C, appeared to be as thermally stable as the Pt/C catalysts. After three temperature cycles, from 400 to 700°C, the CO yield at 700°C obtained using the Cu50Ni50/C catalyst was comparable to that obtained using a Pt/C catalyst.


2010 ◽  
Vol 156 (1-2) ◽  
pp. 2-7 ◽  
Author(s):  
Shanthakumar Sithambaram ◽  
Wen Wen ◽  
Eric Njagi ◽  
Xiong-Fei Shen ◽  
Jonathan C. Hanson ◽  
...  

2014 ◽  
Vol 2014 ◽  
pp. 1-6 ◽  
Author(s):  
R. Bouarab ◽  
S. Bennici ◽  
C. Mirodatos ◽  
A. Auroux

Unsupported and supported iron oxide catalysts were prepared by incipient wetness impregnation method and studied in the water-gas shift reaction (WGSR) in the temperature range 350–450°C. The techniques of characterization employed were BET, X-ray diffraction, acid-base measurements by microcalorimetry and in situ diffuse reflectance infrared Fourier transform spectroscopy. MgO, TiO2, or SiO2 was added in order to (i) obtain a catalyst exempt of chromium oxide and (ii) study the effect of their acid-base properties on catalytic activity of Fe2O3. X-ray diffraction studies, and calorimetric and diffuse reflectance infrared Fourier transform measurements reveal a complete change in the physicochemical properties of the iron oxide catalyst after MgO addition due to the formation of the spinel oxide phase. These results could indicate that the MgFe2O4 phase stabilizes the reduced iron phase, preventing its sintering under realistic WGSR conditions (high H2O partial pressures).


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