Studies on the reactive polyvinylidene fluoride-polyamide 6 interfaces: rheological properties and interfacial width

Polymer ◽  
2005 ◽  
Vol 46 (7) ◽  
pp. 2365-2371 ◽  
Author(s):  
Yang Wu ◽  
Xiaobo Yu ◽  
Yuming Yang ◽  
Binyao Li ◽  
Yanchun Han
2006 ◽  
Vol 13 (8-9) ◽  
pp. 773-782 ◽  
Author(s):  
J. S. Choi ◽  
S. T. Lim ◽  
H. J. Choi ◽  
A. Pozsgay ◽  
L. Százdi

2019 ◽  
Vol 27 (9) ◽  
pp. 567-581 ◽  
Author(s):  
RDS Zwane ◽  
ER Sadiku ◽  
SS Ray ◽  
NE Luruli

Thermal and rheological properties of polyamide 6/layered double hydroxide (PA6/LDH) composites were studied. Pristine (U-LDH) and organically modified (M-LDH) clays were used in this study. Some evidence of intercalation was observed on the microstructure of PA6/M-LDH samples, while PA6/U-LDH was characterised by microcomposite morphology as shown by the transmission electron microscopy results. The scanning electron microscopy results showed a complete delamination of the M-LDH in the PA6 matrix while U-LDH was evenly dispersed as immiscible tactoids. In the melt state, the M-LDH had a significant influence on the melt microstructure of PA6 matrix when compared to U-LDH. Differential scanning calorimetry results, both dynamic and isothermal experiments, showed that LDH had a heterogeneous nucleating effect on the PA6 matrix, with the U-LDH showing better nucleating effect when compared to M-LDH. The thermogravimetric analysis results showed that M-LDH had a negative influence on the thermal stability of the composites, while U-LDH improved their thermal stability. The X-ray diffraction and dynamic mechanical analysis results showed that the presence of M-LDH promoted the formation of γ-crystallites in the PA6 matrix, while U-LDH composites were dominated by the α-crystallites. This phenomenon had a positive correlation with increasing content of both LDH clays. An overall improved dynamic mechanical properties were observed for PA6/U-LDH when compared to PA6/M-LDH composites.


Nanomaterials ◽  
2020 ◽  
Vol 10 (7) ◽  
pp. 1257 ◽  
Author(s):  
Milad Kamkar ◽  
Soheil Sadeghi ◽  
Mohammad Arjmand ◽  
Ehsan Aliabadian ◽  
Uttandaraman Sundararaj

This study seeks to unravel the effect of carbon nanotube’s physical and chemical features on the final electrical and rheological properties of polymer nanocomposites thereof. Nitrogen-doped carbon nanotubes (N-CNTs) were synthesized over two different types of catalysts, i.e., Fe and Ni, employing chemical vapor deposition. Utilizing this technique, we were able to synthesize N-CNTs with significantly different structures. As a result, remarkable differences in the network structure of the nanotubes were observed upon mixing the N-CNTs in a polyvinylidene fluoride (PVDF) matrix, which, in turn, led to drastically different electrical and rheological properties. For instance, no enhancement in the electrical conductivity of poorly-dispersed (N-CNT)Ni/PVDF samples was observed even at high nanotube concentrations, whereas (N-CNT)Fe/PVDF nanocomposites exhibited an insulative behavior at 1.0 wt%, a semi-conductive behavior at 2.0 wt%, and a conductive behavior at 2.7 wt%. In terms of rheology, the most substantial differences in the viscoelastic behavior of the systems were distinguishable in the medium amplitude oscillatory shear (MAOS) region. The stress decomposition method combined with the evaluation of the elastic and viscous third-order Chebyshev coefficients revealed a strong intra-cycle elastic nonlinearity in the MAOS region for the poorly-dispersed systems in small frequencies; however, the well-dispersed systems showed no intra-cycle nonlinearity in the MAOS region. It was shown that the MAOS elastic nonlinearity of poorly-dispersed systems stems from the confinement of N-CNT domains between the rheometer’s plates for small gap sizes comparable with the size of the agglomerates. Moreover, the intra-cycle elastic nonlinearity of poorly-dispersed systems is frequency-dependent and vanished at higher frequencies. The correlation between the microstructure and viscoelastic properties under large shear deformations provides further guidance for the fabrication of high-performance 3D-printed electrically conductive nanocomposites with precisely controllable final properties for engineering applications.


2005 ◽  
Vol 290 (2) ◽  
pp. 122-127 ◽  
Author(s):  
Wen Shyang Chow ◽  
Zainal A. Mohd Ishak ◽  
J�zsef Karger-Kocsis

2004 ◽  
Vol 36 (9) ◽  
pp. 754-760 ◽  
Author(s):  
Hongzhi Liu ◽  
Tingxiu Xie ◽  
Yuchun Ou ◽  
Xiaoping Fang ◽  
Guisheng Yang

2012 ◽  
Vol 125 (5) ◽  
pp. 4060-4073 ◽  
Author(s):  
Isil Isik-Gulsac ◽  
Ulku Yilmazer ◽  
Goknur Bayram

Author(s):  
Małgorzata Rabiej ◽  
Stanisław Rabiej

To decompose a wide-angle X-ray diffraction (WAXD) curve of a semi-crystalline polymer into crystalline peaks and amorphous halos, a theoretical best-fitted curve, i.e. a mathematical model, is constructed. In fitting the theoretical curve to the experimental one, various functions can be used to quantify and minimize the deviations between the curves. The analyses and calculations performed in this work have proved that the quality of the model, its parameters and consequently the information on the structure of the investigated polymer are considerably dependent on the shape of an objective function. It is shown that the best models are obtained employing the least-squares method in which the sum of squared absolute errors is minimized. On the other hand, the methods in which the objective functions are based on the relative errors do not give a good fit and should not be used. The comparison and evaluation were performed using WAXD curves of seven polymers: isotactic polypropylene, polyvinylidene fluoride, cellulose I, cellulose II, polyethylene, polyethylene terephthalate and polyamide 6. The methods were compared and evaluated using statistical tests and measures of the quality of fitting.


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