23 research outputs found

    Does dynamic vulcanization induce phase separation?

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    Immiscible and miscible blends of poly(vinylidene fluoride) (PVDF) and acrylic rubber (ACM) were subjected to dynamic vulcanization to investigate the effect of crosslinking on phase separation. As a result of different processability, mixing torque behavior of miscible and immiscible blends was significantly different from one another. Scanning electron microscopy (SEM) was used to investigate the morphology of the system. After dynamic vulcanization, submicron ACM droplets were observed in the samples near the binodal curve of the system under mixing conditions. Small angle X-ray scattering (SAXS) and differential scanning calorimetry (DSC) analysis were used to investigate the effect of dynamic vulcanization on the lamellar structure of the system. It was shown that for samples near the boundary of phase separation, increasing the crosslink density led to a decrease in the lamellar long period (L) as a sign of increment of crosslink density induced phase decomposition. Effects of shear rate on the final morphology of the system were investigated by changing the mixing temperature and by comparing the results of dynamic vulcanization at one phase and two phase regions

    Crystalline Structures and α → ÎČ and Îł polymorphs transformation induced by nanoclay in PVDF-based nanocomposite

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    Poly(vinylidene fluoride) (PVDF) nanocomposites were prepared by melt-mixing. The dispersion of clay platelets and rheology of nanocomposites were analyzed using X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and rheometric mechanical spectrometer (RMS). The transformation of α to β and γ phase in PVDF was induced by the addition of nanoclay and subsequently the isothermal crystallization kinetics of neat PVDF and its nanocomposite have been investigated. The interaction between clay nanofillers and PVDF macromolecular chains induced the change of conformation from trans-gauche to all-trans crystal structure in PVDF segment. The isothermal crystallization of PVDF/clay nanocomposites was carried out by Differential Scanning Calorimetry (DSC) technique. The influence of clay platelets on nucleation crystallization rate and Avrami exponent were studied. PVDF/clay nanocomposite showed higher crystallization rate indicating that nanoclay has acted as an effective nucleation agent. This nucleation effect of nanoclay increased the Avrami exponent and decreased the degree of crystallinity. © 2014 World Scientific Publishing Company

    PVDF composite fibers for wireless fall-alert detection

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    As the demand for healthcare devices continues to rise, novel technologies centered on personalized motion monitoring systems are being developed, wherein wearable sensors play a pivotal role. In the present investigation, an innovative wireless apparatus for detecting falls is introduced, which encompasses a specifically engineered pressure sensor composed of polyvinylidene fluoride (PVDF) composite fibers. Our design consists of high ÎČ-phase content of electrospun composites including 0.1 wt% of zinc oxide/reduced graphene oxide (ZnO/rGO) hybrid (mass ratio 90/10) which shows enhanced electrical voltage of 11.36 ± 0.72 V compared to pristine PVDF fiber. This piezoelectric pressure sensor is integrated with a wireless embedded system capable of transmitting an “SOS” message to a mobile phone upon the user's fall experience. Such wearable fall alert detection systems with improved characteristics could benefit the elderly and patients requiring continuous monitoring for possible falls

    Beyond 17% stable perovskite solar module via polaron arrangement of tuned polymeric hole transport layer

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    Operational stability of perovskite solar cells (PSCs) is rapidly becoming one of the pressing bottlenecks for their upscaling and integration of such promising photovoltaic technology. Instability of the hole transport layer (HTL) has been considered as one of the potential origins of short life-time of the PSCs. In this work, by varying the molecular weight (MW) of doped poly(triarylamine) (PTAA) HTL, we improved by one order of magnitude the charge mobility inside the HTL and the charge transfer at the perovskite/HTL interface. We demonstrate that this occurs via the enhancement of polaron delocalization on the polymeric chains through the combined effect of doping strategy and MW tuning. By using high MW PTAA doped combining three different dopant, we demonstrate stable PSCs with typical power conversion efficiencies above 20%, retain more than 90% of the initial efficiency after 1080 hours thermal stress at 85 ⁰C and 87% of initial efficiency after 160 hours exposure against 1 sun light soaking. By using this doping-MW strategy, we realized perovskite solar modules with an efficiency of 17% on an active area of 43 cm2, keeping above 90% of the initial efficiency after 800 hours thermal stress at 85 ⁰C. These results, obtained in ambient conditions, pave the way toward the industrialization of PSC-based photovoltaic technology.Horizon 2020, Ministry of Education and Science of the Russian Federation, Alexander von Humboldt Foundation, German Federal Ministry of Education and Research, Winton Studentship, Lloyd's Register Foundation, Jardine Foundation, Cambridge Trust, EPSR
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