A thermodynamically consistent framework for non-isothermal modelling of local heat generation and electromotive force in SOFC single electrodes

Mathematical models for single electrode reversible heat and non-isothermal electromotive force (EMF) of a solid oxide fuel cell (SOFC) are developed. These models estimate the volumetric reversible heat generation and EMF of electrochemical reactions, within each electrode at local conditions of temperature and pressure, based on entropy change of half reactions. The resulting equations are thermodynamically consistent. They inherently obey the conservation of energy law as the electrochemical energy released added to the heat of reactions at each electrode equate the enthalpy change of the reacted species. The equations are implemented to model electrodes in a tubular micro- solid oxide fuel cell (TμSOFC). The thermodynamic consistency of the model is numerically confirmed as the enthalpy of the reactants equates the electric energy released by the cell plus the sum of electrode heats plus electrolyte Ohmic heat. The effect of thermal gradients on the cell's overall EMF is found to be negligible. The reversible and irreversible heat generation of each electrode are distinguished. Overall, the anode is found to be endothermic, and the cathode exothermic.     

Phospholipids and oxophospholipids in atherosclerotic plaques at different stages of plaque development

We identified and quantified the hydroperoxides, hydroxides, epoxides, isoprostanes, and core aldehydes of the major phospholipids as the main components of the oxophospholipids (a total of 5–25 pmol/μmol phosphatidylcholine) in a comparative study of human atheroma from selected stages of lesion development. The developmental stages examined included fatty streak, fibrous plaque, necrotic core, and calcified tissue. The lipid analyses were performed by normal-phase HPLC with on-line electrospray MS using conventional total lipid extracts. There was great variability in the proportions of the various oxidation products and a lack of a general trend. Specifically, the early oxidation products (hydroperoxides and epoxides) of the glycerophosphocholines were found at the advanced stages of the plaques in nearly the same relative abundance as the more advanced oxidation products (core aldehydes and acids). The anticipated linear accumulation of the more stable oxidation products with progressive development of the atherosclerotic plaque was not apparent. It is therefore suggested that lipid infiltration and/or local peroxidation is a continuous process characterized by the formation and destruction of both early and advanced products of lipid oxidation at all times. The process of lipid deposition appears to have been subject to both enzymatic and chemical modification of the normal tissue lipids. Clearly, the appearance of new and disproportionate old lipid species excludes randomness in any accumulation of oxidized LDL lipids in atheroma.     

Effect of different modified nanoclays on the kinetics of preparation and properties of polymer-based nanocomposites

Polymer-clay nanocomposites have been prepared by free radical and RAFT polymerizations. To investigate the effects of nanoclay content and its modification system on the kinetics of polymerization, two different commercial grades of clay including Na-MMT and Cloisite 30B have been used and a method has been developed for further modification of Na-MMT with two commercial modifiers containing either a long organic chain or a vinyl group. Also, kinetics of free radical and RAFT polymerizations of both styrene and methyl methacrylate in the presence of these nanoclays was studied. Morphology of the nanocomposites has been studied by XRD and the results have been assessed with TEM observations. Exfoliated structure was obtained for the nanocomposites with 1?wt.% of vinyl-containing clays. Thermogravimetric behavior of the nanocomposites has been studied by TGA. Incorporation of clays has resulted in an evident increase in thermal stability of both polymers.     

A study on the effect of compositing silver oxide nanoparticles by carbon on the ‎electrochemical behavior and electronic properties of zinc‐silver oxide batteries ‎

In this study, the effect of compositing silver oxide nanoparticles by carbon on the electrochemical behavior and electronic properties of zinc‐silver oxide batteries have been investigated. For this purpose, firstly four silver oxide electrodes containing 5, 10, 15, and 20 wt% carbon powder were produced by powder metallurgy method. For the next step, all four silver oxide electrodes were sintered at 500°C for 10 minutes. Afterward and in order to investigate the microstructure, phase and elemental analysis of the electrodes were carried out using Transmission Electron Microscopy (TEM), Scanning Electron Microscopy (SEM), X‐ray Diffraction (XRD), and Energy Dispersive Spectroscopy (EDS), respectively. Moreover, in order to investigate the effect of compositing silver oxide nanoparticles by carbon on the electrochemical behavior and electronic properties of zinc‐silver oxide, electrochemical tests (potentiodynamic polarization and electrochemical impedance spectroscopy) and electric discharge test in 1.4 wt%KOH electrolyte were carried out respectively. The microstructural observations revealed that increasing carbon content in the silver oxide electrodes results in increasing the apparent porosities in these electrodes. Investigating the phase and elemental analysis results showed that by increasing the content of carbon in the silver oxide electrode, the amount of Ag₂O and AgO phases in this electrode reduces and also the extent of pure silver formation increases. Investigations on the results of electrochemical tests showed that increasing carbon content results in the reduction of corrosion resistance in silver oxide electrodes. Moreover, the results of electric discharge test revealed that the silver oxide electrode containing 10wt% carbon yields the highest energy efficiency in the zinc‐silver oxide batteries.     

Recovery and partial purification of thermophilic β-xylosidase derived from recombinant Bacillus megaterium MS941 by aqueous two-phase system

A polymer–salt-based aqueous two-phase system (ATPS) was developed for the effective extraction and purification of extracellular β-xylosidase from the fermentation broth of recombinant Bacillus megaterium MS941. The effect of molecular weight (MW) of polyethylene glycol (PEG), tie-line length (TLL), volume ratio (V_R), crude loading and pH on the recovery performance was evaluated. Under the optimal extraction conditions, β-xylosidase was successfully purified up to 23-fold with a recovery yield of 99% in the bottom salt-rich phase at PEG 4,000/potassium phosphate ATPS comprising TLL of 41.8, V_R of 2.3, crude loading (C_L) of 30% (w/w) at pH 6.     

Improvement in volume resistivity and morphology of a blend of polyolefin elastomer with linear low-density polyethylene

A silane moisture-cured polyolefin elastomer/linear low-density polyethylene (LLDPE) blend was prepared through a two-step silane-grafting method (Sioplas Process) in an industrial scale twin-screw extruder. The silane-grafted compound was used to make wire and cable coatings. In this work, the effect of some interactive parameters on quality of the products prepared by the above method has been studied, while so far, there have been less experimental investigations. The volume resistivity of cross-linked compound was changed from 2.96 × 10¹⁴ to 7.41 × 10¹⁴ Ω cm with increasing LLDPE component by maximum 10 wt%. Surface morphology of the product was corrected with reduction in benzoyl peroxide (BPO) concentration from 0.2 wt% to 0.13 wt%. BPO at this level acted as an initiator in grafting reaction of vinyl trimethoxysilane. The curing condition and specimen preparation method by injection molding and/or extrusion were factors which influenced the hot-set test results at 200 °C. The results of tensile and elongation studies showed a maximum value of 9 MPa and 397% for the tests, after 6 h curing. With increases in curing time at a specified temperature, the gel content of the cross-linked compound was increased and reached its maximum value. The maximum gel content values were found to be approximately 60%, 80%, and 82% at temperatures of 25, 60, and 85 °C, respectively. The hardness, density, and tear strength of the samples did not vary significantly with the curing temperature.

     

功能梯度金属泡沫填充管在冲击载荷下的高效吸能

研究功能梯度泡沫填充管(FGFTs)在落锤冲击载荷作用下的变形行为和耐撞性.采用液态工艺制备的闭孔泡沫铝、A356合金泡沫和锌泡沫作为轴向梯度填料,用于制备不同构造的单层和多层结构.结果表明,多层泡沫填充管的变形由低强度部位开始,然后通过应力的逐渐增加在高强度部位中扩展.使用更多的A356合金和泡沫铝层可为梯度结构提供...     

Copolymerization of ethylene/α‐olefins using bis(2‐phenylindenyl)zirconium dichloride metallocene catalyst: structural study of comonomer distribution

Catalysts have a major role in the polymerization of olefins and exert their influence in three ways: (1) polymerization behaviour, including polymerization activity and kinetics; (2) polymer particle morphology, including bulk density, particle size, particle size distribution and particle shape; and (3) polymer microstructure, including molecular weight regulation, chemical composition distribution and short‐ and long‐chain branching. By tailoring the catalyst structure, such as the creation of a bridge or introducing a substituent on the ligand, metallocene catalysts can play a major role in the achievement of desirable properties. Kinetic profiles of the metallocene catalyst used in this study showed decay‐type behaviour for copolymerization of ethylene/α‐olefins. It was observed that increasing the comonomer ratio in the feedstock affected physical properties such as reducing the melting temperature, crystallinity, density and molecular weight of the copolymers. It was also observed that the heterogeneity of the chemical composition distribution and the physical properties were enhanced as the comonomer molecular weight was increased. In particular, 2‐phenyl substitution on the indenyl ring reduced somewhat the melting point of the copolymers. In addition, the copolymer produced using bis(2‐phenylindenyl)zirconium dichloride (bis(2‐PhInd)ZrCl₂) catalyst exhibited a narrower distribution of lamellae (0.3–0.9 nm) than the polymer produced using bisindenylzirconium dichloride catalyst (0.5–3.6 nm). The results obtained indicate that the bis(2‐PhInd)ZrCl₂ catalyst showed a good comonomer incorporation ability. The heterogeneity of the chemical composition distribution and the physical properties were influenced by the type of comonomer and type of substituent in the catalyst. Copyright © 2010 Society of Chemical Industry     

Effect of hexagonal structure nanoparticles on the morphological performance of the ceramic scaffold using analytical oscillation response

Porous bony scaffolds are utilized to manage the growth and migration of cells from adjacent tissues to a defective position. In the current investigation, the effect of titanium oxide (TiO₂) nanoparticles on mechanical and physical properties of porous bony implants made of polymeric polycaprolactone (PCL) is studied. The bio-nanocomposite scaffolds are prepared with composition of nanocrystalline hydroxyapatite (HA) and TiO₂ powder using the freeze-drying technique for different weight fractions of TiO₂ (0 wt%, 5 wt%, 10 wt%, and 15 wt%). In order to identify the microstructure and morphology of the fabricated porous bio-nanocomposites, the X-ray diffraction (XRD), atomic force microscope (AFM) and scanning electron microscopy (SEM) are employed. Also, the biocompatibility and biodegradability of the manufactured scaffolds are examined by placing them in a simulated body fluid (SBF) for 21 days, their weight and pH changes are measured. The rate of degradation of the PCL-HA scaffold can be controlled by varying the percentage of its constituent components. Due to an increasing growth and activity of bone cells and the apatite formation on the free surface of the fabricated bio-nanocomposite implants as well as their reasonable mechanical properties, they have the potential to be used as a bone substitute. Additionally, with the aid of the experimentally extracted mechanical properties of the scaffolds, the vibrational characteristics of a beam-type implant made of the proposed porous bio-nanocomposites are explored. The results obtained from SEM image indicate that the scaffolds produced by the employed method have high total porosity (70%–85%) and effective porosity. The pore size is obtained between 60 and 200 μm, which is desirable for the growth and propagation of bone cells. Also, it is revealed that the addition of TiO₂ nanoparticles leads to reduce the rate of dissolution of the fabricated bio-nanocomposite scaffolds.