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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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)

  • 2015Stability of star-shaped RAFT polystyrenes under mechanical and thermal stresscitations
  • 2014Stability of star-shaped RAFT polystyrenes under mechanical and thermal stress21citations
  • 2014Time-resolved SAXS characterization of the shell growth of silica-coated magnetite nanocomposites15citations
  • 2013Anomalous small-angle x-ray scattering from mesoporous noble metal catalysts5citations
  • 2013Linear and nonlinear rheological behavior and crystallization of semicrystalline poly(styrene)-poly(L-lactide) block copolymers11citations
  • 2008Determination of the structure factor of polymeric systems in solution by small-angle scattering: a SANS-study of a dendrimer of fourth generationcitations
  • 2005Analysis of the correlation of counterions to macroions by anomalous small-angle scatteringcitations

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Chart of shared publication
Goldmann, Anja S.
1 / 3 shared
Riazi, Kamran
2 / 4 shared
Wilhelm, Manfred
3 / 39 shared
Abbasi, Mahdi
2 / 9 shared
Altintas, Ozcan
2 / 9 shared
Barner-Kowollik, Christopher
1 / 11 shared
Daikeler, Alexander
1 / 1 shared
Gutsche, Alexander
1 / 2 shared
Nirschl, Hermann
1 / 11 shared
Guo, Xiaoai
1 / 1 shared
Ballauff, Matthias
3 / 15 shared
Vogtt, Karsten
1 / 1 shared
Gläser, Roger
1 / 8 shared
Goerigk, Guenter
1 / 2 shared
Fehrenbacher, Ulrich
1 / 2 shared
Beskers, Timo
1 / 1 shared
Malek, A.
1 / 1 shared
Likos, C. N.
1 / 4 shared
Voegtle, F.
1 / 1 shared
Lindner, P.
1 / 4 shared
Rosenfeldt, Sabine
2 / 13 shared
Werner, N.
1 / 4 shared
Narayanan, Theyencheri
1 / 4 shared
Plamper, Felix A.
1 / 1 shared
Müller, Axel H. E.
1 / 11 shared
Patel, Mushtaq
1 / 1 shared
Chart of publication period
2015
2014
2013
2008
2005

Co-Authors (by relevance)

  • Goldmann, Anja S.
  • Riazi, Kamran
  • Wilhelm, Manfred
  • Abbasi, Mahdi
  • Altintas, Ozcan
  • Barner-Kowollik, Christopher
  • Daikeler, Alexander
  • Gutsche, Alexander
  • Nirschl, Hermann
  • Guo, Xiaoai
  • Ballauff, Matthias
  • Vogtt, Karsten
  • Gläser, Roger
  • Goerigk, Guenter
  • Fehrenbacher, Ulrich
  • Beskers, Timo
  • Malek, A.
  • Likos, C. N.
  • Voegtle, F.
  • Lindner, P.
  • Rosenfeldt, Sabine
  • Werner, N.
  • Narayanan, Theyencheri
  • Plamper, Felix A.
  • Müller, Axel H. E.
  • Patel, Mushtaq
OrganizationsLocationPeople

article

Linear and nonlinear rheological behavior and crystallization of semicrystalline poly(styrene)-poly(L-lactide) block copolymers

  • Fehrenbacher, Ulrich
  • Beskers, Timo
  • Wilhelm, Manfred
  • Dingenouts, Nico
  • Malek, A.
Abstract

The rheological behavior of a poly(styrene)-poly(L-lactide) (PS-PLLA) block copolymer was investigated in the viscoelastic linear and nonlinear regime. Large amplitude oscillatory shear (LAOS) experiments in the nonlinear regime led to an exponential decay of the G moduli and the nonlinearity parameter I-3/1. During LAOS, the lamellar microstructure of a low molecular weight PS-PLLA copolymer was orientated parallel to the shear field to achieve a macroscopically ordered material. The degree of orientation was analyzed via small angle X-ray scattering (SAXS) measurements. The crystallization kinetics could be accurately described by the Avrami equation as determined by DSC and rheology. These experiments revealed that the crystallization process was slower for the PS-PLLA copolymers than for the PLLA homopolymers. SAXS was also used to monitor the crystallization of the PS-PLLA copolymers. When the temperature of the crystallization experiments, T-c, was lower than the glass transition temperature of the amorphous PS block, 7; (hard confinement), the lamellar microstructure of the low molecular weight PS-PLLA was maintained apart from a small increase in the domain spacing. When T-c was higher than T-g(a) of PS (soft confinement), the block copolymer also retained its lamellar structure, but the increase in the domain spacing was unexpectedly increased compared to what occurred for crystallization under hard confinement conditions. In addition, two-dimensional (2-D) SAXS diffractograms indicated a loss of the structure periodicity during crystallization under soft confinement.

Topics
  • amorphous
  • experiment
  • glass
  • glass
  • glass transition temperature
  • differential scanning calorimetry
  • two-dimensional
  • molecular weight
  • copolymer
  • homopolymer
  • block copolymer
  • crystallization
  • small angle x-ray scattering
  • lamellae
  • semicrystalline