CO2 capture on polyethylenimine-impregnated hydrophobic mesoporous silica: Experimental and kinetic modeling

被引:208
作者
Heydari-Gorji, Aliakbar [1 ]
Sayari, Abdelhamid [1 ]
机构
[1] Univ Ottawa, Dept Chem, Ottawa, ON K1N 6N5, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
CO2; removal; Pore-expanded MCM-41; adsorption; Polyethylenimine; Hydrophobic mesoporous silica; SOLID AMINE SORBENT; CARBON-DIOXIDE; HIGH-CAPACITY; PORE-SIZE; ADSORPTION; REMOVAL; GAS; EQUILIBRIUM; PERFORMANCE; SEPARATION;
D O I
10.1016/j.cej.2011.07.038
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
CO2 adsorption measurements for polyethylenimine (PEI)-impregnated pore-expanded MCM-41 were conducted by gravimetry to investigate the effects of (i) amine loading, (ii) CO2 partial pressure, (iii) adsorption and desorption temperatures. Amine impregnation was conducted on ethanol-extracted pore-expanded MCM-41, referred to as PME which is a mesoporous silica whose internal surface is laden by a layer of cetyltrimethylammonium cations (CTMA). The well-dispersed PEI inside the PME hydrophobic channels exhibited a CO2 adsorption capacity at 75 degrees C as high as 206 mg/g for 55 wt.% PEI loading. Moreover, the current PEI-impregnated PME materials had high CO2 adsorption efficiency (g CO2/g PEI) than any other PEI-containing adsorbent reported in the literature. In contrast to most PEI-impregnated materials reported in the literature, which because of diffusion resistance showed little or no CO2 adsorption at room temperature, the PEI-impregnated PME material showed high potential for CO2 removal at ambient temperature. Also a new adsorption kinetic model was proposed to describe the adsorption of CO2 over amine-impregnated materials. The model was found to be in good agreement with experimental data under a wide range of conditions including different PEI loadings, CO2 pressures and adsorption temperatures. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:72 / 79
页数:8
相关论文
共 39 条
[1]   Separation of CO2 from flue gas:: A review [J].
Aaron, D ;
Tsouris, C .
SEPARATION SCIENCE AND TECHNOLOGY, 2005, 40 (1-3) :321-348
[2]  
[Anonymous], 2010, World Development Report 2010: Development and Climate Change
[3]   Effect of pore expansion and amine functionalization of mesoporous silica on CO2 adsorption over a wide range of conditions [J].
Belmabkhout, Youssef ;
Sayari, Abdelhamid .
ADSORPTION-JOURNAL OF THE INTERNATIONAL ADSORPTION SOCIETY, 2009, 15 (03) :318-328
[4]   Dramatic tuning of carbon dioxide uptake via metal substitution in a coordination polymer with cylindrical pores [J].
Caskey, Stephen R. ;
Wong-Foy, Antek G. ;
Matzger, Adam J. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2008, 130 (33) :10870-+
[5]   Adsorption equilibrium of methane, carbon dioxide, and nitrogen on zeolite 13X at high pressures [J].
Cavenati, S ;
Grande, CA ;
Rodrigues, AE .
JOURNAL OF CHEMICAL AND ENGINEERING DATA, 2004, 49 (04) :1095-1101
[6]   Carbon dioxide capture using amine-impregnated HMS having textural mesoporosity [J].
Chen, Chao ;
Son, Won-Jin ;
You, Kwang-Seok ;
Ahn, Ji-Whan ;
Ahn, Wha-Seung .
CHEMICAL ENGINEERING JOURNAL, 2010, 161 (1-2) :46-52
[7]   Amine-impregnated silica monolith with a hierarchical pore structure: enhancement of CO2 capture capacity [J].
Chen, Chao ;
Yang, Seung-Tae ;
Ahn, Wha-Seung ;
Ryoo, Ryong .
CHEMICAL COMMUNICATIONS, 2009, (24) :3627-3629
[8]   Suitability of a Solid Amine Sorbent for CO2 Capture by Pressure Swing Adsorption [J].
Ebner, A. D. ;
Gray, M. L. ;
Chisholm, N. G. ;
Black, Q. T. ;
Mumford, D. D. ;
Nicholson, M. A. ;
Ritter, J. A. .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2011, 50 (09) :5634-5641
[9]   Applications of pore-expanded mesoporous silica.: 2.: Development of a high-capacity, water-tolerant adsorbent for CO2 [J].
Franchi, RS ;
Harlick, PJE ;
Sayari, A .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2005, 44 (21) :8007-8013
[10]   Nanostructured silica as a support for regenerable high-capacity organoamine-based CO2 sorbents [J].
Goeppert, Alain ;
Meth, Sergio ;
Prakash, G. K. Surya ;
Olah, George A. .
ENERGY & ENVIRONMENTAL SCIENCE, 2010, 3 (12) :1949-1960