journal article·2015-07-15

Reversible Thermal Stiffening in Polymer Nanocomposites

Erkan Senses, Andrew Isherwood, Pinar Akcora

Publisher page

Abstract

Miscible polymer blends with different glass transition temperatures (Tg) are known to create confined interphases between glassy and mobile chains. Here, we show that nanoparticles adsorbed with a high-Tg polymer, poly(methyl methacrylate), and dispersed in a low-Tg matrix polymer, poly(ethylene oxide), exhibit a liquid-to-solid transition at temperatures above Tg's of both polymers. The mechanical adaptivity of nanocomposites to temperature underlies the existence of dynamically asymmetric bound layers on nanoparticles and more importantly reveals their impact on macroscopic mechanical response of composites. The unusual reversible stiffening behavior sets these materials apart from conventional polymer composites that soften upon heating. The presented stiffening mechanism in polymer nanocomposites can be used in applications for flexible electronics or mechanically induced actuators responding to environmental changes like temperature or magnetic fields.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Tribology and Wear Analysis · Advanced Theoretical and Applied Studies in Material Sciences and Geometry · Material Properties and Applications

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Chemical Engineering and Materials Science, Stevens Institute of Technology, Hoboken, New Jersey 07030, United States

Funding

Division of Materials Research · Stevens Institute of Technology

References (36)

Show source-provided references
1. 10.1002/adma.20030556010.1002/adma.200305560 ↗
2. 10.1021/nn204938j10.1021/nn204938j ↗
3. 10.1021/mz400596g10.1021/mz400596g ↗
4. 10.1039/c4tb00067f10.1039/c4tb00067f ↗
5. 10.1038/nchem.131410.1038/nchem.1314 ↗
6. 10.1021/ja903080c10.1021/ja903080c ↗
7. 10.1021/ma021067510.1021/ma0210675 ↗
8. 10.1021/ma802767210.1021/ma8027672 ↗
9. 10.1021/bm400694r10.1021/bm400694r ↗
10. 10.1021/nn103104g10.1021/nn103104g ↗
11. 10.1038/nchem.172010.1038/nchem.1720 ↗
12. 10.1038/ncomms277210.1038/ncomms2772 ↗
13. 10.1002/1527-2648(200108)3:8<571::AID-ADEM571>3.0.CO;2-M10.1002/1527-2648(200108)3:8<571::AID-ADEM571>3.0.CO;2-M ↗
14. 10.1021/ma101332s10.1021/ma101332s ↗
15. 10.1021/ma101240j10.1021/ma101240j ↗
16. 10.1103/PhysRevLett.110.10830310.1103/PhysRevLett.110.108303 ↗
17. 10.1039/C4RA07157C10.1039/C4RA07157C ↗
18. 10.1021/j100439a01110.1021/j100439a011 ↗
19. 10.1021/ma302275f10.1021/ma302275f ↗
20. 10.1063/1.193165610.1063/1.1931656 ↗
21. 10.1021/ma070539i10.1021/ma070539i ↗
22. 10.1021/ma052642i10.1021/ma052642i ↗
23. 10.1021/ma021634o10.1021/ma021634o ↗
24. 10.1103/PhysRevLett.98.16830110.1103/PhysRevLett.98.168301 ↗
25. 10.1021/ma035774p10.1021/ma035774p ↗
26. 10.1063/1.47990810.1063/1.479908 ↗
27. 10.1021/ma992170610.1021/ma9921706 ↗
28. 10.1021/ma201912310.1021/ma2019123 ↗
29. 10.1016/0032-3861(94)90134-110.1016/0032-3861(94)90134-1 ↗
30. 10.1002/app.1986.07032061810.1002/app.1986.070320618 ↗
31. Fetters L. · 2007 · 44710.1007/978-0-387-69002-5_25 ↗
32. 10.1039/c2sm06885k10.1039/c2sm06885k ↗
33. 10.1021/ma902072d10.1021/ma902072d ↗
34. 10.1021/ma201200m10.1021/ma201200m ↗
35. 10.1021/acsmacrolett.5b0000210.1021/acsmacrolett.5b00002 ↗
36. 10.1016/S0266-3538(03)00032-010.1016/S0266-3538(03)00032-0 ↗