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Posts Tagged ‘MECHANICAL alloying’

Thermodynamic feasibility of solid solubility extension of nb in cu and their thermal stability






Abstract: A series of Cu–xNb (x =1–15at.% 2 [2] All the compositions are expressed in at.% after this unless otherwise stated. ) alloys have been investigated to study the metastable solid solubility extension of Nb in Cu by mechanical alloying. Analysis of X-ray diffraction and Gibbs free energy change confirmed that 7.5% of Nb was metastably dissolved in Cu after 8h of milling at room temperature although Cu–Nb is a system with positive heat of mixing. The solid solubility could be extended up to 10% after enhancing milling duration to 16h. Detailed thermodynamic analysis revealed that the additional energy stored during mechanical alloying could overcome the required energy barrier as per Miedema”s model for the formation of disordered solid solution. The extended solid solubility has been explained along with the other possible mechanisms. Extensive annealing experiments and structural investigation revealed that the supersaturated solid solution is completely stable up to 400°C. The matrix grains were stabilized and retained their size, ∼25nm, even after annealing at 600°C. Microhardness measurement and grain size analysis show that the dissolution of Nb in Cu has a larger strengthening effect than that of free Nb in the compositions. [Copyright &y& Elsevier]


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Hot deformation behavior of mechanically alloyed al6063/0.75al2o3/0.75y2o3 nano-composite—a study using constitutive modeling and processing map

Abstract: The hot deformation behavior of mechanically alloyed (MA’ed) Al6063/0.75Al2O3/0.75Y2O3 nano-composite was characterized in the temperature and strain rate ranges of 300–500°C and 0.001–1s−1 using compression test. Hot workability is interpreted by processing maps based on dynamic material modeling (DMM) and constitutive model was established based on sine-hyperbolic Arrhenius kinetic rate equation. Dynamic recrystallization (DRX) occurs in the temperature range of 400–500°C and strain rate range of 0.001–0.1s−1. The optimum processing parameters for hot working of MA’ed Al6063/0.75Al2O3/0.75Y2O3 nano-composite was identified to be in two domains, viz.: (i) T =395–440°C and and (ii) T =440–500°C and respectively with maximum efficiency of about 37–39% respectively. At strain rates ranging from 0.1 to 1s−1 the nano-composite exhibits flow instability for all temperatures investigated. The average apparent activation energy for hot deformation is calculated to be 181kJ/mol and flow behavior of the material was styled through a constitutive model. The reasons for the flow instability have been observed to be the surface cracking, void formation, matrix cracking, pores and wedge cracking. [Copyright &y& Elsevier]

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Hydrogen storage properties of libh4–li3alh6 composites

Abstract: To improve the dehydrogenation properties of LiBH4, a novel hydrogen storage system, LiBH4–Li3AlH6, was synthesized by mechanical ball milling. The dehydrogenation/rehydrogenation properties of LiBH4–Li3AlH6 (molar rato: 1:1) composites were studied via thermogravimetry (TG), differential scanning calorimetry (DSC), mass spectral analysis (MS), powder X-ray diffraction (XRD), and Fourier transform infrared spectroscopy (FTIR). The experimental results show that the hydrogen desorption capacity reaches 8.5wt% and that the whole dehydrogenation is a three-step process: (1) a decomposition reaction Li3AlH6 →3LiH+Al+3/2H2, occurring at 160°C; (2) formation of an intermediate product from 300°C to 350°C, and then subsequent transformation into Al, AlB2, and H2. (2LiBH4 +Al→[Li2B2AlH4]→ x(AlB2 +2LiH+3H2)+(1− x) [Li2B2AlH4], (0< x <1)); and (3) final dehydrogenation of LiH+Al→LiAl+1/2H2, occurring at 415°C, with sequential decomposition of the remaining intermediate ((1− x)[Li2B2AlH4]→(1− x)(AlB2 +2LiH+3H2), (0< x <1)). Furthermore, the dehydrogenated products can be rehydrogenated to LiBH4 at 8MPa H2 and 400°C. [Copyright &y& Elsevier]

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