skip to main content
US FlagAn official website of the United States government
dot gov icon
Official websites use .gov
A .gov website belongs to an official government organization in the United States.
https lock icon
Secure .gov websites use HTTPS
A lock ( lock ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.

Explore Research Products in the PAR
It may take a few hours for recently added research products to appear in PAR search results.


  • NSF Public Access
  • Search Results
  • Emerging investigator series: capacitive deionization for selective removal of nitrate and perchlorate: impacts of ion selectivity and operating constraints on treatment costs
Title: Emerging investigator series: capacitive deionization for selective removal of nitrate and perchlorate: impacts of ion selectivity and operating constraints on treatment costs
Treating toxic monovalent anions such as NO 3 − or ClO 4 − in drinking water remains challenging due to the high capital and environmental costs associated with common technologies such as reverse osmosis or ion exchange. Capacitive deionization (CDI) is a promising technology for selective ion removal due to high reported ion selectivity for these two contaminants. However, the impacts of ion selectivity and influent water characteristics on CDI life cycle cost have not been considered. In this study we investigate the impact of ion selectivity on CDI system cost with a parameterized process model and technoeconomic analysis framework. Simulations indicate millimolar concentration contaminants such as nitrate can be removed at costs in the range of $0.01–0.30 per m 3 at reported selectivity coefficient ranges ( S = 6–10). Since perchlorate removal involves micromolar scale concentration changes, higher selectivity values than reported in literature ( S > 10 vs. S = 4–6.5) are required for comparable treatment costs. To contextualize simulated results for CDI treatment of NO 3 − , CDI unit operations were sized and costed for three case studies based on existing treatment facilities in Israel, Spain, and the United States, showing that achieving a nitrate selectivity of 10 could reduce life cycle treatment costs below $0.2 per m 3 .  more » « less
Award ID(s):
1931941
PAR ID:
10293463
Author(s) / Creator(s):
;
Date Published:
Journal Name:
Environmental Science: Water Research & Technology
Volume:
6
Issue:
4
ISSN:
2053-1400
Page Range / eLocation ID:
925 to 934
Format(s):
Medium: X
Sponsoring Org:
National Science Foundation
More Like this
  1. ; ; ; ; (, Environmental Science: Water Research & Technology)
    Capacitive deionization (CDI) technologies have gained intense attention for water purification and desalination in recent years. Inexpensive and widely available porous carbon materials have enabled the fast growth of electrosorption research, highlighting the promise of CDI as a potentially cost-effective technology to remove ions. Whereas the main focus of CDI has been on bulk desalination, there has been a recent shift towards electrosorption for selective ion separations. Heavy metals are pollutants that can have severe health impacts and are present in both industrial wastewater and groundwater leachates. Heavy metal ions, such as chromium, cadmium, or arsenic, are of great concern to traditional treatment technologies, due to their low concentration and the presence of competing species. The modification/functionalization of porous carbon and recent developments of faradaic and redox-active materials have offered a new avenue for selective ion-binding of heavy metal contaminants. Here, we review the progress in electrosorptive technologies for heavy metal separations. We provide an overview of the wide applicability of carbon-based electrodes for heavy metal removal. In parallel, we highlight the trend toward modification of carbon materials, new developments in faradaic interfaces, and the underlying physico-chemical mechanisms that promote selective heavy metal separations. 
    more » « less
  2. ; ; ; (, RSC Advances)
    Capacitive deionization (CDI) is an energy saving and environmentally friendly technology for water desalination. However, classical CDI is challenged by a low salt removal capacity. To improve the desalination capacity, electrode materials utilizing the battery mechanism for salt ion removal have emerged as a new direction more recently. In this work, we report a study of amorphous iron phosphate (FePO 4 ) as a promising electrode material for pseudocapacitive sodium ion removal. Sodium ions can be effectively, reversibly intercalated and de-intercalated upon its electrochemical reduction and oxidation, with an excellent sodium ion capacity under half-cell testing conditions. By assembling a hybrid CDI (HCDI) system utilizing the FePO 4 electrode for pseudocapacitive sodium ion removal and active carbon electrode for capacitive chloride ion removal, the cell exhibited a high salt removal capacity and good reversibility and durability, which was attributed to the advantageous features of amorphous FePO 4 . The HCDI system achieved a high deionization capacity (82 mg g −1 ) in 10 mM NaCl, a fast deionization rate (0.046 mg g −1 s −1 ), and good stability and cyclability. 
    more » « less
  3. ; ; ; (, Microsystems & Nanoengineering)
    Abstract Current potentiometric sensing methods are limited to detecting nitrate at parts-per-billion (sub-micromolar) concentrations, and there are no existing potentiometric chemical sensors with ultralow detection limits below the parts-per-trillion (picomolar) level. To address these challenges, we integrate interdigital graphene ion-sensitive field-effect transistors (ISFETs) with a nitrate ion-sensitive membrane (ISM). The work aims to maximize nitrate ion transport through the nitrate ISM, while achieving high device transconductance by evaluating graphene layer thickness, optimizing channel width-to-length ratio (RWL), and enlarging total sensing area. The captured nitrate ions by the nitrate ISM induce surface potential changes that are transduced into electrical signals by graphene, manifested as the Dirac point shifts. The device exhibits Nernst response behavior under ultralow concentrations, achieving a sensitivity of 28 mV/decade and establishing a record low limit of detection of 0.041 ppt (4.8 × 10−13M). Additionally, the sensor showed a wide linear detection range from 0.1 ppt (1.2 × 10−12M) to 100 ppm (1.2 × 10−3M). Furthermore, successful detection of nitrate in tap and snow water was demonstrated with high accuracy, indicating promising applications to drinking water safety and environmental water quality control. 
    more » « less
  4. ; ; ; ; ; ; (, ECS Meeting Abstracts)
    In our study, an exceptionally high selectivity of the electrocatalytic nitrate-to-nitrite transformation was discovered on Ag surfaces, among eighteen metals screened. It was demonstrated that this electrocatalytic step on oxide-derived Ag (OD-Ag), which possesses extended surface area (13 times) and enhanced specific activity (3 times) relative to Ag foil, can be coupled with a catalytic nitrite-to-dinitrogen step on a Pd catalyst using renewable hydrogen generated on-site by a water electrolyzer. We thereby proposed and demonstrated a combined electrocatalytic-catalytic process as an alternative strategy for innovative nitrate removal from agricultural wastewater with high selectivity of >95%. With future research and development, the combined process may hold the potential of tackling the ever-increasing nitrate pollution in water bodies to address its linked environmental and health issues. Strategically returning reactive nitrogen from wastewater back to the atmosphere in the inert form, this combined process is well-positioned to help close the global nitrogen cycle, one of the grand engineering challenges in the 21st century. In parallel with the applications in wastewater treatment, the Ag-based electrocatalytic nitrate-to-nitrate conversion with ultrahigh selectivity may be widely employed for designing cost-effective and energy-efficient syntheses of various nitrogen-based compounds in a distributed manufacturing fashion. The kinetics studies and computational insights could also be beneficial to advancing nitrogen-centric electrochemistry, materials science, and technologies. 
    more » « less
  5. ; ; ; ; (, Nanomaterials)
    Anionic carboxylated cellulose nanofibers (CNF) are effective media to remove cationic contaminants from water. In this study, sustainable cationic CNF-based adsorbents capable of removing anionic contaminants were demonstrated using a simple approach. Specifically, the zero-waste nitro-oxidization process was used to produce carboxylated CNF (NOCNF), which was subsequently converted into a cationic scaffold by crosslinking with aluminum ions. The system, termed Al-CNF, is found to be effective for the removal of fluoride ions from water. Using the Langmuir isotherm model, the fluoride adsorption study indicates that Al-CNF has a maximum adsorption capacity of 43.3 mg/g, which is significantly higher than that of alumina-based adsorbents such as activated alumina (16.3 mg/g). The selectivity of fluoride adsorption in the presence of other anionic species (nitrate or sulfate) by Al-CNF at different pH values was also evaluated. The results indicate that Al-CNF can maintain a relatively high selectivity towards the adsorption of fluoride. Finally, the sequential applicability of using spent Al-CNF after the fluoride adsorption to further remove cationic contaminant such as Basic Red 2 dye was demonstrated. The low cost and relatively high adsorption capacity of Al-CNF make it suitable for practical applications in fluoride removal from water. 
    more » « less
  • Citation Formats
  • MLA
  • APA
  • Chicago
  • BibTeX
  • Save / Share this Record
  • Send to Email