Mechanical performance of Nano‐Al2O3‐modified composites at cryogenic and room temperatures
Source abstract
Abstract
Mechanical properties of fiber‐reinforced plastic composites at room temperature can be enhanced by adding nanoparticles. However, the damage mechanisms of nanocomposites at low temperatures are still not understood. In this article, different contents of nano‐Al2O3 particles were added on fiber surface by solid–liquid separation method, and vacuum‐assisted resin injection was adopted to manufacture composites laminates. A comparative study on the mechanical behavior of nano‐Al2O3‐filled composite at room and low temperatures was presented. Effect of nano‐Al2O3 particle contents (0, 0.5, 1, and 2 wt%) on the mechanical properties of glass fiber‐reinforced vinyl ester resin (GF/vinyl ester) composite laminates at different temperatures was investigated. The damage mechanism of these composite laminates in various environments was studied. The results showed that to a certain extent, nanoparticles could improve the mechanical properties of composites at 25 and −60°C. With assistance of scanning electron microscope (SEM) observation, the damage mechanisms of the composite laminates in various temperature conditions were further analyzed. POLYM. COMPOS., 39:3006–3012, 2018. © 2017 Society of Plastics Engineers
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Natural Fiber Reinforced Composites · Mechanical Behavior of Composites · Polymer Nanocomposites and Properties
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Smart Structures and Advanced Composites Laboratory, College of Aerospace and Civil Engineering Harbin Engineering University Harbin 150001 China
Key Laboratory of Superlight Materials and Surface Technology, Ministry of Education College of Materials Science and Chemical Engineering Harbin Engineering University Harbin 150001 China
Funding
National Natural Science Foundation of China
References (32)
Show source-provided references
1. 10.1023/A:100468670863910.1023/A:1004686708639 ↗
2. 10.1002/app.2788210.1002/app.27882 ↗
3. 10.1016/j.polymer.2010.08.03810.1016/j.polymer.2010.08.038 ↗
4. 10.1007/BF0111429410.1007/BF01114294 ↗
5. 10.1016/S0266-3538(00)00169-X10.1016/S0266-3538(00)00169-X ↗
6. 10.1016/0032-3861(96)00295-910.1016/0032-3861(96)00295-9 ↗
7. 10.1016/j.carbon.2009.06.03910.1016/j.carbon.2009.06.039 ↗
8. 10.1016/j.carbon.2011.06.04710.1016/j.carbon.2011.06.047 ↗
9. 10.1016/j.polymer.2012.02.05210.1016/j.polymer.2012.02.052 ↗
10. 10.1016/j.carbon.2012.10.00410.1016/j.carbon.2012.10.004 ↗
11. 10.1016/j.compscitech.2012.05.02510.1016/j.compscitech.2012.05.025 ↗
12. 10.1016/j.compstruct.2012.12.01810.1016/j.compstruct.2012.12.018 ↗
13. 10.1177/002199831038908810.1177/0021998310389088 ↗
14. 10.1016/j.matdes.2014.07.01710.1016/j.matdes.2014.07.017 ↗
15. 10.1016/j.compscitech.2006.08.02610.1016/j.compscitech.2006.08.026 ↗
16. 10.2320/matertrans.MBW20081710.2320/matertrans.MBW200817 ↗
17. Brown H.R. · Compos. Mater. · 2013 · 002199831348526
18. 10.1016/S0266-3538(02)00063-510.1016/S0266-3538(02)00063-5 ↗
19. 10.1016/j.compstruct.2008.03.00510.1016/j.compstruct.2008.03.005 ↗
20. 10.1080/01694243.2014.88021910.1080/01694243.2014.880219 ↗
21. 10.1177/073168441245034910.1177/0731684412450349 ↗
22. Tomo T. · Compos. Mater. · 2014 · 10 · 1
23. 10.1016/j.compstruct.2014.02.00710.1016/j.compstruct.2014.02.007 ↗
24. 10.1016/j.compstruct.2013.08.01510.1016/j.compstruct.2013.08.015 ↗
25. 10.1016/j.compositesb.2013.03.04410.1016/j.compositesb.2013.03.044 ↗
26. 10.1016/j.compstruct.2013.08.01710.1016/j.compstruct.2013.08.017 ↗
27. 10.1016/j.compscitech.2009.04.01010.1016/j.compscitech.2009.04.010 ↗
28. 10.1016/j.cryogenics.2013.09.00810.1016/j.cryogenics.2013.09.008 ↗
29. 10.1016/j.cryogenics.2005.03.00310.1016/j.cryogenics.2005.03.003 ↗
30. 10.1016/j.cryogenics.2009.12.00310.1016/j.cryogenics.2009.12.003 ↗
31. 10.1002/jbm.a.3455210.1002/jbm.a.34552 ↗
32. 10.1177/073168440504355210.1177/0731684405043552 ↗