Properties of amorphous and crystallizable hydrocarbon polymers. III. Studies of the hydrogenation of polybutadiene

Abstract

Abstract Three methods for hydrogenating anionically prepared polybutadiene (containing about 8% vinyl double bonds) were investigated: homogeneous catalysis (alkylated transition metal salts), heterogeneous catalysis (nickel on kieselguhr; paladium on calcium carbonate), and stoichiometric reaction with in situ generated diimide. The products were characterized by intrinsic viscosity, gel permeation chromatography, infrared spectroscopy, and melt viscosity. Only the heterogeneous catalysts were found to yield completely hydrogenated products without incorporation of foreign groups and without significant change in the large‐scale molecular structure of the chain. The 195°C melt viscosity of linear polybutadiene hydrogenated with heterogeneous catalysts is virtually identical with that of linear polyethylene with the same intrinsic viscosity in trichlorobenzene at 135°C. The solid state properties of hydrogenated polybutadiene, containing about 20 ethyl branches/1000 main chain atoms, closely resemble those of commercial branched polyethylene.