<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>Caimi, Stefano</dc:creator>
  <dc:creator>Cingolani, Alberto</dc:creator>
  <dc:creator>Jaquet, Baptiste</dc:creator>
  <dc:creator>Siggel, Marc</dc:creator>
  <dc:creator>Lattuada, Marco</dc:creator>
  <dc:creator>Morbidelli, Massimo</dc:creator>
  <dc:date>2017-12-12</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Surface chemistry is believed to be the key parameter affecting the aggregation and  breakage of colloidal suspensions when subjected to shear. To date, only a few works  dealt with the understanding of the role of the physical and chemical properties of the  particles’ surface upon aggregation under shear. Previous studies suggested that  surface modifications strongly affect polymer particles’ adhesion, but it was very  challenging to demonstrate this effect and monitor these alterations upon prolonged  exposure to shear forces. More importantly, the mechanisms leading to these changes  remain elusive. In this work, shear-induced aggregation experiments of polymer  colloidal particles have been devised with the specific objective of highlighting material  transfer and clarifying the role of the softness of the particle’s surface. To achieve this  goal, polymer particles with a core–shell structure comprising fluorescent groups have  been prepared so that the surface’s softness could be tuned by the addition of  monomer acting as a plasticizer and the percentage of fluorescent particles could be  recorded over time via confocal microscopy to detect eventual material transfer  among different particles. For the first time, material exchange occurring on the soft  surface of core–shell polymer microparticles upon aggregation under shear was  observed and proved. More aptly, starting from a 50% labeled/nonlabeled mixture, an  increase in the percentage of particles showing a fluorescent signature was recorded  over time, reaching a fraction of 70% after 5 h.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/global/documents/306399</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/306399/files/lat_tfl.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1021/acs.langmuir.7b03054</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>Langmuir. - 2017, vol. 33, no. 49, p. 14038–14044</dc:source>
  <dc:subject>info:eu-repo/classification/udc/54</dc:subject>
  <dc:title xmlns:ns1="xml" ns1:lang="en">Tracking of fluorescently labeled polymer particles reveals surface effects during shear-controlled aggregation</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
