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Ozone and stratosphere

There is also a significant correlation between temperature fluctuations in the lower stratosphere and fluctuations in total ozone. There are two sources of this correlation, radiative and dynamical (McCormack and Hood, 1994). Thus, increased ozone leads to increased absorption of solar radiation and increased heating. In addition, dynamical effects associated with vertical and meridional air motions also give a positive correlation between ozone and stratospheric temperature. For example, Randel and Cobb (1994) analyzed total column 03 and temperatures in the lower stratosphere from 1979 to 1992. Correlations between 03... [Pg.736]

NAS, Committee on Ozone and Stratospheric Aviation. 1971-75 NAS Committee on Motor Vehicle Emissions. 1969-73 California Statewide Air Pollution Research Center. 1965-67 NAS Panel to National Bureau of Standards. [Pg.252]

Explain the difference between the effects of ground-level ozone and stratospheric ozone. Why is one beneficial to human life, while the other is not ... [Pg.318]

Perfluorinated ethers and perfluorinated tertiary amines do not contribute to the formation of ground level ozone and are exempt from VOC regulations (32). The commercial compounds discussed above have an ozone depletion potential of zero because they do not contain either chlorine or bromine which take part in catalytic cycles that destroy stratospheric ozone (33). [Pg.298]

Most ozone is formed near the equator, where solar radiation is greatest, and transported toward the poles by normal circulation patterns in the stratosphere. Consequendy, the concentration is minimum at the equator and maximum for most of the year at the north pole and about 60°S latitude. The equihbrium ozone concentration also varies with altitude the maximum occurs at about 25 km at the equator and 15—20 km at or near the poles. It also varies seasonally, daily, as well as interaimuaHy. Absorption of solar radiation (200—300 nm) by ozone and heat Hberated in ozone formation and destmction together create a warm layer in the upper atmosphere at 40—50 km, which helps to maintain thermal equihbrium on earth. [Pg.495]

The demand for trichloroethylene grew steadily until 1970. Since that time trichloroethylene has been a less desirable solvent because of restrictions on emissions under air pollution legislation and the passage of the Occupational Safety and Health Act. Whereas previously the principal use of trichloroethylene was for vapor degreasing, currentiy 1,1,1-trichloroethane is the most used solvent for vapor degreasing. The restrictions on production of 1,1,1-trichloroethane [71-55-6] from the 1990 Amendments to the Montreal Protocol on substances that deplete the stratospheric ozone and the U.S. [Pg.22]

The discovery of ozone holes over Antarctica in the mid-1980s was strong observational evidence to support the Rowland and Molina hypothesis. The atmosphere over the south pole is complex because of the long periods of total darkness and sunlight and the presence of a polar vortex and polar stratospheric clouds. However, researchers have found evidence to support the role of CIO in the rapid depletion of stratospheric ozone over the south pole. Figure 11-3 shows the profile of ozone and CIO measured at an altitude of 18 km on an aircraft flight from southern Chile toward the south pole on September 21, 1987. One month earlier the ozone levels were fairly uniform around 2 ppm (vol). [Pg.160]

Fig. 11-3. Stratospheric ozone and CIO concentrations at an altitude of 18 km measured by aircraft flying south over Antarctica on September 27,1987. The dramatic decrease in ozone at a latitude of 71 degrees is attributed to the role of CIO in catalytic destruction of ozone. Adapted from Anderson et al. (13). Fig. 11-3. Stratospheric ozone and CIO concentrations at an altitude of 18 km measured by aircraft flying south over Antarctica on September 27,1987. The dramatic decrease in ozone at a latitude of 71 degrees is attributed to the role of CIO in catalytic destruction of ozone. Adapted from Anderson et al. (13).
The EPA summary (4) for stratospheric ozone and global climate protection lists the basics of the title ... [Pg.404]

Title VI Stratospheric Ozone and Global Climate Protection - The law builds on the market-based structure and requirements currently contained in EPA s regulations to phase out the production of substances that deplete the ozone layer. [Pg.7]

Title VI - Stratospheric Ozone and Global Climate Title VII - Provisions Relating to Enforcement... [Pg.9]

The oxygen atom produced in this step can react with oxygen molecules to produce more ozone, and so the ozone concentration in the stratosphere normally remains constant, with seasonal variations. Because the decomposition of ozone... [Pg.688]

The Antarctic ozone hole is the result of anthropogenic release of trace gases into the atmosphere (CFCs in particular), causing a decrease in stratospheric ozone and a subsequent increase in solar ultraviolet radiation reaching the earth s surface. [Pg.204]

Goldsmith, P., Tuck, A. F., Foot, J. S., Simmons, E. L., and Newson, R. L. (1973). Nitrogen oxides, nuclear weapon testing, Concorde, and stratospheric ozone. Nature 244, 545-551. [Pg.104]

The atmospheric chemistry of nitrogen is quite complex and involves literally hundreds or thousands of chemical reactions. Although the fluxes are much smaller than the biological fluxes, these processes are important for a variety of reasons, including impacts on climate, stratospheric ozone, and photochemical smog. In this section we present an overview of the most important processes. [Pg.329]

Describe the trends in the ozone concentrations in the troposphere and stratosphere, and the total ozone column. What roles do nitrogen oxides play in these changes ... [Pg.340]

It is not difficult to see that ozone initially forms from the oxygen present in the air. Chapman [115] introduced the photochemical model of stratospheric ozone and suggested that the ozone mechanism depended on two photochemical and two chemical reactions ... [Pg.485]

This report deals primarily with the origins and effects of ozone and other photochemical oxidants. It is limited, more or less, to the problem of urban pollution and to such closely related topics as natural background in the earth s boundary layer. No consideration is given to the stratospheric ozone layer and the effects produced by supersonic transport (sst) emission or halocarbons. [Pg.2]

The main purpose of this chapter is to survi atmospheric concentrations of photochemical oxidants, with emphasis on surface concentrations and the distribution patterns associated with them. The reason for that em> phasis is that the photochemical oxidants that affect public health and welfare are largely concentrated in this region. The whole subject of stratospheric ozone (and its filtering of ultraviolet light and interactions with supersonic-transport exhaust products), nuclear weapon reaction products, and halogenated hydrocarbon decomposition pr ucts is not treated here. [Pg.126]

The concentration of ozone near the Earth s surface is very low, typically in the range of 15-45 pphv (parts per billion by volume). In contrast, ozone is more abundant in the Earth s stratosphere, where it is formed by the action of ultraviolet radiation on molecules of dioxygen. A distinction is sometimes made between stratospheric ozone ("good ozone") and tropospheric (low-level or surface ozone "bad ozone"). This distinction arises from the fact that stratospheric ozone reduces the amount of ultraviolet radiation that reaches the Earth, reducing the rate of skin cancer and other medical problems... [Pg.46]

CFCs are nearly ideal substances for attacking ozone molecules and damaging the ozone layer. On the one hand, they tend to be very stable, even in the stratosphere. Many CFCs have half-lives of 100 years or more that means that once they have escaped into the upper atmosphere, they are likely to remain there for very long periods. On the other hand, some small number of CFC molecules do dissociate to form chlorine free radicals, with the ability to destroy ozone molecules. Although the number of CFC molecules that do dissociate is relatively small, the actual number is not important since chlorine free radicals that are generated in the process are used over and over again. That is, they are catalysts in the destruction of ozone and are not, themselves, used up in their reactions with ozone molecules. [Pg.74]

The actual destruction of ozone in the stratosphere actually involves hundreds of different reactions. Besides the Chapman reactions and destruction by CFCs, many other chemical species can destroy ozone. In 1970, Paul Crutzen (193 3-) showed that nitrogen oxides could destroy ozone. Nitric oxide can remove an oxygen atom from ozone and be regenerated according to the following reactions ... [Pg.266]


See other pages where Ozone and stratosphere is mentioned: [Pg.246]    [Pg.55]    [Pg.94]    [Pg.246]    [Pg.55]    [Pg.94]    [Pg.286]    [Pg.496]    [Pg.15]    [Pg.331]    [Pg.32]    [Pg.602]    [Pg.689]    [Pg.135]    [Pg.204]    [Pg.204]    [Pg.347]    [Pg.463]    [Pg.50]    [Pg.75]    [Pg.280]    [Pg.330]    [Pg.452]    [Pg.213]    [Pg.300]    [Pg.277]    [Pg.765]    [Pg.159]    [Pg.163]    [Pg.1]   
See also in sourсe #XX -- [ Pg.54 ]




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