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| Content Provider | Royal Society of Chemistry (RSC) |
|---|---|
| Author | Bartlett, Paul Zhang, Isla Faers, Malcolm A. Royall, C. Patrick |
| Copyright Year | 2013 |
| Abstract | Colloid–polymer mixtures may undergo either fluid–fluid phase separation or gelation. This depends on the depth of the quench (polymer concentration) and the polymer–colloid size ratio. We present a real-space study of dynamics in phase separating colloid–polymer mixtures with medium- to long-range attractions (polymer–colloid size ratio qR = 0.45–0.89), with the aim of understanding the mechanism of gelation as the range of attraction is changed. In contrast to previous studies of short-range attractive systems, where gelation occurs shortly after crossing the equilibrium phase boundary, we find a substantial region of fluid–fluid phase separation. Upon quenching deeper, the system undergoes a continuous crossover to gel formation. We identify two regimes, ‘classical’ phase separation, where single particle relaxation is much faster than the dynamics of phase separation, and ‘viscoelastic’ phase separation, where demixing is slowed down appreciably due to slow dynamics in the colloid-rich phase. Particles at the surface of the strands of the network exhibit significantly greater mobility than those buried inside the gel strand which presents a method for coarsening. |
| Starting Page | 2076 |
| Ending Page | 2084 |
| Page Count | 9 |
| File Format | HTM / HTML PDF |
| ISSN | 1744683X |
| Volume Number | 9 |
| Issue Number | 6 |
| Journal | Soft Matter |
| DOI | 10.1039/c2sm27119b |
| Language | English |
| Publisher | Royal Society of Chemistry |
| Access Restriction | Open |
| Subject Keyword | Viscoelasticity Classical mechanics Polymer |
| Content Type | Text |
| Resource Type | Article |
| Subject | Chemistry Condensed Matter Physics |
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