2010
DOI: 10.1016/j.crci.2010.02.001
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Nature du dépôt formé au cours de l’oxydation en voie humide catalysée du phénol

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Cited by 9 publications
(6 citation statements)
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“…In many studies, traditional HDO catalysts have been deactivated by rapid coke formation 14. The same problem was reported for ceria catalysts in the wet oxidation of phenol at 120–160 °C 71. 72 In the present study, oligomeric products were only detected over pure ceria, and no such species were detected over the ceria–zirconia catalysts.…”
Section: Discussionsupporting
confidence: 75%
See 1 more Smart Citation
“…In many studies, traditional HDO catalysts have been deactivated by rapid coke formation 14. The same problem was reported for ceria catalysts in the wet oxidation of phenol at 120–160 °C 71. 72 In the present study, oligomeric products were only detected over pure ceria, and no such species were detected over the ceria–zirconia catalysts.…”
Section: Discussionsupporting
confidence: 75%
“…Kaev et al. reported that this pathway leads to the formation of chromenones, xanthones, and fluorenones as the oligomerization products from the wet oxidation of phenol over ceria‐based catalysts at 160 °C 71…”
Section: Discussionmentioning
confidence: 99%
“…Note that these substances are present on the chromatograms of the reaction mixture at the initial stages over low active catalysts. There may be further polymerization of phenols and intermediate phenol derivatives to form carbonaceous deposits of aromatic nature [6,49]. We cannot completely exclude the oxidation of the carbon support itself during the reaction.…”
Section: Discussionmentioning
confidence: 98%
“…3. 75 Chen et al compared EDS spectra obtained from the same catalyst before and after phenol WAO experiments and noticed the apparition of a C element corresponding peak. 40 According to Pintar and Levec, the adsorbed species are not soluble into conventional organic solvents.…”
Section: Quintanilla Et Al Attributed the Non Deactivation Of A Fouledmentioning
confidence: 99%
“…4, they extracted and identified aromatic polycyclic compounds from the chromenone, xanthone and fluorenone families. 75 Although of different structures, aromatic dimers and trimers such as hydroxylated biphenyls, diphenyl ethers, dibenzofurans and dibenzodioxins were identified during the phenol liquid-phase elimination by (i) molecular oxygen in supercritical conditions, 77 (ii) Fenton reaction 78 and (iii) adsorption over activated carbon in an oxidizing medium. 79 The formation of these species was attributed to oxidative coupling reactions.…”
Section: Quintanilla Et Al Attributed the Non Deactivation Of A Fouledmentioning
confidence: 99%