Organics in orogenic gold systems: characterization of organic matter associated with gold (Au) deposits

A Robert, H Grotheer, R Lockhart… - Goldschmidt 2014 …, 2014 - researchgate.net
Goldschmidt 2014 Abstracts. Sacramento, California, USA, 2014researchgate.net
Organic compounds can react with metal and sulfur species through a variety of processes
including redox reactions and may influence physico-chemical properties important to
mineralisation. The association of organic matter (OM) with metallogenic systems is well-
observed and studied in low to moderate (< 350 C) temperature regimes. Thermally mature
systems (> 350 C), common to most orogenic Au in Australia, challenge analytical methods
traditionally used for OM analyses. Presently, the characterisation provided by various state …
Organic compounds can react with metal and sulfur species through a variety of processes including redox reactions and may influence physico-chemical properties important to mineralisation. The association of organic matter (OM) with metallogenic systems is well-observed and studied in low to moderate (< 350 C) temperature regimes. Thermally mature systems (> 350 C), common to most orogenic Au in Australia, challenge analytical methods traditionally used for OM analyses. Presently, the characterisation provided by various state-of-the-art techniques (eg, catalytic Hydropyrolysis (HyPy), Gas Chromatography (GC) isotope ratio Mass Spectrometry (irMS), Scanning Electrom Microscopy (SEM) combined with Energy-dispersive X-ray spectroscopy (EDS)) was explored through application to OM from typically high temperature (> 550 C) orogenic Au deposits. Data obtained with the new methods show promising links between OM and mineralisation, despite the low organic carbon content and high relative thermal maturity of the samples.
HyPy released hydrocarbons (HCs) display a homologous series of C15 to C36 n-alkanes (n-C18, δ13C=-28.4‰) with a distinctive even carbon number preference. Other HCs detected in the HyPy fraction included polyaromatic HCs, mainly pyrene (δ13C=-16.3‰) and its hydrogenated products. These HCs were not detected in the bitumen fractions which showed essentially no GC-MS products and are structurally distinct from the carbonaceous “graphite” like material in the matrix and infills to mineral grains detected in SEM-EDS. The-20 to-30‰ bulk δ13C of OM reveal isotopically lighter carbon with increasing distance from the ore zone. Further experiments and analysis are currently conducted on samples from the mineralised and unmineralised zones and will be scrutinised for possible hydrothermal footprints in the petrogenic markers, as well as other clues on the role of OM in Au mineralisation.
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