Energy Consumption in Batch-Mode Capacitive Deionization

2016 ◽  
Vol 868 ◽  
pp. 43-49 ◽  
Author(s):  
Hai Bo Li ◽  
Sen Liang ◽  
Mang Mang Gao ◽  
Chang Yeoul Kim

Capacitive deionization (CDI) is a water desalination technique in which salt ions are removed from brackish water by flowing through a spacer channel with porous electrodes on each side. Upon applying a small 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. Therefore, one of the advanced merits of CDI is the low driven energy by compared to other desalination technologies. Inspired this, we have performed the calculation on energy consumption of activated carbon based CDI in different operation conditions. The results show that the energy consumptions are significantly related to cell voltage as well as solution concentration. Furthermore, the round trip efficiency as a vital indication in terms of energy consumption have been introduced and discussed as well.

2019 ◽  
Vol 5 (5) ◽  
pp. 873-883
Author(s):  
G. R. Iglesias ◽  
S. Ahualli ◽  
M. M. Fernández ◽  
M. L. Jiménez ◽  
A. V. Delgado

The capacitive deionization (CDI) method, in which the capacitance of the electrical double layers is used for removing ions from aqueous solutions, can be more efficient if some procedures are devised to help the bare electrode double layers in adsorbing ions.


2014 ◽  
Vol 71 (1) ◽  
pp. 83-88 ◽  
Author(s):  
Haibo Li ◽  
Sen Liang ◽  
Mangmang Gao ◽  
Guolong Li ◽  
Jin Li ◽  
...  

In this work, the capacitive deionization (CDI) performance of a single-walled carbon nanotube (CNT) electrode has been studied from the point view of charge efficiency theory. It is revealed here that the charge efficiency of a CNT electrode is strongly dependent upon the cell voltage and solution concentration. Either the high cell voltage or the low ionic strength results in a high charge efficiency, implying that CDI is expected to be a promising technique for an aqueous solution with low ionic strength. Additionally, it is found that the high decay constant and high electrical double-layer capacity are beneficial to enhance electrosorption performance.


2018 ◽  
Vol 18 (6) ◽  
pp. 2028-2034 ◽  
Author(s):  
Shaojie Jiang ◽  
Hongwu Wang ◽  
Guanquan Xiong ◽  
Xinlei Wang ◽  
Siying Tan

Abstract The removal performance of nitrate using capacitive deionization (CDI) of activated carbon (AC)-based electrodes were studied. The AC electrode was prepared and the effect of cell voltage, flow rate and initial solution concentration on ion removal were investigated. Furthermore, the AC was modified with phosphoric acid (ACP) and the surface structure of AC and ACP were analyzed. The results showed that the specific surface area of AC increased by 10.71% after the modification. The mesopore ratio and micropore ratio increased by 14.69% and 24.06%, respectively. The optimal conditions of AC electrode was a voltage of 1.4 V and flow rate of 20 mL/min while the ACP electrode was a voltage of 1.4 V and flow rate of 10 mL/min. The electrosorption capacity of ACP electrode was improved and the unit of electrosorption load was high to 19.28 mg/L. For the AC or ACP electrode, the nitrate removal efficiency decreases with the increase in the initial feed solutions, but the unit electrosorption load gradually increased with the improvement of initial feed solutions' concentration and the ACP electrode was superior to the AC electrode. Therefore, the ACP electrode would be suitable for the application of CDI on the nitrate removal.


2016 ◽  
Vol 3 (5) ◽  
pp. 222-226 ◽  
Author(s):  
Di He ◽  
Chi Eng Wong ◽  
Wangwang Tang ◽  
Peter Kovalsky ◽  
T. David Waite

Author(s):  
Yasamin Salamat ◽  
Carlos A. Rios Perez ◽  
Carlos Hidrovo

Due to the increasing demand for clean and potable water stemming from population growth and exacerbated by the scarcity of fresh water resources, more attention has been drawn to different and innovative methods for water desalination. Capacitive deionization (CDI) is a relatively new, low maintenance, and energy efficient technique for desalinating brackish water. In this technique, an electrical field is employed to adsorb ions into a high-porous media. After the saturation of the porous electrodes, their adsorption capacity can be restored through a regeneration process. Various parameters affect the overall performance of CDI. The flow rate at which water is purified in CDI plays an essential role in its ultimate performance. Many studies have shown that desalination percentage decreases as flow rate increases in CDI, since the advection of ions in the flow becomes more dominant than their diffusion toward the electrodes. However, herein, based on a physical model previously developed, we conjecture that for a given amount of time and volume of water, multiple desalination cycles in a high flow rate regime will outperform desalinating in a single cycle at a low flow rate. Moreover, splitting a CDI unit into two sub-units, with the same total length, will lead to higher desalination. Based on these premises, we introduce a new approach aimed at enhancing the overall performance of CDI. An array of CDI cells are sequentially connected to each other with intermediate solutions placed in between them. These intermediate solutions act as buffers to homogenize the outlet concentration of the preceding cell and maintain a constant inlet concentration for the following cell. Desalination tests were conducted to compare the performance of the proposed system, consisting of two CDI units and one intermediate solution buffer, with a two-cascaded-CDI unit system with no intermediate solution. Desalination tests were performed in a high flow rate regime with a low salinity initial solution of NaCl in water. In the buffered arrangement, the concentration of the solution buffer was set at the minimum average outlet concentration of the first CDI test. Experimental data demonstrated the improved performance of the buffered system over the non-buffered system, in terms of desalination percentage and energy consumption. Increasing the number of CDI units and solution buffers in a buffered system, the new proposed method will lead to lower amount of energy consumed per unit volume of the desalinated water.


Materials ◽  
2020 ◽  
Vol 13 (22) ◽  
pp. 5185
Author(s):  
Gbenro Folaranmi ◽  
Mikhael Bechelany ◽  
Philippe Sistat ◽  
Marc Cretin ◽  
Francois Zaviska

Capacitive deionization is an emerging brackish water desalination technology whose principle lies in the utilization of porous electrodes (activated carbon materials) to temporarily store ions. Improving the properties of carbon material used as electrodes have been the focus of recent research, as this is beneficial for overall efficiency of this technology. Herein, we have synthesized a composite of activated carbon/graphene oxide electrodes by using a simple blending process in order to improve the hydrophilic property of activated carbon. Graphene oxide (GO) of different weight ratios was blended with commercial Activated carbon (AC) and out of all the composites, AC/GO-15 (15 wt.% of GO) exhibited the best electrochemical and salt adsorption performance in all operating conditions. The as prepared AC and AC/GO-x (x = 5, 10, 15 and 20 wt.% of GO) were characterized by cyclic voltammetry and their physical properties were also studied. The salt adsorption capacity (SAC) of AC/GO-15 at an operating window of 1.0 V is 5.70 mg/g with an average salt adsorption rate (ASAR) of 0.34 mg/g/min at a 400 mg/L salt initial concentration and has a capacitance of 75 F/g in comparison to AC with 3.74 mg/g of SAC, ASAR of 0.23 mg/g/min and a capacitance of 56 F/g at the same condition. This approach could pave a new way to produce a highly hydrophilic carbon based electrode material in CDI.


Nanomaterials ◽  
2021 ◽  
Vol 11 (5) ◽  
pp. 1090
Author(s):  
Gbenro Folaranmi ◽  
Mikhael Bechelany ◽  
Philippe Sistat ◽  
Marc Cretin ◽  
Francois Zaviska

Capacitive deionization is a second-generation water desalination technology in which porous electrodes (activated carbon materials) are used to temporarily store ions. In this technology, porous carbon used as electrodes have inherent limitations, such as low electrical conductivity, low capacitance, etc., and, as such, optimization of electrode materials by rational design to obtain hybrid electrodes is key towards improvement in desalination performance. In this work, different compositions of mixture of reduced graphene oxide (RGO) and activated carbon (from 5 to 20 wt% RGO) have been prepared and tested as electrodes for brackish water desalination. The physico-chemical and electrochemical properties of the activated carbon (AC), reduced graphene oxide (RGO), and as-prepared electrodes (AC/RGO-x) were characterized by low-temperature nitrogen adsorption measurement, scanning electron microscope (SEM), X-ray diffraction (XRD), Raman spectroscopy, X-ray photoelectron spectroscopy (XPS), Fourier transform infra-red (FT-IR), cyclic voltammetry (CV), and electrochemical impedance spectroscopy (EIS). Among all the composite electrodes, AC/RGO-5 (RGO at 5 wt%) possessed the highest specific capacitance (74 F g−1) and the highest maximum salt adsorption capacity (mSAC) of 8.10 mg g−1 at an operating voltage ∆E = 1.4 V. This shows that this simple approach could offer a potential way of fabricating electrodes of accentuated carbon network of an improved electronic conductivity that’s much coveted in CDI technology.


2019 ◽  
Author(s):  
Jie Jin ◽  
Man Li ◽  
Mengting Tang ◽  
Yang Li ◽  
Yangyang Liu ◽  
...  

Hybrid capacitive deionization (HCDI) is an emerging and promising technology for water desalination and has been extensively explored in recent years. Designing a structure tailorable electrode material has been proved to be a valid strategy for achieving a higher salt adsorption capacity (SAC). In this study, <a></a><a>MnO<sub>2</sub> materials with tailorable phase compositions and regulatory microstructures were prepared hydrothermally and then evaluated as electrodes for removal of ions from NaCl solution in a membrane-free HCDI cell.</a> MnO<sub>2</sub> electrode materials tested in HCDI system include poorly crystalline δ-MnO<sub>2</sub> with a lot of amorphous phases (MnO<sub>2</sub>-1h), crystalline δ-MnO<sub>2</sub> with amorphous MnO<sub>2</sub> (MnO<sub>2</sub>-2h), MnO<sub>2</sub> mixtures of α-, δ-, and amorphous MnO<sub>2</sub> (MnO<sub>2</sub>-5h), and <a></a><a>α-MnO<sub>2</sub> nanowire</a> with minor amorphous MnO<sub>2</sub> (MnO<sub>2</sub>-12h). It is notable that the phase composition along with the microstructures of MnO<sub>2</sub> materials rather than their surface areas determines the SAC values. When the cell voltage is 1.2 V, the <a></a><a>lamellar</a> structured MnO<sub>2</sub>-1h electrode demonstrates the highest SACs of 13.84 mg g<sup>-1</sup> in 100 mg L<sup>-1</sup> NaCl, and 21.32 mg g<sup>-1</sup> in 500 mg L<sup>-1</sup> NaCl solution, respectively. The desalination efficiencies are remarkable and far greater than other MnO<sub>2</sub>-based electrodes under similar conditions (e.g., NaCl concentrations, cell voltage, etc.). This study sheds light on the significance of understanding the fundamental of both phase composition and microstructure in governing the desalination performance of MnO<sub>2</sub> electrodes.


Author(s):  
Huizhong Zhang ◽  
Jiayu Tian ◽  
Xiujuan Hao ◽  
Dongmei Liu ◽  
Fuyi Cui

Abstract Capacitive deionization (CDI) has been investigated for brackish water desalination, selective removal of ions, and water softening. We used humic acid (HA) and alginate sodium (SA) to simulate different kinds of natural organic matter to investigate the fouling phenomena during CDI operation. Adsorption amount and energy efficiency were studied. Results showed that both SA and HA could decrease the removal of NaCl during CDI operation. There existed a slight decrease of energy consumption in SA solutions which was opposite to that in HA solutions. HA can compete with ions adsorbed by electrodes and attach to electrodes adhesively, resulting in co-ion repulsion. SA is not sensitive to electrical field and its fouling is not obvious. The amount of adsorbed Mg2+ would increase from 0.927 mg/g to 1.508 mg/g in ten cycles' operation and the increment of Ca2+ was from 1.885 mg/g to 2.878 mg/g in SA solutions. This increase of adsorption was due to the complexation between SA and cations. Simultaneously, energy consumption was decreased. In HA solutions, energy consumption of Mg2+ and Ca2+ adsorption increased. In ten cycles' operations, both HA and SA could reduce the efficiency of CDI operation. The types of organic substances are important factors in fouling of CDI electrodes.


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