Abstract
Polyacrylamide gel (PAMG) method is a simple, fast and cheap method used for the synthesis of a wide variety of nanopowders. However, no adequate results have been reported on the thermal degradation behavior of PAMG which can be very effective on the final product properties. In this work, thermal degradation behavior of PAMG in the presence of TiCl4 as a precursor salt for synthesis of TiO2 nanoparticles was examined in comparison with linear polyacrylamide (LPAM) and pure PAMG by thermogravimetry/differential thermal analysis. Their thermal degradation kinetics was investigated, as well. The results showed that thermal degradation of all samples occurred in two stages at different onset temperatures. Despite the high thermal stability of pure PAMG compared to LPAM, the presence of TiCl4 as a mineral material in PAMG structure decreases the thermal degradation onset temperature, considerably. Furthermore for LPAM and PAMG, majority of weight loss occurs in the second stage, but in PAMG with TiCl4 the weight loss occurs mainly at the first stage. For more detailed investigation, residual materials were characterized by Fourier transform infrared spectroscopy and X-ray diffraction (XRD) techniques, attributing this trend to the presence of mineral materials in PAMG structure. XRD and transmission electron microscopy were also applied to confirm anatase crystalline structure and nanoscale distribution of the TiO2 particles synthesized via PAMG method.
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Acknowledgments
The authors wish to thank Sahand University of Technology (SUT) for financial support of this work. Also, thank coworkers and technical staff in nanostructure materials research center and institute of polymeric materials of SUT for their help during various stages of this study.
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Rakhshani, M., Kamrannejad, M.M., Babaluo, A.A. et al. Thermal degradation behavior and kinetic studies of polyacrylamide gel in TiO2 nanoparticles synthesis. Iran Polym J 21, 821–828 (2012). https://doi.org/10.1007/s13726-012-0086-2
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DOI: https://doi.org/10.1007/s13726-012-0086-2