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F. Dulong

Publications and source records attributed to F. Dulong.

3 recordsLinked to original sources

Origin and significance of high nickel and chromium concentrations in pliocene lignite of the Kosovo Basin, Serbia

Trace element data from 59 Pliocene lignite cores from the lignite field in the Kosovo Basin, southern Serbia, show localized enrichment of Ni and Cr (33-304 ppm and 8-176 ppm, respectively, whole-coal basis). Concentrations of both elements decrease from the western and southern boundaries of the lignite field. Low-temperature ash and polished coal pellets of selected bench and whole-coal samples were analyzed by X-ray diffraction and scanning electron microscopy with energy-dispersive X-ray analyses. These analyses show that most of the Ni and Cr are incorporated in detrital and, to a lesser degree, in authigenic minerals. The Ni- and Cr-bearing detrital minerals include oxides, chromites, serpentine-group minerals and rare mixed-layer clays. Possible authigenic minerals include Ni-Fe sulfates and sulfides. Analyses of three lignite samples by a supercritical fluid extraction technique indicate that some (1-11%) of the Ni is organically bound. Ni- and Cr-bearing oxides, mixed-layer clays, chromites and serpentine-group minerals were also identified in weathered and fresh samples of laterite developed on serpentinized Paleozoic peridotite at the nearby Glavica and C??ikatovo Ni mines. These mines are located along the western and northwestern rim, respectively, of the Kosovo Basin, where Ni contents are highest. The detrital Ni- and Cr-bearing minerals identified in lignite samples from the western part of the Kosovo Basin may have been transported into the paleoswamp by rivers that drained the two Paleocene laterites. Some Ni may have been transported directly into the paleoswamp in solution or, alternatively, Ni may have been leached from detrital minerals by acidic peat water and adsorbed onto organic matter and included into authigenic mineral phases. No minable source of Ni and Cr is known in the southern part of the lignite field; however, the mineral and chemical data from the lignite and associated rocks suggest that such a source area may exist.

International Journal of Coal Geology↗

Superparamagnetic Fe 3 O 4 particles formed by oxidation of pyrite heated in an anoxic atmosphere

As a follow-up to previous gas analysis experiments in which pyrite was heated to 681 K in an anoxic (oxygen starved) atmosphere, the first oxidation product, FeSO 4 , was studied as a bulk material. No decomposition of FeSO 4 to Fe 3 O 4 was observed in the temperature range studied. The lack of decomposition of bulk FeSO 4 to Fe 3 O 4 suggests that FeS 2 oxidizes directly to Fe 3 O 4 , or that FeSO 4 , FeS 2 and O 2 react together to form Fe 3 O 4 . Magnetic susceptibility and magnetization measurements, along with magnetic hysteresis curves, show that small particles of Fe 3 O 4 form on the pyrite surface, rather than a continuous layer of bulk Fe 3 O 4 . A working model describing the oxidation steps is presented.

Fuel↗

The 57 Fe Mössbauer parameters of pyrite and marcasite with different provenances

Eighteen pyrite and twelve marcasite samples which have different provenances have been investigated to determine the systematics of the influence of mineralogical and geological factors on the 57 Fe Mössbauer spectra at 298 K. The following results have been obtained: there is no ambiguity in distinguishing single phase pyrite from single phase marcasite by means of 57 Fe Mössbauer spectroscopy at 298 K. At 298 K the average electric quadrupole splitting, 〈 ΔE Q 〉, and average isomer shift, 〈δ〉, with respect to Fe metal, are 0.6110 ± 0.0030 mm s −1 and 0.313 ± 0.008 mm s −1 , respectively, for the 18 pyrites; 〈 ΔE Q 〉 = 0.5030 ± 0.0070 mm s −1 and 〈 δ 〉 = 0.2770 ± 0.0020 mm s −1 for the 12 marcasites. At 77 K, ΔE Q is 0.624 mm s −1 for pyrite and 0.508 mm s −1 for marcasite. In distinguishing pyrites from marcasites, spectra obtained at 77 K are not warranted. The Mössbauer parameters of pyrite and marcasite exhibit appreciable variations, which bear no simple relationship to the geological environment in which they occur but appear to be selectively influenced by impurities, especially arsenic, in the pyrite lattice. Quantitative and qualitative determinations of pyrite/marcasite mechanical mixtures are straightforward at 298 K and 77 K but do require least-squares computer fittings and are limited to accuracies ranging from ±5 to ±15 per cent by uncertainties in the parameter values of the pure phases. The methodology and results of this investigation are directly applicable to coals for which the presence and relative amounts of pyrite and marcasite could be of considerable genetic significance.

Geochimica et Cosmochimica Acta↗