nanocomposite fibers
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Author(s):  
Giovanni Spiaggia ◽  
Patricia Taladriz-Blanco ◽  
Dedy Septiadi ◽  
Roberto Diego Ortuso ◽  
Aaron Lee ◽  
...  
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Materials ◽  
2021 ◽  
Vol 14 (19) ◽  
pp. 5699
Author(s):  
Paulina Latko-Durałek ◽  
Povilas Bertasius ◽  
Jan Macutkevic ◽  
Juras Banys ◽  
Anna Boczkowska

Polymer composites containing carbon nanofillers are extensively developed for electromagnetic shielding applications, where lightweight and flexible materials are required. One example of the microwave absorbers can be thermoplastic fibers fabricated from copolyamide hot melt adhesives and 7 wt % of multi-walled carbon nanotubes, as presented in this paper. A broadband dielectric spectroscopy confirmed that the addition of carbon nanotubes significantly increased microwave electrical properties of the thin (diameter about 100 μm) thermoplastic fibers. Moreover, the dielectric properties are improved for the thicker fibers, and they are almost stable at the frequency range 26–40 GHz and not dependent on the temperature. The variances in the dielectric properties of the fibers are associated with the degree of orientation of carbon nanotubes and the presence of bundles, which were examined using a high-resolution scanning microscope. Analyzing the mechanical properties of the nanocomposite fibers, as an effect of the carbon nanotubes addition, an improvement in the stiffness of the fibers was observed, together with a decrease in the fibers’ elongation and tensile strength.


2021 ◽  
pp. 1-12
Author(s):  
Chengfei Yue ◽  
Changkun Ding ◽  
Bowen Cheng ◽  
Xuan Du ◽  
Jieliang Su

2021 ◽  
Vol 899 ◽  
pp. 381-386
Author(s):  
Gleb Vaganov ◽  
Elena Ivan’kova ◽  
Vladimir Yudin ◽  
Vyacheslav Vaganov

In the present work, fibers based on heat-resistant amorphous polyimide brand Ultem-1000 were prepared by melt extrusion. Vapor-grown carbon nanofibers (VGCFs) and single-wall carbon nanotubes (SWCNTs) were used to increase the mechanical characteristics of the polymer fibers. The fibers were characterized by scanning electron microscopy (SEM), thermophysical and mechanical tensile analysis. SEM study revealed very good distribution of the carbon nanofillers throughout the polyimide fiber volume. The mechanical testing of the unoriented nanocomposite fibers showed that the introduction of VGCFs or SWCNTs led to an increase in tensile strength and modulus. High-temperature drawing allows obtaining polyimide nanocomposite fibers with significantly increased mechanical properties (»300 MPa for strength and »4.6 GPa for modulus).


Nanomaterials ◽  
2021 ◽  
Vol 11 (8) ◽  
pp. 2153
Author(s):  
Fatemeh Mokhtari ◽  
Geoffrey M Spinks ◽  
Sepidar Sayyar ◽  
Javad Foroughi

Piezoelectric fibers have an important role in wearable technology as energy generators and sensors. A series of hybrid nanocomposite piezoelectric fibers of polyinylidene fluoride (PVDF) loaded with barium–titanium oxide (BT) and reduced graphene oxide (rGO) were prepared via the melt spinning method. Our previous studies show that high-performance fibers with 84% of the electroactive β-phase in the PVDF generated a peak output voltage up to 1.3 V and a power density of 3 W kg−1. Herein, the dynamic mechanical and creep behavior of these fibers were investigated to evaluate their durability and piezoelectric performance. Dynamic mechanical analysis (DMA) was used to provide phenomenological information regarding the viscoelastic properties of the fibers in the longitudinal direction. DSC and SEM were employed to characterize the crystalline structure of the samples. The storage modulus and the loss tangent increased by increasing the frequency over the temperature range (−50 to 150 °C) for all of the fibers. The storage modulus of the PVDF/rGO nanocomposite fibers had a higher value (7.5 GPa) in comparison with other fibers. The creep and creep recovery behavior of the PVDF/nanofillers in the nanocomposite fibers have been explored in the linear viscoelastic region at three different temperatures (10–130 °C). In the PVDF/rGO nanocomposite fibers, strong sheet/matrix interfacial interaction restricted the mobility of the polymer chains, which led to a higher modulus at temperatures 60 and 130 °C.


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