@article { ISI:000300529100034, title = {Polymeric ionic liquids (PILs): effect of anion variation on their CO2 sorption}, journal = {Journal of Membrane Science}, volume = {389}, year = {2012}, month = {FEB}, pages = {305-315}, publisher = {ELSEVIER SCIENCE BV}, address = {PO BOX 211, 1000 AE AMSTERDAM, NETHERLANDS}, abstract = {

A series of polymeric ionic liquids (PILs) based on poly(diallyldimethylammonium chloride), P[DADMA][Cl] as a precursor was investigated by varying anions categorized into carboxylates, sulphonates and inorganic type. For the exchange of chloride from P[DADMA][Cl] by another anion, silver salt of the corresponding anion was preferred. Obtained PILs were investigated for physical properties which are anticipated to affect gas sorption. PILs possessing carboxylate (especially acetate) anion exhibited attractive CO2 sorption capacity as well as sorption selectivity over H-2 and N-2, in Comparison to Other two Categories. PIL with acetate anion, P[DADMA][Ac] possessed appreciable CO2 sorption coupled with high selectivity (S-CO2/S-N2 = 114.3). This crucial finding from this series of PILs was further substantiated by making PIL based on poly(vinylbenzyltrimethylammonium chloride), P[VBTMA][Cl] as a precursor. (C) 2011 Elsevier B.V. All rights reserved.

}, keywords = {Anion exchange, CO2 sorption, Polymeric ionic liquid}, issn = {0376-7388}, doi = {10.1016/j.memsci.2011.10.042}, author = {Bhavsar, Rupesh S. and Kumbharkar, Santosh C. and Kharul, Ulhas K.} } @article { ISI:000363852200028, title = {Polybenzimidazole based polymeric ionic liquids possessing partial ionic character: effects of anion exchange on their gas permeation properties}, journal = {Journal of Membrane Science}, volume = {497}, year = {2016}, month = {JAN}, pages = {282-288}, publisher = {ELSEVIER SCIENCE BV}, address = {PO BOX 211, 1000 AE AMSTERDAM, NETHERLANDS}, abstract = {

Polymeric ionic liquids (PILs) are emerging as promising membrane materials for CO2 separation. Present work is in continuation with our earlier efforts on evaluating gas permeation properties (especially, CO2) of film forming PILs based on polybenzimidazoles and efforts towards improving their permeability by structural tuning. This work specifically aims at evaluating effect of anion variation in chosen PILs possessing partial N-quaternization of imidazole moiety of PBI-Bul. Three anions (viz., Tf2N-, BF4- and Ac-) were chosen for the bromide exchange of two PILs, viz., [TBzPBI-Bul][Br](10) and [TBzPBI-Bul][Br](18), possessing degree of PEI N-quaternization (DQ) as 10 and 18\%, respectively. Concurrent effects of variation in anion and DQ were analyzed in terms of physical and gas permeation properties of the resulting PILs. All of them possessed amorphous nature, adequate thermal stability ( \>= 250 degrees C) and solvent solubility, which are primary requisites towards their applicability as a membrane material. PILs possessing BF4- anion exhibited improved CO2 permeability coefficient as well as its permselectivity over CH4 and N-2, in comparison to their counterparts with other anions. (C) 2015 Elsevier B.V. All rights reserved.

}, keywords = {Anion exchange, Gas separation, Polybenzimidazole, Polymeric ionic liquids (PILs)}, issn = {0376-7388}, doi = {10.1016/j.memsci.2015.09.019}, author = {Rewar, Anita S. and Shaligram, Sayali V. and Kharul, Ulhas K.} } @article {49710, title = {Enhanced electrocatalytic performances of NiCr layered double hydroxides by oxalate intercalation in anion exchange membrane water electrolysis}, journal = {ACS Applied Materials \& Interfaces}, volume = {17}, year = {2025}, month = {JUN}, pages = {37863-37878}, type = {Article}, abstract = {

Layered double hydroxides (LDHs) have attracted much attention these days in the field of water electrolysis due to easy modulation in their layered structure and properties. Herein, NiCr-LDH has been developed, and its interlayer spacing has been considerably increased by oxalate intercalation. Such increased interlayer spacing allows easy access of hydroxides to a large number of electroactive sites and thereby boosts the electrocatalytic performances both for oxygen and hydrogen evolution reactions. Being very active toward both the electrocatalytic reactions, the oxalate-intercalated NiCr-LDH was further explored in an alkaline anion exchange membrane water electrolyzer (AEMWE), achieving 800 mA cm-2 at 1.88 V cell voltage at an operating temperature of 60 degrees C. In fact, the electrolyzer efficiency has been determined to be as high as 69.66\%, and the calculated H2 production cost was found to be \$0.97 per gasoline-gallon equivalent, which is well below the targeted cost by the Department of Energy, USA. The electrocatalyst was also examined in harsh alkaline media, like highly saline or seawater, which also indicated its ability to carry out sustainable seawater electrolysis, restricting chlorides to a great extent. Interestingly, post-electrolysis characterization reveals the fact that oxalate decomposition aided carbonate formation within interlayers of NiCr-LDH, and high affinity toward hydroxides is responsible for restricting chlorides during the electrolysis process, apart from the great electrocatalytic activity.

}, keywords = {Anion exchange, hydrogen production, interlayerspacing, Layered double hydroxide, Sustainable, water electrolyzer}, issn = {1944-8244}, doi = {10.1021/acsami.5c04189}, author = {Pal, Santanu and Sinha, Nibedita and Das, Chandni and Chauhan, Inderjeet and Ahmed, Tanbir and Roy, Poulomi} }