Sorption of natural organic matter fractions to goethite (α-FeOOH):: effect of chemical composition as revealed by liquid-state 13C NMR and wet-chemical analysis

被引:93
作者
Kaiser, K [1 ]
机构
[1] Univ Bayreuth, Inst Soil Sci & Soil Geog, D-95440 Bayreuth, Germany
关键词
D O I
10.1016/S0146-6380(03)00120-7
中图分类号
P3 [地球物理学]; P59 [地球化学];
学科分类号
0708 ; 070902 ;
摘要
In order to quantify the potential influence of the chemical composition of natural organic matter (NOM) on the extent of its sorption to mineral surfaces, I compared the interaction with synthetic goethite (alpha-FeOOH) of 18 different NOM (hydrophilic and hydrophobic fractions, fulvic and humic acids) samples from soil and terrestrial surface waters. The chemical composition of NOM was characterised by elemental analysis, titration of acidity, wet chemical analyses of lignin and carbohydrate constituents, and liquid-state C-13 NMR spectroscopy. The proportions of resonances due to carboxyl C ranged from 7 to 21% and signals for total aromatic C varied from 0 to 38%. Signals due to O,N-alkyl C comprised 5-65% of the spectral area. The sorption of all tested NOM was adequately described by the Langmuir model. In general, hydrophobic fractions and fulvic and humic acids rich in carboxyl and aromatic C, probably derived from lignin, sorbed much more strongly to goethite than the hydrophilic fractions which were characterised by high abundance of 0,N-alkyl C, probably due to carbohydrates, and low abundance of aromatic C. A sample of fulvic acids rich in alkyl C sorbed more weakly than samples rich in aromatic C. Consequently, the strong sorption of the hydrophobic fractions and fulvic acids seemed to be caused by the presence of aromatic structures. Within the groups of samples, however, the major determinant of the extent of the sorption proved to be acidic groups, as revealed by the close relationship between maximum sorption and total acidity and the content of carboxyl C. The maximum sorption of hydrophobic, fulvic and humic acids was inversely related to the ratio of aromatic to carboxyl C, which suggests that the number (and probably the position) of acidic groups attached to aromatics controls the interactions of hydrophobic, fulvic and humic acids with goethite. (C) 2003 Elsevier Ltd. All rights reserved.
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页码:1569 / 1579
页数:11
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共 41 条
[1]  
Abbt-Braun G., 2002, REFRACTORY ORGANIC S, P1, DOI DOI 10.1002/9783527611195.CH1A
[2]   Determination of neutral and acidic sugars in soil by capillary gas-liquid chromatography after trifluoroacetic acid hydrolysis [J].
Amelung, W ;
Cheshire, MV ;
Guggenberger, G .
SOIL BIOLOGY & BIOCHEMISTRY, 1996, 28 (12) :1631-1639
[3]   Lignin in particle-size fractions of native grassland soils as influenced by climate [J].
Amelung, W ;
Flach, KW ;
Zech, W .
SOIL SCIENCE SOCIETY OF AMERICA JOURNAL, 1999, 63 (05) :1222-1228
[4]  
[Anonymous], REFRACTORY ORGANIC S
[5]   ADSORPTION OF POTENTIAL-DETERMINING IONS AT FERRIC OXIDE-AQUEOUS ELECTROLYTE INTERFACE [J].
ATKINSON, RJ ;
POSNER, AM ;
QUIRK, JP .
JOURNAL OF PHYSICAL CHEMISTRY, 1967, 71 (03) :550-&
[6]   Desorption of humic acids from an iron oxide surface [J].
Avena, MJ ;
Koopal, LK .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1998, 32 (17) :2572-2577
[7]   Adsorption of natural organic matter on preformed aluminum hydroxide flocs [J].
Bose, P ;
Reckhow, DA .
JOURNAL OF ENVIRONMENTAL ENGINEERING-ASCE, 1998, 124 (09) :803-811
[8]   Analysis of carboxyl groups in soil humic acids by a wet chemical method, Fourier-transform infrared spectrophotometry, and solution-state carbon-13 nuclear magnetic resonance. A comparative study [J].
Celi, L ;
Schnitzer, M ;
Negre, M .
SOIL SCIENCE, 1997, 162 (03) :189-197
[9]   Reaction of forest floor organic matter at goethite, birnessite and smectite surfaces [J].
Chorover, J ;
Amistadi, MK .
GEOCHIMICA ET COSMOCHIMICA ACTA, 2001, 65 (01) :95-109
[10]   Acidity characteristics of soluble organic substances in spruce-fir forest floor leachates [J].
Dai, KH ;
David, MB ;
Vance, GF ;
McLaughlin, JW ;
Fernandez, IJ .
SOIL SCIENCE, 1996, 161 (10) :694-704