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硫酸盐还原条件下多环芳烃在土壤中的迁移转化
Transportation of PAHs in Soil under Sulfate-Reducing Conditions
【摘要】 为研究硫酸盐还原条件下多环芳烃(Polycyclic Aromatic Hydrocarbons,PAHs)类有机污染物在土壤中的污染分布规律和迁移转化过程,设计了室内土柱淋溶试验,选择菲、蒽和芘作为PAHs的代表,模拟硫酸盐还原条件下PAHs在土壤中的迁移转化过程.监测土壤中PAHs的垂直分布、淋出液中ρ(PAHs)和ρ(SO42-)、淋出液的氧化还原电位(Eh)和总体积,并通过质量平衡计算出PAHs的降解率.结果表明:①菲和蒽的相对淋出率总体都不超过2%.120 d后菲和蒽在土壤中的残留率分别为51.87%和51.21%,而芘有90%以上吸附在土壤中,在淋出液中未检出.②随着淋溶时间的延长,土壤中的氧气逐渐被消耗,淋出液中ρ(SO42-)和Eh逐渐降低,并趋于稳定,硫酸盐还原作用发生.③3种PAHs在硫酸盐还原条件下都存在一定程度的降解.菲和蒽的降解率相差不大且随淋溶时间的延长逐渐增大,120 d后菲和蒽的降解率分别为47.41%和48.10%,而4环的芘降解速率非常低,120 d后降解率仅为3.61%.
【Abstract】 The distribution and transportation of polycyclic aromatic hydrocarbon(PAH) contamination in soil under sulfate-reducing conditions were studied through column experimentation.Phenanthrene,anthracene and pyrene were selected as representative PAHs,and their vertical distributions in the soil column,their mass concentrations,and sulfate radical ion and Eh values in leaching solution were detected under simulated sulfate-reducing conditions.Also,the mass balance of PAHs was analyzed to calculate the biodegradation rate of PAHs.The result showed that the leaching ratios of phenanthrene and anthracene were not more than 2%,and their residual ratios after 120 days were 51.87% and 51.21%,respectively.However,more than 90% of pyrene was absorbed in the soil and not detected in the leaching solution.The concentrations of sulfate radical ion and Eh of the leaching solution decreased with leaching time;this was attributed to O2 depletion.Phenanthrene,anthracene and pyrene degraded under sulfate-reducing conditions,and,after 120 days,their biodegradation ratios were 47.41%,48.10% and 3.61%,respectively.Pyrene degradation was slowest.The experiment result indicated that phenanthrene,anthracene and pyrene could be degraded by acclimated native microorganisms in soil under sulfate-reducing conditions,which provided a theoretical basis for in-situ remediation of PAHs pollution in soil.
【Key words】 polycyclic aromatic hydrocarbons(PAHs); sulfate-reducing; biodegradation;
- 【文献出处】 环境科学研究 ,Research of Environmental Sciences , 编辑部邮箱 ,2009年02期
- 【分类号】X53
- 【被引频次】13
- 【下载频次】568