Precursors carbons

Titanium carbide may also be made by the reaction at high temperature of titanium with carbon titanium tetrachloride with organic compounds such as methane, chloroform, or poly(vinyl chloride) titanium disulfide [12039-13-3] with carbon organotitanates with carbon precursor polymers (31) and titanium tetrachloride with hydrogen and carbon monoxide. Much of this work is directed toward the production of ultrafine (<1 jim) powders. The reaction of titanium tetrachloride with a hydrocarbon-hydrogen mixture at ca 1000°C is used for the chemical vapor deposition (CVD) of thin carbide films used in wear-resistant coatings. 

Petroleum pitch was obtained from Kureha Company, Japan (designated here as KS pitch). A second petroleum pitch was obtained from the Crowley Tar Company, U.S.A. (designated here as CRO pitch). Polyvinyl chloride (PVC) was obtained from the Aldrich Chemical Company (U.S.A.). These samples are all soft carbon precursors. 

Microporous Carbons from Pyrolyzed Hard-Carbon Precursors... 

Contrary to the expectation that a sulfur-containing substituent will be a catalyst poison, a phenylthio group serves as an effective selectivity control element in TMM cycloadditions. A single regioisomer (30) was obtained from the carbonate precursor (31) in good yield. The thermodynamically more stable sulfide (32) is readily accessible from (30) via a 1,3-sulfide shift catalyzed by PhSSPh. A wide array of synthetically useful intermediates could be prepared from the sulfides (30) and (32) with simple transformations (Scheme 2.10) [20]. 

The use of carbonate precursor (56) allows the introduction of a carboxylic function in the cycloadduct. The proposed mechanism involves internal delivery of a Pd-bound carbon dioxide to the TMM unit as depicted in Scheme 2.17 [27, 28]. 

In the Chapter 6 Focus On, "Terpenes Naturally Occurring Alkenes," we looked briefly at terpenoids, a vast and diverse group of lipids found in all living organisms. Despite their apparent structural differences, all terpenoids are related. All contain a multiple of five carbons and are derived biosynthetically from the five-carbon precursor isopentenyl diphosphate (Figure 27.6). Note that formally, a... 

Eicosanoids and terpenoids are still other classes of lipids. Eicosanoids, of which prostaglandins are the most abundant kind, are derived biosynthetically from arachidonic acid, are found in all body tissues, and have a wide range of physiological activity. Terpenoids are often isolated from the essential oils of plants, have an immense diversity of structure, and are produced biosynthetically from the five-carbon precursor isopentenyl diphosphate (IPP). lsopentenyl diphosphate is itself biosynthesized from 3 equivalents of acetate in the mevalonate pathway. 

Figure 29.5 MECHANISM The pathway for fatty-acid biosynthesis from the two-carbon precursor, acetyl CoA. Individual steps are explained in the text.

Higher organisms are not able to synthesize glucose from acetyl CoA but must instead use one of the three-carbon precursors lactate, glycerol, or alanine, all of which are readily converted into pyruvate. 

The physicochemical properties of carbon are highly dependent on its surface structure and chemical composition [66—68], The type and content of surface species, particle shape and size, pore-size distribution, BET surface area and pore-opening are of critical importance in the use of carbons as anode material. These properties have a major influence on (9IR, reversible capacity <2R, and the rate capability and safety of the battery. The surface chemical composition depends on the raw materials (carbon precursors), the production process, and the history of the carbon. Surface groups containing H, O, S, N, P, halogens, and other elements have been identified on carbon blacks [66, 67]. There is also ash on the surface of carbon and this typically contains Ca, Si, Fe, Al, and V. Ash and acidic oxides enhance the adsorption of the more polar compounds and electrolytes [66]. 

Transalkylation might be expected another kind of the solvolitic reaction. However, the present results suggest low probability with alkylated pyrenes as suggested by the NMR analyses. Instead, the increased polarity by alkyl group or the enhanced reactivity of the carbonization precursor from alkylpyrene, especially ethylpyrene, may be responsible for a considerable liquefaction yield. The recovery of the solvent becomes difficult by its latter conversion as observed in the present study. 

In the sixth paper of this chapter, Kierzek et al., mainly focus on modeling of pore formation vs surface area growth phenomena upon activation of coal and pitch-derived carbon precursors. These authors briefly touch on other precursor carbons as well. The properties of newly synthesized materials are being looked at from the point of view of their application as active materials in the supercapacitor electrodes. Editors thought this work by the Institute of Chemistiy and Technology of Petroleum and Coal in Poland, could be of genuine interest to the practical developers of carbon materials for the supercapacitor industry. 

High porosity carbons ranging from typically microporous solids of narrow pore size distribution to materials with over 30% of mesopore contribution were produced by the treatment of various polymeric-type (coal) and carbonaceous (mesophase, semi-cokes, commercial active carbon) precursors with an excess of KOH. The effects related to parent material nature, KOH/precursor ratio and reaction temperature and time on the porosity characteristics and surface chemistry is described. The results are discussed in terms of suitability of produced carbons as an electrode material in electric double-layer capacitors. 

A departure from traditional approaches of depositing a significant amount of metal onto carbon precursor differentiated our experiments from the state of the art literature. Through several trial and error experiments, it was possible to formulate several key principles, which should constitute a design of the metal/carbon composites. Among those are ... 

From this point of view a one-stage process of simultaneous GIC exfoliation, impregnation of EG by amorphous carbon precursor and its subsequent carbonization would be very attractive. But up to now this simple one-stage process could not be realized because of high exfoliation temperature of the ordinary GICs needed (900 - 1200°C), which leads to almost complete burnout of AC precursor at the atmospheric air conditions. 

Combined with appropriate amorphous carbon precursors graphite intercalation compounds could be used in one-stage process of production of carbon-carbon composites, which could possess attractive properties for such applications as supercapacitors elements, sorbents as well as catalyst supports and materials for energy- and gas-storage systems. 

Nitrogen-containing carbon replicas of SBA-15 and MLV prepared from pyrrole as carbon precursor... 

Incorporation of nitrogen into the carbons prepared via chemical vapour deposition (CVD) or into the carbon nanotubes yields highly graphitised materials with excellent structure ordering. For example, ordered mesoporous carbons containing 7.0-8.8 wt,% N have been obtained by the CVD method, using the SBA-12, SBA-15, MCM-41, MCM-48, and HMS materials as matrices and acetonitrile as carbon precursor [1],... 

A similar pathway involving a microwave-driven molybdenum-catalyzed asymmetric allylic alkylation as the key step was elaborated by Moberg and coworkers for the preparation of the muscle relaxant (R)-baclofen (Scheme 6.52) [108]. The racemic form of baclofen is used as a muscle relaxant (antispasmodic) lipophilic derivative of y-aminobutyric acid (GABA). Pharmacological studies have shown that the (R)-enantiomer is the therapeutically useful agonist of the GABAb receptor. Asymmetric alkylation of the allylic carbonate precursor with dimethyl malonate afforded... 

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