Akademik Veri Yönetim Sistemi
Chemical Engineering Journal, cilt.174, sa.1, ss.281-288, 2011 (SCI-Expanded)
The difference in the basal spacing (8.79Å) and a higher mass loss (6.2%) in the temperature range of 200-750°C of naproxen-bentonite (N-bentonite) comparing to that of Unye bentonite (UB) signified the existence of thermally stable organic species in the interlamellar space of the bentonite clay. The asymmetric OCO- stretching band (1607cm-1) of N-bentonite became stronger in the temperature interval of 100-400°C as a result of binding via the CO group of the ligand to exchangeable cation and/or water molecule whereas the OH bending peak of water (1633cm-1) and the CC stretching vibration of aromatic ring (1531cm-1) became weaker on thermal treatment. The effect of ionic strength on the desorption of naproxen species and the related kinetic data revealed that the release mechanism at pH=7.4 is unrestricted diffusion controlled and governed by the repulsive interactions between the bentonite surface and the negatively charged species. The pore structure characteristics of the bentonite samples corresponding to the surface area, pore volume and pore size were determined by using the conventional analysis of the nitrogen adsorption-desorption isotherms. © 2011 Elsevier B.V.