A GPU-based hyperbolic SVD algorithm

A one-sided Jacobi hyperbolic singular value decomposition (HSVD) algorithm, using a massively parallel graphics processing unit (GPU), is developed. The algorithm also serves as the final stage of solving a symmetric indefinite eigenvalue problem. Numerical testing demonstrates the gains in speed and accuracy over sequential and MPI-parallelized variants of similar Jacobi-type HSVD algorithms. Finally, possibilities of hybrid CPU–GPU parallelism are discussed.     

Influence of phenylenediamine additions on the morphology and on the catalytic effect of polyaniline

The influence of para‐, ortho‐, and meta‐phenylenediamine (p‐, o‐, and m‐PDA) additions on the electrochemical synthesis of polyaniline has been investigated by the use of cyclic voltametry. It has been found that small additions (1 and 5 mmol L^?1) of PDA monomers influence significantly the polymerization rate. Whereas p‐PDA increases the polymerization rate, the addition of o‐ or m‐PDA slows it down. Therefore, a different number of potential cycling is necessary to obtain similar thickness of layers. The layers exhibit very different morphology, which changes from “spaghetti‐like” for polyaniline to “sponge‐like” for p‐PDA, to “pebble‐like” for o‐PDA and to “cauliflower‐like” for m‐PDA additions, respectively. The catalytic effect of the synthesized polymer layers has been tested. It has been found that all the layers exhibit catalytic effect in lowering the redox potential of hydroquinone/quinone tested reaction, but the rate of the electrocatalytic reaction varies depending on the PDA monomer added. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 1599–1608, 2004     

Morphology of polythiophene and polyphenyl films produced via surface polymerization by ion-assisted deposition

Conducting polymer films are grown by either mass-selected or non-mass-selected, hyperthermal thiophene ions coincident on a surface with a thermal beam of organic monomers of either alpha-terthiophene (3T) or p-terphenyl (3P) neutrals. Previous experiments verified polymerization of both 3T and 3P by 200 eV C(4)H(4)S(+) during surface polymerization by ion-assisted deposition (SPIAD). A wide variety of structures are observed by scanning electron microscopy to form in the SPIAD polythiophene and polyphenyl films. These structures include microscale islands, lamellar structures, fractal-like growth patterns, and nanoscale crystallites. Some of the deposited films diffract X-rays while others show electron micrographs of crystallites. The variation of these patterns with deposition conditions clearly indicate that ion-induced polymerization mediates film morphology through control of ion energy and ion/neutral ratio. Furthermore, these ion-assisted events mediate important thermal processes such as sublimation.     

Nonlinear reynolds equation for lubrication of a rapidly rotating shaft

Using the homogenization theory, we derive the nonlinear Reynolds equation governing the process of lubrication of a slipper bearing with rapidly rotating shaft. We prove that this nonliner lubrication law is an approximation of the full Navier-Stokes equations in a thin cylinder with periodic roughness. The analyticity of the nonlinear function giving the relation between the velocity and the pressure drop is proved. The first term in its Taylor's expansion is the classical linear Reynolds law. Boundary layer correctors are computed.     

Sonochemical effectiveness factor (eUS) in the reactors for wastewater treatment by sono-Fenton oxidation: Novel considerations

A comprehensive algorithm was recently proposed for calculation of the sonochemical effectiveness factor and wastewater treatment modeling. The presented approach implies that ultrasound is an auxiliary source of free radicals in Fenton type reactions; introduction of ultrasound represents an enhancement of pollutant degradation rates. The sonochemical effectiveness factor was introduced in kinetic models as the e_US factor (Gr?i? et al., 2012 [1]). As a substantial follow-up, this study presents novel considerations. The e_US factor was modeled as a function of employed frequency, actual cavitation-related power intensity of ultrasound and a portion of the cavitationally active zone, i.e. dimensionless active volume. The effect of temperature was disregarded in the present model considerations. Cavitationally active zone in reactors was determined based on the erosion of aluminum foil, resulting in cone-shaped space arising from transducer.In the present study, sonochemical treatment of industrial wastewater containing HCOONa as organic pollutant was performed using different equipment: ultrasonic baths (UB1, UB2 and UB3), cylindrical reactor with homogenizer (HCR) and three-frequency hexagonal cell, i.e. ultrasonic pilot reactor prototype (PP). Explored frequency range was from 20 to 120 kHz. Homogeneous and heterogeneous Fenton-type sonochemical processes, US/Fe(II)(FeSO₄,aq.)/H₂O₂ and US/Fe(II)(steel-plate)/H₂O₂, respectively, applied to industrial wastewater were investigated in terms of mineralization kinetics. Newly modeled e_US factor was introduced in corresponding kinetic models and the overall model was validated. Kinetic parameters of Fenton process were treated as independent of ultrasound, since e_US factor consists of cavitation-related phenomena responsible for the mineralization rate enhancement. In average, a 21% increase of mineralization efficiency was achieved using a single frequency, while more than 70% increase can be achieved by combining 20, 68 and 120 kHz in PP.     

Synthesis,characterization and cytotoxic activity of organoruthenium(II)-halido complexes with 5-chloro-1H-benzimidazole-2-carboxylic acid

Three new ruthenium(II)-arene halido complexes, [(η⁶-p-cymene) RuX(L)] (1–3), were synthesized in a reaction of [(η⁶-p-cymene)RuX₂]₂ with 5-chloro-1H-benzimidazole-2-carboxylic acid (HL) in ethanol (X^– = Cl^– (1), Br^– (2), I^– (3)). The complexes were characterized by elemental analysis, mass spectrometry, IR, ¹H and ¹³C NMR spectroscopy. The cytotoxic activity of the ligand precursor and its ruthenium complexes was tested by MTT assay in human cancer cell lines: lung adenocarcinoma (A549), myelogenous leukemia (K562) as well as in one normal human fetal lung fibroblast cell line (MRC-5). The results show that ruthenium(II)-arene complexes possess enhanced cytotoxicity when compared to HL in the range of concentrations up to 300 µM. In terms of halido ligand substitution, cytotoxic activity toward A549 and K562 cell lines in 1–3 serie significantly increased (e.g., IC₅₀ values for K562: 1: 205.76 µM; 2: 174.77 µM; 3: 83.97 µM). All studied compounds were found to be ineffective toward MRC-5. Hydrolysis of 1–3 was followed by UV-vis spectroscopy at 25?°C, revealing ligand-substitution reactions at the Ru(II) center. Compounds 2 and 3 underwent rapid hydrolysis ranging from a few minutes for the aquation to ca. 20?min, confirming typical Ru-arene behavior in aqueous solutions.     

Classification of auxin plant hormones by interaction property similarity indices

Although auxins were the first type of plant hormone to be identified, little is known about the molecular mechanism of this important class of plant hormones. We present a classification of a set of about 50 compounds with measured auxin activities, according to their interaction properties. Four classes of compounds were defined: strongly active, weakly active with weak antiauxin behaviour, inactive and inhibitory. All compounds were modeled in two low-energy conformations, P and T, so as to obtain the best match to the planar and tilted conformations, respectively, of indole 3-acetic acid. Each set of conformers was superimposed separately using several different alignment schemes. Molecular interaction energy fields were computed for each molecule with five different chemical probes and then compared by computing similarity indices. Similarity analysis showed that the classes are on average distinguishable, with better differentiation achieved for the T conformers than the P conformers. This indicates that the T conformation might be the active one. Further, a screening was developed which could distinguish compounds with auxin activity from inactive compounds and most antiauxins using the T conformers. The classifications rationalize ambiguities in activity data found in the literature and should be of value in predicting the activities of new plant growth substances and herbicides.     

Particulate matter analysis at elementary schools in Curitiba,Brazil

The particulate matter indoors and outdoors of the classrooms at two schools in Curitiba, Brazil, was characterised in order to assess the indoor air quality. Information concerning the bulk composition was provided by energy-dispersive x-ray fluorescence (EDXRF). From the calculated indoor/outdoor ratios and the enrichment factors it was observed that S-, Cl- and Zn-rich particles are of concern in the indoor environment. In the present research, the chemical compositions of individual particles were quantitatively elucidated, including low-Z components like C, N and O, as well as higher-Z elements, using automated electron probe microanalysis low Z EPMA. Samples were further analysed for chemical and morphological aspects, determining the particle size distribution and classifying them according to elemental composition associations. Five classes were identified based on major elemental concentrations: aluminosilicate, soot, organic, calcium carbonate and iron-rich particles. The majority of the respirable particulate matter found inside of the classroom was composed of soot, biogenic and aluminosilicate particles. In view of the chemical composition and size distribution of the aerosol particles, local deposition efficiencies in the human respiratory system were calculated revealing the deposition of soot at alveolar level. The results showed that on average 42% of coarse particles are deposited at the extrathoracic level, whereas 24% are deposited at the pulmonary region. The fine fraction showed a deposition rate of approximately 18% for both deposition levels.     

Barzilai–Borwein method with variable sample size for stochastic linear complementarity problems

A smoothing method for solving stochastic linear complementarity problems is proposed. The expected residual minimization reformulation of the problem is considered, and it is approximated by the sample average approximation (SAA). The proposed method is based on sequential solving of a sequence of smoothing problems where each of the smoothing problems is defined with its own sample average approximation. A nonmonotone line search with a variant of the Barzilai–Borwein (BB) gradient direction is used for solving each of the smoothing problems. The BB search direction is efficient and low cost, particularly suitable for nonmonotone line search procedure. The variable sample size scheme allows the sample size to vary across the iterations and the method tends to use smaller sample size far away from the solution. The key point of this strategy is a good balance between the variable sample size strategy, the smoothing sequence and nonmonotonicity. Eventually, the maximal sample size is used and the SAA problem is solved. Presented numerical results indicate that the proposed strategy reduces the overall computational cost.     

Thermal dileptons in high-energy nuclear collisions

Clear signs of excess dileptons above the known sources have been found at the SPS for a long time. However, a real clarification of these observations was only recently achieved by NA60, measuring dimuons with unprecedented precision in 158A GeV In-In collisions. The excess mass spectrum in the region is consistent with a dominant contribution from π⁺π⁻→ρ→μ⁺μ⁻ annihilation. The associated ρ spectral function shows a strong broadening, but essentially no shift in mass. In the region , the excess is found to be prompt, not due to enhanced charm production. The inverse slope parameter associated with the transverse momentum spectra rises with mass up to the ρ, followed by a sudden decline above. While the initial rise, coupled to a hierarchy in hadron freeze-out, points to radial flow of a hadronic decay source, the decline above signals a transition to a low-flow source, presumably of partonic origin. The mass spectra show a steep rise towards low masses characteristic of Planck-like radiation. The polarization of the excess referred to the Collins Soper frame is found to be isotropic. All observations are consistent with a global interpretation of the excess as thermal radiation. We conclude with a short discussion of a possible link to direct photons.