Thermodynamic analysis of absorption refrigeration cycles using ionic liquid plus supercritical CO2 pairs

被引:71
作者
Martin, Angel [1 ]
Dolores Bermejo, Maria [1 ]
机构
[1] Univ Valladolid, Dept Chem Engn & Environm Technol, High Pressure Proc Grp, E-47011 Valladolid, Spain
关键词
Group-Contribution equation of state; Coefficient of Performance; Circulation ratio; 1-Alkyl-1-methyl-pyrrolidinium bis(trifluoromethylsulfonyl)-imide; 1-Alkyl-3-methylimidazolium tetrafluoroborate; 1-Alkyl-3-methylimidazolium nitrate; GROUP-CONTRIBUTION EQUATION; BINARY-SYSTEMS; CARBON-DIOXIDE; PHASE-BEHAVIOR; OF-STATE; TEMPERATURE; TETRAFLUOROBORATE; SOLUBILITIES; PRESSURE;
D O I
10.1016/j.supflu.2010.10.012
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Absorption refrigerators are alternative systems to conventional compression cycles in which the energy necessary for the refrigeration is provided by heating instead of mechanical power. Commercial absorption refrigerators use two absorbent/refrigerant pairs: NH3-H2O and H2O-LiBr. These systems have some limitations due to the difficulty of separating absorbent and refrigerant, the narrow refrigeration temperature range, or the possibility of corrosion and salt deposition. The application of ionic liquids as absorbents with supercritical carbon dioxide as refrigerant can solve some of these problems because separation of ionic liquid from CO2 is easy due to the negligible vapor pressure of ionic liquids. In this work, suitable ionic liquids-CO2 pairs have been selected considering their phase equilibrium properties, calculated with the Group-Contribution equation of state developed by Skjold-Jorgensen. The energetic efficiency of the process with ionic liquids has been estimated by calculation of the Coefficient of Performance (COP) of the process. It has been found that the process with ionic liquids has a lower COP than conventional NH3-H2O systems due to the necessity of operating with a higher solution flowrate. Nevertheless, near-optimum performance is obtained in a wide range of process conditions. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:852 / 859
页数:8
相关论文
共 30 条
[1]   Application of a group contribution equation of state for the thermodynamic modeling of the binary systems CO2-1-butyl-3-methyl imidazolium nitrate and CO2-1-hydroxy-1-propyl-3-methyl imidazolium nitrate [J].
Bermejo, M. D. ;
Martin, A. ;
Foco, G. ;
Cocero, M. J. ;
Bottini, S. B. ;
Peters, C. J. .
JOURNAL OF SUPERCRITICAL FLUIDS, 2009, 50 (02) :112-117
[2]  
Bogart M., 1981, AMMONIA ABSORPTION R
[3]   Thermodynamic modeling of the phase behavior of binary systems of ionic liquids and carbon dioxide with the group contribution equation of state [J].
Breure, Bianca ;
Bottini, Susana B. ;
Witkamp, Geert-Jan ;
Peters, Cor J. .
JOURNAL OF PHYSICAL CHEMISTRY B, 2007, 111 (51) :14265-14270
[4]  
CAI W, 2007, P 2007 ASME INT MECH
[5]   High pressure phase behavior of carbon dioxide in 1-butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide and 1-butyl-3-methylimidazolium dicyanamide ionic liquids [J].
Carvalho, Pedro J. ;
Alvarez, Victor H. ;
Marrucho, Isabel M. ;
Aznar, Martin ;
Coutinho, Joao A. P. .
JOURNAL OF SUPERCRITICAL FLUIDS, 2009, 50 (02) :105-111
[6]  
Chase M.W., 1998, J. of Physical and Chemical Reference Data, DOI 10.18434/T42S31
[7]   Application of a Group Contribution Equation of State for the Thermodynamic Modeling of Gas plus Ionic Liquid Mixtures [J].
Dolores Bermejo, Maria ;
Mendez, David ;
Martin, Angel .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2010, 49 (10) :4966-4973
[8]   Synthesis of 1,3-Dimethylimidazolium Chloride and Volumetric Property Investigations of Its Aqueous Solution [J].
Dong, L. ;
Zheng, D. X. ;
Wei, Z. ;
Wu, X. H. .
INTERNATIONAL JOURNAL OF THERMOPHYSICS, 2009, 30 (05) :1480-1490
[9]   Heat capacities of ionic liquids as a function of temperature at 0.1 MPa. measurement and prediction [J].
Ge, Rile ;
Hardacre, Christopher ;
Jacquemin, Johan ;
Nancarrow, Paul ;
Rooney, David W. .
JOURNAL OF CHEMICAL AND ENGINEERING DATA, 2008, 53 (09) :2148-2153
[10]  
Holbrey J. D., 1999, CLEAN PRODUCTS PROCE, V1, P223, DOI DOI 10.1007/S100980050036