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使用生物炭负载的绿色合成磁铁矿催化剂对实际工业废水中的有机污染物进行高效氧化降解。

Efficient oxidative degradation of organic pollutants in real industrial effluents using a green-synthesized magnetite supported on biochar catalyst.

作者信息

Gaber Mohamed Mohamed, Toghan Arafat, Shokry Hassan, Samy Mahmoud

机构信息

Environmental Engineering Department, Faculty of Engineering, Egypt-Japan University of Science and Technology (E-JUST) P.O. Box 179, New Borg El-Arab City 21934 Alexandria Egypt

Chemistry Department, College of Science, Imam Mohammad Ibn Saud Islamic University (IMSIU) Riyadh 11623 Saudi Arabia.

出版信息

RSC Adv. 2025 Sep 2;15(38):31522-31538. doi: 10.1039/d5ra04070a. eCollection 2025 Aug 29.

Abstract

This study investigated the degradation of tetracycline (TCN) antibiotic catalytic activation of periodate (PI, IO ) using a novel composite catalyst composed of green-synthesized magnetite nanoparticles supported on water lettuce-derived biochar (MWLB). Characterization results revealed that the magnetic biochar possessed a porous structure, abundant surface functional groups, and high carbon and iron contents. Compared to conventional oxidants such as persulfate, hydrogen peroxide, and peroxymonosulfate, the PI-activated system demonstrated superior degradation efficiency. Process optimization response surface methodology identified the optimal conditions as follows: PI concentration of 2.05 mM, TCN concentration of 16.52 mg L, and catalyst dosage of 0.83 g L. Under these conditions, the system achieved 99.64% TCN degradation and 72.14% total organic carbon mineralization. Additionally, the system effectively degraded other persistent organic pollutants, including paracetamol, chlorpyrifos, atrazine, and methylene blue, demonstrating its universality. Mechanistic investigations identified iodate radicals as the dominant reactive species responsible for TCN degradation. The magnetized biochar displayed a remarkable reusability with only a 2.5% reduction in TCN degradation ratio after five repeated cycles. The TCN degradation by-products were identified, and the proposed TCN degradation pathways indicated its transformation into simpler intermediates. A removal ratio of 73.95% was accomplished in the case of tetracycline-laden real pharmaceutical effluent confirming the system's practical applicability. This study presents a sustainable, cost-effective, and efficient PI activator for wastewater remediation that can be utilized in real applications.

摘要

本研究使用一种新型复合催化剂——负载在水葫芦衍生生物炭上的绿色合成磁铁矿纳米颗粒(MWLB),研究了过碘酸盐(PI,IO₄⁻)催化活化对四环素(TCN)抗生素的降解情况。表征结果表明,磁性生物炭具有多孔结构、丰富的表面官能团以及高碳和铁含量。与过硫酸盐、过氧化氢和过一硫酸盐等传统氧化剂相比,PI活化体系表现出更高的降解效率。采用响应面法对工艺进行优化,确定了最佳条件如下:PI浓度为2.05 mM,TCN浓度为16.52 mg/L,催化剂用量为0.83 g/L。在此条件下,该体系实现了99.64%的TCN降解率和72.14%的总有机碳矿化率。此外,该体系还能有效降解其他持久性有机污染物,包括对乙酰氨基酚、毒死蜱、阿特拉津和亚甲基蓝,证明了其通用性。机理研究确定碘酸根自由基是导致TCN降解的主要活性物种。磁化生物炭具有显著的可重复使用性,经过五次重复循环后,TCN降解率仅降低2.5%。鉴定了TCN降解副产物,并提出了TCN降解途径,表明其转化为更简单的中间体。对于含四环素的实际制药废水,去除率达到73.95%,证实了该体系的实际适用性。本研究提出了一种可持续、经济高效的PI活化剂用于废水修复,可应用于实际场景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39df/12403054/2d6a08d8124d/d5ra04070a-f1.jpg

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