468
Views
60
CrossRef citations to date
0
Altmetric
Original Articles

Conditions and mechanism of formation of nano-polycrystalline diamonds on direct transformation from graphite and non-graphitic carbon at high pressure and temperature

, , , &
Pages 63-69 | Received 18 Feb 2006, Published online: 21 Aug 2006
 

Abstract

The conditions and mechanism of formation of nano-polycrystalline diamonds directly from graphite and non-graphitic carbon (carbon black, glassy carbon, C60 and carbon nanotubes) at high pressure and high temperature have been investigated. The onset temperature for diamond formation at Pq 15 GPa is 1500–1600 °C for all carbon materials, although the required temperature conditions for pure polycrystalline diamond are Tq 2200 °C for graphite and Tq 1600 °C for non-graphitic carbon. Polycrystalline diamond forms as a result of simultaneous diffusion and two-step martensitic processes from graphite, whereas it forms only due to diffusion without graphitization or formation of intermediate phases from non-graphitic carbon. Nano-polycrystalline diamonds consisting only of very fine particles (<10 nm in size) can be obtained from non-graphitic carbon at T∼ 1600–2000 °C under pressures≥q15 GPa.

Acknowledgement

The authors thank A. Saiyama, H. Namura and A. Kurio for experimental assistance on this work.

Log in via your institution

Log in to Taylor & Francis Online

PDF download + Online access

  • 48 hours access to article PDF & online version
  • Article PDF can be downloaded
  • Article PDF can be printed
USD 61.00 Add to cart

Issue Purchase

  • 30 days online access to complete issue
  • Article PDFs can be downloaded
  • Article PDFs can be printed
USD 1,965.00 Add to cart

* Local tax will be added as applicable

Related Research

People also read lists articles that other readers of this article have read.

Recommended articles lists articles that we recommend and is powered by our AI driven recommendation engine.

Cited by lists all citing articles based on Crossref citations.
Articles with the Crossref icon will open in a new tab.