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环境修复中锰氧化物与变价重金属交互作用的研究进展 被引量:12

Interaction of manganese oxides with multiple valences heavy metals in environmental remediation
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摘要 氧化-还原过程是影响重金属环境行为的重要过程.锰氧化物作为重要的天然氧化剂,通过对变价重金属的氧化还原和吸附作用,影响着其在环境中的形态、生物有效性乃至归趋,具有很高的环境修复潜力和应用价值.近年来对锰氧化物和变价重金属元素的研究主要集中在以下几个方面:生物氧化锰的形成与多铜氧化酶体系的关系;锰氧化物与变价重金属的交互作用的机制及其影响因素,尤其锰氧化物的空间结构和作用位点的影响.目前,锰氧化物在环境修复中的应用主要集中在水环境修复方面,土壤体系及土壤微界面还很鲜见.同时土壤体系中影响锰氧化物与重金属交互作用的因素更多,其过程也更为复杂.本文通过总结锰氧化物与变价重金属交互作用的研究进展,对比不同重金属种类之间反应机制的差别,为更好的理解锰氧化物的环境作用提供基础,也期望能够进一步拓展其在污染环境的修复中的应用范围. Redox reaction plays an important role in the biogeochemical cycles of heavy metals.Manganese oxides,as an important natural oxidant,affect the speciation and bioavailability of the multiple valences heavy metals by redox reactions and adsorption,thus are provided with a high potential for environmental remediation.This study is mainly focused on the interaction of manganese oxides with multiple valences heavy metals,including the relationship between biogenic manganese oxide formation and multi-copper oxidase and the influences from the spatial structures of manganese oxides and their active sites.Currently,the application of manganese oxides in the environment is mainly in the remediation of aquatic environment,while the application in the soil system remains rare.However,since the complicated characteristics of soil system,more factors should exist in affecting the interaction of manganese oxides with heavy metals.In this review,we summarize the research progresses of the interaction mechanisms of manganese oxides with multiple valences heavy metals and compare their differences,and then provide a basis for a better understanding of environmental behaviors of the manganese oxides and further promotion of their application in environment remediation.
出处 《环境科学学报》 CAS CSCD 北大核心 2013年第6期1519-1526,共8页 Acta Scientiae Circumstantiae
基金 国家自然科学基金项目(No.41071163) 中国科学院青年创新促进会人才项目~~
关键词 环境修复 锰氧化物 变价重金属 氧化还原 生物氧化锰 environment remediation manganese oxides multiple valences heavy metal redox reaction biogenic manganese oxides
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  • 1Apte A D, Tare V, Bose P. 2006. Extent of oxidation of Cr(Ⅲ) to Cr (VI) under various conditions pertaining to natural environment [ J]. Journal of Hazardous Materials, 128 (2/3) : 164-174.
  • 2Arai Y, Elzinga E J, Sparks D L. 2001. X-ray absorpt ion spectroscopic investigation of arsenite and arsenate adsorption at the aluminum oxidewater interface [ J]. Colloid Interface Science, 235 : 80-88.
  • 3Banerjee D, Nesbitt H W. 1999a. Oxidation of aqueous Cr(Ⅲ) at birnessite surfaces: Constraints on reaction mechanism [ J ]. Geochimica et Cosmochimica Acta, 63 : 1671-1687.
  • 4Banerjee D, Nesbitt H W. 1999b. XPS study of reductive dissolution of birnessite by oxalate: Rates and mechanistic aspects of dissolution and redox processes [ J]. Geochlmica et Cosmochimica Acta, 63: 3025 -3038.
  • 5Bartlett R, James B. 1979. Behavior of chromium in soils: Ⅲ. Oxidation [J]. Environment Quality, 8:31-35.
  • 6Borch T, Kretzschmar R, Kapple A,et al. 2010. Biogeochemical redox processes and their impact on contaminant Dynamics [ J ]. Environmental Science & Technology, 44:15-23.
  • 7Cooper G R. 2002. Oxidation and toxicity of chromium in uhramafic soils in Zimbabwe [ J ]. Applied Geochemistry, 17 : 981-986.
  • 8Chinni S, Anderson C R, Ulrich K, et al. 2005. Indirect UO2 oxidation by Mn( Ⅱ )-oxidizing spores of bacillussp: Strain SG- 1 and the Effect of U and Mn concentrations [ J ]. Environmental Science & Technology, 42 : 8709-8714.
  • 9Chiu V Q, Hering J G. 2000. Arsenic adsorption and oxidation atmanganite surfaces 1. Method for simultaneous determination of adsorbed and dissolved arsenic species [ J]. Environmental Science & Technology, 34:2029-2034.
  • 10Christ A G. 2003. Arsenic - a Review Part I: Occurrence, toxicity, speciation, mobility [ J]. Acta Hydrochimica Hydrobilogica, 31 : 9- 18.

二级参考文献20

  • 1贺纪正,李学垣,徐凤琳,王贻俊.1.4-nm Intergrade Mineral Derived From Smectite in Soils[J].Chinese Science Bulletin,1994,39(8):676-680. 被引量:1
  • 2肖雪毅,陈保冬,朱永官.丛枝菌根真菌对铜尾矿上植物生长和矿质营养的影响[J].环境科学学报,2006,26(2):312-317. 被引量:33
  • 3Haag W R, Yao C C D. 1992. Rate constants for reaction of hydroxyl radicals with several drinking water contaminants [ J ]. Environmental Science & Technology, 26 (5) : 1005-1013
  • 4Kim M J, Nriagu J. 2000. Oxidation of arsenite in groundwater using ozone and oxygen[ J]. The Science of The Total Environment, 247 : 71-79
  • 5Kusic H, Koprivanac N, Srean L. 2006. Azo dye degradation using Fenton type processes assisted by UV irradiation: A kinetic study [J]. J Photochem Photobiol A, 181 (2-3) : 195-202
  • 6Li W, Gibbs G V, Oyama S T. 1998. Mechanism of ozone decomposition on a manganese oxide catalyst. 1. in situ raman spectroscopy and ab initio molecular orbital calculations [ J ]. J of the American Chemical Soiety, 120 : 9041-9046
  • 7Moura F C C, Araujo M H, Costa R C C,et al. 2005. Efficient use of Fe metal as an electron transfer agent in a heterogeneous Fenton system based on Fe^0/Fe3 O4 composites [J]. Chemosphere, 60 (8) : 1118-1123
  • 8Nie Y, Hu C, Qu J H,et al. 2007. Photoassisted degradation of azodyes over FeO2H2x-3/Fe^0 in the presence of H2O2 at neutral pH values [J]. Environmental Science & Technology, 41:4715-4719
  • 9Nie Y, Hu C. 2008. An efficient electron transfer at the Fe^/iron oxide interface for the photoassisted degradation of pollutants with HE O2 [ J]. Applied Catalysis (B : Environmental) , 82 : 151-156
  • 10Stumm W, Sulzberger B. 1992. The cycling of iron in natural environments: considerations based on laboratory studies of heterogeneous redox processes [ J]. Geochim Cosmochim Acta, 56 : 3233-3257

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