Raman study of the variation in anatase structure of TiO2 nanopowders due to the changes of sol–gel synthesis conditions

2008 ◽  
Vol 49 (3) ◽  
pp. 311-319 ◽  
Author(s):  
A. Golubović ◽  
M. Šćepanović ◽  
A. Kremenović ◽  
S. Aškrabić ◽  
V. Berec ◽  
...  
2020 ◽  
Vol 30 (6) ◽  
pp. 812-814
Author(s):  
Ekaterina S. Dolinina ◽  
Anton S. Kraev ◽  
Elena V. Parfenyuk

2007 ◽  
Vol 1007 ◽  
Author(s):  
Aracely Hernandez ◽  
Patricia Esquivel-Ferriño ◽  
Idalia Gomez ◽  
Lucia Cantu

ABSTRACTIn the present work, sol-gel method was used to incorporate in a ceramic material a non steroidal anti-inflammatory drug (piroxicam) as model drug. The incorporation of the drug in the SiO2 network was carried out at different sol-gel synthesis parameters, such as pH (3 and 5) and the alkoxide/water ratio (1:6 and 1:8). The biomaterial obtained was analyzed by thermal analysis TGA-DTA, infrared spectroscopy (FTIR), Scanning Electronic Microscopy (SEM) and X-ray diffraction (XRD); specific surface area and porosity were analyzed from nitrogen adsorption isotherm. Better drug incorporation into the material was achieved at the synthesis conditions of pH 5 and 1:6 alkoxide/water molar ratio.


2012 ◽  
Vol 9 (2) ◽  
pp. 659-668 ◽  
Author(s):  
A. Elsagh

The aim of the present research was optimization of practical conditions of the sol-gel synthesis. In so doing, silica particles were synthesized using sol-gel method and their size and morphology were investigated by use of SEM and TEM images. The effect of changing molar ratio of reactive including acids and silica pre-matter on the particles' morphology and size was studied. Also, acid type and silica pre-matter used in reaction was examined and the result product of the reaction were investigated in the presence of several acids and two types of silica pre-matter. The reaction time was studied as a very important factor in products' digestion phase which plays a significant role in determining particles’ size and rate of cracking products. Finally, in optimized conditions 50-80 nm diameter nanostructures were synthesized. These products can be used as drug delivery systems.


2016 ◽  
Vol 22 (1) ◽  
pp. 65-73
Author(s):  
Aleksandar Golubovic ◽  
Ivana Veljkovic ◽  
Maja Scepanovic ◽  
Mirjana Grujic-Brojcin ◽  
Natasa Tomic ◽  
...  

The titanium dioxide (TiO2) nanopowders were produced by sol-gel technique from tetrabutyl titanate as a precursor by varying some parameters of the sol-gel synthesis like the temperature (500 and 550 ?C) and the duration of the calcination (1.5, 2, and 2.5 h). X-ray powder diffraction (XRPD) results have shown that all synthesized nanopowders are dominantly in anatase phase, with the presence of a small amount of rutile in samples calcined at 550 ?C. According to the results obtained by Williamson-Hall method, the anatase crystallite size was increased with the duration of the calcination (from 24 to 29 nm in samples calcined at lower, and from 30 to 35 nm in samples calcined at higher temperature). The analysis of the shift and linewidth of the most intensive anatase Eg Raman mode confirmed the XRPD results. The analysis of pore structure from nitrogen sorption experimental data described all samples as mesoporous, with mean pore diameters in the range of 5-8 nm. Nanopowder properties have been related to the photocatalytic activity, tested in degradation of the textile dye (C.I. Reactive Orange 16), carbofuran and phenol.


2018 ◽  
Vol 57 (2) ◽  
pp. 183-192 ◽  
Author(s):  
R.R. Kapaev ◽  
S.A. Novikova ◽  
A.A. Chekannikov ◽  
D.Yu. Gryzlov ◽  
T.L. Kulova ◽  
...  

Abstract The sol-gel synthesis and precipitation from dimethyl sulfoxide (DMSO)-water mixture were used to obtain LiFePO4. Sucrose (sucr), citric acid (CA), phthalic acid (phth), polyvinyl alcohol (PVA), polyvinylpyrrolidone (PVP), polyvinylidene fluoride (PVDF), polyethylene glycol (PEG), polyacrylic acid (PAA) were investigated as carbon precursors. Increasing of the annealing temperature from 600 °» to 800 °» leads to a certain perfection of graphite structure with simultaneous particle size growth. Higher capacities were observed for the materials synthesized at 600 °». The best results for the sol-gel synthesis were obtained when PVDF was used as a source of carbon coating due to the partial fluorination of LiFePO4 (discharge capacity of LiFePO4/ C-PVDF was ~160 and 70 mAh g-1 at 20 mA g-1 and 800 mA g-1 currents, respectively). For nanocrystalline LiFePO4 obtained by precipitation from DMSO-water mixture the best results were obtained when PEG was used as carbon source (discharge capacity LiFePO4/C-PEG was 158 and 77 mAh g-1 at 20 mA g-1 and 800 mA g-1, respectively).


2000 ◽  
Vol 15 (8) ◽  
pp. 1842-1848 ◽  
Author(s):  
Gustavo Larsen ◽  
Edgar Lotero ◽  
Manuel Marquez

Commercially available poly(propylene)imine (DAB-Am-32 and DAB-Am-64) dendrimers were used as single-molecule templates to tailor the porosity of silicas via a nonacidic sol-gel method. X-ray diffraction on both the as-prepared (oven-dried at 373 K) and the calcined (833 K) materials revealed that modest contraction took place on template removal and that the cavities created did not achieve three-dimensional ordering under the current synthesis conditions. Transmission electron microscopy of “Pt-stained” samples supported this picture. A modified Horvath–Kawazoe analysis of the argon adsorption isotherms indicated that DAB-Am-64 is a much more effective template than DAB-Am-32. Pyrolysis and oxidation protocols for template removal are also presented.


2003 ◽  
Vol 18 (12) ◽  
pp. 2743-2746 ◽  
Author(s):  
Donglin Li ◽  
Haoshen Zhou ◽  
Mitsuhiro Hibino ◽  
Itaru Honma

Porous TiO2–P2O5 oxide was synthesized by the sol-gel method in the presence of tri-block copolymer (EO)20(PO)70(EO)20 (Pluronic123) in queous solution. The TiO2 nanocrystals with anatase structure precipitated in the as-synthesized TiO2–P2O5 materials at 80°C, considerably lower than that for traditional heat treatment in the solid state, which maintained a stable size of 3.6–4 nm upon calcinations below 500°C. It is believed that P2O5 glass phase prevents the coarsening of TiO2 nanocrystals below 500°C. The mixed oxide exhibited a specific surface area of 170–200 m2/g after calcining in the temperature range of 300–500°C.


Author(s):  
О.P. Linnik ◽  
◽  
N.P. Smirnova ◽  
A.М. Eremenko ◽  
◽  
...  

According to the XPS investigation of titania films co-modified by nitro gen and metal ions obtained via sol-gel method, the formation of common bonds between elements occurs due to the presence of metal ions. The mechanism of urea thermolysis is changed as a result of the ability of metal ions to form the complex compounds with urea molecules under the reported synthesis conditions that, in turn, depends on the nature of metal ions, leading to the different chemical compositions of materials’ surface. The XPS data show that nitrogen atoms are surrounded by nonmetal ones on the surface of the films modi fied by Zn2+ or Zr4+ ions. It is suggested that no formation of the complexes between Ті, Zn, or Zr atoms with urea occurs due to its protonation through an oxygen atom leading to the formation of O,N-containing reaction products. In the case of Pt2+ doping, the substitutional nitrogen incorporation in the titania lattice, as well as the formation of N-containing fragments, have been detected. The chemical nature of Pt ions allows them to interact with urea molecules through an N atom of the amino group. As a result, the transformation of urea molecules in the complexes occurs at higher temperatures concurrently with the titania crystallization that is recognized as a catalyst for the intermediates of the urea decomposition leading to the formation of common bonds between N and Ti atoms.


2013 ◽  
Vol 214 ◽  
pp. 364-375 ◽  
Author(s):  
D.M. Tobaldi ◽  
R.C. Pullar ◽  
A.F. Gualtieri ◽  
M.P. Seabra ◽  
J.A. Labrincha

Molecules ◽  
2021 ◽  
Vol 26 (16) ◽  
pp. 5090
Author(s):  
Jolanta Doneliene ◽  
Egle Fataraite-Urboniene ◽  
Matas Rudzikas ◽  
Saulius Pakalka ◽  
Nina Danchova ◽  
...  

The aim of this investigation was to synthesize high porosity TiO2 aerogel by applying sol-gel and subcritical drying methods and to identify the influence of reagent’s nature and synthesis conditions on their structural and optical properties. Methods of XRD, FT-IR, BET, STA, SEM, and UV-vis were applied to investigate and compare the properties of synthesized TiO2 aerogels and to determine the most effective synthesis route. The structural parameters of the synthesized materials can be varied by changing the precursor type (titanium (IV), isopropoxide (TIP), or tetrabutylorthotitanate (TBOT)) and the nature of the solvent used for additional exchange (n-hexane (nH), cyclohexane (CH), or diethyl ether (DE)). All of the subcritical dried samples show the amorphous structure, which tends to crystallize into the anatase phase after calcination. The number of micro and mesopores and the specific surface area depends on the synthesis conditions. The pores with the highest diameter have been found for additionally nH exchanged and aged aerogel synthesized from precursor TIP. Despite the imperfections in the structure, the produced aerogels show structural and optical properties typical of the TiO2 structures mentioned in the literature.


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