scholarly journals Extrusion of poly(vinylidene fluoride) recycled filaments: Effect of the processing cycles on the degree of crystallinity and electroactive phase content

2013 ◽  
Vol 32 (6) ◽  
pp. 1041-1044 ◽  
Author(s):  
M.P. Silva ◽  
R.S. Martins ◽  
H. Carvalho ◽  
J.M. Nobrega ◽  
S. Lanceros-Mendez
2006 ◽  
Vol 949 ◽  
Author(s):  
Marco Pinto Silva ◽  
Vitor Sencadas ◽  
Anabela G Rolo ◽  
Gabriela Botelho ◽  
Ana Vera Machado ◽  
...  

ABSTRACTThe kinetics of the isothermal crystallization from the melt at different crystallisation temperatures and the melting behaviour of Poly(vinylidene fluoride) (PVDF) in the alpha phase has been investigated. The variation of the microstructure of the samples crystallized at different temperatures was monitored with time by Optical Microscopy. The correlation between microstructure and kinetic parameters allows the tailoring of the microstructure by choosing the crystallisation conditions of the samples. Raman and Infrared Transmission Spectroscopy also show the appearance of the γ-phase for higher crystallisation temperatures. The influence of the crystallisation kinetics on the degree of crystallinity of the samples will be also presented and discussed.


2006 ◽  
Vol 514-516 ◽  
pp. 951-955 ◽  
Author(s):  
Carlos M. Costa ◽  
Vitor Sencadas ◽  
João F. Mano ◽  
Senentxu Lanceros-Méndez

In this work, mechanical and thermal experimental techniques have been applied in order to relate the mechanical response with the microscopic variations of the material. Stress-strain results along the main directions of β-poly(vinylidene fluoride), β-PVDF, in poled and non-poled samples enables to investigate the influence of the poling process on the mechanical response of the material. Further, differential scanning calorimetry experiments allow the investigation of the effect of poling in the degree of crystallinity of the material as well as on the stability of the crystalline phase. Thermogravimetric analysis was used to investigate the kinetics of the thermal degradation of poled and non-poled β-PVDF samples. The differences observed between the two materials suggest that the poling affects the mechanical properties of the material especially in the direction parallel to the polymeric chains and originates changes at a molecular level that remain beyond the melting of the material.


2013 ◽  
Vol 313-314 ◽  
pp. 117-120 ◽  
Author(s):  
Narges Ataollahi ◽  
Azizan Ahmad ◽  
Harun Haji Hamzah ◽  
Mohd Yusri Rahman ◽  
Nor Sabirin Mohamed

Poly (vinylidene fluoride-hexafluoro propylene) (PVDF-HFP), Poly (methyl methacrylate)-grafted natural rubber (MG49) (70/30) complexed with different compositions of lithium trifluoromethane sulfonate (LiCF3SO3) based solid polymer electrolyte has been prepared using solution casting method. This work has demonstrated that conductivity values were found to depend upon the concentration of LiCF3SO3. The highest ionic conductivity was 1.97×10ˉ4 S cm-1at 25 wt. % of LiCF3SO3 at room temperature. X-ray diffraction (XRD) indicates decrease in the degree of crystallinity by increasing of salt concentration.


2015 ◽  
Vol 35 (5) ◽  
pp. 451-461 ◽  
Author(s):  
Bin Hu ◽  
Ning Hu ◽  
Liangke Wu ◽  
Feng Liu ◽  
Yaolu Liu ◽  
...  

Abstract The effects of some important factors in the initial crystallization process of the solution casting method on the piezoelectricity of poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) films were extensively explored. The experimental results revealed that there is an optimal initial crystallization temperature at around 90°C. The slow cooling speed can moderately enhance the degree of crystallinity. The most important finding was that a bilayer crystalline structure caused by an asymmetrical heating pattern can enhance the formation of packed micro-fibrillar morphologies after drawing. These three points can increase the piezoelectricity of the PVDF-HFP films, indicating the increase of the extended-chain crystals (β-phase).


ChemPhysChem ◽  
2013 ◽  
Vol 14 (9) ◽  
pp. 1926-1933 ◽  
Author(s):  
Ana Catarina Lopes ◽  
Sonia A. C. Carabineiro ◽  
Manuel Fernando R. Pereira ◽  
Gabriela Botelho ◽  
Senentxu Lanceros-Mendez

Polymers ◽  
2021 ◽  
Vol 13 (19) ◽  
pp. 3292
Author(s):  
Wu Guo ◽  
Zhaogang Liu ◽  
Yan Zhu ◽  
Li Li

Based on poly(vinylidene fluoride)/graphene (PVDF/GP) nano-composite powder, with high β-phase content (>90%), prepared on our self-designed pan-mill mechanochemical reactor, the micro-injection molding of PVDF/GP composite was successfully realized and micro-parts with good replication and dimensional stability were achieved. The filling behaviors and the structure evolution of the composite during the extremely narrow channel of the micro-injection molding were systematically studied. In contrast to conventional injection molding, the extremely high injection speed and small cavity of micro-injection molding produced a high shear force and cooling rate, leading to the obvious “skin-core” structure of the micro-parts and the orientation of both PVDF and GP in the shear layer, thus, endowing the micro-parts with a higher melting point and crystallinity and also inducing the transformation of more α-phase PVDF to β-phase. At the injection speed of 500 mm/s, the β-phase PVDF in the micro-part was 78%, almost two times of that in the macro-part, which was beneficial to improve the dielectric properties. The micro-part had the higher tensile strength (57.6 MPa) and elongation at break (53.6%) than those of the macro-part, due to its increased crystallinity and β-phase content.


RSC Advances ◽  
2017 ◽  
Vol 7 (77) ◽  
pp. 48712-48722 ◽  
Author(s):  
Ji Eun Lee ◽  
Yanting Guo ◽  
Richard Eungkee Lee ◽  
Siu Ning Leung

A new strategy using non-isothermal crystallization and supercritical CO2 processing is found to promote the electroactive phase content in PVDF.


Polymers ◽  
2020 ◽  
Vol 12 (2) ◽  
pp. 384 ◽  
Author(s):  
Roberto Morales-Cerrada ◽  
Vincent Ladmiral ◽  
Florence Gayet ◽  
Christophe Fliedel ◽  
Rinaldo Poli ◽  
...  

The use of [Mn(RF)(CO)5] (RF = CF3, CHF2, CH2CF3, COCF2CH3) to initiate the radical polymerization of vinylidene fluoride (F2C=CH2, VDF) and the radical alternating copolymerization of vinyl acetate (CH2=CHOOCCH3, VAc) with tert-butyl 2-(trifluoromethyl)acrylate (MAF-TBE) by generating primary RF• radicals is presented. Three different initiating methods with [Mn(CF3)(CO)5] (thermal at ca. 100 °C, visible light and UV irradiations) are described and compared. Fair (60%) to satisfactory (74%) polyvinylidene fluoride (PVDF) yields were obtained from the visible light and UV activations, respectively. Molar masses of PVDF reaching 53,000 g·mol−1 were produced from the visible light initiation after 4 h. However, the use of [Mn(CHF2)(CO)5] and [Mn(CH2CF3)(CO)5] as radical initiators produced PVDF in a very low yield (0 to 7%) by both thermal and photochemical initiations, while [Mn(COCF2CH3)(CO)5] led to the formation of PVDF in a moderate yield (7% to 23%). Nevertheless, complexes [Mn(CH2CF3)(CO)5] and [Mn(COCHF2)(CO)5] efficiently initiated the alternating VAc/MAF-TBE copolymerization. All synthesized polymers were characterized by 1H and 19F NMR spectroscopy, which proves the formation of the expected PVDF or poly(VAc-alt-MAF-TBE) and showing the chaining defects and the end-groups in the case of PVDF. The kinetics of VDF homopolymerization showed a linear ln[M]0/[M] versus time relationship, but a decrease of molar masses vs. VDF conversion was noted in all cases, which shows the absence of control. These PVDFs were rather thermally stable in air (up to 410 °C), especially for those having the highest molar masses. The melting points ranged from 164 to 175 °C while the degree of crystallinity varied from 44% to 53%.


2020 ◽  
Vol 20 (12) ◽  
pp. 7535-7543
Author(s):  
Guihai Gan ◽  
Cheng Wang ◽  
Pengpeng Chen ◽  
Jichang Liu

The crystallization behaviours of amorphous poly(vinylidene fluoride) (PVDF) nanocompositesmodified with two different kinds of molybdenum disulfide (MoS2) at different filler loadings were investigated in detail in this work. The crystallinity, melting temperature and crystallization temperature of the PVDF/MoS2 nanocomposites were transformed from α-phase to β-phase with the addition of MoS2, MoS2-COOH and MoS2-NH2. During isothermal cold crystallization, the overall crystallization rate of PVDF was slowed with increased MoS2 loading relative to that of neat PVDF. Moreover, the crystallization temperature of the PVDF nanocomposites increased with the addition of MoS2 despite the cooling rate during nonisothermal cold crystallization. DMA tests showed that the storage modulus of PVDF was decreased with the addition of MoS2, while those of PVDF/MoS2-COOH and PVDF/MoS2-NH2 were enhanced to different degrees. The decomposition of the PVDF/MoS2 nanocomposites were also discussed. Relative to neat PVDF, the thermal stability of PVDF was obviously improved with the addition of MoS2, MoS2-COOH and MoS2-NH2, which could be ascribed to the increased degree of crystallinity.


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