Abstract
The influence of СО2 and Н2О on the morphology of diamond dissolution in carbonate melts was studied experimentally at pressure 5.7-7.0 GPa and temperature 1400-1750 °С, using a BARS multi-anvil apparatus. It has been established that diamond dissolution in fluid-free carbonate melts starts with the development of positive trigons on the {111} diamond faces, followed by truncation of crystal edges by trigon-trioctahedral surfaces, and finally by the transformation of diamond into spherical dodecahedroid-like morphology. Diamond dissolution in СО2-bearing carbonate melts also begins with the formation of positive trigons on the {111} faces and development trigon-trioctahedron surfaces on the edges. Dissolution form changes from trigon-trioctahedron to dodecahedroid with increasing loss of initial weight. Addition of more than 8 wt% of Н2О into the carbonate medium changes the orientation of the trigons and the secondary morphology of diamond. At the beginning of the process, negative trigons and ditrigonal (shield-shaped) dissolution layers developed on the {111} faces. Dissolution form of diamond in water-bearing melts is tetrahexahedroid, which is most similar to rounded natural diamonds. The results obtained allow us to regard the morphology of trigons and dissolution forms as an indicator of the composition of the diamond dissolution medium. The experiments suggest that the morphology of diamond during dissolution is controlled by the presence of water in a system. Our data show that the СО2/(СО2+Н2О) ratio by weight value was <0.81 during natural diamond dissolution.
© 2015 by Walter de Gruyter Berlin/Boston
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Artikel in diesem Heft
- Ti-Al zoning of experimentally grown titanite in the system CaO-Al2O3-TiO2-SiO2-NaCl-H2O-(F): Evidence for small-scale fluid heterogeneity
- A new method for quantitative petrography based on image processing of chemical element maps: Part I. Mineral mapping applied to compacted bentonites
- A new method for quantitative petrography based on image processing of chemical element maps: Part II. Semi-quantitative porosity maps superimposed on mineral maps
- Enhancement of solid-state reaction rates by non-hydrostatic stress effects on polycrystalline diffusion kinetics
- (H3O)Fe(SO4)2 formed by dehydrating rhomboclase and its potential existence on Mars
- Crystal chemistry and low-temperature behavior of datolite: A single-crystal X-ray diffraction study
- Density and seismic velocities of chromitite body in oceanic mantle peridotite
- Packing schemes of cavities in selected clathrasils and zeolites and the analogous packings of atoms in crystal structures
- Temperature dependence of IR absorption of OH species in clinopyroxene
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- Kinetics of Fe-oxidation/deprotonation process in Fe-rich phlogopite under isothermal conditions
- On the crystal chemistry of londonite [(Cs,K,Rb)Al4Be5B11O28]: A single-crystal neutron diffraction study at 300 and 20 K
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- Primary Nb-Ta minerals in the Szklary pegmatite, Poland: New insights into controls of crystal chemistry and crystallization sequences
- Evolution of the interlayer space of hydrated montmorillonite as a function of temperature
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- Lead-tellurium oxysalts from Otto Mountain near Baker, California: IV. Markcooperite, Pb(UO2)Te6+O6, the first natural uranyl tellurate
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