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Electrophoretic mobility of aqueous colloidal suspensions in the gas and liquid-like phases

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Trends in Colloid and Interface Science VI

Part of the book series: Progress in Colloid & Polymer Science ((PROGCOLLOID,volume 89))

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Abstract

New electrophoretic light scattering (ELS) measurements are reported on aqueous colloidal suspensions down to salt concentrations lower than n s = 10−6 M, where the polyions are liquid-like ordered due to screened Coulomb forces. Mobility data are presented for spherical polystyrene latices of different radius a and rodlike tobacco mosaic virus (TMV) particles (length l = 300 nm and radius a = 9 nm), and they are discussed in relation to the small ion concentration or ka. The salt concentration n s is determined via electric conductivity measurements. Static light scattering (SLS) combined with computer calculations are used to characterize the structure; they also yield the salt concentration of the suspensions. The suspensions of latex spheres show, with decreasing salt concentration, a minimum in mobility. For lowering hte salt content below 10−4 M an increase up to a factor of 3 is observed. The mobility of a dilute suspension of rodlike TMV is found to be about 5 μm/s/V/cm. Increasing the particle concentration leads to a decrease in mobility. In the limit of negligible salt concentration for a particle concentration below 0.1 mg/ml the mobilities lie above 5 μm/s/V/cm. At higher concentrations they are smaller than this value. A qualitative comparison with the theory is made.

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C. Helm M. Lösche H. Möhwald

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© 1992 Dr. Dietrich Steinkopff Verlag GmbH & Co. KG

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Deggelmann, M., Kramer, H., Martin, C., Weber, R. (1992). Electrophoretic mobility of aqueous colloidal suspensions in the gas and liquid-like phases. In: Helm, C., Lösche, M., Möhwald, H. (eds) Trends in Colloid and Interface Science VI. Progress in Colloid & Polymer Science, vol 89. Steinkopff. https://doi.org/10.1007/BFb0116298

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  • DOI: https://doi.org/10.1007/BFb0116298

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  • Publisher Name: Steinkopff

  • Print ISBN: 978-3-7985-0913-9

  • Online ISBN: 978-3-7985-1680-9

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