Nanopore-Based Power Generation from Salinity Gradient: Why It Is Not Viable

被引:135
作者
Wang, Li [1 ]
Wang, Zhangxin [1 ]
Patel, Sohum K. [1 ]
Lin, Shihong [2 ]
Elimelech, Menachem [1 ]
机构
[1] Yale Univ, Dept Chem & Environm Engn, New Haven, CT 06520 USA
[2] Vanderbilt Univ, Dept Civil & Environm Engn, Nashville, TN 37235 USA
关键词
salinity gradient energy; nanopore; power generation; multiscale modeling; power density; energy efficiency;
D O I
10.1021/acsnano.0c08628
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In recent years, the development of nanopore-based membranes has revitalized the prospect of harvesting salinity gradient (blue) energy. In this study, we systematically analyze the energetic performance of nanopore-based power generation (NPG) at various process scales, beginning with a single nanopore, followed by a multipore membrane coupon, and ending with a full-scale system. We confirm the high power densities attainable by a single nanopore and demonstrate that, at the coupon scale and above, concentration polarization severely hinders the power density of NPG, revealing the common, yet significant, error in linearly extrapolating single-pore performance to multipore membranes. Through our consideration of concentration polarization, we also importantly show that the development of materials with exceptional nanopore properties provides limited enhancement of practical process performance. For a full-scale NPG membrane module, we find an inherent tradeoff between power density and thermodynamic energy efficiency, whereby achieving a high power density sacrifices the energy efficiency. Furthermore, we derive a simple expression for the theoretical maximum energy efficiency of NPG, showing it is solely related to the membrane selectivity (i.e., S-2/2). Through this relation, it is apparent that the energy efficiency of NPG is limited to only 50% (for a completely selective membrane, i.e., S = 1), reinforcing our optimistic full-scale simulations which result in a (practical) maximum energy efficiency of 42%. Finally, we assess the net extractable energy of a full-scale NPG system which mixes river water and seawater by including the energy losses from pretreatment and pumping, revealing that the NPG process-both in its current state of development and in the case of highly optimistic performance with minimized external energy losses-is not viable for power generation.
引用
收藏
页码:4093 / 4107
页数:15
相关论文
共 112 条
[1]   Power generation with pressure retarded osmosis: An experimental and theoretical investigation [J].
Achilli, Andrea ;
Cath, Tzahi Y. ;
Childress, Amy E. .
JOURNAL OF MEMBRANE SCIENCE, 2009, 343 (1-2) :42-52
[2]   Layer-by-Layer Assembly of Polyelectrolytes into Ionic Current Rectifying Solid-State Nanopores: Insights from Theory and Experiment [J].
Ali, Mubarak ;
Yameen, Basit ;
Cervera, Javier ;
Ramirez, Patricio ;
Neumann, Reinhard ;
Ensinger, Wolfgang ;
Knoll, Wolfgang ;
Azzaroni, Omar .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2010, 132 (24) :8338-8348
[3]   Current-Induced Membrane Discharge [J].
Andersen, M. B. ;
van Soestbergen, M. ;
Mani, A. ;
Bruus, H. ;
Biesheuvel, P. M. ;
Bazant, M. Z. .
PHYSICAL REVIEW LETTERS, 2012, 109 (10)
[4]  
[Anonymous], 2011, Seawater Desalination Costs
[5]  
Baker R.W., 2012, Membrane Technology, DOI [10.1016/S0958-2118(96)90133-0, DOI 10.1016/S0958-2118(96)90133-0]
[6]   Large osmotic energy harvesting from functionalized conical nanopore suitable for membrane applications [J].
Balme, Sebastien ;
Ma, Tianji ;
Balanzat, Emmanuel ;
Janot, Jean-Marc .
JOURNAL OF MEMBRANE SCIENCE, 2017, 544 :18-24
[7]  
Bejan A., 1997, ADV ENG THERMODYNAMI, P850
[8]   Analysis of ionic conductance of carbon nanotubes [J].
Biesheuvel, P. M. ;
Bazant, M. Z. .
PHYSICAL REVIEW E, 2016, 94 (05)
[9]   Nanofluidics, from bulk to interfaces [J].
Bocquet, Lyderic ;
Charlaix, Elisabeth .
CHEMICAL SOCIETY REVIEWS, 2010, 39 (03) :1073-1095
[10]   'Blue energy' from ion adsorption and electrode charging in sea and river water [J].
Boon, Niels ;
van Roij, Rene .
MOLECULAR PHYSICS, 2011, 109 (7-10) :1229-1241