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Pyrolysis, acetone mechanisms

It is now clearly demonstrated through the use of free radical traps that all organic liquids will undergo cavitation and generate bond homolysis, if the ambient temperature is sufficiently low (i.e., in order to reduce the solvent system s vapor pressure) (89,90,161,162). The sonolysis of alkanes is quite similar to very high temperature pyrolysis, yielding the products expected (H2, CH4, 1-alkenes, and acetylene) from the well-understood Rice radical chain mechanism (89). Other recent reports compare the sonolysis and pyrolysis of biacetyl (which gives primarily acetone) (163) and the sonolysis and radiolysis of menthone (164). Nonaqueous chemistry can be complex, however, as in the tarry polymerization of several substituted benzenes (165). [Pg.94]

Chemical, Physical, and Mechanical Tests. Manufactured friction materials are characterized by various chemical, physical, and mechanical tests in addition to friction and wear testing. The chemical tests include thermogravimetric analysis (tga), differential thermal analysis (dta), pyrolysis gas chromatography (pgc), acetone extraction, liquid chromatography (lc), infrared analysis (ir), and x-ray or scanning electron microscope (sem) analysis. Physical and mechanical tests determine properties such as thermal conductivity, specific heat, tensile or flexural strength, and hardness. Much attention has been placed on noise /vibration characterization. The use of modal analysis and damping measurements has increased (see Noise POLLUTION AND ABATEMENT). [Pg.275]

Whereas acetone shows little tendency to undergo chain decomposition in photolysis or pyrolysis, acetaldehyde has been found to decompose by a chain mechanism which tends to quite sizable chain lengths as the temperature is raised. As a consequence of this behavior, the dec(3mposition has been found to be remarkably sensitive to the presence of small amounts of substances that can form free radicals more readily than pure acetaldehyde does. A further result of this sensitivity is that the data on the pyrolysis obtained under different conditions or in different laboratories show quite important discrepancies. In compensation for these difficulties the stoichiometry of the pyrolysis seems to be quite simple, the products being CO + CH4, together with very small amounts of C2H6 and also some II2 at temperatures near 500°C. These can be represented by ... [Pg.379]

A 10% solution of each hexafluoropropylene-vinylidene fluoride copolymer is prepared by dissolving 10 g of polymer in 100 ml of reagent grade acetone. A vial 58 mm high is filled with the sample solution. A pyrolysis wire, previously cleaned in a bunsen burner until red hot, then cooled, is dipped into the vial. The dipped wire is then dried in a vacuum oven at 90°C for 30 min. Use of lower drying temperatures or shorter times results in an acetone peak in the pyrogram. This is due to mechanically trapped... [Pg.420]

Because citric acid is considered as relatively cheap and abundant material, it was catalytically dehydrated to aconitic acid in the 120-150 °C temperature range by Umbdenstock and Bruin [61]. Aconitic acid can be readily decaiboxylated to a mixture of isomeric itaconic acids (itaconic, citraconic and mesaconic acids). These acids and their esters are nsed to produce alkyl resins and plasticizers. The mechanism of thermal rearrangement of citraconic acid to itaconic acid in aqueous solution was in a great detail investigated by Sakai [62]. In some cases, the applied catalyst caused excessive pyrolysis of citric acid and in the dehydration and decarboxylation reactions acetone dicarboxylic acid (P-ketoglutaric acid) was initially formed and from it acetone. The catalytic pyrolysis of citric acid monohydrate heated up to 140 °C to obtain itaconic and citraconic acids was reported by Askew and Tawn [63],... [Pg.220]


See other pages where Pyrolysis, acetone mechanisms is mentioned: [Pg.275]    [Pg.451]    [Pg.451]    [Pg.234]    [Pg.69]    [Pg.174]    [Pg.70]    [Pg.30]    [Pg.174]    [Pg.419]    [Pg.265]    [Pg.9]    [Pg.62]    [Pg.600]    [Pg.1100]    [Pg.313]    [Pg.276]    [Pg.410]    [Pg.50]   
See also in sourсe #XX -- [ Pg.98 ]




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Pyrolysis mechanism

Pyrolysis, acetone

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