Jump to content

Capacitive deionization

From Wikipedia, the free encyclopedia

This is an old revision of this page, as edited by Ranzhao (talk | contribs) at 19:45, 20 April 2010. The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

Capacitive deionization (CDI), sometimes called electrosorption desalination, is a technology for desalination and water treatment in which salts and minerals are removed from water by applying an electric field between two porous (often, carbon) electrodes, similar to Electric double-layer capacitor. Counterions are stored in the electrical double layers which form at the solution/matrix interface inside the porous electrodes, with the ions of positive charge (cations) stored in the negatively charged electrode, and vice-versa for the anions, which are stored in the positively biased electrode (anode).

The electrodes used in CDI are typically prepared from porous carbon particles with internal areas for ion adsorption of the order of 1000 m2/gram, but other materials are also possible, such as carbon nanotubes and nanofibers. The two oppositely placed (planar) electrodes are separated by a thin open structure, “spacer”, or flow channel, through which the water flows. Upon applying an electrical potential difference between the two electrodes of the order of 0.8–1.5 V, anions are adsorbed in the anode and cations into the cathode, thereby producing a (partially) ion-depleted product stream. After the ion adsorption capacity of the electrodes has been reached, the applied voltage difference can be reduced to zero and a small product stream concentrated in salt is obtained in the ion release-step. In this way the inflowing stream of brackish water is split into a partially deionized stream and a more concentrated brine.



Membrane capacitive deionization

Membrane capacitive deionization (MCDI), sometimes called “flowthrough capacitor-technology”, is a modification of CDI by inserting an anion-exchange membrane in front of the anode, and a cation exchange membrane in front of the cathode. In this way, the ions of equal charge sign as the electrode, the socalled coions (e.g., the anions in the cathode) are inhibited from leaving the electrode region. This coion expulsion-effect, which at low voltages negatively influences the salt adsorption rate and removal capacity in CDI, is absent in MCDI. Another advantage of MCDI is that during ion release, it is possible to use a reversed voltage which leads to a faster and more complete rejection of the counterions back into the flow channel.


Reference

1. Arnold, B. B. and G. W. Murphy (1961). "Studies on the Electrochemistry of carbon and carbon chemically modified surfaces. Journal of Physical Chemistry 65 (1): 135 - &.
2. Biesheuvel, P. M. (2009). "The analysis of the thermodynamic cycle for the capacitive deionization." Journal of Colloid and Interface Science 332 (1): 258-264.
3. Biesheuvel, P. M. B. van Limpt, et al. (2009). Dynamic adsorption / desorption process model for capacitive deionization. " Journal of Physical Chemistry C 113 (14): 5636-5640.
5. H. Li, Y. Gao, L. Pan, Y. Zhang, Y. Chen, and Z. Sun, "Desalination Electrosorptive nanotubes and carbon nanofibers electrodes and ion-exchange membranes," Water Research 42 4923 (2008).
6. J.-B. Lee, K.-K. Park, H.-M. Eum and CW Lee, "Desalination of a thermal power station wastewa-ter membrane capacitive deionization," Desalination 196 125 (2006).
7. MD Andelman, "the flow through the barrier charge-capacitor," Can. CA Patent 2444390 (2002).
8. Oren, Y. (2008). "Delonization capacitive (CDI) for the desalination and water treatment - past, present and future (a review)." Desalination 228 (1-3): 10-29.
9. Postel, S. (1992). Last Oasis: Facing Water Scarcity. New York, W.W. Norton & Company.
Welgemoed, T. J. and C. F. Schutte (2005). "Delonization Capacitive Technology (TM): An alternative desalination." Desalination 183: 327-340.
10.Zhao,R et al. "The efficiency of charge: a functional tool to probe the internal structure of double layer porous electrodes, and the application in the modeling of capacitive deionization" J. Phys. Chem. Lett, accepted (2010)