Environmental Chemistry Acid rain APCH211 Dr PG Ndungu Acid Rain Acidic Deposition “Acid rain" – General term applied to any form of wet precipitation, usually in the troposphere, with acidic species stronger than CO2 ± Includes rain, sleet, snow, fog, or dew ± ± Wet deposition Acid rain is particularly damaging to lakes, streams, and forests and the plants and animals that live in these ecosystems. Nitrogen species: NOx Sources include burning of fossil fuels, biomass, etc Sulfur Species SO2 H2S, & CS2: ± Natural Sources; Anorexic waters, t soils, il etc t NH3 ± If the acidic chemicals in the air are blown into areas where the weather is wet, the acids can fall to the ground in the form of rain, snow, fog, g or mist. In areas where the weather is dry, the acid chemicals may become incorporated into dust or smoke and fall to the ground through dry deposition sticking to the ground, buildings, homes, cars, and trees. Later, when moisture content i increases, acid id solution l ti iis produced. d d Aqueous and dry deposition are collectively termed acid deposition The precursors or chemical forerunners of acid rain formation result from both natural sources, such as volcanoes and decaying vegetation and man-made sources, primarily emissions of sulfur dioxide (SO2) and nitrogen oxides (NOx) resulting from fossil fuel combustion. ± Can have deposition of dry gases and compounds – so called dry deposition ± refers to acidic rain, fog and snow. Natural pH of rain water ~ 5.6 (from dissolved CO2) Main Culprits in Acidic Precipitation Dry deposition Animal excreta, fertilizers and microbiological release ± Fossil fuels & sulfur ore smelting The principle reaction sequence contributing to production of nitric acid starts with nitric oxide, NO from combustion processes. Nitric oxide Chemistry: Daytime NO is oxidized by O2, O3 or ROO – e.g. This NO2 radical can then contribute to ozone and OH radical production i.e. plays a role in smog formation NO + O3 Æ NO2 + O2 Wetlands and submerged soils Dimethylsulfide, (CH3)2S, carbonyl sulfide, COS, methyl mercaptan, CH3SH and Dimethyl disulfide, CH3SSCH3. ± Atmospheric Production Of Nitric Acid Ocean and soils. Short lifetime, thus smog events don’t last, & not that frequent Main removal sequence for NO is via catalyst (M), OH rxns NO2 + OH + M Æ HNO3 + M 1 Nitric acid Production at Night Key species is the nitrate radical (NO3). Formed via O3 & NO2 Atmospheric production of dinitrogen pentoxide (N2O5) occurs when NO3 reacts with NO2 is the only way to form in the atmosphere. atmosphere N2O5 is a store of NO3. Reactions of NO3 with hydrocarbons Easily removes an H from alkanes o NO3 + RH Æ R + HNO3 o The R radical can then react with O2 to form peroxyl radicals With alkenes the NO3 radical reacts via an addition mechanism producing nitro-oxy substituted organic radicals which can regenerate NO2, or relatively stable organic nitrate compounds (see - Paul S. Monks. Gas-phase radical chemistry in the troposphere. Chem. Soc. Rev., 2005, 34, 376-395, for e.g. with propene) o NO3 + CnH2n Æ CnH2nNO3 o With aldehydes, typically form nitric acid and the corresponding radical o Overall nighttime chemistry of NO3 can recycle NOx, or form HNO3, depending on the mix of hydrocarbons Can decompose back to NO3 and NO2 NO3 + RCHO Æ RCO + HNO3 Can react with water to form nitric acid Can be a nighttime source of OH radicals o Easily zapped by the rising sun! (λ ~ 600 -700nm) Removal of Nitric Acid Atmospheric Production of Sulfuric Acid Oxidation of reduced sulfur species • ¾ Removal is accomplished by either wet or dry deposition ¾ One of the main contributors to acid precipitation. ¾ Nitric acid can react with ammonia: ¾ The ammonium nitrate, NH4NO3 can act as a condensation nucleus for the formation of a water droplet or it can be deposited as part of the solid aerosol • NH3 + HNO3 Æ NH4NO3 Production of sulfuric acid is more complex than that of nitric acid as the starting materials cover a wide range of reduced sulfur and partially oxidized sulfur compounds. These include hydrogen sulfide, carbon disulfide, carbonyl sulfide, methyl mercaptan, di th l disulfide, dimethyl di lfid and d dimethyl di th l sulfide. All these compounds contain sulfur in its oxidation state (-2). • Mostly from natural sources S H Sequence of Reactions of Sulfur Cmpds • Once sulfur compounds are in the air, a sequence of reaction begin as follows: SH + O3 Æ SHO + O2 CS2 + OH Æ COS + SH SHO + O2 Æ SO + HOO COS + OH Æ CO2 + SH The SO radical can then react with either O2, O3 or NO2 to give SO2 and other products. The above reactions release thionyl radical, SH as the initial product. Importance of OH! Hydrogen sulfide and carbon disulfide unlike carbonyl sulfide, are very reactive and therefore are quickly consumed 2SO + O2 Æ 2SO2 SO + O3 Æ SO2 + O2 SO + NO2 Æ SO2 + NO NB. SO2 is ultimately converted to sulfuric acid, H2SO4. S C S O C S More About SOx… • Dimethyl sulfide is produced by phytoplankton living in surface waters of the ocean. It is oxidized by hydroxyl radical (OH) with a final product being sulfuric acid. • Sulfur dioxide SO2 is also released in large quantities directly into the atmosphere from sulfide ore smelting and fossil-fuel combustion. SH + O2 Æ SO + OH H2S + OH Æ H2O + SH NB: Further oxidation of thionyl radical eventually produces sulfur dioxide: H Where is the OH coming from? 2 Peer to Peer Assignment: Mount Pinatubo Reducing Acid Rain There are several ways to reduce acid rain (i.e. acid deposition). These range from government policy to societal changes and individual action. e.g. given by epa (http://www.epa.gov/acidrain/reducing/): Understand acid deposition deposition’ss causes and effects • • Clean up smokestacks and exhaust pipes • Use alternative energy sources • Restore a damaged environment • Look to the future • Take action as individuals Recycle, Reuse, Reduce or the 3 R’s of waste management has evolved from the initial concepts championed in the 1970’s & now includes, amongst other things, prevention & minimization The steps involved in reduction of acid deposition are: Steps to solve acid deposition problem Reducing Acid rain Understand acid deposition’s causes and effects understand acid deposition’s causes and effects, and to track changes in the environment. Scientist Æ collect air, water & soil samples and measure them for various characteristics such as pH and chemical composition, and investigate the effects of acid deposition on human-made materials. Scientists Æ understand the effects of sulfur dioxide (SO2) and nitrogen oxides (NOx), and any other acid causing species People to understand the process of how acid rain damages the environment (Need to educate Policy Makers!). People to find out what changes could be made to the air pollution sources that cause the problem (Need to educate Policy Makers!). WHY? Almost all of the electricity that powers modern life comes from burning fossil fuels such as coal (Over 80% in RSA), RSA) natural gas, and oil. Sulfur dioxide (SO2) and nitrogen oxides (NOx) are the main acid chemicals. • • Use alternative energy sources • Other sources of electricity besides fossil fuels. They include nuclear power, hydropower, wind energy, tidal, geothermal energy, and solar energy. • Alternatives to internal combustion engines • batteries, solar cells, and fuel cells Options for reducing SO2 emissions, include: using coal containing less sulfur, washing the coal, and using devices called “scrubbers” to chemically remove the SO2 from the gases leaving the smokestack. Power plants to change type of fuels e.g, burning natural gas creates much less SO2 than burning coal. Steps to solve acid deposition… Steps to solve acid deposition… b) Clean up smokestacks and exhaust pipes a) Restore a damaged environment c) NB! It takes many years for ecosystems to recover from acid deposition, even after emissions are reduced and the rain pH is restored to normal. There are some things that people can do to bring back lakes and streams more quickly. i kl • Limestone or lime (a naturally occurring basic compound) can be added to acidic lakes to “cancel out” the acidity. Liming, has been used extensively in Norway and Sweden. NB: All sources of energy have environmental costs as well as benefits. 3 Steps to solve acid deposition… • e) Take action as individuals Yes! You too can make a difference! 9 Turn off lights, computers, and other appliances when you're not using them (Unplug chargers when not in use!). 9 Use energy-efficient appliances for lighting, air conditioners, heaters, refrigerators, washing machines, etc. If the depositions are reduced, reduced environmental protection agency (EPA) scientists must assess the reductions to make sure they are achieving the anticipated results. 9 Use public transportation, transportation or better yet, yet walk or bicycle whenever possible 9 Buy vehicles with low NOx emissions, and properly maintain your vehicle (In the News, Mercedes, VW, etc, complaining RSA fuel quality has too much sulfur for latest technologies). If no changes, to consider additional ways to reduce emissions that cause acid deposition. Example: focus on energy efficiency and alternative energy. 9 6. Be well informed. Evaluation of the progress made on acid rain reduction process d) Monitoring Very Important! • • Steps to solve acid deposition… WHAT ABOUT TALKING TO GOVERNMENT What Policies, Programs, or commitment in general has RSA made (PEER TO PEER ASSIGNMENT)? The Chemistry of Urban & Indoor Atmospheres THE CHEMISTRY OF URBAN AND INDOOR ATMOSPHERES Urban & Indoor Atmospheres… Use of petroleum products especially in motor vehicles result in groundlevel emissions of carbon monoxides, volatile hydrocarbons, nitrogen oxides and sometimes, lead compounds. These emissions are accompanied by aldehydes and other secondary pollutants. The combustion of biomass and coal produces substantial concentrations p of solid particulate matter along with nitrogen oxides, polyaromatic hydrocarbon (PAHs) compounds as well as sulphur dioxide. Open burning refuse or garbage cause air pollution is a source of volatile organic carbon compounds and solid particulate matter (SPM). Hurricanes and wind are the source of particulate matter such as dust especially in dry areas. The chemical composition of air in places where people live & work (urban areas, homes, offices, etc) vary with modernization or industrialization of the locality. Urban areas are likely to be affected by atmospheric pollution due to the following major factors: Combustion of fossil fuels (mostly cars) In-space heating and cooling Power generation and industrialization Incineration of waste materials Pollutants In The Urban Atmosphere World Health Organization (WHO) Standards for Air Quality The WHO guidelines for air quality take into account time period over which measurements is done. This is known as human exposure. Potential toxicity depend on both atmospheric concentration and duration of contact with the atmosphere. That is; Exposure = Concentration x time 4 Quality guidelines The quality guidelines must specify the acceptable concentration to be exposed to humans over a specified period. Example: carbon monoxide at 20mg.m-3 (20ppbv) may be acceptable if exposure time is 1 hour but not acceptable t bl ffor llonger period i d times. ti For longer exposure such as 8hrs, the allowed concentration of carbon dioxide should not exceed 10mg.m-3, that is, 0.01ppmv or 10ppbv. WHO works closely with United Nations Environmental Program (UNEP) to carry out air quality monitoring. Table 1 is a summary of WHO guideline values for air quality-values in µg.m-3 or parts per trillion in volume (pptv). Pollutant Max. time Average weighted time (µg/. m-3) SO2 500 10 min CO 30,000 1 hr NO2 400 1 hr O3 150-200 1 hr SPM (black smoke) 100-150 24hr SPM=Suspended particulate matter TSP=Total suspended particulate RSP; PM10 150-230 24hr RSP = Respirable suspended particulate, PM10 with particle size Pb 70 24hr < 10µm 0.5-1 1yr TSP Updated values (2005) can be found at: http://www.who.int/mediacentre/factsheets/fs313/en/index.html You Need it! Air quality parameters Suspended Particles Matter (SPM) •Concentration of atmospheric particulates is severe in some megacities (cities > 10million population) and average levels may range from 200 to 600 µg.m-3 or pptv. Carbon Monoxide (CO): depend on high traffic density – vary from city to city. Sulphur dioxide (SO2): Usually produced by coal. Sulfur dioxide conc. Is low in cities that use low coal fuels Nitrogen dioxide (NO2): Higher levels expected indoors with poor ventilation where kerosene or natural gas used for heating and cooking. Ozone (O3): from reaction of gases in the troposphere; trace amounts may result from mass transfer from stratosphere. Lead (Pb): Airborne lead depends on the population of cars, the concentration of lead additives in the fuel and availability of unleaded fuel. Concentrations in leaded gasoline vary between 0.1 and 2.0 g.L-1. •Human health associated with high values depend on the nature of particulates. particulates Examples: those derived from coal and those in the PM10 or PM2.5 categories, have been shown to be hazardous. NB: PM10 is particulate matter size < 10µm ; PM2.5 < 2.5µm. NB. Use of tetraethyl lead to augment the octane number (?) is becoming less. More info from: http://www.bbc.co.uk/dna/h2g2/A16407173 You Need it! Major factors that determine the quality of indoor air INDOOR AIR QUALITY • Many people spend most of their time indoors (home, office, etc.). The atmospheres encountered indoor vary a great deal. • The materials of house construction may vary from clay-rich soils or other fresh or baked earth materials. • In some cases cases, the homes are open and air exchange is rapid while in others heating may be done over an open fire in a room without a chimney and also a variety of fuels may be used. • The building materials may range from bricks, stones, wood, various plastics and metals. • Activities in the homes include: cleaning, cooking, heating over open or closed fires with varying smoke conditions. • • • • • • The nature of the ambient air, outdoor around the building plays a role. In this case, the outdoor atmosphere is influenced by air outside. Design and site of the building is important. This will dictate the quality of exchange of indoor atmosphere. Nature of materials present in the building such as polymers. The latter could be a source of formaldehydes or other partially oxidized organic compounds. Building materials from clays, clays concrete, concrete etc., etc may contain traces of radioactive elements such as uranium. Activities that take place inside the house. These may include combustion of wood for heating, cooking gas, electric cookers, etc. Cleaning of the house may involve mechanical devices such as vacuum cleaner, that create dust. Use of cleaning solvents and detergents, insecticide sprays, toilet sprays and air fresheners. Another reference you will need: Indoor Air Quality Guidelines: selected pollutants(PDF) http://www.who.int/indoorair/publications/en/index.html 5 COMMON INDOOR AIR CONTAMINANTS Radioactivity Air contaminants refer to levels above the outdoor background level. 1. Radioactive compounds: • Radioactivity is usually associated with Radon noble gas, Rn released by Uranium isotope 238 and also by Thorium isotope 232 with half-lifes of 4.5 and 14 billion years, respectively. These elements are found in geological materials such as rocks and fossils Radioactive elements Radioactive elements, such as uranium (239U) thorium (234Th) and potassium (40K) break down (decay) fairly readily to form lighter atoms e.g Be, B. The energy that is released in the process is made up of small, fast-moving particles and high-energy waves. These particles and waves are, of course, invisible. (The level of radioactivity of an element varies according to how stable its atoms are). Other elements with naturally occurring radioactive forms, (isotopes) are carbon (C13), bismuth (210Bi), radon (223R) and strontium (88Sr). Example: Calculation of HalfHalf- Life of Radioactive Elelemnts • Consider strontium-90 which has a half-life of approximately 28 years. Initially, at time t=0, the sample is 100% strontium-90 • After 28 years, only half the original amount of strontium will remain: ½ x 100% = 50% • After another 28 years, only half of this amount of strontium-90 will remain: ½ x 50% = 25% • After another 28 years, only half of this amount of strontium will remain: ½ x 25% = 12.5% • and so on. • At any given time, the amount of strontium-90 that has undergone decay can be calculated: amount of strontium-90 decayed = the original amount the amount remaining. The spontaneous emission of particles and/or energy from atomic nuclei. The spontaneous emission of radiation from the nucleus of an atom. Radionuclides lose particles and energy through this process of radioactive decay. Conti… Radioactivity process Radioactivity is a random process that happens naturally as the isotopes in particular elements decay. The isotopes continue to break down over time. The length of time that is taken for half of the nuclei in an element to decay is called its 'half-life'. A half half-life life can be very short (milliseconds to hours) or very long (hundreds of thousands of years). Radiation also arises from nuclear fission. Fission can be spontaneous but is usually initiated in a nuclear reactor. Fission is a radioactive process; it releases energy as the heavy nucleus is split into two. Calculations The amount of radioactive isotope remaining can be calculated: Nt = No x (0.5)number of half-lives Nt = amount of radioisotope remaining No = original amount of radioisotope number of half-lives = time ÷ half-life Example p Calculate the percentage of strontium-90 remaining after 280 years. Nt = No x (0.5)number of half-lives Nt = ? % No = 100% number of half-lives = time ÷ half-life = 280 ÷ 28 =10 Nt = 100 x (0.5)10 = 0.098% 6 Strontium-90 half-lifes Strontium-90 half-lifes % % Number StrontiumTime Strontiumof Half90 that (years) 90 lives has remaining decayed 0 0 100 0 1 28 50 50 2 56 25 75 3 84 12.5 87.5 4 112 6.25 93.75 5 140 3.125 96.875 6 168 1.5625 98.4375 2. Volatile Organic Compounds (VOCs) 3. Polybrominated diphenyl ether Sources are: Polybrominated diphenyl ether (PBDE) is toxic. General structure is shown below. PBDE is used in commercial household products such as plastics casings for appliances, in fabrics used for clothing, carpets, etc. • Paints: toluene, ethylbenzene, 2-isopropanol and butanone. • Cleaning agents: households solvents, detergents. • Wood-building materials such as plywood produce formaldehyde. Chemical structure of PBDEs Conti…air contaminants 4. Emissions from indoor combustion. 5. Indoor particulates These include: solid aerosols from dust; combustion of coal & biomass material. This is combustion of fuel that contains VOCs; burning of coal, wood and biomass. • Tobacco smoking is a source of many VOCs iincluding l di aldehydes, ld h d ketones, k t organic i bases b such h as nicotine, organic acids. Particle size is usually in the range PM10 (<10µm). Particle size <2µm, can easily enter p y track. respiratory • Smoking contributes to respirable particulate matter inside a building. • Polyaromatic hydrocarbons emitted from coal & biomass. (PAHs) are 7 Particles in the atmosphere • Particulate is a term that has come to stand for particles in the atmosphere. • Particulate matter makes up the most visible and obvious form of air pollution. • Particles in the atmosphere range from 0.5 mm (size of sand) down to molecular size level (nanometer). • Particles may consist of either solids or liquid droplets. • Atmospheric aerosols are solid or liquid particles smaller than 100 µm in diameter. • Pollutant particles in the 1 nm to 10 µm range are commonly suspended in the air near sources of pollution such as the urban atmosphere, industrial plants, highways and power plants. Nature of particles • • D ESC R IPT IO N PA R T IC L ES Very small solid particles include (1 nm-10 µm ): carbon black, silver iodide, combustion nuclei, sea-salt nuclei- tend to be acidic. Larger particles include (100 µm -500 µm ) : cement dust, wind blown soil dust, foundry dust and pulverized coal- tend to be basic. • Li id particles-mist, Liquid i l i include i l d raindrops, i d fog f andd sulfuric lf i acid id mixture • Particles of biological origin: viruses, bacteria, bacterial spores, fungal spores and pollen. • Important atmospheric contaminants- mainly inorganic and organic particles. Effects of atmospheric particles… OF A TM O SPH E R IC T erm s 1. A erosol M eaning Colloidal-sized atm ospheric particle 2. C ondensation Form ed by condensation of aerosol vapors or reactions of gases. 3. D ispersion Form ed by grinding of solids, aerosoll atom t ization i ti off liquids li id or dispersion of dusts. 4. Fog D enotes high level of w ater droplets 5. H aze D enotes decreased visibility due to presence of particles 6. M ists Liquid particles 7. Sm oke Particles form ed by incom plete com bustion of fuel Effects of atmospheric particles • Effects on climate • Damage buildings • Impact on human health (people with asthma) • Reduced visibility & causes undesirable aesthetic effects NB: Aerosols, natural and anthropogenic, can affect the climate by changing the way a radiation is transmitted through thro gh the atmosphere. atmosphere Physical behaviour of particles All aerosols both absorb and scatter solar and terrestrial radiation. • If a substance absorbs a significant amount of radiation, as well as scattering, it is called absorbing. Small colloidal particles undergo diffusion processes and coagulate together to form larger particles. • This is quantified as the ratio of scattering alone to scattering plus absorption (extinction) of radiation by a particle. Mechanism for removal of particles from the atmosphere is mainly through sedimentation & scavenging by rain drops and then precipitation. • Particle size refers to diameter of the particle but in some cases radius may b used. be d 8 Composition of Inorganic Particles Process for particle formation • Physical Process: particle formation is mainly through disintegration of larger particles > 1 µm • Many dispersion aerosols originate from natural sources: sea-spray, windblown dust, volcanic dust. • Chemical process: Inorganic particles are mainly metal oxides formed by oxidation of the metal by oxygen. • • Aluminium oxide, iron oxide, calcium oxide and silicon dioxide are due to soil erosion, rock dust, coal combustion. • Carbon particles- due to incomplete combustion • Sodium and chlorine compounds- due to marine aerosols • Antimony and selenium- due to combustion of oil, coal or refuse. • Lead from combustion of leaded fuels & wastes Organic particles are produced mainly through internal combustion engines. N.B. Recall: PHOTOCHEMICAL SMOG Composition of Organic Particles A wide variety of organic compounds most of which are toxic: polycyclic aromatic hydrocarbons (PAHs) such as benzo(a)pyrene, chrysene, benzo-fluoranthene, acridine. Control of Particulate Emissions • Removal of particulate matter from gas streams is the most practiced means of air pollution control. • Techniques for removal depends on particle size, loading, nature of particles and type of scrubbing system. Radioactive particles • Main source of radionuclides in atmosphere is randon: it is a noble gas produced from radium decay. • Cosmic rays in the atmosphere produce radionuclides which are isotopes of: 7Be , 10Be, 14C, 39Cl, 3H, 22Na, 32P and 33P Methods of particle removal Air Pollution Control for Particulate Emissions These include: • Sedimentation and inertia, i.e gravitational settling as a continuous process. • Particle filtration using fabric filters that allow gas molecules to pass through but retain the particulate matter. • Scrubbers- this involves use of scrubbing liquid which forms small droplets g gp particles from the g gas stream. for scavenging It is possible to minimize emissions of aerosol particles from point of source such as thermal electrical generating stations or industrial smelting units. Containment of particulate matter is achieved using devises that remove the aerosols from fast moving stack gas stream. Common collection methods include: settling chambers, cyclones, fabric filter, scrubbers, and electrostatic precipitators as shown in the slides that follow. 9 Settling Chambers Are the simplest and commonly used. Advantages ± Types of Settling Chambers Simple to build, low cost, low maintenance, low pressure drop, simple to dispose of collected materials Disadvantages Construction includes variety of baffles and open space designed to allow the particles sufficient time to settle under the force of gravity. Settling rates are limited by gravity therefore method effective for large particle size >10µm. They come in different design. The mechanism include adsorption and absorption. ± Simple expansion chamber Multiple-tray settling chamber. Limited to removal of particles larger than40-60 μm diameter Supp Slide 1 Combustion Momentum Separators These differ slightly from your typical settling chambers via the addition of simple chamber features that allow for directional changes in air flow that add a downward inertial force to supplement the gravitational force. Supp Slide 2 Fabric Filters: Filtration Fabric filter or bags operate in a similar principle as vacuum cleaner. The air stream is made to pass thro a porous fabric material and is effective for particulates size in the range 0.01 - 10µm range. Bags or fabric filters are sensitive to temperature and humidity. The fine particles clog the filters and there4 must be periodically cleaned. Advantages Disadvantages High Collection Efficiency (>99%) Effective for a Wide Range of Dust Types Modules Can be Factory Assembled Operates Over Wide Range of Gas Flow Rates • Reasonably Low Pressure Drop • Good Efficiency for Small Particles • Dry Collection and Disposal • • • • • • • • • Filtration Large Footprint Temperature Limitations Requires Dry Environment Fire or Explosion Potential High Maintenance Cost 10 Electrostatic Precipitator Electrostatic precipitator causes the particles in a gas stream to become charged by electrons produced thro an electrical discharge between two electrodes. The negatively charged particles then migrate to the positive electrode and are collected and removed from the emission stream. Positively charged particles move to negative electrode. Advantages Disadvantages High Collection Efficiency Dry Collection and Disposal Small Pressure Drop Capable of Handling Large Gas Flow Rates • Low Electrical Power Requirements • Low Maintenance • Disadvantages • High Capital Cost • Particle Resistivity Limitations • May Require Injection of SO3 or NH3 to Control Resistivity • Relatively Large Footprint • Special Precautions for Safe Operating at High Voltage • • • • Absorption Method Scrubbers Scrubbers allow gas stream to be in contact with a fine mist or spray of water. The water droplets capture many small particles and these settle more rapidly into a collector container. Scrubbers come in different designs as shown below. Advantages Disadvantages • High Collection Efficiency • Capable of Handling Flammable and Explosive Dusts • Can Handle Mists • Low Maintenance • Simple Design and Easy to Install • Provides Cooling for Hot Gases • Neutralizes Corrosive Gases and Dusts • Waste Water Must be Treated • Collected Particulates are in Sludge Form • High Corrosion Potential • High Pressure Drop • May Require Protection Against Freezing • Final Exhaust Must be Reheated • Sludge Disposal May be Expensive Adsorption Electrostatic Precipitator Liquid Scrubber 11 Cyclones Cyclones are cone-shaped devices that cause the waste gas stream to swirl rapidly in spiral fashion causing larger particles to move towards the wall of the cone by centrifugal force. Stokes Law νt = ( ρ p - ρ a ) C g d 2p 18η Where Once in contact with the wall, the particles slide down the inner surface of the cone to a collection container below it. vt = terminal velocity of particles in m.s-1; Stoke’s law determines the extent of removal of particles but the settling rates can be greatly enhanced by the increased force due to cyclone action. In this case removal of particles <10µm can be achieved. C = Stokes correction factor for assuming spherical shape and discontinous of fluid interactions when the particle size is small compared with the molecular mean path in air. pp = density d it off particle ti l in i g.cm-33 Pa = density of air = 1.2 x 103 g.m-3 at Po and 25° C; g = acceleration due to gravity = 9.8 m.s-2 dp = particle diameter in meters and = viscosity of air = 1.9 x 10-2 g.m-1.s-1 at P° and 25° C Cyclone Combustion Minimize Emission from point Source: example SO2 EXAMPLE: Sulfur Dioxide Control Minimize emissions of aerosol particles from point of source such as thermal electrical generating stations or industrial smelting units. http://www.apt.lanl.gov/projects/cctc/factsheets/puair/adflugasdemo.html 12 Clean Coal Technologies Advanced Flue Gas Desulfurization Demonstration Project - e.g. of a series of initiatives Others Include ± Carbon Capture and storage ± Underground coal gasification Why Clean Coal? Coal Usage CO2 Sequestration In RSA Coal used to generate over 85% of th electricity the l t i it Globally Coal accounts for more than 40% of Electricity produced Impact of Coal Mining ± Water scarcity ± Water Pollution Burning ± Only realistic technology for next 20 – 50 years SOx, NOx, particulates, CO2, fly ash Underground Coal Gasification (UCG) Historically a lot of the work was done in the former USSR Resurgence in interest (China, Australia, Europe, Americas & RSA • • • • Clean and treat the CO2 then store it Currently used in enhanced oil recovery Options to use saline (very salty) aquifers Abandoned coal mines, other geologic caverns etc SASOL Majuba http://www.eskom.co.za/live/content.php?Item_ID=14077 13