Tuning surface V5+ concentration in M1 phase MoVSbOx catalysts for ethylene production from ethane through oxidative dehydrogenation reaction

2021 ◽  
Vol 610 ◽  
pp. 117946
Author(s):  
Chunyu Xin ◽  
Fagen Wang ◽  
Guo Qin Xu
2020 ◽  
Author(s):  
Leelavathi Annamalai ◽  
Sopuruchukwu Ezenwa ◽  
Yanliu Dang ◽  
Haiyan Tan ◽  
Steven L. Suib ◽  
...  

2017 ◽  
Vol 4 (7) ◽  
pp. 6966-6974 ◽  
Author(s):  
Luman Zhang ◽  
Dong Chen ◽  
Leewoon Jang ◽  
Mattias Vervaele ◽  
Jean-Pierre Locquet ◽  
...  

1969 ◽  
Vol 12 (12) ◽  
pp. 932-934
Author(s):  
Eiichiro Nishikawa ◽  
Toru Ueki ◽  
Keiichi Shibuya ◽  
Yoshiro Morita

ACS Catalysis ◽  
2016 ◽  
Vol 6 (7) ◽  
pp. 4775-4781 ◽  
Author(s):  
Mimoun Aouine ◽  
Thierry Epicier ◽  
Jean-Marc M. Millet

2020 ◽  
Vol 63 (19-20) ◽  
pp. 1754-1764
Author(s):  
Daniel Melzer ◽  
Gerhard Mestl ◽  
Klaus Wanninger ◽  
Andreas Jentys ◽  
Maricruz Sanchez-Sanchez ◽  
...  

AbstractThe pathways of ethane oxidative dehydrogenation and total combustion have been elucidated for M1 phase type Mo–V oxide catalysts with different metal composition. The ethane oxidation mechanism is not affected by the presence of Te or Nb. Conversely, the selectivity is strongly affected by stoichiometry of M1 catalysts. This is attributed to the facile oxidation of ethene to COx upon formation of unselective VOx species in the absence of Te and Nb.


ChemCatChem ◽  
2014 ◽  
Vol 6 (8) ◽  
pp. 2270-2275 ◽  
Author(s):  
Xiaoyan Sun ◽  
Rui Wang ◽  
Bingsen Zhang ◽  
Rui Huang ◽  
Xing Huang ◽  
...  

2017 ◽  
Vol 53 (70) ◽  
pp. 9737-9740 ◽  
Author(s):  
Lirong Yu ◽  
Yanglizhi Li ◽  
Xi Wang ◽  
Xingyong Wang ◽  
Panpan Zhou ◽  
...  

An elegant synthetic route to a ladder-type di-borate compound 2a was reported based on the reduction, radical-cyclization, and oxidative-dehydrogenation reaction of 1.


2021 ◽  
Vol 19 (2) ◽  
pp. 101-106
Author(s):  
A.M. Aliyev ◽  
◽  
G.A. Ali-zade ◽  
M.Q. Aliyeva ◽  
A.R. Safarov ◽  
...  

The article studied and compared the reactivity of cyclohexanol and methylcyclohexanol isomers in the oxidative dehydrogenation reaction over modified zeolite catalysts. It found that rates of oxidative dehydrogenation of all methylcyclohexanol isomers are practically the same and exceed rates of oxidative dehydrogenation of cyclohexanol into cyclohexanone.


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