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Titanate nanotubes were synthesized by hydrothermal method using various TiO2 precursors as starting materials. The electrochemical properties were investigated by cyclic voltammetric methods. The microstructure and morphology of the synthesized powders were characterized by XRD, TEM. Titanate nanotubes composed of H2Ti2O5 x H2O with outer and inner diameter of approximately 10 nm and 6 nm, and the interlayer spacing was about 0.65 approximately 0.74 nm. Also, the titanate nanotubes showed a discharge capacity of 303 mAh/g and the highest cycle stability because of the open-end and rolled layers with suitable spacing. The relationships between morphology and electrochemical properties have been also discussed.
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PMID:Structural characterization of titanate nanotubes for lithium storage. 1919 83

Titanate nanotubes and nanofibers were synthesized by hydrothermal method using various alkaline solutions (NaOH and KOH) in order to study the effect of synthesis condition for hydrogen storage. The microstructures of titanate nanotube and nanofibers were characterized by XRD, TEM, FE-SEM. It was found that interlayer spacing of titanate nanotubes and nanofibers depended on the alkaline solution, because some of the Ti-O-Ti bonds were broken and layered titanate nanosheet of Ti-O-A (Na+ and K+) bonds were formed. The sorption of hydrogen of the titanate nanotubes and nanofibers were studied by the conventional volumetric pressure-composition isothermal method at RT, 30 atm. The relationships between interlayer spacing, ionic radius of alkaline solution and hydrogen capacity have been discussed.
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PMID:Synthesis and characterization of titanate nanotube for hydrogen storage using hydrothermal method with various alkaline treatment. 1919 98

Diatoms are single-celled algae that make silica shells or frustules with intricate nanoscale features imbedded within periodic two-dimensional pore arrays. A two-stage photobioreactor cultivation process was used to metabolically insert titanium into the patterned biosilica of the diatom Pinnularia sp. In Stage I, diatom cells were grown up on dissolved silicon until silicon starvation was achieved. In Stage II, soluble titanium and silicon were continuously fed to the silicon-starved cell suspension (approximately 4 x 10(5) cells/mL) for 10 h. The feeding rate of titanium (0.85-7.3 micromol Ti L(-1) h(-1)) was designed to circumvent the precipitation of titanate in the liquid medium, and feeding rate of silicon (48 micromol Si L(-1) h(-1)) was designed to sustain one cell division. The addition of titanium to the culture had no detrimental effects on cell growth and preserved the frustule morphology. Cofeeding of Ti and Si was required for complete intracellular uptake of Ti. The maximum bulk composition of titanium in the frustule biosilica was 2.3 g of Ti/100 g of SiO(2). Intact biosilica frustules were isolated by treatment of diatom cells with SDS/EDTA and then analyzed by TEM and STEM-EDS. Titanium was preferentially deposited as a nanophase lining the base of each frustule pore, with estimated local TiO(2) content of nearly 80 wt %. Thermal annealing in air at 720 degrees C converted the biogenic titanate to anatase TiO(2) with an average crystal size of 32 nm. This is the first reported study of using a living organism to controllably fabricate semiconductor TiO(2) nanostructures by a bottom-up self-assembly process.
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PMID:Metabolic insertion of nanostructured TiO2 into the patterned biosilica of the diatom Pinnularia sp. by a two-stage bioreactor cultivation process. 1920 57

The vanadium (V)-doped mesoporous titanium dioxide (TiO(2)) nanoparticles with V/Ti ratios from 0-2 wt% were prepared using sol-gel method in the presence of triblock polymers, Pluronic F127. SEM images showed that the V-doped TiO(2) nanoparticles were porous structures. The surface areas and pore sizes were in the range 85-107 m(2)/g and 12-14 nm, respectively. From XRPD, the V-doped mesoporous TiO(2) after calcination at 500 degrees C was mainly anatase phase, and the crystallite sizes were in the range 14-16 nm. TEM images showed that vanadia was doped both on the surface and in the lattice of anatase TiO(2). A slight red-shift in wavelength absorption was observed when V/Ti ratio increased from 0 to 2 wt%. Addition of vanadium ion slightly decreased the photocatalytic activity of TiO(2) toward the decolorization of MB under the illumination of UV light at 305 nm. However, a 1.6-1.8 times increase in rate constants for MB photodegradation was observed when 0.5-1.0 wt% V-doped TiO(2) was illumined by solar simulator at AM 1.5. These results demonstrated that the doping of low concentrations of V ion into mesoporous TiO(2) enhance the photocatalytic activity of mesoporous TiO(2) towards photodecomposition of azo dye in the visible range.
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PMID:Characterization and photocatalytic activity of vanadium-doped titanium dioxide nanocatalysts. 1921 7

Our recent work suggests limited uptake of unstabilized metal oxide nanoparticles via water into fish, however, some other studies have indicated such exposures can induce oxidative stress. To investigate tissue distribution and toxicity of titanium dioxide (TiO(2)) nanoparticles that may enter into fish, we conducted a series of injection studies. Rainbow trout (Oncorhynchus mykiss) were intravenously injected with 100 microg TiO(2) nanoparticles and the content of titanium in blood, brain, gills, liver, and kidney quantified at time points between 6 h and 90 days using inductively coupled plasma optical emission spectroscopy. Injected Ti was concentrated in the kidneys and remained there up to 21 days, however, there was evidence of clearance of TiO(2) at 90 days. Ti accumulation in the liver was 15 times lower than in the kidney with no apparent clearance. Using TEM we showed nanoparticles were localized in tissue vesicles surrounding the kidney tubules. In a second injection study, rainbow trout were injected with 100 microg TiO(2) and plasma samples from individual fish analyzed for total protein and creatinine content at time points between 6 h and 21 days to assess for possible effects on kidney function. No effect of TiO(2) on total plasma protein content or creatinine concentrations were found indicating that neither urine production nor glomerular filtration rate were affected. We conclude that in trout upon a single high dose exposure of TiO(2) nanoparticles via the bloodstream, TiO(2) accumulates in the kidneys but has minimal effect on kidney function.
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PMID:High doses of intravenously administered titanium dioxide nanoparticles accumulate in the kidneys of rainbow trout but with no observable impairment of renal function. 1933 50

Mesoporous titanosilicates with high titanium content were synthesized under mild acidic conditions (pH=4.4, HAc-NaAc buffer solution) by co-condensation of acetylacetone-modified titanium isopropoxide (Ti(OBu(n))(3) (acac)) and mixture of sodium silicate with tetramethoxysilane (TMOS) or tetraethoxysilane (TEOS) or tetrakis(2-hydroxyethyl)orthosilicate (EGMS), using block copolymer Pluronic P123 as template. The combined results of XRD, N(2) sorption and TEM show that the highly regular structure of the mesoporous titanosilicates can still be obtained when Ti/Si molar ratio in the final product is as high as 0.059. The results of UV-vis diffuse reflectance spectra and UV resonance Raman spectra show that the framework titanium species are predominant in the mesoporous titanosilicates when Ti/Si molar ratio in the final product is less than 0.042. The mixture of sodium silicate and EGMS was proved to be the best silicon source for the synthesis of titanosilicates with ordered mesostructure and high titanium content. The efficiency of this synthetic method may be attributed to the mild acidic medium as well as the modified hydrolysis-condensation rate and hydrophility of the precursors.
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PMID:Mesoporous titanosilicates with high loading of titanium synthesized in mild acidic buffer solution. 1939 14

Hierarchical morphologies in metal oxides are advantageous for many applications, including controlled drug release, photocatalysis, catalysis, synthetic biomaterials, and adsorption and separation technologies. In this study, agarose gel has been used as a template to prepare zirconium titanium mixed oxide pellets with bimodal porosity. Sol-gel chemistry conducted within the agarose gel produced "coral-like" interconnected networks of oxide nanoparticles with controllable quantities of zirconium and titanium. The materials were characterized using N(2) sorption, extended X-ray absorption fine structure, X-ray diffraction, TEM, SEM, zeta potential, and thermogravimetric analysis (to measure surface hydroxyl group density). The oxides were then tested for the adsorption of vanadyl and vanadate to determine which Zr mole fraction exhibited the highest capacity and fastest kinetics. The material containing 25 mol % Zr exhibited the highest surface area (322 +/- 8 m(2)/g) of the compositions investigated and also displayed a superior adsorption rate and capacity. Vanadate adsorption occurred with faster kinetics than did vanadyl adsorption. A comparative study demonstrated that the macro/meso pore structure had improved transport properties over a monomodal mesopore structure of similar Zr/Ti composition. The faster vanadate adsorption kinetics is attributed to enhanced surface accessibility in a hierarchical material.
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PMID:Template synthesis and adsorption properties of hierarchically porous zirconium titanium oxides. 1939 63

Vertically-oriented high aspect ratio titania nanotube bundles have been grown by a potentiostatic anodization of titanium sheet in fluoride-free electrolytes. The anodization conditions like the applied voltage were optimized for the synthesis of titania nanotubes in HClO4 and NaCl electrolyte. The resulting nanotubes have a length of about 30 microm, outer diameter about 40 nm, inner pore size of about 10 nm and the aspect ratio was 750:1 by anodization in 0.1 M perchloric acid of pH approximaately 1 at applied voltage of 20 V. While for nanotubes prepared in 0.3 M NaCl of pH 4.3, the length was above 50 microm with the aspect ratio of 1250:1. A method to increase the uniformity of nanotube was demonstrated by pretreatment the titanium sheet by (4 wt% HF + 5 M HNO3) solution prior to anodization. Titania nanotubes were prepared, for the first time, by anodization in aqueous H2SO4 electrolyte alone with tube length above 500 nm. Annealing studies were performed, on high aspect ratio Titania nanotube layers produced in HClO4 electrolyte, in the temperature interval of 300 to 550 degrees C. The XRD patterns and TEM data confirmed the formation of single anatase phase after annealing at 450 degrees C with perfect nanoubular structure. While the rutile titania phase starts to emerege after annealing at about 500 degrees C and the evidence for the appearance of rutile phase due to the oxidation of the underlying Ti metal at the interface between nanotube/Ti-metal was given. On the other hand, the nanotubular structure starts to destroy upon annealing temperature of approximate 550 degrees C by tube flattening and losing of roll-up characteristics as indicated in SEM images. The superior morphology of these high aspect ratio nanotubes and their rapid growth rate foreshadow a bright future in wide applications like dye-sensitized solar cells, water photolysis and nanobiomedical.
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PMID:Electrochemical growth of vertically-oriented high aspect ratio titania nanotubes by rabid anodization in fluoride-free media. 1943 43

Phosphorus-doped titania powders were prepared by a sol-gel method using titanium (IV) tetrabutoxide and sodium hypophosphite as starting materials. The as-prepared products were characterized by XRD, XPS, TEM and UV-vis spectroscopy. The TiO2 powders calcined at 400 degrees C for 5 h in an N2 atmosphere showed an anatase structure. The crystallinity of TiO2 was improved by calcination both in air and in N2 atmospheres. Furthermore, UV-vis spectroscopy analysis indicated that the absorption edge of the samples shifted to a longer wavelength after calcination. The XRD results suggested that phosphorus was doped into the crystal lattice of TiO2. The electronic states of phosphorus were determined by XPS, which indicated that the phosphorus in the prepared titania powders was in a lower oxidization state than the pentavalent oxidation state of phosphorus. Also, the photocatalytic activity was tested by observing the photodecomposition of methylene blue.
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PMID:Preparation and photocatalytic property of phosphorus-doped TiO2 particles. 1949 34

Very stable titania hydrosols were prepared by fast hydrolysis of titanium isopropoxide in a large excess of water. XRD patterns show that these sols contain nanocrystals (5-6 nm) of anatase (70%) and brookite (30%). TEM images indicate that these primary particles form aggregates whose mean hydrodynamic diameter, determined by photon correlation spectroscopy, is in the range of 80-90 nm. The flow curves of these colloids, recorded for several volume fractions of nanoparticles, can be perfectly fitted, in the range 0-100 s(-1), with a power-law model. In this range the behavior is Newtonian but for larger shear rates a shear thinning is observed. The viscosity dependence on particle concentration can be predicted by a Batchelor-type model were the volume fraction of particles is replaced by an effective volume fraction of aggregates, taking into account their fractal dimension. Addition of polyethylene glycol (PEG 2000) induced a marked decrease (more than 50%) of the sol viscosity down to a minimum. This is explained by assuming that PEG adsorbs on the surface of TiO(2) particles producing stabilization by steric effects and leading to formation of more compact aggregates. Without PEG the sol viscosity strongly decreases on aging. This effect is not caused by the growth of primary particles. It is rather interpreted as a progressive reorganization of the aggregates toward a more compact packing.
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PMID:Effect of PEG on rheology and stability of nanocrystalline titania hydrosols. 1950 38


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