Effect of VOx surface density and structure on VOx/TiO2 catalysts for H2S selective oxidation reaction

2020 ◽  
Vol 92 ◽  
pp. 252-262
Author(s):  
Hanki Eom ◽  
Sang Moon Lee ◽  
Hyerin Kang ◽  
Ye Hwan Lee ◽  
Soon Woong Chang ◽  
...  
ChemCatChem ◽  
2018 ◽  
Vol 10 (16) ◽  
pp. 3539-3545 ◽  
Author(s):  
Li-Bing Lv ◽  
Shi-Ze Yang ◽  
Wen-Yu Ke ◽  
Hong-Hui Wang ◽  
Bing Zhang ◽  
...  

2017 ◽  
Vol 9 (44) ◽  
pp. 38992-38998 ◽  
Author(s):  
Satoshi Yasuda ◽  
Takahiro Yoshii ◽  
Shohei Chiashi ◽  
Shigeo Maruyama ◽  
Kei Murakoshi

AIChE Journal ◽  
2014 ◽  
Vol 61 (2) ◽  
pp. 572-581 ◽  
Author(s):  
Matic Krivec ◽  
Andrej Pohar ◽  
Blaž Likozar ◽  
Goran Dražić

2017 ◽  
Vol 8 (1) ◽  
Author(s):  
Linping Qian ◽  
Zhen Wang ◽  
Evgeny V. Beletskiy ◽  
Jingyue Liu ◽  
Haroldo J. dos Santos ◽  
...  

Abstract The ability of Au catalysts to effect the challenging task of utilizing molecular oxygen for the selective epoxidation of cyclooctene is fascinating. Although supported nanometre-size Au particles are poorly active, here we show that solubilized atomic Au clusters, present in ng ml−1 concentrations and stabilized by ligands derived from the oxidized hydrocarbon products, are active. They can be formed from various Au sources. They generate initiators and propagators to trigger the onset of the auto-oxidation reaction with an apparent turnover frequency of 440 s−1, and continue to generate additional initiators throughout the auto-oxidation cycle without direct participation in the cycle. Spectroscopic characterization suggests that 7–8 atom clusters are effective catalytically. Extension of work based on these understandings leads to the demonstration that these Au clusters are also effective in selective oxidation of cyclohexene, and that solubilized Pt clusters are also capable of generating initiators for cyclooctene epoxidation.


2014 ◽  
Vol 16 (6) ◽  
pp. 3024-3030 ◽  
Author(s):  
Ajay K. Singh ◽  
K. C. Basavaraju ◽  
Siddharth Sharma ◽  
Seungwook Jang ◽  
Chan Pil Park ◽  
...  

Here, we demonstrate that graphene oxide (GO) can be converted to N-doped reduced GO (rGO) that could become a substitute for N-doped graphene.


RSC Advances ◽  
2014 ◽  
Vol 4 (93) ◽  
pp. 51544-51547 ◽  
Author(s):  
Weijie Zhang ◽  
Pingping Jiang ◽  
Ying Wang ◽  
Jian Zhang ◽  
Yongxue Gao ◽  
...  

We synthesized a readily accessible molybdenum-doped covalent-organic framework catalyst (Mo-COF) linked by a hydrazine linkage via a facile two-step bottom-up approach. This Mo-COF catalyst as an open nanochannel-reactor showed promising catalytic properties for the selective oxidation reaction.


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