Microcellular foams of glass–fiber reinforced poly(phenylene sulfide) composites generated using supercritical carbon dioxide
Source abstract
Abstract
Microcellular foaming of poly(phenylene sulfide) (PPS) and its glass–fiber (GF) reinforced composites using supercritical CO2 as a blowing agent presents a promising approach to produce novel cellular materials with tailored microstructures. This study investigated the effects of the material composition and process conditions on the foaming behaviors and final morphologies of the microcellular foamed PPS and PPS/GF composites. The rheological and thermal properties as well as the saturation and desorption behaviors of CO2 in the pure PPS and PPS/GF composites were also detailedly discussed. The results show that microcellular foams with various relative densities, cell sizes, cell‐size distributions, and cell densities can be attained by tailoring the fiber content and key process parameters. At low foaming temperatures below the cold crystallization temperature, the microcellular foamed PPS and PPS/GF composites both present a unimodal cell‐size distribution. At elevated temperatures, the generated crystalline superstructures including spherulites in the polymer matrix and transcrystals around the GF will cause a secondary heterogeneous cell nucleation. This leads to the observations of bimodal and trimodal cell‐size distributions in the pure PPS and the PPS/GF composites, respectively. The mechanisms for the solid‐state foaming behaviors of pure PPS and PPS/GF composites have been illustrated by establishing theoretical models. POLYM. COMPOS., 37:2527–2540, 2016. © 2015 Society of Plastics Engineers
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Research context
OpenAlex topics: Polymer Foaming and Composites · Phase Equilibria and Thermodynamics · Carbon dioxide utilization in catalysis
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Applied Chemistry MOE Key Lab of Applied Physics and Chemistry in Space, School of Science, Northwestern Polytechnical University Xi'an 710072 People's Republic of China
Funding
National Natural Science Foundation of China · Shaanxi Provincial Natural Science Foundation
References (50)
Show source-provided references
1. 10.1021/am501610p10.1021/am501610p ↗
2. 10.1002/pi.318710.1002/pi.3187 ↗
3. 10.1039/c4ra02907k10.1039/c4ra02907k ↗
4. 10.1002/app.3121410.1002/app.31214 ↗
5. 10.1016/j.msea.2011.01.08510.1016/j.msea.2011.01.085 ↗
6. 10.1177/0021955X1245964210.1177/0021955X12459642 ↗
7. 10.1177/0021955X0505903310.1177/0021955X05059033 ↗
8. 10.1002/pen.1175810.1002/pen.11758 ↗
9. 10.1016/j.msec.2010.03.00810.1016/j.msec.2010.03.008 ↗
10. J.E.Martini Master's Thesis Massachusetts Institute of Technology MA (1981).
11. 10.1021/ie040040210.1021/ie0400402 ↗
12. 10.1039/c4ra00285g10.1039/c4ra00285g ↗
13. 10.1016/j.biortech.2007.07.06210.1016/j.biortech.2007.07.062 ↗
14. 10.1002/1521-4095(20020805)14:15<1041::AID-ADMA1041>3.0.CO;2-A10.1002/1521-4095(20020805)14:15<1041::AID-ADMA1041>3.0.CO;2-A ↗
15. 10.1016/j.polymer.2009.09.02010.1016/j.polymer.2009.09.020 ↗
16. 10.1002/pen.2168810.1002/pen.21688 ↗
17. 10.1016/j.compscitech.2012.12.00810.1016/j.compscitech.2012.12.008 ↗
18. 10.1039/C4CS00100A10.1039/C4CS00100A ↗
19. 10.1016/j.progpolymsci.2010.12.00410.1016/j.progpolymsci.2010.12.004 ↗
20. 10.1002/pc.2282610.1002/pc.22826 ↗
21. 10.1016/j.progpolymsci.2005.08.00210.1016/j.progpolymsci.2005.08.002 ↗
22. 10.1039/b801895b10.1039/b801895b ↗
23. 10.1016/j.progpolymsci10.1016/j.progpolymsci ↗
24. 10.1002/app.3296910.1002/app.32969 ↗
25. 10.1002/pc.2060110.1002/pc.20601 ↗
26. 10.1002/pc.2118810.1002/pc.21188 ↗
27. 10.1177/0021955X1350477510.1177/0021955X13504775 ↗
28. 10.1016/j.compositesa.2005.08.01010.1016/j.compositesa.2005.08.010 ↗
29. 10.1002/pc.2116910.1002/pc.21169 ↗
30. 10.1016/j.carbon.2014.01.03110.1016/j.carbon.2014.01.031 ↗
31. 10.1016/j.carbon.2013.04.05010.1016/j.carbon.2013.04.050 ↗
32. 10.1177/0021955X1452893110.1177/0021955X14528931 ↗
33. Itoh M. · Furukawa Rev. · 2005 · 28 · 32
34. 10.1080/03602559.2012.74880310.1080/03602559.2012.748803 ↗
35. 10.1002/pen.1066410.1002/pen.10664 ↗
36. 10.1177/0021955X1350384910.1177/0021955X13503849 ↗
37. 10.1016/j.compscitech.2006.12.00910.1016/j.compscitech.2006.12.009 ↗
38. 10.1016/j.ces.2012.02.04010.1016/j.ces.2012.02.040 ↗
39. 10.1021/ma001291z10.1021/ma001291z ↗
40. 10.1016/j.polymer.2007.08.00410.1016/j.polymer.2007.08.004 ↗
41. 10.1021/ie101723g10.1021/ie101723g ↗
42. 10.1002/polb.1012910.1002/polb.10129 ↗
43. 10.1063/1.44602310.1063/1.446023 ↗
44. 10.1002/pen.76027070210.1002/pen.760270702 ↗
45. 10.1021/ie101637f10.1021/ie101637f ↗
46. 10.1002/pc.2058610.1002/pc.20586 ↗
47. 10.1021/ma102345710.1021/ma1023457 ↗
48. 10.1021/ma034597p10.1021/ma034597p ↗
49. 10.1021/jp409021q10.1021/jp409021q ↗
50. 10.1016/0032-3861(91)90450-W10.1016/0032-3861(91)90450-W ↗