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通过响应面法利用过氧化钙纳米颗粒优化多西环素在水体系中的降解

Optimized Degradation of Doxycycline in Aqueous Systems Using Calcium Peroxide Nanoparticles via Response Surface Methodology.

作者信息

Nuar Nurul Nazihah Amerhaider, Jamil Siti Nurul Ain Md, Choong Thomas Shean Yaw, Mahadzir Syazana Ishami, Azmi Intan Diana Mat, Basri Mohd Salahuddin Mohd, Hamid Mohamad Rezi Abdul

机构信息

Department of Chemistry, Faculty of Science, Universiti Putra Malaysia (UPM), Serdang, Selangor 43400, Malaysia.

Centre for Foundation Studies in Science, Universiti Putra Malaysia (UPM), Serdang, Selangor 43400, Malaysia.

出版信息

ACS Omega. 2025 Mar 7;10(10):10205-10219. doi: 10.1021/acsomega.4c09460. eCollection 2025 Mar 18.

Abstract

The presence of antibiotic residues in aqueous systems, particularly doxycycline (DOX), is harmful to the environment and public health. In this study, dextran-coated calcium peroxide nanoparticles (DEX@nCPs(DEX)), Fe(II), and oxalic acid (OA) were combined to improve the heterogeneous Fenton-like degradation of DOX. X-ray photoelectron spectroscopy (XPS) demonstrated the successful synthesis of DEX@nCPs(DEX), showing the presence of Ca, O, and C functional groups associated with dextran. Using response surface methodology with a central composite design (RSM-CCD), the optimal conditions (DEX@nCPs(DEX) dosage: 2 g/L, pH: 5, contact time: 420 min) achieved 90% DOX removal, which was 20% higher than using DEX@nCPs(DEX)/Fe(II) alone. The degradation process followed first-order kinetics with a rate constant of = 0.0047 min. Model validation showed high predictive accuracy ( = 0.996; adjusted = 0.987). Scavenger and photoluminescence analyses revealed hydroxyl radicals (OH) to be the primary reactive species, accounting for over 80% of the degradation activity. The DEX@nCPs(DEX)/Fe(II)/OA system offers a promising approach for mitigating pharmaceutical pollutants in water, contributing to more sustainable environmental management practices.

摘要

水系统中抗生素残留的存在,尤其是多西环素(DOX),对环境和公众健康有害。在本研究中,将葡聚糖包覆的过氧化钙纳米颗粒(DEX@nCPs(DEX))、Fe(II)和草酸(OA)结合起来,以改善DOX的非均相类芬顿降解。X射线光电子能谱(XPS)证明成功合成了DEX@nCPs(DEX),显示出与葡聚糖相关的Ca、O和C官能团的存在。采用中心复合设计的响应面方法(RSM-CCD),最佳条件(DEX@nCPs(DEX)剂量:2 g/L,pH:5,接触时间:420分钟)实现了90%的DOX去除率,比单独使用DEX@nCPs(DEX)/Fe(II)高出20%。降解过程遵循一级动力学,速率常数k = 0.0047 min⁻¹。模型验证显示出较高的预测准确性(R² = 0.996;调整后R² = 0.987)。清除剂和光致发光分析表明,羟基自由基(·OH)是主要的反应物种,占降解活性的80%以上。DEX@nCPs(DEX)/Fe(II)/OA系统为减轻水中的药物污染物提供了一种有前景的方法,有助于实现更可持续的环境管理实践。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec1c/11923643/6dc6f8662775/ao4c09460_0001.jpg

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