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Characterization of Monodisperse Aqueous Latex Dispersions Prepared with N-Isopropylacrylamide

Published online by Cambridge University Press:  15 February 2011

D. Kiminta
Affiliation:
Imperial College of Sci., Tech. & Medicine, Chem. Eng. Dept., Prince Consort Road, London SW7 2BY
B. Costello
Affiliation:
Imperial College of Sci., Tech. & Medicine, Chem. Eng. Dept., Prince Consort Road, London SW7 2BY
S. Lenon*
Affiliation:
ICI Paints Division, Wexham Road, Slough, Bucks (UK)
P.F. Luckham
Affiliation:
Imperial College of Sci., Tech. & Medicine, Chem. Eng. Dept., Prince Consort Road, London SW7 2BY
*
To whom all correspondence should be addressed.
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Abstract

Poly-N-isopropylacrylamide (poly-NIPAM) is a water soluble nonionic polymer that exhibits a lower consolute solution temperature (LCST) of about 31°C. This paper describes the preparation and characterization of a monodisperse, hydrophilic polymer latex of poly-NIPAM, crosslinked by N,N'-methylenebisacrylamide. The presence of these crosslinking moieties will prevent dissolution of the particles at low temperatures; rather the particles will be swollen with solvent such that a microgel is formed. The swelling and rheological behaviour of the latex has been studied. The results show that at high temperatures the particles are ˜ 30 nm whilst at 25°C, the particles were ˜ 130 nm in diameter. This four fold increase in the particle diameter correspond to a ˜ sixty fold increase in volume. The rheological properties, both continuous and oscillatory shear, of these systems have also been studied and is strongly temperature dependant, reflecting the changes in phase volume of the NIPAM latex.

Type
Research Article
Copyright
Copyright © Materials Research Society 1993

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References

1. Kreiger, I. M., Adv. Colloid Interface Sci., 3, 111, (1972).Google Scholar
2. Buscall, R., Goodwin, J. W., Hawkins, J. W., and Ottewill, R. H., J. Chem Soc Faraday Trans. I, 78, 2887, (1982).Google Scholar
3. Strivens, T. A., Colloid Polymer Sci., 265, 553 (1987).Google Scholar
4. Frith, W. J., Strivens, T. A. and Mewis, J., J. Colloid Interface Sci. 139, 55, (1990).Google Scholar
5. Russel, W. B., W. B., Powder Technology, 51, 15, (1987).Google Scholar
6. Prestidge, C. and Tadros, Th. F., J. Colloid Interface Sci., 124, 660, (1988)Google Scholar
7. Kim, I. T. and Luckham, P. F., J. Colloid Interface Sci., 144, 174, (1991)Google Scholar
8. Ansarifar, M. A. and Luckham, P. F., Colloid and Polm Sci., 267, (1989)Google Scholar
9. Tadros, Th. F., Langmuir, 6, 28, (1990).Google Scholar
10. Liang, W., Tadros, Th. F. and Luckham, P. F., J. Colloid Interface Sci., 153, 131, (1992).Google Scholar
11. Pelton, R. H. and Chibante, P., Colloids and Surfaces, 20, 247, (1986).Google Scholar
12. Kawaguchi, H., Fujimoto, K. and Muzuhara, Y., Colloid & Polym. Sci., 270, 53, (1992)Google Scholar
13. Snowden, M. J., J. Chem Soc, Chem Com., (12), 803, (1992).Google Scholar
14. Snowden, M. J. and Vincent, B., J. Chem. Soc. Chem. Com., (16), 1103 (1992).Google Scholar
15. Heskins, M. and Guillet, J. E., J. Macromol. Sci.-Chem., A2, 1441, (1968).Google Scholar