Neutron-mapping polymer flow: Scattering, flow visualization, and molecular theory

被引:151
作者
Bent, J
Hutchings, LR
Richards, RW
Gough, T
Spares, R
Coates, PD
Grillo, I
Harlen, OG
Read, DJ
Graham, RS
Likhtman, AE
Groves, DJ
Nicholson, TM
McLeish, TCB [1 ]
机构
[1] Univ Leeds, Dept Phys & Astron, Leeds LS2 9JT, W Yorkshire, England
[2] Univ Queensland, Div Chem Engn, St Lucia, Qld 4072, Australia
[3] Univ Leeds, Dept Appl Math, Leeds LS2 9JT, W Yorkshire, England
[4] Univ Durham, Dept Chem, Durham DH1 3HP, England
[5] Univ Bradford, Dept Mech Engn, Bradford BD7 1DP, W Yorkshire, England
[6] Inst Max Von Laue Paul Langevin, F-38042 Grenoble 9, France
关键词
D O I
10.1126/science.1086952
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Flows of complex fluids need to be understood at both macroscopic and molecular scales, because it is the macroscopic response that controls the fluid behavior, but the molecular scale that ultimately gives rise to rheological and solid-state properties. Here the flow field of an entangled polymer melt through an extended contraction, typical of many polymer processes, is imaged optically and by small-angle neutron scattering. The dual-probe technique samples both the macroscopic stress field in the flow and the microscopic configuration of the polymer molecules at selected points. The results are compared with a recent "tube model" molecular theory of entangled melt flow that is able to calculate both the stress and the single-chain structure factor from first principles. The combined action of the three fundamental entangled processes of reptation, contour length fluctuation, and convective constraint release is essential to account quantitatively for the rich rheological behavior. The multiscale approach unearths a new feature: Orientation at the length scale of the entire chain decays considerably more slowly than at the smaller entanglement length.
引用
收藏
页码:1691 / 1695
页数:5
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