An Assessment of the International Space Station's Trace Contaminant Control Subassembly Process Economics

Science.gov (United States)

Perry J. L.; Cole, H. E.; El-Lessy, H. N.

2005-01-01

The International Space Station (ISS) Environmental Control and Life Support System includes equipment speci.cally designed to actively remove trace chemical contamination from the cabin atmosphere. In the U.S. on-orbit segment, this function is provided by the trace contaminant control subassembly (TCCS) located in the atmosphere revitalization subsystem rack housed in the laboratory module, Destiny. The TCCS employs expendable adsorbent beds to accomplish its function leading to a potentially signi.cant life cycle cost over the life of the ISS. Because maintaining the TCCSs proper can be logistically intensive, its performance in .ight has been studied in detail to determine where savings may be achieved. Details of these studies and recommendations for improving the TCCS s process economics without compromising its performance or crew health and safety are presented and discussed.

40 CFR 227.6 - Constituents prohibited as other than trace contaminants.

Science.gov (United States)

2010-07-01

... trace contaminants. 227.6 Section 227.6 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Environmental Impact § 227.6 Constituents prohibited as other than trace contaminants. (a) Subject to the..., of materials containing the following constituents as other than trace contaminants will not be...

An anaerobic membrane bioreactor - membrane distillation hybrid system for energy recovery and water reuse: Removal performance of organic carbon, nutrients, and trace organic contaminants.

Science.gov (United States)

Song, Xiaoye; Luo, Wenhai; McDonald, James; Khan, Stuart J; Hai, Faisal I; Price, William E; Nghiem, Long D

2018-07-01

In this study, a direct contact membrane distillation (MD) unit was integrated with an anaerobic membrane bioreactor (AnMBR) to simultaneously recover energy and produce high quality water for reuse from wastewater. Results show that AnMBR could produce 0.3-0.5L/g COD added biogas with a stable methane content of approximately 65%. By integrating MD with AnMBR, bulk organic matter and phosphate were almost completely removed. The removal of the 26 selected trace organic contaminants by AnMBR was compound specific, but the MD process could complement AnMBR removal, leading to an overall efficiency from 76% to complete removal by the integrated system. The results also show that, due to complete retention, organic matter (such as humic-like and protein-like substances) and inorganic salts accumulated in the MD feed solution and therefore resulted in significant fouling of the MD unit. As a result, the water flux of the MD process decreased continuously. Nevertheless, membrane pore wetting was not observed throughout the operation. Crown Copyright © 2018. Published by Elsevier B.V. All rights reserved.

Techniques for removing contaminated concrete surfaces

International Nuclear Information System (INIS)

Halter, J.M.; Sullivan, R.G.

1981-01-01

This discussion compares various techniques that have been used to clean concrete surfaces by removing the surface. Three techniques which have been investigated by the Pacific Northwest Laboratory for removing surfaces are also described: the water cannon, the concrete spaller, and high-pressure water jet. The equipment was developed with the assumption that removal of the top 1/8 to 1/4 in. of surface would remove most of the contamination. If the contamination has gone into cracks or deep voids in the surface, the removal processes can be repeated until the surface is acceptable

Trace element removal from coal ash leachate by the 10-year-old construction wetland

Energy Technology Data Exchange (ETDEWEB)

Ye, Z.H.; Whiting, S.N.; Qian, J.H.; Lytle, C.M.; Lin, Z.-Q.; Terry, N. [University of California at Berkeley, Berkeley, CA (USA). Dept. of Plant and Microbial Biology

2001-10-01

The study investigated the ability of a 10-year old constructed wetland to treat metal-contaminated leachate emanating from a coal ash pile at the Widows Creek electric utility, Alabama (USA). The two vegetated cells, which were dominated by cattail (Typha latifolia L.) and soft rush (Juncus effusus L.), were very effective at removing Fe and Cd from the wastewater, but less efficient for Zn, S, B, and Mn. The concentrations were decreased by up to 99% for Fe, 91% for Cd, 63% for Zn, 61% for S, 58% for Mn, and 50% for B. Higher pH levels ({gt} 6) in standing water substantially improved the removing efficiency of the wetland for Mn only. The belowground tissues of both cattail and soft rush had high concentrations of all elements; only for Mn, however, did the concentration in the shoots exceed those in the belowground tissues. The concentrations of trace elements in fallen litter were higher than in the living shoots, but lower than in the belowground tissues. The trace element accumulation in the plants accounts for less than 2.5% of the annual loading of each trace element into the wetland. The sediments were the primary sinks for the elements removed from the wastewater. Except for Mn, the concentrations of trace elements in the upper layer (0-5 cm) of the sediment profile tended to be higher than the lower layers (5-10 and 10-15 cm). The conclusion was that constructed wetlands are still able to efficiently remove metals in the long term (i.e. {gt} 10 years after construction). 34 refs., 7 figs., 2 tabs.

The use of transgenic plants in the bioremediation of soils contaminated with trace elements

Energy Technology Data Exchange (ETDEWEB)

Kraemer, U. [Max Planck Inst. of Molecular Plant Physiology, Potsdam (Germany); Chardonnens, A.N. [Faculty of Biology, Bielefeld Univ. (Germany)

2001-07-01

The use of plants to clean-up soils contaminated with trace elements could provide a cheap and sustainable technology for bioremediation. Field trials suggested that the rate of contaminant removal using conventional plants and growth conditions is insufficient. The introduction of novel traits into high biomass plants in a transgenic approach is a promising strategy for the development of effective phytoremediation technologies. This has been exemplified by generating plants able to convert organic and ionic forms of mercury into the less toxic, volatile, elemental mercury, a trait that occurs naturally only in some bacteria and not at all in plants. The engineering of a phytoremediator plant requires the optimization of a number of processes, including trace element mobilization in the soil, uptake into the root, detoxification and allocation within the plant. A number of transgenic plants have been generated in an attempt to modify the tolerance, uptake or homeostasis of trace elements. The phenotypes of these plants provide important insights for the improvement of engineering strategies. A better understanding, both of micronutrient acquisition and homeostasis, and of the genetic, biochemical and physiological basis of metal hyperaccumulation in plants, will be of key importance for the success of phytoremediation. (orig.)

Trace organic removal by photochemical oxidation

International Nuclear Information System (INIS)

Gupta, S.K. Sen; Peori, R.G.; Wickware, S.L.

1995-02-01

Photochemical oxidation methods can be used for the destruction of dissolved organic contaminants in most process effluent streams, including those originating from the nuclear power sector. Evaporators can be used to separate organic contaminants from the aqueous phase if they are non volatile, but a large volume of secondary waste (concentrate) is produced, and the technology is capital-intensive. This paper describes two different types of photochemical oxidation technologies used to destroy trace organics in wastewater containing oil and grease. (author). 9 refs., 4 figs

Estuaries as filters: the role of tidal marshes in trace metal removal.

Directory of Open Access Journals (Sweden)

Johannes Teuchies

Full Text Available Flux calculations demonstrate that many estuaries are natural filters for trace metals. Yet, the underlying processes are poorly investigated. In the present study, it was hypothesized that intertidal marshes contribute significantly to the contaminant filter function of estuaries. Trace metal concentrations and sediment characteristics were measured along a transect from the subtidal, over an intertidal flat and marsh to a restored marsh with controlled reduced tide. Metal concentrations in the intertidal and restored marsh were found to be a factor two to five higher than values in the subtidal and intertidal flat sediments. High metal concentrations and high accretion rates indicate a high metal accumulation capacity of the intertidal marshes. Overbank sedimentation in the tidal marshes of the entire estuary was calculated to remove 25% to 50% of the riverine metal influx, even though marshes comprise less than 8% of the total surface of the estuary. In addition, the large-scale implementation of planned tidal marsh restoration projects was estimated to almost double the trace metal storage capacity of the present natural tidal marshes in the estuary.

Estuaries as Filters: The Role of Tidal Marshes in Trace Metal Removal

Science.gov (United States)

Teuchies, Johannes; Vandenbruwaene, Wouter; Carpentier, Roos; Bervoets, Lieven; Temmerman, Stijn; Wang, Chen; Maris, Tom; Cox, Tom J. S.; Van Braeckel, Alexander; Meire, Patrick

2013-01-01

Flux calculations demonstrate that many estuaries are natural filters for trace metals. Yet, the underlying processes are poorly investigated. In the present study, it was hypothesized that intertidal marshes contribute significantly to the contaminant filter function of estuaries. Trace metal concentrations and sediment characteristics were measured along a transect from the subtidal, over an intertidal flat and marsh to a restored marsh with controlled reduced tide. Metal concentrations in the intertidal and restored marsh were found to be a factor two to five higher than values in the subtidal and intertidal flat sediments. High metal concentrations and high accretion rates indicate a high metal accumulation capacity of the intertidal marshes. Overbank sedimentation in the tidal marshes of the entire estuary was calculated to remove 25% to 50% of the riverine metal influx, even though marshes comprise less than 8% of the total surface of the estuary. In addition, the large-scale implementation of planned tidal marsh restoration projects was estimated to almost double the trace metal storage capacity of the present natural tidal marshes in the estuary. PMID:23950927

NSF-RANN Trace Contaminants Program directory

International Nuclear Information System (INIS)

Purnell, P.A.; Smith, S.K.; Wilkes, C.F.

1976-10-01

This directory is designed to aid effective communication throughout the National Science Foundation's Trace Contaminants Program, Research Applied to National Needs. The majority of the participants in the Program are represented by name, address, telephone number, and a very brief description of research interest. The directory has five major divisions to facilitate its use. Section I contains a listing of the program managers associated with the NSF-RANN Trace Contaminants Program. Section II lists the principal investigators, co-principal investigators, and coordinators of each of the research grants in the Program. Section III lists the personnel by individual projects. Section IV contains a total alphabetic listing complete with project titles and Section V contains a keyword index. This directory is maintained by the Toxic Materials Information Center as part of the Environmental Resource Center of the Information Center Complex, Information Division, Oak Ridge National Laboratory

Impact of hydraulic and carbon loading rates of constructed wetlands on contaminants of emerging concern (CECs) removal

International Nuclear Information System (INIS)

Sharif, Fariya; Westerhoff, Paul; Herckes, Pierre

2014-01-01

Constructed wetlands remove trace organic contaminants via synergistic processes involving plant biomass that include hydrolysis, volatilization, sorption, biodegradation, and photolysis. Wetland design conditions, such as hydraulic loading rates (HLRs) and carbon loading rates (CLRs), influence these processes. Contaminant of emerging concern (CEC) removal by wetland plants was investigated at varying HLRs and CLRs. Rate constants and parameters obtained from batch-scale studies were used in a mechanistic model to evaluate the effect of these two loading rates on CEC removal. CLR significantly influenced CEC removal when wetlands were operated at HLR >5 cm/d. High values of CLR increased removal of estradiol and carbamazepine but lowered that of testosterone and atrazine. Without increasing the cumulative HLR, operating two wetlands in series with varying CLRs could be a way to improve CEC removal. -- Highlights: • A fate-predictive model was developed to evaluate the effect of loading rates on CEC removal in constructed wetlands. • Carbon loading rates (CLRs) can influence CEC removal when wetlands are operated at higher hydraulic loading rates (HLRs). • The effect of CLRs varies among CECs with different physico-chemical properties. • Combination of wetlands with different CLRs can optimize CEC removal without changing the net HLR. -- This article evaluates the effect of design loading rates on contaminant of emerging concern (CEC) removal in constructed wetlands

Method of removing contaminants from plastic resins

Science.gov (United States)

Bohnert, George W.; Hand, Thomas E.; DeLaurentiis, Gary M.

2008-11-18

A method for removing contaminants from synthetic resin material containers using a first organic solvent system and a second carbon dioxide system. The organic solvent is utilized for removing the contaminants from the synthetic resin material and the carbon dioxide is used to separate any residual organic solvent from the synthetic resin material.

Method for removing contaminants from plastic resin

Science.gov (United States)

Bohnert, George W.; Hand, Thomas E.; DeLaurentiis, Gary M.

2008-12-30

A method for removing contaminants from synthetic resin material containers using a first organic solvent system and a second carbon dioxide system. The organic solvent is utilized for removing the contaminants from the synthetic resin material and the carbon dioxide is used to separate any residual organic solvent from the synthetic resin material.

study on trace contaminants control assembly for sealed environment chamber

Science.gov (United States)

Pang, L. P.; Wang, J.; Liu, L. K.; Liu, H.

The biological and Physicochemical P C life support technologies are all important parts to establish a human Closed Ecological Life Support System CELSS for long-duration mission The latter has the advantages of lower power consumption lower mass and higher efficiency therefore researchers often incorporate the use of biological systems with P C life support technologies to continuously recycle air water and part of the solid waste stream generated such as the Russian BLSS and the NASA-sponsored Lunar-Mars Life Support Test Project LMLSTP In short these tests were very successful in integrating biological and P C life support technologies for long-duration life support Therefore we should use a combination of integrated biological with P C life support technologies in a human CELSS Human construction materials plants animals and soils release much trace toxic gases in a CELSS and they will inhibit plant growth and badly affect human health when their concentrations rise over their threshold levels The effect of biological trace contaminant control technologies is slower especially for a human sealed chamber because human produce much more methane and other contaminants A regenerative Trace Contaminant Control Subsystem TCCS with P C technology is a more important part in this case to control quickly the airborne contaminants levels and assure human in good condition in a sealed chamber This paper describes a trace contaminant control test facility incorporated a 8 m3 sealed environment chamber a regenerative TCCS with P C

Radiolabelled substrates for studying biological effects of trace contaminants

International Nuclear Information System (INIS)

1975-01-01

A programme of coordinated isotopic tracer-aided investigations of the biological side-effects of foreign chemical residues in food and agriculture, initiated in 1973, was reviewed. The current status of representative investigations from the point of view of techniques and priorities was assessed. Such investigations involved radioactive substrates for studying DNA injury and its repair; 14 C-labelled acetylcholine as substrate for measuring enzyme inhibition due to the presence of, or exposure to, anticholinesteratic contaminants; radioactive substrates as indication of side-effects in non-target organisms and of their comparative susceptibilities; radioactive substrates as indicators of persistence or biodegradability of trace contaminants of soil or water; and labelled pools for studying the biological side-effects of trace contaminants. Priorities were identified

Removal of organic contaminants from secondary effluent by anodic oxidation with a boron-doped diamond anode as tertiary treatment

Energy Technology Data Exchange (ETDEWEB)

Garcia-Segura, Sergi, E-mail: sergigarcia@ub.edu [Advanced Water Management Centre, The University of Queensland, Level 4, Gehrmann Bld. (60), St Lucia, QLD 072 (Australia); Laboratori d’Electroquímica dels Materials i del Medi Ambient, Departament de Química Física, Facultat de Química, Universitat de Barcelona, Martí i Franquès 1-11, 08028 Barcelona (Spain); Keller, Jürg [Advanced Water Management Centre, The University of Queensland, Level 4, Gehrmann Bld. (60), St Lucia, QLD 072 (Australia); Brillas, Enric [Laboratori d’Electroquímica dels Materials i del Medi Ambient, Departament de Química Física, Facultat de Química, Universitat de Barcelona, Martí i Franquès 1-11, 08028 Barcelona (Spain); Radjenovic, Jelena, E-mail: j.radjenovic@awmc.uq.edu.au [Advanced Water Management Centre, The University of Queensland, Level 4, Gehrmann Bld. (60), St Lucia, QLD 072 (Australia)

2015-02-11

Graphical abstract: - Highlights: • Mineralization of secondary effluent by anodic oxidation with BDD anode. • Complete removal of 29 pharmaceuticals and pesticides at trace level concentrations. • Organochlorine and organobromine byproducts were formed at low μM concentrations. • Chlorine species evolution assessed to evaluate the anodic oxidation applicability. - Abstract: Electrochemical advanced oxidation processes (EAOPs) have been widely investigated as promising technologies to remove trace organic contaminants from water, but have rarely been used for the treatment of real waste streams. Anodic oxidation with a boron-doped diamond (BDD) anode was applied for the treatment of secondary effluent from a municipal sewage treatment plant containing 29 target pharmaceuticals and pesticides. The effectiveness of the treatment was assessed from the contaminants decay, dissolved organic carbon and chemical oxygen demand removal. The effect of applied current and pH was evaluated. Almost complete mineralization of effluent organic matter and trace contaminants can be obtained by this EAOP primarily due to the action of hydroxyl radicals formed at the BDD surface. The oxidation of Cl{sup −} ions present in the wastewater at the BDD anode gave rise to active chlorine species (Cl{sub 2}/HClO/ClO{sup −}), which are competitive oxidizing agents yielding chloramines and organohalogen byproducts, quantified as adsorbable organic halogen. However, further anodic oxidation of HClO/ClO{sup −} species led to the production of ClO{sub 3}{sup −} and ClO{sub 4}{sup −} ions. The formation of these species hampers the application as a single-stage tertiary treatment, but posterior cathodic reduction of chlorate and perchlorate species may reduce the risks associated to their presence in the environment.

Microlith-based Structured Sorbent for Carbon Dioxide, Humidity, and Trace Contaminant Control in Manned Space Habitats

Science.gov (United States)

Junaedi, Christian; Roychoudhury, SUbir; Howard, David F.; Perry, Jay L.; Knox, James C.

2011-01-01

To support continued manned space exploration, the development of atmosphere revitalization systems that are lightweight, compact, durable, and power efficient is a key challenge. The systems should be adaptable for use in a variety of habitats and should offer operational functionality to either expel removed constituents or capture them for closedloop recovery. As mission durations increase and exploration goals reach beyond low earth orbit, the need for regenerable adsorption processes for continuous removal of CO2 and trace contaminants from cabin air becomes critical. Precision Combustion, Inc. (PCI) and NASA Marshall (MSFC) have been developing an Engineered Structured Sorbents (ESS) approach based on PCI s patented Microlith technology to meet the requirements of future, extended human spaceflight explorations. This technology offers the inherent performance and safety attributes of zeolite and other sorbents with greater structural integrity, regenerability, and process control, thereby providing potential durability and efficiency improvements over current state-of-the-art systems. The major advantages of the ESS explored in this study are realized through the use of metal substrates to provide structural integrity (i.e., less partition of sorbents) and enhanced thermal control during the sorption process. The Microlith technology also offers a unique internal resistive heating capability that shows potential for short regeneration time and reduced power requirement compared to conventional systems. This paper presents the design, development, and performance results of the integrated adsorber modules for removing CO2, water vapor, and trace chemical contaminants. A related effort that utilizes the adsorber modules for sorption of toxic industrial chemicals is also discussed. Finally, the development of a 4-person two-leg ESS system for continuous CO2 removal is also presented.

System for removing contaminants from plastic resin

Science.gov (United States)

Bohnert, George W.; Hand, Thomas E.; DeLaurentiis, Gary M.

2010-11-23

A resin recycling system that produces essentially contaminant-free synthetic resin material in an environmentally safe and economical manner. The system includes receiving the resin in container form. A grinder grinds the containers into resin particles. The particles are exposed to a solvent in one or more solvent wash vessels, the solvent contacting the resin particles and substantially removing contaminants on the resin particles. A separator is used to separate the resin particles and the solvent. The resin particles are then placed in solvent removing element where they are exposed to a solvent removing agent which removes any residual solvent remaining on the resin particles after separation.

Trace organics removal using three membrane bioreactor configurations: MBR, IFAS-MBR and MBMBR.

Science.gov (United States)

de la Torre, T; Alonso, E; Santos, J L; Rodríguez, C; Gómez, M A; Malfeito, J J

2015-01-01

Seventeen pharmaceutically active compounds and 22 other trace organic pollutants were analysed regularly in the influent and permeate from a semi-real plant treating municipal wastewater. The plant was operated during 29 months with different configurations which basically differed in the type of biomass present in the system. These processes were the integrated fixed-film activated sludge membrane bioreactor (IFAS-MBR), which combined suspended and attached biomass, the moving bed membrane bioreactor (MBMBR) (only attached biomass) and the MBR (only suspended biomass). Moreover, removal rates were compared to those of the wastewater treatment plant (WWTP) operating nearby with conventional activated sludge treatment. Reverse osmosis (RO) was used after the pilot plant to improve removal rates. The highest elimination was found for the IFAS-MBR, especially for hormones (100% removal); this was attributed to the presence of biofilm, which may lead to different conditions (aerobic-anoxic-anaerobic) along its profile, which increases the degradation possibilities, and also to a higher sludge age of the biofilm, which allows complete acclimation to the contaminants. Operating conditions played an important role, high mixed liquor suspended solids (MLSS) and sludge retention time (SRT) being necessary to achieve these high removal rates. Although pharmaceuticals and linear alkylbenzene sulfonates showed high removal rates (65-100%), nonylphenols and phthalate could only be removed to 10-30%. RO significantly increased removal rates to 88% mean removal rate.

Removal of trace element by isolates of Aspergillus brasiliensis ...

African Journals Online (AJOL)

Coffee beans processing generates a large volume of wastewater composed of trace elements which can be detrimental to human health. The present study aimed at evaluating the capacity of strains of Aspergillus brasiliensis and Penicillium citrinum in tolerating and removing trace elements namely: Cu, Mn and Zn from ...

Energy efficient trace removal by extractive distillation

NARCIS (Netherlands)

Jongmans, M.T.G.

2012-01-01

Separation processes contribute for about 40–70 % to the total energy requirements of the chemical process industry. Especially when trace removal is required to manufacture high purity products, traditional separation technologies become extremely expensive and are not providing satisfying

Use of biomimetic forward osmosis membrane for trace organics removal

DEFF Research Database (Denmark)

Madsen, Henrik T.; Bajraktari, Niada; Helix Nielsen, Claus

2015-01-01

The use of forward osmosis for the removal of trace organics from water has recently attracted considerable attention as an alternative to traditional pressure driven membrane filtration. However, the existing forward osmosis membranes have been found to be ineffective at rejecting small neutral...... organic pollutants, which limits the applicability of the forward osmosis process. In this study a newly developed biomimetic membrane was tested for the removal of three selected trace organics that can be considered as a bench marking test for a membrane[U+05F3]s ability to reject small neutral organic....... This difference is caused by differences in the transport mechanisms. For the cellulose acetate membrane rejection is controlled by steric hindrance, which results in a size dependent rejection of the trace organics, whereas rejection by the aquaporin membrane is controlled by diffusion of the trace organics...

Trace Contaminant Control During the International Space Station's On-Orbit Assembly and Outfitting

Science.gov (United States)

Perry, J. L.

2017-01-01

Achieving acceptable cabin air quality must balance competing elements during spacecraft design, assembly, ground processing, and flight operations. Among the elements that contribute to the trace chemical contaminant load and, therefore, the cabin air quality aboard crewed spacecraft are the vehicle configuration, crew size and activities, mission duration and objectives, materials selection, and vehicle manufacturing and preflight ground processing methods. Trace chemical contaminants produced from pervasive sources such as equipment offgassing, human metabolism, and cleaning fluids during preflight ground processing present challenges to maintaining acceptable cabin air quality. To address these challenges, both passive and active contamination control techniques are used during a spacecraft's design, manufacturing, preflight preparation, and operational phases. Passive contamination control methods seek to minimize the equipment offgassing load by selecting materials, manufacturing processes, preflight preparation processes, and in-flight operations that have low chemical offgassing characteristics. Passive methods can be employed across the spacecraft's entire life cycle from conceptual design through flight operations. However, because the passive contamination control techniques cannot fully eliminate the contaminant load, active contamination control equipment must be deployed aboard the spacecraft to purify and revitalize the cabin atmosphere during in-flight operations. Verifying that the passive contamination control techniques have successfully maintained the total trace contaminant load within the active contamination control equipment's capabilities occurs late in the preflight preparation stages. This verification consists of subjecting the spacecraft to an offgassing test to determine the trace contaminant load. This load is then assessed versus the active contamination control equipment's capabilities via trace contaminant control (TCC) engineering

Trace metal contamination of Beaufort's Dyke, North Channel, Irish Sea: A legacy of ordnance disposal

International Nuclear Information System (INIS)

Callaway, Alexander; Quinn, Rory; Brown, Craig J.; Service, Matthew; Benetti, Sara

2011-01-01

Highlights: → Our samples are the first trace metal concentrations taken from the valley of Beaufort's Dyke. → There is no clear trend between concentrations of trace metals in Dyke and NMMP sediments. → Particle transport simulations show dispersal of trace metals from Beaufort's Dyke is possible. → Disposed ordnance may also contribute to contamination of surrounding areas. → These methods could help predict areas at risk of future trace metal contamination as a result of ordnance disposal. - Abstract: Beaufort's Dyke is a disused ordnance disposal ground within the North Channel of the Irish Sea. Over 1 million tonnes of ordnance were disposed of in the dyke over a 40 year period representing a substantial volume of trace metal pollutants introduced to the seabed. Utilising particle transport modelling software we simulated the potential transport of metal particles from Beaufort's Dyke over a 3 month period. This demonstrated that Beaufort's Dyke has the potential to act as a source for trace metal contamination to areas beyond the submarine valley. Trace metal analysis of sediments from the Dyke and surrounding National Marine Monitoring Programme areas demonstrate that the Dyke is not the most contaminated site in the region. Particle transport modelling enables the transport pathways of trace metal contaminants to be predicted. Implementation of the technique in other munitions disposal grounds will provide valuable information for the selection of monitoring stations.

Methods for removing radioactive isotopes from contaminated streams

International Nuclear Information System (INIS)

Hoy, D.R.; Hickey, T.N.; Spulgis, I.S.; Parish, H.C.

1979-01-01

Methods for removing radioactive isotopes from contaminated gas streams for use in atmospheric containment and cleanup systems in nuclear power plants are provided. The methods provide for removal of radioactive isotopes from a first portion of the contaminated stream, separated from the remaining portion of the stream, so that adsorbent used to purify the first portion of the contaminated stream by adsorption of the radioactive isotopes therefrom can be tested to determine the adsorbing efficacy of the generally larger portion of adsorbent used to purify the remaining portion of the stream

Removal of Microbial Contamination from Surface by Plasma

Science.gov (United States)

Feng, Xinxin; Liu, Hongxia; Shen, Zhenxing; Wang, Taobo

2018-01-01

Microbial contamination is closely associated with human and environmental health, they can be tested on food surfaces, medical devices, packing material and so on. In this paper the removal of the microbial contamination from surface using plasma treatment is investigated. The Escherichia coli (E. coli) has been chosen as a bio-indicator enabling to evaluate the effect of plasma assisted microbial inactivation. Oxygen gas was as the working gas. The plasma RF power, plasma exposition time, gas flow and the concentration of organic pollutant were varied in order to see the effect of the plasma treatment on the Gram-negative germ removal. After the treatment, the microbial abatement was evaluated by the standard plate count method. This proved a positive effect of the plasma treatment on Gram-negative germ removal. The kinetics and mathematical model of removal were studied after plasma treatment, and then the removing course of E. coli was analyzed. This work is meaningful for deepening our understanding of the fundamental scientific principles regarding microbial contamination from surface by plasma.

Trace Contaminant Monitor for Air in Spacecraft, Phase I

Data.gov (United States)

National Aeronautics and Space Administration — A need exists for analyzers that can measure trace contaminants in air on board spacecraft. Toxic gas buildup can endanger the crew particularly during long...

NSF-RANN Trace Contaminants Program directory. [Personnel directory

Energy Technology Data Exchange (ETDEWEB)

Purnell, P.A.; Smith, S.K.; Wilkes, C.F.

1976-10-01

This directory is designed to aid effective communication throughout the National Science Foundation's Trace Contaminants Program, Research Applied to National Needs. The majority of the participants in the Program are represented by name, address, telephone number, and a very brief description of research interest. The directory has five major divisions to facilitate its use. Section I contains a listing of the program managers associated with the NSF-RANN Trace Contaminants Program. Section II lists the principal investigators, co-principal investigators, and coordinators of each of the research grants in the Program. Section III lists the personnel by individual projects. Section IV contains a total alphabetic listing complete with project titles and Section V contains a keyword index. This directory is maintained by the Toxic Materials Information Center as part of the Environmental Resource Center of the Information Center Complex, Information Division, Oak Ridge National Laboratory.

Significantly improving trace thallium removal from surface waters during coagulation enhanced by nanosized manganese dioxide.

Science.gov (United States)

Huangfu, Xiaoliu; Ma, Chengxue; Ma, Jun; He, Qiang; Yang, Chun; Jiang, Jin; Wang, Yaan; Wu, Zhengsong

2017-02-01

Thallium (Tl) is an element of high toxicity and significant accumulation in human body. There is an urgent need for the development of appropriate strategies for trace Tl removal in drinking water treatment plants. In this study, the efficiency and mechanism of trace Tl (0.5 μg/L) removal by conventional coagulation enhanced by nanosized manganese dioxide (nMnO 2 ) were explored in simulated water and two representative surface waters (a river water and a reservoir water obtained from Northeast China). Experimental results showed that nMnO 2 significantly improve Tl(I) removal from selected waters. The removal efficiency was dramatically higher in the simulated water, demonstrating by less than 0.1 μg/L Tl residual. The enhancement of trace Tl removal in the surface waters decreased to a certain extent. Both adjusting water pH to alkaline condition and preoxidation of Tl(I) to Tl(III) benefit trace Tl removal from surface waters. Data also indicated that competitive cation of Ca 2+ decreased the efficiency of trace Tl removal, resulting from the reduction of Tl adsorption on nMnO 2 . Humic acid could largely low Tl removal efficiency during nMnO 2 enhanced coagulation processes. Trace elemental Tl firstly adsorbed on nMnO 2 and then removed accompanying with nMnO 2 settling. The information obtained in the present study may provide a potential strategy for drinking water treatment plants threatened by trace Tl. Copyright © 2016 Elsevier Ltd. All rights reserved.

Trace Elements Removal from Waster water by Ceratophyllum ...

African Journals Online (AJOL)

Michael Horsfall

Submerged aquatic plants can be used for the removal of Trace elements. The aim of this study was ... such as electroplating, metal finishing, textile, storage batteries, lead .... metals, Randomized Complete Block Design was used. Statistical ...

Measurements of trace contaminants in closed-type plant cultivation chambers

Science.gov (United States)

Tani, A.; Kiyota, M.; Aiga, I.; Nitta, K.; Tako, Y.; Ashida, A.; Otsubo, K.; Saito, T.

Trace contaminants generated in closed facilities can cause abnormal plant growth. We present measurement data of trace contaminants released from soils, plants, and construction materials. We mainly used two closed chambers, a Closed-type Plant and Mushroom Cultivation Chamber (PMCC) and Closed-type Plant Cultivation Equipment (CPCE). Although trace gas budgets from soils obtained in this experiment are only one example, the results indicate that the budgets of trace gases, as well as CO_2 and O_2, change greatly with the degree of soil maturation and are dependent on the kind of substances in the soil. Both in the PMCC and in the CPCE, trace gases such as dioctyl phthalate (DOP), dibutyl phthalate (DBP), toluene and xylene were detected. These gases seemed to be released from various materials used in the construction of these chambers. The degree of increase in these trace gas levels was dependent on the relationship between chamber capacity and plant quantity. Results of trace gas measurement in the PMCC, in which lettuce and shiitake mushroom were cultivated, showed that ethylene was released both from lettuce and from the mushroom culture bed. The release rates were about 90 ng bed^-1 h^-1 for the shiitake mushroom culture bed (volume is 1700 cm^3) and 4.1 ~ 17.3 ng dm^-2h^-1 (leaf area basis) for lettuce. Higher ethylene release rates per plant and per unit leaf area were observed in mature plants than in young plants.

Analytical analysis of soil-moisture and trace-contaminant transport

International Nuclear Information System (INIS)

Larson, N.M.; Reeves, M.

1976-03-01

A transport model is presented which predicts the coupled movement of both water and trace contaminants through a layered and unsaturated soil-moisture zone. In order to achieve computation speeds suitable for watershed implementations, moisture properties are approximated as exponential functions of pressure head, and lateral flows are treated as sinks in a basically vertical one-dimensional analysis. In addition, only advection by the Darcy-flow velocities and linear adsorption by the soil matrix are considered in depicting movement of the trace contaminant. Formal solution of the resulting transport equations is obtained through use of both eigenfunction-expansion and coordinate-transformation methods. Numerical solution is effected by means of a program written in FORTRAN IV and implemented on an IBM 360/91 computer. Two example calculations illustrate both strengths and weaknesses of our model

Application of molecularly imprinted and non-imprinted polymers for removal of emerging contaminants in water and wastewater treatment: a review.

Science.gov (United States)

Murray, Audrey; Ormeci, Banu

2012-11-01

Over the past decade, several studies have reported trace levels of endocrine disrupting compounds, pharmaceuticals, and personal care products in surface waters, drinking water, and wastewater effluents. There has also been an increased concern about the ecological and human health impact of these contaminants, and their removal from water and wastewater has become a priority. Traditional treatment processes are limited in their ability to remove emerging contaminants from water, and there is a need for new technologies that are effective and feasible. This paper presents a review on recent research results on molecularly imprinted (MIP) and non-imprinted (NIP) polymers and evaluates their potential as a treatment method for the removal of emerging contaminants from water and wastewater. It also discusses the relative benefits and limitations of using MIP or NIP for water and wastewater treatment. MIP, and in particular NIP, offer promising applications for wastewater treatment, but their toxicity and possible health effects should be carefully studied before they are considered for drinking water treatment. More research is also required to determine how best to incorporate MIP and NIP in treatment plants.

Aqueous adsorption and removal of organic contaminants by carbon nanotubes

International Nuclear Information System (INIS)

Yu, Jin-Gang; Zhao, Xiu-Hui; Yang, Hua; Chen, Xiao-Hong; Yang, Qiaoqin; Yu, Lin-Yan; Jiang, Jian-Hui; Chen, Xiao-Qing

2014-01-01

Organic contaminants have become one of the most serious environmental problems, and the removal of organic contaminants (e.g., dyes, pesticides, and pharmaceuticals/drugs) and common industrial organic wastes (e.g., phenols and aromatic amines) from aqueous solutions is of special concern because they are recalcitrant and persistent in the environment. In recent years, carbon nanotubes (CNTs) have been gradually applied to the removal of organic contaminants from wastewater through adsorption processes. This paper reviews recent progress (145 studies published from 2010 to 2013) in the application of CNTs and their composites for the removal of toxic organic pollutants from contaminated water. The paper discusses removal efficiencies and adsorption mechanisms as well as thermodynamics and reaction kinetics. CNTs are predicted to have considerable prospects for wider application to wastewater treatment in the future. - Highlights: • We summarize the most recent research progress of CNTs for removal of organics. • Adsorption mechanisms between CNTs and organics were elucidated in detail. • The developing trends and prospects of CNTs for removal of organics were discussed

Aqueous adsorption and removal of organic contaminants by carbon nanotubes

Energy Technology Data Exchange (ETDEWEB)

Yu, Jin-Gang, E-mail: yujg@csu.edu.cn [College of Chemistry and Chemical Engineering, Central South University, Changsha, Hunan 410083 (China); College of Chemistry and Chemical Engineering, Hunan University, Changsha, Hunan 410082 (China); Key Laboratory of Resources Chemistry of Nonferrous Metals, Ministry of Education, Central South University, Changsha, Hunan 410083 (China); Zhao, Xiu-Hui; Yang, Hua [College of Chemistry and Chemical Engineering, Central South University, Changsha, Hunan 410083 (China); Key Laboratory of Resources Chemistry of Nonferrous Metals, Ministry of Education, Central South University, Changsha, Hunan 410083 (China); Chen, Xiao-Hong [Collaborative Innovation Center of Resource-conserving and Environment-friendly Society and Ecological Civilization, Changsha, Hunan 410083 (China); Yang, Qiaoqin [Department of Mechanical Engineering, University of Saskatchewan, Saskatoon, SK S7N 5A9 (Canada); Yu, Lin-Yan [College of Chemistry and Chemical Engineering, Central South University, Changsha, Hunan 410083 (China); Key Laboratory of Resources Chemistry of Nonferrous Metals, Ministry of Education, Central South University, Changsha, Hunan 410083 (China); Jiang, Jian-Hui [College of Chemistry and Chemical Engineering, Hunan University, Changsha, Hunan 410082 (China); Chen, Xiao-Qing, E-mail: xqchen@csu.edu.cn [College of Chemistry and Chemical Engineering, Central South University, Changsha, Hunan 410083 (China); Key Laboratory of Resources Chemistry of Nonferrous Metals, Ministry of Education, Central South University, Changsha, Hunan 410083 (China)

2014-06-01

Organic contaminants have become one of the most serious environmental problems, and the removal of organic contaminants (e.g., dyes, pesticides, and pharmaceuticals/drugs) and common industrial organic wastes (e.g., phenols and aromatic amines) from aqueous solutions is of special concern because they are recalcitrant and persistent in the environment. In recent years, carbon nanotubes (CNTs) have been gradually applied to the removal of organic contaminants from wastewater through adsorption processes. This paper reviews recent progress (145 studies published from 2010 to 2013) in the application of CNTs and their composites for the removal of toxic organic pollutants from contaminated water. The paper discusses removal efficiencies and adsorption mechanisms as well as thermodynamics and reaction kinetics. CNTs are predicted to have considerable prospects for wider application to wastewater treatment in the future. - Highlights: • We summarize the most recent research progress of CNTs for removal of organics. • Adsorption mechanisms between CNTs and organics were elucidated in detail. • The developing trends and prospects of CNTs for removal of organics were discussed.

Reconstructing Early Industrial Contributions to Legacy Trace Metal Contamination in Southwestern Pennsylvania

Science.gov (United States)

Rossi, R.; Bain, D.; Hillman, A. L.; Pompeani, D. P.; Abbott, M. B.

2015-12-01

The remobilization of legacy contamination stored in floodplain sediments remains a threat to ecosystem and human health, particularly with potential changes in global precipitation patterns and flooding regimes. Vehicular and industrial emissions are often the dominant, recognized source of anthropogenic trace metal loadings to ecosystems today. However, loadings from early industrial activities are poorly characterized and potential sources of trace metal inputs. While potential trace metal contamination from these activities is recognized (e.g., the historical use of lead arsenate as a pesticide), the magnitude and distribution of legacy contamination is often unknown. This presentation reconstructs a lake sediment record of trace metal inputs from an oxbow lake in Southwestern Pennsylvania. Sediment cores were analyzed for major and trace metal chemistry, carbon to nitrogen ratios, bulk density, and magnetic susceptibility. Sediment trace metal chemistry in this approximately 250 year record (180 cm) record changes in land use and industry both in the 19th century and the 20th century. Of particular interest is early 19th century loadings of arsenic and calcium to the lake, likely attributable to pesticides and lime used in tanning processes near the lake. After this period of tanning dominated inputs, sediment barium concentrations rise, likely reflecting the onset of coal mining operations and resulting discharge of acid mine drainage to surface waters. In the 20th century portion of our record (70 -20 cm), patterns in sediment zinc, cadmium, and lead concentrations are dominated by the opening and closing of the nearby Donora Zinc Works and the American Steel & Wire Works, infamous facilities in the history of air quality regulation. The most recent sediment chemistry records periods include the enactment of air pollution legislation (~ 35 cm), and the phase out of tetraethyl leaded gasoline (~30 cm). Our study documents the impact of early industry in the

Root Cause Assessment of Pressure Drop Rise of a Packed Bed of Lithium Hydroxide in the International Space Station Trace Contaminant Control System

Science.gov (United States)

Aguilera, Tatiana; Perry, Jay L.

2009-01-01

The trace contaminant control system (TCCS) located in the International Space Station s (ISS) U.S. laboratory module employs physical adsorption, thermal catalytic oxidation, and chemical adsorption to remove trace chemical contamination produced by equipment offgassing and anthropogenic sources from the cabin atmosphere. The chemical adsorption stage, consisting of a packed bed of granular lithium hydroxide (LiOH), is located after the thermal catalytic oxidation stage and is designed to remove acid gas byproducts that may be formed in the upstream oxidation stage. While in service on board the ISS, the LiOH bed exhibited a change in flow resistance that leading to flow control difficulties in the TCCS. Post flight evaluation revealed LiOH granule size attrition among other changes. An experimental program was employed to investigate mechanisms hypothesized to contribute to the change in the packed bed s flow resistance. Background on the problem is summarized, including a discussion of likely mechanisms. The experimental program is described, results are presented, and implications for the future are discussed.

Treatment techniques for the removal of radioactive contaminants from drinking water

International Nuclear Information System (INIS)

Logsdon, Gary S.

1978-01-01

Maximum contaminant levels have been set for radioactive contaminants, as required by the Safe Drinking Water Act (PL 93-523). Treatment techniques are available for removing radium and beta-gamma emitters. Presently-used methods of removing radium-226 are precipitative lime softening (80-90% removal) ion exchange softening (95% removal) and reverse osmosis (95% removal). The 5 p Ci/l limit for radium can be met with conventional technology for raw waters in the 5-100 p Ci/l concentration range. Treatment for removal of beta or gamma emitters must be based upon chemical rather than radioactive characteristics of the contaminant. Reverse osmosis can remove a broad spectrum of ions and molecules from water, so it is the process most likely to be used. The maximum contaminant level for beta and gamma radioactivity is an annual dose equivalent to the total body or any organ not to exceed 4 m rem/year. The fate of radionuclides after removal from drinking water should be considered. Presently radium is disposed with other process wastes at softening plants removing radium. Confinement and disposal as a radioactive waste would be very expensive. (author)

System for removing contaminated surface layers

International Nuclear Information System (INIS)

Yoshikawa, Kozo.

1987-04-01

The object of the present invention is to offer a new type of useful decontamination system, with which the contaminated surface layers can be removed effectively by injection of such solid microparticles. Liquid carbon dioxide is passed from a liquid carbon dioxide tank via the carbon dioxide supply line into the system for injecting solid carbon dioxide particles. Part of the liquid carbon dioxide introduced into the system is converted to solid carbon dioxide particles by the temperature drop resulting from adiabatic expansion in the carbon dioxide expansion space of the injection system. The solid carbon dioxide particles reach the injection nozzle, which is connected through the expansion space. The carbon dioxide microparticles are further cooled and accelerated by nitrogen gas injected from the nitrogen gas nozzle at the tip of the nitrogen gas supply line, which is connected to a liquid nitrogen tank. The cooled and accelerated solid carbon dioxide microparticles are injected from the injection nozzle for the solid carbon dioxide and directed against the contaminated surface to be cleaned, and, as a result, the surface contamination is removed

Removal of trace metals and improvement of dredged sediment dewaterability by bioleaching combined with Fenton-like reaction.

Science.gov (United States)

Zeng, Xiangfeng; Twardowska, Irena; Wei, Shuhe; Sun, Lina; Wang, Jun; Zhu, Jianyu; Cai, Jianchao

2015-05-15

Bioleaching by Aspergillus niger strain SY1 combined with Fenton-like reaction was optimized to improve trace metal removal and dewaterability of dredged sediments. The major optimized parameters were the duration of bioleaching and H₂O₂ dose in Fenton-like process (5 days and 2g H₂O₂/L, respectively). Bioleaching resulted in the removal of ≈90% of Cd, ≈60% of Zn and Cu, ≈20% of Pb, and in decrease of sediment pH from 6.6 to 2.5 due to organic acids produced by A. niger. After addition of H₂O₂, Fenton-like reaction was initiated and further metal removal occurred. Overall efficiency of the combined process comprised: (i) reduction of Cd content in sediment by 99.5%, Cu and Zn by >70% and Pb by 39% as a result of metal release bound in all mobilizable fractions; (ii) decrease of sediment capillary suction time (CST) from 98.2s to 10.1s (by 89.8%) and specific resistance to filtration (SRF) from 37.4×10(12)m/kg to 6.2×10(12)m/kg (by 83.8%), due to reducing amount of extracellular polymeric substances (EPS) by 68.7% and bound water content by 79.1%. The combined process was found to be an efficient method to remove trace metals and improve dewaterability of contaminated dredged sediments. Copyright © 2015 Elsevier B.V. All rights reserved.

Integrating electrochemical oxidation into forward osmosis process for removal of trace antibiotics in wastewater.

Science.gov (United States)

Liu, Pengxiao; Zhang, Hanmin; Feng, Yujie; Shen, Chao; Yang, Fenglin

2015-10-15

During the rejection of trace pharmaceutical contaminants from wastewater by forward osmosis (FO), disposal of the FO concentrate was still an unsolved issue. In this study, by integrating the advantages of forward osmosis and electrochemical oxidation, a forward osmosis process with the function of electrochemical oxidation (FOwEO) was established for the first time to achieve the aim of rejection of trace antibiotics from wastewater and treatment of the concentrate at the same time. Results demonstrated that FOwEO (current density J=1 mA cm(-2)) exhibited excellent rejections of antibiotics (>98%) regardless of different operation conditions, and above all, antibiotics in the concentrate were well degraded (>99%) at the end of experiment (after 3h). A synergetic effect between forward osmosis and electrochemical oxidation was observed in FOwEO, which lies in that antibiotic rejections by FO were enhanced due to the degradation of antibiotics in the concentrate, while the electrochemical oxidation capacity was improved in the FOwEO channel, of which good mass transfer and the assist of indirect oxidation owing to the reverse NaCl from draw solution were supposed to be the mechanism. This study demonstrated that the FOwEO has the capability to thoroughly remove trace antibiotics from wastewater. Copyright © 2015 Elsevier B.V. All rights reserved.

Contaminant transport, revegetation, and trace element studies at inactive uranium mill tailings piles

International Nuclear Information System (INIS)

Dreesen, D.R.; Marple, M.L.; Kelley, N.E.

1978-01-01

The stabilization of inactive uranium mill tailings piles is presently under study. These studies have included investigations of stabilizing tailings by attempting to establish native vegetation without applying irrigation. Examination of processes which transport tailings or associated contaminants into the environment has been undertaken to better understand the containment provided by various stabilization methods. The uptake of toxic trace elements and radionuclides by vegetation has been examined as a mechanism of contaminant transport. The source terms of 222 Rn from inactive piles have been determined as well as the attenuation of radon flux provided by shallow soil covers. The possibility of shallow ground water contamination around an inactive pile has been examined to determine the significance of ground water transport as a mode of contaminant migration. The rationale in support of trace element studies related to uranium milling activities is presented including the enrichment, migration, and toxicities of trace elements often associated with uranium deposits. Some concepts for the stabilization of inactive piles are presented to extrapolate from research findings to practical applications. 25 references, 8 tables

Nanofiltration vs. reverse osmosis for the removal of emerging organic contaminants in water reuse

KAUST Repository

Yangali-Quintanilla, Victor

2011-10-01

Reverse osmosis (RO) in existing water reuse facilities is a water industry standard. However, that approach may be questioned taking into consideration that "tight" NF can be equal or "better" than RO. NF can achieve the same removals of RO membranes when dealing with emerging organic contaminants (pharmaceuticals, pesticides, endocrine disruptors and others). Experiments using 18 emerging contaminants were performed using membranes NF200 and NF90 at bench-scale units, and for a more complete study, results of NF and RO pilot and full-scale experiments where compared to our experimental results. The removal results showed that NF can remove many emerging contaminants. The average removal by tight NF was 82% for neutral contaminants and 97% for ionic contaminants. The average removal by RO was 85% for neutral contaminants and 99% for ionic contaminants. Aquifer recharge and recovery (ARR) followed by NF can effectively remove emerging contaminants with removals over 90% when loose NF membranes are used.

Nanofiltration vs. reverse osmosis for the removal of emerging organic contaminants in water reuse

KAUST Repository

Yangali-Quintanilla, Victor

2011-01-01

Reverse osmosis (RO) in existing water reuse facilities is a water industry standard. However, that approach may be questioned taking into consideration that "tight" NF can be equal or "better" than RO. NF can achieve the same removals of RO membranes when dealing with emerging organic contaminants (pharmaceuticals, pesticides, endocrine disruptors and others). Experiments using 18 emerging contaminants were performed using membranes NF200 and NF90 at bench-scale units, and for a more complete study, results of NF and RO pilot and fullscale experiments where compared to our experimental results. The removal results showed that NF can remove many emerging contaminants. The average removal by tight NF was 82% for neutral contaminants and 97% for ionic contaminants. The average removal by RO was 85% for neutral contaminants and 99% for ionic contaminants. Aquifer recharge and recovery (ARR) followed by NF can effectively remove emerging contaminants with removals over 90% when loose NF membranes are used. © 2011 2011 Desalination Publications. All rights reserved.

The role of plant-associated bacteria in the mobilization and phytoextraction of trace elements in contaminated soils.

Science.gov (United States)

Sessitsch, Angela; Kuffner, Melanie; Kidd, Petra; Vangronsveld, Jaco; Wenzel, Walter W; Fallmann, Katharina; Puschenreiter, Markus

2013-05-01

Phytoextraction makes use of trace element-accumulating plants that concentrate the pollutants in their tissues. Pollutants can be then removed by harvesting plants. The success of phytoextraction depends on trace element availability to the roots and the ability of the plant to intercept, take up, and accumulate trace elements in shoots. Current phytoextraction practises either employ hyperaccumulators or fast-growing high biomass plants; the phytoextraction process may be enhanced by soil amendments that increase trace element availability in the soil. This review will focus on the role of plant-associated bacteria to enhance trace element availability in the rhizosphere. We report on the kind of bacteria typically found in association with trace element - tolerating or - accumulating plants and discuss how they can contribute to improve trace element uptake by plants and thus the efficiency and rate of phytoextraction. This enhanced trace element uptake can be attributed to a microbial modification of the absorptive properties of the roots such as increasing the root length and surface area and numbers of root hairs, or by increasing the plant availability of trace elements in the rhizosphere and the subsequent translocation to shoots via beneficial effects on plant growth, trace element complexation and alleviation of phytotoxicity. An analysis of data from literature shows that effects of bacterial inoculation on phytoextraction efficiency are currently inconsistent. Some key processes in plant-bacteria interactions and colonization by inoculated strains still need to be unravelled more in detail to allow full-scale application of bacteria assisted phytoremediation of trace element contaminated soils.

Effective removal of hazardous trace metals from recovery boiler fly ashes.

Science.gov (United States)

Kinnarinen, Teemu; Golmaei, Mohammad; Jernström, Eeva; Häkkinen, Antti

2018-02-15

The objective of this study is to introduce a treatment sequence enabling straightforward and effective recovery of hazardous trace elements from recovery boiler fly ash (RBFA) by a novel method, and to demonstrate the subsequent removal of Cl and K with the existing crystallization technology. The treatment sequence comprises two stages: dissolution of most other RBFA components than the hazardous trace elements in water in Step 1 of the treatment, and crystallization of the process chemicals in Step 2. Solid-liquid separation has an important role in the treatment, due to the need to separate first the small solid residue containing the trace elements, and to separate the valuable crystals, containing Na and S, from the liquid rich in Cl and K. According to the results, nearly complete recovery of cadmium, lead and zinc can be reached even without pH adjustment. Some other metals, such as Mg and Mn, are removed together with the hazardous metals. Regarding the removal of Cl and K from the process, in this non-optimized case the removal efficiency was satisfactory: 60-70% for K when 80% of sodium was recovered, and close to 70% for Cl when 80% of sulfate was recovered. Copyright © 2017 Elsevier B.V. All rights reserved.

Laser assisted removal of fixed contamination from metallic substrate

International Nuclear Information System (INIS)

Kumar, Aniruddha; Prasad, Manisha; Prakash, Tej; Shail, Shailini; Bhatt, R.B.; Behere, P.G.; Mohd Afzal; Kumar, Arun; Biswas, D.J.

2015-01-01

A single mode pulsed fiber laser was used to remove fixed contamination from stainless steel substrate by ablation. Samples were simulated by electro-deposition technique with 232 U as the test contaminant. Laser power, repetition rate, laser beam scanning speed and number of passes were optimised to obtain the desired ablation depth in the substrate. Ablation depth varying between few microns to few hundreds of microns could be achieved through careful control of these processing parameters. The absence of any activity in laser treated samples provided experimental signature of the efficacy of the laser assisted removal of fixed contamination. (author)

Methods for removing contaminant matter from a porous material

Science.gov (United States)

Fox, Robert V [Idaho Falls, ID; Avci, Recep [Bozeman, MT; Groenewold, Gary S [Idaho Falls, ID

2010-11-16

Methods of removing contaminant matter from porous materials include applying a polymer material to a contaminated surface, irradiating the contaminated surface to cause redistribution of contaminant matter, and removing at least a portion of the polymer material from the surface. Systems for decontaminating a contaminated structure comprising porous material include a radiation device configured to emit electromagnetic radiation toward a surface of a structure, and at least one spray device configured to apply a capture material onto the surface of the structure. Polymer materials that can be used in such methods and systems include polyphosphazine-based polymer materials having polyphosphazine backbone segments and side chain groups that include selected functional groups. The selected functional groups may include iminos, oximes, carboxylates, sulfonates, .beta.-diketones, phosphine sulfides, phosphates, phosphites, phosphonates, phosphinates, phosphine oxides, monothio phosphinic acids, and dithio phosphinic acids.

Fiber-Based Adsorbents Tailored for PLSS Ammonia and Formaldehyde Removal, Phase II

Data.gov (United States)

National Aeronautics and Space Administration — Development of advanced lightweight Trace Contaminant Control (TCC) filters plays an important role in removing ammonia and formaldehyde contaminants?both those...

Next Generation Hybrid Photo-Catalytic Oxidation (PCO) for Trace Contaminant Control

Data.gov (United States)

National Aeronautics and Space Administration — Photocatalytic oxidation (PCO) is a primary candidate as an alternative to thermal-catalytic or sorbent- based technologies for VOC trace contaminant control due to...

Development of contaminated concrete removing system 'Clean cut method'

International Nuclear Information System (INIS)

Kinoshita, Takehiko; Tanaka, Tsutomu; Funakawa, Naoyoshi; Idemura, Hajime; Sakashita, Fumio; Tajitsu, Yoshiteru

1989-01-01

In the case of decommissioning nuclear facilities such as nuclear power stations, nuclear fuel facilities and RI handling facilities and carrying out reconstruction works, if there is radioactive contamination on the surfaces of concrete structures such as the floors and walls of the buildings for nuclear facilities, it must be removed. Since concrete is porous, contamination infiltrates into the inside of concrete, and the wiping of surfaces only or chemical decontamination cannot remove it, therefore in most cases, contaminated concrete must be removed. The removal of concrete surfaces has been carried out with chipping hammers, grinders and so on, but many problems arise due to it. In order to solve these problems, the mechanical cutting method was newly devised, and clean cut method (CCRS) was completed. The depth of cutting from concrete surface is set beforehand, and the part to be removed is accurately cut, at the same time, the concrete powder generated is collected nearly perfectly, and recovered into a drum. The outline of the method and the constitution of the system, the features of the clean cut method, the development of the technology for cutting concrete and the technology for recovering concrete powder, and the test of verifying decontamination are reported. (K.I.)

Efficient removal of trace antimony(III) through adsorption by hematite modified magnetic nanoparticles

International Nuclear Information System (INIS)

Shan, Chao; Ma, Zhiyao; Tong, Meiping

2014-01-01

Graphical abstract: - Highlights: • Sb(III) adsorption capacity of MNP@hematite was twice that of commercial Fe 3 O 4 . • pH, ionic strength, coexisting anions and NOM did not inhibit Sb(III) removal. • MNP@hematite could remove trace Sb(III) and As(III) from water simultaneously. • Efficient removal of Sb(III) from real tap water was achieved. • MNP@hematite could be easily recycled with a magnet and could be used repeatedly. - Abstract: Hematite coated magnetic nanoparticle (MNP@hematite) was fabricated through heterogeneous nucleation technique and used to remove trace Sb(III) from water. Powder X-ray diffraction, transmission electron microscopy (TEM), and alternating gradient magnetometry were utilized to characterize the prepared adsorbent. TEM image showed that MNP@hematite particles were spherical with size of 10–30 nm. With saturation magnetization of 27.0 emu/g, MNP@hematite particles could be easily separated from water with a simple magnetic process in short time (5 min). At initial concentration of 110 μg/L, Sb(III) was rapidly decreased to below 5 μg/L by MNP@hematite in 10 min. Sb(III) adsorption capacity of MNP@hematite was 36.7 mg/g, which was almost twice that of commercial Fe 3 O 4 nanoparticles. The removal of trace Sb(III) was not obviously affected by solution pH (over a wide range from 3 to 11), ionic strength (up to 100 mM), coexisting anions (chloride, nitrate, sulfate, carbonate, silicate, and phosphate, up to 10 mM) and natural organic matters (humic acid and alginate, up to 8 mg/L as TOC). Moreover, MNP@hematite particles were able to remove Sb(III) and As(III) simultaneously. Trace Sb(III) could also be effectively removed from real tap water by MNP@hematite. The magnetic adsorbent could be recycled and used repeatedly

Efficient removal of trace antimony(III) through adsorption by hematite modified magnetic nanoparticles

Energy Technology Data Exchange (ETDEWEB)

Shan, Chao; Ma, Zhiyao; Tong, Meiping, E-mail: tongmeiping@pku.edu.cn

2014-03-01

Graphical abstract: - Highlights: • Sb(III) adsorption capacity of MNP@hematite was twice that of commercial Fe{sub 3}O{sub 4}. • pH, ionic strength, coexisting anions and NOM did not inhibit Sb(III) removal. • MNP@hematite could remove trace Sb(III) and As(III) from water simultaneously. • Efficient removal of Sb(III) from real tap water was achieved. • MNP@hematite could be easily recycled with a magnet and could be used repeatedly. - Abstract: Hematite coated magnetic nanoparticle (MNP@hematite) was fabricated through heterogeneous nucleation technique and used to remove trace Sb(III) from water. Powder X-ray diffraction, transmission electron microscopy (TEM), and alternating gradient magnetometry were utilized to characterize the prepared adsorbent. TEM image showed that MNP@hematite particles were spherical with size of 10–30 nm. With saturation magnetization of 27.0 emu/g, MNP@hematite particles could be easily separated from water with a simple magnetic process in short time (5 min). At initial concentration of 110 μg/L, Sb(III) was rapidly decreased to below 5 μg/L by MNP@hematite in 10 min. Sb(III) adsorption capacity of MNP@hematite was 36.7 mg/g, which was almost twice that of commercial Fe{sub 3}O{sub 4} nanoparticles. The removal of trace Sb(III) was not obviously affected by solution pH (over a wide range from 3 to 11), ionic strength (up to 100 mM), coexisting anions (chloride, nitrate, sulfate, carbonate, silicate, and phosphate, up to 10 mM) and natural organic matters (humic acid and alginate, up to 8 mg/L as TOC). Moreover, MNP@hematite particles were able to remove Sb(III) and As(III) simultaneously. Trace Sb(III) could also be effectively removed from real tap water by MNP@hematite. The magnetic adsorbent could be recycled and used repeatedly.

A comparative assessment of chemical contaminant removal by ...

African Journals Online (AJOL)

This study was aimed at modifying the design of, constructing, evaluating and comparing chemical contaminant removal efficiency by, 3 household water treatment filters. The filters were: 1) biosand filter (BSF); 2) the ceramic candle filter (CCF); 3) bucket filter (BF). The filters were evaluated for their efficiency in removal of ...

Can Microalgae Remove Pharmaceutical Contaminants from Water?

Science.gov (United States)

Xiong, Jiu-Qiang; Kurade, Mayur B; Jeon, Byong-Hun

2018-01-01

The increase in worldwide water contamination with numerous pharmaceutical contaminants (PCs) has become an emerging environmental concern due to their considerable ecotoxicities and associated health issues. Microalgae-mediated bioremediation of PCs has recently gained scientific attention, as microalgal bioremediation is a solar-power driven, ecologically comprehensive, and sustainable reclamation strategy. In this review, we comprehensively describe the current research on the possible roles and applications of microalgae for removing PCs from aqueous media. We summarize several novel approaches including constructing microbial consortia, acclimation, and cometabolism for enhanced removal of PCs by microalgae, which would improve practical feasibility of these technologies. Some novel concepts for degrading PCs using integrated processes and genetic modifications to realize algal-based bioremediation technologies are also recommended. Copyright © 2017 Elsevier Ltd. All rights reserved.

Comparison of trace element contamination levels (Cu, Zn, Fe, Cd ...

African Journals Online (AJOL)

Comparison of trace element contamination levels (Cu, Zn, Fe, Cd and Pb) in the soft tissues of the gastropods Tympanotonus fuscatus fuscatus and Tf radula collected in the Ebrié Lagoon (Côte d'Ivoire): Evidence of the risks linked to linked to lead and.

Regenerable Air Purification System for Gas-Phase Contaminant Control

Science.gov (United States)

Constantinescu, Ileana C.; Finn, John E.; LeVan, M. Douglas; Lung, Bernadette (Technical Monitor)

2000-01-01

Tests of a pre-prototype regenerable air purification system (RAPS) that uses water vapor to displace adsorbed contaminants from an adsorbent column have been performed at NASA Ames Research Center. A unit based on this design can be used for removing trace gas-phase contaminants from spacecraft cabin air or from polluted process streams including incinerator exhaust. During the normal operation mode, contaminants are removed from the air on the column. Regeneration of the column is performed on-line. During regeneration, contaminants are displaced and destroyed inside the closed oxidation loop. In this presentation we discuss initial experimental results for the performance of RAPS in the removal and treatment of several important spacecraft contaminant species from air.

Unbiased contaminant removal for 3D galaxy power spectrum measurements

Science.gov (United States)

Kalus, B.; Percival, W. J.; Bacon, D. J.; Samushia, L.

2016-11-01

We assess and develop techniques to remove contaminants when calculating the 3D galaxy power spectrum. We separate the process into three separate stages: (I) removing the contaminant signal, (II) estimating the uncontaminated cosmological power spectrum and (III) debiasing the resulting estimates. For (I), we show that removing the best-fitting contaminant (mode subtraction) and setting the contaminated components of the covariance to be infinite (mode deprojection) are mathematically equivalent. For (II), performing a quadratic maximum likelihood (QML) estimate after mode deprojection gives an optimal unbiased solution, although it requires the manipulation of large N_mode^2 matrices (Nmode being the total number of modes), which is unfeasible for recent 3D galaxy surveys. Measuring a binned average of the modes for (II) as proposed by Feldman, Kaiser & Peacock (FKP) is faster and simpler, but is sub-optimal and gives rise to a biased solution. We present a method to debias the resulting FKP measurements that does not require any large matrix calculations. We argue that the sub-optimality of the FKP estimator compared with the QML estimator, caused by contaminants, is less severe than that commonly ignored due to the survey window.

Trace elements contamination of soils around gold mine tailings ...

African Journals Online (AJOL)

This study investigated the issue of tailings dams as a potential source of trace elements contamination in soils at the Obuasi gold mine in Ghana. Soil samples taken from depths of up to 12 cm and within a radius of 400 m from the tailings dams (active and recommissioned), were analysed for As, Cu, Pb and. Zn using ...

Arsenic Removal from Water by Adsorption on Iron-Contaminated Cryptocrystalline Graphite

Science.gov (United States)

Yang, Qiang; Yang, Lang; Song, Shaoxian; Xia, Ling

This work aimed to study the feasibility of using iron-contaminated graphite as an adsorbent for As(V) removal from water. The adsorbent was prepared by grinding graphite concentrate with steel ball. The study was performed through the measurements of adsorption capacity, BET surface area and XPS analysis. The experimental results showed that the iron-contaminated graphite exhibited significantly high adsorption capacity of As(V). The higher the iron contaminated on the graphite surface, the higher the adsorption capacity of As(V) on the material obtained. It was suggested that the ion-contaminated graphite was a good adsorbent for As(V) removal.

Removing Contamination-Induced Reconstruction Artifacts from Cryo-electron Tomograms

Science.gov (United States)

Fernandez, Jose-Jesus; Laugks, Ulrike; Schaffer, Miroslava; Bäuerlein, Felix J.B.; Khoshouei, Maryam; Baumeister, Wolfgang; Lucic, Vladan

2016-01-01

Imaging of fully hydrated, vitrified biological samples by electron tomography yields structural information about cellular protein complexes in situ. Here we present a computational procedure that removes artifacts of three-dimensional reconstruction caused by contamination present in samples during imaging by electron microscopy. Applying the procedure to phantom data and electron tomograms of cellular samples significantly improved the resolution and the interpretability of tomograms. Artifacts caused by surface contamination associated with thinning by focused ion beam, as well as those arising from gold fiducial markers and from common, lower contrast contamination, could be removed. Our procedure is widely applicable and is especially suited for applications that strive to reach a higher resolution and involve the use of recently developed, state-of-the-art instrumentation. PMID:26743046

Coagulation / flocculation process in the removal of trace metals ...

African Journals Online (AJOL)

Attempts were made in this study to examine the effectiveness of polymer addition to coagulation process during treatment of a beverage industrial wastewater to remove some of its trace metals content such as lead, cadmium, total iron, total chromium, nickel and zinc. Experiments were conducted using the standard Jar ...

Trace element contamination in feather and tissue samples from Anna’s hummingbirds

Science.gov (United States)

Mikoni, Nicole A.; Poppenga, Robert H.; Ackerman, Joshua T.; Foley, Janet E.; Hazlehurst, Jenny; Purdin, Güthrum; Aston, Linda; Hargrave, Sabine; Jelks, Karen; Tell, Lisa A.

2017-01-01

Trace element contamination (17 elements; Be, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, As, Se, Mo, Cd, Ba, Hg, Tl, and Pb) of live (feather samples only) and deceased (feather and tissue samples) Anna's hummingbirds (Calypte anna) was evaluated. Samples were analyzed using inductively coupled plasma-mass spectrometry (ICP-MS; 17 elements) and atomic absorption spectrophotometry (Hg only). Mean plus one standard deviation (SD) was considered the benchmark, and concentrations above the mean + 1 SD were considered elevated above normal. Contour feathers were sampled from live birds of varying age, sex, and California locations. In order to reduce thermal impacts, minimal feathers were taken from live birds, therefore a novel method was developed for preparation of low mass feather samples for ICP-MS analysis. The study found that the novel feather preparation method enabled small mass feather samples to be analyzed for trace elements using ICP-MS. For feather samples from live birds, all trace elements, with the exception of beryllium, had concentrations above the mean + 1 SD. Important risk factors for elevated trace element concentrations in feathers of live birds were age for iron, zinc, and arsenic, and location for iron, manganese, zinc, and selenium. For samples from deceased birds, ICP-MS results from body and tail feathers were correlated for Fe, Zn, and Pb, and feather concentrations were correlated with renal (Fe, Zn, Pb) or hepatic (Hg) tissue concentrations. Results for AA spectrophotometry analyzed samples from deceased birds further supported the ICP-MS findings where a strong correlation between mercury concentrations in feather and tissue (pectoral muscle) samples was found. These study results support that sampling feathers from live free-ranging hummingbirds might be a useful, non-lethal sampling method for evaluating trace element exposure and provides a sampling alternative since their small body size limits traditional sampling of blood and tissues. The

Simultaneous removal of phenanthrene and cadmium from contaminated soils by saponin, a plant-derived biosurfactant

International Nuclear Information System (INIS)

Song Saisai; Zhu Lizhong; Zhou Wenjun

2008-01-01

Batch experiments were conducted to evaluate the performance of saponin, a plant-derived biosurfactant, for simultaneously removing phenanthrene and cadmium from the combined contaminated soils. Results showed that phenanthrene was desorbed from the contaminated soils by saponin with the partition of phenanthrene into surfactant micelle, meanwhile cadmium was effectively removed from the contaminated soils by the complexation of cadmium with the external carboxyl groups of saponin micelle. The efficiencies of saponin for the removal of phenanthrene and cadmium from the contaminated soils were greater than that of Triton X100 and citric acid, respectively. At concentration of 3750 mg/L, saponin has a removal rate of 87.7% and 76.2% of cadmium and phenanthrene, respectively, from the combined contaminated soil. The removals of cadmium and phenanthrene from the soils were not obviously constrained each other. Thus, saponin has the potential for the removal of heavy metal and PAHs from the combined contaminated soils. - Saponin has great potential for the simultaneous removal of cadmium and phenanthrene from the combined contaminated soils

Simultaneous removal of phenanthrene and cadmium from contaminated soils by saponin, a plant-derived biosurfactant

Energy Technology Data Exchange (ETDEWEB)

Song Saisai [Department of Environmental Science, Zhejiang University, Hangzhou, Zhejiang 310028 (China); Zhu Lizhong [Department of Environmental Science, Zhejiang University, Hangzhou, Zhejiang 310028 (China)], E-mail: zlz@zju.edu.cn; Zhou Wenjun [Department of Environmental Science, Zhejiang University, Hangzhou, Zhejiang 310028 (China)

2008-12-15

Batch experiments were conducted to evaluate the performance of saponin, a plant-derived biosurfactant, for simultaneously removing phenanthrene and cadmium from the combined contaminated soils. Results showed that phenanthrene was desorbed from the contaminated soils by saponin with the partition of phenanthrene into surfactant micelle, meanwhile cadmium was effectively removed from the contaminated soils by the complexation of cadmium with the external carboxyl groups of saponin micelle. The efficiencies of saponin for the removal of phenanthrene and cadmium from the contaminated soils were greater than that of Triton X100 and citric acid, respectively. At concentration of 3750 mg/L, saponin has a removal rate of 87.7% and 76.2% of cadmium and phenanthrene, respectively, from the combined contaminated soil. The removals of cadmium and phenanthrene from the soils were not obviously constrained each other. Thus, saponin has the potential for the removal of heavy metal and PAHs from the combined contaminated soils. - Saponin has great potential for the simultaneous removal of cadmium and phenanthrene from the combined contaminated soils.

Removal of iron contaminant from zirconium chloride solution

International Nuclear Information System (INIS)

Voit, D.O.

1992-01-01

This patent describes a process for eliminating iron contaminant from an aqueous zirconium chloride solution that has been contaminated with FeCl 3 in a plant in which zirconium and hafnium chloride solutions are separated by a main MINK solvent extraction system and the FeCl 3 is normally removed from the zirconium chloride solution by a secondary MINK solvent extraction system

Trace and low concentration co2 removal methods and apparatus utilizing metal organic frameworks

KAUST Repository

Eddaoudi, Mohamed

2016-03-10

In general, this disclosure describes techniques for removing trace and low concentration CO2 from fluids using SIFSIX-n-M MOFs, wherein n is at least two and M is a metal. In some embodiments, the metal is zinc or copper. Embodiments include devices comprising SIFSIX-n-M MOFs for removing CO2 from fluids. In particular, embodiments relate to devices and methods utilizing SIFSIX-n-M MOFs for removing CO2 from fluids, wherein CO2 concentration is trace. Methods utilizing SIFSIX-n-M MOFs for removing CO2 from fluids can occur in confined spaces. SIFSIX-n-M MOFs can comprise bidentate organic ligands. In a specific embodiment, SIFSIX-n-M MOFs comprise pyrazine or dipryidilacetylene ligands.

The effects of mediator and granular activated carbon addition on degradation of trace organic contaminants by an enzymatic membrane reactor.

Science.gov (United States)

Nguyen, Luong N; Hai, Faisal I; Price, William E; Leusch, Frederic D L; Roddick, Felicity; Ngo, Hao H; Guo, Wenshan; Magram, Saleh F; Nghiem, Long D

2014-09-01

The removal of four recalcitrant trace organic contaminants (TrOCs), namely carbamazepine, diclofenac, sulfamethoxazole and atrazine by laccase in an enzymatic membrane reactor (EMR) was studied. Laccases are not effective for degrading non-phenolic compounds; nevertheless, 22-55% removal of these four TrOCs was achieved by the laccase EMR. Addition of the redox-mediator syringaldehyde (SA) to the EMR resulted in a notable dose-dependent improvement (15-45%) of TrOC removal affected by inherent TrOC properties and loading rates. However, SA addition resulted in a concomitant increase in the toxicity of the treated effluent. A further 14-25% improvement in aqueous phase removal of the TrOCs was consistently observed following a one-off dosing of 3g/L granular activated carbon (GAC). Mass balance analysis reveals that this improvement was not due solely to adsorption but also enhanced biodegradation. GAC addition also reduced membrane fouling and the SA-induced toxicity of the effluent. Copyright © 2014 Elsevier Ltd. All rights reserved.

Source Evaluation and Trace Metal Contamination in Benthic Sediments from Equatorial Ecosystems Using Multivariate Statistical Techniques.

Directory of Open Access Journals (Sweden)

Nsikak U Benson

Full Text Available Trace metals (Cd, Cr, Cu, Ni and Pb concentrations in benthic sediments were analyzed through multi-step fractionation scheme to assess the levels and sources of contamination in estuarine, riverine and freshwater ecosystems in Niger Delta (Nigeria. The degree of contamination was assessed using the individual contamination factors (ICF and global contamination factor (GCF. Multivariate statistical approaches including principal component analysis (PCA, cluster analysis and correlation test were employed to evaluate the interrelationships and associated sources of contamination. The spatial distribution of metal concentrations followed the pattern Pb>Cu>Cr>Cd>Ni. Ecological risk index by ICF showed significant potential mobility and bioavailability for Cu, Cu and Ni. The ICF contamination trend in the benthic sediments at all studied sites was Cu>Cr>Ni>Cd>Pb. The principal component and agglomerative clustering analyses indicate that trace metals contamination in the ecosystems was influenced by multiple pollution sources.

Method for removal of beryllium contamination from an article

Science.gov (United States)

Simandl, Ronald F.; Hollenbeck, Scott M.

2012-12-25

A method of removal of beryllium contamination from an article is disclosed. The method typically involves dissolving polyisobutylene in a solvent such as hexane to form a tackifier solution, soaking the substrate in the tackifier to produce a preform, and then drying the preform to produce the cleaning medium. The cleaning media are typically used dry, without any liquid cleaning agent to rub the surface of the article and remove the beryllium contamination below a non-detect level. In some embodiments no detectible residue is transferred from the cleaning wipe to the article as a result of the cleaning process.

Removable coating for contamination protection of concrete surface

International Nuclear Information System (INIS)

Brambilla, G.; Beaulardi, L.

1985-01-01

In order to research protective coatings for concrete surfaces, assuring an effective protection against contamination and that it be easily removed before dismantling the structures, commercial stripping paints have been characterized for their conventional and nuclear properties: water and chemicals, abrasion, impact, tensile stress resistance, stripping capacity, decontaminability. The protective power of the coatings against contamination has been checked by recording the surface activity before and after stripping the paint film: the activity filtered through the coating was, in any case, very low (< 1% of the deposited activity). Indications from large scale application of a stripping paint in NUCLEO (Rome) establishments and technical evaluation of the possible utilization of removable coatings in the CAORSO Nuclear Power Station, are also reported

Removal of emerging contaminants in sewage water subjected to advanced oxidation with ozone.

Science.gov (United States)

Ibáñez, M; Gracia-Lor, E; Bijlsma, L; Morales, E; Pastor, L; Hernández, F

2013-09-15

Advanced oxidation processes (AOP) based on ozone treatments, assisted by ultrasounds, have been investigated at a pilot-plant scale in order to evaluate the removal of emerging contaminants in sewage water. Around 60 emerging contaminants, mainly pharmaceuticals from different therapeutically classes and drugs of abuse, have been determined in urban wastewater samples (treated and untreated) by LC-MS/MS. In a first step, the removal efficiency of these contaminants in conventional sewage water treatment plants was evaluated. Our results indicate that most of the compounds were totally or partially removed during the treatment process of influent wastewater. Up to 30 contaminants were quantified in the influent and effluent samples analysed, being antibiotics, anti-inflammatories, cholesterol lowering statin drugs and angiotensin II receptor antagonists the most frequently detected. Regarding drugs of abuse, cocaine and its metabolite benzoylecgonine were the most frequent. In a second step, the effectiveness of AOP in the removal of emerging contaminants remaining in the effluent was evaluated. Ozone treatments have been proven to be highly efficient in the removal, notably decreasing the concentrations for most of the emerging contaminants present in the water samples. The use of ultrasounds, alone or assisting ozone treatments, has been shown less effective, being practically unnecessary. Copyright © 2013 Elsevier B.V. All rights reserved.

Nanofiltration vs. reverse osmosis for the removal of emerging organic contaminants in water reuse

KAUST Repository

Yangali-Quintanilla, Victor; Maeng, Sung Kyu; Fujioka, Takahiro; Kennedy, Maria; Li, Zhenyu; Amy, Gary L.

2011-01-01

study, results of NF and RO pilot and full-scale experiments where compared to our experimental results. The removal results showed that NF can remove many emerging contaminants. The average removal by tight NF was 82% for neutral contaminants and 97

Contaminant removal by wastewater treatment plants in the Stillaguamish River Basin, Washington

Science.gov (United States)

Barbash, Jack E.; Moran, Patrick W.; Wagner, Richard J.; Wolanek, Michael

2015-01-01

Human activities in most areas of the developed world typically release nutrients, pharmaceuticals, personal care products, pesticides, and other contaminants into the environment, many of which reach freshwater ecosystems. In urbanized areas, wastewater treatment plants (WWTPs) are critical facilities for collecting and reducing the amounts of wastewater contaminants (WWCs) that ultimately discharge to rivers, coastal areas, and groundwater. Most WWTPs use multiple methods to remove contaminants from wastewater. These include physical methods to remove solid materials (primary treatment), biological and chemical methods to remove most organic matter (secondary treatment), advanced methods to reduce the concentrations of various contaminants such as nitrogen, phosphorus and (or) synthetic organic compounds (tertiary treatment), and disinfection prior to discharge (Metcalf and Eddy, Inc., 1979). This study examined the extent to which 114 organic WWCs were removed by each of three WWTPs, prior to discharge to freshwater and marine ecosystems, in a rapidly developing area in northwestern Washington State. Removal percentages for each WWC were estimated by comparing the concentrations measured in the WWTP influents with those measured in the effluents. The investigation was carried out in the 700-mi2Stillaguamish River Basin, the fifth largest watershed that discharges to Puget Sound (fig. 1).

Facilitation drives the positive effects of plant richness on trace metal removal in a biodiversity experiment.

Directory of Open Access Journals (Sweden)

Jiang Wang

Full Text Available BACKGROUND: Phytoextraction is an environmentally acceptable and inexpensive technique for mine tailing rehabilitation that uses metallophyte plants. These plants reduce the soil trace metal contents to environmentally acceptable levels by accumulating trace metals. Recently, whether more trace metals can be removed by species-rich communities of these plants received great attention, as species richness has been reported having positive effects on ecosystem functions. However, how the species richness affects trace metals removal of plant communities of mine tailing is rarely known. METHODOLOGY/PRINCIPAL FINDINGS: We examined the effects of species richness on soil trace metal removal in both natural and experimental plant communities. The root lengths and stem heights of each plant species were measured in order to calculate the functional diversity indices. Our results showed that trace metal (Cu, Cd, Pb and Zn concentrations in mine tailing soil declined as species richness increased in both the natural and experimental plant communities. Species richness, rather than functional diversity, positively affected the mineralomass of the experimental plant communities. The intensity of plant-plant facilitation increased with the species richness of experimental communities. Due to the incremental role of plant-plant facilitation, most of the species had higher biomasses, higher trace metal concentrations in their plant tissues and lower malondialdehyde concentrations in their leaves. Consequently, the positive effects of species richness on mineralomass were mostly attributable to facilitation among plants. CONCLUSIONS/SIGNIFICANCE: Our results provide clear evidence that, due to plant-plant facilitation, species richness positively affects the removal of trace metals from mine tailing soil through phytoextraction and provides further information on diversity conservation and environmental remediation in a mine tailing environment.

Phytostabilization of semiarid soils residually contaminated with trace elements using by-products: Sustainability and risks

Energy Technology Data Exchange (ETDEWEB)

Perez-de-Mora, Alfredo, E-mail: perezdemora@gmail.com [Instituto de Recursos Naturales y Agrobiologia de Sevilla (IRNAS), CSIC, PO Box 1052, 41080 Sevilla (Spain); Madejon, Paula; Burgos, Pilar; Cabrera, Francisco [Instituto de Recursos Naturales y Agrobiologia de Sevilla (IRNAS), CSIC, PO Box 1052, 41080 Sevilla (Spain); Lepp, Nicholas W. [35, Victoria Road, Formby, Liverpool L37 7DH (United Kingdom); Madejon, Engracia [Instituto de Recursos Naturales y Agrobiologia de Sevilla (IRNAS), CSIC, PO Box 1052, 41080 Sevilla (Spain)

2011-10-15

We investigated the efficiency of various by-products (sugarbeet lime, biosolid compost and leonardite), based on single or repeated applications to field plots, on the establishment of a vegetation cover compatible with a stabilization strategy on a multi-element (As, Cd, Cu, Pb and Zn) contaminated soil 4-6 years after initial amendment applications. Results indicate that the need for re-treatment is amendment- and element-dependent; in some cases, a single application may reduce trace element concentrations in above-ground biomass and enhance the establishment of a healthy vegetation cover. Amendment performance as evaluated by % cover, biomass and number of colonizing taxa differs; however, changes in plant community composition are not necessarily amendment-specific. Although the translocation of trace elements to the plant biotic compartment is greater in re-vegetated areas, overall loss of trace elements due to soil erosion and plant uptake is usually smaller compared to that in bare soil. - Highlights: > By-products enhance vegetation dynamics in contaminated semiarid soils. > Depending on the situation single or repeated incorporations may be required. > The structure of the plant community established is not amendment-dependent. > Phytostabilization reduces overall loss of trace elements in semiarid soils. - Phytostabilization using by-products as amendments is a suitable approach for long-term immobilization of various trace elements in semiarid contaminated soils.

Phytostabilization of semiarid soils residually contaminated with trace elements using by-products: Sustainability and risks

International Nuclear Information System (INIS)

Perez-de-Mora, Alfredo; Madejon, Paula; Burgos, Pilar; Cabrera, Francisco; Lepp, Nicholas W.; Madejon, Engracia

2011-01-01

We investigated the efficiency of various by-products (sugarbeet lime, biosolid compost and leonardite), based on single or repeated applications to field plots, on the establishment of a vegetation cover compatible with a stabilization strategy on a multi-element (As, Cd, Cu, Pb and Zn) contaminated soil 4-6 years after initial amendment applications. Results indicate that the need for re-treatment is amendment- and element-dependent; in some cases, a single application may reduce trace element concentrations in above-ground biomass and enhance the establishment of a healthy vegetation cover. Amendment performance as evaluated by % cover, biomass and number of colonizing taxa differs; however, changes in plant community composition are not necessarily amendment-specific. Although the translocation of trace elements to the plant biotic compartment is greater in re-vegetated areas, overall loss of trace elements due to soil erosion and plant uptake is usually smaller compared to that in bare soil. - Highlights: → By-products enhance vegetation dynamics in contaminated semiarid soils. → Depending on the situation single or repeated incorporations may be required. → The structure of the plant community established is not amendment-dependent. → Phytostabilization reduces overall loss of trace elements in semiarid soils. - Phytostabilization using by-products as amendments is a suitable approach for long-term immobilization of various trace elements in semiarid contaminated soils.

Effects of ozone and ozone/peroxide on trace organic contaminants and NDMA in drinking water and water reuse applications.

Science.gov (United States)

Pisarenko, Aleksey N; Stanford, Benjamin D; Yan, Dongxu; Gerrity, Daniel; Snyder, Shane A

2012-02-01

An ozone and ozone/peroxide oxidation process was evaluated at pilot scale for trace organic contaminant (TOrC) mitigation and NDMA formation in both drinking water and water reuse applications. A reverse osmosis (RO) pilot was also evaluated as part of the water reuse treatment train. Ozone/peroxide showed lower electrical energy per order of removal (EEO) values for TOrCs in surface water treatment, but the addition of hydrogen peroxide increased EEO values during wastewater treatment. TOrC oxidation was correlated to changes in UV(254) absorbance and fluorescence offering a surrogate model for predicting contaminant removal. A decrease in N-nitrosodimethylamine (NDMA) formation potential (after chloramination) was observed after treatment with ozone and ozone/peroxide. However, during spiking experiments with surface water, ozone/peroxide achieved limited destruction of NDMA, while in wastewaters net direct formation of NDMA of 6-33 ng/L was observed after either ozone or ozone/peroxide treatment. Once formed during ozonation, NDMA passed through the subsequent RO membranes, which highlights the significance of the potential for direct NDMA formation during oxidation in reuse applications. Copyright © 2011 Elsevier Ltd. All rights reserved.

Occurrence and removal of emerging contaminants in wastewaters

OpenAIRE

Janna, Hussein

2011-01-01

This thesis was submitted for the degree of Doctor of Philosophy and awarded by Brunel University. Over the past decade, the occurrence and removal of emerging contaminants in the environment has received much attention. Both natural and synthetic progestogens, which are hormones, and also benzotriazoles are two examples of such emerging contaminants. Sewage treatment works are recognised as one of the main routes of these compounds to the environment. Low concentrations (nanograms per lit...

A multi-process phytoremediation system for removal of polycyclic aromatic hydrocarbons from contaminated soils

International Nuclear Information System (INIS)

Huang Xiaodong; El-Alawi, Yousef; Penrose, Donna M.; Glick, Bernard R.; Greenberg, Bruce M.

2004-01-01

To improve phytoremediation processes, multiple techniques that comprise different aspects of contaminant removal from soils have been combined. Using creosote as a test contaminant, a multi-process phytoremediation system composed of physical (volatilization), photochemical (photooxidation) and microbial remediation, and phytoremediation (plant-assisted remediation) processes was developed. The techniques applied to realize these processes were land-farming (aeration and light exposure), introduction of contaminant degrading bacteria, plant growth promoting rhizobacteria (PGPR), and plant growth of contaminant-tolerant tall fescue (Festuca arundinacea). Over a 4-month period, the average efficiency of removal of 16 priority PAHs by the multi-process remediation system was twice that of land-farming, 50% more than bioremediation alone, and 45% more than phytoremediation by itself. Importantly, the multi-process system was capable of removing most of the highly hydrophobic, soil-bound PAHs from soil. The key elements for successful phytoremediation were the use of plant species that have the ability to proliferate in the presence of high levels of contaminants and strains of PGPR that increase plant tolerance to contaminants and accelerate plant growth in heavily contaminated soils. The synergistic use of these approaches resulted in rapid and massive biomass accumulation of plant tissue in contaminated soil, putatively providing more active metabolic processes, leading to more rapid and more complete removal of PAHs. - Persistent PAH contaminants in soils can be removed more completely and rapidly by using multiple remediation processes

Mapping human health risks from exposure to trace metal contamination of drinking water sources in Pakistan

International Nuclear Information System (INIS)

Bhowmik, Avit Kumar; Alamdar, Ambreen; Katsoyiannis, Ioannis; Shen, Heqing; Ali, Nadeem; Ali, Syeda Maria; Bokhari, Habib; Schäfer, Ralf B.; Eqani, Syed Ali Musstjab Akber Shah

2015-01-01

The consumption of contaminated drinking water is one of the major causes of mortality and many severe diseases in developing countries. The principal drinking water sources in Pakistan, i.e. ground and surface water, are subject to geogenic and anthropogenic trace metal contamination. However, water quality monitoring activities have been limited to a few administrative areas and a nationwide human health risk assessment from trace metal exposure is lacking. Using geographically weighted regression (GWR) and eight relevant spatial predictors, we calculated nationwide human health risk maps by predicting the concentration of 10 trace metals in the drinking water sources of Pakistan and comparing them to guideline values. GWR incorporated local variations of trace metal concentrations into prediction models and hence mitigated effects of large distances between sampled districts due to data scarcity. Predicted concentrations mostly exhibited high accuracy and low uncertainty, and were in good agreement with observed concentrations. Concentrations for Central Pakistan were predicted with higher accuracy than for the North and South. A maximum 150–200 fold exceedance of guideline values was observed for predicted cadmium concentrations in ground water and arsenic concentrations in surface water. In more than 53% (4 and 100% for the lower and upper boundaries of 95% confidence interval (CI)) of the total area of Pakistan, the drinking water was predicted to be at risk of contamination from arsenic, chromium, iron, nickel and lead. The area with elevated risks is inhabited by more than 74 million (8 and 172 million for the lower and upper boundaries of 95% CI) people. Although these predictions require further validation by field monitoring, the results can inform disease mitigation and water resources management regarding potential hot spots. - Highlights: • Predictions of trace metal concentration use geographically weighted regression • Human health risk

Mapping human health risks from exposure to trace metal contamination of drinking water sources in Pakistan

Energy Technology Data Exchange (ETDEWEB)

Bhowmik, Avit Kumar [Institute for Environmental Sciences, University of Koblenz-Landau, Fortstrasse 7, D-76829 Landau in der Pfalz (Germany); Alamdar, Ambreen [Key Lab of Urban Environment and Health, Institute of Urban Environment, Chinese Academy of Sciences, Xiamen 361021 (China); Katsoyiannis, Ioannis [Aristotle University of Thessaloniki, Department of Chemistry, Division of Chemical Technology, Box 116, Thessaloniki 54124 (Greece); Shen, Heqing [Key Lab of Urban Environment and Health, Institute of Urban Environment, Chinese Academy of Sciences, Xiamen 361021 (China); Ali, Nadeem [Department of Environmental Sciences, FBAS, International Islamic University, Islamabad (Pakistan); Ali, Syeda Maria [Center of Excellence in Environmental Studies, King Abdulaziz University, Jeddah (Saudi Arabia); Bokhari, Habib [Public Health and Environment Division, Department of Biosciences, COMSATS Institute of Information Technology, Islamabad (Pakistan); Schäfer, Ralf B. [Institute for Environmental Sciences, University of Koblenz-Landau, Fortstrasse 7, D-76829 Landau in der Pfalz (Germany); Eqani, Syed Ali Musstjab Akber Shah, E-mail: ali_ebl2@yahoo.com [Key Lab of Urban Environment and Health, Institute of Urban Environment, Chinese Academy of Sciences, Xiamen 361021 (China); Public Health and Environment Division, Department of Biosciences, COMSATS Institute of Information Technology, Islamabad (Pakistan)

2015-12-15

The consumption of contaminated drinking water is one of the major causes of mortality and many severe diseases in developing countries. The principal drinking water sources in Pakistan, i.e. ground and surface water, are subject to geogenic and anthropogenic trace metal contamination. However, water quality monitoring activities have been limited to a few administrative areas and a nationwide human health risk assessment from trace metal exposure is lacking. Using geographically weighted regression (GWR) and eight relevant spatial predictors, we calculated nationwide human health risk maps by predicting the concentration of 10 trace metals in the drinking water sources of Pakistan and comparing them to guideline values. GWR incorporated local variations of trace metal concentrations into prediction models and hence mitigated effects of large distances between sampled districts due to data scarcity. Predicted concentrations mostly exhibited high accuracy and low uncertainty, and were in good agreement with observed concentrations. Concentrations for Central Pakistan were predicted with higher accuracy than for the North and South. A maximum 150–200 fold exceedance of guideline values was observed for predicted cadmium concentrations in ground water and arsenic concentrations in surface water. In more than 53% (4 and 100% for the lower and upper boundaries of 95% confidence interval (CI)) of the total area of Pakistan, the drinking water was predicted to be at risk of contamination from arsenic, chromium, iron, nickel and lead. The area with elevated risks is inhabited by more than 74 million (8 and 172 million for the lower and upper boundaries of 95% CI) people. Although these predictions require further validation by field monitoring, the results can inform disease mitigation and water resources management regarding potential hot spots. - Highlights: • Predictions of trace metal concentration use geographically weighted regression • Human health risk

Trace Element Removal in Distributed Drinking Water Treatment Systems by Cathodic H2O2 Production and UV Photolysis.

Science.gov (United States)

Barazesh, James M; Prasse, Carsten; Wenk, Jannis; Berg, Stephanie; Remucal, Christina K; Sedlak, David L

2018-01-02

As water scarcity intensifies, point-of-use and point-of-entry treatment may provide a means of exploiting locally available water resources that are currently considered to be unsafe for human consumption. Among the different classes of drinking water contaminants, toxic trace elements (e.g., arsenic and lead) pose substantial operational challenges for distributed drinking water treatment systems. Removal of toxic trace elements via adsorption onto iron oxides is an inexpensive and robust treatment method; however, the presence of metal-complexing ligands associated with natural organic matter (NOM) often prevents the formation of iron precipitates at the relatively low concentrations of dissolved iron typically present in natural water sources, thereby requiring the addition of iron which complicates the treatment process and results in a need to dispose of relatively large amounts of accumulated solids. A point-of-use treatment device consisting of a cathodic cell that produced hydrogen peroxide (H 2 O 2 ) followed by an ultraviolet (UV) irradiation chamber was used to decrease colloid stabilization and metal-complexing capacity of NOM present in groundwater. Exposure to UV light altered NOM, converting ∼6 μM of iron oxides into settable forms that removed between 0.5 and 1 μM of arsenic (As), lead (Pb), and copper (Cu) from solution via adsorption. After treatment, changes in NOM consistent with the loss of iron-complexing carboxylate ligands were observed, including decreases in UV absorbance and shifts in the molecular composition of NOM to higher H/C and lower O/C ratios. Chronoamperometric experiments conducted in synthetic groundwater revealed that the presence of Ca 2+ and Mg 2+ inhibited intramolecular charge-transfer within photoexcited NOM, leading to substantially increased removal of iron and trace elements.

Novel, Vacuum-Regenerable Trace Contaminant Control System for Advanced Spacesuit Applications, Phase I

Data.gov (United States)

National Aeronautics and Space Administration — Trace contaminants that are introduced into the ventilation loop of a spacesuit (primarily ammonia and formaldehyde) via metabolic processes, off-gassing of...

Post-CMP cleaning for metallic contaminant removal by using a remote plasma and UV/ozone

International Nuclear Information System (INIS)

Lim, Jong Min; Jeon, Bu Yong; Lee, Chong Mu

2000-01-01

For the chemical mechanical polishing (CMP) process to be successful, it is important to establish a good post-CMP cleaning process that will remove not only slurry and particles but also metallic impurities from the polished surface. The common metallic contaminants found after oxide CMP and Cu CMP include Cu, K, and Fe. Scrubbing, a popular method for post-CMP cleaning, is effective in removing particles, but removal of metallic contaminants using this method is not so effective. In this study, the removal of Fe metallic contaminants like Fe, which are commonly found on the wafer surface after CMP processes, was investigated using remote-hydrogen-plasma and UV/O 3 cleaning techniques. Our results show that metal contaminants, including Fe, can be effectively removed by using a hydrogen-plasma or UV/O 3 cleaning technique performed under optimal process conditions. In remote plasma H 2 cleaning, contaminant removal is enhanced with decreasing plasma exposure time and increasing rf-power. The optimal process condition for the removal of the Fe impurities existing on the wafer surface is an rf-power of 100 W. Plasma cleaning for 5 min or less is effective in removing Fe contaminants, but a plasma exposure time of 1 min is more appropriate than 5 min in view of the process time, The surface roughness decreased by 30∼50 % after remote-H 2 -plasma cleaning. On the other hand, the highest efficiency of Fe-impurity removal was achieved for an UV exposure time of 30 s. The removal mechanism for the Fe contaminants in the remote-H 2 -plasma and the UV/O 3 cleaning processes is considered to be the liftoff of Fe atoms when the SiO is removed by evaporation after the chemical or native SiO 2 formed underneath the metal atoms reacts with H + and e - to form SiO

Novel, Vacuum-Regenerable Trace Contaminant Control System for Advanced Spacesuit Applications, Phase II

Data.gov (United States)

National Aeronautics and Space Administration — Precision Combustion, Inc. (PCI) proposes a new material paradigm for the Trace Contaminant Control System (TCCS) based upon its novel adsorbent nanomaterials that...

Removal of emerging perfluorooctanoic acid and perfluorooctane sulfonate contaminants from lake water.

Science.gov (United States)

Pramanik, Biplob Kumar; Pramanik, Sagor Kumar; Sarker, Dipok Chandra; Suja, Fatihah

2017-08-01

Perfluorooctanoic acid (PFOA) and perfluorooctane sulfonate (PFOS) are the major polyfluoroalkyl substances (PFASs) contaminating global water environment. This study investigated the efficiency of granular activated carbon (GAC), ultrafiltration (UF) and nanofiltration (NF) treatment for removing PFOS and PFOA contaminants from lake water. NF gave greater removal of all contaminant types (in terms of organic matter, PFOS and PFOA) than GAC treatment which in turn was greater than UF treatment. The lower removal by UF was due to larger pore size of the membrane compared to the size of the target contaminants. For all treatment processes, lower pH (4) in the feedwater showed greater rejection of the organics and selected PFASs. This was likely due to increase in the electrostatic repulsion between solute and sorbent. It could be observed that on increasing the concentration of organics in the feed solution, the rejection of PFOA/PFOS decreased which was due to competition between organics and PFOS/PFOA for binding sites on the membrane/activated carbon surface. It was also noted that protein content led to greater influence for lower rejection of the PFOA/PFOS than carbohydrate or DOC content. This study demonstrated the potential use of membrane processes for removing emerging persistent organic pollutant removal from lake water.

Trace contaminants of agriculture, fisheries and food with particular reference to isotope studies

International Nuclear Information System (INIS)

Winteringham, F.P.W.

1977-01-01

Growing world population, industrilization and intensification of agricultural and fisheries practices have greatly increased the need during recent decades to protect the resources concerned, and the quality of food and agricultural environment. These trends have also resulted in a growing range of trace contaminants and excessive nutrient problems of agriculture and fisheries. Isotopic tracer and nuclear analytical techniques are powerful and often unique tools for the study and control of the problems, especially in relation to trace elements, nutrients and contaminants. In addition to the conventional use of radioactive and stable isotopes as tracers there appears to be considerable scope for the use of environmental or natural isotope ratio techniques and the use of labelled reagents and substrates as monitoring tools. Representative applications are described. (author)

Soil amendments reduce trace element solubility in a contaminated soil and allow regrowth of natural vegetation

International Nuclear Information System (INIS)

Madejon, Engracia; Perez de Mora, Alfredo; Felipe, Efrain; Burgos, Pilar; Cabrera, Francisco

2006-01-01

We tested the effects of three amendments (a biosolid compost, a sugar beet lime, and a combination of leonardite plus sugar beet lime) on trace element stabilisation and spontaneous revegetation of a trace element contaminated soil. Soil properties were analysed before and after amendment application. Spontaneous vegetation growing on the experimental plot was studied by three surveys in terms of number of taxa colonising, percentage vegetation cover and plant biomass. Macronutrients and trace element concentrations of the five most frequent species were analysed. The results showed a positive effect of the amendments both on soil chemical properties and vegetation. All amendments increased soil pH and TOC content and reduced CaCl 2 -soluble-trace element concentrations. Colonisation by wild plants was enhanced in all amended treatments. The nutritional status of the five species studied was improved in some cases, while a general reduction in trace element concentrations of the aboveground parts was observed in all treated plots. The results obtained show that natural assisted remediation has potential for success on a field scale reducing trace element entry in the food chain. - Soil amendments affect soil chemistry and allow revegetation of soils contaminated by trace elements

Experimental analysis on removal factor of smear method in measurement of surface contamination

International Nuclear Information System (INIS)

Sugiura, Nobuyuki; Taira, Junichi; Takenaka, Keisuke; Yamanaka, Kazuo; Sugai, Kenji; Kosako, Toshiso

2007-01-01

The smear test is one of the important ways to measure surface contamination. The loose contamination under the high background radiation, which is more significant in handling non-sealed radioisotopes, can be evaluated by this method. The removal factor is defined as the ratio of the activity removed from the surface by one smear to the whole activity of the removable surface contamination. The removal factor is greatly changed by the quality and condition of surface materials. In this study, the values of removal factor at several typical surface conditions were evaluated experimentally and the practical application of those values was considered. It is required the smear should be pressed by moderate pressure when wiping the surface. The pressure from 1.0 kg to 1.5 kg per filter paper was recommended. The removal factor showed lower value in wiping by the pressure below 1.0 kg. The value of 0.5 for the removal factor could be applied to the smooth surface of linoleum, concrete coated with paint or epoxy resin, stainless steel and glass with the statistical allowance. (author)

Contaminated Sediment Management in Dam Removals and River Restoration Efforts: Critical Need for Research and Policy Development

Science.gov (United States)

Evans, J. E.

2015-12-01

Over 1,000 U.S. dams have been removed (1975-2015) for reasons including obsolescence, liability concerns, water quality upgrades, fisheries, or ecosystem enhancements. Contaminated sediment can significantly complicate the approval process, cost, and timeline of a dam removal, or stop it entirely. In a dam removal, reservoir sediment changes from a sink to a source of contaminants. Recently, the Sierra Club sued to stop the removal of a large dam in Ohio because of the potential impact of phosphate releases on toxic algal blooms in Lake Erie. Heavy metals, PCBs, PAHs, pesticides, and petroleum hydrocarbons can be present in reservoir sediments. In a non-dam removal scenario, reservoir management tools range from "no action" to dredging, dewatering and removal, or sediment capping. But it is not clear how these reservoir management techniques apply to dam removals. Case studies show typically >80% of the reservoir sediment is eventually eroded, precluding sediment capping as a containment option. However, the released contaminants are diluted by mixing with "clean" sediment and are transported to different physio-chemical environments which may immobilize or biodegrade the contaminants. Poorly understood options include phased drawdown/reseeding the former reservoir to contain sediments, diking contaminant "hot spots," and addressing contaminant stratigraphy (where historical use created "hot layers" in the reservoir sediment). Research and policy development needs include: (1) assessment methods based on synergistic effects of multiple contaminants being present; (2) ways to translate the pre-removal contaminant concentrations to post-removal health risks downstream; (3) evaluation of management practices for contaminant "hot spots" and "hot layers;" (4) tools to forecast the presence of contaminated sediment using easily accessible information; and (5) ways to limit liability risk for organizations participating in dam removals involving contaminated sediment.

Radioisotope studies of some effects and interactions of trace contaminants

International Nuclear Information System (INIS)

1976-01-01

The coordinated programme of ''isotopic tracer-aided studies of the biological side-effects of foreign chemical residues in food and agriculture'', initiated in 1973, had involved the participation of 12 scientists from 10 countries. Pesticide residues, toxic metals, atmospheric sulphur dioxide were studied, and the use of radiotracer techniques as monitoring tools for existing contaminant levels or for their biological effects. The programme had been successful in the development and application of selected labelled substrate techniques. Specific aspects studied were the effects of environmental contaminants at the molecular level of the cell nucleus, the development and significance of radioimmunoassay procedure for trace contaminants, action and joint action of toxic elements, and the radiometric analysis of cholinesterase as an index of exposure to organophosphorus and carbamate pesticides. Ten papers were presented and 12 coordinated investigations discussed. A number of recommendations were made

Removal of petroleum-derived hydrocarbons from contaminated soils by solvent extraction

International Nuclear Information System (INIS)

Ladanowski, C.; Petti, L.

1993-01-01

Laboratory studies were conducted using hexane for the removal of light crude oil from contaminated sand, peat, and clay soils. The bench-scale process tested consists of three major steps: solvent washing, settling/decantation/filtration of extract, and solvent recycle. The results indicate that the use of solvent extraction for cleanup of oil-contaminated soils is an effective technology at the bench-scale level. Using a 1,000 g batch system, extremely high oil removal efficiencies were obtained from contaminated sand (up to 98.9%) and peat soil (up to 83.9%). The final oil contaminant concentration for sand varied between 0.06% and 0.39%, while that for peat soil varied between 1.52% and 5.21%. The guidelines for the decommissioning and cleanup of sites in Ontario for oil and grease (1 wt %) were met in all instances for the treated sand. Hexane recovery from diesel-contaminated sand and peat soil experiments was ca 81% and 67% respectively. 4 refs., 6 figs., 10 tabs

Removal of polonium contamination by lead-bismuth eutectic in nuclear systems

International Nuclear Information System (INIS)

Miura, Terumitsu; Obara, Toru; Sekimoto, Hiroshi

2003-01-01

Lead-Bismuth eutectic (LBE) is considered as a promising candidate of the coolant of liquid metal cooled fast reactor, and the coolant and/or target of accelerator driven system. LBE has various good characters for coolant, but it has also some problems such as polonium production. It is necessary to take polonium contamination into consideration, when LBE is used as the coolant. In the present paper, the removal of contaminating polonium from material surface is studied. Baking method is investigated for polonium removal from contaminated quartz glass plate in vacuum. Before and after baking, the mass of the contaminants on the surface and alpha particle counts from contaminated surface is measured. When the contaminated quartz glass plates are baked at more than 400degC for a few minutes, alpha particle counts from the surface decreases by more than 99.7%, and the mass of contaminants decreases by more than 50%. When the baking was performed at 300degC for 15 minutes and more, alpha particle count decreases by more than 80%, and the mass decreases in little. When, the baking temperature is lower than 200degC, alpha particle counts and mass do not decrease. (author)

Removal of trace mercury (II) from aqueous solution by in situ MnO(x) combined with poly-aluminum chloride.

Science.gov (United States)

Lu, Xixin; Huangfu, Xiaoliu; Zhang, Xiang; Wang, Yaan; Ma, Jun

2015-06-01

Removal of trace mercury from aqueous solution by Mn (hydr)oxides formed in situ during coagulation with poly-aluminum chloride (PAC) (in situ MnO(x) combined with PAC) was investigated. The efficiency of trace mercury removal was evaluated under the experimental conditions of reaction time, Mn dosage, pH, and temperature. In addition, the ionic strength and the initial mercury concentration were examined to evaluate trace mercury removal for different water qualities. The results clearly demonstrated that in situ MnO(x) combined with PAC was effective for trace mercury removal from aqueous solution. A mercury removal ratio of 9.7 μg Hg/mg Mn was obtained at pH 3. Furthermore, at an initial mercury concentration of 30 μg/L and pH levels of both 3 and 5, a Mn dosage of 4 mg/L was able to lower the mercury concentration to meet the standards for drinking water quality at less than 1 μg/L. Analysis by Fourier transform infrared spectroscopy and X-ray photoelectron spectroscopy suggests that the hydroxyls on the surface of Mn (hydr)oxides are the active sites for adsorption of trace mercury from aqueous solution.

The Development of Magnetic Molecules for the Selective Removal of Contaminants

International Nuclear Information System (INIS)

Bushart, S.P.; Bradbury, D.; Elder, G.; Duffield, J.; Pascual, I.; Ratcliffe, N.

2006-01-01

'Magnetic molecules' are a new type of decontaminant for removing dilute dissolved contaminants from solution. Magnetic molecules have a specific ion exchange function to selectively react with a particular type of ionic contamination in a liquid solution. The magnetic molecules also have a very small magnetic ferritin core (ferritin is an iron-III mammalian storage protein having about 10 nm diameter), which enables the magnetic molecule to be removed from solution by magnetic filtration. The ion exchange function is attached to the magnetic ferritin core by organic reaction sequences. The ion exchange function selectively bonds to a specific type of contaminant ion. For example, ion exchange functions can selectively target radioactive contaminant ions such as cobalt, cesium and plutonium. The procedure for decontamination is that the appropriate magnetic molecule (which targets the contaminant which it is desired to remove) is added to the solution and the solution is then passed through a magnetic filter. The contaminant binds to the magnetic molecule and is then removed by the magnetic filter. The magnetic molecule/contaminant can then be recovered from the magnetic filter by back-washing. Work has been undertaken towards the development of magnetic molecules for use as radioactive decontaminants for radioactive waste management purposes. Previously we have reported on the functionalization of ferritin with the chelating agent DTPA and have shown that this can be used to bind Ca(II) in solution and separate it from Na(I) ions by the process of equilibrium dialysis. Approximately 100 DTPA molecules could be bound to the surface of the ferritin molecule. Synthetic conditions have been optimised, and which will be reported here, ferritin has been functionalized with approximately 1200 DTPA molecules per mole of ferritin and used successfully to achieve a quantitative separation of Co(II) from Cs(I) ions by equilibrium dialysis. This separation has been carried

Removal of contaminated asphalt layers by using heat generating powder metallic systems

International Nuclear Information System (INIS)

Barinov, A.S.; Karlina, O.K.; Ojovan, M.I.

1996-01-01

Heat generating systems on the base of powder metallic fuel were used for the removal of contaminated asphalt layers. Decontamination of spots which had complex geometric form was performed. Asphalt layers with deep contamination were removed essentially all radionuclides being retained in asphalt residue. Only a small part (1 - 2 %) of radionuclides could pass to combustion slag. No radionuclides were detected in aerosol-gas phase during decontamination process

Effects of electrocardiography contamination and comparison of ECG removal methods on upper trapezius electromyography recordings.

Science.gov (United States)

Marker, Ryan J; Maluf, Katrina S

2014-12-01

Electromyography (EMG) recordings from the trapezius are often contaminated by the electrocardiography (ECG) signal, making it difficult to distinguish low-level muscle activity from muscular rest. This study investigates the influence of ECG contamination on EMG amplitude and frequency estimations in the upper trapezius during muscular rest and low-level contractions. A new method of ECG contamination removal, filtered template subtraction (FTS), is described and compared to 30 Hz high-pass filter (HPF) and averaged template subtraction (ATS) methods. FTS creates a unique template of each ECG artifact using a low-pass filtered copy of the contaminated signal, which is subtracted from contaminated periods in the original signal. ECG contamination results in an over-estimation of EMG amplitude during rest in the upper trapezius, with negligible effects on amplitude and frequency estimations during low-intensity isometric contractions. FTS and HPF successfully removed ECG contamination from periods of muscular rest, yet introduced errors during muscle contraction. Conversely, ATS failed to fully remove ECG contamination during muscular rest, yet did not introduce errors during muscle contraction. The relative advantages and disadvantages of different ECG contamination removal methods should be considered in the context of the specific motor tasks that require analysis. Copyright © 2014 Elsevier Ltd. All rights reserved.

Bio-mechanical removing of contaminated soils: a field experiment

International Nuclear Information System (INIS)

Jouve, A.; Maubert, H.; Schulte, E.

1992-01-01

If, in spite of safety precautions, a major nuclear accident would occur, countermeasures should be taken to attenuate the impact of radioactive deposits. The European RESSAC program (REhabilitation of Soils and Surfaces after an ACcident) aims at studying actions for normal life return in contaminated zones. One of them, called the Decontaminating Vegetal Network (D.V.N.) associates the biological action of turfing plants, producing a dense root-network capable to trap the top contaminated soil particles, and the mechanical efficiency of a turf harvester which can remove only 1 cm of soil. This performance, not associated with other techniques of soil removal such as scrapers or bulldozers, leads to minimize the waste production. The D.V.N is a vegetal cover spread over the contaminated soil, using the hydro-seeding technique. The growing plants are forming a pleasant lawn which may have a positive impact on the public opinion compared to techniques using bitumen mixtures to cover the soil. Field experiments involving labelling solutions of stable molybdenum salts simulating the contamination of the soil have shown that this technique can be applied as well on homogeneous cultivated soil surfaces as on roughly ploughed soils. 4 refs., 3 figs., 2 tabs

Experimental Investigation of Phenanthrene Pollutant Removal Efficiency for Contaminated Sandy Soil by Enhanced Soil Washing

Directory of Open Access Journals (Sweden)

Saif salah Alquzweeni

2016-12-01

Full Text Available Polycyclic aromatic hydrocarbons (PAHs are environmental concerns that must be removed to acceptable level. This research assesses two agents (Na2EDTA and SDS to remediate contaminated sandy soil, spiked with 500mg/kg phenanthrene. Five sets of experiments (batch are applied to investigate the optimal of five influencing factors on soil remediation: Na2EDTA-SDS concentration, liquid/Solid ratio, stirring speed, pH value of flushing solution and mixing time. The results of batch experiments showed that SDS has high phenanthrene removal efficiency (90%, while Na2EDTA shows no phenanthrene removal. pH has no effect on phenanthrene removal. To study the influence of flow rates on the removal efficiency of contaminants, two column tests with hydraulic gradient of 0.2 and 1.2 conducted by SDS solution. The results illustrate that high phenanthrene removal from soil obtained by 1.2 hydraulic gradient condition. The SDS flushing solution removed approximately 69% and 81% of phenanthrene from soil under low and high hydraulic gradients, respectively. It was concluded that phenanthrene removal depend on surfactant micelles formation. Overall, the study showed that soil flushing removal efficiency for contaminants depends on the flushing agents selectivity and affinity to the contaminants and the condition of hydraulic gradient.

Johor strait as a hotspot for trace elements contamination in peninsular Malaysia.

Science.gov (United States)

Zulkifli, Syaizwan Zahmir; Ismail, Ahmad; Mohamat-Yusuff, Ferdaus; Arai, Takaomi; Miyazaki, Nobuyuki

2010-05-01

Present study was conducted to evaluate current status of trace elements contamination in the surface sediments of the Johor Strait. Iron (2.54 +/- 1.24%) was found as the highest occurring element, followed by those of zinc (210.45 +/- 115.4 microg/g), copper (57.84 +/- 45.54 microg/g), chromium (55.50 +/- 31.24 microg/g), lead (52.52 +/- 28.41 microg/g), vanadium (47.76 +/- 25.76 microg/g), arsenic (27.30 +/- 17.11 microg/g), nickel (18.31 +/- 11.77 microg/g), cobalt (5.13 +/- 3.12 microg/g), uranium (4.72 +/- 2.52 microg/g), and cadmium (0.30 +/- 0.30 microg/g), respectively. Bioavailability of cobalt, nickel, copper, zinc, arsenic and cadmium were higher than 50% of total concentration. Vanadium, copper, zinc, arsenic and cadmium were found significantly different between the eastern and western part of the strait (p Johor Strait is suitable as a hotspot for trace elements contamination related studies.

Tracing contamination sources in soils with Cu and Zn isotopic ratios

Energy Technology Data Exchange (ETDEWEB)

Fekiacova, Z.; Cornu, S. [INRA, UR 1119 Géochimie des Sols et des Eaux, F-13100 Aix en Provence (France); Pichat, S. [Laboratoire de Géologie de Lyon (LGL-TPE), Ecole Normale Supérieure de Lyon, CNRS, UMR 5276, 69007 Lyon (France)

2015-06-01

Copper (Cu) and zinc (Zn) are naturally present and ubiquitous in soils and are important micronutrients. Human activities contribute to the input of these metals to soils in different chemical forms, which can sometimes reach a toxic level for soil organisms and plants. Isotopic signatures could be used to trace sources of anthropogenic Cu and Zn pollution. The aim of this paper is to determine whether it is possible to identify (i) Cu and Zn contamination in soils and their sources, on the basis of their isotopic signatures, and (ii) situations that are a priori favorable or not for tracing Cu and Zn pollution using the isotopic approach. Therefore, we compiled data from the literature on Cu and Zn isotopes in soils, rocks and pollutants and added to this database the results of our own research. As only a few studies have dealt with agricultural contamination, we also studied a soil toposequence from Brittany, France, that experienced spreading of pig slurry for tens of years. In the surface horizons of the natural soils, the δ{sup 65}Cu values vary from − 0.15 to 0.44‰ and the δ{sup 66}Zn from − 0.03 to 0.43‰. Furthermore, vertical variations along soil profiles range from − 0.95 to 0.44‰ for δ{sup 65}Cu and from − 0.53 to 0.64‰ for δ{sup 66}Zn values. We concluded that pedogenetic processes can produce isotopic fractionation, yet, it is not always discernible and can be overprinted by an exogenous isotopic signature. Furthermore, some contaminants are enriched in heavy Cu or in light Zn compared to the rock or soil, but no generalization can be made. The anthropogenic inputs can be identified based on stable Cu and Zn isotope ratios if the isotope ratios of the sources are different from those of the soil, which needs to be tested for each individual case. - Highlights: • Pedogenetic processes produce some Cu and Zn isotope fractionation. • Pollution with distinct isotopic signatures can be traced using Cu and Zn isotopes. • Tracing

Tracing contamination sources in soils with Cu and Zn isotopic ratios

International Nuclear Information System (INIS)

Fekiacova, Z.; Cornu, S.; Pichat, S.

2015-01-01

Copper (Cu) and zinc (Zn) are naturally present and ubiquitous in soils and are important micronutrients. Human activities contribute to the input of these metals to soils in different chemical forms, which can sometimes reach a toxic level for soil organisms and plants. Isotopic signatures could be used to trace sources of anthropogenic Cu and Zn pollution. The aim of this paper is to determine whether it is possible to identify (i) Cu and Zn contamination in soils and their sources, on the basis of their isotopic signatures, and (ii) situations that are a priori favorable or not for tracing Cu and Zn pollution using the isotopic approach. Therefore, we compiled data from the literature on Cu and Zn isotopes in soils, rocks and pollutants and added to this database the results of our own research. As only a few studies have dealt with agricultural contamination, we also studied a soil toposequence from Brittany, France, that experienced spreading of pig slurry for tens of years. In the surface horizons of the natural soils, the δ 65 Cu values vary from − 0.15 to 0.44‰ and the δ 66 Zn from − 0.03 to 0.43‰. Furthermore, vertical variations along soil profiles range from − 0.95 to 0.44‰ for δ 65 Cu and from − 0.53 to 0.64‰ for δ 66 Zn values. We concluded that pedogenetic processes can produce isotopic fractionation, yet, it is not always discernible and can be overprinted by an exogenous isotopic signature. Furthermore, some contaminants are enriched in heavy Cu or in light Zn compared to the rock or soil, but no generalization can be made. The anthropogenic inputs can be identified based on stable Cu and Zn isotope ratios if the isotope ratios of the sources are different from those of the soil, which needs to be tested for each individual case. - Highlights: • Pedogenetic processes produce some Cu and Zn isotope fractionation. • Pollution with distinct isotopic signatures can be traced using Cu and Zn isotopes. • Tracing of the metal

Microlith-Based Catalytic Reactor for Air Quality and Trace Contaminant Control Applications

Science.gov (United States)

Vilekar, Saurabh; Hawley, Kyle; Junaedi, Christian; Crowder, Bruce; Prada, Julian; Mastanduno, Richard; Perry, Jay L.; Kayatin, Matthew J.

2015-01-01

Traditionally, gaseous compounds such as methane, carbon monoxide, and trace contaminants have posed challenges for maintaining clean air in enclosed spaces such as crewed spacecraft cabins as they are hazardous to humans and are often difficult to remove by conventional adsorption technology. Catalytic oxidizers have provided a reliable and robust means of disposing of even trace levels of these compounds by converting them into carbon dioxide and water. Precision Combustion, Inc. (PCI) and NASA - Marshall (MSFC) have been developing, characterizing, and optimizing high temperature catalytic oxidizers (HTCO) based on PCI's patented Microlith® technology to meet the requirements of future extended human spaceflight explorations. Current efforts have focused on integrating the HTCO unit with a compact, simple recuperative heat exchanger to reduce the overall system size and weight while also reducing its energy requirements. Previous efforts relied on external heat exchangers to recover the waste heat and recycle it to the oxidizer to minimize the system's power requirements; however, these units contribute weight and volume burdens to the overall system. They also result in excess heat loss due to the separation of the HTCO and the heat recuperator, resulting in lower overall efficiency. Improvements in the recuperative efficiency and close coupling of HTCO and heat recuperator lead to reductions in system energy requirements and startup time. Results from testing HTCO units integrated with heat recuperators at a variety of scales for cabin air quality control and heat melt compactor applications are reported and their benefits over previous iterations of the HTCO and heat recuperator assembly are quantified in this paper.

Effective removal of trace thallium from surface water by nanosized manganese dioxide enhanced quartz sand filtration.

Science.gov (United States)

Huangfu, Xiaoliu; Ma, Chengxue; Ma, Jun; He, Qiang; Yang, Chun; Zhou, Jian; Jiang, Jin; Wang, Yaan

2017-12-01

Thallium (Tl) has drawn wide concern due to its high toxicity even at extremely low concentrations, as well as its tendency for significant accumulation in the human body and other organisms. The need to develop effective strategies for trace Tl removal from drinking water is urgent. In this study, the removal of trace Tl (0.5 μg L -1 ) by conventional quartz sand filtration enhanced by nanosized manganese dioxide (nMnO 2 ) has been investigated using typical surface water obtained from northeast China. The results indicate that nMnO 2 enhanced quartz sand filtration could remove trace Tl(I) and Tl(III) efficiently through the adsorption of Tl onto nMnO 2 added to a water matrix and onto nMnO 2 attached on quartz sand surfaces. Tl(III)-HA complexes might be responsible for higher residual Tl(III) in the effluent compared to residual Tl(I). Competitive Ca 2+ cations inhibit Tl removal to a certain extent because the Ca 2+ ions will occupy the Tl adsorption site on nMnO 2 . Moreover, high concentrations of HA (10 mgTOC L -1 ), which notably complexes with and dissolves nMnO 2 (more than 78%), resulted in higher residual Tl(I) and Tl(III). Tl(III)-HA complexes might also enhance Tl(III) penetration to a certain extent. Additionally, a higher pH level could enhance the removal of trace Tl from surface water. Finally, a slight increase of residual Tl was observed after backwash, followed by the reduction of the Tl concentration in the effluent to a "steady" state again. The knowledge obtained here may provide a potential strategy for drinking water treatment plants threatened by trace Tl. Copyright © 2017. Published by Elsevier Ltd.

PAMAM dendrimers and graphene: materials for removing aromatic contaminants from water.

Science.gov (United States)

DeFever, Ryan S; Geitner, Nicholas K; Bhattacharya, Priyanka; Ding, Feng; Ke, Pu Chun; Sarupria, Sapna

2015-04-07

We present results from experiments and atomistic molecular dynamics simulations on the remediation of naphthalene by polyamidoamine (PAMAM) dendrimers and graphene oxide (GrO). Specifically, we investigate 3rd-6th generation (G3-G6) PAMAM dendrimers and GrO with different levels of oxidation. The work is motivated by the potential applications of these emerging nanomaterials in removing polycyclic aromatic hydrocarbon contaminants from water. Our experimental results indicate that GrO outperforms dendrimers in removing naphthalene from water. Molecular dynamics simulations suggest that the prominent factors driving naphthalene association to these seemingly disparate materials are similar. Interestingly, we find that cooperative interactions between the naphthalene molecules play a significant role in enhancing their association to the dendrimers and GrO. Our findings highlight that while selection of appropriate materials is important, the interactions between the contaminants themselves can also be important in governing the effectiveness of a given material. The combined use of experiments and molecular dynamics simulations allows us to comment on the possible factors resulting in better performance of GrO in removing polyaromatic contaminants from water.

Removal of polycyclic aromatic hydrocarbons from aged-contaminated soil using cyclodextrins: Experimental study

International Nuclear Information System (INIS)

Viglianti, Christophe; Hanna, Khalil; Brauer, Christine de; Germain, Patrick

2006-01-01

The removal of polycyclic aromatic hydrocarbons (PAHs) from soil using water as flushing agent is relatively ineffective due to their low aqueous solubility. However, addition of cyclodextrin (CD) in washing solutions has been shown to increase the removal efficiency several times. Herein are investigated the effectiveness of cyclodextrin to remove PAH occurring in industrially aged-contaminated soil. β-Cyclodextrin (BCD), hydroxypropyl-β-cyclodextrin (HPCD) and methyl-β-cyclodextrin (MCD) solutions were used for soil flushing in column test to evaluate some influent parameters that can significantly increase the removal efficiency. The process parameters chosen were CD concentration, ratio of washing solution volume to soil weight, and temperature of washing solution. These parameters were found to have a significant and almost linear effect on PAH removal from the contaminated soil, except the temperature where no significant enhancement in PAH extraction was observed for temperature range from 5 to 35 o C. The PAHs extraction enhancement factor compared to water was about 200. - An innovative method using a biodegradable and non-toxic flushing agent for the depollution of industrially aged-contaminated soil

Use of the modified BCR three-step sequential extraction procedure for the study of trace element dynamics in contaminated soils

International Nuclear Information System (INIS)

Pueyo, M.; Mateu, J.; Rigol, A.; Vidal, M.; Lopez-Sanchez, J.F.; Rauret, G.

2008-01-01

The modified BCR three-step sequential extraction procedure was used to examine the temporal dynamics of trace elements in soils contaminated by an accidental spill from an opencast mine in south-west Spain. Soils were mainly contaminated with pyritic sludge and acidic wastewater, whereas some soils were affected only by acidic wastewater. The distributions obtained for both some major (Ca, Fe and Mn) and trace elements (As, Cd, Cu, Pb and Zn) in the sludge and soil samples taken at different times after the accident, 1-3 months and 21 months, were compared. Sequential extractions were useful in identifying different sources of contamination, and in obtaining additional information on the solubility of secondary minerals formed by pyrite oxidation. Thus, the effectiveness of the BCR procedure has proved to be a useful tool for predicting short- and long-term mobility of trace elements, even in complex environmental scenarios. - The modified BCR three-step sequential extraction procedure has proved a useful prediction tool for short- and long-term mobility of trace elements in contaminated soils

Optimizing the use of biosurfactants to remove diesel contamination in porous media

International Nuclear Information System (INIS)

Cote, A.L.; Tumeo, M.A.

1995-01-01

It has been demonstrated that biosurfactants can be used to successfully enhance the removal of hydrocarbon contamination from soils. The Environmental Technology Laboratory (ETL) at the University of Alaska Fairbanks is currently involved in a multiyear study of surfactant usage in oil spill remediation in cold climates. Funding for this work is provided by the National Science Foundation, Petroleum Environmental Services, Inc., the Alaska Department of Conservation, and the University of Alaska Fairbanks. In the Summer of 1993, researchers from ETL successfully used a biologically derived surfactant to remove weathered crude oil contamination remaining from the Exxon Valdez oil spill. This same technology may be applicable to other hydrocarbon-contaminated sites. Subsequent laboratory studies are being performed using soil columns to quantify the interaction between surfactant usage and soil characteristics. Specifically, the amount of surfactant applied, the method of application, the level of diesel contamination, and the type of soil matrix are being investigated. Diesel fuel has been chosen as a common type of hydrocarbon contamination. Adsorption of the surfactant on particle surfaces within the soil matrix can increase the cost of surfactant application and potentially diminish oil recovery. Four soil types are being used in these studies; a well-sorted, medium-grained sand; a moderately-sorted gravel, a volcanically-derived soil and a silt representative of tundra conditions. All of these soils are frequently encountered in oil spill remediation. This paper focuses on the relationships being identified between the level of contamination, soil matrix type, and the effectiveness of contaminant removal by biologically-derived surfactants

Preparation of hair and nail samples for trace element analysis

International Nuclear Information System (INIS)

Scoble, H.A.; Litman, R.

1978-01-01

The method of washing of human hair and nail samples is examined by neutron activation and γ-ray analysis. The amounts of Na, K, Br, Au, Zn, and La that are removed by successive washings determine the optimum number of washing for removing these trace elements as surface contaminants. A total solution contact time with the nails is 5 minutes, and leaching effcts are observed after 6 washings

Contaminated sediment removal from a spent fuel storage canal

International Nuclear Information System (INIS)

Geber, K.R.

1993-01-01

A leaking underground spent fuel transfer canal between a decommissioned reactor and a radiochemical separations building at the Oak Ridge National Laboratory (ORNL) was found to contain RCRA-hazardous and radioactive sediment. Closure of the Part B RCRA permitted facility required the use of an underwater robotic vacuum and a filtration-containment system to separate and stabilize the contaminated sediment. This paper discusses the radiological controls established to maintain contamination and exposures As Low As Reasonably Achievable (ALARA) during the sediment removal

Arbuscular mycorrhizal fungi in phytoremediation of contaminated areas by trace elements: mechanisms and major benefits of their applications.

Science.gov (United States)

Cabral, Lucélia; Soares, Claúdio Roberto Fonsêca Sousa; Giachini, Admir José; Siqueira, José Oswaldo

2015-11-01

In recent decades, the concentration of trace elements has increased in soil and water, mainly by industrialization and urbanization. Recovery of contaminated areas is generally complex. In that respect, microorganisms can be of vital importance by making significant contributions towards the establishment of plants and the stabilization of impacted areas. Among the available strategies for environmental recovery, bioremediation and phytoremediation outstand. Arbuscular mycorrhizal fungi (AMF) are considered the most important type of mycorrhizae for phytoremediation. AMF have broad occurrence in contaminated soils, and evidences suggest they improve plant tolerance to excess of certain trace elements. In this review, the use of AMF in phytoremediation and mechanisms involved in their trace element tolerance are discussed. Additionally, we present some techniques used to study the retention of trace elements by AMF, as well as a summary of studies showing major benefits of AMF for phytoremediation.

Removal of contaminated concrete surfaces by microwave heating: Phase 1 results

International Nuclear Information System (INIS)

White, T.L.; Grubb, R.G.; Pugh, L.P.; Foster, D. Jr.; Box, W.D.

1992-01-01

Oak Ridge National Laboratory (ORNL) is developing a microwave heating process to remove radiologically contaminated surface layers from concrete. The microwave energy is directed at the concrete surface and heats the concrete and free water present in the concrete matrix. Continued heating produces steam-pressure-induced mechanical stresses that cause the concrete surface to burst. The concrete particles from this steam explosion are small enough to be removed by a vacuum system, yet less than 1% of the debris is small enough to pose an airborne contamination hazard. The first phase of this program has demonstrated reliable removal of noncontaminated concrete surfaces at frequencies of 2.45 GHz and 10.6 GHz. Continuous concrete removal rates of 1.07 cm 3 /s with 5.2 kW of 2.45.-GHz power and 2.11 cm 3 /s with 3.6 kW of 10.6-GHz power have been demonstrated. Figures-of-merit for microwave removal of concrete have been calculated to be 0.21 cm 3 /s/kW at 2.45 GHz and 0.59 cm 3 /s/kW at 10.6 GHz. The amount of concrete removed in a single pass can be controlled by choosing the frequency and power of the microwave system

Zinc removal from wastewater by complexation-microfiltration process

OpenAIRE

Trivunac Katarina; Sekulić Zoran; Stevanović Slavica

2012-01-01

As a result of its wide industrial applications, zinc has become an important contaminant in aquatic environment since it is a toxic heavy metal and some of its compounds such as zinc arsenate and zinc cyanide, may be extremely hazardous. Therefore, there is a growing need for developing simple methods capable of separating and recovering trace zinc from environmental waters. Nowadays, the ultra and microfiltration method for trace metals removal from waters by the addition of water-sol...

Interactive effects of Cd and PAHs on contaminants removal from co-contaminated soil planted with hyperaccumulator plant Sedum alfredii

Energy Technology Data Exchange (ETDEWEB)

Wang, Kai; Huang, Huagang; Li, Tingqiang; Yang, Xiaoe [Zhejiang Univ., Hangzhou (China). MOE Key Lab. of Environment Remediation and Ecosystem Health; Zhu, Zhiqiang [Zhejiang Univ., Hangzhou (China). MOE Key Lab. of Environment Remediation and Ecosystem Health; Hainan Univ., Haikou (China). College of Agriculture; He, Zhenli [Florida Univ., Port Pierce, FL (United States). Inst. of Food and Agricultural Sciences; Alva, Ashok [US Department of Agriculture, Prosser, WA (United States). Agricultural Research Service

2012-04-15

Purpose: Soil contamination by multiple organic and inorganic contaminants is common but its remediation by hyperaccumulator plants is rarely reported. The growth of a cadmium (Cd) hyperaccumulator Sedum alfredii and removal of contaminants from Cd and polycyclic aromatic hydrocarbons (PAHs) co-contaminated soil were reported in this study. Materials and methods: Soil slightly contaminated by Cd (0.92 mg kg{sup -1} DW) was collected from a vegetable field in Hangzhou and was spiked with two levels (0 and 6 mg kg{sup -1} DW) of Cd and three levels (0, 25, and 150 mg kg{sup -1} DW) of phenanthrene (PHE) or pyrene (PYR). A pot experiment was conducted in a greenhouse using S. alfredii with unplanted controls for 60 days. Shoot and root biomass of plants, dehydrogenase activity (DHA), and microbial biomass carbon in the soil were measured. Concentrations of Cd and PAHs in the plant and soil were determined. Results and discussion: Elevated Cd level (6.38 mg kg{sup -1} DW) increased S. alfredii growth. The presence of PAHs decreased the stimulatory effects of Cd on plant biomass and Cd concentrations in shoots in Cd spiked soil, thus decreasing Cd phytoextraction efficiency. Cadmium removal by S. alfredii after 60 days of growth varied from 5.8% to 6.7% and from 5.7% to 9.6%, in Cd unspiked and spiked soils, respectively. Removal rate of PAHs in the soil was similar with or without the plants. Removal rate of PYR decreased at the elevated Cd level in the soil. This appears to be due to a decrease in soil microbial activity. This is confirmed by a decrease in DHA, which is a good indicator of soil microbial activity. Conclusions: Our results demonstrate that S. alfredii could effectively extract Cd from Cd-contaminated soils in the presence of PHE or PYR; however, both PAHs exhibited negative effects on phytoextraction of Cd from Cd spiked soil (6.38 mg kg{sup -1} DW). S. alfredii is not suitable for remediation of PAHs. The effects of Cd and PAHs concentrations on the

Effect of Co-Contaminant on Denitrification Removal of Nitrate in Drinking Water

Directory of Open Access Journals (Sweden)

Arzu KILIÇ

2012-12-01

Full Text Available In recent years, nitrogenous fertilizers used in agriculture, unconscious and without treatment wastewater is discharged led to an increase in groundwater nitrate pollution. In many countries, nitrate concentration in the ground waters used as drinking water source exceeded the maximum allowable concentration of 10 mg/L NO3-N. According to a study, some wells in the Harran Plain contain nitrate as high as 180 mg/L NO3--N and the average concentration for whole plain is 35 mg/L NO3--N (Yesilnacar et al., 2008. Additionally, increased water consumption, unconscious use of fertilizers and pesticides has led to the emergence of co-contaminant in drinking water. Recently, hazardous to human health co-contaminant such as arsenic, pesticides, perchlorate, selenate, chromate, uranium are observed in the nitrate pollution drinking water. There are many processes used for the removal of nitrate. The physical–chemical technologies that can be used for nitrate removal are reverse osmosis, ion exchange and electrodialysis (Alvarez et al., 2007. Important disadvantages of these processes are their poor selectivity, high operation and maintenance costs and the generation of brine wastes after treatment. Consequently, biological treatment processes to convert nitrates to benign dinitrogen gas, could be an interesting alternative for the remediation of groundwater contaminated with nitrates. The aim of this article, effective and cheap method for the removal of nitrate from drinking water biological denitrification is to examine the usability of contaminated drinking water with co-contaminant pollutions.

Removal of radium-226 from radium-contaminated soil using humic acid by column leaching method

International Nuclear Information System (INIS)

Esther Phillip; Muhamad Samudi Yasir

2012-01-01

In this study, evaluation of radium-226 removal from radium-contaminated soil using humic acid extracted from peat soil by column leaching method was carried out. Humic acid of concentration 100 ppm and pH 7 was leached through a column packed with radium-contaminated soil and leachates collected were analysed with gamma spectrometer to determine the leached radium-226. Results obtained indicated low removal of radium-226 between 1 - 4 %. Meanwhile, leaching profile revealed that radium-226 was bound to soil components with three different strength, thus resulting in three phases of radium-226 removal. It was estimated that the total removal of radium-226 from 10 g radium-contaminated soil sample studied could be achieved using approximately 31500 - 31850 ml HA solutions with leaching rate of 1 ml/ min. (author)

Molecular-level removal of proteinaceous contamination from model surfaces and biomedical device materials by air plasma treatment.

Science.gov (United States)

Banerjee, K K; Kumar, S; Bremmell, K E; Griesser, H J

2010-11-01

Established methods for cleaning and sterilising biomedical devices may achieve removal of bioburden only at the macroscopic level while leaving behind molecular levels of contamination (mainly proteinaceous). This is of particular concern if the residue might contain prions. We investigated at the molecular level the removal of model and real-life proteinaceous contamination from model and practical surfaces by air plasma (ionised air) treatment. The surface-sensitive technique of X-ray photoelectron spectroscopy (XPS) was used to assess the removal of proteinaceous contamination, with the nitrogen (N1s) photoelectron signal as its marker. Model proteinaceous contamination (bovine serum albumin) adsorbed on to a model surface (silicon wafer) and the residual proteinaceous contamination resulting from incubating surgical stainless steel (a practical biomaterial) in whole human blood exhibited strong N1s signals [16.8 and 18.5 atomic percent (at.%), respectively] after thorough washing. After 5min air plasma treatment, XPS detected no nitrogen on the sample surfaces, indicating complete removal of proteinaceous contamination, down to the estimated XPS detection limit 10ng/cm(2). Applying the same plasma treatment, the 7.7at.% nitrogen observed on a clinically cleaned dental bur was reduced to a level reflective of new, as-received burs. Contact angle measurements and atomic force microscopy also indicated complete molecular-level removal of the proteinaceous contamination upon air plasma treatment. This study demonstrates the effectiveness of air plasma treatment for removing proteinaceous contamination from both model and practical surfaces and offers a method for ensuring that no molecular residual contamination such as prions is transferred upon re-use of surgical and dental instruments. Crown Copyright © 2010. Published by Elsevier Ltd. All rights reserved.

Superfine powdered activated carbon (S-PAC) coatings on microfiltration membranes: Effects of milling time on contaminant removal and flux.

Science.gov (United States)

Amaral, Pauline; Partlan, Erin; Li, Mengfei; Lapolli, Flavio; Mefford, O Thompson; Karanfil, Tanju; Ladner, David A

2016-09-01

In microfiltration processes for drinking water treatment, one method of removing trace contaminants is to add powdered activated carbon (PAC). Recently, a version of PAC called superfine PAC (S-PAC) has been under development. S-PAC has a smaller particle size and thus faster adsorption kinetics than conventionally sized PAC. Membrane coating performance of various S-PAC samples was evaluated by measuring adsorption of atrazine, a model micropollutant. S-PACs were created in-house from PACs of three different materials: coal, wood, and coconut shell. Milling time was varied to produce S-PACs pulverized with different amounts of energy. These had different particles sizes, but other properties (e.g. oxygen content), also differed. In pure water the coal based S-PACs showed superior atrazine adsorption; all milled carbons had over 90% removal while the PAC had only 45% removal. With addition of calcium and/or NOM, removal rates decreased, but milled carbons still removed more atrazine than PAC. Oxygen content and specific external surface area (both of which increased with longer milling times) were the most significant predictors of atrazine removal. S-PAC coatings resulted in loss of filtration flux compared to an uncoated membrane and smaller particles caused more flux decline than larger particles; however, the data suggest that NOM fouling is still more of a concern than S-PAC fouling. The addition of calcium improved the flux, especially for the longer-milled carbons. Overall the data show that when milling S-PAC with different levels of energy there is a tradeoff: smaller particles adsorb contaminants better, but cause greater flux decline. Fortunately, an acceptable balance may be possible; for example, in these experiments the coal-based S-PAC after 30 min of milling achieved a fairly high atrazine removal (overall 80%) with a fairly low flux reduction (under 30%) even in the presence of NOM. This suggests that relatively short duration (low energy

Contamination of Detained Sediment in Sustainable Urban Drainage Systems

Directory of Open Access Journals (Sweden)

Deonie Allen

2017-05-01

Full Text Available Adsorption is a key water pollution remediation measure used to achieve stormwater quality improvement in Sustainable urban Drainage Systems (SuDS. The level of contamination of detained sediment within SuDS assets is not well documented, with published investigations limited to specific contaminant occurrence in ponds, wetlands or infiltration devices (bioretention cells and generally focused on solute or suspended sediment. Guidance on contamination threshold levels and potential deposited sediment contamination information is not included in current UK SuDS design or maintenance guidance, primarily due to a lack of evidence and understanding. There is a need to understand possible deposited sediment contamination levels in SuDS, specifically in relation to sediment removal maintenance activities and potential impact on receiving waterways of conveyed sediment. Thus, the objective of the research presented herein was to identify what major elements and trace metals were observable in (the investigated SuDS assets detained sediment, the concentration of these major elements and trace metals and whether they met/surpassed ecotoxicity or contaminated land thresholds. The research presented here provides evidence of investigated SuDS sediment major element and trace metal levels to help inform guidance and maintenance needs, and presents a new methodology to identify the general cause (anthropocentric land use and extent of detained SuDS fine urban sediment contamination through use of a contamination matrix.

[The balance of harmful trace contaminants between the air humidity condensate and air in a simulator of the Mir orbit station moisture condensation unit].

Science.gov (United States)

Zlotopol'skiĭ, V M; Smolenskaia, T S

2000-01-01

Subject of the investigation was the balance of harmful trace contaminants (HTC) between the air moisture condensate and air in a simulator of the MIR moisture condensation unit. Experiments involved various classes of water-solvent compounds including alcohols (C1-C4), ketons (C1-C2), aldehydes (C1-C2), fatty acids (C2-C4), esters (acetates C4-C6), and ammonium. For most of the compounds, removal efficiency correlates with air humidity and virtually does not depend on the HTC concentration within the range of 0.25 to 59.1 mg/m3.

Pyrene removal from contaminated soil using electrokinetic process combined with surfactant

Directory of Open Access Journals (Sweden)

Seyed Enayat Hashemi

2015-07-01

Full Text Available Background: Pyrene is one of the stable polycyclic aromatic hydrocarbons that is considered as an important pollutants, because of extensive distribution in the environment and carcinogenic and mutagenic properties. Among the various treatment techniques, electrokinetic method is an environmental- friendly process for organic and mineral pollutants adsorbed to soil with fine pore size the same as clay and low hydraulic conductivity soils. For improving the efficiency of pyrene removal from soil, soulobilization of pyrene from soil could be used by surfactants. Materials and Methods : In this study, clay soil was selected as model because of the specific properties. Combined method using surfactant and electrokinetic was applied for pyrene removal from soil. Experiments were designed using response surface methodology (RSM, and effect of three variables includes surfactant concentration, voltage and surfactant type were evaluated for pyrene removal from contaminated soil. Results: Pyrene removal using anionic surfactants(SDS and nonionic surfactants(TX100 as a solubilizing agents has high removal efficiency. In the optimum condition with 95% confidence coefficient, utilizing mixed surfactants of sodium dodecyl sulfate and triton X-100 with the same volume, induced of 18.54 volt and 6.53 percent surfactant concentration have 94.6% pyrene removal efficiency. Conclusion:: Results of this study shows that electrokinetic process combined with surfactant as solubilizing agent could be applied as an efficient method for treating the pyrene-contaminated soils.

Evaluation of a Candidate Trace Contaminant Control Subsystem Architecture: The High Velocity, Low Aspect Ratio (HVLA) Adsorption Process

Science.gov (United States)

Kayatin, Matthew J.; Perry, Jay L.

2017-01-01

Traditional gas-phase trace contaminant control adsorption process flow is constrained as required to maintain high contaminant single-pass adsorption efficiency. Specifically, the bed superficial velocity is controlled to limit the adsorption mass-transfer zone length relative to the physical adsorption bed; this is aided by traditional high-aspect ratio bed design. Through operation in this manner, most contaminants, including those with relatively high potential energy are readily adsorbed. A consequence of this operational approach, however, is a limited available operational flow margin. By considering a paradigm shift in adsorption architecture design and operations, in which flows of high superficial velocity are treated by low-aspect ratio sorbent beds, the range of well-adsorbed contaminants becomes limited, but the process flow is increased such that contaminant leaks or emerging contaminants of interest may be effectively controlled. To this end, the high velocity, low aspect ratio (HVLA) adsorption process architecture was demonstrated against a trace contaminant load representative of the International Space Station atmosphere. Two HVLA concept packaging designs (linear flow and radial flow) were tested. The performance of each design was evaluated and compared against computer simulation. Utilizing the HVLA process, long and sustained control of heavy organic contaminants was demonstrated.

Trace element mobility in a contaminated soil two years after field-amendment with a greenwaste compost mulch

Energy Technology Data Exchange (ETDEWEB)

Clemente, Rafael, E-mail: rclemente@cebas.csic.e [Faculty of Sciences, Liverpool John Moores University, Liverpool L3 3AF (United Kingdom); Hartley, William [Faculty of Sciences, Liverpool John Moores University, Liverpool L3 3AF (United Kingdom); Riby, Philip [School of Pharmacy and Chemistry, Liverpool John Moores University, Liverpool L3 3AF (United Kingdom); Dickinson, Nicholas M.; Lepp, Nicholas W. [Faculty of Sciences, Liverpool John Moores University, Liverpool L3 3AF (United Kingdom)

2010-05-15

Application of greenwaste compost to brownfield land is increasingly common in soil and landscape restoration. Previous studies have demonstrated both beneficial and detrimental effects of this material on trace element mobility. A pot experiment with homogenised soil/compost investigated distribution and mobility of trace elements, two years after application of greenwaste compost mulch to shallow soils overlying a former alkali-works contaminated with Pb, Cu and As (approx900, 200 and 500 mg kg{sup -1}, respectively). Compost mulch increased organic carbon and Fe in soil pore water, which in turn increased As and Sb mobilization; this enhanced uptake by lettuce and sunflower. A very small proportion of the total soil trace element pool was in readily-exchangeable form (<0.01% As, <0.001% other trace elements), but the effect of compost on behaviour of metals was variable and ambiguous. It is concluded that greenwaste compost should be applied with caution to multi-element contaminated soils. - Arsenic solubility and bioavailability increases in soil two years after application of greenwaste compost mulch.

Trace element mobility in a contaminated soil two years after field-amendment with a greenwaste compost mulch

International Nuclear Information System (INIS)

Clemente, Rafael; Hartley, William; Riby, Philip; Dickinson, Nicholas M.; Lepp, Nicholas W.

2010-01-01

Application of greenwaste compost to brownfield land is increasingly common in soil and landscape restoration. Previous studies have demonstrated both beneficial and detrimental effects of this material on trace element mobility. A pot experiment with homogenised soil/compost investigated distribution and mobility of trace elements, two years after application of greenwaste compost mulch to shallow soils overlying a former alkali-works contaminated with Pb, Cu and As (∼900, 200 and 500 mg kg -1 , respectively). Compost mulch increased organic carbon and Fe in soil pore water, which in turn increased As and Sb mobilization; this enhanced uptake by lettuce and sunflower. A very small proportion of the total soil trace element pool was in readily-exchangeable form (<0.01% As, <0.001% other trace elements), but the effect of compost on behaviour of metals was variable and ambiguous. It is concluded that greenwaste compost should be applied with caution to multi-element contaminated soils. - Arsenic solubility and bioavailability increases in soil two years after application of greenwaste compost mulch.

Combination of biochar amendment and phytoremediation for hydrocarbon removal in petroleum-contaminated soil.

Science.gov (United States)

Han, Tao; Zhao, Zhipeng; Bartlam, Mark; Wang, Yingying

2016-11-01

Remediation of soils contaminated with petroleum is a challenging task. Four different bioremediation strategies, including natural attenuation, biochar amendment, phytoremediation with ryegrass, and a combination of biochar and ryegrass, were investigated with greenhouse pot experiments over a 90-day period. The results showed that planting ryegrass in soil can significantly improve the removal rate of total petroleum hydrocarbons (TPHs) and the number of microorganisms. Within TPHs, the removal rate of total n-alkanes (45.83 %) was higher than that of polycyclic aromatic hydrocarbons (30.34 %). The amendment of biochar did not result in significant improvement of TPH removal. In contrast, it showed a clear negative impact on the growth of ryegrass and the removal of TPHs by ryegrass. The removal rate of TPHs was significantly lower after the amendment of biochar. The results indicated that planting ryegrass is an effective remediation strategy, while the amendment of biochar may not be suitable for the phytoremediation of soil contaminated with petroleum hydrocarbons.

Trace Contaminant Control for the International Space Station's Node 1- Analysis, Design, and Verification

Science.gov (United States)

Perry, J. L.

2017-01-01

Trace chemical contaminant generation inside crewed spacecraft cabins is a technical and medical problem that must be continuously evaluated. Although passive control through materials selection and active control by adsorption and catalytic oxidation devices is employed during normal operations of a spacecraft, contaminant buildup can still become a problem. Buildup is particularly troublesome during the stages between the final closure of a spacecraft during ground processing and the time that a crewmember enters for the first time during the mission. Typically, the elapsed time between preflight closure and first entry on orbit for spacecraft such as Spacelab modules was 30 days. During that time, the active contamination control systems are not activated and contaminants can potentially build up to levels which exceed the spacecraft maximum allowable concentrations (SMACs) specified by NASA toxicology experts. To prevent excessively high contamination levels at crew entry, the Spacelab active contamination control system was operated for 53 hours just before launch.

Removal of trace Cd2+ from aqueous solution by foam fractionation.

Science.gov (United States)

Lu, Jian; Li, Ying; Zhang, Sen; Sun, Yange

2015-04-09

In recent years, aqueous foam was known as an efficient technique with high potential on being used to remove heavy metal ions from the polluted water, not only because of the low cost, simple operation, but also ascribed to the high removal efficiency of trace heavy metal ions and would not cause secondary pollution to the environment. In this paper, the removal of Cd(2+) from aqueous solution by aqueous foam stabilized by a kind of novel anionic-nonionic surfactant sodium trideceth-4 carboxylate (AEC) was investigated. The effect of conditions such as surfactant/metal ions molar ratio, surfactant concentration on the removal efficiency was studied. In large concentration range of surfactant, the removal rate was higher than 90%, and could reach up to 99.8% under the optimum conditions. The Zeta potential of gas bubbles in the AEC solutions was determined to verify the combination between the negative charged group heads of surfactant molecules and heavy metal ions, and isothermal titration calorimeter (ITC) determination was utilized to demonstrate the interaction, which helped to understand the mechanisms more clearly. Copyright © 2015 Elsevier B.V. All rights reserved.

Trace element hydrochemistry indicating water contamination in and around the Yangbajing geothermal field, Tibet, China.

Science.gov (United States)

Guo, Qinghai; Wang, Yanxin

2009-10-01

Thirty-eight water samples were collected at Yangbajing to investigate the water contamination resulting from natural geothermal water discharge and anthropogenic geothermal wastewater drainage. The results indicate that snow or snow melting waters, Yangbajing River waters and cold groundwaters are free from geothermal water-related contamination, whereas Zangbo river waters are contaminated by geothermal wastewaters. Moreover, there may exist geothermal springs under the riverbed of a tributary stream of Zangbo River as shown by its Cd, Li, Mo and Pb concentrations. The efforts made in this study show trace element hydrochemistry can well indicate water quality degradation related to geothermal water exploitation.

Contamination and ecological risk assessment of trace elements in sediments of the rivers of Sundarban mangrove forest, Bangladesh.

Science.gov (United States)

Islam, M A; Al-Mamun, A; Hossain, F; Quraishi, S B; Naher, K; Khan, R; Das, S; Tamim, U; Hossain, S M; Nahid, F

2017-11-15

In this study, total concentrations of 16 trace elements (Al, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, As, Cd, Sb, Hg, Pb, Th and U) in sediments of the rivers of the Sundarban mangrove forest, after the catastrophic oil spill accident in the Sela river of Sundarban, were determined. The overall mean concentrations of V, Cr, Fe and Cd in surface sediments of the Sundarban are remarkably higher than available literature data of those elements. Trace element contamination assessment, using different environmental contamination indices, reveals that As, Sb, Th and U are low to moderately contaminated while Cd is moderately to severely contaminated in the sediments of this area. The multivariate statistical analyses were applied to reveal the origin and behavior of the elements during their transport in the mangrove ecosystem. High Cr, Ni, Cu and As concentrations suggest the risk of potentially adverse biological effects in the ecosystem. Copyright © 2017 Elsevier Ltd. All rights reserved.

Shippingport Station Decommissioning Project: Contaminated concrete removal: Topical report

International Nuclear Information System (INIS)

1989-01-01

This Topical Report is a synopsis of the removal of contaminated concrete from the Shippingport Station Decommissioning Project (SSDP). The information is provided as a part of the Technology Transfer Program to document the decontamination activities in support of site release in the decommissioning of a nuclear power reactor. 4 refs., 8 figs., 2 tabs

Polycyclic aromatic hydrocarbon removal from contaminated soils using fatty acid methyl esters.

Science.gov (United States)

Gong, Zongqiang; Wang, Xiaoguang; Tu, Ying; Wu, Jinbao; Sun, Yifei; Li, Peng

2010-03-01

In this study, solubilization of PAHs from a manufactured gas plant (MGP) soil and two artificially spiked soils using fatty acid methyl esters (FAME) was investigated. PAH removals from both the MGP and the spiked soils by FAME, methanol, soybean oil, hydroxypropyl-beta-cyclodextrin, Triton X-100, and Tween 80 were compared. The effect of FAME:MGP soil ratios on PAH removals was also investigated. Results showed that the FAME mixture synthesized by our lab was more efficient than the cyclodextrin and the two surfactants used for PAH removal from the spiked soils with individual PAH concentrations of 200 and 400 mg kg(-1). However, the difference among three PAH removals by the FAME, soybean oil and methanol was not quite pronounced. The FAME synthesized and market biodiesel exhibited better performance for PAH removals (46% and 35% of total PAH) from the weathered contaminated MGP soil when compared with the other agents (0-31%). Individual PAH removals from the weathered MGP soil were much lower than those from the spiked soils. The percentages of total PAH removals from the MGP soil were 59%, 46%, and 51% for the FAME:MGP soil ratios of 1:2, 1:1, and 2:1, respectively. These results showed that the FAME could be a more attractive alternative to conventional surfactants in ex situ washing of PAH-contaminated soils. 2010 Elsevier Ltd. All rights reserved.

Behavior of nine selected emerging trace organic contaminants in an artificial recharge system supplemented with a reactive barrier.

Science.gov (United States)

Valhondo, Cristina; Carrera, Jesús; Ayora, Carlos; Barbieri, Manuela; Nödler, Karsten; Licha, Tobias; Huerta, Maria

2014-10-01

Artificial recharge improves several water quality parameters, but has only minor effects on recalcitrant pollutants. To improve the removal of these pollutants, we added a reactive barrier at the bottom of an infiltration basin. This barrier contained aquifer sand, vegetable compost, and clay and was covered with iron oxide dust. The goal of the compost was to sorb neutral compounds and release dissolved organic carbon. The release of dissolved organic carbon should generate a broad range of redox conditions to promote the transformation of emerging trace organic contaminants (EOCs). Iron oxides and clay increase the range of sorption site types. In the present study, we examined the effectiveness of this barrier by analyzing the fate of nine EOCs. Water quality was monitored before and after constructing the reactive barrier. Installation of the reactive barrier led to nitrate-, iron-, and manganese-reducing conditions in the unsaturated zone below the basin and within the first few meters of the saturated zone. Thus, the behavior of most EOCs changed after installing the reactive barrier. The reactive barrier enhanced the removal of some EOCs, either markedly (sulfamethoxazole, caffeine, benzoylecgonine) or slightly (trimethoprim) and decreased the removal rates of compounds that are easily degradable under aerobic conditions (ibuprofen, paracetamol). The barrier had no remarkable effect on 1H-benzotriazole and tolyltriazole.

Preliminary studies on trace element contamination in dumping sites of municipal wastes in India and Vietnam

Science.gov (United States)

Agusa, T.; Kunito, T.; Nakashima, E.; Minh, T. B.; Tanabe, S.; Subramanian, A.; Viet, P. H.

2003-05-01

The disposal of wastes in dumping sites has increasingly caused concem about adverse health effects on the populations living nearby. However, no investigation has been conducted yet on contamination in dumping sites of municipal wastes in Asian developing countries. In this study, concentrations of 11 trace elements (V, Cr, Mn, Co, Cu, Zn, Mo, Ag, Cd, Sb and Pb) were detennined in scalp hair from the population living nearby and in soil from dumping sites and control sites of India and Vietnam. Soil samples in dumping site in India showed significantly higher concentrations of some trace elements than soils in control site, whereas this trend was not notable in Vietnam. This is probably due to the fact that the wastes were covered with the soil in the dumping site of Vietnam. Cadmium concentrations in some hair samples of people living near dumping site in India and Vietnam exceeded the level associated with learning disorder in children. Levels of most of the trace elements in hair were significantly higher in dumping site than those in control site in India and Vietnam, suggesting direct or indirect exposure to those elements from dumping wastes. To our knowledge, this is the first study of trace element contamination in dumping sites in India and Vietnam.

Removal of arsenic from contaminated groundwater by solar-driven membrane distillation

International Nuclear Information System (INIS)

Manna, Ajay K.; Sen, Mou; Martin, Andrew R.; Pal, Parimal

2010-01-01

Experimental investigations were carried out on removal of arsenic from contaminated groundwater by employing a new flat-sheet cross flow membrane module fitted with a hydrophobic polyvinylidenefluoride (PVDF) microfiltration membrane. The new design of the solar-driven membrane module in direct contact membrane distillation (DCMD) configuration successfully produced almost 100 per cent arsenic-free water from contaminated groundwater in a largely fouling-free operation while permitting high fluxes under reduced temperature polarization. For a feed flow rate of 0.120 m 3 /h, the 0.13 μm PVDF membrane yielded a high flux of 74 kg/(m 2 h) at a feed water temperature of 40 deg. C and, 95 kg/m 2 h at a feed water temperature of 60 deg. C. The encouraging results show that the design could be effectively exploited in the vast arsenic-affected rural areas of South-East Asian countries blessed with abundant sunlight particularly during the critical dry season. - Solar-driven membrane distillation has the potential of removing arsenic from contaminated groundwater.

Removal of emerging contaminants by simultaneous application of membrane ultrafiltration, activated carbon adsorption, and ultrasound irradiation

International Nuclear Information System (INIS)

Secondes, Mona Freda N.; Naddeo, Vincenzo; Belgiorno, Vincenzo; Ballesteros, Florencio

2014-01-01

Highlights: • Above 99% of the emerging contaminants were removed in the USAMe process. • Influence of PAC dose and US frequency on removal is studied. • Improved performance is due to PAC adsorption enhancement and sonolytic degradation. • US irradiation improved efficiency and delayed declines in the removal of contaminants. • Performance of the hybrid process is better under lower frequency ultrasound irradiation. -- Abstract: Advanced wastewater treatment is necessary to effectively remove emerging contaminants (ECs) with chronic toxicity, endocrine disrupting effects, and the capability to induce the proliferation of highly resistant microbial strains in the environment from before wastewater disposal or reuse. This paper investigates the efficiency of a novel hybrid process that applies membrane ultrafiltration, activated carbon adsorption, and ultrasound irradiation simultaneously to remove ECs. Diclofenac, carbamazepine, and amoxicillin are chosen for this investigation because of their assessed significant environmental risks. Removal mechanisms and enhancement effects are analysed in single and combined processes. The influence of adsorbent dose and ultrasonic frequency to EC removal are also investigated. Results suggest that adsorption is probably the main removal mechanism and is affected by the nature of ECs and the presence of other components in the mixture. Almost complete removals are achieved in the hybrid process for all ECs

Removal of emerging contaminants by simultaneous application of membrane ultrafiltration, activated carbon adsorption, and ultrasound irradiation

Energy Technology Data Exchange (ETDEWEB)

Secondes, Mona Freda N. [Environmental Engineering Graduate Program, Department of Chemical Engineering, University of the Philippines – Diliman, Quezon City (Philippines); Naddeo, Vincenzo, E-mail: vnaddeo@unisa.it [Sanitary and Environmental Engineering Division (SEED), Department of Civil Engineering, University of Salerno, Fisciano 84084 (Saudi Arabia) (Italy); Belgiorno, Vincenzo [Sanitary and Environmental Engineering Division (SEED), Department of Civil Engineering, University of Salerno, Fisciano 84084 (Saudi Arabia) (Italy); Ballesteros, Florencio [Environmental Engineering Graduate Program, Department of Chemical Engineering, University of the Philippines – Diliman, Quezon City (Philippines)

2014-01-15

Highlights: • Above 99% of the emerging contaminants were removed in the USAMe process. • Influence of PAC dose and US frequency on removal is studied. • Improved performance is due to PAC adsorption enhancement and sonolytic degradation. • US irradiation improved efficiency and delayed declines in the removal of contaminants. • Performance of the hybrid process is better under lower frequency ultrasound irradiation. -- Abstract: Advanced wastewater treatment is necessary to effectively remove emerging contaminants (ECs) with chronic toxicity, endocrine disrupting effects, and the capability to induce the proliferation of highly resistant microbial strains in the environment from before wastewater disposal or reuse. This paper investigates the efficiency of a novel hybrid process that applies membrane ultrafiltration, activated carbon adsorption, and ultrasound irradiation simultaneously to remove ECs. Diclofenac, carbamazepine, and amoxicillin are chosen for this investigation because of their assessed significant environmental risks. Removal mechanisms and enhancement effects are analysed in single and combined processes. The influence of adsorbent dose and ultrasonic frequency to EC removal are also investigated. Results suggest that adsorption is probably the main removal mechanism and is affected by the nature of ECs and the presence of other components in the mixture. Almost complete removals are achieved in the hybrid process for all ECs.

Application of multivariate analysis to investigate the trace element contamination in top soil of coal mining district in Jorong, South Kalimantan, Indonesia

Science.gov (United States)

Pujiwati, Arie; Nakamura, K.; Watanabe, N.; Komai, T.

2018-02-01

Multivariate analysis is applied to investigate geochemistry of several trace elements in top soils and their relation with the contamination source as the influence of coal mines in Jorong, South Kalimantan. Total concentration of Cd, V, Co, Ni, Cr, Zn, As, Pb, Sb, Cu and Ba was determined in 20 soil samples by the bulk analysis. Pearson correlation is applied to specify the linear correlation among the elements. Principal Component Analysis (PCA) and Cluster Analysis (CA) were applied to observe the classification of trace elements and contamination sources. The results suggest that contamination loading is contributed by Cr, Cu, Ni, Zn, As, and Pb. The elemental loading mostly affects the non-coal mining area, for instances the area near settlement and agricultural land use. Moreover, the contamination source is classified into the areas that are influenced by the coal mining activity, the agricultural types, and the river mixing zone. Multivariate analysis could elucidate the elemental loading and the contamination sources of trace elements in the vicinity of coal mine area.

Chemical removal of radionuclides in contaminated spinach derived from the Fukushima nuclear accident

International Nuclear Information System (INIS)

Shiba, Kazuhiro; Kitamura, Yoji; Kozaka, Takashi; Uno, Izumi; Miyoshi, Hirokazu; Yanaga, Makoto

2012-01-01

We examined a simple and effective removal method for contaminated farm products to ensure the relief of farmers and the security of consumers. Removal of radionuclides from spinach by chemical methods was investigated. The result of chemical removal showed that antioxidant agents removed radionuclides from spinach by 70–80% for 131 I and more than 80% for radiocesium. In particular, ascorbic acid is promising as a safe and versatile option. (author)

Simultaneous removal of organic contaminants and heavy metals from kaolin using an upward electrokinetic soil remediation process

International Nuclear Information System (INIS)

Wang, J.-Y.; Huang, X.-J.; Kao, Jimmy C.M.; Stabnikova, Olena

2007-01-01

Kaolins contaminated with heavy metals, Cu and Pb, and organic compounds, p-xylene and phenanthrene, were treated with an upward electrokinetic soil remediation (UESR) process. The effects of current density, cathode chamber flushing fluid, treatment duration, reactor size, and the type of contaminants under the vertical non-uniform electric field of UESR on the simultaneous removal of the heavy metals and organic contaminants were studied. The removal efficiencies of p-xylene and phenanthrene were higher in the experiments with cells of smaller diameter or larger height, and with distilled water flow in the cathode chamber. The removal efficiency of Cu and Pb were higher in the experiments with smaller diameter or shorter height cells and 0.01 M HNO 3 solution as cathode chamber flow. In spite of different conditions for removal of heavy metals and organics, it is possible to use the upward electrokinetic soil remediation process for their simultaneous removal. Thus, in the experiments with duration of 6 days removal efficiencies of phenanthrene, p-xylene, Cu and Pb were 67%, 93%, 62% and 35%, respectively. The experiment demonstrated the feasibility of simultaneous removal of organic contaminants and heavy metals from kaolin using the upward electrokinetic soil remediation process

Solvent cleaning system and method for removing contaminants from solvent used in resin recycling

Science.gov (United States)

Bohnert, George W [Harrisonville, MO; Hand, Thomas E [Lee's Summit, MO; DeLaurentiis, Gary M [Jamestown, CA

2009-01-06

A two step solvent and carbon dioxide based system that produces essentially contaminant-free synthetic resin material and which further includes a solvent cleaning system for periodically removing the contaminants from the solvent so that the solvent can be reused and the contaminants can be collected and safely discarded in an environmentally safe manner.

Trace Element Concentration and Speciation in Selected Mining-Contaminated Soils and Water in Willow Creek Floodplain, Colorado

Directory of Open Access Journals (Sweden)

R. Burt

2011-01-01

Full Text Available Long-term mining activities in the mountains around Creede, Colorado have resulted in significant contamination in soils and water in the Willow Creek floodplain. Total major and trace were determined for soils and water and sequential chemical extraction for soils. Objectives were to determine concentrations and potential reactivity of trace elements and investigate their relationship with other soil and water properties. Water trace elements showed significant variability among sites, ranging from 347 to 12108 μg/L. Relative trend showed (Zn > Sr > Ba > (Mn > W > Cd > (Sn > V ≈ Ni ≈ Cu > Co > (Ag. Soil trace elements showed significant short-range spatial variability, ranging from 2819 to 19274 mg/kg. Relative trend showed (Pb ≈ Zn > Mn > Ba > P > (As > Cu > Sr > V > Cd > Sb ≈ Ag > (Co ≈ Cr > Mo ≈ Sn ≈ Ni > (Be ≈ W > Se ≈ Hg. Predominant fractions were oxide, specifically-sorbed/carbonate bound, and residual. Water soluble and exchangeable fractions showed (Zn ≈ Cd > Pb and Cd > Zn > Pb, respectively. Mobility factors for highly contaminated soils showed Cd ≈ Zn > Pb > Cu > As.

Assessment of soil pollution through trace element contamination in a coal mine environment of Jharia

International Nuclear Information System (INIS)

Singh, Gurdeep; Shrivastava, B.K.

1997-01-01

Coal mining environment is associated with liberation of several trace elements. Soils in such regions particularly have been polluted with these trace elements from a wide range of sources. Trace elements such as lead, copper, iron, zinc, chromium, manganese, cobalt, nickel, cadmium, etc. have caused major human health problems in several parts of the world. Concern over such incidents has prompted numerous investigations into the metabolism and toxic effects of these elements. The trace element contamination of soils (e.g. roadside, overburden dump, residential area etc.) in a part of the Jharia coal field running through a large industrial zone was studied. Representative soil samples from several highly polluted spots of the mining areas were collected and analysed. Results of the investigation revealed that the soils are polluted with trace elements to an appreciable level. Pollution index for soil was developed on the basis of observed concentration levels of trace elements of the study area which may help in better understanding of pollution analysis in coal mining areas. (author)

Removal of PAHs from contaminated clayey soil by means of electro-osmosis

KAUST Repository

Lima, Ana T.

2011-06-01

The removal of polycyclic aromatic hydrocarbons (PAHs) from clayey soils is an intricate task. The low porosity of compacted clayey soil hinders bacterial activity and makes convective removal by hydraulic flow impossible. Electro-osmosis is a process that has been used for the mobilization and cleanup of contaminants in clayey soils with varying successes. The present study focuses on the remediation of a contaminated peaty clay soil, located in Olst - the Netherlands, by means of electro-osmosis. The soil was originally contaminated by an asphalt production plant, active from 1903 to 1983, and presents high levels of all 16 priority PAHs indicated by the US Environmental Protection Agency (EPA). Such a long contact times of PAH with the soil (≥100 years) presents a unique study material with well established solid/liquid contaminant partitioning equilibrium, preferable to artificially spiked soil. A batch of 6 electro-osmosis laboratory experiments was carried out to study the removal of 16 PAHs through electro-osmosis. In these experiments, water and a surfactant (Tween 80) were used to enhance the PAH desorption. The electro-osmotic conductivities ranged from 2.88 × 10-10 to a substantial 1.19 × 10-7 m2 V-1 s -1 when applying a current density of 0.005-0.127 A m-2. Electro-osmosis was expected to occur towards the cathode, because of natural soil characteristics (negative zeta potential), but presented scattered directions. The use of reference electrodes proved to be very effective to the prediction of the flow direction. Finally, the addition of Tween 80 as a surfactant enhanced PAH removal up to 30% of the total PAH content of the soil in 9 days. © 2011 Elsevier B.V.

Comparative assessment of LECA and Spartina maritima to remove emerging organic contaminants from wastewater.

Science.gov (United States)

Ferreira, Ana Rita; Guedes, Paula; Mateus, Eduardo P; Ribeiro, Alexandra B; Couto, Nazaré

2017-03-01

The present work aimed to evaluate the capacity of constructed wetlands (CWs) to remove three emerging organic contaminants with different physicochemical properties: caffeine (CAF), oxybenzone (MBPh), and triclosan (TCS). The simulated CWs were set up with a matrix of light expanded clay aggregates (LECA) and planted with Spartina maritima, a salt marsh plant. Controlled experiments were carried out in microcosms using deionized water and wastewater collected at a wastewater treatment plant (WWTP), with different contaminant mass ranges, for 3, 7, and 14 days. The effects of variables were tested isolatedly and together (LECA and/or S. maritima). The presence of LECA and/or S. maritima has shown higher removal (around 61-97%) of lipophilic compounds (MBPh and TCS) than the hydrophilic compound (CAF; around 19-85%). This was attributed to the fact that hydrophilic compounds are dissolved in the water column, whereas the lipophilic ones suffer sorption processes promoting their removal by plant roots and/or LECA. In the control (only wastewater), a decrease in the three contaminant levels was observed. Adsorption and bio/rhizoremediation are the strongest hypothesis to explain the decrease in contaminants in the tested conditions.

Removal of tetracycline from contaminated water by Moringa oleifera seed preparations.

Science.gov (United States)

Santos, Andréa F S; Matos, Maria; Sousa, Ângela; Costa, Cátia; Nogueira, Regina; Teixeira, José A; Paiva, Patrícia M G; Parpot, Pier; Coelho, Luana C B B; Brito, António G

2016-01-01

The aim of this study was to evaluate tetracycline antibiotic (TA) removal from contaminated water by Moringa oleifera seed preparations. The composition of synthetic water approximate river natural contaminated water and TA simulated its presence as an emerging pollutant. Interactions between TA and protein preparations (extract; fraction and lectin) were also evaluated. TA was determined by solid-phase extraction followed by high-performance liquid chromatography-mass spectrometry. Moringa extract and flour removed TA from water. The extract removed TA in all concentrations, and better removal (40%) was obtained with 40 mg L(-1); seed flour (particles  5 mm (0.50 g L(-1)) removed 55% of antibiotic. Interactions between TA and seed preparations were assayed by haemagglutinating activity (HA). Specific HA (SHA) of extract (pH 7) was abolished with tetracycline (5 mg L(-1)); fraction (75%) and lectin HA (97%) were inhibited with TA. Extract SHA decreased by 75% at pH 8. Zeta potential (ZP) of extract 700 mg L(-1) and tetracycline 50 mg L(-1) , pH range 5-8, showed different results. Extract ZP was more negative (-10.73 to -16.00 mV) than tetracycline ZP (-0.27 to -20.15 mV); ZP difference was greater in pH 8. The focus of this study was achieved since Moringa preparations removed TA from water and compounds interacting with tetracycline involved at least lectin-binding sites. This is a natural process, which do not promote environmental damage.

Removal of contaminants from equipment and debris and waste minimization using TechXtract{reg_sign} technology

Energy Technology Data Exchange (ETDEWEB)

Bonem, M.W. [EET, Inc., Bellaire, TX (United States)

1997-10-01

Under this Program Research and Development Agreement (PRDA), EET, Inc., is extending its proprietary TechXtract{reg_sign} chemical decontamination technology into an effective, economical, integrated contaminant removal system. This integrated system will consist of a series of decontamination baths using the TechXtract{reg_sign} chemical formulas, followed by a waste treatment process that will remove the contaminants from the spent chemicals. Sufficient decontamination will result so that materials can be released without restriction after they have been treated, even those materials that have traditionally been considered to be {open_quotes}undecontaminable.{close_quotes} The secondary liquid waste will then be treated to separate any hazardous and radioactive contaminants, so that the spent chemicals and wastewater can be discharged through conventional, permitted outlets. The TechXtract{reg_sign} technology is a unique process that chemically extracts hazardous contaminants from the surface and substrate of concrete, steel, and other solid materials. This technology has been used successfully to remove contaminants as varied as PCBs, radionuclides, heavy metals, and hazardous organics. The process` advantage over other alternatives is its effectiveness in safe and consistent extraction of subsurface contamination. TechXtract{reg_sign} is a proprietary process developed, owned, and provided by EET, Inc. The objective of the PRDA is to demonstrate on a full-scale basis an economical system for decontaminating equipment and debris, with further treatment of secondary waste streams to minimize waste volumes. Contaminants will be removed from the contaminated items to levels where they can be released for unrestricted use. The entire system will be designed with maximum flexibility and automation in mind.

Removal of contaminants from equipment and debris and waste minimization using TechXtract reg-sign technology

International Nuclear Information System (INIS)

Bonem, M.W.

1997-01-01

Under this Program Research and Development Agreement (PRDA), EET, Inc., is extending its proprietary TechXtract reg-sign chemical decontamination technology into an effective, economical, integrated contaminant removal system. This integrated system will consist of a series of decontamination baths using the TechXtract reg-sign chemical formulas, followed by a waste treatment process that will remove the contaminants from the spent chemicals. Sufficient decontamination will result so that materials can be released without restriction after they have been treated, even those materials that have traditionally been considered to be open-quotes undecontaminable.close quotes The secondary liquid waste will then be treated to separate any hazardous and radioactive contaminants, so that the spent chemicals and wastewater can be discharged through conventional, permitted outlets. The TechXtract reg-sign technology is a unique process that chemically extracts hazardous contaminants from the surface and substrate of concrete, steel, and other solid materials. This technology has been used successfully to remove contaminants as varied as PCBs, radionuclides, heavy metals, and hazardous organics. The process' advantage over other alternatives is its effectiveness in safe and consistent extraction of subsurface contamination. TechXtract reg-sign is a proprietary process developed, owned, and provided by EET, Inc. The objective of the PRDA is to demonstrate on a full-scale basis an economical system for decontaminating equipment and debris, with further treatment of secondary waste streams to minimize waste volumes. Contaminants will be removed from the contaminated items to levels where they can be released for unrestricted use. The entire system will be designed with maximum flexibility and automation in mind

Effect of a New Salivary Contaminant Removal Method on Bond Strength

Science.gov (United States)

2014-08-31

was to evaluate the effect of various salivary- contaminant removal methods on the shear bond strength of resin cement to hydrofluoric-acid (HF) etched...mold (Ultradent) to a height of 3mm and light cured . Specimens were stored for 24 hours in 37°C distilled water and then tested in shear in a... contamination which may compromise the bond strength of the resin cement to the ceramic (Aboush, 1998; van Schalkwyk et al., 2003). Saliva affects bond

Removal of arsenic from contaminated water using coagulation enhanced microfiltration

International Nuclear Information System (INIS)

Volchek, K.; Velicogna, D.; Dumouchel, A.; Wong, W.P.; Brown, C.E.

2002-01-01

Results of an innovative arsenic removal process were presented. The process is based on a combination of coagulation and microfiltration processes. Coagulation-Enhanced Microfiltration (CEMF) may eventually become a full-scale commercial technology. This study focused on the process with respect to groundwater treatment because of the importance of arsenic contamination in drinking water. Most experiments were bench-scale using tap water spiked with arsenic. Ferric chloride, which is commonly used in arsenic removal processes was also added. In addition, some tests were conducted on actual arsenic-contaminated water from the effluent treatment plant of a former mining site in Ontario. Results indicate a high arsenic removal efficiency in both spiked and actual water solutions. The microfiltration significantly reduced the level of arsenic in the treatment. This paper described the characteristics of membrane separation. It also presented information regarding chemically enhanced membrane filtration and coagulation-enhanced microfiltration. Bench-scale tests were conducted with both tubular membranes and with immersed capillary membranes. The effect of iron to arsenic ratios on the effectiveness of the system was also tested. It was recommended that future research should include a field study of the process on a pilot-scale to optimize process parameters and to accurately determine the cost of the process. 16 refs., 8 tabs., 9 figs

The removal of plutonium contaminants from Rocky Flats Plant soil

International Nuclear Information System (INIS)

Sunderland, N.R.

1987-01-01

This research was undertaken to determine if the TRUclean process could effectively remove radioactive elements from soils other than derived coral. This is an interim report prior to the project report and discusses the outcome of the tests of the Rocky Flats Plant (RFP) soil. The soil tested contained plutonium particulates in the micron and submicron range. Volume reduction and activity removal were accomplished with an overall efficiency of greater than 90%. The TRUclean process is a very practical and economical solution to soil contamination problems at the Rocky Flats Plant

Application of carbon nanotube technology for removal of contaminants in drinking water: A review

International Nuclear Information System (INIS)

Upadhyayula, Venkata K.K.; Deng, Shuguang; Mitchell, Martha C.; Smith, Geoffrey B.

2009-01-01

Carbon nanotube (CNT) adsorption technology has the potential to support point of use (POU) based treatment approach for removal of bacterial pathogens, natural organic matter (NOM), and cyanobacterial toxins from water systems. Unlike many microporous adsorbents, CNTs possess fibrous shape with high aspect ratio, large accessible external surface area, and well developed mesopores, all contribute to the superior removal capacities of these macromolecular biomolecules and microorganisms. This article provides a comprehensive review on application of CNTs as adsorbent media to concentrate and remove pathogens, NOM, and cyanobacterial (microcystin derivatives) toxins from water systems. The paper also surveys on consideration of CNT based adsorption filters for removal of these contaminants from cost, operational and safety standpoint. Based on the studied literature it appears that POU based CNT technology looks promising, that can possibly avoid difficulties of treating biological contaminants in conventional water treatment plants, and thereby remove the burden of maintaining the biostability of treated water in the distribution systems.

Development of an Integrated Multi-Contaminant Removal Process Applied to Warm Syngas Cleanup for Coal-Based Advanced Gasification Systems

Energy Technology Data Exchange (ETDEWEB)

Meyer, Howard

2010-11-30

This project met the objective to further the development of an integrated multi-contaminant removal process in which H2S, NH3, HCl and heavy metals including Hg, As, Se and Cd present in the coal-derived syngas can be removed to specified levels in a single/integrated process step. The process supports the mission and goals of the Department of Energy's Gasification Technologies Program, namely to enhance the performance of gasification systems, thus enabling U.S. industry to improve the competitiveness of gasification-based processes. The gasification program will reduce equipment costs, improve process environmental performance, and increase process reliability and flexibility. Two sulfur conversion concepts were tested in the laboratory under this project, i.e., the solventbased, high-pressure University of California Sulfur Recovery Process High Pressure (UCSRP-HP) and the catalytic-based, direct oxidation (DO) section of the CrystaSulf-DO process. Each process required a polishing unit to meet the ultra-clean sulfur content goals of <50 ppbv (parts per billion by volume) as may be necessary for fuel cells or chemical production applications. UCSRP-HP was also tested for the removal of trace, non-sulfur contaminants, including ammonia, hydrogen chloride, and heavy metals. A bench-scale unit was commissioned and limited testing was performed with simulated syngas. Aspen-Plus®-based computer simulation models were prepared and the economics of the UCSRP-HP and CrystaSulf-DO processes were evaluated for a nominal 500 MWe, coal-based, IGCC power plant with carbon capture. This report covers the progress on the UCSRP-HP technology development and the CrystaSulf-DO technology.

Groundwater contamination with arsenic and other trace elements in an area of the Pampa, province of Cordoba, Argentina

International Nuclear Information System (INIS)

Nicolli, H.B.; Suriano, J.M.; Gomez Peral, M.A.; Ferpozzi, L.H.; Baleani, O.A.

1989-01-01

A geochemical study of the groundwater of the pampa in the province of Cordoba, Argentina, is reported. Physical-chemical parameters, dissolved solids, and seven trace elements were determined in 60 selected water samples. Systematic and accurate measurements of arsenic, fluorine, and vanadium were performed for the first time. The geographic distribution of the seven trace elements was mapped and its correlation with the anion-cation composition of the water was studied. Eighty-four percent of the water analyzed showed arsenic contents over 0.05 mg/l. The maxima for arsenic, fluorine, vanadium, and uranium contents were found in the western part of the study area, in waters dominated by alkali metal cations. Maximum selenium and antimony contents were found in the eastern part of the areas, whereas molybdenum distribution showed no relationship to the other groups. The movements of the subsoil have disturbed surface and subsurface drainage, thus influencing the water salinity and trace element contents. To investigate the origin of contamination, 54 loess samples were collected at wells in depths ranging from the surface down to the water table. This loess, which has a high proportion of volcanic components, mainly rhyolitic glass, exhibits a chemical composition corresponding to that of a dacite. The loess and volcanic glass show anomalous contents of all contaminant trace elements, mainly arsenic and selenium. For this reason, loess is considered to be the most important source of contamination of this ground water area. 30 refs., 6 figs., 9 tab

Engineering evaluation/cost analysis for the proposed removal of contaminated materials at the Elza Gate site, Oak Ridge, Tennessee

International Nuclear Information System (INIS)

1991-06-01

This engineering evaluation/cost analysis (EE/CA) has been prepared in support of the proposed removal action for cleanup of radioactive and chemically contaminated soil at the Elza Gate site in Oak Ridge, Tennessee. This property became contaminated as a result of storage of ore residues, equipment, and other materials for the US Atomic Energy Commission. The US Department of Energy is responsible for cleanup of portions of the site under its Formerly Utilized Sites Remedial Action Program. In December 1990 an area known as Pad 1 was abrasively scoured to remove surface contamination, and in March 1991 removal of Pad 1 contamination was begun under a separate EE/CA. This EE/CA is intended to cover the remaining portions of the site for which the Department of Energy has responsibility. It has been determined that an EE/CA report is appropriate documentation for the proposed removal action. This EE/CA covers removal of contaminated soils and contaminated concrete rubble from the Elza Gate site. The primary objectives of this EE/CA report are to identify and describe the preferred removal action, and to document the selection of response activities that will mitigate the potential for release of contaminants from the property into the environment and that will minimize the associated threats to human health or welfare and the environment. The preferred alternative is disposition on the Oak Ridge Reservation. 30 refs., 7 figs., 12 tabs

A soil washing pilot plant for removing petroleum hydrocarbons from contaminated soils

International Nuclear Information System (INIS)

Toor, I.A.; Roehrig, G.R.

1992-01-01

A soil washing pilot plant was built and tested for its ability to remove petroleum hydrocarbons from certain soils. The ITEX soil washing pilot plant is a trailer mountable mobile unit which has a washing capacity of two tons per hour of contaminated soils. A benchscale study was carried out prior to the fabrication of the pilot plant. The first sample was contaminated with diesel fuel while the second sample was contaminated with crude oil. Various nonionic, cationic and anionic cleaning agents were evaluated for their ability to remove petroleum hydrocarbons from these materials. The nonionic cleaning agents were more successful in cleaning the soils in general. The ultimate surfactant choice was based on several factors including cost, biodegradability, cleaning efficiency and other technical considerations. The soil samples were characterized in terms of their particle size distributions. Commercial diesel fuel was carefully mixed in this sand to prepare a representative sample for the pilot plant study. Two pilot runs were made using this material. A multistage washing study was also conducted in the laboratory which indicates that the contamination level can be reduced to 100 ppm using only four stages. Because the pilot plant washing efficiency is twice as high, it is believed that ultimate contamination levels can be reduced to lower levels using the same number of stages. However, this hypothesis has not been demonstrated to date

Activation analysis of hair as an indicator of contamination of man by environmental trace element pollutants

Energy Technology Data Exchange (ETDEWEB)

Ryabukhin, Yu S [ed.

1976-10-01

The burning of fossil fuel, discharges from metallurgical and chemical plants, the wide use of chemicals, and other human activities, result in releasing into the biosphere large quantities of elements which are found in relatively low concentrations in the human organism. The pollution of the biosphere by such trace elements, and in particular heavy metals, has reached such proportions that on the scale of significance of the factors causing the 'stressed' state of the environment of heavy metals occupy the second place and, according to forecasts, may in the future move on to the first. In the problem of pollution of the biosphere, man himself undoubtedly occupies the central position as a target. The pollution of air, soil and water, the contamination of micro-organisms, plants and animals are certainly growing into a serious threat and leading to heavy losses. However, it would be a real disaster if man himself became contaminated to levels giving rise to large scale harmful somatic or genetic effects. It is therefore an urgent problem today to determine the initial levels of trace elements in man and the extent of his contamination in areas where these elements are expected to show anomalous concentrations. Attention should be paid in the first place to those trace elements which probably play no physiological role, are particularly abundant in the environment, and have high toxicity (arsenic, mercury, lead, cadmium, etc.). Moreover, it should be born in mind that in anomalously high concentrations even the physiologically necessary trace elements (copper, zinc, manganese, fluorine, etc.) cause harmful effects. This paper justifies the use of hair samples as a biological indicator of environmental pollutants from physiological and morphological aspect and recommends on sample preparation and analysis methods.

Activation analysis of hair as an indicator of contamination of man by environmental trace element pollutants

International Nuclear Information System (INIS)

Ryabukhin, Yu.S.

1976-10-01

The burning of fossil fuel, discharges from metallurgical and chemical plants, the wide use of chemicals, and other human activities, result in releasing into the biosphere large quantities of elements which are found in relatively low concentrations in the human organism. The pollution of the biosphere by such trace elements, and in particular heavy metals, has reached such proportions that on the scale of significance of the factors causing the 'stressed' state of the environment of heavy metals occupy the second place and, according to forecasts, may in the future move on to the first. In the problem of pollution of the biosphere, man himself undoubtedly occupies the central position as a target. The pollution of air, soil and water, the contamination of micro-organisms, plants and animals are certainly growing into a serious threat and leading to heavy losses. However, it would be a real disaster if man himself became contaminated to levels giving rise to large scale harmful somatic or genetic effects. It is therefore an urgent problem today to determine the initial levels of trace elements in man and the extent of his contamination in areas where these elements are expected to show anomalous concentrations. Attention should be paid in the first place to those trace elements which probably play no physiological role, are particularly abundant in the environment, and have high toxicity (arsenic, mercury, lead, cadmium, etc.). Moreover, it should be born in mind that in anomalously high concentrations even the physiologically necessary trace elements (copper, zinc, manganese, fluorine, etc.) cause harmful effects. This paper justifies the use of hair samples as a biological indicator of environmental pollutants from physiological and morphological aspect and recommends on sample preparation and analysis methods

Mapping human health risks from exposure to trace metal contamination of drinking water sources in Pakistan.

Science.gov (United States)

Bhowmik, Avit Kumar; Alamdar, Ambreen; Katsoyiannis, Ioannis; Shen, Heqing; Ali, Nadeem; Ali, Syeda Maria; Bokhari, Habib; Schäfer, Ralf B; Eqani, Syed Ali Musstjab Akber Shah

2015-12-15

The consumption of contaminated drinking water is one of the major causes of mortality and many severe diseases in developing countries. The principal drinking water sources in Pakistan, i.e. ground and surface water, are subject to geogenic and anthropogenic trace metal contamination. However, water quality monitoring activities have been limited to a few administrative areas and a nationwide human health risk assessment from trace metal exposure is lacking. Using geographically weighted regression (GWR) and eight relevant spatial predictors, we calculated nationwide human health risk maps by predicting the concentration of 10 trace metals in the drinking water sources of Pakistan and comparing them to guideline values. GWR incorporated local variations of trace metal concentrations into prediction models and hence mitigated effects of large distances between sampled districts due to data scarcity. Predicted concentrations mostly exhibited high accuracy and low uncertainty, and were in good agreement with observed concentrations. Concentrations for Central Pakistan were predicted with higher accuracy than for the North and South. A maximum 150-200 fold exceedance of guideline values was observed for predicted cadmium concentrations in ground water and arsenic concentrations in surface water. In more than 53% (4 and 100% for the lower and upper boundaries of 95% confidence interval (CI)) of the total area of Pakistan, the drinking water was predicted to be at risk of contamination from arsenic, chromium, iron, nickel and lead. The area with elevated risks is inhabited by more than 74 million (8 and 172 million for the lower and upper boundaries of 95% CI) people. Although these predictions require further validation by field monitoring, the results can inform disease mitigation and water resources management regarding potential hot spots. Copyright © 2015 Elsevier B.V. All rights reserved.

Removal of pharmaceuticals and unspecified contaminants in sewage treatment effluents by activated carbon filtration and ozonation: Evaluation using biomarker responses and chemical analysis.

Science.gov (United States)

Beijer, Kristina; Björlenius, Berndt; Shaik, Siraz; Lindberg, Richard H; Brunström, Björn; Brandt, Ingvar

2017-06-01

Traces of active pharmaceutical ingredients (APIs) and other chemicals are demonstrated in effluents from sewage treatment plants (STPs) and they may affect quality of surface water and eventually drinking water. Treatment of effluents with granular activated carbon (GAC) or ozone to improve removal of APIs and other contaminants was evaluated at two Swedish STPs, Käppala and Uppsala (88 and 103 APIs analyzed). Biomarker responses in rainbow trout exposed to regular and additionally treated effluents were determined. GAC and ozone treatment removed 87-95% of the total concentrations of APIs detected. In Käppala, GAC removed 20 and ozonation (7 g O 3 /m 3 ) 21 of 24 APIs detected in regular effluent. In Uppsala, GAC removed 25 and ozonation (5.4 g O 3 /m 3 ) 15 of 25 APIs detected in effluent. GAC and ozonation also reduced biomarker responses caused by unidentified pollutants in STP effluent water. Elevated ethoxyresorufin-O-deethylase (EROD) activity in gills was observed in fish exposed to effluent in both STPs. Gene expression analysis carried out in Käppala showed increased concentrations of cytochrome P450 (CYP1As and CYP1C3) transcripts in gills and of CYP1As in liver of fish exposed to effluent. In fish exposed to GAC- or ozone-treated effluent water, gill EROD activity and expression of CYP1As and CYP1C3 in gills and liver were generally equal to or below levels in fish held in tap water. The joint application of chemical analysis and sensitive biomarkers proved useful for evaluating contaminant removal in STPs with new technologies. Copyright © 2017 Elsevier Ltd. All rights reserved.

The role of organic matter in the removal of emerging trace organic chemicals during managed aquifer recharge.

Science.gov (United States)

Rauch-Williams, T; Hoppe-Jones, C; Drewes, J E

2010-01-01

This study explored the effect of different bulk organic carbon matrices on the fate of trace organic chemicals (TOrC) during managed aquifer recharge (MAR). Infiltration through porous media was simulated in biologically active column experiments under aerobic and anoxic recharge conditions. Wastewater effluent derived organic carbon types, differing in hydrophobicity and biodegradability (i. e., hydrophobic acids, hydrophilic carbon, organic colloids), were used as feed substrates in the column experiments. These carbon substrates while fed at the same concentration differed in their ability to support soil biomass growth during porous media infiltration. Removal of degradable TOrC (with the exception of diclofenac and propyphenazone) was equal or better under aerobic versus anoxic porous media infiltration conditions. During the initial phase of infiltration, the presence of biodegradable organic carbon (BDOC) enhanced the decay of degradable TOrC by promoting soil biomass growth, suggesting that BDOC served as a co-substrate in a co-metabolic transformation of these contaminants. However, unexpected high removal efficiencies were observed for all degradable TOrC in the presence of low BDOC concentrations under well adopted oligotrophic conditions. It is hypothesized that removal under these conditions is caused by a specialized microbial community growing on refractory carbon substrates such as hydrophobic acids. Findings of this study reveal that the concentration and character of bulk organic carbon present in effluents affect the degradation efficiency for TOrC during recharge operation. Specifically aerobic, oligotrophic microbiological soil environments present favorable conditions for the transformation of TOrC, including rather recalcitrant compounds such as chlorinated flame retardants. (c) 2009 Elsevier Ltd. All rights reserved.

Trace organic chemicals contamination in ground water recharge.

Science.gov (United States)

Díaz-Cruz, M Silvia; Barceló, Damià

2008-06-01

Population growth and unpredictable climate changes will pose high demands on water resources in the future. Even at present, surface water is certainly not enough to cope with the water requirement for agricultural, industrial, recreational and drinking purposes. In this context, the usage of ground water has become essential, therefore, their quality and quantity has to be carefully managed. Regarding quantity, artificial recharge can guarantee a sustainable level of ground water, whilst the strict quality control of the waters intended for recharge will minimize contamination of both the ground water and aquifer area. However, all water resources in the planet are threatened by multiple sources of contamination coming from the extended use of chemicals worldwide. In this respect, the environmental occurrence of organic micropollutants such as pesticides, pharmaceuticals, industrial chemicals and their metabolites has experienced fast growing interest. In this paper an overview of the priority and emerging organic micropollutants in the different source waters used for artificial aquifer recharge purposes and in the recovered water is presented. Besides, some considerations regarding fate and removal of such compounds are also addressed.

Enhanced desorption of PCB and trace metal elements (Pb and Cu) from contaminated soils by saponin and EDDS mixed solution

International Nuclear Information System (INIS)

Cao, Menghua; Hu, Yuan; Sun, Qian; Wang, Linling; Chen, Jing; Lu, Xiaohua

2013-01-01

This study investigated the simultaneous desorption of trace metal elements and polychlorinated biphenyl (PCB) from mixed contaminated soil with a novel combination of biosurfactant saponin and biodegradable chelant S,S-ethylenediaminedisuccinic acid (EDDS). Results showed significant promotion and synergy on Pb, Cu and PCB desorption with the mixed solution of saponin and EDDS. The maximal desorption of Pb, Cu and PCB were achieved 99.8%, 85.7% and 45.7%, respectively, by addition of 10 mM EDDS and 3000 mg L −1 saponin. The marked interaction between EDDS and saponin contributed to the synergy performance. The sorption of EDDS and saponin on soil was inhibited by each other. EDDS could enhance the complexation of metals with the saponin micelles and the solubilization capabilities of saponin micelles for PCB. Our study suggests the combination of saponin and EDDS would be a promising alternative for remediation of co-contaminated soils caused by hydrophobic organic compounds (HOCs) and metals. -- Highlights: ► A novel combination of biosurfactant saponin and EDDS was used to simultaneously remove mixed contaminations from soil. ► Significant synergy on Pb, Cu and PCB desorption were achieved with EDDS/saponin. ► The marked interaction between EDDS and saponin contributed to the synergy performance. -- Significant synergistic effect on Pb, Cu and PCB desorption were achieved with the mixed solution of saponin and EDDS

Arsenic and fluoride contaminated groundwaters: A review of current technologies for contaminants removal.

Science.gov (United States)

Jadhav, Sachin V; Bringas, Eugenio; Yadav, Ganapati D; Rathod, Virendra K; Ortiz, Inmaculada; Marathe, Kumudini V

2015-10-01

Chronic contamination of groundwaters by both arsenic (As) and fluoride (F) is frequently observed around the world, which has severely affected millions of people. Fluoride and As are introduced into groundwaters by several sources such as water-rock interactions, anthropogenic activities, and groundwater recharge. Coexistence of these pollutants can have adverse effects due to synergistic and/or antagonistic mechanisms leading to uncertain and complicated health effects, including cancer. Many developing countries are beset with the problem of F and As laden waters, with no affordable technologies to provide clean water supply. The technologies available for the simultaneous removal are akin to chemical treatment, adsorption and membrane processes. However, the presence of competing ions such as phosphate, silicate, nitrate, chloride, carbonate, and sulfate affect the removal efficiency. Highly efficient, low-cost and sustainable technology which could be used by rural populations is of utmost importance for simultaneous removal of both pollutants. This can be realized by using readily available low cost materials coupled with proper disposal units. Synthesis of inexpensive and highly selective nanoadsorbents or nanofunctionalized membranes is required along with encapsulation units to isolate the toxicant loaded materials to avoid their re-entry in aquifers. A vast number of reviews have been published periodically on removal of As or F alone. However, there is a dearth of literature on the simultaneous removal of both. This review critically analyzes this important issue and considers strategies for their removal and safe disposal. Copyright © 2015 Elsevier Ltd. All rights reserved.

Mixed Contaminants Removal Efficiency Using Bio-FeS Nanoparticles.

Science.gov (United States)

Seo, Hyunhee; Roh, Yul

2018-02-01

Advances in nanotechnology has provided diverse industrial applications including an environmental remediation field. In particular, bio-nanotechnology gives extended eco-friendly remediation practice. Among diverse bio-nanoparticles synthesized by microorganisms, the iron based nanoparticles (NPs) are of great interest because of their availability, low cost and toxicity to human health and the environment. In this study, iron based nanoparticles were biologically synthesized and mineralogically identified. Also, the removal efficiency of mixed contaminants, high As(III)-low Cr(VI) and high As(V)-low Cr(VI), using these bio-nanoparticles were conducted. As a result, biologically synthesized NPs were identified as FeS complex and their catalytic capacity showed highly effective to immobilize more than 97% of mixed contaminants by adsorption/mineralization.

Enhanced Stormwater Contaminant Removal Using Tree Filters And Modified Sorbents

Science.gov (United States)

Schifman, L. A.; Kasaraneni, V. K.; Boving, T. B.; Oyanedel-Craver, V.

2012-12-01

Stormwater runoff, particularly in urban areas, contains several groups of contaminants that negatively impact surface- and groundwater quality if left untreated. Contaminants in runoff are often addressed by structural best management practices (BMP) that capture and treat runoff before discharging it. Many BMPs, such as tree filters, act as primary filtration devices that attenuate total suspended solids, nutrients, and heavy metals from runoff; but typically these BMPs are not designed to treat bacteria and have only minor petroleum hydrocarbon (PH) treatment capabilities. To address this shortcoming, three materials (red cedar wood chips, expanded shale, and crushed concrete) were modified with either Quaternary Ammonium Silane (QAS) or Silver Nanoparticles (AgNPs) to provide antimicrobial properties to the matrix and/or exploit their affinity to sorb PH, particularly polycyclic aromatic hydrocarbons (PAH). Results show that of the three materials investigated, wood chips exhibit the highest sorption capacity for QAS, making this material favorable for treating bacteria, while at the same time attenuating PAHs by sorption processes. In case of AgNP amendments to wood, less uptake and more desorption from the wood matrix was observed. Relative to wood, expanded shale and crushed concrete exhibited less affinity for QAS (results for AgNPs are pending). Currently, batch isotherm and unsaturated flow column studies are under way to determine the performance of the amended materials with regard to removal of bacteria, nutrients, heavy metals, and PAH from artificially contaminated runoff. In this presentation, the contaminant removal efficiency of all modified and unmodified materials will be discussed on the background of how these materials may find use in enhanced treatment of stormwater in tree filter BMPs.

Trace metal contamination in mangrove sediments, Guanabara Bay, Rio de Janeiro, Brazil

OpenAIRE

Farias,Cassia O.; Hamacher,Claudia; Wagener,Angela de Luca R.; Campos,Reinaldo C. de; Godoy,José M.

2007-01-01

The Guanabara Bay in Rio de Janeiro has undergone profound alterations of its natural environmental conditions. Metal concentration increase in sediments has been reported to be among these alterations. Trace-metal contamination and availability were studied in sediments of 3 mangrove areas of the bay. Cd, Zn, Pb, Ni, Cu and Al concentrations were determined in segments of sediment cores, after treatment with 1 mol L-1 HCl and with concentrated HNO3. Fe and Mn were determined in the leach wit...

The cleaning of burned and contaminated archaeological maize prior to 87Sr/86Sr analysis

Science.gov (United States)

Benson, Larry V.; Taylor, Howard E.; Plowman, Terry I.; Roth, David A.; Antweiler, Ronald C.

2010-01-01

Accurate trace-metal and strontium-isotope analyses of archaeological corn cobs require that metal contaminants be removed prior to chemical analysis. Archaeological cobs are often coated with construction debris, dust, or soil which contains mineral particles. In addition, most archaeological cobs are partially or completely burned and the burned parts incorporate mineral debris in their hardened residual structures. Unburned cobs are weak ion exchangers and most metals within a cob are not firmly bound to cob organic matter; therefore, immersing cobs in acids and rinsing them in deionized water to remove mineral contaminants may result in the undesirable loss of metals, including strontium, from the cob.In this paper we show that some cob metal-pair ratios are not substantially changed when the cob is “cleaned” with deionized water, if the water-cob contact time does not exceed five minutes. Additionally, we introduce a method for eliminating mineral contaminants in both burned and unburned cobs, thus rendering them acceptable for strontium-isotope analysis. However, the decontamination procedure results in the rapid non-stoichiometric leaching of trace metals from the unburned cobs and it is possible that most metals will be extracted from the cobs during the lengthy decontamination process. Trace metals, in particular Al and Ca, should be analyzed in order to determine the presence and level of mineral contamination after cleaning.

The removal of radionuclides from contaminated milk and meat

International Nuclear Information System (INIS)

Long, S.C.; Sequeira, S.; Pollard, D.; Fedin, F.A.; Krylova, N.V.

1996-01-01

The transfer of radiocesium and radiostrontium from milk to a number of commonly consumed European and Ukrainian cheeses was quantified. The F f 1 for radiocesium in these cheeses was typically between 0.5 and 0.7, while that for radiostrontium ranged from 0.7 to 8.3. Those steps during the cheese making process that resulted in removal of radiocesium were then identified. The production of cheeses by modified technologies succeeded in reducing the radiostrontium transfer by a small amount. Acidification of the milk (to a pH < 5.1) prior to coagulation resulted in a significantly smaller transfer of radiostrontium to the cheese. The coagulation process varied by up to 20% for duplicate experiments. At least 50% of radiocesium may be removed from contaminated meat by soaking in NaCI solution (brine). Greater removal (up to 90%) may be achieved by varying treatment parameters. The losses of vitamins and minerals associated with this treatment were quantified

Tracing contamination sources in soils with Cu and Zn isotopic ratios.

Science.gov (United States)

Fekiacova, Z; Cornu, S; Pichat, S

2015-06-01

Copper (Cu) and zinc (Zn) are naturally present and ubiquitous in soils and are important micronutrients. Human activities contribute to the input of these metals to soils in different chemical forms, which can sometimes reach a toxic level for soil organisms and plants. Isotopic signatures could be used to trace sources of anthropogenic Cu and Zn pollution. The aim of this paper is to determine whether it is possible to identify (i) Cu and Zn contamination in soils and their sources, on the basis of their isotopic signatures, and (ii) situations that are a priori favorable or not for tracing Cu and Zn pollution using the isotopic approach. Therefore, we compiled data from the literature on Cu and Zn isotopes in soils, rocks and pollutants and added to this database the results of our own research. As only a few studies have dealt with agricultural contamination, we also studied a soil toposequence from Brittany, France, that experienced spreading of pig slurry for tens of years. In the surface horizons of the natural soils, the δ(65)Cu values vary from -0.15 to 0.44‰ and the δ(66)Zn from -0.03 to 0.43‰. Furthermore, vertical variations along soil profiles range from -0.95 to 0.44‰ for δ(65)Cu and from -0.53 to 0.64‰ for δ(66)Zn values. We concluded that pedogenetic processes can produce isotopic fractionation, yet, it is not always discernible and can be overprinted by an exogenous isotopic signature. Furthermore, some contaminants are enriched in heavy Cu or in light Zn compared to the rock or soil, but no generalization can be made. The anthropogenic inputs can be identified based on stable Cu and Zn isotope ratios if the isotope ratios of the sources are different from those of the soil, which needs to be tested for each individual case. Copyright © 2015 Elsevier B.V. All rights reserved.

Design, construction and monitoring of temporary storage facilities for removed contaminants

International Nuclear Information System (INIS)

Saegusa, Hiromitsu; Funaki, Hironori; Kurikami, Hiroshi; Sakamoto, Yoshiaki; Tokizawa, Takayuki

2013-01-01

Since the Fukushima Daiichi nuclear power plant accident caused by the Tohoku Region Pacific Coast Earthquake on March 11, 2011, decontamination work has been conducted in the surrounding environment within the Fukushima prefecture. Removed contaminants including soil, grass and trees are to be stored safely at temporary storage facilities for up to three years, after which they will be transferred to a planned interim storage facility. The decontamination pilot project was carried out in both the restricted and planned evacuation areas in order to assess decontamination methods and demonstrate measures for radiation protection of workers. Fourteen temporary storage facilities of different technical specifications were designed and constructed under various topographic conditions and land use. In order to support the design, construction and monitoring of temporary storage facilities for removed contaminants during the full-scale decontamination within the prefecture of Fukushima, technical know-how obtained during the decontamination pilot project has been identified and summarized in this paper. (author)

Genesis Solar Wind Sample 61422: Experiment in Variation of Sequence of Cleaning Solvent for Removing Carbon-Bearing Contamination

Science.gov (United States)

Allton, J. H.; Kuhlman, K. R.; Allums, K. K.; Gonzalez, C. P.; Jurewicz, A. J. G.; Burnett, D. S.; Woolum, D. S.

2015-01-01

The recovered Genesis collector fragments are heavily contaminated with crash-derived particulate debris. However, megasonic treatment with ultra-pure-water (UPW; resistivity (is) greater than18 meg-ohm-cm) removes essentially all particulate contamination greater than 5 microns in size [e.g.1] and is thus of considerable importance. Optical imaging of Si sample 60336 revealed the presence of a large C-rich particle after UPW treatment that was not present prior to UPW. Such handling contamination is occasionally observed, but such contaminants are normally easily removed by UPW cleaning. The 60336 particle was exceptional in that, surprisingly, it was not removed by additional UPW or by hot xylene or by aqua regia treatment. It was eventually removed by treatment with NH3-H2O2. Our best interpretation of the origin of the 60336 particle was that it was adhesive from the Post-It notes used to stabilize samples for transport from Utah after the hard landing. It is possible that the insoluble nature of the 60336 particle comes from interaction of the Post-It adhesive with UPW. An occasional bit of Post-It adhesive is not a major concern, but C particulate contamination also occurs from the heat shield of the Sample Return Capsule (SRC) and this is mixed with inorganic contamination from the SRC and the Utah landing site. If UPW exposure also produced an insoluble residue from SRC C, this would be a major problem in chemical treatments to produce clean surfaces for analysis. This paper reports experiments to test whether particulate contamination was removed more easily if UPW treatment was not used.

Removal Efficiency of Microbial Contaminants from Hospital Wastewaters

KAUST Repository

Timraz, Kenda

2016-02-01

This study aims to evaluate the removal efficiency of microbial contaminants from two hospitals on-site Wastewater Treatment Plants (WWTPs) in Saudi Arabia. Hospital wastewaters often go untreated in Saudi Arabia as in many devolving countries, where no specific regulations are imposed regarding hospital wastewater treatment. The current guidelines are placed to ensure a safe treated wastewater quality, however, they do not regulate for pathogenic bacteria and emerging contaminants. Results from this study have detected pathogenic bacterial genera and antibiotic resistant bacteria in the sampled hospitals wastewater. And although the treatment process of one of the hospitals was able to meet current quality guidelines, the other hospital treatment process failed to meet these guidelines and disgorge of its wastewater might be cause for concern. In order to estimate the risk to the public health and the impact of discharging the treated effluent to the public sewage, a comprehensive investigation is needed that will facilitate and guide suggestions for more detailed guidelines and monitoring.

Reductions in fish-community contamination following lowhead dam removal linked more to shifts in food-web structure than sediment pollution.

Science.gov (United States)

Davis, Robert P; Sullivan, S Mažeika P; Stefanik, Kay C

2017-12-01

Recent increases in dam removals have prompted research on ecological and geomorphic river responses, yet contaminant dynamics following dam removals are poorly understood. We investigated changes in sediment concentrations and fish-community body burdens of mercury (Hg), selenium (Se), polychlorinated biphenyls (PCB), and chlorinated pesticides before and after two lowhead dam removals in the Scioto and Olentangy Rivers (Columbus, Ohio). These changes were then related to documented shifts in fish food-web structure. Seven study reaches were surveyed from 2011 to 2015, including controls, upstream and downstream of the previous dams, and upstream restored vs. unrestored. For most contaminants, fish-community body burdens declined following dam removal and converged across study reaches by the last year of the study in both rivers. Aldrin and dieldrin body burdens in the Olentangy River declined more rapidly in the upstream-restored vs. the upstream-unrestored reach, but were indistinguishable by year three post dam removal. No upstream-downstream differences were observed in body burdens in the Olentangy River, but aldrin and dieldrin body burdens were 138 and 148% higher, respectively, in downstream reaches than in upstream reaches of the Scioto River following dam removal. The strongest relationships between trophic position and body burdens were observed with PCBs and Se in the Scioto River, and with dieldrin in the Olentangy River. Food-chain length - a key measure of trophic structure - was only weakly related to aldrin body burdens, and unrelated to other contaminants. Overall, we demonstrate that lowhead dam removal may effectively reduce ecosystem contamination, largely via shifts in fish food-web dynamics versus sediment contaminant concentrations. This study presents some of the first findings documenting ecosystem contamination following dam removal and will be useful in informing future dam removals. Copyright © 2017 Elsevier Ltd. All rights reserved.

Effects of incubation on solubility and mobility of trace metals in two contaminated soils

International Nuclear Information System (INIS)

Ma, Lena Q.; Dong Yan

2004-01-01

Much research has focused on changes in solubility and mobility of trace metals in soils under incubation. In this experiment, changes in solubility and mobility of trace metals (Pb, Cu and As) and Fe in two contaminated soils from Tampa, Florida and Montreal, Canada were examined. Soils of 30 g were packed in columns and were incubated for 3-80 days under water-flooding incubation. Following incubation, metal concentrations in pore water (water soluble) and in 0.01 M CaCl 2 leachates (exchangeable+water soluble) were determined. While both soils were contaminated with Pb (1600-2500 mg kg -1 ), Tampa soil was also contaminated with As (230 mg kg -1 ). Contrast to the low pH (3.8) of Tampa soil, Montreal soil had an alkaline pH of 7.7 and high Ca of 1.6%. Concentrations of Fe(II) increased with incubation time in the Tampa soil mainly due to reductive Fe dissolution, but decreased in the Montreal soil possibly due to formation of FeCO 3 . The inverse relationship between concentrations of Pb and Fe(II) in pore water coupled with the fact that Fe(II) concentrations were much greater than those of Pb in pore water may suggest the importance of Fe(II) in controlling Pb solubility in soils. However, changes in concentrations of Fe(II), Pb, Cu and As in pore water with incubation time were similar to those in leachate, i.e. water soluble metals were positively related to exchangeable metals in the two contaminated soils. This research suggests the importance of Fe in controlling metal solubility and mobility in soils under water-flooded incubation. - Iron is important in controlling metal solubility and mobility in flooded soils

Environmental projects. Volume 14: Removal of contaminated soil and debris

Science.gov (United States)

Kushner, Len

1992-01-01

Numerous diverse activities at the Goldstone Deep Space Communications Complex (GDSCC) are carried out in support of six parabolic dish antennas. Some of these activities can result in possible spills or leakages of hazardous materials and wastes stored both above ground in steel drums and below ground in underground storage tanks (UST's). These possible leaks or spills, along with the past practice of burial of solid debris and waste in trenches and pits, could cause local subsurface contamination of the soil. In 1987, the Jet Propulsion Laboratory (JPL), retained Engineering-Science, Inc. (E-S), Pasadena, California, to identify the specific local areas within the GDSCC with subsurface soil contamination. The E-S study determined that some of the soils at the Apollo Site and the Mars Site were contaminated with hydrocarbons, while soil at a nonhazardous waste dumpsite at the Mojave Base site was contaminated with copper. This volume is a JPL-expanded version of the PE209 E-S report, and it also reports that all subsurface contaminated soils at the GDSCC were excavated, removed, and disposed of in an environmentally acceptable way, and the excavations were backfilled and covered in accordance with accepted Federal, State, and local environmental rules and regulations.

Effects of iron and calcium carbonate on contaminant removal efficiencies and microbial communities in integrated wastewater treatment systems.

Science.gov (United States)

Zhao, Zhimiao; Song, Xinshan; Zhang, Yinjiang; Zhao, Yufeng; Wang, Bodi; Wang, Yuhui

2017-12-01

In the paper, we explored the influences of different dosages of iron and calcium carbonate on contaminant removal efficiencies and microbial communities in algal ponds combined with constructed wetlands. After 1-year operation of treatment systems, based on the high-throughput pyrosequencing analysis of microbial communities, the optimal operating conditions were obtained as follows: the ACW10 system with Fe 3+ (5.6 mg L -1 ), iron powder (2.8 mg L -1 ), and CaCO 3 powder (0.2 mg L -1 ) in influent as the adjusting agents, initial phosphorus source (PO 4 3- ) in influent, the ratio of nitrogen to phosphorus (N/P) of 30 in influent, and hydraulic retention time (HRT) of 1 day. Total nitrogen (TN) removal efficiency and total phosphorus (TP) removal efficiency were improved significantly. The hydrolysis of CaCO 3 promoted the physicochemical precipitation in contaminant removal. Meanwhile, Fe 3+ and iron powder produced Fe 2+ , which improved contaminant removal. Iron ion improved the diversity, distribution, and metabolic functions of microbial communities in integrated treatment systems. In the treatment ACW10, the dominant phylum in the microbial community was PLANCTOMYCETES, which positively promoted nitrogen removal. After 5 consecutive treatments in ACW10, contaminant removal efficiencies for TN and TP respectively reached 80.6% and 57.3% and total iron concentration in effluent was 0.042 mg L -1 . Copyright © 2017 Elsevier Ltd. All rights reserved.

A review of biosensing techniques for detection of trace carcinogen contamination in food products.

Science.gov (United States)

Li, Zhanming; Yu, Yue; Li, Zhiliang; Wu, Tao

2015-04-01

Carcinogen contaminations in the food chain, for example heavy metal ions, pesticides, acrylamide, and mycotoxins, have caused serious health problems. A major objective of food-safety research is the identification and prevention of exposure to these carcinogens, because of their impossible-to-reverse tumorigenic effects. However, carcinogen detection is difficult because of their trace-level presence in food. Thus, reliable and accurate separation and determination methods are essential to protect food safety and human health. This paper summarizes the state of the art in separation and determination methods for analyzing carcinogen contamination, especially the advances in biosensing methods. Furthermore, the application of promising technology including nanomaterials, imprinted polymers, and microdevices is detailed. Challenges and perspectives are also discussed.

Contamination by arsenic and other trace elements of tube-well water along the Mekong River in Lao PDR

International Nuclear Information System (INIS)

Chanpiwat, Penradee; Sthiannopkao, Suthipong; Cho, Kyung Hwa; Kim, Kyoung-Woong; San, Vibol; Suvanthong, Boukeo; Vongthavady, Chantha

2011-01-01

Arsenic and other trace element concentrations were determined for tube-well water collected in the Lao PDR provinces of Attapeu, Bolikhamxai, Champasak, Savannakhet, Saravane, and Vientiane. Water samples, especially from floodplain areas of central and southern Laos, were significantly contaminated not only with As, but with B, Ba, Mn, U, and Fe as well. Total As concentrations ranged from -1 to 278 μg L -1 , with over half exceeding the WHO guideline of 10 μg L -1 . 46% of samples, notably, were dominated by As(III). Samples from Vientiane, further north, were all acceptable except on pH, which was below drinking water limits. A principal component analysis found associations between general water characteristics, As, and other trace elements. Causes of elevated As concentrations in Lao tube wells were considered similar to those in other Mekong River countries, particularly Cambodia and Vietnam, where young alluvial aquifers give rise to reducing conditions. - Research highlights: → Tube-well waters were significantly contaminated with As, B, Ba, Mn, U and Fe. → As contaminated areas were mostly floodplains in the central and southern parts of Laos. → As (III) was a predominant species in 46% of tube-well water samples. → A positive association between water characteristics, B and Sr contents was found. → Total As, As (III) and Fe concentrations were positively associated among each other. - In the first international research on As and other trace element contamination of tube-well water in Lao PDR, concentrations of As, B, Ba, Mn, U, and Fe exceeding drinking water guidelines were found in samples taken mostly from Mekong River floodplain areas.

Contamination by arsenic and other trace elements of tube-well water along the Mekong River in Lao PDR

Energy Technology Data Exchange (ETDEWEB)

Chanpiwat, Penradee [School of Environmental Science and Engineering, Gwangju Institute of Science and Techonology (GIST), 261 Cheomdan-gwagiro (Oryong-dong), Buk-gu, Gwangju 500-712 (Korea, Republic of); Sthiannopkao, Suthipong, E-mail: suthi@gist.ac.k [International Environmental Research Center (IERC), Gwangju Institute of Science and Technology (GIST), 261 Cheomdan-gwagiro - Oryong-dong, Buk-gu, Gwangju 500-712 (Korea, Republic of); Cho, Kyung Hwa [School of Environmental Science and Engineering, Gwangju Institute of Science and Techonology (GIST), 261 Cheomdan-gwagiro (Oryong-dong), Buk-gu, Gwangju 500-712 (Korea, Republic of); Kim, Kyoung-Woong, E-mail: kwkim@gist.ac.k [School of Environmental Science and Engineering, Gwangju Institute of Science and Techonology (GIST), 261 Cheomdan-gwagiro (Oryong-dong), Buk-gu, Gwangju 500-712 (Korea, Republic of); San, Vibol [Department of Environmental Science, Royal University of Phnom Penh (Cambodia); Suvanthong, Boukeo; Vongthavady, Chantha [Environmental Health Division, Center for Environmental Health and Water Supply, Ministry of Health, NongBone Road, Vientiane (Lao People' s Democratic Republic)

2011-02-15

Arsenic and other trace element concentrations were determined for tube-well water collected in the Lao PDR provinces of Attapeu, Bolikhamxai, Champasak, Savannakhet, Saravane, and Vientiane. Water samples, especially from floodplain areas of central and southern Laos, were significantly contaminated not only with As, but with B, Ba, Mn, U, and Fe as well. Total As concentrations ranged from <0.5 {mu}g L{sup -1} to 278 {mu}g L{sup -1}, with over half exceeding the WHO guideline of 10 {mu}g L{sup -1}. 46% of samples, notably, were dominated by As(III). Samples from Vientiane, further north, were all acceptable except on pH, which was below drinking water limits. A principal component analysis found associations between general water characteristics, As, and other trace elements. Causes of elevated As concentrations in Lao tube wells were considered similar to those in other Mekong River countries, particularly Cambodia and Vietnam, where young alluvial aquifers give rise to reducing conditions. - Research highlights: Tube-well waters were significantly contaminated with As, B, Ba, Mn, U and Fe. As contaminated areas were mostly floodplains in the central and southern parts of Laos. As (III) was a predominant species in 46% of tube-well water samples. A positive association between water characteristics, B and Sr contents was found. Total As, As (III) and Fe concentrations were positively associated among each other. - In the first international research on As and other trace element contamination of tube-well water in Lao PDR, concentrations of As, B, Ba, Mn, U, and Fe exceeding drinking water guidelines were found in samples taken mostly from Mekong River floodplain areas.

Removal of heavy metals and radionuclides by seeded magnetic filtration

International Nuclear Information System (INIS)

Bibler, J.P.; Norrell, G.; Hemmings, R.L.; Bradbury, D.; Dunn, M.J.; Kalinauskas, G.L.

1991-01-01

Removal of traces of heavy metal or radionuclide contamination from solution at high flow rate presents a considerable technical challenge. Low flow methods of treatment such as particle gravity settling require expensive large volume equipment, whereas traditional methods of filtration can cause significant energy costs. Magnetic filtration can be used to provide a low cost method of solid-liquid separation at high flow rate, provided contaminants can be selectively bound to a magnetic solid particle. This paper describes the use of such selective magnetic particles made up of inorganic particles coupled with organic polymers

Removal of uranium from uranium-contaminated soils -- Phase 1: Bench-scale testing

International Nuclear Information System (INIS)

Francis, C.W.

1993-09-01

To address the management of uranium-contaminated soils at Fernald and other DOE sites, the DOE Office of Technology Development formed the Uranium in Soils Integrated Demonstration (USID) program. The USID has five major tasks. These include the development and demonstration of technologies that are able to (1) characterize the uranium in soil, (2) decontaminate or remove uranium from the soil, (3) treat the soil and dispose of any waste, (4) establish performance assessments, and (5) meet necessary state and federal regulations. This report deals with soil decontamination or removal of uranium from contaminated soils. The report was compiled by the USID task group that addresses soil decontamination; includes data from projects under the management of four DOE facilities [Argonne National Laboratory (ANL), Los Alamos National Laboratory (LANL), Oak Ridge National Laboratory (ORNL), and the Savannah River Plant (SRP)]; and consists of four separate reports written by staff at these facilities. The fundamental goal of the soil decontamination task group has been the selective extraction/leaching or removal of uranium from soil faster, cheaper, and safer than current conventional technologies. The objective is to selectively remove uranium from soil without seriously degrading the soil's physicochemical characteristics or generating waste forms that are difficult to manage and/or dispose of. Emphasis in research was placed more strongly on chemical extraction techniques than physical extraction techniques

High-temperature removal of H2S from syngas by means of zinc-contaminated soils

International Nuclear Information System (INIS)

Tzu-Hsing Ko; Hsin-Ta Hsueh

2006-01-01

Hydrogen sulfide (H 2 S) is one of the most common compounds and can be easily found in advanced power generation plants, such as integrated gasification combined cycle (IGCC) and molten-carbonate fuel cell (MCFC) plants. Generally, in these systems raw materials with high heating value (HHV) or biomass were gasified under high temperature and produced a useful mixture gas. During the gasification, hydrogen sulfide accompanies with a great quantity of reductive gases at high temperature including CO, H 2 , CH 4 and N 2 , etc. This mixture gas is so-call syngas. Syngas is a valuable resource for electric power generation. Prior to using, H 2 S needs to be removed because its harmful effect. In addition, H 2 S is not only the malodorous and corrosive gas but also is the sources of the acid rain when it is oxidized into SO 2 and reacted with water. It has been known for many years that certain soils have the ability to absorb reductive sulfur-containing species such as hydrogen sulfide (H 2 S), carbonyl sulfide (COS), carbon disulfide (CS 2 ), dimethyl sulfide (CH 3 SCH 3 ) and dimethyl disulfide (CH 3 SSCH 3 ) at room temperature. Therefore, soils could act as an important sorption media for the removal of waste gases before they are released into the atmosphere. In this study, we further use the contaminated soils as regenerable sorbent for the removal of H 2 S from syngas under high temperature. Results indicate that contaminated soils could be used to remove H 2 S as well as maintain at least 90% regeneration efficiency after regeneration cycles. Additionally, zinc and iron appeared to be the major active species to react with H 2 S. The chemical structure of zinc and iron after removal of H 2 S could be expressed as ZnS and FeS. In addition to removal of H 2 S, it is also established that contaminated soil can be used for application which reduce the problem of heavy metal contaminated soils (Full text of contribution)

Trace elements in nail polish as a source of contamination of nail clippings when used in epidemiological studies

International Nuclear Information System (INIS)

Favaro, P.C.; Bode, P.; De Nadai Fernandes, E.A.

2005-01-01

Trace elements were determined in 27 brands of nail polish using INAA so as to estimate the impact of nail polish remainders when using (finger, toe) nail clippings as a bioindicator for epidemiological studies. Fe was found to be present up to almost 1.7% in one brand. No unambiguous correlation between trace elements and color was established, though transparent polish has the lowest trace element concentrations. An estimate of the maximum effect (no removal of the paint) indicates that over-estimates of some trace element levels in nail with more than 200.000% may occur. If nail clippings will be used to study trace elements, very high demands have to be set to the efficiency and selectivity of the cleaning procedure. (author)

Selective flotation for the removal of radionuclides from contaminated soil

International Nuclear Information System (INIS)

Miller, J.D.; Yu, Q.; Lu, Y.Q.

1995-01-01

Low-level radioactive contaminated soils (10--500 pci/gm) created by defense-related activities at certain Superfund sites, such as Nevada Test Site (NTS), is a current environmental concern. Many of these contaminated sites may require appropriate cleanup and restoration, which could cost billions of dollars and put tremendous pressure on limited financial resources. Therefore, the development of a selective flotation process to separate such radionuclides from contaminated soils should be considered. In this study, both a pure depleted UO 2 sample and three synthetic UO 2 /soil mixtures were used to evaluate surface chemistry features and to examine the possibility for the flotation of fine UO 2 particles from selected soils. It was intended that this model system would be a reasonable representation of contaminated soils such as those found the Nevada Test Site which are reported to be contaminated by PuO 2 fallout. The effect of reagent schedule, particle size distribution, and surface charge are discussed with respect to the flotation separation of the UO 2 /soil mixtures. It was found that both commercial fatty acids and reagent grade sodium oleate are effective collectors for UO 2 flotation provided the pH is adjusted to the range of pH 8--9. The bench-scale flotation results successfully demonstrated that froth flotation technology can be used to remove UO 2 from such model contaminated soils with appropriate flotation chemistry conditions which depend on the soil characteristics and other pretreatment procedures

Citric-acid preacidification enhanced electrokinetic remediation for removal of chromium from chromium-residue-contaminated soil.

Science.gov (United States)

Meng, Fansheng; Xue, Hao; Wang, Yeyao; Zheng, Binghui; Wang, Juling

2018-02-01

Electrokinetic experiments were conducted on chromium-residue-contaminated soils collected from a chemical plant in China. Acidification-electrokinetic remediation technology was proposed in order to solve the problem of removing inefficient with ordinary electrokinetic. The results showed that electrokinetic remediation removal efficiency of chromium from chromium-contaminated soil was significantly enhanced with acidizing pretreatment. The total chromium [Cr(T)] and hexavalent chromium [Cr(VI)] removal rate of the group acidized by citric acid (0.9 mol/L) for 5 days was increased from 6.23% and 19.01% in the acid-free experiments to 26.97% and 77.66% in the acidification-treated experiments, respectively. In addition, part of chromium with the state of carbonate-combined will be converted into water-soluble state through acidification to improve the removal efficiency. Within the appropriate concentration range, the higher concentration of acid was, the more chromium was released. So the removal efficiency of chromium depended on the acid concentration. The citric acid is also a kind of complexing agent, which produced complexation with Cr that was released by the electrokinetic treatment and then enhanced the removal efficiency. The major speciation of chromium that was removed from soils by acidification-electrokinetics remediation was acid-soluble speciation, revivification speciation and oxidation speciation, which reduced biological availability of chromium.

Washing enhanced electrokinetic remediation for removal cadmium from real contaminated soil

International Nuclear Information System (INIS)

Giannis, Apostolos; Gidarakos, Evangelos

2005-01-01

The main objective of this study is to evaluate the combination of electrokinetic remediation and soil washing technology in order to remove cadmium from contaminated soil. This paper presents the results of an experimental research undertaken to evaluate different washing and purging solutions to enhance the removal of cadmium from a real contaminated soil during electrokinetic remediation. Two different experimental modules were applied in the laboratory. Soil was saturated with tap water, while acetic and hydrochloric acids, as well as ethylenediaminetetraacetic acid (EDTA) were used as purging solutions in the first module. Results show that there was a decrease of cadmium concentration near anode, but a significant increase in the middle of the cell, due to the increasing pH. Citric, nitric and acetic acids were used for soil washing and purging solutions in the second module. In this case, an 85% reduction of cadmium concentration was achieved. Therefore, results indicate that soil pH and washing solutions are the most important factors in governing the dissolution and/or desorption of Cd in a soil system under electrical fields

Spectroscopic Determination of Trace Contaminants in High Purity Oxygen

Science.gov (United States)

Hornung, Steven D.

2011-01-01

Oxygen used for extravehicular activities (EVA) must be free of contaminants because a difference in a few tenths of a percent of argon or nitrogen content can mean significant reduction in available EVA time. These inert gases build up in the extravehicular mobility unit because they are not metabolized or scrubbed from the atmosphere. Measurement of oxygen purity above 99.5% is problematic, and currently only complex instruments such as gas chromatographs or mass spectrometers are used for these determinations. Because liquid oxygen boil-off from the space shuttle will no longer be available to supply oxygen for EVA use, other concepts are being developed to produce and validate high purity oxygen from cabin air aboard the International Space Station. A prototype optical emission technique capable of detecting argon and nitrogen below 0.1% in oxygen was developed at White Sands Test Facility. This instrument uses a glow discharge in reduced pressure gas to produce atomic emission from the species present. Because the atomic emission lines from oxygen, nitrogen, and argon are discrete and in many cases well-separated, trace amounts of argon and nitrogen can be detected in the ultraviolet and visible spectrum. This is a straightforward, direct measurement of the target contaminants and may lend itself to a device capable of on-orbit verification of oxygen purity. System design and optimized measurement parameters are presented.

Method and apparatus for removal of gaseous, liquid and particulate contaminants from molten metals

Science.gov (United States)

Hobson, D.O.; Alexeff, I.; Sikka, V.K.

1987-08-10

Method and apparatus for removal of nonelectrically-conducting gaseous, liquid, and particulate contaminants from molten metal compositions by applying a force thereto. The force (commonly referred to as the Lorentz Force) exerted by simultaneous application of an electric field and a magnetic field on a molten conductor causes an increase, in the same direction as the force, in the apparent specific gravity thereof, but does not affect the nonconducting materials. This difference in apparent densities cause the nonconducting materials to ''float'' in the opposite direction from the Lorentz Force at a rapid rate. Means are further provided for removal of the contaminants and prevention of stirring due to rotational forces generated by the applied fields. 6 figs.

Alleviation of environmental risks associated with severely contaminated mine tailings using amendments: Modeling of trace element speciation, solubility, and plant accumulation.

Science.gov (United States)

Pardo, Tania; Bes, Cleménce; Bernal, Maria Pilar; Clemente, Rafael

2016-11-01

Tailings are considered one of the most relevant sources of contamination associated with mining activities. Phytostabilization of mine spoils may need the application of the adequate combination of amendments to facilitate plant establishment and reduce their environmental impact. Two pot experiments were set up to assess the capability of 2 inorganic materials (calcium carbonate and a red mud derivate, ViroBind TM ), alone or in combination with organic amendments, for the stabilization of highly acidic trace element-contaminated mine tailings using Atriplex halimus. The effects of the treatments on tailings and porewater physico-chemical properties and trace-element accumulation by the plants, as well as the processes governing trace elements speciation and solubility in soil solution and their bioavailability were modeled. The application of the amendments increased tailings pH and decreased (>99%) trace elements solubility in porewater, but also changed the speciation of soluble Cd, Cu, and Pb. All the treatments made A. halimus growth in the tailings possible; organic amendments increased plant biomass and nutritional status, and reduced trace-element accumulation in the plants. Tailings amendments modified trace-element speciation in porewater (favoring the formation of chlorides and/or organo-metallic forms) and their solubility and plant uptake, which were found to be mainly governed by tailing/porewater pH, electrical conductivity, and organic carbon content, as well as soluble/available trace-element concentrations. Environ Toxicol Chem 2016;35:2874-2884. © 2016 SETAC. © 2016 SETAC.

Development of HUMASORB trademark, a lignite derived humic acid for removal of metals and organic contaminants from groundwater

International Nuclear Information System (INIS)

Sanjay, H.G.; Srivastave, K.C.; Walia, D.S.

1995-01-01

Heavy metal and organic contamination of surface and groundwater systems is a major environmental concern. The contamination is primarily due to improperly disposed industrial wastes. The presence of toxic heavy metal ions, volatile organic compounds (VOCs) and pesticides in water is of great concern and could affect the safety of drinking water. Decontamination of surface and groundwater can be achieved using a broad spectrum of treatment options such as precipitation, ion-exchange, microbial digestion, membrane separation, activated carbon adsorption, etc. The state of the art technologies for treatment of contaminated water however, can in one pass remediate only one class of contaminants, i.e., either VOCs (activated carbon) or heavy metals (ion exchange). This would require the use of at a minimum, two different stepwise processes to remediate a site. The groundwater contamination at different Department of Energy (DOE) sites (e.g., Hanford) is due to the presence of both VOCs and heavy metals. The two-step approach increases the cost of remediation. To overcome the sequential treatment of contaminated streams to remove both organics and metals, a novel material having properties to remove both classes of contaminants in one step is being developed as part of this project.The objective of this project is to develop a lignite-derived adsorbent, Humasorb TM to remove heavy metals and organics from ground water and surface water streams

Removal of lead and fluoride from contaminated water using exhausted coffee grounds based bio-sorbent.

Science.gov (United States)

Naga Babu, A; Reddy, D Srinivasa; Kumar, G Suresh; Ravindhranath, K; Krishna Mohan, G V

2018-07-15

Water pollution by industrial and anthropogenic actives has become a serious threat to the environment. World Health Organization (WHO) has identified that lead and fluoride amid the environmental pollutants are most poisonous water contaminants with devastating impact on the human race. The present work proposes a study on economical bio-adsorbent based technique using exhausted coffee grounds in the removal of lead and fluoride contaminants from water. The exhausted coffee grounds gathered from industrial wastes have been acid-activated and examined for their adsorption capacity. The surface morphology and elemental characterization of pre-and-post adsorption operations by FESEM, EDX and FTIR spectral analysis confirmed the potential of the exhausted coffee ground as successful bio-sorbent. However, thermodynamic analysis confirmed the adsorption to be spontaneous physisorption with Langmuir mode of homogenous monolayer deposition. The kinetics of adsorption is well defined by pseudo second order model for both lead and fluoride. A significant quantity of lead and fluoride is removed from the synthetic contaminated water by the proposed bio-sorbent with the respective sorption capabilities of 61.6 mg/g and 9.05 mg/g. However, the developed bio-sorbent is also recyclable and is capable of removing the lead and fluoride from the domestic and industrial waste-water sources with an overall removal efficiency of about 90%. Copyright © 2018 Elsevier Ltd. All rights reserved.

SITE demonstration of the Dynaphore/Forager Sponge technology to remove dissolved metals from contaminated groundwater

Energy Technology Data Exchange (ETDEWEB)

Esposito, C.R. [Environmental Protection Agency, Edison, NJ (United States); Vaccaro, G. [Science Applications International Corp., Hackensack, NJ (United States)

1995-10-01

A Superfund Innovative Technology Evaluation (SITE) demonstration was conducted of the Dynaphore/Forager Sponge technology during the week of April 3, 1994 at the N.L. Industries Superfund Site in Pedricktown, New Jersey. The Forager Sponge is an open-celled cellulose sponge incorporating an amine-containing chelating polymer that selectively absorbs dissolved heavy metals in both cationic and anionic states. This technology is a volume reduction technology in which heavy metal contaminants from an aqueous medium are concentrated into a smaller volume for facilitated disposal. The developer states that the technology can be used to remove heavy metals from a wide variety of aqueous media, such as groundwater, surface waters and process waters. The sponge matrix can be directly disposed, or regenerated with chemical solutions. For this demonstration the sponge was set up as a mobile pump-and-treat system which treated groundwater contaminated with heavy metals. The demonstration focused on the system`s ability to remove lead, cadmium, chromium and copper from the contaminated groundwater over a continuous 72-hour test. The removal of heavy metals proceeded in the presence of significantly higher concentrations of innocuous cations such as calcium, magnesium, sodium, potassium and aluminum.

Supported Photocatalyst for Removal of Emerging Contaminants from Wastewater in a Continuous Packed-Bed Photoreactor Configuration

OpenAIRE

Borges, Mª; García, Dulce; Hernández, Tania; Ruiz-Morales, Juan; Esparza, Pedro

2015-01-01

Water pollution from emerging contaminants (ECs) or emerging pollutants is an important environmental problem. Heterogeneous photocatalytic treatment, as advanced oxidation treatment of wastewater effluents, has been proposed to solve this problem. In this paper, a heterogeneous photocatalytic process was studied for emergent contaminants removal using paracetamol as a model contaminant molecule. TiO2 photocatalytic activity was evaluated using two photocatalytic reactor configurations: Photo...

Blast furnace residues for arsenic removal from mining-contaminated groundwater.

Science.gov (United States)

Carrillo-Pedroza, Fco Raúl; Soria-Aguilar, Ma de Jesús; Martínez-Luevanos, Antonia; Narvaez-García, Víctor

2014-01-01

In this work, blast furnace (BF) residues were well characterized and then evaluated as an adsorbent material for arsenic removal from a mining-contaminated groundwater. The adsorption process was analysed using the theories of Freundlich and Langmuir. BF residues were found to be an effective sorbent for As (V) ions. The modelling of adsorption isotherms by empirical models shows that arsenate adsorption is fitted by the Langmuir model, suggesting a monolayer adsorption of arsenic onto adsorbents. Arsenate adsorption onto BF residue is explained by the charge density surface affinity and by the formation of Fe (II) and Fe (III) corrosion products onto BF residue particles. The results indicate that BF residues represent an attractive low-cost absorbent option for the removal of arsenic in wastewater treatment.

Removal of Cu(II) ions from contaminated waters using a conducting microfiltration membrane.

Science.gov (United States)

Wang, Xueye; Wang, Zhiwei; Chen, Haiqin; Wu, Zhichao

2017-10-05

Efficient removal of toxic metals using low-pressure membrane processes from contaminated waters is an important but challenging task. In the present work, a conducting microfiltration membrane prepared by embedding a stainless steel mesh in the active layer of a polyvinylidene fluoride membrane is developed to remove Cu(II) ions from contaminated waters. Results showed that the conducting membrane had favorable electrochemical properties and stability as cathode. Batch tests showed that Cu(II) removal efficiency increased with the increase of voltages and leveled off with the further enhancement of electric field. The optimal voltages were determined to be 1.0V and 2.0V for the influent Cu(II) concentrations of 5mg/L and 30mg/L, respectively. X-ray photoelectron spectroscopy and X-ray diffraction results demonstrated the presence of Cu(0) and Cu(OH) 2 on the membrane surface. The removal mechanisms involved the intrinsic adsorption of membrane, electrosorption of membrane, adsorption of deposited layer, chemical precipitation of Cu(OH) 2 and deposition of Cu(0) which were aided by electrophoresis and electrochemical oxidation-reduction. Long-term tests showed that the major contributors for Cu(II) removal were the deposition of Cu(0) by electrochemical reduction-oxidation (47.3%±8.5%) and chemical precipitation (41.1%±0.2%), followed by electrosorption, adsorption by the fouling layer and membrane intrinsic sorption. Copyright © 2017 Elsevier B.V. All rights reserved.

Fundamental Studies of the Removal of Contaminants from Ground and Waste Waters via Reduction by Zero-Valent Metals

International Nuclear Information System (INIS)

Yarmoff, Jory A.; Amrhein, Christopher

1999-01-01

Contaminated groundwater and surface waters are a problem throughout the United States and the world. In many instances, the types of contamination can be directly attributed to man's actions. For instance, the burial of chemical wastes, casual disposal of solvents in unlined pits, and the development of irrigated agriculture have all contributed to groundwater and surface water contamination. The kinds of contaminants include chlorinated solvents and toxic trace elements (including radioisotopes) that are soluble and mobile in soils and aquifers. Oxyanions of uranium, selenium, chromium, arsenic, technetium, and chlorine (as perchlorate) are frequently found as contaminants on many DOE sites. Uranium is a particularly widespread contaminant at most DOE sites including Oak Ridge, Rocky Flats, Hanford, Idaho (INEEL), and Fernald. The uranium contamination is associated with mining and milling of uranium ore (UMTRA sites), isotope separation and enrichment, and mixed waste and TRU waste burial. In addition, the careless disposal of halogenated solvents, such as carbon tetrachloride and trichloroethylene, has further contaminated many groundwaters at these sites. A potential remediation method for many of these oxyanions and chlorinated-solvents is to react the contaminated water with zero-valent iron. In this reaction, the iron serves as both an electron source and as a catalyst. Elemental iron is already being used on an experimental basis at many DOE sites. Both in situ reactive barriers and above-ground reactors are being developed for this purpose. However, the design and operation of these treatment systems requires a detailed process-level understanding of the interactions between the contaminants and the iron surfaces. We are performing fundamental investigations of the interactions of the relevant chlorinated solvents and trace element-containing compounds with single- and poly-crystalline Fe surfaces. The aim of this work is to develop th e fundamental

Contamination by trace elements at e-waste recycling sites in Bangalore, India.

Science.gov (United States)

Ha, Nguyen Ngoc; Agusa, Tetsuro; Ramu, Karri; Tu, Nguyen Phuc Cam; Murata, Satoko; Bulbule, Keshav A; Parthasaraty, Peethmbaram; Takahashi, Shin; Subramanian, Annamalai; Tanabe, Shinsuke

2009-06-01

The recycling and disposal of electronic waste (e-waste) in developing countries is causing an increasing concern due to its effects on the environment and associated human health risks. To understand the contamination status, we measured trace elements (TEs) in soil, air dust, and human hair collected from e-waste recycling sites (a recycling facility and backyard recycling units) and the reference sites in Bangalore and Chennai in India. Concentrations of Cu, Zn, Ag, Cd, In, Sn, Sb, Hg, Pb, and Bi were higher in soil from e-waste recycling sites compared to reference sites. For Cu, Sb, Hg, and Pb in some soils from e-waste sites, the levels exceeded screening values proposed by US Environmental Protection Agency (EPA). Concentrations of Cr, Mn, Co, Cu, In, Sn, Sb, Tl, Pb and Bi in air from the e-waste recycling facility were relatively higher than the levels in Chennai city. High levels of Cu, Mo, Ag, Cd, In, Sb, Tl, and Pb were observed in hair of male workers from e-waste recycling sites. Our results suggest that e-waste recycling and its disposal may lead to the environmental and human contamination by some TEs. To our knowledge, this is the first study on TE contamination at e-waste recycling sites in Bangalore, India.

Alternatives Generation Analysis Long Length Contaminated Equipment Removal System Storage

International Nuclear Information System (INIS)

BOGER, R.M.

1999-01-01

Major pieces of Characterization sampling equipment are currently stored outdoors. This includes the Long Length Contaminated Equipment receiver trailer and transportation trailer. A decision is required to determine the preferred alternative for facilities to store and maintain this equipment. The Long Length Contaminated Equipment Removal System (LLCERS) consists of many tools, mechanisms, and controllers currently stored in various locations. Much of this equipment should be protected from the elements while being stored. Some of the LLCERS equipment should be protected with some kind of roof cover. This decision analysis is to determine the best alternative for weather protection for the large equipment requiring a cover. Additional details are included in Sections 2.0 and 5.0. Key assumptions used in this analysis are detailed in Section 3.2

Contamination and Health Risks from Heavy Metals (Cd and Pb and Trace Elements (Cu and Zn in Dairy Products

Directory of Open Access Journals (Sweden)

Hamid Reza Ghafari

2017-08-01

Conclusion: Considering the serious contamination of some brands of butter and cheese by Cu and Pb, a control of heavy metals and trace elements levels during the whole production processing of dairy products must be applied.

Removing gaseous contaminants in 3He by cryogenic stripping

International Nuclear Information System (INIS)

Benapfl, M.; Biltoft, P.; Coombs, A.

1995-01-01

The Tritium Operations Group at LLNL, Tritium Facility has recently developed a 3 He recovery system to remove argon, xenon, neon, hydrogen, and all other contaminants from the 3 He stream in an Accelerator Production of Tritium (APT) experimental apparatus. In this paper the authors will describe in detail the background information, technical requirements, the design approach, and the results of their experimental tests. The authors believe this gas purification system may have other applications as it provides at a reasonable cost an efficient method for purification of gaseous helium

Removal of emerging contaminants from the environment by adsorption.

Science.gov (United States)

Sophia A, Carmalin; Lima, Eder C

2018-04-15

Emerging contaminants (EC's) are pollutants of growing concern. They are mainly organic compounds such as: pesticides, pharmaceuticals and personal care products, hormones, plasticizers, food additives, wood preservatives, laundry detergents, surfactants, disinfectants, flame retardants, and other organic compounds that were found recently in natural wastewater stream generated by human and industrial activities. A majority of ECs does not have standard regulations and could lead to lethal effects on human and aquatic life even at small concentrations. The conventional primary and secondary water treatment plants do not remove or degrade these toxic pollutants efficiently and hence need cost effective tertiary treatment method. Adsorption is a promising method worldwide for EC removal since it is low initial cost for implementation, highly-efficient and has simple operating design. Research has shown that the application of different adsorbents such as, activated carbons(ACs), modified biochars (BCs), nanoadsorbents (carbon nanotubes and graphene), composite adsorbents, and other are being used for EC's removal from water and wastewater. The current review intends to investigate adsorption process as an efficient method for the treatment of ECs. The mechanism of adsorption has also been discussed. Copyright © 2017 Elsevier Inc. All rights reserved.

The potential of compost-based biobarriers for Cr(VI) removal from contaminated groundwater: Column test

International Nuclear Information System (INIS)

Boni, Maria Rosaria; Sbaffoni, Silvia

2009-01-01

This paper presents the results of a column reactor test, aiming at evaluating the performance of a biological permeable barrier made of low-cost waste materials, for Cr(VI) removal from contaminated groundwater. A 1:1 by volume mixture of green compost and siliceous gravel was tested as reactive medium in the experimental activity. A 10 mg/l Cr(VI) contaminated solution was used and the residual Cr(VI) concentration along the column height and in the outlet was determined in the water samples collected daily. Also pH, redox potential and COD were analyzed. At the end of the test, the reactive medium was characterized in terms of Cr(VI) and total chromium. The Cr(VI) removal efficiency was higher than 99% during the entire experimental activity. The influence of the biological activity on Cr(VI) removal efficiency was evaluated by varying the organic carbon and nitrogen dosages in the contaminated solution fed to the system; a removal decrease was observed when the organic carbon was not enough to sustain the microbial metabolism. The Cr(VI) removal was strictly linked to the biological activity of the native biomass of compost. No Cr(III) was detected in the outlet: the Cr(III) produced was entrapped in the solid matrix. Two main processes involved were: adsorption on the organic-based matrix and reduction into Cr(III) mediated by the anaerobic microbial metabolism of the bacteria residing in green compost. Siliceous gravel was used as the structure matrix, since its contribution to the removal was almost negligible. Thanks to the proven efficiency and to the low-cost, the reactive medium used can represent a valid alternative to conventional approaches to chromium remediation.

Effect of some operational parameters on the arsenic removal by electrocoagulation using iron electrodes

OpenAIRE

Can, Berrin Zeliha; Boncukcuoglu, Recep; Yilmaz, Alper Erdem; Fil, Baybars Ali

2014-01-01

Arsenic contamination of drinking water is a global problem that will likely become more apparent in future years as scientists and engineers measure the true extent of the problem. Arsenic poisoning is preventable though as there are several methods for easily removing even trace amounts of arsenic from drinking water. In the present study, electrocoagulation was evaluated as a treatment technology for arsenic removal from aqueous solutions. The effects of parameters such as initial pH, curr...

An improved SOIL*EX trademark process for the removal of hazardous and radioactive contaminants from soils, sludges and other materials

International Nuclear Information System (INIS)

Bloom, R.R.; Bonnema, B.E.; Navratil, J.D.; Falconer, K.L.; Van Vliet, J.A.; Diel, B.N.

1995-01-01

Rust's patented SOIL*EX process is designed to remove hazardous and radioactive contaminants from soils, sludges and a matrix of other materials while destroying volatile organic compounds often associated with contaminated soil and debris. The process is comprised of three major process operations. The first operation involves the dissolution of contaminants that are chemically or mechanically bonded to the solid phase. The second process operation involves separation of the solid phase from the dissolution solution (mother liquor), which contains the dissolved contaminants. The final operation concentrates and removes the contaminants from the mother liquor. A pilot-scale SOIL*EX system was constructed at Rust's Clemson Technical Center for a Proof-of-Process demonstration. The demonstration program included the design, fabrication, and operation of pilot scale and demonstration equipment and systems. The pilot plant, an accurate scaled-down version of a proposed full-scale treatment system, was operated for five months to demonstrate the efficiency of the overall process. The pilot plant test program focused on demonstrating that the SOIL*EX process would remove and concentrate the contaminants and destroy volatile organic compounds. The pilot plant processed nearly 20 tons of soils and sludges, and test results indicated that all contaminants of concern were removed. Additionally, Rust completed numerous bench scale tests to optimize the chemistry. This paper discusses the pilot plant test criteria and results along with the salient design features of the SOIL*EX system and planned improvements

Engineering hyporheic zones for the attenuation of urban pesticides and other stormwater trace organic contaminants

Science.gov (United States)

Portmann, A. C.; Halpin, B. N.; Herzog, S.; Higgins, C.; McCray, J. E.

2017-12-01

The hyporheic zone (HZ) is a natural bioreactor that can provide in-stream attenuation of various nonpoint source contaminants. Main contributions of nonpoint source pollution are coming from urban stormwater and agricultural runoff, which both adversely impact aquatic life. Stormwater pollutants of concern commonly include nutrients, metals, pathogens, and trace organic contaminants (TOrCs). Despite substantial water quality challenges, current stormwater management typically focuses on water quantity issues rather than pollutant removal. Furthermore, current HZ restoration best management practices do not explicitly control HZ residence times, and generally only induce localized effects. To increase hyporheic exchange and therefore improving water quality, we introduced engineered streambeds featuring modifications to subsurface hydraulic conductivity (K) and reactivity - termed Biohydrochemical Enhancements for Streamwater Treatment (BEST). BEST modifications comprise subsurface modules that employ 1) low-permeability sediments to drive hyporheic exchange and control subsurface residence times, and 2) permeable reactive geomedia to change reaction rates within the HZ. Here we present performance data collected in constructed stream experiments, comparing an all-sand control condition with a stream containing BEST modules and a mixture of 70/30 sand/woodchips (v/v). We evaluated the attenuation of a suite of TOrCs in the BEST versus the control system for two different streambed media: a coarse sand with K = 0.48 cm/s and a fine sand with K = 0.16 cm/s. The range of TOrCs investigated comprises urban pesticides and other stormwater relevant TOrCs. Benefits of applying BEST include increased exchange between streamwater and HZ water, leading to diverse redox conditions that are beneficial for aquatic organisms and will facilitate in-stream pollutant transformation. Future work will focus on tailoring the BEST design for specific pollutants, thereby controlling HZ

Removing high-level contaminants

International Nuclear Information System (INIS)

Wallace, Paula

2013-01-01

Full text: Using biomimicry, an Australian cleantech innovation making inroads intoChinas's industrial sector offers multiple benefits to miners and processors in Australia. Stephen Shelley, the executive chairman of Creative Water Technology (CWT), was on hand at a recent trade show to explain how his Melbourne company has developed world-class techniques in zero liquid discharge and fractional crystallization of minerals to apply to a wide range of water treatment and recycling applications. “Most existing technologies operate with high energy distillation, filters or biological processing. CWT's appliance uses a low temperature, thermal distillation process known as adiabatic recovery to desalinate, dewater and/or recycle highly saline and highly contaminated waste water,” said Shelley. The technology has been specifically designed to handle the high levels of contaminant that alternative technologies struggle to process, with proven water quality results for feed water samples with TDS levels over 300,000ppm converted to clean water with less than 20ppm. Comparatively, reverse osmosis struggles to process contaminant levels over 70,000ppm effectively. “CWT is able to reclaim up to 97% clean usable water and up to 100% of the contaminants contained in the feed water,” said Shelley, adding that soluble and insoluble contaminants are separately extracted and dried for sale or re-use. In industrial applications CWT has successfully processed feed water with contaminant levels over 650,000 mg/1- without the use of chemicals. “The technology would be suitable for companies in oil exploration and production, mining, smelting, biofuels, textiles and the agricultural and food production sectors,” said Shelley. When compared to a conventional desalination plant, the CWT system is able to capture the value in the brine that most plants discard, not only from the salt but the additional water it contains. “If you recover those two commodities... then you

CONTAMINATED PROCESS EQUIPMENT REMOVAL FOR THE DECOMMISSIONG AND DECONTAMINATION OF THE 232-Z CONTAMINATED WASTE RECOVERY PROCESS FACILITY AT THE PLUTONIUM FINISHING PLANT

International Nuclear Information System (INIS)

HOPKINS, A.M.; MINETTE, M.J.; KLOS, D.B.

2007-01-01

This paper describes the unique challenges encountered and subsequent resolutions to accomplish the deactivation and decontamination of a plutonium ash contaminated building. The 232-Z Contaminated Waste Recovery Process Facility at the Plutonium Finishing Plant was used to recover plutonium from process wastes such as rags, gloves, containers and other items by incinerating the items and dissolving the resulting ash. The incineration process resulted in a light-weight plutonium ash residue that was highly mobile in air. This light-weight ash coated the incinerator's process equipment, which included gloveboxes, blowers, filters, furnaces, ducts, and filter boxes. Significant airborne contamination (over 1 million derived air concentration hours [DAC]) was found in the scrubber cell of the facility. Over 1300 grams of plutonium held up in the process equipment and attached to the walls had to be removed, packaged and disposed. This ash had to be removed before demolition of the building could take place

Removal of Cyclohexane from a Contaminated Air Stream Using a Dense Phase Membrane Bioreactor

National Research Council Canada - National Science Library

Roberts, Michael G

2005-01-01

The purpose of this research was to determine the ability of a dense phase membrane bioreactor to remove cyclohexane, a volatile organic compound in JP-8 jet fuel, from a contaminated air stream using...

Identification and Removal of Contaminant Sequences From Ribosomal Gene Databases: Lessons From the Census of Deep Life.

Science.gov (United States)

Sheik, Cody S; Reese, Brandi Kiel; Twing, Katrina I; Sylvan, Jason B; Grim, Sharon L; Schrenk, Matthew O; Sogin, Mitchell L; Colwell, Frederick S

2018-01-01

Earth's subsurface environment is one of the largest, yet least studied, biomes on Earth, and many questions remain regarding what microorganisms are indigenous to the subsurface. Through the activity of the Census of Deep Life (CoDL) and the Deep Carbon Observatory, an open access 16S ribosomal RNA gene sequence database from diverse subsurface environments has been compiled. However, due to low quantities of biomass in the deep subsurface, the potential for incorporation of contaminants from reagents used during sample collection, processing, and/or sequencing is high. Thus, to understand the ecology of subsurface microorganisms (i.e., the distribution, richness, or survival), it is necessary to minimize, identify, and remove contaminant sequences that will skew the relative abundances of all taxa in the sample. In this meta-analysis, we identify putative contaminants associated with the CoDL dataset, recommend best practices for removing contaminants from samples, and propose a series of best practices for subsurface microbiology sampling. The most abundant putative contaminant genera observed, independent of evenness across samples, were Propionibacterium , Aquabacterium , Ralstonia , and Acinetobacter . While the top five most frequently observed genera were Pseudomonas , Propionibacterium , Acinetobacter , Ralstonia , and Sphingomonas . The majority of the most frequently observed genera (high evenness) were associated with reagent or potential human contamination. Additionally, in DNA extraction blanks, we observed potential archaeal contaminants, including methanogens, which have not been discussed in previous contamination studies. Such contaminants would directly affect the interpretation of subsurface molecular studies, as methanogenesis is an important subsurface biogeochemical process. Utilizing previously identified contaminant genera, we found that ∼27% of the total dataset were identified as contaminant sequences that likely originate from DNA

Evaluation of trace organic contaminants in ultra-pure water production processes by measuring total organic halogen formation potential

International Nuclear Information System (INIS)

Urano, Kohei; Iwase, Yoko

1984-01-01

A new procedure for the determination of organic substances in water with high accuracy and high sensitivity was proposed, in which a hypochlorite is added to water, and the resultant total amount of organic halogen compounds (TOX formation potential) was measured, and it was applied to the evaluation of trace organic contaminants in ultra-pure water production process. In this investigation, the TOX formation potential of the raw water which was to be used for the ultra-pure water production process, intermediately treated water and ultra-pure water was measured to clarify the behavior of organic substances in the ultra-pure water production process and to demonstrate the usefulness of this procedure to evaluate trace organic contaminants in water. The measurement of TOX formation potential requires no specific technical skill, and only a short time, and gives accurate results, therefore, it is expected that the water quality control in the ultra-pure water production process can be performed more exactly by applying this procedure. (Yoshitake, I.)

Prioritizing research for trace pollutants and emerging contaminants in the freshwater environment

Energy Technology Data Exchange (ETDEWEB)

Murray, Kyle E., E-mail: Kyle.Murray@utsa.ed [Center for Water Research, University of Texas at San Antonio, One UTSA Circle, San Antonio, TX 78249-0663 (United States); Thomas, Sheeba M [San Antonio River Authority, San Antonio, TX (United States); Bodour, Adria A [Air Force Center for Engineering and the Environment (AFCEE), Brooks City-Base, TX (United States)

2010-12-15

Organic chemicals have been detected at trace concentrations in the freshwater environment for decades. Though the term trace pollutant indicates low concentrations normally in the nanogram or microgram per liter range, many of these pollutants can exceed an acceptable daily intake (ADI) for humans. Trace pollutants referred to as emerging contaminants (ECs) have recently been detected in the freshwater environment and may have adverse human health effects. Analytical techniques continue to improve; therefore, the number and frequency of detections of ECs are increasing. It is difficult for regulators to restrict use of pollutants that are a human health hazard; scientists to improve treatment techniques for higher priority pollutants; and the public to modify consumption patterns due to the vast number of ECs and the breadth of literature on the occurrence, use, and toxicity. Hence, this paper examines literature containing occurrence and toxicity data for three broad classes of trace pollutants and ECs (industrials, pesticides, and pharmaceuticals and personal care products (PPCPs)), and assesses the relevance of 71 individual compounds. The evaluation indicates that widely used industrials (BPF) and PPCPs (AHTN, HHCB, ibuprofen, and estriol) occur frequently in samples from the freshwater environment but toxicity data were not available; thus, it is important to establish their ADI. Other widely used industrials (BDE-47, BDE-99) and pesticides (benomyl, carbendazim, aldrin, endrin, ethion, malathion, biphenthrin, and cypermethrin) have established ADI values but occurrence in the freshwater environment was not well documented. The highest priority pollutants for regulation and treatment should include industrials (PFOA, PFOS and DEHP), pesticides (diazinon, methoxychlor, and dieldrin), and PPCPs (EE2, carbamazepine, {beta}E2, DEET, triclosan, acetaminophen, and E1) because they occur frequently in the freshwater environment and pose a human health hazard at

Prioritizing research for trace pollutants and emerging contaminants in the freshwater environment

International Nuclear Information System (INIS)

Murray, Kyle E.; Thomas, Sheeba M.; Bodour, Adria A.

2010-01-01

Organic chemicals have been detected at trace concentrations in the freshwater environment for decades. Though the term trace pollutant indicates low concentrations normally in the nanogram or microgram per liter range, many of these pollutants can exceed an acceptable daily intake (ADI) for humans. Trace pollutants referred to as emerging contaminants (ECs) have recently been detected in the freshwater environment and may have adverse human health effects. Analytical techniques continue to improve; therefore, the number and frequency of detections of ECs are increasing. It is difficult for regulators to restrict use of pollutants that are a human health hazard; scientists to improve treatment techniques for higher priority pollutants; and the public to modify consumption patterns due to the vast number of ECs and the breadth of literature on the occurrence, use, and toxicity. Hence, this paper examines literature containing occurrence and toxicity data for three broad classes of trace pollutants and ECs (industrials, pesticides, and pharmaceuticals and personal care products (PPCPs)), and assesses the relevance of 71 individual compounds. The evaluation indicates that widely used industrials (BPF) and PPCPs (AHTN, HHCB, ibuprofen, and estriol) occur frequently in samples from the freshwater environment but toxicity data were not available; thus, it is important to establish their ADI. Other widely used industrials (BDE-47, BDE-99) and pesticides (benomyl, carbendazim, aldrin, endrin, ethion, malathion, biphenthrin, and cypermethrin) have established ADI values but occurrence in the freshwater environment was not well documented. The highest priority pollutants for regulation and treatment should include industrials (PFOA, PFOS and DEHP), pesticides (diazinon, methoxychlor, and dieldrin), and PPCPs (EE2, carbamazepine, βE2, DEET, triclosan, acetaminophen, and E1) because they occur frequently in the freshwater environment and pose a human health hazard at

Selective Removal of Uranium from the Washing Solution of Uranium-Contaminated Soil

Energy Technology Data Exchange (ETDEWEB)

Kim, Seung Soo; Han, G. S.; Kim, G. N.; Koo, D. S.; Jeong, J. W.; Choi, J. W. [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of)

2015-10-15

This study examined selective removal methods of uranium from the waste solution by ion exchange resins or solvent extraction methods to reduce amount of the 2{sup nd} waste. Alamine-336, known as an excellent extraction reagent of uranium from the leaching solution of uranium ore, did not remove uranium from the acidic washing solution of soil. Uranyl ions in the acidic waste solution were sorbed on ampholyte resin with a high sorption efficiency, and desorbed from the resin by a washing with 0.5 M Na{sub 2}CO{sub 3} solution at 60 .deg. C. However, the uranium dissolved in the sulfuric acid solution was not sorbed onto the strong anion exchanger resins. A great amount of uranium-contaminated (U-contaminated) soil had been generated from the decommissioning of a uranium conversion plant. Our group has developed a decontamination process with washing and electrokinetic methods to decrease the amount of waste to be disposed of. However, this process generates a large amount of waste solution containing various metal ions.

Improved removal of sticky and light contaminants from wastepaper. Final report, April 1, 1995--December 31, 1997

Energy Technology Data Exchange (ETDEWEB)

Seifert, P.; Kelly, A.

1998-03-01

Work under this two-year cooperative agreement addresses improved removal of light and sticky contaminants from waste paper. Such contaminants occur in ever-increasing amounts, resulting from glues, labels, book bindings, packaging tapes, etc., all associated with the waste paper stream. Despite various cleaning steps in the paper mill recycling systems, residual contamination remains, causing big problems with the product quality and with paper machine and converting operations. Some grades cannot be recycled at all. Stickies are truly a barrier against increased paper recycling. The stickies problem was attacked in four project segments--three of those have yielded tangible results. One segment has been outstanding in its success; namely, the development of a centrifugal reverse cleaning system consisting of primary and secondary stages, which have unparalleled high efficiency in the removal of light and sticky contaminants. This cleaning system, consists of primary XTREME and secondary XX-Clone units. Another segment of this work, washing wax contaminated old corrugated wastepaper (OCC), also has resulted in the new Xtrax process which was released for sale.

Application of Metal Oxide Heterostructures in Arsenic Removal from Contaminated Water

Directory of Open Access Journals (Sweden)

Lei Chen

2014-01-01

Full Text Available It has become one of the major environmental problems for people worldwide to be exposed to high arsenic concentrations through contaminated drinking water, and even the long-term intake of small doses of arsenic has a carcinogenic effect. As an efficient and economic approach for the purification of arsenic-containing water, the adsorbents in adsorption processes have been widely studied. Among a variety of adsorbents reported, the metal oxide heterostructures with high surface area and specific affinity for arsenic adsorption from aqueous systems have demonstrated a promising performance in practical applications. This review paper aims to summarize briefly the metal oxide heterostructures in arsenic removal from contaminated water, so as to provide efficient, economic, and robust solutions for water purification.

Microbial contamination of removable dental prosthesis at different interval of usage: An in vitro study

Directory of Open Access Journals (Sweden)

Vijita Vijay Nair

2016-01-01

Conclusion: There is a linear increase in microbial contamination of removable dental prosthesis as the duration of usage increases and might increase the susceptibility of individuals' to many diseases.

Evaluation of the seasonal performance of a water reclamation pond-constructed wetland system for removing emerging contaminants.

Science.gov (United States)

Matamoros, Víctor; Salvadó, Victòria

2012-01-01

The capacity of a full-scale reclamation pond-constructed wetland (CW) system to eliminate 27 emerging contaminants (i.e. pharmaceuticals, sunscreen compounds, fragrances, antiseptics, fire retardants, pesticides, and plasticizers) and the seasonal occurrence of these contaminants is studied. The compounds with the highest concentrations in the secondary effluent are diclofenac, caffeine, ketoprofen, and carbamazepine. The results show that the constructed wetland (61%) removes emerging contaminants significantly more efficiently than the pond (51%), presumably due to the presence of plants (Phragmites and Thypa) as well as the higher hydraulic residence time (HRT) in the CW. A greater seasonal trend to the efficient removal of these compounds is observed in the pond than in the CW. The overall mass removal efficiency of each individual compound ranged from 27% to 93% (71% on average), which is comparable to reported data in advanced treatments (photo-fenton and membrane filtration). The seasonal average content of emerging contaminants in the river water (2488 ng L(-1)) next to the water reclamation plant is found to be higher than the content in the final reclaimed water (1490 ng L(-1)), suggesting that the chemical quality of the reclaimed water is better than available surface waters. Copyright © 2011 Elsevier Ltd. All rights reserved.

The Use of Modified Bentonite for Removal of Aromatic Organics from Contaminated Soil.

Science.gov (United States)

Gitipour; Bowers; Bodocsi

1997-12-15

This study investigates the clay-aromatic interactions with a view to the use of bentonite clay for binding benzene, toluene, ethylbenzene, and o-xylene (BTEX compounds) in contaminated soils. BTEX compounds are the most toxic aromatic constituents of gasoline present in many underground storage tanks. Modified (organophilic) and ordinary bentonites are used to remove these organics. The organophilic bentonites are prepared by replacing the exchangeable inorganic cations present in bentonite particles with a quaternary ammonium salt. Various clay-to-soil ratios were applied to determine the efficiency of the modified bentonite in enhancing the cement-based solidification/stabilization (S/S) of BTEX contaminated soils. Toxicity characteristics leaching procedure (TCLP) tests were performed on soil samples to evaluate the leaching of the organics. In addition, X-ray diffraction analyses were conducted to assess the changes in the basal spacing of the clays as a result of their interaction with BTEX compounds. The findings of this study reveal that organophilic bentonite can act as a successful adsorbent for removing the aromatic organics from contaminated soil. Thus, this material is viable for enhancing the performance of cement-based S/S processes, as an adsorbent for petroleum spills, and for landfill liners and slurry walls. Copyright 1997 Academic Press.

The use of modified bentonite for removal of aromatic organics from contaminated soil

International Nuclear Information System (INIS)

Gitipour, S.; Bowers, M.T.; Bodocsi, A.

1997-01-01

This study investigates the clay-aromatic interactions with a view to the use of bentonite clay for binding benzene, toluene, ethylbenzene, and o-xylene (BTEX compounds) in contaminated soils. BTEX compounds are the most toxic aromatic constituents of gasoline present in many underground storage tanks. Modified (organophilic) and ordinary bentonites are used to remove these organics. The organophilic bentonites are prepared by replacing the exchangeable inorganic cations present in bentonite particles with a quaternary ammonium salt. Various clay-to-soil ratios were applied to determine the efficiency of the modified bentonite in enhancing the cement-based solidification/stabilization (S/S) of BTEX contaminated soils. Toxicity characteristics leaching procedure (TCLP) tests were performed on soil samples to evaluate the leaching of the organics. In addition, X-ray diffraction analyses were conducted to assess the changes in the basal spacing of the clays as a result of their interaction with BTEX compounds. The findings of this study reveal that organophilic bentonite can act as a successful adsorbent for removing the aromatic organics from contaminated soil. Thus, this material is viable for enhancing the performance of cement-based S/S processes, as an adsorbent for petroleum spills, and for landfill liners and slurry walls

Removal of Radium-226 from Radium-Contaminated Soil using Distilled Water and Humic Acid: Effect of pH

International Nuclear Information System (INIS)

Phillips, E.; Muhammad Samudi Yasir; Muhamat Omar

2011-01-01

Effect of washing solutions' pH removal of radium-226 from radium-contaminated soil using distilled water and humic acid extracted from Malaysian peat soil was studied by batch washing method. The study encompassed the extraction of humic acid and the washing of radium-contaminated soil using distilled water and humic acid solutions of 100 ppm, both with varying pHs in the range of 3 to 11. The radioactivity concentration of radium-226 was determined by gamma spectrometer.The removal of radium-226 was greater when humic acid solutions were used compared to distilled water at the pH range studied and both washing solutions showed greater removal of radium-226 when basic solutions were used. Nevertheless, comparable removal efficiencies were observed when neutral and highly basic humic acid solutions were used. (author)

Method for selectively removing fluorine and fluorine-containing contaminants from gaseous UF/sub 6/. [ClF/sub 3/

Science.gov (United States)

Jones, R.L.; Otey, M.G.; Perkins, R.W.

1980-11-24

This invention is a method for effecting preferential removal and immobilization of certain gaseous contaminants from gaseous UF/sub 6/. The contaminants include fluorine and fluorides which are more reactive with CaCO/sub 3/ than is UF/sub 6/. The method comprises contacting the contaminant-carrying UF/sub 6/ with particulate CaCO/sub 3/ at a temperature effecting reaction of the contaminant and the CaCO/sub 3/.

Development of HUMASORB trademark, a lignite derived humic acid for removal of metals and organic contaminants from groundwater

International Nuclear Information System (INIS)

Sanjay, H.G.; Srivastava, K.C.; Walia, D.S.

1995-01-01

Heavy metal and organic contamination of surface and groundwater systems is a major environmental concern. The contamination is primarily due to improperly disposed industrial wastes. The presence of toxic heavy metal ions, volatile organic compounds (VOCs) and pesticides in water is of great concern and could affect the safety of drinking water. Decontamination of surface and groundwater can be achieved using a broad spectrum of treatment options such as precipitation, ion-exchange, microbial digestion, membrane separation, activated carbon adsorption, etc. The state of the art technologies for treatment of contaminated water however, can in one pass remediate only one class of contaminants, i.e., either VOCs (activated carbon) or heavy metals (ion exchange). This would require the use of at a minimum, two different stepwise processes to remediate a site. The groundwater contamination at different Department of Energy (DOE) sites (e.g., Hanford) is due to the presence of both VOCs and heavy metals. The two-step approach increases the cost of remediation. To overcome the sequential treatment of contaminated streams to remove both organics and metals, a novel material having properties to remove both classes of contaminants in one step is being developed as part of this project

Effects of cleaning methods upon preservation of stable isotopes and trace elements in shells of Cyprideis torosa (Crustacea, Ostracoda): Implications for palaeoenvironmental reconstruction

Science.gov (United States)

Roberts, L. R.; Holmes, J. A.; Leng, M. J.; Sloane, H. J.; Horne, D. J.

2018-06-01

The trace element (Sr/Ca and Mg/Ca) and stable isotope (δ18O and δ13C) geochemistry of fossil ostracod valves provide valuable information, particularly in lacustrine settings, on palaeo-water composition and palaeotemperature. The removal of sedimentary and organic contamination prior to geochemical analysis is essential to avoid bias of the results. Previous stable isotope and trace element work on ostracod shells has, however, employed different treatments for the removal of contamination beyond simple 'manual' cleaning using a paint brush and methanol under a low-power binocular microscope. For isotopic work pre-treatments include chemical oxidation, vacuum roasting and plasma ashing, and for trace element work sonication, chemical oxidation and reductive cleaning. The impact of different treatments on the geochemical composition of the valve calcite has not been evaluated in full, and a universal protocol has not been established. Here, a systematic investigation of the cleaning methods is undertaken using specimens of the ubiquitous euryhaline species, Cyprideis torosa. Cleaning methods are evaluated by undertaking paired analyses on a single carapace (comprising two valves); in modern ostracods, whose valves are assumed to be unaltered, the two valves should have identical geochemical and isotopic composition. Hence, when one valve is subjected to the chosen treatment and the other to simple manual cleaning any difference in composition can confidently be assigned to the treatment method. We show that certain cleaning methods have the potential to cause alteration to the geochemical signal, particularly Mg/Ca and δ18O, and hence have implications for palaeoenvironmental reconstructions. For trace-element determinations we recommend cleaning by sonication and for stable isotope analysis, oxidation by hydrogen peroxide. These methods remove contamination, yet do not significantly alter the geochemical signal.

Simultaneous removal of selected oxidized contaminants in groundwater using a continuously stirred hydrogen-based membrane biofilm reactor.

Science.gov (United States)

Xia, Siqing; Liang, Jun; Xu, Xiaoyin; Shen, Shuang

2013-01-01

A laboratory trial was conducted for evaluating the capability of a continuously stirred hydrogen-based membrane biofilm reactor to simultaneously reduce nitrate (NO(3-)-N), sulfate (SO4(2-)), bromate (BrO3-), hexavalent chromium (Cr(VI)) and parachloronitrobenzene (p-CNB). The reactor contained two bundles of hollow fiber membranes functioning as an autotrophic biofilm carrier and hydrogen pipe as well. On the condition that hydrogen was supplied as electron donor and diffused into water through membrane pores, autohydrogenotrophic bacteria were capable of reducing contaminants to forms with lower toxicity. Reduction occurred within 1 day and removal fluxes for NO(3-)-N, SO4(2-), BrO3-, Cr(VI), and p-CNB reached 0.641, 2.396, 0.008, 0.016 and 0.031 g/(day x m2), respectively after 112 days of continuous operation. Except for the fact that sulfate was 37% removed under high surface loading, the other four contaminants were reduced by over 95%. The removal flux comparison between phases varying in surface loading and H2 pressure showed that decreasing surface loading or increasing H2 pressure would promote removal flux. Competition for electrons occurred among the five contaminants. Electron-equivalent flux analysis showed that the amount of utilized hydrogen was mainly controlled by NO(3-)-N and SO4(2-) reduction, which accounted for over 99% of the electron flux altogether. It also indicated the electron acceptor order, showing that nitrate was the most prior electron acceptor while suIfate was the second of the five contaminants.

Formerly utilized MED/AEC sites remedial action program. Removal of a contaminated industrial waste line, Los Alamos, New Mexico. Final report

International Nuclear Information System (INIS)

Gunderson, T.C.; Ahlquist, A.J.

1979-04-01

In 1977 parts of an abandoned industrial waste line (IWL) that carried laboratory or process chemical and radiochemical wastes were removed from Los Alamos Scientific Laboratory property and from the townsite of Los Alamos in north-central New Mexico. Most of the IWL was removed between 1964 and 1967. Some IWL segments in the townsite, which at that time were buried under newly paved roads, were left for removal during future construction projects involving these roads to minimize traffic problems and road damage, and because they posed no public health hazard. In 1977, prior to impending major road construction in several areas, 400 m (1300 ft) of IWL and two IWL manhole structures were removed from Laboratory and Los Alamos County property. Associated soil contamination was removed to levels considered to be as low as practicable. Contaminated or potentially contaminated material was removed to an approved radioactive waste disposal site on Department of Energy property. Full details of the methods, findings, and as-left conditions are documented in this report

Is halogen content the most important factor in the removal of halogenated trace organics by MBR treatment?

Science.gov (United States)

Hai, Faisal I; Tadkaew, Nichanan; McDonald, James A; Khan, Stuart J; Nghiem, Long D

2011-05-01

This study investigated the relationship between physicochemical properties (namely halogen content and hydrophobicity) of halogenated trace organics and their removal efficiencies by a laboratory scale membrane bioreactor (MBR) under stable operating conditions. The reported results demonstrated a combined effect of halogen content and hydrophobicity on the removal. Compounds with high halogen content (>0.3) were well removed (>85%) when they possessed high hydrophobicity (Log D>3.2), while those with lower Log D values were also well removed if they had low halogen content (BIOWIN index (which is based on only biodegradation) or a more specific index such as the halogen content (which captures a chemical aspect) appeared insufficient to predict the removal efficiency of halogenated compounds in MBR. Experimental data confirmed that the ratio of halogen content and Log D, which incorporates two important physico-chemical properties, is comparatively more suitable. Copyright © 2011 Elsevier Ltd. All rights reserved.

REMOVAL OF ORGANIC DYES FROM CONTAMINATED WATER USING COFE2O4 /REDUCED GRAPHENE OXIDE NANOCOMPOSITE

Directory of Open Access Journals (Sweden)

F. Sakhaei

2016-12-01

Full Text Available Up to now, lots of materials such as active carbon, iron, manganese, zirconium, and metal oxides have been widely used for removal of dyes from contaminated water. Among these, ferrite nanoparticle is an interesting magnetic material due to its moderate saturation magnetization, excellent chemical stability and mechanical hardness. Graphene, a new class of 2D carbonaceous material with atom thick layer features, has attracted much attention recently due to its high specific surface area. Reduced graphene oxide (rGO has also been of great interest because of its unique properties, which are similar to those of graphene, such as specific surface area, making it an ideal candidate for dye removal. Thus far, few works have been carried out on the preparation of CoFe2O4-rGO composite and its applications in removal of contaminants from water. In this paper, CoFe2O4 reduced graphene oxide nanocomposite was fabricated using hydrothermal process. During the hydrothermal process, the reduction of graphene oxide and growth of CoFe2O4 simultaneously occurred on the carbon basal planes under the conditions generated in the hydrothermal system. The samples were characterized by X-ray diffraction (XRD, scanning electron microscopy (SEM, and Fourier transform infrared spectroscopy contaminant and UV-Vis spectroscopy as the analytical method. The experimental results suggest that this material has great potential for treating Congo red contaminated water.

A combined process coupling phytoremediation and in situ flushing for removal of arsenic in contaminated soil.

Science.gov (United States)

Yan, Xiulan; Liu, Qiuxin; Wang, Jianyi; Liao, Xiaoyong

2017-07-01

Phytoremediation and soil washing are both potentially useful for remediating arsenic (As)-contaminated soils. We evaluated the effectiveness of a combined process coupling phytoremediation and in situ soil flushing for removal of As in contaminated soil through a pilot study. The results showed that growing Pteris vittata L. (P.v.) accompanied by soil flushing of phosphate (P.v./Flushing treatment) could significantly decrease the total As concentration of soil over a 37day flushing period compared with the single flushing (Flushing treatment). The P.v./Flushing treatment removed 54.04% of soil As from contaminated soil compared to 47.16% in Flushing treatment, suggesting that the growth of P. vittata was beneficial for promoting the removal efficiency. We analyzed the As fractionation in soil and As concentration in soil solution to reveal the mechanism behind this combined process. Results showed that comparing with the control treatment, the percent of labile arsenate fraction significantly increased by 17% under P.v./Flushing treatment. As concentration in soil solution remained a high lever during the middle and later periods (51.26-56.22mg/L), which was significantly higher than the Flushing treatment. Although soil flushing of phosphate for more than a month, P. vittata still had good accumulation and transfer capacity of As of the soil. The results of the research revealed that combination of phytoremediation and in situ soil flushing is available to remediate As-contaminated soils. Copyright © 2016. Published by Elsevier B.V.

Rate of Contamination Removal of Two Phyto-remediation Sites at the DOE Portsmouth Gaseous Diffusion Plant

International Nuclear Information System (INIS)

Lewis, A.C.; Baird, D.R.

2006-01-01

This paper describes applications of phyto-remediation at the Portsmouth Gaseous Diffusion Plant (PORTS), a Department of Energy (DOE) Facility that enriched uranium from the early 1950's until 2000. Phyto-remediation has been implemented to assist in the removal of TCE (trichloroethylene) in the groundwater at two locations at the PORTS facility: the X-740 area and the X-749/X-120 area. Phyto-remediation technology is based on the ability of certain plants species (in this case hybrid poplar trees) and their associated rhizo-spheric microorganisms to remove, degrade, or contain chemical contaminants located in the soil, sediment, surface water, groundwater, and possibly even the atmosphere. Phyto-remediation technology is a promising clean-up solution for a wide variety of pollutants and sites. Mature trees, such as the hybrid poplar, can consume up to 3,000 gallons of groundwater per acre per day. Organic compounds are captured in the trees' root systems. These organic compounds are degraded by ultraviolet light as they are transpired along with the water vapor through the leaves of the trees. The phyto-remediation system at the X-740 area encompasses 766 one-year old hybrid poplar trees (Populus nigra x nigra, Populus nigra x maximowiczii, and Populus deltoides x nigra) that were planted 10 feet apart in rows 10 feet to 20 feet apart, over an area of 2.6 acres. The system was installed to manage the VOC contaminant plume. At the X749/X-120 area, a phyto-remediation system of 2,640 hybrid poplar trees (Populus nigra x maximowiczii) was planted in seven areas/zones to manage the VOC contaminant plume. The objectives of these systems are to remove contamination from the groundwater and to prevent further migration of contaminants. The goal of these remediation procedures is to achieve completely mature and functional phyto-remediation systems within two years of the initial planting of the hybrid poplar trees at each planting location. There is a direct

Trace contaminant concentration affects mineral transformation and pollutant fate in hydroxide-weathered Hanford sediments

International Nuclear Information System (INIS)

Perdrial, Nicolas; Rivera, Nelson; Thompson, Aaron; O’Day, Peggy A.; Chorover, Jon

2011-01-01

Highlights: ► Fate of Sr, Cs and I tracked during hydroxide-weathering of sediments. ► pCO 2 and contaminant concentration affected mineral transformation. ► Sodalite/cancrinite formed at μM levels, chabazite at mM levels. ► Absence of CO 2 resulted in calcite dissolution and strätlingite formation. ► Trace contaminant concentrations modified their own sequestration path. - Abstract: Prior work has shown that when silicaceous sediments are infused with caustic radioactive waste, contaminant fate is tightly coupled to ensuing mineral weathering reactions. However, the effects of local aqueous geochemical conditions on these reactions are poorly studied. Thus, we varied contaminant concentration and pCO 2 during the weathering of previously uncontaminated Hanford sediments over 6 months and 1 year in a solution of caustic waste (pH 13, high ionic strength). Co-contaminants Sr, Cs and I were added at “low” (Cs/Sr: 10 −5 m; I: 10 −7 m) and “high” (Cs/Sr: 10 −3 m; I: 10 −5 m) concentrations, and headspace was held at atmospheric or undetectable ( 2 partial pressure. Solid phase characterization revealed the formation of the zeolite chabazite in “high” samples, whereas feldspathoids, sodalite and cancrinite, were formed preferentially in “low” samples. Sr, Cs and I were sequestered in all reacted sediments. Native calcite dissolution in the CO 2 -free treatment drove the formation of strätlingite (Ca 2 Al 2 SiO 7 ·8H 2 O) and diminished availability of Si and Al for feldspathoid formation. Results indicate that pCO 2 and contaminant concentrations strongly affect contaminant speciation in waste-weathered sediments, and are therefore likely to impact reaction product stability under any remediation scenario.

A Market Basket Survey of Horticultural Fruits for Arsenic and Trace Metal Contamination in Southeast Nigeria and Potential Health Risk Implications

OpenAIRE

Chigozie Damian Ezeonyejiaku; Maximilian Obinna Obiakor

2017-01-01

Background. Elevated arsenic and trace metal contamination of the terrestrial food chain represents one of the most significant environmental risk exposures for human populations in developing countries. Metalloid and metal contamination in horticultural crop produce such as fruit is a public health concern in Nigeria. Local fruits are cheap sources of vitamins and minerals for the resident population and pose an important dietary threat of metal(loid) toxicity through consumption. Objecti...

Tracey - a simulation model of trace element fluxes in soil-plant system for long-term assessment of a radioactive groundwater contamination

International Nuclear Information System (INIS)

Gaerdenaes, Annemieke; Eckersten, Henrik; Reinlert, Andre; Gustafsson, David; Jansson, Per-Erik; Ekstroem, Per-Anders; Avila, Rodolfo; Greger, Maria

2009-10-01

We developed a general trace element model called Tracey to simulate dynamically the possible accumulation of radionuclides as a result of an long-term radioactive contamination of groundwater in terrestrial ecosystems. The overall objectives of the study are to: 1) Develop and evaluate a multi-compartmental model that dynamically simulates the transport and accumulation of a radionuclide in the soil-plant system at a time scale relevant for risk assessment of nuclear fuel waste; and 2) Asses the possible accumulation of radionuclide in terrestrial ecosystems due to an eventual long-term continuous radioactive groundwater contamination. Specific objectives were to assess: - The proportion of the contamination accumulated and where it is stored in the ecosystem. - The importance of the plant uptake approach for accumulation of radionuclides. - The most important radionuclide properties and ecosystem characteristics for accumulation and losses. - The proportion of the contamination lost and how is it lost. - The circumstances which stimulated export of radionuclides to other ecosystems. The model presented here, called Tracey, is a stand-alone version to allow for long simulation periods relevant for the time scale of risk assessment of nuclear waste (i.e. several thousand years) with time steps as short as one day. Tracey is a multi-compartmental model in which fluxes and storage of radionuclide are described for different plant parts and for several soil layers. Each layer includes pools of slowly and quickly decomposing litter, humus, solved and absorbed trace element. The trace element fluxes are assumed to be proportional to either water or carbon fluxes, these fluxes are simulated using the dynamic model CoupModel for fluxes of water, carbon, nitrogen and carbon in terrestrial ecosystems. Two different model approaches were used to describe plant uptake of radionuclides. The one called passive uptake approach is driven by water uptake and the one called active

Sensitive Multi-Species Emissions Monitoring: Infrared Laser-Based Detection of Trace-Level Contaminants

Energy Technology Data Exchange (ETDEWEB)

Steill, Jeffrey D. [Sandia National Lab. (SNL-CA), Livermore, CA (United States); Huang, Haifeng [Sandia National Lab. (SNL-CA), Livermore, CA (United States); Hoops, Alexandra A. [Sandia National Lab. (SNL-CA), Livermore, CA (United States); Patterson, Brian D. [Sandia National Lab. (SNL-CA), Livermore, CA (United States); Birtola, Salvatore R. [Sandia National Lab. (SNL-CA), Livermore, CA (United States); Jaska, Mark [Sandia National Lab. (SNL-CA), Livermore, CA (United States); Strecker, Kevin E. [Sandia National Lab. (SNL-CA), Livermore, CA (United States); Chandler, David W. [Sandia National Lab. (SNL-CA), Livermore, CA (United States); Bisson, Soott [Sandia National Lab. (SNL-CA), Livermore, CA (United States)

2014-09-01

This report summarizes our development of spectroscopic chemical analysis techniques and spectral modeling for trace-gas measurements of highly-regulated low-concentration species present in flue gas emissions from utility coal boilers such as HCl under conditions of high humidity. Detailed spectral modeling of the spectroscopy of HCl and other important combustion and atmospheric species such as H 2 O, CO 2 , N 2 O, NO 2 , SO 2 , and CH 4 demonstrates that IR-laser spectroscopy is a sensitive multi-component analysis strategy. Experimental measurements from techniques based on IR laser spectroscopy are presented that demonstrate sub-ppm sensitivity levels to these species. Photoacoustic infrared spectroscopy is used to detect and quantify HCl at ppm levels with extremely high signal-to-noise even under conditions of high relative humidity. Additionally, cavity ring-down IR spectroscopy is used to achieve an extremely high sensitivity to combustion trace gases in this spectral region; ppm level CH 4 is one demonstrated example. The importance of spectral resolution in the sensitivity of a trace-gas measurement is examined by spectral modeling in the mid- and near-IR, and efforts to improve measurement resolution through novel instrument development are described. While previous project reports focused on benefits and complexities of the dual-etalon cavity ring-down infrared spectrometer, here details on steps taken to implement this unique and potentially revolutionary instrument are described. This report also illustrates and critiques the general strategy of IR- laser photodetection of trace gases leading to the conclusion that mid-IR laser spectroscopy techniques provide a promising basis for further instrument development and implementation that will enable cost-effective sensitive detection of multiple key contaminant species simultaneously.

Osmotic versus conventional membrane bioreactors integrated with reverse osmosis for water reuse: Biological stability, membrane fouling, and contaminant removal.

Science.gov (United States)

Luo, Wenhai; Phan, Hop V; Xie, Ming; Hai, Faisal I; Price, William E; Elimelech, Menachem; Nghiem, Long D

2017-02-01

This study systematically compares the performance of osmotic membrane bioreactor - reverse osmosis (OMBR-RO) and conventional membrane bioreactor - reverse osmosis (MBR-RO) for advanced wastewater treatment and water reuse. Both systems achieved effective removal of bulk organic matter and nutrients, and almost complete removal of all 31 trace organic contaminants investigated. They both could produce high quality water suitable for recycling applications. During OMBR-RO operation, salinity build-up in the bioreactor reduced the water flux and negatively impacted the system biological treatment by altering biomass characteristics and microbial community structure. In addition, the elevated salinity also increased soluble microbial products and extracellular polymeric substances in the mixed liquor, which induced fouling of the forward osmosis (FO) membrane. Nevertheless, microbial analysis indicated that salinity stress resulted in the development of halotolerant bacteria, consequently sustaining biodegradation in the OMBR system. By contrast, biological performance was relatively stable throughout conventional MBR-RO operation. Compared to conventional MBR-RO, the FO process effectively prevented foulants from permeating into the draw solution, thereby significantly reducing fouling of the downstream RO membrane in OMBR-RO operation. Accumulation of organic matter, including humic- and protein-like substances, as well as inorganic salts in the MBR effluent resulted in severe RO membrane fouling in conventional MBR-RO operation. Crown Copyright © 2016. Published by Elsevier Ltd. All rights reserved.

Development of an Electrochemical Ceramic Membrane Filtration System for Efficient Contaminant Removal from Waters.

Science.gov (United States)

Zheng, Junjian; Wang, Zhiwei; Ma, Jinxing; Xu, Shaoping; Wu, Zhichao

2018-04-03

Inability to remove low-molecular-weight anthropogenic contaminants is a critical issue in low-pressure membrane filtration processes for water treatment. In this work, a novel electrochemical ceramic membrane filtration (ECMF) system using TiO 2 @SnO 2 -Sb anode was developed for removing persistent p-chloroaniline (PCA). Results showed that the ECMF system achieved efficient removal of PCA from contaminated waters. At a charging voltage of 3 V, the PCA removal rate of TiO 2 @SnO 2 -Sb ECMF system under flow-through mode was 2.4 times that of flow-by mode. The energy consumption for 50% of PCA removal for TiO 2 @SnO 2 -Sb ECMF at 3 V under flow-through mode was 0.38 Wh/L, much lower than that of flow-by operation (1.5 Wh/L), which was attributed to the improved utilization of the surface adsorbed HO· and dissociated HO· driven by the enhanced mass transfer of PCA toward the anode surface. Benefiting from the increased production of reactive oxygen species such as O 2 •- , H 2 O 2 , and HO· arising from excitation of anatase TiO 2 , TiO 2 @SnO 2 -Sb ECMF exhibited a superior electrocatalytic activity to the SnO 2 -Sb ECMF system. The degradation pathways of PCA initiated by OH· attack were further proposed, with the biodegradable short-chain carboxylic acids (mainly formic, acetic, and oxalic acids) identified as the dominant oxidized products. These results highlight the potential of the ECMF system for cost-effective water purification.

Means to remove electrode contamination effect of Langmuir probe measurement in space

Energy Technology Data Exchange (ETDEWEB)

Oyama, K.-I.; Lee, C. H.; Fang, H. K.; Cheng, C. Z. [Plasma and Space Science Center, National Cheng Kung University, No.1 Ta-Hsueh Rd., Tainan 70101, Taiwan (China)

2012-05-15

Precaution to remove the serious effect of electrode contamination in Langmuir probe experiments has not been taken in many space measurements because the effect is either not understood or ignored. We stress here that one should pay extra attention to the electrode contamination effect to get accurate and reliable plasma measurements so that the long time effort for sounding rocket/satellite missions does not end in vain or becomes less fruitful. In this paper, we describe two main features of voltage-current characteristic curves associated with the contaminated Langmuir probe, which are predicted from the equivalent circuit model, which we proposed in 1970's. We then show that fast sweeping dc Langmuir probes can give reliable results in the steady state regime. The fast sweeping probe can also give reliable results in transient situations such as satellite moves through plasma bubble in the ionosphere where the electron density drastically changes. This fact was first confirmed in our laboratory experiment.

Efficiency of lipopeptide biosurfactants in removal of petroleum hydrocarbons and heavy metals from contaminated soil.

Science.gov (United States)

Singh, Anil Kumar; Cameotra, Swaranjit Singh

2013-10-01

This study describes the potential application of lipopeptide biosurfactants in removal of petroleum hydrocarbons and heavy metals from the soil samples collected from industrial dumping site. High concentrations of heavy metals (like iron, lead, nickel, cadmium, copper, cobalt and zinc) and petroleum hydrocarbons were present in the contaminated soil samples. Lipopeptide biosurfactant, consisting of surfactin and fengycin was obtained from Bacillus subtilis A21. Soil washing with biosurfactant solution removed significant amount of petroleum hydrocarbon (64.5 %) and metals namely cadmium (44.2 %), cobalt (35.4 %), lead (40.3 %), nickel (32.2 %), copper (26.2 %) and zinc (32.07 %). Parameters like surfactant concentration, temperature, agitation condition and pH of the washing solution influenced the pollutant removing ability of biosurfactant mixture. Biosurfactant exhibited substantial hydrocarbon solubility above its critical micelle concentration. During washing, 50 % of biosurfactant was sorbed to the soil particles decreasing effective concentration during washing process. Biosurfactant washed soil exhibited 100 % mustard seed germination contradictory to water washed soil where no germination was observed. The results indicate that the soil washing with mixture of lipopeptide biosurfactants at concentrations above its critical micelle concentration can be an efficient and environment friendly approach for removing pollutants (petroleum hydrocarbon and heavy metals) from contaminated soil.

Tracey - a simulation model of trace element fluxes in soil-plant system for long-term assessment of a radioactive groundwater contamination

Energy Technology Data Exchange (ETDEWEB)

Gaerdenaes, Annemieke (Dept. of Soil and Environment, Swedish Univ. of Agricultural Sciences, Uppsala (Sweden)); Eckersten, Henrik (Dept. of Ecology and Crop Production, Swedish Univ. of Agricultural Sciences, Uppsala (Sweden)); Reinlert, Andre (Dept. of Physical Geography and Ecosystems Analysis, Lund Univ., Lund (Sweden)); Gustafsson, David; Jansson, Per-Erik (Dept. Land and WaterResources, Royal Inst. of Technology, Stockholm (Sweden)); Ekstroem, Per-Anders; Avila, Rodolfo (Facilia AB, Bromma (Sweden)); Greger, Maria (Dept. of Botany, Stockholm Univ., Stockholm (Sweden))

2009-10-15

We developed a general trace element model called Tracey to simulate dynamically the possible accumulation of radionuclides as a result of an long-term radioactive contamination of groundwater in terrestrial ecosystems. The overall objectives of the study are to: 1) Develop and evaluate a multi-compartmental model that dynamically simulates the transport and accumulation of a radionuclide in the soil-plant system at a time scale relevant for risk assessment of nuclear fuel waste; and 2) Asses the possible accumulation of radionuclide in terrestrial ecosystems due to an eventual long-term continuous radioactive groundwater contamination. Specific objectives were to assess: - The proportion of the contamination accumulated and where it is stored in the ecosystem. - The importance of the plant uptake approach for accumulation of radionuclides. - The most important radionuclide properties and ecosystem characteristics for accumulation and losses. - The proportion of the contamination lost and how is it lost. - The circumstances which stimulated export of radionuclides to other ecosystems. The model presented here, called Tracey, is a stand-alone version to allow for long simulation periods relevant for the time scale of risk assessment of nuclear waste (i.e. several thousand years) with time steps as short as one day. Tracey is a multi-compartmental model in which fluxes and storage of radionuclide are described for different plant parts and for several soil layers. Each layer includes pools of slowly and quickly decomposing litter, humus, solved and absorbed trace element. The trace element fluxes are assumed to be proportional to either water or carbon fluxes, these fluxes are simulated using the dynamic model CoupModel for fluxes of water, carbon, nitrogen and carbon in terrestrial ecosystems. Two different model approaches were used to describe plant uptake of radionuclides. The one called passive uptake approach is driven by water uptake and the one called active

Trace Metals in Urban Stormwater Runoff and their Management

Science.gov (United States)

Li, T.; Hall, K.; Li, L. Y.; Schreier, H.

2009-04-01

In past decades, due to the rapid urbanization, land development has replaced forests, fields and meadows with impervious surfaces such as roofs, parking lots and roads, significantly affecting watershed quality and having an impact on aquatic systems. In this study, non-point source pollution from a diesel bus loop was assessed for the extent of trace metal contamination of Cu, Mn, Fe, and Zn in the storm water runoff. The study was carried out at the University of British Columbia (UBC) in the Greater Vancouver Regional District (GVRD) of British Columbia, Canada. Fifteen storm events were monitored at 3 sites from the diesel bus loop to determine spatial and temporal variations of dissolved and total metal concentrations in the storm water runoff. The dissolved metal concentrations were compared with the provincial government discharge criteria and the bus loop storm water quality was also compared with previous studies conducted across the GVRD urban area. To prevent storm water with hazardous levels of contaminants from being discharged into the urban drainage system, a storm water catch basin filter was installed and evaluated for its efficiency of contaminants removal. The perlite filter media adsorption capacities for the trace metals, oil and grease were studied for better maintenance of the catch basin filter. Dissolved copper exceeded the discharge criteria limit in 2 out of 15 cases, whereas dissolved zinc exceeded the criteria in 4 out of 15 cases, and dissolved manganese was below the criteria in all of the events sampled. Dissolved Cu and Zn accounted for 36 and 45% of the total concentration, whereas Mn and Fe only accounted for 20 and 4% of their total concentration, respectively. Since they are more mobile and have higher bioaccumulation potentials, Zn and Cu are considered to be more hazardous to the aquatic environment than Fe and Mn. With high imperviousness (100%) and intensive traffic at the UBC diesel bus loop, trace metal concentrations

Spectroscopic Determination of Trace Contaminants in High-Purity Oxygen

Science.gov (United States)

Hornung, Steven

2013-01-01

Oxygen used for extravehicular activities (EVAs) must be free of contaminants because a difference in a few tenths of a percent of argon or nitrogen content can mean significant reduction in available EVA time. These inert gases build up in the extravehicular mobility unit because they are not metabolized or scrubbed from the atmosphere. A prototype optical emission technique capable of detecting argon and nitrogen below 0.1% in oxygen has been developed. This instrument uses a glow discharge in reduced-pressure gas to produce atomic emission from the species present. Because the atomic emission lines from oxygen, nitrogen, and argon are discrete, and in many cases well-separated, trace amounts of argon and nitrogen can be detected in the ultraviolet and visible spectrum. This is a straightforward, direct measurement of the target contaminants, and may lend itself to a device capable of on-orbit verification of oxygen purity. A glow discharge is a plasma formed in a low-pressure (1 to 10 Torr) gas cell between two electrodes. Depending on the configuration, voltages ranging from 200 V and above are required to sustain the discharge. In the discharge region, the gas is ionized and a certain population is in the excited state. Light is produced by the transitions from the excited states formed in the plasma to the ground state. The spectrum consists of discrete, narrow emission lines for the atomic species, and broader peaks that may appear as a manifold for molecular species such as O2 and N2, the wavelengths and intensities of which are a characteristic of each atom. The oxygen emission is dominated by two peaks at 777 and 844 nm.

Chelating agent-assisted electrokinetic removal of cadmium, lead and copper from contaminated soils

International Nuclear Information System (INIS)

Giannis, Apostolos; Nikolaou, Aris; Pentari, Despina; Gidarakos, Evangelos

2009-01-01

An integrated experimental program was conducted to remove Cd, Pb and Cu from contaminated soil. The chelate agents nitrilotriacetic acid (NTA), diethylenetriamine pentaacetic acid (DTPA) and ethyleneglycol tetraacetic acid (EGTA) were used as washing solutions under different pH conditions and concentrations. Results showed that the extraction efficiency for Cd in decreasing order was NTA > EGTA > DTPA, while for Pb and Cu it was DTPA > NTA > EGTA. The use of higher chelate concentrations did not necessarily result in greater extraction efficiency. Electrokinetic remediation was applied by conditioning anolyte-catholyte pH to neutral values in order to avoid any potential alterations to the physicochemical soil properties. The removal efficiency for Cd was 65-95%, for Cu 15-60%, but for Pb was less than 20%. The phytotoxicity of the treated soil showed that the soil samples from the anode section were less phytotoxic than the untreated soil, but the phytotoxicity was increased in the samples from the cathode section. - Cadmium, lead and copper were extracted from contaminated soil by integrated electrokinetic and soil washing studies.

Chelating agent-assisted electrokinetic removal of cadmium, lead and copper from contaminated soils

Energy Technology Data Exchange (ETDEWEB)

Giannis, Apostolos, E-mail: apostolos.giannis@enveng.tuc.g [Laboratory of Toxic and Hazardous Waste Management, Department of Environmental Engineering, Technical University of Crete, Politechnioupolis, Chania 73100 (Greece); Nikolaou, Aris [Laboratory of Toxic and Hazardous Waste Management, Department of Environmental Engineering, Technical University of Crete, Politechnioupolis, Chania 73100 (Greece); Pentari, Despina [Laboratory of Inorganic and Organic Geochemistry and Organic Petrography, Department of Mineral Resources Engineering, Technical University of Crete, Politechnioupolis, Chania 73100 (Greece); Gidarakos, Evangelos, E-mail: gidarako@mred.tuc.g [Laboratory of Toxic and Hazardous Waste Management, Department of Environmental Engineering, Technical University of Crete, Politechnioupolis, Chania 73100 (Greece)

2009-12-15

An integrated experimental program was conducted to remove Cd, Pb and Cu from contaminated soil. The chelate agents nitrilotriacetic acid (NTA), diethylenetriamine pentaacetic acid (DTPA) and ethyleneglycol tetraacetic acid (EGTA) were used as washing solutions under different pH conditions and concentrations. Results showed that the extraction efficiency for Cd in decreasing order was NTA > EGTA > DTPA, while for Pb and Cu it was DTPA > NTA > EGTA. The use of higher chelate concentrations did not necessarily result in greater extraction efficiency. Electrokinetic remediation was applied by conditioning anolyte-catholyte pH to neutral values in order to avoid any potential alterations to the physicochemical soil properties. The removal efficiency for Cd was 65-95%, for Cu 15-60%, but for Pb was less than 20%. The phytotoxicity of the treated soil showed that the soil samples from the anode section were less phytotoxic than the untreated soil, but the phytotoxicity was increased in the samples from the cathode section. - Cadmium, lead and copper were extracted from contaminated soil by integrated electrokinetic and soil washing studies.

Trace elements in agroecosystems and impacts on the environment.

Science.gov (United States)

He, Zhenli L; Yang, Xiaoe E; Stoffella, Peter J

2005-01-01

Trace elements mean elements present at low concentrations (mg kg-1 or less) in agroecosystems. Some trace elements, including copper (Cu), zinc (Zn), manganese (Mn), iron (Fe), molybdenum (Mo), and boron (B) are essential to plant growth and are called micronutrients. Except for B, these elements are also heavy metals, and are toxic to plants at high concentrations. Some trace elements, such as cobalt (Co) and selenium (Se), are not essential to plant growth but are required by animals and human beings. Other trace elements such as cadmium (Cd), lead (Pb), chromium (Cr), nickel (Ni), mercury (Hg), and arsenic (As) have toxic effects on living organisms and are often considered as contaminants. Trace elements in an agroecosystem are either inherited from soil parent materials or inputs through human activities. Soil contamination with heavy metals and toxic elements due to parent materials or point sources often occurs in a limited area and is easy to identify. Repeated use of metal-enriched chemicals, fertilizers, and organic amendments such as sewage sludge as well as wastewater may cause contamination at a large scale. A good example is the increased concentration of Cu and Zn in soils under long-term production of citrus and other fruit crops. Many chemical processes are involved in the transformation of trace elements in soils, but precipitation-dissolution, adsorption-desorption, and complexation are the most important processes controlling bioavailability and mobility of trace elements in soils. Both deficiency and toxicity of trace elements occur in agroecosystems. Application of trace elements in fertilizers is effective in correcting micronutrient deficiencies for crop production, whereas remediation of soils contaminated with metals is still costly and difficult although phytoremediation appears promising as a cost-effective approach. Soil microorganisms are the first living organisms subjected to the impacts of metal contamination. Being responsive and

Use of polymeric resins for removing contaminants from oily waters

Energy Technology Data Exchange (ETDEWEB)

Clarisse, M.D.; Queiros, Y.G.C.; Mauro, A.C.; Lucas, E.F. [Universidade Federal do Rio de Janeiro (UFRJ), RJ (Brazil). Inst. de Macromoleculas; Barbosa, C.C.R. [Instituto de Engenharia Nuclear (IEN/CNEN-RJ), Rio de Janeiro, RJ (Brazil); Barbosa, L.C.F.; Louvisse, A.M.T. [PETROBRAS, Rio de Janeiro, RJ (Brazil). Centro de Pesquisas (CENPES)

2004-07-01

Polymeric resins are being tried as an alternative material for treating oily waters from the petroleum industry, which have already been treated by conventional methods. The objective of this work has been to evaluate the purification degree of synthetic oily waters when treated in fixed bed columns packed with polymeric resins made up of hydrophilic and lipophilic moieties. The analysis used for characterizing the total grease and oil content (TOG) was fluorimetry. Starting oily waters of average TOG 40 ppm were prepared. Data obtained from eluted waters did not outweigh 1% of the TOG values of starting solutions. The kinetic study showed that the contaminant removal efficiency depends on the system elution flow rate; optimum removal values were reached at a 7.0 mL/min flow rate. High efficiency and speed in the purification process were obtained at this optimum flow rate. The passage of a water volume 1,000 times the volume of the column bed was not sufficient to observe its saturation level. (author)

Quantitative Structure--Activity Relationship (QSAR) for the Oxidation of Trace Organic Contaminants by Sulfate Radical.

Science.gov (United States)

Xiao, Ruiyang; Ye, Tiantian; Wei, Zongsu; Luo, Shuang; Yang, Zhihui; Spinney, Richard

2015-11-17

The sulfate radical anion (SO4•–) based oxidation of trace organic contaminants (TrOCs) has recently received great attention due to its high reactivity and low selectivity. In this study, a meta-analysis was conducted to better understand the role of functional groups on the reactivity between SO4•– and TrOCs. The results indicate that compounds in which electron transfer and addition channels dominate tend to exhibit a faster second-order rate constants (kSO4•–) than that of H–atom abstraction, corroborating the SO4•– reactivity and mechanisms observed in the individual studies. Then, a quantitative structure activity relationship (QSAR) model was developed using a sequential approach with constitutional, geometrical, electrostatic, and quantum chemical descriptors. Two descriptors, ELUMO and EHOMO energy gap (ELUMO–EHOMO) and the ratio of oxygen atoms to carbon atoms (#O:C), were found to mechanistically and statistically affect kSO4•– to a great extent with the standardized QSAR model: ln kSO4•– = 26.8–3.97 × #O:C – 0.746 × (ELUMO–EHOMO). In addition, the correlation analysis indicates that there is no dominant reaction channel for SO4•– reactions with various structurally diverse compounds. Our QSAR model provides a robust predictive tool for estimating emerging micropollutants removal using SO4•– during wastewater treatment processes.

A combination of bioleaching and bioprecipitation for deep removal of contaminating metals from dredged sediment

Energy Technology Data Exchange (ETDEWEB)

Fang Di, E-mail: dfang@ouc.edu.cn [Department of Environmental Engineering, Ocean University of China, Qingdao 266100 (China); State Key Laboratory of Soil and Sustainable Agriculture, Institute of Soil Science, Chinese Academy of Sciences, Nanjing 210008 (China); Zhang Ruichang [Department of Environmental Engineering, Ocean University of China, Qingdao 266100 (China); Zhou Lixiang [Department of Environmental Engineering, Nanjing Agricultural University, Nanjing 210095 (China); Li Jie [Department of Environmental Engineering, Ocean University of China, Qingdao 266100 (China)

2011-08-15

Highlights: {yields} Bioleaching-bioprecipitation can deeply cleanup sediment-borne metal contaminants. {yields} Bioleaching results in a sufficient solubilisation of sediment-borne metals. {yields} Bioprecipitation removes most of solubilised metals from sediment leachate at pH 3.7. {yields} Bioremoval of soluble Zn, Cu and Cr is due to the formation of ZnS, Cu{sub 2}S and CrOOH. {yields} Alkalization of bioleached sediment by Ca(OH){sub 2} excludes the risk of re-acidification. - Abstract: A linked microbial process comprising bioleaching with sulfate-oxidizing bacteria and bioprecipitation with sulfate-reducing bacteria operating sequentially was investigated to deeply remove contaminating metals from dredged sediment. The results showed that sediment bioleaching resulted in a sharp decrease in sediment pH from an initial pH {approx}7.6 to pH {approx}2.5 within 10-20 days, approximately 65% of the main heavy metals present (Zn + Cu + Cr) were solubilized, and most of the unsolubilized metals existed in residual form of sediment. The acidic leachate that resulted from sediment bioleaching was efficiently stripped of metal sulfates using a bioprecipitation reactor when challenged with influent as low as pH {approx}3.7. More than 99% of Zn{sup 2+}, 99% of Cu{sup 2+} and 90% of Cr{sup 3+} were removed from the leachate, respectively, due to the formation of ZnS, Cu{sub 2}S and CrOOH precipitates, as confirmed by SEM-EDS and XRD detection. It was also found that alkalization of bioleached sediment using Ca(OH){sub 2} excluded the risk of sediment re-acidification. The ability of the combined process developed in this study to deeply remove heavy metals in insoluble sulfides or hydroxides forms makes it particularly attractive for the treatment of different types of metal contaminants.

A combination of bioleaching and bioprecipitation for deep removal of contaminating metals from dredged sediment

International Nuclear Information System (INIS)

Fang Di; Zhang Ruichang; Zhou Lixiang; Li Jie

2011-01-01

Highlights: → Bioleaching-bioprecipitation can deeply cleanup sediment-borne metal contaminants. → Bioleaching results in a sufficient solubilisation of sediment-borne metals. → Bioprecipitation removes most of solubilised metals from sediment leachate at pH 3.7. → Bioremoval of soluble Zn, Cu and Cr is due to the formation of ZnS, Cu 2 S and CrOOH. → Alkalization of bioleached sediment by Ca(OH) 2 excludes the risk of re-acidification. - Abstract: A linked microbial process comprising bioleaching with sulfate-oxidizing bacteria and bioprecipitation with sulfate-reducing bacteria operating sequentially was investigated to deeply remove contaminating metals from dredged sediment. The results showed that sediment bioleaching resulted in a sharp decrease in sediment pH from an initial pH ∼7.6 to pH ∼2.5 within 10-20 days, approximately 65% of the main heavy metals present (Zn + Cu + Cr) were solubilized, and most of the unsolubilized metals existed in residual form of sediment. The acidic leachate that resulted from sediment bioleaching was efficiently stripped of metal sulfates using a bioprecipitation reactor when challenged with influent as low as pH ∼3.7. More than 99% of Zn 2+ , 99% of Cu 2+ and 90% of Cr 3+ were removed from the leachate, respectively, due to the formation of ZnS, Cu 2 S and CrOOH precipitates, as confirmed by SEM-EDS and XRD detection. It was also found that alkalization of bioleached sediment using Ca(OH) 2 excluded the risk of sediment re-acidification. The ability of the combined process developed in this study to deeply remove heavy metals in insoluble sulfides or hydroxides forms makes it particularly attractive for the treatment of different types of metal contaminants.

A Review of Removable Surface Contamination on Radioactive Materials Transportation Containers

Energy Technology Data Exchange (ETDEWEB)

Kennedy, Jr, W. E.; Watson, E. C.; Murphy, D. W.; Harrer, B. J.; Harty, R.; Aldrich, J. M.

1981-05-01

This report contains the results of a study sponsored by the U.S. Nuclear Regulatory Commission (NRC) of removable surface contamination on radioactive materials transportation containers. The purpose of the study is to provide information to the NRC during their review of existing regulations. Data was obtained from both industry and literature on three major topics: 1) radiation doses, 2) economic costs, and 3) contamination frequencies. Containers for four categories of radioactive materials are considered including radiopharmaceuticals, industrial sources, nuclear fuel cycle materials, and low-level radioactive waste. Assumptions made in this study use current information to obtain realistic yet conservative estimates of radiation dose and economic costs. Collective and individual radiation doses are presented for each container category on a per container basis. Total doses, to workers and the public, are also presented for spent fuel cask and low-level waste drum decontamination. Estimates of the additional economic costs incurred by lowering current limits by factors of 10 and 100 are presented. Current contamination levels for each category of container are estimated from the data collected. The information contained in this report is designed to be useful to the NRC in preparing their recommendations for new regulations.

Off-Gas Treatment: Evaluation of Nano-structured Sorbents for Selective Removal of Contaminants

Energy Technology Data Exchange (ETDEWEB)

Utgikar, Vivek; Aston, D. Eric; Sabharwall, Piyush

2018-03-30

Reprocessing of used nuclear fuel (UNF) is expected to play an important role for sustainable development of nuclear energy by increasing the energy extracted from the fuel and reducing the generation of the high level waste (HLW). However, aqueous reprocessing of UNF is accompanied by emission of off-gas streams containing radioactive nuclides including iodine, krypton, xenon, carbon, and tritium. Volatile iodine (129I), and krypton (85Kr) are long lived isotopes which have adverse effects on the environment as well as human health. Development of methods for the capture and long-term storage of radioactive gases is of crucial importance in order to manage their emissions that are anticipated to increase significantly with the growth of nuclear energy. For more than 70 years, porous solid sorbents have been in the forefront of radioactive contaminant removal due to promising results and their advantages such as high removal efficiency, low maintenance cost, simple equipment design and operation over other techniques. The research conducted in this project has focused on development of a novel nanostructured sorbent and its application for the capture of the above two contaminants of interest. Nanostructured carbon polyhedrons supported on Engelhard Titanosilicate-10 sorbent was synthesized using hydrothermal methods and subjected to structural and compositional characterization using various techniques including electron microscopy, Raman, x-ray diffraction and BET surface area analysis. Dynamic sorption experiments conducted using a flow-through column setup yielded information on the thermodynamics and kinetics of sorption in single-contaminant and multi-contaminant streams. Parameters varied in the study included carbon loading, temperature, contact time, contaminant concentration and humidity. The behavior of the system was modeled using models available in literature as well as development of a mass-transfer model from fundamental principles. Experimental

Demolition and removal of radioactively contaminated concrete soil: Aerosol control and monitoring

Energy Technology Data Exchange (ETDEWEB)

Newton, G.J.; Hoover, M.D.; Grace, A.C. III

1995-12-01

From 1963 to 1985, two concrete-lined ponds were used to reduce the volume of radioactive liquids from the Institute`s research programs. Following withdrawal of the {open_quotes}hot ponds{close_quotes} from active use, the residual sludges and plastic liners of the ponds were removed and shipped to a radioactive waste disposal site. From 1987 to 1994, the concrete structures remained undisturbed pending environmental restoration on the site. Restoration began in 1994 and was completed in 1995. Restoration involved mechanical breakup and removal of the concrete structures and removal of areas of contaminated soils from the site. This report describes the design and results of the aerosol control and monitoring program that was conducted to ensure protection of workers and the environment during the restoration process. The aerosol control and monitoring strategy developed for remediation of the ITRI hot ponds was successful both in preventing dispersion of radioactive dusts and in demonstrating that exposures of workers and offsite releases were within statutory limits.

Potential of Ranunculus acris L. for biomonitoring trace element contamination of riverbank soils: photosystem II activity and phenotypic responses for two soil series.

Science.gov (United States)

Marchand, Lilian; Lamy, Pierre; Bert, Valerie; Quintela-Sabaris, Celestino; Mench, Michel

2016-02-01

Foliar ionome, photosystem II activity, and leaf growth parameters of Ranunculus acris L., a potential biomonitor of trace element (TE) contamination and phytoavailability, were assessed using two riverbank soil series. R. acris was cultivated on two potted soil series obtained by mixing a TE (Cd, Cu, Pb, and Zn)-contaminated technosol with either an uncontaminated sandy riverbank soil (A) or a silty clay one slightly contaminated by TE (B). Trace elements concentrations in the soil-pore water and the leaves, leaf dry weight (DW) yield, total leaf area (TLA), specific leaf area (SLA), and photosystem II activity were measured for both soil series after a 50-day growth period. As soil contamination increased, changes in soluble TE concentrations depended on soil texture. Increase in total soil TE did not affect the leaf DW yield, the TLA, the SLA, and the photosystem II activity of R. acris over the 50-day exposure. The foliar ionome did not reflect the total and soluble TE concentrations in both soil series. Foliar ionome of R. acris was only effective to biomonitor total and soluble soil Na concentrations in both soil series and total and soluble soil Mo concentrations in the soil series B.

Controlled Contamination of Epoxy Composites with PDMS and Removal by Laser Ablation

Science.gov (United States)

Palmieri, Frank; Ledesma, Rodolfo; Cataldo, Daniel; Lin, Yi; Wohl, Christopher; Gupta, Mool; Connell, John

2016-01-01

Surface preparation is critical to the performance of adhesively bonded composites. During manufacturing, minute quantities of mold release compounds are inevitably deposited on faying surfaces and may compromise bond performance. To ensure safety, mechanical fasteners and other crack arrest features must be installed in the bondlines of primary structures, which negates some advantages of adhesively bonded construction. Laser ablation is an automated, repeatable, and scalable process with high potential for the surface preparation of metals and composites in critical applications such as primary airframe structures. In this study, laser ablation is evaluated on composite surfaces for the removal of polydimethylsiloxane (PDMS), a common mold release material. Composite panels were contaminated uniformly with PDMS film thicknesses as low as 6.0 nm as measured by variable angle spectroscopic ellipsometry. Bond performance was assessed by mechanical testing using a 250 F cure, epoxy adhesive and compared with pre-bond surface inspection results. Water contact angle, optically stimulated electron emission, and laser induced breakdown spectroscopy were used to characterize contaminated and laser ablated surfaces. The failure mode obtained from double cantilever beam tests correlated well with surface characterization data. The test results indicated that even low levels of PDMS were not completely removed by laser ablation.

Final report: survey and removal of radioactive surface contamination at environmental restoration sites, Sandia National Laboratories/New Mexico. Volume 1

International Nuclear Information System (INIS)

Lambert, K.A.; Mitchell, M.M.; Jean, D.; Brown, C.; Byrd, C.S.

1997-09-01

This report describes the survey and removal of radioactive surface contamination at Sandia's Environmental Restoration (ER) sites. Radiological characterization was performed as a prerequisite to beginning the Resource Conservation and Recovery Act (RCRA) corrective action process. The removal of radioactive surface contamination was performed in order to reduce potential impacts to human health and the environment. The predominant radiological contaminant of concern was depleted uranium (DU). Between October 1993 and November 1996 scanning surface radiation surveys, using gamma scintillometers, were conducted at 65 sites covering approximately 908 acres. A total of 9,518 radiation anomalies were detected at 38 sites. Cleanup activities were conducted between October 1994 and November 1996. A total of 9,122 anomalies were removed and 2,072 waste drums were generated. The majority of anomalies not removed were associated with a site that has subsurface contamination beyond the scope of this project. Verification soil samples (1,008 total samples) were collected from anomalies during cleanup activities and confirm that the soil concentration achieved in the field were far below the target cleanup level of 230 pCi/g of U-238 (the primary constituent of DU) in the soil. Cleanup was completed at 21 sites and no further radiological action is required. Seventeen sites were not completed since cleanup activities wee precluded by ongoing site activity or were beyond the original project scope

Final report: survey and removal of radioactive surface contamination at environmental restoration sites, Sandia National Laboratories/New Mexico. Volume 1

Energy Technology Data Exchange (ETDEWEB)

Lambert, K.A.; Mitchell, M.M. [Brown and Root Environmental, Albuquerque, NM (United States); Jean, D. [MDM/Lamb, Inc., Albuquerque, NM (United States); Brown, C. [Environmental Dimensions, Inc., Albuquerque, NM 87109 (United States); Byrd, C.S. [Sandia National Labs., Albuquerque, NM (United States)

1997-09-01

This report describes the survey and removal of radioactive surface contamination at Sandia`s Environmental Restoration (ER) sites. Radiological characterization was performed as a prerequisite to beginning the Resource Conservation and Recovery Act (RCRA) corrective action process. The removal of radioactive surface contamination was performed in order to reduce potential impacts to human health and the environment. The predominant radiological contaminant of concern was depleted uranium (DU). Between October 1993 and November 1996 scanning surface radiation surveys, using gamma scintillometers, were conducted at 65 sites covering approximately 908 acres. A total of 9,518 radiation anomalies were detected at 38 sites. Cleanup activities were conducted between October 1994 and November 1996. A total of 9,122 anomalies were removed and 2,072 waste drums were generated. The majority of anomalies not removed were associated with a site that has subsurface contamination beyond the scope of this project. Verification soil samples (1,008 total samples) were collected from anomalies during cleanup activities and confirm that the soil concentration achieved in the field were far below the target cleanup level of 230 pCi/g of U-238 (the primary constituent of DU) in the soil. Cleanup was completed at 21 sites and no further radiological action is required. Seventeen sites were not completed since cleanup activities wee precluded by ongoing site activity or were beyond the original project scope.

Removal and treatment of radioactive, organochlorine, and heavy metal contaminants from solid surfaces

International Nuclear Information System (INIS)

Grieco, S.A.; Neubauer, E.D.

1996-01-01

The U.S. Department of Energy (DOE) is defining decontamination and decommissioning (D ampersand D) obligations at its sites. Current D ampersand D activities are generally labor intensive, use chemical reagents that are difficult to treat, and may expose workers to radioactive and hazardous chemicals. Therefore, new technologies are desired that minimize waste, allow much of the decommissioned materials to be reused rather than disposed of as waste, and produce wastes that will meet disposal criteria. The O'Brien ampersand Gere companies tested a scouring decontamination system on concrete and steel surfaces contaminated with radioactive and hazardous wastes under the sponsorship of Martin Marietta Energy Systems, Inc. (MMES) at DOE's K-25 former gaseous diffusion plant in Oak Ridge, Tennessee. The scouring system removes fixed radioactive and hazardous contamination yet leaves the surface intact. Blasting residuals are treated using physical/chemical processes. Bench- and pilot-scale testing of the system was conducted on surfaces contaminated with uranium, technetium, heavy metals, and PCBs. Areas of concrete and metal surfaces were blasted. Residuals were dissolved in tap water and treated for radioactive, hazardous, and organochlorine constituents. The treatment system comprised pH adjustment, aeration, solids settling, filtration, carbon adsorption, and ion exchange. This system produced treated water and residual solid waste. Testing demonstrated that the system is capable of removing greater than 95% of radioactive and PCB surface contamination to below DOE's unrestricted use release limits; aqueous radionuclides, heavy metals, and PCBs were below DOE and USEPA treatment objectives after treatment. Waste residuals volume was decreased by 71 %. Preliminary analyses suggest that this system provides significant waste volume reduction and is more economical than alternative surface decontamination techniques that are commercially available or under development

Urban environmental geochemistry of trace metals

International Nuclear Information System (INIS)

Wong, Coby S.C.; Li Xiangdong; Thornton, Iain

2006-01-01

As the world's urban population continues to grow, it becomes increasingly imperative to understand the dynamic interactions between human activities and the urban environment. The development of urban environmental geochemistry has yielded a significant volume of scientific information about geochemical phenomena found uniquely in the urban environment, such as the distribution, dispersion, and geochemical characteristics of some toxic and potentially toxic trace metals. The aim of this paper is to provide an overview of the development of urban environmental geochemistry as a field of scientific study and highlight major transitions during the course of its development from its establishment to the major scientific interests in the field today. An extensive literature review is also conducted of trace metal contamination of the urban terrestrial environment, in particular of urban soils, in which the uniqueness of the urban environment and its influences on trace metal contamination are elaborated. Potential areas of future development in urban environmental geochemistry are identified and discussed. - Urban environmental geochemistry as a scientific discipline provides valuable information on trace metal contamination of the urban environment and its associated health effects

O problema da contaminação na determinação de traços de alumínio The problem of contamination in the aluminium trace analysis

Directory of Open Access Journals (Sweden)

Solange Cristina Garcia

1997-08-01

Full Text Available The most common difficulties which occur in trace analysis are those which involve contamination, mainly when the measurement is at very low concentration of ubiquitous elements as aluminium. The worst situation is when a separation step is necessary, because it requires extra-manipulations of the sample. This article describes the degree of contamination and its control for the aluminium trace analysis in dialysis solutions, when aluminium content of about 15 µg/l must be determinated.

Effect of the ultrasound-Fenton oxidation process with the addition of a chelating agent on the removal of petroleum-based contaminants from soil.

Science.gov (United States)

Li, Ying; Li, Fangmin; Li, Fanxiu; Yuan, Fuqian; Wei, Pingfang

2015-12-01

The effects of ultrasonic irradiation, the chelating agent modified Fenton reaction, and a combination of ultrasound and the Fenton method in removing petroleum contaminants from a soil were studied. The results showed that the contaminant removal rate of the Fenton treatment combined with an oxalic acid chelating agent was 55.6% higher than that without a chelating agent. The average removal rate of the contaminants using the ultrasound-Fenton treatment was 59.0% higher than that without ultrasonic treatment. A combination of ultrasound and an Fe(2+)/Fe(3+)-oxalate complex-modified Fenton reagent resulted in significantly higher removal rates of n-alkanes (C(n)H(2n+2), n Fenton method. The Fenton reaction and the ultrasound-Fenton treatment can unselectively remove multiple components of residual hydrocarbons and a number of benzene rings in polycyclic aromatic hydrocarbons. The chemistry of the heterocyclic compounds and the position and number of substituents can affect the degradation process.

Analysis of Leading Edge and Trailing Edge Cover Glass Samples Before and After Treatment with Advanced Satellite Contamination Removal Techniques

Science.gov (United States)

1993-04-01

surface analysis, 40 contamination control, ANCC ( Aerogel Mesh Contamination Collector) iPRICECODE 17. SECURITY CLASSIFICATION 1 & SECURITY CLASSIFICATION...operational parameter space (temperature, vibration, radiation, vacuum and micrometorite environments). One embodiment of this device, the Aerogel Mesh...Lippey and Dan Demeo of Hughes Aircraft Corporation for their kind hospitality and research collaboration on the contamination removal phase of this work

Arsenic contamination of underground water in Bangladesh: cause, effect, separation, determination and remedy

International Nuclear Information System (INIS)

Ahmed, M.J.

2003-01-01

Arsenic contamination of underground water of Bangladesh has become the gravest concern for the lives of millions of people of this land. Probable causes and effects of arsenic contamination of underground water of Bangladesh have been extensively discussed. The extent of current knowledge regarding the specification of arsenic in environmental waters in delineated. A simple, non-extractive, highly sensitive and selective quench photometric methods for the rapid determination of arsenic at trace levels in aqueous medium has been developed. This paper also presents a short review of the technologies used for arsenic removal of underground water in Bangladesh. (author)

Air suctioning during colon biopsy forceps removal reduces bacterial air contamination in the endoscopy suite.

Science.gov (United States)

Vavricka, S R; Tutuian, R; Imhof, A; Wildi, S; Gubler, C; Fruehauf, H; Ruef, C; Schoepfer, A M; Fried, M

2010-09-01

Bacterial contamination of endoscopy suites is of concern; however studies evaluating bacterial aerosols are lacking. We aimed to determine the effectiveness of air suctioning during removal of biopsy forceps in reducing bacterial air contamination. This was a prospective single-blinded trial involving 50 patients who were undergoing elective nontherapeutic colonoscopy. During colonoscopy, endoscopists removed the biopsy forceps first without and then with suctioning following contact with the sigmoid mucosa. A total of 50 L of air was collected continuously for 30 seconds at 30-cm distance from the biopsy channel valve of the colonoscope, with time starting at forceps removal. Airborne bacteria were collected by an impactor air sampler (MAS-100). Standard Petri dishes with CNA blood agar were used to culture Gram-positive bacteria. Main outcome measure was the bacterial load in endoscopy room air. At the beginning and end of the daily colonoscopy program, the median (and interquartile [IQR] range) bioaerosol burden was 4 colony forming units (CFU)/m (3) (IQR 3 - 6) and 16 CFU/m (3) (IQR 13 - 18), respectively. Air suctioning during removal of the biopsy forceps reduced the bioaerosol burden from a median of 14 CFU/m (3) (IQR 11 - 29) to a median of 7 CFU/m (3) (IQR 4 - 16) ( P = 0.0001). Predominantly enterococci were identified on the agar plates. The bacterial aerosol burden during handling of biopsy forceps can be reduced by applying air suction while removing the forceps. This simple method may reduce transmission of infectious agents during gastrointestinal endoscopies. Copyright Georg Thieme Verlag KG Stuttgart . New York.

Spectroscopic techniques for assessing the possible use of phosphate rock by-products for the removal of trace elements in soils.

Science.gov (United States)

Martinez-Sanchez, M. J.; Perez-Sirvent, C.; Garcia-Lorenzo, M. L.; Bech, J.; Hernandez-Cordoba, M.

2012-04-01

The production of fertilizers from apatite results in the obtention of considerable amounts of phosphate rock byproducts, representing a serious environmental problem. In addition, soil contamination with heavy metals due to mining or metallurgical activities is a severe environmental problem, increased when soil use is changed to agricultural or urban uses. The aim of this work was to study the possibility of using phosphate rock byproducts for the in situ treatment of soils polluted by heavy metals, allowing to revalorise phosphate rock residues and at the same time, providing a low-cost solution for the contaminated soil. The following methodologies were applied in order to characterise minerals phases present in phosphate rock residues: Wavelength Dispersive X-Ray Spectrometry (WDXRF), Scanning Electron Microscopy (SEM), Energy Dispersive X-Ray Spectrometry (EDS), thermogravimetry (TG) and Fourier Transform Infrared Spectroscopy (FTIR). The results obtained showed that the samples studied had a fine texture, showing average contents of 71%, 24% of sand and 5% for silt, sand and clay, respectivaly. In addition, these materials showed basic-neutral pH values (7.5-9) and a cationic interchange capacity of 20.4 meq/100g. Studied samples showed a 22% of carbonates and a 13% of apatite in their composition and all of them showed 4 bands at 1.100, 1.044, 674 y 576 cm-1, corresponding to P-O vibrations in PO4 groups. OH band vibrations appeared at 3.700-3.550 cm-1, and detected band at 3.400 cm-1 and 633 cm-1 could correspond to occluded water. On the other hand, detected bands at 1.460-1.430, 874 cm-1 suggested the presence of CaCO3 and carbonates in the apatite. After sample characterization, the performance of these residues to adsorb trace element ions (Cd+2 and Pb+2) from acidic aqueous solutions (simulating acidic mine drainage) was studied. The use of spectroscopic techniques after mixing soils and phosphate rock products demonstrate that these residues could be

A multi-disciplinary approach to the removal of emerging contaminants in municipal wastewater treatment plans in New York State, 2003-2004

Science.gov (United States)

Philips, Patrick J.; Stinson, Beverley; Zaugg, Steven D.; Furlong, Edward T.; Kolpin, Dana W.; Esposito, Kathleen; Bodniewicz, B.; Pape, R.; Anderson, J.

2005-01-01

Across the United States, there is a rapidly growing awareness of the occurrence and the toxicological impacts of natural and synthetic trace compounds in the environment. These trace compounds, referred to as emerging contaminants (ECs), are reported to cause a range of negative impacts in the environment, such as adverse effects on biota in receiving streams and interference with the normal functions of the endocrine system, which controls growth and development in living organisms.

A review on the application of constructed wetlands for the removal of priority substances and contaminants of emerging concern listed in recently launched EU legislation

International Nuclear Information System (INIS)

Gorito, Ana M.; Ribeiro, Ana R.; Almeida, C.M.R.; Silva, Adrián M.T.

2017-01-01

The presence of organic pollutants in the aquatic environment, usually found at trace concentrations (i.e., between ng L −1 and μg L −1 or even lower, known as micropollutants), has been highlighted in recent decades as a worldwide environmental concern due to their difficult elimination by conventional water and wastewater treatment processes. The relevant information on constructed wetlands (CWs) and their application for the removal of a specific group of pollutants, 41 organic priority substances/classes of substances (PSs) and 8 certain other substances with environmental quality standards (EQS) listed in Directive 2013/39/EU as well as 17 contaminants of emerging concern (CECs) of the Watch List of Decision 2015/495/EU, is herein reviewed. Studies were found for 24 PSs and 2 other substances with EQS: octylphenol, nonylphenol, perfluorooctane sulfonic acid, di(2-ethylhexyl)phthalate, trichloromethane, dichloromethane, 1,2-dichloroethane, pentachlorobenzene, benzene, polychlorinated dibenzo-p-dioxins, naphthalene, fluoranthene, trifluralin, alachlor, isoproturon, diuron, tributyltin compounds, simazine, atrazine, chlorpyrifos (chlorpyrifos-ethyl), chlorfenvinphos, hexachlorobenzene, pentachlorophenol, endosulfan, dichlorodiphenyltrichloroethane (or DDT) and dieldrin. A few reports were also published for 8 CECs: imidacloprid, erythromycin, clarithromycin, azithromycin, diclofenac, estrone, 17-beta-estradiol and 17-alpha-ethinylestradiol. No references were found for the other 17 PSs, 6 certain other substances with EQS and 9 CECs listed in EU legislation. - Highlights: • Directive 2013/39/EU includes 41 organic priority substances/classes of substances. • Watch List of Decision 2015/495/EU defines 17 contaminants of emerging concern. • Removal of these water micropollutants by constructed wetlands (CWs) is reviewed. • The need to study removal by CWs of more of these substances is emphasized. • More works with realistic concentrations

Vegetated Treatment Systems for Removing Contaminants Associated with Surface Water Toxicity in Agriculture and Urban Runoff.

Science.gov (United States)

Anderson, Brian S; Phillips, Bryn M; Voorhees, Jennifer P; Cahn, Michael

2017-05-15

Urban stormwater and agriculture irrigation runoff contain a complex mixture of contaminants that are often toxic to adjacent receiving waters. Runoff may be treated with simple systems designed to promote sorption of contaminants to vegetation and soils and promote infiltration. Two example systems are described: a bioswale treatment system for urban stormwater treatment, and a vegetated drainage ditch for treating agriculture irrigation runoff. Both have similar attributes that reduce contaminant loading in runoff: vegetation that results in sorption of the contaminants to the soil and plant surfaces, and water infiltration. These systems may also include the integration of granulated activated carbon as a polishing step to remove residual contaminants. Implementation of these systems in agriculture and urban watersheds requires system monitoring to verify treatment efficacy. This includes chemical monitoring for specific contaminants responsible for toxicity. The current paper emphasizes monitoring of current use pesticides since these are responsible for surface water toxicity to aquatic invertebrates.

Contamination analysis unit

International Nuclear Information System (INIS)

Gregg, H.R.; Meltzer, M.P.

1996-01-01

The portable Contamination Analysis Unit (CAU) measures trace quantities of surface contamination in real time. The detector head of the portable contamination analysis unit has an opening with an O-ring seal, one or more vacuum valves and a small mass spectrometer. With the valve closed, the mass spectrometer is evacuated with one or more pumps. The O-ring seal is placed against a surface to be tested and the vacuum valve is opened. Data is collected from the mass spectrometer and a portable computer provides contamination analysis. The CAU can be used to decontaminate and decommission hazardous and radioactive surfaces by measuring residual hazardous surface contamination, such as tritium and trace organics. It provides surface contamination data for research and development applications as well as real-time process control feedback for industrial cleaning operations and can be used to determine the readiness of a surface to accept bonding or coatings. 1 fig

Octanol-solubility of dissolved and particulate trace metals in contaminated rivers: implications for metal reactivity and availability

International Nuclear Information System (INIS)

Turner, Andrew; Mawji, Edward

2005-01-01

The lipid-like, amphiphilic solvent, n-octanol, has been used to determine a hydrophobic fraction of dissolved and particulate trace metals (Al, Cd, Co, Cu, Mn, Ni, Pb, Zn) in contaminated rivers. In a sample from the River Clyde, southwest Scotland, octanol-solubility was detected for all dissolved metals except Co, with conditional octanol-water partition coefficients, D ow , ranging from about 0.2 (Al and Cu) to 1.25 (Pb). In a sample taken from the River Mersey, northwest England, octanol-solubility was detected for dissolved Al and Pb, but only after sample aliquots had been spiked with individual ionic metal standards and equilibrated. Spiking of the River Clyde sample revealed competition among different metals for hydrophobic ligands. Metal displacement from hydrophobic complexes was generally most significant following the addition of ionic Al or Pb, although the addition of either of these metals had little effect on the octanol-solubility of the other. In both river water samples hydrophobic metals were detected on the suspended particles retained by filtration following their extraction in n-octanol. In general, particulate Cu and Zn (up to 40%) were most available, and Al, Co and Pb most resistant ( 3.3 -10 5.3 ml g -1 . The presence of hydrophobic dissolved and particulate metal species has implications for our understanding of the biogeochemical behaviour of metals in aquatic environments. Specifically, such species are predicted to exhibit characteristics of non-polar organic contaminants, including the potential to penetrate the lipid bilayer. Current strategies for assessing the bioavailability and toxicity of dissolved and particulate trace metals in natural waters may, therefore, require revision. - New approaches are presented for fractionating trace metals in natural waters

Diagnostic de contamination des agrosystèmes périurbains de Dakar par les éléments traces métalliques

Directory of Open Access Journals (Sweden)

Hodomihou, NR.

2016-01-01

Full Text Available Diagnosis of periurban Dakar (Senegal agrosystem contamination by trace elements. Description of the subject. Urban and periurban market gardening is widespread in the Dakar area of Senegal. Repeated long-term application of organic matter results in high inputs of trace elements (TE. Objectives. The aim is to assess TE contamination in suburban agrosystems. Method. At four sites, we compared the Cu, Zn, Pb and Cd content in the surface layers and sublayers of plots cultivated over a long period with the content found in adjacent uncultivated plots. Results. The two prevailing soil types (Arenosol and Fluvisol were characterized by significantly different background soil geochemical TE content. In the 0 – 20 and 20 – 40 cm soil layers at the four studied sites, TE content was significantly higher (p < 0.05 in the cultivated plots than in the non-cultivated plots. Arenosols showed a significantly higher (p < 0.05 TE content than Fluvisols. An exception to these results was found in cultivated Arenosols, where Cd, Cu, Zn and Pb contamination was observed. This could be explained by the frequent input into these soils of sewage sludge, poultry droppings, and irrigation with only partially treated wastewater. Cadmium contamination of cultivated Fluvisols was the result of regular natural phosphate inputs, as observed throughout the soil profile. Conclusions. Analysis of soils and organic matters would enable adjustment of the quantities of organic matter applied and could lead to a reduction in TE contamination within these agroecosystems.

Removal factor determination of some local smear papers for surface contamination smear test

International Nuclear Information System (INIS)

Suratman; Indriyotomo, D.; Aminjoyo, S.

1996-01-01

Removal factor determination of some local smear papers has been done, using dry smear test method. The aim of this research is to find removal values of local smear papers on some surfaces, to replace import smear papers. Smear test was done on the various surfaces i.e.: porcelain, formica, glass, stainless steel, steel and PVC, with the local smear papers I.e.: Padalarang, Diagonal, Concorde, Marga, Hard Cloth, and import smear paper. The artificial contaminant which used were I-131 and P-32. The removal factor values of Padalarang paper for surfaces: porcelain, formica, glass stainless steel, steel and PVC were: 24.5%, 20.0%, 27.0%, 6.8%, 4.9%, and 13.6% respectively. The removal factor values of Diagonal paper were:18.4%, 15.9%, 5.7%, 3.5%, and 9.1% respectively. The removal factor values of concord paper were: 18.5%, 20.3%, 23.1%, 6.6%, 3.8%, and 9.0% respectively. The removal factor values of Marga paper were: 16.7%, 13.5%, 21.1%, 4.2%, 4.1% and 8.1% respectively. The removal factor values of Hard Cloth were: 18.6%, 12.6%, 20.5%, 8.2%, and 10.1% respectively. The removal factor values of import smear paper were: 17.8%, 15.0%, 18.8%, 9.1%, 4.8%, and 14.4% respectively . Substitution alternative of import smear paper is Padalarang. (author)

The Removal of Confidor Pesticide by Different Species of Trichoderma Fungi from Contaminated Waters

Directory of Open Access Journals (Sweden)

Hossein Banejad

2017-01-01

Full Text Available Introduction: Pesticides are considered as the most important pollutants in surface water and groundwater. Neonicotinoids are new group of insecticides, derived from nicotine. Their physicochemical properties render them useful for a wide range of application techniques, including foliar, seed treatment, soil drench and stem applications. Confidor, the representative of the first generation of neonicotinoid insecticides, was patented in 1985 by Bayer and was placed on the market in 1991. The Canadian Pest Management Regulatory Agency considers confidor to have high potential for surface water contamination, leaching to groundwater and persistence in soils. Biodegradation is one of the most effective ways to destroy pesticides in the environment. The application of Bioremediation techniques is taken into consideration as an option to reduce or remove pollutants from the environment due to their low cost, high efficiency and environmentally friendly features. Bioremediation by using microorganisms has not any adverse effect after cleanup. The accumulator microorganism species, haven’t pathogenic properties and aren’t the cause of disease on the other organisms. The selection of a biomass for using in bioremediation is very important, it should be abundant in environment and adapted to environmental conditions. The aim of this study was to investigate the ability of various species of Trichoderma fungi to remove Confidor from contaminated water influenced by variables like pH, concentration of the confidor and time. Materials and Methods: In order to conduct this study three different fungal species belonging to the genus Trichoderma were used. The samples were transferred to PDA (Potato Dextrose Agar sterile solid media for in vitro testing usage. The samples were kept in refrigerator at 4◦C temperature, after the fungal biomass reached to maximal growth; the colonies were transferred to new media and used in our experiments as resources

REMOVAL OF MERCURY FROM CONTAMINATED SOILS AT THE PAVLODAR CHEMICAL PLANT.

Energy Technology Data Exchange (ETDEWEB)

KHRAPUNOV, V. YE.; ISAKOVA, R.A.; LEVINTOV, B.L.; KALB, P.D.; KAMBEROV, I.M.; TREBUKHOV, A.

2004-09-25

Soils beneath and adjacent to the Pavlodar Chemical Plant in Kazakhstan have been contaminated with elemental mercury as a result of chlor alkali processing using mercury cathode cell technology. The work described in this paper was conducted in preparation for a demonstration of a technology to remove the mercury from the contaminated soils using a vacuum assisted thermal distillation process. The process can operate at temperatures from 250-500 C and pressures of 0.13kPa-1.33kPa. Following vaporization, the mercury vapor is cooled, condensed and concentrated back to liquid elemental mercury. It will then be treated using the Sulfur Polymer Stabilization/Solidification process developed at Brookhaven National Laboratory as described in a companion paper at this conference. The overall project objectives include chemical and physical characterization of the contaminated soils, study of the influence of the soil's physical-chemical and hydro dynamical characteristics on process parameters, and laboratory testing to optimize the mercury sublimation rate when heating in vacuum. Based on these laboratory and pilot-scale data, a full-scale production process will be designed for testing. This paper describes the soil characterization. This work is being sponsored by the International Science and Technology Center.

Removal of contaminants in a paper mill effluent by Azolla caroliniana

Directory of Open Access Journals (Sweden)

D. Sivakumar

2015-09-01

Full Text Available This study was focused on removal of various parameters in paper mill effluent using a method called bioremediation by Azolla caroliniana.  The experimental investigations have been carried out using Azolla caroliniana for conducting the sorption study with various dilution ratios (2, 4, 6, 8, and 10, pH (3, 4, 5, 6, 7, 8 and 9 and biomass (200, 400, 600, 800 and 1000 g. The maximum removal percentage of TDS, BOD and COD in a paper mill effluent was obtained at the optimum dilution ratio of 6, pH of 8 and biomass of 800 g. The results of this study indicated that the maximum removal percentage of TDS, BOD and COD in a paper mill effluent was 82.3 %, 88.6 % and 79.1 % respectively.  Also, the study focused on uptake of TDS, BOD and COD in paper mill effluent by Azolla caroliniana through bioaccumulation factor and translocation factor. The results of bioaccumulation factor revealed that TDS, BOD and COD in paper mill effluent were adsorbed by Azolla caroliniana.  The results of translocation factor revealed that the roots of Azolla caroliniana translocate the TDS, BOD and COD in a paper mill effluent to the shoots of Azolla caroliniana. From the results, this study concluded that bioremediation by Azolla caroliniana could be effectively used for removing TDS, BOD and COD in a paper mill effluent. This study also suggested that Azolla caroliniana may be used for removing various contaminants, not only from paper mill effluent, but also from any other industrial effluents.

Natural and anthropogenic trace metal contamination and load assessment in the Oum Er-Rbia river basin, Morocco

International Nuclear Information System (INIS)

Schone, Selina; Zahry, Fatiha; Matschullat, Jorg; Bounakhla, Moussa

2008-01-01

Due to natural constraints and its fast socio-economic development Morocco is confronted with serious problems both in terms of water quantity and water quality management. In order to counteract the water quality degradation a comprehensive understanding of the geochemical and hydrological functioning as well as the bahavior of inorganic contaminants in large riverine systems under semiarid conditions shall be developed within the scope of this pilot study. Within the scope of a dissertation project Mrs Zahry has already investigated the physical and geochemical characteristics of the oum Er-Rbia river basin in Morocco. Water, sediment and suspended matter samples were analyzed in order to assess the trace metal contamination of the river. Due to the lack of the local geochemical backgrounds levels the results were normalised to common international standards. But because of the spatial and temporal variability of the geochemical background global standards are not appropriate to answer regional and local problems. Following up the work of Mrs Zahry the project shall for the first time ever in Morocco provide local geochemical backgrounds levels of various media in the large-scale Oum ErRbia river basin to establish regional geochemical standards and to assess the watercourse contamination in terms of anthropogenic contributions of trace metals. The research project will be conducted in cooperation between the CNESTEN, Morocco and the Technical University Bergakademie Freiberg in Germany. The project has started of the aquisation of geo-basis data to develop a sampling strategy. All field investigations (sampling, run-off measurements), analytical work and data analysis will be done in direct collaboration with the Moroccan Scientists [fr

The use of some local plants for removal of radioactive and trace elements from aqueous media

International Nuclear Information System (INIS)

Al-Masri, M. S.; Amin, Y.; Al-Akel, B; Al-Naama, T.

2008-02-01

The removal of metal ions from aqueous solutions by biosorption plays an important role in water pollution control. In this study, dried leaves of Barbary, Jew's mallow and poplar, branches of poplar trees and creeping club as biomass for removal of toxic elements (Cd, Pb and U) and some radionuclides ( 133 Ba, 137 Cs and 226 Ra) from aqueous solution have been evaluated. The results show that all studied plants can be effectively used for removing U and Ba from aqueous solutions, while Pb was removed using branches of poplar trees. In addition, Cd was removed using Barbary, Jew's mallow and branches of poplar trees. The adsorption of U and Cd by leaves of Barbary reached 3.3 mg g -1 and 3.5 mg g -1 , respectively. Moreover, the leaves of poplar trees were the best plant for biosorping Pb, its maximum capacity reached a value 1.7 mg g -1 . On the other hand, the maximum capacity for studied radionuclide was less than 10-6 mg g -1 . Further more, the effect of many factors such as, plant pretreatment, solution temperature, pH, plant particles size and contact time, on biosorption process were performed and the best conditions of biosorption were recognized. The studied plants were used for removing 226 Ra and some trace elements from real polluted water. The results show that the method is effective.(author)

Supported Photocatalyst for Removal of Emerging Contaminants from Wastewater in a Continuous Packed-Bed Photoreactor Configuration

Directory of Open Access Journals (Sweden)

Mª Emma Borges

2015-02-01

Full Text Available Water pollution from emerging contaminants (ECs or emerging pollutants is an important environmental problem. Heterogeneous photocatalytic treatment, as advanced oxidation treatment of wastewater effluents, has been proposed to solve this problem. In this paper, a heterogeneous photocatalytic process was studied for emergent contaminants removal using paracetamol as a model contaminant molecule. TiO2 photocatalytic activity was evaluated using two photocatalytic reactor configurations: Photocatalyst solid suspension in wastewater in a stirred photoreactor and TiO2 supported on glass spheres (TGS configuring a packed bed photoreactor. The surface morphology and texture of the TGS were monitored by scanning electron microscope (SEM. The influence of photocatalyst amount and wastewater pH were evaluated in the stirred photoreactor and the influence of wastewater flowrate was tested in the packed bed photoreactor, in order to obtain the optimal operation conditions. Moreover, results obtained were compared with those obtained from photolysis and adsorption studies, using the optimal operation conditions. Good photocatalytic activities have been observed and leads to the conclusion that the heterogeneous photocatalytic system in a packed bed is an effective method for removal of emerging pollutants.

Tracing and analytical results of the dioxin contamination incident in 2008 originating from the Republic of Ireland.

Science.gov (United States)

Heres, L; Hoogenboom, R; Herbes, R; Traag, W; Urlings, B

2010-12-01

High levels of dioxins (PCDD/Fs) in pork were discovered in France and the Netherlands at the end of 2008. The contamination was rapidly traced back to a feed stock in the Republic of Ireland (RoI). Burning oil, used for the drying of bakery waste, appeared to be contaminated with PCBs. Consequently, very high levels up to 500 pg TEQ g⁻¹ fat were found in pork. The congener pattern clearly pointed to PCB-oil as a source, but the ratio between the non-dioxin-like indicator PCBs (PCBs 28, 52, 101, 138, 152 and 180) and PCDD/Fs was much lower than observed during the Belgian incident, thereby limiting the suitability of indicator PCBs as a marker for the presence of dioxins and dioxin-like PCBs. This paper describes the tracking and tracing of the incident, the public-private cooperation, the surveillance activities and its results. A major lesson to be learned from this incident is the importance of good private food safety systems. In this incident, it was the private surveillance systems that identified the origin of contamination within 10 days after the first signal of increased dioxin levels in a product. On the other hand, retrospective analyses showed that signals were missed that could have led to an earlier detection of the incident and the source. Above all, the incident would not have occurred when food safety assurance systems had been effectively implemented in the involved feed chain. It is discussed that besides primary responsibility for effective private food safety systems, the competent authorities have to supervise whether the food safety procedures are capable of coping with these kinds of complex food safety issues, while private food companies need to implement the law, and public authorities should supervise and enforce them. Finally, it is discussed whether the health risks derived from consumption of the contaminated batches of meat may have been underestimated during the incident due to the unusually high intake of dioxins.

Combination of biochar amendment and phytoremediation for hydrocarbon removal in petroleum-contaminated soil

OpenAIRE

Han, Tao; Zhao, Zhipeng; Bartlam, Mark; Wang, Yingying

2016-01-01

Remediation of soils contaminated with petroleum is a challenging task. Four different bioremediation strategies, including natural attenuation, biochar amendment, phytoremediation with ryegrass, and a combination of biochar and ryegrass, were investigated with greenhouse pot experiments over a 90-day period. The results showed that planting ryegrass in soil can significantly improve the removal rate of total petroleum hydrocarbons (TPHs) and the number of microorganisms. Within TPHs, the rem...

Kinetics of trace metal removal from tidal water by mangrove sediments under different redox conditions

International Nuclear Information System (INIS)

Suzuki, K.N.; Machado, E.C.; Machado, W.; Bellido, A.V.B.; Bellido, L.F.; Osso, J.A.; Lopes, R.T.

2014-01-01

The extent in which redox conditions can affect the removal kinetics of 58 Co and 65 Zn from tidal water by mangrove sediments was evaluated in microcosm experiments, simulating a tidal flooding period of 6 h. The average half-removal time (t 1/2 ) of 58 Co from overlaying water was slightly higher (7.3 h) under an N 2 -purged water column than under an aerated water column (5.4 h). A lower difference was found for 65 Zn (1.9 h vs. 1.5 h, respectively). Average removals of 58 Co activities from water were 54.6% (N 2 treatment) and 43.5% (aeration treatment), whereas these values were 88.0% and 92.7% for 65 Zn, respectively. Very contrasting sorption kinetics of different radiotracers occurred, while more oxidising conditions favoured only a slightly higher removal. Average 58 Co and 65 Zn inventories within sediments were 30.4% and 18.8% higher in the aeration treatment, respectively. A stronger particle-reactive behaviour was found for 65 Zn that was less redox-sensitive and more efficiently removed by sediments than 58 Co. - Highlights: ► Radiotracer experiments evidenced the role of mangrove sediments in trapping trace metals. ► Very contrasting removal kinetics from tidal water were observed for 65 Zn and 58 Co. ► Nearly 40%–50% of 58 Co activities and nearly 90% of 65 Zn activities in overlying water were removed. ► 65 Zn showed a stronger particle-reactive behaviour than observed for 58 Co. ► 58 Co was more sensitive to redox conditions in tidal water than observed for 65 Zn

Engineering evaluation/cost analysis for the proposed removal of contaminated materials from Pad 1 at the Elza Gate site, Oak Ridge, Tennessee

International Nuclear Information System (INIS)

1990-06-01

This engineering evaluation/cost analysis (EE/CA) has been prepared in support of the proposed removal action for cleanup of radioactively contaminated concrete and soil beneath a building on privately owned commercial property in Oak Ridge, Tennessee. The property, known as the Elza Gate site, became contaminated with uranium-238, radium-226, thorium-232, thorium-230, and decay products as a result of the Manhattan Engineer District storing uranium ore and ore processing residues at the site in the early 1940s. The US Department of Energy (DOE) has responsibility for cleanup of the property under its Formerly Utilized Sites Remedial Action Program (FUSRAP). The DOE plans to remove the cracked and worn concrete pad and contaminated subsoil beneath the pad, after which the property owner/tenant will provide clean backfill and new concrete. Portions of the pad and subsoil are contaminated and, if stored or disposed of improperly, may represent a potential threat to public health or welfare and the environment. The EE/CA report is the appropriate documentation for the proposed removal action, as identified in guidance from the US Environmental Protection Agency. the objective of the EE/CA report, in addition to identifying the planned removal action, is to document the selection of response activities that will mitigate the potential for release of contaminants from the property into the environment and minimize the related threats to public health or welfare and the environment. 7 refs., 2 figs., 3 tabs

Engineering evaluation/cost analysis for the proposed removal of contaminated materials from pad 1 at the Elza Gate site, Oak Ridge, Tennessee

International Nuclear Information System (INIS)

1990-09-01

This engineering evaluation/cost analysis (EE/CA) has been prepared in support of the proposed removal action for cleanup of radioactively contaminated concrete and soil beneath a building on privately owned commercial property in Oak Ridge, Tennessee. The property, known as the Elza Gate site, became contaminated with uranium-238, radium-226, thorium-232, thorium-230, and decay products as a result of the Manhattan Engineer District storing uranium ore and ore processing residues at the site in the early 1940s. The US Department of Energy (DOE) has responsibility for cleanup of the property under its Formerly Utilized Sites Remedial Action Program (FUSRAP). The DOE plans to remove the cracked and worn concrete pad and contaminated subsoil beneath the pad, after which the property owner/tenant will provide clean backfill and new concrete. Portions of the pad and subsoil are contaminated and, if stored or disposed of improperly, may represent a potential threat to public health or welfare and the environment. The EE/CA report is the appropriate documentation for the proposed removal action, as identified in guidance from the US Environmental Protection Agency. The objective of the EE/CA report, in addition to identifying the planned removal action, is to document the selection of response activities that will mitigate the potential for release of contaminants from the property into the environment and minimize the related threats to public health or welfare and the environment. 7 refs., 2 figs., 3 tabs

In situ electro-osmotic cleanup of tar contaminated soil—Removal of polycyclic aromatic hydrocarbons

KAUST Repository

Lima, Ana T.

2012-12-01

An in situ electro-osmosis experiment was set up in a tar contaminated clay soil in Olst, the Netherlands, at the site of a former asphalt factory. The main goal of this experiment was to remove polycyclic aromatic hydrocarbons (PAHs) from the contaminated clay layer by applying an electric gradient of 12 V m-1 across the soil over an electrode distance of 1 m. With the movement of water by electro-osmosis and the addition of a non-ionic surfactant (Tween 80), the non-polar PAHs were dragged along by convection and removed from the fine soil fraction. Soil samples were taken at the start and after 159 days at the end of the experiment. Water at the electrode wells was sampled regularly during the course of the experiment. The results reflect the heterogeneity of the soil characteristics and show the PAH concentrations within the experimental set up. After first having been released into the anolyte solution due to extraction by Tween 80 and subsequent diffusion, PAH concentrations increased significantly in the electrode reservoirs at the cathode side after 90 days of experiment. Although more detailed statistical analysis is necessary to quantify the efficiency of the remediation, it can be concluded that the use of electro-osmosis together with a non-ionic surfactant is a feasible technique to mobilize non-polar organic contaminants in clayey soils. Crown Copyright © 2011 Published by Elsevier Ltd. All rights reserved.

Octanol-solubility of dissolved and particulate trace metals in contaminated rivers: implications for metal reactivity and availability

Energy Technology Data Exchange (ETDEWEB)

Turner, Andrew [School of Earth, Ocean and Environmental Sciences, University of Plymouth, Drake Circus, Plymouth PL4 8AA (United Kingdom)]. E-mail: aturner@plymouth.ac.uk; Mawji, Edward [School of Earth, Ocean and Environmental Sciences, University of Plymouth, Drake Circus, Plymouth PL4 8AA (United Kingdom)

2005-05-01

The lipid-like, amphiphilic solvent, n-octanol, has been used to determine a hydrophobic fraction of dissolved and particulate trace metals (Al, Cd, Co, Cu, Mn, Ni, Pb, Zn) in contaminated rivers. In a sample from the River Clyde, southwest Scotland, octanol-solubility was detected for all dissolved metals except Co, with conditional octanol-water partition coefficients, D{sub ow}, ranging from about 0.2 (Al and Cu) to 1.25 (Pb). In a sample taken from the River Mersey, northwest England, octanol-solubility was detected for dissolved Al and Pb, but only after sample aliquots had been spiked with individual ionic metal standards and equilibrated. Spiking of the River Clyde sample revealed competition among different metals for hydrophobic ligands. Metal displacement from hydrophobic complexes was generally most significant following the addition of ionic Al or Pb, although the addition of either of these metals had little effect on the octanol-solubility of the other. In both river water samples hydrophobic metals were detected on the suspended particles retained by filtration following their extraction in n-octanol. In general, particulate Cu and Zn (up to 40%) were most available, and Al, Co and Pb most resistant (<1%) to octanol extraction. Distribution coefficients defining the concentration ratio of octanol-soluble particle-bound metal to octanol-soluble dissolved metal were in the range 10{sup 3.3}-10{sup 5.3} ml g{sup -1}. The presence of hydrophobic dissolved and particulate metal species has implications for our understanding of the biogeochemical behaviour of metals in aquatic environments. Specifically, such species are predicted to exhibit characteristics of non-polar organic contaminants, including the potential to penetrate the lipid bilayer. Current strategies for assessing the bioavailability and toxicity of dissolved and particulate trace metals in natural waters may, therefore, require revision. - New approaches are presented for fractionating

Waste treatment process for removal of contaminants from aqueous, mixed-waste solutions using sequential chemical treatment and crossflow microfiltration, followed by dewatering

Science.gov (United States)

Vijayan, S.; Wong, C.F.; Buckley, L.P.

1994-11-22

In processes of this invention aqueous waste solutions containing a variety of mixed waste contaminants are treated to remove the contaminants by a sequential addition of chemicals and adsorption/ion exchange powdered materials to remove the contaminants including lead, cadmium, uranium, cesium-137, strontium-85/90, trichloroethylene and benzene, and impurities including iron and calcium. Staged conditioning of the waste solution produces a polydisperse system of size enlarged complexes of the contaminants in three distinct configurations: water-soluble metal complexes, insoluble metal precipitation complexes, and contaminant-bearing particles of ion exchange and adsorbent materials. The volume of the waste is reduced by separation of the polydisperse system by cross-flow microfiltration, followed by low-temperature evaporation and/or filter pressing. The water produced as filtrate is discharged if it meets a specified target water quality, or else the filtrate is recycled until the target is achieved. 1 fig.

The use of carbonate lixiviants to remove uranium from uranium-contaminated soils

International Nuclear Information System (INIS)

Francis, C.W.; Lee, S.Y.; Wilson, J.H.; Timpson, M.E.; Elless, M.P.

1997-01-01

The objective of this research was to design an extraction media and procedure that would selectively remove uranium without adversely affecting the soils' physicochemical characteristics or generating secondary waste forms difficult to manage or dispose of. Investigations centered around determining the best lixivant and how the various factors such as pH, time, and temperature influenced extraction efficiency. Other factors investigated included the influence of attrition scrubbing, the effect of oxidants and reductants and the recycling of lixiviants. Experimental data obtained at the bench- and pilot-scale levels indicated 80 to 95% of the uranium could be removed from the uranium-contaminated soils by using a carbonate lixiviant. The best treatment was three successive extractions with 0.25 M carbonate-bicarbonate (in presence of KMnO 4 as an oxidant) at 40 C followed with two water rinses

Tritium removal from contaminated water via infrared laser multiple-photon dissociation

International Nuclear Information System (INIS)

Maienschein, J.L.; Magnotta, F.; Herman, I.P.; Aldridge, F.T.; Hsiao, P.

1983-01-01

Isotope separation by means of infrared-laser multiple-photon dissociation offers an efficient way to recover tritium from contaminated light or heavy water found in fission and fusion reactors. For tritium recovery from heavy water, chemical exchange of tritium into deuterated chloroform is followed by selective laser dissociation of tritiated chloroform and removal of the tritiated photoproduct, TCl. The single-step separation factor is at least 2700 and is probably greater than 5000. Here we present a description of the tritium recovery process, along with recent accomplishments in photochemical studies and engineering analysis of a recovery system

Removal of both cationic and anionic contaminants by amphoteric starch.

Science.gov (United States)

Peng, Huanlong; Zhong, Songxiong; Lin, Qintie; Yao, Xiaosheng; Liang, Zhuoying; Yang, Muqun; Yin, Guangcai; Liu, Qianjun; He, Hongfei

2016-03-15

A novel amphoteric starch incorporating quaternary ammonium and phosphate groups was applied to investigate the efficiency and mechanism of cationic and anionic contaminant treatment. Its flocculation abilities for kaolin suspension and copper-containing wastewater were evaluated by turbidity reduction and copper removal efficiency, respectively. And the kinetics of formation, breakage and subsequent re-formation of aggregates were monitored using a Photometric Dispersion Analyzer (PDA) and characterized by flocculation index (FI). The results showed that amphoteric starch possessed the advantages of being lower-dosages-consuming and being stronger in shear resistance than cationic starch, and exhibited a good flocculation efficiency over a wide pH range from 3.0 to 11.0. Copyright © 2015 Elsevier Ltd. All rights reserved.

Phytotoxicity of trace metals in spiked and field-contaminated soils: Linking soil-extractable metals with toxicity.

Science.gov (United States)

Hamels, Fanny; Malevé, Jasmina; Sonnet, Philippe; Kleja, Dan Berggren; Smolders, Erik

2014-11-01

Soil tests have been widely developed to predict trace metal uptake by plants. The prediction of metal toxicity, however, has rarely been tested. The present study was set up to compare 8 established soil tests for diagnosing phytotoxicity in contaminated soils. Nine soils contaminated with Zn or Cu by metal mining, smelting, or processing were collected. Uncontaminated reference soils with similar soil properties were sampled, and series of increasing contamination were created by mixing each with the corresponding soil. In addition, each reference soil was spiked with either ZnCl2 or CuCl2 at several concentrations. Total metal toxicity to barley seedling growth in the field-contaminated soils was up to 30 times lower than that in corresponding spiked soils. Total metal (aqua regia-soluble) toxicity thresholds of 50% effective concentrations (EC50) varied by factors up to 260 (Zn) or 6 (Cu) among soils. For Zn, variations in EC50 thresholds decreased as aqua regia > 0.43 M HNO3  > 0.05 M ethylenediamine tetraacetic acid (EDTA) > 1 M NH4 NO3  > cobaltihexamine > diffusive gradients in thin films (DGT) > 0.001 M CaCl2 , suggesting that the last extraction is the most robust phytotoxicity index for Zn. The EDTA extraction was the most robust for Cu-contaminated soils. The isotopically exchangeable fraction of the total soil metal in the field-contaminated soils markedly explained the lower toxicity compared with spiked soils. The isotope exchange method can be used to translate soil metal limits derived from soils spiked with metal salts to site-specific soil metal limits. © 2014 SETAC.

Demonstration/Validation of a Surface Cleaning Control to Mitigate Storm Water Metal Contaminants

Science.gov (United States)

2014-04-01

added to a pre- weighed 125-ml low density polyethylene (LDPE) bottle. The particles were digested with 1.0 ml of concentrated trace metal grade (TMG...Sorenson. 2005. “ Residential Street-Dirt Accumulation Rates and Chemical Composition, and Removal Efficiencies by Mechanical- and Vacuum-Type...Bay, and M. Kayhanian. 2003. “A Review of the Contaminants and Toxicity Associated with Particles in Stormwater Runoff.” Caltrans CTSW-RT-03-059.73.15

Geochemical distribution of trace metals and organochlorine contaminants of a lake ontario shoreline marsh

Energy Technology Data Exchange (ETDEWEB)

Glooschenko, W A; Capocianco, J; Coburn, J; Glooschenko, V

1981-02-01

Rattray Marsh, an 8 ha marsh on the Lake Ontario shoreline at Mississauga, Ontario, is an important local habitat for waterfowl and shorebirds during spring and fall migration. A study was conducted to determine the distribution of nutrients (carbon, nitrogen, and phosphorus) and potential trace metal and organochlorine pollutants in the marsh as evidenced by the sedimentary concentrations of these compounds. Generally, copper, zinc, lead, and mercury were higher in concentration in local soils than in Lake Ontario sediments. Metals and organic carbon levels did not correlate, and the metals appeared to be associated with silts and clays. Organochlorine contaminants include p,p1-DDE, p,p1-DDD, p,p1-DDT, alpha-chlordane, PCB, mirex, and HCB.

Sequential injection on-line matrix removal and trace metal preconcentration using a PTFE beads packed column as demonstrated for the determination of cadmium by electrothermal atomic absorption spectrometry

DEFF Research Database (Denmark)

Wang, Jianhua; Hansen, Elo Harald

2002-01-01

A sequential injection (SI) on-line matrix removal and trace metal preconcentration procedure by using a novel microcolumn packed with PTFE beads is described, and demonstrated for trace cadmium analysis with detection by electrothermal atomic absorption spectrometry (ETAAS). The analyte...

Removal of heavy metals and organic contaminants from aqueous streams by novel filtration methods. 1998 annual progress report

International Nuclear Information System (INIS)

Rodriguez, N.M.

1998-01-01

'Graphite nanofibers are a new type of material consisting of nanosized graphite platelets where only edges are exposed. Taking advantage of this unique configuration the authors objective is: (1) To produce graphite nanofibers with structural properties suitable for the removal of contaminants from water. (2) To test the suitability of the material in the removal of organic from aqueous solutions. (3) To determine the ability of the nanofibers to function as an electrochemical separation medium the selective removal of metal contaminants from solutions. This report summarizes work after 1.5 of a 3-year project. During this period, efforts have been concentrated on the production, characterization and optimization of graphite nanofibers (GNF). This novel material has been developed in the laboratory from the metal catalyzed decomposition of certain hydrocarbons (1). The structures possess a cross-sectional area that varies between 5 to 100 nm and have lengths ranging from 5 to 100 mm (2). High-resolution transmission electron microscopy studies have revealed that the nanofibers consist of extremely well-ordered graphite platelets, which are oriented in various directions with respect to the fiber axis (3). The arrangement of the graphene layers can be tailored to a desired geometry by choice of the correct catalyst system and reaction conditions, and it is therefore possible to generate structures where the layers are stacked in a ribbon, herring-bone, or stacked orientation. The research has been directed on two fronts: (a) the use of the material for the removal of organic contaminants, and (b) taking advantage of the high electrical conductivity as well as high surface area of the material to use it as electrode for the electrochemical removal of metal pollutants from aqueous streams.'

A comparison of phytoremediation capability of selected plant species for given trace elements

International Nuclear Information System (INIS)

Fischerova, Zuzana; Tlustos, Pavel; Jirina Szakova; Kornelie Sichorova

2006-01-01

In our experiment, As, Cd, Pb, and Zn remediation possibilities on medium contaminated soil were investigated. Seven plant species with a different trace element accumulation capacity and remediation potential were compared. We found good accumulation capabilities and remediation effectiveness of Salix dasyclados similar to studied hyperaccumulators (Arabidopsis halleri and Thlaspi caerulescens). We have noticed better remediation capability in willow compared to poplar for most of the elements considered in this experiment. On the contrary, poplar species were able to remove a larger portion of Pb as opposed to other species. Nevertheless, the removed volume was very small. The elements found in plant biomass depend substantially on the availability of these elements in the soil. Different element concentrations were determined in natural soil solution and by inorganic salt solution extraction (0.01 mol L -1 CaCl 2 ). Extracted content almost exceeded the element concentration in the soil solution. Element concentrations in soil solution were not significantly affected by sampling time. - Selected accumulator trees grown on medium contaminated soil may have remediation capacity similar to hyperaccumulator species

Development of sustainable Palladium-based catalysts for removal of persistent contaminants from drinking water

Science.gov (United States)

Shuai, Danmeng

Pd-based catalytic reduction has emerged as an advanced treatment technology for drinking water decontamination, and a suite of persistent contaminants including oxyanions, N-nitrosoamines, and halogenated compounds are amenable to catalytic reduction. The primary goal of this study is to develop novel Pd-based catalysts with enhanced performance (i.e., activity, selectivity, and sustainability) to remove contaminants from drinking water. The effects of water quality (i.e., co-contaminants in water matrix), catalyst support, and catalyst metal were explored, and they provide insights for preparing catalysts with faster kinetics, higher selectivity, and extended lifetime. Azo dyes are wide-spread contaminants, and they are potentially co-exisiting with target contaminants amenable for catalytic removal. The probe azo dye methyl orange (MO) enhanced catalytic reduction kinetics of a suite of oxyanions (i.e., nitrate, nitrite, bromate, chlorate, and perchlorate) and diatrizoate significantly but not N-nitrosodimethylamine (NDMA) with a variety of Pd-based catalysts. Nitrate was selected as a probe contaminant, and several different azo dyes (i.e., (methyl orange, methyl red, fast yellow AB, metanil yellow, acid orange 7, congo red, eriochrome black T, acid red 27, acid yellow 11, and acid yellow 17) were evaluated for their ability to enhance reduction. A hydrogen atom shuttling mechanism was proposed and a kinetic model was proposed based on Bronsted-Evans-Polanyi (BEP) theory, and they suggest sorbed azo dyes and reduced hydrazo dyes shuttle hydrogen atoms to oxyanions or diatrizoate to enhance their reduction kinetics. Next, vapor-grown carbon nanofiber (CNF) supports were used to explore the effects of Pd nanoparticle size and interior versus exterior loading on nitrite reduction activity and selectivity (i.e., dinitrogen over ammonia production). In order to evaluate the amount of interior versus exterior loading of Pd nanoparticles, a fast and accurate geometric

Field testing the effectiveness of pumping to remove sulfur hexafluoride traced drilling air from a prototype borehole near superior, Arizona

International Nuclear Information System (INIS)

Peters, C.A.; Striffler, P.; Yang, I.C.; Ferarese, J.

1993-01-01

The US Geological Survey (USGS), Department of the Interior is conducting studies at Yucca Mountain, Nevada, to provide hydrologic, hydrochemical, and geologic information to evaluate the suitability of Yucca Mountain for development as a high-level nuclear-waste repository. The USGS unsaturated-zone hydrochemistry study involves the collection of gas and water samples from the unsaturated zone for chemical and isotopic analyses. Results from these analyses will aid in the understanding of the movement of gas and water in the rock units at Yucca Mountain. A prototype borehole designated USW UZP5 was drilled by the US Department of Energy, Yucca Mountain Site Characterization Project Office (DOE, YMSCPO) in June 1990 in the Apache Leap Tuff of southcentral Arizona. The hole was dry drilled with air using sulfur hexafluoride (SF 6 ) as a tracer. This drilling method simulated that which will be used to drill boreholes for the collection of gas and water samples at Yucca Mountain. The purpose of tracing the drilling air is to quantify its removal by pumping, prior to sampling of in situ gases. The objectives of our work in Arizona were to: (1) Determine the amount of time and the pumping rates required to remove the SF 6 -enriched drilling air without inducing additional atmospheric contamination; (2) collect core samples for uniaxial compression to determine the amount of SF 6 gas that penetrated the core during drilling; (3) test the effectiveness of the SF 6 injection and sampling system; (4) test the installation and effectiveness of the prototype packer system; and (5) test the effectiveness of several core sealing methods. 1 fig., 1 tab

Improved removal of blood contamination from ThinPrep cervical cytology samples for Raman spectroscopic analysis.

Science.gov (United States)

Traynor, Damien; Duraipandian, Shiyamala; Martin, Cara M; O'Leary, John J; Lyng, Fiona M

2018-05-01

There is an unmet need for methods to help in the early detection of cervical precancer. Optical spectroscopy-based techniques, such as Raman spectroscopy, have shown great potential for diagnosis of different cancers, including cervical cancer. However, relatively few studies have been carried out on liquid-based cytology (LBC) pap test specimens and confounding factors, such as blood contamination, have been identified. Previous work reported a method to remove blood contamination before Raman spectroscopy by pretreatment of the slides with hydrogen peroxide. The aim of the present study was to extend this work to excessively bloody samples to see if these could be rendered suitable for Raman spectroscopy. LBC ThinPrep specimens were treated by adding hydrogen peroxide directly to the vial before slide preparation. Good quality Raman spectra were recorded from negative and high grade (HG) cytology samples with no blood contamination and with heavy blood contamination. Good classification between negative and HG cytology could be achieved for samples with no blood contamination (sensitivity 92%, specificity 93%) and heavy blood contamination (sensitivity 89%, specificity 88%) with poorer classification when samples were combined (sensitivity 82%, specificity 87%). This study demonstrates for the first time the improved potential of Raman spectroscopy for analysis of ThinPrep specimens regardless of blood contamination. (2018) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE).

Enhanced removal of lead from contaminated soil by polyol-based deep eutectic solvents and saponin

Science.gov (United States)

Mukhopadhyay, Soumyadeep; Mukherjee, Sumona; Hayyan, Adeeb; Hayyan, Maan; Hashim, Mohd Ali; Sen Gupta, Bhaskar

2016-11-01

Deep eutectic solvents (DESs) are a class of green solvents analogous to ionic liquids, but less costly and easier to prepare. The objective of this study is to remove lead (Pb) from a contaminated soil by using polyol based DESs mixed with a natural surfactant saponin for the first time. The DESs used in this study were prepared by mixing a quaternary ammonium salt choline chloride with polyols e.g. glycerol and ethylene glycol. A natural surfactant saponin obtained from soapnut fruit pericarp, was mixed with DESs to boost their efficiency. The DESs on their own did not perform satisfactory due to higher pH; however, they improved the performance of soapnut by up to 100%. Pb removal from contaminated soil using mixture of 40% DES-Gly and 1% saponin and mixture of 10% DES-Gly and 2% saponin were above 72% XRD and SEM studies did not detect any major corrosion in the soil texture. The environmental friendliness of both DESs and saponin and their affordable costs merit thorough investigation of their potential as soil washing agents.

Sedimentation and contamination patterns of dike systems along the Rhône River (France)

Science.gov (United States)

Seignemartin, Gabrielle; Tena, Alvaro; Piégay, Hervé; Roux, Gwenaelle; Winiarski, Thierry

2017-04-01

Humans have historically modified the Rhône River, especially in the last centuries. In the 19th century, the river was systematically embanked for flood protection purposes, and works continued along the 20th century with dike system engineering work for navigation. The Rhône was canalised and its historical course by-passed by a series of hydroelectric dams. Besides, industrial activity polluted the river. For example, high levels of PCB's were attributed to the inputs of the heavily industrialized zone downstream from Lyon. During floods, these contaminants, associated with the suspended sediment, were trapped by the engineering works and the floodplain. Currently, a master plan to reactivate the river dynamics in the alluvial margins by removing the groyne-fields and dikes in the by-passed sections is being implemented. Within this context, this work aims to assess historical dynamics of sediment and associated contaminants in the floodplain (e.g. trace metal elements), notably in the dike system, in order to evaluate the contamination risk related to bank protection removal. With this objective, a transversal methodology has been applied coupling GIS diachronic analysis (old maps, bathymetric data, Orthophotos, LIDAR, etc.) to understand the historical floodplain evolution, sediment survey to obtain sediment thickness (metal rod and Ground Penetrating Radar), and sediment sampling (manual auger and core sampling) to obtain the metal element concentrations (X-Ray Fluorescence and Inductively Coupled Plasma Mass Spectrometry). By this way, metal element patterns were defined and used as contamination tracing indicators to apprehend the contamination history but also as geochemical background indicators to define the sediment source influence. We found that sediment temporal patterns are directly related with the by-pass construction year. Spatially, fine sediment deposition predominates in the dike systems, being lower in the floodplain already disconnected in

A Study on the Removal of Cesium in Soil Contaminated with Radiation Using a Soil Washing Process

International Nuclear Information System (INIS)

Park, Ukryang; Kim, Gyenam; Kim, Seungsoo; Park, Hyemin; Kim, Wansuk; Moon, Jaikwon

2013-01-01

The first principle is related with the washing process which is carried out to transfer the contaminated mass from the soil to water by dissolving it with a cleansing solution. The second is concerned with the size of the separation process which focuses on the reduction of the volume by separating the subject matters based on the different sizes of the soil. The complex agents used in the soil washing process include HCl, Oxalic acid, Citric acid, CaCl 2 , BaCl 2 , NH 4 NO 3 , and NaOH. It is known that the complex-forming capacity of such complex agents and radionuclides influences the decontamination from the soil. Also, since the forms of the chemical species related with the complex agents and the surface potential of the soil vary based on the changes of acidity observed in the cleansing solution, the level of acidity in the cleansing solution can be regarded as a factor that influences the decontamination. Therefore, in this study, H 2 SO 4 was selected as the complex agent and used to check the influence of the temperature when the subject contaminated soil was washed. Then, by applying the sieve grading process with a sieve-shaker, the size separation process was carried out to measure the level of radiation for each size. By washing the contaminated soil separated into different sizes with the complex agent H 2 SO 4 , the different removal tendencies for each size were considered. After selecting the complex agent H 2 SO 4 and checking the influence of temperature when the contaminated soil was washed based on the solid-liquid ratio of 1g:2ml, it was found that the heat washing process at a temperature of 95 .deg. C showed a higher level of efficiency for the removal of Cs compared to the case of the non-heat washing process. Also, according to the results given by the process of considering the different removal tendencies for each size based on the heat washing process after the sieve grading process was applied with the sieve-shaker prior for the size

Removal effectiveness and mechanisms of naphthalene and heavy metals from artificially contaminated soil by iron chelate-activated persulfate

International Nuclear Information System (INIS)

Yan, Dickson Y.S.; Lo, Irene M.C.

2013-01-01

The effectiveness and mechanisms of naphthalene and metal removal from artificially contaminated soil by FeEDTA/FeEDDS-activated persulfate were investigated through batch experiments. Using FeEDTA-activated persulfate, higher naphthalene removal from the soil at 7 h was achieved (89%), compared with FeEDDS-activated persulfate (75%). The removal was mainly via the dissolution of naphthalene partitioned on mineral surfaces, followed by activated persulfate oxidation. Although EDDS is advantageous over EDTA in terms of biodegradability, it is not preferable for iron chelate-activated persulfate oxidation since persulfate was consumed to oxidize EDDS, resulting in persulfate inadequacy for naphthalene oxidation. Besides, 55 and 40% of naphthalene were removed by FeEDTA and FeEDDS alone, respectively. Particularly, 21 and 9% of naphthalene were degraded in the presence of FeEDTA and FeEDDS alone, respectively, which caused by electrons transfer among dissolved organic matter, Fe 2+ /Fe 3+ and naphthalene. Over 35, 36 and 45% of Cu, Pb and Zn were removed using FeEDTA/FeEDDS-activated persulfate. -- Highlights: ► FeEDTA/FeEDDS-activated persulfate oxidation removed PAH and heavy metal from soil. ► More naphthalene was removed by FeEDTA-activated persulfate compared to FeEDDS. ► Persulfate was consumed to oxidize EDDS in FeEDDS-activated persulfate oxidation. ► Metals can be extracted from soil by free EDTA/EDDS dissociated from FeEDTA/FeEDDS. ► Naphthalene oxidation can be induced by e − transfer among Fe 2+ , DOM and naphthalene. -- This study focuses on the potencies and mechanisms of naphthalene and metal removal from contaminated soil by FeEDTA/FeEDDS-activated persulfate

Removal of heavy metals from contaminated soil by electrodialytic remediation enhanced with organic acids.

Science.gov (United States)

Merdoud, Ouarda; Cameselle, Claudio; Boulakradeche, Mohamed Oualid; Akretche, Djamal Eddine

2016-11-09

The soil from an industrial area in Algeria was contaminated with Cr (8370 mg kg -1 ), Ni (1135 mg kg -1 ) and zinc (1200 mg kg -1 ). The electrodialytic remediation of this soil was studied using citric acid and EDTA as facilitating agents. 0.1 M citric acid or EDTA was added directly to the soil before it was introduced in an electrodialytic cell in an attempt to enhance the heavy metal solubility in the interstitial fluid. The more acidic pH in the soil when citric acid was used as the facilitating agent was not enough to mobilize and remove the metals from the soil. Only 7.2% of Ni and 6.7% of Zn were removed from the soil in the test with citric acid. The best results were found with EDTA, which was able to solubilize and complex Zn and Ni forming negatively charged complexes that were transported and accumulated in the anolyte. Complete removal was observed for Ni and Zn in the electrodialytic treatment with EDTA. Minor amounts of Cr were removed with both EDTA and citric acid.

Low Temperature Catalyst for NH3 Removal

Science.gov (United States)

Monje, Oscar; Melendez, Orlando

2013-01-01

Air revitalization technologies maintain a safe atmosphere inside spacecraft by the removal of C02, ammonia (NH3), and trace contaminants. NH3 onboard the International Space Station (ISS) is produced by crew metabolism, payloads, or during an accidental release of thermal control refrigerant. Currently, the ISS relies on removing NH3 via humidity condensate and the crew wears hooded respirators during emergencies. A different approach to cabin NH3 removal is to use selective catalytic oxidation (SCO), which builds on thermal catalytic oxidation concepts that could be incorporated into the existing TCCS process equipment architecture on ISS. A low temperature platinum-based catalyst (LTP-Catalyst) developed at KSC was used for converting NH3 to H20 and N2 gas by SCO. The challenge of implementing SCO is to reduce formation of undesirable byproducts like NOx (N20 and NO). Gas mixture analysis was conducted using FTIR spectrometry in the Regenerable VOC Control System (RVCS) Testbed. The RVCS was modified by adding a 66 L semi-sealed chamber, and a custom NH3 generator. The effect of temperature on NH3 removal using the LTP-Catalyst was examined. A suitable temperature was found where NH3 removal did not produce toxic NO, (NO, N02) and N20 formation was reduced.

Reactive Distillation and Air Stripping Processes for Water Recycling and Trace Contaminant Control

Science.gov (United States)

Boul, Peter J.; Lange, Kevin E.; Conger, Bruce; Anderson, Molly

2009-01-01

Reactive distillation designs are considered to reduce the presence of volatile organic compounds in the purified water. Reactive distillation integrates a reactor with a distillation column. A review of the literature in this field has revealed a variety of functional reactive columns in industry. Wastewater may be purified by a combination of a reactor and a distiller (e.g., the EWRS or VPCAR concepts) or, in principle, through a design which integrates the reactor with the distiller. A review of the literature in reactive distillation has identified some different designs in such combinations of reactor and distiller. An evaluation of reactive distillation and reactive air stripping is presented with regards to the reduction of volatile organic compounds in the contaminated water and air. Among the methods presented, an architecture is presented for the evaluation of the simultaneous oxidation of organics in air and water. These and other designs are presented in light of potential improvements in power consumptions and air and water purities for architectures which include catalytic activity integrated into the water processor. In particular, catalytic oxidation of organics may be useful as a tool to remove contaminants that more traditional distillation and/or air stripping columns may not remove. A review of the current leading edge at the commercial level and at the research frontier in catalytically active materials is presented. Themes and directions from the engineering developments in catalyst design are presented conceptually in light of developments in the nanoscale chemistry of a variety of catalyst materials.

Separation of heavy metals: Removal from industrial wastewaters and contaminated soil

Energy Technology Data Exchange (ETDEWEB)

Peters, R.W.; Shem, L.

1993-03-01

This paper reviews the applicable separation technologies relating to removal of heavy metals from solution and from soils in order to present the state-of-the-art in the field. Each technology is briefly described and typical operating conditions and technology performance are presented. Technologies described include chemical precipitation (including hydroxide, carbonate, or sulfide reagents), coagulation/flocculation, ion exchange, solvent extraction, extraction with chelating agents, complexation, electrochemical operation, cementation, membrane operations, evaporation, adsorption, solidification/stabilization, and vitrification. Several case histories are described, with a focus on waste reduction techniques and remediation of lead-contaminated soils. The paper concludes with a short discussion of important research needs in the field.

Separation of heavy metals: Removal from industrial wastewaters and contaminated soil

Energy Technology Data Exchange (ETDEWEB)

Peters, R.W.; Shem, L.

1993-01-01

This paper reviews the applicable separation technologies relating to removal of heavy metals from solution and from soils in order to present the state-of-the-art in the field. Each technology is briefly described and typical operating conditions and technology performance are presented. Technologies described include chemical precipitation (including hydroxide, carbonate, or sulfide reagents), coagulation/flocculation, ion exchange, solvent extraction, extraction with chelating agents, complexation, electrochemical operation, cementation, membrane operations, evaporation, adsorption, solidification/stabilization, and vitrification. Several case histories are described, with a focus on waste reduction techniques and remediation of lead-contaminated soils. The paper concludes with a short discussion of important research needs in the field.

Trace elements distribution in environmental compartments

Energy Technology Data Exchange (ETDEWEB)

Queiroz, Juliana C. de; Peres, Sueli da Silva; Godoy, Maria Luiza D.P., E-mail: suelip@ird.gov.br [Instituto de Radioprotecao e Dosimetria (IRD/CNEN-RJ), Rio de Janeiro, RJ (Brazil)

2017-11-01

Trace elements term defines the presence of low concentrations metals at environment. Some of them are considered biologically essential, as Co, Cu and Mn. Others can cause detriment to environment and human health, as Pb, Cd, Hg, As, Ti and U. A large number of them have radioactive isotopes, implying the evaluation of risks for human health should be done considering the precepts of environmental radiological protection. The ecosystem pollution with trace elements generates changes at the geochemistry cycle of these elements and in environmental quality. Soils have single characteristics when compared with another components of biosphere (air, water and biota), cause they introduce themselves not only as a drain towards contaminants, but also as natural buffer that control the transport of chemical elements and other substances for atmosphere, hydrosphere and biota. The main purpose of environmental monitoring program is to evaluate the levels of contaminants in the various compartments of the environment: natural or anthropogenic, and to assess the contribution of a potential contaminant source on the environment. Elemental Composition for the collected samples was determined by inductively coupled plasma mass spectroscopy. The main objective of this work was to evaluate the map baseline of concentration of interest trace elements in environmental samples of water, sediment and soil from Environmental Monitoring Program of Instituto de Radioprotecao e Dosimetria (IRD). The samples were analyzed using an inductively coupled plasma mass spectrometer (ICP-MS) at IRD. >From the knowledge of trace elements concentrations, could be evaluated the environmental quality parameters at the studied ecosystems. The data allowed evaluating some relevant aspects of the study of trace elements in soil and aquatic systems, with emphasis at the distribution, concentration and identification of main anthropic sources of contamination at environment. (author)

Trace elements distribution in environmental compartments

International Nuclear Information System (INIS)

Queiroz, Juliana C. de; Peres, Sueli da Silva; Godoy, Maria Luiza D.P.

2017-01-01

Trace elements term defines the presence of low concentrations metals at environment. Some of them are considered biologically essential, as Co, Cu and Mn. Others can cause detriment to environment and human health, as Pb, Cd, Hg, As, Ti and U. A large number of them have radioactive isotopes, implying the evaluation of risks for human health should be done considering the precepts of environmental radiological protection. The ecosystem pollution with trace elements generates changes at the geochemistry cycle of these elements and in environmental quality. Soils have single characteristics when compared with another components of biosphere (air, water and biota), cause they introduce themselves not only as a drain towards contaminants, but also as natural buffer that control the transport of chemical elements and other substances for atmosphere, hydrosphere and biota. The main purpose of environmental monitoring program is to evaluate the levels of contaminants in the various compartments of the environment: natural or anthropogenic, and to assess the contribution of a potential contaminant source on the environment. Elemental Composition for the collected samples was determined by inductively coupled plasma mass spectroscopy. The main objective of this work was to evaluate the map baseline of concentration of interest trace elements in environmental samples of water, sediment and soil from Environmental Monitoring Program of Instituto de Radioprotecao e Dosimetria (IRD). The samples were analyzed using an inductively coupled plasma mass spectrometer (ICP-MS) at IRD. >From the knowledge of trace elements concentrations, could be evaluated the environmental quality parameters at the studied ecosystems. The data allowed evaluating some relevant aspects of the study of trace elements in soil and aquatic systems, with emphasis at the distribution, concentration and identification of main anthropic sources of contamination at environment. (author)

Trace Metals Bioaccumulation Potentials of Three Indigenous ...

African Journals Online (AJOL)

User

grasses as bioaccumulators of trace metals from polluted soils. Seeds of ... transfer factor (TF) showed that Zn was the most bioaccumulated trace metals by all the grasses followed by. Pb, Mn ... was used to de-contaminate copper (Cu) and.

Removal of uranium from uranium-contaminated soils -- Phase 1: Bench-scale testing. Uranium in Soils Integrated Demonstration

Energy Technology Data Exchange (ETDEWEB)

Francis, C. W.

1993-09-01

To address the management of uranium-contaminated soils at Fernald and other DOE sites, the DOE Office of Technology Development formed the Uranium in Soils Integrated Demonstration (USID) program. The USID has five major tasks. These include the development and demonstration of technologies that are able to (1) characterize the uranium in soil, (2) decontaminate or remove uranium from the soil, (3) treat the soil and dispose of any waste, (4) establish performance assessments, and (5) meet necessary state and federal regulations. This report deals with soil decontamination or removal of uranium from contaminated soils. The report was compiled by the USID task group that addresses soil decontamination; includes data from projects under the management of four DOE facilities [Argonne National Laboratory (ANL), Los Alamos National Laboratory (LANL), Oak Ridge National Laboratory (ORNL), and the Savannah River Plant (SRP)]; and consists of four separate reports written by staff at these facilities. The fundamental goal of the soil decontamination task group has been the selective extraction/leaching or removal of uranium from soil faster, cheaper, and safer than current conventional technologies. The objective is to selectively remove uranium from soil without seriously degrading the soil`s physicochemical characteristics or generating waste forms that are difficult to manage and/or dispose of. Emphasis in research was placed more strongly on chemical extraction techniques than physical extraction techniques.

Mitigation of cesium and cobalt contamination on the surfaces of RAM packages

International Nuclear Information System (INIS)

Krumhansl, J.; Bonhomme, F.; McConnell, P.; Kapoor, A.

2004-01-01

Techniques for mitigating the adsorption of 137 Cs and 60 Co on metal surfaces (e.g., RAM packages) exposed to contaminated water (e.g., spent-fuel pools) has been developed and experimentally verified. The techniques are also effective in removing some of the 60 Co and 137 Cs that may have been adsorbed on the surfaces after removal from the contaminated water. The principle for the 137 Cs mitigation technique is based upon ion-exchange processes. In contrast, 60 Co contamination primarily resides in minute particles of CRUD that become lodged on cask surfaces. CRUD is an insoluble Fe-Ni-Cr oxide that forms colloidal-sized particles as stainless steels corrode. Because of the similarity between Ni +2 and Co +2 , CRUD is able to scavenge and retain traces of cobalt as it forms. A number of organic compounds have a great specificity for combining with nickel and cobalt. Ongoing research is investigating the effectiveness of chemical complexing agent, EDTA, with regard to its ability to dissolve the host phase (CRUD) thereby liberating the entrained 60Co into a solution where it can be rinsed away

Removal of heavy metals and arsenic from a co-contaminated soil by sieving combined with washing process.

Science.gov (United States)

Liao, Xiaoyong; Li, You; Yan, Xiulan

2016-03-01

Batch experiments were conducted with a heavy metals and arsenic co-contaminated soil from an abandoned mine to evaluate the feasibility of a remediation technology that combines sieving with soil washing. Leaching of the arsenic and heavy metals from the different particle size fractions was found to decrease in the order: 2mm. With increased contact time, the concentration of heavy metals in the leachate was significantly decreased for small particles, probably because of adsorption by the clay soil component. For the different particle sizes, the removal efficiencies for Pb and Cd were 75%-87%, and 61%-77% for Zn and Cu, although the extent of removal was decreased for As and Cr at 2mm, although good metal removal efficiencies were also achieved in the small particle size fractions. Through SEM-EDS observations and correlation analysis, the leaching regularity of the heavy metals and arsenic was found to be closely related to Fe, Mn, and Ca contents of the soil fractions. The remediation of heavy metal-contaminated soil by sieving combined with soil washing was proven to be efficient, and practical remediation parameters were also recommended. Copyright © 2015. Published by Elsevier B.V.

Early versus delayed dressing removal after primary closure of clean and clean-contaminated surgical wounds.

Science.gov (United States)

Toon, Clare D; Lusuku, Charnelle; Ramamoorthy, Rajarajan; Davidson, Brian R; Gurusamy, Kurinchi Selvan

2015-09-03

Most surgical procedures involve a cut in the skin that allows the surgeon to gain access to the deeper tissues or organs. Most surgical wounds are closed fully at the end of the procedure (primary closure). The surgeon covers the closed surgical wound with either a dressing or adhesive tape. The dressing can act as a physical barrier to protect the wound until the continuity of the skin is restored (within about 48 hours) and to absorb exudate from the wound, keeping it dry and clean, and preventing bacterial contamination from the external environment. Some studies have found that the moist environment created by some dressings accelerates wound healing, although others believe that the moist environment can be a disadvantage, as excessive exudate can cause maceration (softening and deterioration) of the wound and the surrounding healthy tissue. The utility of dressing surgical wounds beyond 48 hours of surgery is, therefore, controversial. To evaluate the benefits and risks of removing a dressing covering a closed surgical incision site within 48 hours permanently (early dressing removal) or beyond 48 hours of surgery permanently with interim dressing changes allowed (delayed dressing removal), on surgical site infection. In March 2015 we searched the following electronic databases: The Cochrane Wounds Group Specialised Register; The Cochrane Central Register of Controlled Trials (CENTRAL) (The Cochrane Library); Database of Abstracts of Reviews of Effects (DARE) (The Cochrane Library); Ovid MEDLINE; Ovid MEDLINE (In-Process & Other Non-Indexed Citations); Ovid EMBASE; and EBSCO CINAHL. We also searched the references of included trials to identify further potentially-relevant trials. Two review authors independently identified studies for inclusion. We included all randomised clinical trials (RCTs) conducted with people of any age and sex, undergoing a surgical procedure, who had their wound closed and a dressing applied. We included only trials that compared

Covalent organic polymer functionalized activated carbon: A novel material for water contaminant removal and CO2 capture

DEFF Research Database (Denmark)

Mines, Paul D.; Thirion, Damien; Uthuppu, Basil

Covalent organic polymers (COPs) have emerged as one of the leading advanced materials for environmental applications, such as the capture and recovery of carbon dioxide and the removal of contaminants from polluted water. COPs exhibit many remarkable properties that other leading advanced materi...

Is there a risk of trace element contamination in herbal preparations? A test study on the lichen Cetraria islandica.

Science.gov (United States)

Giordani, Paolo; Minganti, Vincenzo; Brignole, Daniele; Malaspina, Paola; Cornara, Laura; Drava, Giuliana

2017-08-01

Lichens are a source of unique secondary metabolites, which have been proved to have many biological properties with possible pharmaceutical roles, including e.g. antioxidant, antimicrobial, antifungal or anti-inflammatory activities and to be worth of consideration for potential human use. However, lichens lack cuticolar tissues and are exposed to several atmospheric contaminants, including trace elements. This work aims at exploring the potential toxicity of herbal preparations derived by the lichen Cetraria islandica due to trace element contamination, testing whether different concentrations may be observed, depending on the origin of the raw material. Fourteen samples of C. islandica, as cut dried thalli occurring on the European market, have been bought from different providers. For each sample, the concentrations of As, Cd, Co, Cu, Fe, Mn, Ni, P, Pb, V and Zn were measured on comminuted herbal substance and on the corresponding decoction, using atomic emission spectrometry (ICP-OES). The elemental concentrations in decoctions were significantly lower than those measured in raw materials, dropping down to levels of negligible health concern. Differences observed in raw materials were not observed anymore in the corresponding decoctions. Also, the elemental transfer rate from dried lichen to decoction was extremely element-specific, ranging from 2% for Cu to 95% for Zn. Copyright © 2017 Elsevier Ltd. All rights reserved.

Contamination and ecological risk assessment of toxic trace elements in the Xi River, an urban river of Shenyang city, China.

Science.gov (United States)

Lin, Chunye; He, Mengchang; Liu, Xitao; Guo, Wei; Liu, Shaoqing

2013-05-01

The objectives of this study were to assess the enrichment, contamination, and ecological risk posed by toxic trace elements in the sediments of the Xi River in the industrialized city of Shenyang, China. Surface sediment and sediment core were collected; analyzed for toxic trace elements; and assessed with an index of geoaccumulation (Igeo), enrichment factor (EF) value, potential ecological risk factor (Er), ecological risk index (RI), and probable effect concentration quotient (PECQ). Elemental concentrations (milligram per kilogram) were 8.5-637.9 for As, 6.5-103.9 for Cd, 12.2-21.9 for Co, 90.6-516.0 for Cr, 258.1-1,791.5 for Cu, 2.6-19.0 for Hg, 70.5-174.5 for Ni, 126.9-1,405.8 for Pb, 3.7-260.0 for Sb, 38.4-100.4 for V, and 503-4,929 for Zn. The Igeo, EF, Er, and PECQ indices showed that the contamination of Cd and Hg was more serious than that of As, Cr, Cu, Ni, Pb, Sb, and Zn, whereas the presence of Co and V might be primarily from natural sources. The Igeo index for Cr and Ni might underestimate the degree of contamination, potentially as a result of high concentrations of these elements in the shale. The RI index was higher than 600, indicating a notably high ecological risk of sediment for the river. The average PECQ for As, Cd, Cr, Cu, Hg, Ni, Pb, and Zn ranged from 1.4 to 4.1 for surface sediment and from 5.2 to 9.6 in the sediment cores, indicating a high potential for an adverse biological effect. It was concluded that the sediment in the Xi River was severely contaminated and should be remediated as a hazardous material.

Removing Copper from Contaminated Water Using Activated Carbon Sorbent by Continuous Flow

Directory of Open Access Journals (Sweden)

M.H. Salmani

2012-07-01

Full Text Available Introduction: A major concern of human being is accumulation and toxicity of heavy metals in their body. Copper is a heavy metal ion that in concentration of 2 mg/l can cause numerous complications. Different treatment methods have been proposed for removing metals from contaminated water by researchers. Among these methods, sorption seems a better method with high removal efficiency. In this study, conditions for removal of copper ions by activated carbon sorbent were studied with continuous flow. Materials & Methods: This was a laboratory – experimental study. A 20mg/l solution of copper ions was prepared and passed through a 5 × 10 cm column with average output rate of 1.85 ml/min. Output of column was sampled every 30 minutes and the remaining amount of copper ion in each sample was measured by flame atomic absorption. Results: The empty bed volume (EBV was equal to 138 ml. The highest removal efficiency was 99.7 percent at 127 minutes. From equilibrium time, the removal efficiency was constant with time. The adsorption capacity of activated carbon was 0.25mg.g-1. The isotherm study indicated that the sorption data can be obeyed by both Langmuir and Freundlich isotherms (R2>0.95 but Langmuir model had higher agreement with this experimental data (R2= 0.988. Conclusion: The binding of ions to the sorbent in the adsorption process is extremely important. For this column 62.5 minutes after filling was appropriate, so the highest removal efficiency was obtained. Equilibrium time was dependent on the speed of influent through the column in the continuous flow. For selected column, the rate of 1.85 ml/min is a good performance.

In situ biosurfactant production and hydrocarbon removal by Pseudomonas putida CB-100 in bioaugmented and biostimulated oil-contaminated soil.

Science.gov (United States)

Ángeles, Martínez-Toledo; Refugio, Rodríguez-Vázquez

2013-01-01

In situ biosurfactant (rhamnolipid) production by Pseudomonas putida CB-100 was achieved during a bioaugmented and biostimulated treatment to remove hydrocarbons from aged contaminated soil from oil well drilling operations. Rhamnolipid production and contaminant removal were determined for several treatments of irradiated and non-irradiated soils: nutrient addition (nitrogen and phosphorus), P. putida addition, and addition of both (P. putida and nutrients). The results were compared against a control treatment that consisted of adding only sterilized water to the soils. In treatment with native microorganisms (non-irradiated soils) supplemented with P. putida, the removal of total petroleum hydrocarbons (TPH) was 40.6%, the rhamnolipid production was 1.54 mg/kg, and a surface tension of 64 mN/m was observed as well as a negative correlation (R = -0.54; p soil treated with P. putida, TPH removal was 24.5% with rhamnolipid generation of 1.79 mg/kg and 65.6 mN/m of surface tension, and a correlation between bacterial growth and biosurfactant production (R = -0.64; p soils, in situ rhamnolipid production by P. putida enhanced TPH decontamination of the soil.

Synthesis and application of magnetic hydrogel for Cr(VI) removal from contaminated water

KAUST Repository

Tang, Samuel C N; Wang, Peng; Yin, Ke; Lo., Irene Man Chi

2010-01-01

Many magnetic adsorbents reported in the literature, such as iron oxides, for Cr(VI) removal have been found effective only in low pH environments. Moreover, the application of polymeric hydrogels on heavy metal removal has been hindered by difficulties in separation by filtration. In this study, a magnetic cationic hydrogel was synthesized for Cr(VI) removal from contaminated water, making use of the advantages of magnetic adsorbents and polymeric hydrogels. The magnetic hydrogel was produced by imbedding 10-nm γ-Fe2O 3 nanoparticles into the polymeric matrix via radical polymerization. Characterization of the hydrogel was undertaken with Fourier transform infrared and vibrating sample magnetometer; swelling properties were tested and anionic adsorption capacity was evaluated. The magnetic hydrogel showed a superior Cr(VI) removal capacity compared to commercial products such as MIEX®. Cr(VI) removal was independent of solution pH. Results show that Cr(VI) removal kinetics was improved drastically by grinding the bulk hydrogel into powder form. At relevant concentrations, common water anions (e.g., Cl-, SO4 2-, PO4 3-) and natural organic matter did not exhibit significant inhibition of Cr(VI) adsorption onto the hydrogel. Results of vibrating sample magnetometer indicate that the magnetic hydrogel can be easily separated from treatment systems. Regeneration of the magnetic hydrogel can be easily achieved by washing the Cr(VI)-loaded hydrogel with 0.5 M NaCl solution, with a recovery rate of about 90% of Cr(VI). © Copyright 2010, Mary Ann Liebert, Inc. 2010.

Synthesis and application of magnetic hydrogel for Cr(VI) removal from contaminated water

KAUST Repository

Tang, Samuel C N

2010-11-01

Many magnetic adsorbents reported in the literature, such as iron oxides, for Cr(VI) removal have been found effective only in low pH environments. Moreover, the application of polymeric hydrogels on heavy metal removal has been hindered by difficulties in separation by filtration. In this study, a magnetic cationic hydrogel was synthesized for Cr(VI) removal from contaminated water, making use of the advantages of magnetic adsorbents and polymeric hydrogels. The magnetic hydrogel was produced by imbedding 10-nm γ-Fe2O 3 nanoparticles into the polymeric matrix via radical polymerization. Characterization of the hydrogel was undertaken with Fourier transform infrared and vibrating sample magnetometer; swelling properties were tested and anionic adsorption capacity was evaluated. The magnetic hydrogel showed a superior Cr(VI) removal capacity compared to commercial products such as MIEX®. Cr(VI) removal was independent of solution pH. Results show that Cr(VI) removal kinetics was improved drastically by grinding the bulk hydrogel into powder form. At relevant concentrations, common water anions (e.g., Cl-, SO4 2-, PO4 3-) and natural organic matter did not exhibit significant inhibition of Cr(VI) adsorption onto the hydrogel. Results of vibrating sample magnetometer indicate that the magnetic hydrogel can be easily separated from treatment systems. Regeneration of the magnetic hydrogel can be easily achieved by washing the Cr(VI)-loaded hydrogel with 0.5 M NaCl solution, with a recovery rate of about 90% of Cr(VI). © Copyright 2010, Mary Ann Liebert, Inc. 2010.

Assessment of trace ground-water contaminants release from south Texas in-situ uranium solution-mining sites

Energy Technology Data Exchange (ETDEWEB)

Kidwell, J.R.; Humenick, M.J.

1981-01-01

The future of uranium solution mining in south Texas depends heavily on the industry's ability to restore production zone ground water to acceptable standards. This study investigated the extent of trace contaminant solubilization during mining and subsequent restoration attempts, first through a literature search centered on uranium control mechanisms, and then by laboratory experiments simulating the mining process. The literature search indicated the complexity of the situation. The number of possible interactions between indigenous elements and materials pointed on the site specificity of the problem. The column studies evaluated three different production area ores. Uranium, molybdenum, arsenic, vanadium, and selenium were analyzed in column effluents. After simulated mining operations were completed, uranium was found to be the most persistent trace element. However, subsequent ground water flushing of the columns could restore in-situ water to EPA recommended drinking water concentrations. Limited data indicated that ground water flowing through mined areas may solubilize molybdenum present in down gradient areas adjacent to the production zone due to increased oxidation potential of ground water if adequate restoration procedures are not followed.

The Use of Haz-Flote to Efficiently Remove Mercury from Contaminated Materials

Energy Technology Data Exchange (ETDEWEB)

Terry Brown

2009-03-03

There are thousands of known contaminated sites in the United Stated, including Superfund sites (1500 to 2100 sites), RCRA corrective action sites (1500 to 3500 sites), underground storage tanks (295,000 sites), U.S. Department of Defense sites (7300 sites), U.S. Department of Energy sites (4,000 sites), mining refuse piles, and numerous other hazardous metals and organic contamination sites. Only a small percentage of these sites has been cleaned up. The development of innovative technologies to handle the various clean-up problems on a national and international scale is commonplace. Many innovative technologies have been developed that can be used to effectively remediate contaminated materials. Unfortunately, many of these technologies are only effective for materials coarser than approximately 200 mesh. In addition, these technologies usually require considerable investment in equipment, and the clean-up costs of soil material are relatively high - in excess of $100 to $500 per yd{sup 3}. These costs result from the elaborate nature of the processes, the costs for power, and the chemical cost. The fine materials are disposed of or treated at considerable costs. As a result, the costs often associated with amelioration of contaminated sites are high. Western Research institute is in the process of developing an innovative soil washing technology that addresses the removal of contaminants from the fine size-fraction materials located at many of the contaminated sites. This technology has numerous advantages over the other ex-situ soil washing techniques. It requires a low capital investment, low operating costs and results in high levels of re-emplacement of the cleaned material on site. The process has the capability to clean the fine fraction (<200 mesh) of the soil resulting in a replacement of 95+% of the material back on-side, reducing the costs of disposal. The Haz-Flote{trademark} technology would expand the application of soil washing technology to heavy

Integration of pneumatic fracturing with bioremediation from the enhanced removal of BTX from low permeability gasoline-contaminated soils

International Nuclear Information System (INIS)

Venkatraman, S.N.; Kosson, D.S.; Schuring, J.R.; Boland, T.M.

1995-01-01

A pilot-scale evaluation of the integrated pneumatic fracturing and bioremediation system was carried out to demonstrate the enhanced removal of BTX from a gasoline contaminated, low permeability soil formation. The fracturing enhanced subsurface permeability by an average of over 36 times, and established an extended bioremediation zone supporting aerobic, denitrifying and methanogenic populations. Subsurface amendment injections consisting of phosphate and nitrogen were made periodically over a 50-week period to stimulate microbial activity. Results indicate that 79% of the soil-phase BTX was removed during the field test, with over 85% of the mass removed attributable to bioremediation

Removal of arsenic and iron removal from drinking water using coagulation and biological treatment.

Science.gov (United States)

Pramanik, Biplob Kumar; Pramanik, Sagor Kumar; Suja, Fatihah

2016-02-01

Effects of biological activated carbon (BAC), biological aerated filter (BAF), alum coagulation and Moringa oleifera coagulation were investigated to remove iron and arsenic contaminants from drinking water. At an initial dose of 5 mg/L, the removal efficiency for arsenic and iron was 63% and 58% respectively using alum, and 47% and 41% respectively using Moringa oleifera. The removal of both contaminants increased with the increase in coagulant dose and decrease in pH. Biological processes were more effective in removing these contaminants than coagulation. Compared to BAF, BAC gave greater removal of both arsenic and iron, removing 85% and 74%, respectively. Longer contact time for both processes could reduce the greater concentration of arsenic and iron contaminants. The addition of coagulation (at 5 mg/L dosage) and a biological process (with 15 or 60 min contact time) could significantly increase removal efficiency, and the maximum removal was observed for the combination of alum and BAC treatment (60 min contact time), with 100% and 98.56% for arsenic and iron respectively. The reduction efficiency of arsenic and iron reduced with the increase in the concentration of dissolved organics in the feedwater due to the adsorption competition between organic molecules and heavy metals.

Evaluation of Macronet polymeric adsorbents for removal of PAHs from contaminated soil and groundwater

International Nuclear Information System (INIS)

Valderrama, C.; Gamisans, X.; Lao, C.; Farran, A.; Cortina, J.L.

2005-01-01

Polycyclic aromatic hydrocarbons (PAHs) represent the largest group of compounds that are mutagenic, carcinogenic, and teratogenic and are included in the priority pollutants lists. Despite their widespread distributions, PAHs can be ultimately deposited and persisted in bed sediments in the aquatic system. This is due largely to the fact that most PAHs sorb strongly to sediments because of their high hydrophobicity, and are resistant to bacterial degradation under anoxic environment. When environmental conditions become favourable PAHs will be released to the overlying water as a long-term source and pose potential threat to water quality and aquatic ecosystem via bioaccumulation in food chains. Faced with these problems adsorption processes are one of the alternatives for PAHs retention. The adsorption of hydrophobic organic contaminants from aqueous phases generally increases with decreasing solubility of the compound and increasing organic carbon content of the aquifer solids. Natural materials with high organic carbon content such as coals or bituminous shales cause significant retardation of organic contaminants from groundwater. Such materials with high sorption capacities have been postulated and used for passive removal of hydrophobic contaminants in groundwater such as PAHs. Much more efficient is adsorption onto activated carbon, which is already a well-established technology for ex situ treatment of drinking water, polluted groundwater or waste water. One major advantages lies in the fact that the persistent compounds are removed from the ground water rather then being converted to still potentially dangerous metabolites as those generated by oxidation or reductive steps. One of the biggest disadvantages of the adsorption processes is the need to dispose or regenerate the adsorbent. In the case of activated carbon, it needs thermal desorption of the sorbed pollutants and thermal activation of the adsorbent. One of the possibilities to overcome this

Removal of copper and nickel contaminants from Si surface by use of cyanide solutions

International Nuclear Information System (INIS)

Fujiwara, N.; Liu, Y.-L.; Nakamura, T.; Maida, O.; Takahashi, M.; Kobayashi, H.

2004-01-01

The cleaning method using cyanide solutions has been developed to remove heavy metals such as copper (Cu) and nickel (Ni) from Si surfaces. Immersion of Si wafers with both Cu and Ni contaminants in potassium cyanide (KCN) solutions of methanol at room temperature decreases these surface concentrations below the detection limit of total reflection X-ray fluorescence spectroscopy of ∼3x10 9 atoms/cm 2 . UV spectra of the KCN solutions after cleaning of the Cu-contaminated Si surface show that stable copper-cyanide complexes are formed in the solution, leading to the prevention of the re-adsorption of copper in the solutions. From the complex stability constants, it is concluded that the Cu(CN) 4 3- is the most dominant species in the KCN solutions

A Study on the Removal of Cesium in Soil Contaminated with Radiation Using a Soil Washing Process

Energy Technology Data Exchange (ETDEWEB)

Park, Ukryang; Kim, Gyenam; Kim, Seungsoo; Park, Hyemin; Kim, Wansuk; Moon, Jaikwon [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of)

2013-05-15

The first principle is related with the washing process which is carried out to transfer the contaminated mass from the soil to water by dissolving it with a cleansing solution. The second is concerned with the size of the separation process which focuses on the reduction of the volume by separating the subject matters based on the different sizes of the soil. The complex agents used in the soil washing process include HCl, Oxalic acid, Citric acid, CaCl{sub 2}, BaCl{sub 2}, NH{sub 4}NO{sub 3}, and NaOH. It is known that the complex-forming capacity of such complex agents and radionuclides influences the decontamination from the soil. Also, since the forms of the chemical species related with the complex agents and the surface potential of the soil vary based on the changes of acidity observed in the cleansing solution, the level of acidity in the cleansing solution can be regarded as a factor that influences the decontamination. Therefore, in this study, H{sub 2}SO{sub 4} was selected as the complex agent and used to check the influence of the temperature when the subject contaminated soil was washed. Then, by applying the sieve grading process with a sieve-shaker, the size separation process was carried out to measure the level of radiation for each size. By washing the contaminated soil separated into different sizes with the complex agent H{sub 2}SO{sub 4}, the different removal tendencies for each size were considered. After selecting the complex agent H{sub 2}SO{sub 4} and checking the influence of temperature when the contaminated soil was washed based on the solid-liquid ratio of 1g:2ml, it was found that the heat washing process at a temperature of 95 .deg. C showed a higher level of efficiency for the removal of Cs compared to the case of the non-heat washing process. Also, according to the results given by the process of considering the different removal tendencies for each size based on the heat washing process after the sieve grading process was

Flexible graphene composites for removal of methylene blue dye-contaminant from water

Science.gov (United States)

Oliva, J.; Martinez, A. I.; Oliva, A. I.; Garcia, C. R.; Martinez-Luevanos, A.; Garcia-Lobato, M.; Ochoa-Valiente, R.; Berlanga, A.

2018-04-01

This work presents the use of flexible graphene composites (FGCs) fabricated by a casting method for the removal of Methylene blue (MB) dye from water. Those FGCs with elastic modulus of 15 MPa had enough mechanical resistance to support the Al2O3:Eu3+ and SrAl2O4:Bi3+ photocatalytic powders. After the incorporation of those powders in the FGCs, their photocatalytic activity was evaluated by monitoring the degradation of MB dye under solar irradiation. Scanning electron microscopy (SEM) images demonstrate that the surface of FGCs with catalysts powders presents pores with sizes in the range of 15-40 μm, which favored the sunlight absorption by scattering effects. Moreover, X-Ray diffraction measurements confirmed the formation of the composites by displacements of their diffraction peaks. The MB dye was completely removed (by photocatalysis and by physical adsorption) from the water after 180 min and 270 min by using the FGCs with Al2O3:Eu3+ and SrAl2O4:Bi3+ catalysts respectively. Hence, the results of photocatalytic activity suggest that our FGCs could be used as an effective support of catalyst powders for the easy removal of dye contaminants in wastewater treatment plants.

Trace-level mercury removal from surface water

International Nuclear Information System (INIS)

Klasson, K.T.; Bostick, D.T.

1998-01-01

Many sorbents have been developed for the removal of mercury and heavy metals from waters; however, most of the data published thus far do not address the removal of mercury to the target levels represented in this project. The application to which these sorbents are targeted for use is the removal of mercury from microgram-per-liter levels to low nanogram-per-liter levels. Sorbents with thiouronium, thiol, amine, sulfur, and proprietary functional groups were selected for these studies. Mercury was successfully removed from surface water via adsorption onto Ionac SR-4 and Mersorb resins to levels below the target goal of 12 ng/L in batch studies. A thiol-based resin performed the best, indicating that over 200,000 volumes of water could be treated with one volume of resin. The cost of the resin is approximately $0.24 per 1,000 gal of water

Liver histopathology of the southern watersnake, Nerodia fasciata fasciata, following chronic exposure to trace element-contaminated prey from a coal ash disposal site

Energy Technology Data Exchange (ETDEWEB)

Ganser, L.R.; Hopkins, W.A.; O' Neil, L.; Hasse, S.; Roe, J.H.; Sever, D.M. [St Marys College, Notre Dame, IN (USA). Dept. of Biology

2003-03-01

Previous studies have demonstrated the accumulation of arsenic, cadmium, selenium, strontium, and vanadium in livers of Southern Watersnakes fed fish from a coal-ash contaminated site. Our study is the first to investigate effects of trace element accumulation on cytology of snake liver. Snakes were born in the laboratory and raised for one or two years on diets consisting of varying proportions of contaminated fish. The majority (71%) of snakes fed contaminated prey did not exhibit any differences in liver histology when compared to control snakes fed an uncontaminated diet. In the remaining contaminant-exposed snakes, some aberrations were noted. The most prevalent pathology involved the proliferation of collagen fibers that resulted in narrowing or occlusion of sinusoids and increasing the mass of the intersinsuoidal parenychma. Fibrosis of the liver as a result of chronic injury has been reported previously in reptiles, but this is the first report that links such tissue damage to dietary contamination.

Assisted phytoremediation of a multi-contaminated soil: Investigation on arsenic and lead combined mobilization and removal.

Science.gov (United States)

Barbafieri, Meri; Pedron, Francesca; Petruzzelli, Gianniantonio; Rosellini, Irene; Franchi, Elisabetta; Bagatin, Roberto; Vocciante, Marco

2017-12-01

The removal of contaminants from an earthy matrix by phytoremediation requires the selection of appropriate plant species and a suitable strategy to be effective. In order to set up an assisted phytoremediation intervention related to a disused industrial site affected by an arsenic and lead complex contamination, an extensive experimental investigation on micro and mesocosm scale has been conducted. Particular attention was given to the choice of plant species: using crop plants (Lupinus albus, Helianthus annuus and Brassica juncea) a series of parallel test campaigns have been realized to investigate different scenarios for the reclamation. With regard to the arsenic contamination, which is certainly the most worrying, the possibility of employing a hyper-accumulator species (Pteris vittata) has also been investigated, highlighting advantages and difficulties associated with such an approach. The application of various mobilizing agents in different concentrations was tested, in order to maximize the extraction efficiency of plants in respect of both contaminants, showing the necessity of a chemically assisted approach to promote their uptake and translocation in the shoots. Phosphate addition appears to produce the desired results, positively affecting As phyto-extraction for both hyper-accumulator and crop plants, while minimizing its toxic effects at the investigated concentrations. With regard to Pb, although tests with EDDS have been encouraging, EDTA should be preferred at present due to lower uncertainties about its effectiveness. The performed tests also improved the addition of mobilizing agents, allowing the simultaneous removal of the two metals despite their great diversity (which in general discourages such approach), with significant saving of time and an obvious improvement of the overall process. Copyright © 2017 Elsevier Ltd. All rights reserved.

Can liming change root anatomy, biomass allocation and trace element distribution among plant parts of Salix × smithiana in trace element-polluted soils?

Science.gov (United States)

Vondráčková, Stanislava; Tlustoš, Pavel; Száková, Jiřina

2017-08-01

Willows (Salix spp.) are considered to be effective for the phytoremediation of trace elements from contaminated soils, but their efficiency is limited in heavily polluted soils because of poor growth. Liming can be a desirable measure to decrease the plant availability of elements, resulting in improved plant development. Notably, large root area and maximum soil penetration are basic parameters that improve the efficiency of phytoremediation. The impact of soil chemical properties on willow root anatomy and the distribution of trace elements below-ground have rarely been studied. The effect of liming on root parameters, biomass allocation and trace element distribution in non-harvestable (coarse roots, fine roots, stumps) and harvestable plant parts (twigs and leaves) of Salix × smithiana was assessed at the end of a 4-year pot experiment with two trace element-polluted soils that differed in terms of soil pH. Stump biomass predominated in weakly acidic soil. In neutral soil, the majority of biomass was located in fine roots and stumps; the difference from other plant parts was minor. Trace elements were the most concentrated in fine roots. Translocation to above-ground biomass increased as follows: Pb roots roots). Lime application decreased the concentrations of mobile Cd and Zn and related levels in plants, improved biomass production and root parameters and increased the removal of all trace elements in weakly acidic soil. None or minimum differences in the monitored parameters were recorded for dolomite treatments in both soils. The dose and source of liming had crucial effects on root anatomy. Growing willows in limed trace element-polluted soils is a suitable measure for combination of two remediation strategies, i.e. phytoextraction of Cd and Zn and assisted phytostabilization of As and Pb.

Searching for traces of life in subglacial Lake Vostok (Antarctica) in terms of forward contamination: the lessons for exploration of icy environments on Mars

Science.gov (United States)

Bulat, S. A.; Alekhina, I. A.; Lipenkov, V. Ya.; Petit, J.-R.

Bacterial 16S ribosomal gene analysis guarded by criteria for trace DNA analysis and Ancient DNA research clearly testifies for the very low biomass in accretion ice from giant subglacial Lake Vostok buried beneath 4-km thick East Antarctic ice sheet. It seems that the accretion ice is essentially germ-free indicating that the water body should also be hosting a highly sparse life, if any, unless the lake water lost its biological contents during accretion process. Due to this the search for life in Lake Vostok is constrained by a high chance of contamination similar to forward-contamination upon searching for life on Mars and other icy planets. Of 16 bacterial phylotypes initially recovered from the accretion ice the only one was kept with confident relevance to the lake environment while 15 others were presumed to be contaminants on the basis of indexing contaminant criteria developed for Lake Vostok and similar icy environments. The current way to avoid contamination appears to use stringent ice chemistry-based decontamination procedures and comprehensive biological controls including establishment of contemporary contaminant database as a prerequisite to identify and categorize sources of contaminants. More challenge would be to advance cleanliness and sterilization approaches and procedures in order to achieve and measure the level of cleanliness appropriate for tools exploring environments like Lake Vostok. As a guide for searching for life in (sub)glacial environments on Earth or Mars and Jovian's Europa our recommendations can be summarized as follows: (i) apply stringent ice decontamination procedures to meet chemistry and trace DNA analysis standards, (ii) document biological contents of various environments including humans in contact with ice samples (development of contaminant database), (iii) ensure in using relevant methods to cover both known and expected biodiversity and (iv) verify microbial findings through their possible metabolic profiles

Risk assessment of particle dispersion and trace element contamination from mine-waste dumps.

Science.gov (United States)

Romero, Antonio; González, Isabel; Martín, José María; Vázquez, María Auxiliadora; Ortiz, Pilar

2015-04-01

In this study, a model to delimit risk zones influenced by atmospheric particle dispersion from mine-waste dumps is developed to assess their influence on the soil and the population according to the concentration of trace elements in the waste. The model is applied to the Riotinto Mine (in SW Spain), which has a long history of mining and heavy land contamination. The waste materials are separated into three clusters according to the mapping, mineralogy, and geochemical classification using cluster analysis. Two of the clusters are composed of slag, fresh pyrite, and roasted pyrite ashes, which may contain high concentrations of trace elements (e.g., >1 % As or >4 % Pb). The average pollution load index (PLI) calculated for As, Cd, Co, Cu, Pb, Tl, and Zn versus the baseline of the regional soil is 19. The other cluster is primarily composed of sterile rocks and ochreous tailings, and the average PLI is 3. The combination of particle dispersion calculated by a Gaussian model, the PLI, the surface area of each waste and the wind direction is used to develop a risk-assessment model with Geographic Information System GIS software. The zone of high risk can affect the agricultural soil and the population in the study area, particularly if mining activity is restarted in the near future. This model can be applied to spatial planning and environmental protection if the information is complemented with atmospheric particulate matter studies.

Effect of arbuscular mycorrhizal fungi on trace metal uptake by sunflower plants grown on cadmium contaminated soil.

Science.gov (United States)

Hassan, Saad Eldin; Hijri, Mohamed; St-Arnaud, Marc

2013-09-25

Trace metal (TM) pollution of soil is a worldwide problem that threatens the quality of human and environmental health. Phytoremediation using plants and their associated microbes has been increasingly used as a green technology for cleaning up TM-polluted soils. In this study, we investigated the effect of inoculating two arbuscular mycorrhizal fungal isolates, Rhizophagus irregularis and Funneliformis mosseae, on trace metal uptake by sunflower plants grown in soils contaminated with three different Cd concentrations in a greenhouse trial. Root colonization, plant dry mass, and plant tissue cadmium (Cd), zinc (Zn), and copper (Cu) concentrations in roots and shoots were determined after sunflower harvesting. We found that root mycorrhizal colonization rates were not significantly affected by Cd treatments. At low soil Cd concentration, R. irregularis-inoculated plants had significantly higher shoot Cd and Zn concentrations than plants inoculated with F. mosseae and non-inoculated plants. However, at high soil Cd concentrations, F. mosseae-inoculated plants had significantly lower shoot Cd and Zn concentrations and biological concentration factor (BCF) values than plants inoculated with R. irregularis and non-inoculated plants. Cadmium was mainly translocated in shoot tissues of R. irregularis-inoculated plants and sequestered in the rhizosphere of F. mosseae-inoculated plants. The results indicate that these AMF strains mediate different tolerance strategies to alleviate TM toxicity in their host plants and that inoculation with the R. irregularis strain can be used for Cd phytoextraction, whereas this F. mosseae strain can be useful for Cd and Zn phytostabilization of contaminated soil. Copyright © 2013 Elsevier B.V. All rights reserved.

Small zeolite column tests for removal of cesium from high radioactive contaminated water in Fukushima Daiichi Nuclear Power Station

International Nuclear Information System (INIS)

Hijikata, Takatoshi; Uozumi, Koichi; Tukada, Takeshi; Koyama, Tadafumi; Ishikawa, Keiji; Ono, Shoichi; Suzuki, Shunichi; Denton, Mark; Raymont, John

2011-01-01

After the earthquake on March 11th 2011, a large amount (more than 0.12 million m 3 ) of highly radioactive contaminated water had pooled in Fukushima Daiichi nuclear power station. As an urgent issue, highly radioactive nuclides should be removed from this contaminated water to reduce radioactivity in the turbine buildings and nuclear reactor buildings. Removal of Cs from this contaminated water is a key issue, because 134 Cs and 137 Cs are highly radioactive γ-emitting nuclides. The zeolite column system was used for Cs and Sr removal from the radioactive water of Three-Mile Island Unit 2, and modified columns were then developed as a Cs removal method for high-level radioactive water in US national laboratories (WRSC, ORNL, PNNL, Hanford, etc.). In order to treat Fukushima's highly contaminated water with a similar system, it was necessary to understand the properties of zeolite to remove Cs from sea salt as well as the applicability of the column system to a high throughput of around 1200 m 3 /d. The kinetic characteristics of the column were another property to be understood before actual operation. Hence, a functional small-scale zeolite column system was installed in CRIEPI for conducting the experiments to understand decontamination behaviors. Each column has a 2- or 3-cm inner diameter and a 12-cm height, and 12 g of zeolite-type media was packed into the column. The column experiments were carried out with Kurion-zeolite, Herschelite, at different feed rates of simulated water with different concentrations of Cs and sea salt. As for the water with 4 ppm Cs and 0 ppm sea salt, only a 10% Cs concentration was observed in the effluent after 20,000 bed volumes were fed at a rate of 33 cm/min, which corresponds to the actual system. On the other hand, a 40% Cs concentration was observed in the effluent after only 50 bed volumes were passed for water with 2 ppm Cs and 3.4 wt.% sea salt at a feed rate of 34 cm/min. As the absorption of Cs is hampered by the

Evaluation of secondary electron filter for removing contaminant electrons from high-energy 6 MV x-ray beam

International Nuclear Information System (INIS)

Kumagai, Kozo

1988-01-01

When using high energy X-rays, the dose increases at the skin surface and build-up region of beam contamination of secondary electrons coming out from the inner surface of the lineac head. At our radiotherapy department, many cases of external otitis from severe skin reactions, particularly resulting from whole brain irradiation of primary and metastatic brain tumors with a 6 MV X-ray lineac, have been encountered. An investigation was made of the physical aspects of a 6 MV X-ray beam using three electron filters, lead lucite, lead glass and lucite to remove secondary electrons. Transparent materials for filters should be preferable for locating the light field. The following results were obtained: 1) For removing secondary electrons, a lead lucite filter was found best. 2) The lead lucite filter proved most effective for removing secondary electrons from the area of treatment. It reduced the dose of irradiation to the skin surface and build-up region, and furthermore improved the depth dose relative to that without filters. 3) From a clinical standpoint, skin reactions such as external otitis remarkably decreased using a lead lucite filter. 4) It thus appears necessary to use a high energy X-ray with newly designed filters to reduce beam contamination of secondary electrons. (author)

Biotransformation of trace organic compounds by activated sludge from a biological nutrient removal treatment system.

Science.gov (United States)

Inyang, Mandu; Flowers, Riley; McAvoy, Drew; Dickenson, Eric

2016-09-01

The removal of trace organic compounds (TOrCs) and their biotransformation rates, kb (LgSS(-)(1)h(-)(1)) was investigated across different redox zones in a biological nutrient removal (BNR) system using an OECD batch test. Biodegradation kinetics of fourteen TOrCs with initial concentration of 1-36μgL(-)(1) in activated sludge were monitored over the course of 24h. Degradation kinetic behavior for the TOrCs fell into four groupings: Group 1 (atenolol) was biotransformed (0.018-0.22LgSS(-)(1)h(-)(1)) under anaerobic, anoxic, and aerobic conditions. Group 2 (meprobamate and trimethoprim) biotransformed (0.01-0.21LgSS(-)(1)h(-)(1)) under anoxic and aerobic conditions, Group 3 (DEET, gemfibrozil and triclosan) only biotransformed (0.034-0.26LgSS(-)(1)h(-)(1)) under aerobic conditions, and Group 4 (carbamazepine, primidone, sucralose and TCEP) exhibited little to no biotransformation (<0.001LgSS(-)(1)h(-)(1)) under any redox conditions. BNR treatment did not provide a barrier against Group 4 compounds. Copyright © 2016 Elsevier Ltd. All rights reserved.

PRTR ion exchange vault water removal

International Nuclear Information System (INIS)

Ham, J.E.

1995-11-01

This report documents the removal of radiologically contaminated water from the Plutonium Recycle Test Reactor (PRTR) ion exchange vault. Approximately 57,000 liters (15,000 gallons) of water had accumulated in the vault due to the absence of a rain cover. The water was removed and the vault inspected for signs of leakage. No evidence of leakage was found. The removal and disposal of the radiologically contaminated water decreased the risk of environmental contamination

Vertical distribution of dehalogenating bacteria in mangrove sediment and their potential to remove polybrominated diphenyl ether contamination.

Science.gov (United States)

Pan, Ying; Chen, Juan; Zhou, Haichao; Farzana, Shazia; Tam, Nora F Y

2017-11-30

The removal and degradation of polybrominated diphenyl ethers (PBDEs) in sediments are not clear. The vertical distribution of total and dehalogenating bacteria in sediment cores collected from a typical mangrove swamp in South China and their intrinsic degradation potential were investigated. These bacterial groups had the highest abundances in surface sediments (0-5cm). A 5-months microcosm experiment also showed that surface sediments had the highest rate to remove BDE-47 than deeper sediments (5-30cm) under anaerobic condition. The deeper sediments, being more anaerobic, had lower population of dehalogenating bacteria leading to a weaker BDE-47 removal potential than surface sediments. Stepwise multiple regression analysis indicated that Dehalococcoides spp. were the most important dehalogenating bacteria affecting the anaerobic removal of BDE-47 in mangrove sediments. This is the first study reporting that mangrove sediments harbored diverse groups of dehalogenating bacteria and had intrinsic potential to remove PBDE contamination. Copyright © 2016 Elsevier Ltd. All rights reserved.

Long-term Records of Trace Metal Elements in Core Sediments: Anthropogenic Impacts in The Eure River Watershed

Science.gov (United States)

Gardes, T.; Debret, M.; Copard, Y.; Patault, E.; Deloffre, J.; Marcotte, S.; Develle, A. L.; Sabatier, P.; Chaumillon, E.; Coulombier, T.; Revillon, S.; Nizou, J.; Laberdesque, Y.; Koltalo, F.

2017-12-01

The Martot Dam is located in the Eure River Watershed (Normandy, France), few hundred meters upstream the Eure-Seine Rivers confluence. In the context of the European Water Framework Directive (2000/60/EC), the French Authorities planned to remove this dam in 2017. Nevertheless, impacts of the removal remain poorly studied. Classically, dam blocked sedimentary transfers downstream, but here, sediments are not blocked behind the dam but stored three hundred meters upstream in a hydraulic annex, called the Martot Pond. Furthermore, this pond is submitted to the tidal flow from the Seine Estuary despite the Martot Dam. The aim of the study is to evaluate the dam removal impacts on sedimentary transfers and re-suspension of contaminated sediments stored in the Martot Pond and the Eure River's channel. Concerning past transfers and sediments accumulation in the Eure River Watershed, sedimentary archives have been cored, before dam removal, at the Martot Pond and the Les Damps Pond (located 10km upstream the latter). Dating of sedimentary cores for both ponds indicates a sedimentation rate around 1 cm y-1. Trace metal elements quantification showed a wide metallic contamination with highest concentrations evidenced during the 1950-1960's (As: 13-22 mg kg-1; Cd: 40-55 mg kg-1; Cr: 170-210 mg kg-1; Cu: 400-490 mg kg-1; Hg: 2.3 mg kg-1; Mn: 1,280-2,200 mg kg-1; Ni: 64-75 mg kg-1; Zn: 905-990 mg kg-1) and the 1990-2000's (Cr: 95-215 mg kg-1; Ni: 100 mg kg-1; Pb: 670-855 mg kg-1). These variations of concentrations along cores can be associated with industrial past of the Eure River Watershed and sources of contamination can be identified. Thereby, Zn, Ni or Hg contamination could be associated with wastes of battery factory released in the Eure River during the economic recovery, while Pb contamination is linked to the activities of a cathode-ray tubes factory. Metals quantification in core materials highlighted anthropogenic impacts in the Eure River Watershed. These

Contaminant removal and hydraulic conductivity of laboratory rain garden systems for stormwater treatment.

Science.gov (United States)

Good, J F; O'Sullivan, A D; Wicke, D; Cochrane, T A

2012-01-01

In order to evaluate the influence of substrate composition on stormwater treatment and hydraulic effectiveness, mesocosm-scale (180 L, 0.17 m(2)) laboratory rain gardens were established. Saturated (constant head) hydraulic conductivity was determined before and after contaminant (Cu, Zn, Pb and nutrients) removal experiments on three rain garden systems with various proportions of organic topsoil. The system with only topsoil had the lowest saturated hydraulic conductivity (160-164 mm/h) and poorest metal removal efficiency (Cu ≤ 69.0% and Zn ≤ 71.4%). Systems with sand and a sand-topsoil mix demonstrated good metal removal (Cu up to 83.3%, Zn up to 94.5%, Pb up to 97.3%) with adequate hydraulic conductivity (sand: 800-805 mm/h, sand-topsoil: 290-302 mm/h). Total metal amounts in the effluent were pH was elevated (up to 7.38) provided by the calcareous sand in two of the systems, whereas the topsoil-only system lacked an alkaline source. Organic topsoil, a typical component in rain garden systems, influenced pH, resulting in poorer treatment due to higher dissolved metal fractions.

Removal of Contaminants from Waste Streams at Gas Evolving Flow-Through Porous Electrodes

International Nuclear Information System (INIS)

Mahmoud Saleh, M.

1999-01-01

Electrochemical techniques have been used for the removal of inorganic and organic toxic materials from industrial waste streams. One of the most important branch of these electrochemical techniques is the flow-through porous electrode. Such systems allow for the continuous operation and hence continuous removal of the contaminants from waste streams at high rates and high efficiency. However, when there is an evolution of gas bubbles with the removal process, the treatment process needs a much different treatment of both the design and the mathematical treatment of the such these systems. The evolving gas bubbles within the electrode decrease the pore electrolyte conductivity of the porous electrodes, decrease the efficiency and make the current more non-uniform. This cause the under utilization of the reaction area and finally make the electrode inoperable. In this work the harmful effects of the gas bubbles on the performance of the porous electrode will be modeled. The model accounts for the effects of kinetic, mass transfer and gas bubbles resistance on the overall performance of the electrode. This will help in optimizing the operating conditions and the cell design

Contamination vs. Exposure

Science.gov (United States)

... into the environment can cause air, water, surfaces, soil, plants, buildings, people, or animals to become contaminated. ... water to remove contamination. This process is called decontamination. Try to avoid spreading contamination to parts of ...

Biomonitoring of selected freshwater macrophytes to assess lake trace element contamination: a case study of Nal Sarovar Bird Sanctuary, Gujarat, India

Directory of Open Access Journals (Sweden)

Rita N. KUMAR

2006-02-01

Full Text Available A biomonitoring study was carried out at Nal Sarovar Bird Sanctuary, a proposed Ramsar site, Gujarat State, India, to ascertain the degree of trace element contamination. The study focused on assessment of trace element contamination in certain aquatic macrophytes to be used as biomonitors, in comparison with the sediments (abiotic monitor for heavy metal pollution. Good information was provided by analyzing roots, stems and leaves of native aquatic plants (biomonitors represented by eight species: Bergia odorata, Hydrilla verticillata, Ipomoea aquatica, Najas graminea, Nelumbo nucifera, Phragmites karka, Typha angustata and Vellisnaria spiralis, alongwith surface sediments and water, were analyzed for Cd, Co, Cu, Cu, Ni, Pb and Zn contamination. The highest concentrations of the trace elements were measured in Ipomoea aquatica and the lowest in Bergia odorata. Based on the concentration and toxicity status observed in the lake's vegetation, the six metals are arranged in the following decreasing order: Zn > Cu > Ni > Co > Pb > Cd. Compared with the standard, normal and critical toxicity range in plants, the detected values of Cd and Pb falls within normal range, while that of Co, Ni and Cu were within the critical range. However, Zn showed the highest concentration and alarming toxicity levels, which is considered as one of the most hazardous pollutants in Nal Sarovar Bird Sanctuary. Certain aquatic macrophytes species are also proposed as biomonitors for the investigated heavy metal pollutants. Such result was significant in the plant species such as Ipomoea aquatica and Phragmites karka, which are the two most useful species in biomonitoring studies due to their ability to accumulate elements in high concentration in the roots and their availability throughout the year. The results showed the significant difference in accumulation rate of some metals like Zn, Cu and Ni in different plant organs, which showed more accumulation in root than

Organic contaminant removal efficiency of sodium bentonite/clay (BC) mixtures in high permeability regions utilizing reclaimed wastewater: A meso-scale study

Science.gov (United States)

Xiao, Yang; Li, Yunkai; Ning, Zigong; Li, Pengxiang; Yang, Peiling; Liu, Chengcheng; Liu, Zhongwei; Xu, Feipeng; Hynds, Paul Dylan

2018-03-01

Wastewater reclamation now represents an effective measure for sustainable water resource management in arid regions, however wastewater components (organic micropollutants) may potentially impact local ecological and/or human health. Previous studies have shown that sodium bentonite/natural clay (BC) mixes may be used to effectively reduce riverbed infiltration in regions characterized by excessively high hydraulic conductivity. Accordingly, the current study sought to investigate the contaminant removal efficiency (Re) of several BC mass ratios in simulated dry riverbeds. Results indicate that the measured Re of NH4+-N, CODcr and BOD5 increased in concurrence with an increasing sodium bentonite ratio, up to a maximum Re of 97.4% (NH4+-N), 55.2% (CODcr), and 51.5% (BOD5). The primary contaminant removal site was shown to be the infiltration-reducing (BC) layer, accounting for approximately 40%, 60%, and 70% of NH4+-N, CODcr and BOD5 removal, respectively. Conversely, the removal efficiency of NO3-N was found to be low (managing recharge of non-potable aquifers with reclaimed wastewater.

Influences of thermal decontamination on mercury removal, soil properties, and repartitioning of coexisting heavy metals.

Science.gov (United States)

Huang, Yu-Tuan; Hseu, Zeng-Yei; Hsi, Hsing-Cheng

2011-08-01

Thermal treatment is a useful tool to remove Hg from contaminated soils. However, thermal treatment may greatly alter the soil properties and cause the coexisting contaminants, especially trace metals, to transform and repartition. The metal repartitioning may increase the difficulty in the subsequent process of a treatment train approach. In this study, three Hg-contaminated soils were thermally treated to evaluate the effects of treating temperature and duration on Hg removal. Thermogravimetric analysis was performed to project the suitable heating parameters for subsequent bench-scale fixed-bed operation. Results showed that thermal decontamination at temperature>400°C successfully lowered the Hg content tosoil particle size was less significant, even when the soils were thermally treated to 550°C. Soil clay minerals such as kaolinite were shown to be decomposed. Aggregates were observed on the surface of soil particles after the treatment. The heavy metals tended to transform into acid-extractable, organic-matter bound, and residual forms from the Fe/Mn oxide bound form. These results suggest that thermal treatment may markedly influence the effectiveness of subsequent decontamination methods, such as acid washing or solvent extraction. Copyright © 2011 Elsevier Ltd. All rights reserved.

Quality assessment of trace Cd and Pb contaminants in Thai herbal medicines using ultrasound-assisted digestion prior to flame atomic absorption spectrometry

Directory of Open Access Journals (Sweden)

Watsaka Siriangkhawut

2017-10-01

Full Text Available A simple, efficient, and reliable ultrasound-assisted digestion (UAD procedure was used for sample preparation prior to quantitative determination of trace Cd and Pb contaminants in herbal medicines using flame atomic absorption spectrometry. The parameters influencing UAD such as the solvent system, sample mass, presonication time, sonication time, and digestion temperature were evaluated. The efficiency of the proposed UAD procedure was evaluated by comparing with conventional acid digestion (CAD procedure. Under the optimum conditions, linear calibration graphs in a range of 2–250 μg/L for Cd, and 50–1000 μg/L for Pb were obtained with detection limits of 0.56 μg/L and 10.7 μg/L for Cd and Pb, respectively. The limit of quantification for Cd and Pb were 1.87 μg/L and 40.3 μg/L, respectively. The repeatability for analysis of 10 μg/L for Cd and 100 μg/L for Pb was 2.3% and 2.6%, respectively. The accuracy of the proposed method was evaluated by rice flour certified reference materials. The proposed method was successfully applied for analysis of trace Cd and Pb in samples of various types of medicinal plant and traditional medicine consumed in Thailand. Most herbal medicine samples were not contaminated with Cd or Pb. The contaminant levels for both metals were still lower than the maximum permissible levels of elements in medicinal plant materials and finished herbal products sets by the Ministry of Public Health of Thailand. The exception was the high level of Cd contamination found in two samples of processed medicinal plants.

1993 Proceedings volume 1--Contamination control; symposium on minienvironments; symposium on biocontamination control

International Nuclear Information System (INIS)

Anon.

1993-01-01

Volume 1 contains the proceedings from three symposia. Contamination Control includes the following topics: Atmospheric pressure ionization mass spectroscopy (APIMS) applications; APIMS development; contamination control in cleanroom air; defect reduction in semiconductor processes; contamination control in the aerospace industry; filtration of gases; ultrapure chemical and DI water; filtration of chemicals; wafer cleaning/trace contaminant effects; wafer cleaning techniques; detection of particles in UHP fluids; detection of surface particles; modeling contamination; detection of surface organics; modeling, particle transport, deposition, and removal; and detection of surface metallics. Symposium on Minienvironments includes the following: design of minienvironments; robotics and I/O transport; testing, methods, and standards. The Symposium on Biocontamination Control includes the following: microbial CC facility requirements in pharmaceutical, biological, and medical device manufacture; cleaning and disinfecting methods and devices for bio CC; biocontamination control devices, methodology, and standards, airborne and surface microbial monitoring methods and devices; and regulatory issues in bio CC--present and future. All papers within the scope of the Energy Data Base have been processed separately for inclusion on the data base

Enhanced Stormwater Contaminant Removal and Improved Runoff Quality Using Modified Sorbents in Tree Filters

Science.gov (United States)

Schifman, L. A.; Kasaraneni, V.; Boving, T. B.; Oyanedel-Craver, V.

2013-12-01

Stormwater runoff, particularly in urban areas, contains high concentrations of pathogens that are often cited as one of the main reasons for beach closings and other water quality issues in coastal areas. Commonly found contaminants in runoff are often addressed by structural best management practices (BMP) that capture and treat the runoff before discharging it. Many BMP, such as tree filters, act as primary filtration devices that attenuate total suspended solids, nutrients, and heavy metals from runoff, but typically these BMPs are not designed to treat bacteria and have only minor petroleum hydrocarbon (PH) treatment capabilities. To address this shortcoming, the contaminant retention of an alternative sorption material was compared to expanded shale that is usually used in tree filters. Red cedar wood chips were modified with either Quaternary Ammonium Silane (QAS) or Silver Nanoparticles (AgNPs) to provide antimicrobial properties to the matrix and/or exploit their affinity to sorb PH, particularly polycyclic aromatic hydrocarbons (PAH). Results show that the wood chips exhibit the highest sorption capacity for QAS, making this material favorable for treating bacteria, while at the same time attenuating PAH by sorption processes. In the case of AgNP amendment to wood, less AgNP uptake and more desorption from the wood matrix was observed, making this amendment less favorable for bacteria deactivation. Batch experiments show that wood chips modified with QAS can remove up to 3 orders of magnitude of bacteria and retain up to 0.1 mg/g of PAH compared to shale, which has very limited bacteria deactivation (less than one order of magnitude) a PAH retention capacity of 0.04 mg/g. In this talk, the contaminant removal efficiency of the modified and unmodified materials will be discussed on the background of how these materials may find use in enhanced treatment of stormwater in tree filter BMPs.

Dynamic Sampling of Trace Contaminants During the Mission Operations Test of the Deep Space Habitat

Science.gov (United States)

Monje, Oscar; Valling, Simo; Cornish, Jim

2013-01-01

The atmospheric composition inside spacecraft during long duration space missions is dynamic due to changes in the living and working environment of crew members, crew metabolism and payload operations. A portable FTIR gas analyzer was used to monitor the atmospheric composition within the Deep Space Habitat (DSH) during the Mission Operations Test (MOT) conducted at the Johnson Space Center (JSC). The FTIR monitored up to 20 gases in near- real time. The procedures developed for operating the FTIR were successful and data was collected with the FTIR at 5 minute intervals. Not all the 20 gases sampled were detected in all the modules and it was possible to measure dynamic changes in trace contaminant concentrations that were related to crew activities involving exercise and meal preparation.

Contamination status of arsenic and other trace elements in drinking water and residents from Tarkwa, a historic mining township in Ghana.

Science.gov (United States)

Asante, Kwadwo Ansong; Agusa, Tetsuro; Subramanian, Annamalai; Ansa-Asare, Osmund D; Biney, Charles A; Tanabe, Shinsuke

2007-01-01

This study was conducted to assess the contamination status of 22 trace elements, especially As in water and residents in Tarkwa, a historic mining town in Ghana. Drinking water and human urine samples were collected from Tarkwa in addition to control samples taken from Accra, the capital of Ghana in March, 2004. Concentrations of As and Mn in some drinking water samples from Tarkwa were found above the WHO drinking water guidelines posing a potential health risk for the people. A potential health risk of As and Mn is a concern for the people consuming the contaminated water in this area. No significant difference of As concentrations in human urine between mining town (Tarkwa) and control site (Accra) was observed. Although As concentrations in drinking water in Tarkwa were low, urinary As levels were comparable to those reported in highly As-affected areas in the world. These results suggest the presence of other sources of As contamination in Ghana. This is the first study on multi-elemental contamination in drinking water and human from a mining town in Ghana.

The use of supercritical carbon dioxide for contaminant removal from solid waste

International Nuclear Information System (INIS)

Adkins, C.L.J.; Russick, E.M.; Smith, H.M.; Olson, R.B.

1994-01-01

Supercritical carbon dioxide is being explored as a waste minimization technique for separating oils, greases and solvents from solid waste. The containments are dissolved into the supercritical fluid and precipitated out upon depressurization. The carbon dioxide solvent can then be recycled for continued use. Definitions of the temperature, pressure, flowrate and potential co-solvents are required to establish the optimum conditions for hazardous contaminant removal. Excellent extractive capability for common manufacturing oils, greases, and solvents has been observed in both supercritical and liquid carbon dioxide. Solubility measurements are being used to better understand the extraction process, and to determine if the minimum solubility required by federal regulations is met

Trace Elements in Marine Sediment and Organisms in the Gulf of Thailand

Science.gov (United States)

Worakhunpiset, Suwalee

2018-01-01

This review summarizes the findings from studies of trace element levels in marine sediment and organisms in the Gulf of Thailand. Spatial and temporal variations in trace element concentrations were observed. Although trace element contamination levels were low, the increased urbanization and agricultural and industrial activities may adversely affect ecosystems and human health. The periodic monitoring of marine environments is recommended in order to minimize human health risks from the consumption of contaminated marine organisms. PMID:29677146

Final Report: Caustic Waste-Soil Weathering Reactions and Their Impacts on Trace Contaminant Migration and Sequestration

International Nuclear Information System (INIS)

O'Day, Peggy A.; Chorover, J.; Mueller, K.T.; Serne, R.J.

2006-01-01

The principal goal of this project was to assess the molecular nature and stability of radionuclide (137-Cs, 90-Sr, and 129-I) immobilization during weathering reactions in bulk Hanford sediments and their high surface area clay mineral constituents. We focused on the unique aqueous geochemical conditions that are representative of waste-impacted locations in the Hanford site vadose zone: high ionic strength, high pH and high Al concentrations. The specific objectives of the work were to (i) measure the coupling of clay mineral weathering and contaminant uptake kinetics of Cs+, Sr2+ and I-; (ii) determine the molecular structure of contaminant binding sites and their change with weathering time during and after exposure to synthetic tank waste leachate (STWL); (iii) establish the stability of neoformed weathering products and their sequestered contaminants upon exposure of the solids to more ''natural'' soil solutions (i.e., after removal of the caustic waste source); and (iv) integrate macroscopic, microscopic and spectroscopic data to distinguish labile from non-labile contaminant binding environments, including their dependence on system composition and weathering time. During this funding period, we completed a large set of bench-scale collaborative experiments and product characterization aimed at elucidating the coupling between mineral transformation reactions and contaminant sequestration/stabilization. Our experiments included three representative Hanford sediments: course and fine sediments collected from the Hanford Formation and Ringold Silt, in addition to investigations with specimen clay minerals illite, vermiculite, smectite and kaolinite. These experiments combined macroscopic measurements of element release, contaminant uptake and subsequent neoformed mineral dissolution behavior, with detailed studies of solid phase products using SEM and TEM microscopy, NMR, XAS and FTIR spectroscopy. Our studies have shown direct coupling between mineral

[Impact of compounded chelants on removal of heavy metals and characteristics of morphologic change in soil from heavy metals contaminated sites].

Science.gov (United States)

Yin, Xue; Chen, Jia-Jun; Lü, Ce

2014-02-01

Na2 EDTA (EDTA) has been extensively applied in remediation of soil contaminated by heavy metals (HMs). However, it poses a threat to the environment due to its difficulty of degradation. In addition, it is of great importance to clarify the morphological distribution of these metals in soil, as it is related to the environmental risk of contaminated sites. Thus, in order to cut back the use of EDTA, a series of batch washing experiments were conducted to evaluate the removal of arsenic, cadmium, copper, and lead from the contaminated soil collected in a chemical plant. Furthermore, adopting the optimal ratio of EDTA/EDDS, the change of morphological distribution of HMs before and after washing was studied. The results indicated that the removal of arsenic, cadmium and lead reached the maximum when the ratio of EDTA/EDDS was 7:3 and the optimal value was 12.67%, 38.71% and 31.09%, respectively. The removal of copper reached 16.91% at an EDTA/EDDS ratio of 9:1. After washing, the absolute Fe-Mn oxide fraction concentration of arsenic was higher, which would increase the environmental risk; the morphological fraction distribution of cadmium was similar to the original soil; the removal of copper and lead was mainly derived from the Fe-Mn oxide fraction; as to lead, the absolute concentration of Fe-Mn oxide fraction decreased dramatically, was and the same was observed for the percentage in the organic fraction. Employing the compounded system, the removal of HMs could be improved, and meanwhile the amounts of bioavailable HMs declined. Hence, it is beneficial for providing theoretical support for HMs remediation.

Selective removal of diclofenac from contaminated water using molecularly imprinted polymer microspheres

International Nuclear Information System (INIS)

Dai Chaomeng; Geissen, Sven-Uwe; Zhang Yalei; Zhang Yongjun; Zhou Xuefei

2011-01-01

A molecularly imprinted polymer (MIP) was synthesized by precipitation polymerization using diclofenac (DFC) as a template. Binding characteristics of the MIP were evaluated using equilibrium binding experiments. Compared to the non-imprinted polymer (NIP), the MIP showed an outstanding affinity towards DFC in an aqueous solution with a binding site capacity (Q max ) of 324.8 mg/g and a dissociation constant (K d ) of 3.99 mg/L. The feasibility of removing DFC from natural water by the MIP was demonstrated by using river water spiked with DFC. Effects of pH and humic acid on the selectivity and adsorption capacity of MIP were evaluated in detail. MIP had better selectivity and higher adsorption efficiency for DFC as compared to that of powdered activated carbon (PAC). In addition, MIP reusability was demonstrated for at least 12 repeated cycles without significant loss in performance, which is a definite advantage over single-use activated carbon. - Highlights: → A MIP was synthesized by precipitation polymerization using DFC as template. → The MIP had better selectivity and higher adsorption efficiency for DFC. → The MIP is an effective method for selective removal of DFC from complex water. → MIP reusability is a definite advantage over single-use activated carbon. - A diclofenac molecularly imprinted polymer synthesized by precipitation polymerization was used for the selective removal of diclofenac from contaminated water.

Selective removal of diclofenac from contaminated water using molecularly imprinted polymer microspheres

Energy Technology Data Exchange (ETDEWEB)

Dai Chaomeng [State Key Laboratory of Pollution Control and Resource Reuse, Tongji University, Shanghai 200092 (China); Department of Environmental Technology, Chair of Environmental Process Engineering, Technical University of Berlin, Berlin (Germany); Geissen, Sven-Uwe, E-mail: sven.geissen@tu-berlin.de [Department of Environmental Technology, Chair of Environmental Process Engineering, Technical University of Berlin, Berlin (Germany); Zhang Yalei, E-mail: zhangyalei@tongji.edu.cn [State Key Laboratory of Pollution Control and Resource Reuse, Tongji University, Shanghai 200092 (China); Zhang Yongjun [Department of Environmental Technology, Chair of Environmental Process Engineering, Technical University of Berlin, Berlin (Germany); Zhou Xuefei [State Key Laboratory of Pollution Control and Resource Reuse, Tongji University, Shanghai 200092 (China)

2011-06-15

A molecularly imprinted polymer (MIP) was synthesized by precipitation polymerization using diclofenac (DFC) as a template. Binding characteristics of the MIP were evaluated using equilibrium binding experiments. Compared to the non-imprinted polymer (NIP), the MIP showed an outstanding affinity towards DFC in an aqueous solution with a binding site capacity (Q{sub max}) of 324.8 mg/g and a dissociation constant (K{sub d}) of 3.99 mg/L. The feasibility of removing DFC from natural water by the MIP was demonstrated by using river water spiked with DFC. Effects of pH and humic acid on the selectivity and adsorption capacity of MIP were evaluated in detail. MIP had better selectivity and higher adsorption efficiency for DFC as compared to that of powdered activated carbon (PAC). In addition, MIP reusability was demonstrated for at least 12 repeated cycles without significant loss in performance, which is a definite advantage over single-use activated carbon. - Highlights: > A MIP was synthesized by precipitation polymerization using DFC as template. > The MIP had better selectivity and higher adsorption efficiency for DFC. > The MIP is an effective method for selective removal of DFC from complex water. > MIP reusability is a definite advantage over single-use activated carbon. - A diclofenac molecularly imprinted polymer synthesized by precipitation polymerization was used for the selective removal of diclofenac from contaminated water.

Use of fluorescence EEM to monitor the removal of emerging contaminants in full scale wastewater treatment plants.

Science.gov (United States)

Sgroi, Massimiliano; Roccaro, Paolo; Korshin, Gregory V; Greco, Valentina; Sciuto, Sebastiano; Anumol, Tarun; Snyder, Shane A; Vagliasindi, Federico G A

2017-02-05

This study investigated the applicability of different techniques for fluorescence excitation/emission matrices data interpretations, including peak-picking method, fluorescence regional integration and PARAFAC modelling, to act as surrogates in predicting emerging trace organic compounds (ETOrCs) removal during conventional wastewater treatments that usually comprise primary and secondary treatments. Results showed that fluorescence indexes developed using alternative methodologies but indicative of a same dissolved organic matter component resulted in similar predictions of the removal of the target compounds. The peak index defined by the excitation/emission wavelength positions (λ ex/ λ em ) 225/290nm and related to aromatic proteins and tyrosine-like fluorescence was determined to be a particularly suitable surrogate for monitoring ETOrCs that had very high removal rates (average removal >70%) (i.e., triclosan, caffeine and ibuprofen). The peak index defined by λ ex/ λ em =245/440nm and the PARAFAC component with wavelength of the maxima λ ex/ λ em =245, 350/450, both identified as humic-like fluorescence, were found remarkably well correlated with ETOrCs such as atenolol, naproxen and gemfibrozil that were moderately removed (51-70% average removal). Finally, the PARAFAC component with wavelength of the maxima λ ex/ λ em =<240, 315/380 identified as microbial humic-like fluorescence was the only index correlated with the removal of the antibiotic trimethoprim (average removal 68%). Copyright © 2016 Elsevier B.V. All rights reserved.

Trace impurity analyzer

International Nuclear Information System (INIS)

Schneider, W.J.; Edwards, D. Jr.

1979-01-01

The desirability for long-term reliability of large scale helium refrigerator systems used on superconducting accelerator magnets has necessitated detection of impurities to levels of a few ppM. An analyzer that measures trace impurity levels of condensable contaminants in concentrations of less than a ppM in 15 atm of He is described. The instrument makes use of the desorption temperature at an indicated pressure of the various impurities to determine the type of contaminant. The pressure rise at that temperature yields a measure of the contaminant level of the impurity. A LN 2 cryogenic charcoal trap is also employed to measure air impurities (nitrogen and oxygen) to obtain the full range of contaminant possibilities. The results of this detector which will be in use on the research and development helium refrigerator of the ISABELLE First-Cell is described

Arbuscular mycorrhizal fungal inoculation protects Miscanthus × giganteus against trace element toxicity in a highly metal-contaminated site.

Science.gov (United States)

Firmin, Stéphane; Labidi, Sonia; Fontaine, Joël; Laruelle, Frédéric; Tisserant, Benoit; Nsanganwimana, Florian; Pourrut, Bertrand; Dalpé, Yolande; Grandmougin, Anne; Douay, Francis; Shirali, Pirouz; Verdin, Anthony; Lounès-Hadj Sahraoui, Anissa

2015-09-15

Arbuscular mycorrhizal fungus (AMF)-assisted phytoremediation could constitute an ecological and economic method in polluted soil rehabilitation programs. The aim of this work was to characterize the trace element (TE) phytoremediation potential of mycorrhizal Miscanthus × giganteus. To understand the mechanisms involved in arbuscular mycorrhizal symbiosis tolerance to TE toxicity, the fatty acid compositions and several stress oxidative biomarkers were compared in the roots and leaves of Miscanthus × giganteus cultivated under field conditions in either TE-contaminated or control soils. TEs were accumulated in greater amounts in roots, but the leaves were the organ most affected by TE contamination and were characterized by a strong decrease in fatty acid contents. TE-induced oxidative stress in leaves was confirmed by an increase in the lipid peroxidation biomarker malondialdehyde (MDA). TE contamination decreased the GSSG/GSH ratio in the leaves of exposed plants, while peroxidase (PO) and superoxide dismutase (SOD) activities were increased in leaves and in whole plants, respectively. AMF inoculation also increased root colonization in the presence of TE contamination. The mycorrhizal colonization determined a decrease in SOD activity in the whole plant and PO activities in leaves and induced a significant increase in the fatty acid content in leaves and a decrease in MDA formation in whole plants. These results suggested that mycorrhization is able to confer protection against oxidative stress induced by soil pollution. Our findings suggest that mycorrhizal inoculation could be used as a bioaugmentation technique, facilitating Miscanthus cultivation on highly TE-contaminated soil. Copyright © 2015. Published by Elsevier B.V.

Dual layer hollow fiber sorbents for trace H2S removal from gas streams

KAUST Repository

Bhandari, Dhaval A.; Bessho, Naoki; Koros, William J.

2013-01-01

Hollow fiber sorbents are pseudo monolithic materials with potential use in various adsorption based applications. Dual layer hollow fiber sorbents have the potential to allow thermal regeneration without direct contact of the regeneration fluid with the sorbent particles. This paper considers the application of dual layer hollow fiber sorbents for a case involving trace amounts of H2S removal from a simulated gas stream and offers a comparison with single layer hollow fiber sorbents. The effect of spin dope composition and core layer zeolite loading on the gas flux, H2S transient sorption capacity and pore structure are also studied. This work can be used as a guide to develop and optimize dual layer hollow fiber sorbent properties beyond the specific example considered here. © 2013 Elsevier Ltd.

Dual layer hollow fiber sorbents for trace H2S removal from gas streams

KAUST Repository

Bhandari, Dhaval A.

2013-05-01

Hollow fiber sorbents are pseudo monolithic materials with potential use in various adsorption based applications. Dual layer hollow fiber sorbents have the potential to allow thermal regeneration without direct contact of the regeneration fluid with the sorbent particles. This paper considers the application of dual layer hollow fiber sorbents for a case involving trace amounts of H2S removal from a simulated gas stream and offers a comparison with single layer hollow fiber sorbents. The effect of spin dope composition and core layer zeolite loading on the gas flux, H2S transient sorption capacity and pore structure are also studied. This work can be used as a guide to develop and optimize dual layer hollow fiber sorbent properties beyond the specific example considered here. © 2013 Elsevier Ltd.

Monitoring the prevalence of nitrosamines in South African waters and their removal using cyclodextrin polyurethanes

Science.gov (United States)

Mhlongo, Sthembile H.; Mamba, Bhekie B.; Krause, Rui W.

The prevalence of nitrosamines, especially N-nitrosodimethylamine (NDMA), was monitored in three South African water supplies. NDMA a disinfection by-product (DBP) and potent carcinogen, has recently been detected in many drinking water supplies internationally. Besides direct industrial or human-derived contamination, nitrosodimethylamine can be formed through a chemical reaction between monochloroamine and an organic based compound such as dimethylamine which is frequently detected in surface water. It has been suggested that chloramination of surface waters with a high concentration of dissolved organic carbon (DOC) could result in elevated NDMA formation. Growing evidence suggests that NDMA occurs more frequently and at higher concentrations in drinking water systems that practise chloramination compared to systems that use chlorination. In gauging the extent of water contamination by nitrosamines in water distribution systems, especially NDMA, water samples collected from three different water treatment plants that practise chemical drinking water disinfection were qualitatively analysed for the presence of nitrosamines. Solid phase microextraction (SPME) was employed in the extraction of nitrosamines from the water samples and gas chromatography-mass spectrometry (GC-MS), was used in the analysis of the water samples. Trace amounts of NDMA were detected at one of the water treatment plants and in the distribution network. The application of water-insoluble cyclodextrin (CD) polymers in the removal of nitrosamines and potential amine precursors from the water samples was tested. Quantitative removal of NDMA (based on peak area) from the water samples was achieved which suggests that in the water treatment train the use of these nanosponges can be applied in the mitigation of trace contaminants such as NDMA.

Assessment of suitability of tree species for the production of biomass on trace element contaminated soils

International Nuclear Information System (INIS)

Evangelou, Michael W.H.; Deram, Annabelle; Gogos, Alexander; Studer, Björn; Schulin, Rainer

2012-01-01

Highlights: ► Birch: lowest metal concentrations in foliage, wood and bark. ► Bark proportion does not have to decline with increasing age of tree. ► Long harvest rotation (>25 y) reduces metal concentrations in stem. ► Birch: most suitable tree for BCL. - Abstract: To alleviate the demand on fertile agricultural land for production of bioenergy, we investigated the possibility of producing biomass for bioenergy on trace element (TE) contaminated land. Soil samples and plant tissues (leaves, wood and bark) of adult willow (Salix sp.), poplar (Populus sp.), and birch (Betula pendula) trees were collected from five contaminated sites in France and Germany and analysed for Zn, Cd, Pb, Cu, Ca, and K. Cadmium concentration in tree leaves were correlated with tree species, whereas Zn concentration in leaves was site correlated. Birch revealed significantly lower leaf Cd concentrations (1.2–8.9 mg kg −1 ) than willow and poplar (5–80 mg kg −1 ), thus posing the lowest risk for TE contamination of surrounding areas. Birch displayed the lowest bark concentrations for Ca (2300–6200 mg kg −1 ) and K (320–1250 mg kg −1 ), indicating that it would be the most suitable tree species for fuel production, as high concentrations of K and Ca decrease the ash melting point which results in a reduced plant lifetime. Due to higher TE concentrations in bark compared to wood a small bark proportion in relation to the trunk is desirable. In general the bark proportion was reduced with the tree age. In summary, birch was amongst the investigated species the most suitable for biomass production on TE contaminated land.

Present and Future Challenges in Trace and Ultra-Trace Analysis

International Nuclear Information System (INIS)

Toulhoat, P.

2005-01-01

The analysis of trace and ultra-trace elements is continuously stimulating the progress in analytical chemistry. Environmental chemistry, radiochemistry, biology, health, agri-food are prescribers of trace analyses, with continuously increasing exigencies: lowering detection limits, lowering costs and analysis time, improving the quality of analytical information. Precise data about the chemical identity and chemical environment of analytes are now requested. Such pieces of information, beyond simple numerical data and confidence intervals, are necessary to understand studied systems, and to predict their evolution. From environmental contamination cases, one can envisage the various aspects of a problem, with for each of them its own exigencies and specificities in terms of analytical methods and approaches. The detection of traces and ultra-traces of actinides and fission products has been recently revisited and stimulates new technological developments (non proliferation issues, waste management). Data on their speciation in geological and biological media are essential for evaluating the safety of nuclear waste repositories. Various techniques are now used to determine speciation in liquid samples or on surfaces, with tremendous spatial resolutions or sensitivities. A new revolution in analytical chemistry is expected with the development of micro- or nano-analytical technologies. (author)

Conditions for effective removal of pyrene from an artificially contaminated soil using Pseudomonas aeruginosa 57SJ rhamnolipids

International Nuclear Information System (INIS)

Bordas, Francois; Lafrance, Pierre; Villemur, Richard

2005-01-01

The efficacy of a new rhamnolipid biosurfactants mixture to enhance the removal of pyrene from a soil artificially contaminated was investigated. The molar solubilization ratio (MSR) and the partition coefficient between the micelles and water (log K m ) were found to be 7.5 x 10 -3 and 5.7, respectively. From soil column studies, the pyrene removal increased linearly with the concentration of the injected biosurfactants solution above the effective critical micellar concentration (0.4 g L -1 ). Flushing with a 5.0 g L -1 biosurfactants solution increased the pyrene concentration in the effluent by 178 times. At high biosurfactants' concentrations (2.5 and 5.0 g L -1 ), the cumulative pyrene recovery reached 70%. This pyrene remobilization takes place independently of the soil organic carbon solubilization. This study provides a combination of batch and column experiments in order to find the conditions for effective soil remediation using a new rhamnolipids mixture. - The potential of newly isolated biosurfactants to mobilize PAHs from contaminated soils was evaluated from the determination in dynamic conditions of their effective critical micellar concentration

Removal of Pb, Zn, and Cd from contaminated soil by new washing agent from plant material.

Science.gov (United States)

Cao, Yaru; Zhang, Shirong; Wang, Guiyin; Huang, Qinling; Li, Ting; Xu, Xiaoxun

2017-03-01

Soil washing is an effective approach to remove soil heavy metals, and the washing agent is generally regarded as one of the primary factors in the process, but there is still a lack of efficient and eco-friendly agents for this technique. Here, we showed that four plant washing agents-from water extracts of Coriaria nepalensis (CN), Clematis brevicaudata (CB), Pistacia weinmannifolia (PW), and Ricinus communis (RC)-could be feasible agents for the removal of soil lead (Pb), zinc (Zn), and cadmium (Cd). The metal removal efficiencies of the agents increased with their concentrations from 20 to 80 g L -1 , decreased with the increasing solution pH, and presented different trends with the reaction time increasing. CN among the four agents had the highest removal efficiencies of soil Pb (62.02%) and Zn (29.18%) but owned the relatively low Cd removal efficiencies (21.59%). The Fourier transform infrared spectroscopy showed that the abilities of plant washing agents for the removal of soil heavy metals may result from bioactive substances with specific functional groups such as -COOH, -NH 2 , and -OH. Our study provided CN as the best washing agents for the remediation of contaminated soil by heavy metals.

A thermodynamic and kinetic study of trace iron removal from aqueous cobalt sulfate solutions using Monophos resin.

Science.gov (United States)

Wang, Guangxin; Zhao, Yunchao; Yang, Bin; Song, Yongfa

2018-01-01

High purity cobalt has many important applications, such as magnetic recording media, magnetic recording heads, optoelectronic devices, magnetic sensors, and integrated circuits, etc. To produce 5N or higher purity cobalt in an electro-refining process, one of the challenges is to effectively reduce the Fe content of aqueous cobalt salt solution before electrolysis. This paper describes thermodynamic and kinetic investigations of the Fe adsorption process of a new sulfonated monophosphonic resin with the trade mark Monophos. Five cobalt sulfate solutions of different Co concentrations were prepared. Fe ions were removed from the solutions by ion exchange method using Monophos resin. Chemical analysis was carried out using a Perkin Elmer ICP-OES. The initial Fe concentrations of about 0.9-2.0 mg/L can be reduced to about 0.3-0.8 mg/L, which is equivalent to an Fe removal rate of 60-67%. The Langmuir isothermal adsorption model applies well to the Fe removal process. A second-order type based on McKay equation fits better with experimental data than other kinetic models. The kinetic curve can be divided into two sections. For t 30 min. Monophos resin is effective for the removal of trace Fe from cobalt sulfate solution. This ion exchange process obeys the Langmuir isothermal adsorption model and the McKay equation of second-order kinetics.

Remediation of the Highland Drive South Ravine, Port Hope, Ontario: Contaminated Groundwater Discharge Management Using Permeable Reactive Barriers and Contaminated Sediment Removal - 13447

Energy Technology Data Exchange (ETDEWEB)

Smyth, David; Roos, Gillian [Golder Associates Ltd., 2390 Argentia Road, Mississauga, ON L5N 5Z7 (Canada); Ferguson Jones, Andrea [MMM Group Ltd., 100 Commerce Valley Drive West, Thornhill, ON L3T 0A1 (Canada); Case, Glenn [AECL Port Hope Area Initiative Management Office, 115 Toronto Road, Port Hope, ON L1A 3S4 (Canada); Yule, Adam [Public Works and Government Services Canada, 4900 Yonge Street, 11th Floor, Toronto, ON, M2N 6A6 (Canada)

2013-07-01

The Highland Drive South Ravine (HDSR) is the discharge area for groundwater originating from the Highland Drive Landfill, the Pine Street North Extension (PSNE) roadbed parts of the Highland Drive roadbed and the PSNE Consolidation Site that contain historical low-level radioactive waste (LLRW). The contaminant plume from these LLRW sites contains elevated concentrations of uranium and arsenic and discharges with groundwater to shallow soils in a wet discharge area within the ravine, and directly to Hunt's Pond and Highland Drive South Creek, which are immediately to the south of the wet discharge area. Remediation and environmental management plans for HDSR have been developed within the framework of the Port Hope Project and the Port Hope Area Initiative. The LLRW sites will be fully remediated by excavation and relocation to a new Long-Term Waste Management Facility (LTWMF) as part of the Port Hope Project. It is projected, however, that the groundwater contaminant plume between the remediated LLRW sites and HDSR will persist for several hundreds of years. At the HDSR, sediment remediation within Hunt's Ponds and Highland Drive South Creek, excavation of the existing and placement of clean fill will be undertaken to remove current accumulations of solid-phase uranium and arsenic associated with the upper 0.75 m of soil in the wet discharge area, and permeable reactive barriers (PRBs) will be used for in situ treatment of contaminated groundwater to prevent the ongoing discharge of uranium and arsenic to the area in HDSR where shallow soil excavation and replacement has been undertaken. Bench-scale testing using groundwater from HDSR has confirmed excellent treatment characteristics for both uranium and arsenic using permeable reactive mixtures containing granular zero-valent iron (ZVI). A sequence of three PRBs containing ZVI and sand in backfilled trenches has been designed to intercept the groundwater flow system prior to its discharge to the ground

Remediation of the Highland Drive South Ravine, Port Hope, Ontario: Contaminated Groundwater Discharge Management Using Permeable Reactive Barriers and Contaminated Sediment Removal - 13447

International Nuclear Information System (INIS)

Smyth, David; Roos, Gillian; Ferguson Jones, Andrea; Case, Glenn; Yule, Adam

2013-01-01

The Highland Drive South Ravine (HDSR) is the discharge area for groundwater originating from the Highland Drive Landfill, the Pine Street North Extension (PSNE) roadbed parts of the Highland Drive roadbed and the PSNE Consolidation Site that contain historical low-level radioactive waste (LLRW). The contaminant plume from these LLRW sites contains elevated concentrations of uranium and arsenic and discharges with groundwater to shallow soils in a wet discharge area within the ravine, and directly to Hunt's Pond and Highland Drive South Creek, which are immediately to the south of the wet discharge area. Remediation and environmental management plans for HDSR have been developed within the framework of the Port Hope Project and the Port Hope Area Initiative. The LLRW sites will be fully remediated by excavation and relocation to a new Long-Term Waste Management Facility (LTWMF) as part of the Port Hope Project. It is projected, however, that the groundwater contaminant plume between the remediated LLRW sites and HDSR will persist for several hundreds of years. At the HDSR, sediment remediation within Hunt's Ponds and Highland Drive South Creek, excavation of the existing and placement of clean fill will be undertaken to remove current accumulations of solid-phase uranium and arsenic associated with the upper 0.75 m of soil in the wet discharge area, and permeable reactive barriers (PRBs) will be used for in situ treatment of contaminated groundwater to prevent the ongoing discharge of uranium and arsenic to the area in HDSR where shallow soil excavation and replacement has been undertaken. Bench-scale testing using groundwater from HDSR has confirmed excellent treatment characteristics for both uranium and arsenic using permeable reactive mixtures containing granular zero-valent iron (ZVI). A sequence of three PRBs containing ZVI and sand in backfilled trenches has been designed to intercept the groundwater flow system prior to its discharge to the ground surface

Uptake of toluene and ethylbenzene by plants: removal of volatile indoor air contaminants.

Science.gov (United States)

Sriprapat, Wararat; Suksabye, Parinda; Areephak, Sirintip; Klantup, Polawat; Waraha, Atcharaphan; Sawattan, Anuchit; Thiravetyan, Paitip

2014-04-01

Air borne uptake of toluene and ethylbenzene by twelve plant species was examined. Of the twelve plant species examined, the highest toluene removal was found in Sansevieria trifasciata, while the ethylbenzene removal from air was with Chlorophytum comosum. Toluene and ethylbenzene can penetrate the plant׳s cuticle. However, the removal rates do not appear to be correlated with numbers of stomata per plant. It was found that wax of S. trifasciata and Sansevieria hyacinthoides had greater absorption of toluene and ethylbenzene, and it contained high hexadecanoic acid. Hexadecanoic acid might be involved in toluene and ethylbenzene adsorption by cuticles wax of plants. Chlorophyll fluorescence analysis or the potential quantum yield of PSII (Fv/Fm) in toluene exposed plants showed no significant differences between the control and the treated plants, whereas plants exposed to ethylbenzene showed significant differences or those parameters, specifically in Dracaena deremensis (Lemon lime), Dracaena sanderiana, Kalanchoe blossfeldiana, and Cordyline fruticosa. The Fv/Fm ratio can give insight into the ability of plants to tolerate (indoor) air pollution by volatile organic chemicals (VOC). This index can be used for identification of suitable plants for treating/sequestering VOCs in contaminated air. Copyright © 2014 Elsevier Inc. All rights reserved.

Phytoremediation removal rates of benzene, toluene, and chlorobenzene.

Science.gov (United States)

Limmer, Matt A; Wilson, Jordan; Westenberg, David; Lee, Amy; Siegman, Mark; Burken, Joel G

2018-06-07

Phytoremediation is a sustainable remedial approach, although performance efficacy is rarely reported. In this study, we assessed a phytoremediation plot treating benzene, toluene, and chlorobenzene. A comparison of the calculated phytoremediation removal rate with estimates of onsite contaminant mass was used to forecast cleanup periods. The investigation demonstrated that substantial microbial degradation was occurring in the subsurface. Estimates of transpiration indicated that the trees planted were removing approximately 240,000 L of water per year. This large quantity of water removal implies substantial removal of contaminant due to large amounts of contaminants in the groundwater; however, these contaminants extensively sorb to the soil, resulting in large quantities of contaminant mass in the subsurface. The total estimate of subsurface contaminant mass was also complicated by the presence of non-aqueous phase liquids (NAPL), additional contaminant masses that were difficult to quantify. These uncertainties of initial contaminant mass at the site result in large uncertainty in the cleanup period, although mean estimates are on the order of decades. Collectively, the model indicates contaminant removal rates on the order of 10 -2 -10 0 kg/tree/year. The benefit of the phytoremediation system is relatively sustainable cleanup over the long periods necessary due to the presence of NAPL.

Isotopic Tracing of Thallium Contamination in Soils Affected by Emissions from Coal-Fired Power Plants.

Science.gov (United States)

Vaněk, Aleš; Grösslová, Zuzana; Mihaljevič, Martin; Trubač, Jakub; Ettler, Vojtěch; Teper, Leslaw; Cabala, Jerzy; Rohovec, Jan; Zádorová, Tereza; Penížek, Vít; Pavlů, Lenka; Holubík, Ondřej; Němeček, Karel; Houška, Jakub; Drábek, Ondřej; Ash, Christopher

2016-09-20

Here, for the first time, we report the thallium (Tl) isotope record in moderately contaminated soils with contrasting land management (forest and meadow soils), which have been affected by emissions from coal-fired power plants. Our findings clearly demonstrate that Tl of anthropogenic (high-temperature) origin with light isotope composition was deposited onto the studied soils, where heavier Tl (ε(205)Tl ∼ -1) naturally occurs. The results show a positive linear relationship (R(2) = 0.71) between 1/Tl and the isotope record, as determined for all the soils and bedrocks, also indicative of binary Tl mixing between two dominant reservoirs. We also identified significant Tl isotope variations within the products from coal combustion and thermo-desorption experiments with local Tl-rich coal pyrite. Bottom ash exhibited the heaviest Tl isotope composition (ε(205)Tl ∼ 0), followed by fly ash (ε(205)Tl between -2.5 and -2.8) and volatile Tl fractions (ε(205)Tl between -6.2 and -10.3), suggesting partial Tl isotope fractionations. Despite the evident role of soil processes in the isotope redistributions, we demonstrate that Tl contamination can be traced in soils and propose that the isotope data represent a possible tool to aid our understanding of postdepositional Tl dynamics in surface environments for the future.

Food product tracing technology capabilities and interoperability.

Science.gov (United States)

Bhatt, Tejas; Zhang, Jianrong Janet

2013-12-01

Despite the best efforts of food safety and food defense professionals, contaminated food continues to enter the food supply. It is imperative that contaminated food be removed from the supply chain as quickly as possible to protect public health and stabilize markets. To solve this problem, scores of technology companies purport to have the most effective, economical product tracing system. This study sought to compare and contrast the effectiveness of these systems at analyzing product tracing information to identify the contaminated ingredient and likely source, as well as distribution of the product. It also determined if these systems can work together to better secure the food supply (their interoperability). Institute of Food Technologists (IFT) hypothesized that when technology providers are given a full set of supply-chain data, even for a multi-ingredient product, their systems will generally be able to trace a contaminated product forward and backward through the supply chain. However, when provided with only a portion of supply-chain data, even for a product with a straightforward supply chain, it was expected that interoperability of the systems will be lacking and that there will be difficulty collaborating to identify sources and/or recipients of potentially contaminated product. IFT provided supply-chain data for one complex product to 9 product tracing technology providers, and then compared and contrasted their effectiveness at analyzing product tracing information to identify the contaminated ingredient and likely source, as well as distribution of the product. A vertically integrated foodservice restaurant agreed to work with IFT to secure data from its supply chain for both a multi-ingredient and a simpler product. Potential multi-ingredient products considered included canned tuna, supreme pizza, and beef tacos. IFT ensured that all supply-chain data collected did not include any proprietary information or information that would otherwise

Atom trap trace analysis

International Nuclear Information System (INIS)

Lu, Z.-T.; Bailey, K.; Chen, C.-Y.; Du, X.; Li, Y.-M.; O'Connor, T. P.; Young, L.

2000-01-01

A new method of ultrasensitive trace-isotope analysis has been developed based upon the technique of laser manipulation of neutral atoms. It has been used to count individual 85 Kr and 81 Kr atoms present in a natural krypton sample with isotopic abundances in the range of 10 -11 and 10 -13 , respectively. The atom counts are free of contamination from other isotopes, elements,or molecules. The method is applicable to other trace-isotopes that can be efficiently captured with a magneto-optical trap, and has a broad range of potential applications

Removal of antibiotics from water in the coexistence of suspended particles and natural organic matters using amino-acid-modified-chitosan flocculants: A combined experimental and theoretical study

International Nuclear Information System (INIS)

Jia, Shuying; Yang, Zhen; Ren, Kexin; Tian, Ziqi; Dong, Chang; Ma, Ruixue; Yu, Ge; Yang, Weiben

2016-01-01

Highlights: • Novel amino-acid-modified-chitosan flocculants are employed to remove antibiotics. • Effects of different structures of amino acids and antibiotics are investigated. • Correlation analysis shows coexisted kaolin and HA have synergistic removal effect. • Theoretical DFT calculation clarifies the interactions in molecular level. - Abstract: Contamination of trace antibiotics is widely found in surface water sources. This work delineates removal of trace antibiotics (norfloxacin (NOR), sulfadiazine (SDZ) or tylosin (TYL)) from synthetic surface water by flocculation, in the coexistence of inorganic suspended particles (kaolin) and natural organic matter (humic acid, HA). To avoid extra pollution caused by petrochemical products-based modification reagents, environmental-friendly amino-acid-modified-chitosan flocculants, Ctrp and Ctyr, with different functional aromatic-rings structures were employed. Jar tests at various pHs exhibited that, Ctyr, owning phenol groups as electron donors, was favored for elimination of cationic NOR (∼50% removal; optimal pH: 6; optimal dosage: 4 mg/L) and TYL (∼60% removal; optimal pH: 7; optimal dosage: 7.5 mg/L), due to π–π electron donator-acceptor (EDA) effect and unconventional H-bonds. Differently, Ctrp with indole groups as electron acceptor had better removal rate (∼50%) of SDZ anions (electron donator). According to correlation analysis, the coexisted kaolin and HA played positive roles in antibiotics’ removal. Detailed pairwise interactions in molecular level among different components were clarified by spectral analysis and theoretical calculations (density functional theory), which are important for both the structural design of new flocculants aiming at targeted contaminants and understanding the environmental behaviors of antibiotics in water.

Removal of antibiotics from water in the coexistence of suspended particles and natural organic matters using amino-acid-modified-chitosan flocculants: A combined experimental and theoretical study

Energy Technology Data Exchange (ETDEWEB)

Jia, Shuying [School of Chemistry and Materials Science, Jiangsu Provincial Key Laboratory of Materials Cycling and Pollution Control, Nanjing Normal University, Nanjing 210023 (China); Yang, Zhen, E-mail: yangzhen@njnu.edu.cn [School of Chemistry and Materials Science, Jiangsu Provincial Key Laboratory of Materials Cycling and Pollution Control, Nanjing Normal University, Nanjing 210023 (China); Ren, Kexin [School of Chemistry and Materials Science, Jiangsu Provincial Key Laboratory of Materials Cycling and Pollution Control, Nanjing Normal University, Nanjing 210023 (China); Tian, Ziqi [Department of Chemistry, University of California, Riverside, CA 92521 (United States); Dong, Chang; Ma, Ruixue; Yu, Ge [School of Chemistry and Materials Science, Jiangsu Provincial Key Laboratory of Materials Cycling and Pollution Control, Nanjing Normal University, Nanjing 210023 (China); Yang, Weiben, E-mail: yangwb007@njnu.edu.cn [School of Chemistry and Materials Science, Jiangsu Provincial Key Laboratory of Materials Cycling and Pollution Control, Nanjing Normal University, Nanjing 210023 (China)

2016-11-05

Highlights: • Novel amino-acid-modified-chitosan flocculants are employed to remove antibiotics. • Effects of different structures of amino acids and antibiotics are investigated. • Correlation analysis shows coexisted kaolin and HA have synergistic removal effect. • Theoretical DFT calculation clarifies the interactions in molecular level. - Abstract: Contamination of trace antibiotics is widely found in surface water sources. This work delineates removal of trace antibiotics (norfloxacin (NOR), sulfadiazine (SDZ) or tylosin (TYL)) from synthetic surface water by flocculation, in the coexistence of inorganic suspended particles (kaolin) and natural organic matter (humic acid, HA). To avoid extra pollution caused by petrochemical products-based modification reagents, environmental-friendly amino-acid-modified-chitosan flocculants, Ctrp and Ctyr, with different functional aromatic-rings structures were employed. Jar tests at various pHs exhibited that, Ctyr, owning phenol groups as electron donors, was favored for elimination of cationic NOR (∼50% removal; optimal pH: 6; optimal dosage: 4 mg/L) and TYL (∼60% removal; optimal pH: 7; optimal dosage: 7.5 mg/L), due to π–π electron donator-acceptor (EDA) effect and unconventional H-bonds. Differently, Ctrp with indole groups as electron acceptor had better removal rate (∼50%) of SDZ anions (electron donator). According to correlation analysis, the coexisted kaolin and HA played positive roles in antibiotics’ removal. Detailed pairwise interactions in molecular level among different components were clarified by spectral analysis and theoretical calculations (density functional theory), which are important for both the structural design of new flocculants aiming at targeted contaminants and understanding the environmental behaviors of antibiotics in water.

Comparison of trace element contamination levels (Cu, Zn, Fe, Cd ...

African Journals Online (AJOL)

SERVER

2008-03-18

Mar 18, 2008 ... Chemical analysis of the trace elements in the soft tissues. The trace elements of interest (Cu, Zn, Fe, Pb, Cd) were then determined in the digested solutions, using Thermoelemental type. M6 brand of an atomic absorption Spectrometer equipped with a flame operated atomisation system and a deuterium ...

Arsenic removal by electrocoagulation process: Recent trends and removal mechanism.

Science.gov (United States)

Nidheesh, P V; Singh, T S Anantha

2017-08-01

Arsenic contamination in drinking water is a major issue in the present world. Arsenicosis is the disease caused by the regular consumption of arsenic contaminated water, even at a lesser contaminated level. The number of arsenicosis patients is increasing day-by-day. Decontamination of arsenic from the water medium is the only one way to regulate this and the arsenic removal can be fulfilled by water treatment methods based on separation techniques. Electrocoagulation (EC) process is a promising technology for the effective removal of arsenic from aqueous solution. The present review article analyzes the performance of the EC process for arsenic removal. Electrocoagulation using various sacrificial metal anodes such as aluminium, iron, magnesium, etc. is found to be very effective for arsenic decontamination. The performances of each anode are described in detail. A special focus has been made on the mechanism behind the arsenite and arsenate removal by EC process. Main trends in the disposal methods of sludge containing arsenic are also included. Comparison of arsenic decontamination efficiencies of chemical coagulation and EC is also reported. Copyright © 2017 Elsevier Ltd. All rights reserved.

Characterization of natural adsorbent material for heavy metal removal in a petrochemical site contamination

Directory of Open Access Journals (Sweden)

Bianchi F.

2013-04-01

Full Text Available Despite of over 25 years of intensive technological efforts, sub-surface environment cleanup still remains a challenge, especially in case of highly contaminated sites. In this context, ion exchanger technologies could provide simple and effective solutions for heavy metal removal in water treatment. The challenge is finding exchanger able to operate in extreme natural environments or in situations involving natural interfering species such as inorganic ions. In this paper we exam the use of natural zeolites as versatile exchanger for environmental protection of coastal refinery's groundwater against pollution of Ni, Cd, Pb. The influence of particle diameter on clinoptilolite performances toward heavy metal removal is studied. Also, we evaluate the exchanger activities in condition of high ionic strength, commonly present in groundwater located under coastal petrol industries. The obtained results confirmed that ion exchangers could provide an effective solutions for remediation in complex environmental conditions.

The validation of forensic DNA extraction systems to utilize soil contaminated biological evidence.

Science.gov (United States)

Kasu, Mohaimin; Shires, Karen

2015-07-01

The production of full DNA profiles from biological evidence found in soil has a high failure rate due largely to the inhibitory substance humic acid (HA). Abundant in various natural soils, HA co-extracts with DNA during extraction and inhibits DNA profiling by binding to the molecular components of the genotyping assay. To successfully utilize traces of soil contaminated evidence, such as that found at many murder and rape crime scenes in South Africa, a reliable HA removal extraction system would often be selected based on previous validation studies. However, for many standard forensic DNA extraction systems, peer-reviewed publications detailing the efficacy on soil evidence is either lacking or is incomplete. Consequently, these sample types are often not collected or fail to yield suitable DNA material due to the use of unsuitable methodology. The aim of this study was to validate the common forensic DNA collection and extraction systems used in South Africa, namely DNA IQ, FTA elute and Nucleosave for processing blood and saliva contaminated with HA. A forensic appropriate volume of biological evidence was spiked with HA (0, 0.5, 1.5 and 2.5 mg/ml) and processed through each extraction protocol for the evaluation of HA removal using QPCR and STR-genotyping. The DNA IQ magnetic bead system effectively removed HA from highly contaminated blood and saliva, and generated consistently acceptable STR profiles from both artificially spiked samples and crude soil samples. This system is highly recommended for use on soil-contaminated evidence over the cellulose card-based systems currently being preferentially used for DNA sample collection. Copyright © 2015 Elsevier Ireland Ltd. All rights reserved.

The integrated contaminant elution and tracer test toolkit, ICET3, for improved characterization of mass transfer, attenuation, and mass removal

Science.gov (United States)

Brusseau, Mark L.; Guo, Zhilin

2018-01-01

It is evident based on historical data that groundwater contaminant plumes persist at many sites, requiring costly long-term management. High-resolution site-characterization methods are needed to support accurate risk assessments and to select, design, and operate effective remediation operations. Most subsurface characterization methods are generally limited in their ability to provide unambiguous, real-time delineation of specific processes affecting mass-transfer, transformation, and mass removal, and accurate estimation of associated rates. An integrated contaminant elution and tracer test toolkit, comprising a set of local-scale groundwater extraction-and injection tests, was developed to ameliorate the primary limitations associated with standard characterization methods. The test employs extended groundwater extraction to stress the system and induce hydraulic and concentration gradients. Clean water can be injected, which removes the resident aqueous contaminant mass present in the higher-permeability zones and isolates the test zone from the surrounding plume. This ensures that the concentrations and fluxes measured within the isolated area are directly and predominantly influenced by the local mass-transfer and transformation processes controlling mass removal. A suite of standard and novel tracers can be used to delineate specific mass-transfer and attenuation processes that are active at a given site, and to quantify the associated mass-transfer and transformation rates. The conceptual basis for the test is first presented, followed by an illustrative application based on simulations produced with a 3-D mathematical model and a brief case study application.

Natural uranium-series radionuclide inventories in coastal and oceanic waters of the south-western Pacific - insights into trace metal flux and removal pathway analysis

International Nuclear Information System (INIS)

Szymczak, R.; Jeffree, R.A.; Peck, G.A.

2003-01-01

Participate scavenging of trace metals plays a major role in determining their ecosystem flux and incident dissolved concentrations. Differences in the half-lives and biogeochemical behaviour of natural uranium series radioisotope pairs (eg. 238 U/ 234 Th, 210 Pb/ 210 Po) allow their application as oceanic process tracers. Coincidental measurements of dissolved and particulate trace element concentrations and inventories of radionuclides in the Noumea coral lagoon and adjacent offshore waters were used to quantify water column flux rates and provide insights on removal pathway analysis. Understanding prevailing pathways and respective flux rates of pollutants in specific coastal and oceanic systems will assist to establish the fate and consequence of pollutants and allow sustainable management strategies to be developed. Both natural and pollutant chemical species introduced to the marine environment may either remain benign in solution or undergo physiological uptake by biota, but most often associate with colloids and fine particles, which subsequent undergo aggregation, sedimentation and removal to the sea floor

Influence of attrition scrubbing, ultrasonic treatment, and oxidant additions on uranium removal from contaminated soils

International Nuclear Information System (INIS)

Timpson, M.E.; Elless, M.P.; Francis, C.W.

1994-01-01

As part of the Uranium in Soils Integrated Demonstration Project being conducted by the US Department of Energy, bench-scale investigations of selective leaching of uranium from soils at the Fernald Environmental Management Project site in Ohio were conducted at Oak Ridge National Laboratory. Two soils (storage pad soil and incinerator soil), representing the major contaminant sources at the site, were extracted using carbonate- and citric acid-based lixiviants. Physical and chemical processes were used in combination with the two extractants to increase the rate of uranium release from these soils. Attrition scrubbing and ultrasonic dispersion were the two physical processes utilized. Potassium permanganate was used as an oxidizing agent to transform tetravalent uranium to the hexavalent state. Hexavalent uranium is easily complexed in solution by the carbonate radical. Attrition scrubbing increased the rate of uranium release from both soils when compared with rotary shaking. At equivalent extraction times and solids loadings, however, attrition scrubbing proved effective only on the incinerator soil. Ultrasonic treatments on the incinerator soil removed 71% of the uranium contamination in a single extraction. Multiple extractions of the same sample removed up to 90% of the uranium. Additions of potassium permanganate to the carbonate extractant resulted in significant changes in the extractability of uranium from the incinerator soil but had no effect on the storage pad soil

Potential of vetiver (vetiveria zizanioides l.) grass in removing selected pahs from diesel contaminated soil

International Nuclear Information System (INIS)

Nisa, W.U.; Rashid, A.

2015-01-01

Phytoremediation has been renowned as an encouraging technology for the remediation of polycyclic aromatic hydrocarbon (PAH)-contaminated soils, little is known about how plant species behave during the process of PAH phytoremediation. Therefore, the aim of this study was to investigate the effectiveness of vetiver (Vetiveria zizanioides L.) plant in PAH phytoremediation and extraction potential of Vetiveria zizanioides for selected PAHs from the diesel contaminated soil. The field soil samples were spiked with varying concentrations (0.5% and 1%) of diesel and used for pot experiment which was conducted in greenhouse. Vetiver grass was used as experimental plant. Physico-chemical analysis of soil was performed before and after the experiment. Concentration of selected PAHs i.e. phenanthrene, pyrene and benzo(a)pyrene in soil was determined using HPLC. Plant parameters such as root/shoot length and dry mass were compared after harvest. Concentrations of PAHs were also determined in plant material and in soils after harvesting. Result showed that initial concentration of phenanthrene was significantly different from final concentration in treatments in which soil was spiked with diesel. Initial and final concentration of pyrene in soil was also significantly different from each other in two treatments in which soil was spiked with 1% diesel. Pyrene concentration was significantly different in roots and shoots of plants while benzo(a)pyrene concentration in treatments in which soil was spiked with diesel was also significantly different from roots and shoots. Phenanthrene was less extracted by the plant in all the treatments and it was present in higher concentration in soil as compared to plant. Our results indicate that vetiver grass has effectively removed PAHs from soil consequently a significantly higher root and shoot uptake of PAHs was observed than control treatments. Study concludes Vetiveria zizanioides as potentially promising plant specie for the removal

Hydrotalcite formation facilitates effective contaminant and radionuclide removal from acidic uranium mine barren lixiviant

International Nuclear Information System (INIS)

Douglas, Grant; Shackleton, Mark; Woods, Peter

2014-01-01

Highlights: • Remediation of barren lixiviant using hydrotalcite precipitation. • High U and rare earth element concentration factor. • Hydrotalcite may be further modified for long-term disposal. • Potential application to U and other commodities. - Abstract: An assessment of hydrotalcite (HT) formation as a method to neutralise acidity and remove trace elements was undertaken using barren lixiviant from Heathgate Resources’ Beverley North in situ recovery (ISR) U mine in South Australia. This study demonstrated proof of concept in terms of the neutralisation of acidity and concomitant removal of a range of trace elements and U–Th series radionuclides from the barren lixiviant using MgCl 2 as a supplementary Mg source to optimise Mg:Al mol ratios and NaOH as the neutralising agent. Hydrotalcite was the predominant mineral formed during neutralisation, hosting a range of elements including substantial U (∼0.2%) and rare earth elements (REE ∼0.1%). High U and REE recovery (∼99%) from barren lixiviant after HT precipitation indicates a potential to both remediate barren lixiviant and to offset remediation costs. Alternatively, HT precipitates formed during barren lixiviant neutralisation may be further stabilised via calcination, silicification or a combination thereof forming minerals potentially amenable for inclusion in a long-term waste repository at the cessation of ISR mining. Importantly, the composition of the neutralised barren lixiviant produced via HT precipitation is similar to that of existing groundwater allowing for the possibility of direct aquifer re-injection after remediation. A potential exists to apply this HT-based remediation technology to conventional or ISR U mines (or mines exploiting other commodities) and allows for the prospect of a fully integrated ISR mining, processing and lixiviant remediation strategy consistent with stringent environmental and mine closure standards

Copper removal from contaminated soils by soil washing process using camellian-derived saponin

Science.gov (United States)

Reyes, Arturo; Fernanda Campos, Maria; Videla, Álvaro; Letelier, María Victoria; Fuentes, Bárbara

2015-04-01

Antofagasta Region in North of Chile has been the main copper producer district in the world. As a consequence of a lack of mining closure regulation, a large number of abandon small-to-medium size metal-contaminated sites have been identified in the last survey performed by the Chilean Government. Therefore, more research development on sustainable reclamation technologies must be made in this extreme arid-dry zone. The objective of this study is to test the effectiveness of soil remediation by washing contaminated soil using camellian-derived saponin for the mobilization of copper. Soil samples were taken from an abandoned copper mine site located at 30 km North Antofagasta city. They were dried and sieved at 75 µm for physico-chemical characterization. A commercial saponin extracted from camellias seed was used as biosurfactant. The soil used contains 67.4 % sand, 26.3 % silt and 6.3 % clay. The soil is highly saline (electric conductivity, 61 mScm-1), with low organic matter content (0.41%), with pH 7.30, and a high copper concentration (2200 mg Kg-1 soil). According to the sequential extraction procedure of the whole soil, copper species are mainly as exchangeable fraction (608.2 mg Kg-1 soil) and reducible fraction (787.3 mg Kg-1 soil), whereas the oxidizable and residual fractions are around 205.7 and 598.8 mg Kg-1 soil, respectively. Soil particles under 75 µm contain higher copper concentrations (1242 mg Kg-1 soil) than the particle fraction over 75 µm (912 mg Kg-1 soil). All washing assays were conducted in triplicate using a standard batch technique with and without pH adjustment. The testing protocols includes evaluation of four solid to liquid ratio (0.5:50; 1.0:50; 2.0:50, and 5.0:50) and three saponin concentrations (0, 1, and 4 mg L-1). After shaking (24 h, 20±1 °C) and subsequently filtration (0.45 µm), the supernatants were analyzed for copper and pH. The removal efficiencies of copper by saponin solutions were calculated in according to the

Analysis of food contaminants

National Research Council Canada - National Science Library

Gilbert, John

1984-01-01

... quantification methods used in the analysis of mycotoxins in foods - Confirmation and quantification of trace organic food contaminants by mass spectrometry-selected ion monitoring - Chemiluminescence...

Use of fugacity model to analyze temperature-dependent removal of micro-contaminants in sewage treatment plants.

Science.gov (United States)

Thompson, Kelly; Zhang, Jianying; Zhang, Chunlong

2011-08-01

Effluents from sewage treatment plants (STPs) are known to contain residual micro-contaminants including endocrine disrupting chemicals (EDCs) despite the utilization of various removal processes. Temperature alters the efficacy of removal processes; however, experimental measurements of EDC removal at various temperatures are limited. Extrapolation of EDC behavior over a wide temperature range is possible using available physicochemical property data followed by the correction of temperature dependency. A level II fugacity-based STP model was employed by inputting parameters obtained from the literature and estimated by the US EPA's Estimations Programs Interface (EPI) including EPI's BIOWIN for temperature-dependent biodegradation half-lives. EDC removals in a three-stage activated sludge system were modeled under various temperatures and hydraulic retention times (HRTs) for representative compounds of various properties. Sensitivity analysis indicates that temperature plays a significant role in the model outcomes. Increasing temperature considerably enhances the removal of β-estradiol, ethinyestradiol, bisphenol, phenol, and tetrachloroethylene, but not testosterone with the highest biodegradation rate. The shortcomings of BIOWIN were mitigated by the correction of highly temperature-dependent biodegradation rates using the Arrhenius equation. The model predicts well the effects of operating temperature and HRTs on the removal via volatilization, adsorption, and biodegradation. The model also reveals that an impractically long HRT is needed to achieve a high EDC removal. The STP model along with temperature corrections is able to provide some useful insight into the different patterns of STP performance, and useful operational considerations relevant to EDC removal at winter low temperatures. Copyright © 2011 Elsevier Ltd. All rights reserved.

Enhancement of Methane Concentration by Removing Contaminants from Biogas Mixtures Using Combined Method of Absorption and Adsorption

Directory of Open Access Journals (Sweden)

Muhammad Rashed Al Mamun

2017-01-01

Full Text Available We report a laboratory scale combined absorption and adsorption chemical process to remove contaminants from anaerobically produced biogas using cafeteria (food, vegetable, fruit, and cattle manure wastes. Iron oxide (Fe2O3, zero valent iron (Feo, and iron chloride (FeCl2 react with hydrogen sulfide (H2S to deposit colloidal sulfur. Silica gel, sodium sulfate (Na2SO4, and calcium oxide (CaO reduce the water vapour (H2O and carbon dioxide (CO2. It is possible to upgrade methane (CH4 above 95% in biogas using chemical or physical absorption or adsorption process. The removal efficiency of CO2, H2S, and H2O depends on the mass of removing agent and system pH. The results showed that Ca(OH2 solutions are capable of reducing CO2 below 6%. The H2S concentration was reduced to 89%, 90%, 86%, 85%, and 96% for treating with 10 g of FeCl2, Feo (with pH, Fe2O3, Feo, and activated carbon, respectively. The H2O concentration was reduced to 0.2%, 0.7%, 0.2%, 0.2%, and 0.3% for treating raw biogas with 10 g of silica gel and Na2SO4 for runs R1, R2, R3, R4, and R5, respectively. Thus, given the successful contaminant elimination, the combined absorption and adsorption process is a feasible system for biogas purification.

Octanol-solubility of dissolved and particulate trace metals in contaminated rivers: implications for metal reactivity and availability.

Science.gov (United States)

Turner, Andrew; Mawji, Edward

2005-05-01

The lipid-like, amphiphilic solvent, n-octanol, has been used to determine a hydrophobic fraction of dissolved and particulate trace metals (Al, Cd, Co, Cu, Mn, Ni, Pb, Zn) in contaminated rivers. In a sample from the River Clyde, southwest Scotland, octanol-solubility was detected for all dissolved metals except Co, with conditional octanol-water partition coefficients, D(ow), ranging from about 0.2 (Al and Cu) to 1.25 (Pb). In a sample taken from the River Mersey, northwest England, octanol-solubility was detected for dissolved Al and Pb, but only after sample aliquots had been spiked with individual ionic metal standards and equilibrated. Spiking of the River Clyde sample revealed competition among different metals for hydrophobic ligands. Metal displacement from hydrophobic complexes was generally most significant following the addition of ionic Al or Pb, although the addition of either of these metals had little effect on the octanol-solubility of the other. In both river water samples hydrophobic metals were detected on the suspended particles retained by filtration following their extraction in n-octanol. In general, particulate Cu and Zn (up to 40%) were most available, and Al, Co and Pb most resistant (octanol extraction. Distribution coefficients defining the concentration ratio of octanol-soluble particle-bound metal to octanol-soluble dissolved metal were in the range 10(3.3)-10(5.3)mlg(-1). The presence of hydrophobic dissolved and particulate metal species has implications for our understanding of the biogeochemical behaviour of metals in aquatic environments. Specifically, such species are predicted to exhibit characteristics of non-polar organic contaminants, including the potential to penetrate the lipid bilayer. Current strategies for assessing the bioavailability and toxicity of dissolved and particulate trace metals in natural waters may, therefore, require revision.

Fate of soluble uranium in the I2/KI leaching process for mercury removal

International Nuclear Information System (INIS)

Bostick, W.D.; Davis, W.H.; Jarabek, R.J.

1997-09-01

General Electric Corporation has developed an extraction and recovery system for mercury, based upon the use of iodine (oxidant) and iodide ion (complexing agent). This system has been proposed for application to select mercury-contaminated mixed waste (i.e., waste containing radionuclides as well as other hazardous constituents), which have been generated by historic activities in support of US Department of Energy (DOE) missions. This system is compared to a system utilizing hypochlorite and chloride ions for removal of mercury and uranium from a sample of authentic mixed waste sludge. Relative to the hypochlorite (bleach) system, the iodine system mobilized more mercury and less uranium from the sludge. An engineering flowsheet has been developed to treat spent iodine-containing extraction medium, allowing the system to be recycled. The fate of soluble uranium in this series of treatment unit operations was monitored by tracing isotopically-enriched uranyl ion into simulated spent extraction medium. Treatment with use of elemental iron is shown to remove > 85% of the traced uranium while concurrently reducing excess iodine to the iodide ion. The next unit operation, adjustment of the solution pH to a value near 12 by the addition of lime slurry to form a metal-laden sludge phase (an operation referred to as lime-softening), removed an additional 57% of soluble uranium activity, for an over-all removal efficiency of ∼ 96%. However, the precipitated solids did not settle well, and some iodide reagent is held up in the wet filtercake

Effects of Humidity Swings on Adsorption Columns for Air Revitalization: Modeling and Experiments

Science.gov (United States)

LeVan, M. Douglas; Finn, John E.

1997-01-01

Air purification systems are necessary to provide clean air in the closed environments aboard spacecraft. Trace contaminants are removed using adsorption. One major factor concerning the removal of trace contaminants is relative humidity. Water can reduce adsorption capacity and, due to constant fluctuations, its presence is difficult to incorporate into adsorption column designs. The purpose of the research was to allow for better design techniques in trace contaminant adsorption systems, especially for feeds with water present. Experiments and mathematical modeling research on effects of humidity swings on adsorption columns for air revitalization were carried out.