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纳米Fe3O4/CeO2-H2O2非均相类Fenton体系对3,4-二氯三氟甲苯的降解
摘要点击 2068  全文点击 937  投稿时间:2014-11-28  修订日期:2015-01-25
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中文关键词  纳米Fe3O4/CeO2  影响因素  非均相类Fenton体系  3,4-二氯三氟甲苯(3,4-DCBTE)
英文关键词  nanoscale Fe3O4/CeO2  influence factor  heterogeneous Fenton-like system  3,4-Dichlorobenzotrifluoride (3,4-DCBTE)
作者单位E-mail
孙正男 中国地质大学(北京)水资源与环境学院, 北京水资源与环境工程重点实验室, 北京 100083 453106324@qq.com 
杨琦 中国地质大学(北京)水资源与环境学院, 北京水资源与环境工程重点实验室, 北京 100083 yq@cugb.edu.cn 
纪冬丽 中国地质大学(北京)水资源与环境学院, 北京水资源与环境工程重点实验室, 北京 100083  
郑琳 中国地质大学(北京)水资源与环境学院, 北京水资源与环境工程重点实验室, 北京 100083  
中文摘要
      以浸渍法制备的新型纳米Fe3O4/CeO2为催化剂,3,4-二氯三氟甲苯(3,4-DCBTE)为目标污染物,在Fe3O4/CeO2-H2O2非均相类Fenton体系中对目标污染物的降解进行研究,考察催化剂的催化效果和温度、pH、H2O2投加量等因素对催化剂催化效果的影响. 结果表明,以纳米Fe3O4/CeO2作为催化剂的非均相类Fenton体系对3,4-二氯三氟甲苯的处理效果极佳;随着温度的升高,纳米Fe3O4/CeO2的催化效果不断提高;在偏酸性环境中,pH越低催化效果越好,pH=2时反应去除效率可达96.67%;随着H2O2投加量的增加, 3,4-二氯三氟甲苯的降解效率先提高后降低,投加量为15 mg·L-1时去除效果最好可达99.47%;随着催化剂投加量的增加,同样出现了处理效果先升高后降低的现象,投加量为0.5 g·L-1时催化效果最好可达99.64%. 在以纳米Fe3O4/CeO2为催化剂的非均相类Fenton体系中, 3,4-二氯三氟甲苯的降解符合一级反应动力学,反应所需活化能较低只需30.26 kJ·mol-1.
英文摘要
      The 3,4-Dichlorobenzotrifluoride (3,4-DCBTE) was dehalogenated with oxidation treatment by heterogeneous Fenton-like system, using nanoscale Fe3O4/CeO2 as a catalyst. This nanoscale catalyst was prepared by the impregnated method. As a highly active new heterogeneous Fenton-like catalyst, nanoscale Fe3O4/CeO2 not only has the characteristics of the traditional Fenton-like catalyst but also can prevent the secondary pollution which caused by Fe2+. To find the optimum catalytic conditions for nanoscale Fe3O4/CeO2, the influence factors were investigated. The results indicated that the degradation ratio of 3,4-DCBTE was significantly improved by adding nanoscale Fe3O4/CeO2, with the removal ratio reaching 97.76% in 120 minutes and 79.85% in 20 minutes. As the temperature increasing, the catalytic effect of nanoscale Fe3O4/CeO2 catalyst had been constantly improved obviously. As the pH decreased, the degradation ratio of 3,4-DCBTE increased. With the increase of dosage of hydrogen peroxide (H2O2), the degradation efficiency of 3,4-DCBTE initially increased and then decreased, because oxygen (O2) was generated in preferential self-reaction when an excess of (H2O2) was added. The optimum removal efficiency was observed with the dosage of 15 mg·L-1. With the increased amount of catalyst, there was a same trend as dosage of hydrogen peroxide (H2O2). The degradation ratio of 3,4-DCBTE initially increased and then decreased, the optimum amount of catalyst was 0.5 g·L-1. The results also suggested that the reaction process followed the first-order kinetics and the thermodynamic analysis demonstrated that the reaction was only needed low reaction activation energy.

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