Gohndrone Thomas R, Bum Lee Tae, DeSilva M Aruni, Quiroz-Guzman Mauricio, Schneider William F, Brennecke Joan F
Department of Chemical and Biomolecular Engineering, University of Notre Dame, Notre Dame, Indiana 46556 (United States).
ChemSusChem. 2014 Jul;7(7):1970-5. doi: 10.1002/cssc.201400009. Epub 2014 May 6.
We show that phosphonium azolide ionic liquids of interest for CO2 capture applications react with CO2 both through the normal anion channel and, at elevated temperatures, through a previously unrecognized cation channel. The reaction is caused by an interaction between the anion and cation that allows proton transfer, and involves a phosphonium ylide intermediate. The cation reaction can be mitigated by using ammonium rather than phosphonium cations. Thus, phosphonium and ammonium cations paired with aprotic heterocyclic anions (AHAs) react with CO2 through different mechanisms at elevated temperatures. This work shows that careful consideration of both physical properties and chemical reactivity of ILs based on AHA anions is needed when designing ionic liquids for CO2 separations.
我们表明,用于二氧化碳捕集应用的唑鎓叠氮化物离子液体与二氧化碳的反应既通过正常的阴离子通道,也在高温下通过一个此前未被认识的阳离子通道进行。该反应是由阴离子与阳离子之间的相互作用引起的,这种相互作用允许质子转移,并且涉及一个磷叶立德中间体。通过使用铵阳离子而非鏻阳离子,可以减轻阳离子反应。因此,与非质子杂环阴离子(AHA)配对的鏻阳离子和铵阳离子在高温下通过不同的机制与二氧化碳反应。这项工作表明,在设计用于二氧化碳分离的离子液体时,需要仔细考虑基于AHA阴离子的离子液体的物理性质和化学反应性。