| People | Locations | Statistics |
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| Naji, M. |
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| Motta, Antonella |
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| Aletan, Dirar |
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| Mohamed, Tarek |
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| Ertürk, Emre |
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| Taccardi, Nicola |
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| Kononenko, Denys |
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| Petrov, R. H. | Madrid |
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| Alshaaer, Mazen | Brussels |
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| Bih, L. |
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| Casati, R. |
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| Muller, Hermance |
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| Kočí, Jan | Prague |
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| Šuljagić, Marija |
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| Kalteremidou, Kalliopi-Artemi | Brussels |
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| Azam, Siraj |
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| Ospanova, Alyiya |
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| Blanpain, Bart |
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| Ali, M. A. |
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| Popa, V. |
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| Rančić, M. |
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| Ollier, Nadège |
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| Azevedo, Nuno Monteiro |
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| Landes, Michael |
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| Rignanese, Gian-Marco |
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Torkelson, John M.
in Cooperation with on an Cooperation-Score of 37%
Topics
Publications (14/14 displayed)
- 2022Functional enzyme–polymer complexescitations
- 2011Effect of gradient sequencing on copolymer order-disorder transitionscitations
- 2009Melt rheology and x-ray analysis of gradient copolymers
- 2009Glass transition breadths and composition profiles of weakly, moderately, and strongly segregating gradient copolymerscitations
- 2008Microphase separation and shear alignment of gradient copolymerscitations
- 2006Confinement, composition, and spin-coating effects on the glass transition and stress relaxation of thin films of polystyrene and styrene-containing random copolymerscitations
- 2005Impacts of polystyrene molecular weight and modification to the repeat unit structure on the glass transition-nanoconfinement effect and the cooperativity length scalecitations
- 2005On the glass transition and physical aging in nanoconfined polymers
- 2004Erratumcitations
- 2004Effects of free-surface and interfacial layers and plasticizer content on the distribution of glass transition temperatures in nanoconfined polymers
- 2004Dramatic reduction of the effect of nanoconfinement on the glass transition of polymer films via addition of small-molecule diluentcitations
- 2004In situ monitoring of sorption and drying of polymer films and coatingscitations
- 2003The distribution of glass-transition temperatures in nanoscopically confined glass formerscitations
- 2002Sensing the glass transition in thin and ultrathin polymer films via fluorescence probes and labelscitations
Places of action
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document
On the glass transition and physical aging in nanoconfined polymers
Abstract
<p>The glass transition temperature (T<sub>g</sub>) and physical aging behavior of nanoconfined polymer films were investigated by novel fluorescence methods. These studies have revealed that there are large modifications in both T<sub>g</sub> and physical aging behavior due to interfacial effects. For example, T<sub>g</sub> was observed to decrease compared to bulk in polymers where free-surface effects dominate (e.g., for polystyrene (PS) on silica substrates), while T<sub>g</sub> was observed to increase compared to bulk for polymers where strong attractive substrate interactions dominate (e.g., for poly(2-vinylpyridine) (P2VP) on silica substrates). Similar interfacial effects were observed for physical aging, where attractive substrate effects retarded physical aging compared to bulk. Furthermore, the T<sub>g</sub>-nanoconfinement effect was observed to be widely tunable by small variations on the repeat unit structure of PS or by the addition of low molecular weight diluents or plasticizers. Finally, T<sub>g</sub> and enthalpy relaxation behavior were investigated by differential scanning calorimetry for PS-silica and P2VP-silica nanocomposites. As in the nanoconfined film studies, interfacial interactions were key in dictating the ultimate properties of the nanocomposite, but it was also observed that preparation method plays a significant role.</p>