2012
DOI: 10.1016/j.cattod.2012.06.011
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Conversion of decalin and 1-methylnaphthalene over AlSBA-15 supported Pt catalysts

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Cited by 19 publications
(13 citation statements)
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“…was already explained in terms of the presence of electronic deficient species that avoid the irreversible adsorption of the hydrocarbon compounds. These sites are also more resistant to poisoning and coke formation [37][38][39][40]. In this way, Nishimura et al [9] affirm that the formation of the electronically poor states in the noble metal in the alloy plays a crucial role in the activation of H2 molecules and/or the enhancement of the hydrogenation reaction pathway.…”
Section: Tablementioning
confidence: 99%
“…was already explained in terms of the presence of electronic deficient species that avoid the irreversible adsorption of the hydrocarbon compounds. These sites are also more resistant to poisoning and coke formation [37][38][39][40]. In this way, Nishimura et al [9] affirm that the formation of the electronically poor states in the noble metal in the alloy plays a crucial role in the activation of H2 molecules and/or the enhancement of the hydrogenation reaction pathway.…”
Section: Tablementioning
confidence: 99%
“…Recently, the bifunctional catalysts 1,7,8,10,[12][13][14][15][16][17][18][19][20][21][22][23][24][25][26][27][28][29][30] has been used in the ring opening of naphthenes which showed good performance because of its more acid sites and higher hydrogenation on metal sites. The studies about bifunctional catalysts mainly focused on some noble metal catalyst, 1,[8][9][10]12,[14][15][16][18][19][20][21][24][25][26][28][29][30][31] which are easier sulfur poisoning.…”
Section: Introductionmentioning
confidence: 99%
“…However, here we observe that using a slightly acidic support, such as TiC, we obtained better results in terms of DMF performance. As we said earlier, the acidity of the support generates electron deficient species that prevent deep hydrogenation or opening of the furan ring [65][66][67][68][69][70]. Despite of the higher acidity values obtained by FTIR of Py for the catalyst modified with Ti, C-C bond cleavage of tertiary carbon of the HMF to the formation of FA products was not observed.…”
Section: Catalytic Activitymentioning
confidence: 97%
“…Despite of the higher acidity values obtained by FTIR of Py for the catalyst modified with Ti, C-C bond cleavage of tertiary carbon of the HMF to the formation of FA products was not observed. These sites are also more resistant to poisoning and coke formation [5,[67][68][69][70][71].…”
Section: Catalytic Activitymentioning
confidence: 99%