Hydrolytic degradation of poly(l‐lactic acid)/poly(methyl methacrylate) blends |
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| Authors: | Naila Boudaoud Samira Benali Rosica Mincheva Hamid Satha Jean‐Marie Raquez Philippe Dubois |
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| Affiliation: | 1. Laboratory of Silicates, Polymers and Nanocomposites (LSPN), Department of Process Engineering, University of 8 Mai 1945, Guelma, Algeria;2. Department of Chemistry, Laboratory of Polymeric and Composite Materials (LPCM), Center of Innovation and Research in Materials and Polymers (CIRMAP), University of Mons, Mons, Belgium |
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| Abstract: | The hydrolytic degradation of poly(l ‐lactic acid)/poly(methyl methacrylate) (PLLA/PMMA) blends was carried out by the immersion of thin films in buffer solutions (pH = 7.24) in a shaking water bath at 60 °C for 38 days. The PLA/PMMA blends (0/100; 30/70; 50/50; 70/30; 100/0) were obtained by melt blending using a Brabender internal mixer and shaped into thin films of about 150 µm in thickness. Considering that PMMA does not undergo hydrolytic degradation, that of PLLA was followed via evolution of PLA molecular weight (recorded by size exclusion chromatography), thermal parameters (differential scanning calorimetry (DSC)) and morphology of the films (scanning transmission electron microscopy). The results reveal a completely different degradation pathway of the blends depending on the polymethacrylate/polyester weight ratio. DSC data suggest that, during hydrolysis at higher PMMA content, the polyester amorphous chains, more sensitive to water, are degraded before being able to crystallize, while at higher PLLA content, the crystallization is favoured leading to a sample more resistant to hydrolysis. In other words, and quite unexpectedly, increasing the content of water‐sensitive PLLA in the PLLA/PMMA blends does not mean de facto faster hydrolytic degradation of the resulting materials. © 2018 Society of Chemical Industry |
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| Keywords: | PLLA PMMA polymer blend hydrolytic degradation crystallization |
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