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.