APPLICATION OF A SEQUENTIAL EXTRACTION PROCEDURE TO THE DETERMINATION OF THE DISTRIBUTION OF SULPHUR FORMS IN SELECTED PEAT MATERIALS

1986 ◽  
Vol 66 (2) ◽  
pp. 337-345 ◽  
Author(s):  
L. E. LOWE

Total S (St), soluble sulphate, pyritic S, elemental S, carbon-bonded S (C-S) and organic sulphate S were determined on four peat samples and three sedimentary gyttja samples, one of which (Ginc.) had been subjected to aerobic incubation. A sequential extraction procedure was used to assess the distribution of St and of organic S forms in a series of peat fractions. Total S varied from 0.42 to 3.67%, with values below 1% associated only with freshwater-derived peats. The S content of brackish peat and of gyttja was consistently high and in some cases, organic S exceeded 6% of the organic matter. With the exception of Ginc., organic S accounted for a very high proportion of St (mean 94%), with C-S the dominant organic S form. Ginc. showed a very different S form distribution from the unincubated gyttja samples, with organic S accounting for only 44.5% of St, and organic sulphate-S exceeding C-S. Ginc. also had a lower pH, suggesting acidification resulting from oxidation of the organic C-S fraction during incubation. The recovery of St in seven peat (or gyttja) fractions averaged 99%, and indicated that humic acid and residue ("humin") fractions together generally accounted for most of the organic S (73.3–90.4%), with the notable exception of Ginc., for which these fractions only accounted for 42–47% of organic S. The proportion of humic acid-S increased with increase in degree of peat decomposition. The fulvic acid fraction contained variable proportions of St and had relatively more oxidized S forms than humic acid or residue fractions. Some oxidation of C-S occurred during alkaline extraction. Minor amounts of organic S were extracted with water, chloroform and ethanol-benzene. Key words: Sulphur forms, peat sulphur, gyttja, peat fractions

2014 ◽  
Vol 97 (4) ◽  
pp. 1034-1038 ◽  
Author(s):  
Yunus Emre Unsal ◽  
Mustafa Tuzen ◽  
Mustafa Soylak

Abstract Total concentration of metal ions at trace levels does not give sufficient information about toxicity and biological availability of these elements in fertilizer samples. In the presented work, a sequential extraction procedure modified by the European Community Bureau of Reference (BCR) was applied to fractionate Cd, Cr, Co, Cu, Fe, Pb, Mn, Ni, and Zn levels in two fertilizer samples collected from cooperative agricultural retailers. The fractions extracted were exchangeable/dilute acid soluble, reducible bound to Fe/Mn oxides, oxidizable bound to organic matter and sulfides, and residual. The determination of analyte elements was done by flame atomic absorption spectrometry. The accuracy of the procedure was validated with BCR-701 sediment certified reference material. The RSD of the procedure was less than 10%.


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