Efficient and Energy-Saving CO2 Capture through the Entropic Effect Induced by the Intermolecular Hydrogen Bonding in Anion-Functionalized Ionic Liquids

2014 ◽  
Vol 5 (2) ◽  
pp. 381-386 ◽  
Author(s):  
Xiao Y. Luo ◽  
Fang Ding ◽  
Wen J. Lin ◽  
Yu Q. Qi ◽  
Hao R. Li ◽  
...  
2014 ◽  
Vol 50 (95) ◽  
pp. 15041-15044 ◽  
Author(s):  
Fang Ding ◽  
Xi He ◽  
Xiaoyan Luo ◽  
Wenjun Lin ◽  
Kaihong Chen ◽  
...  

Carbonyl-containing anion-functionalized ionic liquids exhibit a significant enhancement in CO2 capacity and excellent reversibility.


2019 ◽  
Vol 123 (39) ◽  
pp. 8370-8376 ◽  
Author(s):  
Helen J. Zeng ◽  
Mark A. Johnson ◽  
Jasodra D. Ramdihal ◽  
Rawlric A. Sumner ◽  
Chanele Rodriguez ◽  
...  

2016 ◽  
Vol 13 (1) ◽  
pp. 53
Author(s):  
Siti Nabihah Jamaludin ◽  
Ruzitah Mohd Salleh

Anthropogenic CO2 emissions has led to global climate change and widely contributed to global warming since its concentration has been increasing over time. It has attracted vast attention worldwide. Currently, the different CO2 capture technologies available include absorption, solid adsorption and membrane separation. Chemical absorption technology is regarded as the most mature technology and is commercially used in the industry. However, the key challenge is to find the most efficient solvent in capturing CO2. This paper reviews several types of CO2 capture technologies and the various factors influencing the CO2 absorption process, resulting in the development of a novel solvent for CO2 capture.


Chemistry ◽  
2021 ◽  
Vol 3 (1) ◽  
pp. 149-163
Author(s):  
Duncan Micallef ◽  
Liana Vella-Zarb ◽  
Ulrich Baisch

N,N′,N″,N‴-Tetraisopropylpyrophosphoramide 1 is a pyrophosphoramide with documented butyrylcholinesterase inhibition, a property shared with the more widely studied octamethylphosphoramide (Schradan). Unlike Schradan, 1 is a solid at room temperature making it one of a few known pyrophosphoramide solids. The crystal structure of 1 was determined by single-crystal X-ray diffraction and compared with that of other previously described solid pyrophosphoramides. The pyrophosphoramide discussed in this study was synthesised by reacting iso-propyl amine with pyrophosphoryl tetrachloride under anhydrous conditions. A unique supramolecular motif was observed when compared with previously published pyrophosphoramide structures having two different intermolecular hydrogen bonding synthons. Furthermore, the potential of a wider variety of supramolecular structures in which similar pyrophosphoramides can crystallise was recognised. Proton (1H) and Phosphorus 31 (31P) Nuclear Magnetic Resonance (NMR) spectroscopy, infrared (IR) spectroscopy, mass spectrometry (MS) were carried out to complete the analysis of the compound.


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