Recycling of waste glass and incinerated sewage sludge ash in glass-ceramics.

Disposal of waste glass and incinerated sewage sludge ash (ISSA) in landfills is a waste of resources and poses significant environmental risks. This work aims to recycle waste glass and ISSA together to form value-added glass-ceramics. The physical and mechanical properties, leaching behaviour, and microstructure of the glass-ceramics produced with different proportions of waste glass powder (WGP) and ISSA were investigated. Thermodynamic calculations were performed to predict the formation of crystalline phases and the phase transformation involved. The results showed the potential of WGP and ISSA as raw materials in glass-ceramics production. WGP effectively densified the microstructure of the glass-ceramics by forming a viscous phase. As WGP content increased, the total porosity of glass-ceramics decreased whereas the density increased, accompanied by the formed anorthite transforming into wollastonite. The incorporation of WGP densified and refined the pore structure of the glass-ceramics, thereby improving the mechanical properties and reducing the water absorption. The glass-ceramics produced with a 50:50 blend of WGP and ISSA exhibited the highest compressive strength of 43.7 MPa and the lowest water absorption of 0.3 %. All fabricated glass-ceramics exhibited innocuous heavy metal leaching. The co-sintering of ISSA and WGP can produce additive-free glass-ceramics, characterized by reduced energy consumption and notable heavy metal immobilization capacity. These materials hold promise for utilization in construction as building materials.

Hierarchically Porous Few-Layer Carbon Nitride and Its High H+ Selectivity for Efficient Photocatalytic Seawater Splitting.

Photocatalysts for seawater splitting are severely restricted because of the presence of multiple types of ions in seawater that cause corrosion and deactivation. As a result, new materials that promote adsorption of H+ and hinder competing adsorption of metal cations should enhance utilization of photogenerated electrons on the catalyst surface for efficient H2 production. One strategy to design advanced photocatalysts involves introduction of hierarchical porous structures that enable fast mass transfer and creation of defect sites that promote selective hydrogen ion adsorption. Herein, we used a facile calcination method to fabricate the macro-mesoporous C3N4 derivative, VN-HCN, that contains multiple nitrogen vacancies. We demonstrated that VN-HCN has enhanced corrosion resistance and elevated photocatalytic H2 production performance in seawater. Experimental results and theoretical calculations reveal that enhanced mass and carrier transfer and selective adsorption of hydrogen ions are key features of VN-HCN that lead to its high seawater splitting activity.

Development of Calcium Carbonate-Based Coatings by the Carbonation of Gamma-C2S (γ-C2S).

A calcium carbonate (CaCO3)-based coating with gamma-C2S (γ-C2S) as the main carbonatable binder is proposed to protect the metal substrate against corrosion in this paper. Here, the morphology and phase assemblage of the coatings are studied by scanning electron microscopy (SEM) and X-ray diffraction (XRD), and the corrosion resistance of the coating is evaluated by electrochemical impedance spectroscopy (EIS) and X-ray photoelectron spectroscopy (XPS). Results show that the carbonated coating has excellent properties in terms of ultraviolet (UV) aging resistance, salt fog resistance, and electrochemical corrosion resistance. The porosity of deposited coating on steel substrates decreases by 47.1% after carbonation due to the compacted calcium carbonate formation, which is recognized as a self-compacting process during carbonation. The coating also exhibits rapid strength development within the first 2 h of carbonation; both the CO2 uptake efficiency and degree of carbonation (DOC) can reach more than 95% of the total CO2 uptake efficiency and final DOC values. This study provides a novel insight to extend the category of inorganic coating with additional benefits of CO2 solidification.

The Effect of Interfacial Chemical Bonding in TiO2-SiO2 Composites on Their Photocatalytic NOx Abatement Performance.

The chemical bonding of particulate photocatalysts to supporting material surfaces is of great importance in engineering more efficient and practical photocatalytic structures. However, the influence of such chemical bonding on the optical and surface properties of the photocatalyst and thus its photocatalytic activity/reaction selectivity behavior has not been systematically studied. In this investigation, TiO2 has been supported on the surface of SiO2 by means of two different methods: (i) by the in situ formation of TiO2 in the presence of sand quartz via a sol-gel method employing tetrabutyl orthotitanium (TBOT); and (ii) by binding the commercial TiO2 powder to quartz on a surface silica gel layer formed from the reaction of quartz with tetraethylorthosilicate (TEOS). For comparison, TiO2 nanoparticles were also deposited on the surfaces of a more reactive SiO2 prepared by a hydrolysis-controlled sol-gel technique as well as through a sol-gel route from TiO2 and SiO2 precursors. The combination of TiO2 and SiO2, through interfacial Ti-O-Si bonds, was confirmed by FTIR spectroscopy and the photocatalytic activities of the obtained composites were tested for photocatalytic degradation of NO according to the ISO standard method (ISO 22197-1). The electron microscope images of the obtained materials showed that variable photocatalyst coverage of the support surface can successfully be achieved but the photocatalytic activity towards NO removal was found to be affected by the preparation method and the nitrate selectivity is adversely affected by Ti-O-Si bonding.

Different Roles of Water in Photocatalytic DeNOx Mechanisms on TiO2: Basis for Engineering Nitrate Selectivity?

The nitrate selectivity of TiO2 has important consequences for its efficiency as a NOx depollution photocatalyst. Most emphasis is typically given to photocatalyst activity, a measure of the rate at which NOx concentrations are reduced, but a reduction in NOx concentration (mainly NO + NO2) is not necessarily a reduction in atmospheric NO2 concentration because the catalytic process itself generates NO2. With NO2 being considerably more toxic than NO, more emphasis on nitrate selectivity, a measure of the NOx conversion to nitrate, and how to maximize it, should be given in engineering photocatalytic systems for improved urban air quality. This study, on the importance of adsorbed water in the photocatalytic oxidation of NOx, has identified important correlations which differentiate the role that water plays in the oxidation of NO and NO2. This observation is significant and offers insights into controlling nitrate selectivity on TiO2 and the potential for increased effectiveness in environmental photocatalyst applications.

Phenylamine-Functionalized rGO/TiO2 Photocatalysts: Spatially Separated Adsorption Sites and Tunable Photocatalytic Selectivity.

The preferential adsorption of targeted contaminants on a photocatalyst surface is highly required to realize its photocatalytic selective decomposition in a complex system. To realize the tunable preferential adsorption, altering the surface charge or polarity property of photocatalysts has widely been reported. However, it is quite difficult for a modified photocatalyst to realize the simultaneously preferential adsorption for both cationic and anionic dyes. In this study, to realize the selective adsorption for both cationic and anionic dyes on a photocatalyst surface, the negative reduced graphene oxide (rGO) nanosheets and positive phenylamine (PhNH2) molecules are successfully loaded on the TiO2 surface (PhNH2/rGO-TiO2) with spatially separated adsorption sites, where the negative rGO and positive PhNH2 molecules work as the preferential adsorption sites for cationic and anionic dyes, respectively. It was interesting to find that although all the TiO2 samples (including the naked TiO2, PhNH2/TiO2, rGO-TiO2, and PhNH2/rGO-TiO2) clearly showed a better adsorption performance for cationic dyes than anionic dyes, only the PhNH2/rGO-TiO2 with spatially separated adsorption-active sites exhibited an opposite photocatalytic selectivity, namely, the naked TiO2, PhNH2/TiO2, and rGO-TiO2 showed a preferential decomposition for cationic dyes, while the resultant PhNH2/rGO-TiO2 exhibited an excellently selective decomposition for anionic dyes. In addition, the resultant PhNH2/rGO-TiO2 photocatalyst not only realizes the tunable photocatalytic selectivity but also can completely and sequentially decompose the opposite cationic and anionic dyes.

The Visible-Light Photocatalytic Activity and Antibacterial Performance of Ag/AgBr/TiO2 Immobilized on Activated Carbon.

Visible-light-driven Ag/AgBr/TiO2 /activated carbon (AC) composite was prepared by solgel method coupled with photoreduction method. For comparison, TiO2 , TiO2 /AC, and Ag/AgBr/TiO2 were also synthesized. Their characteristics were analyzed by XRD, SEM-EDS, TG-DSC and UV-vis techniques. Photocatalytic activity and antibacterial performance under visible-light irradiation were investigated by ICP-AES, ATR-FT-IR and spectrophotometry methods using methylene blue and Escherichia coli as target systems, respectively. The results showed that Ag/AgBr was successfully deposited on anatase TiO2 /AC surface, and exhibited a distinct light absorption in the visible region. Ag/AgBr/TiO2 /AC displayed excellent antibacterial performance both in dark and under visible-light illumination. The growth of E. coli cell was inhibited in the presence of Ag/AgBr/TiO2 /AC in dark. Moreover, upon visible-light illumination, a significant damage of cell membrane was noticed. Ag/AgBr/TiO2 /AC was also shown higher photocatalytic efficiency for methylene blue degradation than those of TiO2 , TiO2 /AC, and Ag/AgBr/TiO2 . This is attributed to the synergetic effect between AC and Ag/AgBr/TiO2 , of which AC acts as the role of increasing reaction areas, continuous enriching, and transferring the adsorbed MB molecules to the surface of supported photocatalysts, and the Ag/AgBr/TiO2 acts as a highly active photocatalyst for degrading MB molecules under visible-light irradiation.

An in-situ synthesis of Ag/AgCl/TiO2/hierarchical porous magnesian material and its photocatalytic performance.

The absorption ability and photocatalytic activity of photocatalytic materials play important roles in improving the pollutants removal effects. Herein, we reported a new kind of photocatalytic material, which was synthesized by simultaneously designing hierarchical porous magnesian (PM) substrate and TiO2 catalyst modification. Particularly, PM substrate could be facilely prepared by controlling its crystal phase (Phase 5, Mg3Cl(OH)5 · 4H2O), while Ag/AgCl particles modification of TiO2 could be achieved by in situ ion exchange between Ag(+) and above crystal Phase. Physiochemical analysis shows that Ag/AgCl/TiO2/PM material has higher visible and ultraviolet light absorption response, and excellent gas absorption performance compared to other controls. These suggested that Ag/AgCl/TiO2/PM material could produce more efficient photocatalytic effects. Its photocatalytic reaction rate was 5.21 and 30.57 times higher than that of TiO2/PM and TiO2/imporous magnesian substrate, respectively. Thus, this material and its intergration synthesis method could provide a novel strategy for high-efficiency application and modification of TiO2 photocatalyst in engineering filed.

Microstructure and Characteristic of BiVO4 Prepared under Different pH Values: Photocatalytic Efficiency and Antibacterial Activity.

In the present study, BiVO4 sample was prepared under different pH 0.5-13 without capping agent. Different morphology characteristics were observed, such as sheet crystal structure, cross crystal structure and branching crystal structure. The mechanism of the formation of BiVO4 nanostructure was discussed. Under acid condition, sheet crystal structure was obtained. The phenomenon could be attributed to polymerization of vanadate in the presence of H⁺. In the weak alkaline solution, across structure and branching type morphology was obtained. The photocatalytic efficiency for the samples ranked as pH 5 > pH 3 > pH 7 > pH 9 > pH 1 > pH 11 > pH 13 > blank, which is in good agreement with X-ray diffraction (XRD) result. E. coli envelop was damaged in the presence of BiVO4 under visible light. The protrusion on envelop was diminished by BiVO4. Attenuated Total Reflection Fourier transformed Infrared Spectroscopy (ATR-FTIR) results suggested the intensity was weakened for the amide, phosphoric, -COO- group and C-H bond in lipopolysaccharides (LPS), peptidoglycan and periplasm molecules.