Macromolecules, Vol.53, No.7, 2503-2515, 2020
Thermoplastic Superelastomers Based on Poly(isobutylene)-graft-Poly(L-lactide) Copolymers: Enhanced Thermal Stability, Tunable Tensile Strength, and Gas Barrier Property
A mechanically adjustable reinforced thermoplastic superelastomer system, with tunable gas-permeability, was developed. The superelastomer is based on a graft copolymer structure, using commercial butyl rubbers (or poly(isobutylene-co-isoprene), P(IB-co-I)) and L- or oplactide (LLA or LA) derived from renewable feedstocks, by a "grafting from" controlled polymerization. First, hydroxyl-functionalized PIB (PIB-g-(OH)) macroinitiators were prepared through epoxidation using an economical alternative to m-chloroperoxybenzoic acid and ring-opening reaction. Second, PIB-based graft copolymers with end-hydroxylated poly(lactide) as hard side-chains, PIB-g-(P(L)LA-OH)s, were synthesized to target f(P(L)LA) of 0.18-0.45, to achieve mechanical reinforcement and an additional gas barrier. They were subsequently acetylated with an acetic anhydride to produce PIB-g- (P(L)LA-Ac)s with improved thermal stability. The well-defined molecular structures indicated controlled P(L)LA lengths, and the resulting superelastomers demonstrated improved thermal stability with increased T-d,T-5%; microphase-separated structures having spherical and/or elongated features; thermoplastic behaviors proved by T-ODT, which were much lower than the resulting T-d,T-5%; and superior and adjustable mechanical characterizations, proving to control elastomeric-to-ductile properties. An oxygen permeability value as low as 27 mL mm m(-2) day(-1) atm(-1) was achieved by increasing f(P(L)LA) to 0.45, comparable to polyethylene terephthalate. The partially biodegradable and processable gas barrier films based on these PIB-g-PLLA thermoplastic superelastomers have great potential for the flexible packaging of food and medical products.