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Carbon growth mechanisms

M. Endo. Meeanisme de eroissanee en phase vapeur de fibres de earhone (Tlte growth mechanism of vapor-grown carbon fibers). PhD thesis. University of Orleans, Orleans, France, 1975. (in French). [Pg.87]

Key Words—Carbon nanotubes, vapor-grown carbon fibers, high-resolution transmission electron microscope, graphite structure, nanotube growth mechanism, toroidal network. [Pg.1]

Growth mechanism of a (9n,0) tubule, over 24n coordination sites of the catalyst. The growth of a general (9 ,0) tubule on the catalyst surface is illustrated by that of the (9,0) tubule in Fig. 16 which shows the unsaturated end of a (9,0) tubule in a planar representation. At that end, the carbons bearing a vacant bond are coordinatively bonded to the catalyst (grey circles) or to a growing cis-polyacetylene chain (oblique bold lines in Fig. 16). Tlie vacant bonds of the six c/s-polyacetylene chains involved are taken to be coordinatively bonded to the catalyst [Fig. 16(b)]. These polyacetylene chains are continuously extruded from the catalyst particle where they are formed by polymerization of C2 units assisted by the catalyst coordination sites. Note that in order to reduce the number of representations of important steps, Fig. 16(b) includes nine new Cj units with respect to Fig. 16(a). [Pg.99]

The direct linking of carbon nanotubes to graphite and the continuity in synthesis, structure and properties between carbon nanotubes and vapor grown carbon fibers is reviewed by the present leaders of this area, Professor M. Endo, H. Kroto, and co-workers. Further insight into the growth mechanism is presented in the article by Colbert and Smalley. New synthesis methods leading to enhanced production... [Pg.192]

Although the Langelier index is probably the most frequently quoted measure of a water s corrosivity, it is at best a not very reliable guide. All that the index can do, and all that its author claimed for it is to provide an indication of a water s thermodynamic tendency to precipitate calcium carbonate. It cannot indicate if sufficient material will be deposited to completely cover all exposed metal surfaces consequently a very soft water can have a strongly positive index but still be corrosive. Similarly the index cannot take into account if the precipitate will be in the appropriate physical form, i.e. a semi-amorphous egg-shell like deposit that spreads uniformly over all the exposed surfaces rather than forming isolated crystals at a limited number of nucleation sites. The egg-shell type of deposit has been shown to be associated with the presence of organic material which affects the growth mechanism of the calcium carbonate crystals . Where a substantial and stable deposit is produced on a metal surface, this is an effective anticorrosion barrier and forms the basis of a chemical treatment to protect water pipes . However, the conditions required for such a process are not likely to arise with any natural waters. [Pg.359]

An alternative route to obtain NbS2-sheathed carbon nanotubes (CNT) has been proposed by Zhu et al. [71] with this sonochemical method. In this study, CNTs act as templates to produce the uniform and well-crystallized bS2 nanotubes and the formation of such nanotubes has been explained by means of multi-point nuclei site growth mechanism. [Pg.207]

Charlier JC, Iijima S (2001) Growth mechanisms of carbon nanotubes. Carbon Nanotubes 80 55-80. [Pg.259]

Raiswell R, Fisher QJ (2000) Mudrock-hosted carbonate concretions a review of growth mechanisms and their influence on chemical and isotopic composition. J Geol Soc 157 239-251 Roden EE, Lovley DR (1993) Dissimilatory Fe (111) reduction by the marine microorganism Desulfuromonas acetoxidans. App Environ Microbio 59 734-742... [Pg.407]

Properties of thin layers of lead electrodeposited on vitreous carbon have been found identical with that of metallic lead [304]. Therefore Pb and Pb02 coated reticulated vitreous carbon (RVC) electrodes [185] can be applied as electrodes in lead-acid batteries, as reviewed in [305]. The deposition of lead on carbon is through the diffusion-controlled process with instantaneous or progressive nucleation, for high and low Pb + concentration, respectively, and three-dimensional growth mechanism. The number of nucleation sites increases with deposition overpotential, as shown for vitreous [306] and glassy carbon [307] electrodes. The concentration dependence of the nucleation... [Pg.821]

Fig. 7. Growth mechanism of graphitic carbon nanofibers. The illustration highlights the observation of spontaneous nickel step edge formation at the carbon-nickel interface. The observations in Reference (52) are consistent with a growth mechanism involving surface transport of carbon and nickel atoms along the graphene-nickel interface. Fig. 7. Growth mechanism of graphitic carbon nanofibers. The illustration highlights the observation of spontaneous nickel step edge formation at the carbon-nickel interface. The observations in Reference (52) are consistent with a growth mechanism involving surface transport of carbon and nickel atoms along the graphene-nickel interface.

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Carbon growth

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