Automatic generation and compaction of March tests for memoryarrays

Given a set of memory array faults, the problem of computing a compact March test that detects all specified memory array faults is addressed. In this paper, we propose a novel approach in which every memory array fault is modeled by a set of primitive memory faults. A primitive March test is defined for each primitive memory fault. We show that March tests that detect the specified memory array faults are composed of primitive March tests. A method to compact the March tests for the specified memory array faults is described. A set of examples to illustrate the approach is presented. Experimental results demonstrate the productivity gained using the proposed framework     

Feed Water Chemistry-Related Corrosion Failures in Subcritical 250 MW Coal-Fired Boiler

This paper emphasis on the study of typical premature failure of water wall tubes of two thermal power plant boiler of same capacity (250 MW) and same operational parameter but with different boiler water chemistry. The investigation concludes on the water-side corrosion in both of the cases. One boiler is running with coordinated phosphate treatment (CPT) and another with all volatile treatment (AVT). The causes of corrosion were discovered and proposed measures for their elimination were given. Visual examination, chemical analysis of deposits, oxide scale thickness measurement, and microstructural examination were carried to ascertain the probable cause/causes of failure. From the investigation, it was finally concluded that the combination of localized high tube metal temperature and wall thinning due to under deposit corrosion led to the premature tube failure in boiler running with CPT and localized pitting corrosion in boiler running with AVT. Based on the results and discussions, a possible way to combat the corrosion was proposed.     

Validation of arrayed imaging reflectometry biosensor response for protein-antibody interactions: cross-correlation of theory, experiment, and complementary techniques

One of the critical steps in the development of an analytical technique is to confirm that its experimental response correlates with predictions derived from the theoretical framework on which it is based. This validates the technique quantitatively and, in the case of a biosensor, facilitates a correlation of the sensor's output signal to the concentration of the analyte being tested. Herein we report studies demonstrating that the quantitative response of arrayed imaging reflectometry (AIR), a highly sensitive label-free biosensing method, is a predictable function of the probe and analyte properties. We first incorporated a standard one-site Langmuir binding model describing probe-analyte interactions at the surface into the theoretical model for thickness-dependent reflectance in AIR. This established a hypothetical correlation between the analyte concentration and the AIR response. Spectroscopic ellipsometry, surface plasmon resonance, and AIR were then used to validate this model for two biomedically important proteins, fibroblast growth factor-2 and vascular endothelial growth factor. While our studies demonstrated that the 1:1 one-site Langmuir model accurately described the observed response of macrospot AIR arrays, either a two-site Langmuir model or a Sips isotherm better described the behavior of AIR microarrays. These studies confirmed the quantitative performance of AIR across a range of probe-analyte affinities. Furthermore, the methodology developed here can be extended to other label-free biosensing platforms, thus facilitating a more accurate and quantitative interpretation of the sensor response.     

Exploitation of nano alumina for the chromatographic separation of clinical grade 188Re from 188W: a renaissance of the 188W/188Re generator technology

The (188)W/(188)Re generator using an acidic alumina column for chromatographic separation of (188)Re has remained the most popular procedure world over. The capacity of bulk alumina for taking up tungstate ions is limited (～50 mg W/g) necessitating the use of very high specific activity (188)W (185-370 GBq/g), which can be produced only in very few high flux reactors available in the world. In this context, the use of high-capacity sorbents would not only mitigate the requirement of high specific activity (188)W but also facilitate easy access to (188)Re. A solid state mechanochemical approach to synthesize nanocrystalline γ-Al(2)O(3) possessing very high W-sorption capacity (500 mg W/g) was developed. The structural and other investigations of the material were carried out using X-ray diffraction (XRD), transmission electron microscopy (TEM), Brunauer Emmett Teller (BET) surface area analysis, thermogravimetric-differential thermal analysis (TG-DTA), and dynamic light scattering (DLS) techniques. The synthesized material had an average crystallite size of ～5 nm and surface area of 252 ± 10 m(2)/g. Sorption characteristics such as distribution ratios (K(d)), capacity, breakthrough profile, and elution behavior were investigated to ensure quantitative uptake of (188)W and selective elution of (188)Re. A 11.1 GBq (300 mCi) (188)W/(188)Re generator was developed using nanocrystalline γ-Al(2)O(3), and its performance was evaluated for a period of 6 months. The overall yield of (188)Re was >80%, with >99.999% radionuclidic purity and >99% radiochemical purity. The eluted (188)Re possessed appreciably high radioactive concentration and was compatible for the preparation of (188)Re labeled radiopharmaceuticals.     

Improved correlations for computations of liquid helium two phase flow in cryogenic transfer lines

The available experimental data, Vishnev et al. [6], implies that the widely used homogenous equilibrium model and the Martinelli–Nelson equation do not map correctly the pressure drop data for horizontal liquid helium two phase flow particularly in cases for high vapour fraction. Hence, considering the empirical nature of Martinelli–Nelson equation, suitable parameters and terms have been suggested so that, the pressure drop can be better predicted. The proposed equation being a third order in ‘x’ (vapour fraction) is more accurate to predict the characteristic behavior of liquid helium two phase flow as observed in experiments [6], Mamedov et al. [7], and Deev et al. [8], which the available equations are unable to predict.     

Studies on interfacial interactions of TiO2 nanoparticles with bacterial cells under light and dark conditions

The probable underlying mechanism(s) of bacterial cell–TiO₂ nanoparticles (TiO₂ NPs) interaction in the absence of photo-irradiation has been less studied since most of the prior cytotoxicity studies focused on irradiated TiO₂. The present study draws attention to the possible role of cell surface–TiO₂ NP interactions under dark conditions, through an array of spectroscopic and microscopic investigations. A dominant freshwater bacterial isolate, Bacillus licheniformis, which interacted with environmentally relevant concentrations of TiO₂ NPs (1 μg/mL), was analysed and compared under both light and dark conditions. Aggregation of cells upon NP interaction and adsorption of NPs onto the cell membrane was evident from the scanning electron micrographs under both light and dark conditions. The FT–IR and FT–Raman spectra suggested stress response of bacterial cells by elevated protein and polysaccharide content in the cell–NP interaction. The Xray photoelectron spectroscopic data substantiated the reduction of titanium from Ti(IV) to Ti(III) species which might have contributed to the redox interactions on the cell surface under light as well as dark conditions. The internalization of NPs in the cytoplasm were obvious from the transmission electron micrographs. The consequent cell death/damage was confirmed through fluorescence spectroscopy and microscopy. To conclude, the current study established the substantial role of interfacial interactions in cytotoxicity of the TiO₂ NPs irrespective of the irradiation conditions.     

Improved mode decision algorithm based on residues and early zero block detection in H.264/AVC

Video compression standard H.264/AVC outperforms previous standards in terms of coding efficiency but at the cost of higher computational complexity. In H.264/AVC, the variable block size full motion estimation is the most time-consuming operation. This paper presents a method to reduce the complexity of motion estimation in two stages. The first stage exploits the similarities between frames for early SKIP mode decision for a macroblock (MB) based upon a criteria formulated on the basis of the statistics of the frame difference residues. MBs that fail to qualify for the SKIP mode in the first stage spills over to the second stage where mode decision depends upon the number of zero blocks (ZB) in the MB. The study of the full search motion estimation on different sequences show that there is a strong dependence between the number of ZBs in a MB and the likelihood of a particular mode being selected. The proposed algorithm utilizes this relationship for early mode decision for a MB. The algorithm is evaluated using a wide range of test sequences from different classes. Experimental results show that the proposed algorithm gives considerable saving in encoding time and search points in the range of 36–87%. Furthermore, despite the reduction in computational complexity, the coding efficiency (picture quality and bitrate) in the proposed method is comparable to the H.264/AVC standard software Joint Model (JM12.4).     

Lysine 58 and histidine 66 at the C-terminal alpha-helix of monocyte chemoattractant protein-1 are essential for glycosaminoglycan binding

Monocytes rolling on the endothelial cell layer interact with monocyte chemoattractant protein-1 (MCP-1) that is tethered to the proteoglycans on the luminal side of the endothelial cells and consequently initiate adhesion of monocytes in the early phase of immune response. The amino acid residues in MCP-1 involved in tethering to the proteoglycans have not been elucidated. MCP-1 showed binding to [3H]heparin with a KD of 1.5 microM. We substituted lysine or histidine residues at the C-terminal end of MCP-1 with alanine residues and tested these mutants for their ability to bind heparin, heparan sulfate, hyaluronic acid, and chondroitin sulfate-C. Substitution of Lys-58 or His-66 drastically reduced glycosaminoglycan binding. Substitution of Lys-56 or deletion of the five amino acid residues at the C terminus, including Lys-75, did not alter the heparin binding ability, suggesting that the other lysine residues at the C terminus are not involved in glycosaminoglycan binding. MCP-1 and its mutants did not bind hyaluronic acid as strongly as the other subunits of the GAGs. Substitution of Lys-58 or His-66 by alanine that prevented glycosaminoglycan binding did not affect Ca2+ influx, receptor binding, or chemotactic activity elicited by the chemokine on monocytic THP-1 cells. Therefore, we conclude that the Lys-58 and His-66 residues in the C-terminal alpha-helix of MCP-1 are essential for glycosaminoglycan binding and probably for the binding to the endothelial surface proteoglycans.