Odour nuisance in Scheldt branch Gentbrugge-Melle [POSTER]

The tidal branch of the Sea Scheldt between the lock of Gentbrugge and Melle - part of the complex Ringvaart system around Ghent - has not received any upstream discharge since 1981. Consequently, ebb velocities were reduced, while flood velocities were left unaffected, causing sedimentation in the branch. At some locations along the branch, odour nuisance was regularly reported. In order to address the problem, Division Sea Scheldt of the Flemish Government proposed to dredge the associated muddy material. Flanders Hydraulics Research (FHR) was asked to conduct a study about the necessary upstream discharge at the lock of Gentbrugge needed to ensure the river branch’s self-erosiveness. To answer this question, monitored data were combined with modelling know-how. A 2D numerical morphological model was constructed, for which hydrological and sedimentological parameters, such as discharge, gauge height and sediment concentration, were used as input and for validation. All of these data were provided by FHR. After numerous numerical scenarios, it was concluded that the discharge required, lies between 20 and 25 m3/s. However, as a mean discharge of about 70 m3/s is discharged into the entire water system around Ghent, and as other waterways within this system require sufficient discharges (of which the Canal Ghent-Terneuzen has been determined in a Belgian-Dutch treaty) this discharge is not available in normal circumstances in the tidal branch. Currently, Flanders Hydraulics Research is investigating the possibilities of a lower discharge at the weir of Gentbrugge, that would allow to maintain the branch with a limited dredging

Heat Treated NiP–SiC Composite Coatings: Elaboration and Tribocorrosion Behaviour in NaCl Solution

Tribocorrosion behaviour of heat-treated NiP and NiP–SiC composite coatings was investigated in a 0.6 M NaCl solution. The tribocorrosion tests were performed in a linear sliding tribometer with an electrochemical cell interface. It was analyzed the influence of SiC particles dispersion in the NiP matrix on current density developed, on coefficient of friction and on wear volume loss. The results showed that NiP–SiC composite coatings had a lower wear volume loss compared to NiP coatings. However, the incorporation of SiC particles into the metallic matrix affects the current density developed by the system during the tribocorrosion test. It was verified that not only the volume of co-deposited particles (SiC vol.%) but also the number of SiC particles per coating area unit (and consequently the SiC particles size) have made influence on the tribocorrosion behaviour of NiP–SiC composite coatings

Magnetic and thermal properties of 4f-3d ladder-type molecular compounds

We report on the low-temperature magnetic susceptibilities and specific heats of the isostructural spin-ladder molecular complexes L$_{2}$[M(opba)]_{3\cdot xDMSO$\cdot y$H$_{2}$O, hereafter abbreviated with L$_{2}$M$_{3}$ (where L = La, Gd, Tb, Dy, Ho and M = Cu, Zn). The results show that the Cu containing complexes (with the exception of La$_{2}$Cu$_{3}$) undergo long range magnetic order at temperatures below 2 K, and that for Gd$_{2}$Cu$_{3}$ this ordering is ferromagnetic, whereas for Tb$_{2}$Cu$_{3}$ and Dy$_{2}$Cu$_{3}$ it is probably antiferromagnetic. The susceptibilities and specific heats of Tb$_{2}$Cu$_{3}$ and Dy$_{2}$Cu$_{3}$ above $T_{C}$ have been explained by means of a model taking into account nearest as well as next-nearest neighbor magnetic interactions. We show that the intraladder L--Cu interaction is the predominant one and that it is ferromagnetic for L = Gd, Tb and Dy. For the cases of Tb, Dy and Ho containing complexes, strong crystal field effects on the magnetic and thermal properties have to be taken into account. The magnetic coupling between the (ferromagnetic) ladders is found to be very weak and is probably of dipolar origin.Comment: 13 pages, 15 figures, submitted to Phys. Rev.

Synthesis of La2NiO4+d oxides by sol–gel process: Structural and microstructural evolution from amorphous to nanocrystallized powders

In this paper, the structural and microstructural transition from amorphous to La2NiO4+d nanocrystallized oxides synthesized by a polymeric route based on Pechini’s work has been studied by several experimental techniques including infrared spectroscopy and wide angle X-ray scattering. The synthesis parameters which govern this transition have been identified in order to synthesize La2NiO4+d oxides with various mean crystallite sizes and non stoichiometry levels. Therefore, it has been demonstrated that the control of the nature and the content of organic compounds in the polymeric sols allows the preparation of La2NiO4+d metastable phases with a mean crystallite size ranging from 100 to 220 nm and a non stoichiometry level ranging from 0.15 to 0.22 at 25 8C. As the cathodic performance strongly depends on the physical characteristics of the oxides, this study shows that our versatile process may be suitable to elaborate electrodes with different electrochemical behaviours

Dihydrolipoic acid reduces cytochrome b561 proteins.

Cytochrome b561 (Cyt-b561) proteins constitute a family of trans-membrane proteins that are present in a wide variety of organisms. Two of their characteristic properties are the reducibility by ascorbate (ASC) and the presence of two distinct b-type hemes localized on two opposite sides of the membrane. Here we show that the tonoplast-localized and the putative tumor suppressor Cyt-b561 proteins can be reduced by other reductants than ASC and dithionite. A detailed spectral analysis of the ASC-dependent and dihydrolipoic acid (DHLA)-dependent reduction of these two Cyt-b561 proteins is also presented. Our results are discussed in relation to the known antioxidant capability of DHLA as well as its role in the regeneration of other antioxidant compounds of cells. These results allow us to speculate on new biological functions for the trans-membrane Cyt-b561 proteins

A Cytochrome b561 with Ferric Reductase Activity from the Parasitic Blood Fluke, Schistosoma japonicum

Parasites acquire their food from their hosts, either by feeding directly on tissues of the host, or by competing for ingested food. Adult schistosomes live within the vasculature of humans and rely on the blood cells and plasma they ingest and dissolved solutes they derive across their body surface, the tegument, for their nutrition. Schistosomes require host trace elements, notably iron, which is used as a co-factor in many biological reactions. Iron is especially important for schistosomes, for it has a significant role in egg formation and embryogenesis. In human tissues, iron predominates in the trivalent (ferric) form; however, it is the divalent (ferrous) form that is used as an essential co-factor for multiple biomolecules and enzymes. In order to be acquired from the host environment, the valency of iron must be modified to render it suitable for transport across the parasite membrane. This paper describes the molecular characterisation of a schistosome molecule that is crucial for bringing about this change in iron. Schistosoma japonicum Cytb561 is the first ferric reductase characterised in any parasitic helminth and emphasises the importance of iron, and other divalent cations, in these organisms