Stress-Aware Periodic Test of Interconnects

Journal of Electronic Testing - Safety-critical systems have to follow extremely high dependability requirements as specified in the standards for automotive, air, and space applications. The...     

Performance improvement for recommender systems using ontology

Recommender systems have emerged in the e-commerce domain and have been developed to actively recommend appropriate items to online users. The use of recently developed hybrid recommendation systems has helped overcome the main drawbacks of Content-Based Filtering (CBF) and Collaborative Filtering (CF). In hybrid recommendation systems that combine CF and CBF, the CF part uses two methods, including memory- and model-based approaches. Both approaches have some advantages and disadvantages for item recommendation. Sparsity has been one of the main difficulties associated with these approaches, whereas recommendation with high accuracy has been one of the important advantages of the memory-based approach. However, this approach is not scalable for current recommendation systems as their databases include huge numbers of items and users. In contrast, the model-based approach generates recommendations with low accuracy but is scalable for large databases in e-commerce recommender systems. Accordingly, to address this problem and take advantage of both approaches, in this work, we propose a new hybrid recommendation method and evaluate it using a real-world dataset. The aim is to improve efficiency and accuracy by designing a heuristic hybrid recommender method that combines memory-based and model-based approaches. Specifically, we use ontology in the CF part and improve ontology structure by eliminating uniformity of edges of the hierarchical relation between concepts (IS-A relation) in item ontology in the CBF part. Ontology structure is considered for improving accuracy; according to this, a new method for measuring semantic similarity that is more accurate than the traditional methods is presented. This new method can enhance the accuracy of CF and CBF in our method. In addition, the number of searches required to find similar clusters and neighbor users of the target user is decreased significantly using ontology, enhanced clustering and the new proposed algorithm. We evaluate the proposed method using a real-world dataset. The experimental results show that our method is more scalable and accurate than the benchmark k-Nearest Neighbor (k-NN) and model-based recommendation methods.     

β-Tetra-brominated meso-tetraphenylporphyrin: A conformational study and application to the Mn-porphyrin catalyzed epoxidation of olefins with tetrabutylammonium oxone

X-ray crystallographic studies have shown that the free base β-tetra-brominated meso-tetraphenylporphyrin (H₂TPPBr₄) has a slightly ruffled structure with the dihedral angles of 70.1–79.2° between the phenyl groups and the porphyrin mean plane. The N(pyrrole)–N(pyrrolenine) distance is very similar to that of the standard planar porphyrins. The decreased N–H bond length of H₂TPPBr₄ with respect to that of meso-tetraphenylporphyrin (H₂TPP) seems to be due to the weaker intramolecular hydrogen bond of the former relative to the latter caused by the electron-withdrawing effects of the β-bromine substituents. The large red shifts of the Soret and Q(0,0) bands of H₂TPPBr₄ in comparison with those of H₂TPP, in spite of the nearly planar porphyrin core of the compound, also may be explained on the basis of the electron-withdrawing effects of the bromine atoms. Oxidation of styrene, the para-substituted derivatives and cyclooctene with tetrabutylammonium oxone in the presence of catalytic amounts of β-tetra-brominated meso-tetraphenylporphyrinatomanganese(III) acetate immediately gives the epoxide as the sole product. Terminal double bonds and unconjugated ones are less reactive than the conjugated double bonds and show lower selectivities. Catalytic activity of the electron-deficient Mn(H₂TPPBr₄)OAc dramatically depends on the Co-catalytic activity of the nitrogen donors as the axial base. The best axial bases are the nitrogenous donors with mixed σ- and π-donor ability to the metal centre.     

Sharing spray and wait routing algorithm in opportunistic networks

Due to the instability and intermittent connectivity of links among the nodes and the lack of connectivity in opportunistic network, it is not feasible to use common routing for delivering messages. The only practical method for routing and delivering messages is to use the store-carry-forward routing method. As a case in point, spray and wait is considered to be one of the most appropriate routing methods. The efficiency of this method depends directly on the proper selection of the next hop and the number of copies when it encounters a node. In this paper, a method was proposed that constantly selects the next node and considers the number of copies a node can deliver. In the proposed method, the selection of the next node and the number of message copies to be transmitted by the next hop are based on message carrying time and the probability of message delivery. The network model, based on Markov chain, is extended for analysis. Simulation and analysis results showed that significant enhancement is obtained with the proposed method when measuring metrics such as delay, delivery ratio and copy do comparisons with similar methods.     

Light expanded clay aggregate (LECA) as a support for TiO<Subscript>2</Subscript>, Fe/TiO<Subscript>2</Subscript>, and Cu/TiO<Subscript>2</Subscript> nanocrystalline photocatalysts: a comparative study on the structure,morphology, and activity

In this work, TiO₂ and doped TiO₂ photocatalysts (Fe/TiO₂ and Cu/TiO₂) were synthesized by the sol–gel method. The main objective of this study was to investigate the influence of dopants on the structure, morphology, and activity of the catalysts in powder and immobilized states. XRF, XRD, and SEM methods were used to characterize the catalysts. The structure and phase distribution of the nanocrystalline powders were identified by XRD. Nanoparticles crystallite size and the degree of crystallinity were affected by doping. The anatase contents of catalysts were achieved as follows: TiO₂ (5.89 %) < Fe/TiO₂ (42.17 %) < Cu/TiO₂ (70.28 %). It was indicated that the activity of the catalysts strongly depends on the anatase content. Under the same circumstances, copper-modified TiO₂ exhibited a twofold higher photocatalytic activity compared with TiO₂. The nanostructured catalysts were immobilized on light expanded clay aggregate (LECA) granules in order to investigate the effect of a novel support on the activity of the catalysts. Morphological changes are recognizable in the SEM images. Activity tests indicated that the best catalytic performance was assigned to Cu/TiO₂/LECA. After 120 min of irradiation, 61 % degradation of phenol in synthetic wastewater was achieved. The high photocatalytic activity of Cu/TiO₂/LECA confirms that LECA is as an excellent support.     

Solution of Lane–Emden type equations using rational Bernoulli functions

In this paper, a numerical method for solving Lane‐Emden type equations, which are nonlinear ordinary differential equations on the semi‐infinite domain, is presented. The method is based upon the modified rational Bernoulli functions; these functions are first introduced. Operational matrices of derivative and product of modified rational Bernoulli functions are then given and are utilized to reduce the solution of the Lane‐Emden type equations to a system of algebraic equations. Illustrative examples are included to demonstrate the validity and applicability of the technique. Copyright © 2015 John Wiley & Sons, Ltd.     

Synthesis of 2-Mercaptonicotinic Acid-Capped CdSe Quantum Dots and its Application to Spectrofluorometric Determination of Cr(VI) in Water Samples

The CdSe quantum dots (QDs) capped with 2-mercaptonicotinic acid (H₂MN) were prepared through a controllable process at 80 °C. The prepared QDs were characterized by XRD, TEM, IR, UV–Vis and fluorescence (FL) techniques. It was found that the QDs were nearly mono-disperse with the diameters in the range of 8–10 nm. These QDs are capable to exhibit strong FL even in concentrated acidic media. They exhibit an enhanced fluorescence in the presence of Cr(VI), which was used for the determination of Cr(VI) in water samples. The linear range was found to be 1?×?10^?7–6.0?×?10^?6 M with the RSD and DL of 0.92 % and 5?×?10^?8 M, respectively. Except that Ca²⁺ and Fe³⁺ which can be eliminated through a simple precipitation process, the other co-existent ions present in natural water were not interfered. The recoveries obtained for the added amounts of Cr(VI) were in the range of 96.9–103.2 %, which denote on application of the method, satisfactorily.     

Electrochemical synthesis of 5,6-dihydroxy-2-methyl-1-benzofuran-3-carboxylate derivatives

Electrochemical oxidation of catechols (1a-c) has been studied in the presence of methyl acetoacetate (2a) and ethyl acetoacetate (2b) as nucleophiles in aqueous solution using cyclic voltammetry and controlled-potential coulometry. The results indicate that the quinones derived from catechols (1a-c) participate in Michael addition reactions with 2a and 2b to form the corresponding benzofuran derivatives (3a-f). The electrochemical synthesis of 3a-f has been successfully performed in an undivided cell in good yield and purity. The oxidation mechanism was deduced from voltammetric data and by coulometry at controlled potential. The products have been characterized after purification by IR, ¹H NMR, ¹³C NMR, MS, and single crystal X-ray diffraction.     

Voltammetric determination of hydroxylamine in water samples using a 1-benzyl-4-ferrocenyl-1H-[1,2,3]-triazole/carbon nanotube-modified glassy carbon electrode

A modified glassy carbon electrode has been constructed using a 1-benzyl-4-ferrocenyl-1H-[1,2,3]-triazole along with multiwalled carbon nanotubes. The electrochemical behaviour of modified electrode has been investigated by cyclic voltammetry. Electrocatalytic activity of the modified electrode was investigated for the oxidation of hydroxylamine in 0.1 M phosphate-buffered solution of pH 8. The modified electrode showed electrocatalytic response to the oxidation of hydroxylamine at the potential of 330 mV. The linear range and detection limit for the detection of hydroxylamine in the optimum condition were found to be 4.0?×?10^?7 to 6.75?×?10^?4 M and 28.0?±?1.0 nM, respectively. Finally, the method was employed for the determination of hydroxylamine in water samples.