Continuous precipitation polymerization of vinylidene fluoride in supercritical carbon dioxide: A model for understanding the molecular-weight distribution

Abstract

Poly(vinylidene fluoride) (PVDF) that is synthesized by precipitation polymerization in supercritical carbon dioxide (scCO 2) has a bimodal molecular weight distribution (MWD) and a very broad polydispersity index (PDI) under certain reaction conditions. Different models have been formulated to account for this behavior. This paper presents a homogenous model for a continuous stirred-tank reactor (CSTR) that includes the change of the termination reaction from kinetic control to diffusion control as the chain length of the polymeric radicals increases, and accounts for the change in the termination rate constant with macroradical chain length in the diffusion-controlled region. The model also includes the chain transfer to polymer reaction. Comparison of the model output with experimental data demonstrates that changes of the MWD, including the development of a bimodal distribution, with such reaction conditions as monomer concentration and average residence time are successfully predicted. In addition, the model can capture the occurrence of gelation, which appears to be responsible for a region of inoperability that was observed in the polymerization experiments. The success of this homogeneous model is consistent with recent research demonstrating that the CO 2-rich phase is the main locus of polymerization for the precipitation polymerization of vinylidene fluoride and vinylidene fluoride/hexafluoropropylene mixtures in scCO 2, at the conditions that have been studied to date.