Bamboo leaf-derived biochar/iron silicate composite for an adsorption-degradation synergistic removal of ciprofloxacin

生物炭 吸附 化学 催化作用 降级(电信) 硅酸盐 复合数 核化学 竹子 共价键 化学工程 无机化学 有机化学 材料科学 复合材料 工程类 电信 计算机科学 热解
作者
Meng Xu,Junshu Wu,Jinshu Wang,Wenyuan Zhou,Yongli Li,Hongyi Li
出处
期刊:Chemical Engineering Research & Design [Elsevier BV]
卷期号:186: 1183-1196 被引量:15
标识
DOI:10.1016/j.psep.2024.04.074
摘要

Antibiotics pose significant risks to both the environment and human health. Herein, we develop a collaborative strategy for the enhanced removal of a typical antibiotic, Ciprofloxacin (CIP), by using a bamboo leaf-derived biochar/iron silicate composite (BL-FeSi) with the assistance of peroxymonosulfate (PMS). The rationale behind the design is the construction of composited material with synergistic adsorption-catalysis functions, based on covalent bonding networks of the biochar and specific Fe(III)/Fe(II) redox chemistry of iron silicate in PMS activation system. H2 reduction of pristine BL-FeSi increases Fe(II) content and thus improves catalytic activity. Batch experiments demonstrate that the preferred BL-FeSi400 (H2 treatment at 400 oC) exhibits superior efficiency in activating PMS. The CIP removal efficiency is highly dependent on pH value of reaction solution. A remarkable 97% removal is achieved at pH = 5.5 (CIP: 60 mL, 20 mg/L; BL-FeSi400: 0.2 g/L, PMS: 0.2 g/L), and the pH increase to 11 results in 100% CIP removal. The BL-FeSi400 shows robust resistance to inorganic ions (NO3−, SO42−, HCO3−, and H2PO4−), and the catalytic activity remains consistently high (>82%) even after four consecutive cycles, making it highly promising for practical applications. It is found that both radical pathway (•OH and SO4•−) and non-radical pathway (1O2) contribute to CIP degradation in the BL-FeSi400/PMS system, while the active •OH dominates the oxidization process. The coupling of adsorption and degradation holds great potentials for effective removal of more organic contaminants.
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