A screening study of alcohol solvents for alkanolamine-based CO2 capture

被引:47
作者
Chowdhury, Firoz Alam [1 ]
Goto, Kazuya [1 ]
Yamada, Hidetaka [1 ]
Matsuzaki, Yoichi [2 ]
机构
[1] Res Inst Innovat Technol Earth, Chem Res Grp, 9-2 Kizugawadai, Kizugawa, Kyoto 6190292, Japan
[2] Nippon Steel Corp Ltd, Adv Technol Res Labs, Chiyoda Ku, 2-6-1 Marunouchi, Tokyo 1008071, Japan
关键词
CO2; capture; Non-aqueous solvent; Amine absorbent; NMR speciation; Cyclic capacity; Regeneration efficiency; TEMPERATURE IONIC LIQUID; CARBON-DIOXIDE CAPTURE; CO2-BINDING ORGANIC LIQUIDS; TERTIARY AMINE ABSORBENTS; SPECIES DISTRIBUTION; AQUEOUS-SOLUTIONS; SOLUBILITY; PERFORMANCE; MDEA; VISCOSITY;
D O I
10.1016/j.ijggc.2020.103081
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The present study was aimed at developing a non-aqueous absorbent system that does not form any precipitate/solid upon exposure to CO2. More specifically, the non-aqueous absorbent system must be a homogeneous mixture (single phase) within the whole range of CO2 loading. At the same time, sufficient amine regeneration must occur at a low temperature of 80-90 degrees C compared to reference non-aqueous monoethanolamine (MEA)based absorbents. To achieve this target, 18 alcohols were investigated as solvents and 4 alkyl-linked alkanolamines were evaluated as absorbents. Several experiments mixing alkanolamines with alcohols were performed to evaluate their CO2 capture performance. High-performance non-aqueous liquid absorbents (without solid/precipitate formation) with the advantages of higher absorption rates, higher cyclic capacities, higher regeneration efficiencies, lower specific heats, and lower heats of reaction compared to reference MEA-based non aqueous absorbents were successfully developed herein. The favorable features of these absorbents will provide the basis for the discovery of potential non-aqueous amine-based absorbents.
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页数:9
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共 70 条
[1]   Novel design for the nozzle of a laminar jet absorber [J].
Aboudheir, A ;
Tontiwachwuthikul, P ;
Chakma, A ;
Idem, R .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2004, 43 (10) :2568-2574
[2]  
[Anonymous], 2014, APPL ENERG, DOI DOI 10.1016/J.APENERGY.2014.09.046
[3]   Comparative study of solvent properties for carbon dioxide absorption [J].
Aschenbrenner, Ortrud ;
Styring, Peter .
ENERGY & ENVIRONMENTAL SCIENCE, 2010, 3 (08) :1106-1113
[4]   Room-Temperature Ionic Liquids and Composite Materials: Platform Technologies for CO2 Capture [J].
Bara, Jason E. ;
Camper, Dean E. ;
Gin, Douglas L. ;
Noble, Richard D. .
ACCOUNTS OF CHEMICAL RESEARCH, 2010, 43 (01) :152-159
[5]   KINETICS AND MECHANISMS OF THE REACTIONS OF CARBON-DIOXIDE WITH ALKANOLAMINES - A DISCUSSION CONCERNING THE CASES OF MDEA AND DEA [J].
BARTH, D ;
TONDRE, C ;
DELPUECH, JJ .
CHEMICAL ENGINEERING SCIENCE, 1984, 39 (12) :1753-1757
[6]   CO2 capture by a task-specific ionic liquid [J].
Bates, ED ;
Mayton, RD ;
Ntai, I ;
Davis, JH .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (06) :926-927
[7]   Membrane Gas Separation: A Review/State of the Art [J].
Bernardo, P. ;
Drioli, E. ;
Golemme, G. .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2009, 48 (10) :4638-4663
[8]   Carbon capture and storage update [J].
Boot-Handford, M. E. ;
Abanades, J. C. ;
Anthony, E. J. ;
Blunt, M. J. ;
Brandani, S. ;
Mac Dowell, N. ;
Fernandez, J. R. ;
Ferrari, M. -C. ;
Gross, R. ;
Hallett, J. P. ;
Haszeldine, R. S. ;
Heptonstall, P. ;
Lyngfelt, A. ;
Makuch, Z. ;
Mangano, E. ;
Porter, R. T. J. ;
Pourkashanian, M. ;
Rochelle, G. T. ;
Shah, N. ;
Yao, J. G. ;
Fennell, P. S. .
ENERGY & ENVIRONMENTAL SCIENCE, 2014, 7 (01) :130-189
[9]   Why is CO2 so soluble in imidazolium-based ionic liquids? [J].
Cadena, C ;
Anthony, JL ;
Shah, JK ;
Morrow, TI ;
Brennecke, JF ;
Maginn, EJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (16) :5300-5308
[10]   Room-Temperature Ionic Liquid-Amine Solutions: Tunable Solvents for Efficient and Reversible Capture Of CO2 [J].
Camper, Dean ;
Bara, Jason E. ;
Gin, Douglas L. ;
Noble, Richard D. .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2008, 47 (21) :8496-8498