Thermodynamic model for a reversible desalination cycle using weak polyelectrolyte hydrogels

被引:20
作者
Rud, Oleg [1 ,2 ]
Borisov, Oleg [1 ,3 ,4 ]
Kosovan, Peter [2 ]
机构
[1] Russian Acad Sci, Inst Macromol Cpds, Bolshoy Pr 31, St Petersburg 199004, Russia
[2] Charles Univ Prague, Fac Sci, Dept Phys & Macromol Chem, Hlavova 8, Prague 12800 2, Czech Republic
[3] CNRS, UPPA, UMR 5254, Inst Sci Analyt & Physicochim Environm & Mat, Pau, France
[4] St Petersburg Natl Univ Informat Technol Mech & O, Lomonosova St 9, St Petersburg 197101, Russia
关键词
ELECTROSTATIC INTERACTIONS; DRAW SOLUTES; MICROGELS; OSMOSIS; FIELD; PH; SEAWATER; NANOPARTICLES; PERMEATION; COLLAPSE;
D O I
10.1016/j.desal.2018.05.002
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
The recently proposed use of hydrogels for water desalination is based on the decrease of salt concentration in the gel upon compression. In the first experiments, desalination cycles using hydrogels involved an irreversible mixing step, which inevitably reduced the thermodynamic efficiency. This approach could become competitive with membrane-based desalination methods if it could work close to maximum thermodynamic efficiency. In this work, we develop a thermodynamic model for compression of weak polyelectrolyte hydrogels in open and closed systems. We use this model to design a fully reversible desalination cycle which can, in principle, achieve maximum thermodynamic efficiency. We also show that compressing weak polyelectrolyte hydrogels at low salinity decreases their ionization, thereby leading to a non-monotonic dependence of salt concentration on the gel compression. Therefore, our model shows how to redesign the desalination cycle when using weak polyelectrolytes at low salinities.
引用
收藏
页码:32 / 43
页数:12
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