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Atmosphere volume

It is often taken for granted that the oxygen content of the air is nearly constant at ca. 20% of the atmospheric volume, that most of the liquid water on the planet is aerobic (i.e. contains O2), and that most water has pH values relatively close to neutral" (close to 7). However, these circumstances are not mere coincidences but are in fact consequences of the interaction of key global biogeochemical cycles. For instance, the pH of rainwater is often determined by the relative amounts of ammonia and sulfuric acid cycled through the atmosphere, a clear example of interaction between the nitrogen and sulfur cycles. [Pg.11]

This global average burden of anthropogenic sulfate aerosol can be estimated by considering the entire atmospheric volume as a box. Because the lifetime of sulfate aerosol is short, the sum of all sulfate sources, Q, and its lifetime in the box, f, along with the area of the earth, determine B ... [Pg.449]

In this equation, R is called the ideal gas law constant. Its value depends on the units used, but assuming pressure is measured in atmospheres, volume in liters, and temperature in Kelvins its value is 0.082 atm-L/mol-K. Other forms of the ideal gas law are... [Pg.107]

This equation expresses pressure in atmospheres, volume in liters, temperature in degrees Kelvin, and the quantity of gas in moles. These four quantities are related exactly through the use of the ideal gas constant, R the value for R is 0.0821 L atm/K mole. (Notice that the units for R are in terms of V, P, T, and n.)... [Pg.139]

The value of the constant, R, obviously depends on the system of units employed to express temperature, pressure, and volume. Suppose the pressure is expressed in atmospheres, volume in liters, temperature in degrees Kelvin, and moles in gram-moles. In this system of units Avogadro s Law states that one gram-mole of any gas occupies 22.4 liters at 273° K and one atm pressure. Therefore... [Pg.13]

The exit of the inert gas from the apparatus must be protected by a gas bubbler . The bubbler allows you to monitor the flow of inert gas through the apparatus and prevents the entry of air into the apparatus. Several designs of gas bubbler are available (Fig. 18.2) and it is usual to connect the bubbler to the apparatus at the top of the condenser. You should make sure that the bubbler contains enough mineral oil to create a seal from the atmosphere and that it has a bulb above the mineral oil to collect any mineral oil, which could be sucked back into your apparatus if there is a sudden contraction in the volume of inert gas in the apparatus. Such changes in volume will occur if you suddenly cool the apparatus without increasing the gas flow to compensate for the resulting reduction in inert atmosphere volume. [Pg.126]

Water droplets and particulate matter often influence the rates of chemical transformations in the atmosphere. Whereas homogeneous reactions involve only gaseous chemical species in the atmosphere, reactions involving a liquid phase or a solid surface in conjunction with the gas phase are called heterogeneous reactions. Reactions that occur much more rapidly in water than in air may occur primarily in droplets, even though the droplets constitute only a small fraction of the total atmospheric volume. Solid surfaces also can catalyze reactions that would otherwise occur at negligible rates specific examples are discussed in the following sections on acid deposition and stratospheric ozone chemistry. [Pg.367]

The units of R that are appropriate for ideal gas law calculations are those that involve units of volume, pressure, moles, and temperature. When you use the value R = 0.0821 L atm/mol K, remember to express all quantities in a calculation in these units. Pressures should be expressed in atmospheres, volumes in liters, temperature in kelvins, and amount of gas in moles. In Examples 12-9 and 12-10 we converted pressures from torr to atm. In Example 12-10 the volume was converted from ft to L. [Pg.452]

If the rates of all of these processes are known, then ozone densities can be derived from measurements of the infrared atmospheric volume emission rate (e.g., Evans et al, 1968 Thomas et al, 1983). This provides a useful means of measuring mesospheric ozone abundances (Mlynczak and Olander, 1995). Dayglow production mechanisms by oxygen compounds are shown schematically in Figure 2.10 (Mlynczak et al, 1993). [Pg.46]

The ocean water volume needed to contain all water soluble radionuclides and the volumes of atmosphere needed to contain the gaseous waste products from all nuclear power in the world at a level below the DAC and ALI values recommraded by the ICRP for safe breathing and drinking can be estimated. The basic data are the total toxicity values (7/t and 7n,), which have to be compared with the global (free ocean) water volume (1.4x 10 m ) and the atmospheric volume (the troposphere volume up to 12 km is 6 X10 m ). [Pg.624]

Building onto the concept of molecularly wired sensors for signal amplification, Swager reported in 1998 the synthesis of a series of porous PPE derivatives in which pentiptycene modules are incorporated into the PPE main chain. The incorporation of the pentypticene moieties makes 29 and 30a (Chart 5) efficient solid-state emitters unaffected by aggregation i.e., their emission spectra in solution and in the solid state are almost identical. The authors found that thin films of these highly fluorescent PPEs are excellent sensors for the detection of trinitrotoluene and dinitrotoluene. Both aromatics suppress the fluorescence of 29 or 30a effectively but reversibly. The headspace, i.e., the atmospheric volume above land mines, contains measurable quantities of dinitrotoluene. As a consequence, polymers 29 and 30 coated on top of a fiber optic sensor will allow their simple detection by these very sensitive molecular wire-type materials. This elegant concept should be extendable and applicable to any other analyte, (a) which has the ability to quench fluorescence and (b) for which a receptor can be attached to PPEs. [Pg.223]

Cohesive Energy Density and Solubility Parameters. As a result of attractive or cohesive forces the molecules in pure solvents have a cohesive energy that has to be expended in molecular separation processes (e.g., dilution, evaporation, or addition of another substance). The cohesive energy can be calculated from the enthalpy of vaporization AHy and the work that is required to expand the vapor against the atmosphere (volume work) [14.20], The cohesive energy per unit volume, i.e., the cohesive energy density, is defined as [14,16], [14.21], [14.22] ... [Pg.282]

The subscripts a and b characterize the mean time of the dry periods (non-rainy and/or cloudy-free) and wet periods (clouds, rain), respectively, x et represents the residence time during the wet event, either according to Eq. (4.329) for wet deposition or Eq. (4.303) for aqueous phase chemistry. The constant A corresponds to a fractional time of the dry period time T , which becomes smaller when the ratio between the dry and wet periods decreases. The coefficient B is normally larger than one (if > tt ) Most likely ta r but r tb follows r Xa. Eq. (4.361) represents the flow through two reservoirs according to Eq. (4.357), first a space without wet events (dry period) and then a space with a wet event. For a given atmospheric volume, we might also define a transport residence time as ... [Pg.456]

In the German Storfall-Berechnungsgrundlagen it is postulated that in such an incident all the fuel rods of one outer row of the respective assembly are damaged. It is further assumed that 10% of the fission product noble gas inventories of these rods is released to the containment atmosphere. As for the fission product iodine, 5% of the inventory has to be assumed to be transported to the pool water from there, a fraction of the iodine is assumed to be volatilized, in accordance with a partition coefficient of 1 - 10, which is calculated for a pool water volume of ISOOm and an atmosphere volume limited to 20,000 m. Airborne iodine is assumed to be present as 90% I2 and 10% organically bound iodine. [Pg.471]

Summarizing this chapter, we have derived both analytic and numerical procedures for calculating the emerging radiation field provided we can specify the vertical distributions of the temperature as well as the gas and particle compositions. It is also necessary to know the absorption and scattering properties of atmospheric volume elements on a microscopic scale. In the next chapter we discuss these properties before proceeding with the task of computing the intensity of the outgoing radiation field. [Pg.57]

The atmosphere is nitrogen s largest biospheric reservoir, containing some 3.9 x 10 t of the gas. Stable N2 molecules dominate, forming 78% of atmospheric volume. Highly variable concentrations of nitric oxide (NO) and nitrogen dioxide (NO2), often designated jointly as NOx, nitrous oxide (N2O), nitrates (NOa"),... [Pg.17]


See other pages where Atmosphere volume is mentioned: [Pg.2795]    [Pg.348]    [Pg.104]    [Pg.217]    [Pg.103]    [Pg.11]    [Pg.1937]    [Pg.2258]    [Pg.108]    [Pg.379]    [Pg.70]    [Pg.2795]    [Pg.675]    [Pg.39]    [Pg.418]    [Pg.335]    [Pg.335]    [Pg.335]    [Pg.679]    [Pg.11]    [Pg.33]    [Pg.47]    [Pg.396]    [Pg.106]    [Pg.228]   
See also in sourсe #XX -- [ Pg.24 ]




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Atmosphere, mass, thickness, volume

Pressure, atmospheric volume-mass-temperature

Volume percentages of some variable gases (inorganic and organic) in the atmosphere

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