Textured carbon

Texier-Mandoki, N., J. Dentzer, T. Piquero, S. Saadallah, P. David, C. Vix-Guterl, Hydrogen storage in activated carbon materials Role of the nanoporous texture. Carbon 42(12-13), 2744-2747 2004. 

Job J, Heinrichs B, Lambert S et al (2006) Carbon Xerogels as Catalyst Supports Study of Mass Transfer. American Institute of Chemical Engineers Fluid Mechanics and Transport Phenomena 52 2663-2676 Job N, Heinrichs B, Ferauche F et al (2005) Hydrodechlorination of 1,2-dichloroethane on Pd-Ag catalysts supported on tailored texture carbon xerogels. Catalysis Today 102 234—241... 

Fig. 3. Effect of using either liquid or supercritical carbon dioxide on the textural properties of titania aerogels calcined at the temperatures shown. (—), dried with Hquid carbon dioxide at 6 MPa and 283 K (-------), dried with supercritical carbon dioxide at 30 MPa and 323 K. Reproduced from Ref. 36.

The abihty of algiaates to form edible gels by reaction with calcium salts is an important property. Calcium sources are usually calcium carbonate, sulfate, chloride, phosphate, or tartrate (20). The rate of gel formation as well as the quaUty and texture of the resultant gel can be controlled by the solubihty and availabiUty of the calcium source. 

Calcium carbonate is one of the most common filler/extenders used in the paint and coatings industry. Consumer and contractor paint formulas can include products from submicrometer size to coarse mesh sizes. The main function of calcium carbonate in paint is as a low cost extender. It is also used to improve brightness, appHcation properties, stabiHty, and exposure resistance. Coarse products help to lower gloss and sheen or even provide textured finishes. The selection of product type and particle size is deterrnined by the desired performance and cost of the coating. 

To date, there has been relatively little work reported on the mesophase pitch rheology which takes into account its liquid crystalline nature. However, several researchers have performed classical viscometric studies on pitch samples during and after their transformation to mesophase. While these results provide no information pertaining to the development of texture in mesophase pitch-based carbon fibers, this information is of empirical value in comparing pitches and predicting their spinnability, as well as predicting the approximate temperature at which an untested pitch may be melt-spun. 

The above equations have been solved to predict the commonly observed radial and line-origin textures seen in circular and non-circular mesophase pitch-based carbon fibers [39]. 

The properties of mesophase pitch-based carbon fibers can vary significantly with fiber texture. Inspection of the cross-section of a circular mesophase fiber usually shows that the graphitic structure converges toward the center of the fiber. This radial texture develops when flow is fully developed during extrusion through the spinnerette. Endo [48] has shown that this texture of mesophase pitch-based carbon fibers is a direct reflection of their underlying molecular structure. 

Since PAN-based carbon fibers tend to be fibrillar in texture, they are unable to develop any extended graphitic structure. Hence, the modulus of a PAN-based fiber is considerably less than the theoretical value (a limit which is nearly achieved by mesophase fibers), as shown in Fig. 9. On the other hand, most commercial PAN-based fibers exhibit higher tensile strengths than mesophase-based fibers. This can be attributed to the fact that the tensile strength of a brittle material is eontrolled by struetural flaws [58]. Their extended graphitic structure makes mesophase fibers more prone to this type of flaw. The impure nature of the pitch preciusor also contributes to their lower strengths. 

Mochida, I., Yoon, S. H. and Korai, Y., Control of transversal texture in circular mesophase pitch-based carbon fibre using non-circular spinning nozzles, J Mat Sci, 1993,28, 2331 2336. 

In particular, the laser melting experiment produced two well-differentiated populations of carbon clusters (a) spheroidal diamond particles with a radial texture... 

The quality and quantity of sites which are capable of reversible lithium accommodation depend in a complex manner on the crystallinity, the texture, the (mi-cro)structure, and the (micro)morphology of the carbonaceous host material [7, 19, 22, 40-57]. The type of carbon determines the current/potential characteristics of the electrochemical intercalation reaction and also potential side-reactions. Carbonaceous materials suitable for lithium intercalation are commercially available in many types and qualities [19, 43, 58-61], Many exotic carbons have been specially synthesized on a laboratory scale by pyrolysis of various precursors, e.g., carbons with a remarkably high lithium storage capacity (see Secs. 

Apart from manifold structures, carbons can have various shapes, forms, and textures, including powders with different particle size distributions, foams, whiskers, foils, felts, papers, fibers [76, 77], spherical particles [76] such as mesocarbon microbeads (MCMB s) [78], etc. Comprehensive overviews are given, for example in [67, 71, 72], Further information on the synthesis and structures of carbonaceous materials can be found in [67, 70, 72, 75, 79]. Details of the surface composition and surface chemistry of carbons are reviewed in Chapter II, Sec. 8, and in Chapter III, Sec. 6, of this handbook. Some aspects of surface chemistry of lithiated carbons will also be discussed in Sec. 5.2.2.3. 

As far as conducting fillers are concerned, we have rather a wide range of choice. In addition to the traditional and long used fillers, such as carbon black and metal powders [13] fiber and flaky fillers on organic or metal bases, conducting textures, etc recently appeared and came into use. The shape of the filler particles varies widely, but only the particle aspect ratio, the main parameter which determines the probability... 

Modification techniques for activated carhon were used to increase the removal capacity by surface adsorption and to improve the selectivity to volatile organic compounds (VOCs). Modified activated carbons (MACs) were prepared by modifying the purified activated carbon with various acids or bases. The effects of adsorption capacity and modified contents on the textural properties of the MACs were investigated. Furthermore, VOC adsorption and desorption experiments were carried out to determine the relationship between the adsorption capacity and the chemical properties of the adsorbents. High adsorption capacity for the selected VOCs was obtained over lwt%-H3P04/AC (lwt%-PA/AC). As a result, MAC was found to be very effective for VOC removal by adsorption with the potential for repeated use through desorption by simple heat treatment. 

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