On the nature of the Brønsted acidic groups on native and functionalized mesoporous siliceous SBA-15 as studied by benzylamine adsorption from solution

Jessica M. Rosenholm, Teresa Czuryszkiewicz, Freddy Kleitz, Jarl Rosenholm, Mika Lindén

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Sammanfattning

The concentration and Brønsted acidity of surface silanol groups on mesoporous silica (SBA-15) has been studied by following the adsorption of benzylamine, BA, from water as a function of pH. The adsorbed amount of BA from water was compared to the maximum amount of BA that could be adsorbed from cyclohexane. Furthermore, the surface concentration and acidity of carboxylic acid functions on surface-functionalized SBA-15 was also studied, which allowed the relative surface concentration of remaining silanols to be obtained. Two types of silanols can be identified, where about 1/5 of the silanols have a pKa ≤ 2 and the remaining 4/5 of the silanols have a pK a of about 8.2. According to the literature, these two types of silanols can be identified as Q3 and Q2 silanols, respectively, of which the Q3 silanols are more acidic. For the surface-functionalized materials, pKa values close to their respective intrinsic values are found for the carboxylic acid functions. However, irrespective of the method of surface functionalization, 50% or more of the accessible surface groups are silanols, The results thus suggest that the effective charge density is largely controlled by the (de)protonation of the silanol groups even for surface-functionalized mesoporous silica, which render the surface chemistry of the surface-functionalized silicas to be radically different from what simple schematic representations would suggest. The results are suggested to be of importance for reaching a predictive level of understanding for the behavior of mesoporous silica in a range of applications, as many of the foreseen applications for mesoporous silica involves water as the medium. © 2007 American Chemical Society.
OriginalspråkEngelska
Sidor (från-till)4315-4323
Antal sidor9
TidskriftLangmuir
Volym23
Nummer8
DOI
StatusPublicerad - okt. 2007
MoE-publikationstypA1 Tidskriftsartikel-refererad

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