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Interfacial activity of reactive compatibilizers in polymer blends
Authors:Fereshteh?Karkhaneh-Yousefi,Fatemeh?Goharpey  author-information"  >  author-information__contact u-icon-before"  >  mailto:goharpey@aut.ac.ir"   title="  goharpey@aut.ac.ir"   itemprop="  email"   data-track="  click"   data-track-action="  Email author"   data-track-label="  "  >Email author,Reza?Foudazi  author-information"  >  author-information__contact u-icon-before"  >  mailto:rfoudazi@nmsu.edu"   title="  rfoudazi@nmsu.edu"   itemprop="  email"   data-track="  click"   data-track-action="  Email author"   data-track-label="  "  >Email author
Affiliation:1.Department of Polymer Engineering,Amirkabir University of Technology,Tehran,Iran;2.Department of Chemical and Materials Engineering,New Mexico State University,Las Cruces,USA
Abstract:The influence of a reactive block copolymer compatibilizer on the breakup of polymer fibers in the quiescent conditions is investigated using the breaking thread method (BTM). The compatibilizer is either localized at the interface of two polymers or incorporated in the bulk of thread phase. Moreover, the nominal interfacial tension between two polymers is estimated as a function of compatibilizer concentration for both types of samples using Tomotika theory. It is shown that assembling of compatibilizer molecules at the interface of two immiscible polymers can result in very different dynamic of thread breakup compared to samples containing the compatibilizer in the bulk phase. We observe a reduction in the rate of thread breakup (kinetic of stabilization) when compatibilizer is incorporated in the bulk of thread phase. Such effect is more significant when compatibilizer is localized at the interface of two fluids. Additionally, the mode of thread breakup is sensitive to the compatibilizer location since a beads-on-a-string (BOAS) morphology is observed when compatibilizer is localized at the interface. In conclusion, the usual attribution of interfacial activity of compatibilizer in polymer blends may be originated from their random presence at the interface rather than thermodynamically favored diffusion to the interface.
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