Developing strategies for the regeneration of polyethylenimine based CO2 adsorbents

被引:29
作者
Drage, T. C. [1 ]
Smith, K. M. [1 ]
Arenillas, A. [2 ]
Snape, C. E. [1 ]
机构
[1] Univ Nottingham, Sch Chem Environm & Min Engn, Nottingham NG7 2RD, England
[2] CSIC, Inst Nacl Carbon, Oviedo 33080, Spain
来源
GREENHOUSE GAS CONTROL TECHNOLOGIES 9 | 2009年 / 1卷 / 01期
基金
英国工程与自然科学研究理事会;
关键词
Adsorption; CO2; capture; Gas clean-up; CARBON-DIOXIDE;
D O I
10.1016/j.egypro.2009.01.116
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
Adsorption is considered to be one of the more promising technologies for capturing CO2 from flue gases. The efficient adsorption of CO2 at low partial pressures, associated with post-combustion capture, require chemical type adsorbents containing basic amine functional groups. It has been demonstrated that amine polymers, for example polyethylenimine (PEI), immobilised on various porous substrates, silica, zeolites and fly ash, are effective adsorbents for CO2. When considering the use of adsorption for large scale CO2 capture, the ease of regeneration and the lifetime of the adsorbents are critical factors in determining their efficiency, cost and therefore feasibility for use. In this paper two approaches, thermal swing adsorption (TSA) cycles over a range of temperatures and time in an atmosphere of CO2 and thermally assisted pressure swing desorption, are explored for the regeneration of the PEI based adsorbents. The reactions occurring during the TSA regeneration of PEI based adsorbents in an atmosphere of CO2, especially the formation of a thermostable complex between PEI and CO2 above 130 degrees C are described. Identification of the complex by FTIR, XPS and C-13 NMR as a urea linkage will be described. Overall, the results from this research have implications for the selection of regeneration strategies of all amine based CO2 adsorbents. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:875 / 880
页数:6
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