Montmorillonite nanoclay filler effects on electrical conductivity,thermal and mechanical properties of epoxy‐based nanocomposites

Epoxy‐based nanocomposites with 2, 5, and 7 wt% of montmorillonite (MMT) nanoclay were prepared using high shear melt mixing technique. The microstructural features of the nanocomposites were investigated by transmission electron microscopy (TEM). The thermal and mechanical properties were measured using differential scanning calorimetry (DSC), thermogravimetric analyzer (TGA), and dynamic mechanical analyzer (DMA). Further, the effect of voltage, temperature, seawater aging on the electrical conductivity (σ_DC) of the nanocomposites was also measured. To understand the free volume behavior upon filler loading, and to observe the connectivity between microstructure and other properties, positron annihilation lifetime spectroscopy was used. The TEM results revealed that MMT nanoparticles were uniformly dispersed in the epoxy matrix. Experimental results showed that the inclusion of 2 wt% MMT nanofiller increased the T_g, electrical conductivity, thermal stability, modulus, free volume of the epoxy nanocomposite significantly. This is well explained from the results of T_g (DSC and DMA), thermal stability, TGA residue, free volume analysis, and electrical conductivity. POLYM. ENG. SCI., 2011. © 2011 Society of Plastics Engineers     

Positron annihilation study of iodine sorption in acrylonitrile–butadiene–styrene

The influence of iodine on the free volume of acrylonitrile–butadiene–styrene (ABS) was investigated by positron annihilation lifetime spectroscopy (PALS). The results indicate the filling of free-volume holes, formation of a positronium–iodine compound (PsI₂/PsI), and possible charge-transfer complexes (CTCs) in the initial stages and the swelling of iodine in the final stages of sorption. The present study also revealed that iodine acts as a chemical quencher of o-Ps. The average size of the free volume suggests that I₃⁻ is the predominant species that fills up the free-volume holes during iodination. The diffusion process in the present case shows non-Fickian behavior and deviates from Fujita's free-volume concept as far as the fractional free volume and diffusion coefficient are concerned. © 1998 John Wiley & Sons, Inc. J Appl Polym Sci 68: 2077–2085, 1998     

Diffusion of seawater in unsaturated polyester resin and its glass fiber reinforced composites in the presence of titanium dioxide as UV absorber

Diffusion of seawater in unsaturated polyester resin (UPR) and its glass fiber reinforced composite in the presence of titanium dioxide has been studied by sorption method. Incorporation of glass and TiO₂ to UPR alters the seawater diffusion process from Fickian to non‐Fickian type. The dual mode sorption model is used to separate Fickian‐controlled and relaxation‐controlled diffusion in case of UPR‐T, UPR‐G, and UPR‐GT. The presence of TiO₂ seems to stabilize UPR and its glass reinforced samples but an increase in the rate of seawater diffusion is observed for these systems. The free volume determined from positron lifetime measurements support the diffusion data in these systems. Results further indicate that the contribution to diffusion in the later stages of sorption is due to the increased contribution from the interfaces. The plasticizing effect of TiO₂ is clearly seen even in the glass reinforced composite. DMA results show an increase in flexibility because of TiO₂ presence both in the neat as well as glass reinforced resin which is well supported by decrease in T_g value from DSC data. © 2006 Wiley Periodicals, Inc. J Appl PolymSci 102: 2784–2794, 2006     

Influence of curing agent and compatibilizer on the physicomechanical properties of polypropylene/nitrile butadiene rubber blends investigated by positron annihilation lifetime technique

A series of thermoplastic vulcanizates of polypropylene (PP)/nitrile butadiene rubber (NBR) (50/50) have been prepared by melt‐mixing method, using phenolic resin/SnCl₂ as the curing system and maleic anhydride‐functionalized PP (PP‐g‐MA) and carboxylated NBR (NBRE‐RCOOH) as the compatibilizing system. Triethylenetetramine was also employed to promote the reaction between the functionalized polymers. The effects of curing agent and compatibilizer on the mechanical and morphological properties have been studied. A novel technique based on positron annihilation lifetime spectroscopy has been used to measure the free volume parameters of these systems. The positron results showed minimum free volume size and free volume fraction at 5.0% of the curing agent suggesting some crosslinking in the rubber phase. The reduction in free volume holes at 2.5% of the compatibilizer is interpreted as improvement in the interfacial adhesion between the components of the blend. The observed variation of free volume fraction is opposite to the tensile strength and exhibits the correlation that, lesser the free volume more is the tensile strength at 2.5% of the compatibilizer in the blend. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 4672–4681, 2006     

Compatibilizer‐induced microstructural changes in poly(trimethylene terephthalate)/EPDM blends studied by the positron annihilation lifetime technique and differential scanning calorimetry

Blends of poly(trimethylene terephthalate) (PTT) and ethylene propylene diene monomer (EPDM) with and without the compatibilizer poly (EPM‐graft‐MA) were investigated by positron annihilation lifetime spectroscopy (PALS) and differential scanning calorimetric (DSC) measurements. The DSC results for the blend with 50/50 composition revealed two glass transition temperatures, indicating a two‐phase system. In the presence of compatibilizer, the two glass transition temperatures shifts towards each other, suggesting an increased interaction between the blend components. The PALS results for the blends without compatibilizer showed an increase in free volume hole size and concentration with increasing EPDM content in the blend, suggesting the coalescence of free volumes of EPDM with the PTT to some extent, but the phase‐separation behaviour continued. The free volume of these blends exhibited positive deviation from the known free volume linear additivity rule. However, poly(EPM‐graft‐MA) compatibilized blends of PTT/EPDM had a noticeable decrease in the free volume parameters, which was clearly due to the compatibilizing effect through increased interaction between blend components. Copyright © 2005 Society of Chemical Industry     

Influence of spoliation in poly(2-hydroxy ethyl methacrylate) soft contact lens on its free volume and optical transparency

The calcification in poly(2-hydroxy ethyl methacrylate) contact lens was investigated using positron annihilation spectroscopy (PLS). The two poly(2-hydroxy ethyl methacrylate) (PHEMA) lenses of different companies were calcified employing a simple mechanism of calcification in abiotic aqueous solutions. The calcium deposit was analyzed using energy dispersive X-ray spectroscopy (EDS). Calcified lenses showed decrease in ortho-positronium (o-Ps) lifetime and free volume hole size of the lens material suggesting diffusion of Ca²⁺ into these cavities. The change in optical property viz. refractive index of these calcified lenses were measured and correlated with positron results. To find a better correlation, a series of worn spoilt PHEMA lenses of the same power with mainly calcium deposits, were similarly characterized using PLS and refractive index. These results correlate well with the free volume of the material. For hydrophilic lenses this correlation is reported for the first time.     

Effect of increased manganese addition and mould type on the slurry erosion characteristics of Cr-Mn iron systems

The wear resistance of high chromium iron is well recorded. However, the same is not the case as regards the use of manganese at higher percentages in high chromium irons and its influence on wear behaviour. Hence, this work highlights the slurry wear characteristics of chromium (□ 16–19%) iron following the introduction of manganese at two levels i.e. 5 and 10%. It is known that the wear properties are dictated by the microstructural features. To alter the structure, the cooling rate of casting has been varied by adopting two different types of moulds (i.e. sand and metal) and subsequently subjecting to thermal treatment. The as-cast and heat treated samples are examined for microstructure and then evaluated for hardness and slurry erosion properties. As the manganese content is increased from 5 to 10%, the hardness showed a decrease in value both in the as-cast and heat treated conditions. The slurry erosion loss, expectedly, showed an increase irrespective of the sample condition (i.e. mould type/heat treatment adopted). The findings are corroborated with the microstructural features obtained through optical and scanning electron microscopy.