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Water atmospheric

Water vapor absorbs infrared radiation even more strongly than does carbon dioxide, thus greatly influencing Earth s heat balance. Clouds formed from water vapor reflect light from the sun and have a temperature-lowering effect. On the other hand, water vapor in the atmosphere acts as a kind of blanket at night, retaining heat from Earth s surface by the absorption of infrared radiation. [Pg.175]

As discussed in Section 6.5, water vapor and the heat released and absorbed by transitions of water between the vapor state and the liquid or solid state are strongly involved in atmospheric energy transfer. Condensed water vapor in the form of very small droplets is of considerable concern in atmospheric chemistry. The harmful effects of some air pollutants—for instance, the corrosion of metals by acid-forming gases—requires the presence of water, which may come from the atmosphere. Atmospheric water vapor has an important influence on pollution-induced fog formation under some circumstances. Water vapor interacting with pollutant particulate matter in the atmosphere may reduce visibility to undesirable levels through the formation of very small atmospheric aerosol particles. [Pg.175]

In the very cold tropopause layer at the boundary between the troposphere and the stratosphere, water vapor in the atmosphere is condensed and forms ice crystals, a phenomenon that serves as a barrier to the movement of water into the stratosphere. Thns, little water is transferred from the troposphere to the stratosphere, and the main source of water in the stratosphere is the photochemical oxidation of methane  [Pg.175]

Only a very small percentage of all the water in the climate system is actually present in the atmosphere (Table 2.12). Of the atmospheric water, most is in the vapor phase (Fig. 2.37) the liquid water content (LWC) of clouds is only in the order 1 g the cloud ice water content (IWC) still less, down to 0.0001 g m . But clouds play a huge role in the climate system, whereas precipitation closes the cycle for water and also for substances dissolved in it (wet deposition). Some of the processes (droplet formation, transfer processes, deposition, and chemistry) will be described later. The aim of this chapter is to describe the phenomenology of water in the atmosphere so far as we need it for an understanding of chemical processes. [Pg.157]

John Tyndall wrote the following very clear phrase (Strachan 1866, p. 123)  [Pg.157]

Aqueous water is always diffused through the atmosphere. The cleanest day is not exempt from it indeed, in the Alps, the purest skies are often the most treacherous, the blue deepening with the amount of aqueous vapour in the air. Aqueous vapour is not visible it is not fog it is not cloud, it is not mist of any kind. These are formed of vapour which has been condensed to water but the true vapour is an impalpable transparent gas. It is diffused everywhere throughout the atmosphere, though in very different proportion. [Pg.157]

The content of water vapor in air varies from nearly zero up to about 4 Vol-%, depending on temperature and saturation (Fig. 2.37). Normally the ehemi-cal composition of air is based on dry air (cf Table 1.1). Under normal conditions (20 °C and 60 % RH), air contains around 1 % water vapor (absolute humidity). [Pg.157]

The density of water vapor is less than that of other gaseous air constituents (N2 + O2) hence wet air at the same temperature and pressure has a lower density than dry air. Consequently, at same pressure dry air has a somewhat higher temperature (called virtual temperature) than wet air to obtain the same density. This follows from the ideal gas equation [Pg.157]


Deliquescence and efflorescence. A substance is said to deliquesce (Latin to become liquid) when it forms a solution or liquid phase upon standing in the air. The essential condition is that the vapour pressure of the saturated solution of the highest hydrate at the ordinary temperature should be less than the partial pressure of the aqueous vapour in the atmosphere. Water will be absorbed by the substance, which gradually liquefies to a saturated solution water vapour will continue to be absorbed by the latter until an unsaturated solution, having the same vapour pressure as the partial pressure of water vapour in the air, is formed. In order that the vapour pressure of the saturated solution may be sufficiently low, the substance must be extremely soluble in water, and it is only such substances (e.g., calcium chloride, zinc chloride and potassium hydroxide) that deliquesce. [Pg.43]

Electrica.1 Properties. The bulk electrical properties of the parylenes make them excellent candidates for use in electronic constmction. The dielectric constants and dielectric losses are low and unaffected by absorption of atmospheric water. The dielectric strength is quoted for specimens of 25 p.m thickness because substantially thicker specimens cannot be prepared by VDP. If the value appears to be high in comparison with other materials, however, it should be noted that the usual thickness for such a measurement is 3.18 mm. Dielectric strength declines with the square root of increasing... [Pg.434]

Atmosphere—Water Interaction. Although water is a very minor component of the atmosphere, less than 10 vol % of the atmosphere consisting of water, many important reactions occur ki the water droplets of cloud, fog, and rain. The atmosphere is an oxic environment ki its water phase, gigantic quantities of reductants, such as organic substances, Fe(II), SO2, CH SCH (dimethyl sulfide), and nitrogen oxides, are oxidized by oxidants such as oxygen, OH radicals, H2O2, and Fe(III). [Pg.212]

Fig. 9. Genesis of acid tain (13). From the oxidation of C, S, and N during the combustion of fossil fuels, there is a buildup in the atmosphere (gas phase, aerosol particles, raindrops, snowflakes, and fog) of CO2 and the oxides of S and N, which leads to acid—base interaction. The importance of absorption of gases into the various phases of gas, aerosol, and atmospheric water depends on a number of factors. The genesis of acid rain is shown on the upper right as an acid—base titration. The data given are representative of the environment in the vicinity of Zurich, Switzedand. Fig. 9. Genesis of acid tain (13). From the oxidation of C, S, and N during the combustion of fossil fuels, there is a buildup in the atmosphere (gas phase, aerosol particles, raindrops, snowflakes, and fog) of CO2 and the oxides of S and N, which leads to acid—base interaction. The importance of absorption of gases into the various phases of gas, aerosol, and atmospheric water depends on a number of factors. The genesis of acid rain is shown on the upper right as an acid—base titration. The data given are representative of the environment in the vicinity of Zurich, Switzedand.
The tetrahydrate is stable under normal conditions of storage. Its heat of dehydration has been calculated as 110.8 kJ/mol (26.5 kcal/mol) between 106.5 and 134°C (121). Its thermal stabiUty is highly dependent on the partial pressure of atmospheric water. It is stable when heated ia a vaccum up to 105°C ia an atmosphere saturated with water at 90°C, it is stable up to 170°C. [Pg.206]

Total world production of glycidyl neodecanoate is ca 7—10 thousand metric tons per year, with production by Exxon in the United States and by Shell in The Netherlands. The product is shipped in bulk or in dmms and must be protected from contact with atmospheric water during storage. [Pg.106]

Carbon dioxide is a major greenhouse gas within the atmosphere. Water vapour is a greater contributor to the natural greenhouse effect (55-70% of the total radiative absorption compared to COj s 25%). However, the large inherent variability in atmospheric water vapour compared to the anthropogenically... [Pg.17]

ASME, Performance Test Code on Atmospheric Water Cooling Equipment PTC 23, 1997. [Pg.176]

In the case of an open water system, the problem is compounded due to the addition of micr(X)rganisms from the atmosphere. Water temperature control is critical to stop the water from becoming a breeding soup culture for the microorganisms. [Pg.160]

The medium into which tlie release occurred (atmosphere, water, or land) Any known or anticipated acute or clironic healtli risks associated witli the emergency and, where appropriate, advise regarding medical attention necessaiy for exposed individuals... [Pg.47]

Although the high-silicon irons are often used in circumstances which expose them to atmospheric, water or soil corrosion, they are rarely installed specifically to resist these agencies. Their corrosion resistance is such, however, that in fact no normally occurring environment ever causes serious attack. This is not to say that these irons can be regarded as stainless, and in fact alloys containing less than 14-7% silicon have been reported as becoming rusty in a moist atmosphere ... [Pg.626]

Now consider what happens when we heat a liquid in a container that is open to the atmosphere—water heated in a kettle is an example. When the temperature is raised to the point at which the vapor pressure is equal to the atmospheric pressure (for instance, when water is heated to 100°C and the external pressure is 1 atm), vaporization occurs throughout the liquid, not just from its surface. At this... [Pg.434]

Kucera,V. The Effects of Acidification of the Environment on the Corrosion of the Atmosphere, Water, and Soil, Proc. 9th Scandinavian Corrosion Congress, Copenhagen, Denmark, 1983. [Pg.63]

The enormous volume of the oceans results in an average turnover time of more than 2600 years, compared to less than 10 days for atmospheric water. Although the reservoir is much smaller than the oceans, the cryosphere has the longest turnover time due to the small input flux. Average turnover times for all seven reservoirs, calculated from the data in Fig. 6-3, are shown in Table 6-3. [Pg.115]

The original method of phosphate preparation involved extracting the phosphate and reprecipitating it as a bismuth phosphate (Tudge 1960). Alternatively, it is precipitated as a silver phosphate (Wright and Hoering 1989) which involves fewer steps and, more importantly, silver phosphate is not hygroscopic (as is bismuth phosphate) which minimizes the potential for contamination by atmospheric water. [Pg.126]

About 10% of the ethylene produced in the U.S. is used to make vinyl chloride, which in the chemical trade is usually referred to as vinyl chloride monomer or VCM. The largest use of VCM is for polymerization to poly(vinyl chloride) (PVC), a thermoplastic, which in terms of volume is second only to polyethylene. PVC is used in such diverse areas as containers, floor coverings (linoleum), plastic pipes, raincoats, and many, many others. PVC has an evironmental disadvantage over non-chlorine containing plastics in that when it is disposed of by incineration it produces hydrogen chloride, which dissolves in atmospheric water to give hydrochloric acid. Polyethylene does not have this undesirable feature. [Pg.124]

The analytical wavelength has usually been chosen as that of the strongest band in the spectrum which is free from interference due to atmospheric water and CO... If more than one infra-red absorbing material is present in the air in significant concentration, the use of another analytical wavelength may be necessary. [Pg.235]

Atmospheric O2 has a partial pressure of 0.20 bar, and atmospheric water vapor is saturated with carbon dioxide. This dissolved CO2 forms carbonic acid, which generates a hydronium ion concentration of about 2.0 X 10 M. The Nemst equation allows calculation of the half-cell potential for the reduction of 02(g) under these... [Pg.1404]

A reaction between sodium from the glass and atmospheric water and carbon dioxide can lead to the formation of sodium carbonate, which crystallizes in fine needles. A potash glass forms potassium carbonate, which is too deliquescent to crystallize out. A lead glass can react with hydrogen sulphide, and to a smaller extent with carbon dioxide, sulphur dioxide, and acid vapoiurs. [Pg.13]


See other pages where Water atmospheric is mentioned: [Pg.77]    [Pg.244]    [Pg.435]    [Pg.372]    [Pg.378]    [Pg.62]    [Pg.227]    [Pg.211]    [Pg.220]    [Pg.1414]    [Pg.15]    [Pg.34]    [Pg.34]    [Pg.341]    [Pg.211]    [Pg.94]    [Pg.171]    [Pg.502]    [Pg.28]    [Pg.519]    [Pg.519]    [Pg.13]    [Pg.67]    [Pg.112]    [Pg.144]    [Pg.232]    [Pg.489]    [Pg.493]    [Pg.378]    [Pg.341]   
See also in sourсe #XX -- [ Pg.20 , Pg.448 , Pg.508 ]

See also in sourсe #XX -- [ Pg.6 , Pg.10 , Pg.14 , Pg.16 , Pg.151 , Pg.155 , Pg.165 , Pg.166 , Pg.395 ]




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Atmosphere water droplets

Atmosphere water transport

Atmosphere water vapor, carbon dioxide

Atmosphere water-vapour

Atmosphere-water exchange

Atmospheric Noble Gases and Their Dissolution in Water

Atmospheric Sulfuric Acid-Water-Ammonia Particle Formation Using Quantum Chemistry

Atmospheric Water Molecules and the Morning Dew

Atmospheric Water Vapor

Atmospheric Water and Cloud Microphysics

Atmospheric corrosion water

Atmospheric deposition directly to coastal waters

Atmospheric water iron cycling

Atmospheric water transport, effects

Carbon dioxide water-atmosphere equilibrium

Chemical Potential of Water in Atmospheric Particles

Closed rock-water atmosphere

Coastal waters, atmospheric deposition

Environmental Analysis of Atmospheric and Water Pollution

Equilibrium of a Flat Pure Water Surface with the Atmosphere

Liquid Water in the Atmosphere

Other Forms of Water in the Atmosphere

Precipitation (atmospheric) water

Properties of the Atmosphere and Water

Radioactive materials, atmosphere water

Temperature affects atmospheric water vapor

Water Equilibrium in the Atmosphere

Water In atmosphere

Water atmosphere

Water atmosphere

Water atmosphere interface

Water atmospheric residence time

Water concentration profile atmosphere

Water droplets, atmospheric chemistry

Water early atmosphere

Water in atmospheric corrosion

Water vapor atmosphere

Water vapor atmospheric content

Water, acid atmospheric

Water-soluble organic carbon atmospheric aerosols

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