Using Ultramicroporous Carbon for the Selective Removal of Nitrate with Capacitive Deionization

Hawks, Steven A.; Cerón, Maira R.; Oyarzun, Diego I.; Pham, Tuan Anh; Zhan, Cheng; Loeb, Colin K.; Mew, Daniel; Deinhart, Amanda; Wood, Brandon C.; Santiago, Juan G.; Stadermann, Michael; Campbell, Patrick G.

doi:10.1021/acs.est.9b01374

Title: Using Ultramicroporous Carbon for the Selective Removal of Nitrate with Capacitive Deionization

Journal Article · Thu Jun 06 00:00:00 EDT 2019 · Environmental Science and Technology

DOI:https://doi.org/10.1021/acs.est.9b01374· OSTI ID:1572601

^[1];

^[1]; Oyarzun, Diego I. ^[2];

^[1]; Zhan, Cheng ^[1]; Loeb, Colin K. ^[1]; Mew, Daniel ^[1]; Deinhart, Amanda ^[1]; Wood, Brandon C. ^[1];

^[2]; Stadermann, Michael ^[1];

^[1]

Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States)
Stanford Univ., Stanford, CA (United States). Dept. of Mechanical Engineering

The contamination of water resources with nitrate is a growing and significant problem. Here we report the use of ultramicroporous carbon as a capacitive deionization (CDI) electrode for selectively removing nitrate from an anion mixture. Through moderate activation, we achieve a micropore-size distribution consisting almost exclusively of narrow (<1 nm) pores that are well suited for adsorbing the planar, weakly hydrated nitrate molecule. Cyclic voltammetry measurements reveal an enhanced capacitance for nitrate when compared to chloride as well as significant ion sieving effects when sulfate is the only anion present. We measure high selectivities (S) of both nitrate over sulfate (S_NO₃/SO₄ = 17.8 ± 3.6 at 0.6 V) and nitrate over chloride (S_NO₃/Cl = 6.1 ± 0.4 at 0.6 V) when performing a constant voltage CDI separation on 3.33 mM/3.33 mM/1.67 mM Cl/NO₃/SO₄ feedwater. Furthermore, these results are particularly encouraging considering that a divalent interferant was present in the feed. Using molecular dynamics simulations, we examine the solvation characteristics of these ions to better understand why nitrate is preferentially electrosorbed over sulfate and chloride.

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Research Organization:: Lawrence Livermore National Laboratory (LLNL), Livermore, CA (United States)

Sponsoring Organization:: USDOE National Nuclear Security Administration (NNSA)

Grant/Contract Number:: AC52-07NA27344

OSTI ID:: 1572601

Report Number(s):: LLNL-JRNL-768579; 959495

Journal Information:: Environmental Science and Technology, Vol. 53, Issue 18; ISSN 0013-936X

Publisher:: American Chemical Society (ACS)Copyright Statement

Country of Publication:: United States

Language:: English

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Cited by: 80 works

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