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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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (7/7 displayed)

  • 2023Flexible, ultrathin and light films from one-dimensional nanostructures of polypyrrole and cellulose nanofibers for high performance electromagnetic interference shielding11citations
  • 2023Solid–Liquid Equilibrium in Co-Amorphous Systems: Experiment and Prediction5citations
  • 2022Tailor-made dual doping for morphology control of polyaniline chains in cellulose nanofiber-based flexible electrodes: electrical and electrochemical performance4citations
  • 2021Elaboration and properties of nanofibrillated cellulose composites with polypyrrole nanotubes or their carbonized analogs17citations
  • 2020New approach for the development of reduced graphene oxide/polyaniline nanocomposites via sacrificial surfactant-stabilized reduced graphene oxide16citations
  • 2020Impact of Hot-Melt Extrusion Processing Conditions on Physicochemical Properties of Amorphous Solid Dispersions Containing Thermally Labile Acrylic Copolymer18citations
  • 2020Temperature modulated polymer nanoparticle bonding: A numerical and experimental study3citations

Places of action

Chart of shared publication
Vilčáková, Jarmila
1 / 28 shared
Sedlačík, Michal
2 / 4 shared
Kopecký, Dušan
4 / 7 shared
Lapka, Tomáš
2 / 2 shared
Prokeš, Jan
2 / 8 shared
Dendisova, Marcela
4 / 6 shared
Moučka, Robert
1 / 8 shared
Fulem, Michal
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Zemánková, Alžběta
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Klajmon, Martin
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Prokeš, J.
1 / 12 shared
Ulbrich, Pavel
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Lhotka, Miloslav
1 / 3 shared
Jurča, M.
1 / 1 shared
Soukupová, Gabriela
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Mazúr, Petr
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Bautkinová, Tereza
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Laachachi, A.
1 / 7 shared
Kutorglo, Edith Mawunya
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Sifton, A.
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Růžička, Květoslav
1 / 7 shared
Mathers, Alex
1 / 1 shared
Malinová, Lenka
1 / 1 shared
Merna, Jan
1 / 4 shared
Šoóš, Miroslav
1 / 1 shared
Šrom, Ondřej
1 / 1 shared
Kosek, Juraj
1 / 4 shared
Trunov, Dan
1 / 1 shared
Wilson, Jose Francisco
1 / 1 shared
Štětina, Jiří
1 / 1 shared
Chart of publication period
2023
2022
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2020

Co-Authors (by relevance)

  • Vilčáková, Jarmila
  • Sedlačík, Michal
  • Kopecký, Dušan
  • Lapka, Tomáš
  • Prokeš, Jan
  • Dendisova, Marcela
  • Moučka, Robert
  • Fulem, Michal
  • Zemánková, Alžběta
  • Klajmon, Martin
  • Prokeš, J.
  • Ulbrich, Pavel
  • Lhotka, Miloslav
  • Jurča, M.
  • Soukupová, Gabriela
  • Mazúr, Petr
  • Bautkinová, Tereza
  • Laachachi, A.
  • Kutorglo, Edith Mawunya
  • Sifton, A.
  • Růžička, Květoslav
  • Mathers, Alex
  • Malinová, Lenka
  • Merna, Jan
  • Šoóš, Miroslav
  • Šrom, Ondřej
  • Kosek, Juraj
  • Trunov, Dan
  • Wilson, Jose Francisco
  • Štětina, Jiří
OrganizationsLocationPeople

article

Temperature modulated polymer nanoparticle bonding: A numerical and experimental study

  • Šoóš, Miroslav
  • Hassouna, Fatima
  • Šrom, Ondřej
  • Kosek, Juraj
  • Trunov, Dan
  • Wilson, Jose Francisco
  • Štětina, Jiří
Abstract

In this research, we investigated the impact of nanoparticle adhesive properties on the size of micro-clusters formed during shear-induced aggregation at different temperatures. To precisely control particle adhesion, we used nanoparticles with a core-shell structure, where the core is composed of polymethyl methacrylate and the shell is composed of a combination of polymethyl methacrylate and polybutylacrylate. Due to significantly different glass transition temperature (T-g) of these polymers, the core act as a hard-sphere, while the presence of polybutylacrylate in the shell, with a glass transition temperature of 50 degrees C, gives the surface mechanical softness upon increasing temperature. We observed that the size of the aggregates grow significantly when the temperature rises above T-g, indicating an increase of adhesive force between the nanoparticles. Under these conditions, the surface of the nanoparticles exhibits a transition from plastic to viscous behavior that allows core-shell nanoparticles to bond physically upon contact in a controlled coalescence effect. To further investigate the micro-mechanical behavior of the micro-clusters during aggregation, a numerical study of a simple shear flow setup using CFD-DEM with a customized particle interaction model was carried out. This model has the capability to describe non-contact as well as contact forces present in colloidal systems. Depending on the system temperature, the model can simulate either elastic, elastic-plastic or viscoplastic deformation between the interacting nanoparticles. Using this feature, it is demonstrated that it is possible to reproduce the experimentally observed growth in aggregates with temperature rise by simulating an increase in adhesion using primary particle mechanical parameters. Furthermore, these results clearly demonstrate the direct relation between surface properties of the nanoparticles with the macroscopic behavior of the colloidal system.

Topics
  • nanoparticle
  • impedance spectroscopy
  • surface
  • cluster
  • polymer
  • glass
  • glass
  • glass transition temperature
  • discrete element method