Steady‐state and dynamic rheology of poly(1‐olefin) melts

Abstract

AbstractThe steady‐state and dynamic melt rheology for a series of poly(1‐olefins) has been investigated. The series includes poly(1‐butene), poly(1‐hexene), poly(1‐heptene), poly(1‐octene), Poly(1‐undecene), poly(1‐tridecene), poly(1‐hexadecene), and poly(1‐octadecene). The flow behavior was investigated by use of a Weissenberg rheogoniometer. Measurements on poly(1‐butene) were also made using an Instron capillary rheometer. The empirical relationship developed by Cox and Merz was obeyed for the entire series of poly(1‐olefins) at all temperatures investigated. Graessley's theory was used to calculate the flow curves for the poly(1‐olefins) from the measured molecular weight distributions. The purpose was to investigate the effect of polymer composition on the shear rate dependence of viscosity. It was found that all experimental flow curves except those for poly(1‐hexene) can be fitted with the calculated curves from the individual molecular weight distributions. The conclusion is made that flow curves of poly(1‐olefins) depend predominately on molecular weight distribution and are essentially independent of side‐chain length even for poly(1‐olefins) with pendant groups as long as 16 carbon atoms. The low‐shear limiting Newtonian viscosity η0 for all poly(1‐olefins) was expressed by, η0 = KM̄ or by η0 = K′P̄ where M̄w is the weight‐average molecular weight and P̄w is the weight‐average degree of polymerization. The K and K′ values obtained decrease systematically as the side chain is increased.