The Fered-Fenton process has been shown to be an effective method for leachate treatment, but it still faces problems of inadequate regeneration of ferrous ion. However, the use of the photoassisted Fered-Fenton process could overcome this difficulty and improve the efficiency of chemical oxygen demand (COD) removal since photoassisted Fered-Fenton process induces the production of hydroxyl radicals from the regeneration of ferrous ions and the reaction of hydrogen peroxide with UV light. As there are so many operating parameters in photoassisted Fered-Fenton process, it is necessary to develop a mathematical model in order to produce the most economical process. In the present study, a factorial design was carried out to evaluate leachate treatment by photoassisted Fered-Fenton process. The influence of the following variables: H₂O₂concentration, Fe²⁺concentration, current density, and initial pH in the photoassisted Fered-Fenton process was investigated by measuring COD removal efficiencies after 60-min reaction. The relationship between COD removal and the most significant independent variables was established by means of an experimental design. The H₂O₂concentration, Fe²⁺concentration, initial pH, and the interaction effect between current density and initial pH were all significant factors. The factorial design models were derived based on the COD removal efficiency results and the models fit the data well.

The use of effective disposal of redundant pumpkin husk (PH) to remove pollutants is an important issue for environmental protection and utilization of resource. The aim of this study was to remove a potentially toxic reactive azo dye, Reactive Red (RR) 120, by widespread PH as a low-cost adsorbent. Particle size, adsorbent dose, pH, temperature, initial dye concentration, and contact time affected the sorption process. Amine, amide, hydroxyl, and carboxyl groups of PH played significant roles on the sorption process. Rapid sorption occurred within the first 2 min and equilibrium was reached within 60 min. Sorption kinetic was well represented by logistic equation. Generated secondary logistic model can be used to describe effects of initial dye concentration, contact time, and temperature by a single equation with high R²value. Monolayer sorption capacity was found as 98.61 mg g⁻¹. Activation energy, thermodynamic, and desorption studies showed that this process was physical, endothermic, and spontaneous. This study indicated that redundant PH as a low-cost adsorbent had a great potential for the removal of RR 120 as an alternative eco-friendly process.

Atenolol is a β-blocker drug and an identified emerging pollutant. Advanced oxidation processes (AOPs) utilise the reaction of a highly oxidising species (hydroxyl radicals,•OH) for the mineralisation of emerging pollutants since conventional treatment methodologies generally fail to degrade these compounds. In the present work, degradation of atenolol was carried out using ultrasound with frequencies ranging from 200 kHz to 1 MHz as a source of hydroxyl radical. The degradation was monitored by HPLC, total organic carbon (TOC) and chemical oxygen demand (COD) reduction and ion chromatography (IC). Nearly 90 % of degradation of atenolol was observed with ultrasound having 350 kHz. Both frequency and power of ultrasound affect the efficiency of degradation. Nearly 100 % degradation was obtained at a pH of 4. Presence of various additives such as sodium dodecyl sulphate, chloride, sulphate, nitrate, phosphate and bicarbonate was found to reduce the efficiency of degradation. Although nearly 100 % degradation of atenolol was observed under various experimental conditions, only about 62 % mineralisation (from TOC and COD measurements) was obtained. Nearly eight intermediate products were identified using high-resolution mass spectrometry (LC-Q-TOF). These products were understood as the results of hydroxyl radical addition to atenolol. The degradation studies were also carried out in river water which also showed a similar degradation profile. A mechanism of degradation and mineralisation is presented.

In the present study, the investigation of the levels of the local and regional oxidants concentration at Athens, Greece, is attempted by analyzing the observations obtained at an urban and a rural station, during 2001–2011 and 2007–2011, respectively. A progressive increase of the daytime and nighttime average of [NO₂]/[Oₓ] versus [NOₓ] is observed showing a larger proportion of Oₓin the form of NO₂when the level of NOₓincreases. Similar results are observed when studying the variation of mean values of [NO₂]/[NOₓ] versus [NOₓ]. The results obtained when compared with those that have earlier detected elsewhere, revealed similarities and discrepancies that are discussed in detail. The parameterized curves that are presented for the first time in this paper may be used by the air quality planners to track the trends in other cities also, and to understand what is or was driving them.

Urban particulate matter (PM), asphalt, and tire samples were investigated for their content of benzothiazole and benzothiazole derivates. The purpose of this study was to examine whether wear particles, i.e., tire tread wear or road surface wear, could contribute to atmospheric concentrations of benzothiazole derivatives. Airborne particulate matter (PM₁₀) sampled at a busy street in Stockholm, Sweden, contained on average 17 pg/m³ benzothiazole and 64 pg/m³ 2-mercaptobenzothiazole, and the total suspended particulate-associated benzothiazole and 2-mercaptobenzothiazole concentrations were 199 and 591 pg/m³, respectively. This indicates that tire tread wear may be a major source of these benzothiazoles to urban air PM in Stockholm. Furthermore, 2-mercaptobenzothiazole was determined in urban air particulates for the first time in this study, and its presence in inhalable PM₁₀ implies that the human exposure to this biocide is underestimated. This calls for a revision of the risk assessments of 2-mercaptobenzothiazole exposure to humans which currently is limited to occupational exposure.

This work explores the competitive removal of pharmaceuticals from synthetic and environmental waters by combined adsorption-photolysis treatment. Five drugs usually present in waterways have been used as target compounds, some are pseudo-persistent pollutants (carbamazepine, clofibric acid, and sulfamethoxazole) and others are largely consumed (diclofenac and ibuprofen). The effect of the light source on adsorption of drugs onto activated carbons followed by photolysis with TiO₂ was assessed, being UV-C light the most effective for drug removal in both deionized water and river water. Different composites prepared from titania nanoparticles and powdered activated carbons were tested in several combined adsorption-photocatalysis assays. The composites prepared by calcination at 400 °C exhibited much better performance than those synthesized at 500 °C, being the C400 composite the most effective one. Furthermore, some synthetic waters containing dissolved species and environmental waters were used to investigate the effect of the aqueous matrix on each drug removal. In general, photocatalyst deactivation was found in synthetic and environmental waters. This was particularly evident in the experiments performed with bicarbonate ions as well as with wastewater effluent. In contrast, tests conducted in seawater showed adsorption and photocatalytic degradation yields comparable to those obtained in deionized water. Considering the peculiarities of substrate competition in each aqueous matrix, the combined adsorption-photolysis treatment generally increased the overall elimination of drugs in water.

The influents of plants treating complex industrial wastewaters from third parties may contain a large variety of often unknown or unidentified potentially harmful substances. The conventional approach of assessing and regulating the effluents of these plants is to set emission limit values for a limited set of physicochemical parameters, such as heavy metals, biological oxygen demand, chemical oxygen demand and adsorbable organic halogen compounds. The objective of this study was to evaluate the relevance of physicochemical parameters for setting emission limit values for such plants based on a comparison of effluent analyses by physicochemical and biological assessment tools. The results show that physicochemical parameters alone are not sufficient to evaluate the effectiveness of the water treatment plants for removing hazardous compounds and to protect the environment. The introduction of toxicity limits and limits for the total bioaccumulation potential should be considered to supplement generic parameters such as chemical oxygen demand and adsorbable organic halogens. A recommendation is made to include toxicity screening as a technique to consider in the determination of best available techniques (BAT) during the upcoming revision of the BAT reference document for the waste treatment industries to provide a more rational basis in decisions on additional treatment steps.

This study investigates the ability of Rhodococcus sp. strain p52, a dioxin degrader, to biodegrade petroleum hydrocarbons. Strain p52 can use linear alkanes (tetradecane, tetracosane, and dotriacontane), branched alkane (pristane), and aromatic hydrocarbons (naphthalene and phenanthrene) as sole carbon and energy sources. Specifically, the strain removes 85.7 % of tetradecane within 48 h at a degradation rate of 3.8 mg h⁻¹ g⁻¹dry cells, and 79.4 % of tetracosane, 66.4 % of dotriacontane, and 63.9 % of pristane within 9–11 days at degradation rates of 20.5, 14.7, and 20.3 mg day⁻¹ g⁻¹dry cells, respectively. Moreover, strain p52 consumes 100 % naphthalene and 55.3 % phenanthrene within 9–11 days at respective degradation rates of 16 and 12.9 mg day⁻¹ g⁻¹dry cells. Metabolites of the petroleum hydrocarbons by strain p52 were analyzed. Genes encoding alkane-hydroxylating enzymes, including cytochrome P450 (CYP450) enzyme (CYP185) and two alkane-1-monooxygenases, were amplified by polymerase chain reaction. The transcriptional activities of these genes in the presence of petroleum hydrocarbons were detected by reverse transcription-polymerase chain reaction. The results revealed potential of strain p52 to degrade petroleum hydrocarbons.

Regional material flows are strongly influenced by human diets. To diagnose and prevent environmental problems that threaten urban sustainability, the impact of human diet changes with rapid urbanization on the regional nitrogen (N) and phosphorus (P) flows were quantitatively evaluated. A survey of day-to-day activities was conducted of 450 individuals surveyed (adults over 18 years old) in three representative areas (the central district, the new district, and the suburban/rural areas) of Shanghai, a megacity which has attracted worldwide attention. The lifestyle (eating habits, domestic sanitation, drainage facilities, etc.) pattern was determined and the potential N and P loads from human diets on the environment were calculated. The daily potential nitrogen and phosphorus loads from human diets was 19.36 g-N, 1.80 g-P in the central district, 16.48 g-N, 1.52 g-P in the new district, and 13.04 g-N, 1.20 g-P in the suburban/rural areas of Shanghai. Respondents in all three areas, especially those in the suburban/rural areas reported a preference for increasing the intake of animal-derived as well as processed foods, which means that the potential N and P load from human diets to the environment will increase further. In addition, most respondents consider industrial wastewater discharge as the main cause of eutrophication of waterbodies, though in recent years water pollution caused by domestic wastewater has increased rapidly, but this has received much less attention. Environment-friendly eating habits and improvements in the environmental awareness will be required.

The phenomenon of coagulation settling in liquid suspensions has a variety of applications, including mineral processing, treatment of industrial effluents, and municipal sewage sludge purification. This study was to investigate the coagulation settling characteristics of fine-grind natural zeolite and evaluate the removal efficiency of contaminants simultaneously in static and turbulent flow. A series of column experiments were conducted to pattern the characteristics of spatial and temporal variation of coagulation settling and removal contaminants in static and turbulent flow. The results indicated that the suspended solid concentration presented an apparent exponential decay with coagulation settling time in static flow (R ² > 0.99), coagulation settling rate of the fine zeolite-suspended solid in static flow was between 0.005 and 0.05 cm/s obtained from the repeat depth suction method. The relation between average C/C ₀ of pollutants and suspended solid concentration was exponential before the settlement for 24 h and that was the line after the settlement for 24 h. Several various models were presented to highlight the coagulation settling characteristics of fine-grind natural zeolite in static and turbulent flow. Compared to hydrostatic settling experiments, zeolite-suspended solid presented better removal efficiency of pollutants and greater removal rate of pollutants in turbulent flow.