Carbon, activated product name

Carbon fibers can be produced from a wide variety of precursors in the range from natural materials to various thermoplastic and thermosetting precursors Materials, such as Polyacrylonitrile (PAN), mesophase pitch, petroleum, coal pitches, phenolic resins, polyvinylidene chloride (PVDC), rayon (viscose), etc. [42-43], About 90% of world s total carbon fiber productions are polyacrylonitrile (PAN)-based. To make carbon fibers from PAN precursor, PAN-based fibers are generally subjected to four pyrolysis processes, namely oxidation stabilization, carbonization and graphitiza-tion or activation they will be explained in following sections later [43]. 

The best-known synthetic polymer is nylon, a polyamide. Nylon was the brainchild of Wallace Carothers, who was hired away from Harvard University in 1928 by the DuPont Company. Carothers was asked to develop a substitute for silk. Silk was known to be a protein, so Carothers s group studied ways of making amide bonds. In 1935, they prepared a product that they named nylon 66, illustrated in Active Figure 21.36. The reactants were a dicarboxylic acid and a diamine adipic acid and hexamethylenedi-amine, respectively. Note that each monomer has six carbons, hence the name. 

Eicosanoids, so named because they are all derived from 20-carbon fatty acids, are ubiquitous breakdown products of phospholipids. In response to appropriate stimuli, cells activate the breakdown of selected phospholipids (Figure 25.27). Phospholipase Ag (Chapter 8) selectively cleaves fatty acids from the C-2 position of phospholipids. Often these are unsaturated fatty acids, among which is arachidonic acid. Arachidonic acid may also be released from phospholipids by the combined actions of phospholipase C (which yields diacyl-glycerols) and diacylglycerol lipase (which releases fatty acids). 

Further work in this area showed that only one of the cou-marin rings was needed for biologic activity. Condensation of the hydroxyacetophenone, 4, with diethyl carbonate affords 4-hydroxycoumarin (2). The reaction may involve the 3-ketoester (5) cyclization of this would afford 2. Alternately, the reagent may first give the 0-acyl derivative cyclization as above will give the same product. Michael condensation of the coumarin with benzalacetone (6) affords the anticoagulant warfarin (named after its place of origin Wisconsin Alumni Research Foundation,... 

Three compounds acetoacetate, P-hydroxybutyrate, and acetone, are known as ketone bodies. They are suboxidized metabolic intermediates, chiefly those of fatty acids and of the carbon skeletons of the so-called ketogenic amino acids (leucine, isoleucine, lysine, phenylalanine, tyrosine, and tryptophan). The ketone body production, or ketogenesis, is effected in the hepatic mitochondria (in other tissues, ketogenesis is inoperative). Two pathways are possible for ketogenesis. The more active of the two is the hydroxymethyl glutarate cycle which is named after the key intermediate involved in this cycle. The other one is the deacylase cycle. In activity, this cycle is inferior to the former one. Acetyl-CoA is the starting compound for the biosynthesis of ketone bodies. 

Regarding the first problem, the most elemental treatment consists of focusing on a few points on the gas-phase potential energy hypersurface, namely, the reactants, transition state structures and products. As an example, we will mention the work [35,36] that was done on the Meyer-Schuster reaction, an acid catalyzed rearrangement of a-acetylenic secondary and tertiary alcohols to a.p-unsaturatcd carbonyl compounds, in which the solvent plays an active role. This reaction comprises four steps. In the first, a rapid protonation takes place at the hydroxyl group. The second, which is the rate limiting step, is an apparent 1, 3-shift of the protonated hydroxyl group from carbon Ci to carbon C3. The third step is presumably a rapid allenol deprotonation, followed by a keto-enol equilibrium that leads to the final product. 

No formal termination is given in structure 5.42 because in the absence of contaminants the product is a stable macroanion. Szwarz named such stable active species living polymers. These macroanions or macrocarbanions have been used to produce block copolymers such as Kraton. Kraton is an ABA block copolymer of styrene (A) and butadiene (B) (structure 5.43). Termination is brought about by addition of water, ethanol, carbon dioxide, or oxygen. 

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