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      <dc:title>Probing Nanometer-Thick Polyelectrolyte Layers Adsorbed on Oppositely Charged Particles by Dynamic Light Scattering</dc:title>
      <dc:creator>Hierrezuelo-Osorio, José Manuel</dc:creator>
      <dc:creator>Szilagyi, Istvan</dc:creator>
      <dc:creator>Vaccaro, Andrea</dc:creator>
      <dc:creator>Borkovec, Michal</dc:creator>
      <dc:subject>Hidrodinámica</dc:subject>
      <dc:description>https://v2.sherpa.ac.uk/id/publication/7790</dc:description>
      <dc:description>The thickness of adsorbed polyelectrolyte layers on oppositely charged particles can be&#xd;
measured by dynamic light scattering (DLS) with a precision of fractions of a nanometer. However, such data&#xd;
can be only reliably obtained when effects of particle aggregation are carefully eliminated by working at&#xd;
low particle number concentrations. In order to achieve a sufficient light scattering intensity at the same time,&#xd;
the size of colloidal particles must be chosen relatively large. We find that such measurements are best carried&#xd;
out with latex particles in the range of diameters of 150-300 nm. The precision of the measurement can be&#xd;
further enhanced with multiangle DLS. The thickness of adsorbed polyelectrolyte layers on oppositely&#xd;
charged particles is normally below 10 nm. At low ionic strengths, a typical thickness is merely 1-2 nm, while&#xd;
at higher ionic strengths one observes thicknesses between 6 and 9 nm. The transition between these two&#xd;
regimes occurs at ionic strengths 0.01-0.05 M. These observations were made with various highly charged&#xd;
cationic and anionic polyelectrolytes and can be considered as quite generic.</dc:description>
      <dc:date>2024-09-25T15:56:04Z</dc:date>
      <dc:date>2024-09-25T15:56:04Z</dc:date>
      <dc:date>2010-10-06</dc:date>
      <dc:type>journal article</dc:type>
      <dc:identifier>Macromolecules 2010, 43, 21, 9108–9116</dc:identifier>
      <dc:identifier>https://hdl.handle.net/10630/33290</dc:identifier>
      <dc:identifier>10.1021/ma1014462</dc:identifier>
      <dc:language>eng</dc:language>
      <dc:rights>open access</dc:rights>
      <dc:publisher>ACS</dc:publisher>
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