Removal and removing mechanism of tetracycline residue from aqueous solution by using Cu-13X

被引:43
|
作者
Lv, Jun-Min [1 ,2 ]
Ma, Yu-Long [1 ,2 ]
Chang, Xuan [1 ]
Fan, Su-Bing [2 ]
机构
[1] Ningxia Univ, Coll Chem & Chem Engn, Yinchuan 750021, Peoples R China
[2] Ningxia Univ, State Key Lab Cultivat Base Energy Sources & Chem, Yinchuan 750021, Peoples R China
基金
中国国家自然科学基金;
关键词
Adsorption mechanism; Complexation; Cu-13X; Removal; Tetracycline residue; WASTE-WATER TREATMENT; ELECTROCHEMICAL OXIDATION; ANTIBIOTICS; SORPTION; ZEOLITE; DEGRADATION; ADSORPTION; CHLORTETRACYCLINE; NANOFILTRATION; COPPER(II);
D O I
10.1016/j.cej.2015.03.080
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
In order to improve the removal efficiency of the reported adsorbents via freely physical adsorption, a novel adsorbent, Cu-13X, was applied to remove tetracycline (TC) residue from aqueous solution due to the chemically selective adsorption. The removal behaviors, adsorption kinetics, adsorption isotherm, adsorption thermodynamics of TC on synthesized Cu-13X were studied in batch experiments under different conditions. It was found that the adsorption, capability of Cu-13X increased greatly after exchanging. The amount of Cu(II) cation in Cu-13X and the pH value were important factors. At pH 7.0 and the maximum exchange amount of Cu(II), the maximum adsorption capacity of Cu-13X for TC residue reached about 2400 mg g(-1). The adsorption isotherms were fitted well by the Langmuir model. The adsorption kinetics Was described well by pseudo-second order equation, simultaneously was described well by the intra-particle diffusion model at high initial concentration of TC. The data calculated by adsorption thermodynamics of TC on Cu-13X showed it was exothermic and spontaneous. The probable adsorption mechanism was proposed by Fourier transform infrared (FTIR) analysis, which showed that the adsorbing TC residue on Cu-13X depended on the strong complexation of Cu(II) with NH2 radical of amide group of TC. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:247 / 253
页数:7
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