Literature DB >> 11811494

Reduced heterogeneity of a lignite humic acid by preparative HPSEC following interaction with an organic acid. Characterization of size-separates by Pyr-GC-MS and 1H-NMR spectroscopy.

Alessandro Piccolo1, Pellegrino Conte, Enrico Trivellone, Barend van Lagen, Peter Buurman.   

Abstract

Preparative high performance size exclusion chromatography (HPSEC) was used to size-fractionate a humic acid (HA) solution with 0.05 M ionic strength before and after having made the humic solution 0.5 x 10(-3) M in acetic acid (AcOH). Size-fractions were characterized by pyrolysis-gas-chromatography/mass spectrometry (Pyr-GC-MS) and 1H NMR spectroscopy. Pyr-GC-MS showed that the AcOH treatment altered the distribution of humic molecular components in the size-fractions. The unsaturated alkyl chains were moved from size-fractions of larger molecular-size into those of lower molecular-sizes. Most of the aromatic moieties, which were found in larger molecular-size fractions for the untreated HA, were spread into fractions of lower molecular size after AcOH addition to HA. Carbohydrates, which were undetectable in anyfraction of the untreated HA, appeared instead in the pyrogram of the lowest molecular-size and most hydrophilic fraction after treatment with AcOH. Our results suggested that AcOH disrupted the weakly bound association of humic supramolecularstructures and HPSEC elution separated size-fractions of different composition without losing humic matter by adsorption on the HPSEC column. The fractions with the largest apparent molecular size were the richest in alkyl chains, thereby suggesting that humic molecules were stabilized into supramolecular associations by multiple weak interactions among apolar groups such as alkyl chains and aromatic moieties. 1H NMR spectra of size-fractions were greatly simplified and more resolved after AcOH treatment. This was attributed to a less complex molecular association in the size separates which provided a larger solubility in the NMR solvent and more favorable relaxation times. Combination of the procedure used here for size-fractionation with NMR and Pyr-GC-MS methods appears to be promising to advance knowledge on the molecular composition of humic substances.

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Year:  2002        PMID: 11811494     DOI: 10.1021/es010981v

Source DB:  PubMed          Journal:  Environ Sci Technol        ISSN: 0013-936X            Impact factor:   9.028


  5 in total

1.  Co-polymerization of penta-halogenated phenols in humic substances by catalytic oxidation using biomimetic catalysis.

Authors:  Barbara Fontaine; Alessandro Piccolo
Journal:  Environ Sci Pollut Res Int       Date:  2011-10-04       Impact factor: 4.223

2.  Isolation and fractionation of soil humin using alkaline urea and dimethylsulphoxide plus sulphuric acid.

Authors:  Guixue Song; Michael H B Hayes; Etelvino H Novotny; Andre J Simpson
Journal:  Naturwissenschaften       Date:  2010-11-23

3.  H-binding of size- and polarity-fractionated soil and lignite humic acids after removal of metal and ash components.

Authors:  Marios Drosos; Jerry A Leenheer; Apostolos Avgeropoulos; Yiannis Deligiannakis
Journal:  Environ Sci Pollut Res Int       Date:  2013-12-03       Impact factor: 4.223

4.  Frequency-domain fluorescence lifetime measurements via frequency segmentation and recombination as applied to pyrene with dissolved humic materials.

Authors:  Hadi M Marwani; Mark Lowry; Baoshan Xing; Isiah M Warner; Robert L Cook
Journal:  J Fluoresc       Date:  2008-06-11       Impact factor: 2.217

5.  Antiflammatory activity and potential dermatological applications of characterized humic acids from a lignite and a green compost.

Authors:  Mariavittoria Verrillo; Melania Parisi; Gabriella Fabbrocini; Alessandro Piccolo; Davide Savy; Giuseppina Caiazzo; Roberta Di Caprio; Maria Antonietta Luciano; Sara Cacciapuoti
Journal:  Sci Rep       Date:  2022-02-09       Impact factor: 4.379

  5 in total

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