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In the present paper we report an in-situ high-energy X-ray diffraction analysis of MgB2 tapes during the preparation process. The experiment was performed in a specifically designed furnace working in reducing atmosphere, compatible with the Laue di ffraction condition. The MgB2 synthesis was realized starting from MgH2 and amorphous B in powder form as precursors, varying reaction temperature and testing different cooling processes. We analyzed both the MgB2 synthesis and the sintering process of tapes prepared with these powders. Phase evolution, micro and crystallographic structure were monitored during the different thermal treatments. Among the main results we observed the formation of MgB2 at an extraordinary low temperature (300C), probably as a result of a solid-state reaction between MgH2 and B. Furthermore, we studied the dependence of the micro-structure upon the thermal treatment and its effect on the critical current performance of the superconducting tapes.
We report on the superconducting performance of the ex-situ SiC doped MgB2 monofilamentary tapes. Polycrystalline powders of MgB2 doped with 5 and 10 wt% SiC were synthesized by conventional solid-state reaction route and characterized for their supe rconducting performance. It is found that superconducting parameters i.e. upper critical field (Hc2), irreversibility field (Hirr) and critical current density (Jc) are all improved significantly with SiC addition. Also it was found that relatively lower synthesis temperature (700 C) resulted in further improved superconducting parameters. As synthesized powders are used for ex-situ powder-in-tube (PIT) monofilamentary tapes and superconducting parameters are determined. Albeit the superconducting transition temperature (Tc) is decreased slightly (2K) for SiC doped tapes, the superconducting performance in terms of critical current density (Jc), being determined from both magnetization and transport measurements, is improved significantly. In particular the SiC doped and 700 {deg}C synthesized MgB2 tapes exhibited the transport Jc of nearly 10^4 A/cm2 under applied fields of as high as 7 Tesla. Further it is found that the Jc anisotropy decreases significantly for SiC doped tapes. Disorder due to substitution of C at B site being created from broken SiC and the presence of nano SiC respectively in SiC added ex-situ MgB2 tapes are responsible for decreased anisotropy and improved Jc(H) performance.
In this paper we report a new synthesis route to produce boron powders characterized as being amorphous and having very fine particle size. This route has been developed to improve the performances of superconducting MgB2 powders, which can be direct ly synthesized from this nano-structured boron precursor by following the ex-situ or the in-situ P.I.T. method during the manufacturing of tapes, wires and cables. All the procedure steps are explained and the chemical-physical characterization of the boron powder, using x-ray diffraction (Xrd), scanning electron microscopy (SEM) and transmission electron microscopy (TEM) techniques, is reported. Furthermore, a comparison with commercial boron is given. Preliminary results of the magnetic and electrical characterization, such as the critical temperature (TC) and the transport critical current density (JC t), for the MgB2 tape are reported and compared with the tape prepared with commercial boron.
MgB2 monofilamentary nickel-sheated tapes and wires were fabricated by means of the ex-situ powder-in-tube method using either high-energy ball milled and low temperature synthesized powders. All sample were sintered at 920 C in Ar flow. The milling time and the revolution speed were tuned in order to maximize the critical current density in field (Jc): the maximum Jc value of 6 x 10e4 A/cm2 at 5 K and 4 T was obtained corresponding to the tape prepared with powders milled for 144h at 180rpm. Vorious synthesis temperature were also investigated (730-900 C) finding a best Jc value for the wire prepared with powders synthesized at 745 C. We speculate that this optimal temperature is due to the fluidifying effect of unreacted magnesium content before the sintering process which could better connect the grains.
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