Abstract

Polymeric nanocomposite hydrogels were developed from a hydrophilic natural polymer, sodium alginate (SA) with black nano crystalline titania (black TiO2) by using ionic cross linker CaCl2, in view of the possible enhancement in properties of SA towards water treatment application. The optimum conditions for the preparation of films were done by varying the amount of cross-linking agent, cross-linking time and the amount of black nano crystalline TiO2. The nanocomposite hydrogels were then characterized by X-ray diffraction studies (XRD), fourier transform infrared spectroscopy (FTIR) and thermogravimetric analysis (TGA). The surface morphologies of the nanocomposite have been examined by using scanning electron microscopy (SEM). The swelling studies and its kinetics have been investigated under diverse PH conditions. Permeability of the gels were assessed in terms of film characteristics and PH. The results proved that the gels exhibit PH sensitivity. Based on the results, we have proposed a possible mechanism of water transport through the gels. The developed SA/black TiO2 nanocomposite hydrogels have been successfully employed for the efficient degradation organic dyes such as methylene blue and malachite green. The experimental results of dye degradation studies have been compared with theoretical models and it has been observed that the dye degradation follows pseudo second order kinetics for both methylene blue and malachite green. By altering the PH, the nanocomposite hydrogels can be broken and spent TiO2 can be recovered.

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

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.