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Water concentration profile atmosphere

This problem illustrates the solution approach to a one-dimensional, nonsteady-state, diffusional problem, as demonstrated in the simulation examples, DRY and ENZDYN. The system is represented in Fig. 4.2. Water diffuses through a porous solid, to the surface, where it evaporates into the atmosphere. It is required to determine the water concentration profile in the solid, under drying conditions. The quantity of water is limited and, therefore, the solid will eventually dry out and the drying rate will reduce to zero. [Pg.224]

The aluminum profile shown in Figure 11.18 is an example of a mid-depth minimmn created by two inputs, one at the surfece and one from the sediments. The high simfece-water concentrations are due to a large atmospheric dust flux in the North Atlantic. As... [Pg.291]

Fig. 2. Ozone effect on solar radiation (left) and dependence of ozone concentration on atmospheric altitute (right). In the left part the dotted curve represents the photon distribution of solar energy outside the atmosphere (based on the assumption of black body radiation at T = 5773 K). The full curve gives the photon distribution of solar radiation reaching earth surface (see Ref.8. The ozone effect is shown by shadowed area, the dicline above 800 nm is mainly due to absorption by water vapour. On the right side the full curve represents qualitatively a typical ozone profile, the real ozone distribution significantly depends on the local situation (geography), see Ref.15)... Fig. 2. Ozone effect on solar radiation (left) and dependence of ozone concentration on atmospheric altitute (right). In the left part the dotted curve represents the photon distribution of solar energy outside the atmosphere (based on the assumption of black body radiation at T = 5773 K). The full curve gives the photon distribution of solar radiation reaching earth surface (see Ref.8. The ozone effect is shown by shadowed area, the dicline above 800 nm is mainly due to absorption by water vapour. On the right side the full curve represents qualitatively a typical ozone profile, the real ozone distribution significantly depends on the local situation (geography), see Ref.15)...
The feed is delivered to the atmosphoic distillation column between trays 58 and 62 the column has a total of 80-85 valve trays. The operation of this column is governed by the requirement that the overhead product should not contain more than 10 ppm of ethanol and 1-3 ppm of hydrocarbons while the water collected in the bottom should be largely alcohol-firee. This design basis proved to be more cost-effective than the downstream addition of a so-called water purification column for the bottoms product of the atmospheric column as it has some times been practised. In order to meet the purity requirements for the overhead and bottom products, ethanol and hydrocarbons have to be withdrawn through side outlets. This can be achieved best, i.e. with minimum losses of methanol, if the two components are withdrawn at the points where their concentrations are highest. Figure 4.5 shows the concentration profiles of methanol, water, ethanol and n-decane for the theoretical number of trays required by the operating conditions for the example as described here. In this system, the atmo-... [Pg.142]

HBEF, much of the lead entering the ecosystem from the atmosphere appears to be retained in the forest floor. Concentrations and fluxes of lead in bulk deposition are much greater than in Oa horizon leachate. Solution concentrations and fluxes of Pb decrease through the soil profile and losses in stream water are low. There was a strong correlation between concentrations of Pb and dissolved organic carbon (DOC) in soil solution and stream water at Hubbard Brook Driscoll et al., 1994, 1998). [Pg.382]

A study of the vertical profile of chlorinated solvents in the soil, enables the source of contamination to be distinguished for atmospheric inputs a peak occurred a short distance below ground, whereas for inputs from groundwater the concentration increased progressively as the water table was approached. [Pg.158]

As mentioned, the type of concentration-depth profiles observed in oceans should also be observed in lakes. However, the vertical concentration differences in lakes are often not as pronounced as in the ocean. The reason for this is, that the water column in lakes is much shorter mixing and stagnation in lakes is much more dynamic than in the oceans. Due to the presence of high concentrations of different particles in lakes, the release of trace elements from biogenic particles may not be clearly observed, due to readsorption to other particles. This would mean that low concentrations are observed throughout the water column, but that concentration differences are small. Atmospheric inputs to the upper water layers may also make it more difficult to observe a depletion of certain elements in the epilimnion. [Pg.394]

The boron isotope approach to pC02 estimation relies on the fact that a rise in the atmospheric CO2 concentration will increase pC02 of the surface ocean which in turn causes a reduction of its pH. By measuring the boron isotope composition of planktonic foraminifera Pahner et al. (1998) and Pearson and Palmer (2000) have reconstructed the pH-profile of Eocene sea water and estimated past atmospheric CO2 concentrations. However, Lemarchand et al. (2000) argued that 5 B records of planktonic foraminifera partly reflect changes in the marine boron isotope budget rather than changes in ocean pH. [Pg.172]

If the boundary conditions (i.e., the aldehyde concentration in the atmosphere, [A]a, and in the interior of the water body, [A]w) are given and held constant, steady-state conditions are quickly established in the film 3[A]/3t = 3[D]/3t = 0. Since we assume that the diol cannot escape into the atmosphere, the slope of the [D]-profile must be zero at the water surface. Note that any spatial gradient at z= 0 would mean transport by molecular diffusion from or to the boundary. [Pg.935]

Net sedimentation is defined as the flux of material incorporated into the permanent sediment record. 210Pb and 137Cs geochronologies indicate a mass sedimentation rate of 103 g/m2 per year for profundal sediments in Little Rock Lake. By using the mean Hg concentration (118 ng/g) in the top 1-cm slice of our bulk sediment profile, we estimated an annual net sedimentation of 12 xg of HgT/m2 per year. This net accumulation rate is similar to the calculated atmospheric input rate of about 10 xg/m2 per year (18, 19). Additionally, gross deposition rates (from sediment traps) exceeded these estimates by about a factor of 3 this rate suggests substantial internal recycling of material deposited at the sediment-water interface in this lake. [Pg.441]


See other pages where Water concentration profile atmosphere is mentioned: [Pg.56]    [Pg.212]    [Pg.206]    [Pg.219]    [Pg.142]    [Pg.58]    [Pg.129]    [Pg.318]    [Pg.86]    [Pg.347]    [Pg.189]    [Pg.86]    [Pg.218]    [Pg.99]    [Pg.453]    [Pg.166]    [Pg.593]    [Pg.4148]    [Pg.734]    [Pg.194]    [Pg.27]    [Pg.107]    [Pg.598]    [Pg.36]    [Pg.238]    [Pg.98]    [Pg.358]    [Pg.394]    [Pg.164]    [Pg.355]    [Pg.445]    [Pg.8]    [Pg.86]    [Pg.202]    [Pg.236]    [Pg.304]    [Pg.83]   
See also in sourсe #XX -- [ Pg.214 ]




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