期刊
JOURNAL OF SCIENCE-ADVANCED MATERIALS AND DEVICES
卷 1, 期 3, 页码 351-361出版社
VIETNAM NATL UNIV
DOI: 10.1016/j.jsamd.2016.07.007
关键词
Polystyrene; Layered double hydroxides; Nanocomposites; Kinetic; Rheology
资金
- FIST [SR/FST/ETII-028/2010]
- Department of Science and Technology (DST), Government of India
The present work deals with the development of polystyrene ( PS) nanocomposites through solvent blending technique with diverse contents of modified Co-Al layered double hydroxide (LDH). The prepared PS as well as PS/Co-Al LDH (1-7 wt.%) nanocomposites were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FTIR), rheological analysis, thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC). The XRD results suggested the formation of exfoliated structure, while TEM images clearly indicated the intercalated morphology of PS nanocomposites at higher loading. The presence of various functional groups in the Co-Al LDH and PS/Co-Al LDH nanocomposites was verified by FTIR analysis. TGA data confirmed that the thermal stability of PS composites was enhanced significantly as compared to pristine PS. While considering 15% weight loss as a reference point, it was found that the thermal degradation (T-d) temperature increased up to 28.5 degrees C for PS nanocomposites prepared with 7 wt.% Co-Al LDH loading over pristine PS. All the nanocomposite samples displayed superior glass transition temperature (T-g), in which PS nanocomposites containing 7 wt.% LDH showed about 5.5 degrees C higher Tg over pristine PS. In addition, the kinetics for thermal degradation of the composites was studied using Coats-Redfern method. The Criado method was ultimately used to evaluate the decomposition reaction mechanism of the nanocomposites. The complex viscosity and rheological muduli of nanocomposites were found to be higher than that of pristine PS when the frequency increased from 0.01 to 100 s(-1). (C) 2016 The Authors. Publishing services by Elsevier B.V.
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