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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.


'''Refineries''' are industrial manufacturing facilities composed of a group of [[chemical engineering]] [[unit processes]] and [[unit operation]]s<ref>{{cite book|author=McCabe, W., Smith, J. and Harriott, P.|title=[[Unit Operations of Chemical Engineering]]|edition=7th Edition|publisher= McGraw-Hill|year=2004|id=ISBN 0-07-284823-5}}</ref><ref>{{cite book|author=Perry, R.H. and Green, D.W. (Editors)|title=[[Perry's Chemical Engineers' Handbook]]|edition=8th Edition|publisher=McGraw-Hill|year=2007|id=ISBN 0-07-142294-3}}</ref> used for the conversion certain raw materials such as [[petroleum]] [[crude oil]], mined ores, sugar or salt into finished products of value or for the refining and purification of partially converted raw materials into finished products.
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>


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


* [[Petroleum refinery]]: Converts petroleum [[crude oil]] into [[Octane rating|high-octane]] motor fuel ([[gasoline]]/[[petrol]]), [[diesel oil]], [[liquefied petroleum gas]]es (LPG), jet aircraft fuel, [[naphtha]], [[kerosene]], heating [[fuel oil]]s, [[lubricating oil]]s, [[asphalt]] and [[petroleum coke]].
* 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.
* [[Natural gas processing]] plant: Purifies and converts raw [[natural gas]] into residential, commercial and industrial fuel gas, and also recovers byproduct [[sulfur]] and [[natural gas liquids]] (NGL) such as [[ethane]], [[propane]], [[butane]]s and [[pentane]]s.
* 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.
* [[Sugarcane|Sugar refinery]]: Converts [[sugar cane]] and [[sugar beets]] into crystallized [[sugar]] and sugar syrups.
* Terrain elevations at the source location and at receptor locations, such as nearby homes, schools, businesses and hospitals.
* [[Salt refinery]]: Converts salt ([[Sodium chloride|NaCl]]), produced by underground mining, the [[solar evaporation]] of sea water (or other water ponds) or by [[solution mining ]] and [[Vacuum evaporator|vacuum evaporation]], into crystallized salt used for cooking and the flavoring of food, as well as for various industrial uses (notably for the production of [[chlorine]]).
* 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).
* Various metal refineries converting metallic ores into end product metals such as [[alumina]], [[copper]], [[gold]], [[lead]], [[nickel]], [[silver]], [[uranium]], and [[zinc]].


{{Image|Petroleum refinery.jpg|right|250px|A petroleum refinery.}}
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.


==A typical petroleum refinery==
The atmospheric dispersion models are also known as atmospheric diffusion models, air dispersion models, air quality models, and air pollution dispersion models.
{{main|Petroleum refining processes}}
Petroleum refineries are very large industrial complexes that involve a great many different processing units and auxiliary facilities such as utility units and storage tanks. Each refinery has its own unique arrangement and combination of refining processes largely determined by the refinery location, desired products and economic considerations. There are most probably no two refineries that are identical in every respect.


The image below is a schematic [[Process flow diagram|flow diagram]] of a typical oil refinery that depicts the various [[unit]] processes and the flow of intermediate product streams that occurs between the inlet crude oil feedstock and the final end products.  The diagram depicts only one of the literally hundreds of different oil refinery configurations. It does not include any of the usual refinery facilities providing utilities such as steam, cooling water, and electric power as well as storage tanks for crude oil feedstock and for intermediate products and end products.<ref>{{cite book|author=Gary, J.H. and Handwerk, G.E.|title=Petroleum Refining Technology and Economics|edition=2nd Edition|publisher=Marcel Dekker, Inc|year=1984|isbn=0-8247-7150-8}}</ref><ref>[http://www.chevron.com/products/prodserv/fuels/bulletin/motorgas/3_refining-testing/pg2.asp Guide to Refining] from [[Chevron Corporation|Chevron Oil]]'s website</ref><ref>[http://www.uop.com/refining/1010.html Refinery flowchart] from  [[UOP LLC|Universal Oil Products]]' website</ref><ref>[http://www.cheresources.com/refining15.gif An example flowchart] of fractions from crude oil at a refinery</ref>
==Atmospheric layers==


[[Image:RefineryFlow.png|frame|584px|center|Schematic flow diagram of a typical oil refinery]]
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.


[[Image:NaturalGasProcessingPlant.jpg|thumb|250px|right|A natural gas processing plant]]
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.


==A typical natural gas processing plant==
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.


{{main|Natural gas processing}}
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.
There are a great many ways in which to configure the various unit processes used in the processing of raw natural gas. The image below is a generalized, schematic [[Process flow diagram|block flow diagram]] of a typical natural gas processing plant configuration. It shows the various unit processes used to convert raw natural gas into sales gas pipelined to the end user markets.  


The block flow diagram also depicts how processing of the raw natural gas yields byproduct sulfur, byproduct ethane, and natural gas liquids (NGL) such as propane, butanes and natural gasoline (denoted as pentanes +).<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>[http://www.axens.net/upload/presentations/fichier/axens_gpagcc_2004v2.pdf From Purification to Liquefaction Gas Processing]</ref><ref>[http://www.spe.org/specma/binary/files/5804785Syn10682.pdf Feed-Gas Treatment Design for the Pearl GTL Project]</ref><ref>[http://lnglicensing.conocophillips.com/NR/rdonlyres/B78B6727-E5F4-4505-B9C3-96CC94D7B30D/7357/AICHELNGNGLIntegrationPaper.pdf Benefits of integrating NGL extraction and LNG liquefaction]</ref>
==Gaussian air pollutant dispersion equation==


[[Image:NatGasProcessing.png|frame|center|584px|Schematic flow diagram of a typical natural gas processing plant]]
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.


==Typical refining of sugar==
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.


{{main|Sugar refining}}
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>
Most of the sugar produced worldwide is derived either from [[sugar cane]] or [[sugar beet]]s. However, the sugar produced from sugar cane is at least twice the amount produced by sugar beets. For that reason, this section deals with sugar produced from sugar cane.


The refining of sugar cane into sugar is usually done in two stages. The first stage is the  preparation and milling of freshly harvested sugar cane. In some cases, the preparation and milling may be done locally where the sugar cane is grown and harvested. In the milling stage, the sugar cane is first washed, chopped, and shredded by revolving knives. Then the  shredded cane is mixed with water and crushed to produce a sugar juice.


{|border="0" align="center"
<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>
 
{| 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
|-
|-
|valign="top" |{{Image|Sugar Refinery 1.jpg|right|200px|A sugar refinery in [[New South Wales]], [[Australia.]]}}
!align=right|<math>L</math>
|valign="center" |{{Image|Cut sugar cane.jpg|right|250px|Cut sugar cane.}}
|align=left|= height from ground level to bottom of the inversion aloft, in m
|valign="center" |{{Image|Sugar Cane Refinery.png|right|250px|Flow diagram of sugar refining process.}}
|-
!align=right|<math>\exp</math>
|align=left|= the exponential function
|}
|}


As shown in the above schematic flow diagram,<ref>[http://www.trivenigroup.com/sugar/plant-process.html Process flow diagram for sugar refining]</ref> the juice (containing 10 &ndash; 15 percent [[sucrose]]) is heated to about 65 &ndash; 70 °C and mixed with [[lime (mineral)|lime]] and with gaseous [[sulfur dioxide]] (SO<sub>2</sub>). The lime serves to adjust the [[pH]] of the juice to about 7.0 &ndash; 7.1 which arrests sucrose's decay into [[glucose]] and [[fructose]], and precipitates out some impurities. The sulfur dioxide serves to decolorize the juice. The juice is then further heated to about 100 &ndash; 105 °C and sent through a clarifier where the precipitated impurities and other solids are settled out and removed.  
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 <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.
 
<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.


The clarified juice is next concentrated in a [[multiple-effect evaporator]] to make a syrup with about 60 &ndash; 65 weight percent sucrose.  The syrup is again treated sulfur dioxide for further decolorization and then is further concentrated under [[vacuum]] until it becomes [[supersaturated]] with sugar. Upon cooling, sugar crystallizes out of the syrup.  
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.


The crystallized sugar is separated from the residual liquid syrup (''[[molasses]]'')s by [[Centrifuge|centrifuging]]. The end product is a white, crystalline sugar referred to as ''mill white'', ''plantation white'' or ''crystal sugar''. To produce ''[[granulated sugar]]'', in which the individual sugar grains do not clump together, sugar must be dried. Drying is accomplished by first drying the sugar in a hot [[rotary dryer]], and then by blowing cool air through it for several days.
==Briggs plume rise equations==


The refining process described in this section is sometimes referred to as the ''Double Sulfation (DS)'' process. There are other refining processes that use [[calcium phosphate]] (instead of lime) to remove impurities from the sugar juice (and/or the sugar syrup) and treatment with [[activated carbon]] (rather than gaseous sulfur dioxide) for decolorization.
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).


The fibrous solids, called ''[[bagasse]]'', remaining after the crushing of the shredded sugar cane, are burned for fuel within the sugar  refinery. Any surplus bagasse can be used for animal feed, in paper manufacture, or burned to generate electricity for the local power grid.
[[File:Gaussian Plume.png|thumb|right|333px|Visualization of a buoyant Gaussian air pollutant dispersion plume]]


==Salt production and refining==
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>
{{main|Salt production}}


There are three different methods used for the production of salt: solar evaporation of saline water, underground salt mining and mechanical evaporation of solution mined salt.<ref name=InstituteTechnologies>[http://www.saltinstitute.org/Production-industry/Production-technologies Salt production technologies]</ref><ref name=Morton>[http://www.mortonsalt.com/saltfacts/salt_prodproc.htm Salt Production and Processing]</ref><ref>[http://www.cargillsalt.com/dc_salt_about_howmade.htm How Salt Is Made]</ref>
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


===Solar evaporation and refining===
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'''''.


Solar salt ([[sodium chloride]] or [[NaCl]]) is produced by using sunlight and wind to evaporate [[Salinity|saline]] saline ocean water, open water ponds or saline lakes. This is the oldest method of producing salt and has been used since salt crystals were first observed in trapped ponds of sea water. It requires a climate where there are steady prevailing winds and the evaporation rate of open water exceeds the rate of rainfall for long time periods. Some examples of solar salt production are:
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).


{|border="0" align="center"
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"
|-
|-
|valign="top" |{{Image|SF Bay Salt Ponds.jpg|right|240px|Salt ponds in the [[San Francisco Bay]], [[California]].}}
|align=right|where:
|valign="top" |{{Image|Inca salt ponds.jpg|right|240px|[[Inca]] salt ponds in [[Peru]].}}
|&nbsp;
|valign="top" |{{Image|Dead Sea salt.jpg|right|215px|Salt in the [[Dead Sea]], [[Ein Gadi]], [[Israel]].}}
|-
!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/>


The water in the San Francisco Bay salt ponds is not as saline (i.e., salty) as the Pacific Ocean seawater because it is diluted by fresh water from local rivers, creeks and other sources. The bay water first flows into the intake set of ponds and is subsequently moved progressively through other ponds.  In the first stage of ponds, evaporation over time reduces the water volume by about 70 percent which increases the salinity and impurities such as [[calcium sulfate]] (CaSO<sub>4</sub>) precipitate. As the water is subsequently moved through the other pond stages, other impurities preciptate out and 95 percent of the water is eventually evaporated before the water is moved into the final ponds (referred to as the crystallizing ponds) where the sodium chloride precipitates out at about 40 [[U.S. customary units|ton]]s per [[U.S. customary units|acre]] (90 [[SI units|tonnes]] per [[SI units|hectare]]) and is then mechanically harvested.<ref name=Savesfbay>[http://www.savesfbay.org/atf/cf/%7B2D306CC1-EF35-48CC-B523-32B03A970AE5%7D/SALT%20PONDS%20REPORT.pdf Turning Salt Into Environmental Gold]</ref><ref name=InstituteSolarSalt>[http://www.saltinstitute.org/Production-industry/Production-technologies/Solar-salt-sea-salt Solar Salt]</ref><ref name=CargillTour>[http://www.cargill.com/sf_bay/tour.htm Virtual tour of Cargill's San Francisco Bay salt works]</ref>  It takes up to 5 years for the sun and wind to evaporate the bay water and to harvest the salt.
==References==
 
{{reflist}}
The colors of the salt ponds reflect the interaction of plants, aquatic life and varying salinity. In the low-salinity ponds, [[algae]] creates a green color. In the moderate-salinity ponds, [[Dunaliella algae]] proliferates and the color of this ponds become a lighter shade of green. In the mid-salinity ponds, tiny bay shrimp produce an orange color. In the high- salinity ponds, the Dunaliella algae produce a red color and halophilic bacteria (i.e., organisms requiring a salty environment) contribute a purplish-red color.<ref name=Savesfbay/>
 
To produce high-purity salt (99.9 percent pure) for use in cooking and flavoring of foods, the harvested solar salt must be further purified in a salt refinery. In the refinery,  the solar salt is first washed, which removes dust or other debris and some trace minerals that may have clung to the salt crystals during the harvesting of the solar salt. The cleansed solar salt is then dissolved in tanks of pure drinking water.<ref name=CargillTour/>
 
The salt solution (i.e., ''brine'') from the tanks is then passed through [[vacuum evaporator]]s, which remove the water and crystallize the salt. After the salt re-crystallizes, it is dried, filtered, and air-cooled. A series of vibrating screens is used to segregate the dried crystals into various sizes for packaging and shipment to end-users.<ref name=CargillTour/>
 
==Underground mining of rock salt==


Rock salt (referred to as [[halite]]) is mined from underground deposits reached through a circular shaft, usually about 20 [[U.S. customary units|feet]] (6 [[International System of Units|metre]]) in diameter and as deep as 2,000 feet (610 metre), depending on the depth and location of the salt deposit.<ref name=InstituteRockSalt>[http://www.saltinstitute.org/Production-industry/Production-technologies/Rock-salt-halite Rock salt (halite)]</ref>
== Further reading==


Mining methods depend on whether the salt deposit is ''layered'' horizontally or is a vertical ''salt dome''. Layered deposits are mined using the ''room and pillar'' method in which drilling and blasting creates horizontal rooms of 10 &ndash; 25 feet (3 &ndash; 8 metre) high and about 50 feet (15 metre) wide. Openings or cross-cuts are created perpendicular to the length of the rooms to connect the rooms at planned intervals. Salt pillars are left in place to provide structural support for the overlying roof and other layers. Most room-and-pillar mines recover about 45 &ndash; 65% of the salt available, with the remainder left behind as pillar supports with margins both above and below the mined area. Several rooms may be blasted each day with each blast bringing down 350 &ndash; 900 [[U.S. customary units|tons]] (317 &ndash; 816 [[International System of Units|tonne]]s).<ref name=InstituteRockSalt/>
*{{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}}


For salt dome deposits, a level of room-and-pillar extraction is first completed and the usual practice is to then ''bench'' the mine by drilling and blasting the floor extending the excavation downward and removing vast quantities with each blast.<ref name=InstituteRockSalt/>
*{{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}}
 
Typically, salt mining uses large, diesel-powered equipment for cutting, drilling, blasting and loading the blasted salt onto diesel-powered trucks which transport the salt to crushers. Conveyor belts then carry the crushed salt to the a hoist. Each hoist can lift 18 &ndash; 20 tons (16 &ndash; 18 tonnes). Large salt mines may hoist up to 900 tons (816 tonnes) an hour.<ref name=InstituteRockSalt/>
 
Once the salt has been hoisted to above ground, vibrating screens are used to separate the mined salt into various sizes and each size is conveyed to its designated storage bins. From the storage bins, the salt is subsequently shipped either to various end-user buyers of mined rock salt or to salt refineries for final purification (as described above for solar salt).
 
==The equipment used in refineries==
 
Refineries utilize a great many different types of physical equipment such as:
 
{{col-begin}}
{{col-break|width=50%}}
* [[Centrifuge]]s
* [[Gas compressor|Compressors]]
* [[Industrial cooling tower|Cooling towers]]
* [[Control valve]]s
* [[Crusher]]s
* [[Crystallizers]]
* [[Continuous distillation|Distillation towers]] and other  [[Pressure vessel|pressure vessels]]
* [[Electrical generators|Electric power generators]], [[transformer]]s and [[electric motors]]
* [[Electrolysis]] cells
* [[Evaporators]]
* [[Filter (chemistry)|Filters]]
* [[Flare stack]]s
{{col-break}}
* [[Furnace]]s
* [[Mixer]]s and [[blender]]s
* [[Control system|Monitoring and control systems]]
* [[Piping (engineering)|Piping]] and [[valve]]s
* [[Pump]]s
* [[Relief valve]]s
* [[Rotary dryer]]s
* [[Steam generator]]s
* [[Steam turbine]]s and [[gas turbine]]s
* [[Storage tank]]s
* [[Industrial wastewater treatment|Wastewater treatment]]
{{col-end}}
 
==References==


<references/>
*{{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}}


==See also==
*{{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}}


* [[Aluminium oxide|Alumina]]
*{{cite book | author=R. Barrat| title=Atmospheric Dispersion Modelling | edition=1st Edition | publisher=Earthscan Publications | year=2001 | isbn=1-85383-642-7}}
* [[Bagasse]]
* [[Bayer process]] and [[Hall-Héroult process]] (used to produce aluminium from bauxite ore)
* [[Liquefied Natural Gas]] (LNG)
* [[Liquefied petrolem gas]] (LPG)
* [[Natural gas]]
* [[Petroleum refinery]]
* [[Petroleum]]
* [[Sugar cane]]
* [[Sugar beet]]


==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://www.osha.gov/dts/osta/otm/otm_iv/otm_iv_2.html Complete, detailed oil refinery description]
*{{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://www.naturalgas.org/naturalgas/processing_ng.asp Processing natural gas]
* [http://www.sucrose.com/learn.html Aluminum production process flow sheets]
* [http://www.worldlpgas.com World LP Gas Association]
* [http://www.npga.org/i4a/pages/index.cfm?pageid=1 National Propane Gas Association, USA]]
* [http://www.ferc.gov/for-citizens/lng.asp Liquefied Natural Gas (LNG) Overview]
* [http://www.sucrose.com/learn.html Making sugar]
* [http://www.ussugar.com/sugar/sugar_refining.pdf Sugar refining]

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.