Empreitada de construção de 95 moradias no empreendimento Tróia Resort

O sector da construção é sem dúvida um dos que mais contribui para a criação de emprego, representando um valor significativo em termos de produto interno bruto. Muitas vezes a preocupação excessiva com a gestão financeira e do tempo, leva a que as soluções preconizadas na fase de projecto não sejam devidamente amadurecidas e que em obra não se dê a atenção necessária à componente técnica. Estas questões reflectem-se na qualidade da construção e nos custos que as empresas têm que suportar em termos de serviço pós venda durante o período de garantia da obra. Tendo em conta que o aluno desenvolveu a sua actividade profissional nesta área nos últimos 14 anos, o que lhe dará uma base de trabalho para o tema a desenvolver, pretende-se demonstrar a importância de cada uma das áreas da Direcção Técnica e Gestão de Empreitadas, bem como a interligação que tem de existir entre as mesmas, por forma a que o resultado final seja um sucesso pleno. No caso concreto da obra que o aluno propõe para estudo, trata-se de um complexo de 95 moradias com 8 projectos distintos onde as soluções técnicas são bastante diversas e pouco vulgares, o que terá bastante interesse para um trabalho desta natureza

Caracterização profissional e grau de satisfação dos licenciados em fisioterapia da Escola Superior de Tecnologia da Saúde de Lisboa

Mestrado em Fisioterapia.

The solvation and electrochemical behaviour of Copper acetylacetonate complexes in ionic liquids

The behavior of copper(II) complexes of pentane-2,4-dione and 1,1,1,5,5,5-hexafluoro-2,4-pentanedione, [Cu(acac)(2) (1) and [Cu(HFacac)(2)(H2O)] (2), in ionic liquids and molecular organic solvents, was studied by spectroscopic and electrochemical techniques. The electron paramagnetic resonance characterization (EPR) showed well-resolved spectra in most solvents. In general the EPR spectra of [Cu(acac)(2)] show higher g(z) values and lower hyperfine coupling constants, A(z), in ionic liquids than in organic solvents, in agreement with longer Cu-O bond lengths and higher electron charge in the copper ion in the ionic liquids, suggesting coordination of the ionic liquid anions. For [Cu(HFacac)(2)(H2O)] the opposite was observed suggesting that in ionic liquids there is no coordination of the anions and that the complex is tetrahedrically distorted. The redox properties of the Cu(II) complexes were investigated by cyclic voltammetry (CV) at a Pt electrode (d = 1 mm), in bmimBF(4) and bmimNTf(2) ionic liquids and, for comparative purposes, in neat organic solvents. The neutral copper(II) complexes undergo irreversible reductions to Cu(I) and Cu(0) species in both ILs and common organic solvents (CH2Cl2 or acetonitrile), but, in ILs, they are usually more easier to reduce (less cathodic reduction potential) than in the organic solvents. Moreover, 1 and 2 are easier to reduce in bmimNTf(2) than in bmimBF(4) ionic liquid. (C) 2013 Elsevier B.V. All rights reserved.

The solvation and redox behaviour of mixed ligand COPPER(II) complexes of acetylacetonate and aromatic dimines in ionic liquids

The behavior of two cationic copper complexes of acetylacetonate and 2,2'-bipyridine or 1,10-phenanthroline, [Cu(acac)(bipy)]Cl (1) and [Cu(acac)(phen)]Cl (2), in organic solvents and ionic liquids, was studied by spectroscopic and electrochemical techniques. Both complexes showed solvatochromism in ionic liquids although no correlation with solvent parameters could be obtained. By EPR spectroscopy rhombic spectra with well-resolved superhyperfine structure were obtained in most ionic liquids. The spin Hamiltonian parameters suggest a square pyramidal geometry with coordination of the ionic liquid anion. The redox properties of the complexes were investigated by cyclic voltammetry at a Pt electrode (d = 1 mm) in bmimBF(4) and bmimNTf(2) ionic liquids. Both complexes 1 and 2 are electrochemically reduced in these ionic media at more negative potentials than when using organic solvents. This is in agreement with the EPR characterization, which shows lower A(z) and higher g(z) values for the complexes dissolved in ionic liquids, than in organic solvents, due to higher electron density at the copper center. The anion basicity order obtained by EPR is NTf2-, N(CN)(2)(-), MeSO4- and Me2PO4-, which agrees with previous determinations. (C) 2013 Elsevier B.V. All rights reserved.