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Carbon bulk properties

If the focus of interest is on the carbon clusters themselves, then of course no substitute system can be used. However, for studying the convergence of properties towards bulk values one can minimize the termination effects by saturating the dangling bonds in the simplest possible way, i.e. with hydrogen. By that approach one can both avoid the problem of handling an excessive number of open shells, and obtain a series of molecules that converge towards bulk properties more smoothly than the bare carbon clusters. [Pg.38]

An elastomer is a polymer that is flexible, allowing it to be distorted from one shape to another. Polyisoprene (natural mbber), polybutadiene, and butadiene-styrene copolymer are the most important commercial elastomers. All contain some CDC bonds, and their bulk properties are affected by the varying geometries about the carbon atoms that make up the polymer backbone. [Pg.916]

Supercritical C02 (sc C02) is being used to accelerate the natural aging reactions (i.e., carbonation) of Portland cement. This treatment method alters the bulk properties of cement, producing profound changes in both structure and chemical composition. As a result of these changes, the mechanical and transport properties of these cements are also dramatically affected, and they display reduced porosity, permeability and pH, as well as increased density and compressive strength. [Pg.241]

Figure 21 provides an example of the use of ESCA to define an oxidation state of a freshly reduced palladium-on-carbon hydrogenation catalyst exposed to the air. The metallic palladium peaks (Fig. 21a) are quite evident, indicating no bulk oxidation occurred. There is a strong peak for carbon, probably due to adsorbed CO2 from the air. The presence of a small amount of PdO is suggested at 337 eV in Fig. 21B. This peak is a shoulder on the palladium 3 5/2 peak and most likely represents a surface layer of oxide on the palladium. This information could not be conveniently obtained by XRD because small palladium (or PdO) crystallites cannot diffract X rays. Furthermore, XRD measures bulk properties and would not see surface oxides even if the crystallite sizes were sufficiently large to be XRD sensitive. We can therefore expect to see more frequent use of ESCA or other surface sensitive techniques to monitor the surface of catalytic materials. Figure 21 provides an example of the use of ESCA to define an oxidation state of a freshly reduced palladium-on-carbon hydrogenation catalyst exposed to the air. The metallic palladium peaks (Fig. 21a) are quite evident, indicating no bulk oxidation occurred. There is a strong peak for carbon, probably due to adsorbed CO2 from the air. The presence of a small amount of PdO is suggested at 337 eV in Fig. 21B. This peak is a shoulder on the palladium 3 5/2 peak and most likely represents a surface layer of oxide on the palladium. This information could not be conveniently obtained by XRD because small palladium (or PdO) crystallites cannot diffract X rays. Furthermore, XRD measures bulk properties and would not see surface oxides even if the crystallite sizes were sufficiently large to be XRD sensitive. We can therefore expect to see more frequent use of ESCA or other surface sensitive techniques to monitor the surface of catalytic materials.
The basic problem with activated carbon is that, intrinsically, it is a poor electrical conductor. Moreover, the use of small particles instead of a bulk crystal adds a contribution to the contact resistance. A binder must be mixed with the powder to stick the carbon particles together. The choice of binder material type and amount is influenced by the carbon surface properties. [Pg.432]

Indeed, lattice parameters of both the copper and the zinc oxide were found to depend on the catalyst composition. The lattice extension of copper was attributed to alpha brass formation upon partial reduction of zine oxide, and an attempt was made to correlate the lattice constant of copper with the decomposition rate of methanol to methyl formate. Furthermore, the decomposition rate of methanol to carbon monoxide was found to correlate with the changes of lattice constant of zinc oxide. Although such correlations did not establish the cause of the promotion in the absence of surface-area measurements and of correlations of specific activities, the changes of lattice parameters determined by Frolich et al. are real and indicate for the first time that the interaction of catalyst components can result in observable changes of bulk properties of the individual phases. Frolich et al. did not offer an interpretation of the observed changes in lattice parameters of zinc oxide. Yet these changes accompany the formation of an active catalyst, and much of this review will be devoted to the origin, physicochemical nature, and catalytic activity of the active phase in the zinc oxide-copper catalysts. [Pg.247]

Bulk property detectors, and in particular, the refractive index detector, have an inherently limited sensitivity irrespective of the instmmental technique that is used. Consider a hypothetical bulk property detector that monitors, for example, the density of the eluent leaving the column. Assume it is required to detect the concentration of a dense material, such as carbon tetrachloride (specific gravity 1.595), at a level of 1 pg/ml in w-heptane (specific gravity 0.684). [Pg.259]

The advent of high-strength carbon-based fibers has led to a number of structural applications in medical treatment. The specifications for implanted materials required that they offer acceptable long-term mechanical properties and surfaces that are biocompatible [126]. Surface compatibility affects immediate acceptance, while the long-term mechanical performance is determined by the bulk properties of the implant. [Pg.54]

In Volume 26 we assembled three reviews in which the control of bulk properties of carbon was shown to be the key to succe.s.sfiil and widely varying applications. The common theme in the present volume is that surface properties are crucial in the environmental and electrochemical applications of carbon. [Pg.424]

Considerating the number and relative stringency of the functional criteria satisfied by the protein folds - - self-organizing robustness in conjunction with marginal stabihty, diverse architectures, a hydrophobic core fit for organic synthesis, diverse bulk properties, etc. - it seems likely that few other types of polymer will be equally fit. At present, I think that current knowledge is consistent with the possibility that the protein folds represent an ensemble of natural forms uniquely fit for the mechanism we call life. If correct, this not only would support Henderson s contention that the cosmos is fine-tuned for carbon-based life, but would further restrict this statement to the protein-based variety of life that exists currently on earth. [Pg.275]

There is a major drawback, however, to the preparation of carbon onions by electron bombardment the amounts obtained are extremely small and thus render the examination of bulk properties virtually impossible. Only high-energy electron sources outside an HRTEM would enable the production of macroscopic amounts. S till a further development of this method is of considerable interest as the carbon onions made from diamond are very uniform in quality. [Pg.305]

Catalytic behavior of carbon materials depends on their surface properties, but surface properties are to a large extent a consequence of bulk properties. Therefore, after a brief overview of the ways that carbon materials are formed, I discuss their bulk properties briefly before focusing on their physical and chemical surface properties and their chemical (re)activity. [Pg.2]


See other pages where Carbon bulk properties is mentioned: [Pg.9]    [Pg.388]    [Pg.121]    [Pg.111]    [Pg.30]    [Pg.62]    [Pg.228]    [Pg.542]    [Pg.416]    [Pg.109]    [Pg.360]    [Pg.253]    [Pg.6]    [Pg.244]    [Pg.739]    [Pg.154]    [Pg.168]    [Pg.174]    [Pg.9]    [Pg.361]    [Pg.266]    [Pg.112]    [Pg.81]    [Pg.213]    [Pg.121]    [Pg.847]    [Pg.848]    [Pg.82]    [Pg.185]    [Pg.173]    [Pg.77]    [Pg.266]    [Pg.156]    [Pg.470]    [Pg.546]    [Pg.127]    [Pg.16]    [Pg.18]    [Pg.18]   
See also in sourсe #XX -- [ Pg.16 ]




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