Vinylpyridinium ionomers. III. Influence of the matrix glass transition temperature on the dynamic mechanical properties of random acrylate-based systems

1990 ◽  
Vol 68 (7) ◽  
pp. 1228-1232 ◽  
Author(s):  
Denis Duchesne ◽  
Adi Eisenberg

The thermal and dynamic mechanical properties of random butyl acrylate- and plasticized ethyl acrylate-based vinylpyridinium ionomers have been investigated. The properties of the ionomers were found to be dependent on the glass transition temperature of the matrix material. Ionomers having a glass transition temperature lower than ca. 25 °C exhibited all the features associated with the presence of phase-separated microdomains or clusters while the materials with higher glass transition temperatures were not. It was also observed that the dispersion associated with the vinylpyridinium clusters for a butyl acrylate-based ionomer with 12 mol% of ionic units occurs at ca. 25 °C. This value is very close to that observed previously by Otocka and Eirich in their study of a butadiene-based vinylpyridinium ionomer with the same ion content. Keywords: ionomers, plasticization, clustering, glass transition, dynamic mechanical properties.

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. 28-33
Author(s):  
Huey Ling Chang ◽  
Chih Ming Chen ◽  
Kung Liang Lin ◽  
Bor Kae Chang

Nanocomposite samples containing epoxy resin, glass fiber and 0~2 wt.% SiO2 nanopowder are prepared. The effects of SiO2 addition on the chemical resistance, glass transition temperature (Tg) and dynamic mechanical properties of the various samples are then observed. The chemical resistance of the nanocomposite specimens is compared with that of pure glass fiber/epoxy composite specimens when tested in acetone. The results show that the addition of 2 wt.% SiO2 increases the value of storage modulus by 1646MPa compared to that of the sample containing no silica nanopowder. Following immersion in acetone, all the nanocomposite specimen storage modulus decreased, but the addition of SiO2 reduced the decline, where the 2 wt. % samples decrease from 11.76% reduction to 0.84% and no significant change in the Tg compared to that of the sample with no silica nanopowder. Therefore, the experimental results indicate that 2 wt.% SiO2 addition is beneficial in improving chemical resistance, glass transition temperature, and dynamic mechanical properties of epoxy resin / glass fiber nanocomposites.


Adhesive strength of «epoxy binder-steel wire» joints and the mechanical behavior of the binder during multiple repeated curing have been investigated. It is shown that when the curing temperature is considerably higher than the glass transition temperature of the binder, the adhesive strength decreases monotonically with an increase in the number of curing cycles. In this case the mechanical properties of the matrix also decrease. Possible mechanisms of the observed changes are discussed.


2020 ◽  
Vol 10 (21) ◽  
pp. 7840
Author(s):  
Janis Karl ◽  
Franziska Kirsch ◽  
Norbert Faderl ◽  
Leonhard Perko ◽  
Teresa Fras

Using interlayers of rubber adds a positive effect to the synergy of disruptor–absorber armors. Emerging from its viscoelasticity the material is able to transform mechanical stress into heat. The dynamic mechanical properties of elastomers depend on both ambient temperature and frequency of an applied mechanical load. The damping shows a maximum in the glass transition area. If the frequency of the glass transition is in the magnitude of the mechanical stress rate applied by ballistic impact, the elastomer will undergo the transition and thus show maximized damping. An ideal material for ballistic protection against small calibers is developed by making use of dynamic mechanical analysis and the time–temperature superposition principle. The material is later analyzed by ballistic experiments and compared to other nonideal rubbers with regard to glass transition temperature, hardness and damping. It is shown that by choosing a material correctly with certain glass transition temperature and hardness, the ballistic properties of a steel–rubber–aluminum armor can be enhanced. The chosen material (butyl rubber) with a hardness of 50 °ShA is able to enhance energy absorption during ballistic impact by around 8%, which is twice as good as other rubber with non-optimized properties.


Sign in / Sign up

Export Citation Format

Share Document