journal article·1999-06

Separation of a thermotropic liquid crystalline polymer from polypropylene composites

Monty C. Collier, Donald G. Baird

Polymer Composites· Volume 20· Issue 3
Publisher page

Abstract

Abstract This work is concerned with determining how to effectively recycle wholly thermoplastic composites comprised of a polypropylene (PP) matrix reinforced with a thermotropic liquid crystalline polymer (TLCP). A novel reclamation process was developed in which the TLCP could be recovered from the PP matrix. Reactive extrusion was used to reduce the molecular weight of the PP (Montell 6523) and to facilitate phase separation. The melt was then extruded into a heated mineral oil bath, which separated the TLCP (DuPont HX8000) from the matrix by dissolving the PP. It was found that greater than 70 wt% of the TLCP could be reclaimed from the PP matrix at a purity of greater than 96 wt%. In order to determine the ability to reuse the reclaimed HX8000, injection molded in situ composites were generated and their mechanical properties were determined. When the neat HX8000 component was partially replaced with reclaimed HX8000, the injection molded TLCP/PP composites showed no discernible difference in mechanical properties.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: Polymer Nanocomposites and Properties · Polymer crystallization and properties · Liquid Crystal Research Advancements

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

References (33)

Show source-provided references
1. M. A.McLeod PhD thesis Virginia Polytechnic Institute and State University (1997).10.1002/ir.9405 ↗
2. M. A.McLeodandD. G.Baird Polymer submitted in fall of1997.
3. 10.1002/pen.76027060610.1002/pen.760270606 ↗
4. 10.1016/0032-3861(93)90360-M10.1016/0032-3861(93)90360-M ↗
5. 10.1002/pen.76032241110.1002/pen.760322411 ↗
6. Joseph E. G. · 1985
7. 10.1002/pen.76028170410.1002/pen.760281704 ↗
8. 10.1002/pen.76030090610.1002/pen.760300906 ↗
9. 10.1002/pen.76030220510.1002/pen.760302205 ↗
10. 10.1002/app.1991.07043050110.1002/app.1991.070430501 ↗
11. 10.1002/pen.76031130710.1002/pen.760311307 ↗
12. Baird D. G. · Polymeric Materials Encyclopedia · 1996 · 5 · 3207
13. 10.1002/pc.75011010310.1002/pc.750110103 ↗
14. D. G.BairdandA. M.Sukhadia U.S. Patent 5 225 488 (1993).
15. E. A.Sabol PhD thesis Virginia Polytechnic Institute and State University (1994).
16. 10.1002/pc.75016041110.1002/pc.750160411 ↗
17. 10.1295/koron.50.1110.1295/koron.50.11 ↗
18. 10.1177/08927057940070010410.1177/089270579400700104 ↗
19. Hegberg B. A. · 1992
20. 10.1002/(SICI)1098-2329(199711)16:4<313::AID-ADV5>3.0.CO;2-Y10.1002/(SICI)1098-2329(199711)16:4<313::AID-ADV5>3.0.CO;2-Y ↗
21. 10.1021/ie00067a01910.1021/ie00067a019 ↗
22. 10.1016/0032-3861(83)90104-010.1016/0032-3861(83)90104-0 ↗
23. 10.1016/0032-3861(76)90233-010.1016/0032-3861(76)90233-0 ↗
24. 10.1002/app.1968.07012071110.1002/app.1968.070120711 ↗
25. Rosen S. L. · 1993
26. 10.1002/aic.69043061910.1002/aic.690430619 ↗
27. 10.1002/pen.76028030810.1002/pen.760280308 ↗
28. Tzonganakis C. · Intern. Polym. Process. · 1988 · 3
29. 10.1002/app.1995.07057020510.1002/app.1995.070570205 ↗
30. 10.1002/adv.1985.06005020310.1002/adv.1985.060050203 ↗
31. M. C.CollierandD. G.Baird J. Appl. Polym. Sci. accepted.
32. Atkins P. W. · 1990
33. Xanthos M. · 1992