PHYSICAL CHEMICAL STUDIES OF THE AGGREGATION AND CATALYTIC PROPERTIES OF THE SURFACTANT METHYLDODECYLBENZYLTRIMETHYLAMMONIUM CHLORIDE (MDBTACL)
Abstract:
The micellization of methyldodecylbenzyltrimethylammonium chloride (MDBTACL) in water was studied by means of surface tensiometry. The critical micellar concentration (CMC) was determined at 25°, 32° and 40°C and thermodynamic properties such as the free energy of micellization (∆G°mic), enthalpy (∆H°mic), and entropy (∆S°mic) of micellization were measured The CMC at 25°C was 1.12 x 10-2 M and the corresponding values of the thermodynamic parameters were: ∆G°mic = -2.66 kcal/mol; ∆H°mic = -0.82 kcal/mol and ∆S°mic = +6.17 e.u. Micelles of the surfactant MDBTACL were good catalysts for the alkaline hydrolysis of p-nitrophenyl diphenyl phosphate (NPDPP) with a maximum catalytic factor of approximately 60, comparable to that of CTAB. Typical activation parameters measured for 0.012 M surfactant and 0.005 M NaOH were: Ea = 8.5 kcal/mol; ∆H°≠ = 7.8 kcal/mol; ∆G°≠ = 19.6 kcal/mol and ∆S°≠ = -39. 3 e.u. The kinetic results were also analyzed in terms of the pseudo-phase ion-exchange models (PPIE) and showed that the model is applicable and gave reasonable fits.
The micellization of methyldodecylbenzyltrimethylammonium chloride (MDBTACL) in water was studied by means of surface tensiometry. The critical micellar concentration (CMC) was determined at 25°, 32° and 40°C and thermodynamic properties such as the free energy of micellization (∆G°mic), enthalpy (∆H°mic), and entropy (∆S°mic) of micellization were measured The CMC at 25°C was 1.12 x 10-2 M and the corresponding values of the thermodynamic parameters were: ∆G°mic = -2.66 kcal/mol; ∆H°mic = -0.82 kcal/mol and ∆S°mic = +6.17 e.u. Micelles of the surfactant MDBTACL were good catalysts for the alkaline hydrolysis of p-nitrophenyl diphenyl phosphate (NPDPP) with a maximum catalytic factor of approximately 60, comparable to that of CTAB. Typical activation parameters measured for 0.012 M surfactant and 0.005 M NaOH were: Ea = 8.5 kcal/mol; ∆H°≠ = 7.8 kcal/mol; ∆G°≠ = 19.6 kcal/mol and ∆S°≠ = -39. 3 e.u. The kinetic results were also analyzed in terms of the pseudo-phase ion-exchange models (PPIE) and showed that the model is applicable and gave reasonable fits.
DOI: 10.48141/SBJCHEM.v8.n9.2000.83_2000.pdf
Download PDF