Selective Oxidation of Methanol by Extra Oxygen Species on One-Dimensional Mo Rows of a Mo(112)−(1 × 2)-O Surface

1998 ◽  
Vol 102 (44) ◽  
pp. 8825-8833 ◽  
Author(s):  
Ken-ichi Fukui ◽  
Katsuya Motoda ◽  
Yasuhiro Iwasawa
Keyword(s):  
Selective Oxidation ◽  
Oxygen Species ◽  
One Dimensional ◽  
Oxidation Of Methanol ◽  
Extra Oxygen

Active site densities, oxygen activation and adsorbed reactive oxygen in alcohol activation on npAu catalysts

2016 ◽  
Vol 188 ◽  
pp. 57-67 ◽  
Author(s):  
Lu-Cun Wang ◽  
C. M. Friend ◽  
Rebecca Fushimi ◽  
Robert J. Madix
Keyword(s):  
Selective Oxidation ◽  
Activation Barrier ◽  
Initial Step ◽  
Temporal Analysis ◽  
Adsorbed Oxygen ◽  
Transient Pressure ◽  
Pulse Reaction ◽  
Dissociation Probability ◽  
Oxidation Of Methanol ◽  
Oxygen Atoms

The activation of molecular O2 as well as the reactivity of adsorbed oxygen species is of central importance in aerobic selective oxidation chemistry on Au-based catalysts. Herein, we address the issue of O2 activation on unsupported nanoporous gold (npAu) catalysts by applying a transient pressure technique, a temporal analysis of products (TAP) reactor, to measure the saturation coverage of atomic oxygen, its collisional dissociation probability, the activation barrier for O2 dissociation, and the facility with which adsorbed O species activate methanol, the initial step in the catalytic cycle of esterification. The results from these experiments indicate that molecular O2 dissociation is associated with surface silver, that the density of reactive sites is quite low, that adsorbed oxygen atoms do not spill over from the sites of activation onto the surrounding surface, and that methanol reacts quite facilely with the adsorbed oxygen atoms. In addition, the O species from O2 dissociation exhibits reactivity for the selective oxidation of methanol but not for CO. The TAP experiments also revealed that the surface of the npAu catalyst is saturated with adsorbed O under steady state reaction conditions, at least for the pulse reaction.

CuO/TiO2 heterojunction composites: an efficient photocatalyst for selective oxidation of methanol to methyl formate

2019 ◽  
Vol 7 (5) ◽  
pp. 2253-2260 ◽  
Author(s):  
Quanquan Shi ◽  
Guicheng Ping ◽  
Xiaojia Wang ◽  
Hui Xu ◽  
Jingmei Li ◽  
...  
Keyword(s):  
Selective Oxidation ◽  
Methyl Formate ◽  
Photo Oxidation ◽  
Oxidation Of Methanol

This study demonstrates the synthesis of an efficient photocatalyst, CuO/TiO2 heterojunction, for selective aerobic photo-oxidation of methanol to methyl formate.

On the mechanism of the selective oxidation of methanol over elemental silver

1994 ◽  
Vol 28 (2-4) ◽  
pp. 383-395 ◽  
Author(s):  
H. Schubert ◽  
U. Tegtmeyer ◽  
R. Schl�gl
Keyword(s):  
Selective Oxidation ◽  
Oxidation Of Methanol ◽  
Elemental Silver

Co-Electrospun VTiOx Hollow Nanofibers for Selective Oxidation of Methanol to High Value Chemicals

2019 ◽  
Vol 2 (8) ◽  
pp. 5224-5232 ◽  
Author(s):  
Chunlei Zhang ◽  
Ping Wu ◽  
Guojuan Liu ◽  
Zhigao Zhu ◽  
Gaofeng Zeng
Keyword(s):  
Selective Oxidation ◽  
Hollow Nanofibers ◽  
Oxidation Of Methanol

scholarly journals Operando XAS/XRD and Raman Spectroscopic Study of Structural Changes of the Iron Molybdate Catalyst during Selective Oxidation of Methanol

ChemCatChem ◽  
2019 ◽  
Vol 11 (19) ◽  
pp. 4871-4883 ◽  
Author(s):  
Abhijeet Gaur ◽  
Max Schumann ◽  
Kristian Viegaard Raun ◽  
Matthias Stehle ◽  
Pablo Beato ◽  
...  
Keyword(s):  
Spectroscopic Study ◽  
Selective Oxidation ◽  
Structural Changes ◽  
Iron Molybdate ◽  
Raman Spectroscopic ◽  
Raman Spectroscopic Study ◽  
Oxidation Of Methanol ◽  
Operando Xas

Selective oxidation of methanol to dimethoxymethane over V 2 O 5 /TiO 2 –Al 2 O 3 catalysts

2015 ◽  
Vol 60 (11) ◽  
pp. 1009-1018 ◽  
Author(s):  
Tuo Wang ◽  
Yali Meng ◽  
Liang Zeng ◽  
Jinlong Gong
Keyword(s):  
Selective Oxidation ◽  
Oxidation Of Methanol
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