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ZnFe/BC活化过硫酸盐降解金橙Ⅱ 被引量:10

Degradation of Orange Ⅱ by ZnFe/BC catalyzed persulfate
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摘要 为了研究ZnFe/BC在常温下活化过硫酸盐(PS)产生硫酸根自由基(SO_4^(·-))降解酸性偶氮染料金橙Ⅱ(AOⅡ)的效能,采用水热合成法制备了ZnFe/BC催化剂,并用X射线衍射(XRD)和扫描电子显微镜-能谱分析(SEM-EDS)对其形貌与负载成分进行了表征,结果显示生物炭上负载的球状颗粒物为ZnFe_2O_4和Fe_3O_4.考察了ZnFe/BC投加量、PS投加量、AOⅡ初始浓度以及初始pH对ZnFe/BC/PS体系降解AOⅡ效果的影响.结果显示,ZnFe/BC和PS投量的增加对AOⅡ的去除率均有提升效果,而随着AOⅡ初始浓度的增加,金橙Ⅱ的去除率逐渐降低,在初始pH值在3—10范围内,ZnFe/BC对PS均有较高的催化活性.ZnFe/BC催化剂投加量为0.5 g·L^(-1),PS投加量为5 mmol·L^(-1),溶液pH为初始值为6,反应90 min后,50 mg·L^(-1)金橙Ⅱ的脱色率可达到93.7%,而且其降解速率符合拟一级反应动力学.延长反应时间至180 min,TOC去除率达到39.7%.通过对催化剂ZnFe/BC稳定性研究,发现经4次连续循环使用后,金橙Ⅱ脱色率仍然可保持在85%以上,说明该催化剂具有良好的循环使用性能.通过投加对苯醌、乙醇和叔丁醇等3种不同种类的猝灭剂,证实了ZnFe/BC/PS体系中具有SO_4^(·-)、·OH和O_2^(·-)活性物种.发芽实验证明,在反应时间为180 min内,金橙Ⅱ降解出水对小麦发芽的抑制率随反应时间的进行而先升高而逐渐降低,最后基本无抑制. In order to study the effect of sulfate radical (SO4^·-) on the degradation of acid azo dye orange Ⅱ (AOⅡ) by ZnFe/BC activated sulfate persulfate (PS) at room temperature, ZnFe/BC catalyst was prepared by hydrothermal synthesis method. The structure of ZnFe/BC was characterized by X ray diffraction (XRD) and scanning electron microscope-energy dispersive spectrometer (SEM-EDS). The results showed that spherical particle loaded on biochar (BC) was ZnFe2O4 and Fe3O4. The effect of ZnFe/BC dosage, PS concentration, initial AOⅡ concentration and initial pH on the degradation of AOⅡ in ZnFe/BC/PS system was investigated. The results showed that the removal rate of AOⅡ increased with the increase of ZnFe/BC dosage and PS concentration while it decreased when the initial AOⅡ concentration increased. When the initial pH was in range of 3-10, ZnFe/BC has high catalytic activity for PS. When ZnFe/BC addition was 0.5 g·L^-1, PS concentration was 5 mmol·L-1, the initial pH was 6, and the initial AOⅡ concentration was 50 mg·L^-1, the AOⅡ decolorization could reach 93.7% after reaction 90 min, and the degradation rate was accorded with the pseudo first order reaction kinetics. Extending the reaction time to 180min, the TOC removal rate reached 39.7%. The AOⅡ decolorization rate could still remain above 85% when ZnFe/BC was used for 4 continuous cycles in ZnFe/BC/PS system, which indicating that the catalyst had a good recycling performance. Three different kinds of quenching agents (p-benzoquinone, ethanol and tert-butyl alcohol) were added to the ZnFe/BC/PS system for AOⅡ degradation, respectively, and the result confirmed that active species SO4^·-,·OH and O2^·- consisted in ZnFe/BC/PS system. The germination experiment showed that among 180 min of the AOⅡ degradation reaction time, the inhibition rate of the effluent from AOⅡ degradation to wheat germination increased first, and then gradually decreased. Finally, the inhibition rate dropped down to near 0.
作者 王艳 杨硕 张米雪 李璨 姚真真 周璐璐 WANG Yan;YANG Shuo;ZHANG Mixue;LI Can;YAO Zhenzhen;ZHOU Lulu(College of Resource and Environment Anhui Science and Technology University, Fengyang, 233100, China)
出处 《环境化学》 CAS CSCD 北大核心 2018年第12期2630-2637,共8页 Environmental Chemistry
基金 安徽省自然科学基金(1808085MB49) 安徽省教育厅重点项目(KJ2016A178) 安徽省高校优秀中青年骨干人才国内外访学研修(gxfx ZD2016179) 安徽科技学院优秀中青年骨干教师和国家级大学生创新创业训练计划(201710879023)资助~~
关键词 过硫酸盐 金橙Ⅱ 自由基 催化氧化 persulfate orange Ⅱ free radical catalytic oxidation
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  • 1魏树和,周启星,Pavel V.Koval,Galina A.Belogolova.有机污染环境植物修复技术[J].生态学杂志,2006,25(6):716-721. 被引量:32
  • 2陈连山.炼焦气脱硫废液中的硫氰酸钠和硫代硫酸钠的连续测定[J].分析化学,2002,5(4):288-290.
  • 3Rao Y F, Qu L, Yang H, et al. Degradation of carbamazepine by Fe ( H ) -activated persulfate process [ J ]. Journal of Hazardous Materials, 2014, 268:23-32.
  • 4Liang C, Liang C P, Chen C C. pH dependence of persulfate activation by EDTA/Fe( Ill ) for degradation of trichloroethylene[ J]. Journal of Contaminant Hydrology, 2009, 106(3-4) : 173- 182.
  • 5Waldemer R H, Tratnyek P G, Johnson R L, et al. Oxidation of chlorinated ethenes by heat activated persulfate : kinetics and products [J]. Environ Sci Technol, 2007, 41(3) : 1010-1015.
  • 6Kang S H, Choi W. Oxidative degradation of organic compounds using zero-valent iron in the presence of natural organic matter serving as an electron shuttle [ J ]. Environ Sci Technol, 2009, 43 (3) : 878-883.
  • 7Leng Y, Guo W, Shi X, et al. Polyhydroquinone-coated Fe3 04 nanocatalyst for degradation of rhodamine B based on sulfate radicals [ J ]. Industrial & Engineering Chemistry Research, 2013, 52 (38) :13607-13612.
  • 8Taguchi K, Fujii S, Yamano S, et al. An approach to evaluate two-electron reduction of 9,10-phenanthraquinone and redox activity of the hydroquinone associated with oxidative stress [ J]. Free Radical Bio Med, 2007, 43 (5) :789-799.
  • 9Chen R, Pignatello J J. Role of quinone intermediates as electron shuttles in Fenton and photoassisted Fenton oxidations of aromatic compounds[ J]. Environ Sci Technol, 1997, 31 (8) : 2399-2406.
  • 10Fang G, Gao J, Dionysiou D D, et al. Activation of persulfate by quinones: free radical reactions and implication for the degradation of PCBs[J]. Environ Sci Technol, 2013, 47(9) : 4605-4611.

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