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A green and low-cost removal method for cyanate, a toxic byproduct from the treatment of cyanide, is still needed. Cyanase converts cyanate to CO2 and NH3, but its industrial practicality is limited because the reaction requires HCO3− as a substrate. In this study, we used carbonic anhydrase from Sulfurihydrogenibium azorense (SazCA) to provide HCO3− for cyanase from Thermomyces lanuginosus (TlCyn); both TlCyn and SazCA were purified by one-step heating without prior cell lysis. The heat treatment resulted in higher activities of both enzymes than the conventional two-step process. From a 50 mL-culture, the highest total activity of 147 U and 47,174 WAU was obtained from 5 min of heating at 60 and 80 °C for TlCyn and SazCA, respectively. The coupled enzymatic system was used to degrade cyanate in three different matrices: 50 mM Tris-HCl (pH 8), industrial wastewater, and artificial wastewater. In the industrial wastewater, with the addition of 0.75 WAU (Wilbur-Anderson unit) of SazCA, cyanate degradation using 0.5 mM NaHCO3 was similar to that using 3 mM NaHCO3, indicating an 83% reduction in NaHCO3. We have demonstrated that the dependence on HCO3− of cyanate degradation can be effectively alleviated by using low-cost heat-purified TlCyn and SazCA; the industrial practicality of the coupled enzymatic system is therefore improved. [ABSTRACT FROM AUTHOR]

Metallic glasses (MGs) with a unique atomic structure have been widely used in the catalytic degradation of organic pollutants in the recent years. Fe78Si9B13 MGs exhibited excellent catalytic performance for the degradation of oily wastewater in a Fenton-like system for the first time. The oil removal and chemical oxygen demand (COD) removal from the oily wastewater were 72.67% and 70.18% within 60 min, respectively. Quenching experiments were performed to verify the production of active hydroxyl radicals (·OH) by activating hydrogen peroxide (H2O2). The formation of ·OH species can significantly contribute to the degradation reaction of oily wastewater. Fe78Si9B13 MG ribbons were highly efficient materials that exhibited superior reactivity towards H2O2 activation in oily wastewater treatment. The study revealed the catalytic capability of metallic glasses, presenting extensive prospects of their applications in oily wastewater treatment. [ABSTRACT FROM AUTHOR]

Over the past few decades, enzyme-based green and sustainable chemistry has attracted extensive research attention, which provides a promising alternative to the conventional treatment methods of recalcitrant micropollutants. However, enzyme denaturation and stability loss remain critical challenges for its potential applications in industrial wastewater treatment. In this study, laccase from Trametes versicolor (laccase T.) was cross-linked immobilized by ultraporous alumina (UPA) for the sustainable biodegradation of Remazol Brilliant Blue R (RBBR). Through sequential use of an aminosilane coupling agent (3-aminopropyl)triethoxysilane (APTES) and bifunctional cross-linker glutaraldehyde (GA), the synthesized biocatalysts showed better immobilization performances (about 4-fold to physical adsorption). The GA concentration considerably affected the laccase T. cross-linking degree, while the GA post-treatment protocol showed the highest laccase T. immobilization yield with lower activity recovery. Moreover, the biocatalyst stabilities including pH stability, thermal stability, storage stability, and reusability were also studied. Tolerance to broader pH and temperature ranges, better storage stability, good reusability of laccase T. cross-linked UPA(γ) biocatalysts, and their continuous RBRR biodegradation efficiency highlight the potentials of enzyme-based inorganic materials in industrial wastewater treatment, which can broaden our understanding of their practical applications in environmental fields. [ABSTRACT FROM AUTHOR]

Two-dimensional compounds with nanostructural features are attracting attention from researchers worldwide. Their multitude of applications in various fields and vast potential for future technology advancements are successively increasing the research progress. Wastewater treatment and preventing dangerous substances from entering the environment have become important aspects due to the increasing environmental awareness, and increasing consumer demands have resulted in the appearance of new, often nonbiodegradable compounds. In this review, we focus on using the most promising 2D materials, such as MXenes, Bi2WO6, and MOFs, as catalysts in the modification of the Fenton process to degrade nonbiodegradable compounds. We analyze the efficiency of the process, its toxicity, previous environmental applications, and the stability and reusability of the catalyst. We also discuss the catalyst's mechanisms of action. Collectively, this work provides insight into the possibility of implementing 2D material-based catalysts for industrial and urban wastewater treatment. [ABSTRACT FROM AUTHOR]

4-chlorophenol (4-CP), a hydroxylated aromatic compound (HAC), is a recalcitrant and toxic organic pollutant found in industrial wastewater and various environmental media. In this paper, visible-light-activated photocatalysis using graphitic carbon nitride (GCN) was used to treat 4-CP in an aqueous media. Graphitic carbon nitride from different precursors (dicyanamide, urea, and melamine), as well as GCN/silver nanocomposites (AgBr, Ag3PO4, Ag2CrO4, and Ag), were successfully synthesized and characterized by BET, XRD, SEM, EDS, and UV-Vis DRS. The band gaps of the photocatalysts were estimated using the UV-Vis DRS characterization results and Tauc plots. The evaluation of the efficacy of the GCN-based catalysts in degrading 4-CP was conducted with different photoreactors such as a royal blue light-emitting diode (LED), a UV-A LED, LUZCHEM cool white lamps, and a solar simulator. The results showed that GCNs with royal blue LED can effectively degrade 4-CP from aqueous media. Among the different precursors, urea-derived GCN showed the best performance in degrading 4-CP due to its large surface area. GCN/0.3Ag2CrO4 nanocomposite showed a synergistic effect for the enhanced photocatalytic degradation of 4-CP. The degradation of 4-CP with a rate constant of 2.64 × 10−2 min−1 was achieved with a GCN/0.3Ag2CrO4 nanocomposite under royal blue LED irradiation. [ABSTRACT FROM AUTHOR]

The use of nano-photocatalysts for the water/wastewater purifications, particularly in developing regions, offers promising advantages over conventional technologies. TiO2-based photocatalysts deposited on fabrics represent an efficient solution for obtaining heterogeneous photocatalysts, which are easily adaptable in the already installed water treatment plants or air purification systems. Despite the huge effort spent to develop and characterize novel nano-photocatalysts, which are especially active under solar light, knowledge gaps still persist for their full-scale application, starting from the reactor design and scale-up and the evaluation of the photocatalytic efficiency in pre-pilot scenarios. In this study, we offered easily scalable solutions for adapting TiO2-based photocatalysts, which are deposited on different kinds of fabrics and implemented in a 6 L semi-pilot plant, using the photodegradation of Rhodamine B (RhB) as a model of water pollution. We took advantage of a multi-variable optimization approach to identify the best design options in terms of photodegradation efficiency and turnover frequency (TOF). Surprisingly, in the condition of use, the irradiation with a light-emitting diode (LED) visible lamp appeared as a valid alternative to the use of UV LED. The identification of the best design options in the semi-pilot plant allowed scaling up the technology in a 100 L pilot plant suitable for the treatment of industrial wastewater. [ABSTRACT FROM AUTHOR]

Effective La-doped SrTiO3 (Sr1−xLaxTiO3, x = 0–0.1 mol.% La-doped) nanocubes were successfully synthesized by a hydrothermal method. The influence of different La dopant concentrations on the physicochemical properties of the host structure of SrTiO3 was fully characterized. X-ray photoelectron spectroscopy (XPS) and X-ray diffraction (XRD) revealed that the Sr2+ in the crystal lattice of SrTiO3 was substituted by La3+. As a result, the absorption region of the Sr1−xLaxTiO3 could be extended to visible light. Scanning electron microscopy (SEM) images confirmed that their morphologies are associated with an increased surface area and an increased La-doping concentration. The decrease in the photoluminescence (PL) intensity of the dopant samples showed more defect levels created by the dopant La+3 cations in the SrTiO3 structure. The photocatalytic activities of Sr1−xLaxTiO3 were evaluated with regard to the degradation of 2-naphthol at typical conditions under artificial solar light. Among the candidates, Sr0.95La0.05TiO3 exhibited the highest photocatalytic performance for the degradation of 2-naphthol, which reached 92% degradation efficiency, corresponding to a 0.0196 min−1 degradation rate constant, within 180 minutes of irradiation. Manipulating the structure of Sr1−xLaxTiO3 nanocubes could produce a more effective and stable degradation efficiency than their parent compound, SrTiO3. The parameters remarkably influence the Sr1−xLaxTiO3 nanocubes' structure, and their degradation efficiencies were also studied. Undoubtedly, substantial breakthroughs of Sr1−xLaxTiO3 nanocube photocatalysts toward the treatment of organic contaminants from industrial wastewater are expected shortly. [ABSTRACT FROM AUTHOR]

Background: There is a need for more effective methods of industrial wastewater treatment. Methods: Cosmetic wastewater was collected and subjected to H2O2/Fe3O4/Fe2O3/Fe0 and UV/H2O2/Fe3O4/Fe2O3/Fe0 process treatment. Results: Total organic carbon (TOC) was decreased from an initial 306.3 to 134.1 mg/L, 56.2% TOC removal, after 120 min of treatment for 1:1 H2O2/COD mass ratio and 500/500/1000 mg/L Fe3O4/Fe2O3/Fe0 catalyst doses. The application chromatographic analysis allowed for the detection and identification of pollutants present in the wastewater. Identified pollutants were removed during the treatment processes. Processes carried out at a pH greater than 3.0 were ineffective. The UV process was more effective than the lightless process. Conclusions: The applied processes are effective methods for wastewater treatment. Chromatographic results confirmed the effectiveness of the treatment method. The kinetics of the process were described by the modified second-order model. On the basis of ANOVA results, the hypothesis regarding the accuracy and reproducibility of the research was confirmed. [ABSTRACT FROM AUTHOR]

The direct discharge of industrial wastewater into the environment results in serious contamination. Photocatalytic treatment with the application of sunlight and its enhancement by coupling with electrocatalytic degradation offers an inexpensive and green technology enabling the total removal of refractory pollutants such as surfactants, pharmaceuticals, pesticides, textile dyes, and heavy metals, from industrial wastewater. Among metal oxide—semiconductors, cerium dioxide (CeO2) is one of the photocatalysts most commonly applied in pollutant degradation. CeO2 exhibits promising photocatalytic activity. Nonetheless, the position of conduction bands (CB) and valence bands (VB) in CeO2 limits its application as an efficient photocatalyst utilizing solar energy. Its photocatalytic activity in wastewater treatment can be improved by various modification techniques, including changes in morphology, doping with metal cation dopants and non-metal dopants, coupling with other semiconductors, and combining it with carbon supporting materials. This paper presents a general overview of CeO2 application as a single or composite photocatalyst in the treatment of various pollutants. The photocatalytic characteristics of CeO2 and its composites are described. The main photocatalytic reactions with the participation of CeO2 under UV and VIS irradiation are presented. This review summarizes the existing knowledge, with a particular focus on the main experimental conditions employed in the photocatalytic and photoelectrocatalytic degradation of various pollutants with the application of CeO2 as a single and composite photocatalyst. [ABSTRACT FROM AUTHOR]

The application of Fenton-based advanced oxidation processes (AOPs), such as photo-Fenton or electro-Fenton for wastewater treatment have been extensively studied in recent decades due to its high efficiency for the decomposition of persistent organic pollutants. Usually Fenton-based AOPs are used for the degradation of targeted pollutant or group of pollutants, which often leads to the formation of toxic by-products possessing a potential environmental risk. In this work, we have collected and reviewed recent findings regarding the feasibility of Fenton-based AOPs (photo-Fenton, UVC/H2O2, electro-Fenton and galvanic Fenton) for the detoxification of real municipal and industrial wastewaters. More specifically, operational conditions, relevance and suitability of different bioassays for the toxicity assessment of various wastewater types, cost estimation, all of which compose current challenges for the application of these AOPs for real wastewater detoxification are discussed. [ABSTRACT FROM AUTHOR]