硫化亚铁去除水中TCE的机理研究 |
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引用本文: | 李群,杨琦,刘争,陈海,李博. 硫化亚铁去除水中TCE的机理研究[J]. 安徽农业科学, 2014, 0(35): 12606-12609 |
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作者姓名: | 李群 杨琦 刘争 陈海 李博 |
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作者单位: | 中国地质大学(北京)水资源与环境学院,北京水资源与环境工程重点实验室,北京100083 |
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基金项目: | 北京市产学研项目,国家科技重大专项,中央高校基本科研业务费专项,重点防控重金属汞、铬、铅、镉、砷便携/车载/在线监测仪器开发与应用示范项目 |
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摘 要: | [目的]以地下水中常见氯代烃污染物三氯乙烯(TCE)为目标污染物,采用自制硫化亚铁(FeS)作还原剂,探讨两种物质的反应情况.[方法]在厌氧环境下,通过批试验方法研究不同影响因素下硫化亚铁降解TCE的反应动力学并探讨反应机理.[结果]在50℃下,污染物初始浓度为20 mg/L,硫化亚铁浓度为10 g/L,反应48 h后,TCE的去除率可达到80%.硫化亚铁降解TCE的反应符合伪一级动力学反应,反应速率常数(K)为0.032 8 h-1,半衰期为21.13 h.对比试验结果显示,12 h后硫化亚铁吸附TCE达到吸附/解吸平衡,之后TCE的去除以化学降解为主.[结论]硫化亚铁对TCE有一定的降解和吸附作用,反应的主要产物为乙炔.
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关 键 词: | 硫化亚铁 三氯乙烯(TCE) 影响因素 反应机理 |
Removal Mechanism of Trichloroethylene from Water by Iron Sulfide |
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Affiliation: | LI Qun, YANG Qi, LIU Zheng et al ( Key Laboratory of Water Resources and Environmental Engineering, Institute of Water Resources and Environment, China University of Geosciences, Beijing 100083) |
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Abstract: | [Objective] The most widely existent pollutant trichloroethylene (TCE) was chosen as the target pollutant,and the self-made iron sulfide (FeS) was chosen as reductant to investigate the removal ability of chlorinated hydrocarbons.[Method] The batch experiment was used to investigate the reaction kinetics,influencing factors and dechlorination mechanism of TCE in anaerobic environment.[Result] The experimental results show that when the iron sulfide initial concentration is 10 g/L and the initial concentration of pollutant is 20 mg/L,removal efficiency of TCE reaches 80% at 50 ℃ within 48 h.The removal of TCE by iron sulfide follows the pseudo-first order reaction kinetics.Reaction rate constant (K) is 0.032 8 h-1 and half time (t1/2) is 21.13 h.The results of comparison experiment show that the adsorption of TCE on iron sulfide reached adsorption-desorption equilibrium within 12 h,then the removal of TCE primarily by chemical degradation.[Conclusion] Trichloroethylene can be degraded and absorbed by iron sulfide,and the main reaction product is acetylene. |
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Keywords: | Iron sulfide Trichloroethylene (TCE) Influence factor Reaction mechanism |
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