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Studies on the use of nano zinc oxide and modified silica in NR, CR ...

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Chapter 2<br />

2.2.6 Bound rubber c<strong>on</strong>tent<br />

57<br />

Bound rubber is <strong>the</strong> rubber that is trapped by <strong>the</strong> filler aggregates<br />

after mix<strong>in</strong>g. The rubber cha<strong>in</strong> are attracted ei<strong>the</strong>r physically or chemically to<br />

form a rubber shell <strong>on</strong> <strong>the</strong> surface <strong>of</strong> <strong>the</strong> <strong>silica</strong> particles. The rubber fracti<strong>on</strong><br />

<strong>of</strong> an uncured compound is amount <strong>of</strong> rubber that is not extracted when it is<br />

exposed to a good solvent.<br />

The mixture samples were cut <strong>in</strong> small pieces <strong>and</strong> put over a sta<strong>in</strong>less<br />

steel sieve (40 µm meshes), <strong>the</strong>n extracted with toluene for 4 days <strong>and</strong> f<strong>in</strong>ally<br />

dried for <strong>on</strong>e day at 80°C. C<strong>on</strong>tents <strong>of</strong> bound rubber were determ<strong>in</strong>ed from<br />

<strong>the</strong> weights <strong>of</strong> <strong>the</strong> samples before <strong>and</strong> after <strong>the</strong> extracti<strong>on</strong>.<br />

The BRC is calculated from <strong>the</strong> weight <strong>of</strong> <strong>the</strong> residue after extracti<strong>on</strong><br />

(b), <strong>the</strong> weight <strong>of</strong> <strong>the</strong> <strong>in</strong>itial mixture (m), <strong>and</strong> <strong>the</strong> amount <strong>of</strong> <strong>silica</strong> present <strong>in</strong><br />

<strong>the</strong> <strong>in</strong>itial mixture (a), determ<strong>in</strong>ed by calc<strong>in</strong>ati<strong>on</strong> at 600° C.<br />

BRC %= [(b-a) / (m-a)] x 100………………………….. ……….. 2.5<br />

The BRC can be related to <strong>the</strong> amount <strong>of</strong> rubber <strong>in</strong> <strong>the</strong> mixture before<br />

<strong>the</strong> extracti<strong>on</strong> <strong>and</strong> was calculated us<strong>in</strong>g <strong>the</strong> equati<strong>on</strong> 2.5. 11<br />

2.2.7 Oz<strong>on</strong>e resistance<br />

Oz<strong>on</strong>e resistance was determ<strong>in</strong>ed accord<strong>in</strong>g to ASTM D 518 method<br />

B. Samples were exposed to oz<strong>on</strong>ised air <strong>in</strong> an oz<strong>on</strong>e chamber (MAST Model<br />

700-1) for 12 hrs. The c<strong>on</strong>centrati<strong>on</strong> <strong>of</strong> oz<strong>on</strong>e was ma<strong>in</strong>ta<strong>in</strong>ed at 50 pphm at<br />

20% stra<strong>in</strong> <strong>and</strong> <strong>the</strong> <strong>in</strong>side temperature at 40°C. The oz<strong>on</strong>e cracks developed<br />

<strong>on</strong> <strong>the</strong> samples were observed by a lens <strong>and</strong> <strong>the</strong> photographs were taken.<br />

2.2.8 Thermogravimetric analysis<br />

The <strong>the</strong>rmograms <strong>of</strong> natural rubber, <strong>silica</strong> composites are recorded<br />

with a <strong>the</strong>rmogravimetric analyzer Q–50, TA <strong>in</strong>struments. It is computer

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