Publications by authors named "I Ruiz-Larrea"

Shape memory alloys (SMAs) are functional materials with a wide range of applications, from the aerospace sector to the biomedical field. Nowadays, there is a worldwide interest in developing SMAs through powder metallurgy like additive manufacturing (AM), which allows innovative building processes. However, producing SMAs using AM techniques is particularly challenging because of the microstructure required to obtain optimal functional properties.

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Cu-Al-Ni is a high-temperature shape memory alloy (HTSMA) with exceptional thermomechanical properties, making it an ideal active material for engineering new technologies able to operate at temperatures up to 200 °C. Recent studies revealed that these alloys exhibit a robust superelastic behavior at the nanometer scale, making them excellent candidates for developing a new generation of micro-/nano-electromechanical systems (MEMS/NEMS). The very large-scale integration (VLSI) technologies used in microelectronics are based on thin films.

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Shape memory alloys (SMAs) are functional materials that are being applied in practically all industries, from aerospace to biomedical sectors, and at present the scientific and technologic communities are looking to gain the advantages offered by the new processing technologies of additive manufacturing (AM). However, the use of AM to produce functional materials, like SMAs, constitutes a real challenge due to the particularly well controlled microstructure required to exhibit the functional property of shape memory. In the present work, the design of the complete AM processing route, from powder atomization to laser powder bed fusion for AM and hot isostatic pressing (HIP), is approached for Cu-Al-Ni SMAs.

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A calorimetric study of urea/n-nonadecane, CO(NH(2))(2)/C(19)H(40), and the deuterated derivatives, CO(ND(2))(2)/C(19)D(40) and CO(NH(2))(2)/C(19)D(40), around the structural phase transition temperature is presented. For this purpose differential scanning (DSC), temperature-modulated (AC) and adiabatic calorimetry have been used and the obtained results are compared. Leaving apart the noticeable peak associated with the main phase transition at 158.

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An experimental study of the ferroelastic phase transition in urea/n-heptadecane CO(NH2)2/C17H40 composite around the structural phase transition undergone by this crystal at 159 K is presented. The temperature dependence of the macroscopic spontaneous strain and the optical birefringence around this temperature has been determined. A phenomenological model limited to the hexagonal-orthorhombic change of the urea sublattice leads to a linear relation between these quantities and the phase transition entropy.

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