Lawrence Livermore National Laboratory , 7000 East Avenue, Livermore , California 94550 , United States.
Department of Mechanical Engineering , Stanford University , Stanford , California 94305 , United States.
Environ Sci Technol. 2019 Sep 17;53(18):10863-10870. doi: 10.1021/acs.est.9b01374. Epub 2019 Jun 19.
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 () of both nitrate over sulfate ( = 17.8 ± 3.6 at 0.6 V) and nitrate over chloride ( = 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/NO/SO feedwater. 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.
水资源受到硝酸盐污染是一个日益严重且意义重大的问题。在这里,我们报告了使用超微孔碳作为电容去离子(CDI)电极,从阴离子混合物中选择性去除硝酸盐。通过适度的活化,我们实现了微孔尺寸分布,几乎完全由狭窄(<1nm)的孔组成,这些孔非常适合吸附平面、弱水合的硝酸盐分子。循环伏安测量显示,与氯化物相比,硝酸盐的电容增强,并且当硫酸盐是唯一存在的阴离子时,具有显著的离子筛分效应。当对 3.33mM/3.33mM/1.67mM Cl/NO/SO 进料水进行恒电压 CDI 分离时,我们测量到硝酸盐对硫酸盐(=17.8±3.6 在 0.6V)和硝酸盐对氯化物(=6.1±0.4 在 0.6V)的高选择性。考虑到进料中存在二价干扰物,这些结果尤其令人鼓舞。使用分子动力学模拟,我们研究了这些离子的溶剂化特性,以更好地理解为什么硝酸盐优先于硫酸盐和氯化物被电吸附。