Influence of Rhombohedral Graphite Phase on the Diamond Nucleation

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Abstract:

The high pressure and temperature, synthesis of diamond from carbonaceous materials, is a complex process highly dependent on variables such as the catalyst/solvent, the crystalline structure of the precursor material, the processing conditions and the type of compressive chamber. The optimum susceptible precursors to be transformed into diamond are those possessing the perfect hexagonal graphite structure, which is the thermodynamically most stable form of carbon at atmospheric pressure and ambient temperature. However, the majority of both industrial and natural graphites, presents a mixture of different atomic structural arrangements that greatly influence the process of diamond synthesis. In this works the influence of rhombohedral and hexagonal phases existing in the graphite was performed by means of a software refinement of the crystal structures using the Rietveld method. The thermobaric treatment, which determine the structural parameters, was conducted in a high pressure anvil type device with a central concavity. All experiments were carried out at 1200°C and pressures varying from 4.3 to 5.0 GPa. It was determined that the degree of graphite to diamond transformation is directly associated with the content of rhombohedral phase.

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Materials Science Forum (Volumes 727-728)

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1364-1368

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August 2012

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© 2012 Trans Tech Publications Ltd. All Rights Reserved

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[1] A. L. D. Skury, G. S. Bobrovnitchii, S. N. Monteiro. The role of the graphitation degree, on the high pressure-high temperature diamond synthesis. Diamond and Related Materials, 12, pp.1999-2002 (2003).

DOI: 10.1016/s0925-9635(03)00282-6

Google Scholar

[2] W. Kohs, H.J. Santner, F. Hofer, H. Schrottner, J. Doninger, I. Barsukov, H. Buqa, J.H. Albering, K.C. Moller, J.O. Besenhard, M. Winter. A study on electrolyte interactions with graphite anodes exhibiting structures with various amounts of rhombohedral phase. Journal of Power Sources. 528-537 (2003).

DOI: 10.1016/s0378-7753(03)00278-7

Google Scholar

[3] H.A. Wilhelm, B. Croset, G. Medjahdi. Proportion and dispersion of rhombohedral sequences in the hexagonal structure of graphite powders. Carbon 45, 2356-2364 (2007).

DOI: 10.1016/j.carbon.2007.07.010

Google Scholar

[4] H. Shi, J. Barker, M.Y. Saïdi and R. Koksbang, Structure and lithium intercalation properties of synthetic and natural graphite. J Electrochem Soc, 143 11, p.3466–3472 (1996).

DOI: 10.1149/1.1837238

Google Scholar

[5] B. Kwiecinska and F. Kajzar, The Rhombohedral contribution in natural graphite determined by neutron diffraction technique. Mineral Polonica, 6, p.25–34 (1975).

Google Scholar

[6] A. L. D. Skury, G. S. Bobrovnitchii, S. N. Monteiro. Influence of the graphitation process in the synthesis of diamonds from a C-Ni-Mn system. Jourmal Superhard Materials, 5, pp.3-8 (2001).

Google Scholar

[7] V. I. Kasatotchki, L.E. Shterenberg, V. N. Slesarev, N. Yu., Dependence of the the sinthesis of diamond on the nature of the original carbon. Soviet Physics Doklady, 15(10) 930-932 (1971).

Google Scholar

[8] O. Volher, G. Nutsch, G. Collin, F. Von Sturm, E. Wege, W. Frohs, K.D. Henning, H. Von Kienle, M. Voll, P. Kleinschmitt, Carbon graphite, Ullmann's encyclopedia of industrial chemistry, sixth ed., Electronic Release (2002).

DOI: 10.1002/14356007.a05_095

Google Scholar

[9] S. Chehab, K. Guerin, J. Amiell, S. Flandrois. Magnetic properties o fmixed graphite containing both hexagonal an rhombohedral forms. The European Phisical Journal B, 13, pp.235-243 (2000).

DOI: 10.1007/s100510050028

Google Scholar

[10] H. E. Lipson, A.R. Stokes. Proc. R. Sot. London, Ser. A 181, 101 (1942).

Google Scholar

[11] M. Inagaki, K. Hayashia, S. Naka. High Temperature-High Pressure, 3, p.355 (2000).

Google Scholar