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Nondestructive testing of defects in adhesive joints

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This is further evidenced from the impedance plots (Bode) <strong>in</strong>dicated <strong>in</strong> Figures 5 recorded after<br />

40 hrs exposure to hot sal<strong>in</strong>e conditions. It can be seen from these figures that PANI-TiO2-4.18%<br />

has higher resistance than the coat<strong>in</strong>gs without TiO2 especially at low frequency which is<br />

associated with ionic transport through the film. This cont<strong>in</strong>ues to rema<strong>in</strong> high even after<br />

exposure to the corrosive environment. The accelerated <strong>test<strong>in</strong>g</strong> conditions used <strong>in</strong> the present case<br />

are equivalent to <strong>test<strong>in</strong>g</strong> for more than 800 hrs at room temperature which is derived us<strong>in</strong>g the<br />

reported logarithmic relations for corrosion rate <strong>of</strong> steel with temperature which gives about 10X<br />

as acceleration constant [21,22 ]. Thus, there is excellent corrosion protection obta<strong>in</strong>ed <strong>in</strong> these<br />

coat<strong>in</strong>gs especially when PANI-TiO2 (4.18%) powder is used as an additive even at low level <strong>of</strong><br />

load<strong>in</strong>g (10wt %).<br />

Log IZI (Ohm)<br />

1.00E+06<br />

1.00E+05<br />

1.00E+04<br />

1.00E+03<br />

1.00E+<br />

00<br />

1.00E+<br />

01<br />

1.00E+<br />

02<br />

1.00E+<br />

03<br />

Frequency (Hz)<br />

1.00E+<br />

04<br />

1.00E+<br />

05<br />

2.3% TiO2<br />

2.8% TiO2<br />

4.18% TiO2<br />

0% TiO2<br />

Figure: 5.Bode plots <strong>of</strong> PVB/PANI-NanoTiO2 coat<strong>in</strong>gs after 40 hr immersion at 65 0 C sal<strong>in</strong>e<br />

solution<br />

The low frequency data <strong>in</strong> Bode plots has been associated with the diffusion processes and as<br />

mentioned above it <strong>in</strong>dicates to some extent that nano-TiO2 leads to such improvement. However,<br />

there is also an additional cause for further improvement <strong>of</strong> corrosion resistance especially when<br />

one considers that the total concentration <strong>of</strong> the additive <strong>in</strong> the formulation was same (10%) <strong>in</strong> all<br />

cases.<br />

4. Conclusions:<br />

The conduct<strong>in</strong>g PANI nano-particulate TiO2 hybrid composites prepared by <strong>in</strong> situ<br />

polymerization were used for coat<strong>in</strong>g with PVB as the matrix. The effect <strong>of</strong> addition <strong>of</strong> nano<br />

TiO2 on the improvement <strong>of</strong> has been clearly brought out The novelty <strong>of</strong> these coat<strong>in</strong>gs lies <strong>in</strong><br />

generation <strong>of</strong> corrosion <strong>in</strong>hibition by three mechanisms operat<strong>in</strong>g simultaneously viz.<br />

improvement <strong>of</strong> barrier properties, redox behaviour <strong>of</strong> PANI and formation <strong>of</strong> p-n junctions<br />

prevent<strong>in</strong>g easy charge transport when coat<strong>in</strong>g is threatened to be destroyed due to scratch or<br />

scribble. Even if the ma<strong>in</strong> res<strong>in</strong> is damaged, the additives give a heal<strong>in</strong>g effect and prevent<br />

catastrophic failure. Apart from the prevention <strong>of</strong> corrosion, these coat<strong>in</strong>gs have good gloss and<br />

sh<strong>in</strong>y surface, which is not easily obta<strong>in</strong>ed <strong>in</strong> conventional coat<strong>in</strong>g, prepared with commercial<br />

micron size particle additives. Such systems can be used as a primer coat or even as a s<strong>in</strong>gle<br />

coat<strong>in</strong>g on steel where colour is not a very important criterion.

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