Gautam Sumit Kumar, Suresh Sumathi
Centre for Environmental Sciences and Engineering, Indian Institute of Technology-Bombay, Mumbai 400076, India.
J Hazard Mater. 2007 Jan 2;139(1):146-53. doi: 10.1016/j.jhazmat.2006.06.017. Epub 2006 Jun 10.
The aim of our investigation was to compare the rates of dechlorination of DDT using Mg0/Pd4+ system in two different reaction phases, namely, water-acetone and 0.05% biosurfactant in water. Since palladium is expensive and its toxicity effects are not well known we also examined the reuse efficiency of Pd0 immobilized on alumina for dechlorinating DDT. Studies on the dechlorination of DDT in water-acetone (1:1, v/v) and 0.05% biosurfactant phases revealed that the reaction followed second order kinetics and rate of reaction is dependent upon both initial concentrations of the target compound and Mg0/Pd4+. The presence of acid enhanced the rate of reaction by providing protons and preventing passivation of metal that occurs due to deposition of magnesium hydroxide. GC-MS analyses revealed the formation of completely dechlorinated hydrocarbon skeleton of DDT namely, diphenylethane (DPE), as the end product in both reaction phases (water-acetone and 0.05% biosurfactant in water) thereby implying the removal of all five chlorine atoms (three alkyl and two aryl) of DDT. The optimum ratio of water and acetone to facilitate successful dechlorination reaction was found to be 9:1. Results suggested that salt form (K2PdCl6) of palladium had higher potential to dechlorinate DDT as compared to pellet (Pd0-alumina) form (efficiencies of 95 and 36%, respectively, for 100 ppm initial concentration of DDT). We noted that Pd0-alumina pellets could be reused at least four times for successful dechlorination of DDT provided Mg0 granules are present in sufficient quantity. Technical grade DDT (50 ppm) containing significant amounts of DDD was dechlorinated almost completely by the Mg0/Pd4+ (10mg/0.2mg/ml) within 1h in water-biosurfactant phase. Our studies reveal that Mg/Pd system is a promising option due to its high reactivity and its ability to achieve complete dechlorination of DDT. This bimetallic system may be useful for designing indigenous permeable barriers or reactors for the treatment of DDT contaminated water.
我们研究的目的是比较在水 - 丙酮和水中0.05%生物表面活性剂这两种不同反应相中,使用Mg0/Pd4+体系对滴滴涕进行脱氯的速率。由于钯价格昂贵且其毒性影响尚不明确,我们还研究了负载在氧化铝上的Pd0对滴滴涕脱氯的重复使用效率。对水 - 丙酮(1:1,v/v)和0.05%生物表面活性剂相中滴滴涕脱氯的研究表明,该反应遵循二级动力学,反应速率取决于目标化合物和Mg0/Pd4+的初始浓度。酸的存在通过提供质子和防止因氢氧化镁沉积导致的金属钝化来提高反应速率。气相色谱 - 质谱分析表明,在两个反应相(水 - 丙酮和水中0.05%生物表面活性剂)中,滴滴涕完全脱氯的烃骨架即二苯乙烷(DPE)作为最终产物形成,这意味着滴滴涕的所有五个氯原子(三个烷基和两个芳基)都被去除。发现促进成功脱氯反应的水和丙酮的最佳比例为9:1。结果表明,与颗粒(Pd0 - 氧化铝)形式相比,钯的盐形式(K2PdCl6)对滴滴涕脱氯具有更高的潜力(对于100 ppm初始浓度的滴滴涕,效率分别为95%和36%)。我们注意到,只要有足够数量的Mg0颗粒,Pd0 - 氧化铝颗粒可至少重复使用四次以成功对滴滴涕进行脱氯。在水 - 生物表面活性剂相中,含有大量滴滴滴的工业级滴滴涕(50 ppm)在1小时内几乎被Mg0/Pd4+(10mg/0.2mg/ml)完全脱氯。我们的研究表明,Mg/Pd体系因其高反应活性和实现滴滴涕完全脱氯的能力而具有广阔前景。这种双金属体系可能有助于设计用于处理受滴滴涕污染水的本地渗透屏障或反应器。