Teixeira, Bruno, João Louren{\c c}o, and Diogo Sousa. "
A Static Approach for Detecting Concurrency Anomalies in Transactional Memory."
InForum 2010: Proceedings of InForum Simpósio de Informática. Universidade do Minho, 2010.
AbstractPrograms containing concurrency anomalies will most probably exhibit harmful erroneous and unpredictable behaviors. To ensure program correctness, the sources of those anomalies must be located and corrected. Concurrency anomalies in Transactional Memory (TM) programs should also be diagnosed and fixed. In this paper we propose a framework to deal with two different categories of concurrency anomalies in TM. First, we will address low-level TM anomalies, also called dataraces, which arise from executing programs in weak isolation. Secondly, we will address high-level TM anomalies, also called high-level dataraces, bringing the programmers attention to pairs of transactions that the programmer has misspecified, and should have been combined into a single transaction. Our framework was validated against a set of programs with well known anomalies and demonstrated high accuracy and effectiveness, thus contributing for improving the correctness of TM programs
Drasovean, R. a, R. b Monteiro, and M. c Cherif. "
Structure and morphology study of cobalt oxide doped silica nanocomposite films."
AIP Conference Proceedings. Vol. 1203. 2010. 483-488.
AbstractCobalt oxide doped silica films were synthesized by a dip-coating technique. Initial compounds were cobalt acetate Co(CH3COO)2-4H 2O and tetraethoxysilane Si(OC2H5)4. The chemical composition was studied by X-ray diffraction and UV-Vis spectroscopy. The morphology analyses were carried out by means of atomic force microscopy. The average diameter of cobalt oxide dispersed particles increases with the molar ratio Co:Si and with the aging time of the initial colloidal solution. © 2009 American Institute of Physics.
Pinto, R. M., R. I. Olariu, J. Lameiras, F. T. Martins, A. A. Dias, G. J. Langley, P. Rodrigues, C. D. Maycock, J. P. Santos, M. F. Duarte, M. T. Fernandez, and M. L. Costa. "
Study of selected benzyl azides by UV photoelectron spectroscopy and mass spectrometry."
Journal of Molecular Structure. 980 (2010): 163-171.
AbstractBenzyl azide and the three methylbenzyl azides were synthesized and characterized by mass spectrometry (MS) and ultraviolet photoelectron spectroscopy (UVPES). The electron ionization fragmentation mechanisms for benzyl azide and their methyl derivatives were studied by accurate mass measurements and linked scans at constant B/E. For benzyl azide, in order to clarify the fragmentation mechanism, labelling experiments were performed. From the mass analysis of methylbenzyl azides isomers it was possible to differentiate the isomers ortho, meta and para. The abundance and nature of the ions resulting from the molecular ion fragmentation, for the three distinct isomers of substituted benzyl azides, were rationalized in terms of the electronic properties of the substituent. Concerning the para-isomer, IRC calculations were performed at UHF/6-31G(d) level. The photoionization study of benzyl azide, with He(I) radiation, revealed five bands in the 8-21 eV ionization energies region. From every photoelectron spectrum of methylbenzyl azides isomers it has been identified seven bands, on the same range as the benzyl azide. Interpretation of the photoelectron spectra was accomplished applying Koopmans' theorem to the SCF orbital energies obtained at HF/6-311++G(d, p) level.
Neagu, E. R., C. J. Dias, M. C. Lanca, R. Igreja, P. Inacio, J. N. Marat-Mendes, and Ieee. "
The Study of the Molecular Movements in the Range of Glass Transition by the Final Thermally Stimulated Discharge Current Technique."
Proceedings of the 2010 Ieee International Conference on Solid Dielectrics. IEEE International Conference on Solid Dielectrics-ICSD. 2010.
AbstractThe electrical methods used to study the molecular movements are based on the movement of the dipoles under DC or AC electric field. We have proposed recently a combined measuring protocol to analyze charge injection/extraction, transport, trapping and de-trapping in polar or non-polar dielectric materials. The method is used here to analyze the molecular movements in polyimide in the temperature range from 293 to 572 K. A strong relaxation was observed around 402 K and a very weak relaxation around 345 K. This is the beta relaxation which is quite complex. As concern the behavior at high temperatures, above the beta relaxation, a high peak was observed that shifts continuously to higher temperatures as the charging temperature and/or the charging field increase. The maximum current of the peak increases and the temperature corresponding to the maximum current increases as the charging temperature and/or the charging field increase, given a direct observation of the so called cross-over effect related to current decay for sample charged at high fields and/or high temperatures.
Nunes, Isabel L., and Jurek Kirakowski Usabilidade de interfaces – versão Portuguesa do Software Usability Measurement Inventory (SUMI) [Interfaces Usability – Portuguese version of the Software Usability Measurement Inventory (SUMI)]. Eds. P. Arezes, J. S. Baptista, M. P. Barroso, P. Carneiro, P. Cordeiro, N. Costa, R. Melo, A. S. Miguel, and G. P. Perestrelo. Occupational Safety and Hygiene (SHO10). Guimarães - Portugal: SPOSHO, 2010.
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Santos, J. P., A. M. Costa, J. P. Marques, M. C. Martins, P. Indelicato, and F. Parente. "
X-ray-spectroscopy analysis of electron-cyclotron-resonance ion-source plasmas."
Physical Review A. 82 (2010): 062516.
AbstractAnalysis of x-ray spectra emitted by highly charged ions in an electron-cyclotron-resonance ion source (ECRIS) may be used as a tool to estimate the charge-state distribution (CSD) in the source plasma. For that purpose, knowledge of the electron energy distribution in the plasma, as well as the most important processes leading to the creation and de-excitation of ionic excited states are needed. In this work we present a method to estimate the ion CSD in an ECRIS through the analysis of the x-ray spectra emitted by the plasma. The method is applied to the analysis of a sulfur ECRIS plasma.