Effect of nanoparticles on the morphology and properties of PET/PP in situ microfibrillar reinforced composites
Source abstract
Abstract
In this work, the effect of SiO2 nanoparticles on the morphology and properties of PET/PP in situ microfibrillar reinforced composites (MFC) obtained from slit die extrusion and hot stretching‐quenching was investigated. The scanning electron micrographs revealed that the nanoparticles could have different effects on microfibril formation of PET/PP MFC depending on their concentration. Addition of appropriate content of nanoparticles (e.g., 1.6 and 8 wt%) facilitated the PET droplet‐fibril transition during stretching due to the presence of nanosilica in the PP matrix, which increased the viscosity of PP matrix and then improved the droplet deformability. However, at higher loading (e.g., 12 wt%), the aggregation of silica nanoparticles around the PET droplets prevented disperse phase coalescence during drawing and then reduced the fibrillation ability of PET minor phase. The dynamic rheological test performed at 190°C showed that the increased spatial restriction of the nanoparticles improved the viscoelastic moduli and complex viscosity of PET/PP MFC. DSC results indicated that nanosilica had little heterogeneous nucleation effect on the PP matrix of PET/PP MFC. Additionally, nanoparticles could present drastic improvement in the degradation behavior of PET/PP MFC under thermo‐oxidative conditions and increased the modulus of PET/PP MFC. POLYM. COMPOS., 38:2718–2726, 2017. © 2015 Society of Plastics Engineers
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Research context
OpenAlex topics: Polymer crystallization and properties · Polymer Nanocomposites and Properties · Composite Material Mechanics
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
College of Polymer Science and Engineering, The State Key Laboratory for Polymer Materials Engineering Sichuan University Chengdu 610065 People's Republic of China
Funding
State Key Laboratory of Polymer Materials Engineering · The National Science of China · Sichuan Youth Science and Technology Foundation
References (29)
Show source-provided references
1. Filipe S. · Polymer · 2004 · 2367 · 45
2. Li J. · Polymer · 2001 · 5047 · 42
3. Farasoglou P. · Polym. Compos. · 2000 · 84 · 21
4. Silverstein M.S. · J. Appl. Polym. Sci. · 1991 · 157 · 43
5. Li Z.M. · Macromol. Mater. Eng. · 2004 · 349 · 289
6. Li Z.M. · Mater. Lett. · 2002 · 756 · 56
7. Friedrich K. · Compos. Sci. Technol. · 2005 · 107 · 65
8. Wang K. · Prog. Polym. Sci. · 2014 · 891 · 39
9. Li W.J. · Macromol. Mater. Eng. · 2009 · 582 · 294
10. Jayanarayanan K. · Eur. Polym. J. · 2009 · 1738 · 45
11. Yi X. · Eur. Polym. J. · 2010 · 719 · 46
12. Li W. · Polym. Bull. · 2010 · 483 · 64
13. Ma H. · J. Polym. Res. · 2011 · 1941 · 18
14. Qian J. · J. Polym. Res. · 2011 · 409 · 18
15. Okamoto R.S.S.M. · Prog. Polym. Sci. · 2003 · 1539 · 28
16. Naffakh M. · Prog. Polym. Sci. · 2013 · 1163 · 38
17. Elias L. · Polymer · 2007 · 6029 · 48
18. Xi S. · Indus. Eng. Chem. Res. · 2014 · 5916 · 53
19. Ray S.S. · Polymer · 2004 · 8403 · 45
20. Lee M.W. · Compos. Sci. Technol. · 2003 · 339 · 63
21. Chen J. · Polymer · 2007 · 4242 · 48
22. Li W. · J. Appl. Polym. Sci. · 2009 · 1471 · 113
23. Xu X.B. · Macromol. Mater. Eng. · 2004 · 568 · 289
24. Fenouillot F. · Polymer · 2009 · 1333 · 50
25. Owens D.K. · J. Appl. Polym. Sci. · 1969 · 1741 · 13
26. Xiu H. · Polymer · 2014 · 1593 · 55
27. Gollón I.M. · J. Anal. Appl. Pyrol. · 2001 · 635 · 58
28. Palza H. · Macromol. Mater. Eng. · 2010 · 899 · 295
29. Pavlidou S. · Prog. Polym. Sci. · 2008 · 1119 · 33