Degradation of azo dyes in water by Electro-Fenton process

The degradation of the azo dyes azobenzene, p-methyl red and methyl orange in aqueous solution at room temperature has been studied by an advanced electrochemical oxidation process (AEOPs) under potential-controlled electrolysis conditions, using a Pt anode and a carbon felt cathode. The electrochemical production of Fenton's reagent (H₂O₂, Fe²⁺) allows a controlled in situ generation of hydroxyl radicals (^·OH) by simultaneous reduction of dioxygen and ferrous ions on the carbon felt electrode. In turn, hydroxyl radicals react with azo dyes, thus leading to their mineralization into CO₂ and H₂O. The chemical composition of the azo dyes and their degradation products during electrolysis were monitored by high performance liquid chromatography (HPLC). The following degradation products were identified: hydroquinone, 1,4-benzoquinone, pyrocatechol, 4-nitrocatechol, 1,3,5-trihydroxynitrobenzene and p-nitrophenol. Degradation of the initial azo dyes was assessed by the measurement of the chemical oxygen demand (COD). Kinetic analysis of these data showed a pseudo-first order degradation reaction for all azo dyes. A pathway of degradation of azo dyes is proposed. Specifically, the degradation of dyes and intermediates proceeds by oxidation of azo bonds and aromatic ring by hydroxyl radicals. The results display the efficiency of the Electro-Fenton process to degrade organic matter. Electronic Publication     

Visible-light degradation of azo dyes by imine-linked covalent organic frameworks

Covalent organic frameworks(COFs) are nanoporous crystalline polymers with densely conjugated structures. This work discovers that imine-linked COFs exhibit remarkable photodegradation efficiency to azo dyes dissolved in water. Visible light generates different types of radicals from COFs, and superoxide radicals break N═N bonds in dye molecules, resulting in 100% degradation of azo dyes within 1 h. In contrast, these dyes cannot be degraded by conventionally used photocatalysts, for example, Ti...     

Decolorization of azo dyes by a salt-tolerant Staphylococcus cohnii strain isolated from textile wastewater

The salt-tolerant Staphylococcus cohnii strain, isolated from textile wastewater, has been found effective on decolorizing several kinds of azo dyes with different structures. The optimal conditions for azo dye acid red B (ARB) decolorization by S. cohnii were determined to be pH = 7.0 and 30°C. The decolorization efficiency increased with the increase of the salinity concentration, and around 90% of ARB (100 mg·L^?1) could be decolorized in 24 h when the salinity concentration was up to 50 g·L^?1. Moreover, the strain could still decolorize 19% of ARB in 24 h even when the NaCl concentration was increased to 150 g·L^?1. Meanwhile, the dependence of the specific decolorization rate by S. cohnii on the ARB concentration could be described with Michaelis-Menten kinetics (K _m = 585.7mg·L^?1, V _max = 109.8 mg·g cell^?1·h^?1). The addition of quinone redox mediator, named 2-hydroxy-1,4-naphthoquinone and anthraquinone-2,6-disulfonate, significantly accelerated the decolorization performance of S. cohnii. Furtherly, the activities of azoreductase (0.55 ??mol·mg protein^?1·min^?1) and Nicotineamide adenine dinucleotide-dichlorophenol indophenol (NADH-DCIP) reductase (8.9 ??mol·mg protein^?1·min^?1) have been observed in the crude cell extracts of S. cohnii. The decolorization products of ARB were analyzed by HPLC-MS, and the results indicated the reductive pathway was responsible for azo dye decolorization by S. cohnii.     

Sustainable catalytic oxidation of glycerol: a review

Environmental Chemistry Letters - Valorization of biomass-derived feedstocks for the supply of high-value chemicals, clean fuel and electricity is gaining importance in the context of the circular...     

Structural effect on photocatalytic degradation of metallised azo dyes in aqueous TiO2 suspension

Three metallised azo dyes were investigated under TiO₂‐photocatalytic and photosensitised conditions in aqueous buffering solutions. The degradation follows apparent first‐order kinetics. The size and strength of intramolecular conjugation determine the light‐fastness of the investigated dyes. Compared with ¹O₂ produced in photosensitised process, the more powerful *OH radicals in TiCO₂ photocatalytic process are highly reactive towards the investigated azo dyes. And as a result, the TiO₂‐photocatalysis makes little less distinction in the degradation kinetic data of the azo dyes compared with the photosensitised degradation of them.     

Photo-Fenton oxidation of Orange G azo dye: process optimization and mineralization mechanism

Environmental Chemistry Letters - Textile effluents containing synthetic dyes are one of the most important sources of water pollution. Several dyes are toxic to the aquatic life and...     

Electrochemical reduction of carbon dioxide into valuable chemicals: a review

Environmental Chemistry Letters - Global warming is partly caused by massive emissions of carbon dioxide (CO2), a greenhouse gas, in the atmosphere by industrial and other human activities....     

Application of permanganate in the oxidation of micropollutants: a mini review

As a green oxidant, permanganate has received considerable attention for the removal of micropollutants in drinking water treatment. To provide a better understanding of the oxidation of organic micropollutants with permanganate, the oxidation kinetics of 32 micropollutants were compiled. The pollutants include algal toxins, endocrine disrupting chemicals (EDCs), and pharmaceuticals. The oxidation kinetics of micropollutants by permanganate were found to be first order with respect to both contaminant and permanganate concentrations from which second-order rate constants (k″) were obtained. Permanganate oxidized the heterocyclic aromatics with vinyl moiety (i.e., microcystins, carbamazepine, and dichlorvos) by the addition of double bonds. For the polycyclic aromatic hydrocarbons (PAHs) with alkyl groups, permanganate attacked the benzylic C-H through abstraction of hydrogen. The mechanism for the oxidation of phenolic EDCs by permanganate was a single electron transfer and aromatic ring cleavage. The presence of background matrices could enhance the oxidation of some phenolic EDCs by permanganate, including phenol, chlorinated phenols, bisphenol A, and trichlosan. The toxicity of dichlorvos solution increased after permanganate oxidation, and the estrogenic activity of bisphnol A/estrone increased significantly at the beginning of permanganate oxidation. Therefore, the toxicity of degradation products or intermediates should be determined in the permanganate oxidation processes to better evaluate the applicability of permanganate. The influence of background ions on the permanganate oxidation process is far from clear and should be elucidated in the future studies to better predict the performance of permanganate oxidation of micropollutants. Moreover, methods should be employed to catalyze the permanganate oxidation process to achieve better removal of micropollutants.     

Metal ion-induced enhanced oxidation of organic contaminants by ferrate: a review

Environmental Chemistry Letters - The global contamination of water resources by organic contaminants such as pharmaceuticals and pesticides is calling for advanced remediation techniques, yet...     

Polymeric nanocomposite membranes for water treatment: a review

Environmental Chemistry Letters - Water scarcity is a pressing global challenge. Filtration with actual polymeric membranes shows good capability for pollutant separation, but broad applications of...     

Ruthenium-driven catalysis for sustainable water decontamination: a review

Environmental Chemistry Letters - The worldwide demand for clean water is rising worldwide, yet wastewater decontamination is actually limited by the presence of refractory organic and inorganic...     

Dyes removal from water using polymeric nanocomposites: a review

Environmental Chemistry Letters - Most dyes are pollutants that should be removed from waters due to their mutagenic and carcinogenic properties, requiring advanced adsorption methods. Here, we...     

Piezocatalytic removal of water bacteria and organic compounds: a review

Environmental Chemistry Letters - In the context of climate change, freshwater shrinkage and industrialization, human diseases are increasing due to water pollution by toxic chemicals and...     

Worldwide cases of water pollution by emerging contaminants: a review

Environmental Chemistry Letters - Water contamination by emerging contaminants is increasing in the context of rising urbanization, industrialization, and agriculture production. Emerging...     

Recent advances in electrochemical decontamination of perfluorinated compounds from water: a review

● Recent advances in the electrochemical decontamination of PFAS are reviewed. ● Underlying mechanisms and impacting factors of these processes are discussed. ● Several novel couped systems and electrode materials are emphasized. ● Major knowledge gaps and research prospects on PFAS removal are identified. Per- and polyfluoroalkyl substances (PFAS) pose serious human health and environmental risks due to their persistence and toxicity. Among the available PFAS remediation options, the electrochemical approach is promising with better control. In this review, recent advances in the decontamination of PFAS from water using several state-of-the-art electrochemical strategies, including electro-oxidation, electro-adsorption, and electro-coagulation, were systematically reviewed. We aimed to elucidate their design principles, underlying working mechanisms, and the effects of operation factors (e.g., solution pH, applied voltage, and reactor configuration). The recent developments of innovative electrochemical systems and novel electrode materials were highlighted. In addition, the development of coupled processes that could overcome the shortcomings of low efficiency and high energy consumption of conventional electrochemical systems was also emphasized. This review identified several major knowledge gaps and challenges in the scalability and adaptability of efficient electrochemical systems for PFAS remediation. Materials science and system design developments are forging a path toward sustainable treatment of PFAS-contaminated water through electrochemical technologies.     

水生维管束植物在水污染中的应用

随着水污染的加剧，高效低耗的水污染处理技术逐渐受到人们的重视，水生维管束植物以其特有的组织和生态功能及易于人工操纵等原因而在净化水体污染、防治富营养化方面发挥了重要的作用。文章对水生维管束植物在水质净化中的作用、影响因素、水生植物的综合利用及其在水污染监测中的作用等方面进行了系统分析，提出多种植物组合比单种植物能更好地实现对水体的净化，通过温度、水深的调控措施可以加强水生维管束植物对水质的净化效果，温度、水深、水质状况以及水生植物的经济价值等是水生植物选择的重要因素。指出了当前水生维管束植物研究中存在的一些问题，认为在人为操纵下，对于水生植物的长效管理是其在水污染应用中的一个重要内容。     

Design and mechanism of photocatalytic oxidation for the removal of air pollutants: a review

Environmental Chemistry Letters - Nitric oxide, ammonia and volatile organic compounds are common air pollutants which need to be removed for health security. To reach ultra-low emission standards,...     

Wet oxidation of debarking water: changes in lignin content and biodegradability

The purpose of the research was to estimate optimal conditions for wet oxidation (WO) of debarking water from the paper industry. The WO experiments were performed at various temperatures, partial oxygen pressures and pHs. The experiments showed that lignin degradation and organics removal are affected remarkably by temperature and pH. At different WO conditions (pH 12, T 130–200°C), 78–97% of lignin reduction was detected. pH value of 12 caused faster removal of tannins/lignin content; pH value of five was more effective for removal of total organics, represented by chemical oxygen demand (COD) and total organic carbon. The highest biodegradability [biological oxygen demand (BOD)/COD] of 0.72 was obtained at a pH of ten and temperature of 200°C.     

Supported porphyrins for the photocatalytic degradation of organic contaminants in water: a review

Environmental Chemistry Letters - Porphyrins are differentiated π-conjugated compounds with unique photochemical and redox properties. The tetrapyrrole macrocycle core of porphyrins is...     

Conversion of biomass into hydrogen by supercritical water gasification: a review

Environmental Chemistry Letters - The rising issues of global warming due to the rapid use of fossil fuels are calling for sustainable energies such as dihydrogen, thereafter named...