首页> 外文期刊>Fresenius Environmental Bulletin >DEFINED MECHANOCHEMICAL REDUCTIVE DECHLORINATION OF 1,3,5-TRICHLOROBENZENE AT ROOM TEMPERATURE IN A BALL MILL
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DEFINED MECHANOCHEMICAL REDUCTIVE DECHLORINATION OF 1,3,5-TRICHLOROBENZENE AT ROOM TEMPERATURE IN A BALL MILL

机译:球磨机室温下1,3,5-三氯苯的确定的机械化学还原脱氯

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摘要

1,3,5-Trichlorobenzene (TCB) is completely dechlo-rinated to benzene when treated with magnesium and n-butylamine at room temperature in a ball mill. A full mass balance is observed for its stepwise reductive dechlorina-tion via the intermediates 1,3-dichlorobenzene (DCB) and monochlorobenzene (MCB). This mechanochemical (MC) reaction occurs due to ongoing, simultaneous comminution and mechanical activation of small particle size magnesium during milling. The base metal is utilized as the actual dechlorinating agent whereas n-butylamine as a hydrogen donor. A kinetic study reveals that consecutive and coupled one-pot Grignard-Zerewitinoff reactions occur: MC activated formations of intermediary Grignard components from 1,3,5-TCB, 1,3-DCB and MCB, take place each first, and then stepwise their protonation to DCB, MCB and benzene, respectively, by the amine, which reacts as a (weak) acid towards strong bases such as Grignard reagents. An appropriate reaction model comprising a corresponding set of rate equations (ordinary differential equations (ODEs) representing an initial value problem) could successfully be fitted to two data sets recorded for a representative model degradation reaction of 1,3,5-TCB at two different initial concentrations. The rate constants for the formation of the postulated intermediary Grignard components were computed, hence this method can readily be extended to determine Grignard formation rate constants in general as well. Results are in very good accordance to data recently reported for an analogous MC reductive dechlorination reaction of 1,3-DCB and correspond well, too, to other data previously reported elsewhere. In conclusion, MC reductive dechlorination employing base metals in combination with hydrogen donors can be applied as a promising non-combustion method to the environmentally friendly, defined and well characterized destruction of persistent organic pollutants (POPs) at room temperature.
机译:当在室温下在球磨机中用镁和正丁胺处理时,1,3,5-三氯苯(TCB)被完全脱氯精制为苯。通过中间体1,3-二氯苯(DCB)和一氯苯(MCB)观察到其逐步还原性除氯的质量平衡。这种机械化学(MC)反应是由于在研磨过程中持续进行的同时粉碎和小粒径镁的机械活化而发生的。贱金属用作实际的脱氯剂,而正丁胺用作氢供体。动力学研究表明,发生了连续且偶合的一锅式格氏试剂反应:分别首先发生1,3,5-TCB,1,3-DCB和MCB的MC活化格氏试剂中间组分的形成,然后逐步进行通过胺分别质子化为DCB,MCB和苯,作为(弱)酸与强碱(如格氏试剂)反应。包括一组相应的速率方程组(代表初始值问题的普通微分方程(ODE))的适当反应模型可以成功地拟合到记录的两个数据集,以用于在两个不同的条件下进行1,3,5-TCB的代表性模型降解反应初始浓度。计算了假定的中间格氏试剂组分形成的速率常数,因此一般也可以很容易地扩展该方法来确定格氏试剂的速率常数。结果与最近报道的1,3-DCB的类似的MC还原脱氯反应的数据非常吻合,也与先前在其他地方报道的其他数据非常吻合。总之,采用贱金属与氢供体结合的MC还原脱氯可作为一种有前途的非燃烧方法,用于在室温下对持久性有机污染物(POPs)进行环保,确定和特征明确的破坏。

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