A novel preparation of high surface area TiO2 nanoparticles from alkoxide precursor and using active carbon as additive

TiO₂ nanoparticles have been prepared by a novel alkoxide sol–gel precipitation. The presence of active carbon in different percentages could act as an interesting template. Upon calcination, carbon is eliminated leaving surface features significantly different from TiO₂ prepared in the absence of carbon. Wide surface and structural characterisation of samples have been carried out. Correlations with carbon percentage is pointed out from this characterisation. Interesting spherical aggregates of nanosized TiO₂ are observed from TEM images probably stabilised by the presence of carbon. Physicochemical correlations made will be very useful in further application of these TiO₂ to be used as potential high surface area photocatalyst.     

Preparation and characterization of TiO2–SiO2 nano-composite thin films

TiO₂ nanocrystalline particles dispersed in SiO₂ have been prepared by the sol-gel method using titanium- and silicon-alkoxides as precursors. Nano-composite thin films were formed on the glass substrates by dip-coating technique and heat treated at temperatures up to 500 °C for 1 h. The size of the TiO₂ nanocrystalline particles in the TiO₂–SiO₂ solution ranged from 5 to 8 nm. The crystalline structure of TiO₂ powders was identified as the anatase phase. As the content of SiO₂ increased, the anatase phase tended to be stabilized to higher temperature. TEM results revealed the presence of spherical TiO₂ particles dispersed in a disk-shaped glassy matrix. Photocatalytic activity of the TiO₂–SiO₂ (1:1) thin films showed decomposition of 95% of methylene blue solution in 2 h and a contact angle of 10°. The photocatalytic decomposition of methylene blue increased and the contact angle decreased with the content of TiO₂ phase. TiO₂–SiO₂ with the molar ratio of 1:1 showed a reasonable combination of adhesion, film strength, and the photocatalytic activity.     

The synthesis of Ag-doped mesoporous TiO2

Ag-doped mesoporous titanium oxide was prepared using non-ionic surfactants and easily handled titanium precursors, under mild reaction conditions. The structure of these materials was determined as a function of the concentration of the Ag dopant and calcination temperature. In contrast to the stabilizing effect of Cd-doping on mesoporous TiO₂, Ag doping was found to significantly destabilize the mesoporous structure.     

Spectroscopic ellipsometry characterization of TiO2 thin films prepared by the sol–gel method

TiO₂ thin films were prepared on SiO₂/Si(100) substrates by the sol–gel process. XRD results indicate that the major phase of TiO₂ thin films is anatase. The surface morphology and cross-section are observed by FE-SEM. The surface of thin films is dense, free of cracks and flat. The average grain size is about 60–100 nm in diameter. The thickness of single layer TiO₂ thin films is about 60 nm, which increases with the concentration of solution. Ellipsometric angles ψ, Δ are investigated by spectroscopic ellipsometry. The optical constant and the thickness of TiO₂ thin films are fitted according to Cauchy dispersion model. The results reveal that the refractive index and the extinction coefficient of TiO₂ thin films in wavelength above 800 nm are about 2.09–2.20 and 0.026, respectively. The influences of processing conditions on the optical constants and thicknesses of TiO₂ thin films are also discussed.     

TiO2 optical coating layers for self-cleaning applications

TiO₂ films deposited by various coating techniques were investigated for self-cleaning applications. The optical coating layers of TiO₂ films prepared from a sol–gel precursor were deposited on glass substrates using spin coating, dip coating and screen printing techniques. Effects of film deposition techniques on crystal structure, microstructure, thickness, photocatalytic activity, hydrophilicity and optical properties of the films were investigated using XRD, AFM, SEM, surface profilometer, UV–vis spectrophotometer and contact angle measurement. Dip coating the TiO₂ optical film two and three times resulted in superhydrophilic surfaces. Increasing number of dipping times was found to increase the photocatalytic activity.     

Effect of pre-nitridation treatment on the formation of anatase TiO2 films by anodization

High performance-anatase TiO₂ films were successfully formed on metallic titanium by anodization in an acidic electrolyte composed of H₂SO₄, H₃PO₄ and H₂O₂ subsequent to pre-nitridation treatment. The pre-nitridation treatment was carried out by pre-annealing metallic titanium under a nitrogen atmosphere of 0.1 MPa. The anodized films showed photocatalytic activity in photooxidization of the iodide anion into the tri-iodide anion. The nitridation treatment had a significant effect not only on the formation of anatase TiO₂ films but also on the photocatalytic activity of the anodized films.     

Improvement of response characteristics of TiO2 humidity sensors by simultaneous addition of Li2O and V2O5

Porous TiO₂ ceramics were prepared by adding various amounts of Li₂O and V₂O₅ and the humidity sensitivity of the resulting ceramics was investigated by means of electrical measurements, scanning electron microscopy and mercury intrusion porosimetry. Simultaneous addition of Li₂O and V₂O₅ to TiO₂ enabled sintering at temperatures as low as 700 °C and also decreased the impedance of the ceramics. Furthermore, in the ceramics including these additives simultaneously, excellent humidity sensitivity as well as good response characteristics were observed. The microstructures of these ceramics depended on the firing temperature and the amount and ratio of Li₂O/V₂O₅, and optimum humidity sensitivity was observed for the sample including both 0.25 mol% Li₂O and 0.75 mol% V₂O₅ fired at 700 °C. These results indicated that the humidity sensitivity and its response characteristics were closely related to the microstructure, and that improving the uniformity of microstructure is important for improving humidity sensitivity and its response characteristics.     

Physicochemical properties and photocatalytic activities of TiO2-films prepared by sol–gel methods

The physicochemical properties, the photocatalytic activities in aqueous solution and the adhesion properties of supported TiO₂ films prepared by different sol–gel methods have been studied. The thickness, the TiO₂ loading and the photocatalytic activities are influenced by the nature of the stabilising agent. By contrast, the nature of the organic titanium precursor, as well as the solvent and the absence of stabilising agents are determining for the resulting photocatalytic activities. Titania-sol generated by non-controlled hydrolysis of titanium isopropoxide was used to determine the influence (i) of number of coating, (ii) of the calcination temperature and (iii) of the nature of support on the photocatalytic activity under direct and backside irradiation. The higher the coating number, the thicker the TiO₂-film and the higher the photocatalytic efficiency. the optimum calcination temperature was found to be 400 °C. Migration of cationic species into TiO₂-films and the decrease of thickness at higher temperatures lead to the decline of activity.     

Photocatalytic activity of transparent porous glass supported TiO2

A porous glass tube with a composition of 96SiO₂·4B₂O₃ (wt%) supported TiO₂ shows high photooxidation activity due to its transparency and large surface area. The surface area of the porous glass tube supported TiO₂ is 10,000 times larger than that of conventional materials. TiO₂ crystals supported are anatase type. Transparency of the porous glass tube is very important. Herein, sol–gel and chemical vapor deposition (CVD) processes were employed as TiO₂ supporting processes. CVD process is more effective. For instance, an aqueous methylene blue solution with 1 ppm concentration almost thoroughly decomposes at a contact time of 300 s using porous glass tube supported TiO₂ prepared by CVD process under irradiating with 10 W low-pressure mercury lamp, on the other hand, opaque porous alumina tube supported TiO₂ was only 25%. The smaller the pore size of the porous glass tube, the larger the transparency and the permeation resistance through porous glass tube. Hence, porous glass tube with ca. 40 nm pore diameter is suitable from the standpoint of a practical use.     

EXAFS study and photocatalytic properties of un-doped and iron-doped ZrO2-TiO2 (photo-) catalysts

The local zirconium and iron arrangements of the iron-doped ZrO₂-TiO₂ system, prepared by sol–gel impregnation method, were studied by EXAFS spectroscopy. Only a tetragonal ZrO₂ structure is located on TiO₂ surface. For the iron-doped ZrO₂-TiO₂ system, the presence of the Fe-O-Fe species as well as and Fe-O-Zr species located on the surface/pre-surface region are shown; it seems that iron is heterogeneously distributed, forming small iron oxide nanoclusters and Fe_x/ZrO₂ (tetragonal) spots at the catalyst surface. The photocatalytic activity of the un-doped and iron-doped binary system ZrO₂-TiO₂ was investigated in two kind of photoreactions: the salicylic acid photooxidation and the photocatalytic reduction of Cr(VI). Different photocatalytic behaviour has been found for the un-doped and iron-doped ZrO₂-TiO₂ systems which have been explained in terms of the EXAFS study.

This study represents an example of attempt to prepare a new potential photoactive mixed oxide system, containing two ions (Ti⁴⁺ and Zr⁴⁺) with good photocatalytic activity if it is compared with commercial TiO₂ (Degusssa P25) calcined at 600 °C.     

Local structure and photocatalytic activity of B2O3–SiO2/TiO2 ternary mixed oxides prepared by sol–gel method

The local structure and the photoactivity of B₂O₃–SiO₂/TiO₂ ternary mixed oxides (SiO₂ content was fixed as 30 at.% with respect to TiO₂) was investigated by using XRD, FT-IR, BET, UV-vis spectra, and electron paramagnetic resonance (EPR) measurement. In FT-IR analysis, boron was incorporated into the framework of titania matrix with replacing Ti---O---Si with Si---O---B or Ti---O---B bonds. Also, paramagnetic species such as O⁻ and Ti³⁺ defects were formed by the boron incorporation. In SiO₂/TiO₂ mixed oxides, a blue shift in the light absorption band was observed due to the quantization of band structure. All B₂O₃–SiO₂/TiO₂ samples had pure anatase phase and no rutile phase was formed even though the calcination temperature was over 900 °C. Incorporating boron oxides of more than 10% enlarges the grain size of anatase phase and causes a red shift of the light absorption spectrum. The surface area was monotonically decreased with increasing the content of boron content. As a result, the photoactivity of B₂O₃–SiO₂/TiO₂ ternary mixed oxides was greatly influenced by the content of boron oxide. The highest photoactivity (g moles/min l) was obtained when the boron content was 5% and seven times higher than that of silica/titania binary mixed oxide. In addition, the specific photoactivity (g moles/m² l) was maximum still at 5%. It was concluded that the large reduction of surface area, the change of band structure, and more formation of bulk Ti³⁺ sites are responsible for the deterioration in the photoactivity of B₂O₃–SiO₂/TiO₂ ternary mixed oxides when the content of boron is over 10%, although their crystallinity was enhanced by increasing the calcination temperature with keeping anatase phase.     

Hydrophilic/hydrophobic conversion of Ni-doped TiO2 thin films on glass substrates

Nickel-doped titanium oxide thin films were prepared on soda–lime–silica glass substrates by using a metal naphthenate. Films prefired at 500 °C for 10 min were finally annealed at 600 °C for 30 min in air. Contact angle measurement was used for analyzing hydrophilic/hydrophobic conversion. NiTiO₃, rutile and anatase peaks were obtained for the film after nickel doping. The film containing nickel showed a shift towards the visible in the absorption threshold.     

Effect of pre-sintering temperature on the structural and dielectric properties of (Ba0.5Sr0.5)TiO3 thin films deposited by sol–gel technique

(Ba_0.5Sr_0.5)TiO₃ thin films have been deposited by sol–gel technique and the effect of pre-sintering temperature on the structural and dielectric properties has been studied. The sol was prepared from barium acetate and strontium acetate powders by dissolving them in acetic acid; while titanium isopropoxide was used as titanium source. Acetyl acetone, 2-methoxyethanol, and formamide were used as chelating agent, diluting reagent, and for getting crack free films, respectively. Two sets of films were prepared; one set pre-sintered at 400 °C while the other one at 600 °C. In all the cases, the final sintering temperature was kept fixed at 700 °C for 2 h. These films were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), dielectric constant, and loss measurements and AC conductivity studies. It has been found that with an increase in the pre-sintering temperature from 400 to 600 °C, the dielectric constant increases from 225 to 383 (measured at 100 kHz); whereas, the loss tangent remains nearly constant at 0.03–0.05. The XRD results show better crystallinity and enhanced grain growth in case of films pre-sintered at 600 °C. The FTIR spectra reveals that there is significant removal of organic materials in films with higher pre-sintering temperature as compared to that with lower pre-sintering temperature. The AC conductivity studies show a decrease in the frequency exponent ‘s’ with an increase in the pre-sintering temperature which has been correlated with the reduction in oxygen vacancy densities in the sample with higher pre-sintering temperature.     

Low temperature synthesis of MgxAl2(1−x)Ti(1+x)O5 films by sol–gel processing

Aluminium titanate films thicker than 0.5 μm have been synthesized by sol–gel methods. The films have been deposited via repetitive dip-coating on silicon wafers and their thermal stability has been tested as a function of the annealing time and temperature. The sol–gel approach has allowed the formation of the aluminium titanate phase at temperatures (700 °C) much lower than those necessary for solid-state reactions (1450 °C). Magnesium oxide has been used to improve the thermal stability of the films at high temperatures. The behavior of samples prepared with two different Mg content, i.e. Mg_0.2Al_1.6Ti_0.8O₅ and Mg_0.6Al_0.8Ti_1.6O₅, has been studied. The films have proven to be stable at 1150 °C, for up to 90 h. X-ray photoelectron spectroscopy has shown that after firing at 500 °C the surface chemical composition of the films is in accordance with the nominal one, whilst at higher annealing temperatures some differences, attributed to diffusion effects, have been observed.     

Dielectric behavior of Nb2O5-doped TiO2/epoxy thick films

TiO₂/epoxy composite thick films containing the TiO₂ powders doped with 4 and 10 vol% Nb₂O₅ heat treated under vacuum at 1050 and 1150 °C, were prepared by the screen printing and curing steps. The Nb₂O₅-doped TiO₂ ceramic bulks demonstrated a higher effective dielectric constant at different densification environments, as compared with pure TiO₂. The dielectric properties of the TiO₂/epoxy thick films were improved if the heat-treated 4 vol% Nb₂O₅-doped TiO₂ powder was incorporated instead of the un-doped and heat-treated 10 vol% Nb₂O₅-doped TiO₂ powders. The disadvantage of the doped TiO₂ having higher dielectric loss tangent could be minimized after its powder was properly treated and mixed with epoxy to form the TiO₂/epoxy composite. A best result with the dielectric constant of 23 and the loss tangent of 0.046 was obtained for the 40 vol% TiO₂/epoxy composite thick films, where the TiO₂ powder was doped with 4 vol% Nb₂O₅ followed by calcination at 1000 °C in air and heat treatment at 1150 °C under vacuum.     

Surface sol–gel modification of mesoporous silica molecular sieve SBA-15 with TiO2 in supercritical CO2

Mesoporous silica molecular sieve SBA-15 has been grafted with monolayer and doublelayer of titanium dioxide via surface sol–gel process in supercritical carbon dioxide (SC CO₂). The materials were characterized by nitrogen adsorption, X-ray photoelectron, X-ray diffraction (XRD), and Raman spectroscopy. The results suggest that the incorporated titanium dioxide is present mainly as anatase phase. The pore diameter decreases with the modification cycle number, and the titanium dioxide exists as a 5 Å thick film chemically anchored on the mesopores of SBA-15.     

Effect of solvo-thermal treatment temperature on the properties of sol–gel ZrO2–TiO2 mixed oxides as HDS catalyst supports

ZrO₂–TiO₂ mixed oxide (30–70 mol/mol) was prepared by low-temperature sol–gel followed by solvo-thermal treatment (1 day) at various temperatures (40, 80, 120, 160 and 200 °C). Selected samples of the corresponding single oxides were also prepared. Materials characterization was carried out by N₂ physisorption, XRD, thermal analysis (TG-DTA) and UV–vis DRS, infra-red and Laser-Raman spectroscopies. Binary solids of enhanced pore volume and pore size diameter were obtained by increasing the post-treatment severity. Anatase TiO₂ micro-segregation was evidenced by Raman spectroscopy for the mixed oxide solvo-treated at the highest temperature. This solid also showed the highest crystallization temperature to ZrTiO₄ (702 °C). Mo impregnated (2.8 atom nm⁻²) on various mixed oxides was sulfided under H₂S/H₂ (400 °C, 1 h), the catalysts being tested in the dibenzothiophene hydrodesulfurization (HDS, T = 320 °C, P = 5.59 MPa). By increasing the severity of the solvo-treatment improved supports for MoS₂ phase were obtained. The HDS activity of the catalyst with carrier post-treated at 200 °C was 40% higher (in per total mass basis) than that of sulfided Mo supported on the binary oxide solvo-treated at 80 °C. The ZrO₂–TiO₂-supported catalysts showed higher selectivity to products from the hydrogenation route than their counterparts supported on either single oxide.     

The mechanism of SO2 effect on NO reduction with propene over In2O3/Al2O3 catalyst

An In₂O₃/Al₂O₃ catalyst shows high activity for the selective catalytic reduction of NO with propene in the presence of oxygen. The presence of SO₂ in feed gas suppressed the catalytic activity dramatically at high temperatures; however it was enhanced in the low temperature range of 473–573 K. In TPD and FT-IR studies, the formation of sulfate species on the surface of the catalyst caused an inhibition of NO_X adsorption sites, and the absorbance ability of NO was suppressed by the presence of SO₂, and the amount of ad-NO₃⁻ species decreased obviously. This leads to a decrease of catalytic activity at higher temperatures. However, addition of SO₂ enhanced the formation of carboxylate and formate species, which can explain the promotional effect of SO₂ at low temperature, because active C₃H₆ (partially oxidized C₃H₆) is crucial at low temperature.     

Distinct dispersion stability of various TiO2 nanopowders using ammonium polyacrylate as dispersant

The dispersion stabilities of three titania (TiO₂) nanopowders with different particle sizes and surface chemistries in aqueous suspensions containing a common water-based dispersant, ammonium polyacrylate (PAA-NH₄), have been investigated and compared. According to adsorption isotherm and Fourier transform infrared spectroscopy analyses, the adsorption conformations of PAA-NH₄ are distinct for the different TiO₂ nanopowders. In addition, PAA-NH₄ exhibited the greatest adsorption affinity to the larger, hydrophilic TiO₂ nanopowder and the least affinity to smaller, hydrophobic nanopowder. From sedimentation and rheological results, the dispersion stability of the larger, hydrophilic TiO₂ nanopowder was demonstrated to be the greatest. Based on thermodynamic and kinetic calculations for the stabilization energies, the larger, hydrophilic TiO₂ nanopowder was also shown to be the best-stabilized powder, although it settles faster than the smaller, hydrophilic TiO₂ nanopowder; this is due to the greater affection of sedimentation flux on the larger nanopowder. In contrast, the hydrophobic TiO₂ nanopowder formed a gel-like structure in the aqueous suspension when the solid content was greater than 10 wt%, which is attributed to polymer bridging between PAA-NH₄-adsorbed TiO₂ nanoparticles.     

Phototransformation of metobromuron in the presence of TiO2

The photocatalytic degradation of the herbicide metobromuron was studied, using TiO₂ photocatalysts (Degussa P25 and Millennium PC50, PC100, PC105 and PC500). Intermediate products were identified by means of liquid chromatography–mass spectrometry (LC–MS–MS) using electrospray (ES) interfacing technique. In order of importance, the main reaction pathways were demethoxylation of the urea chain, ring oxidation leading to ortho hydroxylation with respect to the N atom, substitution of Br by OH, ring oxidation with formation of the meta hydroxylated compound. Demethylation of the demethoxylated product occurred as a secondary reaction. Formation of bromide ions was observed too. In the presence of 2-propanol used as a hydroxyl radical scavenger, demethoxylation was drastically inhibited while the other reactions were only partly inhibited. It suggests that demethoxylation was exclusively due to the oxidation by hydroxyl radicals, whereas the other reactions involved positive holes too. The degradation rate of metobromuron varied in the order: PC50 < PC100 < PC105 < PC500 < Degussa P25. TiO₂ Degussa P25 was therefore the most efficient photocatalyst although its surface area was lower than that of most of Millennium TiO₂.