Locating and Estimating Air Emissions from Sources of Benzene pt 2
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Chapter 2
Sources and Emissions of Air Pollutants
LEArning ObjECtivES
By the end of this chapter the reader will be able to:
• distinguishthe“troposphere”fromthe“stratosphere”• define“pollutedair”inrelationtovariousscientificdisciplines• describe“anthropogenic”sourcesofairpollutantsanddistinguishthemfrom“natural”
sources• list10sourcesofindooraircontaminants• identifythreemeteorologicalfactorsthataffectthedispersalofairpollutants
ChAPtEr OutLinE
I. Introduction II. MeasurementBasics III. Unpollutedvs.PollutedAir IV. AirPollutantSourcesandTheirEmissions V. PollutantTransport VI. SummaryofMajorPointsVII. QuizandProblemsVIII. DiscussionTopicsReferencesandRecommendedReading
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i. intrOduCtiOn
Structure of the Earth’s Atmosphere
TheEarth,alongwithMercury,Venus,andMars,isaterrestrial(asopposedtogaseous)planetwithaper-manent atmosphere.The Earth is an oblate (slightlyflattened)spherewithameandiameterof12,700km(about8,000statutemiles).Thehighestsurfacefeature,Mt.Everest,reachesabout8.87km(5.5miles)abovesea
level.Mt.Everestisthusaminutebumpontheglobethataddsonly0.06percenttotheEarth’sdiameter.
TheEarth’satmosphereconsistsofseveraldefinedlayers(Figure 2–1).Thetroposphere,inwhichalllifeexists,andfromwhichwebreathe,reachesanaltitudeofabout7–8kmatthepolestojustover13kmattheequa-tor:themeanthicknessbeing9.1km(5.7miles).Thus,thetroposphererepresentsaverythincoverovertheEarth,barelyhigherthanMt.Everest.IftheEarthisrepresentedbyaballwithadiameterof2m,thethickness
Figure 2–1 A:Layersoftheearth’satmosphere(notdrawntoscale);B:To-scaledepictionoflayersofearth’satmosphere. Source:TheUniversityofCaliforniaAirPollutionHealthEffectsLaboratory,withkindpermission.
Troposphere
Ozonosphere Stratosphere
Chemosphere
Ionosphere
Outer space
Mesosphere
Earth
(A)
Mt. Everest
Troposphere
Chemosphere
Stratosphere
Earth’s surface
(B)
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II. Measurement Basics 23
ofthetropospherewouldbeabout1.3mm(Figure 2–1).Themainpointisthatsurfaceairpollutantsarereleasedintoathinatmosphericskin.
GravitationalattractionbindstheatmospheretotheEarth.Theoutermosttracesoftheatmospherereachtoover100km(60miles)abovethesurface.Theprotec-tiveozonelayerisabovethetroposphereatavariablealtitudeofabout20to30km.
vertical Mixing and inversions
Fromourknowledgeofthermodynamicsandhotairballoonobservations,weknowthatheatingtheaircausesittoexpandandrise.Becausethetemperatureoftheairinthetropospherenormallydecreaseswithincreasingaltitude,warmersurfaceairrisesverticallyuntilitcoolssufficiently.Thisverticalairmovementandsubsequentmixingdilutesaircontaminantsgeneratednearthesur-face,thuspreventingtheiraccumulationintheairwenormallybreathe.However,thesituationischangedbyair temperature inversions,inwhichverticalairmove-mentisimpeded.Inversionsarecharacterizedbylocalparcelsofwarmairovercoolerair,whichpreventsthenormalverticalmixing.InversionscantrapairpollutantsveryclosetotheEarth’ssurface.Inversionsmaybelow,lessthan100mhigh,insomecases.Insuchcases,clearairmaybeseenaboveasharplydefinedsmoggyyellow-brownairlayerthatextendsdowntothesurface.
Inversionsarecausedbymanyphenomena,including(1)movementofawarmfrontintoaregion;(2)solarheatingoftheairaboveashadedvalley;(3)down-wardflowofcoldmountainairintoawarmvalley;and(4)nighttimecoolingof theEarth’s surfaceby theradiationofsurfaceheattospace.Severaltypesofaircontaminants(e.g.,blackcarbonparticles)absorbsolarenergyandheatthesurroundingair,thusitisalsopos-siblethatthetrappingofsolarheatintheupperlayersofaheavilypollutedairmasscanproduceorsustainanairinversion(i.e.,asmog inversion).Whenalow-levelinversioniscoupledwithstagnantwindsandheavylocalemissionsofaircontaminants,theconditionsarerightforanairpollutionepisode.Themajorhistoricalairpollutionepisodesalloccurredduringstagnantinversionsinregionsthathadsignificantsourcesofcombustion-relatedairpollutants(seeChapter1).AlthoughlocaldifferencesinairtemperatureandtheEarth’srotationnormallydrivewindsthattransportanddiluteairpol-lutants,airstagnationandlowwind-speedconditionsarecommoninmanyregions.
tropospheric vs. Stratospheric Pollutant Effects
Justabovethetroposphere,thestratospherereachestoanaltitudeofabout50km(30miles).Theboundarybetweenthetroposphereandthestratosphereiscalledthetropopause.Abovethetropopausethetemperaturerises,creatinganaturalglobalinversionthattrapspol-lutantsinthetroposphere.Largemeteorologicevents,suchasmajorstorms,volcaniceruptions,andnuclearbomb detonations, can penetrate the tropopause andlocallymixtroposphericandstratosphericair.Also,thetropopause does not represent an absolute barrier togaseousmoleculesthatrisethroughit,whichisafactorin the stratosphericozone depletion caused from theriseofchlorofluorocarbons(CFCs)andotherreactivesubstancesfromthetroposphere.
Pollutantsinthetropospherecanhavedirect effectsonlivingthingsandphysicalobjectsonthesurfaceoftheEarth.Thephysicalandchemicalpropertiesofthepollutants,thetimeofcontact,andotherfactorswilldeterminethetypesandmagnitudesofthesedirecteffects.Incontrast,pollutantsinthestratospheredonotusuallycontactthesurfaceorinteractwithlife,buttheycanproduce indirect effects.These indirecteffects relateprimarilytoabsorptionandscatteringofsolarradiation(visiblelight,infrared,andultravioletrays)andcosmicionizingradiation.Thestratosphereprovidesimportantprotectionforlifebyshieldingthesurfacefromsuchdamagingradiations.ItalsoinfluencesandstabilizesthetemperatureoftheEarth,whichhassignificantimplica-tionsforthesustainabilityoflifeonEarth(seeChapter5).Similarly,troposphericpollutantscanaffectsurfacetemperaturesbyscatteringandbyabsorbing thermalenergyfromthesunandbytrappingnighttimeheatthatradiatesfromthesurface.
ii. MEASurEMEnt bASiCS
Quantitation and Scale
Quantitative measurementsareamongtheindispens-abletoolsofscience.Withoutsuchmeasurementsoneonlyhasgeneralitiesandpersonalstatements,suchas“it’stoocold”;“theairisclean”;and“visibilityispoor.”Suchgeneralitiesconveysomeinformation,but theyareimpreciseandoflittleuseinairpollutionscience.Quantitative measurements are based on acceptedunits of measurementthatarepreciselydefined.Suchunitsdonotvaryfromtime-to-time,place-to-place,or
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Onecouldalsoexpressratiosonaweight-to-volumebasis.Forexample,1cubiccmofsulfurdioxidegas(SO2)atstandardlaboratoryconditionshasamassof2.6mg,thusthemeasureofmassofsulfurdioxidetoa1m3volumeofairwouldbe2.6mgper1millioncubiccm(or2.6mg/m3).Suchweightperunitvolumemeasuresarecommonlyreportedforsolidorliquidcontaminantssuspendedintheair.However,thismeasurecanstillbeusedwithgaseouscomponentsinair.Insomecasestheaircontaminantmayexistinboththegaseousandsolidorliquidphaseswithintheair.Theweightpervolumemeasureisoftenusedintheseinstances.
Additionalratiosofmeasurecanalsobeused.Forexample,asam3ofairhasamassofabout1.2kg,theweight-to-weightratioforthesulfurdioxideexampleabovewouldbeabout2.2ppmw.Onecouldalsoexpresstheratioofthenumberofsulfurdioxidemoleculestoairmolecules,butthisisseldomdoneinairpollutionscience.Theweightofanaircontaminantinacubicmeterofair(mg/m3)andthevolumeratio(ppmv,orjustppm)arenormallyused.table 2–2showssomeusefulcon-versionfactorsforchangingmg/m3toppmv.
variations in units of Measurement
Airpollutionscienceinvolvesseveraldisciplinesincludingmeteorology,chemistry,physics,ecology,biology,physiology, toxicology, andmedicine.Eachdisciplineusesitsownmeasuresforpollutantparticles,gases,orvapors.Meteorologistsareinterestedinemis-sionsmeasuredinmassorweightunits,soconcentra-tionsaremeasuredinunitssuchasmg/m3ofairorpartspermillionppmv.Chemiststendtouseunitssuchasmolespercubicmeterandatomsormoleculesperunitvolume.Physicistsmayusethenumber,mass,orsurfaceareaofparticlespercubiccentimeterand thepartialpressureofagas.Biologistsandphysiologists,whoareinterestedintheeffectsofairpollutantsonlivingsystems,usemeasuressuchasmassperunitvolumeofairandpartial pressureforgasesandvapors.Physiciansarefrequentlyinterestedindoses,sotheconcentrationsinorgansandtissues(e.g.,microgramspergramoftissueormassofpollutantdeliveredtoanindividualsubject)areofinterest.Althoughmanymoreexamplescouldbegiven,theimportantpointscanbemade:(1)anumberofmeasuresofpollutantsareincommonuse;(2)convert-ingunitsfromonemeasuretoanotherisoftenrequired.Thisintroductorytextwillusethosespecificunitsthatbestsuitthetopicathand.
observer-to-observer.Theyquantifytime,size,location,temperature,pressure,altitude,mass(orweight,whichismasstimestheaccelerationduetogravity),humidity,particlecount,andmanyothermeasurablefactors.Ratiossuchaspartspermillion(ppm)ormilligramspercubicmeter(mg/m3)arequantitative,andalsofrequentlyusedinairpollutionscience.
Todemonstratetheuseofmeasurementunits,con-sidersulfur.Thetotalmassof10billion,trillionsulfuratomsisonlyabout0.5grams.Incontrast,themassofsulfurreleasedinavolcaniceruptioncanbeseveralbilliongrams.Inordertoexpresssuchwiderangesofscale,powersof10(i.e.,exponents)areused.table 2–1providesthescientificnomenclatureassociatedwithpowersof10.Suchexponentsarecommonplace inairpollutionscience.
Powersof10arealsousedforexpressingratios.Forexample,1cubiccm(cm3)ofagasdispersedin1millioncubiccmofairis1partpermillion(ppmv,volume-to-volumeratio).Theconcentrationsofgas-eouscontaminantsintheairaretypicallyreportedasppmvvalues(usuallywithoutthesubscript,v).Toavoidconfusion, thinkofppmassimilar toapercentage.Insteadofaratioof1/100aswithapercent,ppmisaratioof1/1,000,000.Thescaleisdifferentbyseveralpowersof10.
Table 2–1 Powers of ten, using the International System of Units (SI) nomenclature.
Numerical Equivalent Prefix/Name Symbol
10-12 0.000000000001 pico/trillionth p10-9 0.000000001 nano/billionth n10-6 0.000001 micro/millionth µ10-3 0.001 milli/thousandth m10-2 0.01 centi/hundredth c10-1 0.1 deci/tenth d100 1 unity none101 10 deca/ten da102 100 hecto/hundred h103 1,000 kilo/thousand k106 1,000,000 mega/million M109 1,000,000,000 giga/billion G1012 1,000,000,000,000 tera/trillion T
Note: In the United Kingdom, 1 billion = 1012 (i.e. a million million), and 1 trillion = 1018 (i.e. a billion billion).
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III. Unpolluted vs. Polluted Air 25
iii. unPOLLutEd vS. POLLutEd Air
Clean Air, Can it be harmful?
Unpolluted (clean) tropospheric air isdefined intable 2–3.Ofthetwomajoratmosphericgases,N2andO2,oneisconsideredtobechemically inert(N2),andtheotheroxidizing (O2).However,N2 isnotalwaysbio-logicallyinert.Indeep-seadiving,wherethepressure
isseveralatmospheres,diversbreathingcompressedaircanbecomedisorientedduetothenarcoticeffectsofN2dissolvedinthefattytissueofthebrain.SoN2isbiologicallyinertatatmosphericpressure,buttoxicatelevatedpressures.Theuseof80percentheliumgasplus20percentO2indivingairpreventsgastoxicityproblemsatelevatedpressures.Similarly,O2isbenefi-cialatnormalpartialpressure(20.9percentof1atmo-sphere),buttoxicwhenbreathedforaprolongedtimeat
Table 2–2 When converting mg/m3 (mass of gas/volume of air) to ppm (volume gas/volume of air) multiply by k. Valid for 25°C and 760 mm Hg pressure.
PollutantGas ChemicalFormula GasMol.Wt.(g/mole) k=24.45/MW(ppm/[mg/m3])
Ammonia NH3 17.03 1.44Carbon dioxide CO2 44.01 0.556Carbon monoxide CO 28.01 0.873Chlorine Cl2 70.91 0.345Formaldehyde HCHO 30.03 0.814Hydrogen sulfide H2S 34.08 0.717Methane CH4 16.04 1.52Nitric oxide NO 30.01 0.815Nitrogen N2 28.02 0.873Nitrogen dioxide NO2 46.01 0.531Nitrous oxide N2O 44.02 0.555Oxygen O2 32.00 0.764Ozone O3 48.00 0.509Sulfur dioxide SO2 64.07 0.382
Table 2–3 The gaseous composition of dry and wet (100% RH) unpolluted air.
Substance ppmbyVolume,DryAir µgperm3,DryAir ppmbyVolume,WetAir
Nitrogen 781,000 9 × 108 757,000Oxygen 209,000 2.7 × 108 203,000Water 0 0 31,200Argon 9,300 1.5 × 107 9,000Carbon dioxide 315 5.7 × 105 305Neon 18 1.5 × 104 17Helium 5.2 8.5 × 102 5.0Methane 1.0–1.2 7.0 × 102 1.0Krypton 1.0 3.4 × 103 1.0Nitrous oxide trace trace traceHydrogen trace trace traceXenon trace trace traceOrganic vapors trace trace trace
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100percentconcentrationatapressureof1atmosphere.Intoxicology(thestudyofadverseeffectsofchemicals),notonlymustgasconcentrationsbeconsidered,butalsothegaspressures(orpartialpressuresofeachgasinamixture)mustbetakenintoaccount.Thus,thetoxicologyofagasorvaporinaspacecraft(lowambientpressure)orasubmarine(highambientpressure)maynotapplytootherenvironmentswithdifferentatmosphericpressures.
defining Air Pollutants
Air contaminants(alsoair pollutants)aredifficulttoconciselydefine.Theyexistinseveralformsincludingsolids,liquids,vapors(vaporsaregasesformedbyvol-atileliquids/solids),gases,ions,andmixturesoftheseprimarystatesofmatter.Pollutantsmaypersistintheaironlybriefly(e.g.,short-livedreactivechemicalspecieswithlifetimeslessthan1second),orforseveralyears(e.g.,verysmallparticlesandnonreactivegases).
What makes something an air pollutant? From aregulatory perspective,anairpollutantisasubstancethatis,ormaybe,presentataconcentrationthatexceedsitssafeconcentration.Also,fromaregulatorypointofviewtheairisnotnecessarilypollutedifnoneofitscon-stituentsareoutofcompliancewithanairqualitystan-dard.Notethattheairmayquicklygofrom“unpolluted”to“polluted”ifanairstandardistightened.Regulatoryagenciesmayrefertocriteria pollutants, air toxics,orhazardous air pollutants(HAPs)thathavepublishedstandardsthatareintendedtoprotectsusceptiblepopu-lationsorthegeneralpublic.CriteriaairstandardsarereviewedbytheU.S.EnvironmentalProtectionAgency(U.S.EPA)abouteveryfiveyears.HAPsarereviewedonlywhendeemednecessary.Workersareusuallyper-mittedexposuretohigherlevelsofairpollutantsthanthepublic,asworkersarehealthier(asagroup).Fortheprotectionofworkersfromairbornehazards,essentiallyanysubstancemayaddedatanytimetoliststhatproviderecommended(e.g.,ACGIH®,2010)airconcentrations.
Fromapractical perspective,anairpollutantcanbedefinedasanysubstance,regulatedornot,thatinter-fereswithaperson,process,oranobjectthathasvalue.Thus,forananalyticalchemistatraceofwatervaporintheairmaybeaninterferingpollutant.Foradeepseadiver,N2gasintankairmaybeapollutant.Andforamanufacturerofcomputerchips,verytinyamountsofparticlesintheairareseriouspollutantsthatmayaffectproductquality.Asthepracticalperspectivecan
includeessentiallyanyknownsubstanceasapollutant,it isimpracticaltoconsideritinthecontextofthistextbook:specialtypublicationsshouldbeconsultedasneeded.
Anairpollutantisasubstancethat,atrealisticenviron-mentalconcentrations,isknowntohaveadverseeffectsonhumans,otheranimals,vegetation,visibility,thecli-mate,orotherassets(suchasobjectsofart,machinery,orbuildings).
Becauseregulatedpollutantshavebeensubjectedtothemostintensiveresearch,theyareaprimaryfocusinthistextbook.IftheU.S.EPA,theOccupationalSafetyandHealthAdministration(OSHA),oranothermajorregulatorybodydeemssomethingtobeanairpollutant,sowill the authorsof thisbook.However, themainpointisthatboththesubstanceanditsconcentration,alongwithasubject’sexposureandsensitivity,arewhatactuallyproduceahealthproblem.
iv. Air POLLutAnt SOurCES And thEir EMiSSiOnS
terminology and Pollutant Source Categories
Thesourcesofairpollutantsarenumerousandvaried.Threecategoriesofsourcesmaybedefined:(1)natural(i.e.,thosethatarenotassociatedwithhumanactivities);(2)anthropogenic(i.e.,thoseproducedbyhumanactiv-ities);and(3)secondary(i.e.,thoseformedintheatmo-spherefromnaturalandanthropogenicairpollutants).Eachofthesethreecategoriesofairpollutantscanbefurthersubdivided.Forexample,anthropogenicpollutantsourcescanbeclassifiedasstationary,(e.g.,factories,farms,homes,etc.)vs.mobile(e.g.,cars,trucks,boats,aircraft,etc.).Othersubcategories,suchasindoorvs.outdoor, organicvs.inorganic,orlocalvs.regional,arealsoused.Thefollowingsectionswillprovideanover-viewofthesourcesandemissionsassociatedwiththeseandothercategoriesandclassesofairpollutants.
natural vs. Anthropogenic
table 2–4listssomemajorsourcesandannualnationalemissionestimates(inthousandsoftons)forsomeoftheairpollutantsthatareregulatedbytheU.S.EPA.Thenaturalsourcesofselectedairpollutantsareshownintable 2–5.Severalpointscanbemaderelatedtothesetables.Naturalsourcesaredifficult,ifnotimpossibleto
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IV. Air Pollutant Sources and Their Emissions 27
Table 2–4 Some major anthropogenic sources and emissions of ambient air pollutants in the United States in 1993, including primary particle sources and sources of precursor gases (sulfur and nitrogen oxides) and volatile organic compounds (VOCs) (EPA, 1996). PM10 refers to particles with diameters under 10 micro meters. SOx and NOx are oxides of sulfur and nitrogen, respectively. One ton equals 907 kg.
ThousandsofTons/Year
Source PM10 SOx NOx VOCs
Fuel Combustion Utilities 270 15,836 7,782 36 Industrial 219 2,830 3,176 271 Other sources 723 600 732 341Industrial Processes 553 1,862 905 3,091Solvent Utilization 305 43 90 10,381On-road Vehicles 197 438 7,437 6,094Off-road Vehicles 395 278 2,996 2,207Fugitive Dust Roads 22,568 Construction/Mining 11,368 Agriculture 7,236
Table 2–5 Some major global natural sources and emissions of air pollutants.
MillionsTons/Year
Source Particles Sulfur NOx CO
Dust & Soil 90–450 24Sea Spray 800 48Biological 70–180 108 3–30 40–400
ActionVolcanic * 5.5
EruptionsLightning 24Fires & Other * 35 100–5,700
Oxidation
Note:* = extremely large amounts are released.Data, in short tons (2,000 lbs, 907 kg), are from various
sources including: Finlayson–Pitts and Pitts (1986); U.S. EPA (2000).
control.Naturalemissionsareoftengeneratedatlocationsthatareunpopulated,orsparselypopulatedbypeople.Fortheseandotherreasons,theprimaryfocusofregula-torsisonstudyingandcontrollinganthropogenicsources.However,aproblemariseswhensecondarypollutants(formedintheair)areconsidered.Forexample,anthro-
pogenic(ornatural)SO2isaprecursorofH2SO4(sulfuricacid)andotheracidicsulfates.Butthenatural(andanthropogenic)pollutant,NH3(ammonia)reactswithH2SO4,andneutralizesitsstrongacidity.Proposednetreactionsinclude:
SO2 + H2O + ½O2 → H2SO4 (Eq. 2–1)
H2SO4 + NH3 ↔ (NH4) HSO4 (Eq. 2–2)
2H2SO4 + 3NH3 ↔ (NH4)3 H(SO4)2 (Eq. 2–3)
H2SO4 + 2NH3 ↔ (NH4)2 SO4 (Eq. 2–4)
Equations2–1to2–4representtheformation(andbackreactions)ofgases/vaporstosolidorliquidprod-ucts,inthiscasesulfatesalts.Thesesaltsaretypicallysecondarypollutantsformedbythereactionsofanthro-pogenicandnaturalemissions.Sometimes,itisdiffi-culttoisolatetherolesofhumanactivitiesinproducingpoorairquality.
The foregoingexample,which representsonly afewof essentially countless atmospheric reactions,demonstratestheimportanceofairchemistrymodelingtosupportregulations.AirchemistryiscoveredmorecompletelyinChapter3.
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particulatematterincludestationary-sourcefuelcom-bustion(includingmanagedburning),mobilesources,andindustrialprocesses(whichareresponsibleforabout10percentofthetotal).Sourcesthatarehighly-localized,suchaselectricpowerplantsandindustrialplants,areoftenclassifiedaspoint sources,whileagriculturaloper-ations andurbancenters aredistributed sources.Allsourcescanhaveasignificantimpactonlocalairquality.Thedistinction,pointvs.distributed,isimportantformodelinglocalairconcentrationsofpollutants.Ingen-eral,pointsourcesareeasiertoquantifyandtocontrolthanaredistributedsources.
Enclosed Settings and Workplaces
Overview
Airpollutionisnotjustanoutdoorproblem.Infact,theairinmanyenclosed environmentsismorecontaminated
Stationary vs. Mobile and Point vs. Distributed Sources
Anthropogenicpollutantsourcesareclassifiedasstationaryormobile.ThemajorstationarysourcesasdefinedbytheU.S.EPA(2000)include:
• electricutilitiesthatburnorganicfuels(notethatnuclear,hydroelectric,andwind-poweredutilitiesusuallydonotproduceairpollutants);
• industrialplantsthatburnorganicfuels;• chemicalmanufacturing;• metalsprocessing;• petroleumindustries;• otherindustries(agriculture,textile,wood,rubber,
electronic,construction,etc.);• solventusers(degreasing,graphicarts,drycleaning,
etc.);• storage(terminals,servicestations,chemicalstorage,
etc.);• wastehandling(incinerators,openburning,land-
fills,etc.);and• miscellaneous sources (forestry,health services,
accidentalreleases,repairshops,coolingtowers,etc.).
Mobilesources,whicharevehicles,include:
• on-road gasoline powered trucks, automobiles,andmotorcycles;
• on-roaddiesels;and• off-road vehicles (gasoline and diesel powered
automobilesandtrucks,aircraft,marinevehicles,andrailroadengines).
Foreachsource,dataaregatheredonpollutantssuchascarbonmonoxide;sulfurdioxide;ammonia;volatileorganiccompounds;nitrogenoxides;lead;particulatematter; and hazardous air pollutants. Figures 2–2 through 2–9depict2008U.S.emissionsforseveralairpollutants.Themajorsourceofcarbonmonoxideison-roadvehicles(about60percentofthetotal).Non-roadvehiclesemitanother20percent,andothersourcesemittheremainder.Vehiclesarealsomajoremissionsourcesfornitrogenoxidesandvolatileorganiccom-pounds.Electricutilitiesaremajoremittersofsulfurdioxide.Mostof the leademissionsare frommetalsprocessing,followedbywastedisposal/recycling,vehi-cles,andstationaryfuelcombustionsources.Mostoftheammoniaisemittedbylivestock,organicdecay,andfertilizer-related sources. Sources of anthropogenic
Highway vehicles,57%
Stationary fuelcombustion, 8%
Industrial and othersources, 9%
Non-road mobilesources, 26%
2008 U.S. carbon monoxide emissions
Figure 2–2 U.S.1998COemissions Source:U.S.EPA(2010).
2008 U.S. nitrogen oxides emissionsNon-road mobile
sources, 26%
Stationary fuelcombustion, 33%Industrial and other
sources, 9%
Highway vehicles,32%
Figure 2–3 U.S.1998NOxemissions Source:U.S.EPA(2010).
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IV. Air Pollutant Sources and Their Emissions 29
Figure 2–4 U.S.2008Volatileorganiccompoundemissions. Source:U.S.EPA(2010).
2008 U.S. volatile organic compounds emissions
Non-road mobilesources, 16%
Stationary fuelcombustion, 9%
Industrial and othersources, 54%
Highway vehicles,21%
Figure 2–5 U.S.2008SO2emissions. Source:U.S.EPA(2010).
2008 U.S. sulfur dioxide emissions
Stationary fuelcombustion, 85%
Non-road mobilesources, 4%
Highway vehicles,1%
Industrial and othersources, 10%
Figure 2–6 U.S.2008PM10(particlesunder10μmdiameter)emissionsfromnonfugitivedustsources.
Source:U.S.EPA(2010).
2008 U.S. non-fugative PM10 emissions
Stationary fuelcombustion, 20%
Industrial and othersources, 55%
Highway vehicles,9%
Non-road mobilesources, 16%
Figure 2–7 U.S.2008PM2.5(particlesunder2.5μmdiam-eter)fromnonfugitivedustsources.
Source:U.S.EPA(2010).
Industrial and othersources, 45%
Non-road mobilesources, 28%
2008 U.S. non-fugative PM2.5 emissions
Stationary fuelcombustion, 15%
Highway vehicles,12%
Figure 2–8 U.S.2008Leademissions. Source:U.S.EPA(2010).
Non-road mobilesources, 45%
Stationary fuelcombustion, 7%
Industrial and othersources, 48%
2008 U.S. lead emissions
Figure 2–9 U.S.2008Ammoniaemissions. Source:U.S.EPA(2010).
Stationary fuelcombustion, 2%
2008 U.S. ammonia emissions
Highway vehicles,8%
Industrial and othersources, 90%
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than the localoutdoorenvironment.The reasons forthisare(1)thelimitedvolumesofdilutionair;(2)thelowwindspeedsindoors;and(3)thesometimesintenseindoorsources(e.g.,smoking,cooking,andcleaning).Althoughonemightthinkofresidencesasthemajoroccupiedenclosedsettings,workplaces,publicbuild-ings,andvehiclesarealsoplacesinwhichindoorexpo-suresoccur.
Time-activity patterns(howlongandwherepeopleare exposed) areused to estimatehumanexposures.Peoplespendabout90percentoftheirtimeinenclosedenvironments.Eachtypeofindoorsettinghasitsuniquecharacteristics,andimportantvariationsinsourcesandemissionsoccurwithineach.Considertwoworkplaces,anofficeandametalfoundry;theyhaveverylittleincommon.Similarly,theairqualityforanairconditioned,gas-heatedresidencewilldifferconsiderablyfromonethathasnoairconditioningandwherethesourceofheatcomesfromburningcoalorwoodindoors.Asimilarcontrastcouldbedrawnbetweenairqualityinanupscaleautomobileandanold“clunker.”Becauseenclosedsettingsaresovariable,thischapterwillcoveronlyafewspecificexamplesinordertoexplorebasicprinciples.
Residences
Incontrast tooutdoorairpollution,which isbothsource-dominated and meteorology-dominated, resi-dentialairpollutionissource-dominated.Pollutantsgeneratedinthehomearenotrapidlydispersedbythewind,andresidentialaircleanerscanseldomoverpoweruncontrolledpollutantsources.table 2–6listssomeofthemostcommonsourcesofresidentialaircon-taminants.Figure 2–10illustratessomeindoorsources.
Whetherornotthesesourcesproducehealthproblemsdependsontheaircontaminantconcentrations,whetherco-stresses (suchasexcessiveheat,cold,orextremehumidity)arepresent,andthesensitivityandgeneralhealthstatusoftheoccupants.
Allergensandirritants(table 2–7)canposeasignifi-cantresidentialproblem,especiallyforsensitive indi-viduals.Such“sensitives”includepeoplewithallergies,asthma,bronchitis,emphysema,respiratory-tractinfec-tions,andcardiovasculardiseases.These,andotherhealth-related conditions, may both impair normalrespiratorytractdefensesandleadtoexaggerated(evenlife-threatening) responses to modest levels of aircontaminants.Suchvulnerableindividualsmayrequireaverycleanairenvironment.Insomecases,medicaladviceandtreatmentbyaqualifiedallergistand/orapulmonaryphysicianisneeded.
Itiswisetocontrolindoorsourcesofaircontaminants,bothforthesakeofthehealthyresidentsandanysensitiveorotherwisecompromisedindividuals.table 2–8hasachecklistthatcanbeusedinthehome(alsotheschool,office,etc.)forreducingindoorsources.Inaddition,commercialaircleanerscanbeeffectiveifthemajorpollutantsourceshavebeencontrolled.Suchaircleanersshouldbeselectedfortheirair throughput rateandtheircleaning efficiency.Anaircleanerthatprocessesonlyafewcubicfeetofairperminutemaybetotallyineffec-tiveinaroomwithanairvolumeof3,000cubicfeet(8.5cubicmeters).Similarly,anaircleanerthatisnotcapable of removing fine particles (e.g., those fromsmokingorcooking)ororganicvapors,mayprovidelittlerelieftoindooroccupants.Anuncontrolledsourcewithina poorly ventilated and/or poorly filtered residence
Table 2–6 Common sources of residential air pollutants.
Pollutant Sources
Asbestos and other fibers Old insulation in/on ceilings, walls, stoves, pipes, floor tiles, heaters, etc.Lead Old paint, toys, and other commercial productsBiological aerosols Mold, pets, insects, rodents, people, humidifiers, indoor plants, etc.Volatile organic compounds
(including formaldehyde)Air fresheners, spray products, solvents, glues, new building-materials, paints,
printers, ink, etc.Combustion products Smoking, cooking, wood and gas fireplaces, water heaters, candles, incense, etc.Dust Vacuuming/cleaning, plants, dirt, outdoor air, etc.Gases Off-gassing from water and various products, electrical discharges, combustion,
outdoor air, gas appliances, etc.Radon Intrusion from soil, masonry, and underground water
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IV. Air Pollutant Sources and Their Emissions 31
GAS
1
2
3
4 8
7
9
10
12
13
13
1415
16
17
18
19
20
21
5
6
11
Figure 2–10 Somecommonsourcesofresidentialaircontaminantsinclude:(1)fireplace,candles,andincense;(2)vacuumingandcleaning;(3)smoking;(4)indoorpets;(5)pottedplants;(6)insects,radon,andmethane;(7)foodprepara-tion;(8)gasappliances;(9)storedfuel;(10)vehicles;(11)paint,thinner,etc;(12)humidifier;(13)carpetanddrapes; (14) bedding and furniture; (15) computer/printer; (16) air conditioner; (17) hobbies; (18) fish tank;(19)shower;(20)outdoorair;and(21)insulation.
Source:TheUniversityofCaliforniaAirPollutionHealthEffectsLaboratory,withkindpermission.
Table 2–7 Irritants and allergens in residences.
A.Irritants(examplesonly) Sources
Solvents, alcohols, etc. Cleaning and polishing agents, plastics, liquid fuels, hobbies that involve glue, paint and/or solvents, etc.
Formaldehyde Air fresheners, other spray products, solvents, glues, new building- materials, paints, printers, ink, etc.
Dust Vacuuming/cleaning, plants, dirt, outdoor air, etc.
B.Allergens(examplesonly)
Insect products (droppings, body parts) Dust mites, cockroaches, other insect infestationsPet-related Cat, dog, and rodent allergens from saliva, fur, droppings, bedding,
food, water dishesPlant-related Pollens, molds (from dead plant material and soil), volatile fragrances, etc.
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couldresultinarapidbuildupofcontaminantswithinthelivingspace.Thus,eliminationoreffectivecontrolofacontaminantsourceisoftenmorecriticaltoairqualitythanitsdilutionormechanicalremovalfromtheair.
Workplaces
Thevarietyofairpollutantsandtheirsourcesinwork-placesisgreatenoughtodefyanysuccinctsummary.Officesmayhavesolvents,ozone(fromprintersandcopiers),allergensfrominsectinfestations,dust,micro-organisms from ducts and air conditioners, carbonmonoxidefromair intakesnear truck loadingzones,andavarietyofaircontaminantsfromnearbyindustrial
operations. In addition, crowded offices will havehuman-generatedaircontaminantsfromclothingfibers,dander,coughing,andsometimesbody-generatedodors.Manufacturingoperationsmayproduceairbornesolvents,organicand inorganicdusts, exoticchemicals,metalfumes,andmanyothersubstances.Inaddition,heat,noise,vibration,andextremesinhumiditycanexacer-batethedirecteffectsofairpollutantsonworkers.
Manufacturingandotherheavyindustrialoperationsusually require theparticipationof trainedIndustrialHygieniststocontrolthepotentialrisks.Itisessentialthatworkplacesconformtomodernairqualitycriteriaaswellasstandardsforheat,noise,vibration,andother
Table 2–8 Indoor air pollutant control checklist.
_____ 1. House dust
_____ 2. Deteriorating cloth, rubber, wood, plastic, paper
_____ 3. Indoor animals (birds, dogs, cats, rodents, fish tank bubblers, etc.)
_____ 4. Pet bedding, food, water, and litter boxes
_____ 5. Sprays (air fresheners, paints, insecticides, cleaners, cosmetics)
_____ 6. Smoking (cigarettes, cigars, pipes) and burning incense and candles
_____ 7. Fireplaces, wood, coal, and kerosene stoves
_____ 8. Smoke from cooking food
_____ 9. Poorly-vented or broken ovens, stoves, heaters, clothes dryers, and water heaters
_____10. Dusty or soiled carpets, drapes, blankets, pillows, sheets, or mattresses
_____11. Dirty air filters, soiled or dusty air ducts
_____12. Dirty humidifier and dehumidifier water tanks
_____13. Standing water or evidence of mold
_____14. Damp cloth, paper, wood, carpets, walls, etc.
_____15. Indoor plants with pollen or mold growth on container or soil
_____16. Dust-catching decorations, stuffed toys, and drapery
_____17. Hobby-associated activities and materials
_____18. Paints and solvents that are not tightly sealed
_____19. Insects, including mites, ants, fleas, roaches, spiders, and flies
_____20. Poorly-ventilated rooms
_____21. Garbage and spills
_____22. Odorous building materials, insulation, carpets, drapes or furniture
Note: If completing this checklist does not resolve a residential air problem, air cleaners with sufficient throughput and efficiency should be used. Use of an air cleaner in the bedroom may be particularly effective, if the contaminant sources have been removed. When sensitive or ill residents are present, or when symptoms persist, professional medical help is needed.
Source:The University of California Air Pollution Health Effects Laboratory, with kind permission.
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IV. Air Pollutant Sources and Their Emissions 33
hazards.IntheUnitedStates,privateprofessionalorgani-zations, suchas theAmerican Conference of Govern-mental Industrial Hygienists(ACGIH®)andtheAmerican Industrial Hygiene Association(AIHA)publishvolun-taryguidelinesthatareapplicabletoworkplaces.Also,governmental organizations, such as the National Institute for Occupational Safety and Health(NIOSH),the Occu pational Safety and Health Administration(OSHA),theCenters for Disease Control and Prevention(CDC), the Mine Safety and Health Administration(MSHA),andnumerousstateagenciespublishimportantreports,guidelines,andregulations.Althoughthecostofmaintainingahealthfulworkplacemaybesubstantial,itisusuallynegligibletothealternative(i.e.,significantworker illnesses).A good example of air quality andotherworkplacerecommendationscanbefoundintheACGIH®publicationTLVs® and BEIs®(2010).TLVs®are8-houraveragedthreshold limitvalues(airconcentra-tions)nottobeexceededforaircontaminants,andBEIs®arebiological exposure indices,whichareconcentrationsinblood,urine,etc.,thatcanbemeasuredinworkerstodeterminetheiractualexposures.TheACGIH®publica-tionalsocoversother“agents”suchas(1)noise;(2)elec-tromagnetic radiation and fields (including lasers,ultravioletlight,andionizingradiation);(3)thermal(heatandcold)stress;and(4)ergonomics(lifting,vibration,etc.).Theseotheragents,ifnotcontrolled,canproducedirectharmandincreasetherisksassociatedwithexpo-suretoairpollutants.
Evenifalloftherecommendationsforworkplaceairarefollowed,someworkersmaynotbeadequatelyprotected.TheTLVs®andBEIs®acknowledgeandcau-tionthattherecommendationsaredesignedtoprotect“healthy”workingadults,andthattheymaynotprotectallworkers.Sensitiveindividualsmayrequirereassign-mentofduties,stringentlocalengineeringcontrols,andifallelsefails,additionalpersonalprotectiveequipment(e.g.,respiratoryprotection)toreduceexposures.
Criteria Air Pollutants vs. hazardous Air Pollutants
Criteria air pollutants (CAPs) and hazardous air pollutants (HAPs)arespecificagents thathavebeendefinedbylegislationsuchastheU.S.Clean Air Act,orsimilar international standards. In theUnitedStates,therearesevencriteriaairpollutants(seeExhibit6–1,Chapter6).EachonehasassociatedNational Ambient Air Quality Standards(NAAQS)thataretoberevisited
andpossiblyrevisedbytheU.S.EPAatleasteveryfiveyears.TheNAAQSincludeprimary pollutant criteriaforprotectinghumanhealthandsecondary pollutant criteriaforothereffectssuchasreducedvisibility,and/ordamagetomonuments,crops,orlivestock.PrimaryNAAQSmustprotect sensitive subpopulationsandincludeamargin of safety.ConsiderationsofthecostandfeasibilityofattainmentforprimaryandsecondaryNAAQSarecurrentlyprohibitedbylaw.
Hazardous air pollutants(HAPs),alsodesignatedbytheU.S.EPA,currentlycompriseabout200substances,includingbothspecificagents(suchasasbestos,benzene,andformaldehyde)andchemicalclasses(suchasarseniccompounds,cokeovenemissions,nickelcompounds,andradionuclides).ThedistinctionbetweenCAPsandHAPsistwofold:(1)CAPshavebeendeterminedtopresentageneralrisktothehealthofthepublic,andHAPsarebelievedtocauseadversehealthand/orenvi-ronmentaleffects;and(2)unlikeCAPs,HAPsmaybeaddedtoordeletedfromtheirlistings,andtheydonothavethemandatedfive-yearreviewcycle.
SimilarapproachestolistingairpollutantshavebeenestablishedbyCanada,theUnitedKingdom,andtheWorldHealthOrganization,tonameafew.However,nations differ in their standards, often significantly.Twomainpointsare(1)thatairstandardsareconstantlyevolving; and (2) that different approaches are usedthroughouttheworld.
Accidents and disasters
Anaccidentalreleaseofairpollutantscanproducea major health catastrophe for a local community.Explosions,fires,industrialcontainmentfailures,rail-roadcarderailments,andtruckingaccidentscanreleasesubstantial quantities of fuels, solvents, combustionproducts,radionuclides,and/ortoxicaircontaminants.Similarly,naturalaccidents,suchasvolcaniceruptions,earthquakes,forestfires,andhurricanescangeneratehighlevelsofairpollutants.Suchaccidentscantakehundredsto thousandsof lives.Warfareandterroristattacksmustalsobeincludedinthelistofcausesofairpollutiondisasters.Poisongases(e.g.,sulfurandnitro-genmustards,phosgene,chlorine,hydrogencyanideand nerve agents), biological aerosols (e.g., botulin,ricin,anthraxbacteria,andviruses),andradionuclides(fromatomic,hydrogenandso-called“dirty”bombs)areamongthepotentialairpollutants.Warfareagentsaresoughtbyterroristsinordertoachievetheirends.
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Airpollutionisnotsimplyaproblemcausedbyindustry,transportation,agriculture,andotheractivitiesthatareoftenessentialtomaintainingpublichealth.
Anespecially-tragicindustrialdisasteroccurredin1984inBhopal,India.Anexplosionatapesticidefacil-ityduringanatmosphericinversionreleasedtonsofmethylisocyanateintotheairofanearbycommunity,andabout200,000peoplewereexposed.Thehighly-irritantchemicalmostlikelyproducedover3,000deaths,includ-ingthoseatthetimeoftheexplosionandthoseoverthefollowingfouryears.ThousandsmoredelayedBhopalfatalitiesareprojectedintothefuture.Suchdisastersleadtopublicfear,andtheyresultinpressureongovern-mentstoprovidebetterprotection.
v. POLLutAnt trAnSPOrt
Overview
Thetransportofairpollutantsislargelydrivenbyweatherphenomena.Verticalairmotionsalongwithprevailingwindsbothdiluteanddisperseparticlesandgasesemittedfromanygivensource.Onaglobalscale,unequalsolarheatingcauseswarmairneartheequatortoriseandthendescendasitcoolsandtravelstowardthenorthandsouthpoles.Thiseffectalonewouldpro-ducewindcirculationtowardthepolesathighaltitudesandtowardtheequatoratlowaltitudes.Butseveralotherphenomenacomplicatetheglobalweatherpicture.TheEarth’srotationhastwoeffects,surfacefrictionthatdragssurfaceairinthedirectionofrotationandaCoriolis forcethat,ingeneral,turnsairmovementtotherightintheNorthernhemisphereandtowardstheleftintheSouthernhemisphere.TheCoriolis forceoccursasaconsequenceoftheEarth’srotation.Surfacecharacter-istics(e.g.,oceansandotherlargebodiesofwatervs.landareas) that modify the air temperature and moisturecontentalsoinfluencelargeairflowpatterns.Mountains,forests,andevencitiesaffectwindpatternsmorelocally;Figure 2–11depictsthemajorconvectivecellsandthegeneral climate systems.Although the principles ofweatherphenomenaareunderstood,long-rangeweatherpredictionsarehighlyuncertaindueto theeffectsofsmall-scalephenomena.Weatherisachaotic system,inthatsmallchangesininitialconditionscanproducelargelong-termconsequences.
Ifemittedparticlesandgasesstrictlyfollowedthewinds,concentrationsdownwindcouldbeaccuratelypredictedoverthetimescaleofafewdays.However,
suchpredictionsareriskybecauseairborneparticlesandgasescanseparatefromtheirairparcels(thevolumeofairintowhichtheywereemitted),duetodiffusionandsedimentation.Also,localmeteorologycaninfluencetheriseandtransportofaironalocalscale.Suchlocalmeteorology includes air inversions and convectivephenomena(asproducedbylocalheatingeffects,eddies,terraineffects,andotherphenomena).
Gasesandvaporsmorecloselyfollowwindpatterns,buttheyhavediffusionvelocitiesthatcancausethemtospreadbeyondtheairparcelintowhichtheyareemitted.
Particleswithlargeaerodynamicdiameters(20μmandabove;seeChapter3onaerodynamicdiameters)havebehaviorsstronglyinfluencedbygravityandbytheparticle’sinertia.Therefore,theyreadilysettleoutoftheairparcelsinwhichtheyareentrained.Particlesinthissizeregimesettleoutoftheairatvelocitiesthatexceed3mperhour.Thus,ifsuchparticlesareemitted
Subtropical high
Polar high
South pole
Subpolar low
Subtropical high
Intertropical convergence zone
Polar high
Subpolar low
Equator
30° N
30° S
60° S
60° N
North pole
Figure 2–11 The large-scale motion of the Earth’s atmo-sphere.Thismotion is influencedby thermalgradients,frictionbetweentheairandrotatingEarth,andtheCoriolisforce.
Source: The University of California AirPollutionHealthEffectsLaboratory,withkindpermission.
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V. Pollutant Transport 35
1mabovethesurfacetheywillsettletothegroundinabout 20 minutes, unless they encounter substantialupdraftsordescendingterrain.Smallparticles,e.g.,those1μmorsmallerindiameterhavesettlingvelocities(seeChapter3)oflessthanafewcmperhour.Suchparticlescantravelinthewindformorethanseveralkmbeforesettlingtotheground.Verysmallparticlescantravelthousandsofkmbeforesettlingoutoftheair.
Otherphenomenathatproducethelossofcontami-nantparticles,gases,andvaporsfromtheairinclude:
• evaporationofvolatileparticles;• chemicaltransformations;• capturebyvegetationandotherobjects(bothanthro-
pogenicandnatural);• capturebyprecipitation(rain,snow,etc.);and• attachmenttoparticlesthatsettleout.
gaussian Plume Model
TheGaussianplumemodel isused forestimatingdownwindpollutantconcentrationsemittedfrompointsources.Themodelisthree-dimensionalinthatdown-wind,crosswind,andverticaldispersingcomponentsareconsidered.Attheemissionpoint,pollutantdilutionoccursindirectproportionwiththewindspeed.TheplumeshapenearthesourceisGaussian(i.e.,bell-shapednormal-distributions)initscross-sections.Thestandarddeviationsofthenormaldistributionsincreasewithdistancefromtheemissionpointsource.Themodelisusefulforpredictingairpollutantconcentrationsdown-
windfromsmokestacks.However,thebasicmodeldoesnotincludepollutantlosses(orformations)intheplumecausedbychemicalreactionsandparticlesedimenta-tion.Chemicalreactionsinplumescanleadtosignifi-cantacidificationandhencedownwindaciddeposition(seeExhibit 2–1).
Plumes and Smokestacks
Plumesfromsmokestackspresentagoodcasestudyinwhichtoexamineairpollutanttransport.Increasingtheheightofasmokestackwillusuallydecreasethenear-stackgroundlevelconcentrationsofemittedparticlesandgasesandcauseemissionstodiluteanddepositfurtherdownwind,whichiswhysmokestackstendtobetall.Ambientairvelocityhaseffectsonstackemis-sions.Lowwindstendtoincreasenearbygroundlevelconcentrations,butathighwindspeedstheadditionaldilutionoftheemissionsdecreasesdownwindconcen-trations.Asanexample,ifthepollutantconcentrationdownwindfromapointemissionsourceis10mg/m3ofair,thendoublingthewindspeedshouldresultinaconcentrationof about5mg/m3,orhalf theoriginalconcentration.
Thebuoyancyofaplumeisafactorininitialplumerise.Awarmerorotherwiselower-densityplumewillrise toaheightwhereitmatches thedensityof theair.Interestingly,humidairhasalowerdensitythandryair.ThisisbecausethemolecularweightofH2Ovapor(18atomicmassunits)islessthanthatofboth
Exhibit 2–1 Aciddeposition(acidrain,snow,andaerosols).
Thedepositionofacidicairpollutioncanhaveadverseeffectsonsoilandfreshwaterlakesthataredownwindfromlargesourcesofsulfurdioxide,sulfuricacid,NO,NO2,andnitricacid.Aciddeposition,whichreferstothedepositionofrain,snow,fog,oracidaerosols,cancauseimmediateand/ordelayeddecreasesinthepHofwaterandsoil.Thedelayedeffectsaremainlyduetothemeltingofacidifiedsnowandthesubsequentrunoff.Theeffects,whichdependonthebufferingcapacityoflakesandsoil,includedecreases(orelimination)ofsensitivespeciesoffishanddecreasedgrowthofforests.TheEasternUnitedStatesandEasternEuropehavebeenmostheavilyimpactedbyaciddeposition,primarilyduetothepresenceofemissionsofacidsandacidprecursors.Emissioncontrols,e.g.,sulfurreductionsincoal,arepartiallydirectedtowardreducingtheadverseeffectsofaciddepositioninimpactedareas.
Thechemistryofacidrain,snow,fog,andaerosolshasbeenextensivelystudied.TheneutralpHofpurewater,i.e.,neitheracidicnorbasic,is7.0.Evenpristinerainhasaslightly-acidicpHof5.0to5.65,duetothenaturalCO2andothersubstancesintheair.Downwindofsometypesofindustriesandelectricpowerplants,thepHofraincanbeaslowas4.2.Thisacidityformsover time inplumes. Interestingly, tallersmokestackscanproducemoreacidicconditionsdownwindbecauseof thelongertimesavailableforacidstoform.
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N2(28atomicmassunits)andO2(32atomicmassunits),whichmakeupmostoftheair;therefore,watervapordisplacestheseheaviergases.
Whenthesmokestackemitsaplumeatalowupwardvelocityandatatemperatureanddensitynearambientconditionsonecanobservetheinteractionoftheplumewiththewindandtheverticalairtemperatureprofile.Figure 2–12showstwolikelyverticaltemperaturepro-filesintheatmosphere.Thesolidlineshowsthestandardlapse rate,whichisthenormaldecreaseinairtemperaturewithaltitudeinthetroposphere.Thestandardlapserateis9.8°Cperkm,butitcanvary.Thedashedlinerepresentsthetemperatureprofileinalow-level(400m)inversioncondition.Suchinversions,whichcanbelowerorhigherthan400m,arenotuncommon.Figure 2–13showsatopviewofatypicalsmokestackplumecarriedbyawindmovingfromlefttoright.Notethattheplumespreadsoutwardandisdilutedasittravelswiththewind.Theconcentrationofpollutantsintheplumeisusuallygreat-estalongitscenterline,taperingtolowconcentrationsatitsperiphery,aspredictedbytheGaussianplumemodel.Similarly,ifviewedfromtheside,thecenter-lineoftheplumewillhavethehighestconcentrationofstackemissions.
Figure 2–14showstheeffectofwindonaplumeinthenormallapse-ratecase.Withnowind,thetypical
plumewillriseandspreadlaterally.Inawind,theplumewillalsospreadas it isblown.Thespreadingplumemaytouchthenearbygroundifthesmokestackisshort,whichcanproducehighlevelsofemissionsatgroundlevelnearthestack.
Figure 2–15 demonstrates plume behavior in aninversionconditionwhenthesmokestackisaboveorbelowtheinversionheight.Asfortheshortsmokestack,anemissionbelowtheinversionlayercanproducesub-stantiallocalground-levelconcentrations.Theconditionofalowinversionheightandanevenshortersmokestackiscalledtrapping.
0 2 4
Distance downwind (km)
Top view
6
Figure 2–13 Topviewofapoint-sourceplumeinalightwind. Source: The University of California Air
PollutionHealthEffectsLaboratory,withkindpermission.
Tall stack,no wind
Tall stack,light wind
Short stack,light wind
A. B. C.
Figure 2–14 Plumesfrom:A:tallstackwithnowind;B:tallstackwithalightwind;andC:shortstack,withalightwind.
Source: The University of California AirPollutionHealthEffectsLaboratory,withkindpermission.
0
500
1000
Alti
tude
in m
eter
s 1500
2000
5 10
Neutrallapse rate
15
Temperature �C
20 25 30
Inversion topat 400 m
Figure 2–12 Variationofairtemperaturevs.heightabovetheEarth’ssurface.Theslopeofthesolidlineistheneutrallapserateof9.8°Cperkm.Thedashedline depicts a hypothetical inversion layer at400mabovegroundlevel.
Source: The University of California AirPollutionHealthEffectsLaboratory,withkindpermission.
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VII. Quiz and Problems 37
dispersionalsoapplytootheremissionpointsources,suchasfactories,vehicles,andfires.
vi. SuMMAry OF MAjOr POintS
ThesurfaceoftheEarthhasalimitedairvolume,thetroposphere,whichsupportslife.Abovethetroposphere,the stratosphere is also essential to life because itshieldsthesurfacefromharmfulradiationsandhelpstostabilizethetemperatureoftheplanet.Severalscientificdisciplines,eachwiththeirownnomenclature,studyairpollutantsintheatmosphere.Airpollutionstudiesrequirequantitationandpreciseunitsofmeasurementinordertodevelopreliableknowledgeandtodeviseacceptableairqualitystandards.Thereareseveralwaystodefinetheterm“airpollution”dependingonone’sperspective.Regulated(e.g.,criteriaandtoxic)airpol-lutantsareamainfocusofmodernresearch.Airpol-lutantsareemittedbyavarietyofsources,whichmaybe“natural”or“anthropogenic,”“outdoor”or“indoor,”“stationary”or“mobile,”and“point”or“distributed.”Enclosedspacesandworkplacesarehighlyvariedwithrespect to sources and emissions of air pollutants.However,duetothelackofeffectivedilutionandwinddispersal,strictsourcecontrolisusuallyneededinordertoprotectoccupantsintheseenvironments.Althoughgovernmentalregulationhasbeeneffectiveincontrol-ling“normal”emissions,periodicaccidentsandnaturaldisastersaddtothecontinuinghealth-relatedtollofairpollution.
Thetransportofaircontaminantsmustbeconsideredinorder tounderstandtheirdownwindconcentrations,andthusexposuresofpeople,animals,andplants.Oneaspectoftransportthathasbeenwellstudiedisthedisper-sionofplumes.Smokestackplumesaredispersedundertheinfluenceofmeteorologicalconditions(e.g.,windspeedandverticalairtemperatureprofiles)andsmoke-stackdesign(specificallysmokestackheightabovethesurface).
vii. Quiz And PrObLEMS
Quiz Questions
(select the best answer)
1. The“troposphere”:a. isatermthatdescribestheuppermostregion
oftheEarth’sair.
Figure 2–16showstheeffectofthestrength(steepnessoftheairtemperatureprofile)oftheenvironmentallapserate.Ifthelapserateisstrong,loopingoftheplumecanoccur,whichcancausetheplumetodescendtothesurface, rise, and descend again. If the lapse rate isweak,theplumetendstoremainaloft.
Themostseriousconditions,suchasashortsmoke-stack,anemissionbelowalowinversion,andastronglapserate,havethepotentialforproducinghighground-levelconcentrationsofemissions.Intheidealcasethesmokestackwillbetallenoughtoallowsubstantialdilutionoftheplumebeforeitreachesthesurface.Theexamplesgivendemonstratejustsomeofthefatesofsmokestackplumes.Theprinciplesofsmokestackplume
Effect of stack height
Inversion layer
A. B.
Figure 2–15 Effectofstackheight:A:aboveinversionlayer;andB:belowinversionlayer.
Source: The University of California AirPollutionHealthEffectsLaboratory,withkindpermission.
Effect of lapse rate on a smokestack plume
A. B.
Figure 2–16 Effect of lapse rate on a smokestack plume:A:forastronglapserateinwhichthedecreaseintemperaturevs.altitudeismuchgreaterthannormal,producingloopingoftheplume;B:foranormallapse-ratecondition.
Source: The University of California AirPollutionHealthEffectsLaboratory,withkindpermission.
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c. negligible in comparison to outdoor airpollution.
d. independentoftheactivitiesofoccupants. 9. Theuseofaircleanersindoors:
a. isthebestwaytodealwithbuilding-relatedillnesses.
b. istheprimarymeansofcontrollingindoorairqualityinthehome.
c. isagoodmethodforcontrollingindoorcar-bonmonoxide,butnotindoorallergens.
d. areeffectiveifthemajorsourcesofairpollut-antshavebeenremovedandthefilteringrateandefficiencyaresufficient.
10. TheU.S.EPA’sdesignatedhazardousairpollut-ants(HAPs):a. arealsocalled“secondaryNAAQS.”b. isalistofsubstancesthatcanchangethrough
bothadditionsanddeletionsbytheU.S.EPA.c. includeclassesofairpollutants,butnotindi-
vidualsubstances.d. havebeendeterminedtocauseadverseenvi-
ronmental effects but not adverse humanhealtheffects.
11. Howdoestheheightofasmokestackinfluencethe ground-level concentrations of its emittedparticlesandgases?a. Itisnotanimportantfactor.b. It isonly important if there isan inversion
condition.c. It is only importantwhenwind speeds are
low.d. Noneoftheabovearetrue.
12. Which meteorological factors are importantin influencing ground-level air pollutantconcentrations?a. precipitation.b. windspeed.c. inversions.d. Alloftheabovearetrue.
Problems
1. Convertthefollowingtoppm.10percent100percent1ppb
b. isover1,000kmthick.c. providestheairinwhichtheEarth’sliving
thingsexist.d. consistsof80percentoxygenand20percent
ozone. 2. Anairinversioniscausedby:
a. stagnantwinds.b. lowatmosphericpressure.c. coolerairontopofwarmerair.d. warmerairontopofcoolerair.
3. Thethreeaircontaminants,ozone,sulfurdioxide,andcarbonaceousfineparticles,are:a. onlynaturalaircontaminants.b. onlyanthropogenicaircontaminants.c. both natural and anthropogenic air con-
taminants.d. neithernaturalnoranthropogenicaircon-
taminants. 4. Howdoairpollutantconcentrationsof10-3and
10-6mg/m3comparetoeachother?a. 10-3isathousandtimesgreaterthan10-6.b. 10-6istwotimesgreaterthan10-3.c. 10-3istwotimesgreaterthan10-6.d. 10-6isthreetimesgreaterthan10-3.
5. Whatfactorscanclassifyasubstanceasanairpollutant?a. presenceintheair.b. interferencewithhumanhealthorwelfare,
damagetomaterialsorobjectsofvalue,orinterferencewithimportantscientificprocesses.
c. bothaandb.d. Noneoftheabovearetrue.
6. Howwouldoneclassifythepopulationofcross-countrymotorcyclesassourcesofairpollution?a. stationary,distributed,andnatural.b. mobile,distributed,andanthropogenic.c. mobile,point,andnatural.d. stationary,point,andanthropogenic.
7. Themajoranthropogenicsourcesofparticulateairpollutantsare:a. stationary-sourcefuelcombustion.b. mobile-sourcefuelcombustion.c. volcaniceruptionsandnaturalfires.d. bothaandb.
8. Indoorairpollutionis:a. source-dominated.b. meteorologydominated.
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VIII. Discussion Topics 39
references and recommended reading
ACGIH® (American Conference of GovernmentalIndustrialHygienists),ACGIH®, TLVs®, and BEIs®,American Conference of Governmental IndustrialHygienists,Cincinnati,OH,2010.
Costa,D.L.,“Airpollution,”inCasarett and Doull’s Essentials of Toxicology,Klaassen,C.D.,andWatkins,J.B., III, eds., McGraw–Hill, New York, 2003,Chapter28,pp.407–418.
Finlayson–Pitts,B.J.andPitts,J.N.Jr.,Atmospheric Chemistry: Fundamentals and Experimental Tech-niques,JohnWiley&Sons,NewYork,1986.
Gammage,R.B.andBerven,B.A.,eds.,Indoor Air and Human Health, 2nd Edition,LewisPublishers,BocaRaton,FL,1996.
Grant,L.D.,Shoaf,C.R.,andDavis,J.M.,“UnitedStatesandinternationalapproachestoestablishingair standardsandguidelines,” inAir Pollution and Health,Holgate,S.T.,Samet,J.M.,Koren,H.S.,andMaynard,R.L.,eds.,AcademicPress,SanDiego,CA,1999,Chapter42,pp.947–982.
HindsW.C.,Aerosol Technology: Properties, Behavior and Measurement of Airborne Particles, 2nd Edition,Wiley–Interscience,NewYork,1999.
Lippmann,M.andMaynard,R.L.,“Airqualityguide-linesandstandards,”inAir Pollution and Health,Holgate, S.T., Samet, J.M., Koren, H.S., andMaynard,R.L.,eds.,AcademicPress,SanDiego,CA,1999,Chapter43,pp.983–1017.
(NOAA)NationalOceanicandAtmosphericAdmin-istration,NationalAeronauticsandSpaceAdminis-trationandU.S.AirForce,U.S. Standard Atmosphere,1976,NOAA–S/T76–1562,WashingtonDC,1976.
Perkins, J.L., Modern Industrial Hygiene, Vol. I: Recognition and Evaluation of Chemical Agents, 2nd Edition,AmericanConferenceofGovernmentalIndustrialHygienists,Cincinnati,OH,2008.
Rom,W.N. andMarkowitz,S., eds.,Environmental and Occupational Medicine, 4th Edition,LippincottWilliams&Wilkins,Hagerstown,MD,2006.
Samet, J.M. and Spengler, J.D., eds., Indoor Air Pollution: A Health Perspective, Johns HopkinsUniversityPress,Baltimore,MD,1991.
Scaillet,B.,Arevolcanicgasesserialkillers?Science,319:1628–1629,2008.
Seinfeld,J.H.andPandis,S.N.,Atmospheric Chem-istry and Physics, 2nd Edition,Wiley–Interscience,NewYork,2006.
2. If the Earth and its atmosphere shrunk to thesize of an apple, how thick would the tropo-spherebe?
3. Howmuchtimeisrequiredforanaircleanerwithathroughputairrateof15cubicfeetperminute(1cubicfoot=0.0283m3)tofilterthevolumeofairinaroom20feetby20feetby10feet(1foot=0.305m)?
4. Using Table 2–4, estimate the percent of totalPM10emissionsthatcomefromvehicles.
5. Ifanasthmaticchildlivedinyourhome,namesixsourcesofairpollutantsthatshouldbeeliminatedorgreatlyreduced.
6. Recommendationsforchildrenatschoolincludeallowingthemtogooutsideduringrecesseveninsmoggycities.Howcanthisrecommendationbejustified?
7. If gasoline-powered cars were all replaced byelectric vehicles, what air pollutants would bereduced?Whatairpollutants,ifany,wouldnotbereduced?
viii. diSCuSSiOn tOPiCS
1. Whatarethemajorsourcesandemissionsofairpollutants in your community? Do the sourcesbenefitthecommunity?Howwouldonedecideon whether or not a specific pollutant sourceshould be shut down or required to reduce itsemissions?
2. What jobs/occupations expose workers to thepoorest air quality? Contrast the air quality-relatedhazardsforanelementaryschoolteacher,afarmer,aparamedic,andaconstructionworker.Whichoccupationismostlikelytodeveloplungdisease?
3. Shouldindoorpottedplantsberecommendedfortreatingpeoplewithasthma?Discusstheprosandconsassociatedwithyourselection.
4. Cantheairinacitybetooclean?5. You are charged with the task of designing a
smokestackforanewchemicalplantthatwillbebuilt somewhereneara largecity.Theadversepublichealtheffectsareaconcern.Whatfactorswouldyoutakeintoaccountthatwouldinfluenceyourdesign?
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40 Chapter 2 SourCeS and emiSSionS of air pollutantS
2ND REVISE
U.S.EnvironmentalProtectionAgency,WashingtonDC,1991.
U.S. EPA (United States Environmental ProtectionAgency) National Air Pollutant Emission Trends,EPA–454/R–00–02,U.S.EnvironmentalProtectionAgency,officeofAirQualityPlanningandStandards,ResearchTrianglePark,NC,2000.
U.S. EPA (United States Environmental ProtectionAgency),Our Nation’s Air: Status and Trends Through 2008, EPA–454/R–09–002, U.S. EnvironmentalProtectionAgency,ResearchTrianglePark,NC,2010.
Sidel,V.W.,Onel,E.,Geiger,H.J.,Leaning,J.,andFoege,W.H.,“Publichealthresponsestonaturalandhuman-madedisasters,”inPublic Health and Pre-ventive Medicine, 13th Edition, Last, J.M., andWallace,R.B.,eds.,Appleton&Lange,Norwalk,CT,1992,Chapter74,pp.1173–1186.
Stern,A.C., ed., Air Pollution, Vol. I., 3rd Edition,AcademicPress,NewYork,1976.
U.S. EPA (United States Environmental ProtectionAgency)Building Air Quality: A Guide for Building Owners and Facility Managers,EPA/400/1–91/033,
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