2014
DOI: 10.1016/j.cej.2014.04.116
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An examination of catalyst deactivation in p-chloronitrobenzene hydrogenation over supported gold

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Cited by 37 publications
(29 citation statements)
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“…Many 3 efforts have been devoted to performing the hydrogenation of halogenated nitro compounds over a variety of supported noble metals (e.g. Ag, Au, Pd, Pt and Ru) [24][25][26][27][28][29][30][31][32][33][34]. In addition to their high cost in industrial applications, the problem often arising is that highly active noble metals are not selective toward haloanilines and must be modified by alloying or poisoning with other metal oxides or the application of several promoters [23,35,36], but in most cases at the expenses of catalytic activity.…”
Section: Introductionmentioning
confidence: 99%
“…Many 3 efforts have been devoted to performing the hydrogenation of halogenated nitro compounds over a variety of supported noble metals (e.g. Ag, Au, Pd, Pt and Ru) [24][25][26][27][28][29][30][31][32][33][34]. In addition to their high cost in industrial applications, the problem often arising is that highly active noble metals are not selective toward haloanilines and must be modified by alloying or poisoning with other metal oxides or the application of several promoters [23,35,36], but in most cases at the expenses of catalytic activity.…”
Section: Introductionmentioning
confidence: 99%
“…6). In contrast, temporal deactivation in hydrogenation over oxide supported Au [29,[66][67][68][69] and Ag [70] has been reported and attributed to coke formation [29,66], metal sintering [67,70] and reactant poisoning of active sites [68,69]. Given the higher conversions achieved we focused our attention on a comparison of 0.1%wt.…”
Section: Catalyst Activitymentioning
confidence: 80%
“…Catalyst activation by temperature programmed reduction (TPR) employed a 2 K min −1 ramp to 623 K in 60 cm 3 min −1 H 2 . The temperature requirements for reduction of supported Au and Ag precursors have been discussed elsewhere [7,29]. Post-activation the samples were cooled to ambient temperature and passivated in 1% v/v O 2 /He for 1 h for ex situ characterisation.…”
Section: Catalyst Preparation and Activationmentioning
confidence: 99%
“…As compared with bulk gold, The downward shifts of Au 4 f in these catalysts suggest a modification of the electronic states of Au due to interactions between the gold nanoparticles and the supports . A similar negative shift in binding energy for Au on γ‐Al 2 O 3 (Au 4f 7/2 =83.4 eV) have also been reported, which was attributed to electron transfer from the support . The sample of 1.5 wt.…”
Section: Resultsmentioning
confidence: 99%