Solution properties of nafion in methanol/water mixture solvent

Dilute solution properties of Nafion in methanol/water (4/1 wt ratio) mixture solvent with Nafion concentrations ranging from 0.2 to 9.0 mg/ml was studied using membrane osmometer, viscoelasticity analyzer, and dynamic light scattering. Two aggregation processes were observed. The primary aggregatio...

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Published inPolymer (Guilford) Vol. 45; no. 8; pp. 2853 - 2862
Main Authors Lee, Su-Jen, Yu, T.Leon, Lin, Hsiu-Li, Liu, Wen-Horng, Lai, Chen-Lan
Format Journal Article
LanguageEnglish
Published Oxford Elsevier Ltd 01.04.2004
Elsevier
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Summary:Dilute solution properties of Nafion in methanol/water (4/1 wt ratio) mixture solvent with Nafion concentrations ranging from 0.2 to 9.0 mg/ml was studied using membrane osmometer, viscoelasticity analyzer, and dynamic light scattering. Two aggregation processes were observed. The primary aggregation process causes formation of smaller sizes (∼10 3 nm) rod-like aggregation particles, which can be dissociated into single molecular chains by dissolving Nafion in propanol/water mixture solvents, is attributed to the hydrophobic interaction of fluorocarbon backbone. The secondary aggregation process causes formation of larger aggregation particles (∼10 4 nm), which can be dissociated into primary aggregation particles by mixing NaCl salt into Nafion/methanol/water solutions, is attributed to the ionic aggregation of primary aggregation particles which arise from the electrostatic attraction of Nafion side chain –SO 3 − ion pairs. Two critical concentrations were observed in this concentration regime, i.e. C ∗∼ around 1.0 mg/ml and C ∗∗∼ around 5.0 mg/ml in the present study, where transitions of Nafion aggregation conformations occur. C ∗ is the concentration at which most of the Nafion primary rod-like perfluoro backbone aggregation particles aggregate to form secondary ionic aggregations. C ∗∗ is the concentration at which the disordered segments of primary aggregation particles start to overlap and self-assemble.
Bibliography:ObjectType-Article-2
SourceType-Scholarly Journals-1
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content type line 23
ISSN:0032-3861
1873-2291
DOI:10.1016/j.polymer.2004.01.076