Zhao Ling, Yu Zhiqiang, Peng Pingán, Huang Weilin, Feng Shunqing, Zhou Haiyan
State Key Laboratory of Organic Geochemistry, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Wushan, Guangdong 510640, People's Republic of China.
Environ Toxicol Chem. 2006 Nov;25(11):2912-9. doi: 10.1897/06-001r.1.
This study examined the abiotic transformation kinetics of pentachlorophenol (PCP) by manganese dioxide (MnO2) at different solution chemistry and initial concentrations of PCP and MnO2. The measured PCP transformation rates were found to be on the order of 1.07 with respect to [PCP] and 0.91 and 0.87 with respect to [MnO2] and [H+], respectively. Dissolved Mn2+ and Ca2+ as background electrolytes considerably decreased the reaction rate because of their adsorption and hence blocking of active sites on MnO2 surfaces. The dechlorination number, 0.59 chloride ions per transformed PCP after a 1-h reaction, suggests that a fraction of the transformed PCP was not dechlorinated and may be coupled directly to dimeric products. Gas chromatography/ mass spectrometry and liquid chromatography/mass spectrometry/mass spectrometry techniques were used to identify two isomeric nonachlorohydroxybiphenylethers as major products and 2,3,5,6-tetrachloro-1,4-hydroquinone and tetrachlorocatechol as minor products. Product identification suggested that the reaction may include two parallel reactions to form either dimers or 2,3,5,6-tetrachloro-1,4-hydroquinone and tetrachlorocatechol via simultaneous dehydrochlorination and hydroxylation.
本研究考察了在不同溶液化学条件以及五氯苯酚(PCP)和二氧化锰(MnO₂)初始浓度下,二氧化锰对五氯苯酚的非生物转化动力学。测得的PCP转化速率相对于[PCP]约为1.07,相对于[MnO₂]和[H⁺]分别为0.91和0.87。作为背景电解质的溶解态Mn²⁺和Ca²⁺由于吸附并因此阻塞了MnO₂表面的活性位点,显著降低了反应速率。脱氯数为反应1小时后每转化一个PCP有0.59个氯离子,这表明一部分转化后的PCP未被脱氯,可能直接偶联形成二聚产物。采用气相色谱/质谱和液相色谱/质谱/质谱技术鉴定出两种异构的九氯羟基联苯醚为主要产物,2,3,5,6-四氯-1,4-对苯二酚和四氯邻苯二酚为次要产物。产物鉴定表明该反应可能包括两个平行反应,通过同时脱氯化氢和羟基化形成二聚体或2,3,5,6-四氯-1,4-对苯二酚和四氯邻苯二酚。