A FTIR study of PVDF irradiated by means of swift heavy ions

Poly(vinylidene difluoride) (PVDF) films were irradiated by means of heavy ions (in the electronic stopping-power range) and electrons. Both types of ionizing radiation induce in the polymer film ionizations and excitations, but swift heavy ions induce a huge density of excitations and ionizations along the ion path. Dose-range goes from 0.3 to 40 MGy. Irradiations were performed with Kr ions in the presence of helium, hydrogen, deuterium, and oxygen. Fourier transform infrared (FTIR) transmission measurements show differences in the nature of the created defects. Triple bonds are characteristic of the Kr ion irradiation. Double bonds, isolated and conjugated, exist for both kinds of radiation, but concentrations are higher with the Kr radiation. The presence of oxygen during irradiation produces oxidization defects. Typical bands of hydroxyls and carbonyls can be seen, respectively, in the 3800-3000 cm^?1 zone and ca. 1850–1730 cm^?1. The formation of conjugated double bonds is enhanced when the Kr irradiation is performed under an O₂ atmosphere. © 1994 John Wiley & Sons, Inc.     

Ferro-electric ceramics versus polymer piezoelectric materials

A wide variety of transducer shapes and applications exists in the field of diagnostic ultrasound. As a basic material ferro-electric ceramics are used almost exclusively, but polymer piezoelectric material seems a new alternative. By comparing in a qualitative way the most relevant parameters of these materials, a state of the art judgement may be made about their applicability in diagnostic ultrasound.     

强脉冲激光在AZ31B镁合金中诱导冲击波的实验研究

为了研究强脉冲激光在镁合金中诱导冲击波的衰减,采用Nd:Glass脉冲激光(1054 nm,23 ns)对AZ31B变形镁合金试样表面进行冲击,并利用响应快、测量范围大的PVDF压电膜传感器以及示波器实时测量了强脉冲激光在镁合金靶中诱导激光冲击波的相对压力.根据冲击波每次在靶材背面反射时,所经过距离的不同得到激光冲击波在镁合金中的衰减规律.结果表明,在激光能量为5J的强脉冲激光作用下,镁合金中冲击波衰减的平均速度为5.83×10³ m/s,与镁合金中应力波纵波的传播速度相符;强脉冲激光诱导冲击波在镁合金中是以指数规律衰减的.试验所得分析结果对激光冲击强化镁合金的应用具有重要意义. 关键词： 激光 镁合金 压电膜传感器 衰减规律     

PVDF压电计的动态响应特性及其在橡胶材料SHPB实验中的应用

通过夹心式PVDF(Polyvinylide Fluoride)压电计的动态分离式Hopkinson压杆(SHPB)标定实验,系统地讨论了传感器的动态响应特性,其中包括测量电路、PVDF表面应力集中、压电计的材料及结构特性和同一压电计受多次撞击对测试信号的影响,为PVDF压电计的制作工艺研究提供参考。利用标定好的压电计测试了橡胶材料在SHPB实验中的动态应力均匀过程。结果表明:调节并联电阻值可以提高压电计的传感精度;增大压电计的敏感面积可以减小因应力集中所造成的信号失真;材料的热粘塑性性质、摩擦效应等将使信号振荡幅度偏小;多次撞击对信号的加载与卸载段都将产生影响,但当传感器表面未发生明显损伤时,测试的应力平台平均值与真实信号近似相同。     

An Atomic Force Microscopy Observation of Poly(Vinylidene Fluoride) Banded Spherulites

We examined the free surface of a banded spherulite of poly (vinylidene fluoride) (PVDF) by atomic force microscopy. The directions of the slope of multilayer terraces of lamellar crystals are retained in each half of a banded spherulite; this evidence confirms the macroscopic selection of one-handedness in the formation of spiral terraces in each growth direction of the sheaf at the center of banded spherulite of PVDF. In a previous paper, it was confirmed that the three-dimensional morphology of all single crystals of PVDF grown from the melt is of chair-type, and hence, it is most probable that the stress in the chair crystal is responsible for the formation of spiral dislocations and terraces keeping the same handedness in each growth direction. The chair-type morphology is created because of the chain tilting to the fold surface, which can introduce symmetry breaking and, consequently, the selection of handedness in nonchiral polymers such as PVDF.     

α to β Phase Transformation and Microestructural Changes of PVDF Films Induced by Uniaxial Stretch

The phase transformation from α to β poly(vinylidene fluoride) (PVDF) through a stretching process at different temperatures was investigated. Samples of originally α-PVDF were stretched uniaxially at different temperatures at draw ratios from 1 to 5. The stretched samples were studied and characterized by infrared spectroscopy, scanning electron microscopy, and differential scanning calorimetry. The maximum β-phase content was achieved at 80°C and a stretch ratio of 5, but the samples still showed 20% of the original α-phase. Accompanying the phase transformation, an orientation of the polymer chains was observed. The stretching process also influenced the degree of crystallinity of the polymer. Poling of the samples also improves the α- to β-phase transformation.     

Protection of Li metal anode by surface-coating of PVDF thin film to enhance the cycling performance of Li batteries

The PVDF thin film on the surface of the lithium metal can highly suppress the lithium dendrites.     

Enhanced antifouling performance of ZnS/GO/PVDF hybrid membrane by improving hydrophilicity and photocatalysis

In order to improve the antifouling performance of PVDF membrane, a novel zinc sulfide/graphene oxide/polyvinylidene fluoride (ZnS/GO/PVDF) composite membrane was prepared by immersed phase inversion method. The surface morphology, crystal structure, photocatalytic activity, and antifouling property of the as‐prepared membranes were systematically studied. Results showed that the ZnS/GO/PVDF hybrid membranes were successfully fabricated with uniform surface. The hybrid membrane surface possessed higher hydrophilicity with water contact angle decreasing from 77.1° to 62.2°. The permeability of the hybrid membrane was therefore enhanced from 222.9 to 326.1 L/(m² hour). Moreover, bovine serum albumin (BSA) retention experiment showed that the hybrid membrane separation was also promoted by 7.2%. The blending of ZnS and GO enhanced the hydrophilic and photocatalytic performances of PVDF membrane, which mitigated the membrane fouling effectively. This novel hybrid membrane could accelerate the practical application of photocatalytic technology in membrane separation process.     

Polyamide 11/Poly(vinylidene fluoride) Blends as Novel Flexible Materials for Capacitors

A novel capacitor with high dielectric constant (ε) has been developed by blending poly(vinylidene fluoride) (PVDF) with polyamide (PA11). The blends show high dielectric constants (ε_blend = 40), which give better frequency stability (1 MHz), and excellent mechanical properties. Based on certain volume fractions, the measured dielectric constants (ε _blend ) were found to exceed those of the corresponding polymers, in contrasted to conventional composites, where ε_polymerA < ε_composite < ε_polymerB. SEM investigations suggest that the enhanced dielectric behavior originates from significant interfacial polymer‐polymer interactions. DSC and XRD demonstrate that blending PA11 with PVDF affects the crystalline behavior of each component. However, the PA11/PVDF blends exhibit a slightly high dielectric loss (tanδ ≈ 0.17), which is a great disadvantage to a capacitor. Adding a copolymer of styrene and maleic anhydride decreased the dielectric loss (tanδ ≈ 0.057) and increased the dielectric constant (ε_blend = 60). Our findings suggest that the high‐ε polymeric blends created represent a novel type of material that is flexible and easy to process, of relatively high dielectric constant, of high breakdown strength and, moreover, is suited to applications in flexible electronics.

     

Iodine-transfer polymerization and CuAAC “click” chemistry: A versatile approach toward poly(vinylidene fluoride)-based amphiphilic triblock terpolymers

This study presents the synthesis and properties of linear PVDF-based amphiphilic triblock terpolymers with PS and PEO, [PVDF-b-PS-b-PEO], by adopting a procedure that involves: (a) iodine-transfer polymerization (ITP) of VDF with 1-iodoperfluorohexane (C₆F₁₃I) serving as chain-transfer agent (CTA) to afford C₆F₁₃-PVDF-I, (b) ITP of styrene with the C₆F₁₃-PVDF-I macromolecular-CTA to obtain C₆F₁₃-PVDF-b-PS-I diblock copolymer, (c) end-group exchange from iodo- to azido-group by nucleophilic substitution reaction with NaN_3, and (d) copper-catalyzed azide-alkyne cycloaddition (CuAAC) with alkyne-terminated PEO to achieve C₆F₁₃-PVDF-b-PS-b-PEO triblock terpolymers. The ¹H and ¹⁹F NMR spectroscopy confirmed the presence of all blocks, while gel permeation chromatography traces showed the living nature of ITP technique. The self-assembly of these terpolymers was investigated in films (atomic force microscopy and DSC), as well as in aqueous and organic solvents (DLS). The analysis of crystalline phases based on the FTIR spectroscopy indicated the conversion of PVDF α-phase into α + β-phases and β + γ-phases upon the incorporation of PS and PEO blocks, respectively. The synthesized amphiphilic copolymers were evaluated (fluorescence spectroscopy) as carriers of small hydrophobic molecules in water. © 2019 Wiley Periodicals, Inc. J. Polym. Sci. 2020 , 58, 163–171