Synthesis and Characterization of Pseudoboehmite and Gamma-Alumina

2015 ◽  
Vol 820 ◽  
pp. 131-136 ◽  
Author(s):  
Antonio Hortêncio Munhoz ◽  
H. de Paiva ◽  
Leila Figueiredo de Miranda ◽  
E.C. de Oliveira ◽  
Raphael Cons Andrades ◽  
...  

Pseudoboehmite (PB) were synthesized through the sol-gel process, using aluminum nitrate as precursor. The pH adjustment of the precursor solution was made by using ammonium carbonate. After the precipitation, the material was dried at 70°C before characterization. The pseudoboehmite obtained were characterized by x-ray diffraction, scanning electron microscopy and afterwards by thermal analysis (DTA and TG). The pseudoboehmite was also calcined at 500oC to obtain gamma-alumina. The specific surface area measurements through the BET process and the desorption-absorption of nitrogen as well the t plot in order to evaluate the pore volume of the calcined samples was realized. Finally, the results showed that the synthesized pseudoboehmite can be used to produce high specific surface material with a crystal structure of gamma-Al2O3(around 324m2/g).

2014 ◽  
Vol 87 ◽  
pp. 54-60 ◽  
Author(s):  
A.H. Munhoz ◽  
H. de Paiva ◽  
L. Figueiredo de Miranda ◽  
E.C. de Oliveira ◽  
Raphael Cons Andrades ◽  
...  

Different samples of pseudoboehmite (PB) were synthesized through the sol-gel process, using aluminum nitrate as precursor. The influence of variables on the synthesis and calcinations of the PB on the specific area of the obtained gamma-Alumina were studied. The variables were the ageing temperature (25 and 130o C), addition or not of polyvinyl alcohol to the precursor solution and the ageing time of the PB. The pH adjustment of the precursor solution was made by using ammonium carbonate. The products, which were obtained on different conditions, were then characterized by x-ray diffraction, specific area measurements through the BET process, and by thermal analysis (DTA and TG). After characterization, the synthesis products were calcined at 500°C; during this process the gamma-Alumina transformation was observed. The calcination products were characterized by the same methods (x-ray diffraction, BET, DTA and TG) and the desorption-absorption curves were obtained as well, in order to measure the pore volume of the samples. Finally, the results were analyzed through an experimental factorial planning, which showed that high specific surface area gamma-Al2O3 (around 330m²/g) can be obtained through this process.


2007 ◽  
Vol 546-549 ◽  
pp. 2007-2010
Author(s):  
Gao Yang Zhao ◽  
Huang Li Zhang ◽  
Ren Zhong Xue ◽  
Yuan Qing Chen ◽  
Li Lei

precursor solution was prepared using barium trifluoroacetae (Ba-TFA) and non-fluorine yttrium (Y) and copper (Cu) organic salts. The precursor solution was modified by benzalacetone (BzAcH), in which the Cu2+ were chelated with BzAcH, which preventing the loss of Cu in the pyrolysis process. Dense YBCO superconducting films with smooth surface, which confirmed by scanning electron microscopy (SEM), were repeatedly obtained through sol-gel process. X-ray diffraction (XRD) 2θ scanning and φ scanning indicated that the as-prepared YBCO films had good c-axis texture. YBCO films with superconducting transition temperature (TC) above 89K were obtained.


Micromachines ◽  
2018 ◽  
Vol 9 (11) ◽  
pp. 601
Author(s):  
Yahua Hu ◽  
Mu Gu ◽  
Xiaolin Liu ◽  
Juannan Zhang ◽  
Shiming Huang ◽  
...  

Uniform Lu2O3:Eu3+ nanowire arrays were successfully prepared by the sol-gel process using anodic aluminum oxide (AAO) templates. The as-synthesized nanowires are homogeneous, highly ordered, and dense and have a uniform diameter of ~300 nm defined by the AAO templates. The X-ray diffraction and selected area electron diffraction results show that the Lu2O3:Eu3+ nanowires have a polycrystalline cubic structure, and the crystallite size of the Lu2O3:Eu3+ nanowires is confined by the AAO template. The nanowires within the AAO template showed good photoluminescence and X-ray-excited optical luminescence performances for Lu2O3:Eu3+. The emission peaks were attributed to the 5D0 → 7FJ transitions of Eu3+ (J = 0, 1, 2, 3).


1997 ◽  
Vol 12 (3) ◽  
pp. 596-599 ◽  
Author(s):  
Ji Zhou ◽  
Qing-Xin Su ◽  
K. M. Moulding ◽  
D. J. Barber

Ba(Mg1/3Ta2/3)O3 thin films were prepared by a sol-gel process involving the reaction of barium isopropoxide, tantalum ethoxide, and magnesium acetate in 2-methoxyethanol and subsequently hydrolysis, spin-coating, and heat treatment. Transmission electron microscopy, x-ray diffraction, and Raman spectroscopy were used for the characterization of the thin films. It was shown that the thin films tend to crystallize with small grains sized below 100 nm. Crystalline phase with cubic (disordered) perovskite structure was formed in the samples annealed at a very low temperature (below 500 °C), and well-crystallized thin films were obtained at 700 °C. Although disordered perovskite is dominant in the thin films annealed below 1000 °C, a low volume fraction of 1 : 2 ordering domains was found in the samples and grows with an increase of annealing temperature.


Materials ◽  
2020 ◽  
Vol 13 (21) ◽  
pp. 4928
Author(s):  
Andrzej Kruk

In this study, pure Y2O3, La0.1Y1.9O3 and La0.1Nd0.12Y1.78O3 nanosized powders were successfully synthesized by a modified sol–gel method. Pure and rare-earth ions doped yttria powders were characterized by X-ray diffraction, scanning electron microscopy and Brunauer–Emmett–Teller methods. The powders were sintered by the hot isostatic pressing process. The highest in-line transmittance of 56% was obtained at 800 nm and increased in the IR region. The influence of the lanthanum and neodymium ions on the physicochemical properties of yttria were discussed. The La-Nd-doped material exhibited a Verdet constant over 4000 deg/T·m at 400 nm and low thermal dependence. An interesting evolution of the Verdet constant across the absorption band with high resolution was studied. A study of the optical and magneto-optical properties of yttria doped with Nd3+ and La3+ is discussed in this paper.


2011 ◽  
Vol 1326 ◽  
Author(s):  
Rene Fabian Cienfuegos ◽  
Leonardo Chávez Guerrero ◽  
Sugeheidy Carranza ◽  
Laurie Jouanin ◽  
Guillaume Marie ◽  
...  

ABSTRACTThe goal in this study was to synthesize a lanthanum - nickel phase (Ruddlesden-Popper phases) La4Ni3O10. This material was prepared using a polymeric route. An easy synthesis method is presented in order to obtain an economical cathode material, which can be used in Solid Oxide Fuel Cells (SOFC). The polymeric precursors were prepared following the Castillo method. The originality of this work was to optimize the ratio HMTA/ metallic salts from 1 to 6. The obtained powders were characterized by thermal analysis; Differential Scanning Calorimetry (DSC Q10 Instrument TA), Thermogravimetric Analysis (TGA - Q50 Instrument TA-) and X-ray diffractometer (Bruker, D8 Advance diffractometer), in order to determine the crystallized phase. Experiments 5 and 6 did not present coagulation but after few days, solution 5 was transformed into a gel. Gels 2 to 5 were heated in order to obtain a solid material. These powders are characterized by thermogravimetric and thermo-differential methods. The powders obtained at 800, 900 and 1000°C were analyzed by X-ray diffraction and it was found that the temperature to get to the La4Ni3O10 phase was 1000ºC.


2017 ◽  
Vol 748 ◽  
pp. 413-417
Author(s):  
Chun Yu Long ◽  
Fang Fang Peng ◽  
Min Min Jin ◽  
Pei Song Tang ◽  
Hai Feng Chen

Using Pr (NO3)3, butyl titanate, ethylene glycol and citric acid as main raw materials, praseodymium titanate (Pr2Ti2O7) was prepared by the sol-gel process. The samples were characterized by means of X-ray diffraction (XRD), scanning electron microscope (SEM), thermal gravity-differential thermal analysis (TG-DTA), diffuse-reflection spectra (DRS) and Fourier transform infrared (FT-IR). The effect of different calcination temperature and illumination time on the photocatalytic properties of Pr2Ti2O7 was investigated. It was found that the single phase Pr2Ti2O7 could be obtained through sol-gel process and calcination at 1000 °C. The Pr2Ti2O7 samples calcination at 1000 °C were uniform , and the resulting product had a particle size of 200 nm and an optical band gap of 3.26 eV. Under ultraviolet light, the degradation of methyl orange arrived to 80.11% after 180 min of photocatalytic reaction. The Pr2Ti2O7 samples showed good photocatalytic activity for decomposition of methyl orange.


2010 ◽  
Vol 17 (01) ◽  
pp. 59-62 ◽  
Author(s):  
YOUNG-JAE KO ◽  
JONG KYU LEE ◽  
MIN-CHEOL CHU ◽  
DONG-SIK BAE

Y 2 SiO 5: Ce 3+ particles was synthesized by sol–gel process. In all samples treated at 1100°C, monoclinic X 1 phase for all cerium concentration. Luminescence spectra shows broad Ce 3+ luminescence in Y 2 SiO 5 host, which picks around 450 nm. The synthesized and calcined powders were characterized by thermogravimetry-differential scanning calorimeter (TG-DSC), X-ray diffraction analysis (XRD), scanning electron microscopy (SEM) and photoluminescence spectra (PL).


2010 ◽  
Vol 148-149 ◽  
pp. 1062-1066 ◽  
Author(s):  
Ren Bo Yang ◽  
Wei Guo Fu ◽  
Xiang Yun Deng ◽  
Zhong Wen Tan ◽  
Yan Jie Zhang ◽  
...  

The (Ba0.88Ca0.12)( Zr0.12Ti0.88)O3 powders and piezoelectric ceramics were prepared by sol-gel process. The reaction process was analyzed with the help of thermo gravimetric and differential scanning calorimetry. X-ray diffraction characterized results showed that the structure of the (Ba0.88Ca0.12)( Zr0.12Ti0.88)O3 powders was perovskite structure and the particle size was approximately 37nm. Piezoelectric measurements revealed that Curie temperature and the maximum piezoelectric coefficient d33 is 95°C and 215pm/V, respectively.


2012 ◽  
Vol 10 (5) ◽  
pp. 1574-1583 ◽  
Author(s):  
Dalia Jonynaite ◽  
Darius Jasaitis ◽  
Rimantas Raudonis ◽  
Algirdas Selskis ◽  
Remigijus Juskenas ◽  
...  

AbstractIn the present work, the formation of cobalt aluminium spinel (CoAl2O4) as well as novel cobalt neodymium-aluminates with nominal compositions of CoAl1.75Nd0.25O4, CoAl1.5Nd0.5O4 and CoAlNdO4 by an aqueous sol-gel process and the sinterability of the products are investigated. The metal ions, generated by dissolving starting materials of metals in the diluted acetic acid were complexed by 1,2-ethanediol to obtain the precursors for the mixed metal ceramics. The phase purity of the synthesized compounds was characterized by powder X-ray diffraction analysis and infrared spectroscopy. The microstructural evolution and morphological features of the products were studied by scanning electron microscopy and atomic force microscopy, which together with the optical characterization of these new compounds showed that the sol-gel-derived materials could be successfully used as effective cobalt-based ceramic pigments.


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