Photocatalytic Degradation of Textile Dye and Wastewater

In this study, the photocatalytic degradation of commercial azo dye (Remazol Red 133) in the presence of titanium dioxide (TiO₂) suspensions as photocatalyst was investigated. The effect of various operational parameters, such as pH of dye solution and catalyst concentration on the photocatalytic degradation process, was examined. The mineralization of dye was also evaluated by measuring the chemical oxygen demand of the dye solutions. The extent of photocatalytic degradation was found to increase with increasing TiO₂ concentration. For the Remazol Red dye solutions, a 120-min treatment resulted in 97.9% decolorization and 87.6% degradation at catalyst loading of 3 g/L. Experiments using real textile wastewater were also carried out. Textile wastewater degradation was enhanced at acidic conditions. The decolorization and degradation efficiencies for textile wastewater were 97.8% and 84.9% at pH 3.0, catalyst loading of 3 g/L, and treatment time of 120 min.     

Biosorption of Reactive Dyes: A Review

Development of treatment technologies to alleviate water pollution has been a challenging and demanding task for researchers. Furthermore, synthetic dyes fabricated of complex aromatic structures turned out to be a great hazard as they impart color to water reservoirs making them abhorrent for human use. Reactive dyes being water soluble prove difficult to be eliminated by conventional treatment technologies. In recent times, biosorption has gained prominence as a finishing technology to remove pollutants being cost-effective and environment friendly. This paper describes the hazards posed by dyeing effluents, exclusively reactive dyes, on the environment and use of various biosorbents to remove reactive dyes from aqueous solution under optimum physicochemical parameters. Enhancement of biosorption capacity by chemical treatment and immobilization; equilibrium, kinetic and thermodynamic modeling of biosorption process; characterization by FTIR and SEM and regeneration of biosorbents is also plainly and comprehensively discussed.     

Degradation of Hazardous Dyes in Wastewater using Nanometer Mixed Crystal TiO2 Powders under Visible Light Irradiation

The partial phase transformation of nanometer TiO₂ powder from anatase phase to rutile phase was realized by heat-treatment and a new TiO₂ photocatalyst which could be excited by visible light was obtained. The heat-treated TiO₂ powder at different stage of transition crystal was characterized and monitored by XRD, TEM, FT-IR and UV–vis DRS methods. The test of photocatalytic activity of the heat-treated TiO₂ powder was carried out by the photocatalytic degradation of rhodamine B and acid orange II dyes, respectively, in aqueous solution under visible light irradiation. The results indicate that the nanometer TiO₂ photocatalyst heat-treated at 500°C for 60 min shows the highest photocatalytic activity, that is, it can effectively degrade the rhodamine B and acid orange II under visible light irradiation. The remarkable improvement of photocatalytic activity of heat-treated TiO₂ powder at 500°C for 60 min was mainly illustrated by the formation of special interphase between rutile and anatase phases, which not only restrains the recombination of photogenerated electrons and holes, but also reduces the adsorbability of nanometer anatase TiO₂ powder properly for various dyes. Additionally, the effects of dye-assisting chemicals such as Na₂CO₃ and NaCl on the photocatalytic degradation were also studied.     

Photocatalytic Degradation of Emerging Contaminants: Artificial Sweeteners

Artificial sweeteners are food additives widely used, mainly in reduced sugar or sugar-free foods and beverages. Acesulfame potassium (ACE-K) and sodium saccharin (SAC) are among the most widely consumed sweeteners worldwide. These compounds when ingested are not metabolized by the body, being excreted unchanged. They arrive at treatment plants, where they are partially degraded and consequently released directly into water bodies. For this reason, artificial sweeteners have been detected in the most diverse aquatic environments, being recognized as emerging contaminants. In this work, aqueous solutions of ACE-K and SAC, submitted to heterogeneous photocatalysis (TiO₂/UV-A) for 60 min, showed degradations of more than 99% and maximum mineralization of 57% for ACE-K and 49% for SAC. The effects of certain variables were evaluated, with pH having a greater influence on the degradation of acesulfame and the mass of semiconductor on that of saccharin. The degradation of ACE-K and SAC followed a pseudo-first-order kinetic model according to the Langmuir–Hinshelwood model. Assays using Artemia salina as the test organism demonstrated the low toxicity of the photocatalyzed solutions of ACE-K and SAC. The contribution of different reactive species to the photocatalysis was investigated using specific radical inhibitors; the results indicate that singlet oxygen (¹O₂) has a fundamental role in the photocatalytic degradation of ACE-K and SAC.

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Structural Influence on Photooxidative Degradation of Halogenated Phenols

The influence of structure on degradation of five halogenated phenols (XPs) by UV/H₂O₂ process was investigated. The combined influence of type or number of substituents and UV/H₂O₂ process parameters (pH and [H₂O₂]) on the degradation kinetics of 2-fluorophenol (2-FP), 2-chlorophenol (2-CP), 2-bromophenol (2-BP), 2,4-dichlorophenol (2,4-DCP), and 2,4,6-trichlorophenol (2,4,6-TCP) was studied using modified miscellaneous 3³ full factorial design and response surface modeling (RSM). Studied XPs obey first-order degradation kinetics within the investigated range of process parameters. Determined degradation rate constants (k _obs) were correlated with process and structural parameters by the quadratic polynomial models. Analysis of variance (ANOVA) demonstrated RSM models’ accuracy and showed that, in addition to pH and [H₂O₂], model terms related with the pollutant structure are highly influential. k _obs of mono-XPs follow the decreasing order 2-FP, 2-CP, and 2-BP, while CPs follow the decreasing order 2-CP, 2,4-DCP, and 2,4,6-TCP. Biodegradability (biochemical oxygen demand (BOD)₅/chemical oxygen demand (COD)) and toxicity (TU) were evaluated prior to the treatment and at the reference time intervals. The observed differences are correlated with the structural characteristics of studied XPs.     

Microbial Degradation of Organophosphate Pesticides: A Review

Pesticides have become an inevitable part of the modern environment as they are widely used in agriculture,household,and public health sectors and,hence,are extensively distributed throughout most ecosystems.Currently,organophosphate pesticides are the most commercially favored group of pesticides,with large application areas all over the world.Depending on their fate,these organophosphorus compounds may become bioavailable for microbial degradation.Environmental microbes,such as Aspergillus,Pseudomonas,Chlorella,and Arthrobacter,are capable of coupling a variety of physical and biochemical mechanisms for the degradation of organophosphate pesticides,including adsorption,hydrolysis of P–O alkyl and aryl bonds,photodegradation,and enzymatic mineralization.Enzymes,such as esterase,diisopropyl fluorophosphatase,phosphotriesterase,somanase,parathion hydrolase,and paraoxonase,have been isolated from microbes to study and understand the catabolic pathways involved in the biotransformation of these xenobiotic compounds.This review highlights various aspects of biodegradation of organophosphate pesticides along with biological and molecular characterization of some organophosphate pesticide-degrading bacteria.     

Removal of Hexavalent Chromium-Contaminated Water and Wastewater: A Review

Cr(VI) is a well-known highly toxic metal, considered a priority pollutant. Industrial sources of Cr(VI) include leather tanning, cooling tower blowdown, plating, electroplating, anodizing baths, rinse waters, etc. This article includes a survey of removal techniques for Cr(VI)-contaminated aqueous solutions. A particular focus is given to adsorption, membrane filtration, ion exchange, and electrochemical treatment methods. The primary objective of this article is to provide recent information about the most widely used techniques for Cr(VI) removal.     

Photocatalytic Decolorization of Commercial Acid Dyes using Solar Irradiation

Four wetland plants were selected to study the effect of Fe plaque formation on phosphorus (P) accumulation in the rhizosphere and P uptake. There were significant positive correlations between the sorbed Fe content in the rhizosphere and the Fe plaque concentration (r ²?=?0.8454, p?<?0.01) and between P accumulation and the amount of the sorbed Fe in the rhizosphere (r ²?=?0.8460, p?<?0.01). The concentration of the Fe plaque on the root surface of four wetland plants species tested followed the order of Zizania cedu Ciflora Turez > Scirpus tabernaemontani Gmel > Iris pseudacorus Linn > Canna indica Linn. The Fe plaque formation increased P uptake, apparently through enhancing the diffusion of P into the roots of the wetland plants; this resulted in increased P concentration in shoots. However, this effect decreased in the higher Fe plaque concentration status, apparently due to physical blocking and immobilization of P by Fe plaque. Therefore, adequate surface coverage of roots of wetland plant by the Fe plaque would increase the uptake of P by wetland plants, which depend on the optimum amendment of Fe. These effects also varied with wetland plant species.     

The Role of Soils in Land Degradation Assessment: A Review

Eurasian Soil Science - Within the framework of the existing concepts of land degradation assessment, the main ideas about its causes and consequences are formulated, methodological provisions for...     

UV-TiO2 Photocatalytic Degradation of Landfill Leachate

Mature landfill leachate contains some macromolecular organic substances that are resistant to biodegradation. The photocatalytic process helps to enhance biodegradability of landfill leachate. Batch experiments were employed to determine the optimum conditions for removal of organic matter by UV-TiO₂ photocatalysis. Under optimum conditions, the removal of chemical oxygen demand (COD), dissolved organic carbon (DOC), biological oxygen demand (BOD), and color was determined. Moreover, gas chromatography coupled with mass spectrometry (GC/MS) was used to analyze the organic matter in the treated leachate before and after treatment by the photocatalysis. The experimental results indicated that the removal of COD, DOC, and color by UV-TiO₂ photocatalysis could reach above 60%, 70% and 97%, respectively. Under optimal conditions, the ratio of biological oxygen demand (BOD)/chemical oxygen demand (COD) was elevated from 0.09 to 0.39, representing substantial improvement in biodegradability. GC/MS analysis revealed that 37 out of 72 kinds of organic pollutants in the leachate remained after 72 h treatment. Esters were produced during photocatalytic process and ketones, hydrocarbons, aromatic hydrocarbons, hydroxybenzenes, and acids were easier to be degraded during photocatalytic oxidation processes. The UV-TiO₂ photocatalysis systems proposed may be a cost-effective approach for pre-treatment of landfill leachate.     

Removal of Dyes Using Graphene-Based Composites: a Review

Water contamination has reached an alarming state due to industrialization and urbanization and has become a worldwide issue. Dyes contaminate water and are addressed extensively by researchers. Various technologies and materials have been developed for the treatment of contaminated water. Among them, adsorption has attracted great attention due to its ease and cost-effective nature. In recent years, graphene-based composites have shown great potential for the removal of contaminants from water. The literature reveals the usefulness of composites of graphene with metal oxides, carbon derivatives, metal hybrids and polymers for the removal of organic dyes from contaminated water. In this review, efforts have been made to compile the studies on the removal of cationic and anionic dyes from water using graphene-based composites.     

Tannin-Based Coagulants in the Depuration of Textile Wastewater Effluents: Elimination of Anthraquinonic Dyes

Two tannin-based coagulants have been tested on anthraquinonic dye elimination from aqueous solutions. Acquapol S5T, derived from Acacia mearnsii de Wild, and Silvafloc, derived from Schinopsis balansae, were found to be excellent agents in the destabilization of Alizarin Violet 3R dye and its elimination through coagulation from textile effluents. Both coagulants showed that high affinity to the dye molecule in a wide pH range and q values reaches significant levels (up to 0.5 mg mg^???1) with reasonable low coagulant doses. Dye?Ccoagulant system presented a consistent behavior if studied under the statistical perspective of a design of experiments, where initial dye concentration and coagulant dose were the operating variables. Finally, both coagulants seemed to follow a predictable theoretical model under the Langmuir hypothesis with an accurate adjusted r ² coefficient above 0.9.     

Soil Retention Capacity of Phenols from Biologically Pre-Treated Kraft Mill Wastewater

Allophanic soil, natural and activated by acidification or calcination was used to adsorb organic recalcitrant compounds (lignin and chlorophenols) from biologically pre-treated kraft mill effluent. A synthetic non crystalline aluminosilicate like allophane coated with iron oxide (Al-Si-Fe) was used as control for comparison purposes. It was observed that the adsorption capacity of the allophanic soil increased at higher solid/solution ratio, and at lower pH values. The highest total phenolic compounds removal was obtained between pH 4.0 and 4.5 for natural and activated soil using a solid/solution ratio of 1:5, and for synthetic aluminosilicate using 300 mg in 30 mL of effluent solution. Soil activated by calcination procedure presented the highest total phenolic compounds adsorption capacity (71–85%) for untreated and aerobic or anaerobic pre-treated effluent. The specific chlorophenols analysis indicated that pentachlorophenol (PCP) was almost completely adsorbed onto the allophanic soil (> 99%), and that over 79% of the 2,3,4,6-tetrachlorophenol (TeCP) was adsorbed, independent of the biological pre-treatment type and the soil activation procedure. On the other hand, 2,4-dichlorophenol (DCP) coming from both aerobic and anaerobic treated effluent was poorly removed (24–30%) when natural soil was used for adsorption; whereas in calcinated and acidified soil DCP removal was more than 71%.     

土壤水资源研究进展及评述

通过分析土壤水的资源属性,回顾土壤水资源研究的主要进展,在此基础上探讨土壤水资源定义,并对未来土壤水在水资源中的研究进行了展望.     

微生物降解石油源多环芳香烃的研究进展

石油源多环芳香烃是存在于石油中的一类致畸、致癌污染物,具有以低环(2~3环)为主且取代基比例明显高于其他来源PAHs的组分特征。石油泄露引发的PAHs污染,其降解主要依赖于微生物的活动。本文对能够降解PAHs的微生物种类、降解机理、代谢途径及编码基因进行了概述。从PAHs作为碳源的角度将微生物降解机理划分为能以PAHs为唯一碳源进行生长的降解机理和共代谢机理。对与PAHs有关的好氧和厌氧微生物降解途径及对应的编码基因簇进行了总结。自然界中细菌、放线菌、真菌及藻类都能够降解PAHs,由加氧酶催化的苯环羟基化和还原酶介导的苯环脱芳烃化是好氧和厌氧降解途径的关键步骤,与降解有关的pca,cat,paa,nah,nah-like和bcr基因簇则分别调控好氧和厌氧降解过程。这些进展有助于系统了解石油源PAHs的降解过程、微生物作用机理和分子遗传机制,为进一步利用微生物促进环境生物修复提供理论依据。     

Biological Degradation and Chemical Oxidation Characteristics of Coke-Oven Wastewater

Biological and chemical oxidation characteristics of two kinds ofcoke-oven wastewaters, A and B, discharged from a conventional batch coke-oven and a newly developed continuous coke-oven, respectively, were studied for selecting effective treatment processes of the wastewaters. Pollutants contained in Wastewater-A could be removed by biological process with a sufficient effluent quality, while those which existed in Wastewater-Bcould not be satisfactorily removed. Microbial community structure investigation using the respiratory quinone profile clarified that Pseudomonas putida (dominant quinone: ubiquinone-9) was a dominant species in the biological treatmentsystem. The refractory organic pollutants, existed in Wastewater-B,were mineralized more effectively by Fenton's reagent than by ozone. A wastewater treatment process, in which Fenton's oxidation is followed by a biological treatment, was proposed forthe treatment of Wastewater-B based on the experimental results.     

Photocatalytic Degradation of Herbicide Quinmerac in Various Types of Natural Water

The efficiency of the photocatalytic degradation of the herbicide quinmerac in aqueous TiO₂ suspensions was examined as a function of the type of light source, TiO₂ loading, pH, temperature, electron acceptors, and hydroxyl radical (^?OH) scavenger. The optimum loading of catalyst was found to be 0.25?mg?mL^?1 under UV light at pH?7.2, with the apparent activation energy of the reaction being 13.7?kJ?mol^?1. In the first stage of the reaction, the photocatalytic degradation of quinmerac (50???M) followed approximately a pseudo-first order kinetics. The most efficient electron acceptor appeared to be H₂O₂ along with molecular oxygen. By studying the effect of ethanol as an ^?OH scavenger, it was shown that the heterogeneous catalysis takes place mainly via ^?OH. The results also showed that the disappearance of quinmerac led to the formation of a number of organic intermediates and ionic byproducts, whereas its complete mineralization occurred in about 120?min. The reaction intermediates (7-chloro-3-methylquinoline-5,8-dione, three isomeric phenols hydroxy-7-chloro-3-methylquinoline-8-carboxylic acids, and 7-chloro-3-(hydroxymethyl)quinoline-8-carboxylic acid) were identified and the kinetics of their appearance/disappearance was followed by LC?CESI?CMS/MS. Tentative photodegradation pathways were proposed and discussed. The study also encompassed the effect of quality of natural water on the rate of removal of quinmerac.     

微生物降解DDT研究进展

DDT是<关于持久性有机污染物(POPs)的斯德哥尔摩公约>规定的12种禁限POPs之一.它的环境毒性越来越引起人们的关注.微生物降解是一种有效的环境友好型去除DDT污染的手段.本文简要综述了国内外在DDT微生物降解方面的研究进展,主要包括降解DDT的微生物、微生物降解DDT的途径以及以影响土壤中微生物降解DDT的因素.并对通过生物强化手段消除土壤中的DDT污染进行了展望.