Environmental Health Criteria 214
Environmental Health Criteria 214
Environmental Health Criteria 214
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HUMAN EXPOSURE ASSESSMENT<br />
impactor is determined by the flow rate, jet size and shape (e.g., the<br />
distance between the jet and the impaction surface) (Pastuska, 1988;<br />
Lehtimäki & Willeke, 1993). The air flow rate must be calibrated<br />
carefully because correct size selection depends largely on precise<br />
flow rates.<br />
Filters are made either from fibre mats of glass, cellulose or<br />
quartz or from synthetic membranes (e.g., Teflon). The selection of<br />
appropriate filters depends on the pump, filter static pressure,<br />
collection efficiency, extraction and analytical requirements, and the<br />
potential for sampling artefacts. Filter mass is determined by<br />
weighing the filter under controlled temperature and humidity<br />
conditions before and after use following a conditioning period of at<br />
least 24 h at those same conditions. The collected mass can be<br />
extracted and analysed for chemical composition. The extraction and<br />
analysis procedures used depend on the analytes of interest. A recent<br />
summary of methods for extraction and analysis of components of<br />
particulate matter may be found in Koutrakis & Sioutas (1996).<br />
7.2.3 Semivolatile compounds<br />
For airborne contaminants that are present in both the particle<br />
and the vapour phase at typical environmental conditions, it is<br />
necessary to use a combination of sampling methods. The most common<br />
approach consists of an aerosol sampling inlet (with or without size<br />
preselector) followed by a sorbent cartridge or tube. Examples of such<br />
contaminants include airborne PAHs, pesticides, polychlorinated<br />
biphenyls (PCBs), dioxins and furans. Semivolatile sampling systems<br />
are commercially available for personal air monitoring. Extraction and<br />
analysis of these samples are done separately for the particle and<br />
vapour phase and then the results are combined to provide a total<br />
concentration. An introduction to sampling and analysis methods for<br />
VOCs in air may be found in Binkova et al. (1995), Wallace & Hites<br />
(1996), Wallace et al. (1996) and Simonich & Hites (1997).<br />
7.2.4 Reactive gas monitoring<br />
Certain gases present in air may react with chemicals present in<br />
particles. For example, sulfuric acid particles collected on filters<br />
can be neutralized by the ammonia gas present in the sample or air<br />
stream. The preferred sampling approach to avoid this is to use a<br />
denuder to remove the reactive gas before it reaches the downstream<br />
filter. In the case of sulfuric acid monitoring, a citric-acid-coated<br />
denuder is used to remove the ammonia gas. Small denuder systems are<br />
commercially available for personal monitors. Denuder technologies are<br />
described in Lodge (1988) and Koutrakis & Sioutas (1996).<br />
7.3 Water<br />
The sampling and analysis of drinking-water characterizes the<br />
extent to which this carrier medium represents a source of specific<br />
chemical exposure. Contaminated drinking-water supplies contribute to<br />
the human intake of numerous chemical contaminants, including heavy<br />
metals, fertilizers, pesticides, aromatic hydrocarbons and<br />
organohalogens, among others. In some cases, drinking-water may be the<br />
primary source of human exposure. Chemical pollutants in water may<br />
originate from one or more of a myriad of sources, as summarized in<br />
Table 25. In the selection of measurement and sampling methods, it is<br />
important to consider raw water sources, water treatment processes,<br />
and distribution and service systems, all of which can either reduce<br />
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