Investigation of Drying of Poly(n-Isoproplacrylamide by Fluorescence Technique
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Date
2013
Authors
Evingür, Gülşen Akin
Pekcan, Önder
Journal Title
Journal ISSN
Volume Title
Publisher
Wiley-Blackwell
Open Access Color
GOLD
Green Open Access
Yes
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OpenAIRE Views
Publicly Funded
No
Abstract
The steady-state fluorescence technique was performed on drying of various molar percentages of poly(N-isopropylacrylamide-co- acrylamide) [poly(NIPA-co-AAc)] to elucidate the mechanism of temperature-induced phase separation and the effect of monomer content. Poly(NIPA-co-AAc) copolymers were prepared by free radical cross-linking copolymerization. The fluorescence intensity I of pyranine introduced as a probe increased as drying time was increased for all samples. The behavior of I was modeled by using the SternVolmer equation combined with the moving boundary diffusion model. The desorption coefficient D increased as NIPA content was increased at a given temperature. Gravimetric and volumetric experiments also supported the results of the fluorescence technique. The energy E values were measured for the drying processes for each molar percentage of NIPA monomer content by using fluorescence gravimetric and volumetric methods respectively. It is understood that E values decrease by increasing NIPA content until 50% NIPA and then increase after 50% NIPA indicating that the phase separation has occurred at 50% NIPA. (c) 2012 Wiley Periodicals Inc. Adv Polym Techn 32: E231E240 2013
View this article online at wileyonlinelibrary.com. DOI 10.1002/adv.21269
View this article online at wileyonlinelibrary.com. DOI 10.1002/adv.21269
Description
Keywords
Copolymerization, Drying, Fluorescence, Hydrophobic effect, Temperature, Copolymerization, Temperature, Hydrophobic effect, Fluorescence, Drying
Fields of Science
0103 physical sciences, 02 engineering and technology, 0210 nano-technology, 01 natural sciences
Citation
WoS Q
Q3
Scopus Q
Q2

OpenCitations Citation Count
1
Source
Advances in Polymer Technology
Volume
32
Issue
Start Page
E231
End Page
E240
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CrossRef : 1
Scopus : 1
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