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Reaction mechanism of 3-chlorophenol with OH, H in aqueous solution

机译:3-氯苯酚与水溶液中OH,H的反应机理

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The reaction mechanism of 3-chlorophenol with OH, H in aqueous solution was studied by transient technology. The 3-chlorophenol aqueous solutions have been saturated with air or N_2 previously. Under alkaline condition, the reaction of OH radical with 3-chlorophenol produces 3-chlorinated phenoxyl radical, with the absorption peaks at 400 nm and 417 nm. Under neutral condition, the reaction of OH radical with 3-chlorophenol produces OH-adduct with the maximal absorption at about 340 nm. And in acid solution, the reaction of H with 3-chlorophenol produces H-adduct with the maximal absorption at about 320 nm. 3-chlorophenol is compared with 4-and 2-chlorophenols from the free radical pathways. The results show that the positions of chlorine on the aromatic ring strongly influence the dehalogenation and degradation process.
机译:通过瞬时技术研究了3-氯苯酚与OH,H在水溶液中的反应机理。事先已将3-氯苯酚水溶液用空气或N_2饱和。在碱性条件下,OH自由基与3-氯苯酚反应生成3-氯代苯氧基自由基,其吸收峰在400 nm和417 nm处。在中性条件下,OH自由基与3-氯苯酚的反应生成OH加合物,在340 nm处具有最大吸收。在酸性溶液中,H与3-氯苯酚的反应生成H-加合物,在约320 nm处具有最大吸收。从自由基途径比较3-氯苯酚与4-和2-氯苯酚。结果表明,氯在芳环上的位置强烈影响脱卤和降解过程。

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