Direct Observation of Crystal Transformation Process of Poly (vinylidene fluoride) under High Pressure by PSPC X-Ray System

1978 ◽  
Vol 17 (3) ◽  
pp. 467-472 ◽  
Author(s):  
Kazumi Matsushige ◽  
Kiyofumi Nagata ◽  
Tetuo Takemura
1980 ◽  
Vol 51 (10) ◽  
pp. 5508 ◽  
Author(s):  
J. M. Schultz ◽  
J. S. Lin ◽  
R. W. Hendricks ◽  
R. R. Lagasse ◽  
R. G. Kepler

Author(s):  
A. M. Kuvshinov ◽  
S. S. Chebotaryov ◽  
L. A. Pesin ◽  
I. V. Gribov ◽  
N. A. Moskvina ◽  
...  

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.


Nanomaterials ◽  
2021 ◽  
Vol 11 (8) ◽  
pp. 2099
Author(s):  
Teng-Hui Wang ◽  
Wei-Xiang Wang ◽  
Hai-Chou Chang

The nanostructures of ionic liquids (ILs) have been the focus of considerable research attention in recent years. Nevertheless, the nanoscale structures of ILs in the presence of polymers have not been described in detail at present. In this study, nanostructures of ILs disturbed by poly(vinylidene fluoride) (PVdF) were investigated via high-pressure infrared spectra. For 1-(2-hydroxyethyl)-3-methylimidazolium bis(trifluoromethanesulfonyl)imide ([HEMIm][TFSI])-PVdF mixtures, non-monotonic frequency shifts of the C4,5-H vibrations upon dilution were observed under ambient pressure. The experimental results suggest the presence of microheterogeneity in the [HEMIm][TFSI] systems. Upon compression, PVdF further influenced the local structure of C4,5–H via pressure-enhanced IL–PVdF interactions; however, the local structures of C2–H and hydrogen-bonded O–H were not affected by PVdF under high pressures. For choline [TFSI]–PVdF mixtures, PVdF may disturb the local structures of hydrogen-bonded O–H. In the absence of the C4,5–H⋯anion and C2–H⋯anion in choline [TFSI]–PVdF mixtures, the O–H group becomes a favorable moiety for pressure-enhanced IL–PVdF interactions. Our results indicate the potential of high-pressure application for designing pressure-dependent electronic switches based on the possible changes in the microheterogeneity and electrical conductivity in IL-PVdF systems under various pressures.


Polymer ◽  
1980 ◽  
Vol 21 (12) ◽  
pp. 1391-1397 ◽  
Author(s):  
K. Matsushige ◽  
K. Nagata ◽  
S. Imada ◽  
T. Takemura

2006 ◽  
Vol 13 (02n03) ◽  
pp. 259-263 ◽  
Author(s):  
KOJI KAMIYA OKUDAIRA ◽  
EIICHI KOBAYASHI ◽  
KAZUHIKO MASE ◽  
SATOSHI KERA ◽  
NOBUO UENO

Poly(vinylidene fluoride) (PVDF, –( CH 2– CF 2)n–) shows the effective H + desorption induced by the irradiation of photon corresponding to the transition from carbon ( C ) 1s to σ( C – H )*. In order to clarify the effect of the C – H bond scission by the irradiation, near-edge X-ray absorption fine structure (NEXAFS) spectra and the kinetic energy (Ek) distribution of desorbed ion were observed. By the irradiation of photon near C 1s region, a new peak appears in the C 1s NEXAFS spectra at photon energy of 285 eV, which is about 3 eV lower than that of the lowest peak in the NEXAFS spectrum of the pristine PVDF film. The appearance of the lowest NEXAFS peak of irradiated PVDF film is assigned to the transition to π*. It indicates that the irradiation of photons near C 1s region introduces carbon–carbon double bonds into the backbone chain of PVDF. At early stage of X-ray exposure the yield of desorbed ion with low Ek (~ 2 eV) decreases rapidly. The ion with low Ek is assigned to H + desorbed from the sp3-hybrid state, which is characteristics of the pristine PVDF. It indicates that formation of double bonds in PVDF backbone chain makes the number of sp3-hybrid state decrease. This variation occurs by irradiation of photons corresponding to the transition from C 1s to σ( C – H )* more rapidly than that to the transition to σ( C – F )*.


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