Reaction mechanism and kinetics of the degradation of bromoxynil initiated by OH radical

RSC Advances ◽  
2014 ◽  
Vol 4 (15) ◽  
pp. 7749 ◽  
Author(s):  
L. Sandhiya ◽  
K. Senthilkumar
Keyword(s):  
Reaction Mechanism ◽  
Oh Radical ◽  
Mechanism And Kinetics ◽  
Kinetics Of

scholarly journals Atmospheric chemical reaction mechanism and kinetics of 1,2-bis(2,4,6-tribromophenoxy)ethane initiated by OH radical: a computational study

RSC Advances ◽  
2017 ◽  
Vol 7 (16) ◽  
pp. 9484-9494 ◽  
Author(s):  
Qi Yu ◽  
Hong-Bin Xie ◽  
Tianchi Li ◽  
Fangfang Ma ◽  
Zihao Fu ◽  
...  
Keyword(s):  
Reaction Mechanism ◽  
Chemical Reaction ◽  
Computational Study ◽  
Oh Radical ◽  
Chemical Reaction Mechanism ◽  
Mechanism And Kinetics ◽  
Kinetics Of

The mechanism and kinetics of OH-initiated oxidation of BTBPE, an alternative of PBDEs, were investigated.

Investigation of the Reaction Mechanism and Kinetics of Iodic Acid with OH Radical Using Quantum Chemistry

2017 ◽  
Vol 1 (4) ◽  
pp. 227-235 ◽  
Author(s):  
Sarah Khanniche ◽  
Florent Louis ◽  
Laurent Cantrel ◽  
Ivan Černušák
Keyword(s):  
Reaction Mechanism ◽  
Quantum Chemistry ◽  
Oh Radical ◽  
Iodic Acid ◽  
Mechanism And Kinetics ◽  
Kinetics Of

Theoretical study on the reaction mechanism of OH radical with Z(E)-CF3CHCHF

2019 ◽  
Vol 21 (3) ◽  
pp. 1367-1374 ◽  
Author(s):  
Chao Xu ◽  
Chaoyang Wang ◽  
Bo Li ◽  
Linping Hu ◽  
Feng Long Gu
Keyword(s):  
Reaction Mechanism ◽  
Quantum Chemical Calculations ◽  
Quantum Chemical ◽  
Theoretical Study ◽  
Oh Radicals ◽  
Oh Radical ◽  
Transformation Mechanism ◽  
Mechanism And Kinetics ◽  
Kinetics Of

The comprehensive transformation mechanism and kinetics of Z(E)-CF3CHCHF initiated by OH radicals were investigated by performing quantum chemical calculations.

scholarly journals Influence of RANEY Nickel on the Formation of Intermediates in the Degradation of Lignin

2012 ◽  
Vol 2012 ◽  
pp. 1-8 ◽  
Author(s):  
Daniel Forchheim ◽  
Ursel Hornung ◽  
Philipp Kempe ◽  
Andrea Kruse ◽  
David Steinbach
Keyword(s):  
Molecular Structure ◽  
Reaction Mechanism ◽  
Enzymatic Hydrolysis ◽  
Raney Nickel ◽  
High Selectivity ◽  
Main Product ◽  
Hydrolysis Lignin ◽  
Renewable Source ◽  
Mechanism And Kinetics ◽  
Kinetics Of

Lignin forms an important part of lignocellulosic biomass and is an abundantly available residue. It is a potential renewable source of phenol. Liquefaction of enzymatic hydrolysis lignin as well as catalytical hydrodeoxygenation of the main intermediates in the degradation of lignin, that is, catechol and guaiacol, was studied. The cleavage of the ether bonds, which are abundant in the molecular structure of lignin, can be realised in near-critical water (573 to 673 K, 20 to 30 MPa). Hydrothermal treatment in this context provides high selectivity in respect to hydroxybenzenes, especially catechol. RANEY Nickel was found to be an adequate catalyst for hydrodeoxygenation. Although it does not influence the cleavage of ether bonds, RANEY Nickel favours the production of phenol from both lignin and catechol. The main product from hydrodeoxygenation of guaiacol with RANEY Nickel was cyclohexanol. Reaction mechanism and kinetics of the degradation of guaiacol were explored.

Study on the reaction mechanism and kinetics of CO hydrogenation on a fused Fe–Mn catalyst

RSC Advances ◽  
2015 ◽  
Vol 5 (115) ◽  
pp. 95287-95299 ◽  
Author(s):  
A. A. Mirzaei ◽  
E. Rezazadeh ◽  
M. Arsalanfar ◽  
M. Abdouss ◽  
M. Fatemi ◽  
...  
Keyword(s):  
Reaction Mechanism ◽  
Co Hydrogenation ◽  
Fixed Bed ◽  
Hydrogenation Reaction ◽  
Mechanism And Kinetics ◽  
Kinetics Of ◽  
Micro Reactor

The kinetics of the CO hydrogenation reaction over a Fe–Mn fused catalyst was investigated in a fixed-bed micro-reactor.

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