journal article·2014-10

Effect of natural oils on the thermal stability and degradation kinetics of recycled polypropylene wood flour composites

Matheus Poletto, Ademir J. Zattera, Ruth M.C. Santana

Polymer Composites· Volume 35· Issue 10
Publisher page

Abstract

Recycled polypropylene was reinforced with wood fibers that were non‐treated and treated with different natural oils (hexanoic, octanoic, decanoic and dodecanoic acids). The thermal properties, morphology, kinetics and thermodynamic parameters were investigated. The use of natural oils as coupling agents clearly improved the interfacial adhesion with the matrix and increased the thermal stability of the composites. Octanoic acid improved the thermal stability of the composite the most compared with the other evaluated natural oils. The improvement caused by this natural oil is similar to that promoted by the addition of PPgMA. The thermal stability of the composite was affected by the boiling temperature and the chain length of the acid used. POLYM. COMPOS., 35:1935–1942, 2014. © 2014 Society of Plastics Engineers
Source: crossref · Quality: baseline

Research context

OpenAlex topics: Natural Fiber Reinforced Composites · Polymer Nanocomposites and Properties · Polymer crystallization and properties

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

Affiliations

Engineering School, Federal University of Rio Grande do Sul – UFRGS Porto Alegre – RS Brazil

Laboratory of Polymers (LPOL), Center of Exact Sciences and Technology (CCET) Caxias do Sul University (UCS) Caxias do Sul – RS Brazil

References (31)

Show source-provided references
1. 10.1016/j.polymdegradstab.2008.07.02110.1016/j.polymdegradstab.2008.07.021 ↗
2. 10.1177/089270571141362710.1177/0892705711413627 ↗
3. 10.1016/j.tca.2006.09.01310.1016/j.tca.2006.09.013 ↗
4. 10.1016/j.carbpol.2010.07.04910.1016/j.carbpol.2010.07.049 ↗
5. 10.1002/app.2479910.1002/app.24799 ↗
6. 10.1016/j.compositesa.2009.03.01110.1016/j.compositesa.2009.03.011 ↗
7. 10.1016/j.polymdegradstab.2012.01.02310.1016/j.polymdegradstab.2012.01.023 ↗
8. 10.1016/j.tca.2009.10.00310.1016/j.tca.2009.10.003 ↗
9. 10.1016/j.polymdegradstab.2010.12.00710.1016/j.polymdegradstab.2010.12.007 ↗
10. 10.1002/pc.2034110.1002/pc.20341 ↗
11. 10.1016/j.biortech.2012.08.13310.1016/j.biortech.2012.08.133 ↗
12. 10.1016/j.polymdegradstab.2007.10.01210.1016/j.polymdegradstab.2007.10.012 ↗
13. 10.1590/S1516-1439201000030001610.1590/S1516-14392010000300016 ↗
14. 10.1016/j.polymdegradstab.2006.11.00410.1016/j.polymdegradstab.2006.11.004 ↗
15. 10.1021/ac60131a04510.1021/ac60131a045 ↗
16. 10.1063/1.174960410.1063/1.1749604 ↗
17. 10.1016/S0040-6031(03)00222-310.1016/S0040-6031(03)00222-3 ↗
18. 10.1016/j.jaap.2007.12.00310.1016/j.jaap.2007.12.003 ↗
19. 10.1155/2011/60571210.1155/2011/605712 ↗
20. 10.1007/s10973-009-0191-410.1007/s10973-009-0191-4 ↗
21. 10.1016/j.biortech.2011.11.12210.1016/j.biortech.2011.11.122 ↗
22. 10.1023/B:JTAN.0000028019.88096.e310.1023/B:JTAN.0000028019.88096.e3 ↗
23. Merck Technical Data Sheet of hexanoic acid(2011).
24. Merck Technical Data Sheet(2011).
25. 10.1016/j.fuproc.2009.01.01610.1016/j.fuproc.2009.01.016 ↗
26. 10.1016/j.compositesa.2007.01.00410.1016/j.compositesa.2007.01.004 ↗
27. 10.1016/j.wasman.2010.10.02710.1016/j.wasman.2010.10.027 ↗
28. 10.3144/expresspolymlett.2008.1810.3144/expresspolymlett.2008.18 ↗
29. 10.1021/ie060528y10.1021/ie060528y ↗
30. 10.1186/1752-153X-6-8110.1186/1752-153X-6-81 ↗
31. 10.1016/j.tafmec.2009.04.00210.1016/j.tafmec.2009.04.002 ↗