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Nondestructive testing of defects in adhesive joints

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<strong>of</strong> 125±2 ºC. Desalt<strong>in</strong>g performance <strong>of</strong> such membranes was studied <strong>in</strong> cont<strong>in</strong>uous mode for a period <strong>of</strong><br />

24 hours. It is observed (Figure 5) that membranes cured for all selected cure time except the lowest one<br />

(10 m<strong>in</strong>utes) show almost constant flux and rejection with time. It is seen from Figure 5B that the<br />

rejection for membranes cured for 30 and 40 m<strong>in</strong>utes are almost the same, whereas there is an average<br />

15% rejection enhancement by vary<strong>in</strong>g the cure time from 20 to 30 m<strong>in</strong>utes without much sacrifice <strong>in</strong> the<br />

flux. Hence 30 m<strong>in</strong>utes cure time was selected as optimum.<br />

Molecular weight cut <strong>of</strong>f: The separation pr<strong>of</strong>ile <strong>of</strong> different organic compounds (vary<strong>in</strong>g molecular<br />

weight from 90 to 600 gm/mole) with the variation <strong>of</strong> curative dose and cure time for different PVA TFC<br />

membranes are shown <strong>in</strong> Figure 6. It is seen that more the cross-l<strong>in</strong>k density <strong>of</strong> the barrier layer (due to<br />

higher cross-l<strong>in</strong>ker dose) higher the rejection <strong>of</strong> any selected organic compound. The lowest selected<br />

cross-l<strong>in</strong>ker dose <strong>of</strong> 2% produces membrane with no specific molecular weight cut <strong>of</strong>f <strong>in</strong> the selected<br />

range i.e. 90-600 Dalton. The higher range <strong>of</strong> cross-l<strong>in</strong>ker doses i.e. 20-50% MA, produce membranes<br />

with MWCO <strong>in</strong> the range <strong>of</strong> 200-300 Dalton. For membranes with MA dose <strong>of</strong> 10%, MWCO values are<br />

between 350-450 Dalton.<br />

Membranes performance with different <strong>in</strong>organic salt solution: The desalt<strong>in</strong>g performances <strong>of</strong> the<br />

membranes were tested with different electrolyte solutions. The performances <strong>of</strong> the membranes (flux and<br />

rejection) vary<strong>in</strong>g <strong>in</strong> their curative dose are presented graphically <strong>in</strong> Figure 7. The % rejections <strong>of</strong><br />

sulphate salts (MgSO4 and Na2SO4) are almost same for all the selected membranes irrespective <strong>of</strong> their<br />

curative dose. The rejection <strong>of</strong> the chloride salts are much lesser than the sulfate salts, which may be due<br />

to higher repulsion <strong>of</strong> sulfate than chloride by the charged surface <strong>of</strong> the membranes. Although the<br />

variation <strong>of</strong> curative dose (2-50%) has negligible effect on the % rejection <strong>of</strong> sulphate salts but there is a<br />

gradual <strong>in</strong>crease <strong>in</strong> rejection <strong>of</strong> chloride salts with <strong>in</strong>crease <strong>in</strong> MA concentration which may be due to a<br />

synchronization <strong>of</strong> charge enhancement and membranes tighten<strong>in</strong>g.<br />

Conclusions:<br />

The overall trend <strong>of</strong> rejection by such membranes is > > R<br />

2 4 SO Na R RMgSO NaCl > R ≅ (R =<br />

4<br />

MgCl R<br />

2 CaCl2<br />

Rejection). The average MWCO <strong>of</strong> the membranes varies between 350-450 Dalton. As for such<br />

membranes 65% difference is observed between the rejection <strong>of</strong> MgSO4<br />

(R 70-90%) and NaCl (R15-<br />

35%), hence, they may be useful for the removal <strong>of</strong> dissolved sulphate hardness and partial desal<strong>in</strong>ation<br />

<strong>of</strong> brackish water.<br />

Acknowledgement: F<strong>in</strong>ancial assistance from CSIR, India is highly acknowledged.<br />

References:<br />

[1] Amjad Z. Ed.; Reverse Osmosis: Membrane Technology, Water Chemistry, and Industrial<br />

Applications, Van Nostrand Re<strong>in</strong>hold: New York, 1993.<br />

[2] Ahn KH, Cha HY, Yeom IT, Song KG. Desal<strong>in</strong>ation 1998; 119(1-3):169-176.<br />

[3] Ikeda K, Kimura S, Ueyama K. Maku 1998; 23:266-272.<br />

[4] Krumova M, Lopez D, Benavente R, Mijangos C, Perena JM. Polymer 2000; 41(26):9265-9272.<br />

[5] Suzuki M, Yoshida T, Koyama T, Kobayashi S, Kimura M, Hanabusa K, Shirai H. Polymer 2000;<br />

41(12):4531-4536.<br />

[6] Radovanovic P, Thiel SW, Hwang ST. Journal <strong>of</strong> Membrane Science 1992; 65(3):213-229.<br />

[7] Kest<strong>in</strong>g RE. A structure perspective' <strong>in</strong>: Synthetic Polymeric membranes, 2 nd . ed. Wiley, 1985.<br />

Biomaterial membrane<br />

3

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