(meteorology) The study of the production, transport, modification, and removal of atmospheric constituents in the troposphere and stratosphere.
| Sci-Tech Dictionary: atmospheric chemistry |
(meteorology) The study of the production, transport, modification, and removal of atmospheric constituents in the troposphere and stratosphere.
| 5min Related Video: Atmospheric chemistry |
| Sci-Tech Encyclopedia: Atmospheric chemistry |
A scientific discipline concerned with the chemical composition of the Earth's atmosphere. Topics include the emission, transport, and deposition of atmospheric chemical species; the rates and mechanisms of chemical reactions taking place in the atmosphere; and the effects of atmospheric species on human health, the biosphere, and climate.
A useful quantity in atmospheric chemistry is the atmospheric lifetime, defined as the mean time that a molecule resides in the atmosphere before it is removed by chemical reaction or deposition. The atmospheric lifetime measures the time scale on which changes in the production or loss rates of a species may be expected to translate into changes in the species concentration. The atmospheric lifetime can also be compared to the time scales for atmospheric transport to infer the spatial variability of a species in the atmosphere; species with lifetimes longer than a decade tend to be uniformly mixed, while species with shorter lifetimes may have significant gradients reflecting the distributions of their sources and sinks.
The principal constituents of dry air are nitrogen (N2; 78% by volume), oxygen (O2; 21%), and argon (Ar; 1%). The atmospheric concentrations of N2 and Ar are largely determined by the total amounts of N and Ar released from the Earth's interior since the origin of the Earth. The atmospheric concentration of O2 is regulated by a slow atmosphere-lithosphere cycle involving principally the conversion of O2 to carbon dioxide (CO2) by oxidation of organic carbon in sedimentary rocks (weathering), and the photosynthetic conversion of CO2 to O2 by marine organisms which precipitate to the bottom of the ocean to form new sediment. This cycle leads to an atmospheric lifetime for O2 of about 4 million years. See also Biosphere; Lithosphere;
Water vapor concentrations in the atmosphere range from 3% by volume in wet tropical areas to a few parts per million by volume (ppmv) in the stratosphere. Water vapor, with a mean atmospheric lifetime of 10 days, is supplied to the troposphere by evaporation from the Earth's surface, and it is removed by precipitation. Because of this short lifetime, water vapor concentrations decrease rapidly with altitude, and little water vapor enters the stratosphere. Oxidation of methane represents a major source of water vapor in the stratosphere, comparable to the source contributed by transport from the troposphere.
The most abundant carbon species in the atmosphere is CO2. It is produced by oxidation of organic carbon in the biosphere and in sediments. The atmospheric concentration of CO2 is rising, and there is concern that this may cause significant warming of the Earth's surface because of the ability of CO2 to absorb infrared radiation emitted by the Earth (the greenhouse effect). The total amount of carbon present in the atmosphere is small compared to that present in the other geochemical reservoirs, and therefore it is controlled by exchange with these reservoirs. Equilibration of carbon between the atmosphere, biosphere, soil, and surface ocean reservoirs takes place on a time scale of decades. See also Carbon dioxide; Greenhouse effect.
Methane is the second most abundant carbon species in the atmosphere and an important greenhouse gas. It is emitted by anaerobic decay of biological carbon (for example, in wetlands, landfills, and stomachs of ruminants), by exploitation of natural gas and coal, and by combustion. It has a mean lifetime of 12 years against atmospheric oxidation by the hydroxyl (OH) radical, its principal sink. See also
Many hydrocarbons other than methane are emitted to the atmosphere from vegetation, soils, combustion, and industrial activities. The emission of isoprene [H2C&dbnd;C(CH3)CH&dbnd;CH2] from deciduous vegetation is particularly significant. Nonmethane hydrocarbons have generally short lifetimes against oxidation by OH (a few hours for isoprene), so that their atmospheric concentrations are low. They are most important in atmospheric chemistry as sinks for OH and as precursors of tropospheric ozone, organic nitrates, and organic aerosols.
Carbon monoxide (CO) is emitted to the atmosphere by combustion, and it is also produced within the atmosphere by oxidation of methane and other hydrocarbons. It is removed from the atmosphere by oxidation by OH, with a mean lifetime of 2 months. Carbon monoxide is the principal sink of OH and hence plays a major role in regulating the oxidizing power of the atmosphere.
Nitrous oxide (N2O) is of environmental importance as a greenhouse gas and as the stratospheric precursor for the radicals NO and NO2. The principal sources of N2O to the atmosphere are microbial processes in soils and the oceans; the main sinks are photolysis and oxidation in the stratosphere, resulting in an atmospheric lifetime for N2O of about 130 years.
About 90% of total atmospheric ozone (O3) resides in the stratosphere, where it is produced by photolysis of O2. The ultraviolet photons (λ < 240 nm) needed to photolyze O2 are totally absorbed by ozone and O2 as solar radiation travels through the stratosphere. As a result, ozone concentrations in the troposphere are much lower than in the stratosphere. See also Photolysis; Stratosphere; Troposphere.
Tropospheric ozone plays a central role in atmospheric chemistry by providing the primary source of the strong oxidant OH. It is also an important greenhouse gas. In surface air, ozone is of great concern because of its toxicity to humans and vegetation. Ozone is supplied to the troposphere by slow transport from the stratosphere, and it is also produced within the troposphere by a chain reaction involving oxidation of CO and hydrocarbons by OH in the presence of NOx. Ozone production by this mechanism is particularly rapid in urban areas, where emissions of NOx and of reactive hydrocarbons are high.
Sulfuric acid produced in the atmosphere by oxidation of sulfur dioxide (SO2) is a major component of aerosols in the atmosphere and an important contributor to acid deposition. Sources of SO2 to the atmosphere include emission from combustion, smelters, and volcanoes, and oxidation of oceanic dimethylsulfide [(CH3)2S] emitted by phytoplankton. It is estimated that about 75% of total sulfur emission to the atmosphere is anthropogenic. See also Aerosol; Air pollution.
| Wikipedia: Atmospheric chemistry |
Atmospheric chemistry is a branch of atmospheric science in which the chemistry of the Earth's atmosphere and that of other planets is studied. It is a multidisciplinary field of research and draws on environmental chemistry, physics, meteorology, computer modeling, oceanography, geology and volcanology and other disciplines. Research is increasingly connected with other areas of study such as climatology.
The composition and chemistry of the atmosphere is of importance for several reasons, but primarily because of the interactions between the atmosphere and living organisms. The composition of the Earth's atmosphere has been changed by human activity and some of these changes are harmful to human health, crops and ecosystems. Examples of problems which have been addressed by atmospheric chemistry include acid rain, photochemical smog and global warming. Atmospheric chemistry seeks to understand the causes of these problems, and by obtaining a theoretical understanding of them, allow possible solutions to be tested and the effects of changes in government policy evaluated.
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| Meteorology (category) |
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| Average composition of dry atmosphere, by volume | ||
|---|---|---|
| Gas | per NASA |
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| Nitrogen, N2 | 78.084% | |
| Oxygen, O2 | 20.946% | |
| Argon, Ar | 0.934% | |
| Minor constituents (in ppmv) | ||
| Carbon Dioxide, CO2 | 383 | |
| Neon, Ne | 18.18 | |
| Helium, He | 5.24 | |
| Methane, CH4 | 1.7 | |
| Krypton, Kr | 1.14 | |
| Hydrogen, H2 | 0.55 | |
| Water | ||
| Water vapour | Highly variable; typically makes up about 1% |
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Notes: the concentration of CO2 and CH4 vary by season and location. The mean molecular mass of air is 28.97 g/mol.
The ancient Greeks regarded air as one of the four elements, but the first scientific studies of atmospheric composition began in the 18th century. Chemists such as Joseph Priestley, Antoine Lavoisier and Henry Cavendish made the first measurements of the composition of the atmosphere.
In the late 19th and early 20th centuries interest shifted towards trace constituents with very small concentrations. One particularly important discovery for atmospheric chemistry was the discovery of ozone by Christian Friedrich Schoenbein in 1840.
In the 20th century atmospheric science moved on from studying the composition of air to a consideration of how the concentrations of trace gases in the atmosphere have changed over time and the chemical processes which create and destroy compounds in the air. Two particularly important examples of this were the explanation of how the ozone layer is created and maintained by Sydney Chapman and Gordon Dobson, and the explanation of Photochemical smog by Arie Jan Haagen-Smit. Further studies on ozone issues led to the 1995 Nobel Prize in Chemistry award shared between Paul Crutzen, Mario Molina and Frank Sherwood Rowland.[1]
In the 21st century the focus is now shifting again. Atmospheric chemistry is increasingly studied as one part of the Earth system. Instead of concentrating on atmospheric chemistry in isolation the focus is now on seeing it as one part of a single system with the rest of the atmosphere, biosphere and geosphere. An especially important driver for this is the links between chemistry and climate such as the effects of changing climate on the recovery of the ozone hole and vice versa but also interaction of the composition of the atmosphere with the oceans and terrestrial ecosystems.
Observations, lab measurements and modeling are the three central elements in atmospheric chemistry. Progress in atmospheric chemistry is often driven by the interactions between these components and they form an integrated whole. For example observations may tell us that more of a chemical compound exists than previously thought possible. This will stimulate new modelling and laboratory studies which will increase our scientific understanding to a point where the observations can be explained.
Observations of atmospheric chemistry are essential to our understanding. Routine observations of chemical composition tell us about changes in atmospheric composition over time. One important example of this is the Keeling Curve - a series of measurements from 1958 to today which show a steady rise in of the concentration of carbon dioxide. Observations of atmospheric chemistry are made in observatories such as that on Mauna Loa and on mobile platforms such as aircraft (e.g. the UK's Facility for Airborne Atmospheric Measurements), ships and balloons. Observations of atmospheric composition are increasingly made by satellites with important instruments such as GOME and MOPITT giving a global picture of air pollution and chemistry. Surface observations have the advantage that they provide long term records at high time resolution but are limited in the vertical and horizontal space they provide observations from. Some surface based instruments e.g. LIDAR can provide concentration profiles of chemical compounds and aerosol but are still restricted in the horizontal region they can cover. Many observations are available on line in Atmospheric Chemistry Observational Databases.
Measurements made in the laboratory are essential to our understanding of the sources and sinks of pollutants and naturally occurring compounds. Lab studies tell us which gases react with each other and how fast they react. Measurements of interest include reactions in the gas phase, on surfaces and in water. Also of high importance is photochemistry which quantifies how quickly molecules are split apart by sunlight and what the products are plus thermodynamic data such as Henry's law coefficients.
In order to synthesise and test theoretical understanding of atmospheric chemistry, computer models (such as chemical transport models) are used. Numerical models solve the differential equations governing the concentrations of chemicals in the atmosphere. They can be very simple or very complicated. One common trade off in numerical models is between the number of chemical compounds and chemical reactions modelled versus the representation of transport and mixing in the atmosphere. For example, a box model might include hundreds or even thousands of chemical reactions but will only have a very crude representation of mixing in the atmosphere. In contrast, 3D models represent many of the physical processes of the atmosphere but due to constraints on computer resources will have far fewer chemical reactions and compounds. Models can be used to interpret observations, test understanding of chemical reactions and predict future concentrations of chemical compounds in the atmosphere. One important current trend is for atmospheric chemistry modules to become one part of earth system models in which the links between climate, atmospheric composition and the biosphere can be studied.
Some models are constructed by automatic code generators (e.g. Autochem or KPP). In this approach a set of constituents are chosen and the automatic code generator will then select the reactions involving those constituents from a set of reaction databases. Once the reactions have been chosen the ordinary differential equations (ODE) that describe their time evolution can be automatically constructed.
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| Paul Jozef Crutzen (Dutch chemist) | |
| Mario Molina (Mexican-American chemist) | |
| Frank Sherwood Rowland (American chemist) |
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