Macromolecules, 2018, vol 51, 17, pp. 6958-6966
DOI:10.1021/acs.macromol.8b01431
Abstract
Linear viscoelastic response and melt microstructure of ultra-high molecular weight poly(α-olefins) (UHMW PO) with bottlebrush architectures, from poly(1-hexene) to poly(1-octadecene) synthesized by metal coordinative insertion polymerization, were measured as a function of side-chain length, Nsc. All these bottlebrush POs are highly entangled, with an average number of entanglements per chain, Z, greater than 50, which allows accurate determination of their rubbery plateau moduli, GN0, and their entanglement molecular weights, Me. Their plateau moduli scale with their side-chain lengths as GN0 ∼ Nsc–1.47, in agreement with the scaling theory for the dense bottlebrush limit that predicts GN0 ∼ Nsc–3/2. Melt structures of these bottlebrush poly(1-olefin)s and their melt structural changes with temperature were determined by wide-angle X-ray scattering. Concomitant with thermal expansion of these bottlebrush PO melts is a nonmonotonic change in backbone-to-backbone distance (d1) and a monotonic increase in side-chain spacing (d2). Both the melt-flow interchain friction coefficient and the viscosity of these UHMW PO bottlebrushes show a very strong dependence on d2, characterized by two exponential decay regimes, with decay constants having an exponential dependence on Nsc.
