We can't find the internet
Attempting to reconnect
Something went wrong!
Hang in there while we get back on track
Hydrolytic degradation of poly(l‐lactic acid)/poly(methyl methacrylate) blends
Summary
Researchers studied how blending poly(lactic acid) with poly(methyl methacrylate) at different ratios alters hydrolytic degradation, finding counterintuitively that increasing the biodegradable PLA fraction does not always accelerate breakdown — at higher PLA content, crystallization is favored during hydrolysis, producing a more degradation-resistant material.
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