Piezoelectric two-layer stacks of cellular polypropylene ferroelectrets: transducer response at audio and ultrasound frequencies

Piezoelectric cellular polypropylene films, so-called ferroelectrets, are assembled in a stack with two active transducer layers. The stack is characterized with respect to its linear and quadratic response in a frequency range from 1 kHz to 80 kHz. A relatively smooth frequency response in the sound-pressure level is found for the individual layers as well as for both layers driven in phase. The piezoelectric response of the two-layer stack is twice the response of an individual layer over a rather broad frequency range. Furthermore, the influence of the preparation conditions on the resonance frequency and the effect of the quadratic distortion on the radiated sound are investigated both for the individual transducer films in the stack and for the stack system as a whole.     

Reentrant phase transition and fast responsive behaviors of poly{N‐[3‐(dimethylaminopropyl)] methacrylamide} hydrogels prepared in poly(ethylene glycol) solutions

Macroporous temperature‐sensitive poly {N‐[3‐(dimethylaminopropyl)] methacrylamide} hydrogels were synthesized by free‐radical crosslinking polymerization of the monomer N‐[3‐(dimethylaminopropyl)] methacrylamide and the crosslinker N,N′‐methylenebisacrylamide in aqueous solutions at 22°C. Poly(ethylene glycol) (PEG) with a molecular weight of 1000 g/mol was used as the pore‐forming agent during the polymerization reaction. The concentration of PEG in the polymerization solutions was varied between 0 and 18 wt %, whereas the crosslinker (N,N′‐methylenebisacrylamide) concentration was fixed at 2 wt % (with respect to the monomer). The effects of the PEG concentration on the thermo‐induced phase‐transition behavior and the chemical structure, interior morphology, and swelling/deswelling kinetics were investigated. Normal‐type hydrogels were also prepared under the same conditions without PEG. An interesting feature of the swelling behavior of both the normal‐type and macroporous hydrogels was the reentrant phase transition, in which the hydrogels collapsed once and reswelled as the temperature was continuously increased. Scanning electron micrographs revealed that the interior network structure of the hydrogels prepared in PEG solutions became more porous with an increase in the PEG concentration in the polymerization solution. This more porous matrix provided numerous water channels for water diffusion in or out of the matrix and, therefore, an improved responsive rate to external temperature changes during the deswelling and swelling processes. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Current scenario and potential of biodiesel production from waste cooking oil in Pakistan: An overview

Biodiesel utilization has been rapidly growing worldwide as the prime alternative to petrodiesel due to a global rise in diesel fuel demand along with hazardous emissions during its thermochemical conversion. Although, several debatable issues including feedstock availability and price, fuel and food competition, changes in land use and greenhouse gas emission have been raised by using edible as well as inedible feedstocks for the production of biodiesel. However, non-crop feedstocks could be a promising alternative. In this article, waste cooking oils have been recommended as a suitable option for biodiesel production bearing in mind the current national situation. The important factors such as the quantity of waste cooking oil produced, crude oil and vegetable oil import expenses, high-speed diesel imports, waste management issues and environmental hazards are considered. Moreover, process simulation and operating cost evaluation of an acid catalyzed biodiesel production unit are also conducted. The simulation results show that the production cost of waste cooking oil-based biodiesel is about 0.66USD·L^-1. We believe that the present overview would open new pathways and ideas for the development of biofuels from waste to energy approach in Pakistan.     

The Influence of Al2O3 and TiO2 Additives on the Electrical Resistivity of Epoxy Resin‐Based Composites at Low Temperature

Electrical insulation is a major security problem in aerospace applications where temperature can reach relatively low values. Epoxy resins are well known as easily formable dielectric materials and can be used to prepare complex insulator parts. In this study, the electrical performance of bisphenol A/epichlorohydrin epoxy resin matrix‐based nanocomposites containing 1, 3, or 6 wt% titanium oxide (TiO₂) or aluminium oxide (Al₂O₃) nanofillers are investigated. Composites are characterized with thermogravimetric analysis, scanning electron microscopy‐coupled electron dispersive spectroscopy, and confocal Raman spectroscopy. Furthermore, the role of additives and their ratio on the resistivity performance of the composites are evaluated from 77 to 500 K by applying a direct current voltage from 1 to 20 V. It is observed that the electrical properties of the matrix are directly influencing the insulation performance of the nanocomposite. For example, the abrupt decrease at 370 K of the positive temperature coefficient of the resin for all nanocomposites. It is found that the most resistive composite contains 3 wt% TiO₂ nanoparticles with a value above 3.7.10¹⁰ Ω from 77 to 370 K at 20 V. As a result, this work gives information on to the choice of appropriate insulator materials in extreme working conditions.     

Polyimide-coated fabrics with multifunctional properties: Flame retardant,UV protective,and water proof

Multifunctional technical textiles are of great interest both by industry and academia and these products are considered as high value-added products that contribute to the economies of countries. In this study, polyamic acid (PAA) was synthesized through polycondensation of pyromellitic dianhydride (PMDA) and 4,4′-oxydianiline (ODA) in dimethyl acetamide (DMAc) at low temperature. Then, PAA was coated onto woven cotton and polyester fabric by padding technique. Finally, polyimide (PI)-coated multifunctional cotton and polyester fabrics were obtained by an easy coating technique and low-temperature imidization. Thus, low cost, easily accessible and widely used cotton and polyester fabrics were converted to high-performance textile products, which are flame retardant, UV protective, acid resistant, and waterproof. The chemical, thermal, morphological, optical, mechanical, wettability, chemical resistance, and flame retardancy properties of developed fabrics were investigated. Optical results showed that both PI-coated cotton and polyester fabrics are UV-A protective compared to noncoated fabrics. Moreover, PI-coated samples have high contact angles which are 111.43° and 113.40° for PI-coated cotton (PI-c-C) and PI-coated polyester (PI-c-PET), respectively. Young's modulus of PI-c-PET fabrics increased four times more than noncoated polyester fabric. PI coating changed the burning behavior of both cotton and polyester fabrics in a positive way. All the test results showed that these developed multifunctional textile products might find an application in different industrial areas such as automotive, aerospace, protective clothing, and so on due to easy and inexpensive production techniques and also superior properties. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47616.     

Boosted hydrogen evolution activity from Sr doped ZnO/CNTs nanocomposite as visible light driven photocatalyst

CNTs were decorated onto Sr doped ZnO nanoparticles to construct an efficient photocatalyst via a facile sol-gel method. The as-fabricated Sr doped ZnO/CNTs with recyclability exhibits Sr and CNTs content dependent hydrogen evolution activit under visible light illumination. The Sr doped ZnO/CNTs photocatalyst shows the highest hydrogen evolution rate of 2732.2 μmolh^?1g^?1, which is 33.7 and 2.83 times higher than pure ZnO and Sr doped ZnO photocatalysts, respectively. The improved hydrogen evolution activity of Sr doped ZnO/CNTs is primarily assigned to high surface area, Sr doping and construction of heterojunction, which can extend the light absorption, decrease the optical band gap and improve the charge separation. Moreover, the underlying photocatalytic mechanism is proposed on the basis of Mott-Schottky study and explains the interfacial charge transfer process from ZnO to CNTs and Sr. This work open new strategies to synthesize CNTs based nanocomposite for hydrogen evolution.     

Silicon Mitigates Drought Stress in Wheat (Triticum aestivum L.) Through Improving Photosynthetic Pigments,Biochemical and Yield Characters

Silicon - Feeling prone to stress differs with plant production stage, water scarcity near commencement of grain filling phase has a significant reduced grain yield through fewer endosperm and sink...     

Hydrogen production employing Cu(BDC) metal–organic framework support in methanol steam reforming process within monolithic micro-reactors

Cu(BDC) metal–organic framework (MOF) was used as a support for the copper (Cu) catalyst applied in the methanol steam reforming (MSR) process at low temperatures (130–250 °C) with a feed WHSV = 9.2 h^?1 within the monolithic reactor. Also, the effects of diverse promoters were examined on the catalytic activities of the Cu/X–Cu(BDC) (X = Ce, Zn, Gd, Sm, La, Y, Pr) catalysts. Results showed that the Ce/Sm–Cu(BDC) supports exhibited highest activities, lowest reduction temperatures and largest specific surface areas, which caused highest distributions of the active copper metal nanoparticles on the supports. The reactor tests displayed that the activities of Cu/X–Cu(BDC) (X = Ce, Zn, Gd, Sm, La, Y, Pr) catalysts followed the order X = Ce > Sm > Y > La > Pr > Cu(BDC) > Zn > Gd. The highest activities of Ce and Sm containing catalysts were attributed to the presence of CeO₂ and Sm₂O₃ caused the oxygen vacancies on the catalyst surface which had positive effects on the methanol reforming process. The time-on-stream stability tests showed the highest resistance of the Cu/Ce–Cu(BDC) catalyst to the carbon formation during 32 h. Consequently, the Cu/Ce–Cu(BDC) with the highest stability, methanol conversion and carbon monoxide selectivity could be used in practical industrial applications.     

Feasibility of Ni/Ti and Ni/GF cathodes in microbial electrolysis cells for hydrogen production from fermentation effluent: A step toward real application

The low cost, low over-potential loss, good catalytic properties for hydrogen evolution reaction (HER), high corrosion stability, commercially available, and could be applied in pH-neutral solution and ambient temperature are important properties for the cathode materials when it is applied in microbial electrolysis cell (MEC) technology. This study has two-pronged objectives: the first is to investigate the feasibility of titanium (Ti) and graphite felt (GF) coated with nickel (Ni), and the second is to generate hydrogen from the fermentation effluent (FE). The electrodeposition (ED) method was used to deposit Ni catalyst onto Ti (Ni/Ti) and GF (Ni/GF) surfaces. The scanning electron microscopy (SEM) and energy dispersive X-ray (EDX) spectroscopy were used to characterize the cathode morphology and element composition. The catalytic properties of Ni/Ti and Ni/GF could be evaluated using the linear sweep voltammetry tests. The maximum volumetric H₂ production rates of MEC using Ni/Ti and Ni/GF cathodes were obtained at 0.39 ± 0.01 and 0.33 ± 0.03 m³ H₂ m⁻³ d⁻¹ respectively. The Ni/Ti and Ni/GF cathodes could be used as alternative cathodes while producing hydrogen from FE.