کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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4482275 | 1316854 | 2013 | 10 صفحه PDF | دانلود رایگان |
The mobility of humic-substance dominated natural organic matter (NOM) concentrated from a freshwater wetland by reverse osmosis was examined in sand columns at pH 5–8, in 0.001 M and 0.01 M NaClO4. Greater mobility was observed at higher pH and lower ionic strength, although breakthrough curves (BTCs) for bulk NOM exhibited extensive tailing under all conditions examined. Based on observations from previous batch experiments indicating preferential adsorption of intermediate to high molecular weight (MW) NOM, we postulate that ‘adsorptive fractionation’ of the NOM pool leads to the observed tailing behavior, and develop a novel approach to assess the effects of polydispersity on transport of NOM and associated contaminants. BTCs for different NOM fractions were constructed by separating column effluent MW distributions determined by high-pressure size exclusion chromatography into five discrete intervals or ‘bins’ and calculating the mass of NOM within each bin at four sampling times. Observed retardation factors (Ro), reflecting median arrival time relative to that of a nonreactive tracer, ranged from 1.4 to 7.9 for the various bins and generally increased with MW. NOM retarded transport of the contaminant metal Cd (2.5 ppm, in 0.01 M NaClO4) slightly at pH 5 and more substantially at pH 8. Although Cd had little or no effect on bulk NOM transport, retention of the more aromatic, IMW-HMW NOM appeared to be slightly enhanced by Cd. Study results demonstrate that heterogeneity in retardation as a function of MW is likely a major factor contributing to bulk NOM BTC tailing and may have important implications for contaminant transport.
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► Preferential adsorption of NOM subcomponents caused tailing of breakthrough curves.
► Differences in retardation of NOM components were quantified for different MW ranges.
► Greater overall retardation of NOM was observed at low pH and high ionic strength.
► Adsorptive fractionation of NOM was slightly enhanced by Cd(II) in solution.
Journal: Water Research - Volume 47, Issue 7, 1 May 2013, Pages 2231–2240