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

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Chapter 9<br />

resistance was studied as per ASTM 573-88. The abrasi<strong>on</strong> resistance <strong>of</strong> <strong>the</strong><br />

vulcanizates was studied us<strong>in</strong>g a DIN abrader as per DIN st<strong>and</strong>ard. The<br />

compressi<strong>on</strong> set <strong>of</strong> <strong>the</strong> samples were determ<strong>in</strong>ed as per ASTM D 395. The<br />

chemical crossl<strong>in</strong>k density was determ<strong>in</strong>ed by equilibrium swell<strong>in</strong>g method.<br />

The heat build-up <strong>of</strong> <strong>the</strong> vulcanizates was determ<strong>in</strong>ed us<strong>in</strong>g Goodrich<br />

flexometer. The flex resistance was determ<strong>in</strong>ed us<strong>in</strong>g Wallace De Mattia<br />

flex<strong>in</strong>g mach<strong>in</strong>e.<br />

174<br />

In <strong>the</strong> present study <strong>nano</strong> <strong>z<strong>in</strong>c</strong> <strong>oxide</strong>s were prepared by two methods,<br />

namely, precipitati<strong>on</strong> method <strong>and</strong> by solid-state pyrolytic method. Nano <strong>z<strong>in</strong>c</strong><br />

<strong>oxide</strong>s from precipitati<strong>on</strong> method (ZnO(p)) <strong>and</strong> solid-state pyrolytic method<br />

(ZnO(s)) were characterized by us<strong>in</strong>g X-ray diffracti<strong>on</strong> (XRD), transmissi<strong>on</strong><br />

electr<strong>on</strong> microscopy (TEM), BET adsorpti<strong>on</strong> <strong>and</strong> <strong>in</strong>frared spectroscopy. Nano<br />

<strong>z<strong>in</strong>c</strong> <strong>oxide</strong>s prepared by <strong>the</strong>se methods had particle size lower than that <strong>of</strong> <strong>the</strong><br />

c<strong>on</strong>venti<strong>on</strong>al <strong>z<strong>in</strong>c</strong> <strong>oxide</strong> (ZnO(c)). Bulk density values are found to be higher<br />

for <strong>z<strong>in</strong>c</strong> <strong>oxide</strong>s prepared <strong>in</strong> <strong>the</strong> laboratory compared to <strong>the</strong> c<strong>on</strong>venti<strong>on</strong>al ZnO.<br />

Natural rubber composites were prepared us<strong>in</strong>g ZnO(p) <strong>and</strong> ZnO(s)<br />

as activator. The cure characteristics <strong>of</strong> <strong>the</strong> natural rubber compounds<br />

c<strong>on</strong>ta<strong>in</strong><strong>in</strong>g a low dosage <strong>of</strong> ZnO(p) <strong>and</strong> ZnO(s) were compared with those <strong>of</strong><br />

natural rubber compound c<strong>on</strong>ta<strong>in</strong><strong>in</strong>g c<strong>on</strong>venti<strong>on</strong>al <strong>z<strong>in</strong>c</strong> <strong>oxide</strong>. The cure<br />

characteristics were found to be comparable. The mechanical properties <strong>of</strong><br />

vulcanizates with ZnO(p) <strong>and</strong> ZnO(s) were compared with those <strong>of</strong><br />

vulcanizates with c<strong>on</strong>venti<strong>on</strong>al ZnO. Abrasi<strong>on</strong> resistance, heat build-up <strong>and</strong><br />

flex resistance were found to be superior for vulcanizates with ZnO(p) <strong>and</strong><br />

ZnO(s). It has been observed that <strong>use</strong> <strong>of</strong> a low dosage <strong>of</strong> ZnO(p) <strong>and</strong> ZnO(s)<br />

as activator <strong>in</strong> natural rubber composites improved <strong>the</strong> cure properties <strong>and</strong><br />

mechanical properties <strong>of</strong> <strong>NR</strong> composites. So low dosages <strong>of</strong> ZnO(p) <strong>and</strong><br />

ZnO(s) were <strong>use</strong>d as curative <strong>in</strong> a selected syn<strong>the</strong>tic polar rubber<br />

(chloroprene rubber) compounds <strong>and</strong> <strong>in</strong> a selected syn<strong>the</strong>tic n<strong>on</strong>-polar rubber<br />

(styrene butadiene) compounds. The cure characteristics <strong>of</strong> polychloroprene

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