Polyethylene Glycol (PEG) Addition to Polyethylenimine (PEI)-Impregnated Silica Increases Amine Accessibility during CO2 Sorption

被引:46
|
作者
Wang, Linxi [1 ]
Al-Aufi, Mohammed [1 ]
Pacheco, Carlos N. [2 ]
Xie, Liyuan [1 ]
Rioux, Robert M. [1 ,2 ]
机构
[1] Penn State Univ, Dept Chem Engn, University Pk, PA 16802 USA
[2] Penn State Univ, Dept Chem, University Pk, PA 16802 USA
来源
基金
美国国家科学基金会;
关键词
Carbon capture; Poly(ethylenimine); Poly(ethylene glycol); Viscosity; Amine efficiency; MESOPOROUS MOLECULAR-SIEVE; CARBON-DIOXIDE; IONIC LIQUIDS; ADSORBED CO2; CAPTURE; SORBENTS; ADSORPTION; PERFORMANCE; VISCOSITY; CAPACITY;
D O I
10.1021/acssuschemeng.9b02798
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Amine-impregnated sorbents can be applied in CO2 sequestration, but they suffer from low amine utility due to slow diffusion of CO2, leading to reduced accessibility of buried amines. We examined silica-supported polyethylenimine (PEI) sorbents and blended them with polyethylene glycol (PEG) as an additive to study the role of PEG in modifying sorption performance. We report an increase in amine efficiency, a decrease in the heat of sorption and regeneration temperature, and a change CO2 amine speciation with the addition of PEG. The increase in viscosity due to CO2 sorption leads to greater diffusion resistance; increases in viscosity were lower during CO2 sorption in blends with higher PEG composition. C-13 NMR results on CO2-saturated PEI PEG blends revealed the formation of carbamic acid and carbamate and showed a larger fraction of carbamic acid in PEG-rich samples. We propose PEG increases the amine efficiency by enabling the diffusion of CO2 due to viscosity reduction and changes in the CO2-amine speciation (carbamate versus carbamic acid), which modifies the theoretical CO2/amine stoichiometry.
引用
收藏
页码:14785 / 14795
页数:21
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