数值模拟铸件充型过程中的液/固两相流动

铸造过程中熔融金属内的固体渣粒的运动轨迹是非常重要的。文中给出了粒子传输轨迹的数学模型,该数学模型采用显示法来确定粒子的位置。模拟研究结果与用其它数学模型的模拟结果比较,吻合良好。该模型可用于固体粒子位置的确定,并应用到SUTCAST软件中。     

Automated optimal design of double-layer latticed domes using particle swarm optimization

Most of the conventional design methods of large-scale domes need deep engineering insight; furthermore, they hardly give the most economical solutions. Therefore, in this paper, a new practical design algorithm is presented to automate optimal geometry and sizing design of the latticed space domes through the idea of using parametric mathematical functions. Moreover, a simple approach is developed for the optimal sizing design of trusses with outsized number of elements. The robust technique of particle swarm optimization is employed to find the solution of the propounded optimization problem. Some numerical examples on the minimum weight design of several famous domes are provided to demonstrate the efficiency of the proposed design algorithm.     

Magnetic and photocatalytic properties of CoFe2O4/Ni nanocomposites

Journal of Electroceramics - In this research, hard/soft CoFe2O4/Ni magnetic nanocomposite samples with different concentrations of Ni were successfully produced by a two-step mechanical alloying...     

Application of mesoporous magnetic carbon composite for reactive dyes removal: Process optimization using response surface methodology

Discharging the effluents of textile wastewaters into potable water resources can endanger the ecosystem, due to their reactivity, toxicity, and chemical stability. In this research, the application of powder activated carbon modified with magnetite nanoparticles (PAC-MNPs) as an adsorbent for removal of reactive dyes (Reactive black 5 (RB5) and reactive red 120 (RR120)) was studied in a batch system. The adsorption performance was evaluated as a function of temperature, contact time and different adsorbent and adsorbate concentrations. The levels of factors were statistically optimized using Box-Behnken Design (BBD) from the response surface methodology (RSM) to maximize the efficiency of the system. The adsorption process of both dyes was fit with the pseudo-second order kinetic and Langmuir isotherm models. The identified optimum conditions of adsorption were 38.7 °C, 46.3 min, 0.8 g/L and 102 mg/L for temperature, contact time, adsorbent dose, and initial dyes concentration, respectively. According to the Langmuir isotherm, the maximum sorption capacities of 175.4 and 172.4 mg/g were obtained for RB5 and RR120, respectively. Thermodynamics studies indicated that the adsorption process of the reactive dyes was spontaneous, feasible, and endothermic. After five cycles, the adsorption efficiency was around 84 and 83% for RB5 and RR120, respectively. A high value of desorption was achieved, suggesting that the PAC-MNPs have a good potential in regeneration and reusability, and also can be effectively utilized in industrial applications. PAC-MNPs also show a good anti-interference potential for removal of reactive dyes in dye-industry wastewaters.     

Ultrathin buffer layer at organic/organic interface for managing the recombination profile in organic light‐emitting diodes: Metal versus dielectric buffer

We report on the utilization of an ultrathin buffer layer at the organic/organic (O/O) interface to enhance device efficiency in organic light‐emitting diodes. Two different kinds of buffer layers are examined: metal and dielectric. It is shown that employment of an ultrathin Ag layer with a thickness of 1–2 nm enhances the device performance, while a MgF₂ dielectric buffer cannot affect the device properties considerably. In particular, the turn‐on voltage of the device with an appropriate buffer layer is reduced about 3 V, its current efficiency increases by a factor of more than three, and the power efficiency increases by a factor of more than five in comparison to the control device when a Ag buffer layer is introduced at the O/O interface. By employment of the buffer layer at the interface, an accumulation of current carriers appears within the device that redistribute the recombination profile toward the interior part of the emissive layer. Also, morphological examinations reveal that distinguishable phase segregation occurs in the blend of the hole‐transport layer. In particular, the polymer component remains at the surface and facilitates the hole transport into the successive layers. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43894.     

MnO2 Nanoparticles as Efficient Oxidant for Ultrasound-Assisted Synthesis of 2-substituted Benzimidazoles under Mild Conditions

In this article, a novel method for synthesis of 2-substituted benzimidazoles using MnO₂ nanoparticles as a convenient oxidant agent in ethanol-water (1:1) as solvent under ultrasound irradiation was demonstrated. In this protocol the desired products were purely obtained in high yields. The main advantages of this research are: mild procedure, simplicity of method, easily work-up, high yields, and short reaction times. The MnO₂ nanoparticles were synthesized through a solid-state reaction route using simple strarting materials. Furthermore, their structure was characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), and Fourier transform infrared spectroscopy (FT-IR).     

Using weighted pseudo‐inverse method for reconstruction of reflectance spectra and analyzing the dataset in terms of normality

Most of spectral estimation methods are based on improving the learning‐based procedures which mainly modify the training sets used by the basic methods. In this article, a new method is developed for analyzing of superiority of these modified processes to the basic methods in terms of normality of datasets. Hence, two qualitative terms, named generality and similarity are introduced to interpret the recovery achievements of different databases and their roles as training and testing sets. Also, a simple technique based on dataset modification of pseudo‐inverse method is introduced for the recovery of reflectance spectra of samples from their corresponding colorimetric data. The method modifies the training dataset according to the color specifications of test sample. In fact, different weighting matrices are employed as dynamic modifiers to improve the pseudo‐inverse estimation as a simple recovery method. The employed datasets are examined in the self as well as cross test conditions and the results are spectrally and colorimetrically evaluated. The root mean square errors between the reconstructed and actual spectra along with the corresponding color difference values under different illuminants decrease by employing the suggested modification method in comparison to classical pseudo‐inverse technique as well as the recently improved version named optimized adaptive Wiener method. © 2010 Wiley Periodicals, Inc. Col Res Appl, 2010     

A new sensor for the simultaneous determination of paracetamol and mefenamic acid in a pharmaceutical preparation and biological samples using copper(II) doped zeolite modified carbon paste electrode

A new chemically modified electrode is constructed based on a copper(II) doped zeolite modified carbon paste electrode (Cu²⁺Y/ZMCPE). It is demonstrated that this novel sensor could be used for the simultaneous determination of the pharmaceutically important compounds paracetamol (PAR) and mefenamic acid (MEF). The measurements were carried out using the differential pulse voltammetry (DPV) method. The prepared modified electrode shows voltammetric responses of high sensitivity, selectivity and stability for PAR and MEF under optimal conditions, which makes it a suitable sensor for simultaneous submicromolar detection of PAR and MEF in solution. The oxidation peak current for PAR in Briton Robinson buffer (pH = 10) was measured at various concentrations between 0.25 and 900 μM. (The detection limit was 0.1 μM and S/N was 3.) It proved linear (the correlation coefficient was 0.9987). For the MEF a linear correlation between oxidation peak current and concentration of MEF over the range 0.3–100 μM, with a correlation coefficient of 0.9991 and a detection limit of 0.04 μM, was obtained. The analytical performance of this sensor has been evaluated for the detection of PAR and MEF in human serum, human urine and a pharmaceutical preparation.