2004
DOI: 10.1016/j.orggeochem.2003.06.001
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Kinetic effect of alkylaromatics on the thermal stability of hydrocarbons under geological conditions

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Cited by 41 publications
(52 citation statements)
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“…Perez and Raimondo also observed that a molecule which has some structural similarity to that of biphenyl, such as 1-phenylnaphthalene, converted to only 1.5% when pyrolyzed at 450 ºC. 34 The condensed polyaromatic model compounds naphthalene, phenanthrene and pyrene also showed important selectivities to benzene, though smaller than those of the other reactants, given their higher thermal stability and minor H/C (refer to Figure 3). In the case of 1PhO minor yields of toluene, ethylbenzene, xylenes and C 2 -C 8 olefins and paraffins besides benzene were also observed, which can be explained based on the scission of the C8 side chain.…”
Section: Thermal Crackingmentioning
confidence: 94%
“…Perez and Raimondo also observed that a molecule which has some structural similarity to that of biphenyl, such as 1-phenylnaphthalene, converted to only 1.5% when pyrolyzed at 450 ºC. 34 The condensed polyaromatic model compounds naphthalene, phenanthrene and pyrene also showed important selectivities to benzene, though smaller than those of the other reactants, given their higher thermal stability and minor H/C (refer to Figure 3). In the case of 1PhO minor yields of toluene, ethylbenzene, xylenes and C 2 -C 8 olefins and paraffins besides benzene were also observed, which can be explained based on the scission of the C8 side chain.…”
Section: Thermal Crackingmentioning
confidence: 94%
“…They confirm that the conversion of noctane in the presence of H 2 S is lower than that of pure n-octane at identical pyrolysis duration: the n-octane pyrolysis is inhibited by H 2 S. In order to quantify this inhibition effect, the inhibition factor (I.F.) can be used [24][25][26][27]. It is defined as the ratio of pure n-octane conversion to n-octane conversion in binary mixture at identical pyrolysis conditions.…”
Section: Kinetic Effect Of H 2 S On N-octane Pyrolysismentioning
confidence: 69%
“…In the case of a chain reaction, the inhibition mechanism was highlighted by Niclause et al [63] and used to explain the inhibition effect of some compounds (toluene, decylbenzene and tetralin) on n-alkane pyrolysis [24][25][26][27]. To summarize, an inhibitor is a coreactant that can easily convert a chain carrier radical into a less reactive radical which leads to new terminations.…”
Section: Mechanisms Of Net Inhibition Effect Of H 2 S On the N-octanementioning
confidence: 99%
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“…The results of an experimental study of the thermal stability and decomposition of individual hydrocarbons at temperatures up to 450 • C are presented in the literature [11][12][13]. In another study, experiments have been conducted under a pressure of 70 MPa at temperatures up to 330 • C [14]. One of the main conclusions from the above-mentioned experimental results could be summarized as follows: the thermal stability of individual hydrocarbons differs greatly from that of the same hydrocarbons in a mixture.…”
Section: Introductionmentioning
confidence: 99%