Other
Scientific paper
Sep 1981
adsabs.harvard.edu/cgi-bin/nph-data_query?bibcode=1981gecoa..45.1411t&link_type=abstract
Geochimica et Cosmochimica Acta, vol. 45, Issue 9, pp.1411-1419
Other
9
Scientific paper
The ferric oxide formed by oxidation of Fe(II) in Esthwaite Water, U.K., during the lake's seasonal thermal stratification and deep-water anoxia consists of amorphous particles which are approximately spherical or ellipsoidal, with diameters in the range 0.05-0.5 m. Concentrations in the lake are 10 11 -10 12 particles per litre, corresponding to 3 mg l -1 Fe. Unlike iron oxides of similar chemical composition formed by oxidative mechanisms in soil-borne waters, the particles do not appear to be composed of small primary particles. This is possibly because in the lake they form slowly, at low supersaturation. The particles contain 30-40% by weight Fe. The carbon content is uncertain because of contamination but is in the range 4-18%. Humic carbon contributes at least 4-7% of the total weight. Other major elements present are P, N, Mn, Si, S. Ca and Mg, comprising between them up to 8% of the total weight. The particles are negatively charged probably because of adsorbed humic substances, and also phosphate and silicate. Their electrophoretic mobility-pH dependence is similar to those of synthetic iron oxides added to samples of surface Esthwaite Water. The calculated zeta potential is - 27 mV, which is sufficiently high to make flocculation slow under lake conditions. The low flocculation rate partially accounts for the formation of a well-defined peak of particulate iron in the water column of the lake.
Cooke David
Tipping Edward
Woof Colin
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