Microcosmic morphology and properties of hollow glass beads‐reinforced polylactic acid–based foam composites
Source abstract
Abstract
Polylactic acid (PLA)–based foam composites reinforced with hollow glass beads (HGBs) were prepared via a two‐step process. First, the glass beads, PLA, foaming agent, and other additives were blended, supplanted, and pelletized. Second, the foaming masterbatch was introduced into the mold using thermocompressor to make the microfoam composites. The foam morphology, mechanical properties, and heat resistance were investigated. The experimental results show that the compressive strength of the composites achieved an optimal value when the mass fraction of HGBs was 15%, and that the elastic modulus of the composites increases with increasing bead contents. In addition, after doing a comparative analysis of composites with different bead contents, it was discovered that the foam morphology quality became more uniform and fine with the addition of the beads. Finally, it was found that inclusion of the beads enhanced the thermal stability of the composites and improved their thermal decomposition temperature by about 50°C. POLYM. COMPOS., 37:692–699, 2016. © 2014 Society of Plastics Engineers
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Polymer Foaming and Composites · biodegradable polymer synthesis and properties · Carbon dioxide utilization in catalysis
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
College of Materials and Technology, Nanjing University of Aeronautics and Astronautics Nanjing 211100 China
Funding
Jiangsu Science and Technology Department
References (31)
Show source-provided references
1. Agarwal S. · Process. Mater. · 2011 · 32 · 553
2. Yang B. · 2007
3. 10.1016/j.compscitech.2013.10.01910.1016/j.compscitech.2013.10.019 ↗
4. 10.1002/pc.2122410.1002/pc.21224 ↗
5. 10.1016/j.compositesb.2013.02.03410.1016/j.compositesb.2013.02.034 ↗
6. 10.1016/j.ultsonch.2012.06.00110.1016/j.ultsonch.2012.06.001 ↗
7. 10.1016/j.polymer.2013.08.05010.1016/j.polymer.2013.08.050 ↗
8. 10.1016/j.matlet.2012.01.08510.1016/j.matlet.2012.01.085 ↗
9. 10.1002/pc.2116410.1002/pc.21164 ↗
10. 10.1016/j.compscitech.2013.01.01310.1016/j.compscitech.2013.01.013 ↗
11. 10.1016/j.matdes.2013.10.06510.1016/j.matdes.2013.10.065 ↗
12. 10.1016/j.jmbbm.2013.07.01410.1016/j.jmbbm.2013.07.014 ↗
13. 10.1016/j.eurpolymj.2013.07.03610.1016/j.eurpolymj.2013.07.036 ↗
14. Keshtkar M. · Polymer · 2014 · 45 · 1734
15. 10.1016/j.vibspec.2014.02.00910.1016/j.vibspec.2014.02.009 ↗
16. 10.1016/j.ultsonch.2012.06.00110.1016/j.ultsonch.2012.06.001 ↗
17. 10.1016/j.compositesb.2013.08.07210.1016/j.compositesb.2013.08.072 ↗
18. 10.1016/j.matdes.2010.03.02910.1016/j.matdes.2010.03.029 ↗
19. 10.1016/j.msea.2005.05.01510.1016/j.msea.2005.05.015 ↗
20. 10.1016/j.compscitech.2008.10.01410.1016/j.compscitech.2008.10.014 ↗
21. 10.1016/j.compositesb.2009.03.00410.1016/j.compositesb.2009.03.004 ↗
22. 10.1016/S0079-6700(02)00012-610.1016/S0079-6700(02)00012-6 ↗
23. 10.1002/pen.76027070410.1002/pen.760270704 ↗
24. 10.1002/pen.76027070210.1002/pen.760270702 ↗
25. 10.1002/pen.76027070310.1002/pen.760270703 ↗
26. 10.1016/j.indcrop.2008.01.00910.1016/j.indcrop.2008.01.009 ↗
27. 10.1016/j.carbpol.2004.10.00310.1016/j.carbpol.2004.10.003 ↗
28. 10.1016/j.supflu.2010.05.00510.1016/j.supflu.2010.05.005 ↗
29. 10.1016/j.actbio.2008.03.00710.1016/j.actbio.2008.03.007 ↗
30. 10.1016/j.supflu.2011.03.01010.1016/j.supflu.2011.03.010 ↗
31. 10.1002/pc.2073610.1002/pc.20736 ↗