Simulations of High-Strain Electrostrictive Chlorinated Terpolymers

2003 ◽  
Vol 785 ◽  
Author(s):  
George J. Kavarnos ◽  
Thomas Ramotowski

ABSTRACTChlorinated poly(vinylidene fluoride/trifluoroethylene) terpolymers are remarkable examples of high strain electrostrictive materials. These polymers are synthesized by copolymerizing vinylidene fluoride and trifluoroethylene with small levels of a third chlorinated monomer. The electromechanical responses of these materials are believed to originate from the chlorine atom, which, by its presence in the polymer chains and by virtue of its large van der Waals radius, destroys the long-range crystalline polar macro-domains and transforms the polymer from a normal to a high-strain relaxor ferroelectric. To exploit the strain properties of the terpolymer, it is desirable to understand the structural implications resulting from the presence of the chlorinated monomer. To this end, computations have been performed on model superlattices of terpolymers using quantum-mechanical based force fields. The focus has been on determining the energetics and kinetics of crystallization of the various polymorphs that have been identified by x-ray diffraction and fourier transform infrared spectroscopy. The chlorinated monomer is shown to act as a defect that can be incorporated into the lamellar structures of annealed terpolymer without a high cost in energy. The degree of incorporation of the chlorinated monomer into the crystal lattice is controlled by annealing conditions and ultimately determines the ferroelectric behavior of the terpolymers.

2007 ◽  
Vol 124-126 ◽  
pp. 1117-1120 ◽  
Author(s):  
Dong Wook Chae ◽  
Young Wan Nam ◽  
Seung Sangh Wang ◽  
S.M. Hong

Poly(vinylidene fluoride) (PVDF) / multi-walled carbon nanotube (MWNT) thermoplastic composites was melt compounded in an internal mixer. The percolation level for this system in electrical conductivity clearly occured between 2 and 2.5 wt%. PVDF/MWNT thermoplastic composites exhibited an increased crystallization temperature with the loading level, at 10 wt% loading by ca. 6. In addition, they presented a shoulder posterior to the main melting peak and an increased endpoint of the peak. In the Wide Angle X-ray Diffraction (WAXD) patterns, the incorporation of MWNT produced a larger shoulder at 2θ =20.7° with increasing the loading level, corresponding to the β-form crystal of PVDF.


Author(s):  
Anubha Bhatla ◽  
Y. Lawrence Yao

Crystallinity of semicrystalline polymers such as aliphatic homopolymer poly(L-lactic acid) (PLLA) affects their degradation and physical properties. In this paper, the effects of laser irradiation using the third harmonic of a Nd:YAG laser on the crystallinity, long-range order, and short-range conformations at the surface of PLLA films are investigated. The factors affecting the transformation are also studied. Detailed characterization of the effect of laser treatment is accomplished using microscopy, X-ray diffraction, and infrared spectroscopy. The cooling rates in the process and the spatial and temporal temperature profiles are numerically examined. The simulation results in conjunction with melting and crystallization kinetics of PLLA are used to understand the effect on sample crystallinity. The effects of laser fluence and annealing conditions on the crystallinity of the processed films are examined. Since degradation profiles depend on crystallinity, laser processing can potentially be used to achieve a modified spatially controlled polymer surface with promising applications such as controlled drug delivery.


Polimery ◽  
2021 ◽  
Vol 66 (10) ◽  
pp. 532
Author(s):  
Aminatul Sobirah Zahari ◽  
Muhammad Hafiz Mazwir ◽  
Izan Izwan Misnon

A significant influence of the molecular weight on the dielectric properties and piezoelectric constant of poly(vinylidene fluoride) (PVDF) membranes obtained by electrospinning was demonstrated. Electrochemical impedance spectroscopy and d33 meter were used to evaluate dielectric properties and piezoelectric constant respectively. The presence of the β-phase was determined by Fourier transform infrared spectroscopy (FTIR) and X-Ray diffraction (XRD). The membranes with the lowest molecular weight (180,000 g/mol) possessed the best dielectric properties. They also had the highest piezoelectric constant (21 pC/N) and dielectric constant (2.9 at 50 Hz) as well as the highest β-phase content (80.25%).


2012 ◽  
Vol 591-593 ◽  
pp. 1113-1116
Author(s):  
Si Chen Cheng ◽  
Yin Zheng Liang ◽  
Yi Ping Qiu

The electrospinning technique was used to produce poly (vinylidene fluoride) (PVDF) membrane. Thermal treatment was introduced to improve the mechanical property and dimensional stability. In this paper, the PVDF membranes before and after thermal treatment were characterized by Scanning electron microscope (SEM), differential scanning calorimeter (DSC) and wide angle X-ray diffraction (WAXD), tensile testing. The crystallinity, tensile property, as well as melting temperature changed with the treated temperature. The results hows that thermal treatment could notably increase the tensile property of electrospun PVDF membrane and 160°C is a proper temperature for thermal treating


2014 ◽  
Vol 1070-1072 ◽  
pp. 589-593
Author(s):  
Fei Peng Wang ◽  
Zheng Yong Huang ◽  
Jian Li

Commercial poly (vinylidene fluoride) (PVDF) films are uniaxially stretched with varying rates at 110 °C in order to endow PVDF piezo-and pyroelectric by crystalline-phase transition from α to β during the stretching. The crystalline phases are determined by infrared spectroscopy. The β-phase content and its fraction in films increase as a result of stretching with high rates. In addition, higher stretching rates yield a slight increase of γ phase. The crystallite size is evaluated by means of X-ray diffraction. It is found that the β-phase crystallites become smaller with fast stretching, whereas the α-phase crystallites are cracked and disappear at high-speed stretching of 2.5 /min.


2016 ◽  
Vol 23 (03) ◽  
pp. 1650005 ◽  
Author(s):  
IBTISAM YAHYA ABDULLAH ◽  
MUHAMMAD YAHAYA ◽  
MOHAMMAD HAFIZUDDIN HJ JUMALI ◽  
HAIDER MOHAMMED SHANSHOOL

The effect of substrate on the crystalline phase and morphology of the poly (vinylidene fluoride) (PVDF) thin film has been investigated. The solution of PVDF/Hexamethyl phosphoramide (HMPA) was deposited on four different substrates, namely, silicon (Si), glass (SiO2), indium tin oxide (ITO) coated glass and silver (Ag) coated glass respectively by using the spin coating technique. The crystalline structure was investigated using X-ray diffraction (XRD) and Fourier transform infrared (FTIR) techniques. The morphology was determined using scanning electron microscopy (SEM). XRD demonstrated that the structure of PVDF thin films on each substrate is [Formula: see text]-phase with different orientations of the molecular chains. FTIR results confirmed XRD that the samples contain [Formula: see text]-phase. SEM shows spherulites structure, which is rough and porous, besides, the size of spherulites and the porosity are different for each sample. The size of spherulites is in average diameter range (1–6[Formula: see text][Formula: see text]m) and this range is attributed to the [Formula: see text]-phase. The nucleation process of [Formula: see text]-phase on the various substrates attributed either to the match of polymer-substrate or to the electrostatic interaction. Among the substrates used, the ITO substrate exhibited a greater tendency for [Formula: see text]-phase formation.


Author(s):  
Rachel C. Huber ◽  
Erik B. Watkins ◽  
Dana M. Dattelbaum ◽  
Richard L. Gustavsen

Abstract Understanding the kinetics of phase transitions, including decomposition from reactants to products under extreme condition events is challenging. Capturing these processes require: 1) diagnostics that probe on the timescales and at energies capable of interacting with the dynamically evolving products, penetrating the opaqueness of the changing system; and 2) detectors sensitive enough to observe these events. Synchrotrons and free electron lasers provide ke-V-energy x-ray beams capable of penetrating the optical-opaqueness of the temporally evolving products. At the Dynamic Compression Sector at the Advanced Photon Source, the x-ray beam is coupled to single and two-stage gas guns capable of producing planar shocks at a range of projectile velocities while capturing in situ x-ray diffraction/scattering of the evolving material under dynamic compression. In this work, we demonstrate the utility of this approach in measuring the evolution of crystalline domains in shocked high-density polyethylene to P = 7.45 GPa, and have observed the compression and orientation of the polymer chains in real time.


2018 ◽  
Vol 33 (1) ◽  
pp. 138-149 ◽  
Author(s):  
MA Ramazanov ◽  
AM Maharramov ◽  
HA Shirinova ◽  
Luca Di Palma

In the present study, the effect of magnetite (Fe3O4) nanoparticles on the structural and dielectric properties of poly(vinylidene fluoride) (PVDF) matrix was investigated. Distribution of Fe3O4 nanoparticles in the polymer matrix has been studied by scanning electron microscopy (JEOL JSM-7600 F). The structure of the nanocomposite samples was investigated by the X-ray diffraction and Fourier-transform infrared spectroscopy. It was shown that the dielectric permittivity of PVDF + Fe3O4 nanocomposite samples was gradually increased up to 7 wt% of Fe3O4 content. Further increase in the concentration of the filler leads to decrease in the dielectric permittivity. The subsequent decrease in dielectric permittivity at higher Fe3O4 content can be explained by the increase in defects in the structure of the nanocomposite. The comparison of experimental data and the results of theoretical calculations show that the reduction in the empirical value of dielectric permittivity of the nanocomposite is obviously linked with the threshold value of filler. While calculating the theoretical value of the dielectric permittivity for the higher content of the filler, defects in the nanocomposite structure should be considered.


2005 ◽  
Vol 59 (3) ◽  
pp. 275-279 ◽  
Author(s):  
C. J. L. Constantino ◽  
A. E. Job ◽  
R. D. Simões ◽  
J. A. Giacometti ◽  
V. Zucolotto ◽  
...  

The phase transition from the non-polar α-phase to the polar β-phase of poly(vinylidene fluoride) (PVDF) has been investigated using micro-Raman spectroscopy, which is advantageous because it is a nondestructive technique. Films of α-PVDF were subjected to stretching under controlled rates at 80 °C, while the transition to β-PVDF was monitored by the decrease in the Raman band at 794 cm−1 characteristic of the α-phase, along with the concomitant increase in the 839 cm−1 band characteristic of the β-phase. The α→β transition in our PVDF samples could be achieved even for the sample stretched to twice (2×-stretched) the initial length and it did not depend on the stretching rate in the range between 2.0 and 7.0 mm/min. These conclusions were corroborated by differential scanning calorimetry (DSC) and X-ray diffraction experiments for PVDF samples processed under the same conditions as in the Raman scattering measurements. Poling with negative corona discharge was found to affect the α-PVDF morphology, improving the Raman bands related to this crystalline phase. This effect is minimized for films stretched to higher ratios. Significantly, corona-induced effects could not be observed with the other experimental techniques, i.e., X-ray diffraction and infrared spectroscopy.


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