scholarly journals Testing the Suitability of Zerovalent Iron Materials for Reactive Walls

2005 ◽  
Vol 2 (1) ◽  
pp. 71 ◽  
Author(s):  
Chicgoua Noubactep ◽  
Günther Meinrath ◽  
Peter Dietrich ◽  
Martin Sauter ◽  
B. J. Merkel

Environmental Context. Groundwater remediation is generally a costly, long-term process. In situ remediation using permeable reactive barriers, through which the groundwaters pass, is a potential solution. For redox-sensitive contaminants in groundwater, a metallic iron barrier (zerovalent iron, ZVI) can immobilize or degrade these dissolved pollutants. Scrap iron materials are a low-cost ZVI material but, because of the wide variation of scrap metal compositions, testing methods for characterizing the corrosion behaviour need to be developed. Abstract. Zerovalent iron (ZVI) has been proposed as reactive material in permeable in situ walls for contaminated groundwater. An economically feasible ZVI-based reactive wall requires cheap but efficient iron materials. From an uranium treatability study and results of iron dissolution in 0.002 M EDTA by five selected ZVI materials, it is shown that current research and field implementation is not based on a rational selection of application-specific iron metal sources. An experimental procedure is proposed which could enable a better material characterization. This procedure consists of mixing ZVI materials and reactive additives, including contaminant releasing materials (CRMs), in long-term batch experiments and characterizing the contaminant concentration over the time.

2019 ◽  
Vol 136 ◽  
pp. 06021
Author(s):  
Qianfeng He ◽  
Shihui Si ◽  
Jun Yang ◽  
Xiaoyu Tu

As a new in-situ remediation of groundwater, compared with the traditional “pump and treat” technology, the permeable reactive barrier (PRB) has the advantages of low cost, no external power, the small disturbance to groundwater, small secondary pollution and long-term operation, this paper introduces the basic concept of PRB, technical principle, structure type, the principle of active materials selection and mechanisms of remediation, design and installation factors, it provides ideas for further research and application of PRB technology in groundwater remediation projects in China.


Author(s):  
Bruno Kursten ◽  
Frank Druyts ◽  
Pierre Van Iseghem

Abstract The current worldwide trend for the final disposal of conditioned high-level, medium-level and long-lived alpha-bearing radioactive waste focuses on deep geological disposal. During the geological disposal, the isolation between the radioactive waste and the environment (biosphere) is realised by the multibarrier principle, which is based on the complementary nature of the various natural and engineered barriers. One of the main engineered barriers is the metallic container (overpack) that encloses the conditioned waste. In Belgium, the Boom Clay sediment is being studied as a potential host rock formation for the final disposal of conditioned high-level radioactive waste (HLW) and spent fuel. Since the mid 1980’s, SCK•CEN has developed an extensive research programme aimed at evaluating the suitability of a wide variety of metallic materials as candidate overpack material for the disposal of HLW. A multiple experimental approach is applied consisting of i) in situ corrosion experiments, ii) electrochemical experiments (cyclic potentiodynamic polarisation measurements and monitoring the evolution of ECORR as a function of time), and iii) immersion experiments. The in situ corrosion experiments were performed in the underground research facility, the High Activity Disposal Experimental Site, or HADES, located in the Boom clay layer at a depth of 225 metres below ground level. These experiments aimed at predicting the long-term corrosion behaviour of various candidate container materials. It was believed that this could be realised by investigating the medium-term interactions between the container materials and the host formation. These experiments resulted in a change of reasoning at the national authorities concerning the choice of over-pack material from the corrosion-allowance material carbon steel towards corrosion-resistant materials such as stainless steels. The main arguments being the severe pitting corrosion during the aerobic period and the large amount of hydrogen gas generated during the subsequent anaerobic period. The in situ corrosion experiments however, did not allow to unequivocally quantify the corrosion of the various investigated candidate overpack materials. The main shortcoming was that they did not allow to experimentally separate the aerobic and anaerobic phase. This resulted in the elaboration of a new laboratory programme. Electrochemical corrosion experiments were designed to investigate the effect of a wide variety of parameters on the localised corrosion behaviour of candidate overpack materials: temperature, SO42−, Cl−, S2O32−, oxygen content (aerobic - anaerobic),… Three characteristic potentials can be derived from the cyclic potentiodynamic polarisation (CPP) curves: i) the open circuit potential, OCP, ii) the critical potential for pit nucleation, ENP, and iii) the protection potential, EPP. Monitoring the open circuit potential as a function of time in clay slurries, representative for the underground environment, provides us with a more reliable value for the corrosion potential, ECORR, under disposal conditions. The long-term corrosion behaviour of the candidate overpack materials can be established by comparing the value of ECORR relative to ENP and EPP (determined from the CPP-curves). The immersion tests were developed to complement the in situ experiments. These experiments aimed at determining the corrosion rate and to identify the corrosion processes that can occur during the aerobic and anaerobic period of the geological disposal. Also, some experiments were elaborated to study the effect of graphite on the corrosion behaviour of the candidate overpack materials.


Sensors ◽  
2020 ◽  
Vol 20 (6) ◽  
pp. 1755 ◽  
Author(s):  
Romwald Lihakanga ◽  
Yuan Ding ◽  
Gabriela M. Medero ◽  
Samuel Chapman ◽  
George Goussetis

This paper presents an in-situ wireless sensor network (WSN) for building envelope thermal transmission analysis. The WSN is able to track heat flows in various weather conditions in real-time. The developed system focuses on long-term in-situ building material variation analysis, which cannot be readily achieved using current approaches, especially when the number of measurement hotspots is large. This paper describes the implementation of the proposed system using the heat flow method enabled through an adaptable and low-cost wireless network, validated via a laboratory experiment.


2020 ◽  
Author(s):  
Lisa C. Füllenbach ◽  
Jeffrey Paolo H. Perez ◽  
Helen M. Freeman ◽  
Andrew N. Thomas ◽  
Liane G. Benning ◽  
...  

<p>Anthropological use of land and resources releases vast amounts of waste into surface waters and aquifers. Copper(II) is one of the most widely occurring heavy metal contaminants, introduced into the environment from industrial discharge, landfill leakage, agricultural and mining sources. Common remediation strategies for redox-sensitive Cu(II) are based on adsorption or phytoremediation methods. To experimentally test the efficiency of Cu(II) retention by inorganic redox reaction processes suitable for in situ surface- and groundwater remediation applications, we used siderite (FeCO<sub>3</sub>), which is abundant in anoxic sediments and soils and as a carbonate highly soluble in acidic environments. Its dissolution increases alkalinity and releases highly reactive, redox sensitive Fe(II). This aqueous ferrous iron can act as 1) a precursor for Fe(III) (hydr)oxides in oxic conditions, which are effective sorbents of heavy metals, and 2) a reducing agent under reducing conditions, where it can form a strong redox couple with Cu(II). We investigated the long term (1008 h) removal of aqueous Cu(II) through siderite dissolution batch experiments under oxic and anoxic conditions and monitored changes in the aqueous concentrations of Cu and Fe, pH and the reacted solids morphology over time. Cu adsorption and speciation on the reaction products was determined by X-ray absorption and photoelectron spectroscopies.</p><p>Under oxic conditions, increasing alkalinity led to a rapid increase in solution pH and the precipitation of nanoparticulate goethite and hematite from the released ferrous iron. After 1008 h of reaction, 80 % of the dissolved Cu(II) were removed from solution by sorption, whereby up to >30 % of this sorbed Cu(II) was reduced to Cu(I). Under anoxic conditions, the solution pH increased abruptly and copper uptake occurred more than twice as fast as under oxic conditions. Notably, the released Fe(II) was oxidized by Cu(II) leading to the precipitation of lepidocrocite, while all copper was removed from solution with >70 % of Cu(II) being reduced to Cu(0).</p><p>Our results suggest that 1) redox reactions between aqueous Cu(II) and Fe(II) promote coupled dissolution-precipitation and adsorption mechanisms responsible for Cu(II) removal, and that 2) siderite is a low-cost and effective material that is potentially useful for in situ remediation in either oxygenated or reduced environments.</p>


NANO ◽  
2008 ◽  
Vol 03 (04) ◽  
pp. 287-289 ◽  
Author(s):  
STEPANKA KLIMKOVA ◽  
MIROSLAV CERNIK ◽  
LENKA LACINOVA ◽  
JAROSLAV NOSEK

It is known that the reductive effects of zero-valent iron ( Fe 0) and the sorptive capability of iron and its oxides can be used for both the dehalogenation of chlorinated hydrocarbons (CHC), especially of chlorinated ethenes (PCE → TCE → DCE → VC → ethene, ethane), and the removing of heavy metals from groundwater by turning them into a less-soluble form through changes of their oxidation state, or by adsorption. These consequences are being exploited in the construction of iron filling permeable reactive barriers for a longer time.1 The advantages of nanoscale zero-valent iron ( nanoFe 0) over the macroscopic one consist not only in the better reactivity implicit in their greater specific surface area but also in their mobility in rock environment.2,3 Numerous laboratory experiments, especially the batch-agitated experiments, with samples from seven various contaminated localities in Europe have been carried out with the aim to discover the measurement of the reductive effect of the nanoFe 0 on selected contaminants. It was found that the nanoFe 0 can be reliably usable as a reductive reactant for in-situ chemical decontamination of sites polluted by chlorinated ethenes (CEs), or hexa-valent chromium ( Cr VI ). The rate of reductive reaction and the optimal concentrations for the real remediation action were determined. On the basis of these laboratory experiments, the methods for pilot application of nanoFe 0 have been specified. Subsequently the pilot experiments were accomplished in surveyed localities.


Author(s):  
Bobbie Corbett ◽  
Nicholas Wellwood ◽  
David Shing ◽  
Leslie Angus Jackson

Munna Point is a premiere recreational beach in the Noosa River which has been maintained by regular nourishment for over 20 years. As longevity of each nourishment was less than 6 months, the long-term costs were high and efforts were eventually suspended resulting in loss of the beach. In an effort to reinstate the amenity and provide a more stable beach, a groyne field accompanied by nourishment was proposed. To provide a low-impact, low-risk and low-cost solution, the groynes were designed with a low crest using sand-filled geotextile containers. To achieve the design, containers and scour mattresses were filled in-situ using a dredge, which was an innovative application of a methodology typically adopted for much larger containers. The first 3 groynes have successfully been installed as part of the first stage and 12 months of monitoring subsequently undertaken. The groynes have clearly been effective at extending the longevity of the nourishment and the wider intertidal profile has remained very stable. The beach is now successfully enhancing the amenity of the community and experiencing a high level of usage.


2005 ◽  
Vol 2 (3) ◽  
pp. 235 ◽  
Author(s):  
Chicgoua Noubactep ◽  
Günther Meinrath ◽  
Broder J. Merkel

Environmental Context.Groundwater is the water that fills the spaces between sand, soil, and rock below the water table. It discharges into ecologically sensitive wetlands and is used as drinking water or in agriculture and industry. Inappropriate waste disposal and poor land management can contaminate groundwater and may minimize its use for decades. The common method for pumping contaminated groundwater to the surface for treatment is costly and labour intensive. Zerovalent iron is a new, more cost-effective method of groundwater remediation. Abstract. Zerovalent iron (ZVI) has been proposed as a reactive material in permeable in situ walls for groundwater contaminated by metal pollutants. For such pollutants that interact with corrosion products, the determination of the actual mechanism of their removal is very important to predict their stability in the long term. From a study of the effects of pyrite (FeS2) and manganese nodules (MnO2) on the uranium removal potential of a selected ZVI material, a test methodology (FeS2–MnO2 method) is suggested to follow the pathway of contaminant removal by ZVI materials. An interpretation of the removal potential of ZVI for uranium in the presence of both additives corroborates coprecipitation with iron corrosion products as the initial removal mechanism for uranium.


2016 ◽  
Vol 563-564 ◽  
pp. 713-723 ◽  
Author(s):  
Milica Velimirovic ◽  
Doris Schmid ◽  
Stephan Wagner ◽  
Vesna Micić ◽  
Frank von der Kammer ◽  
...  

Chemosphere ◽  
2014 ◽  
Vol 111 ◽  
pp. 243-259 ◽  
Author(s):  
Franklin Obiri-Nyarko ◽  
S. Johana Grajales-Mesa ◽  
Grzegorz Malina

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