Hostname: page-component-78c5997874-j824f Total loading time: 0 Render date: 2024-11-02T23:56:45.297Z Has data issue: false hasContentIssue false

Neutron-Scattering Measurements of “Soft Matter”

Published online by Cambridge University Press:  29 November 2013

Get access

Extract

Neutron scattering had its origin in 1932, the year that marked the discovery of the neutron by Chadwick, and the first nuclear reactors were successfully operated in Chicago and Oak Ridge, Tenn., in the early 1940s. During its initial stages, neutron scattering was used mainly for the study of “hard” crystalline materials. For example, Shull and Wollan's pioneering research, which led to the 1994 Nobel Prize in physics, began with studies of iron, chromium, and iridium, and was followed by the development of polarization analysis to determine the structure of magnetic materials. Such studies continue to yield important structural information (see the articles on magnetism by Aeppli and Hayden and on crystallography by Radaelli and Jorgensen in this issue of MRS Bulletin), although during the last two decades, the technique has been increasingly used by scientists from other disciplines (chemistry, biology, polymer science), and many of these newer applications have involved “soft” matter such as polymers, colloids, and gels. By definition, these substances are “plastic” or “squishy,” and easy to mold into different shapes; because of this flexibility, they have become some of the most practical and widely used materials today.

Type
Neutron Scattering in Materials Research
Copyright
Copyright © Materials Research Society 1999

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.Kirste, R.G., Kruse, W.A., and Schelten, J., Kolloid Z.Z. Polym. 251 (1973) p. 919 and Polymer 16 (1975) p. 120.Google Scholar
2.Wignall, G.D., Ballard, D.G.H., and Schelten, J., Eur. Polym. J. 10 (1974) p. 861 and Eur. Polym. J. 9 (1973) p. 965.CrossRefGoogle Scholar
3.Benoit, H., Cotton, J.P., Decker, D., Farnoux, B., Higgins, J.S., Jannink, G., Ober, R., and Picot, C., Nature 245 (1973) p. 23.Google Scholar
4.Lieser, G., Fischer, E.W., and Ibel, K., J. Polym. Sci. 13 (1975) p. 29.Google Scholar
5.de Gennes, P.G., Scaling Concepts in Polymer Physies, Chap. 4 (Cornell University Press, Ithaca, NY, 1979) p. 96.Google Scholar
6.Lohse, D. J., Polym. News 12 (1986) p. 8.Google Scholar
7.Sinha, S.K., Lohse, D.J., and Lin, M.Y., Physica B 213–214 (1995) p. 1.CrossRefGoogle Scholar
8.Alamo, R.G., Graessley, W.W., Krishnamoorti, R., Lohse, D.J., Londono, J.D., Mandelkern, L., Stehling, F.C., and Wignall, G.D., Macromolecules 30 (1997) p. 561.CrossRefGoogle Scholar
9.Bates, F.S. and Frederickson, G.H., Macromolecules 27 (1994) p. 1065.CrossRefGoogle Scholar
10.Weimann, P.A., Jones, T.D., Hillmyer, M.A., Bates, F.S., Londono, J.D., Melnichenko, Y., Wignall, G.D., and Almdal, K., Macromolecules 30 (1997) p. 3650.CrossRefGoogle Scholar
11.Melnichenko, Y.B., Wignall, G.D., Van Hook, W.A., Szydlowski, J., Rebello, L.P., and Wilczura, H., Macromolecules 31 (1998) p. 8436.CrossRefGoogle Scholar
12.Melnichenko, Y.B., Kiran, E., Wignall, G.D., Heath, K.D., Salaniwal, S., Cochran, H.D., and Stamm, M., Macromolecules 16 (1999) p. 5344.CrossRefGoogle Scholar
13.Kiran, E. and Sen, Y.L., in Supercritical Fluid and Engineering Science (ACS Symposium Series 514), Chap. 9, edited by Kiran, E. and Brennecke, J.F. (American Chemical Society, Washington, DC, 1993).Google Scholar
14.DeSimone, J.M., Guan, Z., and Eisbernd, C.S., Science 257 (1992) p. 945.CrossRefGoogle Scholar
15.McClain, J.B., Londono, J.D., Chillura-Martino, D., Triolo, R., Betts, D.E., Canelas, D.A., Cochran, H.D., Samulski, E.T., DeSimone, J.M., and Wignall, G.D., Science 274 (1996) p. 2049.CrossRefGoogle Scholar
16.Londono, J.D., Dharmapurikar, R., Cochran, H.D., Wignall, G.D., McClain, J.B., Combes, J.R., Betts, D.E., Canelas, D.A., DeSimone, J.M., Samulski, E.T., Chillura-Martino, D., and Triolo, R., J. Appl. Crystallogr. 30 (1997) p. 690.CrossRefGoogle Scholar
17.Wignall, G.D., J. Condens. Matter 11 (1999) p. R157.CrossRefGoogle Scholar
18.McCoy, M., Chem. Eng. News (April 26, 1999) p. 10.Google Scholar
19.Wignall, G.D., in The Physical Properties of Polymers, Chap. 7, edited by Mark, J.E. (American Chemical Society, Washington, DC, 1993) p. 313.Google Scholar
20.Lindner, P. and Zemb, T., eds., Neutron, X-Ray and Light Scattering; North-Holland Delta Series (Elsevier Publishers, New York, 1991).Google Scholar
21.Rieger, J., Hädicke, E., Ley, G., and Lindner, P., Phys. Rev. Lett. 68 (1) (1992) p. 2782.CrossRefGoogle Scholar
22.Zipfel, J., Lindner, P., Tsianou, M., Alexandridis, P., and Richtering, W., Langmuir 15 (8) (1999) p. 2599.CrossRefGoogle Scholar
23.Zipfel, J., Berghausen, J., Schmidt, G., Lindner, P., Alexandridis, P., Tsianou, M., and Richtering, W., Phys. Chem. Chem. Phys. 1 (1999) p. 3905.CrossRefGoogle Scholar