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Synthesis and characterization <strong>of</strong> polypropylene/ionomer/ organoclay<br />

nanocomposites<br />

S. R. Mallikarjuna, N. Ramesh, C. Ramesh and S. Sivaram<br />

Divison <strong>of</strong> Polymer Science and Eng<strong>in</strong>eer<strong>in</strong>g, National Chemical Laboratory,<br />

Pune-411 008, Maharashtra, India.<br />

Email: c.ramesh@ncl.res.<strong>in</strong><br />

Abstract:<br />

The compatibilization effects provided by ionomer-g-polypropylenes versus those <strong>of</strong> a maleated<br />

polypropylene, PPMA, for form<strong>in</strong>g polypropylene-based nanocomposites were compared. We<br />

have prepared a novel compatibilizer by graft<strong>in</strong>g ionic functional groups on to the PP and<br />

evaluated its efficiency as compatibilizer <strong>in</strong> the preparation <strong>of</strong> PP/clay nanocomposites. The<br />

PP/ionomer/organoclay nanocomposites were prepared by direct melt mix<strong>in</strong>g and by masterbatch<br />

methods and the structure obta<strong>in</strong>ed were characterized by WAXD and TEM and were compared<br />

with nanocomposites prepared us<strong>in</strong>g PPMA as compatibilizer. Mechanical properties <strong>of</strong> the<br />

nanocomposites prepared were studied us<strong>in</strong>g INSTRON and the crystallization behavior was<br />

studied us<strong>in</strong>g Differential Scann<strong>in</strong>g Calorimetry (DSC) and Polarized Optical Microscopy<br />

(POM). Thermal stabilities were characterized us<strong>in</strong>g TGA. The dispersion <strong>of</strong> clay was found to<br />

be dependent on the method <strong>of</strong> preparation, type <strong>of</strong> compatibilizer used and the amount <strong>of</strong><br />

compatibilizer used. The dispersion <strong>of</strong> the organoclay was better with the ionomer than PPMA<br />

and the dispersion was better when the nanocomposites were prepared by two step masterbatch<br />

route than the s<strong>in</strong>gle step direct mix<strong>in</strong>g method. The dispersion <strong>of</strong> the organoclay improved with<br />

<strong>in</strong>crease <strong>in</strong> the amount <strong>of</strong> compatibilizer. The nanocomposites obta<strong>in</strong>ed with ionomer as<br />

compatibilizer showed better enhancements <strong>in</strong> nucleation, thermal properties and mechanical<br />

properties as compared to the nanocomposites obta<strong>in</strong>ed us<strong>in</strong>g PPMA as compatibilizer.<br />

Introduction:<br />

Polypropylene (PP) is a fast grow<strong>in</strong>g thermoplastic and dom<strong>in</strong>at<strong>in</strong>g the <strong>in</strong>dustrial applications due<br />

to its attractive comb<strong>in</strong>ation <strong>of</strong> properties such as low density, high thermal stability, resistance to<br />

corrosion etc. and low cost. There is a strong need to improve their mechanical properties for its<br />

applications <strong>in</strong> automotive <strong>in</strong>dustry 1 . Researchers <strong>in</strong> the recent decade have shown that<br />

re<strong>in</strong>forcement with dispersed clay <strong>in</strong> the polymer matrix enhances the mechanical properties<br />

without much affect<strong>in</strong>g the density <strong>of</strong> the polymer 2 . Therefore, various research efforts were<br />

made to disperse clay <strong>in</strong> the PP matrix. However it was very difficult to disperse clay <strong>in</strong> the PP<br />

matrix, as the polymer was highly non polar and there are no polar groups available to <strong>in</strong>teract<br />

with the clay surface. The usual organo-modification <strong>of</strong> clay did not sufficiently lower the surface<br />

energy <strong>of</strong> the clay to <strong>in</strong>teract with PP cha<strong>in</strong>s. Unmodified polyolef<strong>in</strong>s lack the <strong>in</strong>tr<strong>in</strong>sic<br />

thermodynamic aff<strong>in</strong>ity with currently available organoclays to form well dispersed<br />

nanocomposites 3 . The surface energy <strong>of</strong> PP cha<strong>in</strong>s was improved by <strong>in</strong>troduc<strong>in</strong>g polar<br />

functionalities and used them for the preparation <strong>of</strong> nanocomposites 4-10 . To improve the surface<br />

energy <strong>of</strong> semi crystall<strong>in</strong>e polymers <strong>in</strong> the preparation <strong>of</strong> nanocomposites, many researchers<br />

<strong>in</strong>troduced ionic groups on to the polymer cha<strong>in</strong>s 11-19 . However compatibilizers such as am<strong>in</strong>e and<br />

ammonium functionalized PP had failed to enhance the dispersion <strong>of</strong> clay <strong>in</strong> the PP matrix as<br />

compared to maleic anhydride grafted polypropylene via melt mix<strong>in</strong>g 20 .<br />

Therefore <strong>in</strong> the present work, we have evaluated a novel metallic ionomer <strong>of</strong> PP as<br />

compatibilizer for prepar<strong>in</strong>g PP/organoclay nanocomposite by two different mix<strong>in</strong>g routes. The<br />

properties <strong>of</strong> the obta<strong>in</strong>ed nanocomposites were compared with the nanocomposites, which are<br />

prepared us<strong>in</strong>g PPMA as compatibilizer.

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