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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 9 (1995), S. 581-590 
    ISSN: 0268-2605
    Keywords: inorganic tin ; monomethyltin cation ; model studies ; salt marsh ; sediment ; Spartina alterniflora ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: This study describes experiments on sedimentestuarine water slurries originating from a Spartina alterniflora salt marsh. We investigated the fate of tin(IV) or monomethyltin cation (MeSn3+) chlorides after their additon to slurries under anaerobic and aerobic conditions. We did not observe methylation of tin in anaerobic or aerobic slurries with and without added tin(IV). MeSn3+-amended samples occasionally formed small amounts of Me2Sn2+ or Me3Sn+ after extended periods of time, particularly when MeSn3+ remained in solution. The stability of MeSn3+ in slurries demonstrates that the absence of net methylation of tin(IV) is not due to rapid demethylation of MeSn3+ or its further methylation. Inorganic tin concentrations in the aqueous phase of anaerobic slurries spiked with MeSn3+ and unspiked slurries decreased by about 85% in 21 days and remained relatively constant until the end of the 59-day experiments. In similar anaerobic experiments about 25% of the MeSn3+ spike was adsorbed to sediment within 1 h and about 75% was adsorbed within 10 days. The lack of methylation and demethylation reactions in our aerobic and anaerobic slurries, which contrasts with two previous reports, undoubtedly reflects the absence of added nutrients and low concentrations of added tin(IV) in our experiments. We believe that our model experiments more accurately reflect conditions in salt marshes than do previous studies. We conclude that future model studies on methylation of inorganic tin should include. S. alterniflora because it is so prominent in observations of methyltin compounds in the estuary.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 11 (1997), S. 761-769 
    ISSN: 0268-2605
    Keywords: methylmercury ; dimethylmercury ; mercury speciation ; estuarine sediment ; sodium borohydride derivatization ; atomic fluorescence spectrometry ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: This paper presents a method capable of quantitatively separating sub-nanogram amounts of monomethylmercury cation (MeHg+) and dimethylmercury from sediments by vacuum distillation at 40 °C and 6 μm Hg pressure followed by hydride derivatization and atomic fluorescence spectrometric detection. Concentrations of MeHg+ in Great Bay Estuarine sediments ranged from 2.2 to 7.3 ng g-1 (dry weight) with a 4.7 ng g-1 average for samples taken over nine weeks of the 1996 summer. The RSD for replicate determinations of a homogenized estuarine sediment is typically less than 6%. The detection limit for the routine determinations on MeHg+ is 0.2 ng g-1 dry weight of sediment. We validated the method by determining MeHg+ concentration in reference sediment S-19, by confirming our method against an established extraction method, and by recovering 85% of 10 ng MeHgCl spiked into estuarine sediments. This paper also includes significant improvements in the hydride derivatization method for mercury compounds relative to previous work with respect to faster analysis time and lower detection limits. © 1997 John Wiley & Sons, Ltd.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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