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Atmosphere removal

Deposition is the atmospheric removal process by which gaseous and particulate contaminants are transferred from the atmosphere to surface receptors - soil, vegetation, and surface waters (22,27,28, 32). This process has been conveniently separated into two categories dry and wet deposition. Dry deposition is a direct transfer process that removes contaminants from the atmosphere without the intervention of precipitation, and therefore may occur continuously. Wet deposition involves the removal of contaminants from the atmosphere in an aqueous form and is therefore dependent on the precipitation events of rain, snow, or fog. [Pg.140]

Brubaker WW, RA Hites (1997) Polychlorinated dibenzo-/)-dioxins and dibenzofurans gas-phase hydroxyl radical reactions and related atmospheric removal. Environ Sci Technol 31 1805-1810. [Pg.39]

The atmospheric and chemical processes controlling the spatial and temporal variability of psychoactive substances in urban atmospheres are largely uncertain, mostly due to the fact that the atmospheric residence time of these compounds is so far unclear. The transport, transformation and deposition/atmospheric removal... [Pg.450]

Dichlorobenzene will exist predominantly in the vapor-phase in the atmosphere, and its detection in rainwater suggests that atmospheric removal via washout is possible (Ligocki et al. 1985). Depending on soil type, the compound is expected to be moderately mobile in soil and to volatilize from surface water and soil surfaces to the atmosphere. Volatilization, sorption, biodegradation, and bioaccumulation are likely to be competing processes, with the dominant fate being determined by local environmental conditions. [Pg.177]

Carbon monoxide, which is predominantly produced during combustion processes, may exhibit an 0 excess of up to 7.5%c in summer at high northern latitudes (Rockmann et al. 1998). The major source of this fractionation is its atmospheric removal reaction CO + OH = CO2 + H2, in which the remaining CO gains excess 0. [Pg.176]

Exhaust gases are treated to minimize SO2 emissions into the atmosphere. Removal of SO2 is achieved by the utilization of a scrubber system and will be discussed below in greater detail. Although numerous variations of both wet and dry scrubbers are commercially available, most rely on the adsorption of S02 onto A1-, Na-, or Ca-based adsorbents. Ca-based adsorbents, such as lime (CaO) or calcite (CaC03), are usually preferred due to their low cost and high availability. [Pg.227]

Despite the growth of HCFCs, the National Oceanic Atmospheric Administration (NOAA) researchers data show that ozone-depleting chemicals in the atmosphere have declined overall about 3% since 1994. But that decrease is due almost entirely to a dramatic drop in the amount of methylchloroform, which was used as a cleaning solvent. Natural oxidation processes in the atmosphere remove methylchloroform so efficiently that its atmospheric concentration has been falling rapidly since production stopped. [Pg.44]

Brubacker, W. W. Jr., and R. A. Hites, Polychlorinated dibenzo-p-dioxins and dibenzofurans Gas phase hydroxyl radical reactions and related atmospheric removal , Environ. Sci. Technol., 31, 1805-1810 (1997). [Pg.1217]

Allow all the gas to escape into the atmosphere. Remove the cover and wash it with distd w into a 25ml volumetric flask with the aid of a funnel. Transfer (quantitatively) the contents of the bomb into the same flask and fill it with w to mark. After mixing the contents, pipet a 50ml aliquot into a tall beaker and titrate with std HC1 soln using successively two indicators, first phpht and then methyl orange Calculation. If reading with phpht indicator is n and with methyl orange n , then... [Pg.452]

Bidleman T.F., Christinsen E.J. (1979) Atmospheric removal process for high molecular weight organochlorines. J. Geophysical Res. 84(cl2), 7857-7862. [Pg.1134]

Methane is found throughout the troposphere in concentrations now exceeding 1.6 parts per million by volume (1 ppmv = 10" ), and is the most abundant source of C-H bonds in the atmosphere. Its primary atmospheric removal process is also reaction with HO radicals, as in (6). The atmospheric lifetimes for CHa and CILCCh can be connected through the relative rates of reactions (5) and (6), and the value observed in the laboratory... [Pg.307]

Atmospheric fate If released to the atmosphere, 2-heptanone is expected to undergo a gas-phase reaction with photochemically produced hydroxyl radicals the estimated half-life for this process is 1.9 days. 2-Heptanone has relatively high water solubility (4300 mgl at 25°C), which indicates that it may undergo atmospheric removal by wet deposition processes. Although 2-heptanone has the potential of being removed from the atmosphere by direct photochemical degradation, the rate of this process is not expected to be able to compete with atmospheric removal by the reaction with hydroxyl radicals. [Pg.1318]

Given its high vapor pressure of over 2 atm at 25°C, methylamine will remain in the vapor phase, if released to the atmosphere where it will react with photochemically produced hydroxyl radicals (Tyx of 18h). Dissolution into rain droplets is also an important removal process. Other atmospheric removal processes, for example, photolysis and hydrolysis are not significant. [Pg.1672]

The earth s forests and jungles play a crucial role in maintaining the balance of gases in the atmosphere, removing CO2 and supplying O2. The massive destruction, for economic reasons, of heavily forested areas such as the Amazon rain forest in South America is cited as another long-term contributor to global environmental problems. Worldwide, more than 3 million square miles of once-forested land is now barren for some reason at least 60% of this land is now unused. [Pg.438]

A solution of 3-(methylsulfanylmethyl)-l, 2,3-triphenylcyclopropene (120 mg, 0.37 mmol) and thioxanthone (15 mg) in benzene (170 mL) was irradiated with a 450-W Hanovia lamp, equipped with a uranium glass filter, for 1 h under an argon atmosphere. Removal of the solvent left a yellow oil which was subjected to chromatography (silica gel, hexane). The major component isolated was the title compound as a crystalline solid yield 108 mg (90%) mp 203-204°C. [Pg.202]

Public Comment on Atmospheric Removal Processes. A public comment questioned whether photolysis is the dominant removal pathway for airborne PCBs, as the profile currently suggests (page 306). One panelist thought precipitation, not photolysis, is the dominant removal pathway. [Pg.966]

Electrical lines and water Maintenance done on wrong equipment Inadequate isolation of equipment venting of atmosphere removal of toxics... [Pg.1330]


See other pages where Atmosphere removal is mentioned: [Pg.186]    [Pg.440]    [Pg.442]    [Pg.65]    [Pg.461]    [Pg.461]    [Pg.134]    [Pg.134]    [Pg.41]    [Pg.1122]    [Pg.360]    [Pg.255]    [Pg.170]    [Pg.170]    [Pg.177]    [Pg.64]    [Pg.55]    [Pg.1122]    [Pg.286]    [Pg.2209]    [Pg.1494]    [Pg.1878]    [Pg.322]    [Pg.43]   
See also in sourсe #XX -- [ Pg.424 ]




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Annotated bibliography of aerosol removal from the containment atmosphere

Atmosphere removal processes

Atmosphere wet removal

Atmospheric Physical Removal Processes

Atmospheric lead removal

Atmospheric lead transport removal processes

Atmospheric pollution hydrogen sulfide removal

Atmospheric removal Deposition processes

Atmospheric removal mechanisms

Atmospheric removal processes

Carbon dioxide removal from atmosphere

Carbon dioxide: atmospheric 1398 removal

Gases, atmospheric removal mechanisms

Nitrogen oxides removal atmosphere

Particles, atmospheric removal

Particles, atmospheric removal mechanisms

Physical Removal of Chemicals from the Atmosphere

Rainout, atmospheric pollution removal

Removal mechanisms atmospheric oxidation

Removal of trace substances from the atmosphere

Sedimentation atmospheric pollution removal

Transformation atmospheric pollution removal

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