Quantifying reaction kinetics of the non-enzymatic decarboxylation of pyruvate and production of peroxymonocarbonate with hyperpolarized13C-NMR

2017 ◽  
Vol 19 (29) ◽  
pp. 19316-19325 ◽  
Author(s):  
Nicholas Drachman ◽  
Stephen Kadlecek ◽  
Ian Duncan ◽  
Rahim Rizi
Keyword(s):  
Reaction Mechanism ◽  
Reaction Kinetics ◽  
Mechanism And Kinetics ◽  
Kinetics Of ◽  
Enzymatic Decarboxylation ◽  
C Nmr

Hyperpolarized13C-NMR is used to study the reaction mechanism and kinetics for non-enzymatic decarboxylation of pyruvate and formation of peroxymonocarbonate.

Elucidating the reaction kinetics of lithium–sulfur batteries by operando XRD based on an open-hollow S@MnO2 cathode

2019 ◽  
Vol 7 (12) ◽  
pp. 6651-6658 ◽  
Author(s):  
Shaozhuan Huang ◽  
Lixiang Liu ◽  
Ye Wang ◽  
Yang Shang ◽  
Lin Zhang ◽  
...  
Keyword(s):  
Quantitative Analysis ◽  
Reaction Mechanism ◽  
Reaction Kinetics ◽  
Lithium Sulfur Batteries ◽  
Mechanism And Kinetics ◽  
Kinetics Of ◽  
Lithium Sulfur

This work studied the reaction mechanism and kinetics of Li–S batteries via operando XRD and quantitative analysis based on different cathode structures.

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.

scholarly journals Reaction mechanism and kinetics of pressurized pyrolysis of Chinese oil shale in the presence of water

2012 ◽  
Vol 9 (4) ◽  
pp. 532-534 ◽  
Author(s):  
Chaohe Fang ◽  
Shuyuan Li ◽  
Guili Ma ◽  
Hongyan Wang ◽  
Zhilong Huang
Keyword(s):  
Reaction Mechanism ◽  
Oil Shale ◽  
Mechanism And Kinetics ◽  
Kinetics Of

scholarly journals Solvent Effect on Reaction Mechanism and Kinetics of Triplet Ion Pairs between Chloranil and Acenaphthene

1990 ◽  
Vol 63 (8) ◽  
pp. 2173-2182 ◽  
Author(s):  
Harumichi Kobashi ◽  
Shunichi Okabe ◽  
Youichi Ohsugi ◽  
Haruo Shizuka
Keyword(s):  
Reaction Mechanism ◽  
Solvent Effect ◽  
Ion Pairs ◽  
Mechanism And Kinetics ◽  
Kinetics Of
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