Investigating the thermodynamic causes behind the anomalously large shifts in pKa values of benzoic acid-modified graphite and glassy carbon surfaces

The difference between the values of 4-carboxyphenyl groups, covalently attached to either graphite (BAcarbon) or glassy carbon (BA-GC) surfaces, and benzoic acid in solution is explored using potentiometric titration and cyclic voltammetry. In solution, benzoic acid has a pKa of 4.20 at 25 degrees...

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Veröffentlicht in:Langmuir : the ACS journal of surfaces and colloids. - 1992. - 23(2007), 14 vom: 03. Juli, Seite 7847-52
1. Verfasser: Abiman, Poobalasingam (VerfasserIn)
Weitere Verfasser: Crossley, Alison, Wildgoose, Gregory G, Jones, John H, Compton, Richard G
Format: Aufsatz
Sprache:English
Veröffentlicht: 2007
Zugriff auf das übergeordnete Werk:Langmuir : the ACS journal of surfaces and colloids
Schlagworte:Journal Article
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100 1 |a Abiman, Poobalasingam  |e verfasserin  |4 aut 
245 1 0 |a Investigating the thermodynamic causes behind the anomalously large shifts in pKa values of benzoic acid-modified graphite and glassy carbon surfaces 
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500 |a Date Completed 14.09.2007 
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500 |a ErratumIn: Langmuir. 2009 Jul 7;25(13):7768 
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520 |a The difference between the values of 4-carboxyphenyl groups, covalently attached to either graphite (BAcarbon) or glassy carbon (BA-GC) surfaces, and benzoic acid in solution is explored using potentiometric titration and cyclic voltammetry. In solution, benzoic acid has a pKa of 4.20 at 25 degrees C. However, the observed pKa value on the graphitic surfaces shows significant deviations, with BAcarbon exhibiting a large shift to higher pKa values (pKa = 6.45) in contrast to BA-GC, which is shifted to lower pKa values (pKa = 3.25). Potentiometric titrations at temperatures between 25 and 50 degrees C allowed us to determine the surface pKa of these materials at each temperature studied and hence to determine the enthalpy, entropy, and Gibbs' energy changes associated with the ionization of the carboxylic acid groups. It was found that the enthalpic contribution is negligible and that the changes in surface pKa values are entropically controlled. This suggests that solvent ordering/disordering around the interface strongly influences the observed pKa value, which then reflects the relative hydrophobicity/hydrophilicity of the different graphitic surfaces 
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700 1 |a Crossley, Alison  |e verfasserin  |4 aut 
700 1 |a Wildgoose, Gregory G  |e verfasserin  |4 aut 
700 1 |a Jones, John H  |e verfasserin  |4 aut 
700 1 |a Compton, Richard G  |e verfasserin  |4 aut 
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