Abstract

The orthorhombic perovskite, Gadolinium aluminum oxide (GdAlO3, GAP) material was successfully prepared by hydrothermal supercritical fluid method using co-precipitated gel of GAP. All experiments were carried out in the pressure and temperature ranges of 100–150 MPa and 180–650 °C respectively. The as-prepared GAP samples were systematically characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FT-IR), X-ray spectroscopy (EDS), thermo gravimetry (TGA) and differential thermo gravimetry analysis (DTA). The XRD profile confirms fully crystalline and orthorhombic nature of as-prepared materials, which is well correlated to the reported results. The SEM studies reveal that the GAP materials synthesized at 650 °C/150 MPa for 92 hrs possesses polycrystalline nature with average particle size in the range of 5–20 µm. The DTA shows a crystallization peak at 361 °C at this temperature the agglomerated GAP gel starts to crystallize into polycrystalline GAP materials. When compared with other methods, like sol-gel and solid-state reactions our crystallization temperature is very much lower and feasible. This work not only demonstrates a simple way to fabricate GAP polycrystalline materials from co-precipitated gels but also shows a possible utilization of same technique for synthesis of other high temperature materials.

Highlights

  • Ceramic based materials on the Ln2O3-Al2O3 system (Ln-Lanthanide element) have shown their potential applications as a neutron absorber, flux suppressors, and high-temperature container materials [1]

  • The as-prepared Gadolinium aluminum perovskite (GAP) samples were systematically characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FT-IR), X-ray spectroscopy (EDS), thermo gravimetry (TGA) and differential thermo gravimetry analysis (DTA)

  • The DTA shows a crystallization peak at 361 °C at this temperature the agglomerated GAP gel starts to crystallize into polycrystalline GAP materials

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Summary

Introduction

Ceramic based materials on the Ln2O3-Al2O3 system (Ln-Lanthanide element) have shown their potential applications as a neutron absorber, flux suppressors, and high-temperature container materials [1]. To avoid the problem associated with solid-state synthesis of GAP powder, several wet-chemical techniques, such as polymerized complex route, combustion system, sol-gel, flux methods, melt technique, citrate-nitrate solution and microwave technique have been used to synthesize GAP [7,9,15,20,21,22,23,24,25,26,27] These are high-temperature methods which consume a lot of energy and lead to certain thermally induced strain in the resultant products thereby affecting their quality and indorsing crystal defects. The as-prepared samples were subjected to systematic characterization using thermal analysis/differential scanning calorimetry (TG/DSC), powder X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), scanning electron microscope and energy dispersive X-ray spectroscopy (SEM/EDAX)

Materials
Material Characterization
TG-DSC Curve Analysis of Co-precipitate Gel
X-ray Diffraction
Infrared Spectra and SEM with EDAX Analysis
Conclusions
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