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Preparation and properties of electrospun poly(vinylidene fluoride) membranes
Author(s) -
Zhao Zhizhen,
Li Jingqing,
Yuan Xiaoyan,
Li Xiang,
Zhang Yuanyuan,
Sheng Jing
Publication year - 2005
Publication title -
journal of applied polymer science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.575
H-Index - 166
eISSN - 1097-4628
pISSN - 0021-8995
DOI - 10.1002/app.21762
Subject(s) - membrane , materials science , electrospinning , scanning electron microscope , differential scanning calorimetry , ultimate tensile strength , polymer chemistry , composite material , capillary action , chemical engineering , polymer , fiber , fluoride , polyvinylidene fluoride , chemistry , inorganic chemistry , biochemistry , physics , engineering , thermodynamics
Poly(vinylidene fluoride) (PVDF) was electrospun into fibrous membranes from its solutions in a mixture of N , N ‐dimethylformamide (DMF) and acetone. The electrospun PVDF membranes were viewed under a scanning electron microscope. Effects of acetone amount, polymer concentration, and capillary‐collector distance on the morphology of the membranes were studied. It was suggested that uniform fibrous membranes with fiber diameters ranging mainly from 50 nm to 300 nm were formed from a 15% (wt/v) PVDF solutions in 8 : 2 (v/v) DMF/acetone at 5‐kV voltage, 0.3‐mL/h flow rate, and 10 ∼ 20‐cm capillary‐collector distance. After about 10 h of electrospinning, fibrous PVDF membranes with thickness of approximate 46 μm were obtained. The tensile moduli and the tensile strengths of the electrospun PVDF membranes were 100 ∼ 170 MPa and 4 ∼ 5 MPa, respectively, from the 13% PVDF solution. Analysis of differential scanning calorimeter and wide angle X‐ray diffraction showed that the crystallization of PVDF in the electrospun membranes was weakened compared to the casting film and the raw material. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 97: 466–474, 2005