Characterization of the acidic sites in organic acid functionalized mesoporous silica in an aqueous media

[Display omitted] ► Method developed to characterize the aqueous phase acidity of solid acid catalysts. ► Bulk aqueous phase pK a of solid Brönsted acid catalysts can be reliably determined. ► Appropriate titration conditions are established for solid acid characterization. ► Method validated by mea...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Applied catalysis. A, General General, 2011-04, Vol.396 (1), p.76-84
Hauptverfasser: Cinlar, Basak, Shanks, Brent H.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:[Display omitted] ► Method developed to characterize the aqueous phase acidity of solid acid catalysts. ► Bulk aqueous phase pK a of solid Brönsted acid catalysts can be reliably determined. ► Appropriate titration conditions are established for solid acid characterization. ► Method validated by measuring pK as of tethered organic acid functional groups. ► Improved acid characterization method over gas phase surrogate measurement. Exploring the catalytic potential of organic acid functionalized mesoporous silica in condensed phase necessitates characterization of their acidic properties in a similar environment. In this study, potentiometric titration is used as a direct measurement technique to determine the acidic strength and total acid capacity of propylsulfonic, arenesulfonic, ethylphosphonic, and butylcarboxylic functionalized mesoporous silica catalysts in water. While the method can provide direct insight into the acidic properties of the materials the characterization conditions must be carefully chosen to yield reliable results. The addition of salts are required for enhancing the ion-exchange in the titration procedure, but their over-addition leads to significant deviation of the activity coefficients leading to incorrect results. Titrations, which are performed under reliable characterization conditions, demonstrate that network interactions can exist between the organic acid functional groups, but their interaction with surface silanols does not appear to play a significant role on acidic properties. While the strongest acidity is observed for the arenesulfonic acid functionalized material, none of the acidic materials are leveled in an aqueous solvent.
ISSN:0926-860X
1873-3875
DOI:10.1016/j.apcata.2011.01.044