journal article·2014-01-02

Effect of PCL and EVA Molar Mass on the Development of Sustainable Polymers

I. Moura, R. Nogueira, V. Bounor-Legare, A. V. Machado

Soft Materials· Volume 12· Issue 1
Publisher page

Abstract

Biodegradable grafted copolymers, EVA-g-PCL, have been synthesized by reactive extrusion, through transesterification reaction between ethylene-vinyl acetate copolymer (EVA) and poly(ϵ-caprolactone) (PCL) using titanium propoxide (Ti(OPr)4) as catalyst. The effect of EVA and PCL molar mass on the amount of grafted copolymer and materials properties was investigated. The prepared blends were characterized by several analytical techniques, such as, selective extractions, rheology, TGA, DSC, SEM, mechanical properties, and the biodegradability was evaluated based on biochemical oxygen demand method. The results showed that the amount of copolymer increases as the amount of catalyst increases. Moreover, using EVA and PCL with high and low molar mass, respectively, allowed to obtain a material exhibiting properties similar to conventional polymers and higher biodegradability.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: biodegradable polymer synthesis and properties · Microplastics and Plastic Pollution · Advanced Polymer Synthesis and Characterization

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

References (34)

Show source-provided references
1. Smith R. · 2005
2. 10.1016/j.polymdegradstab.2005.04.03510.1016/j.polymdegradstab.2005.04.035 ↗
3. 10.3139/217.206110.3139/217.2061 ↗
4. 10.1016/S0141-3910(98)00201-810.1016/S0141-3910(98)00201-8 ↗
5. 10.1016/S0169-409X(03)00036-X10.1016/S0169-409X(03)00036-X ↗
6. 10.1016/S0014-3057(99)00155-X10.1016/S0014-3057(99)00155-X ↗
7. 10.1016/j.polymdegradstab.2004.01.01110.1016/j.polymdegradstab.2004.01.011 ↗
8. 10.1002/pol.1982.18020071210.1002/pol.1982.180200712 ↗
9. 10.1002/1521-4095(200109)13:18<1386::AID-ADMA1386>3.0.CO;2-X10.1002/1521-4095(200109)13:18<1386::AID-ADMA1386>3.0.CO;2-X ↗
10. 10.1023/A:100473082260010.1023/A:1004730822600 ↗
11. 10.1002/app.1974.07018040210.1002/app.1974.070180402 ↗
12. 10.1016/S0032-3861(97)00251-610.1016/S0032-3861(97)00251-6 ↗
13. 10.1002/pen.1148910.1002/pen.11489 ↗
14. 10.1002/pen.76028050410.1002/pen.760280504 ↗
15. 10.1002/app.1130710.1002/app.11307 ↗
16. 10.1002/app.1008710.1002/app.10087 ↗
17. 10.1016/S0014-3057(02)00061-710.1016/S0014-3057(02)00061-7 ↗
18. shulman J. · US Patent. · 1964 · 137 · 664
19. 10.1016/0032-3861(96)87626-910.1016/0032-3861(96)87626-9 ↗
20. 10.1007/BFb002755010.1007/BFb0027550 ↗
21. Mueller R.J. · 2003
22. 10.1016/j.reactfunctpolym.2011.03.01210.1016/j.reactfunctpolym.2011.03.012 ↗
23. 10.1016/j.matchemphys.2012.02.03610.1016/j.matchemphys.2012.02.036 ↗
24. Campbell A.N. · 2006
25. 10.1016/0032-3861(82)90330-510.1016/0032-3861(82)90330-5 ↗
26. 10.1016/S0141-3910(00)00020-310.1016/S0141-3910(00)00020-3 ↗
27. 10.1295/polymj.34.68210.1295/polymj.34.682 ↗
28. 10.1016/S0254-0584(03)00326-210.1016/S0254-0584(03)00326-2 ↗
29. 10.1016/S0141-3910(97)00220-610.1016/S0141-3910(97)00220-6 ↗
30. 10.1016/S0014-3057(02)00215-X10.1016/S0014-3057(02)00215-X ↗
31. 10.1016/0964-8305(95)00089-510.1016/0964-8305(95)00089-5 ↗
32. 10.1002/app.1219610.1002/app.12196 ↗
33. 10.4028/www.scientific.net/MSF.636-637.81910.4028/www.scientific.net/MSF.636-637.819 ↗
34. 10.1016/S0141-3910(98)00029-910.1016/S0141-3910(98)00029-9 ↗