Browse
Submit Data
Databases
API
Help

Dataset Information

26 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Capacitive Deionization of Divalent Cations for Water Softening Using Functionalized Carbon Electrodes.

ABSTRACT: Water softening is a relatively untapped area of research in capacitive deionization (CDI). In this work, we demonstrate how an asymmetric combination of oxidized and aminated carbon can be used for selective removal of divalent cations for water softening. We first show how higher electrosorption performances can be achieved in single-salt experiments involving NaCl, KCl, MgCl2, and CaCl2 before proceeding to multi-salt experiments using different combinations of the four salts. The salt combinations are chosen to investigate one of the three factors: (1) ionic mass, (2) ionic charge, or (3) concentration. We show how divalent selectivity can be achieved due to high local electrostatic attraction between negatively charged oxygen moieties and divalent cations. Additionally, an ion-exchange process between the oxidized carbon surface and cations can result in lower pH values, which prevent the precipitation of scale-forming ions.

SUBMITTER: Leong ZY

PROVIDER: S-EPMC7016927 | biostudies-literature |

REPOSITORIES: biostudies-literature

ACCESS DATA

Json Xml

Similar Datasets

Freestanding Activated Carbon Nanocomposite Electrodes for Capacitive Deionization of Water.

Project description: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 electrodes. Moreover, the electrical conductivity and specific surface area changed with PVDF concentration, which ultimately affected the desalination capacity using the freestanding electrodes. This study paves the way to produce cost effective carbon-based freestanding electrodes for capacitive deionization and other applications including battery electrodes.

| S-EPMC9319057 | biostudies-literature

Theoretical Analysis of Constant Voltage Mode Membrane Capacitive Deionization for Water Softening.

Project description:Water softening is desirable to reduce scaling in water infrastructure and to meet industrial water quality needs and consumer preferences. Membrane capacitive deionization (MCDI) can preferentially adsorb divalent ions including calcium and magnesium and thus may be an attractive water softening technology. In this work, a process model incorporating ion exclusion effects was applied to investigate water softening performance including ion selectivity, ion removal efficiency and energy consumption in a constant voltage (CV) mode MCDI. Trade-offs between the simulated Ca2+ selectivity and Ca2+ removal efficiency under varying applied voltage and varying initial concentration ratio of Na+ to Ca2+ were observed. A cut-off CV mode, which was operated to maximize Ca2+ removal efficiency per cycle, was found to lead to a specific energy consumption (SEC) of 0.061 kWh/mole removed Ca2+ for partially softening industrial water and 0.077 kWh/m3 removed Ca2+ for slightly softening tap water at a water recovery of 0.5. This is an order of magnitude less than reported values for other softening techniques. MCDI should be explored more fully as an energy efficient means of water softening.

| S-EPMC8064386 | biostudies-literature

Fabrication of Activated Carbon Decorated with ZnO Nanorod-Based Electrodes for Desalination of Brackish Water Using Capacitive Deionization Technology.

Project description:Capacitive deionization (CDI) is a promising and cost-effective technology that is currently being widely explored for removing dissolved ions from saline water. This research developed materials based on activated carbon (AC) materials modified with zinc oxide (ZnO) nanorods and used them as high-performance CDI electrodes for water desalination. The as-prepared electrodes were characterized by cyclic voltammetry, and their physical properties were studied through SEM and XRD. ZnO-coated AC electrodes revealed a better specific absorption capacity (SAC) and an average salt adsorption rate (ASAR) compared to pristine AC, specifically with values of 123.66 mg/g and 5.06 mg/g/min, respectively. The desalination process was conducted using a 0.4 M sodium chloride (NaCl) solution with flow rates from 45 mL/min to 105 mL/min under an applied potential of 1.2 V. Furthermore, the energy efficiency of the desalination process, the specific energy consumption (SEC), and the maximum and minimum of the effluent solution concentration were quantified using thermodynamic energy efficiency (TEE). Finally, this work suggested that AC/ZnO material has the potential to be utilized as a CDI electrode for the desalination of saline water.

| S-EPMC9866127 | biostudies-literature

Assembly of Soft Electrodes and Ion Exchange Membranes for Capacitive Deionization.

Project description:The responsible use of water, as well as its reuse and purification, has been a major problem for decades now. In this work, we study a method for adsorbing ions from aqueous solutions on charged interfaces using highly porous electrodes. This water purification process is based on the electric double layer concept, using the method known as capacitive deionization (CDI): If we pump salty solutions through the volume comprised between two porous electrodes while applying a potential difference to them, ions present in the solution are partially removed and trapped on the electrode surfaces. It has been well established that the use of carbon electrodes in combination with ion exchange membranes (membrane-CDI) improves the efficiency of the method above that achieved with bare activated carbon. Another approach that has been tested is based on coating the carbon with polyelectrolyte layers, converting them into "soft electrodes" (SEs). Here we investigate the improvement found when combining SEs with membranes, and it is shown that the amount of ions adsorbed and the ratio between ions removed and electrons transported reach superior values, also associated with a faster kinetics of the process. The method is applied to the partial desalination of up to 100 mM NaCl solutions, something hardly achievable with bare or membrane-covered electrodes. A theoretical model is presented for the ion transport in the presence of both the membrane and the polyelectrolyte coating.

| S-EPMC6836081 | biostudies-literature

Reducing impedance to ionic flux in capacitive deionization with Bi-tortuous activated carbon electrodes coated with asymmetrically charged polyelectrolytes.

Project description:Capacitive deionization (CDI) with electric double layers is an electrochemical desalination technology in which porous carbon electrodes are polarized to reversibly store ions. Planar composite CDI electrodes exhibit poor energetic performance due the resistance associated with salt depletion and tortuous diffusion in the macroporous structure. In this work, we investigate the impact of bi-tortuosity on desalination performance by etching macroporous patterns along the length of activated carbon porous electrodes in a flow-by CDI architecture. Capacitive electrodes were also coated with thin asymmetrically charged polyelectrolytes to improve ion-selectivity while maintaining the bitortuous macroporous channels. Under constant current operation, the equivalent circuit resistance in CDI cells operating with bi-tortuous electrodes was approximately 2.2 times less than a control cell with unpatterned electrodes, leading to significant increases in working capacitance (20-22 to 26.7-27.8 F g-1), round-trip efficiency (52-71 to 71-80%), and charge efficiency (33-59 to 35-67%). Improvements in these key performance indicators also translated to enhanced salt adsorption capacity, rate, and most importantly, the thermodynamic efficiency of salt separation (1.0-2.0 to 2.2-4.1%). These findings demonstrate that the use of bi-tortuous electrodes is a novel approach of reducing impedance to ionic flux in CDI.

| S-EPMC6549939 | biostudies-literature

Chitosan-based activated carbon as economic and efficient sustainable material for capacitive deionization of low salinity water.

Project description:Capacitive deionization (CDI) is a novel low-energy green desalination technology that has attracted much attention in recent years, especially for the desalination of low salinity water. One of the key issues in CDI is the electrode materials, and many efforts have been devoted to developing materials with high specific surface areas, appropriate pore distributions, and good electronic conductivity, in order to obtain a high salt adsorption capacity. In this study, chitosan was selected as a precursor for the preparation of high-performance chitosan-based activated carbon (CTS-AC) for use in CDI electrodes via pyrolysis and KOH activation. The results show that CTS-AC800 (activated at 800 °C) has the largest BET specific surface area (2727 m2 g-1), and exhibits an appropriate pore size distribution (<10 nm), nitrogen doping (2.0%) and good electronic conductivity (2.09 S cm-1). The CDI performance results show that the CTS-AC800 electrode has a saturated salt adsorption capacity of 14.12 mg g-1 in a 500 mg L-1 NaCl solution and retains 95% capacity after 150 adsorption-desorption cycles. Thus, chitosan is a promising, sustainable precursor for CDI electrode materials.

| S-EPMC9070448 | biostudies-literature

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

Project description: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 6.5-fold (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 NaNO3 concentrations from ∼170 ppm to below the limit of maximum allowed values for nitrate in drinking water of about 50 ppm NaNO3.

| S-EPMC6549908 | biostudies-other

Activated Carbon Blended with Reduced Graphene Oxide Nanoflakes for Capacitive Deionization.

Project description: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.

| S-EPMC8144981 | biostudies-literature

Single-Walled Carbon Nanotube (SWCNT) Loaded Porous Reticulated Vitreous Carbon (RVC) Electrodes Used in a Capacitive Deionization (CDI) Cell for Effective Desalination.

Project description:Acid-functionalized single-walled carbon nanotube (a-SWCNT)-coated reticulated vitreous carbon (RVC) composite electrodes have been prepared and the use of these electrodes in capacitive deionization (CDI) cells for water desalination has been the focus of this study. The performance of these electrodes was tested based on the applied voltage, flow rate, bias potential and a-SWCNT loadings, and then evaluated by electrosorption dynamics. The effect of the feed stream directly through the electrodes, between the electrodes, and the distance between the electrodes in the CDI system on the performance of the electrodes has been investigated. The interaction of ions with the electrodes was tested through Langmuir and Freundlich isotherm models. A new CDI cell was developed, which shows an increase of 23.96% in electrosorption capacity compared to the basic CDI cells. Moreover, a comparison of our results with the published results reveals that RVC/a-SWCNT electrodes produce 16 times more pure water compared to the ones produced using only CNT-based electrodes. Finally, it can be inferred that RVC/a-SWCNT composite electrodes in newly-developed CDI cells can be effectively used in desalination technology for water purification.

| S-EPMC6071079 | biostudies-other

Particulate-free porous silicon networks for efficient capacitive deionization water desalination.

Project description:Energy efficient water desalination processes employing low-cost and earth-abundant materials is a critical step to sustainably manage future human needs for clean water resources. Here we demonstrate that porous silicon - a material harnessing earth abundance, cost, and environmental/biological compatibility is a candidate material for water desalination. With appropriate surface passivation of the porous silicon material to prevent surface corrosion in aqueous environments, we show that porous silicon templates can enable salt removal in capacitive deionization (CDI) ranging from 0.36% by mass at the onset from fresh to brackish water (10 mM, or 0.06% salinity) to 0.52% in ocean water salt concentrations (500 mM, or ~0.3% salinity). This is on par with reports of most carbon nanomaterial based CDI systems based on particulate electrodes and covers the full salinity range required of a CDI system with a total ocean-to-fresh water required energy input of ~1.45 Wh/L. The use of porous silicon for CDI enables new routes to directly couple water desalination technology with microfluidic systems and photovoltaics that natively use silicon materials, while mitigating adverse effects of water contamination occurring from nanoparticulate-based CDI electrodes.

| S-EPMC4840374 | biostudies-other

OmicsDI is part of the ELIXIR infrastructure

OmicsDI is an Elixir interoperability service. Learn more ›

Tweets

OmicsDI Databases

PRIDE
PeptideAtlas
MassIVE
JPOST Repository
Physiome Model Repository

EGA
EVA
ENA
LINCS
PAXDB
Cell Collective

MetaboLights
Metabolomics Workbench
MetabolomeExpress
GNPS
BioModels
FAIRDOMHub

ArrayExpress
dbGaP
ExpressionAtlas
GEO
NODE

Information

Databases
Help
API
Contact us
Code on GitHub
Terms of use
Submit Data