Fast X-ray transients towards the Galactic bulge with the Rossi X-ray Timing Explorer

In X-ray binaries, rapid variability in X-ray flux of greater than an order of magnitude on time-scales of a day or less appears to be a signature of wind accretion from a supergiant companion. When the variability takes the form of rare, brief, bright outbursts with only faint emission between them, the systems are called supergiant fast X-ray transients (SFXTs). We present data from twice-weekly scans of the Galactic bulge by the Rossi X-ray Timing Explorer that allow us to compare the behaviour of known SFXTs and possible SFXT candidates with the persistently bright supergiant X-ray binary 4U 1700−377. We independently confirm the orbital periods reported by other groups for SFXTs SAX J1818.6−1703 and IGR J17544−2619. The new data do not independently reproduce the orbital period reported for XTE J1739−302, but slightly improve the significance of the original result when the data are combined. The bulge source XTE J1743−363 shows a combination of fast variability and a long-term decline in activity, the latter behaviour not being characteristic of supergiant X-ray binaries. A far-red spectrum of the companion suggests that it is a symbiotic neutron star binary rather than a high-mass binary, and the reddest known of this class: the spectral type is approximately M8 III.

Towards the Design of a Textile Chemical Ontology

The main goal of this paper is to present the initial version of a Textile Chemical Ontology, to be used by textile professionals with the purpose of conceptualising and representing the banned and harmful chemical substances that are forbidden in this domain. After analysing different methodologies and determining that “Methontology” is the most appropriate for the purposes, this methodology is explored and applied to the domain. In this manner, an initial set of concepts are defined, together with their hierarchy and the relationships between them. This paper shows the benefits of using the ontology through a real use case in the context of Information Retrieval. The potentiality of the proposed ontology in this preliminary evaluation encourages extending the ontology with a higher number of concepts and relationships, and validating it within other Natural Language Processing applications.

Palladium(II) pincer complexes of α-amino acids: towards the synthesis of catalytically active artificial peptides

NCN palladium(II) complexes have been covalently attached to the N- and C-terminus of the dipeptide L-Phe-L-Va-OMe. Remarkably, the hydrolysis of the NCN-Pd(II) L-Val-OMe afforded the corresponding, palladated free amino acid without affecting the metal site. This deprotected amino acid could be coupled to any protein, enzyme or peptidic chain by simple peptide chemistry. This bioorganometallic systems were active as catalysts in the aldol reaction between methyl isocianate and benzaldehyde.

Towards the understanding of the interfacial pH scale at Pt(1 1 1) electrodes

The determination of the potentials of zero total and free charge, pztc and pzfc respectively, were made in a wide pH range by using the CO displacement method and the same calculation assumptions used previously for Pt(1 1 1) electrodes in contact with non-specifically adsorbing anions. Calculation of the pzfc involves, in occasions, long extrapolations that lead us to the introduction of the concept of potential of zero extrapolated charge (pzec). It was observed that the pztc changes with pH but the pzec is independent of this parameter. It was observed that the pztc > pzec at pH > 3.4 but the opposite is true for pH > 3.4. At the latter pH both pzec and pztc coincide. This defines two different pH regions and means that adsorbed hydrogen has to be corrected in the “acidic” solutions at the pztc while adsorbed OH is the species to be corrected in the “alkaline” range. The comparison of the overall picture suggests that neutral conditions at the interface are attained at significantly acidic solutions than those at the bulk.