Shear-Induced Alignment of Block Copolymer Worms in Mineral Oil

Matthew Derry*, Oleksandr O. Mykhaylyk, Steven P. Armes

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review


Poly(stearyl methacrylate)-poly(benzyl methacrylate) [PSMA-PBzMA] diblock copolymer worms were synthesized directly in mineral oil via reversible addition-fragmentation chain transfer (RAFT) dispersion polymerization at 90 °C. Free-standing gels were obtained from this polymerization-induced self-assembly (PISA) formulation when targeting PSMA13-PBzMA65 dispersions at 5% w/w to 20% w/w copolymer concentration. Gel permeation chromatography (GPC) studies indicated that almost identical copolymer chains were obtained in all cases, while transmission electron microscopy (TEM) and small-angle X-ray scattering (SAXS) studies confirmed that highly anisotropic worms were formed with mean cross-sectional diameters of 11.9-13.1 nm. These worms undergo a thermoreversible worm-to-sphere transition on heating up to 150 °C. Rheological studies were conducted to characterize the shear rate- and concentration-dependent behaviour caused by this change in copolymer morphology, where the initial shear-thinning worm gels form spheres (i.e. a Newtonian fluid) on heating up to 150 °C. Complementary shear-induced polarized light imaging (SIPLI) experiments confirmed the formation of aligned linear worms under applied shear between 80 °C and 110 °C, with high-viscosity dispersions of branched worms being obtained at 20-60 °C and low-viscosity spheres being produced at 150 °C. This study informs the use of such block copolymer worms as rheology modifiers for non-polar oils, which is of potential interest for the automotive industry.
Original languageEnglish
Pages (from-to)8867-8876
Number of pages10
JournalSoft matter
Issue number39
Early online date15 Sept 2021
Publication statusPublished - 21 Oct 2021

Bibliographical note

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence.

Funding: The Lubrizol Corporation is thanked for funding a PhD
studentship for M.J.D. and for permission to publish this work.
The Leverhulme Trust is also thanked for post-doctoral funding
of M.J.D. (RPG-2016-330). S.P.A. acknowledges an EPSRC
Established Career Fellowship (EP/R003009/1).


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