scholarly journals Poly(vinylidene fluoride-trifluoroethylene) (72/28) interconnected porous membranes obtained by crystallization from solution

2011 ◽  
Vol 1312 ◽  
Author(s):  
Armando Ferreira ◽  
Jaime Silva ◽  
Vitor Sencadas ◽  
José Luís Gómez-Ribelles ◽  
Senentxu Lanceros-Méndez
Keyword(s):  
Room Temperature ◽  
Vinylidene Fluoride ◽  
Polymer Concentration ◽  
Porous Membranes ◽  
Membrane Thickness ◽  
Solvent Ratio ◽  
Scanning Calorimetry ◽  
Poly Vinylidene Fluoride ◽  
Crystallization From Solution ◽  
Polymer Solvent

ABSTRACTElectroactive macroporous poly[(vinylidene fluoride)-co-trifluoroethylene] membranes have been processed by solvent evaporation at room temperature with different polymer/solvent concentrations. The pore architecture consists on interconnected spherical pores and this morphology is independent of the membrane thickness. The porosity of the produced membranes increases from 72% for the higher polymer concentration in the polymer/solvent solution (15/85), up to 80% for the lowest polymer concentration in the polymer/solvent solution.Fourier transform infrared spectroscopy and differential scanning calorimetry measurements reveal that the polymer crystallizes in the ferroelectric phase and the polymer/solvent ratio does not influences the Curie transition and the melting temperature of the polymer.

Mechanical Relaxations and Transitions in Poly(Vinylidene Fluoride) PVDF

2006 ◽  
Vol 115 ◽  
pp. 151-156 ◽  
Author(s):  
A. Gasmi ◽  
M. Gouasmia ◽  
S. Etienne
Keyword(s):  
Differential Scanning Calorimetry ◽  
Room Temperature ◽  
Vinylidene Fluoride ◽  
Low Frequency ◽  
Mechanical Spectroscopy ◽  
Scanning Calorimetry ◽  
Dynamic Mechanical Spectroscopy ◽  
Poly Vinylidene Fluoride ◽  
Reversible Melting

Dynamic mechanical spectroscopy and differential scanning calorimetry measurements carried out on PVDF films are reported. Several mechanical relaxations are observed around - 100° C, -40° C, and 17° C at 1 Hz, respectively. It is shown that thermomechanical treatments induce variation of material morphology as revealed by calorimetry and low-frequency mechanical spectroscopy. The effect of long-term ageing at room temperature is attributed to reversible melting and formation of small crystallites. The molecular rearrangements involved in ageing at room temperature are characterized by a slow dynamics.

Preparation and Characterization of Modified PVDF-g-PSSA Membrane

2010 ◽  
Vol 152-153 ◽  
pp. 44-50 ◽  
Author(s):  
Gui Bao Guo ◽  
Er Ding Han ◽  
Sheng Li An
Keyword(s):  
Relative Humidity ◽  
Sodium Silicate ◽  
Room Temperature ◽  
Proton Exchange Membrane ◽  
Vinylidene Fluoride ◽  
Proton Exchange ◽  
Poly Vinylidene Fluoride ◽  
Relative Humidity Range ◽  
Exchange Membrane

A new method based on a solution graft technique was used to prepare poly (vinylidene fluoride) grafted polystyrene sulfonated acid (PVDF-g-PSSA) proton exchange membrane. Polystyrene is grafted into PVDF modified by plain sodium silicate (Na4SiO4). There is a linear relationship between the degree of grafting and the content of Na4SiO4. Fourier transform infrared spectroscopy is used to characterize changes of the membrane's microstructures after grafting and sulfonation. The morphology of the membrane's microstructures after grafting and sulfonation is studied by scanning electrolytic microscope (SEM). The effect of plain sodium silicate (Na4SiO4) concentration and relative humidity on the conductivity of the electrolyte was investigated by the impedance at room temperature. The results show that the styrene has been grafted into PVDF. The conductivity of PVDF-g-PSSA electrolyte doped 10% plain sodium silicate (Na4SiO4) is 0.016 S/cm at room temperature. The conductivity of the electrolyte changes slightly at a relative humidity range of 20%-70%. The weightlessness of PVDF-g-PSSA electrolyte heated to 40°C was less than 2%, which indicated that water capacity was good.

scholarly journals Graphene Nanoplatelet-Reinforced Poly(vinylidene fluoride)/High Density Polyethylene Blend-Based Nanocomposites with Enhanced Thermal and Electrical Properties

Nanomaterials ◽  
2019 ◽  
Vol 9 (3) ◽  
pp. 361 ◽  
Author(s):  
Kartik Behera ◽  
Mithilesh Yadav ◽  
Fang-Chyou Chiu ◽  
Kyong Rhee
Keyword(s):  
Isothermal Crystallization ◽  
High Density Polyethylene ◽  
Vinylidene Fluoride ◽  
High Density ◽  
Scanning Calorimetry ◽  
Melt Mixing ◽  
Graphene Nanoplatelet ◽  
Polyethylene Blend ◽  
Poly Vinylidene Fluoride ◽  
Mixing Method

In this study, a graphene nanoplatelet (GNP) was used as a reinforcing filler to prepare poly(vinylidene fluoride) (PVDF)/high density polyethylene (HDPE) blend-based nanocomposites through a melt mixing method. Scanning electron microscopy confirmed that the GNP was mainly distributed within the PVDF matrix phase. X-ray diffraction analysis showed that PVDF and HDPE retained their crystal structure in the blend and composites. Thermogravimetric analysis showed that the addition of GNP enhanced the thermal stability of the blend, which was more evident in a nitrogen environment than in an air environment. Differential scanning calorimetry results showed that GNP facilitated the nucleation of PVDF and HDPE in the composites upon crystallization. The activation energy for non-isothermal crystallization of PVDF increased with increasing GNP loading in the composites. The Avrami n values ranged from 1.9–3.8 for isothermal crystallization of PVDF in different samples. The Young’s and flexural moduli of the blend improved by more than 20% at 2 phr GNP loading in the composites. The measured rheological properties confirmed the formation of a pseudo-network structure of GNP-PVDF in the composites. The electrical resistivity of the blend reduced by three orders at a 3-phr GNP loading. The PVDF/HDPE blend and composites showed interesting application prospects for electromechanical devices and capacitors.

scholarly journals Polyamide 6/Poly(vinylidene fluoride) Blend-Based Nanocomposites with Enhanced Rigidity: Selective Localization of Carbon Nanotube and Organoclay

Polymers ◽  
2020 ◽  
Vol 12 (1) ◽  
pp. 184 ◽  
Author(s):  
Hung-Ming Lin ◽  
Kartik Behera ◽  
Mithilesh Yadav ◽  
Fang-Chyou Chiu
Keyword(s):  
Carbon Nanotube ◽  
Vinylidene Fluoride ◽  
Domain Size ◽  
Polyamide 6 ◽  
Vital Role ◽  
Scanning Electron Micrographs ◽  
Scanning Calorimetry ◽  
Poly Vinylidene Fluoride ◽  
Twin Screw ◽  
Diffraction Patterns

Polyamide 6 (PA6)/poly(vinylidene fluoride) (PVDF) blend-based nanocomposites were successfully prepared using a twin screw extruder. Carbon nanotube (CNT) and organo-montmorillonite (30B) were used individually and simultaneously as reinforcing nanofillers for the immiscible PA6/PVDF blend. Scanning electron micrographs showed that adding 30B reduced the dispersed domain size of PVDF in the blend, and CNT played a vital role in the formation of a quasi-co-continuous PA6-PVDF morphology. Transmission electron microscopy observation revealed that both fillers were mainly located in the PA6 matrix phase. X-ray diffraction patterns showed that the presence of 30B facilitated the formation of γ-form PA6 crystals in the composites. Differential scanning calorimetry results indicated that the crystallization temperature of PA6 increased after adding CNT into the blend. The inclusion of 30B retarded PA6 nucleation (γ-form crystals growth) upon crystallization. The Young’s and flexural moduli of the blend increased after adding CNT and/or 30B. 30B exhibited higher enhancing efficiency compared with CNT. The composite with 2 phr 30B exhibited 21% higher Young’s modulus than the blend. Measurements of the rheological properties confirmed the development of a pseudo-network structure in the CNT-loaded composites. Double percolation morphology in the PA6/PVDF blend was achieved with the addition of CNT.

scholarly journals Preparation and Characterization of TiO2-PVDF/PMMA Blend Membranes Using an Alternative Non-Toxic Solvent for UF/MF and Photocatalytic Application

Molecules ◽  
2019 ◽  
Vol 24 (4) ◽  
pp. 724 ◽  
Author(s):  
Ouassila Benhabiles ◽  
Francesco Galiano ◽  
Tiziana Marino ◽  
Hacene Mahmoudi ◽  
Hakim Lounici ◽  
...  
Keyword(s):  
Phase Separation ◽  
Vinylidene Fluoride ◽  
Membrane Surface ◽  
Polymer Concentration ◽  
Inversion Method ◽  
Membrane Morphology ◽  
Photocatalytic Application ◽  
Poly Vinylidene Fluoride ◽  
Dope Solution ◽  
Phase Inversion Method

The approach of the present work is based on the use of poly (methylmethacrylate) (PMMA) polymer, which is compatible with PVDF and TiO2 nanoparticles in casting solutions, for the preparation of nano-composites membranes using a safer and more compatible solvent. TiO2 embedded poly (vinylidene fluoride) (PVDF)/PMMA photocatalytic membranes were prepared by phase inversion method. A non-solvent induced phase separation (NIPS) coupled with vapor induced phase separation (VIPS) was used to fabricate flat-sheet membranes using a dope solution consisting of PMMA, PVDF, TiO2, and triethyl phosphate (TEP) as an alternative non-toxic solvent. Membrane morphology was examined by scanning electron microscopy (SEM). Backscatter electron detector (BSD) mapping was used to monitor the inter-dispersion of TiO2 in the membrane surface and matrix. The effects of polymer concentration, evaporation time, additives and catalyst amount on the membrane morphology and properties were investigated. Tests on photocatalytic degradation of methylene blue (MB) were also carried out using the membranes entrapped with different concentrations of TiO2. The results of this study showed that nearly 99% MB removal can be easily achieved by photocatalysis using TiO2 immobilized on the membrane matrix. Moreover, it was observed that the quantity of TiO2 plays a significant role in the dye removal.

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