Publication: SANS/WANS time-resolving neutron scattering studiesof polymer phase transitions using NIMROD
Issued Date
2013-01-01
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ISSN
02729172
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2-s2.0-84900300648
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Mahidol University
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SCOPUS
Bibliographic Citation
Materials Research Society Symposium Proceedings. Vol.1528, (2013), 83-88
Suggested Citation
Geoffrey Robert Mitchell, Daniel Bowron, Artur Mateus, Paulo Bartolo, Thomas Gkourmpis, Khamphee Phomphrai, Daniel Lopez, Fred Davis SANS/WANS time-resolving neutron scattering studiesof polymer phase transitions using NIMROD. Materials Research Society Symposium Proceedings. Vol.1528, (2013), 83-88. doi:10.1557/opl.2013.363 Retrieved from: https://repository.li.mahidol.ac.th/handle/20.500.14594/31784
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Title
SANS/WANS time-resolving neutron scattering studiesof polymer phase transitions using NIMROD
Abstract
We use new neutron scattering instrumentation to follow in a single quantitative time-resolving experiment, the three key scales of structural development which accompany the crystallisation of synthetic polymers. These length scales span 3 orders of magnitude of the scattering vector. The study of polymer crystallisation dates back to the pioneering experiments of Keller and others who discovered the chain-folded nature of the thin lamellae crystals which are normally found in synthetic polymers. The inherent connectivity of polymers makes their crystallisation a multiscale transformation. Much understanding has developed over the intervening fifty years but the process has remained something of a mystery. There are three key length scales. The chain folded lamellar thickness is ∼ 10nm, the crystal unit cell is ∼ 1nm and the detail of the chain conformation is ∼ 0.1nm. In previous work these length scales have been addressed using different instrumention or were coupled using compromised geometries. More recently researchers have attempted to exploit coupled time-resolved small-angle and wide-angle x-ray experiments. These turned out to be challenging experiments much related to the challenge of placing the scattering intensity on an absolute scale. However, they did stimulate the possibility of new phenomena in the very early stages of crystallisation. Although there is now considerable doubt on such experiments, they drew attention to the basic question as to the process of crystallisation in long chain molecules. We have used NIMROD on the second target station at ISIS to follow all three length scales in a time-resolving manner for poly(e-caprolactone). The technique can provide a single set of data from 0.01 to 100Å-1 on the same vertical scale. We present the results using a multiple scale model of the crystallisation process in polymers to analyse the results. © 2013 Materials Research Society.