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dc.creatorPremović, Pavle I.
dc.creatorAllard, T
dc.creatorNikolic, ND
dc.creatorTonsa, Ivana R.
dc.creatorPavlović, Mirjana S.
dc.date.accessioned2018-03-01T18:50:25Z
dc.date.available2018-03-01T18:50:25Z
dc.date.issued2000
dc.identifier.issn0016-2361
dc.identifier.urihttps://vinar.vin.bg.ac.rs/handle/123456789/2338
dc.description.abstractWe describe a new, rapid method for determining the concentration of vanadyl porphyrins (VO2+-P) associated with the kerogen of bituminous sedimentary rocks using electron spin resonance (ESR). The method is simple, straightforward and inexpensive. Several concentrations of a vanadyl (VO2+) standard dissolved in glycerol-lignite mixture were prepared. The VO2+ concentrations ranged from 100 to 1000 ppm. The anisotropic ESR spectra of both the standards and kerogen samples were recorded at room temperature and the integrated areas of the pre-selected ESR line (attributed to nuclear spin m(t) = -5/2) were computed. The concentrations of VO2+ found in the kerogen samples were calculated using the relative ratio of the integrated areas for the standards and the kerogen samples. The VO2+-P concentrations of the kerogen materials were then calculated using 350 as the mean molecular weight of these species. Quantitative determination of VO2+-P in the kerogen fractions in the range of 800-8000 ppm and higher is feasible by the method reported. The method of analysis was also extended to the asphaltene samples (enriched with VO2+-P) and a coal sample containing non-porphyrin VO2+ associated with its organic fraction. (C) 2000 Elsevier Science Ltd. All rights reserved.en
dc.rightsrestrictedAccessen
dc.sourceFuelen
dc.subjectvanadyl porphyrinsen
dc.subjectkerogenen
dc.subjectestimationen
dc.subjectconcentrationen
dc.titleEstimation of vanadyl porphyrin concentration in sedimentary kerogens and asphaltenesen
dc.typearticleen
dcterms.abstractAллард, Т; Николиц, НД; Тонса, ИР; Павловиц, МС; Премовиц, ПИ;
dc.citation.volume79
dc.citation.issue7
dc.citation.spage813
dc.citation.epage819
dc.identifier.wos000086311100011
dc.identifier.doi10.1016/S0016-2361(99)00205-7
dc.citation.rankM21
dc.identifier.scopus2-s2.0-0342758526


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