20 research outputs found
Influence of halloysite nanotubes on physical and mechanical properties of cellulose fibres reinforced vinyl ester composites
Natural fibres are generally added to polymer matrix composites to produce materials with the desirable mechanical properties of higher specific strength and higher specific modulus while at the same time to maintain a low density and low cost. The physical and mechanical properties of polymer composites can be enhanced through the addition of nanofillers such as halloysite nanotubes. This article describes the fabrication of vinyl ester eco-composites and eco-nanocomposites and characterizes these samples in terms of water absorption, mechanical and thermal properties. Weight gain test and Fourier transform infrared analysis indicated that 5% halloysite nanotube addition gave favourable reduction in the water absorption and increased the fibre–matrix adhesion leading to improved strength properties in the eco-nanocomposites. However, halloysite nanotube addition resulted in reduced toughness but improved thermal stability
Thermal stability and flammability of nanocomposites made of diene rubbers and modified halloysite nanotubes
Thermal properties and flammability of nanocomposites based on diene rubbers and naturally occurring and activated halloysite nanotubes
Rheological behavior of compatibilized and non-compatibilized PA6/EPM blends
The rheological properties of PA-6/EPM polymer
blends, non-compatibilized and compatibilized with grafted
ethylene propylene rubber (EPM-g-MA), have been investigated.
Linear and non-linear (relaxation both in shear
and extension) experiments were realized. Stress relaxation
experiments coupled with scanning electron microscopy
(SEM) analysis showed the existence of one relaxation time
and non-deformed droplets for the immiscible blend, and
two relaxation times and deformed droplets for the compatibilized
ones, the second relaxation being more pronounced
for higher compatibilizer contents. These results clearly
indicate that, despite the high viscosity and elasticity ratios,
if high amounts of compatibilizer are added to the blend,
interfacial slip is suppressed and a high-enough adhesion
between the phases is achieved for the high-viscosity dispersed
phase to be deformed
Interfacial tension reduction in PBT/PE/clay nanocomposite
We investigated the effect of organically modified nanoclay (organoclay) on immiscible polymer blends [polybutylene terephthalate (PBT)/polyethylene (PE)] with a special focus on the role of clay as a compatibilizer. When organoclay (Nanofil 919; Sud-Chemie, Inc.) is added to the blend, the clay first locates at the interface and then selectively locates in the PBT phase due to its affinity with PBT. This results in effective size reduction and narrowed size distribution of the dispersed phase. However, with a small amount of organoclay, it is observed that the clay locates at the interface regardless of its affinity for a specific component to minimize the chemical potential. The interfacial tension change of the blend with the addition of organoclay was quantitatively predicted from extensional force measurement. When the blend is subjected to an extension, the interfacial tension functions as a resistance against drop deformation. When we added organoclay to the blend, the extensional force was significantly reduced, which means that the contribution of the interfacial tension to the total force is reduced. For a 10/90 PBT/PE blend, the interfacial tension was reduced from 5.76 to 0.14 cN m(-1) when 1 wt% of organoclay was added. This interfacial tension reduction arises from the localization of the organoclay at the interface and its nonhomogeneous distribution along the interface, suppressing the coalescence between the droplets, which is a role of a compatibilizer. Conclusively, the immiscible polymer blends can be compatibilized with organoclay. The organoclay changes the blend morphology by interfacial tension reduction due to the localization of the organoclay at the interface and by the viscosity ratio change due to the selective localization by its affinity to a specific component in the blend