Synthesis of Mesoporous Titanium Dioxide

The objective of this research is to synthesize mesoporous Titanium Dioxide using sol-gel method while investigating the effect of pH and calcinations temperature to the characteristic of the synthesized mesoporous Titanium Dioxide. Mesoporous Titanium Dioxide have been tested previously to have photocatalytic activity in sunlight and promote widespread use in solar technology. A simple sol-gel method has been conducted to synthesize the mesoporous Titanium Dioxide using apparatus available in the Reaction Engineering Lab inside UTP campus. The sample is then analyzed to identify it's characteristics

One-dimensional metal-organic framework photonic crystals used as platforms for vapor sorption.

We present the fabrication of one-dimensional photonic crystals (Bragg stacks) based on a microporous metal–organic framework material and mesoporous titanium dioxide. The Bragg stack heterostructures were obtained using two complementary synthesis approaches utilizing the bottom-up assembly of heterogeneous, i.e. two-component photonic crystal multilayer structures. Zeolitic imidazolate framework ZIF-8 and mesoporous titanium dioxide were chosen as functional components with different refractive indices. While ZIF-8 is intended to impart molecular selectivity, mesoporous TiO2 is used to ensure high refractive index contrast and to guarantee molecular diffusion within the Bragg stack. The combination of micro- and mesoporosity within one scaffold endows the 1D-MOF PC with characteristic adsorption properties upon exposure to various organic vapors. In this context, the sorption behavior of the photonic material was studied as a function of partial pressure of organic vapors. The results show that the multilayered photonic heterostructures are sensitive and selective towards a series of chemically similar solvent vapors. It is thus anticipated that the concept of multilayer heterogeneous photonic structures will provide a versatile platform for future selective, label-free optical sensors

Osteogenic effects of simvastatin-loaded mesoporous titania thin films

The use of statins in the field of bone regeneration is under current investigation due to the existing demand for non-toxic anabolic agents capable of enhancing bone formation in cases of substantial loss. Simvastatin, a coenzyme currently prescribed in clinics to inhibit cholesterol biosynthesis, has been proven to promote osteogenic differentiation by stimulating bone formation and inhibiting osteoclasts activity. We present the loading of simvastatin in mesoporous TiO2 thin films toward combining the pro-osteogenic properties of this molecule with the demonstrated bioactivity of titania. TiO2 thin films processing and characterization were carried out, as well as evaluation of MC3T3-E1 pre-osteoblasts viability when directly incubated with different concentrations of simvastatin, followed by the analysis of osteogenic activity promoted by simvastatin upon loading in the thin films. The accessible porosity of 36% quantified on the 95 ± 5 nm thick mesoporous thin films, together with pore diameters of 5.5 nm, necks between pores of 2.8 nm and interpore distances of 12 ± 2 nm allow the loading of the simvastatin molecule, as confirmed by FTIR spectroscopy. Simvastatin was found to promote MC3T3-E1 pre-osteoblasts viability at concentrations ≤0.01 g l−1, with a cytotoxicity threshold of 0.05 g l−1. We additionally found that film loadings with 0.001 g l−1 simvastatin promotes statistically higher MC3T3-E1 pre-osteoblast proliferation whereas a higher concentration of 0.01 g l−1 leads to statistically higher osteogenic activity (ALP synthesis), after 21 days of incubation, as compared to unloaded films. These results demonstrate the potential of simvastatin local administration based on bioactive mesoporous thin films to promote pro-osteogenic properties. By focusing this strategy on the coating of metallic prostheses, the supply of simvastatin to the target tissue can be favored and risks of systemic side effects will be reduced while enhancing the osteointegration of the implants.Fil: Lopez Alvarez, Miriam. Universidad de Vigo; EspañaFil: López Puente, Vanesa. Universidad de Vigo; EspañaFil: Rodriguez Valencia, Cosme. Universidad de Vigo; EspañaFil: Angelome, Paula Cecilia. Comisión Nacional de Energía Atómica. Centro Atómico Constituyentes; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Liz Marzan, Luis M. Ikerbasque; EspañaFil: Serra, Julia. Universidad de Vigo; EspañaFil: Pastoriza Santos, Isabel. Universidad de Vigo; EspañaFil: Gonzalez, Pio. Universidad de Vigo; Españ

Nanostructured semiconductor materials for dye-sensitized solar cells

Since O'Regan and Grätzel's first report in 1991, dye-sensitized solar cells (DSSCs) appeared immediately as a promising low-cost photovoltaic technology. In fact, though being far less efficient than conventional silicon-based photovoltaics (being the maximum, lab scale prototype reported efficiency around 13%), the simple design of the device and the absence of the strict and expensive manufacturing processes needed for conventional photovoltaics make them attractive in small-power applications especially in low-light conditions, where they outperform their silicon counterparts. Nanomaterials are at the very heart of DSSC, as the success of its design is due to the use of nanostructures at both the anode and the cathode. In this review, we present the state of the art for both n-type and p-type semiconductors used in the photoelectrodes of DSSCs, showing the evolution of the materials during the 25 years of history of this kind of devices. In the case of p-type semiconductors, also some other energy conversion applications are touched upon. © 2017 Carmen Cavallo et al

Synthesis and characterization of nanometric titania coated on granular alumina for arsenic removal

The adsorption process is widely used for the treatment of drinking water sources containing high levels of arsenic. The choice of the adsorbent is crucial for the efficiency of the process. Very good performances were obtained in the past by activated alumina, while more recent studies have shown that also other media such as titanium oxide can provide high removal rates. In the present work, four types of adsorbents were tested for their removal capability of pentavalent arsenic from liquid solutions. Specifically, it was investigated if modifications of activated alumina by coating with titanium oxide nanoparticles or by reducing particle size might improve their performance. The adsorbents were firstly characterized by X-ray diffraction, BET specific area measurement and SEM analysis. Then, kinetics, equilibrium isotherm experiments were conducted in batch mode at fixed pH. All the tested adsorbents showed satisfactory arsenic removal, with the best performance obtained by the mesoporous gamma-alumina which had the lowest grain size. The titanium coating did not appear to significantly improve adsorption capacity. The kinetic data were best fitted by the pseudo-second order model, while both the Freundlich and the Langmuir equations well represented the adsorption isotherm data

TiO2-doped resorcinol–formaldehyde (RF) polymer and carbon gels with photocatalytic activity

Resorcinol-formaldehyde (RF) polymer gels offer a relatively easy and versatile route for incorporating metals into a carbon aerogel matrix. The hybrid materials thus obtained are ideal candidates for applications involving enhanced adsorption or catalysis. This paper presents a detailed study of Ti-doped RF and carbon aerogels. The metal was introduced into the system at three different stages of the preparation process: during polymerization, by impregnation of the RF gel, or by impregnation of the carbon gel. The structure and morphology of the samples are compared using low temperature N2 adsorption, SEM, and small and wide angle X-Ray scattering (SAXS/WAXS) methods. The TiO2-doped carbon aerogels display photocatalytic activity in breaking down aromatic compounds

Sulphur and cerium co-doped mesoporous titanium dioxide photocatalysts and their photocatalytic activity in the degradation of methylene orange

A series of sulphur and cerium co-doped mesoporous titanium dioxide photocatalysts have been prepared by a template method using thiourea, ammonium ceric nitrate and tetrabutyl titanate as precursors and Pluronic P123 as a template. The morphology, crystal structure, surface structure and optical absorption properties of the prepared samples are characterized by scanning electron microscopy, X-ray diffraction, N2 adsorption-desorption measurements and UV-vis absorption spectra. The microcrystal of the co-doped photocatalyst comprises the anatase­ phase. Compared with mesoporous titanium dioxide, the co-doped samples extends the photoabsorption edge into the visible light region. The photocatalytic activities of the obtained photocatalysts under UV and visible light have been estimated by measuring the degradation rate of methylene orange in aqueous solution. Results show that the co-doped mesoporous titanium dioxide exhibits higher photocatalytic activity than mesoporous titanium dioxide under light irradiation. The synergistic effect of sulphur and cerium co-doping plays an important role in improving the photocatalytic activity.

Application of reverse micelle sol-gel synthesis for bulk doping and heteroatoms Surface Enrichment in Mo-Doped TiO 2 nanoparticles

TiO 2 nanoparticles containing 0.0, 1.0, 5.0, and 10.0 wt.% Mo were prepared by a reverse micelle template assisted sol-gel method allowing the dispersion of Mo atoms in the TiO 2 matrix. Their textural and surface properties were characterized by means of X-ray powder diffraction, micro-Raman spectroscopy, N 2 adsorption/desorption isotherms at -196 °C, energy dispersive X-ray analysis coupled to field emission scanning electron microscopy, X-ray photoelectron spectroscopy, diffuse reflectance UV-Vis spectroscopy, and ζ-potential measurement. The photocatalytic degradation of Rhodamine B (under visible light and low irradiance) in water was used as a test reaction as well. The ensemble of the obtained experimental results was analyzed in order to discover the actual state of Mo in the final materials, showing the occurrence of both bulk doping and Mo surface species, with progressive segregation of MoO x species occurring only at a higher Mo content

All-inorganic core-shell silica-titania mesoporous colloidal nanoparticles showing orthogonal functionality

Colloidal mesoporous silica (CMS) nanoparticles with a thin titania-enriched outer shell showing a spatially resolved functionality were synthesized by a delayed co-condensation approach. The titaniashell can serve as a selective nucleation site for the growth of nanocrystalline anatase clusters. These fully inorganic pure silica-core titania-enriched shell mesoporous nanoparticles show orthogonal functionality, demonstrated through the selective adsorption of a carboxylate-containing ruthenium N3-dye. UV-Vis and fluorescence spectroscopy indicate the strong interaction of the N3-dye with the titania-phase at the outer shell of the CMS nanoparticles. In particular, this interaction and thus the selective functionalization are greatly enhanced when anatase nanocrystallites are nucleated at the titania-enriched shell surface

Nanocrystalline TiO2 and halloysite clay mineral composite films prepared by sol-gel method:Synergistic effect and the case of silver modification to the photocatalytic degradation of basic blue- 41 azo dye in water

Tubular halloysite clay mineral and nanocrystalline TiO2 were incorporated in the preparation of nanocomposite films on glass substrates via sol-gel method at 450 °C. The synthesis involves a simple chemical method employing nonionic surfactant molecule as pore directing agent along with the acetic acid-based sol-gel route without addition of water molecules. Drying and thermal treatment of composite films ensure elimination of organic material and lead to the formation of TiO2 nanoparticles homogeneously distributed on the surface of the halloysite. Nanocomposite films without cracks of active anatase crystal phase and small crystallite size on halloysite nanotubes are characterized by microscopy techniques and porosimetry methods in order to examine their structural properties. The composite halloysite-TiO2 films with variable quantities of halloysite were examined as photocatalysts to the discoloration of Basic Blue 41 azo dye in water. These nanocomposite films proved to be very promising photocatalysts and highly effective to dye's discoloration in spite of small amount of halloysite/TiO2 catalyst immobilized onto glass substrates. It also has been shown that the efficiency of the halloysite/TiO2 films could be further improved when silver particles were deposited on their surface after successful adsorption from an aqueous solution of a silver salt and UV reduction of the adsorbed ions