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{{Image|World Gas Production.png|right|306px|Figure 1: 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 undersea [[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.
__NOTOC__
[[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]] consisting of [[pentane]]s plus higher molecular weight [[hydrocarbon]]s (often referred to as pentanes<sup>+ </sup>), 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).


==Composition of raw 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.


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


*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)'''''.
==Atmospheric layers==
*[[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]], a [[Boiling point|low-boiling point]] mixture of liquid hydrocarbons called ''[[natural gas condensate]]'', sometimes also called ''[[natural gasoline]]'', ''[[casinghead gasoline]]'' or simply ''condensate''.
*[[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==
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.


{{main|Heating value}}
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.
Quantities of natural gas are measured in [[normal cubic meter]]s at 0 [[Celsius|°C ]] and 101.325  k[[Pascal (unit)|Pa]] absolute pressure or in [[standard cubic feet]] at 60 [[Fahrenheit and Rankine temperatures|°F]] and 14.496 [[U.S. customary units|psi]] absolute pressure.<ref>[http://www.air-dispersion.com/formulas.html Air Dispersion Modeling Conversions and Formulas] 1 normal cubic meter at 0 °C and 101.325  kPa  absolute = 37.326 standard cubic feet at 60 °F and 14.695 psi absolute.</ref>


The [[higher heating value]] (HHV)<ref>Also referred to as the gross heating value (GHV)</ref> of commercial, processed natural gas is about 40 M[[joule|J]] per normal cubic meter which, in the United States, is equivalent to about 1,015 [[U.S. customary units|Btu]] per standard cubic foot. However, those values can vary by several percent from one natural gas to another depending upon their source reservoir and upon their degree of processing.
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.


The heating value of a fuel gas when the water formed during combustion does not condense is the called the [[lower heating value]] (LHV)<ref>Also referred to as the net heating value (NHV)</ref> and can be as much as 10% less than the HHV.
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.


In the United States, the retail sales processed natural gas to end users are often in units of [[therm]]s with 1 therm being 100,000 Btu (equivalent to the higher heating value of roughly 100 standard cubic feet).
==Gaussian air pollutant dispersion equation==


==Finding and extracting natural gas==
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.


;Exploration:
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.
Exploration, in the oil and  gas industry, is the search for underground or undersea natural gas reservoirs. Recoverable reserves of natural gas tend to occur where impermeable rocks (called ''caprocks'') constrain the upward movement of gas through the undergorund 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. The various worldwide areas having significantly large reservoirs of natural gas are referred to as ''gas fields'' and most gas fields have been given a unique name, such as the North Field in [[Qatar]].  


{{Image|Drilling rig (Montana BLM).jpg|right|250px|A typical drilling rig located in [[Montana]].}}  
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>


;Extraction
After an initial exploration, wells are drilled to confirm the existence of a reservoir and its size. Once a reservoir of natural gas has been confirmed, production wells are drilled to extract the gas (see adjacent photograph). 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 some compressed gas downward into the reservoir.
<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>


Also over time, as gas is extracted, the pressure in the underground gas reservoir declines. When it decreases to below its [[hydrocarbon dew point]], any propane, butanes and pentanes and higher molecular weight hydrocarbons that it contains will partially condense into liquids. That formation of liquid hydrocarbons in a gas reservoir is called [[retrograde condensation]] because some of the gas condenses into a liquid under isothermal conditions instead of expanding or vaporizing when the pressure is decreased. The liquids thus formed may get trapped by depositing in the pores of the gas reservoir. One method of mitigating this problem is to reinject dried gas, free of condensate, to maintain the underground pressure and to allow re-evaporation and extraction of the condensate.
{| border="0" cellpadding="2"  
 
|-
==Sources of natural gas==
|align=right|where:
{| border="0" width="315" align="right" cellpadding="0" cellspacing="0" style="wrap=no"
|&nbsp;
|
|-
{| class = "wikitable" align="right"
!align=right|<math>f</math> 
|+ Table 1: Proved Reserves<br />of Natural Gas in 2007 <ref name=Proved>Proved reserves are those quantities of natural gas, which, by analysis of geological and engineering data, can be estimated with a high degree of confidence to be commercially recoverable from a given date forward, from known reservoirs and under current economic conditions.</ref><ref>[https://www.cia.gov/library/publications/the-world-factbook/rankorder/2179rank.html CIA World Factbook] Country Comparison :: Natural gas - proved reserves</ref>
|align=left|= crosswind dispersion parameter
! Country!!Reserves<br />(m<sup>3</sup>)
|-
|- align="center"
!align=right|&nbsp;
|Russia||44,650,000,000,000
|align=left|= <math>\exp\;[-\,y^2/\,(2\;\sigma_y^2\;)\;]</math>
|- align="center"
|-
|Iran||26,850,000,000,000
!align=right|<math>g</math>
|- align="center"
|align=left|= vertical dispersion parameter = <math>\,g_1 + g_2 + g_3</math>
|Qatar||25,630,000,000,000
|-
|- align="center"
!align=right|<math>g_1</math>
|Saudi Arabia||7,167,000,000,000
|align=left|= vertical dispersion with no reflections
|- align="center"
|-
|United Arab Emirates||6,071,000,000,000
!align=right|&nbsp;
|- align="center"
|align=left|= <math>\; \exp\;[-\,(z - H)^2/\,(2\;\sigma_z^2\;)\;]</math>  
|United States||5,977,000,000,000
|-
|- align="center"
!align=right|<math>g_2</math>
|Nigeria||5,210,000,000,000
|align=left|= vertical dispersion for reflection from the ground
|- align="center"
|-
|Venezuela||4,708,000,000,000
!align=right|&nbsp;
|- align="center"
|align=left|= <math>\;\exp\;[-\,(z + H)^2/\,(2\;\sigma_z^2\;)\;]</math>
|Algeria||4,502,000,000,000
|-
|- align="center"
!align=right|<math>g_3</math>
|Iraq||3,170,000,000,000
|align=left|= vertical dispersion for reflection from an inversion aloft
|- align="center"
|-
|All other countries||41,465,000,000,000
!align=right|&nbsp;
|- align="center"
|align=left|= <math>\sum_{m=1}^\infty\;\big\{\exp\;[-\,(z - H - 2mL)^2/\,(2\;\sigma_z^2\;)\;]</math>
|World total||175,400,000,000,000
|-
!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
|-
|-
|Colspan=2|<small>m<sup>3</sup> are defined as being at 0 °C and 1 atm (101.325 kPa)<br /> of absolute pressure.</small>
!align=right|<math>\exp</math>
|}
|align=left|= the exponential function
|}
|}


===Types of natural gas sources===
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.


Raw natural gas is presently extracted primarily from any one of three conventional underground sources, namely [[petroleum crude oil]] wells, gas wells, and [[Natural gas condensate|condensate]] wells:
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.


*Raw natural gas that comes from petroleum crude oil wells is typically termed '''''associated gas'''''. This gas can exist separate from the crude oil in the underground formation, or dissolved in the crude oil.  
<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.


*Raw natural gas from gas wells and from condensate wells contains little or no crude oil and is termed '''''non-associated gas'''''. Gas wells typically produce only raw natural gas, while condensate wells produce raw natural gas along with natural gas condensate.
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.


Raw natural gas can also come from methane deposits in the pores of some [[coal]] seams. Such gas is referred to as '''''coalbed gas''''' and it is also called ''sweet gas'' because it is relatively free of hydrogen sulfide. It consists mainly of methane with only trace quantities of ethane, nitrogen and carbon dioxide. It does not contain propane, butanes, pentanes or natural gas condensate.
==Briggs plume rise equations==


'''''Natural gas hydrate''''' (also called '' clathrate hydrate'', ''methane clathrate'' or ''methane hydrate'') is a solid in which methane is trapped within the [[crystal]] structure of [[ice]]. Significant deposits of methane clathrate have been found under sediments on Earth's [[ocean]] floors and in the arctic regions.<ref>[http://walrus.wr.usgs.gov/globalhydrate/ A Global Inventory of Natural Gas Occurrence] As of April, 2008. From the website of the [[U.S. Geological Survey]]</ref> The amount of the worldwide reserves of natural gas hydrates is poorly known, and estimates of those reserves have decreased many [[order of magnitude|orders of magnitude]]<ref>Orders of magnitude are powers of 10. One order of magnitude is factor of 10, two orders of magnitude is a factor of 100, three orders of magnitude is a factor of 1,000, etc.</ref>  since it was first recognized that natural gas hydrates could exist in the oceans during the 1960s. Recent estimates (about 2003) range from 1 to 5 × 10<sup>15</sup> m<sup>3</sup> of methane.<ref name="Milkov 2004">{{cite journal| author= A.V. Milkov| year=2004| title= Global estimates of hydrate-bound gas in marine sediments: how much is really out there?| journal=Earth-Sci Rev| volume= 66| issue=3-4| pages= 183–197| doi= 10.1016/j.earscirev.2003.11.002}}</ref> That amounts to 6 to 29 times the worldwide proven natural gas reserves from conventional sources (175.4 × 10<sup>12</sup> m<sup>3 </sup>) as shown in Table 1. As of 2009, there is no available technology for economically extracting and exploiting natural gas from the hydrate reservoirs.
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).


[[Biogas]], [[landfill gas]], [[town Gas]] and [[synthetic gas]] (produced by [[coal gasification]]) are man-made fuels. They are not natural gases.
[[File:Gaussian Plume.png|thumb|right|333px|Visualization of a buoyant Gaussian air pollutant dispersion plume]]


===Natural gas reserves===
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>


As shown in the Table 1, the world's total proven reserves<ref name=Proved/> of natural gas as of 2007 amounted to 175.4 × 10<sup>12</sup> cubic metres and the country having the largest proven reserves was [[Russia]] with 44.7 × 10<sup>12</sup> cubic metres. As shown in Figure 1, Russia was also the world's largest natural gas producer in 2007.
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


The world's largest gas field is the offshore North Field in Qatar, estimated to have 25 × 10<sup>9</sup> cubic metres of gas in place. The second largest natural gas field is the 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 × 10<sup>9</sup> cubic metres.<ref>{{cite web|url=http://www.pseez.ir/gas-en.html|publisher=Pars Special Economic Energy Zone|accessdate=2007-07-17|title=Pars Special Economic Energy Zone}}</ref>
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'''''.


Because natural gas is not a pure methane, when non-associated gas is extracted from a field under [[supercritical]] (pressure/temperature) conditions, the propane, butanes and pentanes it contains may partially condense upon 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 re-evaporation and extraction of condensates.
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).


==Natural gas processing==
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|NaturalGasProcessingPlant.jpg|right|250px|A natural gas processing plant.}}
==References==
{{main|Natural gas processing}}
{{reflist}}
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>
 
The block flow diagram also shows how processing of the raw natural gas yields these byproducts:
 
*Natural gas condensate
*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)
 
 
{{Image|NatGasProcessing.png|center|584px|Schematic flow diagram of a typical natural gas processing plant.}}
 
==Transportation and storage==
 
The major means of transporting large volumes of natural gas overland is by [[Pipeline transportion|pipelines]] and pipelines have been established as the preferred transportation mode for overland distances of up to about 4,000 [[kilometres]] (2,500 miles).
 
{{Image|LNG tanker Abuja.jpg|right|250px|LNG tanker with 5 spherical LNG tanks. Total length is 285 metres (311 yards).}}
 
However, transporting significant amounts of natural gas across oceans in pipelines is too expensive and using ordinary seagoing tankers is not feasible because of the very large volume of a gas compared to its liquid volume. However, natural gas can be and has been cryogenically cooled to – 161 °C (– 258 °F), condensed into [[liquified natural gas]] (LNG) and transported in large [[LNG tanker]]s capable of carrying about 150,000 m<sup>3</sup> of LNG at that temperature and at essentially atmospheric pressure. Transforming natural gas to a liquid is accompanied by a volume reduction of approximately 600 to 1. Thus, each large tanker can transport LNG which can be reconverted to 90,000,000 m<sup>3</sup> of natural gas at atmospheric pressure when delivered at the end of its journey.
 
For LNG transportation by seagoing tankers, an [[LNG liquefaction plant]] is needed at the exporting end and an [[LNG regasification plant]] is needed at the receiving [[LNG terminal]]. LNG transportation by seagoing LNG tankers has been established as the preferred technology for long distance transportation across oceans.
 
[[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.
[[Compressed natural gas]] (CNG) is a substitute fuel for the use of [[gasoline]], [[diesel fuel]], or propane in automotive vehicles. CNG is natural gas that has been compressed to an absolute pressure of about 200 to 220 [[Bar (unit)|bar]] (2,900 to 3,190 psi) which results in reducing the gas volume to about 0.5% of its volume at atmospheric pressure. CNG is transported by rail or in tanker trucks overland to end-users or to distribution points such as pipelines for further transport. As of 2009, plans and designs have been developed for using seagoing CNG tankers for oversea transport in the near future and such transport is expected to be competitive to LNG oversea transport in LNG tankers.
 
Natural gas is often stored underground inside depleted gas reservoirs from previous gas wells, [[salt domes]], or in storage tanks as [[liquefied natural gas]].  The gas is stored during periods of low demand and extracted during periods of higher demand.
 
==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 [[fuel oil]] 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.
 
;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 [[Liquified petroleum gas|LPG]] which is liquified propane, butane or a mixture of both, LPG is the dominant source of rural gas.
 
;Transportation fuel
Compressed natural gas (CNG) is a cleaner alternative to other automobile fuels such as gasoline (petrol) and diesel fuel. 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 used in fertilizer production.
 
;Hydrogen
Natural gas is also a major feedstock for the production of hydrogen, with one common method being the [[steam-methane reforming]] (SMR) process.. 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.
== Further reading==


;Other
*{{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}}
Natural gas is used as a feedstock in the production of petrochemicals.


==Environmental effects==
*{{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}}


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 oils. 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 M[[Tonne|t]]/year of carbon dioxide emissions, while coal and oil produced 10,600 and 10,200 respectively.
*{{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}}


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 or a petrochemical feedstock 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 most attention over greenhouse gases because it is in much higher concentrations.
*{{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}}


==Safety==
*{{cite book | author=R. Barrat| title=Atmospheric Dispersion Modelling | edition=1st Edition | publisher=Earthscan Publications | year=2001 | isbn=1-85383-642-7}}
{{Image|Natural gas odorant injection.jpg|right|325px|A natural gas pipeline odorant injection station.}}
 
Processed natural gas is colorless and essentially odorless. Since it is also very flammable, it is important that natural gas leaks be detected before a fire or explosion occurs. For that reason, very small amounts of a [[mercaptan]] such as [[t-butyl mercaptan]], with a strongly unpleasant smell, is added to the natural gas as an odorant. Such odorants are considered non-toxic in the extremely low concentrations at which they are used. Odorizing of 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.
 
In [[coal mine]]s, where any coalbed methane that may be present has no odor, [[methane sensor]]s are used, and mining equipment has been specifically developed to avoid ignition sources.
 
Explosions caused by natural gas leaks 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 such 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.
 
Extraction of natural gas leads to a decrease of the pressure in an underground gas reservoir. This in turn may sometimes lead to [[subsidence]] at ground level. Subsidence may affect ecosystems, waterways, sewer and  water supply systems, foundations, etc.
 
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 carbon monoxide 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 unsafe levels of carbon monoxide and/or explosive gas (methane, propane, etc.).
 
==References==
{{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


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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.