Dynamic Mechanical Analysis of Nanosilica Filled Epoxy Nanocomposites

2014 ◽  
Vol 699 ◽  
pp. 239-244 ◽  
Author(s):  
Nurhidayah R. Zamani ◽  
Aidah Jumahat ◽  
Rosnadiah Bahsan

In this study, Dynamic Mechanical Analyzer (DMA) was used to study the effect of nanoparticles, which is nanosilica, on glass transition temperature (Tg) of epoxy polymer. A series of epoxy based nanosilica composite with 5-25 wt% nanosilica content was prepared using mechanical stirring method. The weight fractions of nanosilica in epoxy were 5 wt%, 13 wt% and 25 wt%. 30mm x 10mm x 3mm size specimens were tested using DMA machine from room temperature up to 180oC at 2°C/min heating rate. From the analysis of the results, dynamic modulus and glass transition temperature of pure polymer and nanosilica filled polymer were obtained. The glass transition of a polymer composite is a temperature-induced change in the matrix material from the glassy to the rubbery state during heating or cooling. Glass transition temperature Tg was determined using several method: storage modulus onset, loss modulus peak, and tan δ peak. The results showed that the presence of nanosilica reduced Tg of epoxy polymer.

2013 ◽  
Vol 853 ◽  
pp. 46-52
Author(s):  
Huey Ling Chang ◽  
Chih Ming Chen

Epoxy resin nanocomposite samples containing 0~3wt.% reactive diluent and 0~3wt.% silica nanopowder are prepared. The preparation process is presented for solvent-free and greenmanufacturing. The storage modulus, loss modulus and glass transition temperature of the various samples are then evaluated via Dynamic Mechanical Analysis (DMA). For samples containing 0wt.% and 3wt.% reactive diluent, respectively, 3wt.% nanoSiO2 addition is found to increase the storage modulus by 51.06 % and 22.22 %, respectively. In addition, it is found that the loss modulus is determined principally by the level of SiO2 addition, whereas the glass transition temperature is determined mainly by the level of reactive diluent addition.


Author(s):  
Pragati Priyanka ◽  
Harlal Singh Mali ◽  
Anurag Dixit

Comprehensive experimental results of dynamic mechanical analysis (DMA) of polymer reinforced textile composites are presented in the current investigation. Plain and 2x2 twill woven multilayer fabrics of monolithic kevlar and hybrid carbon-kevlar (C-K) are reinforced into the thermoset polymer matrix. Kevlar/epoxy and C-K/epoxy composite laminates are fabricated using an in-house facility of the vacuum-assisted resin infusion process. Variation of the visco-elastic behaviour (storage modulus, damping factor and glass transition temperature, Tg) along with time, temperature and frequency is studied for the composites. Dynamic mechanical analysis is performed under temperature sweep with frequency ranging from 1-50 Hz. Results depict the effect of inter yarn hybridisation of carbon with kevlar yarns on the storage modulus, damping performance, and creep behaviour of dry textile composites. Temperature swept dynamic characterisation is also performed to evaluate the degradation and damping performance of the composite laminates soaked in the deionised water at glass transition temperature Tg, ½ Tg, and ¾ Tg. The morphological study has been performed post the dynamic mechanical analysis using field emission scanning electron microscope.


2011 ◽  
Vol 6 (2) ◽  
pp. 91-95
Author(s):  
Ion Dranca ◽  
Igor Povar ◽  
Tudor Lupascu

This research has been carried out in order to demonstrate the use of differential scanning calorimetry (DSC) in detecting and measuring α- and β-relaxation processes in amorphous pharmaceutical systems. DSC has been employed to study amorphous samples of poly (vinylpyrrolidone) (PVP), indomethacin (InM), and ursodeoxycholic acid (UDA) that are annealed at temperature (Ta) around 0.8 of their glass transition temperature (Tg). Dynamic mechanical analysis (DMA) is used to measure β- relaxation in PVP. Yet, the DSC has been used to study the glassy indomethacin aged at 0 and -10 oC for periods of time up to 109 and 210 days respectively. The results demonstrate the emergence of a small melting peak of the α-polymorph after aging for 69 days at 0°C and for 147 days at -10°C (i.e., ~55°C below the glass transition temperature) that provides evidence of nucleation occurring in the temperature region of the β-relaxation.


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