Sol-Gel Synthesis of the Strontium-Copper Oxycarbonate Superconductor Sr2CuO2(CO3)1−x(BO3)x

1996 ◽  
Vol 453 ◽  
Author(s):  
Audrey J. Babcock ◽  
Alexander R. Pico ◽  
Catherine J. Page

AbstractWe have developed an ambient-pressure sol-gel synthetic route to superconducting borate-doped Sr2CuO2(CO3) using polyether alkoxide precursors. In our sol-gel preparation, the starting solutions contain strontium and copper alkoxide complexes in 2-(2-methoxy-ethoxy)ethanol. Boron is incorporated into the solution by using an aqueous boric acid solution for hydrolysis. Dried gels were examined by x-ray diffraction and thermal gravimetric analysis. By experimenting with various firing sequences and atmospheres we have established a successful route for reproducibly preparing relatively pure Sr2CuO2CO3 and boron-doped phases. Final products were characterized by x-ray diffraction, elemental analysis and magnetic susceptibility. Samples of nominal composition Sr2CuO2(CO3)0.85(BO2)0.15 are superconducting with a Tc(onset) of ∼25K. Subsequent treatment at 1100°C and 3 GPa for one hour increased Tc(onset) to ∼35K.

1994 ◽  
Vol 346 ◽  
Author(s):  
Carol S. Houk ◽  
Gary A. Burgoine ◽  
Catherine J. Page

ABSTRACTWe have investigated the homogeneity of sol‐gel derived YBa2Cu307‐s from the solution phase to the final product using transmission electron microscopy (TEM), x‐ray diffraction (XRD), and Energy Dispersive X‐ray (EDX) lateral mapping techniques. The starting solutions contain stoichiometric amounts of the metal 2‐(2‐methoxyethoxy)ethoxide components in 2‐(2‐methoxyethoxy)ethanol and appear to be homogeneous by TEM with a uniform distribution of particles having an average size of less than 40 â. Through elemental mapping we see elemental segregation in the high temperature (950 °C) products, which are orthorhombic by XRD. In elemental maps of gel samples fired to 700 °C, which are tetragonal by XRD, we also see elemental inhomogeneity within particles and phase zoning in maps of products from finely ground gels. A comparison of elemental maps and x‐ray diffraction patterns of the products from gel processing and conventional solid state processing is made.


2006 ◽  
Vol 45 ◽  
pp. 260-265 ◽  
Author(s):  
Antônio Hortêncio Munhoz Jr. ◽  
Leila Figueiredo de Miranda ◽  
G.N. Uehara

A pseudoboehmite was obtained by sol-gel synthesis using aluminum nitrate as precursor. It was used a 2n full factorial design for studying the effect of the temperature of synthesis, the concentration of ammonium hydroxide, and the radiation dose in the product of sol-gel synthesis. The product of the synthesis was analyzed by scanning electron microscopy, x-ray diffraction of the product (after firing the pseudoboehmite at different temperatures), and it was also analyzed the temperature of endothermic and exothermic transformations using the thermo gravimetric analysis (TG) and differential scanning calorimetry (DSC). The X-ray diffraction data show that α-alumina was obtained at 1100o C.


2013 ◽  
Vol 284-287 ◽  
pp. 41-45
Author(s):  
Chich Kuan Chen

The bioactive properties of hydroxyapatite [HA, Ca10(PO4)6(OH)2] have been demonstrated to be akin to osseous tissue, and provide quick fixation in prosthesis and orthopedics. In this study, sol-gel preparation of hydroxyapatite were arranged for Ca/P=1.67 molar ratio in calcium nitrate [Ca(NO)3.4H2O ] and triethylphosphate [TEP, C6H15PO4] and then dilute in the solvent of ethylene glycol mono-methyl ether [HOCH2CH2OCH3]. Consequently, sintering process was carried out at different temperature for various sintering time to materialize this inorganic polycrystalline phosphate. Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD) and scanning electron microscopy (SEM) are applied to investigate the as dried amorphous and calcined hydroxyapatite. Results reveal calcinations at 1000oC prolonged for 30 minutes in air can exhibit crystalline hydroxyapatite.


2014 ◽  
Vol 896 ◽  
pp. 541-544
Author(s):  
Is Fatimah ◽  
N. Nunani Yuyun

ZnO-SiO2/Laponite was prepared by sol-gel preparation procedure consit of SiO2 pillarization to laponite followed by ZnO dispersion by using zinc acetate as precursor. The obtained material was characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive spectrometry (EDS), diffuse reflectance UV-Visible (DRUV-Vis) and N2 adsorption-desorption analysis. The photocatalytic performance of the amterial in methylene blue decolorization was also investigated. Compared with ZnO-SiO2 nanoparticles, it is concluded that ZnO-SiO2/Laponite possess higher photocatalytic activity which obey Temkin isotherm model.


2013 ◽  
Vol 2013 ◽  
pp. 1-7 ◽  
Author(s):  
Thilagavathi Thirugnanam

Fibers irregular and seed-like microcrystalline ZnO were synthesized by using a cost-effective and low temperature aqueous sol-gel method. Various polymers, namely, polyethylene glycol 6000 (PEG 6000) and polyvinyl pyrrolidone (PVP), were used as structure directing agents. The samples were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), and scanning electron microscopy (SEM). The X-ray diffraction pattern revealed the formation of phase-pure ZnO micropowders. It is observed that the polymers play an important role in modifying the surface morphology and the size of the crystallites. A compact granular morphology is observed for the ZnO samples without polymer. The samples exhibit microparticles of size 100 nm for PVP and for PEG-mediated growth, whereas microporous corrugated morphology is observed for added PEG-mediated micropowder. FTIR study is used to confirm the structural modifications occurring in the polymers.


2014 ◽  
Vol 40 (4) ◽  
pp. 6115-6125 ◽  
Author(s):  
Lianyi Shao ◽  
Kaiqiang Wu ◽  
Xiaoting Lin ◽  
Miao Shui ◽  
Rui Ma ◽  
...  

2013 ◽  
Vol 2013 ◽  
pp. 1-6 ◽  
Author(s):  
Ekaterina V. Borisova ◽  
Alexey V. Ignatov ◽  
Eugeni I. Get'man ◽  
Stanislav N. Loboda ◽  
Lyudmyla I. Ardanova ◽  
...  

Sodium europium silicate, NaEu9(SiO4)6O2, with apatite structure has been obtained and studied using X-ray diffraction and SEM. It has been shown that sodium sublimation does not take place upon synthesis by the sol-gel method. Rietveld refinement has revealed that sodium atoms are ordered and occupy the 4f position. O(4) atoms not related to silicate ions are placed at the centers of Eu(2) triangles. DC and AC electric conductivity and activation energy have been determined for the compound studied.


NANO ◽  
2020 ◽  
Vol 15 (02) ◽  
pp. 2050017
Author(s):  
Ke-Cheng Yang ◽  
Li-Hui Xu ◽  
Hong Pan ◽  
Li-Ming Wang ◽  
Yong Shen ◽  
...  

In this study, CuS/SiO2 composite modified aerogel was prepared by the incorporation of hollow spherical CuS into methyltrimethoxysilane-based SiO2 sol and modification with hexadecafluorodecyltriethoxysilane via acid-base catalyzed sol–gel reaction and drying under ambient pressure. The CuS/SiO2 composite modified aerogel was characterized by Fourier-transform infrared (FT-IR) spectrometry, scanning electron microscope (SEM), nitrogen gas adsorption and desorption and X-ray diffraction (XRD), respectively. The effects of CuS and fluorosilane concentration on density and porosity of aerogel, oleophobic and photocatalytic properties were evaluated. The results showed that structure and physical properties of aerogel had some effect by introducing CuS and fluorosilane, and the CuS/SiO2 composite modified aerogel with density of 0.146[Formula: see text]g/cm3 and specific surface area of 241[Formula: see text]m2/g achieved super-oleophobicity with oil contact angle of 152.8∘ and sliding angle of 10∘, and good photocatalytic properties for methylene blue.


2014 ◽  
Vol 997 ◽  
pp. 359-362 ◽  
Author(s):  
Chun Hong Ma ◽  
Xue Lin ◽  
Liang Wang ◽  
Yong Sheng Yan

Nanocrystalline bismuth titanate (Bi4Ti3O12; BTO) powders were successfully prepared by the sol-gel method, using bismuth nitrate (Bi(NO3)3·5H2O) and tetrabutyl titanate (Ti(OC4H9)4) as source materials, acetic anhydride and ethanediol as solvents. The thermal decomposition and phase inversion process of the gel precursors were studied by using differential thermal analysis (DTA). The crystal structures and microstructures of BTO powders were investigated by using x-ray diffraction (XRD), and transmission electron microscope (TEM). The crystallization of amorphous bismuth titanate has been discussed. The effect of sintering temperature on the structure and morphology of BTO was investigated. At 644 oC and above, BTO powder undergoes a phase transformation from tetragonal to orthorhombic. At 900 oC, the purified orthorhombic BTO nanocrystals were obtained.


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