281 | 9 | 4 |
下载次数 | 被引频次 | 阅读次数 |
研究了在高压汞灯(300nm)光照下4种FeIII-多羧酸盐络合物(FeIII-柠檬酸,FeIII-草酸钠,FeIII-酒石酸钾,FeIII-EDTA)对CrVI的光还原试验,比较了它们光还原Cr(VI)的反应速率.具体研究了在FeIII-草酸钠体系中CrVI)的光还原.探讨了各种影响因素:初始pH值,FeIII、草酸盐、CrVI的初始浓度,以及FeIII∶草酸盐的配比,光照强度等对CrVI光还原的影响.结果表明:在不同光化学体系中光还原CrVI的速率在不加FeIII时,光还原CrVI的速率由大到小依次为:EDTA、草酸钠、柠檬酸钠、酒石酸钾.在FeIII-多羧酸盐络合物体系中CrVI的光还原速率由大到小依次为FeIII-酒石酸钾、FeIII-EDTA、FeIII-柠檬酸钠、FeIII-草酸钠.在FeIII-草酸钠体系中CrVI的光还原速率随着pH值的增大而减小;随FeIII、草酸钠初始浓度的增加而增加,而随CrVI初始浓度的增加,光还原CrVI的速率是减少的.
Abstract:The photochemical reduction of Cr(VI) by Fe(III)-carboxylic salts under the radiation of high-pressure mercury lamp ( 300 nm) containing Fe(III)-citrate complex, Fe(III)-oxalate complex, Fe(III)-tartrate complex, Fe(III)-EDTA are studied and comparing the photoreduction rates. Fe (III)-oxalate complexes were elected to be studied photoreduct Cr(VI). The effects of the initial solution pH value, the initial concentrations of Fe(III), oxalate and Cr(VI) and the ratio Fe(III): oxalate, the light intensity were studied. The results indicate that the rates of photoreduction Cr(VI) decreased from EDTA, oxalate complexes, citrate to tartrate system without Fe(III); but decreased from Fe III -tartrate complexes, Fe III -EDTA complexes, Fe III -citrate complexes, to Fe(III)-oxalate complexes system with Fe(III). The rates of photoreduction Cr(VI) increased with increasing the initial concentrations of Fe(III) and oxalate, however, decreased with increasing the initial concentrations of Cr(VI).
[1]Kota J,Stasicka Z.Chromium occurrence in the environ-ment and methods of its speciation[J].Environ Pollut,2000,107(3):263-283.
[2]彭国胜.光催化处理含铬废水的研究[J].河南科学,2002,20(4):385-387.
[3]邓南圣,吴峰,封享华,等.铬(Ⅵ)在铁(III)-丙酮酸盐体系中的紫外光还原研究[J].环境科学学报,2005,25(7):896-900.
[4]刘淼,董德明,杨全明,等.光催化处理电镀含铬(Ⅵ)废液[J].吉林大学自然科学学报,1998,(2):99-101.
[5]Eary L E,Rai D.Chromate removal from aqueous wastes by reduction with ferrous ion[J].Environ Sci Technol,1988,22(8):972-977.
[6]Kanki T,Yoneda H,Sano N,et al.Photocatalytic reduction and deposition of metallic ions in aqueous phase[J].Chem Eng J,2004,97(1):77-81.
[7]Faust B C,HoignéJ.Photohysis of Fe(III)-hydroxy com-plex as sources of OH radicals in clouds fog and rain[J].Atmospheric Environment,1990,24A(2):79-89.
[8]Zhang Z,Wu F,Deng N S.Photochemical reduction of Cr(VI)in aqueous solutions containing Fe(III)-hydroxy com-plexes[J].Toxicological and Environ Chem,2001,82(3-4):129-137.
[9]Zuo Y,HoignéJ.Formation of hydrogen peroxide and de-pletion of oxalic acid in atmospheric water by photoysis of iron(III)-oxalate complexes[J].Environ Sci Technol,26(5):1014-1022.
[10]中国标准出版社第二编辑室.中国环境保护标准汇编水质分析方法[M].北京:中国标准出版社,2001.
[11]邓南圣,吴峰,Nikolai Bazhin,等.铁(III)-丙酮酸盐配合物光解引发水中铬(Ⅵ)还原[J].环境化学,2005,24(3):307-310.
[12]Buerge I J,Hug S J.Kinetics and pH dependence of chro-mium(VI)reduction by iron(III)[J].Environ Sci Technol,1997,31(5):1426-1432.
基本信息:
DOI:
中图分类号:O641.4;O643.32
引用信息:
[1]刘延湘,刘君侠,吴荣等.Fe(Ⅲ)-多羧酸盐配合物光催化还原Cr(Ⅵ)[J].江汉大学学报(自然科学版),2006(04):40-43.
基金信息: