Chloride ion enhanced thermal stability of carbon dioxide captured by monoethanolamine in hydroxyl imidazolium based ionic liquids

2011 ◽  
Vol 4 (6) ◽  
pp. 2125 ◽  
Author(s):  
Qing Huang ◽  
Yan Li ◽  
Xianbo Jin ◽  
Di Zhao ◽  
George Z. Chen
2013 ◽  
Vol 25 (8) ◽  
pp. 4779-4782 ◽  
Author(s):  
W.D. Liang ◽  
H.F. Li ◽  
G.J. Gou ◽  
A.Q. Wang

Author(s):  
Yong Huang ◽  
Zhichao Chen ◽  
Jacob M. Crosthwaite ◽  
Sudhir N.V.K. Aki ◽  
Joan F. Brennecke

2017 ◽  
Vol 656 ◽  
pp. 70-84 ◽  
Author(s):  
D. Blanco ◽  
P. Oulego ◽  
D. Ramos ◽  
B. Fernández ◽  
J.M. Cuetos

ARKIVOC ◽  
2012 ◽  
Vol 2012 (8) ◽  
pp. 262-281 ◽  
Author(s):  
Paweł Borowiecki ◽  
Marcin Poterała ◽  
Jan Maurin ◽  
Monika Wielechowska ◽  
Jan Plenkiewicz

2016 ◽  
Vol 86 (6) ◽  
pp. 1314-1318 ◽  
Author(s):  
L. I. Voronchikhina ◽  
O. E. Zhuravlev ◽  
N. V. Verolainen ◽  
N. I. Krotova

2018 ◽  
Vol 19 (12) ◽  
pp. 3723 ◽  
Author(s):  
Shaoyun Chen ◽  
Min Xiao ◽  
Luyi Sun ◽  
Yuezhong Meng

The terpolymerization of carbon dioxide (CO2), propylene oxide (PO), and cyclohexene oxide (CHO) were performed by both random polymerization and block polymerization to synthesize the random poly (propylene cyclohexene carbonate) (PPCHC), di-block polymers of poly (propylene carbonate–cyclohexyl carbonate) (PPC-PCHC), and tri-block polymers of poly (cyclohexyl carbonate–propylene carbonate–cyclohexyl carbonate) (PCHC-PPC-PCHC). The kinetics of the thermal degradation of the terpolymers was investigated by the multiple heating rate method (Kissinger-Akahira-Sunose (KAS) method), the single heating rate method (Coats-Redfern method), and the Isoconversional kinetic analysis method proposed by Vyazovkin with the data from thermogravimetric analysis under dynamic conditions. The values of ln k vs. T−1 for the thermal decomposition of four polymers demonstrate the thermal stability of PPC and PPC-PCHC are poorer than PPCHC and PCHC-PPC-PCHC. In addition, for PPCHC and PCHC-PPC-PCHC, there is an intersection between the two rate constant lines, which means that, for thermal stability of PPCHC, it is more stable than PCHC-PPC-PCHC at the temperature less than 309 °C and less stable when the decomposed temperature is more than 309 °C. Pyrolysis-gas chromatography/mass spectrometry (Py-GC/MS) and thermogravimetric analysis/infrared spectrometry (TG/FTIR) techniques were applied to investigate the thermal degradation behavior of the polymers. The results showed that unzipping was the main degradation mechanism of all polymers so the final pyrolysates were cyclic propylene carbonate and cyclic cyclohexene carbonate. For the block copolymers, the main chain scission reaction first occurs at PC-PC linkages initiating an unzipping reaction of PPC chain and then, at CHC–CHC linkages, initiating an unzipping reaction of the PCHC chain. That is why the T−5% of di-block and tri-block polymers were not much higher than that of PPC while two maximum decomposition temperatures were observed for both the block copolymer and the second one were much higher than that of PPC. For PPCHC, the random arranged bulky cyclohexane groups in the polymer chain can effectively suppress the backbiting process and retard the unzipping reaction. Thus, it exhibited much higher T−5% than that of PPC and block copolymers.


2015 ◽  
Vol 220-221 ◽  
pp. 218-223
Author(s):  
Tomasz Jan Kaldonski ◽  
Stanislaw Cudzilo

Some results of tests of the thermal stability (and volatility) of selected ionic liquids pondered as lubricating substances in comparison with typical lubricating, mineral and synthetic oils, are presented in the article. The research was carried out within the framework of PBR/15–249/2007/WAT–OR00002904 Research Project Financed by the Ministry of Science and Higher Education, during 2007–2011 [1]. The obtained results confirmed high thermal resistance of ionic liquids. It makes it possible to use the liquids as high temperature lubricating substances. At the same time, it has been stated that the thermal resistance of ionic liquids depends on the composition and chemical structure of anion and cation.


2009 ◽  
Vol 105 (10) ◽  
pp. 103504 ◽  
Author(s):  
C.-S. Tu ◽  
R. R. Chien ◽  
V. H. Schmidt ◽  
S.-C. Lee ◽  
C.-C. Huang ◽  
...  

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