The kinetics of the catalytic hydrogenolysis of ethane over Ni/SiO2

The rate of hydrogenolysis of ethane over a Ni/SiO₂ catalyst, studied over a large range of pressure and of temperature, is shown to be related to the degree of hydrogen coverage θ_H, by the equation: with K₀ nearly equal to the number of ethane molecules colliding with the Ni surface, E₀ = 14 ? 1 kcal/mole, Y = ?1 ? 2 and X = 15 ? 2. The rate-limiting step is believed to be the irreversible, dissociative adsorption of ethane on an ensemble of at least 12 adjacent Ni atoms, free from adsorbed hydrogen, resulting in the complete cracking of C₂H₆: C₂H₆ + 12Ni → 2

Irreversible adsorption of ethane is assumed to compete with the reversible adsorption of hydrogen. This mechanism, which is compared with those proposed earlier, is in good agreement with data on ethane adsorption studied by magnetic methods, and with a study of ethane hydrogenolysis over NiCu/SiO₂ catalysts.     

Characterisation of the neutral oil from a low-temperature coal tar

Tar resulting from fluidised-bed, low-temperature carbonisation of coal was treated to yield a neutral oil from which a series of six other samples was extracted. These were examined by proton magnetic resonance (p.m.r.) spectroscopy, low-ionising-voltage (11 eV) mass spectroscopy (m.s.), gel chromatography followed by fluorescent indicator analysis, and cryoscopy. Aliphatic fractions separated chromatographically were also examined by infra-red spectroscopy. Distributions of hydrogen between chemical types were found for the several fractions from 60 MHz p.m.r. spectra and presented in terms of average structural parameters. M.s. analysis indicated negligible cracking of paraffin components, and the average molecular weight of 197 agreed well with cryoscopic determinations. For the carbon ratio, f_a, between aromatic and total, agreement between m.s. and p.m.r. depends on the p.m.r. structural analysis scheme adopted. P.m.r. and m.s. structural analyses of the aromatics emphasise the predominance of di- and tri-nuclears, with about 40% of available sites substituted, and the importance of acenes in lowtemperature carbonisation material. Gas and gel chromatography showed urea-adductable paraffins to be largely straight-chain C₁₀-C₂₆, much as for tars from carbonisation at higher temperature.     

LIQUID PHASE TRANSPORT PROPERTIES IN A HIGH PRESSURE PACKED COLUMN

A mathematical model of fluid flow and mass transfer in a packed bed was derived and used to evaluate the liquid phase axial dispersion and mass transfer coefficients under high pressure conditions. The least-squares method was used to evaluate the rate parameters from experimental breakthrough curves, and the agreement between the concentration curves predicted from rate parameters and those measured experimentally was good. Experiments were performed at 20 and 200°C with water as a solvent and nonporous soda-lime glass beads as packing. Although the axial dispersion coefficient was independent of temperature and pressure, the mass transport parameters were found to be pressure dependent.     

The potentiometric behaviour of copolymers of methacrylic acid in water-ethanol solutions

Summary The synthesis is reported of copolymers of styrene with methacrylic acid and of methyl methacrylate with methacrylic acid by radical copolymerization, of copolymers of methyl methacrylate with methacrylic acid by partial alkaline hydrolysis of poly(methyl methacrylate), and of block copolymers of styrene with methacrylic acid. Modified titration curves of all these copolymers were recorded in water and water-ethanol solutions. In a solution containing 50 mass.% ethanol, only small differences could be observed between the potentiometric behaviour of the individual copolymers and polymethacrylic acid. Also, there were no essential differences in any of the solvents used between the potentiometric behaviour of block copolymers of styrene with methacrylic acid, on the one hand, and polymethacrylic acid, on the other. On the contrary, maxima and minima were always observed on the modified titration curves of statistical copolymers with a higher content of the hydrophobic comonomer in solutions with a high water content. Thus, using the modified titration curves, it is possible to decide whether a given copolymer is of the block or statistical type.     

Molecular modeling of antibody-antigen complexes between the Brucella abortus O-chain polysaccharide and a specific monoclonal antibody

A molecular model of the binding site of an anti-carbohydrateantibody (YsT9.1) has been developed using computer-assistedmodeling techniques and molecular dynamics calculations. Sequencehomologies among YsT9.1 and the Fv regions of McPC603, J539and human Bence-Jones protein REI, all of which have solvedcrystal structures, provided the basis for the modeling. Thegroove-type combining site model had a topography which wascomplementary to low energy confonners of the polysaccharide,a Brucella O-antigen, and the site could be almost completelyfilled by a pentasaccharide epitope in either of two dockingmodes. Putative interactions between this epitope and the antibodyare consistent with the known structural requirements for bindingand lead to the design of oligosaccharide inhibitors that probethe veracity of the modeled docked complex. Ultimately boththe Fv model and the docked complex will be compared with independentcrystal structures of YsT9.1 Fab with and without pentasaccharideinhibitor, currently at the stage of refinement.     

Identification of intra-individual variation in intracranial arterial flow by MRI and the effect on computed hemodynamic descriptors

Magnetic Resonance Materials in Physics, Biology and Medicine - To determine the intra-individual flow variation in serially acquired studies, and the influence of this variation on subsequent...     

Korrosion von ölgefeuerten Zentralheizungskesseln

Corrosion of oil-fired domestic boilers Depending on the surface temperature of the flue gas side the corrosion of oil fired domestic boilers proceeds either mainly by acid corrosion or by oxygen corrosion:

• – At surface temperatures of 60°C and higher the corrosion mechanism of acid corrosion prevails and the corrosion rates amount to 0.1–0.3 mm/year (values referred to continuous burner operation). The corrosion products consist of soluble iron(II)- and iron(III)sulfates. Higher corrosion rates can be attributed to an appreciable catalytic formation of sulfur trioxide on the corrosion products formed on the convective heating surfaces.
• – At surface temperatures of 40°C the mechanism of oxygen corrosion already dominates and the corrosion rates are about ten times higher (1.5–3 mm/year, referred to continous burner operation). The high portion of ioron oxide hydrates, especially goethit (α-FeOOH), makes the corrosion products difficult to remove.
• – Distinctly reduced service lives are also expected for the so called reduced temperature boilers (“Niedertemperaturkessel”) and low temperature boiers (“Tieftemperaturkessel”): According to the manufacturers these boilers may be operated at boiler water temperatures well below 60°C, as they are equipped with constructive measures to enhance the surface temperature on the flue gas side. However, these measures are only fully effective under stationary conditions.

Some of the results were obtained from weight loss measurements on test specimen made from St 35.8 and gray cast iron, that were exposed to the flue gases of an oil fired experimental boiler. Other important results come from field measurements of the sulfuric acid content of about 30 boilers that are in practical use.     

Fracture and mechanical properties of P100 Gr/6061 Al composite

The effects of heat treatments on the mechanical and fracture properties of continuous fiber Pitch 100 graphite/6061 aluminum (P100 Gr/6061 Al) composite were evaluated by varying solution temperature and aging time. All heat treatments resulted in decreased mechanical properties due to the reaction at the fiber/matrix interface during solution treatments. SEM analysis of the fractured samples showed a large degree of fiber pullout, interface failure, and matrix cracking.     

Debugging mixed‐environment programs with Blink

Programmers build large‐scale systems with multiple languages to leverage legacy code and languages best suited to their problems. For instance, the same program may use Java for ease of programming and C to interface with the operating system. These programs pose significant debugging challenges, because programmers need to understand and control code across languages, which often execute in different environments. Unfortunately, traditional multilingual debuggers require a single execution environment. This paper presents a novel composition approach to building portable mixed‐environment debuggers, in which an intermediate agent interposes on language transitions, controlling and reusing single‐environment debuggers. We implement debugger composition in Blink, a debugger for Java, C, and the Jeannie programming language. We show that Blink is (i) simple: it requires modest amounts of new code; (ii) portable: it supports multiple Java virtual machines, C compilers, operating systems, and component debuggers; and (iii) powerful: composition eases debugging, while supporting new mixed‐language expression evaluation and Java native interface bug diagnostics. To demonstrate the generality of interposition, we build prototypes and demonstrate debugger language transitions with C for five of six other languages (Caml, Common Lisp, C#, Perl 5, Python, and Ruby) without modifications to their debuggers. Using real‐world case studies, we show that diagnosing language interface errors require prior single‐environment debuggers to restart execution multiple times, whereas Blink directly diagnoses them with one execution. Copyright © 2014 John Wiley & Sons, Ltd.