Structural study of nanocrystalline solid solution of Cu-Mo obtained by mechanical alloying

This work studied the structural evolution of Cu-xMo (x = 5 and 8 wt.%) alloys processed by mechanical alloying using x-ray diffraction profiles, scanning electron microscopy, differential scanning calorimetric and microhardness. X-ray diffraction analysis was done using the modified Williamson-Hall...

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Detalles Bibliográficos
Autores: Aguilar, C. (Claudio)|||/items/468f7717-6532-4e60-880b-b5e69b365ca9, Castro-Fernández, F. (Francisco)|||/items/30ee64ae-43d0-41e2-bd50-c17a3eeb7f30, Alarcón Martínez, V.|||/items/2c81a6cd-4512-4de7-b5e4-b598b4ab9b8c, Guzmán, D. (Danny)|||/items/a72bbb9f-b7da-4532-9c73-c8c228927997, Cuevas, F. (Fernando) de las|||/items/0b674f50-14cb-4c9b-bbcd-acafcdb533c7, Lozada-Cabezas, L. (Lorena)|||/items/2af86ef6-1b27-4e86-bc0e-3de77c3d4521, Vielma, N. (Nirco)|||/items/1c4fe2dd-5542-47ae-a50f-3f583d95aeaf
Tipo de recurso: artículo
Fecha de publicación:2012
País:España
Institución:Universidad de Navarra
Repositorio:Dadun. Depósito Académico Digital de la Universidad de Navarra
Idioma:inglés
OAI Identifier:oai:dadun.unav.edu:10171/120578
Acceso en línea:https://hdl.handle.net/10171/120578
Access Level:acceso abierto
Palabra clave:Non-ferrous alloys
Solid solubility extension
Mechanical alloying
X-ray diffraction
Descripción
Sumario:This work studied the structural evolution of Cu-xMo (x = 5 and 8 wt.%) alloys processed by mechanical alloying using x-ray diffraction profiles, scanning electron microscopy, differential scanning calorimetric and microhardness. X-ray diffraction analysis was done using the modified Williamson-Hall and Warren-Averbach methods. These were used to determine structural properties, such as crystallite size, stacking fault probability and energy, dislocation density of metallic powder as a function of the amount of Mo and milling time. The main results obtained for both alloys were higher dislocation density and Vickers microhardness values were measured and crystallites sizes of around 10 nm were measured for both systems at 50 h of milling. Lattice defects increase the free energy and the free energy curves shift upwards, therefore the solubility limits change and Cu-Mo solid solution is formed.