Oxidative Coupling of Methane by Adsorbed Oxygen Species on SrTi1-xMgxO3-δCatalysts

Author(s):  
Keiichi Tomishige ◽  
Xiao-hong Li ◽  
Kaoru Fujimoto
Catalysts ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 388
Author(s):  
Yuqiao Fan ◽  
Changxi Miao ◽  
Yinghong Yue ◽  
Weiming Hua ◽  
Zi Gao

In this work, Ho2O3 nanosheets were synthesized by a hydrothermal method. A series of Sr-modified Ho2O3 nanosheets (Sr-Ho2O3-NS) with a Sr/Ho molar ratio between 0.02 and 0.06 were prepared via an impregnation method. These catalysts were characterized by several techniques such as XRD, N2 adsorption, SEM, TEM, XPS, O2-TPD (temperature-programmed desorption), and CO2-TPD, and they were studied with respect to their performances in the oxidative coupling of methane (OCM). In contrast to Ho2O3 nanoparticles, Ho2O3 nanosheets display greater CH4 conversion and C2-C3 selectivity, which could be related to the preferentially exposed (222) facet on the surface of the latter catalyst. The incorporation of small amounts of Sr into Ho2O3 nanosheets leads to a higher ratio of (O− + O2−)/O2− as well as an enhanced amount of chemisorbed oxygen species and moderate basic sites, which in turn improves the OCM performance. The optimal catalytic behavior is achievable on the 0.04Sr-Ho2O3-NS catalyst with a Sr/Ho molar ratio of 0.04, which gives a 24.0% conversion of CH4 with 56.7% selectivity to C2-C3 at 650 °C. The C2-C3 yield is well correlated with the amount of moderate basic sites present on the catalysts.


2020 ◽  
Vol 22 (34) ◽  
pp. 19349-19358
Author(s):  
Zunrong Sheng ◽  
Hyun-Ha Kim ◽  
Shuiliang Yao ◽  
Tomohiro Nozaki

Abundant carbonate species are generated over lanthanum by vibrationally excited CO2, which increase adsorbed oxygen species fixation for surface reaction.


1974 ◽  
Vol 13 (S2) ◽  
pp. A911A
Author(s):  
M. Che ◽  
B. Shelimov ◽  
J. F. Kibblewhite ◽  
A. J. Tench

RSC Advances ◽  
2017 ◽  
Vol 7 (24) ◽  
pp. 14809-14815 ◽  
Author(s):  
Min Wang ◽  
Lingxia Zhang ◽  
Weimin Huang ◽  
Yajun Zhou ◽  
Han Zhao ◽  
...  

The obtained catalyst Pt/MnO2-48 h demonstrated complete removal of 20 ppm C2H4at 50 °C for at least 12 h due to the large amount of adsorbed oxygen species and synergetic catalytic effect between Pt and the MnO2support.


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