Adsorption behavior and mechanism of p-arsanilic acid on a Fe-based framework

被引:21
|
作者
Gao, Mengwei [1 ]
Li, Bing [1 ]
Liu, Jue [2 ]
Hu, Yuanan [1 ]
Cheng, Hefa [3 ]
机构
[1] China Univ Geosci Beijing, Sch Water Resources & Environm, MOE Lab Groundwater Circulation & Evolut, Beijing 100083, Peoples R China
[2] Hebei University, Sch Qual & Techn Supervis, Baoding 071002, Hebei, Peoples R China
[3] Peking Univ, Coll Urban & Environm Sci, MOE Key Lab Earth Surface Proc, Beijing 100871, Peoples R China
基金
中国国家自然科学基金;
关键词
MOF; Annealing; P-arsanilic acid; Adsorption; Coordination; METAL-ORGANIC-FRAMEWORK; ZEOLITIC IMIDAZOLATE FRAMEWORK-8; CARBON NANOTUBES; AQUEOUS-SOLUTION; ARSENIC REMOVAL; OXIDE; IRON; FABRICATION; COMPOSITES; ROXARSONE;
D O I
10.1016/j.jcis.2022.08.133
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Hypothesis: Organic arsenic pollutant p-arsanilic acid (p-ASA) in wastewater can be converted into highly toxic inorganic arsenic under natural conditions, causing serious harm to the environment and human health. In this study, an Fe-based metal-organic framework (MOF) material, activated MIL-88A, was synthesized as an adsorbent to remove p-ASA in water. Experiments: Various influencing factors in the material synthesis process, including temperature, time, solution, and annealing process, were investigated to obtain the optimal reaction conditions. The synthesized activated MIL-88A had great porosity and excellent adsorption capacity for p-ASA in a wide pH range (3 similar to 10). When the pH of the solution was 6, the activated MIL-88A achieved a great adsorption capacity of 813 mg?g(-1) for the p-ASA solution with an initial concentration of 0.334 mmol?L-1. In addition, it still had excellent adsorption capacity after 4 times of repeated usage and washing. Findings: The adsorption kinetics of p-ASA on the activated MIL-88A followed the pseudo-second-order models, and the adsorption isotherms can be fitted by the Langmuir models well. The adsorption behavior was spontaneous and endothermic, and was dominated by Fe-O-As coordination and hydrogen bonding. (C) 2022 Elsevier Inc. All rights reserved.
引用
收藏
页码:616 / 627
页数:12
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