English
 
Help Privacy Policy Disclaimer
  Advanced SearchBrowse

Item

ITEM ACTIONSEXPORT

Released

Journal Article

Colloidal crystallite suspensions studied by high pressure small angle x-ray scattering

MPS-Authors
/persons/resource/persons188182

Westermeier,  Fabian
Miller Group, Atomically Resolved Dynamics Department, Max Planck Institute for the Structure and Dynamics of Matter, Max Planck Society;

External Resource
Fulltext (restricted access)
There are currently no full texts shared for your IP range.
Fulltext (public)

1.4941563.pdf
(Publisher version), 4MB

Supplementary Material (public)
There is no public supplementary material available
Citation

Schroer, M. A., Westermeier, F., Lehmkühler, F., Conrad, H., Schavkan, A., Zozulya, A. V., et al. (2016). Colloidal crystallite suspensions studied by high pressure small angle x-ray scattering. The Journal of Chemical Physics, 144(8): 084903. doi:10.1063/1.4941563.


Cite as: https://hdl.handle.net/11858/00-001M-0000-002A-1728-E
Abstract
We report on high pressure small angle x-ray scattering on suspensions of colloidal crystallites in water. The crystallites made out of charge-stabilized poly-acrylate particles exhibit a complex pressure dependence which is based on the specific pressure properties of the suspending medium water. The dominant effect is a compression of the crystallites caused by the compression of the water. In addition, we find indications that also the electrostatic properties of the system, i.e. the particle charge and the dissociation of ions, might play a role for the pressure dependence of the samples. The data further suggest that crystallites in a metastable state induced by shear-induced melting can relax to a similar structural state upon the application of pressure and dilution with water. X-ray cross correlation analysis of the two-dimensional scattering patterns indicates a pressure-dependent increase of the orientational order of the crystallites correlated with growth of these in the suspension. This study underlines the potential of pressure as a very relevant parameter to understand colloidal crystallite systems in aqueous suspension.