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Ambient contaminant concentrations

In contrast to studies of ambient contaminant concentrations in urban areas, comparatively little work has determined rates of contaminant emissions, with the exception of PCBs (e.g. Offenberg et ah, 2005 Totten et al, 2006 Gasic et ah, 2009). This information is of critical importance to risk assessment studies and the design of effective policies and programmes aimed at emissions reductions. There are numerous examples of national scale emissions inventories of single-chemical or point-source. These do not account for many of the important non-point sources of contaminants in urban areas, nor are they comparable due to differences in categorization and research priorities in different jurisdictions (Seika et al., 1996). [Pg.197]

For maximum protection of human health from the potential carcinogenic effects of exposure to arsenic through drinking water or contaminated aquatic organisms, the ambient water concentration should be zero, based on the nonthreshold assumption for arsenic. But a zero level may not be attainable. Accordingly, the levels established are those that are estimated to increase cancer risk over a lifetime to only one additional case per 100,000 population. These values are estimated at 0.022 pg As/L for drinking water and 0.175 pg As/L for water containing edible aquatic resources (USEPA 1980 Table 28.7). [Pg.1529]

It is not passive. The driving force, its continued operation, is based on the difference between the contaminant concentration at the velocity barrier (assumed to be equal to the ambient concentration) and the sorbent surface (the principle of diffusion). That difference is maintained by the continuous adsorption of the contaminant vapors by the sorbent. [Pg.196]

Photocatalytic oxidation over illuminated titanium dioxide has been demonstrated to be effective at removing low concentrations of a variety of hazardous aromatic contaminants from air at ambient temperatures. At low contaminant concentration levels and modest humidity levels, complete or nearly complete oxidation of aromatic contaminants can be obtained in photocatalytic systems. Although aromatic contaminants are less reactive than many other potential air pollutants, and apparent catalyst deactivation may occur in simations where recalcitrant reaction intermediates build up on the catalyst surface, several approaches have already been developed to counter these potential problems. The introduction of a chlorine source, either in the form of a reactive chloro-olefin cofeed or an HCl-pretreated catalyst, has been demonstrated to promote the photocatalytic oxidation of... [Pg.279]

Reverse osmosis molecular weight >200 ambient temperature, high concentration, low contamination ambient temperature, concentration salt concentration, 12-14... [Pg.16]

The procedures used to determine ambient carbonyl concentrations involve a collection step with silica or C18 cartridges impregnated with 2,4-dinitrophenylhydrazine. Contamination is inevitable with this system, and blanks must be used to compensate for the degree of contamination. Selection of the appropriate blank values to subtract is a difficult and uncertain process. Consequently, development of a gas chromatographic system that will resolve and respond to the low-molecular-weight aldehydes and ketones is needed. The mercuric oxide and atomic emission detectors should provide adequate response for the carbonyls. [Pg.297]

That is, changes in humidity and ambient carbon impurity contaminant concentrations will have little influence upon the wafer surface leading to improved photoresist adhesion reproducibility. [Pg.259]

Reduction of mercury emissions and other contaminants from municipal waste incinerators using the best available technology is not always completely successful. For example, the Angers, France, solid waste incinerator plant in operation since 1974 was upgraded in 2000 to comply with the new European standards. Mean mercury emissions were reduced about 13% from 26.8 (18.6-69.4) kg/year to 23.3 (< 1.0-72.5) kg/year, and mean ambient air concentrations by about 62% from 0.0004 ig/m (max. 0.001 xg/m ) to 0.00015 ig/m (max. 0.0028 xg/m ) however, the maximum values in both comparisons were larger in 2000-2001 than in 1975-79. [Pg.415]

Respiratory protection devices are rated as to the effectiveness of the protection provided. A typical protection factor for a full-face air purifying respirator, those with filter cartridges and no separate air supply is a factor of 100, impl3dng that the contaminant concentration inside the respirator is no more than 1/100th of the concentration in the ambient air 10 CFR 20 Appendix A contains a table of respiratory protection factors for different types of respiratory protection. As the degree of inhalation risk increases, the risk of skin contamination also increases. Therefore, half-face respirators, those without a covering for the eyes, are not commonly worn. In addition, some form of anti-contamination... [Pg.927]

Small plastic pieces in the oceans can have high concentrations of toxic chemicals that are floating in the waters. The workshop illustrated the research, which concluded that plastic debris can absorb and transport organic contaminants, such as PCBs, up to 105-106 times the ambient seawater concentrations. [Pg.30]

Ain pollution (qv), lecognized in the National Ambient Aii Quality Standards (NAAQS) as being chaiactetized by a time—dosage lelationship, is defined as the presence in the atmosphere (or ambient ain) of one or more contaminants of such quantity and duration as may be injutious to human, plants, or animal life, property, or conduct of business (1,2). Thus, ain pollutants may be rendered less harmhil by reducing the concentration of contaminants, the exposure time, or both. [Pg.384]

Colorimetric methods have led to the development of visual devices for measurement of benzene concentration. These visual detection tubes have been popular since the 1960s and have provided a simple and rehable method for evaluating ambient aromatic vapor contamination. These products are available from anumber of manufacturers such as Drager (Lubeck, Germany), Gastec (Tokyo, Japan), Kitagawa (Kawasaki, Japan), DuPont (Wilmington, Delaware, USA), and 3M (St. Paul, Minnesota, USA) (85). [Pg.46]

The terms ambient air, ambient air pollution, ambient levels, ambient concentrations, ambient air monitoring, ambient air quality, etc. occur frequently in air pollution parlance. The intent is to distinguish pollution of the air outdoors by transport and diffusion by wind (i.e., ambient air pollution) from contamination of the air indoors by the same substances. [Pg.40]

The Canadian Clean Air Act allows the minister to formulate air quality objectives reflecting three ranges of ambient air quality for any contaminant. The tolerable range denotes a concentration that requires abatement without... [Pg.378]

Trace contaminants are also significant at charged solid surfaces, affecting both the charging process and the surface conductivity. In ambient air atmospheres their effect is often determined by interaction with adsorbed water vapor, whose dominant concentration may be sufficiently large to form a monolayer. Topical antistatic agents for solids typically rely on interaction with adsorbed water and can lose effectiveness at low relative humidity (4-2.1). [Pg.10]


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Ambient

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