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Mobile targets

Mobilization Target, Buna Rubber from 70,000 tons in 1937 to 120 000 tons in 11138. [Pg.307]

Metal bioavailability is the fraction of the total metal occurring in the soil matrix, which can be taken up by an organism and can react with its metabolic system (Campbell, 1995). Metals can be plant-bioavailable, if they come in contact with plants (physical accessibility) and have a form which can be uptaken by plant roots (chemical accessibility). Soil metals become accessible for humans by ingestion, inhalation and dermal contact. Available forms of PTMs are not necessarily associated with one particular chemical species or a specific soil component. Main soil PTMs pools of different mobility, target organisms and routes of transfer are sketched in Fig. 9.2. The most labile fraction, corresponding to the soluble metal pool, occurs as either free ions or soluble complexed ions and is considered the... [Pg.177]

Figure 9.2 Potentially toxic metals (PTMs ) pools of different mobility, target organisms and routes of transfer in and from the soil. Figure 9.2 Potentially toxic metals (PTMs ) pools of different mobility, target organisms and routes of transfer in and from the soil.
Figure 13.5 Schematic presentation of the procedure involved in coupled-column RPLC AS, autosampler C-1 and C-2, first and second separation columns, respectively M-1 and M-2, mobile phases S-1 and S2, interferences A, target analytes HV, high-pressure valve D, detector. Reprinted from Journal of Chromatography, A 703, E. A. Hogendoom and R van Zoonen, Coupled-column reversed-phase liquid cliromatography in environmental analysis , pp. 149-166, copyright 1995, with permission from Elsevier Science. Figure 13.5 Schematic presentation of the procedure involved in coupled-column RPLC AS, autosampler C-1 and C-2, first and second separation columns, respectively M-1 and M-2, mobile phases S-1 and S2, interferences A, target analytes HV, high-pressure valve D, detector. Reprinted from Journal of Chromatography, A 703, E. A. Hogendoom and R van Zoonen, Coupled-column reversed-phase liquid cliromatography in environmental analysis , pp. 149-166, copyright 1995, with permission from Elsevier Science.
As with GC/MS, LC/MS offers the possibility of unequivocal confirmation of analyte identity and accurate quantiation. Similarly, both quadrupole and ion-trap instruments are commercially available. However, the responses of different analytes are extremely dependent on the type of interface used to remove the mobile phase and to introduce the target analytes into the mass spectrometer. For pesticide residue analyses, the most popular interfaces are electrospray ionization (ESI) and atmospheric pressure chemical ionization (APCI). Both negative and positive ionization can be used as applicable to produce characteristically abundant ions. [Pg.742]


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See also in sourсe #XX -- [ Pg.27 ]




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