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Palladium-catalyzed hydrodehalogenation of 1,2,4,5-tetrachlorobenzene in water-ethanol mixtures

机译:钯催化水-乙醇混合物中的1,2,4,5-四氯苯加氢脱卤

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Palladium-catalyzed hydrodehalogenation (HDH) was applied for destroying 1,2,4,5-tetrachlorobenzene (TeCB) in mixtures of water and ethanol. This investigation was performed as a critical step in the development of a new technology for clean-up of soil contaminated by halogenated hydrophobic organic contaminants. The main goals of the investigation were to demonstrate the feasibility of the technology, to determine the effect of the solvent composition (watenethanol ratio), and to develop a model for the kinetics of the dehalogenation process. All experiments were conducted in a batch reactor at ambient temperature under mild hydrogen pressure. The experimental results are all consistent with a Langmuir-Hinshelwood model for heterogeneous catalysis. Major findings that can be interpreted within the Langmuir-Hinshelwood framework include: (1) the rate of hydrodehalogenation depends strongly on the solvent composition, increasing as the water fraction of the solvent increases; (2) the HDH rate increases as the catalyst concentration in the reactor increases; (3) when enough catalyst is present, the HDH reaction appears to follow first-order kinetics, but the kinetics appear to be zero-order at low catalyst concentrations. TeCB is converted rapidly and quantitatively to benzene, with only trace concentrations of 1,2,4-trichlorobenzene appearing as a reactive intermediate. The results obtained here have important implications for the further development of the proposed soil remediation technology, and may also be important for the treatment of other hazardous waste streams.
机译:钯催化的加氢脱卤(HDH)用于破坏水和乙醇混合物中的1,2,4,5-四氯苯(TeCB)。这项调查是开发新技术的关键步骤,该新技术用于清理被卤化的疏水有机污染物污染的土壤。该研究的主要目的是证明该技术的可行性,确定溶剂组成(watenethanol比率)的影响,并开发脱卤过程动力学的模型。所有实验均在间歇反应器中于环境温度和适度的氢气压力下进行。实验结果均与用于非均相催化的Langmuir-Hinshelwood模型一致。在Langmuir-Hinshelwood框架内可以解释的主要发现包括:(1)加氢脱卤的速率在很大程度上取决于溶剂的组成,随着溶剂中水含量的增加而增加; (2)随着反应器中催化剂浓度的增加,HDH速率增加; (3)当存在足够的催化剂时,HDH反应似乎遵循一级动力学,但是在低催化剂浓度下动力学似乎为零级。 TeCB快速定量地转化为苯,只有痕量的1,2,4-三氯苯作为反应性中间体出现。此处获得的结果对拟议的土壤修复技术的进一步发展具有重要意义,对于其他危险废物流的处理也可能很重要。

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