Hostname: page-component-7bb8b95d7b-495rp Total loading time: 0 Render date: 2024-09-10T21:23:17.638Z Has data issue: false hasContentIssue false

Up Close: Institute C. Sadron Takes a Comprehensive Approach to Polymer Blends

Published online by Cambridge University Press:  29 November 2013

Get access

Extract

If one defines a polymeric material as a piece of matter designed for a given and usable property, this property is not related simply to the chemical formula of the polymer. The chemical and stereochemical defects occurring during synthesis, structural organization, and processing must all be characterized, understood, and controlled.

Institute C. Sadron (ICS), established in 1954 by the French National Research organization (CNRS) as the Centre de Recherches sur les Macromolécules under the inspiration and direction of Prof. Ch. Sadron, has progressively shifted from polymer synthesis and characterization toward the understanding of the structure-property relationship in the sense just described. This has involved the creation of an engineering school staffed with equipment and research teams in rheology, processing, and mechanical properties. More than 60 permanent scientists and university professors work in the Institute; about 20 theses are submitted each year. ICS now covers a broad range of competencies, from synthesis to processing through most techniques of characterization and theoretical modeling at the molecular and macroscopic levels. This opens the way to a comprehensive research effort, which is illustrated here for polymer blends.

Type
Features
Copyright
Copyright © Materials Research Society 1994

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

1.Galin, M., 18th Europhysics Conference on Macromolecular Physics, Abstracts 11c (1987) p. 26.Google Scholar
2.Palierne, J.E and Lequeux, F., J. Non-Newtonian Fluid Mechanics 40 (1991) p. 289.CrossRefGoogle Scholar
3.Delaby, I., Ernst, B., Germain, Y., and Muller, R., J. Rheol., in press.Google Scholar
4.Nair, C.P. Reghunadhan and Clouet, G., JMS Rev. Macromol. Chem. Phys. C31 (1991) p. 311.CrossRefGoogle Scholar
5.Marie, P. and Rouault, Y., “Interfacial Tension between Immiscible Molten Polymers. Time, Temperature and Molecular Weight Dependence,” Macromolecules, in press.Google Scholar
6.Jin, S.R., Widmaier, J.M., and Meyer, G.C., Polym. 29 (1988) p. 346.CrossRefGoogle Scholar
7.Weill, G., JMS Rev. Macromol. Chem. Phys. A 27 (1990) p. 1769.Google Scholar
8.Graebling, D., Froelich, D., and Muller, R., J. Rheol. 33 (1989) p. 1283.CrossRefGoogle Scholar
9.Palierne, J.F., Rheologica Acta 29 (1990) p. 204.CrossRefGoogle Scholar
10.Lambla, M. and Seadan, M., Polym. Eng. Sci. 32 (22) (1992) p. 1687.CrossRefGoogle Scholar
11.Perez, J., Physique et Mécanique des Polyméres Amorphes, (Lavoisier, Paris, 1992).Google Scholar
12.Mauzac, O. and Schirrer, R., J. Mater. Sci. 25 (1990) p. 5125.CrossRefGoogle Scholar
13.Wittmann, J.C. and Lotz, B., Prog. Polym. Sci. 15 (1990) p. 909.CrossRefGoogle Scholar
14.Thierry, A., Fillon, B., Strauṕ, C., Lotz, B., and Wittmann, J.C., Prog. Colloid Polym. Sci. 87 (1992) p. 28.CrossRefGoogle Scholar