A re-entrant glass transition in colloidal disks with adsorbing polymerElectronic supplementary information (ESI) available. See DOI: 10.1039/c2sm25311a
A re-entrant colloidal glass transition has been observed in dispersions of a model disk shaped colloid, laponite ® , with the addition of an adsorbing low molecular weight polymer, poly(ethylene oxide) (PEO). In basic solutions laponite ® forms a repulsive colloidal glass. With the addition of low...
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Main Authors | , , , |
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Format | Journal Article |
Language | English |
Published |
08.08.2012
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Online Access | Get full text |
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Summary: | A re-entrant colloidal glass transition has been observed in dispersions of a model disk shaped colloid, laponite
®
, with the addition of an adsorbing low molecular weight polymer, poly(ethylene oxide) (PEO). In basic solutions laponite
®
forms a repulsive colloidal glass. With the addition of low molecular weight PEO, we observe a retardation in formation of the glass, and the system behaves as a viscous fluid. Upon aging, a glassy phase re-forms, with the time scale depending on the concentration of polymer. For samples with polymer concentration high enough to saturate the laponite
®
surface, we believe this arrested state to be an attractive glass where excess PEO chains in the suspension lead to a weak interparticle attraction. For the polymer molecular weight we considered, all the samples eventually age to form a disordered state. We combine our results with previous work on laponite
®
-PEO dispersions to propose qualitative state diagrams with attractive glass, repulsive glass, liquid and gel regimes as a function of polymer molecular weight, polymer concentration, and aging time. To our knowledge, the progression of repulsive glass-liquid-attractive glass states has not been previously observed in colloids with adsorbing polymers.
Rheology and dynamics studies show a repulsive glass-liquid-attractive glass progression of states for colloidal disks with adsorbed polymer, with the liquid aging to an arrested state at very long times. |
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Bibliography: | 10.1039/c2sm25311a Electronic supplementary information (ESI) available. See DOI |
ISSN: | 1744-683X 1744-6848 |
DOI: | 10.1039/c2sm25311a |