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Graphite morphology

Cerium or misch metal as innoculant to modify the graphite morphology from flakes to nodular... [Pg.9]

Machining of Spheroidal Ductile Iron, Fig. 1 Possible graphite morphologies (SEM images) grey cast iron (a), compacted cast iron (b), spheroidal cast iron (c). Above adequate optical images (Nayyar et al. 2012)... [Pg.803]

Fig. 14. Titanium carbide coating on graphite showing the nodular growth with a columnar morphology and the fracturing resulting from a coefficient of... Fig. 14. Titanium carbide coating on graphite showing the nodular growth with a columnar morphology and the fracturing resulting from a coefficient of...
Crystal Morphology. Size, shape, color, and impurities are dependent on the conditions of synthesis (14—17). Lower temperatures favor dark colored, less pure crystals higher temperatures promote paler, purer crystals. Low pressures (5 GPa) and temperatures favor the development of cube faces, whereas higher pressures and temperatures produce octahedral faces. Nucleation and growth rates increase rapidly as the process pressure is raised above the diamond—graphite equiUbrium pressure. [Pg.563]

It has been established that, when mesophase pitch is carbonized, the morphology of the pitch is the primary factor [20] in determining the microstructure of the resulting graphitic material. This may be attributed to the stacking behavior of mesophase molecules (quite similar to the planar stacking in turbostratic graphite), which may be visualized as shown in Fig. 5. [Pg.125]

Structure and morphology. Most of the rare-earth elements were encapsulated in multilayered graphitic cages, being in the form of single-domain carbides. The carbides encapsulated were in the phase of RC2 (R stands for rare-earth elements) except for Sc, for which Sc3C4(20] was encapsulated[21]. [Pg.155]

Fig. 4. Typical tip morphology obtained after high-temperature treatment (2000 °C) of oxidation opened CNTs. Note the elimination of dangling bonds by a bending of graphitic layer (marked with arrows). Fig. 4. Typical tip morphology obtained after high-temperature treatment (2000 °C) of oxidation opened CNTs. Note the elimination of dangling bonds by a bending of graphitic layer (marked with arrows).
Optimisation of SWCNT production has been attempted within the framework of the arc-discharge method in which anode and cathode were made of graphite rods, a hole in the anode being filled with metal catalysts such as Y (1 at.%) and Ni (4.2 at.%) [7]. A dense collar deposit (ca. 20% of the total mass of graphite rod) formed around the eathode under He (ca. 500 Torr), with 30 V and 100 A de eurrent. It was eonfirmed that this optimal eollar eontained large amounts of SWCNT bundles eonsisting of (10, 10) SWCNTs (diameter 1.4 nm). Such morphology resembles that produced by the laser ablation teehnique [4,5]. [Pg.144]

Perhaps the first practical application of carbonaceous materials in batteries was demonstrated in 1868 by Georges Le-clanche in cells that bear his name [20]. Coarsely ground MnO, was mixed with an equal volume of retort carbon to form the positive electrode. Carbonaceous powdered materials such as acetylene black and graphite are commonly used to enhance the conductivity of electrodes in alkaline batteries. The particle morphology plays a significant role, particularly when carbon blacks are used in batteries as an electrode additive to enhance the electronic conductivity. One of the most common carbon blacks which is used as an additive to enhance the electronic conductivity of electrodes that contain metal oxides is acetylene black. A detailed discussion on the desirable properties of acetylene black in Leclanche cells is provided by Bregazzi [21], A suitable carbon for this application should have characteristics that include (i) low resistivity in the presence of the electrolyte and active electrode material, (ii) absorption and retention of a significant... [Pg.236]

Apart from reactions with the electrolyte at the carbon surface, the irreversible specific charge is furthermore strongly affected by the possible co-intercalation of polar solvent molecules between the graphene layers of highly graphitic matrices [139]. This so-called "solvated intercalation reaction" depends (i) on the crystallinity and the morphology of the parent carbonaceous material, which will be discussed in Sec. [Pg.394]


See other pages where Graphite morphology is mentioned: [Pg.369]    [Pg.587]    [Pg.19]    [Pg.21]    [Pg.23]    [Pg.23]    [Pg.31]    [Pg.35]    [Pg.208]    [Pg.620]    [Pg.234]    [Pg.247]    [Pg.164]    [Pg.60]    [Pg.369]    [Pg.587]    [Pg.19]    [Pg.21]    [Pg.23]    [Pg.23]    [Pg.31]    [Pg.35]    [Pg.208]    [Pg.620]    [Pg.234]    [Pg.247]    [Pg.164]    [Pg.60]    [Pg.383]    [Pg.332]    [Pg.524]    [Pg.369]    [Pg.299]    [Pg.66]    [Pg.124]    [Pg.140]    [Pg.141]    [Pg.143]    [Pg.144]    [Pg.144]    [Pg.144]    [Pg.161]    [Pg.987]    [Pg.3]    [Pg.7]    [Pg.8]    [Pg.113]    [Pg.153]    [Pg.156]    [Pg.159]    [Pg.163]    [Pg.93]    [Pg.586]    [Pg.93]    [Pg.234]   
See also in sourсe #XX -- [ Pg.31 ]

See also in sourсe #XX -- [ Pg.383 ]




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