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Sediments chemical analysis

Parkinson D-R, Dust JM (2010) Overview of the current status of sediment chemical analysis trends in analytical techniques. Environ Rev 18(NA) 37-59... [Pg.46]

In addition to tartaric acid another compound named paratartaric acid was found in wine sediments. Chemical analysis showed this compound to have the same composition as tartaric acid, so most scientists assumed the two compounds were identical. Strangely enough, however, paratartaric acid did not rotate plane-polarized fight. Pasteur would not accept the idea that such an experimental result could be an accident or unimportant. He guessed that even though the two compounds had the same chemical composition, they must somehow have different structures—and he set out to find evidence to prove his hypothesis. [Pg.917]

Fernandez P, M Grifoll, AM Solanas, JM Bayiona, J Albalges (1992) Bioassay-directed chemical analysis of genotoxic compounds in coastal sediments. Environ Sci Technol 26 817-829. [Pg.41]

Chen L, Yu C, Shen C, Zhang C, Liu L, Shen K, Tang X, Chen Y (2010) Study on adverse impact of e-waste disassembly on surface sediment in East China by chemical analysis and bioassays. J Soils Sediments 10(3) 359-367. doi 10.1007/sll368-009-0176-8... [Pg.311]

In this case, a likely explanation for the apparent supersaturation is that the chemical analysis included not only dissolved aluminum and iron, but also a certain amount of aluminum and iron suspended in the water as colloids and fine sediments. Analytical error of this type occurs because the standard sampling procedure calls for passing the sample through a rather coarse filter of 0.45 tun p0re size and then adding acid to preserve it during transport and storage. [Pg.95]

As a final note, a variant of the calculation is useful in many cases. Suppose a chemical analysis of a groundwater is available, giving the amount of a component in solution, and we wish to compute how much of the component is sorbed to the sediment. We can solve this problem by eliminating the summations over the sorbed species (the over q terms) from each of the mass balance equations,... [Pg.149]

Chemical analysis of the Meza River and its tributaries revealed significant heavy metal pollution of the upper Meza River sediments with lead, zinc, and some molybdenum, cadmium and arsenic enrichments. The trend of Cd and As is similar to trend of Pb and Zn, which is in agreement with the fact that Cd and As are associated with Pb and Zn in ore minerals (Strucl, 1984 Fux Gosar, 2007). In the lower Meza valley, these heavy metal concentrations decreased somewhat. [Pg.213]

Having as necessary, dried, homogenized or comminuted the samples, they must now be digested in a suitable reagent to extract elements in a suitable form for chemical analysis. In many organizations we have reached the point where the analyses pass from the hands of the person who took the sample to those of the analytical chemist. In the author s experience, however, it must be emphasized that to ensure best-quality results the whole procedure from, for example, statistically sampling a sediment to the final chemical analysis, should be handled by the same person. [Pg.443]

Reference Material Material or substance whose property values are sufficiently homogeneous and well-established so as to be used for the calibration of an apparatus, the assessment of a measurement method, or for assigning values to materials. (Note A reference material may be in the form of a pure or mixed gas, liquid, or solid. Examples include synthetic mixtures such as calibration solutions used in chemical analysis as well as materials based on natural environmental samples such as sediments.)... [Pg.25]

Samples of drainage sediments and pan concentrates of heavy minerals were collected. Chemical analysis was undertaken on the fine fraction (-270 and... [Pg.261]

To be added in cases of indications for relevance and bioavailability In vivo bioassays with relevant exposure conditions, routes and endpoints Prolonged ELS and metamorphosis In vivo bioassays with sediment extracts In vitro bioassays specific mechanisms Internal effect levels Specific chemicals (e.g. PFACs, HBCDs, PBDEs) ELS not longer than free feeding Chemicals that only are toxic in high concentration (narcotics, nanoparticles) Chemical analysis of lipophillic POPs in water... [Pg.100]

It is eoncluded that the determination of dioxin-like activity in cleaned sediment extracts using the DR-Luc bioassay has a consistent reproducibility, and can be used as a reliable and robust tool in the hazard assessment of dredged materials in a licensing system. Its advantage over ehemical analysis is that it also detects the effects of combined exposure as well as the effect of unidentified congeners or chemicals present in concentrations below the limit of detection of chemical analysis with a similar mode of action. In addition the use of cleaned sediment extracts circumvents the problem of disturbing sediment matrix effects. [Pg.118]

Chapter 6 addresses the issue of the applieability of in vitro and in vivo bioassays for hazard, risk and local impact assessment of dredged polluted sediments to be disposed of at sea. It discusses how and to what extent selected bioassays can fill in the gaps left open by chemical analysis and the way in which the bioassays may contribute to the present licensing system for disposal (Schipper et al., 2009b). [Pg.120]

For hazard assessment in a licensing system chemical analysis on total sediment extracts or bioanalysis in order to quantify the bioavailability of the chemicals does not need to be included because the bioavailability will change greatly after disposal of the sediments. [Pg.124]

Local sediment impact assessment can direct the fine-tuning of the selection of chemical and bioassay analyses and the setting of safe levels in the licensing system. This could eventually lead to the decision to include some additional chemical analysis or bioassay in the routine screening. [Pg.124]


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