Synthesis and hydrolytic degradation of poly (glycerol succinate) based polyesters
Journal of the Indian Chemical Society, ISSN: 0019-4522, Vol: 100, Issue: 1, Page: 100841
2023
- 10Citations
- 13Captures
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Article Description
The limited availability of petroleum resources motivates the research towards value-added products production from bio-resources. This study reports the synthesis of glycerol and succinic acid-based polyesters and their detailed characterization. The modification of poly (glycerol succinate) was done by using other diacids like glutaric acid, adipic acid, azelaic acid, sebacic acid, and dodecanedioic acid. The sysnthesized polyesters were characterized using various techniques such as thermogravimetric analysis (TGA), Fourier-transform infrared spectroscopy (FTIR), Nuclear magnetic resonance (NMR), differential scanning calorimetry (DSC), and scanning electron microscopy (SEM). The addition of different dicarboxylic acids to poly (glycerol succinate) based co-polyesters increased the thermal stability of poly (Glycerol succinate). Glass transition temperatures were obtained in the range of −17.2 to −22.5 °C and it increased with chain length. The progress of reaction was monitored by determining acid number, ester number, and degree of esterification. The hydrolytic degradation of polyesters was carried out in acidic and basic medium. The polyesters was found to degrade under basic conditions whereas no weight loss of poly (glycerol succinate) was found under acidic conditions. Particularly, about 40% of poly (glycerol succinate) was degraded within 24 h under basic conditions (pH = 12). The analysis of morphology of polyesters during degradation showed that the increase in hydrolysis time increased the heterogeneity in polyester matrix.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0019452222005039; http://dx.doi.org/10.1016/j.jics.2022.100841; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85144068631&origin=inward; https://linkinghub.elsevier.com/retrieve/pii/S0019452222005039; https://dx.doi.org/10.1016/j.jics.2022.100841
Elsevier BV
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