The effects of binaural spectral resolution mismatch on Mandarin speech perception in simulated electric hearing

This study assessed the effects of binaural spectral resolution mismatch on the intelligibility of Mandarin speech in noise using bilateral cochlear implant simulations. Noise-vocoded Mandarin speech, corrupted by speech-shaped noise at 0 and 5?dB signal-to-noise ratios, were presented unilaterally or bilaterally to normal-hearing listeners with mismatched spectral resolution between ears. Significant binaural benefits for Mandarin speech recognition were observed only with matched spectral resolution between ears. In addition, the performance of tone identification was more robust to noise than that of sentence recognition, suggesting factors other than tone identification might account more for the degraded sentence recognition in noise.     

Molybdenum Cofactor Deficiency in Humans

Molybdenum cofactor (Moco) deficiency (MoCD) is characterized by neonatal-onset myoclonic epileptic encephalopathy and dystonia with cerebral MRI changes similar to hypoxic–ischemic lesions. The molecular cause of the disease is the loss of sulfite oxidase (SOX) activity, one of four Moco-dependent enzymes in men. Accumulating toxic sulfite causes a secondary increase of metabolites such as S-sulfocysteine and thiosulfate as well as a decrease in cysteine and its oxidized form, cystine. Moco is synthesized by a three-step biosynthetic pathway that involves the gene products of MOCS1, MOCS2, MOCS3, and GPHN. Depending on which synthetic step is impaired, MoCD is classified as type A, B, or C. This distinction is relevant for patient management because the metabolic block in MoCD type A can be circumvented by administering cyclic pyranopterin monophosphate (cPMP). Substitution therapy with cPMP is highly effective in reducing sulfite toxicity and restoring biochemical homeostasis, while the clinical outcome critically depends on the degree of brain injury prior to the start of treatment. In the absence of a specific treatment for MoCD type B/C and SOX deficiency, we summarize recent progress in our understanding of the underlying metabolic changes in cysteine homeostasis and propose novel therapeutic interventions to circumvent those pathological changes.     

Ordinary Papers

This paper deals with the systems of algebraic equations arising in the application of implicit Runge-Kutta methods.Equivalent conditions under which three wide classes of differential equations have unique solutions are presented. In addition, sufficient conditions for their existence are given.     

Spontaneous Metal‐Free Transfer Hydrogenation of Iminoboranes with Ammonia Borane and Amine Boranes

The first spontaneous, metal‐free, room‐temperature hydrogen transfer from ammonia borane to an iminoborane is reported. Mechanistic studies of the reaction indicate a concerted transfer of H⁺ and H^? from donor to acceptor with an activation energy far below those of comparable concerted transfer hydrogenations. This reaction was employed in the syntheses and isolation of new B,N‐disubstituted aminoboranes, a comparatively rare subset within the aminoborane family. This successful transfer hydrogenation to a highly dehydrogenated BN system may serve as a starting point for the design of new systems capable of reversible dehydrogenation/rehydrogenation.     

Hydrogen formation during pyrolysis of polystyrene

Hydrogen was identified as a product of the pyrolysis of polygyrene, especially at high pyrolysis temperatures. With a high interface temperature of the Pyroprobe foil pyrolyser and a high pyrolysis temperature, almost 100% of the pyrolysed polymer could be accounted for. It is then assumed that hydrogen (up to 26%) produces a corresponding amount of carbon, which remains on the foil.     

Continuous production of butanol with immobilized cells ofClostridium acetobutylicum

Spores ofClostridium acetobutylicum were immobilized in calcium alginate. An active gel preparation was obtained after outgrowth of the spores to vegetative cells within the gel matrix. A 100 mL column containing the immobilized cells was used for continuous production. At steady-state conditions the productivity of butanol was 67 g/L reactor volume/day.     

A study of the stereochemistry of 2-aryl-4,5-dimethyl-1,3-dioxolanes by cholesteric induction in nematic phases and circular dichroism spectroscopy

[Chemical reaction: See text] The circular dichroism spectra and the twisting ability of a series of 2-aryl-4,5-dimethyl-1,3-dioxolanes used as dopants in nematic solvents have been related to their absolute configuration. Whereas the circular dichroism (CD) spectra are deeply affected by the substituents present in the aromatic ring, which in several cases cause sign inversion, the helical twisting power beta is only marginally influenced. The values of beta also seem not very sensitive to the rotamer population around the aromatic ring; this indicates the predominant importance of the chiral dioxolane ring in determining the cholesteric induction. These facts can be explained by the different nature of the two observables: in CD, the chirality is read by the absorbing chromophore and is deeply influenced even by small changes of this group. In cholesteric induction we are dealing instead with chiral solute-solvent interactions that determine a twist in the solvent. In light of the present and previous results, this process seems predominantly determined by short-range interactions, which are modulated by the molecular shape. From a practical point of view, a configurational correlation using CD for the present series of compounds seems problematic, while the values of beta are nicely correlated to the absolute configurations. Calculations with the surface chirality method predict well the sign and order of magnitude of beta and their limited sensitivity to the phenyl substituents and rotamer population.     

Synthèse de copolymères greffés à base de polyéthylène—1

Polyethylene macromolecular free radical initiators, obtained by ozonization, are used to prepare graft copolymers with methyl methacrylate, styrene and vinyl chloride. The reactions parameters are the number of initiator groups (found by DPPH), peroxide and hydroperoxide proportions (respectively 36 and 64%), decomposition rate (K_d at 90° 10⁻¹sec⁻¹) and monomer concentration. The molecular structure of these copolymers is defined.     

Structure and catalytic properties of nanosized alumina supported platinum and palladium particles synthesized by reaction in microemulsion

Mixtures of nanosized platinum and palladium particles have been prepared by reduction of salt-containing microemulsion droplets using hydrazine as the reducing agent. To avoid possible negative effects of the presence of sulfur compounds during the preparation the microemulsion was made using the sulfur-free nonionic polyoxyethylene 4 lauryl ether surfactant. Transmission electron microscopy showed that the as-prepared mixtures contained crystalline platinum particles of fairly homogeneous size (20 to 40 nm) with adsorbed amorphous palladium particles 2 to 5 nm in size. Catalyst samples were prepared by depositing the nanoparticles on a gamma-Al(2)O(3) support followed by heating in air at 600 degrees C. Alloyed particles of platinum and palladium with sizes ranging from 5 to 80 nm were obtained during the heating. The majority of the particles had the fcc structure and their compositional range was dependent upon the Pt:Pd molar ratio of the microemulsion. A catalyst prepared from a microemulsion with a 20:80 Pt:Pd molar ratio showed the highest catalytic activity for CO oxidation, while pure platinum and palladium catalysts showed higher sulfur resistance. These results differ from the performance of conventional wet-impregnated catalysts, where a 50:50 Pt:Pd molar ratio resulted in the highest catalytic activity as well as the highest sulfur resistance.     

Matériaux composites à base de graves et de liants polymères II: Ozonisation du polyéthylène et dosage des hydropéroxydes et des péroxydes derivés

The study of the oxidation of low density polyethylene is carried out under fluidized conditions in air and ozone. Special attention is paid to the formation of peroxides and hydroperoxides. Their production is optimized according to various parameters (temperature, time, quantity of ozone, flow of the gaseous current) using an experimental design method. Peroxides and hydroperoxides are titrated by a colorimetric method using diphenylpicrylhydrazyl as reagent. A correlation between i.r. carbonyl ratio and the yield of peroxides has been established.