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首页> 外文期刊>Water Research >Electrochemical enhanced heterogeneous activation of peroxydisulfate by Fe-Co/SBA-15 catalyst for the degradation of Orange Ⅱ in water
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Electrochemical enhanced heterogeneous activation of peroxydisulfate by Fe-Co/SBA-15 catalyst for the degradation of Orange Ⅱ in water

机译:Fe-Co / SBA-15催化剂对过氧二硫酸盐的电化学增强非均相活化,以降解水中的橙Ⅱ

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摘要

Mesoporous silica SBA-15 supported iron and cobalt catalysts (Fe-Co/SBA-15) were prepared and used in the electrochemical (EC) enhanced heterogeneous activation of peroxydisulfate (PDS, S_2O_8~(2-)) process for the removal of Orange Ⅱ. The effects of some important reaction parameters such as initial pH, current density, PDS concentration and dosage of Fe-Co/SBA-15 catalysts were investigated. The results showed that the decolorization efficiency was not significantly affected by the initial pH value, and it did increase with the higher PDS concentration, current density and Fe-Co/SBA-15 dosage. Both the sulfate radical (SO_4~-) and the hydroxyl radical (·OH) are considered as the primary reactive oxidants for the Orange Ⅱ decolorization. The Fe-Co/SBA-15 catalyst maintained its high activity during repeated batch experiments. The intermediate products were identified by GC-MS analysis and a plausible degradation pathway is proposed accordingly. The removal efficiencies of chemical oxygen demand (COD) and total organic carbon (TOC) were 52.1% and 31.9%, respectively after 60 min of reaction time but reached 82.9% and 51.5%, respectively when the reaction time was extended to 24 h. Toxicity tests with activated sludge indicated that the toxicity of the solution increased during the first 30 min and then decreased as the oxidation proceeded.
机译:制备了介孔二氧化硅SBA-15负载的铁和钴催化剂(Fe-Co / SBA-15),并用于过氧二硫酸盐(PDS,S_2O_8〜(2-))的电化学(EC)增强的非均相活化过程中,以去除橙子Ⅱ。研究了一些重要反应参数的影响,如初始pH,电流密度,PDS浓度和Fe-Co / SBA-15催化剂的用量。结果表明,脱色效率不受初始pH值的显着影响,并且随着PDS浓度,电流密度和Fe-Co / SBA-15剂量的增加而增加。硫酸根(SO_4〜-)和羟基(·OH)被认为是OrangeⅡ脱色的主要反应氧化剂。在重复的分批实验中,Fe-Co / SBA-15催化剂保持了高活性。通过GC-MS分析鉴定了中间产物,并据此提出了合理的降解途径。反应60分钟后,化学需氧量(COD)和总有机碳(TOC)的去除效率分别为52.1%和31.9%,而将反应时间延长至24 h则分别达到82.9%和51.5%。活性污泥的毒性试验表明,溶液的毒性在最初30分钟内增加,然后随着氧化的进行而降低。

著录项

  • 来源
    《Water Research》 |2014年第1期|473-485|共13页
  • 作者单位

    Department of Environmental Engineering, Hubei Biomass-Resource Chemistry and Environmental Biotechnology Key Laboratory, Wuhan University, Wuhan 430079, China;

    Department of Environmental Engineering, Hubei Biomass-Resource Chemistry and Environmental Biotechnology Key Laboratory, Wuhan University, Wuhan 430079, China;

    Department of Environmental Engineering, Hubei Biomass-Resource Chemistry and Environmental Biotechnology Key Laboratory, Wuhan University, Wuhan 430079, China;

    Department of Environmental Engineering, Hubei Biomass-Resource Chemistry and Environmental Biotechnology Key Laboratory, Wuhan University, Wuhan 430079, China;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Fe-Co/SBA-15; Sulfate radicals; Electrochemical; Peroxydisulfate; Mineralization;

    机译:Fe-Co / SBA-15;硫酸根;电化学;过氧二硫酸盐;矿化;

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