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<sub></sub>{{Image|World Gas Production.png|right|306px|Worldwide natural gas production data for 2007.}}
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'''Natural gas''' is a [[gas]] consisting primarily of [[methane]] (CH<sub>4</sub>). It is found as raw natural gas in underground reservoirs, as gas associated with underground reservoirs of [[petroleum crude oil]], as [[methane hydrates]] and as [[coalbed methane]] in underground [[Coal mining|coal mines]]. It is an important fuel source and a major feedstock for producing [[ammonia]], [[hydrogen]], [[petrochemicals]]and [[fertilizer]]s.
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[[File:Crude oil-fired power plant.jpg|thumb|right|225px|Industrial air pollution source]]
Atmospheric dispersion modeling is the mathematical simulation of how air pollutants disperse in the ambient atmosphere. It is performed with computer programs that solve the mathematical equations and algorithms which simulate the pollutant dispersion. The dispersion models are used to estimate or to predict the downwind concentration of air pollutants emitted from sources such as industrial plants, vehicular traffic or accidental chemical releases.  


Natural gas is often informally referred to as simply '''''gas''''' or '''''fuel gas''''', especially when compared to other energy sources such as electricity.  
Such models are important to governmental agencies tasked with protecting and managing the ambient air quality. The models are typically employed to determine whether existing or proposed new industrial facilities are or will be in compliance with the National Ambient Air Quality Standards (NAAQS) in the United States or similar regulations in other nations. The models also serve to assist in the design of effective control strategies to reduce emissions of harmful air pollutants. During the late 1960's, the Air Pollution Control Office of the U.S. Environmental Protection Agency (U.S. EPA) initiated research projects to develop models for use by urban and transportation planners.<ref>J.C. Fensterstock et al, "Reduction of air pollution potential through environmental planning", ''JAPCA'', Vol. 21, No. 7, 1971.</ref> 


There are a great many different natural gas reservoirs worldwide and each of those gas deposits has a different composition. However, in general, most of them contain at least 90 volume percent of methane. Before raw natural gas from extracted from those reservoirs can be used as a fuel, it must undergo extensive [[natural gas processing|processing]] to remove almost all materials other than methane. The by-products of that processing include [[ethane]], [[propane]], [[butane]]s, [[natural gasoline]] (referred to as [[pentane]]s +) and higher molecular weight [[hydrocarbon]]s, elemental [[sulfur]], and sometimes [[helium]] and [[nitrogen]].
Air dispersion models are also used by emergency management personnel to develop emergency plans for accidental chemical releases. The results of dispersion modeling, using worst case accidental releases and meteorological conditions, can provide estimated locations of impacted areas and be used to determine appropriate protective actions. At industrial facilities in the United States, this type of consequence assessment or emergency planning is required under the Clean Air Act (CAA) codified in Part 68 of Title 40 of the Code of Federal Regulations.


==Formation of natural gas==
The dispersion models vary depending on the mathematics used to develop the model, but all require the input of data that may include:


While the origins of natural gas deposits are not known with certainty, and the different reservoirs vary in their geologic history, it is generally believed<ref name=PGE>http://www.pge.com/microsite/pge_dgz/more/gas.html Natural Gas Formation, Exploration, and Distribution] From the website of the Pacific Gas and Electricity Company.</ref><ref name=ClimateLab>[http://climatelab.org/Natural_Gas Natural Gas] From the website of the Climate Lab</ref> that the gas is formed over millions of years from organic matter, usually from former marine or coastal ecosystems. Decomposed organic matter from dead plants and animals became covered in layers of mud and other sediments, and as more mud and other sediments piled on top of the organic matter, the pressure and temperature increased. The increased pressure and temperature is thought to have caused the organic matter to slowly transform into natural gas and oil. Once formed, gas deposits tended to rise towards the surface of the earth through fissures and pores, until they become trapped underneath less permeable rock layers and formed gas reservoirs.
* Meteorological conditions such as wind speed and direction, the amount of atmospheric turbulence (as characterized by what is called the "stability class"), the ambient air temperature, the height to the bottom of any inversion aloft that may be present, cloud cover and solar radiation.
* The emission parameters such the type of source (i.e., point, line or area), the mass flow rate, the source location and height, the source exit velocity, and the source exit temperature.
* Terrain elevations at the source location and at receptor locations, such as nearby homes, schools, businesses and hospitals.
* The location, height and width of any obstructions (such as buildings or other structures) in the path of the emitted gaseous plume as well as the terrain surface roughness (which may be characterized by the more generic parameters "rural" or "city" terrain).


==Finding and extracting natural gas==
Many of the modern, advanced dispersion modeling programs include a pre-processor module for the input of meteorological and other data, and many also include a post-processor module for graphing the output data and/or plotting the area impacted by the air pollutants on maps. The plots of areas impacted usually include isopleths showing areas of pollutant concentrations that define areas of the highest health risk. The isopleths plots are useful in determining protective actions for the public and first responders.


;Exploration:
The atmospheric dispersion models are also known as atmospheric diffusion models, air dispersion models, air quality models, and air pollution dispersion models.
Exploration, in the oil and  gas industry, is the search for natural gas reservoirs. Recoverable reserves of natural gas tend to occur where impermeable rocks (called ''caprocks'') constrain the upward movement of gas through the undergound soil and rocks. [[Geologist]]s and [[geophysicist]]s usually use [[seismology]] to find areas which have the right conditions for a gas or oil deposit. High-speed computers that help develop three-dimensional underground maps as well as satellite image technology are also widely used to search for natural gas reservoirs.  


;Extraction
==Atmospheric layers==
After an initial exploration, wells are drilled to confirm the existence of a reservoir and its size. Once a resevoir of natural gas has been confirmed, production wells are drilled to extract the gas. Once reached by a well, the gas comes up to the surface under its own pressure.


Over time, the gas flow rate decreases, but may be maintained by drilling reinjection wells and using [[gas compressors]] to reinject compressed gas downward into the reservoir.
Discussion of the layers in the Earth's atmosphere is needed to understand where airborne pollutants disperse in the atmosphere. The layer closest to the Earth's surface is known as the ''troposphere''. It extends from sea-level up to a height of about 18 km and contains about 80 percent of the mass of the overall atmosphere. The ''stratosphere'' is the next layer and extends from 18 km up to about 50 km. The third layer is the ''mesosphere'' which extends from 50 km up to about 80 km. There are other layers above 80 km, but they are insignificant with respect to atmospheric dispersion modeling.


==Composition of raw natural gas==
The lowest part of the troposphere is called the ''atmospheric boundary layer (ABL)'' or the ''planetary boundary layer (PBL)'' and extends from the Earth's surface up to about 1.5 to 2.0 km in height. The air temperature of the atmospheric boundary layer decreases with increasing altitude until it reaches what is called the ''inversion layer'' (where the temperature increases with increasing altitude) that caps the atmospheric boundary layer. The upper part of the troposphere (i.e., above the inversion layer) is called the ''free troposphere'' and it extends up to the 18 km height of the troposphere.


Raw natural gas typically consists primarily of methane (CH<sub>4</sub>), the shortest and lightest [[hydrocarbon]] molecule. It also contains varying amounts of:
The ABL is the most important layer with respect to the emission, transport and dispersion of airborne pollutants. The part of the ABL between the Earth's surface and the bottom of the inversion layer is known as the ''mixing layer''. Almost all of the airborne pollutants emitted into the ambient atmosphere are transported and dispersed within the mixing layer. Some of the emissions penetrate the inversion layer and enter the free troposphere above the ABL.


*Heavier gaseous hydrocarbons: [[ethane]] (C<sub>2</sub>H<sub>6</sub>), [[propane]] (C<sub>3</sub>H<sub>8</sub>), [[Butane|normal butane]] (n-C<sub>4</sub>H<sub>10</sub>), [[isobutane]] (i-C<sub>4</sub>H<sub>10</sub>), [[pentane]]s and even higher [[molecular weight]] hydrocarbons. When processed and purified into finished by-products, all of these are collectively referred to as '''''NGL (Natural Gas Liquids)'''''.
In summary, the layers of the Earth's atmosphere from the surface of the ground upwards are: the ABL made up of the mixing layer capped by the inversion layer; the free troposphere; the stratosphere; the mesosphere and others. Many atmospheric dispersion models are referred to as ''boundary layer models'' because they mainly model air pollutant dispersion within the ABL. To avoid confusion, models referred to as ''mesoscale models'' have dispersion modeling capabilities that can extend horizontally as much as  a few hundred kilometres. It does not mean that they model dispersion in the mesosphere.
*[[Acid gas]]es: [[carbon dioxide]] (CO<sub>2</sub>), [[hydrogen sulfide]] (H<sub>2</sub>S) and [[mercaptan]]s such as [[methanethiol]] (CH<sub>3</sub>SH) and [[ethanethiol]]  (C<sub>2</sub>H<sub>5</sub>SH).
*Other gases: [[nitrogen]] (N<sub>2</sub>) and [[helium]] (He).
*[[Water]]: water vapor and liquid water.
*Liquid hydrocarbons: perhaps some natural gas condensate (also referred to as ''casinghead gasoline'' or ''natural gasoline'') and/or [[crude oil]].
*[[Mercury]]: very small amounts of mercury primarily in elemental form, but chlorides and other species are possibly present.<ref name=UOPHg>[http://www.uop.com/objects/87MercuryRemoval.pdf Mercury Removal from Natural Gas and Liquids] UOP website page</ref>


==Measurement units and heating values==
==Gaussian air pollutant dispersion equation==


Quantities of natural gas are measured in [[normal cubic meter]]s (corresponding to 0 [[Celsius|°C ]]at 101.325  k[[Pascal (unit)|Pa]] absolute) or in [[standard cubic feet]] (corresponding to 60 [[Fahrenheit and Rankine temperatures|°F]] and 14.496 [[U.S. customary units|psi]] absolute).
The technical literature on air pollution dispersion is quite extensive and dates back to the 1930s and earlier. One of the early air pollutant plume dispersion equations was derived by Bosanquet and Pearson.<ref>C.H. Bosanquet and J.L. Pearson, "The spread of smoke and gases from chimneys", ''Trans. Faraday Soc.'', 32:1249, 1936.</ref> Their equation did not assume Gaussian distribution nor did it include the effect of ground reflection of the pollutant plume.


The [[higher heating value]] of commercial, processed natural gas is about 39 M[[joule|J]] per normal cubic meter which is equivalent to about 1000 [[U.S. customary units|Btu]] per standard cubic foot, but those values can vary by several percent from one natural gas to another.
Sir Graham Sutton derived an air pollutant plume dispersion equation in 1947<ref>O.G. Sutton, "The problem of diffusion in the lower atmosphere", ''QJRMS'', 73:257, 1947.</ref><ref>O.G. Sutton, "The theoretical distribution of airborne pollution from factory chimneys", ''QJRMS'', 73:426, 1947.</ref> which did include the assumption of Gaussian distribution for the vertical and crosswind dispersion of the plume and also included the effect of ground reflection of the plume.


The actual heating value when the water formed does not condense is the [[lower heating value|net heat of combustion]] and can be as much as 10% less.
Under the stimulus provided by the advent of stringent environmental control regulations, there was an immense growth in the use of air pollutant plume dispersion calculations between the late 1960s and today. A great many computer programs for calculating the dispersion of air pollutant emissions were developed during that period of time and they were commonly called "air dispersion models". The basis for most of those models was the '''Complete Equation For Gaussian Dispersion Modeling Of Continuous, Buoyant Air Pollution Plumes''' shown below:<ref name=Beychok>{{cite book|author=M.R. Beychok|title=Fundamentals Of Stack Gas Dispersion|edition=4th Edition| publisher=author-published|year=2005|isbn=0-9644588-0-2}}.</ref><ref>{{cite book|author=D. B. Turner| title=Workbook of atmospheric dispersion estimates: an introduction to dispersion modeling| edition=2nd Edition |publisher=CRC Press|year=1994|isbn=1-56670-023-X}}.</ref>


In the United States, retail sales are often in units of [[therm]]s (th); 1 therm = 100,000&nbsp;BTU. [[Gas meter]]s measure the volume of gas used, and this is converted to therms by multiplying the volume by the energy content of the gas used during that period, which varies slightly over time. Wholesale transactions are generally done in [[decatherm]]s (Dth), or in thousand decatherms (MDth), or in million decatherms (MMDth). A million decatherms is roughly a billion cubic feet of natural gas.


==Sources==
<math>C = \frac{\;Q}{u}\cdot\frac{\;f}{\sigma_y\sqrt{2\pi}}\;\cdot\frac{\;g_1 + g_2 + g_3}{\sigma_z\sqrt{2\pi}}</math>


In the past, natural gas was almost always a byproduct of [[Oil well|producing oil]], since the small, light gas carbon chains come out of solution as it undergoes pressure reduction from the [[Petroleum reservoir|reservoir]] to the surface, similar to uncapping a bottle of soda pop where the carbon dioxide [[effervesce]]s. Unwanted natural gas can be a disposal problem at the well site. If there is not a market for natural gas near the [[wellhead]] it is virtually valueless since it must be piped to the end user. Until recently, such unwanted gas was burned off at the wellsite, but due to environmental concerns this practice is becoming less common. Often, unwanted (or 'stranded' gas without a market) gas is pumped back into the reservoir with an 'injection' well for disposal or repressurizing the producing formation. Another solution is to export the natural gas as a [[LNG|liquid]]. [http://en.wikipedia.org/wiki/Gas_to_liquid]Gas-to-liquid, (GTL) is a developing technology that converts stranded natural gas into synthetic gasoline, diesel or jet fuel through the [[Fischer-Tropsch]] process developed in World War II Germany. Such fuels can be transported through conventional pipelines and tankers to users. Proponents claim GTL fuels burn cleaner than comparable petroleum fuels. Most major international oil companies are in advanced development stages of GTL production, with a world-scale (140,000 bbl/day) GTL plant in Qatar scheduled to come online before 2010. In locations such as the United States with a high natural gas demand, pipelines are constructed to take the gas from the wellsite to the [[end consumer]].
{| border="0" cellpadding="2"
|-
|align=right|where:
|&nbsp;
|-
!align=right|<math>f</math> 
|align=left|= crosswind dispersion parameter
|-
!align=right|&nbsp;
|align=left|= <math>\exp\;[-\,y^2/\,(2\;\sigma_y^2\;)\;]</math>
|-
!align=right|<math>g</math>
|align=left|= vertical dispersion parameter = <math>\,g_1 + g_2 + g_3</math>
|-
!align=right|<math>g_1</math>
|align=left|= vertical dispersion with no reflections
|-
!align=right|&nbsp;
|align=left|= <math>\; \exp\;[-\,(z - H)^2/\,(2\;\sigma_z^2\;)\;]</math>
|-
!align=right|<math>g_2</math>
|align=left|= vertical dispersion for reflection from the ground
|-
!align=right|&nbsp;
|align=left|= <math>\;\exp\;[-\,(z + H)^2/\,(2\;\sigma_z^2\;)\;]</math>
|-
!align=right|<math>g_3</math>
|align=left|= vertical dispersion for reflection from an inversion aloft
|-
!align=right|&nbsp;
|align=left|= <math>\sum_{m=1}^\infty\;\big\{\exp\;[-\,(z - H - 2mL)^2/\,(2\;\sigma_z^2\;)\;]</math>
|-
!align=right|&nbsp;
|align=left|&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; <math>+\, \exp\;[-\,(z + H + 2mL)^2/\,(2\;\sigma_z^2\;)\;]</math>
|-
!align=right|&nbsp;
|align=left|&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; <math>+\, \exp\;[-\,(z + H - 2mL)^2/\,(2\;\sigma_z^2\;)\;]</math>
|-
!align=right|&nbsp;
|align=left|&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; <math>+\, \exp\;[-\,(z - H + 2mL)^2/\,(2\;\sigma_z^2\;)\;]\big\}</math>
|-
!align=right|<math>C</math>
|align=left|= concentration of emissions, in g/m³, at any receptor located:
|-
!align=right|&nbsp;
|align=left|&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; x meters downwind from the emission source point
|-
!align=right|&nbsp;
|align=left|&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; y meters crosswind from the emission plume centerline
|-
!align=right|&nbsp;
|align=left|&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; z meters above ground level
|-
!align=right|<math>Q</math>
|align=left|= source pollutant emission rate, in g/s
|-
!align=right|<math>u</math>
|align=left|= horizontal wind velocity along the plume centerline, m/s
|-
!align=right|<math>H</math>
|align=left|= height of emission plume centerline above ground level, in m
|-
!align=right|<math>\sigma_z</math>
|align=left|= vertical standard deviation of the emission distribution, in m
|-
!align=right|<math>\sigma_y</math>
|align=left|= horizontal standard deviation of the emission distribution, in m
|-
!align=right|<math>L</math>
|align=left|= height from ground level to bottom of the inversion aloft, in m
|-
!align=right|<math>\exp</math>
|align=left|= the exponential function
|}


Fossil natural gas can be "associated" (found in [[oil field]]s) or "non-associated" (isolated in [[natural gas field]]s), and is also found in [[coal bed]]s (as [[coalbed methane]]).  It sometimes contains significant quantities of [[ethane]], [[propane]], [[butane]], and [[pentane]]—heavier hydrocarbons removed prior to use as a consumer fuel—as well as [[carbon dioxide]], [[nitrogen]], [[helium]] and [[hydrogen sulfide]].<ref>[http://www.naturalgas.org/overview/background.asp Natural gas overview]</ref>
The above equation not only includes upward reflection from the ground, it also includes downward reflection from the bottom of any inversion lid present in the atmosphere.
Natural gas is commercially produced from [[oil field]]s and [[natural gas field]]s.  Gas produced from oil wells is called casinghead gas or associated gas. The natural gas industry is producing gas from increasingly more challenging [[History of the petroleum industry in Canada (natural gas)#Unconventional gas|resource types]]: [[sour gas]], [[tight gas]], [[shale gas]] and [[coalbed methane]].


The world's largest proven gas reserves are located in [[Russia]], with 4.757{{e|13}} m³ (1.6{{e|15}} cu ft). Russia is also the world's largest natural gas producer, through the [[Gazprom]] company. Major proven resources (with year of estimate) (in billion cubic metres) are world 175,400 (2006), Russia 47,570 (2006), Iran 26,370 (2006), Qatar 25,790 (2007), Saudi Arabia 6,568 (2006) and United Arab Emirates 5,823 (2006).
The sum of the four exponential terms in <math>g_3</math> converges to a final value quite rapidly. For most cases, the summation of the series with '''''m''''' = 1, '''''m''''' = 2 and '''''m''''' = 3 will provide an adequate solution.


The world's largest gas field is [[Qatar]]'s offshore [[South Pars / North Dome Gas-Condensate field|North Field]], estimated to have 25 trillion cubic metres<ref>[http://www.state.gov/r/pa/ei/bgn/5437.htm Background note: Qatar]</ref> (9.0{{e|14}}<!--1500 needs reference-->&nbsp;cu&nbsp;ft) of gas in place—enough to last more than 200 years at optimum production levels. The second largest natural gas field is the [[Asalouyeh|South Pars Gas Field]] in [[Iran]]ian waters in the [[Persian Gulf]]. Connected to Qatar's North Field, it has estimated reserves of 8 to 14 trillion cubic metres<ref>{{cite web|url=http://www.pseez.ir/gas-en.html|publisher=Pars Special Economic Energy Zone|accessdate=2007-07-17|title=   
<math>\sigma_z</math> and <math>\sigma_y</math> are functions of the atmospheric stability class (i.e., a measure of the turbulence in the ambient atmosphere) and of the downwind distance to the receptor. The two most important variables affecting the degree of pollutant emission dispersion obtained are the height of the emission source point and the degree of atmospheric turbulence. The more turbulence, the better the degree of dispersion.
Pars Special Economic Energy Zone}}</ref> {{nowrap|(2.8{{e|14}} to 5.0{{e|14}} cu ft)}} of gas.


Because natural gas is not a pure product, when non-associated gas is extracted from a field under [[supercritical]] (pressure/temperature) conditions, it may partially condense upon isothermic depressurizing—an effect called [[retrograde condensation]]. The liquids thus formed may get trapped by depositing in the pores of the gas reservoir. One method to deal with this problem is to reinject dried gas free of condensate to maintain the underground pressure and to allow reevaporation and extraction of condensates.
Whereas older models rely on stability classes for the determination of <math>\sigma_y</math> and <math>\sigma_z</math>, more recent models increasingly rely on Monin-Obukhov similarity theory to derive these parameters.


[[Landfill gas]] is created from the decomposition of waste in [[landfill]]s. If the gas is not removed, the pressure may get so high that it works its way to the surface, causing damage to the landfill structure, unpleasant odor, vegetation die-off and an [[explosion]] hazard. The gas can be vented to the atmosphere, [[gas flare|flared]] or burned to produce [[electricity]] or [[heat]]. Experimental systems were being proposed for use in parts [[Hertfordshire]], UK and [[Lyon]] in France.
==Briggs plume rise equations==


Once [[water vapor]] is removed, about half of landfill gas is methane. Almost all of the rest is [[carbon dioxide]], but there are also small amounts of [[nitrogen]], [[oxygen]] and [[hydrogen]]. There are usually trace amounts of [[hydrogen sulfide]] and [[siloxane]]s, but their concentration varies widely. Landfill gas cannot be distributed through natural gas pipelines unless it is cleaned up to the same quality. It is usually more economical to combust the gas on site or within a short distance of the landfill using a dedicated pipeline. Water vapor is often removed, even if the gas is combusted on site.  If low temperatures  condense water out of the gas, [[siloxanes]] can be lowered as well because they tend to condense out with the water vapor. Other non-methane components may also be removed in order to meet [[emission standard]]s, to prevent fouling of the equipment or for environmental considerations. Co-firing landfill gas with natural gas improves combustion, which lowers emissions.
The Gaussian air pollutant dispersion equation (discussed above) requires the input of ''H'' which is the pollutant plume's centerline height above ground level. ''H'' is the sum of ''H''<sub>s</sub> (the actual physical height of the pollutant plume's emission source point) plus Δ''H'' (the plume rise due the plume's buoyancy).


Huge quantities of natural gas (primarily methane) exist in the form of [[methane clathrate|hydrates]] under sediment on offshore continental shelves and on land in arctic regions that experience [[permafrost]] such as those in [[Siberia]] (hydrates require a combination of high pressure and low temperature to form). However, {{as of|2009|lc=on}} no technology has been developed to produce natural gas economically from hydrates.
[[File:Gaussian Plume.png|thumb|right|333px|Visualization of a buoyant Gaussian air pollutant dispersion plume]]


==Natural gas processing==
To determine Δ''H'', many if not most of the air dispersion models developed between the late 1960s and the early 2000s used what are known as "the Briggs equations." G.A. Briggs first published his plume rise observations and comparisons in 1965.<ref>G.A. Briggs, "A plume rise model compared with observations", ''JAPCA'', 15:433–438, 1965.</ref> In 1968, at a symposium sponsored by CONCAWE (a Dutch organization), he compared many of the plume rise models then available in the literature.<ref>G.A. Briggs, "CONCAWE meeting: discussion of the comparative consequences of different plume rise formulas", ''Atmos. Envir.'', 2:228–232, 1968.</ref> In that same year, Briggs also wrote the section of the publication edited by Slade<ref>D.H. Slade (editor), "Meteorology and atomic energy 1968", Air Resources Laboratory, U.S. Dept. of Commerce, 1968.</ref> dealing with the comparative analyses of plume rise models.  That was followed in 1969 by his classical critical review of the entire plume rise literature,<ref>G.A. Briggs, "Plume Rise", ''USAEC Critical Review Series'', 1969.</ref> in which he proposed a set of plume rise equations which have become widely known as "the Briggs equations".  Subsequently, Briggs modified his 1969 plume rise equations in 1971 and in 1972.<ref>G.A. Briggs, "Some recent analyses of plume rise observation", ''Proc. Second Internat'l. Clean Air Congress'', Academic Press, New York, 1971.</ref><ref>G.A. Briggs, "Discussion: chimney plumes in neutral and stable surroundings", ''Atmos. Envir.'', 6:507–510, 1972.</ref>


{{Image|NaturalGasProcessingPlant.jpg|right|250px|A natural gas processing plant.}}
Briggs divided air pollution plumes into these four general categories:
{{main|Natural gas processing}}
* Cold jet plumes in calm ambient air conditions
There are a great many ways in which to configure the various unit processes used in the processing of raw natural gas. The schematic [[Process flow diagram|block flow diagram]] below is a generalized, typical configuration for the processing of raw natural gas from non-associated gas wells. It shows how raw natural gas is processed into sales gas pipelined to the end user markets.<ref>[http://www.eia.doe.gov/pub/oil_gas/natural_gas/feature_articles/2006/ngprocess/ngprocess.pdf Natural Gas Processing: The Crucial Link Between Natural Gas Production and Its Transportation to Market]</ref><ref>[http://www.uop.com/gasprocessing/6070.html Example Gas Plant]</ref><ref name=NatGasOrg>[http://www.naturalgas.org/naturalgas/processing_ng.asp NaturalGas.org - Processing Natural Gas]</ref>
* Cold jet plumes in windy ambient air conditions
* Hot, buoyant plumes in calm ambient air conditions
* Hot, buoyant plumes in windy ambient air conditions


The block flow diagram also shows how processing of the raw natural gas yields these byproducts:
Briggs considered the trajectory of cold jet plumes to be dominated by their initial velocity momentum, and the trajectory of hot, buoyant plumes to be dominated by their buoyant momentum to the extent that their initial velocity momentum was relatively unimportant.  Although Briggs proposed plume rise equations for each of the above plume categories, '''''it is important to emphasize that "the Briggs equations" which become widely used are those that he proposed for bent-over, hot buoyant plumes'''''.


*Natural gas condensate
In general, Briggs's equations for bent-over, hot buoyant plumes are based on observations and data involving plumes from typical combustion sources such as the flue gas stacks from steam-generating boilers burning fossil fuels in large power plants.  Therefore the stack exit velocities were probably in the range of 20 to 100 ft/s (6 to 30 m/s) with exit temperatures ranging from 250 to 500 °F (120 to 260 °C).
*Sulfur
*Ethane
*Natural gas liquids (NGL): propane, butanes and C<sub>5</sub>+ (which is the commonly used term for pentanes plus higher molecular weight hydrocarbons)  


A logic diagram for using the Briggs equations<ref name=Beychok/> to obtain the plume rise trajectory of bent-over buoyant plumes is presented below:
[[Image:BriggsLogic.png|none]]
:{| border="0" cellpadding="2"
|-
|align=right|where:
|&nbsp;
|-
!align=right| Δh
|align=left|= plume rise, in m
|-
!align=right| F<sup>&nbsp;</sup> <!-- The HTML is needed to line up characters. Do not remove.-->
|align=left|= buoyancy factor, in m<sup>4</sup>s<sup>−3</sup>
|-
!align=right| x
|align=left|= downwind distance from plume source, in m
|-
!align=right| x<sub>f</sub>
|align=left|= downwind distance from plume source to point of maximum plume rise, in m
|-
!align=right| u
|align=left|= windspeed at actual stack height, in m/s
|-
!align=right| s<sup>&nbsp;</sup> <!-- The HTML is needed to line up characters. Do not remove.-->
|align=left|= stability parameter, in s<sup>−2</sup>
|}
The above parameters used in the Briggs' equations are discussed in Beychok's book.<ref name=Beychok/>


{{Image|NatGasProcessing.png|center|584px|Schematic flow diagram of a typical natural gas processing plant.}}
==References==
 
{{reflist}}
==Uses of natural gas==
{{Main|Ammonia production|Petrochemicals|Haber process|Hydrogen production}}
;Power generation
Natural gas is a major source of [[electricity generation]] through the use of [[gas turbine]]s and [[steam]] [[turbines]]. Most grid [[peaking power plant]]s and some off-grid [[engine-generator]]s use natural gas. Particularly high efficiencies can be achieved through combining gas turbines with a steam turbine in [[combined cycle]] mode. Natural gas burns more cleanly than other [[fossil fuel]]s, such as oil and coal, and produces less carbon dioxide per unit energy released.  For an equivalent amount of heat, burning natural gas produces about 30% less [[carbon dioxide]] than burning [[petroleum]] and about 45% less than burning [[coal]].<ref name=gasdotorg>[http://www.naturalgas.org/environment/naturalgas.asp#greenhouse/ Natural Gas and the Environment]</ref> Combined cycle power generation using natural gas is thus the cleanest source of power available using fossil fuels, and this technology is widely used wherever gas can be obtained at a reasonable cost. [[Fuel cell]] technology may eventually provide cleaner options for converting natural gas into electricity, but as yet it is not price-competitive. (Please note: some [[algal fuel]] producers are considering feeding the carbon dioxide resulting from natural gas burning to [[algae]] to promote growth.)
 
;Domestic use
Natural gas is supplied to homes, where it is used for such purposes as [[cooking]] in natural gas-powered ranges and/or ovens, natural gas-heated [[clothes dryer]]s, [[HVAC|heating]]/[[air conditioning|cooling]] and [[central heating]].  Home or other building heating may include boilers, [[furnace]]s, and [[water heater]]s.  [[compressed natural gas|CNG]] is used in [[rural]] homes without connections to [[plumbing|pipe]]d-in [[public utility]] services, or with portable [[Grill (cooking)|grill]]s.  However, due to CNG being less economical than [[Liquefied petroleum gas|LPG]], LPG (Propane) is the dominant source of rural gas.
 
;Transportation fuel
[[Compressed natural gas]] ([[methane]]) is a cleaner alternative to other automobile fuels such as [[gasoline]] (petrol) and [[Diesel fuel|diesel oil]]. As of December 2008, the countries with the highest number of CNG vehicles, ranked numerically, were [[Pakistan]] <ref>{{cite web|url=http://www.iangv.org/tools-resources/statistics.html|title=NATURAL GAS VEHICLE STATISTICS|publisher=International Association for Natural Gas Vehicles]]|date=2008-12-31 |accessdate=2009-06-11}}</ref>, [[Argentina]], [[Brazil]], [[Iran]] and [[India]]. The energy efficiency is generally equal to that of gasoline engines, but lower compared with modern diesel engines. Gasoline/petrol vehicles converted to run on natural gas suffer because of the low [[compression ratio]] of their engines, resulting in a cropping of delivered power while running on natural gas (10%-15%).  CNG-specific engines, however, use a higher compression ratio due to this fuel's higher [[octane number]] of 120–130.<ref>[http://www.imrt.ethz.ch/research/engine/CNG/cev Clean Engine Vehicle], Measurement and Control Laboratory</ref>
 
;Fertilizer
Natural gas is a major feedstock for the production of [[ammonia]], via the [[Haber process]], for use in [[fertilizer]] production.
 
;Hydrogen
Natural gas is also a major feedstock for the production of [[hydrogen]], with one common method being the [[steam-methane reformer]] (SMR). Hydrogen has various applications: it is a primary feedstock for the chemical industry, a hydrogenating agent, an important commodity for oil refineries, and a fuel source in [[hydrogen vehicle]]s.
 
;Aviation
[[Russia]]n aircraft manufacturer [[Tupolev]] is currently running a development program to produce LNG- and [[hydrogen]]-powered aircraft.<ref> [http://www.tupolev.ru/English/Show.asp?SectionID=82&Page=1 PSC Tupolev - Development of Cryogenic Fuel Aircraft]</ref> The program has been running since the mid-1970s, and seeks to develop LNG and hydrogen variants of the [[Tupolev Tu-204|Tu-204]] and [[Tupolev Tu-334|Tu-334]] passenger aircraft, and also the [[Tupolev Tu-330|Tu-330]] cargo aircraft.
 
The advantages of liquid methane as a jet engine fuel are that it has more specific energy than the standard [[kerosene]] mixes and that its low temperature can help cool the air which the engine compresses for greater volumetric efficiency, in effect replacing an [[intercooler]]. Alternatively, it can be used to lower the temperature of the exhaust.
 
;Other
Natural gas is used as a feedstock in the production of [[petrochemicals]].
 
==Storage and transport==
 
The major difficulty in the  use of natural gas is [[transport]]ation and [[Natural gas storage|storage]] because of its low density. Natural gas [[pipeline transport|pipelines]] are economical, but are impractical across [[ocean]]s.  Many [[List of North American natural gas pipelines|existing pipelines in North America]] are close to reaching their capacity, prompting some politicians representing colder areas to speak publicly of potential shortages. In [[Europe]] gas pipeline network is already dense in the West<ref>[http://www.gie.eu.com/ Gas Infrasturcture Europe], retrieved June 18. 2009</ref>. New pipelines are planned or under construction  in the Eastern Europe and between gas fields in [[Russia]], [[Near East]] and [[Northern Africa]] and Western Europe. (See also: [[List of natural gas pipelines]] )
 
[[LNG carrier]]s can be used to transport [[liquefied natural gas]] (LNG) across oceans, while [[tank truck]]s can carry liquefied or [[compressed natural gas]] (CNG) over shorter distances. Sea transport using [[CNG carrier]] ships that are now under development may be competitive with LNG transport in specific conditions.
For LNG transport a [[liquefaction of gases|liquefaction]] plant is needed at the exporting end and [[gasification|regasification]] equipment at the receiving [[LNG terminal|terminal]]. Shipborne regasification equipment is also practicable. LNG transportation is established as the preferred technology for long distance, high volume transportation of natural gas, whereas pipeline transport is preferred for transport for distances up to typically 4.000 km overland and approximately half that distance over seas.
 
For CNG transport high pressure, typically above 200 [[bar (unit)|bars]], is used. Compressors and decompression equipment are less capital intensive and may be economical in smaller unit sizes than liquefaction/regasification plants. For CNG mode the crucial problem is the investment and operating cost of carriers. Natural gas trucks and carriers may transport natural gas directly to end-users, or to distribution points such as pipelines for further transport.
 
In the past, the natural gas which was recovered in the course of recovering [[petroleum]] could not be profitably sold, and was simply burned at the oil field (known as [[gas flare|flaring]]). This wasteful practice is now illegal in many countries<ref>{{cite book|last=Hyne|first=Norman J. |title=Dictionary of petroleum exploration, drilling & production|publisher=PennWell Books|location=pg. 190|date=1991|pages=625|isbn=0878143521}}</ref>. Additionally, companies now recognize that value for the gas may be achieved with LNG, CNG, or other transportation methods to end-users in the future.  The gas is now re-[[Wiktionary:inject|inject]]ed back into the formation for later recovery. This also assists oil pumping by keeping underground pressures higher. In [[Saudi Arabia]], in the late 1970s, a "Master Gas System" was created, ending the need for flaring. Satellite observation unfortunately shows that some large gas-producing countries still use flaring<ref>[http://www.ethanzuckerman.com/blog/wp-content/2007/11/flares.jpg Satellite observation of flares in the world]</ref> and venting<ref>[[Methane#Methane_in_Earth.27s_atmosphere|satellite observation of methane in earth's atmosphere]]</ref> routinely. The natural gas is used to generate electricity and heat for [[desalination]]. Similarly, some landfills that also discharge methane gases have been set up to capture the methane and generate electricity.
 
Natural gas is often stored underground inside depleted gas reservoirs from previous gas wells, [[salt domes]], or in tanks as [[liquefied natural gas]].  The gas is injected during periods of low demand and extracted during periods of higher demand.  Storage near the ultimate end-users helps to best meet volatile demands, but this may not always be practicable.
 
With 15 nations accounting for 84% of the worldwide production, access to natural gas has become a significant factor in international economics and politics. In this respect, control over the pipelines is a major strategic factor.<ref>[http://www.imi-online.de/2007.php3?id=1589 The Contours of the New Cold War]</ref>  In particular, in the 2000s, [[Gazprom]], the Russian national energy company, has engaged in disputes with [[Ukraine]] and [[Belarus]] over the price of its natural gas, which have created worries that gas deliveries to parts of Europe could be cut off for political reasons.<ref>[http://www.npr.org/templates/story/story.php?storyId=99026745 Gazprom and Russian Foreign Policy]</ref>
 
==Environmental effects==
 
The use of natural gas as [[combustion]] fuel produces far less emissions of [[air pollutant]]s such as [[sulfur dioxide]] and [[nitrogen oxides]] than does the combustion of [[coal]] or [[fuel oil]]s. However, in it does contribute significantly to global [[carbon dioxide]] emissions.  According to the [[IPCC Fourth Assessment Report]], in 2004 natural gas produced about 5,300 Mt/yr of CO<sub>2</sub> emissions, while coal and oil produced 10,600 and 10,200 respectively.
 
In addition, natural gas is a greenhouse gas more potent than carbon dioxide when released into the atmosphere. It is inevitable that, in using natural gas as a combustion fuel on a large scale, some of it will leak into the atmosphere. However, it is not of large concern due to the small amounts of such leakage. Carbon dioxide receives the the most attention over greenhouse gases because it is in much higher concentrations.
 
==Safety==
{{Image|Natural gas odorant injection.jpg|right|350px|A natural gas pipeline odorant injection station.}}
 
In any form, a minute amount of [[aroma compound|odorant]] such as [[butanethiol|t-butyl mercaptan]], with a rotting-cabbage-like smell, is added to the otherwise colorless and almost odorless gas, so that [[leak]]s can be detected before a fire or [[explosion]] occurs.  Sometimes a related compound, [[tetrahydrothiophene|thiophane]] is used, with a rotten-egg smell.  Adding odorant to natural gas began in the United States after the 1937 [[New London School explosion]].  The buildup of gas in the school went unnoticed, killing three hundred students and faculty when it ignited. Odorants are considered non-toxic in the extremely low concentrations occurring in natural gas delivered to the end user.


In [[mining|mine]]s, where methane seeping from rock formations has no odor, [[sensor]]s are used, and mining apparatuses have been specifically developed to avoid ignition sources, e.g., the [[Davy lamp]].
== Further reading==


Explosions caused by natural [[gas leak]]s occur a few times each year. Individual homes, small businesses and boats are most frequently affected when an internal leak builds up gas inside the structure.  Frequently, the blast will be enough to significantly damage a building but leave it standing.  In these cases, the people inside tend to have minor to moderate injuries.  Occasionally, the gas can collect in high enough quantities to cause a deadly explosion, disintegrating one or more buildings in the process.  The gas usually dissipates readily outdoors, but can sometimes collect in dangerous quantities if weather conditions are right.  However, considering the tens of millions of structures that use the fuel, the individual risk of using natural gas is very low.
*{{cite book | author=M.R. Beychok| title=Fundamentals Of Stack Gas Dispersion | edition=4th Edition | publisher=author-published | year=2005 | isbn=0-9644588-0-2}}


Some gas fields yield [[sour gas]] containing hydrogen sulfide, which is toxic. [[Amine gas treating]], an industrial process, is often used to remove hydrogen sulfide from natural gas.<ref name=NatGasOrg/>
*{{cite book | author=K.B. Schnelle and P.R. Dey| title=Atmospheric Dispersion Modeling Compliance Guide  | edition=1st Edition| publisher=McGraw-Hill Professional | year=1999 | isbn=0-07-058059-6}}


Extraction of natural gas (or oil) leads to decrease in pressure in the [[oil reservoir|reservoir]]. This in turn may lead to [[subsidence]] at ground level. Subsidence may affect ecosystems, waterways, sewer and  water supply systems, foundations, etc.
*{{cite book | author=D.B. Turner| title=Workbook of Atmospheric Dispersion Estimates: An Introduction to Dispersion Modeling | edition=2nd Edition | publisher=CRC Press | year=1994 | isbn=1-56670-023-X}}


Natural gas heating systems are a minor source of [[carbon monoxide]] deaths in the United States. According to the US Consumer Product Safety Commission (2008), 56% of unintentional deaths from non-fire CO poisoning were associated with engine-driven tools like gas-powered generators and lawn mowers.  Natural gas heating systems accounted for 4% of these deaths. Improvements in natural gas furnace designs have greatly reduced CO poisoning concerns. [[Carbon monoxide detector|Detectors]] are also available that warn of carbon monoxide and/or explosive gas (methane, propane, etc.).
*{{cite book | author= S.P. Arya| title=Air Pollution Meteorology and Dispersion | edition=1st Edition | publisher=Oxford University Press | year=1998 | isbn=0-19-507398-3}}


==References==
*{{cite book | author=R. Barrat| title=Atmospheric Dispersion Modelling | edition=1st Edition | publisher=Earthscan Publications | year=2001 | isbn=1-85383-642-7}}
{{reflist}}
---------------------------------------


;External links
*{{cite book | author=S.R. Hanna and R.E. Britter| title=Wind Flow and Vapor Cloud Dispersion at Industrial and Urban Sites  | edition=1st Edition | publisher=Wiley-American Institute of Chemical Engineers | year=2002 | isbn=0-8169-0863-X}}


*[http://cera.ecnext.com/coms2/browse_RS_GAS_ CERA] - collection of market and industry reports
*{{cite book | author=P. Zannetti| title=Air pollution modeling : theories, computational methods, and available software | edition= | publisher= Van Nostrand Reinhold | year=1990 | isbn=0-442-30805-1 }}
*[http://tonto.eia.doe.gov/oog/info/ngw/ngupdate.asp DOE/EIA EIA Natural Gas Weekly Update] - current NG prices and market analysis
*[http://www.naturalgasmedia.com Natural Gas Insight and Intelligence] - Natural Gas Media - updated Natural Gas Industry News and Analysis for Traders, Investors, and Institutions

Latest revision as of 04:25, 22 November 2023


The account of this former contributor was not re-activated after the server upgrade of March 2022.


Industrial air pollution source

Atmospheric dispersion modeling is the mathematical simulation of how air pollutants disperse in the ambient atmosphere. It is performed with computer programs that solve the mathematical equations and algorithms which simulate the pollutant dispersion. The dispersion models are used to estimate or to predict the downwind concentration of air pollutants emitted from sources such as industrial plants, vehicular traffic or accidental chemical releases.

Such models are important to governmental agencies tasked with protecting and managing the ambient air quality. The models are typically employed to determine whether existing or proposed new industrial facilities are or will be in compliance with the National Ambient Air Quality Standards (NAAQS) in the United States or similar regulations in other nations. The models also serve to assist in the design of effective control strategies to reduce emissions of harmful air pollutants. During the late 1960's, the Air Pollution Control Office of the U.S. Environmental Protection Agency (U.S. EPA) initiated research projects to develop models for use by urban and transportation planners.[1]

Air dispersion models are also used by emergency management personnel to develop emergency plans for accidental chemical releases. The results of dispersion modeling, using worst case accidental releases and meteorological conditions, can provide estimated locations of impacted areas and be used to determine appropriate protective actions. At industrial facilities in the United States, this type of consequence assessment or emergency planning is required under the Clean Air Act (CAA) codified in Part 68 of Title 40 of the Code of Federal Regulations.

The dispersion models vary depending on the mathematics used to develop the model, but all require the input of data that may include:

  • Meteorological conditions such as wind speed and direction, the amount of atmospheric turbulence (as characterized by what is called the "stability class"), the ambient air temperature, the height to the bottom of any inversion aloft that may be present, cloud cover and solar radiation.
  • The emission parameters such the type of source (i.e., point, line or area), the mass flow rate, the source location and height, the source exit velocity, and the source exit temperature.
  • Terrain elevations at the source location and at receptor locations, such as nearby homes, schools, businesses and hospitals.
  • The location, height and width of any obstructions (such as buildings or other structures) in the path of the emitted gaseous plume as well as the terrain surface roughness (which may be characterized by the more generic parameters "rural" or "city" terrain).

Many of the modern, advanced dispersion modeling programs include a pre-processor module for the input of meteorological and other data, and many also include a post-processor module for graphing the output data and/or plotting the area impacted by the air pollutants on maps. The plots of areas impacted usually include isopleths showing areas of pollutant concentrations that define areas of the highest health risk. The isopleths plots are useful in determining protective actions for the public and first responders.

The atmospheric dispersion models are also known as atmospheric diffusion models, air dispersion models, air quality models, and air pollution dispersion models.

Atmospheric layers

Discussion of the layers in the Earth's atmosphere is needed to understand where airborne pollutants disperse in the atmosphere. The layer closest to the Earth's surface is known as the troposphere. It extends from sea-level up to a height of about 18 km and contains about 80 percent of the mass of the overall atmosphere. The stratosphere is the next layer and extends from 18 km up to about 50 km. The third layer is the mesosphere which extends from 50 km up to about 80 km. There are other layers above 80 km, but they are insignificant with respect to atmospheric dispersion modeling.

The lowest part of the troposphere is called the atmospheric boundary layer (ABL) or the planetary boundary layer (PBL) and extends from the Earth's surface up to about 1.5 to 2.0 km in height. The air temperature of the atmospheric boundary layer decreases with increasing altitude until it reaches what is called the inversion layer (where the temperature increases with increasing altitude) that caps the atmospheric boundary layer. The upper part of the troposphere (i.e., above the inversion layer) is called the free troposphere and it extends up to the 18 km height of the troposphere.

The ABL is the most important layer with respect to the emission, transport and dispersion of airborne pollutants. The part of the ABL between the Earth's surface and the bottom of the inversion layer is known as the mixing layer. Almost all of the airborne pollutants emitted into the ambient atmosphere are transported and dispersed within the mixing layer. Some of the emissions penetrate the inversion layer and enter the free troposphere above the ABL.

In summary, the layers of the Earth's atmosphere from the surface of the ground upwards are: the ABL made up of the mixing layer capped by the inversion layer; the free troposphere; the stratosphere; the mesosphere and others. Many atmospheric dispersion models are referred to as boundary layer models because they mainly model air pollutant dispersion within the ABL. To avoid confusion, models referred to as mesoscale models have dispersion modeling capabilities that can extend horizontally as much as a few hundred kilometres. It does not mean that they model dispersion in the mesosphere.

Gaussian air pollutant dispersion equation

The technical literature on air pollution dispersion is quite extensive and dates back to the 1930s and earlier. One of the early air pollutant plume dispersion equations was derived by Bosanquet and Pearson.[2] Their equation did not assume Gaussian distribution nor did it include the effect of ground reflection of the pollutant plume.

Sir Graham Sutton derived an air pollutant plume dispersion equation in 1947[3][4] which did include the assumption of Gaussian distribution for the vertical and crosswind dispersion of the plume and also included the effect of ground reflection of the plume.

Under the stimulus provided by the advent of stringent environmental control regulations, there was an immense growth in the use of air pollutant plume dispersion calculations between the late 1960s and today. A great many computer programs for calculating the dispersion of air pollutant emissions were developed during that period of time and they were commonly called "air dispersion models". The basis for most of those models was the Complete Equation For Gaussian Dispersion Modeling Of Continuous, Buoyant Air Pollution Plumes shown below:[5][6]


where:  
= crosswind dispersion parameter
  =
= vertical dispersion parameter =
= vertical dispersion with no reflections
  =
= vertical dispersion for reflection from the ground
  =
= vertical dispersion for reflection from an inversion aloft
  =
           
           
           
= concentration of emissions, in g/m³, at any receptor located:
            x meters downwind from the emission source point
            y meters crosswind from the emission plume centerline
            z meters above ground level
= source pollutant emission rate, in g/s
= horizontal wind velocity along the plume centerline, m/s
= height of emission plume centerline above ground level, in m
= vertical standard deviation of the emission distribution, in m
= horizontal standard deviation of the emission distribution, in m
= height from ground level to bottom of the inversion aloft, in m
= the exponential function

The above equation not only includes upward reflection from the ground, it also includes downward reflection from the bottom of any inversion lid present in the atmosphere.

The sum of the four exponential terms in converges to a final value quite rapidly. For most cases, the summation of the series with m = 1, m = 2 and m = 3 will provide an adequate solution.

and are functions of the atmospheric stability class (i.e., a measure of the turbulence in the ambient atmosphere) and of the downwind distance to the receptor. The two most important variables affecting the degree of pollutant emission dispersion obtained are the height of the emission source point and the degree of atmospheric turbulence. The more turbulence, the better the degree of dispersion.

Whereas older models rely on stability classes for the determination of and , more recent models increasingly rely on Monin-Obukhov similarity theory to derive these parameters.

Briggs plume rise equations

The Gaussian air pollutant dispersion equation (discussed above) requires the input of H which is the pollutant plume's centerline height above ground level. H is the sum of Hs (the actual physical height of the pollutant plume's emission source point) plus ΔH (the plume rise due the plume's buoyancy).

Visualization of a buoyant Gaussian air pollutant dispersion plume

To determine ΔH, many if not most of the air dispersion models developed between the late 1960s and the early 2000s used what are known as "the Briggs equations." G.A. Briggs first published his plume rise observations and comparisons in 1965.[7] In 1968, at a symposium sponsored by CONCAWE (a Dutch organization), he compared many of the plume rise models then available in the literature.[8] In that same year, Briggs also wrote the section of the publication edited by Slade[9] dealing with the comparative analyses of plume rise models. That was followed in 1969 by his classical critical review of the entire plume rise literature,[10] in which he proposed a set of plume rise equations which have become widely known as "the Briggs equations". Subsequently, Briggs modified his 1969 plume rise equations in 1971 and in 1972.[11][12]

Briggs divided air pollution plumes into these four general categories:

  • Cold jet plumes in calm ambient air conditions
  • Cold jet plumes in windy ambient air conditions
  • Hot, buoyant plumes in calm ambient air conditions
  • Hot, buoyant plumes in windy ambient air conditions

Briggs considered the trajectory of cold jet plumes to be dominated by their initial velocity momentum, and the trajectory of hot, buoyant plumes to be dominated by their buoyant momentum to the extent that their initial velocity momentum was relatively unimportant. Although Briggs proposed plume rise equations for each of the above plume categories, it is important to emphasize that "the Briggs equations" which become widely used are those that he proposed for bent-over, hot buoyant plumes.

In general, Briggs's equations for bent-over, hot buoyant plumes are based on observations and data involving plumes from typical combustion sources such as the flue gas stacks from steam-generating boilers burning fossil fuels in large power plants. Therefore the stack exit velocities were probably in the range of 20 to 100 ft/s (6 to 30 m/s) with exit temperatures ranging from 250 to 500 °F (120 to 260 °C).

A logic diagram for using the Briggs equations[5] to obtain the plume rise trajectory of bent-over buoyant plumes is presented below:

BriggsLogic.png
where:  
Δh = plume rise, in m
F  = buoyancy factor, in m4s−3
x = downwind distance from plume source, in m
xf = downwind distance from plume source to point of maximum plume rise, in m
u = windspeed at actual stack height, in m/s
s  = stability parameter, in s−2

The above parameters used in the Briggs' equations are discussed in Beychok's book.[5]

References

  1. J.C. Fensterstock et al, "Reduction of air pollution potential through environmental planning", JAPCA, Vol. 21, No. 7, 1971.
  2. C.H. Bosanquet and J.L. Pearson, "The spread of smoke and gases from chimneys", Trans. Faraday Soc., 32:1249, 1936.
  3. O.G. Sutton, "The problem of diffusion in the lower atmosphere", QJRMS, 73:257, 1947.
  4. O.G. Sutton, "The theoretical distribution of airborne pollution from factory chimneys", QJRMS, 73:426, 1947.
  5. 5.0 5.1 5.2 M.R. Beychok (2005). Fundamentals Of Stack Gas Dispersion, 4th Edition. author-published. ISBN 0-9644588-0-2. .
  6. D. B. Turner (1994). Workbook of atmospheric dispersion estimates: an introduction to dispersion modeling, 2nd Edition. CRC Press. ISBN 1-56670-023-X. .
  7. G.A. Briggs, "A plume rise model compared with observations", JAPCA, 15:433–438, 1965.
  8. G.A. Briggs, "CONCAWE meeting: discussion of the comparative consequences of different plume rise formulas", Atmos. Envir., 2:228–232, 1968.
  9. D.H. Slade (editor), "Meteorology and atomic energy 1968", Air Resources Laboratory, U.S. Dept. of Commerce, 1968.
  10. G.A. Briggs, "Plume Rise", USAEC Critical Review Series, 1969.
  11. G.A. Briggs, "Some recent analyses of plume rise observation", Proc. Second Internat'l. Clean Air Congress, Academic Press, New York, 1971.
  12. G.A. Briggs, "Discussion: chimney plumes in neutral and stable surroundings", Atmos. Envir., 6:507–510, 1972.

Further reading

  • M.R. Beychok (2005). Fundamentals Of Stack Gas Dispersion, 4th Edition. author-published. ISBN 0-9644588-0-2. 
  • K.B. Schnelle and P.R. Dey (1999). Atmospheric Dispersion Modeling Compliance Guide, 1st Edition. McGraw-Hill Professional. ISBN 0-07-058059-6. 
  • D.B. Turner (1994). Workbook of Atmospheric Dispersion Estimates: An Introduction to Dispersion Modeling, 2nd Edition. CRC Press. ISBN 1-56670-023-X. 
  • S.P. Arya (1998). Air Pollution Meteorology and Dispersion, 1st Edition. Oxford University Press. ISBN 0-19-507398-3. 
  • R. Barrat (2001). Atmospheric Dispersion Modelling, 1st Edition. Earthscan Publications. ISBN 1-85383-642-7. 
  • S.R. Hanna and R.E. Britter (2002). Wind Flow and Vapor Cloud Dispersion at Industrial and Urban Sites, 1st Edition. Wiley-American Institute of Chemical Engineers. ISBN 0-8169-0863-X. 
  • P. Zannetti (1990). Air pollution modeling : theories, computational methods, and available software. Van Nostrand Reinhold. ISBN 0-442-30805-1.