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2种水稻土胶体界面五氯酚的还原脱氯转化
引用本文:曾芳,王旭刚,李芳柏,黎晓峰,刘亮,顾明华.2种水稻土胶体界面五氯酚的还原脱氯转化[J].生态毒理学报,2007,2(1):49-56.
作者姓名:曾芳  王旭刚  李芳柏  黎晓峰  刘亮  顾明华
作者单位:1. 广西大学农学院,南宁,530005;广东省生态环境与土壤研究所,广东省农业环境综合治理重点实验室,广州,510650
2. 广东省生态环境与土壤研究所,广东省农业环境综合治理重点实验室,广州,510650
3. 广西大学农学院,南宁,530005
基金项目:国家自然科学基金项目(No.20577007)
摘    要:研究了紫泥田和浅脚紫泥田2种水稻土胶体界面五氯酚(PCP)的还原转化效果,以及添加Fe2+或草酸对五氯酚还原转化效果的影响.采用表观一级反应动力学描述土壤胶体界面五氯酚的转化过程.结果表明,紫泥田和浅脚紫泥田土壤胶体界面五氯酚的还原转化动力学常数分别为0.0375d-1和0.0430d-1,半衰期分别为18.5d和16.1d;厌氧条件下水稻土胶体中铁氧化物还原溶解产生的吸附态Fe2+对五氯酚具有一定的还原转化能力.添加1.0mmol·L-1Fe2+或1.0mmol·L-1草酸均能显著促进土壤胶体界面五氯酚的还原转化和氯离子的产生,紫泥田土壤胶体界面五氯酚的还原转化半衰期分别减少到9.6d和6.0d,浅脚紫泥田土壤胶体界面五氯酚的转化半衰期分别减少到7.9d和3.0d.草酸促进作用更加显著的原因是铁-草酸配合物的生成.土壤胶体界面五氯酚的还原转化、脱氯效率与土壤胶体的比表面积、吸附态亚铁离子浓度有一定的正相关关系.促进土壤中吸附态亚铁离子和草酸等低分子量有机酸的产生能显著促进有机氯的还原转化.

关 键 词:土壤胶体  五氯酚  界面  还原转化  脱氯
文章编号:1673-5897(2007)1-049-08
收稿时间:1/8/2007 12:00:00 AM
修稿时间:2007-02-13

Reductive Transformation of Pentachlorophenol in the Interface of Paddy Soil Colloids and Water
ZENG Fang,WANG Xu-gang,LI Fang-bai,LI Xiao-feng,LIU Liang and GU Ming-hua.Reductive Transformation of Pentachlorophenol in the Interface of Paddy Soil Colloids and Water[J].Asian Journal of Ecotoxicology,2007,2(1):49-56.
Authors:ZENG Fang  WANG Xu-gang  LI Fang-bai  LI Xiao-feng  LIU Liang and GU Ming-hua
Abstract:A series of batch experiments were carried out to investigate the reductive transformation of pentachlorophenol (PCP)in the interface of soil colloids from purple paddy soil(PPS)and flat purple paddy soil(FPPS)and water. The effect of additional 1.0mmol·L-1 Fe2+ and oxalate on the reductive transformation of PCP and the generation of chlorine were also investigated. Reductive transformation could be well described by first-order kinetics model. Results showed that PCP could be reductively transformed and dechlorinated in the interface of both soil colloids and water. The kinetics rate constants of PCP transformation were 0.0375, 0.0430d-1, respectively, and half-life time were 18.5, 16.1d for PPS and FPPF, respectively. Obviously, the additional 1.0mmol·L-1 Fe2+ or oxalate could significantly enhance the reductive transformation of PCP and the generation of chlorine. The half-life time for PCP transformation decreased significantly to be 9.6 and 6.0d in the PPF-water interface, while that decreased to be 7.9 and 3.0d in the FPPS-water interface owing to additional Fe2+ and oxalate, respectively. The enhanced effect of additional Fe2+ and oxalate should be attributable to the formation of adsorbed Fe2+ with a higher concentration. It is very interesting that the enhanced effect of oxalate should be more significant than that of Fe2+ because the generated Fe-oxalate complex have a lower reductive potential than Fe2+. This investigation will give some new insights in soil remediation on site.
Keywords:soil colloid  pentachlorophenol  interface  reductive transformation  dechlorination
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