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Effect of Coupling Agents on Mechanical Properties and Morphology ...

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134<br />

PHUEAKBUAKHAO, N. et al.<br />

chemical b<strong>on</strong>ding can be improved the interacti<strong>on</strong><br />

at interface areas between the polymer matrix <strong>and</strong><br />

CaCO 3 particles more than physical b<strong>on</strong>ding or van<br />

der waals forces.<br />

Using other coupling agents at c<strong>on</strong>centrati<strong>on</strong>s<br />

<str<strong>on</strong>g>of</str<strong>on</strong>g> 2, 3, 4 <strong>and</strong> 5 wt.% to study the possibility <str<strong>on</strong>g>of</str<strong>on</strong>g><br />

increasing the polymer-CaCO 3 interacti<strong>on</strong>. It was<br />

found that the mechanical properties <str<strong>on</strong>g>of</str<strong>on</strong>g> composite<br />

can be improved, especially impact resistance when<br />

increase the c<strong>on</strong>centrati<strong>on</strong>s <str<strong>on</strong>g>of</str<strong>on</strong>g> coupling agents.<br />

Table 4 summarizes the mechanical properties<br />

<str<strong>on</strong>g>of</str<strong>on</strong>g> the r-HDPE filled CaCO 3 treated with the<br />

optimum c<strong>on</strong>centrati<strong>on</strong>s <str<strong>on</strong>g>of</str<strong>on</strong>g> each coupling agent.<br />

The results show that each coupling agent gives<br />

rise to increase in a particular mechanical properties<br />

due to its characteristics. The r-HDPE/treated-<br />

CaCO 3 composites show the best mechanical<br />

properties when CaCO 3 were treated with SA,<br />

AMPTES, GPTMS <strong>and</strong> MA-g-HDPE at 1, 2, 3 <strong>and</strong><br />

4 wt.%, respectively. This behavior can be<br />

explained based <strong>on</strong> the fact that increasing the<br />

c<strong>on</strong>centrati<strong>on</strong>s <str<strong>on</strong>g>of</str<strong>on</strong>g> coupling agents can improve the<br />

interacti<strong>on</strong> between the polymer matrix <strong>and</strong> CaCO 3<br />

particle, which are physical forces or van der waals<br />

forces as well as chemical forces but have to use<br />

more c<strong>on</strong>centrati<strong>on</strong>s. This indicates that selecti<strong>on</strong><br />

the type <strong>and</strong> quantity <str<strong>on</strong>g>of</str<strong>on</strong>g> coupling agents for the<br />

composites is important to gets the optimum<br />

property <str<strong>on</strong>g>of</str<strong>on</strong>g> final products.<br />

<strong>and</strong> the surface was rather smooth. This shows that<br />

the polymer matrix <strong>and</strong> CaCO 3 particles didn’t<br />

restrain together. On the other h<strong>and</strong>, the rough<br />

surfaces are observed for the r-HDPE/treated<br />

CaCO 3 composites, as presented in Figure 4(b) -<br />

Figure 4(e). This indicates the ductile fracture. The<br />

morphologies <str<strong>on</strong>g>of</str<strong>on</strong>g> the fractured surfaces were<br />

c<strong>on</strong>sistent with the impact strength listed in Table 2<br />

<strong>and</strong> Table 3. High magnified SEM micrographs<br />

(x3500) <str<strong>on</strong>g>of</str<strong>on</strong>g> the r-HDPE/CaCO 3 composites are<br />

illustrated in Figure 5. Phase separati<strong>on</strong> can be<br />

seen when the untreated CaCO 3 was incorporated<br />

in the r-HDPE matrix (Figure 5(a)). This<br />

phenomen<strong>on</strong> is not visible when the treated CaCO 3<br />

was used (Figure 5(b) - Figure 5(e)). The interfacial<br />

interacti<strong>on</strong> between the r-HDPE matrix <strong>and</strong> CaCO 3<br />

particles was str<strong>on</strong>ger, resulted from the<br />

pretreatment <str<strong>on</strong>g>of</str<strong>on</strong>g> CaCO 3 particles. This would be<br />

another reas<strong>on</strong> for the improvement in the<br />

mechanical properties, particularly impact strength,<br />

<str<strong>on</strong>g>of</str<strong>on</strong>g> the r-HDPE/CaCO 3 composites. (9)<br />

(a) untreated<br />

Table 4. <strong>Mechanical</strong> properties <str<strong>on</strong>g>of</str<strong>on</strong>g> r-HDPE/CaCO 3<br />

composites (CaCO 3 treated with optimum<br />

c<strong>on</strong>tent <str<strong>on</strong>g>of</str<strong>on</strong>g> coupling agents)<br />

<str<strong>on</strong>g>Coupling</str<strong>on</strong>g><br />

Agent<br />

Tensile<br />

strength<br />

(MPa)<br />

Flexural<br />

strength<br />

(MPa)<br />

Impact<br />

strength<br />

(kJ/m 2 )<br />

El<strong>on</strong>gati<strong>on</strong><br />

at Break<br />

(%)<br />

Untreated 14.01 19.87 10.28 18.77<br />

1. wt%<br />

Stearic acid<br />

2. wt%<br />

AMPTES<br />

3. wt%<br />

GPTMS<br />

4. wt%<br />

MA-g-HDPE<br />

15.68 24.93 13.23 21.65<br />

16.17 25.54 15.00 22.32<br />

15.87 25.28 14.67 21.95<br />

16.03 25.84 14.89 23.24<br />

(b) 1 wt.% SA<br />

(c) 2 wt.% AMPTES<br />

<strong>Morphology</strong> <str<strong>on</strong>g>of</str<strong>on</strong>g> r-HDPE/CaCO 3 Composites<br />

The fractured surfaces <str<strong>on</strong>g>of</str<strong>on</strong>g> the r-HDPE/CaCO 3<br />

composites after the impact test were examined by<br />

SEM. Figure 4(a) shows that the r-HDPE filled<br />

with the untreated CaCO 3 exhibits brittle fracture<br />

(d) 3 wt.% GPTMS<br />

(e) 4 wt.% MA-g-HDPE<br />

Figure 4. SEM micrographs (x500) <str<strong>on</strong>g>of</str<strong>on</strong>g> r-HDPE/CaCO 3<br />

composites when CaCO 3 treated with different<br />

coupling agents

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