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聚多巴胺/聚乙烯亚胺复合非织造布/Fe^2+活化过硫酸盐催化氧化酸性红B的效果分析 被引量:2

Effect analysis of catalytic oxidation of acid red B by polydopamine/polyethyleneimine nonwoven/Fe^2+activated persulfate
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摘要 以聚丙烯(PP)非织造布为基体,采用多巴胺聚乙烯亚胺共沉积法制备了聚多巴胺/聚乙烯亚胺复合非织造布(PDA/PEI@PP),研究了PDA/PEI@PP在Fe^2+活化过硫酸盐(PS)降解酸性红B(ARB)的中的性能和反应机理。通过SEM对材料结构进行了表征,考察了不同体系(PS、PDA/PEI@PP/PS、Fe^2+/PS和PDA/PEI@PP/Fe^2+/PS)中ARB的降解效果,通过电子自旋共振波谱(ESR)和傅里叶红外光谱(FT-IR)分析了PDA/PEI@PP活化PS及自由基生成的机理,此外,考察了PDA/PEI@PP对Fe^3+的还原作用。结果表明:PDA/PEI@PP非织造材料具有贯穿的孔道结构,利于PDA/PEI@PP表面官能团对PS的活化;PDA/PEI@PP对Fe^2+/PS体系的催化氧化具有促进作用,当Fe^2+初始浓度为0.5 mmol·L^−1时,90 min内对ARB的降解率为98%,反应速率常数为0.040 min^−1;在不添加Fe^2+的情况下,PDA/PEI@PP可直接活化PS产生自由基降解ARB,降解率为56%;PDA/PEI@PP表面的邻苯二酚基团与邻醌基反应生成半醌,从而活化PS产生硫酸根自由基(SO4^-)和羟基自由基(·OH);同时PDA/PEI@PP表面的邻苯二酚基团也对Fe^3+具有还原作用,生成Fe^2+持续活化PS。因此,PDA/PEI@PP对于Fe^2+活化PS的促进作用主要是通过PDA/PEI@PP对PS协同活化和对Fe^3+的还原作用来实现的。本研究为进一步提高Fe^2+活化PS氧化降解染料废水的效率提供了一种较好的解决方案。 In this study,polypropylene(PP)nonwoven was taken as matrix,the co-deposition method of dopamine and polyethyleneimine was used to prepare the polydopamine/polyethyleneimine-functionalized polypropylene nonwoven(PDA/PEI@PP).The performance and mechanism of PDA/PEI@PP on Fe^2+activated persulfate(PS)and degrading acid red B(ARB)were studied.SEM was used to characterize the PDA/PEI@PP material.The ARB degradation effects in different systems of PS,PDA/PEI@PP/PS,Fe^2+/PS and PDA/PEI@PP/Fe^2+/PS were also studied.Electron spin-resonance spectroscopy(ESR)and Fourier transform infrared(FT-IR)were used to identify the mechanism of PDA/PEI@PP activated PS and radicals formation.In addition,the reduction of Fe^3+by PDA/PEI@PP was investigated.The results showed that the throughout pore structure was presented in PDA/PEI@PP nonwoven material,which facilitated PS activation by the surface functional groups of PDA/PEI@PP.PDA/PEI@PP could promote the catalytic oxidation of Fe^2+/PS system,the degradation rate of ARB could reach 98%within 90 min when the initial content of Fe^2+was 0.5 mmol·L^−1,and the reaction rate constant was 0.040 min^−1.Without the addition of Fe^2+,PDA/PEI@PP could directly activate PS,produce radicals for ARB degradation with a rate of 56%.On the surface of PDA/PEI@PP,the catechol groups reacted with o-quinone groups to produce semiquinone,which could activate PS and produce sulfate radical(SO4^-)and hydroxyl radical(·OH).At the same time,the catechol groups on the surface of PDA/PEI@PP also could reduce the Fe3+to Fe2+,which could sustainably activate PS.Therefore,the promoting effects of PDA/PEI@PP on Fe^2+activated PS are mainly due to the synergetic activation of PS and Fe^3+reduction by PDA/PEI@PP.The study provides a better solution for further improving the efficiency of oxidation degradation of dye wastewater by Fe^2+activated PS.
作者 秦文欣 张环 李欣 胥京福 屈静 吴茜 QIN Wenxin;ZHANG Huan;LI Xin;XU Jingfu;QU Jing;WU Qian(School of Environmental Science and Engineering,Tiangong University,Tianjin 300387,China;State Key Laboratory of Separation Membranes and Membrane Processes,Tiangong University,Tianjin 300387,China)
出处 《环境工程学报》 CAS CSCD 北大核心 2020年第12期3290-3297,共8页 Chinese Journal of Environmental Engineering
基金 国家自然科学基金资助项目(51678409) 天津市高等学校创新团队培养计划项目(TD13-5042)。
关键词 聚多巴胺/聚乙烯亚胺复合非织造布(PDA/PEI@PP) 邻苯二酚基团 邻醌基 FE^2+ 过硫酸盐 酸性红B polydopamine/polyethyleneimine-functionalized polypropylene nonwoven(PDA/PEI@PP) catechol group o-quinone group ferrous iron persulfate acid red B
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  • 1李华文,刘燕群,石丹,张江华,郝巧玲,吕斌,周宜开.双酚A对人胚肝细胞L-02的毒性作用研究[J].环境与职业医学,2005,22(2):102-104. 被引量:11
  • 2潘晶,陈永强,索艳丽,孙铁珩.溶液中阴离子对UV/H_2O_2降解十二烷基苯磺酸钠的影响及其机理[J].环境污染与防治,2007,29(8):575-577. 被引量:5
  • 3Liang Chenju, Wang Z. S. , Mohanty N. Influences of car- bonate and chloride ions on persulfate oxidation of trichloro- ethylene at 20~C. Science of the Total Environment, 2006, 370 ( 2-3 ) : 271-277.
  • 4Khan N. E. , Adewuyi Y. G. Absorption and oxidation of nitric oxide (NO) by aqueous solutions of sodium persul- fate in a bubble column reactor. Industrial & Engineering Chemistry Research, 2010, 49 ( 18 ) : 8749-8759.
  • 5Waldemer R. H. , Tratnyek P. G. , Johnson R. L. , et al. Oxidation of chlorinated ethenes by heat-activated persul- fate: Kinetics and products. Environmental Science & Technology, 2007, 41(3) : 1010-1015.
  • 6House D. A. Kinetics and mechanism of oxidations by per- oxydisulfate. Chemical Reviews, 1962, 62 (3) : 185-203.
  • 7Tsitonaki A. , Petri B. , Crimi M. , et al. In situ chemical oxidation of contaminated soil and groundwater using per- sulfate: A review. Critical Reviews in Environmental Sci- ence and Technology, 2010, 40( 1 ) : 55-91.
  • 8Liang Chenju, Bruell C. J. , Marley M. C. , et al. Persul- fate oxidation for in situ remediation of TCE. I. Activatedby ferrous ion with and without a persulfate-thiosulfate red- ox couple. Chemosphere, 2004, 55(9) : 1213-1223.
  • 9Kent D. B. , DavisJ. A. , JoyeJ. L., et al. Influence of variable chemical conditions on EDTA-enhanced transport of metal ions in mildly acidic groundwater. Environmental Pollution, 2008, 153( 1 ) : 44-52.
  • 10Tsang D. C. W., Zhang Weihua, Lo I. M. C. Copper ex- traction effectiveness and soil dissolution issues of EDTA- flushing of artificially contaminated soils. Chemosphere, 2007, 68 ( 2 ) : 234-243.

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