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Acetylene benzene

On the other hand, organic materials of relatively low molecular weight such as acetylene, benzene, ethylene and methane, can produce vapour-grown carbon materials by imperfect combustion or by exposing their vapour to a heated substrate in an electric furnace in the presence of a metal catalyst. The latter process generates VGCFs. Other precursors to VGCF include polyacrylonitrile (PAN), isotropic or mesophase pitch, rayon or nylon [8]. [Pg.145]

Anunonia Acetylene Benzene n-Butane Carbon disulfide Ethane Ethylene n-Hexane Hydrogen Methane Propane... [Pg.211]

Table II must be used with care in anomalous cases in which the transition probability for ionization of the molecule is very low in some energy ranges (e.g., acetylene, benzene, methylamine). In such cases higher RE s, not included in the table and normally of small importance, may be responsible for the charge exchange processes although with small cross-sections (cf. 9, 13). Table II must be used with care in anomalous cases in which the transition probability for ionization of the molecule is very low in some energy ranges (e.g., acetylene, benzene, methylamine). In such cases higher RE s, not included in the table and normally of small importance, may be responsible for the charge exchange processes although with small cross-sections (cf. 9, 13).
FIGURE 8.14 Critical sooting equivalence ratio l c at 2200K as a function of the number C—C bonds in hydrocarbon fuels. +, 0, and - indicate ethane/l-octane mixtures in molar ratios of 5 to 1, 2 to 1 and 1 to 2, respectively x, acetylene/benzene at a molar ratio of 1 to 3. The O symbol for 2 to 1, falls on top of the butene symbol. [Pg.465]

Order the following compounds in their tendency to soot under diffusion flame conditions vinyl acetylene, ethene, phenyl acetylene, benzene, and acetylene. [Pg.491]

However, direct calculations of accurate bond energies represent a major challenge. Examples are given [13,14] where the ratios of carbon-carbon bond energies, relative to that of ethane, were successfully calculated for ethylene, acetylene, benzene, and... [Pg.4]

Certain compounds do not show two-stage ignition. These include methane, acetylene, benzene, hydrogen, methanol, formaldehyde, and glyoxal (106, 108). Higher aromatics show the effects of their aliphatic side chains and act like aliphatics. [Pg.195]

Werner objected to the older theory because it inadequately explained the racemization of optically active substances, the isomerization of geometric isomers, and the properties and reactions of cyclic compounds as well as of unsaturated compounds including olefins, acetylenes, benzene. [Pg.49]

Benzene from Acetylene.—Benzene may be prepared directly from one of the unsaturated open chain compounds, viz., from acetylene, CH = CH. When this hydrocarbon is passed through a red hot tube it is simply broken down into its elements. If, however, it is heated more slowly, it polymerizes and benzene is obtained. [Pg.478]

The first theories of petroleum origin suggested inorganic sources. These theories are no longer considered probable. The idea of an inorganic source came from the hydrocarbons themselves, since methane, ethane, acetylene, benzene can be made from inorganic substances. [Pg.47]

Authors Location Ethene Propene Butenes Alkadienes Acetylene Benzene Toluene Ethyl- benzene... [Pg.239]

Ethylene is a colorless gas which possesses a peculiar, sweetish odor. One volume of water dissolves one-fourth volume of the gas, and one volume of alcohol about three and one-half volumes. It is much less stable toward heat than methane. At about 400° it decomposes methane, acetylene, benzene,... [Pg.47]

Production of hydrocarbons (linear or ring shaped, saturated or unsaturated, aliphatic or aromatic) Acetylene, benzene, ethylene, toluene, hydrogen 100 0.8 100 0.07... [Pg.620]

If the pyrolysis of poly(a-methylstyrene) is conducted at around 830-1,230 "C, then considerable quantities of fractions with a molecular mass exceeding that of the monomer are formed. This is a result of the volatilisation of chain fragments produced during pyrolysis of the polymer from the high temperature zone before chain decay to monomer can take place. At temperatures of 830-1230 °C a definite quantity of small molecules such as acetylene, benzene, ethylene, hydrogen and methane are formed as products of the secondary, more extensive decomposition of monomer. [Pg.27]

Synthetic chemical methods for the preparation of carbon-14-labeled chemicals utilize a number of basic building components that are prepared from barium carbonate ( " C). These are versions of carbon dioxide, acetylene, benzene, sodium acetate (1- and 2- " C), methyl iodide, methanol, sodium cyanide, and urea. Many complicated labeled compounds may be synthesized from these materials. [Pg.4196]


See other pages where Acetylene benzene is mentioned: [Pg.234]    [Pg.7]    [Pg.80]    [Pg.324]    [Pg.166]    [Pg.166]    [Pg.233]    [Pg.296]    [Pg.33]    [Pg.918]    [Pg.406]    [Pg.124]    [Pg.124]    [Pg.166]    [Pg.124]    [Pg.336]    [Pg.382]    [Pg.254]    [Pg.364]    [Pg.238]    [Pg.177]    [Pg.337]    [Pg.252]    [Pg.438]    [Pg.917]    [Pg.336]    [Pg.3]    [Pg.528]    [Pg.105]    [Pg.370]    [Pg.247]    [Pg.7]    [Pg.986]   
See also in sourсe #XX -- [ Pg.31 , Pg.88 ]




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Acetylene derivatives benzene ring (trimerization

Acetylene derivs benzene ring

Acetylene derivs benzene ring (from

Acetylene-benzene conversion

Benzene from acetylene

Dewar benzene from acetylene + cyclobutadiene

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