Permanganate-Induced Efficient Mineralization of Poly(vinylidene fluoride) and Vinylidene-Fluoride Based Copolymers in Low-Temperature Subcritical Water

2019 ◽  
Vol 58 (29) ◽  
pp. 13030-13040 ◽  
Author(s):  
Ryo Honma ◽  
Hisao Hori ◽  
Fernando Reis da Cunha ◽  
Naoki Horiike ◽  
Lucia Steinbach ◽  
...  
2017 ◽  
Vol 94 ◽  
pp. 322-331 ◽  
Author(s):  
Hisao Hori ◽  
Hirotaka Tanaka ◽  
Takahiro Tsuge ◽  
Ryo Honma ◽  
Sanjib Banerjee ◽  
...  

2015 ◽  
Vol 54 (35) ◽  
pp. 8650-8658 ◽  
Author(s):  
Hisao Hori ◽  
Hirotaka Tanaka ◽  
Kengo Watanabe ◽  
Takahiro Tsuge ◽  
Takehiko Sakamoto ◽  
...  

Polymers ◽  
2019 ◽  
Vol 11 (6) ◽  
pp. 1065 ◽  
Author(s):  
Igor O. Pariy ◽  
Anna A. Ivanova ◽  
Vladimir V. Shvartsman ◽  
Doru C. Lupascu ◽  
Gleb B. Sukhorukov ◽  
...  

This study was dedicated to the investigation of poly(vinylidene fluoride) (PVDF) micropillar arrays obtained by soft lithography followed by phase inversion at a low temperature. Reduced graphene oxide (rGO) was incorporated into the PVDF as a nucleating filler. The piezoelectric properties of the PVDF-rGO composite micropillars were explored via piezo-response force microscopy (PFM). Fourier transform infrared spectroscopy (FTIR) and X-ray diffraction (XRD) showed that α, β, and γ phases co-existed in all studied samples, with a predominance of the γ phase. The piezoresponse force microscopy (PFM) data provided the local piezoelectric response of the PVDF micropillars, which exhibited a temperature-induced downward dipole orientation in the pristine PVDF micropillars. The addition of rGO into the PVDF matrix resulted in a change in the preferred polarization direction, and the piezo-response phase angle changed from −120° to 20°–40°. The pristine PVDF and PVDF loaded with 0.1 wt % of rGO after low-temperature quenching were found to possess a piezoelectric response of 86 and 87 pm/V respectively, which are significantly higher than the |d33eff| in the case of imprinted PVDF 64 pm/V. Thus, the addition of rGO significantly affected the domain orientation (polarization) while quenching increased the piezoelectric response.


2020 ◽  
Vol 91 (3) ◽  
pp. 31301
Author(s):  
Nabil Chakhchaoui ◽  
Rida Farhan ◽  
Meriem Boutaldat ◽  
Marwane Rouway ◽  
Adil Eddiai ◽  
...  

Novel textiles have received a lot of attention from researchers in the last decade due to some of their unique features. The introduction of intelligent materials into textile structures offers an opportunity to develop multifunctional textiles, such as sensing, reacting, conducting electricity and performing energy conversion operations. In this research work nanocomposite-based highly piezoelectric and electroactive β-phase new textile has been developed using the pad-dry-cure method. The deposition of poly (vinylidene fluoride) (PVDF) − carbon nanofillers (CNF) − tetraethyl orthosilicate (TEOS), Si(OCH2CH3)4 was acquired on a treated textile substrate using coating technique followed by evaporation to transform the passive (non-functional) textile into a dynamic textile with an enhanced piezoelectric β-phase. The aim of the study is the investigation of the impact the coating of textile via piezoelectric nanocomposites based PVDF-CNF (by optimizing piezoelectric crystalline phase). The chemical composition of CT/PVDF-CNC-TEOS textile was detected by qualitative elemental analysis (SEM/EDX). The added of 0.5% of CNF during the process provides material textiles with a piezoelectric β-phase of up to 50% has been measured by FTIR experiments. These results indicated that CNF has high efficiency in transforming the phase α introduced in the unloaded PVDF, to the β-phase in the case of nanocomposites. Consequently, this fabricated new textile exhibits glorious piezoelectric β-phase even with relatively low coating content of PVDF-CNF-TEOS. The study demonstrates that the pad-dry-cure method can potentially be used for the development of piezoelectric nanocomposite-coated wearable new textiles for sensors and energy harvesting applications. We believe that our study may inspire the research area for future advanced applications.


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