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  • 1
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    Unknown
    Publication Date: 2021-03-29
    Keywords: letter; apology letter ; 551 ; Chlorine ; Iron ; Lindane ; Palladium ; Water Pollutants, Chemical ; Water Purification
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  • 2
    Publication Date: 2021-03-29
    Description: Despite two decades of intensive laboratory investigations, several aspects of contaminant removal from aqueous solutions by elemental iron materials (e.g., in Fe(0)/H2O systems) are not really understood. One of the main reasons for this is the lack of a unified procedure for conducting batch removal experiments. This study gives a qualitative and semi-quantitative characterization of the effect of the mixing intensity on the oxidative dissolution of iron from two Fe(0)-materials (materials A and B) in a diluted aqueous ethylenediaminetetraacetic solution (2 mM EDTA). Material A (fillings) was a scrap iron and material B (spherical) a commercial material. The Fe(0)/H2O/EDTA systems were shaken on a rotational shaker at shaking intensities between 0 and 250 min(-1) and the time dependence evolution of the iron concentration was recorded. The systems were characterized by the initial iron dissolution rate (k(EDTA)). The results showed an increased rate of iron dissolution with increasing shaking intensity for both materials. The increased corrosion through shaking was also evidenced through the characterization of the effects of pre-shaking time on k(EDTA) from material A. Altogether, the results disprove the popular assumption that mixing batch experiments is a tool to limit or eliminate diffusion as dominant transport process of contaminant to the Fe(0) surface.
    Keywords: Co-precipitation; EDTA; corrosion products; Reactivity; Zerovalent iron ; 551 ; Chelating Agents ; Corrosion ; Edetic Acid ; Iron ; Kinetics ; Metals ; Oxidation-Reduction ; Rotation ; Solubility ; Solutions
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  • 3
    Publication Date: 2021-03-29
    Keywords: Thiobencarb; Herbicides; Zero valent iron (ZVI); Removal; Wastewater treatment ; 551 ; Iron ; Magnesium ; Thiocarbamates ; Water Pollutants, Chemical ; Water Purification ; Zinc
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  • 4
    Publication Date: 2021-03-29
    Description: A central aspect of the contaminant removal by elemental iron materials (Fe0 or Fe0 materials) is that reduction reactions are mediated by the iron surface (direct reduction). This premise was introduced by the pioneers of the reactive wall technology and is widely accepted by the scientific community. In the meantime enough evidence has been provided to suggest that contaminant reduction through primary corrosion products (secondary reductants) does indeed occur (indirect reduction). It was shown for decades that iron corrosion in the pH range of natural waters (4-9) inevitably yields an obstructive oxide film of corrosion products at the metal surface (oxide film). Therefore, contaminant adsorption on to corrosion products and contaminant co-precipitation with corrosion products inevitably occurs. For adsorbed and coprecipitated contaminants to be directly reduced the oxide film should be electronic conductive. This study argues through a literature review a series of points which ultimately lead to the conclusion that, if any quantitative contaminant reduction occurs in the presence of Fe0 materials, it takes place within the matrix of corrosion products and is not necessarily a direct reduction. It is concluded that Fe0 materials act both as source of corrosion products for contaminant adsorption/coprecipitation and as a generator of FeII and H2 (H) for possible catalytic contaminant reduction.
    Keywords: Adsorption; Co-precipitation; Elemental Iron; Groundwater; Remediation ; 551 ; Adsorption ; Corrosion ; Iron ; Oxidation-Reduction ; Water ; Water Pollutants
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  • 5
    Publication Date: 2021-03-29
    Keywords: Adsorption; Co-precipitation, Nanoscale iron; Reduction; Zerovalent iron ; 551 ; Environmental Remediation ; Iron ; Nanotechnology ; Water Pollutants
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  • 6
    Publication Date: 2021-03-29
    Description: The further development of Fe(0)-based remediation technology depends on the profound understanding of the mechanisms involved in the process of aqueous contaminant removal. The view that adsorption and co-precipitation are the fundamental contaminant removal mechanisms is currently facing a harsh scepticism. Results from electrochemical cementation are used to bring new insights in the process of contaminant removal in Fe(0)/H(2)O systems. The common feature of hydrometallurgical cementation and metal-based remediation is the heterogeneous nature of the processes which inevitably occurs in the presence of a surface scale. The major difference between both processes is that the surface of remediation metals is covered by layers of own oxide(s) while the surface of the reducing metal in covered by porous layers of the cemented metal. The porous cemented metal is necessarily electronic conductive and favours further dissolution of the reducing metal. For the remediation metal, neither a porous layer nor a conductive layer could be warrant. Therefore, the continuation of the remediation process depends on the long-term porosity of oxide scales on the metal surfaces. These considerations rationalized the superiority of Fe(0) as remediation agent compared to thermodynamically more favourable Al(0) and Zn(0). The validity of the adsorption/co-precipitation concept is corroborated.
    Keywords: Adsorption; Cementation, Co-precipitation; Surface scale; Zerovalent Iron ; 551 ; Adsorption ; Aluminum ; Chemical Precipitation ; Electrochemical Techniques ; Environmental Remediation ; Iron ; Metals ; Water Pollutants, Chemical ; Zinc
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  • 7
    Publication Date: 2021-03-29
    Keywords: Nano zero valent iron; Nitrate reduction; Nitrogen balance; Kinetic modelling ; 551 ; Iron ; Nitrates
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  • 8
    Publication Date: 2021-03-29
    Description: The author used a recent article on lindane reductive dechlorination by Fe/Pd bimetallics to complain that dozen of published works in several journals are not conform to the state-of-the-art knowledge on the mechanism of aqueous contaminant removal by metallic iron (e.g. in Fe(0)/H(2)O systems). It is shown that the contribution of adsorbed Fe(II) to the process of contaminant reduction has been neglected while discussing the whole process of contaminant reduction in the presence of bimetallics.
    Keywords: Adsorption; Bimetallic Co-precipitation; Iron corrosion; Zerovalent iron ; 551 ; Chlorine ; Hazardous Substances ; Insecticides ; Iron ; Lead ; Lindane ; Nanoparticles
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  • 9
    Publication Date: 2021-03-29
    Description: The term mixing (shaking, stirring, agitating) is confusing because it is used to describe mass transfer in systems involving species dissolution, species dispersion and particle suspension. Each of these mechanisms requires different flow characteristics in order to take place with maximum efficiency. This work was performed to characterize the effects of shaking intensity on the process of aqueous discoloration of methylene blue (MB) by metallic iron (Fe(0)). The extent of MB discoloration by three different materials in five different systems and under shaking intensities varying from 0 to 300 min(-1) was directly compared. Investigated materials were scrap iron (Fe(0)), granular activated carbon (GAC), and deep sea manganese nodules (MnO(2)). The experiments were performed in essay tubes containing 22 mL of the MB solution (12 mg/L or 0.037 mM). The essay tubes contained either: (i) no reactive material (blank), (ii) 0-9.0 g/L of each reactive material (systems I, II and III), or (iii) 5g/L Fe(0) and 0 to 9.0g/L GAC or MnO(2) (systems IV and V). The essay tubes were immobilized on a support frame and shaken for 0.8-5 days. Non-shaken experiments lasted for duration up to 50 days. Results show increased MB discoloration with increasing shaking intensities below 50 min(-1), a plateau between 50 and 150 min(-1), and a sharp increase of MB discoloration at shaking intensities 〉or=200 min(-1). At 300 min(-1), increased MB discoloration was visibly accompanied by suspension of dissolution products of Fe(0)/MnO(2) and suspension of GAC fines. The results suggest that, shaking intensities aiming at facilitating contaminant mass transfer to the Fe(0) surface should not exceed 50 min(-1).
    Keywords: Adsorption; Co-precipitation; Methylene Blue; Shaking Intensity; Zerovalent Iron. ; 551 ; Color ; Coloring Agents ; Iron ; Manganese Compounds ; Methods ; Methylene Blue ; Oxides
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  • 10
    Publication Date: 2021-03-29
    Keywords: EDTA; Electrochemical reactivity; Operational parameters; Water Remediation; Zerovalent iron ; 551 ; Edetic Acid ; Iron ; Kinetics ; Solubility
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  • 11
    Publication Date: 2021-03-29
    Description: The syntrophic community between anaerobic methanotrophic archaea and sulfate reducing bacteria forms thick, black layers within multi-layered microbial mats in chimney-like carbonate concretions of methane seeps located in the Black Sea Crimean shelf. The microbial consortium conducts anaerobic oxidation of methane, which leads to the formation of mainly two biomineral by-products, calcium carbonates and iron sulfides, building up these chimneys. Iron sulfides are generated by the microbial reduction of oxidized sulfur compounds in the microbial mats. Here we show that sulfate reducing bacteria deposit biogenic iron sulfides extra- and intracellularly, the latter in magnetosome-like chains. These chains appear to be stable after cell lysis and tend to attach to cell debris within the microbial mat. The particles may be important nuclei for larger iron sulfide mineral aggregates.
    Keywords: Biogenic Iron Minerals; Methane; Microbial Mat ; 551 ; Anaerobiosis ; Archaea ; Bacteria ; Black Sea ; Calcium Carbonate ; Geologic Sediments ; Iron ; Methane ; Microbial Consortia ; Oxidation-Reduction ; Seawater ; Sulfates ; Sulfides ; Sulfur-Reducing Bacteria
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  • 12
    Publication Date: 2021-03-29
    Description: The interpretation of processes yielding aqueous contaminant removal in the presence of elemental iron (e.g. in Fe(0)/H(2)O systems) is subject to numerous complications. Reductive transformations by Fe(0) and its primary corrosion products (Fe(II) and H/H(2)) as well as adsorption onto and co-precipitation with secondary and tertiary iron corrosion products (iron hydroxides, oxyhydroxides, and mixed valence Fe(II)/Fe(III) green rusts) are considered the main removal mechanisms on a case-to-case basis. Recent progress involving adsorption and co-precipitation as fundamental contaminant removal mechanisms have faced a certain scepticism. This work shows that results from electrocoagulation (EC), using iron as sacrificial electrode, support the adsorption/co-precipitation concept. It is reiterated that despite a century of commercial use of EC, the scientific understanding of the complex chemical and physical processes involved is still incomplete.
    Keywords: Adsorption; Co-precipitation; Electrocoagulation; Flocculation; Zerovalent iron ; 551 ; Adsorption ; Electrochemistry ; Electrocoagulation ; Electrodes ; Environmental Remediation ; Flocculation ; Hydrogen-Ion Concentration ; Iron ; Metals ; Oxides ; Water ; Water Pollutants, Chemical ; Water Purification
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  • 13
    Publication Date: 2021-03-29
    Keywords: 1,1,2,2-Tetrachloroethane Reactions; ; 551 ; Carbon Isotopes ; Chemical Fractionation ; Chemistry Techniques, Analytical ; Chromium ; Copper ; Environmental Monitoring ; Ethane ; Hydrocarbons, Chlorinated ; Hydrogen-Ion Concentration ; Hydroxides ; Iron ; Water Pollutants, Chemical
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  • 14
    Publication Date: 2021-03-29
    Description: A simple method is proposed for testing the reactivity of elemental iron materials (Fe(0) materials) using methylene blue (MB) as reagent. The method is based on the oxidative reactivity of Fe(II) for reductive dissolution of MnO(2). Fe(II) is produced in-situ by the oxidation of a Fe(0) material. The in-situ formed Fe(II) reacted with MnO(2) delaying the bulk precipitation of iron corrosion products and thus MB co-precipitation (MB discoloration). For a given MnO(2), the extent of MB discoloration delay is a characteristic of individual Fe(0) materials under given experimental conditions. The MB discoloration method for testing the reactivity of Fe(0) materials is facile, cost-effective and does not involve any stringent reaction conditions.
    Keywords: Adsorption; Co-precipitation; Methylene blue; Manganese oxides; Reactivity; Zerovalent iron ; 551 ; Color ; Iron ; Manganese Compounds ; Methylene Blue ; Oxides ; Water
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  • 15
    Publication Date: 2021-03-29
    Description: Metallic iron (Fe(0)) is a moderately reducing agent that has been reported to be capable of reducing many environmental contaminants. Reduction by Fe(0) used for environmental remediation is a well-known process to organic chemists, corrosion scientists and hydrometallurgists. However, considering Fe(0) as a reducing agent for contaminants has faced considerable scepticism because of the universal role of oxide layers on Fe(0) in the process of electron transfer at the Fe(0)/oxide/water interface. This communication shows how progress achieved in developing the Becher process in hydrometallurgy could accelerate the comprehension of processes in Fe(0)/H(2)O systems for environmental remediation. The Becher process is an industrial process for the manufacture of synthetic rutile (TiO(2)) by selectively removing metallic iron (Fe(0)) from reduced ilmenite (RI). This process involves an aqueous oxygen leaching step at near neutral pH. Oxygen leaching suffers from serious limitations imposed by limited mass transport rates of dissolved oxygen across the matrix of iron oxides from initial Fe(0) oxidation. In a Fe(0)/H(2)O system pre-formed oxide layers similarly act as physical barrier limiting the transport of dissolved species (including contaminants and O(2)) to the Fe(0)/H(2)O interface. Instead of this universal role of oxide layers on Fe(0), improper conceptual models have been developed to rationalize electron transfer mechanisms at the Fe(0)/oxide/water interface.
    Keywords: Becher process; Leaching; Oxide layers; Remediation; Zerovalent Iron ; 551 ; Environmental Remediation ; Iron ; Oxidation-Reduction
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  • 16
    Publication Date: 2021-03-29
    Description: Precipitation of exceptionally 13C-depleted authigenic carbonate is a result of, and thus a tracer for, sulphate-dependent anaerobic methane oxidation, particularly in marine sediments. Although these carbonates typically are less depleted in 13C than in the source methane, because of incorporation of C also from other sources, they are far more depleted in 13C (δ13C as light as -69‰ V-PDB) than in carbonates formed where no methane is involved. Here we show that oxidation of biogenic methane in carbon-poor deep groundwater in fractured granitoid rocks has resulted in fracture-wall precipitation of the most extremely 13C-depleted carbonates ever reported, δ13C down to -125‰ V-PDB. A microbial consortium of sulphate reducers and methane oxidizers has been involved, as revealed by biomarker signatures in the carbonates and S-isotope compositions of co-genetic sulphide. Methane formed at shallow depths has been oxidized at several hundred metres depth at the transition to a deep-seated sulphate-rich saline water. This process is so far an unrecognized terrestrial sink of methane.
    Keywords: carbonates; biogenic methane; fractured granite ; 551 ; Calcium Carbonate ; Carbon Isotopes ; Crystallization ; Geologic Sediments ; Groundwater ; Iron ; Isotope Labeling ; Methane ; Oxidation-Reduction ; Silicon Dioxide ; Sulfides ; Time Factors
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  • 17
    Publication Date: 2021-03-29
    Keywords: Organochlorine pesticides; Zero-valent iron; Dechlorination; Modeling ; 551 ; Chemical Industry ; DDT ; Environmental Remediation ; Hydrocarbons, Chlorinated ; Ions ; Iron ; Lindane ; Pesticides ; Soil Pollutants
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  • 18
    Publication Date: 2021-03-29
    Keywords: electron transfer; oxidative degradation ; 551 ; Chlorides ; Chlorophenols ; Clofibric Acid ; Electrons ; Environmental Pollutants ; Hydrogen-Ion Concentration ; Iron ; Organic Chemicals ; Oxidation-Reduction
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  • 19
    Publication Date: 2021-03-29
    Keywords: groundwater; biosand filter; arsenic contamination ; 551 ; Arsenic ; Biodegradation, Environmental ; Iron ; Phosphates ; Silicon Dioxide ; Water Pollutants, Chemical
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  • 20
    Publication Date: 2021-03-29
    Description: Aqueous contaminant removal in the presence of metallic iron (e.g. in Fe(0)/H(2)O systems) is characterized by the large diversity of removing agents. This paper analyses the synergistic effect of adsorption, co-precipitation and reduction on the process contaminant removal in Fe(0)/H(2)O systems on the basis of simple theoretical calculations. The system evolution is characterized by the percent Fe(0) consumption. The results showed that contaminant reduction by Fe(0) is likely to significantly contribute to the removal process only in the earliest stage of Fe(0) immersion. With increasing reaction time, contaminant removal is a complex interplay of adsorption onto iron corrosion products, co-precipitation or sequestration in the matrix of iron corrosion products and reduction by Fe(0), Fe(II) or H(2)/H. The results also suggested that in real world Fe(0)/H(2)O systems, any inflowing contaminant can be regarded as foreign species in a domain of precipitating iron hydroxides. Therefore, current experimental protocols with high contaminant to Fe(0) ratios should be revisited. Possible optimising of experimental conditions is suggested.
    Keywords: Adsorption; Co-precipitation; Iron Reactivity; Reduction; Zerovalent iron ; 551 ; Adsorption ; Chemical Precipitation ; Iron ; Water
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