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Soil metal contamination

The finer soil fraction contains adsorbed organics, small metallic particles, and bound ionic metals. This fraction may be treated further to remove the contaminants, or it may be incinerated or landfilled. The "clean" coarse fraction may contain some residual metallic fragments. With metal contamination, both the fine and coarse soil fractions may be leached with an acid solution to remove the metals. [Pg.173]

A further application of the manipulation of microbial activity in the rhizo-sphere is their potential to remediate contaminated land. Bioremediation involves the u.se of microorganisms that break down contaminants. Radwan et al. (255) found that the soil associated with the roots of plants grown in soil heavily contaminated with oil in Kuwait was free of oil residues, presumably as a result of the ability of the resident rhizosphere microflora to degrade hydrocarbons. The use of plants as a means to accumulate pollutants such as heavy metals (256,257) to degrade hydrocarbons and pesticides (255) is already widely implemented and has proven to be successful. In some cases, there is no doubt that it is the plant itself that is responsible for the removal of the contaminants. However, in most... [Pg.125]

Biological activity can be used in two ways for the bioremediation of metal-contaminated soils to immobilize the contaminants in situ or to remove them permanently from the soil matrix, depending on the properties of the reduced elements. Chromium and uranium are typical candidates for in situ immobilization processes. The bioreduction of Cr(VI) and Ur(VI) transforms highly soluble ions such as CrO and UO + to insoluble solid compounds, such as Cr(OH)3 and U02. The selenate anions SeO are also reduced to insoluble elemental selenium Se°. Bioprecipitation of heavy metals, such as Pb, Cd, and Zn, in the form of sulfides, is another in situ immobilization option that exploits the metabolic activity of sulfate-reducing bacteria without altering the valence state of metals. The removal of contaminants from the soil matrix is the most appropriate remediation strategy when bioreduction results in species that are more soluble compared to the initial oxidized element. This is the case for As(V) and Pu(IV), which are transformed to the more soluble As(III) and Pu(III) forms. This treatment option presupposes an installation for the efficient recovery and treatment of the aqueous phase containing the solubilized contaminants. [Pg.537]

Chemical and physical properties of the contaminant should also be investigated. Solubility in water (or other washing fluids) is one of the most important physical characteristics. Hydrophobic contaminants can be difficult to separate from the soil particles and into the aqueous washing fluid. Reactivity with wash fluids may, in some cases, be another important characteristic to consider. Other contaminant characteristics such as volatility and density may be important for the design of remedy screening studies and related residuals treatment systems. Speciation is important in metal-contaminated sites. [Pg.563]

U.S. EPA, Recent Developments for In Situ Treatment of Metal Contaminated Soils, EPA-542-R-97-004, Technology Innovation Office, Washington, 1997. [Pg.568]

U.S. EPA, Recent developments for in-situ treatment of metal contaminated soils, U.S. EPA, Office of Solid Waste and Emergency Response, Technology Innovation Office, EPA Contract No. 68-W5-006, 1997, pp. 1-47. [Pg.570]

There is some uncertainty about the potential presence of metal in the TCE-contaminated soil of Area 2. If metal concentrations of concern are present, only Alternatives 2 and 5 would protect against direct contact and further groundwater contamination through a cap and incineration, respectively. Incineration of metal-contaminated soil may result in a hazardous waste residue, which would have to be disposed of in a hazardous waste landfill. Alternatives 3 and 4 rely on vapor extraction and would not lower risks from metal to human health or the environment. [Pg.649]

Pierzynski GM, Schwab AP. 1993. Bioavailability of zinc, cadmium, and lead in a metal contaminated alluvial soil. J Environ Qual 22 247-254. [Pg.563]

Jinhui L, Huabo D, Pixing S (2011) Heavy metal contamination of surface soil in electronic waste dismantling area site investigation and source-apportionment analysis. Waste Manag... [Pg.311]

Ahnstrom and Parker (2001) studied Cd reactivity in metal-contaminated soils using a coupled stable isotope dilution-sequential extraction procedure. They found that in uncontaminated arid soil and in... [Pg.132]

RESIDENCE TIME OF METALS IN SOIL SOLUTION OF METAL-CONTAMINATED ISRAELI ARID SOILS... [Pg.200]

Ahnstrom Z.A.S., Parker D.R. Cadmium Reactivity in Metal-Contaminated Soils Using a Coupled Stable Isotope Dilution-Sequential Extraction Procedure. Environ Sci... [Pg.329]

Cartwright B., Merry R.H., Tiller K.G. Heavy metal contamination of soils around a lead smelter at Port Pirie, South Australia. Aust J Soil Res. 1976 15 69-81. [Pg.333]

Hardiman R.T., Banin A., Jacoby B. The effect of soil type and degree of metal contamination upon uptake of Cd, Pb and Cu in bush beans. Plant Soil 1984b 81 3-15. [Pg.338]

Mench M.J., Didier V.L., Loftier M., Gomez A., Masson P. A mimicked in-situ remediation study of metal-contaminated soils with emphasis on cadmium and lead. J Environ Qual 1994 23 58-63. [Pg.345]

Chapter 3 Role of Bacteria and Bacteria-Soil Composites in Metal Biosorption and Remediating Toxic Metal-Contaminated... [Pg.1]

Lebeau et al. (2002) investigated the sorption of cadmium by viable microbial cells that were free or immobilized in alginate beads by incubating the bacteria in a liquid soil extract medium at pH 5 7 and Cd concentrations of 1 to 10 mg L-1. The percentage of Cd biosorbed reached a maximum (69%) at low Cd concentrations and neutral pH. Thus, the effectiveness of bacteria, inoculated into metal-contaminated soils, would largely depend on the concentration of the metal and its distribution between the biomass and the medium. [Pg.89]

Bacteria and their composites with soil minerals or organic matter are capable of taking up a wide range and variety of toxic metals in soil environments. Research done over the last decade or so has greatly improved our understanding of the mechanisms on biosorption of metals and bacte-ria-metal-soil component interactions. However, more studies from molecular level are needed in order to enhance the ability of bacteria and their association with soil components to remediate toxic metals-contaminated soils. The focus of future investigations should be on the mechanisms by which metals are sorbed and bound by bacterial cell surfaces and bacteria-soil/mineral composites. In this connection, X-ray absorption spectroscopy (XAS) is a promising technique because it can provide information about... [Pg.92]

Srinath T, Verma T, Ramteke PW, Garg SK (2002) Chromium biosorption and bioaccumulation by chromate resistant bacteria. Chemosphere 48 427-435 Stephen JR, Macnaughton SJ (1999) Developments in terrestrial bacterial remediation of metals. Curr Opinion Biotechnol 10 230-233 Tabak HH, Lens P, van Hullebusch ED, Dejonghe W (2005) Developments in bioremediation of soils and sediments polluted with metals and radionuclides 1. Microbial processes and mechanisms affecting bioremediation of metal contamination and influencing metal toxicity and transport. Rev Environ Sci Bio/Technol. 4 115-156... [Pg.97]

Frostegard A, Tunlid A, Baath E (1996) Changes in microbial community structure during long term incubation in two soils experimentally contaminated with metals. Soil Biol Biochem 28 55-63... [Pg.313]

Kelly JJ, Tate RL (1998) Effects of heavy metal contamination and remediation on soil microbial communities in the vicinity of a zinc smelter. J Environ Qual 27 609-617... [Pg.314]


See other pages where Soil metal contamination is mentioned: [Pg.58]    [Pg.58]    [Pg.25]    [Pg.172]    [Pg.288]    [Pg.166]    [Pg.421]    [Pg.553]    [Pg.624]    [Pg.638]    [Pg.646]    [Pg.821]    [Pg.404]    [Pg.311]    [Pg.178]    [Pg.178]    [Pg.178]    [Pg.220]    [Pg.296]    [Pg.137]    [Pg.21]    [Pg.28]    [Pg.79]    [Pg.303]    [Pg.306]    [Pg.306]    [Pg.312]   


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