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Heavy metals in surface waters

Hygienic standards for dissolved concentrations of heavy metals in surface water are shown in Table 3. [Pg.63]

The range in critical limits for dissolved species of heavy metals in surface waters is large, especially for zinc and nickel. In general, values used by Denmark and the Czech Republic are much higher than for other countries, except for Zn and Ni. For these elements, Canada and the USA also use much higher values. These limits may refer to action values. [Pg.63]

Table 3. Critical limits for heavy metals in surface waters of various countries, related to multifunctional uses. Table 3. Critical limits for heavy metals in surface waters of various countries, related to multifunctional uses.
Processes Coefficients and Models for Simulating Toxic Organics and Heavy Metals in Surface Waters... [Pg.221]

Schnoor, J.L., Sato, C., McKechnie, D., Sahoo, D. (1987) Processes, Coefficients, and Models for Simulating Toxic Organics and Heavy Metals in Surface Waters. EPA 600/3-87-015. US EPA, Athens, Georgia. [Pg.828]

Voltammetry and polarography are particularly important for the analysis of water samples for heavy metals. In surface waters with organic contamination, they can only be analyzed after digestion, Sampling and storage is of prime importance for correct analytical results. [Pg.811]

Industries are constantly dumping heavy metal ions into lakes, rivers and reservoirs, thereby polluting them. Heavy metals are broadly defined as materials whose density is above 5 g/cm (Barakat 2011). Conmion heavy metals present in aqueous streams include chromium, mercury, lead and cadmium (Bailey et al. 1999). Table 2.1 (Kumiawan et al. 2006a) shown below describes the maximum contaminant level of heavy metals in surface water and their toxicides. [Pg.59]

Schnoor, J.L. 1987 Processes, coefficients and models for simulating toxic organics and heavy metals in surface waters. US EPA report EPA/600/3-87/015. [Pg.587]

Sorption can significantly diminish the mobility of certain dissolved components in solution, especially those present in minor amounts. Sorption, for example, may retard the spread of radionuclides near a radioactive waste repository or the migration of contaminants away from a polluting landfill (see Chapters 21 and 32). In acid mine drainages, ferric oxide sorbs heavy metals from surface water, helping limit their downstream movement (see Chapter 31). A geochemical model useful in investigating such cases must provide an accurate assessment of the effects of surface reactions. [Pg.137]

The sorptive nature of bacterial or algal exterior membranes is well-documented [118-122]. Biological particles can influence the distribution of heavy metals in natural waters because the functional groups on the cell surfaces are able to bind certain metal ions [124]. [Pg.128]

Kersten, M., Irion, G. and Forstner, U. (1991) Particulate trace metals in surface waters of the North Sea. In Heavy Metals in the Environment (ed. Vernet, J.-E). Elsevier, Amsterdam, pp.137-160. [Pg.319]

Because many heavy metals are toxic to man, animals and plants, it is necessary to monitor continually potable water, river water and trade and sewage effluents to check that the metal levels are below the predefined safe limits. In this way, water quality is preserved and the health of the population is safeguarded. It is because of the public health aspects that toxic limits for metals in surface waters have been introduced and those set by the European Economic Community are displayed in Table 1. It can be seen that all limits are at the trace level and in order to comply with these directives there will be a need for the regular analysis of raw and potable waters for these metals. This is the function of quality-control water laboratories. [Pg.68]

Concentration of methylated heavy metals in surface sea water of the Southern Ocean... [Pg.203]

Figure 8.18 Dissolved Fe, Mn, and Zn versus discharge for (a) Tobey Creek, (b) Little Licking Creek, and (c) Welch Run. Dashed lines show theoretical dilution of base-flow concentrations. From M.A. Gang and D. Langmuir. Controls on heavy metals in surface and ground waters affected by coal mine drainage. Prov. 5th Syrnp- Coal Mine Drainage Research. Copyright 1974 by Natl. Coal Assck. Used by permission. Figure 8.18 Dissolved Fe, Mn, and Zn versus discharge for (a) Tobey Creek, (b) Little Licking Creek, and (c) Welch Run. Dashed lines show theoretical dilution of base-flow concentrations. From M.A. Gang and D. Langmuir. Controls on heavy metals in surface and ground waters affected by coal mine drainage. Prov. 5th Syrnp- Coal Mine Drainage Research. Copyright 1974 by Natl. Coal Assck. Used by permission.
What are the main sources of heavy metals in surface and ground waters in various Asian countries Discuss the natural and anthropogenic causes. [Pg.215]

Figure 39. Flow diagram of the procedure for the polaro-graphic/voltammetric determination of heavy metals in drinking water, groundwater, and surface water according to DIN 38406 Part 16... Figure 39. Flow diagram of the procedure for the polaro-graphic/voltammetric determination of heavy metals in drinking water, groundwater, and surface water according to DIN 38406 Part 16...
Chelant Control. Chelants are the prime additives in a solubilizing boiler water treatment program. Chelants have the abihty to complex many cations (hardness and heavy metals under boiler water conditions). They accomplish this by locking metals into a soluble organic ring stmcture. The chelated cations do not deposit in the boiler. When apphed with a dispersant, chelants produce clean waterside surfaces. [Pg.263]

Table 3. Comparative assessment of heavy metal contents in surface waters of various ecosystems from the East European Plain and average values for the similar global... Table 3. Comparative assessment of heavy metal contents in surface waters of various ecosystems from the East European Plain and average values for the similar global...
The iron cycle shown in Fig. 10.14 illustrates some redox processes typically observed in soils, sediments and waters, especially at oxic-anoxic boundaries. The cycle includes the reductive dissolution of iron(lll) hydr)oxides by organic ligands, which may also be photocatalyzed in surface waters, and the oxidation of Fe(II) by oxygen, which is catalyzed by surfaces. The oxidation of Fe(II) to Fe(III)(hydr)-oxides is accompanied by the binding of reactive compounds (heavy metals, phosphate, or organic compounds) to the surface, and the reduction of the ferric (hydr) oxides is accompanied by the release of these substances into the water column. [Pg.362]


See other pages where Heavy metals in surface waters is mentioned: [Pg.13]    [Pg.34]    [Pg.13]    [Pg.34]    [Pg.217]    [Pg.312]    [Pg.211]    [Pg.217]    [Pg.303]    [Pg.27]    [Pg.214]    [Pg.218]    [Pg.254]    [Pg.390]    [Pg.916]    [Pg.1323]    [Pg.198]    [Pg.296]    [Pg.97]    [Pg.163]    [Pg.183]    [Pg.247]    [Pg.146]    [Pg.149]    [Pg.649]    [Pg.84]    [Pg.42]    [Pg.160]    [Pg.509]   
See also in sourсe #XX -- [ Pg.131 ]




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