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Carbon C

Various blends of the C,—C, carbon numbers are also available. 1-Butene and 1-hexene are... [Pg.439]

Product Temperature range, °C Carbon number range... [Pg.159]

The radioactive isotopes available for use as precursors for radioactive tracer manufacturing include barium [ C]-carbonate [1882-53-7], tritium gas, p2p] phosphoric acid or pP]-phosphoric acid [15364-02-0], p S]-sulfuric acid [13770-01 -9], and sodium [ I]-iodide [24359-64-6]. It is from these chemical forms that the corresponding radioactive tracer chemicals are synthesized. [ C]-Carbon dioxide, [ C]-benzene, and [ C]-methyl iodide require vacuum-line handling in weU-ventilated fume hoods. Tritium gas, pH]-methyl iodide, sodium borotritide, and [ I]-iodine, which are the most difficult forms of these isotopes to contain, must be handled in specialized closed systems. Sodium p S]-sulfate and sodium [ I]-iodide must be handled similarly in closed systems to avoid the Uberation of volatile p S]-sulfur oxides and [ I]-iodine. Adequate shielding must be provided when handling P P]-phosphoric acid to minimize exposure to external radiation. [Pg.437]

Phase Behavior. One of the pioneering works detailing the phase behavior of ternary systems of carbon dioxide was presented ia the early 1950s (12) and consists of a compendium of the solubiHties of over 260 compounds ia Hquid (21—26°C) carbon dioxide. This work contains 268 phase diagrams for ternary systems. Although the data reported are for Hquid CO2 at its vapor pressure, they yield a first approximation to solubiHties that may be encountered ia the supercritical region. Various additional sources of data are also available (1,4,7,13). [Pg.221]

Thermodynamic calculations for reactions forming carbon disulfide from the elements are compHcated by the existence of several known molecular species of sulfur vapor (23,24). Thermochemical data have been reported (12). Although carbon disulfide is thermodynamically unstable at room temperature, the equiHbtium constant of formation increases with temperature and reaches a maximum corresponding to 91% conversion to carbon disulfide at about 700°C. Carbon disulfide decomposes extremely slowly at room temperature in the absence of oxidizing agents. [Pg.27]

When treated with aluminum bromide at 100°C, carbon tetrachloride is converted to carbon tetrabromide [558-13-4], reaction with calcium iodide, Cal2, at 75°C gives carbon tetraiodide [507-25-5]. With concentrated hydroiodic acid at 130°C, iodoform [75-47-8], CHI, is produced. Carbon tetrachloride is unaffected by gaseous fluorine at ordinary temperatures. Replacement of its chlorine by fluorine is brought about by reaction with hydrogen fluoride at a... [Pg.530]

Fibers produced from pitch precursors can be manufactured by heat treating isotropic pitch at 400 to 450°C in an inert environment to transform it into a hquid crystalline state. The pitch is then spun into fibers and allowed to thermoset at 300°C for short periods of time. The fibers are subsequendy carbonized and graphitized at temperatures similar to those used in the manufacture of PAN-based fibers. The isotropic pitch precursor has not proved attractive to industry. However, a process based on anisotropic mesophase pitch (30), in which commercial pitch is spun and polymerized to form the mesophase, which is then melt spun, stabilized in air at about 300°C, carbonized at 1300°C, and graphitized at 3000°C, produces ultrahigh modulus (UHM) carbon fibers. In this process tension is not requited in the stabilization and graphitization stages. [Pg.6]

Caustic, 50% Misco C Misco C 18-8 Misco C Ring Misco C Carbon Steel Misco C... [Pg.110]

Radovic, L. R. and Sudhakar, C., Carbon as a catalyis support production, properties and applications. In Introduction to Carbon Technologies, ed. H. Marsh, E. A. Heintz and F. Rodriguez-Reinoso, University of Alicante (Spain) Publications, 1997, pp. 103 165. [Pg.111]

Donnett, JB and Bansal, R.C., Carbon Fibers, 2nd edition, Marcel Dekker, Inc., New York, 1990. [Pg.201]

Furnace mortars are used over a very wide range of conditions. They are resistant to nonoxidizing acids, alkalis, and solvents up to 190°C. Carbon fillers should be used for conditions involving strong alkalis and compounds containing fluorine. [Pg.104]

Fig. 2. Raman spectra (T = 300 K) from various sp carbons using Ar-ion laser excitation (a) highly ordered pyrolytic graphite (HOPG), (b) boron-doped pyrolytic graphite (BHOPG), (c) carbon nanoparticles (dia. 20 nm) derived from the pyrolysis of benzene and graphitized at 2820°C, (d) as-synthesized carbon nanoparticles ( 850°C), (e) glassy carbon (after ref. [24]). Fig. 2. Raman spectra (T = 300 K) from various sp carbons using Ar-ion laser excitation (a) highly ordered pyrolytic graphite (HOPG), (b) boron-doped pyrolytic graphite (BHOPG), (c) carbon nanoparticles (dia. 20 nm) derived from the pyrolysis of benzene and graphitized at 2820°C, (d) as-synthesized carbon nanoparticles ( 850°C), (e) glassy carbon (after ref. [24]).
In the aUyl radical, the spin density is divided between the two terminal carbon atoms In the four other compounds, the C2 carbon atom retains an unpaired electron. Foi the Mg and Be cases, both the C2 carbon atom and the substituent have an unpairec electron. In the Be compound, the spin density is localized mostly on the substitueni atoms, while for the Mg compound, a bit more of the density remains near the C carbon. [Pg.131]

Both the oxygen and sulfur atoms have two lone pairs while the C/ carbon has ar unpaired electron, and in both cases the double bond shifts from the two carbor atoms to the carbon and the substituent. In acetyl radical, the electron density i centered primarily on the C2 carbon, and the spin density is drawn toward the lattei more than toward the former. In contrast, the density is more balanced between thf two terminal heavy atoms with the sulfur substituent (similar to that in allyl radical with a slight bias toward the sulfur atom. These trends can be easily related to th< varying electronegativity of the heavy atom in the substituent. [Pg.131]


See other pages where Carbon C is mentioned: [Pg.74]    [Pg.519]    [Pg.522]    [Pg.1252]    [Pg.1146]    [Pg.283]    [Pg.353]    [Pg.321]    [Pg.511]    [Pg.53]    [Pg.280]    [Pg.327]    [Pg.4]    [Pg.29]    [Pg.29]    [Pg.530]    [Pg.2232]    [Pg.2233]    [Pg.199]    [Pg.31]    [Pg.33]    [Pg.111]    [Pg.137]    [Pg.559]    [Pg.76]    [Pg.65]    [Pg.1298]    [Pg.87]    [Pg.54]    [Pg.54]    [Pg.1252]    [Pg.644]    [Pg.1]    [Pg.53]    [Pg.33]    [Pg.74]   
See also in sourсe #XX -- [ Pg.49 ]

See also in sourсe #XX -- [ Pg.49 ]

See also in sourсe #XX -- [ Pg.88 ]

See also in sourсe #XX -- [ Pg.88 ]




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