| 1. |
- Bundschuh, J., et al.
(författare)
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Arsenic in Latin America : New findings on source, mobilization and mobility in human environments in 20 countries based on decadal research 2010-2020
- 2020
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Ingår i: Critical reviews in environmental science and technology. - : Taylor and Francis Inc.. - 1064-3389 .- 1547-6537. ; , s. 1-119
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Forskningsöversikt (refereegranskat)abstract
- Today (year 2020), the globally recognized problem of arsenic (As) contamination of water resources and other environments at toxic levels has been reported in all of the 20 Latin American countries. The present review indicates that As is prevalent in 200 areas across these countries. Arsenic is naturally released into the environment and mobilized from geogenic sources comprising: (i) volcanic rocks and emissions, the latter being transported over thousands of kilometers from the source, (ii) metallic mineral deposits, which get exposed to human beings and livestock through drinking water or food chain, and (iii) As-rich geothermal fluids ascending from deep geothermal reservoirs contaminate freshwater sources. The challenge for mitigation is increased manifold by mining and related activities, as As from mining sites is transported by rivers over long distances and even reaches and contaminates coastal environments. The recognition of the As problem by the authorities in several countries has led to various actions for remediation, but there is a lack of long-term strategies for such interventions. Often only total As concentration is reported, while data on As sources, mobilization, speciation, mobility and pathways are lacking which is imperative for assessing quality of any water source, i.e. public and private.
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| 2. |
- Aad, G, et al.
(författare)
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- 2015
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swepub:Mat__t
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| 3. |
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| 4. |
- Ahmad, Arslan, et al.
(författare)
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Advanced Oxidation-Coagulation-Filtration (AOCF) - An innovative treatment technology for targeting drinking water with <1 μg/L of arsenic
- 2014
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Ingår i: One Century of the Discovery of Arsenicosis in Latin America (1914-2014). - : CRC Press. - 9781138001411 ; , s. 817-819
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Konferensbidrag (refereegranskat)abstract
- Advanced Oxidation-Coagulation-Filtration (AOCF) has been investigated for producing drinking water with less than 1 μg L-1 of As through a series of bench scale and pilot scale experiments. At bench scale, the suitable coagulant, its combination dose with KMnO4 oxidant, the optimum process pH and kinetics of As removal were determined. The optimized AOCF technique was capable of consistently reducing the As concentration to below 1 μg L-1 when implemented at pilot scale and did not adversely affect the already existing removal processes of Fe, Mn and NH4 +. Dual media filter solved the filter run time reduction issue.
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| 5. |
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| 6. |
- Ahmad, Arslan, et al.
(författare)
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Arsenic reduction to < 1 mu g/L in Dutch drinking water
- 2020
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Ingår i: Environment International. - : Elsevier. - 0160-4120 .- 1873-6750. ; 134
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Forskningsöversikt (refereegranskat)abstract
- Arsenic (As) is a highly toxic element which naturally occurs in drinking water. In spite of substantial evidence on the association between many illnesses and chronic consumption of As, there is still a considerable uncertainty about the health risks due to low As concentrations in drinking water. In the Netherlands, drinking water companies aim to supply water with As concentration of < 1 mu g/L - a water quality goal which is tenfold more stringent than the current WHO guideline. This paper provides (i) an account on the assessed lung cancer risk for the Dutch population due to pertinent low-level As in drinking water and cost-comparison between health care provision and As removal from water, (ii) an overview of As occurrence and mobility in drinking water sources and water treatment systems in the Netherlands and (iii) insights into As removal methods that have been employed or under investigation to achieve As reduction to < 1 mu g/L at Dutch water treatment plants. Lowering of the average As concentration to < 1 mu g/L in the Netherlands is shown to result in an annual benefit of 7.2-14 M(sic). This study has a global significance for setting drinking water As limits and provision of safe drinking water.
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| 7. |
- Ahmad, Arslan, et al.
(författare)
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Arsenite removal in groundwater treatment plants by sequential Permanganate-Ferric treatment
- 2018
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Ingår i: Journal of Water Process Engineering. - : ELSEVIER SCIENCE BV. - 2214-7144. ; 26, s. 221-229
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Tidskriftsartikel (refereegranskat)abstract
- The Dutch drinking water sector is actively investigating methods to reduce arsenic (As) to < 1 mu g/L in drinking water supply. We investigated (1) the effectiveness of sequential permanganate (MnO4-)-ferric (Fe(III)) dosing during aeration-rapid sand filtration to achieve < 1 mu g/L As (2) the influence of MnO4--Fe(III) dosing on preestablished removal patterns of As(III), Fe(II), Mn(II) and NH4+ in rapid sand filters and (3) the influence of MnO4--Fe(III) dosing on the settling and molecular-scale structural properties of the filter backwash solids. We report that MnO4--Fe(III) dosing is an effective technique to improve arsenite [As(III)] removal at groundwater treatment plants. At a typical aeration-rapid sand filtration facility in the Netherlands effluent As concentrations of < 1 mu g/L were achieved with 1.2 mg/L MnO4--and 1.8 mg/L Fe(III). The optimized combination of MnO4-and Fe(III) doses did not affect the removal efficiency of Fe(II), Mn(II) and NH4+ in rapid sand filters, however, the removal patterns of Fe(II) and Mn(II) in rapid sand filter were altered, as well as the settling behaviour of backwash solids. The characterization of backwash solids by Fe K-edge X-ray absorption spectroscopy (XAS) and X-ray diffraction (XRD) showed that the changed settling velocity of backwash solids with MnO4-Fe(III) in place was not due to changes in the molecular-scale structure of Fe-precipitates that constitute the major portion of the backwash solids.
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| 8. |
- Ahmad, Arslan, et al.
(författare)
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Characteristics of Fe and Mn bearing precipitates generated by Fe(II) and Mn(II) co-oxidation with O-2, MnO4 and HOCl in the presence of groundwater ions
- 2019
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Ingår i: Water Research. - : Elsevier. - 0043-1354 .- 1879-2448. ; 161, s. 505-516
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Tidskriftsartikel (refereegranskat)abstract
- In this work, we combined macroscopic measurements of precipitate aggregation and chemical composition (Mn/Fe solids ratio) with Fe and Mn K-edge X-ray absorption spectroscopy to investigate the solids formed by co-oxidation of Fe(II) and Mn(II) with O-2, MnO4, and HOCl in the presence of groundwater ions. In the absence of the strongly sorbing oxyanions, phosphate (P) and silicate (Si), and calcium (Ca), O-2 and HOCl produced suspensions that aggregated rapidly, whereas co-oxidation of Fe(II) and Mn(II) by MnO4 generated colloidally stable suspensions. The aggregation of all suspensions decreased in P and Si solutions, but Ca counteracted these oxyanion effects. The speciation of oxidized Fe and Mn in the absence of P and Si also depended on the oxidant, with O-2 producing Mn(III)-incorporated lepidocrocite (Mn/Fe = 0.01-0.02 mol/mol), HOCl producing Mn(III)-incorporated hydrous ferric oxide (HFO) (Mn/Fe = 0.08 mol/mol), and MnO4 producing poorly-ordered MnO2 and HFO (Mn/Fe > 0.5 mol/mol). In general, the presence of P and Si decreased the crystallinity of the Fe(III) phase and increased the Mn/Fe solids ratio, which was found by Mn K-edge XAS analysis to be due to an increase in surface-bound Mn(II). By contrast, Ca decreased the Mn/Fe solids ratio and decreased the fraction of Mn(II) associated with the solids, suggesting that Ca and Mn(II) compete for sorption sites. Based on these results, we discuss strategies to optimize the design (i.e. filter bed operation and chemical dosing) of water treatment plants that aim to remove Fe(II) and Mn(II) by co-oxidation.
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| 9. |
- Ahmad, Arslan, et al.
(författare)
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Deep-dive into iron-based co-precipitation of arsenic : A review of mechanisms derived from synchrotron techniques and implications for groundwater treatment
- 2024
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Ingår i: Water Research. - : Elsevier Ltd. - 0043-1354 .- 1879-2448. ; 249
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Forskningsöversikt (refereegranskat)abstract
- The co-precipitation of Fe(III) (oxyhydr)oxides with arsenic (As) is one of the most widespread approaches to treat As-contaminated groundwater in both low- and high-income settings. Fe-based co-precipitation of As occurs in a variety of conventional and decentralized treatment schemes, including aeration and sand filtration, ferric chloride addition and technologies based on controlled corrosion of Fe(0) (i.e., electrocoagulation). Despite its ease of deployment, Fe-based co-precipitation of As entails a complex series of chemical reactions that often occur simultaneously, including electron-transfer reactions, mineral nucleation, crystal growth, and As sorption. In recent years, the growing use of sophisticated synchrotron-based characterization techniques in water treatment research has generated new detailed and mechanistic insights into the reactions that govern As removal efficiency. The purpose of this critical review is to synthesize the current understanding of the molecular-scale reaction pathways of As co-precipitation with Fe(III), where the source of Fe(III) can be ferric chloride solutions or oxidized Fe(II) sourced from natural Fe(II) in groundwater, ferrous salts or controlled Fe(0) corrosion. We draw primarily on the mechanistic knowledge gained from spectroscopic and nano-scale investigations. We begin by describing the least complex reactions relevant in these conditions (Fe(II) oxidation, Fe(III) polymerization, As sorption in single-solute systems) and build to multi-solute systems containing common groundwater ions that can alter the pathways of As uptake during Fe(III) co-precipitation (Ca, Mg bivalent cations; P, Si oxyanions). We conclude the review by providing a perspective on critical knowledge gaps remaining in this field and new research directions that can further improve the understanding of As removal via Fe(III) co-precipitation.
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| 10. |
- Ahmad, Arslan, et al.
(författare)
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Environmental arsenic in a changing world
- 2019
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Ingår i: Groundwater for Sustainable Development. - : Elsevier. - 2352-801X. ; 8, s. 169-171
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