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铁钴金属氧化物活化过硫酸盐降解水中苯并噻唑

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随着经济的发展,各类化学品的大量使用产生了许多新兴污染物,目前如何处理这些新兴污染物已成为环境领域研究的热点.作为一种常用的化工产品,苯并噻唑(BZA)已成为水中新兴的有毒化合物,对水生生态环境和饮用水安全构成了较大的威胁.试验通过溶胶凝胶法制备FeCo2O4纳米材料,利用XPS(X射线光电子能谱)、HRTEM(高分辨率透射电镜能谱)、SEM(扫描电镜能谱)和XRD(X射线衍射)对BZA进行表征.以水中的BZA为目标物,基于过单硫酸盐(PMS)的高级氧化技术,对FeCo2O4活化PMS降解BZA的效果进行试验,并探讨了影响因素和降解机理.试验结果表明:当加入0.3 g/L的FeCo2O4和3 mmol/L的PMS时,在90 min内能完全降解BZA,同时FeCo2O4在循环使用4次后仍对污染物有76.90%的降解率,FeCo2O4纳米材料活化PMS对水中的BZA降解效果明显.其中自由基SO·-4对降解BZA起着主导作用,水中常见的阴离子HCO-3会促进体系对BZA的降解,而腐殖酸和Cl-起抑制作用.
Iron-cobalt metal oxide activated persulfate degrades benzothiazole in water
With the development of the economy,the extensive use of various chemicals has led to the emergence of new pollutants,creating a challenge in environmental research.One such contaminant is benzothiazole (BZA)that poses a significant threat to aquatic ecosystems and the safety of drinking water.In this study,FeCo2O4 nanomaterials were prepared by sol-gel method and characterized by XPS (X-ray photoelectron spectroscopy ),HRTEM (High resolution transmission electron microscopy ),SEM (Scanning electron microscopy ) and XRD (X-ray diffraction).The degradation of BZA in water was tested using persulfate (PMS)advanced oxidation technology,with FeCo2O4 acting as catalyst to activate PMS.Various influencing factors and degradation mechanism were also discussed.Results show that with the addition of 0.3 g/L FeCo2O4 and 3 mmol/L PMS,BZA was completely removed within 90 min.Even after four cycles FeCo2O4 maintained a 76.90% removal efficacy.The degradation process primarily involved SO·-4,which played a leading role in BZA degradation.Additionally,common anion HCO-3 promoted BZA degradation,whereas humic acid and Cl-inhibited the process.

iron-cobalt metal oxidesbenzothiazolepersulfateinfluencing factorsdegradation mechanism

丁春生、潘宇强、雷佳、张航天

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浙江工业大学 土木工程学院,浙江 杭州 310023

铁钴金属氧化物 苯并噻唑 过单硫酸盐 影响因素 降解机理

2025

浙江工业大学学报
浙江工业大学

浙江工业大学学报

北大核心
影响因子:0.704
ISSN:1006-4303
年,卷(期):2025.53(1)