Fabrication of MIL-53(Al) based composites from biomass activated carbon (AC) for efficient p-nitrophenol adsorption from aqueous solution

被引:21
|
作者
Qi, Lihua [1 ]
Jiang, Hailin [1 ]
Lin, Tianni [1 ]
Chang, Xinyu [1 ]
Jiang, Bolong [2 ]
机构
[1] Qingdao Univ Technol, Inst Environm & Municipal Engn, Qingdao 266000, Shandong, Peoples R China
[2] Qingdao Univ Technol, Innovat Inst Sustainable Maritime Architecture Re, Qingdao 266000, Shandong, Peoples R China
关键词
MIL-53(Al) based composite; Biomass activated carbon; Wastewater treatment; p-nitrophenol; METAL-ORGANIC FRAMEWORKS; REMOVAL; DESULFURIZATION; EXTRACTION; GASOLINE; PHENOL;
D O I
10.1016/j.jtice.2021.08.020
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Background: The aim of this study was to develop a class of novel MIL-53(Al) based composite with high phenolic compound adsorption capacity to treat highly toxic phenolic wastewater. Method: MIL-53(Al)@AC-x composites with different AC loading (x) were constructed by combining MIL-53 (Al) with cheap biomass AC derived from cheap rice husk. The adsorbents were characterized by various methods. Significant findings: The results showed that the surface area and pore volume of all MIL-53(Al)@AC-x composites increased remarkably, which are much higher than those of pristine AC and MIL-53(Al). The p-nitrophenol adsorption rate of MIL-53(Al)@AC-10 was higher than pristine MIL-53(Al) by 36%. The adsorption performance decreased in the order of MIL-53(Al)@AC-10 > MIL-53(Al)@AC-15 > MIL-53(Al)@AC-5 > MIL-53(Al). The maximum adsorption capacity for p-nitrophenol of MIL-53(Al)@AC-10 reached 250 mg.g(-1), which are higher than the data reported in most literature. The fabrication of AC into MIL-53(Al) is a promising method to obtain a composite with high adsorption capacity and stability. The adsorption kinetics and isotherms fitted well with pseudo-second-order model and Langmiur model. The adsorption is mainly through the pi-pi and hydrogen bond interactions, and hydrophobic effect. (C) 2021 Taiwan Institute of Chemical Engineers. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:220 / 227
页数:8
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