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高锰酸钾对污染物的降解动力学

Kinetics of contaminant degradation by permanganate.

作者信息

Waldemer Rachel H, Tratnyek Paul G

机构信息

Department of Environmental and Biomolecular Systems, OGI School of Science and Engineering, Oregon Health and Science University, 20000 NW Walker Road, Portland, Oregon 97006, USA.

出版信息

Environ Sci Technol. 2006 Feb 1;40(3):1055-61. doi: 10.1021/es051330s.

Abstract

To provide a more complete understanding of the kinetics of in situ chemical oxidation (ISCO) with permanganate (MnO4-), we measured the kinetics of oxidation of 24 contaminants-many for which data were not previously available. The new data reported here were determined using an efficient method based on continuous measurement of the MnO4- concentration by absorbance spectrometry. Under these conditions, the kinetics were found to be first-order with respect to both contaminant and MnO4- concentrations, from which second-order rate constants (k") were readily obtained. Emerging contaminants forwhich k" was determined (at 25 degrees C and pH 7) include 1,4-dioxane (4.2 x 10(-5) M(-1) s(-1)), methyl t-butyl ether (MTBE) (1.0 x 10(-4) M(-1) s(-1)), and methyl ethyl ketone (MEK) (9.1 x 10(-5) M(-1) s(-1)). Contaminants such as 2,4,6-trinitrotoluene (TNT), the pesticides aldicarb and dichlorvos, and many substituted phenols are oxidized with rate constants comparable to tetrachloroethene (PCE) and trichloroethene (TCE) (i.e., 0.03-1 M(-1) s(-1)) and therefore are good candidates for remediation with MnO4- in the field. There are several--sometimes competing--mechanisms by which MnO4- oxidizes contaminants, including addition to double bonds, abstraction of hydrogen or hydride, and electron transfer.

摘要

为了更全面地理解用高锰酸盐(MnO₄⁻)进行原位化学氧化(ISCO)的动力学,我们测量了24种污染物的氧化动力学——其中许多污染物的数据以前并不存在。此处报告的新数据是使用一种基于吸光光谱法连续测量MnO₄⁻浓度的有效方法确定的。在这些条件下,发现动力学对污染物和MnO₄⁻浓度均为一级,由此很容易获得二级速率常数(k")。已确定k"(在25℃和pH 7下)的新兴污染物包括1,4 - 二氧六环(4.2×10⁻⁵ M⁻¹ s⁻¹)、甲基叔丁基醚(MTBE)(1.0×10⁻⁴ M⁻¹ s⁻¹)和甲乙酮(MEK)(9.1×10⁻⁵ M⁻¹ s⁻¹)。诸如2,4,6 - 三硝基甲苯(TNT)、农药涕灭威和敌敌畏以及许多取代酚等污染物的氧化速率常数与四氯乙烯(PCE)和三氯乙烯(TCE)相当(即0.03 - 1 M⁻¹ s⁻¹),因此是现场用MnO₄⁻进行修复的良好候选物。MnO₄⁻氧化污染物有几种——有时相互竞争的——机制,包括加成到双键、夺取氢或氢化物以及电子转移。

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