CHEMISORPTION OF DIVALENT-CATIONS ON N-(2-PYRIDYL)ACETAMIDE IMMOBILIZED ON SILICA-GEL - A THERMODYNAMIC STUDY

Citation
C. Airoldi et Efc. Alcantara, CHEMISORPTION OF DIVALENT-CATIONS ON N-(2-PYRIDYL)ACETAMIDE IMMOBILIZED ON SILICA-GEL - A THERMODYNAMIC STUDY, Journal of Chemical Thermodynamics, 27(6), 1995, pp. 623-632
Citations number
37
Categorie Soggetti
Chemistry Physical
ISSN journal
00219614
Volume
27
Issue
6
Year of publication
1995
Pages
623 - 632
Database
ISI
SICI code
0021-9614(1995)27:6<623:CODONI>2.0.ZU;2-L
Abstract
N-(2-Pyridyl)acetamide covalently immobilized on silica gel (''=Si-pa' ') has a great ability to chemisorb cations from propanonic or ethanol ic solutions through the amount of substance divided by mass 1.57 . 10 (-4) mol . g(-1) of bidentate groups attached to this inorganic suppor t. The chemisorption isotherms obtained with MCl(2) (M: Ni, Co, Cu, Zn , Cd, Hg) in each solvent are similar and adjustable to a modified Lan gmuir equation. The sequence of the maximum capacity is Cu > Co > Zn i n propanone and Hg > Cd > Zn > Co > Cu > Ni in ethanol. The enthalpies of chemisorption of the cations by ''=Si-pa'' at T = (298.15 +/- 0.02 ) K showed larger values in ethanol. With the exception of cobalt (Del ta H-m = +(6.12 +/- 0.01) kJ . mol(-1)} in propanone, all other cation -surface interactions are enthalpically favourable in both solvents. T he enthalpic sequence is Cu > Zn > Co in each solvent and the complete series Cu > Cd > Hg > Ni > Zn > Co was found in ethanol. The standard molar Gibbs free energies are in agreement with the spontaneity of th e proposed reactions between a cation and a basic centre, which has a favourable enthalpic contribution to these chelating processes.