Effect of temperature-cycling on the morphology of polymeric thermotropic glazings for overheating protection applications

  • Andreas WeberEmail author
  • Katharina Resch
Original Paper


In this paper, the morphology of thermotropic systems with fixed domains (TSFD) was evaluated applying high resolution Atomic Force Microscopy (AFM) also upon heating and cooling. Furthermore nano-mechanical characteristics of the samples were determined by means of Force/Distance spectrometry. TSFD formulated with additive types exhibiting a short chain length displayed roughly spherical scattering particles with dimensions between 0.6 μm and 4 μm. By means of Force Distance spectroscopy stiffness values of 0.6 N/m and 7.8 N/m were determined for the scattering domains and the matrix, respectively. Upon heating, melting and deliquescence of the additive along with migration was ascertained. After cooling to ambient temperature the formation and growth of terrace-like additive domains on the surface was recorded. Additive types with long-chain molecules developed anisotropic scattering domains resembling distorted disks without predominating orientation. Diameters up to 50 μm and a thickness between 200 nm and 600 nm were ascertained. Determination of stiffness yielded values of 0.9 N/m and 13.1 N/m of the scattering domains and the matrix, respectively. Upon heating, swelling and deliquescence of the additive were detected. After cooling to ambient temperature a partial recovery of swelling was observed. Force-Distance spectroscopy yielded a 5 to 10 nm thick additive layer which coated wide areas of the surface after the heating cycle for all samples investigated.


Thermotropic systems with fixed domains Atomic force microscopy Scattering domain size Force distance curve Phase imaging 



The research work of this paper was performed at the Polymer Competence Center Leoben GmbH (PCCL, Austria) within the framework of the Kplus-program of the Austrian Ministry of Traffic, Innovation and Technology with contributions by the University of Leoben. The PCCL is funded by the Austrian Government and the State Governments of Styria and Upper Austria.

The investigated samples were obtained from a project of the non Kplus-program, which is funded by the State Government of Styria, Department Zukunftsfonds Steiermark. The authors wish to express their acknowledgements to Cytec Surface Specialties (Drogenbos, BEL), Sasol Germany GmbH (Hamburg, GER) and Chemson Polymer Additive AG (Arnoldstein, AUT), for providing the materials. Special thanks go to the Austrian Center for Electron Microscopy and Nanoanalysis (Graz, AUT) for sample preparation. The authors are grateful to Franz Schmied (Institute of Physics, University of Leoben, Austria) for technical support on the Atomic Force Microscope.


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Copyright information

© Springer Science+Business Media B.V. 2012

Authors and Affiliations

  1. 1.Polymer Competence Center Leoben GmbHLeobenAustria
  2. 2.Materials Science and Testing of Polymers, Department Polymer Engineering and ScienceUniversity of LeobenLeobenAustria

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