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Atmospheric Sections

Coil Shed Towers - These are composed of a combination structure of a cooling tower installed on top of a substmcture that contains atmospheric section coils (refer to Figure 7). [Pg.74]

Acceptor doping in perovskite oxides gives materials with a vacancy population that can act as proton conductors in moist atmospheres (Section 6.9). In addition, the doped materials are generally p-type semiconductors. This means that in moist atmospheres there is the possibility of mixed conductivity involving three charge carriers (H+, O2-, and h ) or four if electrons, e, are included. [Pg.385]

The stability of powders can be determined by adiabatic storage tests or Dewar flask tests under an air atmosphere (Section 2.3.2.2). Several other dedicated tests have been developed [10,133-136]. [Pg.76]

In an atmospheric spray tower the air movement - is dependent on atmospheric conditions and the aspirating effect of the spray nozzles. Natural-draft cooling tower operation depends on a chimney or stack to induce air movement. Mechanical-draft cboling towers utilize fans to move ambient air through the tower. Deck-filled towers contain tiers of splash bars or decks to assist in the breakup of water drops to increase the total water surface and subsequently the evaporation rate. Spray-filled towers depend only on spray nozzles for water breakup. Coil shed towers are comprised of a combination structure of a cooling tower installed on top of a substructure that contains atmospheric section coils. Hyperbolic natural-draft cooling towers are typically large-capacity systems. [Pg.59]

The complexes and derivatives of borane (BH3) are now among the most useful and versatile reagents available to the organic chemist. The reader is referred to key monographs and reviews for a full account of the variety and scope of these reagents.4 A very wide range of boranes is now available commercially, but it is often convenient and less expensive to prepare them as and when needed. Most reactions with boranes should be carried out under an inert atmosphere. Section 2.17.8, p. 120 should be consulted for details of the experimental procedures for these reactions. [Pg.418]

From a simple 40Ar inventory in the Earth, we also concluded that a majority of the terrestrial Ar has been degassed from the mantle to the atmosphere (Section 6.6 and 6.8). Hence, the assumption that, except for He and Xe, atmospheric noble gas is a good proxy of the terrestrial noble gas inventory serves as a useful working hypothesis. [Pg.250]

Methanol has advantages as a carrier of hydrogen because it is a liquid and stable at room temperature. Instead of manufacturing methanol from a fossil fuel such as methane or coal, it would be possible to extract C02 from the atmosphere (Section 15.3.2), produce H2 from solar-based water decomposition, and combine H2 and C02 to CH3OH. The C02 used up to do this would be re-injected to the atmosphere again upon the re-forming of methanol to H2 for the fuel cells, but there would be no net buildup of C02. Further, we would not have to worry about the exhaustion of fossil fuels, which, as far as oil at an acceptable price is concerned, will occur before 2040. [Pg.333]

Halogenated solvents are an example of a class of chemicals that with a few exceptions (such as methyl chloride, CH3Cl, produced by some marine algae) are not naturally present in the atmosphere. Currently, such solvents are released in large amounts (Table 4-4). Many are degraded in the lower atmosphere (Section 4.6). Some, however, such as the CFCs, pose a unique set of problems because their low reactivity allows them to escape destruction in the troposphere therefore, they can enter the stratosphere, where they take part in a catalytic cycle that destroys beneficial high-altitude ozone (Section 4.6.4). [Pg.293]

Roasting sulfide ores causes air pollution. Enormous quantities of SO2 escape into the atmosphere (Section 6-8, part 4), where it causes great environmental damage (Figure 22-3). Federal regulations now require limitation of the amount of SO2 that escapes with stack gases and fuel gases. Now most of the SO2 is trapped and used in the manufacture of sulfuric acid (Section 24-12). [Pg.905]

The above sections describe the utility of models in predicting the transport of biological and chemical threat threats in the atmosphere (Section 3.2), and under given... [Pg.90]

The sections of this chapter deal with the following elements of atmospheric dynamics vertical structure of the atmosphere (Section 3.2), fundamental equations of atmospheric motions (Section 3.3), transport of chemical constituents and the relative importance of dynamical and chemical effects on photochemical species (Section 3.4), atmospheric waves (Section 3.5), the mean meridional circulation and the use of the transformed Eulerian formalism to illustrate the roles of mean meridional and eddy transports (Section 3.6), the important role of wave transience and dissipation (Section 3.7), vertical transport by molecular diffusion in the thermosphere (Section 3.8), and finally, models of the middle atmosphere (Section 3.9). [Pg.52]

Single-waUed nanotubes prepared by vapor deposition are of high quahty and, contrary to materials made by other methods, far less entangled. Hence the purification of CVD-SWNT is facilitated. Still the samples often bear defects, and they always contain considerable amounts of catalyst material, which has to be removed through a time-consuming purification procedure. The defects can be cured by annealing at high temperatures under an inert atmosphere (Section 3.3.6). [Pg.148]

The reaction of simple nitriles with ammonium chloride and SC12 under a chlorine atmosphere (Section II.B) has previously been shown to yield [2]C1 in moderate yields. However, reaction of p-dicyanobenzene with ammonium chloride in refluxing SC12 (or directly with 11) has been reported to yield only small quantities ( 1%) of [2]C1 (R = p-NC.C6H4) within the S02-soluble fraction, and no [78]C12 was observed [91JCS(D)1099]. [Pg.220]

This year, reactions of noble gases are covered in this section, but, as before, reactions of , H, and N atoms are covered in the atmospheric section (Section... [Pg.124]

Large-scale experimental releases of fission product activity are clearly ruled out because of the implications on the safety of the public, described in Section V,F, as are also the smaller scale releases referred to earlier in Section V. Therefore, for verification of our conclusions we have to rely on limited experience from those few accidents that have occurred and that have released fission products (see Section I,D), but much more on our store of knowledge of all the factors involved, i.e., types of reactor accidents (Section II) through fission product release (Section III) and dispersion of a release in the atmosphere (Section IV), to analysis of the radiation and radiobiological hazards and risks to exposed members of the population. In view of these several steps involved in the estimation of hazard, it is reassuring that the many different authors who have written on the topie reach conclusions which are generally similar and differ only in limited areas. [Pg.67]

Convert between pressure units with an emphasis on torr and atmospheres. (Section 10.2)... [Pg.414]

Describe the processes of photodissociation and photoionization and their role in the upper atmosphere. (Section 18.1)... [Pg.776]


See other pages where Atmospheric Sections is mentioned: [Pg.1032]    [Pg.1087]    [Pg.70]    [Pg.235]    [Pg.15]    [Pg.219]    [Pg.70]    [Pg.422]    [Pg.855]    [Pg.910]    [Pg.39]    [Pg.160]    [Pg.1405]    [Pg.4345]    [Pg.1198]    [Pg.1256]    [Pg.184]    [Pg.39]    [Pg.417]    [Pg.49]    [Pg.1199]    [Pg.1257]    [Pg.1036]    [Pg.1091]    [Pg.60]    [Pg.98]   


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