Coadsorption of Cu(II) and tylosin/sulfamethoxazole on biochar stabilized by nano-hydroxyapatite in aqueous environment

泰乐菌素 吸附 化学 离子强度 生物炭 水溶液 傅里叶变换红外光谱 核化学 Zeta电位 X射线光电子能谱 吸附 腐植酸 纳米颗粒 化学工程 有机化学 热解 抗生素 工程类 生物化学 肥料
作者
Zhen Li,Miao Li,Zhaoyan Wang,Xiang Liu
出处
期刊:Chemical Engineering Journal [Elsevier]
卷期号:381: 122785-122785 被引量:64
标识
DOI:10.1016/j.cej.2019.122785
摘要

Antibiotics and heavy metals are frequently detected simultaneously in water environment. In this study, a biochar stabilized by nano-hydroxyapatite ([email protected]) was used for the coadsorption of tylosin (TYL)/sulfamethoxazole (SMX) and Cu(II) in aqueous environment, which was well suited for real water samples. The physicochemical properties of [email protected] were characterised by SEM image, zeta potential, FTIR, BET analysis, XPS and XRD. The pseudo-second-order model was better fit for the sorption kinetics data. Background electrolytes, ionic strength, humic acid (HA) and addition sequences presented a significant effect on the adsorption of TYL/SMX and Cu(II) when with or without Cu(II). The adsorption of TYL and Cu(II) increased with the increasing of ionic strength and HA, and compared with TYL, the influence on SMX was not obvious. Adsorption results exhibited that TYL obviously enhanced the Cu(II) adsorption capability and Cu(II) obviously enhanced the SMX adsorption capability. According to the results of FTIR and XPS, H-bond may be one of the main interactions of TYL with [email protected] adsorption and weak π-π interactions and H-bond were two of the main interaction of SMX. TYL/SMX-Cu complexes were formed. In the system, the complexes were more on the formation of [email protected] and [email protected], rather than on [email protected] and [email protected], respectively.
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