Fish oil thermosetting polymers: synthesis, structure, properties and their relationships

Citation
F. Li et al., Fish oil thermosetting polymers: synthesis, structure, properties and their relationships, POLYMER, 41(22), 2000, pp. 7925-7939
Citations number
14
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
POLYMER
ISSN journal
00323861 → ACNP
Volume
41
Issue
22
Year of publication
2000
Pages
7925 - 7939
Database
ISI
SICI code
0032-3861(200010)41:22<7925:FOTPSS>2.0.ZU;2-K
Abstract
The cationic copolymerization of native or conjugated fish oil (FO or CFO) with divinylbenzene (DVB), norbornadiene (NBD) or dicyclopentadiene (DCP) c omonomers initiated by boron trifluoride diethyl etherate (BF3.OEt2) was co nducted in an effort to develop useful biodegradable polymers with rational ly designed structures from natural renewable resources. Polymers ranging f rom rubbers to hard plastics have been obtained. H-1 NMR,C-13 NMR, solid st ate C-13 MMR, differential scanning calorimetry (DSC), and dynamic mechanic al analysis (DMA) have been used to characterize the structures and physica l properties of the fish oil polymers. The results indicate that the produc ts are typical thermosetting polymers with densely crosslinked structures. These polymer materials have densities of approximately 1000 kg/m(3) which appear to be independent of their compositions. The structure of the bulk p olymer is composed of 40-85 wt% of crosslinked polymer networks plasticized by 15-60 wt% of unreacted free oil. The moduli of the FO (similar to 0.8 G Pa) and CFO (similar to 1.1 GPa) polymers at room temperature are found to be comparable to those of conventional petroleum-based plastics. The glass transition temperatures of the polymers range from 50 to 150 degrees C with a broad transition region. Thermogravimetric analysis (TGA) indicates thre e distinct decomposition temperature regions, i.e. 200-400 degrees C, 400-5 60 degrees C, and 560-800 degrees C, which correspond to evaporation of the unreacted free oil, carbonization of the crosslinked polymer network, and oxidation of the carbon, respectively. The thermal stability of these mater ials is found to be largely dependent on the amount of unreacted free oil m olecules present in the bulk polymers. The CFO polymers have higher moduli and thermal stability than the FO polymers due to the lower amount of free oil present in the CFO bulk polymers. (C) 2000 Elsevier Science Ltd. All ri ghts reserved.