Search

Glauconite mineral is one of the most sensitive indicators of low sedimentation rate in the marine environment. The time of residence of glauconites at the sea bottom before burial is reflected by their so-called maturity that is differentiated based on their K2O content. The present work aims to investigate the evolution of glauconites during the transition toward the highly evolved level. Complementary electron microprobe, Raman, and Thermogravimetric analysis were performed on glauconitic grains from the Belluno basin (N Italy) with different K2O content in order to verify whether the level of glauconites evolution affects the results of these surveys. The obtained results show that Raman spectra are sensitive to the grade of glauconite maturations. First, spectra of mature glauconites are more structured, due to the lower degree of Al substitution in the octahedral sites. Moreover, the position of the strongest Raman peak (Si–Ob–Si mode) at ~700 cm-1 shows two contrasting behaviors in the early (K2O 8%) stages of glauconites maturation, respectively. TGA measurements reveals that the presence of interlayer water is also related to the state of glauconites maturations. The obtained results were explained in the light of different isomorphic substitutions occurring at octahedral level in the mature and non-mature glauconites, thus allowing to obtain a deeper insight onto the mechanism of glauconites evolution.

Ladder-like polysilsesquioxanes (LPSQs) are characterized by a double-stranded siloxane backbone, whose chemical and structural properties depend on both the synthesis parameters and the nature of the organic side-chains. In the case of ladder-like (methacryloxypropyl) polysilsesquioxanes (LPMASQ), polymer matrices can be produced by exploiting the presence of photocurable methacrylate groups. Consequently, they can be used to prepare functional nanocomposites (NCs), either by blending with organic polymers such as polybutadiene or exploiting the inorganic fillers’ dispersion. Since the properties of LPMASQ-based NCs are strongly related to their structure, the structural changes of polymerized LPMASQ were investigated upon addition of low loadings of TiO2 nanoparticles (up to 3 wt%) by solid state nuclear magnetic resonance and X-ray diffraction. The filler addition leads to the reduction of the polymerization capacity of the LPMASQ organic side-chains. Moreover, a different organization of ladder chains has been highlighted, ascribable to the increase in fully condensed linear ladder units at the expenses of folded chains and defective structures. The methodological approach here adopted can be extended to other composite systems and may help to describe the properties at the filler-matrix interface, offering valuable hints for a better design of these materials. Graphical Abstract

Ceramic aerogels possess intriguing thermophysical properties which make them excellent candidates for high temperature thermal insulators. However, their properties can degrade at high temperature because of crystallization phenomena or because of densification (causing a sensible reduction of their specific surface area and porosity). The polymer derived ceramic (PDC) route is a relatively new way of developing ceramic aerogels. Several aspects influence the properties of the final product when dealing with preceramic polymers, among them their chemical composition and molecular architecture. In this work, we investigated the possibility of producing aerogels belonging to the SiCN system from polysilazanes mixtures, namely perhydropolysilazane (PHPS) and a methyl/vinyl-containing polysilazane, namely Durazane 1800®, thus changing the C/Si ratio of the amorphous pyrolyzed products. It is shown that the chemical composition of the ceramic aerogel affects the main properties of the porous materials, such as thermal stability and specific surface area (SSA). Results show that the presence of carbon in the aerogels inhibits crystallization of Si3N4 up to 1600 °C in N2 and allows to maintain a SSA of ~90 m2/g up to this temperature.

Au nanoparticles supported on CeO2 have been prepared and investigated as photocatalysts for the photocatalytic selective oxidation of benzyl alcohol and 4-methoxybenzyl alcohol to the correspondent benzaldehydes, in aqueous suspensions and room conditions under UV, visible and natural solar light irradiation. Au nanoparticles have been supported by impregnation (1 and 3 wt.%) on two types of CeO2 (i.e., a commercial one and a home prepared oxide obtained in the presence of NaOH as precipitation agent). The Au impregnated samples showed strong visible radiation absorption at 565–570 nm associated to localized surface plasmon resonance (LSPR). The bare CeO2 samples are activated by UV light and resulted virtually inactive under visible irradiation, whereas the presence of Au improved both the conversion of the alcohols and the selectivity of the reaction towards the aldehyde, giving rise to good results, particularly under visible and natural solar light irradiation. The activity of the materials increased by increasing the Au content.

International audience; Fluorination of the TiO2 surface has been often reported as a tool to increase the photocatalytic efficiency due to the beneficial effects in terms of production of oxidizing radicals. Moreover, it is shown that the unique amphiphilic properties of the fluorinated TiO2 (TiO2-F) surface allow one to use this material as a stabilizer for the formulation of Pickering emulsions of poorly soluble pollutants such as nitrobenzene (NB) in water. The emulsions have been characterized in terms of size of the droplets, type of emulsion, possibility of phase inversion, contact angle measurements, and optical microscopy. The emulsified system presents micrometer-sized droplets of pollutant surrounded by the TiO2-F photocatalyst. Consequently, the system can be considered to be composed of microreactors for the degradation of the pollutant, which maximize the contact area between the photocatalyst and substrate. The enhanced photocatalytic activity of TiO2-F was confirmed in the present paper as the apparent rate constants of NB photodegradation were 16 × 10–3 and 12 × 10–3 min–1 for fluorinated and bare TiO2, respectively. At NB concentrations largely exceeding its solubility, the rate constant was 0.04 × 10–3 min–1 in the presence of both TiO2 and TiO2-F. However, unlike TiO2, TiO2-F stabilized NB/water emulsions and, under these conditions, the efficiency of NB photocatalytic degradation in the emulsified system was ca. 18 times higher than in the nonemulsified one. This result is relevant also in terms of practical applications because it opens the route to one-pot treatments of biphasic polluted streams without the need of preliminary physical separation treatments.

The influence of bromide ions on systems containing highly reactive radical species is of great interest for environmental remediation, atmospheric chemistry, and the synthesis of high-added-value ...

The most investigated materials used as heterogeneous photocatalysts for the formation of high-value chemicals under mild experimental conditions are presented in this survey. Only papers reporting reactions carried out in harmless solvents such as water, the green solvent par excellence, are reported. Metal oxides have been used often, but carbon-based materials such as carbon nitride and graphene, metal nanoparticles, sulphides and selenides also have received a great attention mainly due to their good performances both in partial oxidations and reductions. The results presented indicate that an appropriate choice of the photocatalytic material is the main problem to be faced to efficiently perform the desired photocatalytic synthesis. Moreover, the highly specific nature of the interaction between the surface of the photocatalyst and the molecules involved in the process must be carefully considered in order to maximize conversion and selectivity and to make these processes green and sustainable competitive alternatives to traditional synthetic methods. Many structural and physicochemical parameters can be tailored such as the initial pH in the case of liquid-solid systems, concentration of reagent(s), induction of defects in the photocatalyst, crystallinity, addition of loading or dopant species to tune the opto-electronic features of semiconductors, and specific surface area.

Environmental catalysis has drawn a great deal of attention due to its clean ways to produce useful chemicals or carry out some chemical processes. Photocatalysis and electrocatalysis play important roles in these fields. They can decompose and remove organic pollutants from the aqueous environment, and prepare some fine chemicals. Moreover, they also can carry out some important reactions, such as O2 reduction reaction (ORR), O2 evolution reaction (OER), H2 evolution reaction (HER), CO2 reduction reaction (CO2RR), and N2 fixation (NRR). For catalytic reactions, it is the key to develop high-performance catalysts to meet the demand for targeted reactions. In recent years, two-dimensional (2D) materials have attracted great interest in environmental catalysis due to their unique layered structures, which offer us to make use of their electronic and structural characteristics. Great progress has been made so far, including graphene, black phosphorus, oxides, layered double hydroxides (LDHs), chalcogenides, bismuth-based layered compounds, MXenes, metal organic frameworks (MOFs), covalent organic frameworks (COFs), and others. This content drives us to invite many famous groups in these fields to write the roadmap on two-dimensional nanomaterials for environmental catalysis. We hope that this roadmap can give the useful guidance to researchers in future researches, and provide the research directions.

Photocatalytic chemical transformations in the presence of irradiated TiO2 are generally considered in terms of interfacial electron transfer. However, more elusive energy-transfer-driven reactions have been also hypothesized to occur, mainly on the basis of the indirect evidence of detected reaction products whose existence could not be justified simply by electron transfer. Unlike in homogeneous and colloidal systems, where energy transfer mechanisms have been investigated deeply for several organic syntheses, understanding of similar processes in heterogeneous systems is at only a nascent level. However, this gap of knowledge can be filled by considering the important achievements of synthetic heterogeneous photocatalysis, which bring the field closer to industrial exploitation. The present manuscript summarizes the main findings of previous literature reports and, also on the basis of some novel experimental evidences, tentatively proposes that the energy transfer in TiO2 photocatalysis could possess a Förster-like nature.

The present review summarizes some of the main results achieved in electrochemical, photocatalytic, and (photo)-electrocatalytic systems for the reduction of carbon dioxide. After a preliminary survey of the electrocatalytic and photocatalytic systems in terms of materials used, efficiencies, operating conditions, and product distribution, it is shown how the combination of the two approaches affords often higher efficiency than the single technologies and allows better control of the product distribution. In fact, the peculiar energetic distribution at the interface of irradiated semiconductors under opportune electrical bias enables enhancement of the spatial separation of the photogenerated charges and minimization of the external energy required in electrochemical applications. Even though the efficiency of CO2 reduction is still far away from being industrially appealing, in some cases the photoelectrocatalytic systems are promising tools to be further investigated for sustainable green chemistry based CO2 utilization. The aim of this review is to examine the strengths and the weaknesses of the different approaches considering that sometimes one of the three methods can be used more successfully than the others, depending on the desired product(s) and the materials used as photocatalysts or as the (photo)electrode.

Photocatalytic chemical transformations in the presence of irradiated TiO

A long-term test at a laboratory scale with a closed system (a coral reef aquarium) has been carried out to study the potentialities of photocatalytic ozonation and photocatalysis for the removal of noxious organic compounds in recirculating systems (aquaria and recirculating aquaculture systems) working with a minimum make up of new water. Attention has been focused not only on the depuration capabilities but also on possible negative phenomena, some of which could become apparent only at long times. After having tuned the system by setting appropriate operating conditions and procedures, positive results were obtained. In particular, it was observed that the alternation of photocatalytic ozonation with photocatalysis with definite cycle allowed to severely limit the presence of the organic compounds, which otherwise could accumulate in the system, and at the same time to control the formation of bromate, the ozonation side-product of main concern. In addition, the values of other parameters, which are important for water quality, remained at satisfactory values. It was also verified that the prepared photocatalytic films maintained a good photocatalytic activity even after several months of utilization in seawater. These results demonstrate that photocatalytic ozonation is a good candidate for water purification in recirculating systems in view of sustainable aquaculture.

This study investigated the treatment of a shipboard slop containing commercial gasoline in a pilot plant scale consisting of a membrane biological reactor (MBR) and photocatalytic reactor (PCR) acting in series. The MBR contributed for approximately 70% to the overall slop purification. More precisely, the biological process was able to remove approximately 40%, on average, of the organic pollution in the slop. Nevertheless, the membrane was capable to retain a large amount of organic molecules within the system, amounting for a further 30% of the influent total organic content removal. However, this affected the membrane fouling, thus resulting in the increase of the pore blocking mechanism that accounted for approximately 20% to the total resistance to filtration (2.85∙10 13 m −1 ), even if a significant restoration of the original membrane permeability was obtained after chemical cleanings. On the other hand, the biological treatment produced a clear solution for the photocatalytic system, thereby optimizing the light penetration and generation of highly oxidizing active oxygen species that enabled the degradation of bio-recalcitrant compounds. Indeed, low total organic carbon (TOC) values (

Biochar application to soil can be considered as a means to improve soil quality, thereby optimizing irrigation management and reducing irrigation needs, especially in dryland regions. This paper is aimed at investigating the effect of biochar (BC) on a desert sandy soil (Al Foah, United Arab Emirates) in terms of bulk density, porosity, water retention, plant available water (AWmax), aggregate stability (AS) and specific surface area (BET-SSA). BC was produced from forest biomass (Italy). Soil water retention was measured by the High Energy Moisture Characteristic (HEMC) and by pressure plate measurements, by using BC fractions equal to 0 (soil only), 0.014, 0.091, 0.23, 0.33 and 1 (BC only). The results indicated that BC significantly (p = 0.05) increased soil porosity and the amount of storage pores. As a consequence, water retention was enhanced and AWmax from 19.3 mm/m for the sandy soil (fbc = 0), to 60.8, 102.3 and 107.6 at fbc = 0.091, 0.23, and 0.33, respectively, was raised. No significant effects of BC were detected on the soil water retention curve of the BC-amended soil at fbc = 0.014, compared to the original condition. The significant increase in the structural index (SI) at fbc, ≥0.091, indicated that BC improved soil aggregate stability. The BET-SSA was measured by nitrogen adsorption measurements and indicated that the connected porosity was significantly increased by the 0.091 BC fraction. Both AWmax and SI were found to be correlated with BET-SSA. This showed an outcome that has been so far little investigated, namely that the BET-SSA played a significant role in the mechanism affecting the soil response to BC addition. The results showed that application of BC can improve soil structure and water retention and therefore optimize irrigation management by reducing irrigation needs, in the Al-Foah area and/or in similar dryland regions.

Heterogeneous photocatalysis is the result of an inextricable connection of several factors differently contributing to the overall process. Photon absorption is the “sine qua non” condition for the reaction to occur. In fact, photons can be considered as immaterial reactants, and all of the phenomena related to the interaction of light–matter play a prominent role. However, other factors contribute in a concerted way to address the reaction, so that the relative contribution of each of them is often difficult to evaluate. In this framework, the present paper highlights some aspects of the interaction of TiO 2 surface-adsorbate species that could be underestimated and their influence on the conversion, selectivity, and mechanisms of photocatalytic reactions. To this aim, some paradigmatic examples on the adsorption of water and organics on TiO 2 are reported.

PFAS substances, which have been under investigation in recent years, are certainly some of the most critical emerging contaminants. Their presence in drinking water, correlated with diseases, is consistently being confirmed by scientific studies in the academic and health sectors. With the aim of developing new technologies to mitigate the water contamination problem, research activity based on advanced oxidation processes for PFAS dealkylation and subsequent mineralization is active. While UV radiation could be directly employed for decontamination, there are nevertheless considerable problems regarding its use, even from a large-scale perspective. In contrast, the use of cheap, robust, and green photocatalytic materials active under near UV-visible radiation shows interesting prospects. In this paper we take stock of the health problems related to PFAS, and then provide an update on strategies based on the use of photocatalysts and the latest findings regarding reaction mechanisms. Finally, we detail some brief considerations in relation to the economic aspects of possible solutions.

Dielectric barrier discharge plasma and photocatalysis have been proposed as tools for decontamination of process water, especially in food industry. The present investigation aims to redefine and identify the features of coupling the two technologies in terms of degradation efficiency of a model compound. Results show that, when the process is carried out in plasma activated water in the presence of irradiated TiO2, the efficiency of the integrated process is lower than the sum of the two processes acting separately. It is proposed that afterglow species, e.g. hydrogen peroxide and/or peroxynitrites could be activated by UVA light irradiation producing hydroxyl radicals in the liquid phase. Even if TiO2 limits this additional effect by acting as UVA screen barrier material, its decontamination efficiency under certain conditions results higher than that obtained with plasma systems. These results open the route to chlorine-free decontamination processes and redefine the application framework of this integrated approach.

Ladder-like silsesquioxanes (SSQs) and TiO2 have been functionalized with methacryloyloxypropyl chains and embedded in a polybutadiene (PB) matrix giving rise to hybrid (organic–inorganic) nanocomposites (NCs) capable of acting as oxygen scavenging materials. The joint use of infrared spectroscopy, small-angle X-ray scattering, and permittivity measurements highlighted that the presence of TiO2, regardless of its modification, does not significantly alter the structure of the NCs, but just reduces the crosslinking degree and induces a local disorganization of the ladder-like SSQ stacks. The introduction of an optimum amount (0.5 wt%) of modified TiO2 within the polymeric matrix enhanced the oxygen uptake rate of ca. 70% with respect to the sole polymeric material. Moreover, the uptake kinetics changes from the first to second order with respect to the PB amount, clearly indicating different oxidation mechanisms. NCs containing modified TiO2 showed an oxygen uptake rate ranging from 30 to 60% higher than that achievable in the presence of bare TiO2. The superior activity of the materials containing modified TiO2 has been related to mechanistic aspects. Fluorescence and electron spin resonance spectroscopies allowed to underline the role of singlet oxygen within the polymeric matrix, although the known photochemical oxidation of PB and the TiO2 induced hydroxyl radical mediated oxidation cannot be excluded. These results open the route to highly efficient flexible oxygen scavenging materials for the protection of electronic devices such as organic based light emitting diodes, solar cells, and liquid crystal displays, which require high targets of protection from oxygen and water.

"Properties of titanium dioxide" presents a survey of the main physicochemical properties of TiO2 upon which rely all of the applications of this material. Structures and morphologies of titanium dioxide have been taken into account, also in correlation with thermodynamic properties. Bulk and surface defectivity has been described in detail, because of its relevant consequences in terms of catalytic activity. The basic mechanisms of interaction between photons and TiO2 have been discussed on the basis of the optoelectronic features of the semiconductor. Finally, electrical, mechanical, and rheological properties of TiO2 have been presented.

Photocatalysis emerged in the last decades as a versatile technology, whose applications range from environmental remediation to hydrogen production, energy harvesting, and organic synthesis, with exciting examples also in medicine, electronics, and advanced functional materials [...]

In this work, three different functionalized mesoporous silica nanoparticles (MSNs) were synthesized through the co-condensation synthesis in oil/water emulsion. Hexadecyltrimethoxysilane, triethoxy-3-(2-imidazolin-1-yl)propylsilane and (3-mercaptopropyl)triethoxysilane were used as organo-substituted silica precursors with variable molar ratio with respect to tetraethylorthosilicate (TEOS, 1:4, 1:9, 1:19). The occurred functionalization was investigated by Infrared Spectroscopy and FT-Raman and 29Si {1H} CP-MAS-NMR spectroscopy. Results show that the three materials were successfully functionalized. The influence of the different pendant groups and their concentration on the mesostructured pore organization of the obtained nanoparticles respect to the non-functionalized mesoporous silica was evaluated by means of Transmission Electron Microscopy and N2 sorption measurements. Bulky aliphatic C16 chains, especially in higher concentration, causes severe changes in mesoporous structure, leading to a more heterogeneous material. The imidazoline groups, instead, change the mesostructured morphology of the pores to an irregular but more interconnected one, while the presence of mercaptopropyl groups does not bring significant modifications. The different structural modifications in pore morphology observed between the samples is due to the different interactions between derivatized silica precursors and the components of the emulsion.

The present study explores the exploitation of ladder-like polysilsesquioxanes (PSQs) bearing reactive functional groups in conjunction with SiO2 nanoparticles (NPs) to produce UV-curable nanocomposite coatings with increased hydrophobicity and good thermal resistance. In detail, a medium degree regular ladder-like structured poly (methacryloxypropyl) silsesquioxane (LPMASQ) and silica NPs, either naked or functionalized with a methacrylsilane (SiO2@TMMS), were blended and then irradiated in the form of a film. Material characterization evidenced significant modifications of the structural organization of the LPMASQ backbone and, in particular, a rearrangement of the silsesquioxane chains at the interface upon introduction of the functionalized silica NPs. This leads to remarkable thermal resistance and enhanced hydrophobic features in the final nanocomposite. The results suggest that the adopted strategy, in comparison with mostly difficult and expensive surface modification and structuring protocols, may provide tailored functional properties without modifying the surface roughness or the functionalities of silsesquioxanes, but simply tuning their interactions at the hybrid interface with silica fillers.

International audience; Surface fluorination improves the photocatalytic activity of TiO2, and the influences of various features of fluorinated TiO2 (TiO2–F) have often been discussed in the literature. The present paper addresses the changes induced by surface fluorination on the morphological, structural, surface, and electronic features of TiO2. In particular, X-ray diffraction, specific surface area analysis, and transmission and scanning electron microscopy give evidence that surface fluorination does not affect the structural properties and the morphology of TiO2 nanoparticles. In contrast, fluorination induces changes of surface and electronic properties. Chemical and thermogravimetric analyses show that surface fluorination can reach up to 50% of original Ti–OH surface sites. The surface charge of TiO2 turns more negative upon fluorination, as shown by a shift of the point of zero charge toward lower pH. Electronic properties are deeply characterized by combining diffuse reflectance, X-ray, and UV photoelectron spectroscopies, as well as time-resolved fluorescence spectroscopy, and photoelectrochemical measurements. Results show the presence of intra-band-gap energy states induced by the local interaction of chemisorbed fluorine atoms. Such energy levels are close to the valence band. The unique surface and electronic properties of TiO2–F make it a promising material for the photocatalytic degradation of poorly soluble emerging pollutants such as 1-methylnaphtalene. In particular, TiO2–F demonstrates faster degradation kinetics with respect to both the pristine material and TiO2 P25 used as a benchmark standard.

Composites comprised of Ag3PO4 and bare TiO2 (TiO2@Ag3PO4) or silver doped TiO2 (Ag@TiO2&ndash, Ag3PO4) have been synthesized by coupling sol&ndash, gel and precipitation methods. For the sake of comparison, also the bare components have been similarly prepared. All the samples have been characterized by X-ray diffraction (XRD), UV-vis diffuse reflectance spectroscopy (DRS), scanning electron microscopy (SEM), Fourier transformed infrared spectroscopy (FTIR), photoelectrochemical measurements, and specific surface area (SSA) analysis. The optoelectronic and structural features of the samples have been related to their photocatalytic activity for the degradation of 4&ndash, nitrophenol under solar and UV light irradiation. Coupling Ag3PO4 with silver doped TiO2 mitigates photocorrosion of the Ag3PO4 counterpart, and remarkably improves the photocatalytic activity under solar light irradiation with respect to the components, to the TiO2&ndash, Ag3PO4 sample, and to the benchmark TiO2 Evonik P25. These features open the route to future applications of this material in the field of environmental remediation.

In the present work, dialysis was used to recover vanillin while being produced by partial photocatalytic oxidation of ferulic acid in an aqueous solution at ambient temperature. The relatively high value of the permeate flux through a dense polyether-block amide membrane allowed continuously extracting vanillin from the reacting solution, thus avoiding its successive oxidation. The rate of vanillin formation was improved, compared to other reactor configurations, because intermediate compounds permeated from the reacting solution and did not hinder the reaction, while ferulic acid permeated in the opposite direction to partially replenish the reactor with the substrate. The photocatalytic membrane reactor obtained by the effective coupling of dialysis with the photocatalytic reaction improved the production yield. For instance, with the utilized experimental set up, the total amount of vanillin produced after 5 h in the membrane reactor was more than one-third higher than in the photocatalytic reactor without dialysis. The results obtained with a mathematical model agree with the experimentally observed behavior. The model allowed estimating vanillin diffusivity in the membrane and showed that concentration polarization might limit the process.

Photocatalytic waterborne coating based on anatase titania nanoparticles imparting self-cleaning, antifogging, and air depolluting properties is now a mature technology that, we argue in this chapter, will shortly become ubiquitous. A number of doubts still surround these coatings. For example, are they health-beneficial via air depollution or do they actually pose health threats through incomplete volatile organic compound oxidation and titania nanoparticle release in the environment? This study offers a critical perspective and identifies the technology and economic drivers that will drive growth in demand and applications. The study is also an educational tool aiding in chemistry undergraduate education renewal process via recent research outcomes and critical thinking.

Mesoporous silica nanoparticles (MSN) were used as a platform to design novel active materials for the catalytic and photocatalytic epoxidation of limonene. Binary systems comprised of TiO2 and MSN were used for the catalytic reaction when doped with manganese, and for the photocatalytic reaction when functionalised with hexadecyl chains or imidazolinyl groups. All of the MSN based systems were synthesized by condensation in emulsion. A thorough characterization of the powders has been performed by means of Inductively Coupled Plasma – Optical Emission Spectroscopy (ICP-OES), X-ray diffraction (XRD), FT-IR, Raman and EPR Spectroscopy, Fluorescence and diffuse reflectance UV–vis (DRS) Spectroscopy, gas Porosimetry, and Transmission Electron Microscopy (TEM). The obtained morphological and structural information have been related to the catalytic and photocatalytic performances for the epoxidation of limonene. MSN support finely distributes the manganese active centres in the case of the catalytic epoxidation, while acts as functional co-catalyst in the case of the photocatalytic reaction. Upon careful optimization of the experimental conditions, the catalytic process afforded conversion and selectivity values up to 90 and 84%, respectively, while the photocatalytic process provided in the best case conversions up to 80% and selectivity values of ca. 50%. Both the catalytic and photocatalytic approaches were performed under relatively mild experimental conditions and use molecular oxygen as the oxidant. Therefore, both of them represent promising green alternatives to traditional methods for the industrially relevant production of limonene epoxide. This compound, in fact, is the starting material for the production of poly(limonene carbonates), biopolymers with outstanding properties which are promising substitutes of oil derived polycarbonates.

The present chapter reports some economical aspects of the cerium oxide market. Porter’s and PESTEL analyses have been used to evidence the strengths and weaknesses of the ceria market, along with the potentiality and opportunities within the years to come. The wide use of CeO2 nanoparticles in many applications requires to consider also issues related to their toxicity and environmental fate. In this regard, some contradictory reports in the relevant literature have been surveyed, thus highlighting the need for further and detailed investigation on these topics in order to propose effective strategies of risk assessment and environmental remediation.

This review presents a survey of some heterogeneous photocatalytic processes for the synthesis of high-value added compounds carried out in photocatalytic membrane reactors (PMRs). The two technologies can be easily integrated due to the similar conditions at which they usually operate. Furthermore, significant advantages derive from the coupling and in some cases also synergistic effects can be observed. These features have been highlighted for the photocatalytic syntheses reviewed along with engineering and design aspects investigated for some industrially relevant high-value added compounds. Notably, photocatalytic syntheses carried out in PMRs are still rare mainly because interdisciplinary competences and collaborations are often required in this field. However, we hope that a survey of the recently reported examples may inspire researchers for future developments and new opportunities.

This chapter deals with water treatments by advanced oxidation processes (AOPs) based on chemical and photochemical reactions. The most used processes are described, and for each of them, the main reaction mechanisms, principles, advantages, drawbacks, performances and formation of by-products, coupled with technologies and their applications to waters and wastewater depollution, have been analysed, supporting the main results of studies published in the pertinent literature.