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预磁化 Fe-C 激活过硫酸盐强化降解 2,4-二氯苯氧乙酸:影响因素、机制和降解途径。

Enhanced degradation of 2,4-dichlorophenoxyacetic acid by pre-magnetization Fe-C activated persulfate: Influential factors, mechanism and degradation pathway.

机构信息

School of Environment, Henan Normal University, Xinxiang 453000, China; Key Laboratory of Yellow River and Huai River Water Environment and Pollution Control, Ministry of Education, Xinxiang 453000, China; Henan Key Laboratory for Environmental Pollution Control, Xinxiang 453000, China; Key Laboratory of Pollution Process and Environmental Criteria, Ministry of Education, College of Environmental Science and Engineering, Nankai University, Tianjin 300350, China; Tianjin Key Laboratory of Urban Ecology Environmental Remediation and Pollution Control, College of Environmental Science and Engineering, Nankai University, Tianjin 300350, China; Tianjin Advanced Water Treatment Technology International Joint Research Center, College of Environmental Science and Engineering, Nankai University, Tianjin 300350, China.

Key Laboratory of Pollution Process and Environmental Criteria, Ministry of Education, College of Environmental Science and Engineering, Nankai University, Tianjin 300350, China; Tianjin Key Laboratory of Urban Ecology Environmental Remediation and Pollution Control, College of Environmental Science and Engineering, Nankai University, Tianjin 300350, China; Tianjin Advanced Water Treatment Technology International Joint Research Center, College of Environmental Science and Engineering, Nankai University, Tianjin 300350, China.

出版信息

J Hazard Mater. 2018 Jul 5;353:454-465. doi: 10.1016/j.jhazmat.2018.04.035. Epub 2018 Apr 21.

Abstract

2,4-dichlorophenoxyacetic acid (2,4-D) is one of the most applicable herbicides in the world, its residue in aquatic environment threatens the human health and ecosystems. In this study, for the first time, inexpensive Fe-C after pre-magnetization (Pre-Fe-C) was used as the heterogeneous catalyst to activate persulfate (PS) for 2,4-D degradation, proving that Pre-Fe-C could significantly improve the degradation and dechlorination. The results indicated the stability and reusability of Pre-Fe-C were much better than pre-magnetization Fe (Pre-Fe), while the leaching iron ion was lower, indicating that using Pre-Fe-C not only reduced the post-treatment cost, but also enhanced the removal and dechlorination efficiency of 2,4-D. Several important parameters including initial pH, Fe-C dosage, PS concentration affecting 2,4-D degradation and dechlorination by Pre-Fe-C/PS were investigated and compared with that of Fe-C/PS, observing a 1.2-2.7 fold enhancement in the degradation rate of 2,4-D. The Fe-C and Pre-Fe-C were characterized by scanning electron microscopy (SEM), energy dispersive X-ray (EDX) and SEM-EDX-mapping, suggesting that the content of Fe and O changed more obviously after magnetization. The degradation intermediates, such as chloroquinol, 2-chlorophenol, were identified by a gas chromatography mass spectrometry (GC/MS) and an ion chromatography (IC), and a possible degradation pathway was proposed.

摘要

2,4-二氯苯氧乙酸(2,4-D)是世界上应用最广泛的除草剂之一,其在水生环境中的残留威胁着人类健康和生态系统。在这项研究中,首次使用廉价的预磁化 Fe-C(Pre-Fe-C)作为非均相催化剂来激活过硫酸盐(PS)降解 2,4-D,证明 Pre-Fe-C 可以显著提高降解和脱氯效率。结果表明,Pre-Fe-C 的稳定性和可重复使用性明显优于预磁化 Fe(Pre-Fe),而浸出铁离子较低,表明使用 Pre-Fe-C 不仅降低了后处理成本,而且提高了 2,4-D 的去除和脱氯效率。研究了初始 pH 值、Fe-C 用量、PS 浓度等几个重要参数对 Pre-Fe-C/PS 降解和脱氯 2,4-D 的影响,并与 Fe-C/PS 进行了比较,观察到 2,4-D 的降解速率提高了 1.2-2.7 倍。通过扫描电子显微镜(SEM)、能谱(EDX)和 SEM-EDX 映射对 Fe-C 和 Pre-Fe-C 进行了表征,表明磁化后 Fe 和 O 的含量变化更为明显。通过气相色谱质谱(GC/MS)和离子色谱(IC)鉴定了降解中间体,如氯喹醇、2-氯苯酚等,并提出了可能的降解途径。

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