Acetylene from aromatic hydrocarbons

Another use is in various extraction and absorption processes for the purification of acetylene or butadiene and for separation of aHphatic hydrocarbons, which have limited solubiHty in DMF, from aromatic hydrocarbons. DMF has also been used to recover CO2 from flue gases. Because of the high solubiHty of SO2 iu DMF, this method can even be used for exhaust streams from processes using high sulfur fuels. The CO2 is not contaminated with sulfur-containing impurities, which are recovered from the DMF in a separate step (29). 

Alcohols, primary, 56,40 ALDEHYDES, acetylenic, 55, 52 aromatic, aromatic hydrocarbons from, 55,7... 

This review deals with metal-hydrocarbon complexes under the following headings (1) the nature of the metal-olefin and -acetylene bond (2) olefin complexes (3) acetylene complexes (4) rr-allylic complexes and (5) complexes in which the ligand is not the original olefin or acetylene, but a molecule produced from it during complex formation. ir-Cyclopentadienyl complexes, formed by reaction of cyclopentadiene or its derivatives with metal salts or carbonyls (78, 217), are not discussed in this review, neither are complexes derived from aromatic systems, e.g., benzene, the cyclo-pentadienyl anion, and the cycloheptatrienyl cation (74, 78, 217), and from acetylides (169, 170), which have been reviewed elsewhere. 

KETENE, feef-butylcyano-, 55, 32 37, 38 Ketene 1 1-dimethylpropylcyano-, 55, 38 7-KETOESTERS, 58, 79, 81, 82 7-KETOESTERS TO PREPARE CYCLIC DIKETONES, 58, 83 KETONE terf-butyl phenyl, 55, 122 Ketone, methyl ethyl- 55, 25 Ketone, methyl vinyl, 56, 36 KETONES, acetylenic, 55, 52 Ketones, alkylation of, 56, 52 KETONFS aromatic, aromatic hydrocarbons from 55, 7... 

In Tables 10 to 12 we show the heats of formation calculated by the various methods, together with their deviation from the experimentally observed values for alkanes and cycloalkanes, alkenes and cydoalkenes, and acetylenes and aromatic compounds. Table 13 shows a comparison of heats of formation of hydrocarbon radicals calculated by the MINDO methods. Finally, in Tables 14 and 15 we show the results of MINDO/1 calculations on a selection of oxygen- and nitrogen-containing compounds. 

Roithova and Schroder have demonstrated that a dicationic species can participate in carbon-carbon bond forming reactions in the gas-phase and that this is a potential route to polycyclic aromatic hydrocarbons.45 When C7H62+ is generated (from double ionization of toluene) and allowed to react with acetylene, new ions, CgRj1+ and CyHf,2+, are detected (eq 44). 

Pyrolysis of acetylene to a mixture of aromatic hydrocarbons has been the subject of many studies, commencing with the work of Berthelot in 1866 (1866a, 1866b). The proposed mechanisms have ranged from formation of CH fragments by fission of acetylene (Bone and Coward, 1908) to free-radical chain reactions initiated by excitation of acetylene to its lowest-lying triplet state (Palmer and Dormisch, 1964 Palmer et al., 1966) and polymerization of monomeric or dimeric acetylene biradicals (Minkoff, 1959 see also Cullis et al., 1962). Photosensitized polymerization of acetylene and acetylene-d2 and isotopic analysis of the benzene produced indicated involvement of both free-radical and excited state mechanisms (Tsukuda and Shida, 1966). 

High quality MWNT were obtained from acetylene on Co3C>4/MgO catalyst [3], However, commercial acetylene often contains impurities which sometimes have harmful influence on the process. For instance, we observed poisoning of a catalyst, probably by phosphine, when obtaining CNF from commercial acetylene on Fe/C/Si02 catalyst. After careful purifying of acetylene the process proceeded normally. Further, sometimes aromatic hydrocarbons form if the catalyst used is not sufficiently selective. In our experiments formation of aromatics was observed frequently in case of acetylene. This creates ecological problems. 

Based on earlier studies on the total synthesis of benzene (2), which he called the keystone of the total aromatic edifice , Berthelot in 1867 carried out a remarkable experiment heating acetylene (1) - which he had prepared from the elements - in a bent bell-jar at a temperature where the glass began to soften , he noticed the formation of polymeric substances . When these were subjected to fractional distillation, benzene, styrene, and other aromatic hydrocarbons could be isolated, with 2 constituting approximately half of the product mixture (Scheme 1) [1]. 

They noted that in dimethoxyethane or in iso-octane (path a), the major product was dicarbonylcyclopentadienylcobalt (2) which must arise as a result of a retro Diels-Alder reaction of the norbornadiene (which would lead to the formation of acetylene and cyclopentadiene). When the solvent was changed to an aromatic hydrocarbon such as benzene or toluene (path b), the major cobalt-containing product was shown to be a complex derived from Co4(CO)i2, with three CO ligands on an apical cobalt being replaced by a molecule of the aromatic solvent (3). The group noted that they were also obtaining hydrocarbon and ketonic products derived from norbornadiene, acetylene and carbon monoxide .1,2... 

In aromatic hydrocarbons, some substituted alkenes, dienes, substituted acetylenes and ketones, one half of the n orbitals are empty and an electron can easily be placed in these antibonding orbitals. The capture of an electron by the acceptor molecule is an exothermic process because the energy of the antibonding orbitals lies below the level of the ionization potential of the acceptor radical anion. Many radical anions formed from unsaturated molecules are themselves stable they do not decompose and may exist indefinitely under suitable experimental conditions [182a],On the other hand, they react easily with other molecules. 

Zinc dichromate tiihydrate, ZnCr207<3H20, is obtained as an orange-red solid by adding zinc carbonate to a cold solution of chromium trioxide in dilute sulfuric acid [660]. The applications are oxidations of acetylenes lo a-diketones, of aromatic hydrocarbons to quinones, of alcohols to aldehydes, and of ethers to esters and the oxidative regeneration of carbonyl compounds from their oximes [660]. 

The applications of ruthenium tetroxide range from the common types of oxidations, such as those of alkenes, alcohols, and aldehydes to carboxylic acids [701, 774, 939, 940] of secondary alcohols to ketones [701, 940, 941] of aldehydes to acids (in poor yields) [940] of aromatic hydrocarbons to quinones [942, 943] or acids [701, 774, 941] and of sulfides to sulfoxides and sulfones [942], to specific ones like the oxidation of acetylenes to vicinal dicarbonyl compounds [9JS], of ethers to esters [940], of cyclic imines to lactams [944], and of lactams to imides [940]. 

In the steam cracking of hydrocarbons, a small portion of the hydrocarbon feed gases decomposes to produce coke that accumulates on the interior walls of the coils in the radiant zone and on the inner surfaces of the transferline exchanger (TLX). Albright et identified three mechanisms for coke formation. Mechanism 1 involves metal-catalyzed reactions in which metal carbides are intermediate compounds and for which iron and nickel are catalysts. The resulting filamentous coke often contains iron or nickel positioned primarily at the tips of the filaments. This filamenteous coke acts as excellent collection sites for coke formed by mechanisms 2 and 3. Mechanism 2 results in the formation of tar droplets in the gas phase, often from aromatics. These aromatics are often produced by trimerization and other reactions involving acetylene. Some, but not all, of these droplets collect... 

Therefore, hydrocarbon-containing materials have the potential to be used in carbon black production. Raw materials can be in the form of hydrocarbon gases, such as methane and acetylene, but mostly viscous residual aromatic hydrocarbons are used. Depending on chemical composition, the reaction is exo- or endothermic. Only when carbon black is produced from acetylene the reaction is exothermic and the process demands intensive cooling, whereas in other cases the reaction is endothermic and needs a substantial amount of energy in order to form carbon black. 

Crude Oil. Crude petroleum consists essentially of mixtures of paraffinic, naphthenic, and aromatic hydrocarbons containing from 1 to over 70 carbon atoms per molecule and may contain dissolved gases or solids. The naphthenic hydrocarbons are based on cyclopentane or cyclohexane or on fused C5 and Ce rings. There is no evidence of the existence of C3, C4, C7, or C7+ cycloparaffins in crude oil. Olefins, diolefins, and acetylenes are absent. The aromatics are mainly benzene derivatives naphthalene, tetralin, and their substituted derivatives have been isolated in a few cases. 

The flyer plate velocity range employed in these simulations, from 8 to 25 km/s, is comparable to the speeds expected for cometary impact into planetary atmospheres [42]. It is clear from the simulations that significant shock-induced pol5nnerization can occur in cometary acetylene under these conditions. Ring structures characteristic of polycyclic aromatic hydrocarbons (PAHs) were not found in the simulations, but unsamrated oligomer precursors would presumably react to form these more complex structures over a much longer time interval than could be followed in the shock impact simulations. 

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