Abstract
ObjectiveThe aim of this study is to analyze different strategies of modification of bentonite (Bent) combining reactions of cationic exchange, silylation and acid activation. MethodsSix samples of modified bentonite were prepared: silylated bentonite (S-Bent), acid-activated bentonite (A-Bent), exchanged clay (E-Bent), silylated and acid-activated clay (S–A-Bent), exchanged and acid-activated clay (E–A-Bent), and exchanged, silylated and acid-activated bentonite (E–S–A-Bent). To study the effectiveness of the different treatments, X-ray diffraction analysis, thermogravimetric analysis, Fourier transform infrared spectroscopy and water absorption tests were performed. ResultsThe silylated bentonite presented a significant reduction in the equilibrium water uptake percentage with respect to the unmodified clay, even when small amounts of silane were incorporated to the clay. On the other hand, no significant changes in the organic content were obtained when the silylation reaction was performed on previously acid-activated bentonite. When a sample of silylated and activated bentonite was further modified by cationic exchange reaction, it was found that the previous treatments allowed increasing the uptaken amount of surfactant cations during the exchange reaction. In fact, the combination of the three treatments (acid-activation, silylation and cationic exchange) gave place to the modified bentonite with the biggest basal spacing and the lower equilibrium water uptake percentage. SignificanceThe results obtained in the present study reveal the potential usefulness of the E–S–A-Bent sample as promising filler for the formulation of clay polymer nanocomposites. Work is in progress in this direction.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.