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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University of Strathclyde

in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (7/7 displayed)

  • 2024Probing the role of the so-called inactive transition metal in conversion reactions: Not so inactive!1citations
  • 2023Filler-induced heterogeneous nucleation of polymer crystals investigated by molecular dynamics simulations7citations
  • 2022Controlling urea crystallisation via heterogeneous nucleationcitations
  • 2022Polyhydroxybutyrate32citations
  • 2020Glass transition temperature of a polymer thin film20citations
  • 2016Phase behaviour of self-assembled monolayers controlled by tuning physisorbed and chemisorbed states12citations
  • 2013Hierarchical multiscale modeling of polymer-solid interfaces54citations

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Chart of shared publication
Grey, Clare
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Stievano, Lorenzo
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Griffith, Kent
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Darwiche, Ali
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Monconduit, Laure
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Dupré, Nicolas
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Mulheran, Paul
3 / 7 shared
Wadkin-Snaith, Dominic
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Anker, Samira
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Mckechnie, David
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Majerczak, Katarzyna
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Magueijo, Vitor
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Liggat, John J.
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Cree, Jordan
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Cheung, David
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Fortuna, Sara
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Co-Authors (by relevance)

  • Grey, Clare
  • Stievano, Lorenzo
  • Griffith, Kent
  • Darwiche, Ali
  • Monconduit, Laure
  • Dupré, Nicolas
  • Mulheran, Paul
  • Wadkin-Snaith, Dominic
  • Anker, Samira
  • Mckechnie, David
  • Majerczak, Katarzyna
  • Magueijo, Vitor
  • Liggat, John J.
  • Cree, Jordan
  • Cheung, David
  • Fortuna, Sara
  • Harmandaris, Vagelis
OrganizationsLocationPeople

article

Filler-induced heterogeneous nucleation of polymer crystals investigated by molecular dynamics simulations

  • Mulheran, Paul
  • Johnston, Karen
  • Wadkin-Snaith, Dominic
Abstract

Filler particles are known to act as nucleants for polymer crystallisation yet the connection between the filler surface properties and polymer crystallisation are not well understood. In this work, molecular dynamics simulations were used to investigate homogeneous and heterogeneous polymer nucleation and crystallisation using a generic linear bead-spring polymer model with a bond bending potential. The polymer systems were equilibrated at high temperature and then cooled at a constant rate. Without a surface present, polymers with stiff chains were found to crystallise more readily than more flexible polymers. The degree of crystallinity was estimated based on the mass fraction of straight chain segments which we equate to stem mass fraction. At a temperature Tc a sharp increase in density, radius of gyration and stem mass fraction occurred. After cooling, the systems were reheated and some systems showed hysteresis with a sharp decrease in these properties occurring upon melting at Tm &gt; Tc. For slower heating rates, crystal growth occurred during heating from between the glass transition temperature, Tg, and Tc until just before melting at Tm. The presence of an isotropic surface was found to promote crystallisation in flexible systems that did not crystallise in the bulk, where the stem mass fraction and Tc increased with the interaction strength between the surface and the polymer beads. Changes in Tc and degree of crystallinity with cooling rate are consistent with experimental observations. This model captures polymer crystallisation phenomena and provides insight into heterogeneous nucleation, demonstrating that strong interfacial interactions promote crystallisation, thus aiding the choice or design of nucleants for control of polymer crystallisation and microstructure.<br/>

Topics
  • density
  • surface
  • polymer
  • simulation
  • glass
  • glass
  • molecular dynamics
  • strength
  • thermogravimetry
  • glass transition temperature
  • isotropic
  • crystallinity