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Pedro Morgado

Researcher at Instituto Superior Técnico

Publications -  53
Citations -  1009

Pedro Morgado is an academic researcher from Instituto Superior Técnico. The author has contributed to research in topics: Ionic liquid & Equation of state. The author has an hindex of 17, co-authored 52 publications receiving 826 citations. Previous affiliations of Pedro Morgado include University of Lisbon & Technical University of Lisbon.

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Fluid-Phase Behavior of {1-Hexyl-3-methylimidazolium Bis(trifluoromethylsulfonyl) Imide, [C6mim][NTf2], + C2−C8 n-Alcohol} Mixtures: Liquid−Liquid Equilibrium and Excess Volumes‡

TL;DR: In this article, a model of 1-hexyl-3-methylimidazolium bis(trifluoromethylsulfonyl) imide with linear alkan-1-ols, CnH(2n+1)OH, with n = 4, 5, 6, and 8, was selected as the model ionic liquid to perform round-robin measurements on a series of ionic liquids properties.
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Cation Alkyl Side Chain Length and Symmetry Effects on the Surface Tension of Ionic Liquids

TL;DR: The trend of the derived thermodynamic properties highlights the effect of the structural organization of the IL at the surface with visible trend shifts occurring at a well-defined CACL in both symmetric and asymmetric series of ILs.
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Modelling the phase behaviour and excess properties of alkane + perfluoroalkane binary mixtures with the SAFT-VR approach

TL;DR: In this article, a transferable binary interaction parameter was proposed to predict the phase and volumetric behavior of binary mixtures of n-alkanes and n-perfluoroalkanes at subcritical conditions.
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Liquid phase behavior of perfluoroalkylalkane surfactants.

TL;DR: Through this simple approach, this work is able to predict the thermodynamic behavior of the perfluoroalkylalkanes studied without fitting to any experimental data for the systems being studied.
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Predicting the phase behavior of nitrogen + n-alkanes for enhanced oil recovery from the SAFT-VR approach: examining the effect of the quadrupole moment.

TL;DR: The inclusion of the quadrupolar term in the equation of state therefore reduces the need to use effective parameters by explicitly including at the molecular level interactions due to the quadruplerupole moment.