Lipase-catalyzed synthesis and characterization of flaxseed oil-based structured lipids

The biosynthesis of structured lipids (SLs) was carried out by the interesterification of flaxseed oil (FO) and tricaprylin (TC) in an organic solvent medium (OSM), using selected commercial lipases, including Amano DF, Novozym 435, Lipozyme TL-IM and Lipozyme RM-IM. The fatty acyl chains of the synthesized triacylglycerols (TAGs) were identified by atmospheric pressure chemical ionization/mass spectrometric (APCI/MS) analysis, while the fatty acid positional distribution of the MLM- and MML-SLs (M-medium and L-long chain fatty acids) was determined by silver-ion high-performance liquid chromatographic (Ag⁺/HPLC) analysis. The effects of reaction temperature (T_r, 30–50 °C), enzyme concentration (E_c, 0.5–4%, w/v), initial water activity (a_w, 0.05–0.43) and reaction time (R_t, 0–72 h) on the efficiency of the enzymes, were studied. The bioconversion yield (%) of the synthesized MLM- and MML-SLs was monitored under the established reaction parameters for each lipase. The maximum yield of MLM-SLs was obtained in the order, of Novozym 435 > Lipozyme TL-IM > Lipozyme RM-IM > Amano DF. Moreover, considering the ratio of the MLM- to MML-SLs produced by each enzyme, Novozym 435 and Lipozyme TL-IM were selected as the most effective enzymes for interesterification of FO and TC.     

Aluminum-27 and Silicon-29 Magic-Angle Spinning Nuclear Magnetic Resonance Study of the Kaolinite-Mullite Transformation

The ²⁷Al and ²⁹Si magic-angle spinning nuclear magnetic resonance (MAS-NMR) study of the kaolinite-mullite transformation has shown the presence of Al in tetra- and pentacoordination in dehydroxylated kaolinite. The ²⁹Si NMR signal analysis of samples heated above 400°C demonstrates that the tetrahedral sheet of kaolinite begins to break down near 600°C and continues to do so to 900°C. From the ²⁷Al NMR signal evolution, it can be deduced that the exothermic peak at 980°C in DTA curves is associated with the modification of the coordination of Al, which changes from the tetra- or pentacoordination to the more stable octahedral coordination. Heating the sample at 880°C for 36 h produces the same transformation in the coordination of Al ions and the elimination of the exothermic peak at 980°C in the DTA diagram. After this transformation, all spectra show two tetrahedral lines characteristic of mullite, indicating that nuclei of mullite with low crystallinity are generated during the exothermic process which are not detected by XRD. At higher temperatures tetrahedral NMR peaks increase in intensity, yielding, at 1200°C, the 3:2 mullite NMR spectrum.     

Electrooxidation of formaldehyde as a fuel for fuel cells using Fe2+-nano-zeolite modified carbon paste electrode

This study aimed to investigate the application of nano ZSM-5 zeolite for preparation of modified carbone paste electrode for electrocatalytic oxidation of formaldehyde. The electrochemical behavior of modified carbon paste electrodes in the forms of Fe/FeZSM-5CPE and unmodified carbon paste electrode were studied using cyclic voltammetric and chronoamprometric techniques. The obtained results show that the modified carbon paste electrode (Fe/FeZSM-5CPE) is the suitable electrode for electrooxidation of formaldehyde in the acidic solution. The transfer coefficient and current density for formaldehyde were calculated 0.23 and 19.8 mA/cm², respectively. The rate constant for catalytic reaction was calculated as 3.6 × 10³ cm³ s^?1 mol^?1 via Cottrell equation.     

Service reliability of offshore wind turbines

A probabilistic formulation is proposed to assess the performance of the support structure of offshore wind turbines based on their probability and expected time of exceeding specified drift thresholds. To this end, novel probabilistic models are developed to predict the mean and standard deviation of the drift ratio response of wind turbine support structures operating under day-to-day loads as a function of the wind turbine geometry and material properties, and loading conditions. The proposed models are assessed using a database of virtual experiments generated using detailed three-dimensional (3D) nonlinear finite element (FE) models of a set of representative wind turbine configurations. The developed models are then used in a random vibration formulation to estimate the probability and expected time of exceeding specified drift thresholds. As an example, the probability and expected time of exceeding specified drift thresholds are estimated for a typical offshore wind turbine at different wind speeds. A comparison is made between the results obtained based on the proposed models, those obtained using simulators commonly used in practice and detailed 3D nonlinear FE analyses.     

Role of morphology in electrochemical hydrogen storage using binary DyFeO3-ZnO nanocomposites as electrode materials

Hydrogen storage technology is one of the most challenging issues due to the increasing demand for fossil fuel replacement and the reduction of greenhouse gas emissions. In the current paper, the main aim is one-step and eco-friendly preparation of DyFeO₃-ZnO nanocomposites using Barberry fruit extract as natural precursor (with the role of both fuel and capping agent) to compare with various conventional carboxylic acids. To further examine, the effect of different parameters like calcination temperature and the type of the chelating agent was scrutinized to acquire optimum shape, structure, morphology and size of the obtained products. This is the first effort on the investigation of the hydrogen storage capacity of DyFeO₃-ZnO nanocomposites in terms of role of morphology. The electrochemical hydrogen storage capacity of obtained DyFeO₃-ZnO nanocomposites was studied mediated by chronopotentiometry charge-discharge methods in KOH medium. The synthesis of nanocomposites in the presence of chemical or natural capping agent (carboxylic acids or Barberry fruit extract) led to different morphologies which affects to the electrochemical performance. As a result, the electrode which is provided by plate-like DyFeO₃-ZnO nanocomposites performed 600.11 mAh/g discharge capacity compared with other samples. Based on the obtained results, DyFeO₃-ZnO nanocomposites can be promising compounds to improve the electrochemical performance of hydrogen storage.     

Barium cobaltite nanoparticles: Sol-gel synthesis and characterization and their electrochemical hydrogen storage properties

The study of the effect of different chelating agents in the Pechini method on the morphology has been a promising strategy that can be used for practical tuning of the nanoparticle's morphology and hence the electrochemical hydrogen storage capacity. In the current study, the conventional Pechini sol-gel approach was used to prepare the Ba₂Co₉O₁₄ nanoparticles as a novel hydrogen storage material. The X-ray diffraction investigation approved the formation of Ba₂Co₉O₁₄ with a Hexagonal crystal structure for all of the synthesized samples. The scanning electron microscopy (SEM) revealed when citric acid was used as a chelating agent, nanoparticles with finer and more uniform morphology were obtained rather than other chelating sources. The transmission electron microscopy (TEM) showed in the presence of citric acid; the size of the synthesized nanoparticles was between 14 and 24 nm. According to the Diffuse Reflectance Spectroscopy (DRS) analysis, the calculated bandgap of synthesized nanoparticles was approximately 3.2 eV, which indicates that synthesized nanoparticles were semiconductors in essence. The electrochemical hydrogen adsorption/desorption results showed that the sample synthesized by the citric acid has an enhancement in electrochemical hydrogen storage of approximately 800 mAh/g after 15 cycles.     

Comparing photocatalytic activity consisting of Sb2S3 and Ag2S on the TiO2–SiO2/TiO2 nanotube arrays-support for improved visible-light-induced photocatalytic degradation of a binary mixture of basic blue 41 and basic red 46 dyes

In the present study, a TiO₂ nanotube (TNAs) supported Sb₂S₃–TiO₂–SiO₂ (STS/TNAs), and Ag₂S–TiO₂–SiO₂ (ATS/TNAs) hybrid novel photocatalysts were prepared and characterized by XRD, FT-IR, SEM-EDX, X-ray mapping and, DRS. EIS was employed, and an equivalent circuit model is proposed. Flat-band potential and free carrier concentration were determined by Mott–Schottky plots. The obtained catalysts were used in the photodegradation of a binary mixture of Basic Blue 41 (BB41) and Basic Red 46 (BR46) dyes. Compared with ATS/TNAs, STS/TNAs photocatalyst showed the highest apparent rate constant for BB41 dye, about two times higher, and BR41 dye more than 1.5 times. EIS results agreed with the photodegradation results, so the STS/TNAs system with higher charge transfer ability than the ATS/TNAs system showed the best photodegradation activity. The optimization effect of the amount of Sb₂S₃, TiO₂, and SiO₂ doped on the TNAs on the photocatalytic activity of the STS/TNAs was done using a central composite rotatable design (CCRD) based response surface methodology (RSM). Results have shown catalyst containing 12.2% Sb₂S₃ and 27.1% SiO₂/TNAs (S₃TS₃/TNAs) the best photodegradation activity was obtained. The GC-Mass analysis was done to detect the degradation intermediates formed during the photodegradation process.     

Performance enhancement of a direct absorption solar collector using copper oxide porous foam and nanofluid

The current research proposes the idea of using water-saturated metal oxide foams and water-based nanofluids as solar absorber in the direct absorption solar collectors (DASCs). Specifically, the novel solar collector design utilizes copper oxide (CuO) porous foam and nanoparticle with high optical properties and is expected to have enhanced thermal performance than the conventional collectors utilizing pure water. The finite volume technique is used to solve the governing equations of flow and heat transfer in the radiative participating media. Also, to establish the reliability and accuracy of numerical solutions, the obtained results are compared with the corresponding numerical and experimental data. The computations are carried out for different nanoparticle volume fractions, foam pore sizes, working fluid mass flow rates, and both porous layer thicknesses and positions (inserted at the lower or upper wall of the collector). It is found that the efficiency of DASC partially/fully filled with metal oxide foam is maximized when the collector is completely filled with it. Compared with the water flow, the numerical results show that the collector efficiency using CuO nanofluid and metal oxide foam is improved by up to 26.8% and 23.8%, respectively. Moreover, considering the second law of thermodynamics, the use of CuO nanofluids in the DASC seems to be more effective than the use of CuO porous foam.     

Platinum‐promoted fibrous silica Y zeolite with enhanced mass transfer as a highly selective catalyst for n‐dodecane hydroisomerization

A fibrous silica zeolite Y (HY@KCC‐1) catalyst with a high surface area of 568 m²/g and unique core‐shell morphology was successfully synthesized via a modified KCC‐1 synthesis method. Characterization of the catalysts was achieved with X‐ray powder diffraction (XRD), field emission scanning microscope (FESEM), N₂ adsorption/desorption, and 2,6‐dimethylpyridine adsorbed Fourier‐transform infrared spectroscopy (FTIR). The Pt/HY@KCC‐1 has displayed complete n‐dodecane conversion coupled with an incredibly enhanced isomer yield of 72% at 350°C, nearly two‐fold higher than that of unmodified Pt/HY catalyst. Remarkably, Pt/HY@KCC‐1 had an internal effectiveness factor (η) of unity and negligible internal diffusion limitation, thus suggesting its potential application in hydroisomerization of higher hydrocarbons for enhancing fuel properties.