Triglycerides with acrylate functionality were prepared from various oils and model triglycerides. The triglyceride-acrylates were homopolymerized and copolymerized with styrene. The cross-link densities of the resulting polymer networks were predicted utilizing the Flory-Stockmayer theory. Although the model predictions overestimated the cross-link density, the trends in the cross-link density predictions matched the experimental results. In both cases, the cross-link density was found to increase gradually at low levels of acrylation and then linearly at higher levels of acrylation. The deviation in the experimental results and model predictions were the result of intramolecular cross-linking. Approximately 0.5 and 0.8 acrylates per triglyceride were lost to intramolecular cyclization for homopolymerized triglyceride-acrylates and triglycerides copolymerized with styrene, respectively. The glass transition temperature (T-g) increased approximately linearly with the cross-link density from as low as -50degreesC to as high as 92degreesC. Simple models accurately predicted the effect of cross-link density on T-g. The tensile strength and modulus of triglyceride-based polymers increased exponentially at low levels of acrylate functionality, but increased linearly at higher levels of acrylate functionality, as predicted by vector percolation theory. (C) 2004 Published by Elsevier Ltd.