Assembly of Soft Electrodes and Ion Exchange Membranes for Capacitive Deionization (original) (raw)

Limitations of charge efficiency in capacitive deionization processes III: The behavior of surface oxidized activated carbon electrodes

Electrochimica Acta, 2010

In previous papers we reported on attempts to improve the performance of water desalination using capacitive de-ionization (CDI) processes by understanding the ions transport and adsorption/desorption behavior of activated carbon electrodes as a function of the applied potential. We also investigated the charge efficiency in CDI processes of brackish water in symmetrical cells containing identical highly porous activated carbon electrodes. In this work, we study the influence of oxygen-containing surface groups on activated carbon electrodes on the adsorption/desorption behavior of ions in brackish water. A special methodology was developed in order to estimate the charge efficiency of CDI processes which include the ability to prepare various kinds of activated carbon electrodes (ACEs) with controlled porosity and surface groups, measuring the PZC (potential of zero charge) of ACE in solutions and simultaneous adsorption and desorption of ions into/from them. The presence of polar, oxygen containing surface groups on ACE does not affect the electroadsorption behavior of Na + and Cl − ions into porous carbons whose average pore size is greater than 0.58 nm, apart of considerably changing the PZC. This results in a shift of the entire curves of ion adsorption vs. potential. The possible use of ACE with oxidized surfaces in CDI processes is discussed.

Ion selectivity in capacitive deionization with functionalized electrode: Theory and experimental validation

Water Research X

Capacitive deionization (CDI) is a promising technique for salt removal and may have potential for highly selective removal of ion species. In this work, we take advantage of functional groups usually used with ionic exchange resins and apply these to CDI. To this end, we functionalize activated carbon with a quaternary amines surfactant and use this surface to selectively and passively (no applied field) trap nitrate ions. We then set the cell voltage to a constant value to regenerate these electrodes, resulting in an inverted capacitive deionization (i-CDI) operation. Unlike resins, we avoid use of concentrated chemicals for regeneration. We measure the selectivity of nitrate versus chloride ions as a function of regeneration voltage and initial chloride concentration. We experimentally demonstrate up to about 6.5fold (observable) selectivity in a cycle with a regeneration voltage of 0.4 V. We also demonstrate a novel multi-pass, air-flush i-CDI operation to selectively enrich nitrate with high water recovery. We further present a dynamic, multi-species electrosorption and equilibrium solution-to-surface chemical reaction model and validate the model with detailed measurements. Our i-CDI system exhibits higher nitrate selectivity at lower voltages; making it possible to reduce NaNO 3 concentrations from~170 ppm to below the limit of maximum allowed values for nitrate in drinking water of about 50 ppm NaNO 3 .

Ionic Group Derivitized Nano Porous Carbon Electrodes for Capacitive Deionization

Capacitance for electrostatic adsorption forms primarily within a Debye length of the electrode surface. Capacitive carbon electrodes were derivatized with ionic groups by means of adsorbing a surfactant in order to test the theory that attached ionic groups would exclude co-ions and increase coulombic efficiency without the need for an added charge barrier membrane. It has been discovered that capacitive electrodes surface derivatized with ionic groups become polarized and intrinsically more coulombically efficient.

Ion removal trends in capacitive deionization and its application for treating industrial effluents

2020

Capacitive deionization (CDI) is a relatively new water purification technology based on the principles of super-capacitors that is gaining both scientific and commercial momentum over the last decade. Typically, CDI devices are built using nano-porous and conductive activated carbon materials, which lead to operational flexibility for contaminant removal from different water sources generally requiring lower power for operation with very little needs for maintenance. In this thesis, we have used a unique CDI device architecture and validated its efficacy to remove positive and negative ionic contaminants from synthetic and industrial wastewater. The correlation between the ion size, charge and structure on electrosorption capacity and dynamics were studied to develop an understanding of the optimum operating protocol to treat wastewater from mining industry, using commercially available activated carbon cloth as the CDI electrode material. Results indicate that ions with lower valences are prone to be replaced by higher valence ions, depending on the time of operation and thus could be used to design selectivity in terms of contaminant removal. Application of CDI for mining water treatment was found to be feasible with low power consumption and shows good promise as a candidate for the future of smart water treatment processes.

Capacitive deionization concept based on suspension electrodes without ion exchange membranes

Electrochemistry Communications, 2014

This is an author's version published in: http://oatao.univ-toulouse.fr/20256 a b s t r a c t a r t i c l e i n f o A new type of capacitive deionization (CDI) system, based on capacitive suspension electrodes (CSEs), was developed for the purpose of desalting brackish and seawater through the use of flowable carbon suspensions. CSEs derived from activated carbon and acetylene black demonstrated a specific capacitance of 92 F g −1 in a static mode in a 0.6 M NaCl solution. The novel system introduced here is a proof of concept that capacitive suspension electrodes can be envisioned to desalt water without the aid of ion exchange membranes (IEMs).

Freestanding Activated Carbon Nanocomposite Electrodes for Capacitive Deionization of Water

Polymers

Freshwater reserves are being polluted every day due to the industrial revolution. Man-made activities have adverse effects upon the ecosystem. It is thus the hour of need to explore newer technologies to save and purify water for the growing human population. Capacitive deionization (CDI) is being considered as an emerging technique for removal of excess ions to produce potable water including desalination. Herein, cost-effective activated carbon incorporated with carbon nanotubes (CNT) was used as a freestanding electrode. Further, the desalination efficiency of the designed electrodes was tuned by varying binder concentration, i.e., polyvinylidene difluoride (PVDF) in the activated carbon powder and CNT mixture. PVDF concentration of 5, 7.5, 10, and 12.5 wt% was selected to optimize the freestanding electrode formation and further applied for desalination of water. PVDF content affected the surface morphology, specific surface area, and functional groups of the freestanding elect...

A comparison of multicomponent electrosorption in capacitive deionization and membrane capacitive deionization

Water research, 2017

In this study, the desalination performance of Capacitive Deionization (CDI) and Membrane Capacitive Deionization (MCDI) was studied for a wide range of salt compositions. The comprehensive data collection for monovalent and divalent ions used in this work enabled us to understand better the competitive electrosorption of these ions both with and without ion-exchange membranes (IEMs). As expected, MCDI showed an enhanced salt adsorption and charge efficiency in comparison with CDI. However, the different electrosorption behavior of the former reveals that ion transport through the IEMs is a significant rate-controlling step in the desalination process. A sharper desorption peak is observed for divalent ions in MCDI, which can be attributed to a portion of these ions being temporarily stored within the IEMs, thus they are the first to leave the cell upon discharge. In addition to salt concentration, we monitored the pH of the effluent stream in CDI and MCDI and discuss the potential ...

Water Desalination Using Capacitive Deionization with Microporous Carbon Electrodes

ACS Applied Materials & Interfaces, 2012

Capacitive deionization (CDI) is a water desalination technology in which salt ions are removed from brackish water by flowing through a spacer channel with porous electrodes on each side. Upon applying a voltage difference between the two electrodes, cations move to and are accumulated in electrostatic double layers inside the negatively charged cathode and the anions are removed by the positively charged anode. One of the key parameters for commercial realization of CDI is the salt adsorption capacity of the electrodes. State-of-the-art electrode materials are based on porous activated carbon particles or carbon aerogels. Here we report the use for CDI of carbide-derived carbon (CDC), a porous material with well-defined and tunable pore sizes in the sub-nanometer range. When comparing electrodes made with CDC with electrodes based on activated carbon, we find a significantly higher salt adsorption capacity in the relevant cell voltage window of 1.2−1.4 V. The measured adsorption capacity for four materials tested negatively correlates with known metrics for pore structure of the carbon powders such as total pore volume and BET-area, but is positively correlated with the volume of pores of sizes <1 nm, suggesting the relevance of these sub-nanometer pores for ion adsorption. The charge efficiency, being the ratio of equilibrium salt adsorption over charge, does not depend much on the type of material, indicating that materials that have been identified for high charge storage capacity can also be highly suitable for CDI. This work shows the potential of materials with well-defined sub-nanometer pore sizes for energy-efficient water desalination.

Review on carbon-based electrode materials for application in capacitive deionization process

Most of the electrochemical studies related to porous carbon electrodes are those which can be used for either electrostatic energy storage or for energy conversion [using electrical double layer capacitor (EDLC)]. The techniques, such as electrodialysis, membrane filtration, advanced oxidation process, thermal evaporation, can be used now-a-days to treat salty water. Among which, capacitive deionization (CDI) has emerged as a novel cost effective and environment friendly desalination technology. CDI process involves the removal of inorganic ions from the salty water by applying an electrical potential between two porous carbon electrodes. Because of the passage of electrical potentials in the system, the unwanted ions present in the water sample will be adsorbed on the electrode surfaces. Hence, the electrodes which are having high surface area can exhibit higher desalination capacity. In this article, the application of various carbon-based composite electrode materials such as activated carbon and PVDF composite, carbon–metal oxide composite, carbon– CNT composite, carbon–polymer composite and carbon sheet (carbon aerogel, activated carbon cloth) in CDI process is systematically reviewed and presented. CDI process is being developed now-a-days especially toward commercialization in treating the brackish water.