Date of Award
Winter 5-16-2025
Document Type
Thesis
Degree Name
Master of Science in Chemistry (MSChem)
First Advisor
Dr. Ram Gupta
Second Advisor
Dr. Tim Dawsey
Third Advisor
Dr. Alessandro Martins
Keywords
Bio based
Abstract
In this thesis, we applied 1,4-butanediol, which is an emerging biobased and low-cost monomer, was synthesized with a series of aliphatic dicarboxylic acids, namely succinic acid, adipic acid, and sebacic acid using melt polycondensation to Biobased polyesters. The resulting polymers poly(butylene succinate) (PPeS), poly(butylene adipate) (PPeA), and poly(butylene sebacate) (PPeSe) chemical structures were analysis through Fourier transfer infrared spectroscopy(FT-IR), 1H nuclear magnetic resonance (NMR) revealed the elimination of side reactions in the obtained polyesters. Differential scanning calorimetry (DSC) was employed to analyze physical properties, and the impact of dicarboxylate chain length and long short diol on crystalline structure and thermo-mechanical properties was investigated characterized with intrinsic viscosity, nuclear magnetic resonance (NMR), differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), dynamic mechanical analysis(DMA) and tensile testing. All the polymers had weight-average molecular weight over 50,000 g/mol and melting temperature (Tm) ranging from 50˚C to 116˚C, PPeA exhibited a lower melting temperature due to semicrystalline structure and rapid crystallization. The “even-even” effect was observed, contributing to increased tensile strength of PPeA. All the polymers exhibit good thermal stability, mechanical properties and tensile properties compared to polyethylene. These biobased and potentially biodegradable polyester appear to be promising for practical applications like packaging, biomedical materials, and environmentally friendly plastics.
Recommended Citation
Chaudhari, Vinashkumar Jayantibhai, "EXPLORING SUSTAINABLE BIOPOLYESTERS: SYNTHESIS FROM 1,4-BUTANEDIOL AND ALIPHATIC DIACIDS" (2025). Electronic Theses & Dissertations. 770.
https://digitalcommons.pittstate.edu/etd/770
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