Graphene-TiO2 hybrids for photocatalytic aided removal of VOCs and nitrogen oxides from outdoor environment.

Outdoor and indoor air pollution has become a global concern in modern society. Although many policies and regulations on air quality have been promulgated worldwide over the past decades, airborne pollution still negatively affects health and therefore the life-style of human beings. One of the strategies to challenge this problem might be reducing the amount of airborne pollutant by mineralising them via photoinduced reactions. Photocatalytic oxidation of gaseous pollutants via titanium dioxide is one of the most promising solar photochemical reactions. In this research work, by means of a green sol-gel procedure, we have coupled titania to graphene (0.5 and 1.0 wt%) aiming to increase the solar photocatalytic activity of the produced hybrid materials. Transient paramagnetic species formed upon UV-A irradiation were detected by means of EPR spectroscopy. The photocatalytic reactions were assessed by monitoring the removal of nitrogen oxides and two different volatile organic compounds (benzene and isopropanol), which has never been assessed before. Our results highlight the exceptional characteristics of the TiO2/graphene hybrid material synthesised with 1.0 wt% graphene, and its excellent suitability for multi-purpose applications in the field of environmental remediation. Compared to unmodified titania, it shows a clear enhancement in the photocatalytic removal of those hazardous pollutants, having a photocatalytic degradation rate twice higher. In addition, the same material is highly stable and shows fully recyclability over repeated tests. Hybrid titania-graphene materials could thus be exploited to grant safer outdoor and indoor environments, having thus a beneficial impact on public health and on the quality of our lives.

Synthesis of ceramic pigments from industrial wastes: Red mud and electroplating sludge.

The perception of industrial waste has changed, in the last decades, from an economic and environmental problem to a potential raw material. In this work, the synthesis of a stable pigment was prepared by combining two hazardous and unexplored wastes: red mud (RM, rich in Fe) and electroplating sludge (ES, rich in Ni/Cr). The wastes were mixed in different proportions and calcined at 1200 °C. Black and brown pigments were obtained from the mixture of RM/ES in 1:3 and 1:1 wt proportions, respectively. The color was given by the chrome-iron-nickel spinels, based on Ni2+ 3T1g(3F) transitions (≈13,000 cm-1), Cr3+ 4A2g → 4T1g(4F) transitions (≈24,400 cm-1) and Fe3+ (≈15,000-≈22,500 cm-1). The achieved coloring strength and thermal stability on various ceramic glazes render excellent prospects for the industrial application of such waste-based pigments.

Purely Visible-Light-Induced Photochromism in Ag-TiO2 Nanoheterostructures.

We report titania nanoheterostructures decorated with silver, exhibiting tuneable photochromic properties for the first time when stimulated only by visible white light (domestic indoor lamp), with no UV wavelengths. Photochromic materials show reversible color changes under light exposure. However, all inorganic photochromic nanoparticles (NPs) require UV light to operate. Conventionally, multicolor photochromism in Ag-TiO2 films involves a change in color to brownish-gray during UV-light irradiation (i.e., reduction of Ag+ to Ag0) and a (re)bleaching (i.e., (re)oxidation of Ag0 to colorless Ag+) upon visible-light exposure. In this work, on the contrary, we demonstrate visible-light-induced photochromism (ranging from yellow to violet) of 1-10 mol % Ag-modified titania NPs using both spectroscopic and colorimetric CIEL*a*b* analyses. This is not a bleaching of the UV-induced color but a change in color itself under exposure to visible light, and it is shown to be a completely different mechanism-driven by the interfacial charge transfer of an electron from the valence band of TiO2 to that of the AgxO clusters that surround the titania-to the usual UV-triggered photochromism reported in titania-based materials. The quantity of Ag or irradiation time dictated the magnitude and degree of tuneability of the color change, from pale yellow to dark blue, with a rapid change visible only after a few seconds, and the intensity and red shift of surface plasmon resonance induced under visible light also increased. This effect was reversible after annealing in the dark at 100 °C/15 min. Photocatalytic activity under visible light was also assessed against the abatement of nitrogen oxide pollutants, for interior use, therefore showing the coexistence of photochromism and photocatalysis-both triggered by the same wavelength-in the same material, making it a multifunctional material. Moreover, we also demonstrate and explain why X-ray photoelectron spectroscopy is an unreliable technique with such materials.

Effect of preparation and processing conditions on UV absorbing properties of hydroxyapatite-Fe2O3 sunscreen.

The development of innovative, safe and non-photocatalytic sunscreens is urgently needed, as it is essential to have sunscreen filters offering appropriate UV protection without damaging the environment and/or generating free radicals when in contact with the skin. Hydroxyapatite (Ca10(PO4)6(OH)2, HAp) when substituted with iron has UV protection properties and is not photocatalytic; HAp was used to make a sunscreen filter by treating cod fish bones in an iron-containing solution, and then calcining them at 700°C. Here we present a systematic and advanced study on this material, to obtain a sunscreen with improved UV absorbing properties. Bones were treated with three different iron salts - Fe(II) chloride, Fe(II) lactate and Fe(III) nitrate - under various pH conditions. Results showed that Fe(II) chloride in basic pH led to the most effective iron inclusion. High energy ball milling or ultrasound were investigated to increase surface area and corresponding UV absorption; high energy ball milling treatment led to the best optical properties. The optimum powders were used to formulate UV protection creams, which showed Sun Protection Factor (SPF) values significantly superior to the control cream (up to 4.1). Moreover the critical wavelength (λcrit) was >370nm (388-389nm) and UVA/UVB ratios were very close to 1. With these properties these sunscreens can be classified as broad UV protectors. Results also showed that combining these powders with other sunscreens (i.e. titanium dioxide), a synergic effect between the different components was also observed. This investigation showed that HAp-based sunscreens of marine origin are a valid alternative to commercial products, safe for the health of the customers and, being non-photocatalytic, do not pose a threat to the environment.

Novel nanosynthesis of In2O3 and its application as a resistive gas sensor for sevoflurane anesthetic.

A novel non-aqueous sol-gel route for synthesizing pure indium oxide (In2O3) nanoparticles (NPs) using indium acetylacetonate and n-butylamine as the reactive solvent, under solvothermal conditions, is herein proposed. The samples were characterized by an advanced X-ray method, whole powder pattern modeling (WPPM) and high-resolution transmission electron microscopy (HR-TEM), showing the exclusive presence of pure In2O3. Diffuse reflectance spectroscopy (DRS) was used to determine the optical band gap (Eg) of the sample. Moreover, these investigations also revealed that the In2O3 nanoparticles are quasi-spherical in shape, with a diameter of around 7 nm as prepared and 9.5 nm after thermal treatment at 250 °C. In2O3 NPs worked as highly sensitive sensing interfaces to provide resistance changes during exposure to sevoflurane, a volatile anesthetic agent used in surgical wards. The developed sensor demonstrated a good response and fast response/recovery time towards very low concentrations of sevoflurane in air, suggesting a very attractive application as a real-time monitoring analyzer in a hospital environment.

Fabricating and characterising ZnO-ZnS-Ag2S ternary nanostructures with efficient solar-light photocatalytic activity.

ZnO-ZnS-Ag2S ternary nanostructures were prepared by a simple and low-cost chemical precipitation method. The sample was characterised by X-ray diffraction, energy-dispersive X-ray, UV-Vis-NIR, Raman and Fourier transform infrared spectroscopy. Morphology of the sample was studied by scanning electron microscopy and it was observed that ZnO nanoplates were covered with ZnS and Ag2S nanoparticles. A high resolution transmission electron microscope was used to obtain further information about the crystalline domains of the prepared ternary nanostructure. The Kramers-Kronig method and classical dispersion theory were utilised to study the optical properties of the sample in the far-infrared region. Photocatalytic activity of the prepared samples was also attained in the gas-solid phase by using a solar lamp (simulating outdoor lighting) and monitoring NOx degradation.

A hydroxyapatite-Fe2O3 based material of natural origin as an active sunscreen filter.

The use of sunscreens as protective barriers against skin damage and cancer, by absorbing harmful UVA and UVB rays, is becoming an increasingly important issue. Such products are usually based on TiO2 or ZnO, although both Fe2O3 and hydroxyapatite (Ca10(PO4)6(OH)2, HAp) doped with metal ions have been reported as being ultraviolet (UV) absorbing materials. HAp is the main component of bone; it is, therefore, highly biocompatible. In the present work, an iron-doped HAp-based material, containing both Fe ions substituted into the HAp structure and iron oxide in hematite (α-Fe2O3) form, was successfully developed from waste cod fish bones. This was achieved through a simple process of treating the bones in a Fe(ii) containing solution, followed by heating at 700 °C. The material showed good absorption in the whole UV range and did not form radicals when irradiated. The sunscreen cream formulated with this material could be used as a broad sunscreen protector (λcrit > 370 nm), showing high absorption both in the UVA and UVB ranges. Because of its absorption properties it would be classified as 5 star protection according to the Boots UVA star rating system. The cream is also photostable, and does not cause irritation or erythema formation when in contact with the human skin. These results show that a food by-product such as fish bones could be converted into a valuable product, with potential applications in health care and cosmetics. This is the first time a HAp-based sunscreen cream has been developed and validated as a proof of concept.

Bacteria immobilisation on hydroxyapatite surface for heavy metals removal.

Selected bacterial strains were immobilised on the surface of hydroxyapatite (Ca10(PO4)6(OH)2 - HAp) of natural origin (fish bones). The capacity of the material, alone and in combination with the bacterial strains to act as heavy metal removers from aqueous streams was assessed. Pseudomonas fluorescens (S3X), Microbacterium oxydans (EC29) and Cupriavidus sp. (1C2) were chosen based on their resistance to heavy metals and capacity of adsorbing the metals. These systems were tested using solutions of Zn(II), Cd(II) and in solutions containing both metals. A synergistic effect between the strains and HAp, which is effective in removing the target heavy metals on its own, was observed, as the combination of HAp with the bacterial strains led to higher adsorption capacity for both elements. For the solutions containing only one metal the synergistic effect was greater for higher metal concentrations; 1C2 and EC29 were the most effective strains for Zn(II) and Cd(II) respectively, while S3X was less effective. Overall, an almost four-fold increase was observed for the maximum adsorption capacity for Zn(II) when 1C2 was employed - 0.433 mmol/g in comparison of 0.121 mmol/g for the unmodified HAp. For Cd(II), on the other hand, an almost three-fold increase was registered with EC29 bacterial strain - 0.090 vs 0.036 mmol/g for the unmodified HAp. When the solutions containing both metals were tested, the effect was more marked for lower concentrations.