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Boiling water before drinking or using it for cooking is a general practice especially in areas where portable water is not readily available. However, boiling water in an aluminum pot could be a route of entry of heavy metals into humans. This study assessed the genotoxic and mutagenic potential of boiled water samples from aluminum pots of different duration of use using the SOS chromotest on Escherichia coli PQ37 and the Ames fluctuation test on Salmonella typhimurium strains TA98 and TA100, respectively. Three aluminum pots from the same manufacturer but of different years of use (6-year-old, 3-year-old, and new aluminum pots) were used for the experiment. Six selected heavy metals (Cadmium, Copper, Arsenic, Nickel, Lead, and Aluminum) were also analyzed in the samples using an Atomic Absorption Spectrophotometer (AAS Buck, Scientific model 210 VGP). Cadmium, Copper, Arsenic, Nickel, Lead, and Aluminum were present in all the test water samples at concentrations that were higher than the maximum limit allowable by standard regulatory organizations. The concentrations of these metals in the samples also increased as the duration of use of the aluminum pots increased. The results further showed that the water boiled in the three aluminum pots is mutagenic and genotoxic in both Ames fluctuation and SOS chromotests. The 6-year-old aluminum pot induced the highest mutagenicity and genotoxicity followed by the 3-year-old aluminum pot. The metals in the tested samples were believed to be responsible for the observed mutagenicity and genotoxicity in the microbial assays. The findings of this study revealed that cooking with Aluminum pots could lead to the leaching of heavy metals into food, and pose mutagenic and genotoxic risks to consumers.

It is estimated that around 140 million people are drinking highly contaminated water with arsenic (As) as a natural earth’s crust component. On the other hand, the prevalence of neurodegenerative disorders, especially Alzheimer’s disease, is constantly increasing. The aim of the present study was to investigate the correlation between oral arsenic trioxide exposure and its impact on tau protein phosphorylation at Ser262. Fifty-four male mice were randomly divided into three groups and were freely accessed to food and contaminated water of 1 and 10 ppm arsenic trioxide for 3 months, except for control subjects. At the end of each month, As concentration and tau phosphorylation were checked with graphite furnace atomic absorption spectrometer and western blot analysis, respectively. Surprisingly, it was observed that the amount of measured brain arsenic in 10 ppm-exposed subjects was significantly increased after 3 months (P-value ˂ 0.0001). The significant changes in tau phosphorylation were not seen in the 1 ppm-exposed subjects, and it was observed that Ser262 phosphorylation significantly increased after 2 and 3 months in the 10 ppm group (P-value < 0.05). Our results demonstrated that arsenic accumulated in the brain time-dependently and increased Ser262 tau phosphorylation, which is very important in several tauopathies. In conclusion, it could be inferred that environmental arsenic exposure even at very low concentrations could be considered as a reason for increasing the risk of developing neurodegenerative disease.

An optical colorimetric and smartphone-integrated paper device (SIPD) is demonstrated for determination of As (III) in water and soil samples using sucrose modified gold nanoparticles (AuNPs/Suc) as a nanoprobe. The mechanism for determination of As(III) is experimentally validated by performing UV-Vis, transmission electron microscope (TEM), Fourier transforms infra-red spectroscopy (FTIR) and dynamic light scattering (DLS) measurements. The density function theory (DFT) calculations using B3LYP with 6-311G (2d,2p) and LANL2DZ basis sets is used to theoretically prove the mechanism for determination of As(III). In addition, the paper fabricated with AuNPs/SuC was used as a nanoprobe for quantitative determination of As(III) using smartphone and ImageJ software. Calibration plot was linear over 10–800 μgL−1 for colorimetric determination of As(III) with limit of detection (LOD) of 4 μgL−1 acquired when the absorbance ratio obtained at 594 nm/515 nm. The linearity range of 50–3000 μgL−1 with LOD of 20 μgL−1 was determined using smartphone-integrated paper device. AuNPs/Suc is successfully employed for determination of As (III) from contaminated water and soil samples in colorimetry and SIPD.

Submitted by Vivian Rosa Storti (vivian.storti@unesp.br) on 2019-08-23T15:03:10Z No. of bitstreams: 1 fraceto_lf_preprint_soro_ecodesignedpaper.pdf: 1703375 bytes, checksum: 0750647a29c04919959a376041b2d4d3 (MD5) Approved for entry into archive by Luana Priscila Costa (luana@reitoria.unesp.br) on 2019-08-23T17:53:29Z (GMT) No. of bitstreams: 1 fraceto_lf_preprint_soro_ecodesignedpaper.pdf: 1703375 bytes, checksum: 0750647a29c04919959a376041b2d4d3 (MD5) Made available in DSpace on 2019-08-23T17:53:29Z (GMT). No. of bitstreams: 1 fraceto_lf_preprint_soro_ecodesignedpaper.pdf: 1703375 bytes, checksum: 0750647a29c04919959a376041b2d4d3 (MD5) Previous issue date: 2019-07 Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) In this study we reported the development of a paper-based algal biosensor for the optical detection of nanoencapsulated-atrazine, a forefront nanoformulated herbicide with a high effective postemergence herbicidal activity. In particular, the unicellular green photosynthetic algae Chlamydomonas reinhardtii was immobilised on a paper substrate soaked with an agar thin film and placed in a glass optical measurement cell, obtaining a totally environmental-friendly device. Nanoencapsulated-atrazine was detected by following the variable fluorescence (1-VJ) parameter, which decreased inversely proportional to the herbicide concentrations, in a range between 0.5 and 200 nM, indicating a linear relationship in the measured dose-response curves and a detection limit of 4 pM. Interference studies resulted in a very slight interference in presence of 0.5 ppm copper and 10 ppb arsenic at safety limits, as well as a slight matrix effect and a satisfactory recovery value of 96 ± 5 % for 75 nM nanoencapsulated-atrazine in tap water. Stability studies were also performed obtaining a good storage stability up to 3 weeks. Results demonstrated the suitability of the proposed paper-based optical biosensor as a valid support in smart agriculture for on site, environmentally friendly, cost effective and sensitive nanoencapsulated-atrazine analysis Preprint Institute of Crystallography, National Research Council, Department of Chemical Sciences and Materials Technologies Department of Chemical Science and Technologies, Università di Roma Tor Vergata São Paulo State University (UNESP), Institute of Science and Technology of Sorocaba, Laboratory of Environmental Nanotechnology FAPESP: 2017/21004-5

The efficiency of combining iron sulfate and organic amendments (paper mill sludge, olive mill waste compost and olive tree pruning biochar) for the remediation of an As- and Cu-contaminated soil was evaluated. Changes in As and Cu fractionation and solubility due to the application of the amendments was explored by leachate analysis, single and sequential extractions. Also, the effects on Arrhenatherum elatius growth, germination of Lactuca sativa and toxicity to the bacteria Vibrio fischeri were assessed. The combination of iron sulfate and the organic amendments efficiently reduced As solubility and availability through the formation of amorphous iron oxides, while organic matter did not seem to mobilize As. At the same time, copper fractionation was strongly affected by soil pH and organic matter addition. The soil pH significantly influenced both As and Cu mobility. Within all the amendments tested, FeSO4 in combination with compost showed to be the most suitable treatment for the overall remediation process, as it reduced As and Cu availability andenhanced soil nutrient concentrations and plant growth. In sipte of contradictory trends between chemical analyses and ecotoxicity tests, we can still conclude that the application of organic amendments in combination with reactive iron salts is a suitable approach for the remediation of soils contaminated by Cu and As.

Paper is one of the most commonly used food packaging materials. During the production of packaging paper, it is possible for trace amounts of heavy metals to be incorporated as contaminants. These could migrate into food when packaging paper (food contact paper) is used for cooking, storing and eating. The aim of this study was to determine the migration of lead (Pb) and arsenic (As) from food contact paper into a food simulant and then to assess human safety through the estimated daily intake (EDI) with consumption factor. Migration tests were conducted for 310 samples using 4% acetic acid as a food simulant at 25°C for 10 min and at 95°C for 30 min. Concentrations of Pb and As in a food simulant were quantified by inductively coupled plasma mass spectrometry. LODs for Pb and As were 0.002 and 0.005 µg L

This paper describes the development of simple, sustainable, and low-cost strategies for signal enhancement on paper-based carbon platforms through gold nanoparticles electrogenerated from small volumes of tetrachloroauric (III) acid solutions. Carbon ink is deposited on a hydrophilic working area of the paper delimited with hydrophobic wax. This maskless procedure is fast and cuts down ink waste. The connection of this working electrode to the potentiostat is ensured with the use of screen-printed electrodes (SPEs). Close contact of the whole area of both carbon electrodes improves the precision of the nanostructuration. Resulting gold-modified paper-based carbon working electrodes (AuNPs-PCWEs) were characterized by cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), scanning electron microscopy (SEM), and electron dispersion X-ray spectrometry (SEM/EDX). This methodology was applied for the first time to the inorganic arsenic determination in commercial white wines by chronoamperometric stripping of the electrodeposited As(0). In an optimized system, As(III) was reduced and deposited as As(0) on the nanostructured surface by applying a potential of −0.3 V during 180 s. Then, anodic stripping chronoamperometry was performed at +0.4 V. The analytical signal was the current recorded at 30 s. On the other hand, As(V) was chemically reduced to As(III) with 0.2 M KI, and total determination of arsenic could be carried out. As(V) was determined as the difference between total As and As(III).Then, this fast, simple and low-cost method can be employed for speciation purposes. Limits of detection for As(III) and total arsenic (in the presence of KI) are 2.2 μg L−1 and 2.4 μg L−1, respectively, and indicate that this method is suitable for regulated quality control., This work has been supported by the Spanish Ministry of Economy and Competitiveness (MINECO) under Projects CTQ2011-25814 and CTQ2014-58826-R. E. Nunez-Bajo thanks MINECO for the award of a Ph.D. Grant BES-2012- 056713. Authors thank Prof. E. Blanco-Gonzalez, Prof. M. Montes-Bayon, and J. García-Fernández from the Departamento de Quimica Física y Analí tica, Universidad de Oviedo, for kindly determining the total arsenic concentration in white wines by ICP-MS.

In this study, four ten years test areas with covered tailings were geochemically evaluated. Three areas were covered with a fly ash and an overlying sludge layer, and one only with a sludge cover, originating from paper mills. The accumulation of As, Fe and Pb in sludge layers, originating from air-borne dust and the depletion of K, Na and P from both cover layers were observed. High release of elements from tailings was observed in the comparison profile due to oxidation and weathering of tailings. In only sludge covered area, the leaching of elements from tailings decreased. In the profiles with thin ash (20 cm and 30 cm), most elements were retained in tailings with pH 7–9. In the profile with the thickest ash (50 cm), elements such as As, Cd, Cu, Mg, Mn, Pb, S and Zn were depleted in the uppermost tailings with pH above 11 and retained deeper in the zone with pH 7–8, which implied that large quantities of fly ash increased the oxidation and weathering of tailings and mobility of elements. Elements excluding K, never reached the groundwater in high concentrations in the covered areas, while the comparison area had high Ca, K, Mn and S concentrations.

The objective of this World Bank technical assistance has been to support the Government of Bangladesh’s (GoB) national capacity development framework for improving water and sanitation services (WSS) in Bangladesh, focusing on demand-responsive peer-to-peer or horizontal learning processes and improve horizontal accountability communication and monitoring systems to track progress in the sector. This technical assistance is in line with the World Bank country assistance strategy (CAS) which seeks to support the GoB target of ensuring safe drinking water and sanitation for all. It has contributed to strengthening the long-term capacity of the government, in particular the union Parishad (UP) which is responsible for ensuring water and sanitation services for all in Bangladesh.

Over the last decade, the use of ethylenediaminetetraacetic acid (EDTA) has increased by a factor of three within the Swedish pulp industry. The effects of pulp mill wastewater in combination with EDTA on metal mobility and the consequences for ecologically relevant organisms have been studied. Ethylenediaminetetraacetic acid was added to pulp mill effluent water in the laboratory and compared to wastewater without EDTA. Degradation of the water was followed over a experimental period up to eight weeks and samples were taken five times for chemical analysis and at the beginning and the end for biological tests. Half a year later, the experiment was repeated. The results from both experiments showed that EDTA markedly increased the solubility of zinc, cadmium, lead, iron, nickel, and copper, whereas the solubility of vanadium, molybdenum, thallium, arsenic, and chromium was not changed by the presence of EDTA. No measurable degradation of EDTA occurred even after 5.5 months. The toxicity of the pulp mill effluent water was low, and only a slight toxic effect was observed on the reproduction of Ceramium strictum. The most pronounced effect was a stimulation in the growth of three algal species in 5 to 20% (v/v) total effluent wastewater with and without EDTA. The presence of EDTA in the dissolved fraction of the pulp mill effluent water increased the growth stimulation in 20 to 40% (v/v), possibly because of the increased availability of essential metals like iron, zinc, and copper. The capacity of the pulp mill wastewater to support algal growth was nearly as good as a rich nutrient medium for algae. The combination of poorly degradable EDTA and the increasing availability of metals might further enhance eutrophication in the recipient areas of pulp mills.

A field study was developed in a new landfill for refuse from construction and demolition (C&D) material recovery plants of small size (4 Ha.) in Europe, with the aim of evaluating the liquid and gas emissions in this type of facility at a large scale. It included characterization of the materials, monitoring leachate and gas quantity and composition. Besides thermometers, piezometers and sampling ports were placed in several points within the waste. This paper presents the data obtained for five years of the landfill life. The materials disposed were mainly made up of wood and concrete, similar to other C&D debris sites, but the amount of gypsum drywall (below 3% of the waste) was significantly smaller than other available studies, where percentages above 20% had been reported. Leachate contained typical C&D pollutants, such as different inorganic ions and metals, some of which exceeded other values reported in the literature (conductivity, ammonium, lead and arsenic). The small net precipitation in the area and the leachate recirculation into the landfill surface help explain these higher concentrations, thus highlighting the impact of liquid to solid (L/S) ratio on leachate characteristics. In contrast to previous studies, neither odor nuisances nor significant landfill gas over the surface were detected. However, gas samples taken from the landfill inside revealed sulfate reducing and methanogenic activity.

International audience; The literature on the presence of heavy metals in contaminated wastes is reviewed. Various categories of materials produced from domestic and industrial activities are included, but municipal solid waste, which is a more complex material, is excluded. This review considers among the most abundant the following materials - wood waste including demolition wood, phytoremediation scavengers and chromated copper arsenate (CCA) timber, sludges including de-inking sludge and sewage sludge, chicken litter and spent pot liner. The partitioning of the metals in the ashes after combustion or gasification follows conventional behaviour, with most metals retained, and higher concentrations in the finer sizes due to vaporisation and recondensation. The alkali metals have been shown to catalyse the biomass conversion, particularly lithium and potassium, although other metals are active to a lesser extent. The most prevalent in biomass is potassium, which is not only inherently active, but volatilises to become finely distributed throughout the char mass. Because the metals are predominantly found in the ash, the effectiveness of their removal depends on the efficiency of the collection of particulates. The potential for disposal into soil depends on the initial concentration in the feed material.

International audience; Rivers used for drinking water production might be subject to anthropogenic pollution discharge upstream of the intake point. This problem was investigated in the case of the Moselle River, used for water production in Nancy (350,000 inhabitants) and which might be impacted by industrial activities 60 km upstream. The arsenic flux of a pulp and paper mill discharging in the Moselle River at this location has been more specifically investigated. The main sources of arsenic in that mill seemed to be the recovered papers and the gravel pit water used as feed water. The arsenic input related to wood and bark was limited. The main arsenic outputs from the plant were the paper produced on site and the deinking sludge. The arsenic concentration in the effluent of the wastewater treatment plant (WWTP) was not correlated to the one in the gravel pit water, but may depend on the operating conditions of the WWTP or the changes in processes of the mill. The impact of this anthropogenic source of arsenic on the Moselle River was slightly larger in summer, when the flowrate was lower. Globally the impact of the paper mill on the Moselle River water quality was limited in terms of arsenic.

Article, WASTE MANAGEMENT. 29(3):1192-1197 (2009)

Most arsenic bearing solid residuals (ABSR) from water treatment will be disposed in nonhazardous landfills. The lack of an appropriate leaching test to predict arsenic mobilization from ABSR creates a need to evaluate the magnitude and mechanisms of arsenic release under landfill conditions. This work studies the leaching of arsenic and iron from a common ABSR, granular ferric hydroxide, in a laboratory-scale column that simulates the biological and physicochemical conditions of a mature, mixed solid waste landfill. The column operated for approximately 900 days and the mode of transport as well as chemical speciation of iron and arsenic changed with column age. Both iron and arsenic were readily mobilized under the anaerobic, reducing conditions. During the early stages of operation, most arsenic and iron leaching (80% and 65%, respectively) was associated with suspended particulate matter, and iron was lost proportionately faster than arsenic. In later stages, while the rate of iron leaching declined, the arsenic leaching rate increased greater than 7-fold. The final phase was characterized by dissolved species leaching. Future work on the development of standard batch leaching tests should take into account the dominant mobilization mechanisms identified in this work: solid associated transport, reductive sorbent dissolution, and microbially mediated arsenic reduction.

Due to the enactment of a stricter drinking water standard for arsenic in the United States, larger quantities of arsenic will be treated resulting in larger volumes of treatment residuals. The current United States Environmental Protection Agency recommendation is to dispose spent adsorbent residuals from arsenic treatment into non-hazardous municipal solid waste (MSW) landfills. The potential of microorganisms to alter the speciation affecting the mobility of arsenic in the disposal environment is therefore a concern. The purpose of this paper was to evaluate the potential of an anaerobic microbial consortium to biologically mobilize arsenate (As(V)) adsorbed onto activated alumina (AA), a common adsorbent used for treating arsenic in drinking water. Three anaerobic columns (0.27 l) packed with 100 g dry weight of AA containing 0.657 mg adsorbed As(V) (expressed as arsenic) per gram dry weight were continuously flushed with synthetic landfill leachate for 257 days. The fully biologically active column was inoculated with methanogenic anaerobic sludge (10 g volatile suspended solids l(-1) column) and was operated with a mixture of volatile fatty acids (VFA) in the feed (2.5 g chemical oxygen demand l(-1) feed). At the end of the experiment, 37% of the arsenic was removed from the column, of which 48% was accounted for by arsenical species identified in the column effluent. The most important form of arsenic eluted was arsenite (As(III)), accounting for nearly all of the identified arsenic in periods of high mobilization. Additionally, two methylated metabolites, methylarsonic acid and dimethylarsinic acid were observed. Mobilization of arsenic is attributed to the biological reduction of As(V) to As(III) since literature data indicates that As(III) is more weakly adsorbed to AA compared to As(V). Batch and continuous assays confirmed that VFA, present in landfill leachates, served as an electron donating substrate supporting enhanced rates of As(V) reduction to As(III). Two control columns, lacking inoculum and/or VFA in the feed displayed low mobilization of arsenic compared to the fully biologically active column. Therefore, leachates generated in MSW landfills could potentially result in the biologically catalyzed mobilization of arsenic from As(V)-laden drinking water residuals.

A survey of 32 paper and board materials intended for food contact has been undertaken. Sample composition was analysed to identify chemicals with a potential to migrate to foods. Representative materials covering a range of uses such as aqueous and fatty foods, and use at ambient and elevated temperatures, were obtained from industry. The samples were examined in their unfinished state, even where the final form would have included lamination to plastics, printing, or other treatments. A comprehensive and systematic analytical approach was applied which included determination of volatiles by headspace GC-MS, extraction using water, ethanol and chloroform with subsequent analysis by GC-MS and HPLC, and multi-element screening by ICP-MS. The solvent extracts were also weighed to determine the total amount of material available for migration. A large number of volatile substances were identified with alkyl and aryl aldehydes predominating in the majority of samples. Substances identified in solvent extracts included 2,6-di-tert-butyl-4-hydroxytoluene (BHT), di-tert-butylphenol, benzophenone, 4,4'-bis(dimethyl amino) benzophenone (Michler's ketone), triphenyl methane, bicyclohexylphenylphenanthrene carboxylic acid (and its methyl ester) and abietic acid. Levels of these substances were however generally below 1 mg/kg paper. Of the inorganic elements, arsenic and mercury were not detected above the limits of determination of 1.8 and 0.4 mg/kg respectively in any of the 10 samples examined. Cadmium was detected in teabag tissue and in unbleached Kraft paper at 0.3 mg/kg. Chromium was present in seven samples at 1.1-7.8 mg/kg, whilst lead was present in nine of the 10 samples at levels ranging from 0.3 to 5.9 mg/kg.