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Dechlorination and destruction of 2,4,6-trichlorophenol and pentachlorophenol using hydrogen peroxide as the oxidant catalyzed by molybdate ions under basic condition

机译:碱性条件下以钼酸根离子为氧化剂过氧化氢对2,4,6-三氯苯酚和五氯苯酚的脱氯和破坏

摘要

The dechlorination and destruction of 2,4,6-trichlorophenol (TCP) and pentachlorophenol (PCP) under basic condition using hydrogen peroxide as the oxidant catalyzed by molybdate ions have been studied. Under ambient conditions of temperature and pressure, more than 95% of millimolar solutions of TCP and PCP can be converted to CO2 and CO, chlorinated and nonchlorinated carboxylic acid in 40min. Up to 2.4 chloride ions per TCP and 3.5 chloride ions per PCP were released. TOC measurements indicated that 18% and 11% of the carbon was mineralized for TCP and PCP respectively after an hour of reaction. The results of ESR measurements suggested that the reaction possibly proceeded via the pathway with singlet oxygen. (c) 2004 Elsevier Ltd. All rights reserved.
机译:研究了在碱性条件下以钼酸根离子为氧化剂,过氧化氢对2,4,6-三氯苯酚(TCP)和五氯苯酚(PCP)的脱氯和破坏作用。在温度和压力的环境条件下,TCP和PCP的毫摩尔溶液中的95%可以在40分钟内转化为CO2和CO,氯化和非氯化羧酸。每个TCP最多释放2.4个氯离子,每个PCP最多释放3.5个氯离子。 TOC测量表明,反应一小时后,分别有18%和11%的碳矿化了TCP和PCP。 ESR测量的结果表明,该反应可能通过单线态氧通过该途径进行。 (c)2004 Elsevier Ltd.保留所有权利。

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    Tai C; Jiang GB;

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