Materials Map

Discover the materials research landscape. Find experts, partners, networks.

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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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Materials Map under construction

The Materials Map is still under development. In its current state, it is only based on one single data source and, thus, incomplete and contains duplicates. We are working on incorporating new open data sources like ORCID to improve the quality and the timeliness of our data. We will update Materials Map as soon as possible and kindly ask for your patience.

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Derry, Matthew

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Aston University

in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (7/7 displayed)

  • 2024Block copolymer synthesis in ionic liquid via polymerisation-induced self-assembly: A convenient route to gel electrolytes6citations
  • 2024Harnessing Cytosine for Tunable Nanoparticle Self-Assembly Behavior Using Orthogonal Stimuli4citations
  • 2023Triggered Polymersome Fusion30citations
  • 2022Heterotelechelic homopolymers mimicking high χ – ultralow N block copolymers with sub-2 nm domain size5citations
  • 2021Shear-Induced Alignment of Block Copolymer Worms in Mineral Oil9citations
  • 2021Tuning the vesicle-to-worm transition for thermoresponsive block copolymer vesicles prepared via polymerisation-induced self-assembly17citations
  • 2019In Situ Small-Angle X-ray Scattering Studies During Reversible Addition–Fragmentation Chain Transfer Aqueous Emulsion Polymerization130citations

Places of action

Chart of shared publication
Topham, Paul D.
5 / 29 shared
Worrall, Stephen D.
1 / 10 shared
Liu, Mingyu
1 / 1 shared
Maitland, Georgia Lucy
1 / 1 shared
Hammerton, James
1 / 1 shared
Neal, Thomas
1 / 1 shared
Han, Yisong
1 / 17 shared
Oreilly, Rachel K.
2 / 10 shared
Fielden, Stephen D. P.
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Parkinson, Sam J.
1 / 1 shared
Miller, Alisha J.
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Thomas, Marjolaine
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Haddleton, David M.
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Al-Shok, L.
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Greenall, Martin J.
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Huband, Steven
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Hancox, Ellis
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Town, James S.
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Armes, Steven P.
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Mykhaylyk, Oleksandr O.
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Williams, Clive
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Brown, Steven
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Cunningham, Victoria
1 / 1 shared
Dorsman, Isabella
1 / 1 shared
Cornel, Erik J.
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Hatton, Fiona L.
1 / 1 shared
Cockram, Amy A.
1 / 1 shared
Czajka, Adam
1 / 4 shared
Brotherton, Emma E.
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Chart of publication period
2024
2023
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2019

Co-Authors (by relevance)

  • Topham, Paul D.
  • Worrall, Stephen D.
  • Liu, Mingyu
  • Maitland, Georgia Lucy
  • Hammerton, James
  • Neal, Thomas
  • Han, Yisong
  • Oreilly, Rachel K.
  • Fielden, Stephen D. P.
  • Parkinson, Sam J.
  • Miller, Alisha J.
  • Thomas, Marjolaine
  • Haddleton, David M.
  • Al-Shok, L.
  • Greenall, Martin J.
  • Huband, Steven
  • Hancox, Ellis
  • Town, James S.
  • Armes, Steven P.
  • Mykhaylyk, Oleksandr O.
  • Williams, Clive
  • Brown, Steven
  • Cunningham, Victoria
  • Dorsman, Isabella
  • Cornel, Erik J.
  • Hatton, Fiona L.
  • Cockram, Amy A.
  • Czajka, Adam
  • Brotherton, Emma E.
OrganizationsLocationPeople

article

Shear-Induced Alignment of Block Copolymer Worms in Mineral Oil

  • Derry, Matthew
  • Armes, Steven P.
  • Mykhaylyk, Oleksandr O.
Abstract

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.

Topics
  • impedance spectroscopy
  • mineral
  • dispersion
  • experiment
  • anisotropic
  • viscosity
  • transmission electron microscopy
  • copolymer
  • block copolymer
  • small angle x-ray scattering
  • self-assembly
  • aligned
  • gel filtration chromatography