Kinetic H2S/CO2 selectivity in an exceptionally sterically hindered amine membrane

被引:0
|
作者
Rao, Shraavya [1 ]
Deng, Xuepeng [1 ]
Zou, Changlong [1 ]
Prasad, Babul [1 ,2 ]
Han, Yang [1 ]
Lin, Li-Chiang [1 ,3 ]
Ho, W. S. Winston [1 ,4 ]
机构
[1] Ohio State Univ, William G Lowrie Dept Chem & Biomol Engn, 151 West Woodruff Ave, Columbus, OH 43210 USA
[2] Natl Chem Lab, CSIR, Polymer Sci & Engn Div, Dr Homi Bhabha Rd, Pune 411008, India
[3] Natl Taiwan Univ, Dept Chem Engn, Taipei 10617, Taiwan
[4] Ohio State Univ, Dept Mat Sci & Engn, 2041 Coll Rd, Columbus, OH 43210 USA
关键词
FACILITATED TRANSPORT MEMBRANES; IN-SITU ATR; CO2; CAPTURE; HYDROGEN-SULFIDE; AQUEOUS-SOLUTIONS; GAS STREAMS; COMPOSITE MEMBRANES; THIN-FILM; ABSORPTION; H2S;
D O I
10.1039/d4ta04997g
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Facilitated transport membranes (FTMs) show great promise for H2S/CO2 separation, an industrially important yet challenging process. Herein, we report FTMs with excellent H2S/CO2 separation performance and investigate how contradictory thermodynamic and kinetic reaction preferences affect FTM selectivity. For membranes based on an extremely sterically hindered di-tert-butylamine carrier, CO2 transport occurs exclusively via a slow bicarbonate pathway. Reducing the membrane thickness shifts the reaction preference from the thermodynamically favored bicarbonate pathway to the kinetically favored amine-H2S reaction, leading to a 10-fold improvement in H2S/CO2 selectivity. This unusual trend of increasing selectivity with decreasing thickness, the opposite of typical FTMs, enables simultaneous improvements in membrane permeance and selectivity. This translates to an exceptional H2S/CO2 permselectivity of 20, and an overall separation performance surpassing the H2S/CO2 upper bounds.
引用
收藏
页码:29138 / 29144
页数:7
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