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Carbon dioxide tetrachloromethane

Egli C, T Tschan, R Scholtz, AM Cook, T Leisinger (1988) Transformation of tetrachloromethane to dichloro-methane and carbon dioxide by Acetobacterium woodii. Appl Environ Microbiol 54 2819-2824. [Pg.371]

In contrast with water and ammonia, carbon dioxide and tetrachloromethane (CCI4) have zero dipole moments. Molecules of both substances contain individual polar covalent bonds, but because of the symmetry of their structures, the individual bond polarities exactly cancel. [Pg.383]

FIGURE 4. The effects of co-solvents of supercritical carbon dioxide on the polarity of the medium82. The / of Nile Red in supercritical fluids and the continuous curve methanol + and the dashed curve dichloromethane and for ordinary liquids O cyclohexane, V tetrachloromethane, toluene and A DMSO... [Pg.396]

Passage of the off-gases through a mass of bone-black, coke, or pumice results in the dismutation of the phosgene into tetrachloromethane and carbon dioxide (see Section 8.2). [Pg.259]

Although the reverse of the dismutation reaction (see Section 5.4) was first observed experimentally in 1868 [1824a], when it was observed that phosgene was produced when carbon dioxide and tetrachloromethane vapour were passed over pumice heated to 350-400 "C, the forward reaction has proved more elusive (despite the overwhelmingly favourable thermodynamics). The potential value of the phosgene dismutation was recognised as early as... [Pg.331]

From the foregoing discussion, the propensity of a sample to undergo micro-wave heating is related to its dielectric and physical properties. Compounds with high dielectric constants (e.g. ethanol and dimethylformamide) tend to absorb microwave irradiation readily whereas less polar substances (for example aromatic and aliphatic hydrocarbons) or compounds with no net dipole moment (e.g. carbon dioxide, dioxane, and tetrachloromethane) and highly ordered crystalline materials, are poorly absorbing. [Pg.128]

The valences in Table 1.5 apply whether the bonds are single, double, or triple. For example, carbon has four bonds in each of the structures we have written so far methane, tetrachloromethane, ethane, ethene, ethyne, carbon dioxide, and so on. These common valences are worth remembering, because they will help you to write correct structures. [Pg.12]

Decomposition to tetrachloromethane and carbon dioxide occurs on exposure to alumina [51, 55, 57, 60]. [Pg.16]

Carbon dioxide Nitric oxide Tetrachloromethane Ethylbromide Anthracene... [Pg.126]

Apolar, hydrophobic solutes with sufficient volatility, e.g., aromatics in dilute aqueous solutions, are vaporized into the bubble, where they undergo pyrolysis to acetylene,26 and oxidation to carbon mono- and dioxide.27/28 Tetrachloromethane and other chlorocarbons cleave homolytically. The chlorine atoms and organic radicals decompose, recombine, and disproportionate to give complex mixtures (Fig. 5).28,29,30 In most cases, a monomolecular pyrolytic mechanism is admitted, unaffected by frequency changes. Sc... [Pg.58]


See other pages where Carbon dioxide tetrachloromethane is mentioned: [Pg.21]    [Pg.21]    [Pg.241]    [Pg.229]    [Pg.5097]    [Pg.85]    [Pg.260]    [Pg.264]    [Pg.190]    [Pg.21]    [Pg.613]    [Pg.561]    [Pg.4]    [Pg.151]    [Pg.258]   


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Tetrachloromethane

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