Insights into the Adsorption of Carbon Dioxide in the Presence of Water Vapor Utilizing a Low Molecular Weight Polyethylenimine-Impregnated CARiACT Silica Sorbent

被引:11
作者
Monazam, Esmail R. [3 ]
Breault, Ronald W. [1 ,2 ]
Fauth, Daniel J. [1 ,2 ]
Shadle, Lawrence J. [1 ,2 ]
Bayham, Samuel [1 ,2 ]
机构
[1] US DOE, Natl Energy Technol Lab, 3610 Collins Ferry Rd, Morgantown, WV 26507 USA
[2] US DOE, Natl Energy Technol Lab, 626 Cochrans Mill Rd, Pittsburgh, PA 15236 USA
[3] PLLC, REM Engn Serv, 3537 Collins Ferry Rd, Morgantown, WV 26505 USA
关键词
INDUCED PHASE-TRANSITIONS; SOLID AMINE SORBENT; POLY(ETHYLENE IMINE); NANO-SILICA; CO2; CAPTURE; KINETICS; PERFORMANCE; APPLICABILITY; EQUILIBRIUM; ADSORBENT;
D O I
10.1021/acs.iecr.7b01271
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Thermogravimetric analysis was employed to investigate the CO, and H2O adsorption rates and water vapor equilibrium on anhydrous and prehydrate linear polyethylenimine (LPEI) sorbent impregnated within a commercially functional CARiACT G10 (HPV) silica support. Water vapor experiments utilizing specific humidities of 2%, 8%, and 16% in contact with an anhydrous PEI sorbent resulted inproportional quantities of water vapor uptake. Subsequently, both anhydrous and prehydrated PEI-impregnated sorbents were made available to identical humidified gaseous streams containing a CO2 concentration of 10% at 60 degrees C. CO2 capacity increased dramatically in the presence of different levels of humidity. Various kinetic models were systematically employed to interpret the experimental data including single- and multiple-step models. The rate data was best represented by a reaction mechanism pathway involving the interplay of CO2 with PEI-impregnated sorbents exhibiting a quick adsorption phase followed by a slow approach to equilibrium. Moreover, a phenomenological rate model was developed to describe the dynamic H2O and CO2 uptakes at specific humidity levels studied. The kinetic study showed good agreement with experimental data. Furthermore, the effects observed during the adsorption and hydration are shown to be complementary to known chemical and physical transformations within the polyethylenimine's macromolecule.
引用
收藏
页码:9054 / 9064
页数:11
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