Facile synthesis of MnOx‐loaded biochar for the removal of doxycycline hydrochloride: effects of ambient conditions and co‐existing heavy metals

吸附 生物炭 化学 金属 核化学 水溶液中的金属离子 离子强度 Zeta电位 比表面积 水处理 热解 无机化学 水溶液 纳米颗粒 化学工程 有机化学 催化作用 环境工程 工程类
作者
Si‐jia Liu,Yunguo Liu,Xiaofei Tan,Shaobo Liu,Meifang Li,Ni Liu,Zhihong Yin,Sirong Tian,Yahui Zhou
出处
期刊:Journal of Chemical Technology & Biotechnology [Wiley]
卷期号:94 (7): 2187-2197 被引量:50
标识
DOI:10.1002/jctb.6000
摘要

Abstract BACKGROUND In this study, manganese oxide (MnO x ) nanoparticle loaded biochar (BC) was applied for doxycycline hydrochloride (DOX) removal from water. Biochar composites were synthesized by either pre‐treating biomass using MnCl 2 /KMnO 4 /NaOH (PMBC) or inserting MnO x ultrafine particles after pyrolysis of biomass (AMBC). In complex water environments, the presence of heavy metals may affect the removal of antibiotics. Cu(II) and Cr(VI) were used to study their effect on DOX removal. RESULTS The BC loaded with MnO x exhibited superior adsorption properties for DOX. The adsorption capacity of AMBC and PMBC was ≈93 mg/g and 104 mg g −1 , respectively, which was about nine‐ and ten‐fold higher than that of raw BC (11.48 mg g −1 ). The characterization indicated that AMBC and PMBC had better surface structure and more surface functional groups than raw BC. The main mechanisms for DOX adsorption onto PMBC were surface complexation, H‐bond, π–π interaction and electrostatic interaction. DOX removal by PMBC also involved its degradation effect on DOX. Adsorption experiments were carried out with the influence of pH, ionic strength and background electrolyte. The presence of Cu(II) obviously enhanced the DOX adsorption capability through Cu(II) bridging effect, whereas the presence of Cr(VI) significantly inhibited DOX adsorption through competitive adsorption and electrostatic repulsion. CONCLUSIONS The results suggested that PMBC could be implemented as a cost‐effective and environmentally friendly adsorbent for DOX removal from water. Heavy metal ions can obviously enhance or weaken the adsorption ability of PMBC for DOX. © 2019 Society of Chemical Industry
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