Vittorio Luca

Strong photoresponse of nanostructured tungsten trioxide films prepared via a sol–gel route

A simple route for synthesizing nanostructured tungsten trioxide (WO3) films on conducting glass substrates has been developed. Films with different morphologies were synthesized by the addition of mineral acids (such as HCl) to an aqueous peroxopolytungstic acid precursor solution. The films were characterized by SEM, SAXS, in-situ X-ray diffraction, cyclic voltammetry, optical absorption and photoelectrochemical measurements. The best of these films generated anodic photocurrents as high as 4.0 mA cm−2 for oxidization of methanol and 2.3 mA cm−2 for water splitting, under Xe lamp illumination at 86 mW cm−2. The improvement of photocurrent can be attributed to enhanced light harvesting and charge transport arising due to the nanostructure.

Mesoporous zirconium titanium oxides. Part 3. Synthesis and adsorption properties of unfunctionalized and phosphonate-functionalized hierarchical polyacrylonitrile-F-127-templated beads.

A method is presented for the preparation of zirconium titanate mixed oxides in bead form having hierarchical pore structure. This method entailed the use of both preformed polyacrylonitrile (PAN) polymer beads and surfactants as templates. The templates were removed by calcination at temperatures below about 500 degrees C, resulting in mixed oxide beads with trimodal pore size distributions and interconnected pores. The pore size distributions as determined using nitrogen adsorption-desorption showed clear maxima at 4.5 and 45 nm length scales and also clear evidence of microporosity. The macroporous framework morphology was a replica of the PAN beads with radial structure. The mesoporous framework possessed wormhole-like pores with pore size of about 6 nm that was consistent with the F-127 triblock copolymer template used. The mixed oxide beads exhibited surface areas of 215 and 185 m2/g after calcination at 500 and 600 degrees C. Thermal stability up to 650 degrees C is unprecedented for bulk systems. The adsorption properties were characterized using uranyl as the target cation and the mass transport in the beads with the present hierarchical architectures has been shown to be exceptional. The beads were functionalized with 4-amino,1-hydroxy,1,1-bis-phosphonic acid (HABDP) and amino-tris-methylene phosphonic acid (ATMP) and the adsorption properties for the extraction of uranyl sulfate complexes from acidic solution examined. Of the two molecules investigated, ATMP functionalization resulted in the best extraction efficiency with equilibrium uptake of about 90% of uranium available in solution between pH 1 and 2. The beads could potentially be utilized as catalysts, catalyst supports, adsorbents, and separation materials.

Aerosol-Assisted Production of Mesoporous Titania Microspheres with Enhanced Photocatalytic Activity: The Basis of an Improved Process

An aerosol-based process was used to prepare mesoporous TiO(2) microspheres (MTM) with an average diameter in the range of 0.5-1 microm. The structural characteristics and photocatalytic properties of the synthesized materials were determined. As-prepared MTM materials and those heated in air from 400 to 600 degrees C exhibited mesoporous texture with a narrow size distribution and an inorganic framework that consisted of 4-13 nm anatase crystallites. Pore volumes for the MTM materials were in the range of 0.17-0.34 cm(3) g(-1). Microspheres heated to 400 degrees C presented a locally ordered mesopore structure and possessed X-ray diffraction d spacings between 9.8 and 17.3 nm. Heating above 400 degrees C resulted in a loss of the mesoscopic order, a decrease of the surface area, retention of the porosity, and an increase of the anatase nanoparticle size to 13 nm. The accessibility of the pore volume was measured by monitoring the uptake of gallic acid (GA) using Fourier transform IR. The MTM materials made excellent catalysts for the photodegradation of GA, with the performance being higher than that of an equivalent sample of Degussa P25. The present MTM materials are advantageous in terms of their ease of separation from the aqueous phase, and hence a novel photocatalytic process is proposed based on separate adsorption and photocatalytic decomposition steps with an improved and more rational use of both catalyst and sunlight.

Hybrid Inorganic−Organic Adsorbents Part 1: Synthesis and Characterization of Mesoporous Zirconium Titanate Frameworks Containing Coordinating Organic Functionalities

A series of functional hybrid inorganic-organic adsorbent materials have been prepared through postsynthetic grafting of mesoporous zirconium titanate xerogel powders using a range of synthesized and commercial mono-, bis-, and tris-phosphonic acids, many of which have never before been investigated for the preparation of hybrid phases. The hybrid materials have been characterized using thermogravimetric analysis, diffuse reflectance infrared (DRIFT) and 31P MAS NMR spectroscopic techniques and their adsorption properties studied using a 153Gd radiotracer. The highest level of surface functionalization (molecules/nm2) was observed for methylphosphonic acid (∼3 molecules/nm2). The level of functionalization decreased with an increase in the number of potential surface coordinating groups of the phosphonic acids. Spectral decomposition of the DRIFT and 31P MAS NMR spectra showed that each of the phosphonic acid molecules coordinated strongly to the metal oxide surface but that for the 1,1-bis-phosphonic acids and tris-phosphonic acids the coordination was highly variable resulting in a proportion of free or loosely coordinated phosphonic acid groups. Functionalization of a porous mixed metal oxide framework with the tris-methylenephosphonic acid (ATMP-ZrTi-0.33) resulted in a hybrid with the highest affinity for 153Gd3+ in nitric acid solutions across a wide range of acid concentrations. The ATMP-ZrTi-0.33 hybrid material extracted 153Gd3+ with a Kd value of 1×10(4) in 0.01 M HNO3 far exceeding that of the other hybrid phases. The unfunctionalized mesoporous mixed metal oxide had negligible affinity for Gd3+ (Kd<100) under identical experimental conditions. It has been shown that the presence of free or loosely coordinated phosphonic acid groups does not necessarily translate to affinity for 153Gd3+. The theoretical cation exchange capacity of the ATMP-ZrTi-0.33 hybrid phase for Gd3+ has been determined to be about 0.005 mmol/g in 0.01 M HNO3. This behavior and that of the other hybrid phases suggests that the surface-bound ATMP ligand functions as a chelating ligand toward 153Gd3+ under these acidic conditions.

Microcrystalline hexagonal tungsten bronze. 1. Basis of ion exchange selectivity for cesium and strontium.

The structural basis of selectivity for cesium and strontium of microcrystalline hexagonal tungsten bronze (HTB) phase Na(x)WO(3+x/2).zH(2)O has been studied using X-ray and neutron diffraction techniques, 1D and 2D (23)Na magic angle spinning (MAS) nuclear magnetic resonance (NMR) spectroscopy, and radiochemical ion exchange investigations. For the HTB system, this study has shown that scattering techniques alone provide an incomplete description of the disorder and rapid exchange of water (with tunnel cations) occurring in this system. However, 1D and 2D (23)Na MAS NMR has identified three sodium species within the HTB tunnels-species A, which is located at the center of the hexagonal window and is devoid of coordinated water, and species B and C, which are the di- and monohydrated variants, respectively, of species A. Although species B accords with the traditional crystallographic model of the HTB phase, this work is the first to propose and identify the anhydrous species A and monohydrate species C. The population (total) of species B and C decreases in comparison to that of species A with increasing exchange of either cesium or strontium; that is, species B and C appear more exchangeable than species A. Moreover, a significant proportion of tunnel water is redistributed by these cations. Multiple ion exchange investigations with radiotracers (137)Cs and (85)Sr have shown that for strontium there is a definite advantage in ensuring that any easily exchanged sodium is removed from the HTB tunnels prior to exchange. The decrease in selectivity (wrt cesium) is most probably due to the slightly smaller effective size of Sr(2+); namely, it is less of a good fit for the hexagonal window, ion exchange site. The selectivity of the HTB framework for cesium has been shown unequivocally to be defined by the structure of the hexagonal window, ion exchange site. Compromising the geometry of this window even in the slightest way by either (1) varying the cell volume through changes to hydration or sodium content or (2) introducing disorder in the a-b plane through isomorphous substitution of molybdenum is sufficient to reduce the selectivity. Indeed, it is our hypothesis that this applies for all cations which are strongly bound by the HTB framework.

Nb-substitution and Cs+ ion-exchange in the titanosilicate sitinakite

Cesium-133 MAS NMR and X-ray powder diffraction have been used to investigate Cs+ ion-exchange in synthetic samples of the titanosilicate mineral, sitinakite. The effect of incorporating Nb using Nb(V) ethoxide as the Nb source into the sitinakite framework and its influence on Cs+ ion-exchange was also studied. Refinements of X-ray powder data show that substitution of niobium for titanium in the sitinakite framework occurs to a limited extent using the synthetic method employed. Niobium substitution is also supported by 29Si MAS NMR spectra. Any niobium that was not substituted into the sitinakite structure was present in a distinct Nb-rich oxide/hydroxide phase. NMR studies reveal that in the undoped samples with low Cs loadings, at least four types of Cs+ are present, while at higher levels of Cs+ loadings, an additional two sites are populated. Similar sites appear to be occupied in the Nb-substituted samples but the relative occupancies are strongly modulated relative to the undoped samples. The multiple Cs environments are attributed to Cs+ ions occupying similar structural sites in the titanosilicate channels but experiencing different hydration water coordination environments.

Pore size and volume effects on the incorporation of polymer into macro- and mesoporous zirconium titanium oxide membranes.

Macro- and mesoporous hybrid materials have applications in the fields of drug delivery, catalysis, biosensing, and separations. The pore size requirements must be well-understood to maximize the performance (e.g., load capacity and accessibility) of such materials. Hybrid materials were prepared by coating five distinct macroporous commercial membranes with zirconium titanium oxide through sol-gel chemistry. Calcination of these templated materials produced oxide membranes which had a suite of macropore and mesopore architectures, pore volumes, and surface areas. These differences in physical properties were used to conduct a fundamental study on the relationship between the pore size and volume and the polymer incorporation. Metal oxide membranes were postsynthetically modified with poly(ethyleneimine) (PEI) ranging in molecular weight from 1300 to 1 000 000 Da (1.2-11 nm in hydrodynamic diameter). The incorporation of the polymer from a 9 wt % solution at pH 10 was highly dependent on the pore size and pore volume. As the surface area increased, loading capacity decreased, indicating that much of the increased internal surface, due to small pore diameters (< or = 8 nm), was inaccessible to the macromolecules. Exclusion of PEI from small mesopores was apparent even for the lowest molecular weight polymer. A high maximum loading of 1.25 mg m(-2) of 600 000-1 000 000 Da PEI was achieved in the metal oxide with the largest minimum mesopore diameter. Thus, mesopore diameter and pore volume must be considered when designing a mesoporous solid support.

Monitoring bisphosphonate surface functionalization and acid stability of hierarchically porous titanium zirconium oxides.

To take advantage of the full potential of functionalized transition metal oxides, a well-understood nonsilane based grafting technique is required. The functionalization of mixed titanium zirconium oxides was studied in detail using a bisphosphonic acid, featuring two phosphonic acid groups with high surface affinity. The bisphosphonic acid employed was coupled to a UV active benzamide moiety in order to track the progress of the surface functionalization in situ. Using different material compositions, altering the pH environment, and looking at various annealing conditions, key features of the functionalization process were identified that consequently will allow for intelligent material design. Loading with bisphosphonic acid was highest on supports calcined at 650 °C compared to lower calcination temperatures: A maximum capacity of 0.13 mmol g(-1) was obtained and the adsorption process could be modeled with a pseudo-second-order rate relationship. Heating at 650 °C resulted in a phase transition of the mixed binary oxide to a ternary oxide, titanium zirconium oxide in the srilankite phase. This phase transition was crucial in order to achieve high loading of the bisphosphonic acid and enhanced chemical stability in highly acidic solutions. Due to the inert nature of phosphorus-oxygen-metal bonds, materials functionalized by bisphosphonic acids showed increased chemical stability compared to their nonfunctionalized counterparts in harshly acidic solutions. Leaching studies showed that the acid stability of the functionalized material was improved with a partially crystalline srilankite phase. The materials were characterized using nitrogen sorption, X-ray powder diffraction, and UV-vis spectroscopy; X-ray photoelectron spectroscopy was used to study surface coverage with the bisphosphonic acid molecules.

One-Pot Preparation and Uranyl Adsorption Properties of Hierarchically Porous Zirconium Titanium Oxide Beads using Phase Separation Processes to Vary Macropore Morphology

A simple and engineering friendly one-step process has been used to prepare zirconium titanium mixed oxide beads with porosity on multiple length scales. In this facile synthesis, the bead diameter and the macroporosity can be conveniently controlled through minor alterations in the synthesis conditions. The precursor solution consisted of poly(acrylonitrile) dissolved in dimethyl sulfoxide to which was added block copolymer Pluronic F127 and metal alkoxides. The millimeter-sized spheres were fabricated with differing macropore dimensions and morphology through dropwise addition of the precursor solution into a gelation bath consisting of water (H(2)O beads) or liquid nitrogen (LN(2) beads). The inorganic beads obtained after calcination (550 °C in air) had surface areas of 140 and 128 m(2) g(-1), respectively, and had varied pore architectures. The H(2)O-derived beads had much larger macropores (5.7 μm) and smaller mesopores (6.3 nm) compared with the LN(2)-derived beads (0.8 μm and 24 nm, respectively). Pluronic F127 was an important addition to the precursor solution, as it resulted in increased surface area, pore volume, and compressive yield point. From nonambient XRD analysis, it was concluded that the zirconium and titanium were homogeneously mixed within the oxide. The beads were analyzed for surface accessibility and adsorption rate by monitoring the uptake of uranyl species from solution. The macropore diameter and morphology greatly impacted surface accessibility. Beads with larger macropores reached adsorption equilibrium much faster than the beads with a more tortuous macropore network.

Structural and ion exchange properties of nanocrystalline Si-doped antimony pyrochlore

Antimonic acid Sb2O5·4H2O with the pyrochlore structure is a well known ion-exchanger that is selective for Sr2+ in mildly acidic solution. An enhancement of the ion exchange properties of antimony-based pyrochlore materials, with respect to Cs+ and Sr2+, was previously reported by Moller and co-workers to be achievable if Si4+ is incorporated during synthesis of these materials (T. Moller, R. Harjula, M. Pillinger, A. Dyer, J. Newton, E. Tusa, S. Amin, M. Webb and A. Araya, J. Mater. Chem., 2001, 11, 1526–1532). The present study aims to shed light on the role of Si4+ in the pyrochlore structure and its influence on the ion-exchange properties. A series of samples were prepared with increasing concentrations of Si added during preparation. X-Ray powder diffraction and electron microscope observations indicate that the average particle size of the antimony pyrochlores decreases as Si concentration increases. Refinement of X-ray powder data shows a small and abrupt decrease in unit cell volume at an added Si concentration corresponding to about 10 atom%. For undoped samples 29Si solid-state MAS NMR showed only a single sharp resonance at −75 ppm assigned to Si(OH)4 species located within the hexagonal channels of the pyrochlore structure. The increasing addition of Si to the reactant mixture gave rise to a progressive increase in the intensity of resonances from hydrated amorphous silicate species. Base treatment succeeded in removing only the resonances due to these silicate species, leaving the resonance assigned to structural Si unaffected. These data are taken as confirmation of the assignment of the sharp −75 ppm resonance to isolated species Si(OH)4 within the pyrochlore tunnels. Neutron powder diffraction of partially dehydrated samples shows the existence of two pyrochlore phases that appear to differ slightly in their unit cell parameters and confirms that incorporation of Si4+ into the pyrochlore structure and a reduction in water content cause volume contraction of the cubic cell. The slight unit cell contraction resulting from Si incorporation is hypothesised to be responsible for enhanced Cs+ selectivity of samples containing Si.