土壤中取代硝基苯化合物被零价铁还原的机理

陈少瑾; 陈宜菲; 张二华; 吴双桃; 谢凝子

环境化学

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陈少瑾, 陈宜菲, 张二华, 吴双桃, 谢凝子. 土壤中取代硝基苯化合物被零价铁还原的机理[J]. 环境化学, 2006, 25(3): 288-293.

引用本文:

陈少瑾, 陈宜菲, 张二华, 吴双桃, 谢凝子. 土壤中取代硝基苯化合物被零价铁还原的机理[J]. 环境化学, 2006, 25(3): 288-293.

CHEN Shao-jin, CHEN Yi-fei, ZHANG Er-hua, WU Shuang-tao, XIE Ning-zi. REDUCTION MECHANISMS OF SUBSTITUTED NITROBENZENES BY ZERO-VALENT IRON IN SOILS[J]. Environmental Chemistry, 2006, 25(3): 288-293.

Citation:

CHEN Shao-jin, CHEN Yi-fei, ZHANG Er-hua, WU Shuang-tao, XIE Ning-zi. REDUCTION MECHANISMS OF SUBSTITUTED NITROBENZENES BY ZERO-VALENT IRON IN SOILS[J]. Environmental Chemistry, 2006, 25(3): 288-293.

土壤中取代硝基苯化合物被零价铁还原的机理

1.
韩山师范学院环境化学应用技术研究所, 潮州, 521041
基金项目:
广东省自然科学基金(编号04106270)

韩山师范学院重点课题基金资助项目

REDUCTION MECHANISMS OF SUBSTITUTED NITROBENZENES BY ZERO-VALENT IRON IN SOILS

1.
Research Institute of Environmental Chemistry and Technology, Hanshan Normal University, Chaozhou, 521041, China
Fund Project:

摘要: 以气相色谱-质谱联用仪(GC-MS)分析和密度泛函理论(DFT)计算,探讨了土壤中甲基、氯代硝基苯混合物在常温常压下被零价铁还原的机理.GC-MS数据证明,取代硝基苯在土壤中被零价铁还原的主要产物是苯胺,同时还检测到微量的亚硝基苯、甲基苯二氮烯(对二甲基偶氮苯)、氯苯二氮烯(对二氯偶氮苯)等分解和缩合中间产物.理论计算表明:随还原程度的加深,对硝基甲苯和对氯硝基苯反应体系的能量从高到低,还原反应通过逐步添加质子和电子到硝基而进行,质子亲和力、电子亲和力起主导作用.逐步还原的机理合理地解释了实验中还原反应对土壤pH值的敏感以及微量中间产物的生成过程.苯环上的氯或甲基对还原反应的影响没有明显的差异.
- 零价铁 /
- 还原 /
- 硝基甲苯 /
- 氯代硝基苯
Abstract: The reduction mechanisms of mixed methyl- and chloro-substituted nitrobenzenes(SNBs) in soils at(ambient) temperature and pressure by zero valent iron(ZVI) were investigated using gas chromatography-mass spectrometry(GC-MS) as the analytical method for experiments and computational chemistry especially(density) functional theory(DFT) as the guiding principle.GC-MS data indicated that the major products of SNBs reduction by ZVI were anilines,but trace amounts of nitrosobenzenes,4,4'-dimethylazobenzene,4,4'-dichloroazobenzene and other degradation and condensation compounds were also detected as the intermediate products.DFT calculations showed that the total energies of the intermediates decreased with increasing levels of reduction for the SNBs,and the reduction seemed to be a process of step-wise additions of protons and electrons to the nitro group.This mechanism of step-wise reduction offered a reasonable explanation towards why the reduction reaction was sensitive to the soil pH as well as the formations of the detected trace intermediates.With either methyl- or chloro- substitutions,no significant differences in their impacts on the rates of reduction were observed.
- zero-valent iron /
- reduction /
- nitrobenzene /

[1]

赵珏,傅大放,曾苏,硝基芳香烃废水处理技术研究进展.环境污染治理技术与设备,2002,3 (5):31-35
[2] 肖羽堂,王继徽,二硝基氯苯废水预处理技术研究.化工环保,1997,17(5):264-286

[3] Johnson T L,Scheres M M,Tratnyek P G,Kinetics of Halogenated Organic Compound Degradation by Iron Metal.Environ.Sci.Technol.,1996,30 (8):2634-2640
[4] Hung H M,Ling F H,Hoffmann M R,Kinetics and Mechanism of the Enhanced Reductive Degradation of Nitrobenzene by Elemental Iron in the Presence of Ultrasound.Environ.Sci.Technol.,2000,34(9):1758-1763
[5] Klausen J,Rane J,Schwarzenbach R P,Influence of Solution Composition and Column Aging on the Reduction of Nitroaromatic Compounds by Zero Valent Iron.Chemosphere,2001,44(4):511-517
[6] Agrawal A,Tratnyek P G,Reduction of Nitro Aromatic Compounds by Zero-Valent Iron Metal.Environ.Sci.Technol.,1996,30(1):153-160
[7] Zilberberg Igor,Pelmenschikov Alexander,Mcgrath Christian J et al.,Reduction of Nitroaromatic Compounds on the Surface of Metallic Iron:Quantum Chemical Study.Int.J.Mol.Sci.,2002,3:801-813
[8] Ilchenko M,Gorb L,C McGrath J et al.,Molecular Models of Iron Oxide Interactions with Explosives (TNT,RDX)A Density Functional Theory Investigation.2001.In:Proceedings of the Eleventh Annual V.M.Goldschmidt Conference

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土壤中取代硝基苯化合物被零价铁还原的机理

1. 韩山师范学院环境化学应用技术研究所, 潮州, 521041

基金项目:

广东省自然科学基金(编号04106270)

韩山师范学院重点课题基金资助项目

关键词:

摘要: 以气相色谱-质谱联用仪(GC-MS)分析和密度泛函理论(DFT)计算,探讨了土壤中甲基、氯代硝基苯混合物在常温常压下被零价铁还原的机理.GC-MS数据证明,取代硝基苯在土壤中被零价铁还原的主要产物是苯胺,同时还检测到微量的亚硝基苯、甲基苯二氮烯(对二甲基偶氮苯)、氯苯二氮烯(对二氯偶氮苯)等分解和缩合中间产物.理论计算表明:随还原程度的加深,对硝基甲苯和对氯硝基苯反应体系的能量从高到低,还原反应通过逐步添加质子和电子到硝基而进行,质子亲和力、电子亲和力起主导作用.逐步还原的机理合理地解释了实验中还原反应对土壤pH值的敏感以及微量中间产物的生成过程.苯环上的氯或甲基对还原反应的影响没有明显的差异.

English Abstract

REDUCTION MECHANISMS OF SUBSTITUTED NITROBENZENES BY ZERO-VALENT IRON IN SOILS

1. Research Institute of Environmental Chemistry and Technology, Hanshan Normal University, Chaozhou, 521041, China

Fund Project:

Keywords:

Abstract: The reduction mechanisms of mixed methyl- and chloro-substituted nitrobenzenes(SNBs) in soils at(ambient) temperature and pressure by zero valent iron(ZVI) were investigated using gas chromatography-mass spectrometry(GC-MS) as the analytical method for experiments and computational chemistry especially(density) functional theory(DFT) as the guiding principle.GC-MS data indicated that the major products of SNBs reduction by ZVI were anilines,but trace amounts of nitrosobenzenes,4,4'-dimethylazobenzene,4,4'-dichloroazobenzene and other degradation and condensation compounds were also detected as the intermediate products.DFT calculations showed that the total energies of the intermediates decreased with increasing levels of reduction for the SNBs,and the reduction seemed to be a process of step-wise additions of protons and electrons to the nitro group.This mechanism of step-wise reduction offered a reasonable explanation towards why the reduction reaction was sensitive to the soil pH as well as the formations of the detected trace intermediates.With either methyl- or chloro- substitutions,no significant differences in their impacts on the rates of reduction were observed.

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土壤中取代硝基苯化合物被零价铁还原的机理

REDUCTION MECHANISMS OF SUBSTITUTED NITROBENZENES BY ZERO-VALENT IRON IN SOILS

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土壤中取代硝基苯化合物被零价铁还原的机理

English Abstract

REDUCTION MECHANISMS OF SUBSTITUTED NITROBENZENES BY ZERO-VALENT IRON IN SOILS

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