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'''Graphitizing''' and '''non-graphitizing''' carbons (alternatively graphitizable and non-graphitizable carbon) are the two categories of [[carbon]] produced by [[pyrolysis]] of organic materials. [[Rosalind Franklin]] first identified them in a 1951 paper in ''[[Proceedings of the Royal Society]]''.<ref>{{cite journal|author= R.E. Franklin |title= Crystallite growth in graphitizing and non-graphitizing carbons |journal= Proceedings of the Royal Society A|volume=209|pages=
The precursors for graphitizing carbons pass through a fluid stage during pyrolysis ([[carbonization]]). This fluidity facilitates the molecular mobility of the aromatic molecules, resulting in intermolecular dehydrogenative polymerization reactions to create aromatic, lamellar (disc-like) molecules. These “associate” to create a new liquid crystal phase, the so-called mesophase. A fluid phase is the dominant requirement for production of graphitizable carbons.<ref name= Mesophase >H. Marsh and M.A. Diez (1994) " Mesophase of Graphitizable Carbons" In: Shibaev V.P., Lam L. (eds) Liquid Crystalline and Mesomorphic Polymers. Springer, New York, NY {{DOI| 10.1007/978-1-4613-8333-8_7 }}</ref>
Non-graphitizing carbons generally do not pass through a fluid stage during carbonization. Since the time of Rosalind Franklin, researchers have put forward a number of models for their structure . Oberlin and colleagues emphasised the role of basic structural units (BSU), made of planar aromatic structures consisting of less than 10-20 rings, with four layers or fewer. Cross-linking between the BSUs in non-graphitizing carbons prevents graphitization<ref>{{cite journal|author= A. Oberlin |title= Carbonization and graphitization |journal= Carbon|volume=22|pages=
==See also==
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