Adsorption of organic arsenic acids from water over functionalized metal-organic frameworks

被引:122
|
作者
Sarker, Mithun [1 ]
Song, Ji Yoon [1 ]
Jhung, Sung Hwa [1 ]
机构
[1] Kyungpook Natl Univ, Green Nano Mat Res Ctr, Dept Chem, Daegu 41566, South Korea
基金
新加坡国家研究基金会;
关键词
Adsorption; Hydrogen bonding; MIL-101(OH)(3); Phenylarsonic acid; p-Arsanilic acid; AROMATIC ORGANOARSENIC COMPOUNDS; NITROGEN-CONTAINING COMPOUNDS; P-ARSANILIC ACID; PHOTOCATALYTIC DEGRADATION; PHENYLARSONIC ACID; DICLOFENAC SODIUM; AQUEOUS-SOLUTION; CLOFIBRIC ACID; MODEL FUEL; REMOVAL;
D O I
10.1016/j.jhazmat.2017.04.044
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Organic arsenic acids (OAAs) are regarded as water pollutants because of their toxicity and considerable solubility in water. Adsorption of OAAs such as phenylarsonic acid (PAA) and p-arsanilic acid (ASA) from water was investigated over functionalized (with OH groups) metal-organic framework (MOF, MIL-101), as well as over pristine MIL-101 and commercial activated carbon. The highly porous MIL-101 bearing three hydroxyl groups (MIL-101(OH)(3)) exhibited remarkable PAA and ASA adsorption capacities. Based on the effects of pH on PAA and ASA adsorption, hydrogen bonding was suggested as a plausible mechanism of OAA adsorption. Importantly, OAAs and MIL-101(OH)(3) can be viewed as hydrogen-bond acceptors and donors, respectively. Moreover, MIL-101(OH)(3) could be regenerated by acidic ethanol treatment, being a promising adsorbent for the removal of PAA and ASA from water. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:162 / 169
页数:8
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