Temporary droplet-size hysteresis in immiscible polymer blends

Citation
Aj. Ramic et al., Temporary droplet-size hysteresis in immiscible polymer blends, POLYMER, 41(16), 2000, pp. 6263-6270
Citations number
26
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
POLYMER
ISSN journal
00323861 → ACNP
Volume
41
Issue
16
Year of publication
2000
Pages
6263 - 6270
Database
ISI
SICI code
0032-3861(200007)41:16<6263:TDHIIP>2.0.ZU;2-N
Abstract
The droplet size distribution during steady shearing of model polymer blend s is examined in situ by optical microscopy. The volume-average steady-stat e droplet size during shear is essentially inversely proportional to shear rate, as expected. When the shear rate is increased suddenly, the droplets break up, through a process that involves the transient formation of thread s, and rapidly establish a new steady state, comprising ellipsoidal droplet s that are extended slightly in the direction of shear. When the shear is s topped, the droplets quickly relax to a spherical shape, but virtually no c oalescence is observed, because neither Brownian nor buoyant forces are sig nificant and the volume fraction of the dispersed phase is low. Slow shear, however, induces droplet collisions that lead to coalescence. The coalesce nce process is much slower than breakup. In contrast to some predictions, h owever, there is no permanent droplet size hysteresis. The steady-state siz e produced by breakup of initially larger droplets is eventually produced a t large strain by coalescence of initially smaller droplets. The lack of pe rmanent hysteresis has implications concerning appropriate mathematical mod els of coalescence behavior. (C) 2000 Elsevier Science Ltd. All rights rese rved.