Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Carbon sheets

Electron diffraction studies [3] have revealed that hexagons within the sheets are helically wrapped along the axis of the nanotubes. The interlayer spacing between sheets is 0.34 nm which is slightly larger than that of graphite (0.3354 nm). It was dso reported [2] that the helicity aspect may vary from one nanotube to another. Ijima et al. [2] also reported that in addition to nanotubes, polyhedral particles consisting of concentric carbon sheets were also observed. [Pg.149]

The basic building block of carbon is a planar sheet of carbon atoms arranged in a honeycomb structure (called graphene or basal plane). These carbon sheets are stacked in an ordered or disordered manner to form crystallites. Each crystallite has two different edge sites (Fig. 2) the armchair and zig-zag sites. In graphite and other ordered carbons, these edge sites are actually the crystallite planes, while in disordered soft and hard carbons these sites, as a result of turbostratic disorder, may not... [Pg.430]

A glance at the structure of graphite, illustrated in Fig. 1, reveals the presence of voids between the planar, sp -hybridized, carbon sheets. Intercalation is the insertion of ions, atoms, or molecules into this space without the destruction of the host s layered, bonding network. Stacking order, bond distances, and, possibly, bond direction may be altered, but the characteristic, lamellar identity of the host must in some sense be preserved. [Pg.282]

As with graphite oxide, there are currently two views as to the structure of carbon monofluoride. Although detailed X-ray diffraction work suggested a chair arrangement of the sp -hybridized, carbon sheets (Ml), second-moment calculations of the adsorption mode of the fluorine nuclear magnetic resonance suggested that a boat arrangement is more plausible iE2). The structures are illustrated in Fig. 3. [Pg.284]

The carbon sheets form hexagonal nets, each of which is displaced with respect to the one below. [Pg.454]

The selective deposition of catalyst particles on the inner or on the outer walls of CNTs is the prerequisite for the investigation or utilization of the confinement effect, as discussed in Section 15.2.3. Wet chemistry methods making use of the capillary effect are most effective however, they depend on surface functionalization and tube diameter. In any case, CNT caps as well as radial carbon sheets and walls blocking parts of the inner CNT cavity have to be removed prior to impregnation, e.g., by mild oxidative treatment. The impregnation of this material with a limited amount of liquid can lead... [Pg.413]

X-ray diffraction studies suggested a disordered carbon structure with a large number of single layer carbon sheets. [Pg.244]

Decarburization is intentional in the processing of low-carbon sheet steels for electrical applications. In the production of malleable cast iron by annealing while cast iron deearburizalion is beneficial. [Pg.470]

The carbon sheets in graphite are separated by a distance of 335 pm and are held together by only London dispersion forces. Atmospheric gases can be absorbed between the sheets, thus enabling the sheets to easily slide over one another. As a result, graphite has a slippery feel and can be used as a lubricant. Because the sheets are so far apart, it s relatively difficult for an electron to hop from one sheet to the next and the electrical conductivity in the direction perpendicular to the sheets is therefore about 104 times smaller than the conductivity parallel to the sheets. [Pg.824]

The SiC coating is processed based on the reaction of SiO vapor and carbon materials. Commercial SiO powders (99.9% pure) are provided as the silicon source. The carbon materials are placed on the SiO powder bed via a carbon felt as illustrated in Fig. 10.1. This assembly is covered with carbon sheets in an alumina crucible to keep the SiO gas pressure in the crucible, and heated in a vacuum furnace at various temperatures from 1150 to 1550°C in vacuum (about 0.03 Pa) for periods of time between 1 and 90 minutes. It is necessary to heat at a temperature greater than 1150°C for the vaporization of solid SiO. [Pg.261]

Figure 10.3 shows the relation between temperature and pressure in the furnace when the assembly of SiO powders, carbon sheets and carbon felts is heated. The increase of the total pressure in the furnace at about 1200°C results from the vaporization of SiO according to reaction (10.1). The evolution of CO gas by the formation of SiC according to reaction (10.2) causes the increase of the total pressure after vaporization of SiO.34-36 In this case, the... [Pg.262]

Based on these analyses on the SiC coating, the growth mechanism of the SiC layer on diamond is considered as follows. In the early stage of the SiC formation on diamond, a very thin SiC layer is formed on the diamond surface according to reaction (10.2) between diamond and SiO(g). Once the SiC layer is formed, this reaction does not proceed due to the protective layer of SiC. The carbon sheet and felt in an alumina crucible act as the carbon source. The reaction of C02(g) with these carbon sources will produce further CO(g) and deposit SiC(s) by reaction (10.7). Thin j3-SiC whiskers are observed on the surface of the SiC-coated diamond, suggesting the vapor growth of SiC. [Pg.264]

Figure 9. Organization of carbon sheets in nanocrystalhne carbons. Case (A) represent bent sheets which are stacked concentrically and randomly. In the high-resolution TEM of fullerene black filamentous structures from carbon macrocycles which did not react to fullerene molecules can also be seen (weak contrasts). Case (B) shows the arrangement of stacks of planar graphene units. Only few of these stacks are oriented with the o-axis parallel to the electron beam and can be imaged as illustrated in the sketch, the majority are randomly orientated and give hence an amorphous contrast. Case (C) is the same as (B) with the addition of covalent bonding interactions between the stacks. These bonds are invisible by electron microscopy but influence the graph-iti/ability of the carbon. Figure 9. Organization of carbon sheets in nanocrystalhne carbons. Case (A) represent bent sheets which are stacked concentrically and randomly. In the high-resolution TEM of fullerene black filamentous structures from carbon macrocycles which did not react to fullerene molecules can also be seen (weak contrasts). Case (B) shows the arrangement of stacks of planar graphene units. Only few of these stacks are oriented with the o-axis parallel to the electron beam and can be imaged as illustrated in the sketch, the majority are randomly orientated and give hence an amorphous contrast. Case (C) is the same as (B) with the addition of covalent bonding interactions between the stacks. These bonds are invisible by electron microscopy but influence the graph-iti/ability of the carbon.
Perhaps the recently studied graphitic microtubes [29] with their cylindrical folded two-dimensional carbon sheets will, like the fullarenes, mix quasi-two- and three-dimensional properties. [Pg.33]

Units of permeation rate cm (STP)/cm -s-cm Hg. Substrate 1-mil-thick silicone-carbonate sheet (MEM 213, General Electric). [Pg.752]

The connections between the elements and the plates in special cases can also be made by chemical reaction. For example, carbon membrane tubes can be connected to carbon sheets through cross linking at high temperatures and circumvent the need for gaskets. [Pg.169]

With the uptake of AsFg (to composition C14ASF6 VizAsFs), the carbon-atom sheets move into registry with one another, as well as farther apart. The observed diffracted X-ray intensities require that the As atoms be placed midway between the enclosing carbon sheets. In the ah plane, all of the... [Pg.576]

The presence of graphite-like vibrations, occurring at practically the same frequency as in graphite itself, establishes the planarity of the carbon sheets in Cj,F, (HF), even at C/F ratios of two. [Pg.594]


See other pages where Carbon sheets is mentioned: [Pg.27]    [Pg.369]    [Pg.393]    [Pg.393]    [Pg.70]    [Pg.401]    [Pg.62]    [Pg.134]    [Pg.297]    [Pg.56]    [Pg.58]    [Pg.263]    [Pg.489]    [Pg.180]    [Pg.101]    [Pg.102]    [Pg.104]    [Pg.3]    [Pg.510]    [Pg.609]    [Pg.44]    [Pg.393]    [Pg.393]    [Pg.752]    [Pg.752]    [Pg.222]    [Pg.551]    [Pg.554]    [Pg.575]    [Pg.576]    [Pg.577]    [Pg.592]   
See also in sourсe #XX -- [ Pg.334 ]




SEARCH



Carbon Fibers graphite like sheets

Carbon fiber sheet

Carbon graphene sheets

Carbon materials sheets

Carbon nanofiber sheets

Carbon nanotubes sheets

Carbon sheets aromaticity

Parallel stacked carbon sheets

© 2024 chempedia.info