Evaluation of kinetics and energy consumption of the electrochemical oxidation of Acid Red 73 in aqueous media

A laboratory scale, undivided electrolysis cell with platinum anode and cathode was used for electrochemical oxidation of the azo dye Acid Red 73 in simulated wastewater. The influence of the supporting electrolyte, applied voltage, pH, initial dye concentration and temperature was studied, and decolorization was monitored by UV/Vis spectroscopy. Energy consumption, current efficiency and the electric energy per order have been also determined. With NaCl (1.5 g L^?1) as supporting electrolyte, at a voltage of 6 V, at neutral pH (6.9) and at 25 °C, the solution of the dye (50 mg L^?1) was completely decolorized within 15 min. The apparent activation energy for electrochemical decolorization was determined as ?1.9 kJ mol^?1.     

Seasonal variations in physicochemical characteristics and cyanobacterial diversity of a lake in Northern India

Physicochemical analyses and cyanobacterial diversity of Ramgarh Lake water were performed at five sampling sites during winter, summer, and monsoon seasons. Higher load of solids, carbon, and nutrients were persistent throughout the analysis that indicates the conversion of lake from oligotrophic to eutrophic nature. High nutrients load enhanced cyanobacterial biomass, while low nutrients load produced relatively less biomass. The physicochemical parameters of water samples revealed minimum 2.9 mg L^?1 dissolved oxygen (DO) at site-1 during summer, while maximum (5.6 mg L^?1) at site-4 in monsoon season. Maximum biochemical oxygen demand (BOD) (40 mg L^?1) and chemical oxygen demand (COD) (126 mg L^?1) were recorded at site-1 during summer, whereas minimum BOD (18 mg L^?1) and COD (52 mg L^?1) were evident at site-3 in monsoon season. Minimum concentration of nitrate (0.72 mg L^?1) was recorded at site-3 in summer, whereas maximum 2.7 mg L^?1 was present at site-5 in winter season. The phosphate concentration was maximum (0.52 mg L^?1) at site-5 in summer, and minimum (0.18 mg L^?1) was observed at site-4 in monsoon season. Cyanobacterial diversity was higher during all the seasons, and dominated by the species of Microcystis at all the five sampling sites.     

Development of a complex-based flow injection spectrophotometric method for determination of the herbicide pinoxaden in environmental samples

A flow injection (FI) spectrophotometric method for the determination of the herbicide pinoxaden (PXD) has been proposed. PXD was converted in alkaline media with hydroxylamine hydrochloride to the hydroxamate salt. The salt was reacted with iron(III) chloride, and the absorbance of the red colored tris iron hydroxamate complex was measured at 500?nm using a FI system. The method was found to be linear between 0.5 and 40?mg?L^?1 with a molar absorptivity of 1.53?×?10^4?L?mol^?1?cm^?1. The limit of detection and limit of quantification were found to be 0.1?±?0.01?mg?L^?1 and 0.6?±?0.05?mg?L^?1, respectively. Any interference of fenoxaprop-p-ethyl (FE) was avoided by the separation of PXD by liquid chromatography with a mixture of dichloromethane and n-hexane (1?:?1) as eluent. The method was applied to the determination of PXD in soil, water, and wheat grains with percent recoveries of 98?±?2, 100?±?2, and 98?±?5, respectively. Sample throughput of 60 samples per hour was achieved under optimized conditions.     

Application of water extract of slippery elm tree leaves as a natural reagent for selective spectrophotometric determination of trace amounts of molybdenum(VI) in environmental water samples

A novel spectrophotometric method for the determination of molybdenum(VI) by using a natural reagent, water extract of slippery elm tree leaves, is developed. Molybdenum(VI) reacts with this natural reagent to form an orange colored product. The formed product shows maximum absorbance at 418 nm with a molar absorptivity value of 0.57 × 10⁴ L mol^?1 cm^?1, and this method is linear in the 0.4–10 mg L^?1 concentration range. The detection limit value was found to be 0.0350 mg L^?1. The proposed method is simple, clean, low cost, selective, and sensitive. It was applied to the analytic samples with satisfactory results.     

Daily dietary fluoride intake in rural villages of the Ethiopian Rift Valley

Dental and skeletal fluorosis is widespread in the Ethiopian Rift Valley region. Drinking water has been considered the main reason for the development of fluorosis, but dietary intake may also be a contributor in areas with high concentration of fluoride in water, soil, and biota. The purpose of this study is to assess the total daily dietary fluoride intake by adults in a rural part of the Ethiopian Rift Valley. The food, beverage, and water samples were collected from selected households of three neighboring villages with similar dietary pattern, but with different fluoride content in their water sources. Village A uses water with 1.0 mg L^?1 fluoride, village B uses water with 3.0 mg L^?1 fluoride, and village C uses water with 11.5 mg L^?1 fluoride both for food preparation and for drinking. The level of fluoride was determined in all food ingredients, in the prepared food, beverages, and in the water used for food preparation and drinking. Recipe and food frequency questionnaires were used to gather household food preparation and consumption patterns. An alkali fusion method was used for digestion of food samples and for subsequent determination of fluoride with ion-selective electrode. The daily fluoride intake varied depending on its concentration in the water used for cooking and drinking. In households using water with 1 mg L^?1, 3 mg L^?1, and 11.5 mg L^?1 fluoride, the total personal intake was found to be 10.5, 16.6, and 35.3 mg d^?1, respectively. Contribution of the water to the daily fluoride intake was 33%, 58%, and 86%, respectively. Even in households using water containing fluoride at a concentration of 1 mg L^?1, the daily intake was higher than the recommended safe intake of 1.5–4.0 mg d^?1 for adults, which indicates that the fluoride intake through food may cause health risks. Minimizing the fluoride concentration in water to the lowest possible level will greatly reduce the daily intake. The form of fluorine (organic or inorganic) in the food items and the associated health risk factors need further investigation.     

Acetaldehyde contamination of water,alcoholic, and non-alcoholic beverages stored in glass or plastic bottles

Acetaldehyde is a naturally found chemical in food substances characterized by a fruity aroma at low levels. However, high levels of acetaldehyde can add to or change the taste of foods and beverages. More importantly, acetaldehyde has recently been found to be possibly carcinogenic to humans (Group 2B). In this investigation, the amounts of acetaldehyde in several alcoholic and non-alcoholic beverages consumed in Greece, including red or white wine, retsina, tsipouro, grappa, fruit-based liqueurs, beers with different alcohol content as well as mineral water, soft drinks, and fruit juices were measured. The analytical method used is based on derivatization of acetaldehyde with 2,4-dinitrophenylhydrazine and its subsequent measurement using high performance liquid chromatography. High concentrations (median, min–max) were detected in grappa (29.4, 29.2–52.7 mg L^?1) and tsipouro (17.1, 0.8–55.6 mg L^?1), followed by beer (6.8, 6.7–6.9 mg L^?1) and red wine (3.7, 1.6–29.4 mg L^?1); the lowest levels were detected in soft drinks (0.067, 0.033–0.075 mg L^?1) and mineral water (0.04, 0.002--0.096 mg L^?1). Levels of acetaldehyde in retsina were very high (68.1, 63.9--68.3 mg L^?1) when after opening, the wine remained in plastic bottles for a long time, much higher than in samples taken from just opened bottles (7.2, 7.1–7.4 mg L^?1). The amount of acetaldehyde shows some positive correlation to the alcoholic content. These results suggest that regulatory measures and consumer guidance may be necessary for acetaldehyde in beverages.     

Cloud point extraction of trace cyanide from environmental waters for indirect flame atomic absorption spectrometric determination

A method has been developed for indirect determination of cyanide in environmental waters based on cloud point extraction (CPE), preconcentration and determination by flame atomic absorption spectrometry (FAAS). The method was based on reduction of Cu(II) to Cu(I) in the presence of cyanide and complexation of the produced Cu(I)(CN)₂^? with gallocyanin (GC⁺) as an ion-pairing reagent at pH 4.0, followed by its extraction into polyethyleneglycol mono-p-nonylphenylether (Ponpe 7.5). Selectivity was improved with the use of suitable masking agents. Various factors influencing separation and preconcentration of cyanide have been investigated, and conditions were optimized, allowing determination of cyanide in the range of up to 1.2 mg L^?1 with a detection limit of 0.00045 mg L^?1. The method has been applied to the determination of cyanide in environmental waters, the results being in agreement with those obtained by a reference method.     

Toxicity of cadmium nanoparticles to Bacillus subtilis

The study deals with the toxicological impact of cadmium nanoparticles (Cd NPs) on Bacillus subtilis as a model Gram-positive bacterium. Cadmium oxide (CdO) NPs (～22 nm) and cadmium sulfide (CdS) NPs (～3 nm) were used in this study. Both the NPs were found to inhibit the cell viability of B. subtilis when added to the culture at mid-log phase, the viable cell number declined with increasing concentration of Cd NPs. At mid-log phase, 15 mg L^?1 CdO NPs inhibited growth by ～50%, whereas at 30 mg L^?1 growth completely ceased. Under the same conditions, CdS NPs inhibited growth by ～50% at a concentration of 8 mg L^?1, and at 20 mg L^?1 growth was completely retarded. The cells changed their morphological features to a filamentous form with increasing Cd NPs exposure time, leading to associated with clumping. NPs treated cells when stained with 4′, 6-diamino-2-phenylindole, showed filamentous multinucleated bead structure, suggesting irregularities in cell division. Increasing intracellular oxidative stress due to Cd NPs exposure might be one of the reasons for the cell morphological changes and toxicity in B. subtilis.     

Effect of calcium and magnesium on copper,cadmium, and some essential elements of Indian major carps Labeo rohita (Hamilton) and Catla catla (Hamilton) treated with copper and cadmium

The effect of calcium and magnesium either singly or in combination on accumulation of cadmium and copper in Labeo rohita (rohu) and Catla catla (catla) was investigated in this study under laboratory conditions. The investigation showed that copper accumulation in rohu exposed to 0.25 mg L^?1 of copper for 14 days reduced from 31.0 ± 0.4 mg kg^?1 at no calcium/magnesium treatment to 3.5 ± 0.2 and 2.2 ± 0.1 mg kg^?1, respectively, at 75 mg L^?1 calcium or magnesium treatment. The copper level in catla exposed to 0.20 mg L^?1 of copper for 14 days reduced from 5.7 ± 0.1 mg kg^?1 at no calcium/magnesium treatment to 3.4 ± 0.2 and 3.3 ± 0.1 mg kg^?1, respectively, at 300 mg L^?1 calcium or magnesium treatment. The cadmium accumulation in rohu exposed to 0.20 mg L^?1 of cadmium for 14 days reduced from 1.7 ± 0.1 mg kg^?1 at no magnesium treatment to 1.4 ± 0.1 mg kg^?1 at 120 mg L^?1 magnesium treatment. The cadmium accumulation in catla exposed to 0.20 mg L^?1 of cadmium for 14 days reduced from 0.8 ± 0.2 mg kg^?1 at no magnesium treatment to 0.6 ± 0.2 mg kg^?1 at 80 mg L^?1 magnesium treatment. Copper and cadmium treatments also reduced some essential microelements of rohu and catla. Both the fishes restored these elements at different levels of calcium and magnesium.     

Green chemistry approach to analysis of formic acid and acetic acid in aquatic environment by headspace water-based liquid-phase microextraction and high-performance liquid chromatography

A simple and totally organic-free (green) method, viz. headspace water-based liquid-phase microextraction combined with high-performance liquid chromatography-ultraviolet detection has been successfully developed for analysis of formic acid and acetic acid in environmental water samples. A microdrop of an aqueous solution of sodium hydroxide was suspended from the tip of a microsyringe needle over the headspace of the stirred sample solution containing the analytes at pH 1.0 for a given time. The microdrop was then retracted into the microsyringe, diluted with HPLC mobile phase, and injected to HPLC. Optimum efficiency has been achieved for: 3.0 µL NaOH microdrop (0.1 mol L^?1) exposed for 15 min over the headspace of an aqueous sample of 6.5 mL at 55 °C, containing 15% w/v of Na₂SO₄, adjusted to pH = 1.0 and stirred at 750 rpm. Under these conditions, enrichment factors of 162 and 187, limits of detection of 0.3 and 0.1 µg L^?1 (S/N = 3) with dynamic linear ranges of 1–500 and 0.5–500 µg L^?1 were obtained for formic acid and acetic acid, respectively. A reasonable repeatability (5.8% ≤ RSD ≤ 8.8%, n = 6) and satisfactory linearity (r² ≥ 0.997) illustrated the performance of the method.     

Preconcentration of samarium with modified yeast cells for its determination by atomic emission spectroscopy

A chelating-modified biosorbent is produced by coupling of a dye, procion red, to yeast cells. The resulting modified cells have been characterized by Fourier transform infrared, elemental analysis and thermogravimetric analysis and studied for preconcentration and determination of trace Sm(III). The optimum pH value for sorption of the samarium ions is 6.2. The sorption capacity of functionalized modified yeast cells is 7.2 mg g^?1. Recovery was 99% when Sm(III) was eluted with an aqueous solution of 0.1 mol L^?1 ethylenediaminetetraacetic acid. Scatchard analysis suggested that binding sites were homogeneous. The equilibrium data were analyzed using Langmuir, Freundlich, Temkin, and Redlich–Peterson isotherm models, and the respective constants were determined as 1.0 (L mg^?1), 2.9 [(mg g^?1) (L mg^?1)^1/n], 2.4 × 10⁸ (L g^?1), and 30 (dm³ g^?1) at 20 °C. The method was applied for an Sm(III)-containing sample of ceramic industry effluent.     

Spectrophotometric methods for determination of vanadium: a review

Vanadium (V) is widely used industrially, and plays an important role in the biosphere. Sensitive and reliable analytical methods to determine V in various kinds of samples are of extensive interest. Mainly two spectrophotometric methods developed in the last decade are discussed, namely complex formation methods and catalytic methods. The former is based on either oxidation or reduction of V leading to coloured complexes with proper reagents; they are applicable to determination of V at the mg L^?1 level. Catalytic methods are based on the ability of V to catalyse the oxidation of various organic dyes and are applicable to determination at the μg L^?1 level. Both methods are used for determination of V in environmental and biological samples.     

Mercury pollution in the Sonbhadra district of Uttar Pradesh,India, and its health impacts

The Sonbhadra district in the Singrauli area of Uttar Pradesh, India, has many coal mines and thermal power plants and is a critically polluted area. Many residents of this area reported adverse health conditions which may be linked to metal pollution, especially of mercury investigated here.

In May 2012, samples of water (23), soil (7), blood, hair, and nails from persons showing adverse health conditions selected at random were collected and analyzed for total mercury by atomic absorption spectrometry.

Twenty percent drinking water samples contained mercury from 3 to 26 μg L^?1 (3–26 times the permissible limit). Soil samples had 0.5–10.1 mg kg^?1 Hg.

The average concentrations of mercury in human blood, hair, and nails were found to be 34 μg L^?1, 7.4 mg kg^?1, and 0.8 mg kg^?1, respectively. Mercury concentrations in the blood of these persons were 45 and 28 μg L^?1 on average in the case of men and women. This is much higher than the safe level of 5.8 μg L^?1 set by the United States Environmental Protection Agency (USEPA).

It was concluded that all residents of Sonbhadra sampled could be suffering from mercury toxicity as the area is polluted by Hg released from the coal-fired thermal power plants.     

The effects of evening primrose oil on arsenic-induced oxidative stress in rats

Forty-eight male Wistar albino rats were allocated to the four groups such that each comprised 12 animals. The first group was maintained as the control. In group 2, evening primrose oil was administered at a dose of 0.1 mL rat^?1 day^?1 (～500 mg kg^?1 bw) into the stomach via gavage, whilst in group 3 sodium arsenide was administered at a concentration of 100 mg L^?1 in ad-libitum drinking water for 30 days. The fourth group was given 0.1 mL rat^?1 day^?1 evening primrose oil into the stomach via gavage plus 100 mg L^?1 of sodium arsenide in ad-libitum drinking water for 30 days. At the end of the 30th day, tissue (liver, lung, kidney, brain, heart, spleen, and testis) and blood samples were collected from each group. Malondialdehyde (MDA) and nitric oxide (NO) levels and superoxide dismutase, catalase and glutathione peroxidase activities were measured in the samples. Exposure to arsenic in rats causes oxidative stress by increasing lipid peroxidation (increase of MDA and NO levels) and altering the activity of antioxidant enzymes. Evening primrose oil did not have any adverse effects. Furthermore, it was ascertained that the administration of arsenic with evening primrose oil reduced the severity of oxidative stress.     

Acute toxicity of 30 pharmaceutically active compounds to freshwater planarians,Dugesia japonica

Pharmaceutically active compounds are produced worldwide and consumed in large quantities, so these chemicals are frequently detected in limnic environments posing potential ecological risks. Thirty pharmaceutically active compounds were selected for examination of their acute toxicity for freshwater planarians (Dugesia japonica). Among the 30 compounds tested, diclofenac, mefenamic acid, naproxen, propranolol HCl, and diphenhydramine HCl had a 48-h nominal LC₅₀ below10 mg L^?1, and for 18 chemicals, it exceeded 100 mg L^?1. The 96-h nominal LC₅₀ was below 10 mg L^?1 for diclofenac, mefenamic acid, naproxen, propranolol HCl, diltiazem HCl, diphenhydramine HCl, hydroxyzine HCl, and triprolidine HCl, and for 15 chemicals, it exceeded 100 mg L^?1. Among different therapeutic groups, analgesics were most toxic to planarians, and antibiotics were least toxic. Antihistamines and beta blockers varied in their acute toxicity to planarians. At the current environmental levels, none of the tested pharmaceutically active compounds may have acutely harmful impacts on aquatic invertebrates. To answer the question whether chronic, long-term exposure to pharmaceutically active compounds may entail ecological risks for aquatic ecosystems, further investigations with different end points in multiple species tests are needed.     

Evaluation of the toxicity of tetrabromobisphenol A and some of its oxidation products using a micro-scale algal growth inhibition test

A micro-scale algal growth inhibition (μ-AGI) test using a common micro-plate based fluorometric detection was used to demonstrate the effects of humic substances (HSs) on the toxicity of tetrabromobisphenol A (TBBPA) and its oxidative decomposition products 2,5-dibromo-1,4-benzoquinone (2,5-DBBQ), 2,5-dibromohydroquinone (2,5-DBHQ), 2,6-dibromobenzoquinone (2,6-DBBQ), and 2,6-dibromophenol (2,6-DBP) to Pseudokirchneriella subcapitata. The EC₅₀ values were: EC_50(TBBPA) = 7 mg L^?1, EC_50(2,5-DBHQ) = 7 mg L^?1, EC_50(2,5-DBBQ) = 19 mg L^?1, EC_50(2,6-DBP) = 49 mg L^?1, and EC_50(2,6-DBBQ) = 13 mg L^?1. The toxicity of the chemicals was slightly lower in the presence of HA. The toxicity of TBBPA decomposed by a biomimetic catalytic system consisting of iron (III) 5,10,15,20-tetrakis (p-sulfonatophenyl) porphyrin (Fe(III)-TPPS) and KHSO₅ was also evaluated using P. subcapitata and Chlamydomonas reinhardtii.     

Polyphenol contents of five of medicinal plants from Cameroon and effects of their extracts on antioxidant capacities of human breast cancer cells

The aim of the study was to investigate the antiproliferative properties of extracts of five plants on breast cancer cells (MDA-MB-231) and their effects on antioxidant activities. The total phenol contents of the extracts were determined to establish a correlation to their antiproliferative effects which were evaluated by the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide viability assay. Enzymes involved in oxidative stress were also determined. Total polyphenol contents of the five extracts varied from 170 to 440 mg L^?1 of gallic acid per mg of extract with the highest value for the extract of Sida cordifolia. Cell growth inhibition was observed within 24 h, with inhibitory concentration values ranging from 7.3 to 25 mg L^?1 depending on plant extract. At concentrations between 100 and 200 mg L^?1, all the extracts exhibited significant reduction of cell proliferation in time-dependent and linear manner. The activities of superoxide dismutase and catalase of cells treated for 24 h with the extract of S. cordifolia were 3.5 U per mg protein and 8 mole H₂O₂ consumed per min per mg protein higher than those of cells treated with an extract of Viscum album.     

A fast and reliable method for quantitative determination of total mercury in vegetables

A cloud-point extraction (CPE) process using the nonionic surfactant, polyethylene glycol tert octylphenyl ether (Triton X-114) was employed for determination of Hg(II) ions in aqueous solutions. The method is based on the ion-pairing reaction of Hg(II) with Pyronin B (PyrB⁺) in the presence of excess iodide at pH 6.0 and extraction of the complex formed. The chemical variables affecting CPE efficiency were studied, and the analytical characteristics of the method were obtained. The calibration curves were linear in the range of 1–40 μg L^?1 with the detection limits of 0.35 and 0.30 μg L^?1 at 556 and 521 nm. Selectivity was also tested. The coefficients of variation of the method are 2.4% and 5.2% for five replicate measurements of mercury at levels of 10 and 25 μg L^?1, respectively. The results obtained for two certified reference samples were in a good agreement with the certified values. The method was applied to the determination of total mercury in vegetable samples.     

Impacts of sublethal lead exposure on the hemato-immunological parameters in tilapia (Oreochromis mossambicus)

The effects of exposure of tilapia (Oreochromis mossambicus) to sublethal concentrations of lead on hematological and immunological parameters were investigated. The fish were semistatically exposed to low (L) (0.5 mg L^?1), medium (M) (2.5 mg L^?1), and high (H) (5 mg L^?1) lead concentrations for 14 days. At the end of the trial, red blood cell (RBC) count, hematocrit (Hct) ratio and hemoglobin levels showed significant decreases in M and H groups, while RBC was significantly increased in L group compared to control group. Lysozyme activity showed a decrease in all groups on day 14 compared to control. A decrease in myeloperoxidase activity was seen in M and H groups on day 7, and in all treatment groups on day 14. In conclusion, it was found that exposure of O. mossambicus to lead concentrations affected hematological and immunogical parameters adversely.     

Effects of zinc stress on growth and antioxidant enzyme responses of Kandelia obovata seedlings

This study evaluated the tolerance and accumulation potential in the mangrove Kandelia obovata under moderate and high levels of external Zn. A greenhouse experiment was conducted to investigate the effects of a range of external Zn concentrations (0–400 mg L^?1) on the growth of this species by counting the lateral root number and measuring the root length, leaf area, and total dry biomass. We also determined the Zn accumulation in plant tissues. K. obovata survived with external Zn concentrations of up to 400 mg L^?1, although the excess metal resulted in a biomass reduction of 34%. A significant increase in antioxidant enzyme activities occurred in roots of plants under high-level Zn stress, suggesting that K. obovata seedlings could tolerate up to 200 mg L^?1 zinc treatment.