0000000000291895
AUTHOR
Carla Valentín
Cobalt aluminate spinel-mullite composites synthesized by sol-gel method
Abstract CoAl 2 O 4 spinel-mullite composites were prepared by double substitution of Al by Ti and Ni in stoichiometric 3:2 mullite. Gels with compositions 3(Al 2 − 2 x Co x Ti x O 3 )·2SiO 2 (x = 0.025, 0.05 and 0.2) and 3(Al 2 − 2 x M x O 3 )·2SiO 2 (x = 0.05; M = Co 2+ or Ti 4+ ) were synthesized by sol-gel techniques. The structure of the gels was investigated by infra-red spectroscopy. Heating gels at 750 °C produced an amorphous silicoaluminate network. The reaction sequence was investigated by differential thermal analysis, X-ray diffraction and ultraviolet-visible spectroscopy. All samples crystallized at temperatures lower than 1000 °C from the amorphous state. Al-Si spinel and/or …
Spinel-mullite composites with optical properties
The aim of this paper was to study the synthesis and characterization of spinel-containing mullite based materials, using sol-gel techniques. Several gels were prepared, with nominal compositions 3(Al2−2xMx TixO3)·2SiO2 and 3(Al2−xMxO3)·2SiO2, with M=Ni+2 or Co+2 and 0.0≤x≤0.2, by hydrolysis and condensation of mixtures of aluminum, silicon and titanium alkoxides and nickel chloride. Dried gels were homogeneous and displayed a glass transition at around 750°C, which indicated that the system could be described as an amorphous silicoaluminate network.
Reaction Sequence in the Preparation of NiAl2O4 Spinel-Mullite Composites by Sol-Gel
NiAl 2 O 4 spinel-mullite composites were prepared by simultaneous replacement of Al by Ti and/or Ni in 3:2 stoichiometric mullite. Specimens having nominal compositions 3(Al 2-2x Ni x Ti x O 3 ).2SiO 2 (x = 0, 0.025, 0.05, 0.2) and 3(Al 2-x M x O 3) .2SiO 2 (M = Ni 2+ or Ti 4+ and x = 0.05) were synthesized by sol-gel techniques, which provide homogeneous gels in the SiO 2 -Al 2 O 3 system. Gel structures investigated by infrared (IR) spectroscopy revealed the formation of Al-O-Si bonds in dried gels. The reaction sequence of gel-derived glasses, previously obtained by preheating gels at 750°C for 3 h, was evaluated by X-ray powder diffraction (XRD) and ultraviolet-visible (UV-vis) spectro…
Low-temperature metastabilization of tetragonal V+4-containing ZrO2 solid solutions
Abstract The formation and characterization of tetragonal vanadium–zirconia solid solutions with different vanadium contents have been investigated. Vanadium–zirconia precursors were prepared by gelling mixtures of zirconium n-propoxide and vanadyl acetylacetonate, and studied over the range of temperature up to the tetragonal–monoclinic phase transformation. The formation of the tetragonal phase has been investigated by X-ray powder diffraction (XRD). It was found that it took place after annealing around 450°C for all specimens independently of the vanadium loading. In contrast, the temperature for the subsequent tetragonal to monoclinic transformation was dependent on the nominal vanadiu…