Intergrated approach for microbiological impact assessment of public wastewater treatment plants

Wastewaters are a source of pathogenic micro-organisms in the environment. The microbial load and residues found in the final effluents of wastewater-treatment plants (WWTPs) depend on the WWTPs' abatement capacity and the final disinfection treatment systems applied to wastewaters before discharge into water. A historical database with data on surface and marine-coastal water quality and on the characterization of WWTP effluents was made using data from 1997 to 2004 to assess the microbiologic impact along the coast of the Venice province (Italy, northern Adriatic sea). The monitoring of river and sea discharges along the coast is integrated with the application of the Synthetic Pluriennal Faecalization Index (ISPF). The experimental study was conducted in the period from November 2002 to April 2004 by the Veneto Regional Environmental Prevention and Protection Agency. The results of this investigation on faecal contamination together with previous data are presented with a preliminary performance characterization of the WWTPs' disinfection technologies (sodium hypochlorite, peracetic acid, UV rays, and ozone).     

Seasonal differences in treatment efficiency of a set of stabilization ponds in a semi-arid region

This article aims to determine the significant differences of the seasonal changes of pH, chemical oxygen demand (COD), biological oxygen demand (BOD), and total suspended solids (TSS) parameters in a wastewater stabilization pond. The variation of these parameters followed the seasonal pattern of temperature. The mean seasonal pH of the influent wastewater ranged between 7.8 (in spring) and 7.9 (in summer), while in the final effluents it was between 7.9 (in winter) and 8.3 (in summer). The mean seasonal COD of the influent wastewater ranged between 650?mg?L^?1 in spring and 600?mg?L^?1 in autumn, whereas in the effluents it was between 150?mg?L^?1 in autumn and 270?mg?L^?1 in spring. The mean seasonal BOD₅ of the influent wastewater ranged between 360?mg?L^?1 in autumn and 390?mg?L^?1 in winter, whereas in the effluents it was between 66?mg?L^?1 in summer and 130?mg?L^?1 in winter. The results showed that the percent removals of COD, BOD₅ and TSS from final effluents were maximum in summer for COD and BOD₅ (76%), summer (83%) and for TSS in winter (78%), respectively. Data analysis showed that there were significant differences between parameters of pH, COD, BOD₅ and TSS at four different seasons (p?相似文献   

Photoelectrochemical treatment of ammonium using seawater as a natural supporting electrolyte

In the present study, a photoelectrochemical process containing seawater as a natural low-cost supporting electrolyte was used to remove ammonium from wastewater in a continuous flow mode. Based on central composite design (CCD), response surface methodology (RSM) was employed to evaluate the performance of the process in ammonia removal. The effect of four main independent parameters, including initial ammonium concentration, hydraulic retention time (HRT), current intensity and initial pH on the removal of ammonia was evaluated by the model. The optimal initial ammonium concentration, HRT, current intensity and initial pH were 917 mg NH ₄? N;·L ^?1, 108 min, 1.8 A and 8.4, respectively. The high coefficients (R ²=0.97 and adjusted R ²=0.94) obtained by the analysis of variance (ANOVA) demonstrated close correlation between predicted and experimental values. Also, treating the reject water from the sludge dewatering unit as an ammonium-rich wastewater showed the effectiveness of the process for treating real wastewaters (86% ammonium removal). The results revealed that the present process can be an efficient method for ammonium removal from polluted effluents in coastal areas based on the availability of seawater as a cost-efficient supporting electrolyte.     

Removal and recovery of uranium(VI) by adsorption onto a lignocellulosic-based polymeric adsorbent containing amidoxime chelating functional group

A new adsorbent (ABS) with amidoxime functional group was prepared through graft polymerization of acrylonitrile onto banana stem (BS) using ceric ammonium nitrate (CAN)/HNO₃ initiator system, followed by treatment with hydroxylamine hydrochloride in alkaline solution. Infrared spectroscopy, surface area analyzer, thermogravimetry, and potentiometric titration were used for the characterization of the adsorbent. Effective removal of U(VI) ions was demonstrated at the pH range 4.0–6.0. The mechanism for the removal of U(VI) ions by ABS was based on complexation adsorption model. Equilibrium was achieved in approximately 3 h. The experimental kinetic data were analyzed using first-order, second-order, and Elovich kinetic models, and are well fitted with second-order kinetics. The temperature dependence indicates an exothermic process. U(VI) adsorption was found to decrease with increase of ionic strength. The Freundlich isotherm model fitted the experimental equilibrium data well. The adsorption efficiency was tested using synthetic nuclear industry effluents. The maximum adsorption capacity for U(VI) removal was found to be 80 mg g^-1 at 20°C. Adsorbed U(VI) ions were desorbed effectively, about 99% by 0.2 M HCl. Repeated adsorption/desorption cycles show the feasibility of the ABS for the removal of U(VI) ions from water and nuclear industry effluents.     

Synthesis and characterization of an ion exchanger based on tamarind kernel powder and its application for removal of some metal ions from industrial effluents

A resin synthesized from tamarind kernel powder possesses high selectivity for metal ions. Distribution coefficients for some metal ions has been determined by the batch method. The influence of pH on ion exchange capacity and K _d value of metal ions were studied. The resin has been characterized by Fourier transform infrared spectroscopy, thermogravimetric analysis, chemical composition and ion exchange capacity (IEC). The selectivity order is Pb²⁺?>?Cu²⁺?>?Fe²⁺?>?Zn²⁺?>?Ni²⁺. Removal of metal ions from the aqueous solution and from effluents of a steel mill has been studied.     

The effect of selenium on fluoride — clay interactions: Possible environmental health implications

Previous epidemiological studies have shown that dental fluorosis is endemic in the lowland, dry zone of Sri Lanka, which is considered to be an area in which excessive quantities of fluorides are present in the drinking water supplies. It has been found that kaolinitic clay forms a suitable raw material in the defluoridation of water.It is shown that there is a noticeable effect of selenium and media pH on the reactions involved in the interaction of fluoride with clay. In this study, 1 mM fluoride solutions containing SeO ₃ ^2– (selenite) concentrations of 0 mM, 0.1 mM, 0.5 mM and 1 mM were used in the reactions with kaolinitic clay. The effect of pH was monitored in the range 4 to 8. It was observed that fluoride adsorption was maximum at a pH of 5.6 without either SeO ₃ ^2– or SeO ₄ ^2– , the adsorption capacity being 15.2 mol F^– g^–1 clay. However, when the SeO ₃ ^2– concentration was increased up to 0.5 mM at this optimum pH, the adsorption capacity reduced to 12.8 mol F^– g^–1 clay. Monitoring of the effect of SeO ₄ ^2– and media pH on fluoride adsorption showed that when the SeO ₄ ^2– concentration increases from zero to 0.1 mM, there is a reduction of fluoride adsorption capacity. However, when the SeO ₄ ^2– concentration is further increased from 0.1 mM to 1.0 mM, there was an increase in the fluoride adsorption capacity, indicating a more consistent effect of SeO ₃ ^2– on fluoride-kaolinitic clay interaction than SeO ₄ ^2– .Fluoride concentrations in drinking water supplies have a marked effect on dental health and the geochemistry of selenium appears to play an important role in the geochemical mobility of fluoride ions.     

Ethylenediamine-modified activated carbon for aqueous lead adsorption

This study is to develop a carbon-based adsorbent containing multiple functional ligands for effective removal of lead ions from aqueous media. Activated carbon was oxidized by nitric acid, followed by chlorination with thionyl chloride and reaction with ethylenediamine. Modified activated carbon (MAC) was characterized using scanning electron microscopy in conjunction of energy dispersive spectroscopy (SEM-EDS), Fourier transform infrared spectroscopy (FT-IR), and potentiometric titration. Surface characterizations confirmed that carboxyl, amine, and chlorine functional groups were effectively introduced onto the carbon surface by the treatments. The modifications lowered the pH at the point of zero charge (pH_pzc) from 9.6 to 2.55 and resulted in more negatively charged surfaces. Adsorptive experiments showed that aqueous Pb removal by MAC was faster, with a 62% higher capacity than the original activated carbon (60.2 vs. 37.2 mg g⁻¹).     

Biological treatments of textile industrial effluents in Lagos metropolis, Nigeria

The assessment of the effluents from two textile industries in Ilupeju in Lagos metropolis, Nigeria showed that they were high in conductivity, biochemical oxygen demand (BOD), chemical oxygen demand (COD), total dissolved solids (TDS) and contained traces of heavy metals like Ca, Zn but high concentrations of Cr and Pb. These wastewaters are normally discharged into neighbouring water bodies. Five bacterial groups, namely Micrococcus sp., Enterobacter sp., Alcaligens sp., Bacillus sp. and Acinetobacter sp. were isolated from these effluents. They were used individually for biotreatment and found to be able to utilize the components of the wastewaters for growth, Bacillus sp. and Acinetobacter sp. being the most efficient utilizers as they were able to reduce BOD to zero. The total viable count (TVC) increased significantly depicting growth of the bacterial population. The pH was regulated from 3.4-6.80 for NSF effluent and 12.2-10.29 for STI effluent. The work emphasises the level of industrial pollution in our environment as wastes are indiscrimately dumped into surrounding water bodies in urban areas, the textile industry being a case study. The treatment of any form of waste before disposal into the environment is important and ensures safety of the populace.     

Efficient oxidation of bisphenol A with oxysulfur radicals generated by iron-catalyzed autoxidation of sulfite at circumneutral pH under UV irradiation

There is actually a need for efficient methods to clean waters and wastewaters from pollutants such as the bisphenol A endocrine disrupter. Advanced oxidation processes currently use persulfate or peroxymonosulfate to generate sulfate radicals. There are, however, few reports on the use of sulfite to generate sulfate radicals, instead of persulfate or peroxymonosulfate, except for dyes. Here we studied the degradation of the bisphenol A using iron(III) as catalyst and sulfite as precursor of oxysulfur radicals, at initial pH of 6, under UV irradiation at 395 nm. The occurrence of radicals was checked by quenching with tert-butyl alcohol and ethanol. Bisphenol A degradation products were analyzed by liquid chromatography coupled with mass spectrometry (LC–MS). Results reveal that iron(III) or iron(II) have a similar oxidation efficiency. Quenching experiments show that the oxidation rate of bisphenol A is 47.7 % for SO ₄ ^·? , 37.3 % for SO ₅ ^·? and 15 % for HO^·. Bisphenol A degradation products include catechol and quinone derivatives. Overall, our findings show that the photo-iron(III)–sulfite system is efficient for the oxidation of bisphenol A at circumneutral pH.     

Soil washing of As-contaminated stream sediments in the vicinity of an abandoned mine in Korea

A soil washing process was applied to remediate arsenic (As)-contaminated stream sediments around an abandoned mine in Goro, Korea. Laboratory scale soil washing experiments for As-contaminated stream sediments were performed under various washing conditions in order to maximize As removal efficiency. Stream sediments were taken from two sites (S1 and S5) along the main stream connected to an abandoned mine. Stream sediments at the two sites were divided into two groups (≥0.35 and <0.35 mm in diameter), giving four types of sediments, which were thereupon used for soil washing experiments. The results of soil washing experiments involving various pH conditions suggested that As removal efficiency is very high in both strongly acidic and basic solutions (pH 1 and 13), regardless of sediment type. Removal efficiencies for fine sediments from S1 and S5 were >95% after 1 h of washing with 0.2 M citric acid (C₆H₈O₇). When using 0.2 M citric acid mixed with 0.1 M potassium phosphate (KH₂PO₄), the As removal efficiency increased to 100%. When recycled washing solution was applied, As removal efficiency was maintained at a level greater than 70%, even after eight recycling events. This suggests that the recycling of washing solution could be successfully applied as a means of decreasing the cost of the washing process. Results from the experiments suggest that soil washing is a potentially useful process for the remediation of As-contaminated stream sediments around abandoned mines.     

Differential toxic response of Chironomus travalensis kieffer ( Chironomidae : Diptera ) to some industrial effluents

Acute toxicity testing of some industrial effluents (rubber (Rr), brewery (Br), and bottling (Bt)) on Chironomus travalensis (Diptera larvae) was determined at 96-h using a static bioassay technique. Effluent quality characterization revealed acidic pH values of 4.5 for Rr, 5.64 for Br, and 4.32 for Bt effluents. Tests were carried out in replicates between 10 and 100% effluent concentrations. Mortality rate rose progressively with increasing concentrations. Bt effluent was the most toxic with 96-h LC₅₀ of 61.5%, closely followed by Rr effluent with 96-h LC₅₀ of 87% and the least toxic was Br effluent with 96-h LC₅₀ of 90%.     

Potential fluoride contamination in the drinking water of Marks Nagar,Unnao district,Uttar Pradesh,India

This study was conducted in the summer season (May, 2007). The fluoride concentration along with other physico-chemical parameters in ground water samples was determined in Marks Nagar of Unnao district, Uttar Pradesh (India), since it is the only source of drinking water for the villagers. The fluoride concentration in the water varied from 0.8 to 13.9 mgl⁻¹ with a mean of 4.02 mgl⁻¹. The correlation analysis revealed that fluoride had a positive correlation with pH, CO₃, HCO₃, and sodium adsorption ratio (SAR), whereas a negative correlation with Ca and Mg was found. A soil profile was also dug in the area to assess depth-wise fluoride content in the soil. The soil samples and underneath calcium carbonate (CaCO₃) concretion were analyzed for fluoride content. The percent of soluble fluoride to total fluoride in the soil varied from 25.15 to 4.76% down the soil profile. The soluble fluoride was found to decrease with the increase in the clay content in the soil. The total leachable fluoride in CaCO₃ concretions was found to be 6.08%. It was inferred from this study that the soil and underneath layer of CaCO₃ concretions may be the potential source of fluoride contamination in the shallow drinking water sources of the area.     

Treatment of organic pollutants by homogeneous and heterogeneous Fenton reaction processes

Nowadays, the water ecosystem is being polluted due to the rapid industrialization and massive use of antibiotics, fertilizers, cosmetics, paints, and other chemicals. Chemical oxidation is one of the most applied processes to degrade contaminants in water. However, chemicals are often unable to completely mineralize the pollutants. Enhanced pollutant degradation can be achieved by Fenton reaction and related processes. As a consequence, Fenton reactions have received great attention in the treatment of domestic and industrial wastewater effluents. Currently, homogeneous and heterogeneous Fenton processes are being investigated intensively and optimized for applications, either alone or in a combination of other processes. This review presents fundamental chemistry involved in various kinds of homogeneous Fenton reactions, which include classical Fenton, electro-Fenton, photo-Fenton, electro-Fenton, sono-electro-Fenton, and solar photoelectron-Fenton. In the homogeneous Fenton reaction process, the molar ratio of iron(II) and hydrogen peroxide, and the pH usually determine the effectiveness of removing target pollutants and subsequently their mineralization, monitored by a decrease in levels of total organic carbon or chemical oxygen demand. We present catalysts used in heterogeneous Fenton or Fenton-like reactions, such as H₂O₂–Fe³⁺(solid)/nano-zero-valent iron/immobilized iron and electro-Fenton-pyrite. Surface properties of heterogeneous catalysts generally control the efficiency to degrade pollutants. Examples of Fenton reactions are demonstrated to degrade and mineralize a wide range of water pollutants in real industrial wastewaters, such as dyes and phenols. Removal of various antibiotics by homogeneous and heterogeneous Fenton reactions is exemplified.     

Unexpected toxicity decrease during photoelectrochemical degradation of atrazine with NaCl

This report shows an unexpected toxicity decrease during atrazine photoelectrodegradation in the presence of NaCl. Atrazine is a pesticide classified as endocrine disruptor occurring in industrial effluents and agricultural wastewaters. We therefore studied the effects of the degradation method, electrochemical and electrochemical photo-assisted, and of the supporting electrolyte, NaCl and Na₂SO₄, on the residual toxicity of treated atrazine solutions. We also studied the toxicity of treated atrazine solutions using Artemia nauplii. Results show that at initial concentration of 20 mg L⁻¹, atrazine was completely removed in up to 30 min using 10 mA cm⁻² electrolysis in NaCl medium, regardless of the electrochemical method used. The total organic carbon removal by the photo-assisted method was 82% with NaCl and 95% with Na₂SO₄. The solution toxicity increased during sole electrochemical treatment in NaCl, as expected. However, the toxicity unexpectedly decreased using the photo-assisted method. This finding is a major discovery because electrochemical treatment with NaCl usually leads to the formation of toxic chlorine-containing organic degradation by-products.     

Hydroxyl radical generation by redox cycling of some chemotherapeutic antibiotics

The anticancer drugs: adriamycin, farmorubicin and mitomycin C greatly enhance the generation of hydroxyl radicals (HO^.) from H₂O₂ in the presence of Co(II) ions (CoCl2) at pH 7.4 and 8, as measured by the deoxyribose assay. Catalase, hydroxyl radical scavengers (mannitol, cysteine, glutathione, thiourea, lactic dehydrogenase) inhibited the degradation of deoxyribose confirming that HO‐radicals are responsible for the degradation of the carbohydrate.     

Development and application of cross-linked polyethylenimine for trace metal and metalloid removal from mining and industrial wastewaters

Pollution of water bodies by trace metals is an established problem and several studies have been conducted to deal with it. South Africa is amongst those countries whose water systems are most affected as a result of intensive mining activities. This research was dedicated to the development of an insoluble chelating polymer for use as an adsorbent for abstraction of metal ions from mining and industrial wastewaters. Polyethylenimine (PEI), well known for its metal chelating potential, was cross-linked by epichlorohydrin (ECH) in order to convert it into a water-insoluble form for direct use as an adsorbent. The binding affinity of the cross-linked polyethylenimine (CPEI) to heavy metal ions was assessed as well as its ability to be regenerated for re-use. CPEI exhibited good complexation ability to metal ions with high affinity to Cr and most divalent metal ions. The observed order of complexation was: Cr?>?Zn>?Fe?>?Ni?>?Mn?>?Pb. On the other hand, it showed very poor ability to bind oxo-anions such as SeO₃ ^2? and AsO₂ ^? which has been attributed to the unavailability of suitable functional groups to interact with these ions.     

Treatment of biologically treated effluents from baker's yeast industry by membrane and ozone technologies

This paper presents pilot‐scale membrane treatment results performed on biologically treated effluents from fermentation industry and ozone oxidation on concentrates from the same membrane treatment system. The results obtained from the ultrafiltration (UF) and/or the reverse osmosis (RO) systems indicate that membrane treatment are very effective for COD, Color, NH₃‐N and conductivity removal. Ozone oxidation of the membrane concentrates was tested to increase biodegradability of the wastes. The initial ratios of Biochemical oxygen demand (BOD₅) to Chemical oxygen demand (COD) were increased significantly by applying chemicaloxidation with O₃ and O₃ + H₂O₂.     

Geochemistry of soil around a fluoride contaminated area in Nayagarh District,Orissa, India: Factor analytical appraisal

Fluoride contamination in soil was studied in the vicinity of a hot spring in Nayagarh district of Orissa. Both bulk soil from 0 to 30 cm depth and profile soils from 0 to 90 cm depth were analyzed for total fluoride (F_t) and 0.01 M CaCl₂ extractable fluoride (F_ca), major elements, pH, EC and Organic Carbon (OC). High concentrations of both F_t and F_ca were observed in the area surrounding the hot spring and the village of Singhpur. Principal factor analysis (PFA) on the parameters of the bulk soils suggests that two major chemical processes due to three factors, control the soil geochemistry of the area. Factor-1 contributes 37.11% of the total variance and is strongly loaded with Al, Si, Fe, F_tand F_ca, and explains the fluoride enrichment of the soil, whereas the second and the third factors contribute 16.6 and 12.2%, respectively and explain the controlling process of carbonate precipitation and soil alkalinity. Multiple regression analysis of the scores of the factors was performed to derive a fluoride contamination index in soil. The magnitude of the factor effect on the contamination index follows the order of Factor-1 > Factor-2 > Factor-3. The spatial distribution of the contamination index is used to classify the area into highly contaminated, moderately contaminated and uncontaminated zones.     

Removal of the herbicide amitrole from water by anodic oxidation and electro-Fenton

Here we demonstrate that an aqueous solution of the herbicide amitrole can be completely depolluted at pH 3.0 by anodic oxidation and electro-Fenton process. Anodic oxidation gives faster degradation with a boron-doped diamond anode than with a Pt anode. Electro-Fenton with a Pt anode and 1 mmol l ^–1 Fe²⁺ as catalyst yields the quickest depollution. Amitrole decay always follows a pseudo first-order reaction. NO₃^– and NH₄⁺ are accumulated in the medium during mineralization, although volatile N-products are also formed. These environmentally friendly electrochemical treatments could be applied to the remediation of wastewaters containing amitrole.     

Evaluation of porous cup soil‐water samplers under laboratory conditions: Comparison of ceramic and PTFE cups

Three different types of soil solution samplers (two ceramic cups and PTFE) were tested in the laboratory to validate their use for collecting soil‐water samples and for monitoring the chemical composition of soil solutions. Interactions between porous materials and chemical solutions were examined under different experimental conditions for several major cations (Ca²⁺, Mg²⁺, Na⁺ and K⁺) and anions (HCO^‐ ₃, NO^‐ ₃, SO₄ ^2‐ and Cl^‐) and for several minor ions (NH⁺ ₄, NO^‐ ₄, PO₄ ^3‐and B).

The results show that ceramic cups are not inert for bicarbonate, calcium and phosphate ions. Their use is only valid for a limited number of ions such as chloride and nitrate which, however, are the most studied ions in field experiments. PTFE cups have less restrictions although their use in measuring sulphates, phosphates and ammonium presents some problems.

Choosing the appropriate type of cup depends on the objectives. In any case, laboratory experiments must be performed before installation.