花球状Fe3O4/MoS2活化过一硫酸盐氧化去除环丙沙星
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1.南华大学土木工程学院;2.南华大学 土木工程学院

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Flower-like spherical Fe3O4 / MoS2 catalyst activated PMS for efficient removal of ciprofloxacin
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School of Civil Engineering, University of South China

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    摘要:

    采用水热法将纳米颗粒Fe3O4负载于花球状MoS2,制备出花球状Fe3O4/MoS2复合催化剂。通过SEM、XRD、XPS和VSM等手段对Fe3O4/MoS2进行表征,并考察了花球状Fe3O4/MoS2活化过一硫酸盐(PMS)对环丙沙星(CIP)去除性能。考察了不同体系、pH、Fe3O4/MoS2投加量、PMS投加量、CIP初始浓度和常见阴离子及腐植酸对Fe3O4/MoS2/PMS体系去除 CIP的影响,并探究了花球状Fe3O4/MoS2复合催化剂的循环稳定性。结果表明,在30 ℃、催化剂投加量0.2 g/L、PMS投加量0.25 mmol/L、CIP浓度5 mg/L的条件下,20 min内CIP的去除率可达96.1%,且在较宽的pH范围内(3.0~9.0)该体系仍具有较高的去除率。催化剂经三次循环试验后仍能对CIP有90.27%的去除率。自由基淬灭试验和EPR测试表明,Fe3O4/MoS2活化PMS去除CIP的机制包括自由基途径(?SO4–和?OH)和非自由基途径(1O2),其主要活性物质为1O2。本研究为活化PMS处理水中抗生素提供了一定的理论依据和技术支撑。

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    Nano-Fe3O4 was loaded on globular MoS2 by hydrothermal method to prepare globular Fe3O4/MoS2 composite catalyst. Fe3O4/MoS2 was characterized by SEM, XRD, XPS and VSM, and the removal performance of ciprofloxacin (CIP) by flower globular Fe3O4/MoS2 activated persulfate (PMS) was investigated. The effects of different systems, pH, Fe3O4/MoS2 dosage, PMS dosage, initial CIP concentration, common anions and humic acid on CIP removal in Fe3O4/MoS2/PMS system were investigated, and the cycle stability of flower ball Fe3O4/MoS2 composite catalyst was investigated. The results show that under the conditions of 30℃, 0.2 g/L catalyst dosage,0.25g / L PMS dosage and 5 mg/L CIP concentration, the removal rate of CIP can reach 96.1% within 20 min, and the system still has a high removal rate in a wide range of pH (3.0~9.0). After three cycles, the catalyst can still remove 90.27% of CIP. Free radical quenching test and EPR test showed that the mechanism of CIP removal by Fe3O4/MoS2 activated PMS included free radical pathway (?SO4- and ?OH) and non-free radical pathway (1O2), and the main active substance was 1O2. This study provides some theoretical basis and technical support for activating PMS to treat antibiotics in water.

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郑友臣,余泽旭,段毅,周书葵,周紫璇,闫俊霖.花球状Fe3O4/MoS2活化过一硫酸盐氧化去除环丙沙星[J].精细化工,2025,42(9):

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  • 收稿日期:2024-08-03
  • 最后修改日期:2024-10-17
  • 录用日期:2024-09-29
  • 在线发布日期: 2025-09-01
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