Groundwater constitutes a major source of fresh water globally. However, it faces serious quality challenges from both conventional pollutants and contaminants of emerging concern (CECs) such as pharmaceutically active compounds (PhACs), personal care products (PCPs) and pesticides. There exists a significant knowledge gap regarding the occurrence of CECs in groundwater, especially in Africa. This study presents unique data on the concentration of fourteen PhACs, five PCPs and nine pesticides in groundwater wells in Nzoia River basin, Kenya. Generally, PCPs were the most dominant class with concentrations up to 10 μg/L (methylparaben). Anti(retro)virals, being important in the treatment of HIV/AIDS, were more prevalent among the PhACs as compared to the developed world, with concentrations up to 700 ng/L (nevirapine). In contrast, pesticides were measured at lower concentrations, the maximum being 42 ng/L (metolachlor). A basic risk assessment shows that – among the detected CECs – carbamazepine may pose medium human health risk and requires further investigation among infants and children. Point-of-use (POU) technologies are being increasingly promoted especially in the developing nations to provide drinking water solutions at the household level, but very little data is available on their performance towards CECs removal. Therefore, besides measuring CECs in groundwater, we investigated ceramic filters and solar disinfection (SODIS) as possible POU treatment options. Both techniques show potential to treat CECs in groundwater, with removal efficiencies higher than 90% obtained for 41 and 22 compounds in ceramic filters and SODIS, respectively. Moreover, for the more recalcitrant compounds (e.g. sulfadoxin), the performance is improved by up to three orders of magnitude when using TiO₂ as a photocatalyst in SODIS.

Hydroxyapatite (HAP) is an easily synthesizable, low-cost mineral that has been recognized as a potential material for fluoride removal. Some of the synthesis methods of HAP are quite straightforward and cost-effective, while some require sophisticated synthesis techniques under advanced laboratory conditions. This review assesses the physicochemical characteristics of HAP and HAP-based composites produced via various techniques, their recent development in defluoridation and most importantly, the fluoride removal performances. For the first time, fluoride removal performances of HAP and HAP composites are compared based on partition coefficient (KD) instead of maximum adsorption capacity (Qₘₐₓ), which is significantly influenced by initial loading concentrations. Novel HAP tailored composites exhibit comparatively high KD values indicating the excellent capability of fluoride removal along with specific surface areas above 120 m²/g. HAP doped with aluminium complexes, HAP doped ceramic beads, HAP-pectin nanocomposite and HAP-stilbite nanocomposite, HAP decorated nanotubes, nanowires and nanosheets demonstrated high Qₘₐₓ and KD. The secret of HAP is not the excellent fluoride removal performances but best removal at neutral and near-neutral pH, which most of the defluoridation materials are incapable of, making them ideal adsorbents for drinking water treatment. Multiple mechanisms including physical surface adsorption, ion-exchange, and electrostatic interactions are the main mechanisms involved in defluoridation. Further research work must be focused on upscaling HAP-based composites for defluoridation on a commercial scale.

In this proposed study, erbium (Er³⁺)-doped ZnO nanocomposites were prepared through the effective, basic, and green combustion method. The significant effects of Er dopants on the structural, morphological features, dielectric, and optical behaviors of the pure ZnO matrix as well as Er₂O₃–ZnO nanostructured materials were investigated applying X-ray diffraction (XRD), scanning electron microscopy (SEM), Fourier transformation infrared (FT-IR) spectroscopy, and UV–Vis spectrophotometer techniques. These results showed that the synthesized Er₂O₃–ZnO nanocomposites are well polycrystalline. The Er₂O₃–ZnO nanocomposites are almost uniformly distributed on the surface morphologies. Furthermore, UV–Vis diffuse reflectance spectroscopy, AC electrical conductivity, and dielectric properties’ current–voltage characteristics were utilized to examine the influence of erbium doping on the optical properties, energy bandgaps of the proposed Er₂O₃–ZnO nanostructured powder. The tested nano-samples were applied for the visible light photodegradation of p-chlorophenol(4-CP) and p-nitrophenol (4-NP). The Er-doped ZnO ratio affects the photocatalytic activity of the ZnO matrix. This current research substantiated that more than 99.5% of 4-CP and 4-NP were photodegraded through 30 min of irradiation. Four times, the Er:ZnO nanocatalysts were used and still displayed an efficiency of more than 96.5% for 4-CP and 4-NP degradations in the specified period of 30 min. The as-prepared Er₂O₃–ZnO nanostructures are considered novel potential candidates in broad nano-applications from visible photocatalytic degradation of waste pollutants to the electronic varistor devices.

The present study evaluates the performance of an indigenously developed ceramic ultrafiltration (UF) membrane in a lab-scale membrane bioreactor (MBR) process to treat real tannery effluent with varying organic loading (1500–6000 mg/L). UF membrane was prepared by the coating of bentonite clay on tubular clay-alumina macroporous support. The membrane surface was characterized by scanning electron microscopy, Fourier transform infrared spectroscopy, X-ray diffraction, X-ray photoelectron spectroscopy, BET adsorption–desorption, contact angle measurement, and atomic force microscopy. In the side-stream MBR process, sewage sludge from a local sewage treatment plant was used as an activated sludge source with a constant sludge retention time of 30 days. Membrane filtration was performed in cross-flow mode using a single-channel membrane module. Artificial neural network (ANN) modeling tool was used to analyze the influence of various independent input variables, namely, the hydraulic retention time (4–10 h), mixed liquor suspended solid (MLSS) concentration (2–8 g/L), and influent COD concentration (1500–6000 mg/L) on COD removal (%) with feed-forward backpropagation method. Membrane study was done at a transmembrane pressure of 4.3 bar and feed flow rate of 7.5 L/min to observe the flux declination and fouling of the UF membrane with time. Average COD and BOD concentrations obtained in the treated effluent were 147.56 and 31 mg/L, respectively, and chromium concentration was < 0.1 mg/L; thus, treated effluent quality was found to be suitable for industrial recycling purposes apart from the safe environmental discharge. An in-depth study was undertaken to understand the removal mechanism in the MBR process, nature and extent of membrane fouling, changes in the morphology of the UF membrane, surface wettability, and surface topology by detailed surface characterization of the membrane pre- and post-filtration.

The aim of this study was to recycle dredged sediments as an alternative raw material in the production of ceramic tiles. The effect of the substitution of kaolin by raw sediment (HDS) and calcined sediment (HDSC) in the mixture of the ceramic tile samples sintered at 1100 and 1200 °C was studied. The samples were prepared with different proportions of HDS and HDSC (0, 10, 20 and 30 wt.%) substituting kaolin. The mineralogical analysis of the samples shows that mullite phase disappears in the samples incorporating raw sediments (HDS) and fired sediments (HDSC) leading to the formation of new crystalline phases such as anorthite and diopside.Moreover, ceramic tile samples with 20 wt.% of calcined sediment improve its densification and hence the compressive strength (171 MPa) and thermal conductivity (0.555 W/mK). An evaluation of the leaching was carried out in the ceramic samples, finding that the concentrations of heavy metals in the leachate were within the safety limit established by the USEPA. The heavy metals were immobilised in the ceramic matrix. Therefore, the results showed that dredged sediment (HDS) and calcined sediment (HDSC) could be used as substituent of kaolin to produce eco-friendly ceramic building materials as floor tile ceramics.

This paper presents the removal of nine potential endocrine disruptors including pesticides, pharmaceuticals and industrial chemicals using a submerged membrane bioreactor (MBR) system. Two lab-scale submerged MBRs having ceramic membranes were operated at three different sludge retention times (SRT: 15, 45, 90 days) and two hydraulic retention times (HRT: 12, 6 h) and the effects of SRT and HRT on both micropollutant removal and membrane fouling were investigated. While the effect of SRT and HRT change was observed on the removal of atrazine, fluoxetine, penconazole, no significant change was detected for the other micropollutants studied. It was determined that physicochemical properties such as distribution coefficient (LogD) and hydrophobicity of micropollutants are also effective on the removal efficiency of micropollutants. High removal efficiencies ([Formula: see text] 97.5%) were observed for hydrophobic pollutants (logD > 3.2) except for penconazole (72.1%) and for hydrophilic pollutants (logD < 3.2) except for atrazine (42.5%). Membrane fouling was significantly affected by different operational parameters applied, with the slowest fouling occurring at 45 days of SRT and 12 h of HRT. However, micropollutant addition did not have a significant effect on membrane fouling. It has been shown that the simultaneous and effective treatment performance for micropollutants makes the membrane bioreactor system a promising wastewater treatment process.

The idea of reusing municipal incinerator bottom ash (MIBA), the residue from incinerating municipal solid wastes, fits nicely in a circular economy scheme, which leads to an avoided impact of landfill disposal, and at the same time reduces the demand of natural resources. Past studies have attempted to add 20 to 60% MIBA for ceramic production, and resulted in some inspiring success. Focused on delivering quality interior and exterior floor tiles meeting industrial standards, this study investigated the operative conditions and the optimum amount of MIBA in the mix. In this study, only the kaolinite clay and MIBA were used. Before making specimens, raw materials of clay and MIBA underwent SEM, EDS, and TCLP tests to determine their chemical contents. Six sets of specimens with different replacement levels of MIBA (0%, 5%, 10%, 15%, 20%, and 30%) were then prepared. These specimens were fired at 1000°C, 1050°C,1100°C, and 1150°C and the products underwent a series of mechanical tests to verify their performance. NMR (nuclear magnetic resonance spectroscopy) were also used to determining the organic compound structure after each specimens’ crystallization. Research results showed that proper mix of MIBA up to 20% could result in quality tiles complying with specifications for interior and exterior flooring applications at certain kiln temperatures, while the specimens with 30% MIBA failed to meet either bending strength or size shrinkage requirement at all four kiln temperatures, and could not deliver a satisfactory result.

The use of the ornamental stone wastes, such as the originated from granite or marble, has been the subject of technological studies that evaluated its application in ceramic and cement materials; however, some complementary assessments, such as its life cycle assessment, are still not well explored in the literature. Therefore, the objective of this study was to discuss the main environmental impacts related to the manufacture of ceramic specimens, comparing conventional production versus the production of specimens incorporated with ornamental stone wastes. For this, the life cycle assessment was conducted in accordance with ISO 14.040 and 14.044. For this research, the ornamental stone wastes from the municipality of Cachoeiro do Itapemirim–ES and clay from the municipality of Campos dos Goytacazes–RJ were used. The system was modeled, using the SimaPro 9.0 software and the Ecoinvent database 3.3, for the life cycle assessment of the ceramic specimens and the potentiality regarding the use of ornamental stone wastes in ceramic materials using alternative input energy for burning, contributing to the effectiveness of the solid wastes reuse by the ceramic industry. The evaluation identified that the ornamental stone wastes incorporated into the ceramic specimens had significant potential in reducing environmental impacts and that the alternative input energy in burning stage makes them even more relevant. The study points out as the main result, the reduction of 35.74% of the impacts related to the category of the emission of greenhouse gases, and scarcity of mineral resources, 14.83% reduction, when compared to specimens to conventional brick production and alternative brick production, which emphasizes that the ceramic materials with wastes contribute to the mitigation of impacts.

This work aims to integrate several hydrogen peroxide (H₂O₂) activation mechanisms, photolysis (UVC irradiation), chemical electron transfer (TiO₂-P25 photocatalysis), and reaction with TiO₂-P25 in dark conditions, for reactive oxygen species (ROS) generation towards the removal of contaminants of emerging concern (CECs), in a single unit operated in continuous-flow mode. An H₂O₂ stock solution is fed by the lumen side of a tubular ceramic membrane, delivering the oxidant to the (i) catalyst immobilized in the membrane shell-side and (ii) annular reaction zone (ARZ, space between membrane shell-side and outer quartz tube) where CECs contaminated water flows with a helix trajectory, being activated by UV light provided by four lamps placed symmetrically around the reactor. First, the effect of several parameters in the removal of a CEC target molecule, amoxicillin (AMX), was evaluated using a synthetic solution ([AMX]ᵢₙₗₑₜ = 2.0 mg L⁻¹): (i) light source (UVA or UVC radiation), (ii) H₂O₂ dose, (iii) H₂O₂ injection method (radial permeation vs. upstream injection), and (iv) number of TiO₂-P25 layers deposited on the membrane. The UVC/H₂O₂/TiO₂ system with radial addition of H₂O₂ (20 mg L⁻¹) and 9-TiO₂-P25 layers provided the highest AMX removal efficiency (72.2 ± 0.5%) with a UV fluence of 45 mJ cm⁻² (residence time of 4.6 s), due to the synergic effect of four mechanisms: (i) AMX photolysis, (ii) H₂O₂ photocleavage, (iii) TiO₂-P25 photoactivation, and (iv) chemical reactions between H₂O₂ and TiO₂-P25. The urban wastewater matrix showed a negative effect on AMX removal (~44%) due to the presence of ROS scavengers and light-filtering species.

Currently, recycling of waste materials in construction is being considered very important because waste generation is posing serious threats to our living environment. Hence, to induce sustainability in the ongoing urban development, researchers around the globe are using numerous wastes in concrete as partial substitutes of binders (cement, lime, etc.) and fillers (fine and coarse aggregates) with the aim of reducing the depletion of natural resources and cutting the carbon dioxide emissions emerging from increased demand and production of cement. This review paper has summarized the findings of literature relating to recycling of marble wastes and ceramic tiles wastes in production of concrete. The physical, fresh-state, and strength properties of concrete were reviewed from available extensive literature, and it was found that the concrete prepared from marble waste and ceramic waste as partial substitution of cement and aggregates is expected to perform at least comparable to conventional cement concrete and better if applicable. Both marble wastes and ceramic tiles wastes can be incorporated and recycled in concrete as cementitious materials and aggregate replacing materials. With such approach, the concrete can be made strong and durable, and the issues relating to depletion of natural resources and environmental degradation can also be solved without compromising sustainability in infrastructure development.