Coprecipitated Ni‐Co Bimetallic Nanocatalysts for Methane Dry Reforming

Methane dry reforming was studied over nanostructure bimetallic Ni‐Co‐MgO catalysts. The catalysts were prepared by coprecipitation with different Ni‐Co contents and characterized by XRD, BET, N₂ adsorption/desorption, temperature‐programmed reduction (TPR), SEM, and temperature‐programmed oxidation (TPO) techniques. XRD results let conclude that all samples contained MgO crystallite phases. With a higher Ni content the intensity of the diffraction peaks became stronger, indicating growth of the crystallite size of the prepared solid solutions. BET analysis demonstrated that a higher Ni‐Co content decreased the surface area. The optimal catalyst could be determined which had the highest activity and a good stability in dry reforming reaction.     

A highly active and stable chromium free iron based catalyst for H2 purification in high temperature water gas shift reaction

In this work mesoporous nanocrystalline chromium free Fe–Al–Ni catalysts with various Fe/Al and Fe/Ni ratios were prepared by coprecipitation method for high temperature water gas shift reaction. The prepared catalysts were characterized using X-ray diffraction (XRD), N₂ adsorption (BET), temperature-programmed reduction (TPR) and transmission electron microscopy (TEM) techniques. The catalytic results revealed that the catalyst with Fe/Al = 10 and Fe/Ni = 5 weight ratios exhibited the highest catalytic activity among the prepared catalysts and the commercial chromium containing one. This catalyst possessed a high surface area of 177.4 m² g⁻¹ with an average pore size of 4.3 nm with a high stability during 20 h time on stream. Furthermore, the effect of calcination temperature, GHSV and steam/gas ratio on the structural properties and catalytic performance of the catalyst with the highest activity was investigated.     

Promoted Fe2O3‐Al2O3‐CuO Chromium‐Free Catalysts for High‐Temperature Water‐Gas Shift Reaction

Promoted Fe₂O₃‐Al₂O₃‐CuO (FAC) chromium‐free catalysts were prepared for high‐temperature water‐gas shift reactions and characterized by X‐ray diffraction (XRD), Brunauer‐Emmett‐Teller method (BET), temperature‐programmed reduction (TPR), and transmission electron microscopy (TEM) techniques. The catalytic results revealed that among the investigated promoted catalysts with Ce, La, Zn, Y, and Mn as promoters, the Mn‐promoted sample showed higher activity compared to the other promoted catalysts. Increasing the Mn content improved the surface area and catalytic activity. The FAC catalyst promoted with a high Mn content exhibited maximum activity and relatively high stability in high‐temperature water‐gas shift reaction.     

Efficient synthesis of novel bis(arylmethylidenes) of the 2,2-dimethyl-1,3-dithian-5-one system

In a mixture consisting of catalytic quantities of diethylamine, sodium dodecyl sulfate, and a zirconium salt in water, 2,2-dimethyl-1,3-dithian-5-one undergoes double aldol condensation with two folds of aromatic aldehydes at 50^oC to yield the respective bisarylmethylidene derivatives efficiently within 2?h. The products precipitate in the reaction mixtures spontaneously, perhaps due to high polarity of the medium, avoiding time-consuming and expensive chromatographic separations. Thus, products are isolated easily by a simple filtration and recrystallization from ethyl acetate, while the filtrate was recycled successfully for subsequent reactions.     

Performance of IEEE 802.15.4 Clusters with Power Management and Key Exchange

The IEEE 802.15.4 specification is a recent low data rate wireless personal area network standard.While basic security services are provided for,there is a lack of more advanced techniques which are indispensable in modern personal area network applications.In addition,performance implications of those services are not known.In this paper,we describe a secure data exchange protocol based on the ZigBee specification and built on top of IEEE 802.15.4 link layer.This protocol includes a key exchange mechanism.We assume that all nodes are applying power management technique based on the constant event sensing reliability required by the coordinator.Power management generates random sleep times by every node which in average fairly distributes the sensing load among the nodes.Key exchange is initiated by a cluster coordinator after some given number of sensing packets have been received by the coordinator.We develop and integrate simulation model of the key exchange and power management technique into the cluster's reliable sensing function.We evaluate the impact of security function and its periodicity on cluster performance.     

Spectral-spatial Classification of Hyperspectral Images Using Signal Subspace Identification and Edge-preserving Filter

Machine Intelligence Research - Hyperspectral images in remote sensing include hundreds of spectral bands that provide valuable information for accurately identify objects. In this paper, a new...     

Effect of process parameters on the synthesis of nanocrystalline magnesium oxide with high surface area and plate-like shape by surfactant assisted precipitation method

A surfactant assisted precipitation method was employed for the preparation of nanocrystalline magnesium oxide with high specific surface area and plate-like shape. Ammonium hydroxide and polyvinyl alcohol (PVA) were used as precipitant and polymeric surfactant, respectively. The effects of several process parameters such as refluxing time, refluxing temperature and magnesium oxide to PVA monomer unit mole ratio (MgO/PVA) were investigated on the structural properties of the powders. The obtained results showed that the increase in refluxing time and temperature increased the specific surface area and decreased the crystallite size. The results revealed that the polymeric surfactant (PVA) has a significant effect on the synthesis of MgO nanocrystals and led to obtain a powder with higher surface area and plate-like shape.     

Promotional roles of second metals in catalyzing methane decomposition over the Ni-based catalysts for hydrogen production: A critical review

The thermocatalytic decomposition (TCD) of methane is considered as a milestone towards the production of valuable CO_x-free hydrogen and carbon nanomaterials without the use of steam or O₂. Previous reviews have been aimed at methane decomposition over the different catalysts, such as nickel-based catalysts, non-nickel-based catalysts, metal oxide-supported catalysts, and carbon-supported catalysts. The Ni-based catalysts are suitably applied for methane TCD process due to their high activity and low cost. However, the loss of activity and/or stability with reaction time is one of the most notable challenges in the use of Ni-based catalysts, and a number of studies on the roles of various factors in overcoming such a problem can be found in the literature. Recently, the use of the second metal as a promoter to control catalyst deactivation has attracted much attention. The present review focuses on classification of the different promoters based on the periodic table of elements, such as alkali metals, alkaline earth, transition metals, noble metals, and rare earth metals, and makes a detailed discussion on promotional roles in influencing their physicochemical properties and catalytic performance of the Ni-based catalysts. The generalized structure-performance relationship of the metals-doped catalysts may give an appreciated reference to the design of catalysts with highly pure hydrogen production and carbon nanomaterials. In addition, this review also covers the works on effects of the promoters on nature and morphology of the formed carbon nanomaterials. The use of transition metals (Fe, Co or Cu), noble metal (Pd or Pt), and rare earth metal (La) with a suitable loading as a promoter influenced performance and lifespan of the catalyst and the interaction of Ni particles with the support. Among these promoters, Cu, Pd, La, and Cu–Pd as a dopant have demonstrated superior performance, which was attributed to the capability of these elements in prohibiting carbon accumulation on the active Ni components.     

Photodynamic Antimicrobial Cellulosic Material Through Covalent Linkage of Protoporphyrin IX onto Lyocell Fibers

Here, we report the preparation of porphyrin-functionalized Lyocell fibers according to an azide-alkyne click concept. First, azido-modified Lyocell fibers and alkynylated protoporphyrin building blocks were prepared through alkoxysilane chemistry and Steglich esterification, respectively. Lyocell fibers were pre-activated by swelling in organic solvents in order to increase the accessibility of hydroxyl groups in the subsequent silanization process. The azide-equipped cellulosic matrix reacted with the propargyl groups of the protoporphyrin IX derivative in a copper-catalyzed azide-alkyne cycloaddition reaction (CuAAC), by which protoporphyrin IX was introduced onto the surface of the Lyocell fibers. The modified building blocks and the final functionalized cellulosic materials were comprehensively characterized by FTIR, NMR, UV/Vis spectroscopy and elemental analysis. Photo-bactericidal activity of modified fibers against 2?gram-positive bacteria strains, including Staphylococcus aureus and Bacillus subtilis, were investigated and compared to those of unmodified and azido-modified Lyocell fibers. The results confirmed the photo-antibacterial activity of the synthesized fibers against both bacteria strains.