The kinetics modeling and reactor simulation of propylene chlorination reaction process

AIChE Journal ◽  
2021 ◽  
Author(s):  
Ming Li ◽  
Luchang Han ◽  
Xiao Luo ◽  
He'an Luo
Keyword(s):  
Reaction Process ◽  
Chlorination Reaction ◽  
Kinetics Modeling

Researches on the Synthesis and Biological Activity of 1,2,4-tiadizoles-3,5-disubstituted using Ditiazolium Salts as Precursors

2008 ◽  
Vol 59 (1) ◽  
pp. 101-105
Author(s):  
Irina Zarafu ◽  
Lucia Veronica Ivan ◽  
Iuliana Harasim
Keyword(s):  
Biological Activity ◽  
Comparative Study ◽  
Anticancer Activity ◽  
Reaction Process ◽  
Physical Analysis ◽  
Ultrasound Exposure ◽  
Medium Activity ◽  
Antibacterial And Anticancer Activity

3,5-disubstituted-1,2,4-tiadiazoles with substituted-styril and heterocycle-vinyl were obtained by extending the method which implies the use of 3,5-disubstituted-1,2,4-ditiazolium salts as precursors [1-4]. A comparative study of the reaction process in the case of perchlorates, diacide phosphates, tribromides and 3,5-distyrile-dithiazolium triiodides, taken as etalon, was perfomed. Good yields were obtained when using perchlorates, phosphates and triiodides. The reaction was made by heating the reaction mixture and by ultrasound exposure. The structure of the compounds was confirmed by chemical and physical analysis and the data obtained were identical to those of 3,5-disubstituted-1,2,4-tiadiazoles obtained by another methods [5,6]. The biological (antibacterial and anticancer) activity of the synthesized compounds was tested and the results indicated a medium activity.

Iodine-Mediated Sulfenylation of Imidazo[1,2-a]pyridines with Ethyl Arylsulfinates

Synlett ◽  
2021 ◽  
Author(s):  
Dong Tang ◽  
Jian Sun ◽  
Yangxiu Mu ◽  
Zafar Iqbal ◽  
Jing Hou ◽  
...  
Keyword(s):  
Reaction Process ◽  
Mild Conditions ◽  
Plausible Mechanism

AbstractA simple iodine-mediated approach is reported for the synthesis of sulfenylated imidazo[1,2-a]pyridines through the reaction of imidazo[1,2-a]pyridines with ethyl arylsulfinates under mild conditions. The reaction scope was investigated, and a plausible mechanism is proposed to elucidate the reaction process and activation mode. The results indicate that ethyl sulfinates are efficient sulfur sources for the construction of C–S bonds.

Direct Detection and Visualization of the H+ Reaction Process in a VO2 Cathode for Aqueous Zinc-Ion Batteries

2021 ◽  
pp. 7076-7084
Author(s):  
Shiyong Zuo ◽  
Jun Liu ◽  
Weixin He ◽  
Sahar Osman ◽  
Zhengbo Liu ◽  
...  
Keyword(s):  
Direct Detection ◽  
Zinc Ion ◽  
Reaction Process

Solid-state reaction process for high-quality organometallic halide perovskite thin film

2021 ◽  
Vol 227 ◽  
pp. 111014
Author(s):  
Chien-Chung Hsu ◽  
Sheng-Min Yu ◽  
Kun-Mu Lee ◽  
Chuan-Jung Lin ◽  
Hao-Chien Cheng ◽  
...  
Keyword(s):  
Thin Film ◽  
Solid State ◽  
Solid State Reaction ◽  
Reaction Process ◽  
High Quality ◽  
Halide Perovskite

Chemical kinetics modeling and LES combustion model effects on a perfectly premixed burner

2009 ◽  
Vol 337 (6-7) ◽  
pp. 318-328 ◽  
Author(s):  
Guillaume Albouze ◽  
Thierry Poinsot ◽  
Laurent Gicquel
Keyword(s):  
Chemical Kinetics ◽  
Combustion Model ◽  
Kinetics Modeling

Simulations and process analysis of the carbonation–calcination reaction process with intermediate hydration

Fuel ◽  
2012 ◽  
Vol 92 (1) ◽  
pp. 94-106 ◽  
Author(s):  
William Wang ◽  
Shwetha Ramkumar ◽  
Danny Wong ◽  
Liang-Shih Fan
Keyword(s):  
Process Analysis ◽  
Reaction Process
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