TY - JOUR
T1 - Gelation and Re-entrance in Mixtures of Soft Colloids and Linear Polymers of Equal Size
AU - Parisi, Daniele
AU - Truzzolillo, Domenico
AU - Slim, Ali H.
AU - Dieudonné-George, Phillippe
AU - Narayanan, Suresh
AU - Conrad, Jacinta C.
AU - Deepak, Vishnu D.
AU - Gauthier, Mario
AU - Vlassopoulos, D.
N1 - KAUST Repository Item: Exported on 2023-03-06
Acknowledgements: We would like to thank Professor Nikos Hadjichristidis (KAUST) for providing a linear polymer used in this work and Dr. Julian Oberdisse for fruitful discussions. This research was partly funded by the EU [European Training Network Colldense (H2020-MCSA-ITN-2014), grant number 642774]. A.S. and J.C.C. acknowledge support from the Welch Foundation (E-1869) and the US National Science Foundation (CBET-2004652). This research used resources of the Advanced Photon Source, a user facility operated for the DOE Office of Science by Argonne National Laboratory under contract no. DE-AC02-06CH11357.
This publication acknowledges KAUST support, but has no KAUST affiliated authors.
PY - 2023/2/22
Y1 - 2023/2/22
N2 - Liquid mixtures composed of colloidal particles and much smaller non-adsorbing linear homopolymers can undergo a gelation transition due to polymer-mediated depletion forces. We now show that the addition of linear polymers to suspensions of soft colloids having the same hydrodynamic size yields a liquid-to-gel-to-re-entrant liquid transition. In particular, the dynamic state diagram of 1,4-polybutadiene star-linear polymer mixtures was determined with the help of linear viscoelastic and small-angle X-ray scattering experiments. While keeping the star polymers below their nominal overlap concentration, a gel was formed upon increasing the linear polymer content. Further addition of linear chains yielded a re-entrant liquid. This unexpected behavior was rationalized by the interplay of three possible phenomena: (i) depletion interactions, driven by the size disparity between the stars and the polymer length scale which is the mesh size of its entanglement network; (ii) colloidal deswelling due to the increased osmotic pressure exerted onto the stars; and (iii) a concomitant progressive suppression of the depletion efficiency on increasing the polymer concentration due to reduced mesh size, hence a smaller range of attraction. Our results unveil an exciting new way to tailor the flow of soft colloids and highlight a largely unexplored path to engineer soft colloidal mixtures.
AB - Liquid mixtures composed of colloidal particles and much smaller non-adsorbing linear homopolymers can undergo a gelation transition due to polymer-mediated depletion forces. We now show that the addition of linear polymers to suspensions of soft colloids having the same hydrodynamic size yields a liquid-to-gel-to-re-entrant liquid transition. In particular, the dynamic state diagram of 1,4-polybutadiene star-linear polymer mixtures was determined with the help of linear viscoelastic and small-angle X-ray scattering experiments. While keeping the star polymers below their nominal overlap concentration, a gel was formed upon increasing the linear polymer content. Further addition of linear chains yielded a re-entrant liquid. This unexpected behavior was rationalized by the interplay of three possible phenomena: (i) depletion interactions, driven by the size disparity between the stars and the polymer length scale which is the mesh size of its entanglement network; (ii) colloidal deswelling due to the increased osmotic pressure exerted onto the stars; and (iii) a concomitant progressive suppression of the depletion efficiency on increasing the polymer concentration due to reduced mesh size, hence a smaller range of attraction. Our results unveil an exciting new way to tailor the flow of soft colloids and highlight a largely unexplored path to engineer soft colloidal mixtures.
UR - http://hdl.handle.net/10754/689992
UR - https://pubs.acs.org/doi/10.1021/acs.macromol.2c02491
UR - http://www.scopus.com/inward/record.url?scp=85148873119&partnerID=8YFLogxK
U2 - 10.1021/acs.macromol.2c02491
DO - 10.1021/acs.macromol.2c02491
M3 - Article
C2 - 36938509
SN - 1520-5835
JO - Macromolecules
JF - Macromolecules
ER -