Influence of silane‐coupling agents on the performance of morphological,mechanical, thermal,electrical, and rheological properties of polycarbonate/fly ash composites

Fly ash, waste product of thermal power station, generated in huge quantities has been posing problems of its disposal. As such, it contains a variety of inorganic oxide and is available in finely powder form. Attempts have been made for its utilization, as filler in engineering plastic. The fly ash (FA) fillers reinforced polycarbonate (PC) composites were fabricated using a economically and environmentally viable method of melt extrusion and compression molding technique. The FA surface was chemically modified using vinyltrimethoxysilane and 3–Aminopropyltriethoxysilane. The feasibility of using treated FA/PC composites was examined in terms of scanning electron microscopy, thermogravimetric analysis, differential scanning calorimetry, and rheological behavior. The morphology shows a good dispersion and strong interfacial interaction between PC and modified FA than the unmodified counterpart. Mechanical investigation manifested that modified FAs have strengthening effect (increase in tensile and flexural strength) on the mechanical performance of PC composites. Rheological behavior of PC/FA composites was characterized by parallel plate rheometer system. Addition of treated FA imparted dimensional and thermal stability, which has been observed in scanning electron micrographs and in thermogravimetric analysis plot. The increase of thermal stability has been explained based on increased mechanical interlocking of PC chains inside the structure of FA. This study shows that surface modification of FA is one of the key factors influencing the mechanical and thermal properties of PC/FA composites. POLYM. COMPOS., 2012. © 2012 Society of Plastics Engineers     

Studying the Thermal Properties of a Cotton/Epoxy Composite Inhibitor

The inhibitory effect of double‐base solid propellants is used to control and prevent the burning degree of exposed areas, induced by longer burning time. In recent years, inhibition with cellulose derivatives including cellulose acetate and ethyl cellulose has become popular, but these monolithic systems usually suffer from the drawback of a high erosion rate and demand high thickness and low burning time. A composite inhibitor based on cotton fibers/epoxy resin containing some chlorinated flame retardants (CFR), which were added in inhibitor composition to control its burning process, is described in this article. The thermal properties of the composite inhibitor were studied by thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), thermomechanical analysis (TMA), and flame retardancy. Finally, the inhibited propellant charge, statically fired at ambient temperature, was found to display a smooth and flat pressure‐time profile, confirming the successful performance of the composite inhibition system without the application of any barrier coat.     

Sequence and in vitro function of chicken, ring-necked pheasant, and Japanese quail AHR1 predict in vivo sensitivity to dioxins

There are large differences in sensitivity to the toxic and biochemical effects of dioxins and dioxin-like compounds (DLCs) among vertebrates. Previously, we demonstrated that the difference in sensitivity between domestic chicken (Gallus gallus domesticus) and common tern (Sterna hirundo) to aryl hydrocarbon receptor 1 (AHR1)-dependent changes in gene expression following exposure to 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) is based upon the identities of the amino acids at two sites within the ligand binding domain of AHR1 (chicken--highly sensitive; Ile324_Ser380 vs common tern--250-fold less sensitive than chicken; Val325_Ala381). Here, we tested the hypotheses that (i) the sensitivity of other avian species to TCDD, 2,3,4,7,8-pentachlorodibenzofuran (PeCDF), and 2,3,7,8-tetrachlorodibenzofuran (TCDF) is also determined by the amino acids at sites that are equivalent to sites 324 and 380 in chicken, and (ii) Ile324_Ala380 and Val324_Ser380 genotypes confer intermediate sensitivity to DLCs in birds. We compared ligand-induced transactivation function of full-length AHR1s from chicken, common tern, ring-necked pheasant (Phasianus colchicus; Ile324_Ala380) and Japanese quail (Coturnix japonica; Val324_Ala380), and three Japanese quail AHR1 mutants. The results support our hypothesis that avian species can be grouped into three general classes of sensitivity to DLCs. Both AHR1 genotype and in vitro transactivation assays predict in vivo sensitivity. Contrary to the assumption that TCDD is the most potent DLC, PeCDF was more potent than TCDD at activating Japanese quail (13- to 26-fold) and common tern (23- to 30-fold) AHR1. Our results support and expand previous in vitro and in vivo work that demonstrated ligand-dependent species differences in AHR1 affinity. The findings and methods will be of use for DLC risk assessments.     

Influence of novel surface modifying macromolecules and coagulation media on the gas permeation properties of different polymeric gas separation membranes

Integrally skinned asymmetric membranes for the separation of O₂ and N₂ were fabricated by the phase inversion technique from polysulfone, polyetherimide, and polyimide. Two types of surface modifying macromolecules (SMMs) including hydrophilic SMM (LSMM) and charged SMM (cSMM) were synthesized and blended with the casting solution to modify the membrane surface. The cast film was then immersed in the first coagulant alcohol (methanol, ethanol, or isopropanol) for a predetermined period, before being immersed in the second coagulant (water). The SMMs used in these experiments were laboratory synthesized by the two‐step process of polyurethane prepolymer synthesis and end capping, before being characterized by differential scanning calorimetry. Their molecular structure was determined from the molecular weight obtained by gel permeation chromatography. The membranes were characterized by contact angle measurement and O₂ and N₂ gas permeation performance. Attempts were made to interpret the gas permeation data by delayed demixing affected by solubility parameters of polymer, solvent, and nonsolvent. Furthermore, the permeation performance of cSMM membranes was interpreted by the solvation of the charged sulfonate groups present in cSMM. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Triple-layer proton exchange membranes based on chitosan biopolymer with reduced methanol crossover for high-performance direct methanol fuel cells application

A novel triple-layer proton exchange membrane comprising two thin layers of structurally modified chitosan, as methanol barrier layers, both sides coated with Nafion^®105 is prepared and tested for high-performance direct methanol fuel cell applications. A tight adherence is detected between layers from SEM and EDX data for the cross-sectional area of the newly designed membrane, which are attributed to high affinity of opposite charged polyelectrolyte layers. Proton conductivity and methanol permeability measurements show improved transport properties for the multi-layer membrane compared to Nafion^®117 with approximately the same thickness. Moreover, direct methanol fuel cell tests reveal higher open circuit voltage, power density output, and overall fuel cell efficiency for the triple-layer membrane than Nafion^®117, especially at concentrated methanol solutions. A power output of 68.10 mW cm^?2 at 5 M methanol feed is supplied using multi-layer membrane, which is found to be about 72% more than that of for Nafion^®117. In addition, fuel cell efficiency for multi-layer membrane is measured about 19.55% and 18.45% at 1 and 5 M methanol concentrations, respectively. Owing to the ability to provide high power output, significantly reduced methanol crossover, ease of preparation and low cost, the triple-layer membrane under study could be considered as a promising polyelectrolyte for high-performance direct methanol fuel cell applications.     

Synthesis of kappa-carrageenan-g-poly(acrylamide)/sepiolite nanocomposite hydrogels and adsorption of cationic dye

In this study, nanocomposite hydrogels from grafting of acrylamide onto kappa-carrageenan biopolymer were prepared in the presence of sepiolite clay. Methylenebisacrylamide and ammonium persulfate were used as cross-linker and initiator, respectively. The sepiolite nanoclay was introduced into hydrogel matrix without any chemical treatment. The structure of nanocomposites was investigated by FTIR, SEM, TEM, and TGA techniques. The TEM image showed that sepiolite exists as individual needle’s shape. The swelling of hydrogels were studied in distilled water, salt solutions, and various pHs. The obtained nanocomposites were evaluated to remove of cationic crystal violet (CV) dye from water. The kinetic and isotherm of adsorption of dye onto nanocomposites were studied and analyzed according to kinetic and isotherm models. The results showed that the pseudo-second-order adsorption kinetic was predominated for the adsorption of CV onto nanocomposites. The experimental equilibrated adsorption capacity of nanocomposites was analyzed using Freundlich and Langmuir isotherm models. The results corroborated that the experimental data fit the Langmuir isotherm the best. By varying the pH of initial dye solution, while the clay-free hydrogel showed relatively pH-independent adsorption behavior, the nanocomposites depicted pH-dependent adsorption.     

Design of a Tubular Ceramic Membrane for Gas Separation in a PEMFC System

The objective of this study is to introduce a shortcut in the method of design for a tubular ceramic membrane (TCM) for gas separation. Generally, it explains the permeation of the multi component gas using cross flow models in a porous membrane and the surface area of the membrane required. The novel aspect of this method is that the expression for the length of the membrane is simplified to a number unit (NTU) and a height of transfer unit (HTU). The HTU term for porous membranes is characterised by the physical properties of the membrane; the feed flow rate, n_F, membrane thickness, l_M, feed pressure, P_F, K the permeability of gas and the diameter of the membrane, D_M. The integral for NTU of a porous membrane is the solution for the local permeate along the length of the membrane. It is found that, NTU mainly depends on the rejection stream, x_R,, along the membrane and it describes the relative degree of separation. The Proton Electrolyte Membrane Fuel Cell (PEMFC) system is taken as the case study. CO is the main culprit in reducing the performance of the PEMFC and will act as a catalyst poison for the fuel cell anode at a concentration as low as 100 ppm. Thus, the reformate, from primary reforming, contains a significant amount of CO and must be purified. The effect of some important parameters such as temperature, pressure and the thickness of membrane to the degree of separation are presented in this paper. From the results, it can be seen that the system could reduce the CO concentration from 2000 – 500 ppm. Basically the TCM will operate, in series, with a pressure swing adsorber in order to further reduce the concentration of CO to less than 10 ppm before entering the fuel cell stack. However, this paper only focuses on the design of the TCM. Besides this, it is observed that the purity of the hydrogen increased from 72.8 – 96% (at θ = 0.5) after the membrane.     

Multi-objective modelling of day ahead scheduling of MMG-based distribution networks accompanied by DEA considering economics,emissions and power quality

ABSTRACT

This paper presents the state of the art relating to multi-objective modelling for day ahead scheduling of multi micro grid-based distribution networks, using optimal power flow (OPF) accompanied by data envelopment analysis (DEA). In this paper eco-reliability cost function, power quality enhancement and emission reduction are treated as the objective functions and the uncertainties of renewable distributed generations (DGs), load demand and market price are incorporated into the problem. This method is able to find the optimum operation of DGs in grid-connected or isolated MGs, power transaction between each MG and upstream networks/other MGs and hourly reconfiguration instants. For this purpose, firstly OPF is applied to the problem, then the obtained optimal solutions are prioritised by DEA and ranking is done, based on the efficiencies of the optimal solutions. Finally, the provided results validate the practicability of the proposed method and accuracy of the outcomes.     

Thermal,mechanical, and corrosion resistance properties of vinyl ester/clay nanocomposites for the matrix of carbon fiber‐reinforced composites exposed to electron beam

Vinyl ester/clay nanocomposites with 1, 3, and 5% nanoclay contents were prepared. X‐ray diffractography patterns and Scanning Electron micrographs showed that nanocomposites with the exfoliated structure were formed. Thermogravimetric analysis, water absorption test, and Tafel polarization method, respectively, revealed the improvements in thermal resistance, water barrier properties, and corrosion resistance properties of the samples with an increase in the amount of the incorporated nanoclay. Tensile tests showed that nanoclay also enhanced the mechanical properties of the polymer, so that the tensile strength of the samples with 5% nanoclay was more than 3 times higher than tensile strength of pure vinyl ester samples. Overall, the best properties were observed for the samples containing 5% nanoclay. Pure vinyl ester and nanocomposite with 5% nanoclay content were exposed to the electron beam radiation and their mechanical properties improved up to 500 kGy irradiation dose. Finally, pure vinyl ester and vinyl ester/nanoclay (5%) matrixes were reinforced with carbon fiber and the effect of electron beam irradiation on their mechanical properties was examined. The tensile strength and the modulus of the samples initially increased after exposure to the radiation doses up to 500 kGy and then a decrease was observed as the irradiation dose rose to 1000 kGy. Moreover, nanoclay moderated the effect of the irradiation. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42393.