scholarly journals Catalytic hydrolysis of carbonyl sulphide and carbon disulphide over Fe2O3 cluster: Competitive adsorption and reaction mechanism

2017 ◽  
Vol 7 (1) ◽  
Author(s):  
Ping Ning ◽  
Xin Song ◽  
Kai Li ◽  
Chi Wang ◽  
Lihong Tang ◽  
...  
Keyword(s):  
Reaction Mechanism ◽  
Competitive Adsorption ◽  
Carbon Disulphide ◽  
Catalytic Hydrolysis ◽  
Carbonyl Sulphide ◽  
Hydrolysis Of

scholarly journals Catalytic hydrolysis of s-triazine compounds over Al2O3

1996 ◽  
Vol 27 (1-2) ◽  
pp. 167-173 ◽  
Author(s):  
Zhaoqi Zhan ◽  
Martin Müllner ◽  
Johannes A. Lercher
Keyword(s):  
Catalytic Hydrolysis ◽  
Hydrolysis Of

Catalytic Hydrolysis of 4-Nitrophenyl Phosphate by Lanthanum(III)-Hectorite

Langmuir ◽  
2003 ◽  
Vol 19 (6) ◽  
pp. 2188-2192 ◽  
Author(s):  
Steven T. Frey ◽  
Benjamin M. Hutchins ◽  
Brian J. Anderson ◽  
Teresa K. Schreiber ◽  
Michael E. Hagerman
Keyword(s):  
Catalytic Hydrolysis ◽  
Nitrophenyl Phosphate ◽  
Hydrolysis Of

Thermodynamics Study on Catalytic Hydrolysis of CCl2F2 over Solid Acid MoO3/ZrO2

2013 ◽  
Vol 726-731 ◽  
pp. 535-538
Author(s):  
Tian Cheng Liu ◽  
Yu Jiao Guo ◽  
Ping Ning ◽  
Guang Yang Tang ◽  
Ming Long Yuan
Keyword(s):  
Water Vapor ◽  
Solid Acid ◽  
Exothermic Reaction ◽  
Fixed Bed ◽  
Fixed Bed Reactor ◽  
Catalytic Hydrolysis ◽  
Chemical Adsorption ◽  
Freundlich Model ◽  
Hydrolysis Of

Catalytic hydrolysis decomposition of dichlorodifluoromethane (CCl2F2) in the presence of water vapor and oxygen was studied over solid acid MoO3/ZrO2 using a fixed-bed reactor. The CCl2F2 adsorption was multilayer chemical adsorption and its process was corresponding with Freundlich model. Its heat was from 56.3 to 73.2 KJ.mol-1, and it was exothermic reaction and chemical adsorption.

Vinyl ether hydrolysis. XVII. Oxacyclonon-2,8-diene and the question of the unorthodox reaction mechanism for 9-methoxyoxacyclonon-2-ene

1984 ◽  
Vol 62 (1) ◽  
pp. 74-76 ◽  
Author(s):  
R. A. Burt ◽  
Y. Chiang ◽  
A. J. Kresge ◽  
S. Szilagyi
Keyword(s):  
Reaction Mechanism ◽  
Vinyl Ether ◽  
Membered Ring ◽  
Specific Rate ◽  
Ether Group ◽  
Reaction Proceeds ◽  
Great Reactivity ◽  
Rate Of Hydrolysis ◽  
Acid Catalyzed ◽  
Hydrolysis Of

The acid-catalyzed hydrolysis of the nine-membered ring cyclic vinyl ether, oxacyclonon-2,8-diene, occurs with a normal isotope effect, [Formula: see text], which indicates that this reaction proceeds by the conventional vinyl ether hydrolysis mechanism involving rate-determining proton transfer to carbon. The specific rate of this reaction, [Formula: see text], may then be used to show that there is no significant ring-size effect on the rate of hydrolysis of a vinyl ether group in a nine-membered ring. The previously noted unusually great reactivity of the vinyl ether group in 9-methoxyoxacyclonon-2-ene, for which an unorthodox reaction mechanism has been claimed, must therefore be due to some other cause.

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