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Title: Design of Graft Block Polymer Thermoplastics

Journal Article · · Macromolecules

Graft block polymers are defined by several architectural parameters, including backbone flexibility, graft density, backbone length, side-chain composition, and side-chain length. In this work we probe the impacts of each of these parameters on the phase behavior, rheological properties, and mechanical performance of these materials. Specifically, we examine two sets of materials prepared from backbones of different inherent flexibility. One set was prepared from poly[(n-butyl acrylate)-co-(2-hydroxyethyl acrylate)] (B$$_x$$E$$_y$$) copolymers; the other was prepared from hydroxypropyl methyl cellulose (HPMC) samples. Sequential ring-opening transesterification polymerization from these hydroxyl-functionalized macroinitiatiors yielded a diblock graft architecture containing a rubbery interior block and semicrystalline exterior blocks tethered to a flexible (B$$_x$$E$$_y$$) or rigid (HPMC) backbone. Good control over side-chain molar mass and composition and judicious choice of the graft block segments enabled the preparation of materials that were either ordered or disordered in the melt state. In the former case, crystallization destroys existing order in the material; in the latter case crystallization induces new microphase separation in the bulk. Many of the structure–mechanical property relationships observed for graft block copolymers with rigid backbones are maintained for graft block polymers with semiflexible backbones, including the tendency for samples to remain transparent when stretched. However, interestingly, we note the effects of graft density and backbone length are quite different depending on the rigidity of the backbone.

Research Organization:
Argonne National Lab. (ANL), Argonne, IL (United States). Advanced Photon Source (APS); Univ. of Minnesota, Minneapolis, MN (United States)
Sponsoring Organization:
National Science Foundation (NSF); National Natural Science Foundation of China (NSFC); E.I. DuPont de Nemours & Co.; The Dow Chemical Company; USDOE Office of Science (SC), Basic Energy Sciences (BES)
Grant/Contract Number:
DMR-1420013; 21504013; AC02-06CH11357
OSTI ID:
1340733
Alternate ID(s):
OSTI ID: 1418560
Journal Information:
Macromolecules, Vol. 49, Issue 23; ISSN 0024-9297
Publisher:
American Chemical SocietyCopyright Statement
Country of Publication:
United States
Language:
ENGLISH
Citation Metrics:
Cited by: 55 works
Citation information provided by
Web of Science

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Cited By (6)

Field-theoretic simulations of bottlebrush copolymers journal November 2018
Photocross‐linked polymers based on plant‐derived monomers for potential application in optical 3D printing journal November 2019
Mimicking biological stress–strain behaviour with synthetic elastomers journal September 2017
Integration of metal-free ring-opening metathesis polymerization and organocatalyzed ring-opening polymerization through a bifunctional initiator journal January 2019
The synthesis of bottlebrush cellulose- graft -diblock copolymer elastomers via atom transfer radical polymerization utilizing a halide exchange technique journal January 2019
Natural Polymers from Biomass Resources as Feedstocks for Thermoplastic Materials journal February 2019

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