Preparation of Zinc(II) Oxide Nanoparticles from a New Nano-Size Coordination Polymer Constructed from a Polypyridyl Amidic Ligand; Spectroscopic, Photoluminescence and Thermal Analysis Studies

A new zinc(II) coordination polymer, {[Zn(bpcdp)₂(DMF)₄](ClO₄)₂·(H₂O)₂}_n (1) bpcdp = 2,6-bis(4-pyridinecarboxamide)pyridine has been synthesized and characterized by IR, ¹HNMR and ¹³CNMR spectroscopy. The single crystal X-ray data of compound 1 shows the zinc(II) atom has been considered as octahedral with ZnN₂O₄ coordination sphere. Two nitrogen atoms of bpcdp ligand and four oxygen atoms of DMF molecules have occupied coordination sphere around zinc(II) atoms. The prepared zinc(II) coordination polymer grows in three-dimensional network by hydrogen bonding and π–π stacking interaction. The nanostructure of compound 1 were obtained by sonochemical process and studied by scanning electron microscopy (SEM), X-ray powder diffraction (XRD), IR and NMR spectroscopy. Thermal stabilities of single crystalline and nano-size samples of compound 1 were studied by thermal gravimetric (TG) and differential thermal analyses (DTA). The ZnO nanoparticles were obtained by direct calcination of compound 1 at 400 °C and by thermolysis in oleic acid at 200 °C. The obtained zinc(II) oxide nanoparticles were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM).     

Experimental and modelling studies of carbon dioxide adsorption by porous biomass derived activated carbon

The goal of the study was to produce a low-cost activated carbon from agricultural residues via single stage carbon dioxide (CO₂) activation and to investigate its applicability in capturing CO₂ flue gas. The performance of the activated carbon was characterized in terms of the chemical composition, surface morphology as well as textural characteristics. The adsorption capacity was investigated at three temperatures of 25, 50 and 100 °C for different types of adsorbate, such as purified carbon dioxide and binary mixture of carbon dioxide and nitrogen. The purified CO₂ adsorption study showed that the greatest adsorption capacity of the optimized activated carbon of 1.79 mmol g^?1 was obtained at the lowest operating temperature. In addition, the adsorption study proved that the adsorption capacity for binary mixtures was lower due to the reduction in partial pressure. The experimental values of the purified CO₂ adsorption were modelled by the Lagergren pseudo-first-order model, pseudo-second-order model, and intra-particle diffusion model. Based on the analysis, it inferred that the adsorption of CO₂ followed the pseudo-second-order model with regression coefficient value higher than 0.995. In addition, the adsorption study was governed by both film diffusion and intra-particle diffusion. The activation energy that was lesser than 25 kJ mol^?1 implied that physical adsorption (physisorption) occurred.     

Pulse response of 0°Z cut ADP modulators

Experimental results are presented on the variation of a delay time which is observed between the application of a voltage pulse and the onset of mechanical vibrations in 0° Z cut ADP modulators.     

The role of nanoclay partitioning and fibril formation on dyeability of blend nanocomposite fibres

The aim of the present work was to study the effect of microstructure and microfibril formation on dyeability of polypropylene/poly(butylene terephthalate)/organoclay blend nanocomposite fibres. The blend nanocomposite samples with the same blend ratio but varying in organoclay content were prepared via melt compounding by using a co‐rotating twin screw extruder. The microfibrillar morphology and nanoclay partitioning were studied using scanning electron microscopy and transmission electron microscopy together with rheological results. The presence of nanoclay in the form of tactoids in the polypropylene matrix accelerated the dye sorption but much greater ultimate dye uptake could be achieved for the sample in which the major part of the platelets were preferentially located inside the poly(butylene terephthalate) fibrils. Although increasing the organoclay concentration increased the ultimate dye uptake, it limited the fibril formation at higher organoclay concentration. The utilisation of a compatibiliser was found to have an enhancing effect on ultimate dye uptake. This could be explained in terms of the interfacial role of the compatibiliser in improving microfibril formation as well as partitioning a fraction of nanoclay platelets inside the polypropylene matrix.     

A Novel Approach to the Gas-Lift Allocation Optimization Problem

Abstract

Because compressed gas is a scarce and expensive resource, allocating an optimal amount of gas injection to a group of wells to increase the oil production rate is an important optimization problem in the gas lift operation. In this article, a particle swarm optimization algorithm is employed to assign an optimum gas injection rate for each individual well. Also, a new gas lift performance curve-fit that can reduce the time and volume of the computation is suggested. Finally, the algorithm is tested on five wells in an Iranian oil field.     

Relationship between dye sorption and morphology in polypropylene/poly (butylene terephthalate) microfibrillar blend nanocomposite fibers

In this research work, the relation between microstructural enhancement and dyeing behavior of immiscible blend nanocomposite fibers was investigated using scanning electron microscopy, transmission electron microscopy, X-ray diffraction patterns, and rheometric mechanical spectrometer along with quantitative analysis of dye sorption. A novel microfibrillar morphology blend fiber, in which poly (butylene terephthalate) nanocomposite fibrils uniformly distributed in the cross section of polypropylene matrix, was successfully developed using melt compounding process. Preferred location of nanoclay had improving effect on poly (butylene terephthalate) fibril formation such that there was an organoclay concentration above that fiber with fine microfibrillar morphology could hardly be produced. It was demonstrated that nanoclay melt intercalation and partitioning controlled the activation energy of dyeing. The maximum sorption rate was achieved by utilizing compatibilizer to transfer part of nanoclay platelets into the polypropylene matrix.     

Microstructural features of nanocomposite of alumina@carbon nanotubes/alumina nanoparticles synthesized by a solvothermal method

The present study focuses on the synthesis of nanocomposite gamma alumina (γ-Al₂O₃), boehmite and multi- walled carbon nanotubes (MWCNTs) via a solvothermal procedure. The method is based on the ex situ filling of opened CNTs by liquid reactants. The microstructure and morphology of the synthesized nanocomposite Al₂O₃@CNTs/Al₂O₃ was characterized by high resolution transmission electron microscopy (HRTEM), transmission electron microscopy (TEM), field emission scanning electron microscopy (FESEM), energy-dispersive X-ray spectroscopy (EDX), X-ray diffraction (XRD), Brunauer–Emmett–Teller (BET) and N₂ adsorption–desorption analysis.Based on the experimental results, it was determined that the volume ratio of γ-Al₂O₃/MWCNTs and the surface tension of the solvent both greatly influence the morphology of the nanocomposite. The resultant MWCNTs were coated and filled by homogeneous and uniform boehmite and γ-Al₂O₃ layers and nanoparticles with thicknesses of 1–3 nm and diameters of 20–40 nm, when the volume ratio of γ-Al₂O₃/MWCNT_S is 1 and the surface tension of the solvent is approximately 26 mN m^?1 at 20 °C, far below the maximum value (100–200 mN m^?1) for MWCNT filling.     

The effect of functionalisation method on the stability and the thermal conductivity of nanofluid hybrids of carbon nanotubes/gamma alumina

Based on our previous studies that focused on the synthesis of a nanohybrid of multi-walled carbon nanotubes (MWCNTs) and gamma alumina (γ-Al₂O₃) particles, this paper reports the heat transfer properties and dispersion behaviour of the hybrid. In this study, functionalised CNTs were synthesised via a solvothermal process with various concentrations of carboxylic acid groups (–COOH). The microstructure of the synthesised nanohybrids was characterised via high-resolution transmission electron microscopy (HRTEM), transmission electron microscopy (TEM), and energy-dispersive X-ray spectroscopy (EDX). The MWCNT/γ-Al₂O₃ nanofluid was prepared using a two-step method. The thermal conductivities of different nanohybrids were measured with a KD2 probe using a modified transient hot wire method. The zeta potential and particle size distribution were determined to investigate the stability of the nanofluid.The results showed that the functional groups had a significant influence on the thermal conductivity of the hybrid nanofluid. The data showed that the enhancement in thermal conductivity reached up to 20.68% at a 0.1% volume fraction of hybrid, for a gum arabic (GA) based nanofluid.     

Kinetics of methane decomposition to COx-free hydrogen and carbon nanofiber over Ni–Cu/MgO catalyst

Kinetic modeling of methane decomposition to CO_x-free hydrogen and carbon nanofiber has been carried out in the temperature range 550–650 °C over Ni–Cu/MgO catalyst from CH₄–H₂ mixtures at atmospheric pressure. Assuming the different mechanisms of the reaction, several kinetic models were derived based on Langmuir–Hinshelwood type. The optimum value of kinetic parameters has been obtained by Genetic Algorithm and statistical analysis has been used for the model discrimination. The suggested kinetic model relates to the mechanism when the dissociative adsorption of methane molecule is the rate-determining stage and the estimated activation energy is 50.4 kJ/mol in agreement with the literature. The catalyst deactivation was found to be dependent on the time, reaction temperature, and partial pressures of methane and hydrogen. Inspection of the behavior of the catalyst activity in relation to time, led to a model of second order for catalyst deactivation.