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用电子脉冲辐解测定羟基自由基与苏万尼河富里酸及其他溶解有机物分离物的反应速率常数。

Electron pulse radiolysis determination of hydroxyl radical rate constants with Suwannee River fulvic acid and other dissolved organic matter isolates.

作者信息

Westerhoff Paul, Mezyk Stephen P, Cooper William J, Minakata Daisuke

机构信息

Department of Civil and Environmental Engineering, Arizona State University, Box 5306, Tempe, Arizona 85287-5306, USA.

出版信息

Environ Sci Technol. 2007 Jul 1;41(13):4640-6. doi: 10.1021/es062529n.

DOI:10.1021/es062529n
PMID:17695909
Abstract

Pulse radiolysis experiments were conducted on dissolved organic matter (DOM) samples isolated as hydrophobic and hydrophilic acids and neutrals from different sources (i.e., stream, lake, wastewater treatment plant). Absolute bimolecular reaction rate constants for the reaction of hydroxyl radicals (OH) with DOM (k(OH), DOM) were determined. k*(OH, DOM) values are expressed as moles of carbon. Based on direct measurement of transient DOM radicals (DOM*) and competition kinetic techniques, both using pulse radiolysis, the k*(OH, DOM) value for a standard fulvic acid from the Suwannee River purchased from the International Humic Substances Society was (1.60 +/- 0.24) x 10(8) M(-1) s(-1). Both pulse radiolysis methods yielded comparable k*(OH, DOM) values. The k*(OH, DOM) values for the seven DOM isolates from different sources ranged from 1.39 x 10(8) M(-1) s(-1) to 4.53 x 10(8) M(-1) s(-1), and averaged 2.23 x 108 M(-1) s(-1) (equivalent to 1.9 x 10(4) (mgC/L)(-1) s(-1)). These values represent the first direct measurements of k*(OH, DOM,) and they compare well with literature values obtained via competition kinetic techniques during ozone or ultraviolet irradiation experiments. More polar, lower-molecular-weight DOM isolates from wastewater have higher k*(OH, DOM) values. In addition, the formation (microsecond time scale) and decay (millisecond time scale) of DOM* transients were observed for the first time. DOM* from hydrophobic acids exhibited broader absorbance spectra than transphilic acids, while wastewater DOM isolates had narrower DOM* spectra more skewed toward shorter wavelengths than did DOM* spectra for hydrophobic acids.

摘要

对从不同来源(即溪流、湖泊、污水处理厂)分离得到的疏水酸、亲水酸和亲水中性物质形式的溶解有机物(DOM)样品进行了脉冲辐解实验。测定了羟基自由基(OH)与DOM反应的绝对双分子反应速率常数(k(OH), DOM)。k*(OH, DOM)值以碳的摩尔数表示。基于使用脉冲辐解的瞬态DOM自由基(DOM*)的直接测量和竞争动力学技术,从国际腐殖质协会购买的来自苏万尼河的标准富里酸的k*(OH, DOM)值为(1.60 +/- 0.24) x 10(8) M(-1) s(-1)。两种脉冲辐解方法得到的k*(OH, DOM)值相当。来自不同来源的7种DOM分离物的k*(OH, DOM)值范围为1.39 x 10(8) M(-1) s(-1)至4.53 x 10(8) M(-1) s(-1),平均为2.23 x 108 M(-1) s(-1)(相当于1.9 x 10(4) (mgC/L)(-1) s(-1))。这些值代表了对k*(OH, DOM)的首次直接测量,并且与在臭氧或紫外线照射实验期间通过竞争动力学技术获得的文献值比较良好。来自废水的极性更强、分子量更低的DOM分离物具有更高的k*(OH, DOM)值。此外,首次观察到DOM瞬态的形成(微秒时间尺度)和衰减(毫秒时间尺度)。疏水酸的DOM比亲水酸表现出更宽的吸收光谱,而废水DOM分离物的DOM光谱比疏水酸的DOM光谱更窄,且更偏向较短波长。

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