Kinetics of the reaction between the hydroxyl radical and organic matter standards from the International Humic Substance Society |
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| Authors: | Garrett McKay Jonathan L. Kleinman Kimberly M. Johnston Mei Mei Dong Fernando L. Rosario-Ortiz Stephen P. Mezyk |
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| Affiliation: | 1. Department of Chemistry and Biochemistry, California State University Long Beach, 1250 N. Bellflower Blvd., Long Beach, CA, 90840, USA
2. Department of Civil, Architectural, and Environmental Engineering, University of Colorado Boulder, 1111 Engineering Drive, ECOT 518, Boulder, CO, 80309, USA
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| Abstract: | Purpose The objective of this study was to evaluate the effect of the physicochemical properties of five dissolved organic matter (DOM) isolates on their reactivity with the hydroxyl radical (HO·) in water. Materials and methods Five DOM isolates were purchased from the International Humic Substance Society (IHSS). Weight average molecular weight (M W) of these samples was quantified using size exclusion chromatography based on polyethylene glycols as reference standards. Functional group and elemental composition of the DOM samples were available from the IHSS website. Room temperature rate constants were measured using electron pulse radiolysis. Results and discussion Five IHSS standards were examined in this study: two soil organic and three aquatic organic matters. The composition varied from samples that had primarily aliphatic carbon (Pony Lake fulvic acid) to mostly aromatic carbon moieties (Elliot Soil humic acid). The M W values of the five samples ranged from 2,400 to 4,100 Da, with an average value of 3,060 Da. Second-order reaction rate constants between DOM and HO· (k DOM-HO·) were measured using thiocyanate competition kinetics, giving values ranging from 1.21 to 10.36?×?108 MC ?1?s?1. The k DOM-HO· values were not found to correlate with either M W or the aliphatic-aromatic carbon ratio, which is consistent with previous reports looking at natural organic matter (NOM), but is different to reports on size-fractionated (ultrafiltration through 15–1 kDa membranes) effluent organic matter (EfOM). We attribute this difference to the larger molecular weight distributions in size-fractionated EfOM compared to NOM. Conclusions The k DOM-HO· values in this study ranged over a factor of 10, suggesting that hydroxyl radical reactivity does depend on the sample composition; however, no major correlation was found between the measured reactivity and bulk physicochemical properties of DOM. |
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