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Cited by 30 publications
(28 citation statements)
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“…The experimental facilities of low-pressure laminar premixed flat flames used in this study have been already described in detail in recent work [21]. Chemical species were measured by on-line gas chromatography (GC).…”
Section: Experimental Methodologymentioning
confidence: 99%
“…The experimental facilities of low-pressure laminar premixed flat flames used in this study have been already described in detail in recent work [21]. Chemical species were measured by on-line gas chromatography (GC).…”
Section: Experimental Methodologymentioning
confidence: 99%
“…A very minor channel is the recombination of C 8 H 9 radicals with methyl radical to produce cumene (reaction 40). The decomposition of the obtained hydroperoxide by reaction (35) contributes to only 4% to the formation of acetophenone (mainly formed by reaction (38) and from styrene), but its main reaction is by O-O bond scission to give an alkoxy radical which decompose mainly to yield methyl radicals and benzaldehyde (reaction 37). This last reaction is the major source of benzaldehyde.…”
Section: Discussionmentioning
confidence: 99%
“…Only the reaction of styrene with HO 2 radicals to give phenyloxirane which rapidly isomerize to give phenylacetaldehyde or acetophenone has been added (see Table S2 in Supplementary data). In addition to the sub-mechanisms proposed by Tian et al for naphthalene and indene [35], three submechanisms including the reactions of cumene, methylstyrene (the two first mechanisms being taken from Pousse et al [36]) and benzofuran have been added specifically for this study. Note that no reaction in these primary and secondary mechanisms involves the opening of the aromatic cycle.…”
Section: Modelingmentioning
confidence: 99%
“…24 The aromatic, bicyclic indane molecule as well as its α-methylstyrene (2-phenylpropene) and 1-phenylpropene isomers are considered as important reaction intermediates and toxic byproducts in the combustion of fossil fuel ( Figure 1). 11,12,[25][26][27][28][29][30][31][32] The reaction of the phenyl radcial (C 6 H 5 ) with propylene (C 3 H 6 ) presents a potential synthetic routes to synthesize C 9 H 10 isomers and to access the C 9 H 11 potential energy surface.…”
Section: Introductionmentioning
confidence: 99%