Universal Scaling of Polymer Diffusion in Nanocomposites

被引:75
作者
Choi, Jihoon [1 ]
Hore, Michael J. A. [1 ]
Meth, Jeffrey S. [2 ]
Clarke, Nigel [3 ]
Winey, Karen I. [1 ]
Composto, Russell J. [1 ]
机构
[1] Univ Penn, Dept Mat Sci & Engn, Philadelphia, PA 19104 USA
[2] EI DuPont de Nemours & Co Inc, Cent Res & Dev, DuPont Nanocomposite Technol, Wilmington, DE USA
[3] Univ Sheffield, Dept Phys & Astron, Sheffield S3 7RH, S Yorkshire, England
基金
美国国家科学基金会; 英国工程与自然科学研究理事会;
关键词
MOLECULAR-DYNAMICS; NANOPARTICLES; PARTICLE; SURFACES; TEMPERATURE; TRANSITION; ELASTOMERS; COPOLYMERS; INTERFACES; SCATTERING;
D O I
10.1021/mz400064w
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 [高分子化学与物理];
摘要
Nanoparticles are new and valuable additives that can favorably tune thermomechanical, electric, optical, and magnetic properties of polymeric materials. The addition of nanoparticles can also enhance or slow down polymer dynamics depending on the mixture thermodynamics and key length scales, namely, nanoparticle size, interparticle spacing (ID), and the polymer radius of gyration (R-g). Presently, a framework for understanding how nanoparticles affect polymer dynamics is not available, in part, because of a lack of wide-ranging experimental studies. Here, tracer diffusion is studied in model nanocomposites containing silica nanoparticles grafted with either polymer brushes (soft nanoparticles) or short ligands (hard nanoparticles). Over a wide range of tracer molecular weights and nanoparticle loadings, the normalized diffusion coefficient collapses onto a universal curve for both soft and hard nanoparticles when plotted against a confinement parameter, defined as ID/R-g, which accounts for tracer penetration into the brush. These experimental results provide new insights into the fundamental principles required to construct predictive models of polymer dynamics in nanocomposites.
引用
收藏
页码:485 / 490
页数:6
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