Scheduling component replacement for timely execution in dynamic systems

Timely run‐time software replacement techniques are a corner stone for reconciling real‐time systems development and dynamic behavior. Typical real‐time systems do not consider dynamic behavior because it deeply challenges predictability and timeliness. Current efforts are starting to merge the safe and predictable execution with a controllable level of dynamicity by imposing a set of bounds and limitations to the system dynamic behavior. One of the obstacles for this is how to time‐bound the different operations required to effectively implement component replacement. In this paper, the main challenges for this problem are identified, and a model to ensure that components can be replaced at run time preserving the temporal properties of the system is provided that also avoids failures in replacements. A real example and simulations of our replacement model are provided that validate the presented ideas. Copyright © 2013 John Wiley & Sons, Ltd.     

Modèles Hydrodynamiques pour la Séparation des Courants dans un Décanteur Pilote

Despite of its general use in industry, particle sedimentation is still a not well understood unit operation. Hydrodynamics is complex in essence, mainly because the possible volumes are depending on the operating conditions, which in turn has consequences on the stability of the equipment in unsteady state conditions.     

Vitamin C Enhances Vitamin E Status and Reduces Oxidative Stress Indicators in Sea Bass Larvae Fed High DHA Microdiets

Docosahexaenoic acid (DHA) is an essential fatty acid necessary for many biochemical, cellular and physiological functions in fish. However, high dietary levels of DHA increase free radical injury in sea bass (Dicentrarchus labrax) larvae muscle, even when vitamin E (α-tocopherol, α-TOH) is increased. Therefore, the inclusion of other nutrients with complementary antioxidant functions, such as vitamin C (ascorbic acid, vitC), could further contribute to prevent these lesions. The objective of the present study was to determine the effect of vitC inclusion (3,600?mg/kg) in high DHA (5?% DW) and α-TOH (3,000?mg/kg) microdiets (diets 5/3,000 and 5/3,000?+?vitC) in comparison to a control diet (1?% DHA DW and 1,500?mg/kg of α-TOH; diet 1/1,500) on sea bass larvae growth, survival, whole body biochemical composition and thiobarbituric acid reactive substances (TBARS) content, muscle morphology, skeletal deformities and antioxidant enzymes, insulin-like growth factors (IGFs) and myosin expression (MyHC). Larvae fed diet 1/1,500 showed the best performance in terms of total length, incidence of muscular lesions and ossification degree. IGFs gene expression was elevated in 5/3,000 diet larvae, suggesting an increased muscle mitogenesis that was confirmed by the increase in the mRNA copies of MyHC. vitC effectively controlled oxidative damages in muscle, increased α-TOH larval contents and reduced TBARS content and the occurrence of skull deformities. The results of the present study showed the antioxidant synergism between vitamins E and C when high contents of DHA are included in sea bass larvae diets.     

Raiding the Noosphere: the open development of networked RAID support for the Linux kernel

The Noosphere is a term borrowed by open‐source advocate Eric Raymond to denote the virtual world of the Internet. Fitting a new driver into the Linux kernel requires a ‘noospheric’ strategy as well as an engineering strategy, because the code is part of the open‐source development process, not its end. This article recounts the technology and the development process followed for a ‘fast and intelligent’ driver extension to the existing Linux software RAID subsystem. The development adapts the kernel RAID subsystem for use in the context of network‐attached storage. Copyright © 2005 John Wiley & Sons, Ltd.     

Ternary Gels of a Polymer Blend and a Recycled Oil: Their Use as Bitumen Modifiers

A blend of random ethylene‐vinyl acetate copolymer (EVA) and triblock styrene‐butadiene‐styrene copolymer (SBS) was dissolved in a recycled engine oil to obtain ternary thermoreversible gels. As the temperature was increased, first a network associated with EVA disappeared, and a second one associated with SBS dominated, maintaining the elastic response of the system. The principal advantage of these ternary systems is that their mechanical properties and thermal stability are better than that of binary gels. These gels, made from waste, can be used as bitumen modifiers to obtain binders of improved properties and good stability, which are useful for road surfacing.

Temperature sweeps of elastic modulus performed at a frequency of 1 Hz.     

Catalytic Reduction of 4-Nitrobenzoic Acid by cis-[Rh(CO)2(Amine)2](PF6) Complexes Under Water–Gas Shift Reaction Conditions: Kinetics Study

Rhodium(I) complexes of the type, cis-[Rh(CO)₂(amine)₂](PF₆) where (amine = 3-picoline, 2-picoline, pyridine, 2,6-lutidina or 3,5-lutidine) dissolved in 80% aqueous amine solutions catalyzed the selective reduction of 4-nitrobenzoic acid to 4-aminobenzoic acid under CO atmosphere. The importance of these catalytic systems is their high chemo selectivity for the aromatic nitro group of the 4-nitrobenzoic acid with respect to the carboxylic group, allowing the production of the desired aromatic amine in high yields. The 4-aminobenzoic acid production depends on the nature of the coordinated amine. The Rh/3,5-lutidine system, the most active catalyst among tested, displays turnover frequencies for 4-aminobenzoic acid production of about 173 moles per mole Rh per day for [Rh] = 1 × 10^?4 mol, [4-nitrobenzoic acid] = 3.82 × 10^?3mol, 10 mL of 80% aqueous 3,5-lutidine, P(CO) = 0.9 atm at 100 °C. Analyses of kinetic results for the Rh/3,5-lutidine system show a first order dependence on 4-nitrobenzoic acid concentration, a non-linear dependence on CO pressure, a segmented Arrhenius plot and dependence on the nature of the reducing gas agent. These data are discussed in terms of a possible mechanism.     

Characterising polysaccharides in cherimoya (Annona cherimola Mill.) purée and their enzymatic liquefaction

Polysaccharides isolated in the alcohol-insoluble residues (AIR) from cherimoya (Annona cherimola Mill.) were characterised for contents of soluble pectin, cellulose, hemicellulose and lignin, and the distribution of neutral sugars and uronides in water-soluble pectin (WSP) and water-insoluble AIR (WAIR) fractions. For WSP, the predominant neutral sugar was arabinose and, for WAIR, cellulosic glucose and xylose. Two enzyme preparations were tested for their capacity to release neutral sugars and uronides from WAIR. The optimal incubation temperature (45 °C) and the most effective preparation—rich in pectinase, cellulase and xylanase activities—were selected according to a central composite rotatable design (CCRD). Enzyme was also applied to native cherimoya purée according to another CCRD, varying the enzyme concentration and incubation time. Native purée exhibited strong shear-thinning behaviour with high, extrapolated, yield stress. During enzymatic treatment, behaviour was less shear thinning, and yield stress, consistency index and Bostwick consistency tended to decrease, giving rise to purées of different rheological properties.     

PARTICLE SIZE, SOLVENT, OXYGEN, TEMPERATURE AND PRESSURE EFFECTS ON THE CONTENTS OF INSOLUBLE FRACTIONS FROM SOLID VACUUM RESIDUA

n-Heptane insoluble contents were determined for an extraheavy-oil vacuum residue, one petroleum and one coal pitch as a function of particle size. This variable was found to affect the yields of insoluble material, aspect which was also observed during extractions carried out with aromatic and halogenated solvents. The precision of results was observed to be independent on the operators. A study was carried out to determine the effect of sample drying time on fraction yields. It was found that maltene fractions were strongly dependent on this variable, whereas asphaltene fractions were totally independent

Predissolution in aromatic solvents proved worthless from the repeatability point of view. However, predissolution of the oil residue in CH₂Cl₂ followed by filtration and asphaltene precipitation with simultaneous solvent removal, was deemed to be a suitable technique to remove mineral matter and isolate asphaltenes in a single step

Sample oxidation during asphaltene precipitation and isolation was detected by gravimetric and spectroscopic techniques. This fact is very important since common precipitation techniques do not address this issue

Preliminary accelerated extraction experiments carried out with pitch samples at high temperature and pressure, revealed that this approach can be a very interesting research tool to investigate solubility properties.