environmental chemistry ib option e. e1 air pollution e 1.1 describe the main sources of carbon...
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Environmental Environmental ChemistryChemistry
IB Option EIB Option E
E1 Air PollutionE1 Air Pollution
E 1.1 Describe the main sources of carbon E 1.1 Describe the main sources of carbon monoxide (CO), oxides of nitrogen (NOmonoxide (CO), oxides of nitrogen (NOxx), ), oxides of sulfur (SOoxides of sulfur (SOxx), particulates and ), particulates and volatile organic compounds (VOCs) in the volatile organic compounds (VOCs) in the atmosphere.atmosphere.
E 1.2 Evaluate current methods for the reduction E 1.2 Evaluate current methods for the reduction of air pollution.of air pollution.
Too Much of a Good ThingToo Much of a Good Thing
E.1. Air Pollution
Composition of unpolluted air: 78% Nitrogen 21% Oxygen 1% Argon 0.03% Carbon dioxide Trace amounts of other gases +4%water vapour
Primary air pollutants: Carbon monoxide(CO) Oxides of nitrogen(NOx):N2O, NO, NO2
Oxides of sulfur(SO2) and SO3(oxidation of SO2) Particulates Hydrocarbons and volatile organic compounds
E.1.1E.1.1 Describe the main sources of carbon monoxide (CO), Describe the main sources of carbon monoxide (CO), oxides of nitrogen (NOx), oxides of sulfur (SOx), particulates oxides of nitrogen (NOx), oxides of sulfur (SOx), particulates and volatile organic compounds (VOCs) in the atmosphere.and volatile organic compounds (VOCs) in the atmosphere.
Air pollutant = any chemical in such concentration (greater than its natural levels) in the air that it produces an harmful effect on the environment i.e. humans, animals, vegetation or materials.
Primary air pollutant = an air pollutant which is a waste product from a human activity and which is added directly into the air (as opposed to a secondary air pollutant which is formed in the air as a product of a chemical reaction of a primary pollutant in the air).
E.1.1. Sources:Check out Table 25.2 for a great summary of sources
Carbon Monoxide:
Natural: Incomplete oxidation of methane, produced by anaerobic bacteria from decaying organic material:
CH4 + 1 ½ O2 => CO + 2 H2O
Man-made( Anthropogenic sources): Incomplete combustion of fossil fuels used in internal combustion engines and coal fired electrical generating facilities.
C8H18 + 8 ½ O2 => 8CO + 9 H2O
Oxides of Nitrogen:
Natural: Electrical storms and biological processes.
Man-made: High T inside combustion engines cause a direct reaction between atmospheric oxygen and nitrogen.
Oxides of sulfur:
Natural: Oxidation of hydrogen sulfides produced by decaying organic material and volcanos.
Man –made: Combustion of sulfur containing coal by smelters (furnace) and power plants.
Particulates:
Natural: Soot, ash, dust,asbestos,sand,smoke,pollen,bacterial and fungal spores.
Man-made: Burning fossil fuels, particularly coal and diesel.
Volatile Organic Compounds (VOC’s) aka Hydrocarbons:
Natural: Trees and plants(rice) emit hydrocarbons known as terpines.
Man-made: Unburned or partially burned gasoline, fuels, solvents escaping or evaporating.
E.1.1. Sources:
E.1.1. Effect on HealthCarbon Monoxide: Prevents hemoglobin from carrying oxygen to the cells. Oxides of Nitrogen: Respiratory irritant leading to respiratory tract infections Oxides of Sulfur: Respiratory irritant leading to respiratory tract infections
Particulates: Affects the lungs and the respiratory system causing emphysema, bronchitis, and
lung cancer
Volatile Organic Compounds (VOC’s) aka Hydrocarbons: Some (e.g.benzene) are carcinogenic. Some may form toxic secondary air
pollutants such as PAN’s.(peroxyacetyl nitrate)
Crash Course Nitrogen and Phosphorus Cycles: http://www.youtube.com/watch?v=leHy-Y_8nRs&index=10&list=PL8dPuuaLjXtNdTKZkV_GiIYXpV9w4WxbX
Respiratory Diseases
E.1.2E.1.2 Evaluate current methods for the reduction of air pollution.Evaluate current methods for the reduction of air pollution.
I. Catalytic Converters on vehicles: CO , Oxides of Nitrogen and VOCs Science Channel Deconstructed: http://www.youtube.com/watch?v=rmtFp-SV0tY
The hot exhaust gases are passed over a catalyst of Pt, Rh, or Pd.These fully oxidize CO and unburned volatile organic compounds, VOCs, and catalyse the reaction:
2CO(g) + 2NO(g) => 2CO2(g) + N2(g)
E.1.2E.1.2 Evaluate current methods for the reduction of air pollution.Evaluate current methods for the reduction of air pollution.
I. Catalytic Converters on vehicles: CO , Oxides of Nitrogen and VOCs
Burning fuel releases nitrogen oxides, CO and VOCs (HCs)
1. Stage 1:1. Platinum & rhodium plates are used to…
2. Withhold one atom…
3. Creating N2 and O2
2. Stage 2: 1. Platinum and palladium plates are used to…
2. Help the oxygen (created from stage 1) and hydrocarbons (VOCs) combust…
3. Creating CO2 and H2O
E.1.2E.1.2 Evaluate current methods for the reduction of air pollution.Evaluate current methods for the reduction of air pollution.
Electrostatic Precipitation( Particulates) Particulates are solid or liquid particles suspended in the air. Larger particles can be allowed to settle under the influence of gravity in
sedimentation chambers. Smaller particles can be charged and be attracted to oppositely charged
electrodes, which are shaken periodically so that the aggregated particles fall to the bottom of the precipitator where they can be removed.
E2 Acid DepositionE2 Acid Deposition
E 2.1 State what is meant by the term acid E 2.1 State what is meant by the term acid deposition and outline its origins.deposition and outline its origins.
E 2.2 Discuss the environmental effects of acid E 2.2 Discuss the environmental effects of acid deposition and possible methods to counteract deposition and possible methods to counteract them.them.
Acid deposition refers to how acidic particulars leave the atmosphere. A well known example is acid rain.
The term “acid rain” was coined in 1872 by Robert Angus Smith, an English scientist who observed that acidic precipitation could damage plants and materials.
However it wasn’t around the 1960’s or 70’s that acid deposition become a serious environmental issue, when scientist discover low ph level in lakes and streams.
Acid Rain
Natural rain is acidic with a pH level around 5.6.
H2O+CO2 H2CO3
Only a very small percentage is in rain. Typical acid rain has a pH level of 4.0 and pH level of 4.2 in lakes wouldn’t be able to support life.
DRY DEPOSITION Dry Deposition refers how
the acidic particulars leave the atmosphere without the presence of precipitation.
These particulars leave the atmosphere due to gravity, and these acidic gases such as sulfur dioxide have a direct harmful effect on the environment because the gases haven’t dissolved in the rain water.
WET DEPOSITION Wet deposition refers how
the acidic particulars leave the atmosphere through precipitation. Either by rain, snow, or fog.
The main source of acidity in the atmosphere is sulfur oxides produced from power plants. These sulfur acidity react with react in rain water.
Two types of acids are formed from there sulfur oxide.
SO2 + H2O H2SO3 Sulfurous acid
orSO3 + H2O H2SO4 Sulfuric Acid
Nitrogen oxides also contribute to acid rain. These nitrogen oxides are formed from vehicle engines. This gas combines with hydroxyl radical then forms with nitrous acid. HNO2
Acid deposition effects the environment in 5 ways:
1. pH level of lakes and streams, and organism in them
2. The availability of metal ions in the soil, and therefore affects nearby plant life and water
3. Directly affects plant life
4. Affects buildings & other structures
5. Affects human health
A pH level below 5.5 would kill some species of fish like Salmon, also kill algae and zooplankton which depletes the food for larger organisms. At low pH levels eggs are unable to hatch.
The pH of soil is a key factor whether or not if plants will grow.
Not only does it damage the soil, it lowers the amount of nutrients that plants need. Acid deposition directly affects of plants by turning leaves brown and reduces photosynthetic ability of the plant
Majority of historical buildings are made of limestone and marble which are forms of calcium carbonate which acid rain erodes.
CaCO3+H2SO4 CaSO4+H2O+ CO2 As for metallic building those made of iron or
steel are readily attack by acid deposition by both dry and wet deposition.
Dry depositionFe+ SO2+ O2 FeSO4
Wet depositionFe + H2SO4 FeSO4 + H2
To counteract acid deposition is by reducing the amount of sulfur and nitrogen oxides released in the atmosphere.
Nitrogen oxides have been reduce from vehicle emissions using catalytic converters.
EPA’s acid rain program focuses on power plants, the largest single source of SO2 emissions, and a major source of NOx emissions by issuing permits to power plants of the amount of emissions being released.
Limestone or calcium hydroxide is being use to increase the ph level in soil and lakes.
E3 Greenhouse EffectE3 Greenhouse Effect
E 3.1 Describe the greenhouse effect.E 3.1 Describe the greenhouse effect.
E 3.2 List the main greenhouse gases and their E 3.2 List the main greenhouse gases and their sources, and discuss their relative effects.sources, and discuss their relative effects.
E 3.3 Discuss the influence of increasing E 3.3 Discuss the influence of increasing amounts of greenhouse gases on the amounts of greenhouse gases on the atmosphere.atmosphere.
The greenhouse effect is supposedly the cause of global warming by trapping in high concentration of greenhouse gases, and by doing so it raises earth’s average temperature which could cause natural disasters.
Greenhouse effect is necessary to keep earth hospitable because it able to maintain heat.
However some argue that man has disturbed the natural equilibrium of atmosphere causing the earth to become warmer.
E.4.3. Greenhouse Effect The incoming radiation from the Sun is short wave UV and visible radiation.Some reflects back but some is
absorbed by the atmosphere before it reaches the surface. The energy reflected from the Earth is a longer wavelength infra red radiation. Greenhouse gases allow the passage of incoming short wave but absorb some of the reflected IR and re-radiate
it back to the Earth’s surface See Table on the next slide
http://youtu.be/Hi3ERes0h84
The contribution of a greenhouse gas to the warming of the atmosphere depends on three factors.
1. The amount of gas in the atmosphere
2. The ability of the gas to absorb infrared radiation.
3. The lifetime of the gas molecules in the atmosphere, before they have been chemically removed.
GWP or Global Warming Potential is a measurement of how much heat a green house gas can trap in the atmosphere.
Water Vapor, H2O - The most important greenhouse gas and about 1 to 4% is contains Water Vapor. Its GWP is 0.1 and estimates that it contributes 36 to 75% of global warming.
Carbon Dioxide, CO2- only .035% is in the atmosphere and has the GWP of 1, but more effective at absorbing infrared radiation than water. More importantly CO2 absorbs infrared in a window of wavelengths which water cant absorbed. However an increase of concentration of Carbon Dioxide disrupts the equilibrium absorption and transmission in the atmosphere.
Some human activities have increase the concentration.1. The amount of fossil fuels be burn in the atmosphere2. Manufacture of cement and concrete involves the thermal
decomposition of calcium carbonate to calcium oxide, releasing CaO2 (CaCO3 CaO + CO2)
3. Deforestation in the tropics lowers the rate of photosynthesis. Estimates that CO2 contributes 9% to 26% of Global Warming
Methane, CH4 - The concentration in the atmosphere is around 1.7 X 10-4 though its GWA is 72 but is remove from the atmosphere quickly. Methane is form when cellulose decomposes anaerobically from bacteria.
This reaction can occur from several human activities. 1. Rice cultivation2. Cows3. Leaking gas pipes 4. Fermentation of organic material in covered landfills Though its contribution ranges 4 to 9%
Nitrous oxide, N2O - has a GWP of 296 that can last over 100 years. Its less efficient at absorbing inferred radiation. Its concentration is at .031% however it is increasing. However only contributes 5% of global warming effects. Humans accounts of 10% of the Nitrous oxide being released.
1. Nitrogen-based fertilizers2. Decomposition of organic matter3. Naturally produced by bacteria from the ocean and
the soil
Chlorofluorocarbons, CFC’s- CFC is an important greenhouse gas. This gas is less damaging to the Ozone but has a higher GWP than CO2
1. Human: coolants (in refrigerators and air-conditioners), aerosols, foaming agens
2. Natural: none Ozone, O3-The production of ground level ozone
has dramatically increased since the industrial age. This ozone is formed by the action of sunlight on hydrocarbons and nitrous oxide from the burning of fossil fuels. This helps increase the greenhouse effects.
Gas Main source Heat trapping
Effectiveness compared with CO2
Overall contribution to increased GW
H2O (main)
Evaporation ocean and lakes 0.1 -
CO2
(main)Combustion fossil fuels and biomass 1 50%
CH4 Anaerobic decay of organic matter caused by intensive farming
30 18%
N2O Artificial fertilizers and combustion of biomass
150 6%
O3 Secondary pollutant in photochemical smogs
2000 12%
CFCs Refrigerants, propellants, solvents, foaming agents
10,000-25,000 14%
The increase of green house gases results in the temperature increases and then the sea level increases for two reasons.
1. It causes the acceleration of the polar ice caps melting and deposit in the ocean.
2. As the ocean warms up, the water in them will occupy more volume.
Glaciers undergo a seasonal melting and
refreezing cycle as temp vary throughout the year. Increased melting increases erosion and risks of flooding downriver. A particular problem in low-lying countries.
Because of the increase of greenhouse gases the humidity and rainfall also increases.
This causes a greater chance of fungal crop diseases and migration of tropical insects to higher latitudes.
In addition an increase of weed growth leading to a greater use of herbicide. There is a greater chance of extreme weather like flooding, and storms that can lead to soil erosion that would ruined harvest.
In tropical regions temperature increases may lead fertile land becoming a desert
These are some effects of global warming however there could be more consequences.
http://youtu.be/VuH-ThmNUjM
Gas Main source Heat trapping
Effectiveness compared with CO2
Overall contribution to increased GW
H2O Evaporation ocean and lakes 0.1 -
CO2 Combustion fossil fuels and biomass 1 50%
CH4 Anaerobic decay of organic matter caused by intensive farming
30 18%
N2O Artificial fertilizers and combustion of biomass
150 6%
O3 Secondary pollutant in photochemical smogs
2000 12%
CFCs Refrigerants,propellants,solvents,foaming agents
10000-25000 14%
E4 Ozone DepletionE4 Ozone Depletion
E 4.1 Describe the formation and depletion of E 4.1 Describe the formation and depletion of ozone in the stratosphere by natural processes.ozone in the stratosphere by natural processes.
E 4.2 List the ozone-depleting pollutants and E 4.2 List the ozone-depleting pollutants and their sources.their sources.
E 4.3 Discuss the alternatives to CFCs in terms E 4.3 Discuss the alternatives to CFCs in terms of their properties.of their properties.
E.4. Ozone Depletion D.4.1. Formation and depletion of ozone in the stratosphere:
(CFC’s and oxides of NOx from combustion engines, power stations and jet airplanes)
The ozone layer occurs in the stratosphere between about 12km and 50km above the surface of the Earth. Stratospheric ozone is in dynamic equilibrium with oxygen and is continually being formed and decomposed.
Formation: UV(high energy)
O=O(g) ---------------> 2 O ● (g)
O ●(g) + O2(g) --------> O3(g)
The oxygen free radicals are very reactive. The bonds in ozone are weaker so UV light of less energy breaks them. When they are broken, a reverse process happens forming back oxygen and the radical.
Depletion:
Ozone is depleted in two ways: UV(low energy)
O3(g) ---------------> O2(g) + O●(g)
O3(g) + O●(g) -----------> 2O2(g)
Overall the rate of production of ozone is equal to the rate of ozone destruction
The formation and depletion of ozone absorbs a wide range of UV so the ozone layer protects the surface from damaging radiation.
E.4.2. Ozone Depleting Pollutants
Pollutants :
Chlorofluorocarbons (CFCs)
Nitrogen oxides (NOx)
Sources:
Propellants for aerosol sprays Refrigerants They are volatile and chemically
inert in the troposphere
Nitrogen-based fertilizers Decomposition of organic matter Naturally produced by bacteria
from the ocean and the soil
E.4.3. Alternatives to CFC’s
Montreal Protocol (1987) CFCs banned.CFC’s , low reactivity-remain atmosphere for 80 years.Destroy ozone layer( UV breaks C-Cl bond)
The alternatives should have low reactivity, similar properties but no bonds that can break with UV, low toxicity and no C-Cl bonds, should not absorb infrared so they will not become a global warming gas.
Some alternatives:
Hydrochlorofluorocarbons (HClFCs): chlorodifluoromethane Hydrofluorocarbons (HFCs): 1,1,1,2-tetrafluoromethaneHydrocarbons (HCs): mixtures of propane and butane
E.4.3. Alternatives to CFC’s
Hydrochlorofluorocarbons (HCFCs): chlorodifluoromethane Have stronger C-F bonds so less likely to break and pose a threat to ozone Problems:
Contain C-Cl bonds that reduce ozone layer (thus, a temporary solution)
Hydrofluorocarbons (HFCs): 1,1,1,2-tetrafluoromethane Have stronger C-F & C-H bonds so less likely to break and pose a threat to
ozone No C-Cl bonds, low reactivity, low toxicity, low flammability Problems:
Greenhouse gas that contribute to global warming
Hydrocarbons (HCs): mixtures of propane and butane Have stronger C-H bonds (413 kJ/mol) than C-Cl bonds (346 kJ/mol) Problems:
Volatile Greenhouse gases that contribute to global warming
substance flammable toxicity
HydrocarbonCH3CH(CH3)CH3
yes high
FluorocarbonsCF4
no not known
HydrofluorocarbonsCF3CH2F
no low
E5 Dissolved Oxygen in E5 Dissolved Oxygen in WaterWater
E 5.1 Outline biochemical oxygen demand (BOD) as a measure of oxygen- demanding wastes in water.
E 5.2 Distinguish between aerobic and anaerobic decomposition of organic material in water.
E 5.3 Describe the process of eutrophication and its effects.
E 5.4 Describe the source and effects of thermal pollution in water.
E.5.1. Outline biochemical oxygen demand (BOD) as a measure of oxygen-demanding wastes in water
Dissolved oxygen in water
BOD: the amount of oxygen (in ppm) needed / used by bacteria
to decompose the organic matter aerobically in a fixed volume
of water over a set period of time.
The greater the quantity of degradable organic waste, the higher
the BOD.
BOD versus DO (dissolved oxygen) content of the water.
Rivers: oxygen level is regenerated, lakes: limited.
Measurement: BOD is often measured over a set time period of 5
days. Water with a BOD above 5ppm is regarded as polluted.
E.5.1. Outline biochemical oxygen demand (BOD) as a measure of oxygen-demanding wastes in water
Importance of oxygen in water… At a pressure of 1 atm and 20C the solubility of oxygen in
water is 0.009 gdm-3. Oxygen (DO) is crucial for aquatic plants and animals that
require it for aerobic respiration (fish require at least 3ppm)
BOD- cont.
E.5.2. Distinguish between aerobic and anaerobic decomposition of organic material in water
Aerobic: If there’s sufficient oxygen present in the water, organic matter is broken down by microbes aerobically. This oxidizes the C, N, P, S, and H to produce CO2, NO3
-, PO43-,
SO42-, and H2O.
Anaerobic: If there’s an insufficient amount of oxygen present in the water, organic matter is decomposed by microbes that don’t require oxygen. They break down C, N, S, and P to form CH4, NH3, H2S, and PH3.
See chart on next page
elementaerobic decay
productanaerobic decay
product
Carbon CO2 CH4
Hydrogen H2O CH4, NH3, H2S, H2O
NitrogenNO3
- (oxidation number: +5)
NH3, amines(oxidation number: -3)
SulfurSO4
2-
(oxidation number: +6)H2S
(oxidation number: -2)
PhosphorusPO4
3-
(oxidation number: +5)PH3
(oxidation number: -3)
E.5.3. Describe the process of eutrophication and its effects
Eutrophication: the natural process by which a lake or river becomes
excessively rich in nutrients…
This is not a good thing!
This process is usually very slow, but can be greatly accelerated by
human activity.
Man-made eutrophication usually begins with algal blooms and can be
caused by: Large amounts of nitrates (from fertilizers) and phosphates (from
detergents) accumulating in lakes and streams, or
Large amounts of organic waste from sewage, meat processing, food
packing
E.5.3. Describe the process of eutrophication and its effects
Nutrients can increase the growth of plants and algae
Impacts the BOD because if plant growth increases too fast
DO will not be sufficient to decompose organic material
and waste by aerobic decomposition
Anaerobic decomposition will occur
Producing ammonia & hydrogen sulfide
More species will die
The lake will be stagnant
Little / no life
E.5.4. Describe the source and effects of thermal pollution in water.
Sources of thermal pollution: Many industries use water as a coolant and release the heated
water into rivers
Effects of thermal pollution: Higher temperature = lower solubility of gases
So, warm water holds less DO than cold water Higher temperature = increased metabolism (CR) in aquatic
animals (fish & amphibians) greater consumption rate of food requires more oxygen, which is less available
E.5.4. Describe the source and effects of thermal pollution in water.
As a result one has the problem of compromising food chains of
the old and new environments. Biodiversity (the degree of
variation of life forms within a given ecosystem, biome, or an
entire planet) can be decreased as a result.
Temperature changes of even one to two degrees Celsius can
cause significant changes in organism metabolism.
Producers are affected by warm water because higher water
temperature increases plant growth rates, resulting in a shorter
lifespan and species overpopulation.
This can cause an algae bloom which reduces oxygen levels.
E6 Water TreatmentE6 Water Treatment
E 6.1 List the primary pollutants found in waste water and identify their sources.
E 6.2 Outline the primary, secondary and tertiary stages of waste water treatment, and state the substance that is removed during each stage.
E 6.3 Evaluate the process to obtain fresh water from sea water using multi-stage distillation and reverse osmosis.
E 6.1 List the primary pollutants found in waste water and identify their sources.
Waste water contains floating, suspended, and colloidal organic matter,
dissolved ions with a wide range of microorganisms and bacteria as well as
chemicals.
Pesticides: agriculture (DDT, herbicides, fungicides)
Dioxins: large scale processes, such as waste combustion, manufacture of
herbicides, paper pulp bleaching with chlorine. Very toxic and can
accumulate in the liver.
Polychlorobiphenyls (PCBs): used in electrical insulators, circuit breakers,
transformers and capacitors, which can leak. Persists in the environment and
can accumulate in the liver, also carcinogenic. Overexposure can lead to
chloroacne, a skin condition that creates cysts
E 6.1 List the primary pollutants found in waste water and identify their sources.
Nitrates: from fertilisers or acid rain. They are toxic at high
levels, especially to babies because they have less stomach acid
than adults, can cause blue baby syndrome
Heavy metals: Cadmium (Cd) (rechargeable batteries),
Mercury (Hg) (batteries, paints), Copper (Cu) (household
plumbing), Lead (Pb) (pipes, fuel)
Organic matter: household waste (sewage water),
Phosphates: from fertilisers.
Pollutants Sources Effects
PesticidesAgriculture (DDT, herbicides,
fungicides)
Dioxins
Large scale processes, such as waste combustion, manufacture
of herbicides, paper pulp bleaching with chlorine
Teratogens (deform unborn fetuses), highly poisonous /
toxic
PCBsPlasticisers (now banned),
electrical insulatorsHard to degrade in environment,
build up through food web
Heavy metals Cu, Cd, Hg, Pb
Pretty much anything with metal
Organic matter Sewage
Nitrates Fertilizer or acid rain Toxic at high levels
Phosphorus Fertilizer
E.6.2: Outline the primary , secondary, and tertiary stages of waste water treatment, and state the substance that is
removed during each stage.
Summary: Primary Treatment: Filtration (screening) to
remove solids followed by sedimentation of sand, grit, and sludge.
Secondary Treatment: Use of oxygen and bacteria to remove matter
Tertiary Treatment: Chemical precipitation of remaining organic compounds, heavy metals, nitrates, phosphates.
E 6.2 Outline the primary, secondary and tertiary stages of waste water treatment, and state the substance that is removed during each stage.
Primary treatment: the removal of large solids (filtration & sedimentation)
Primary treatment involves running water through the below mechanisms in
order:
1. Bar screens: these remove large objects and debris from the surface of the water
and remove floating solids.
2. Settling tanks: these are used to settle out sand and small objects from the water
(as they sink to the bottom); these particles are then sent to landfills.
3. Sedimentation tanks: Alum (Ca(OH)2 and Al2(SO4)3) precipitates out and carry
with them solid suspended particles (this process is called flocculation).
Al2(SO4)3 (aq) + 3Ca(OH)2 (aq) → 2Al(OH)3 (s) + 3CaSO4 (s)
E 6.2 Outline the primary, secondary and tertiary stages of waste water treatment, and state the substance that is removed during each stage.
Secondary treatment: the removal of organic materials
using microbes (oxygen and bacteria)
Activated sludge process:
1. Air is bubbled into sewage which has been mixed with
bacteria-filled sludge.
2. Aerobic bacteria oxidize organic material in the sewage.
3. Water-containing decomposed suspended particles are
passed through the sedimentation tanks where the activated
sludge is collected.
E 6.2 Outline the primary, secondary and tertiary stages of waste water treatment, and state the substance that is removed during each stage.
4. Some of the sludge is recycled, and some is sent to
landfills.
5. This removes 90% of organic oxygen-demanding waste,
50% of nitrogen, and 30% of phosphates.
Effluent is then treated with chlorine or ozone to kill pathogenic
bacteria before releasing the water to lakes or rivers.
E 6.2 Outline the primary, secondary and tertiary stages of waste water treatment, and state the substance that is removed during each stage.
Tertiary treatment: the removal of remaining organics, nutrients and toxic
heavy metal ions
Heavy metal ions and phosphates are removed by precipitation, for
example, nickel:
Ni2+(aq) + 2OH−(aq) → Ni(OH)2 (s)
Aluminum sulfate or calcium oxide can be used to precipitate
phosphates:
Al3+ (aq) + PO43- (aq) → AlPO4 (s)
3CaO (aq) + 2PO43- (aq) + 3H2O → Ca3(PO4)2 (s) + 6OH−(aq)
E 6.2 Outline the primary, secondary and tertiary stages of waste water treatment, and state the substance that is removed during each stage.
Heavy metals will precipitate in the presence of hydroxide:
Cr3+(aq) + 3OH−(aq) → Cr(OH)3 (s)
Nitrates are more difficult to remove by precipitation because they’re
quite soluble, however, there are some ways to remove them:
1. Anaerobic denitrifying bacteria can reduce nitrates into nitrogen
2NO3− (aq) → N2 (g) + 3O2 (g)
2. Another method is to pass them into algae ponds where algae uses
nitrate as a nutrient.
Treatment StageSubstance(s)
RemovedMethod(s)
Primary
Secondary
Tertiary
Treatment StageSubstance(s)
RemovedMethod(s)
PrimaryLarge solids / solid waste
Filtration & sedimentation
SecondaryOrganic
substances
Activated sludge process:
oxygen & bacteria used
TertiaryIons (metals &
phosphates)Precipitation
reactions
E 6.2 Outline the primary, secondary and tertiary stages of waste water treatment, and
state the substance that is removed during each stage.
http://www.youtube.com/watch?v=9z14l51ISwg
E 6.3 Evaluate the process to obtain fresh water from sea-water using multi-stage
distillation and reverse osmosis.
DISTILLATION The sea water is heated in
series of coiled pipes and then introduced into a partially evacuated chamber.
Under reduced pressure some of the water boils instantly.
The water vapour is condensed by contact with cold water pipes carrying sea water.
The heat released by the water condensing is used to preheat more sea water.
Multi-stage distillation
E 6.3 Evaluate the process to obtain fresh water from sea-water using multi-stage
distillation and reverse osmosis.
REVERSE OSMOSIS A high pressure is applied to
the solution side of a partially (semi) permeable membrane made of cellulose ethanoate.
Water is forced out of the salt solution through the membrane leaving the salt behind.
Reverse osmosis moves water AWAY from the concentrated solute
Commercial plants: 70atm and 1m3 of membrane-250000L fresh water/day
Reverse osmosis
E7 SoilE7 Soil
E 7.1 Discuss salinization, nutrient depletion and soil pollution as causes of soil degradation.
E 7.2 Describe the relevance of the soil organic matter (SOM) in preventing soil degradation, and outline its physical and biological functions.
E 7.3 List common soil pollutants and their sources.
E 7.1 Discuss salinization, nutrient depletion and soil pollution as causes of soil degradation.
Salinization: this is the result of continually irrigating soils Irrigation waters contain dissolved salts, which are left behind after
water evaporates In poorly drained soils, the salts are not washed away and begin to
accumulate in the topsoil Plants (most) cannot grow in soil that is too salty Salt concentration reaches a toxic level or plants die of dehydration
(osmosis) Treatment for salinization is to flush the soil with large volumes of
water This, however, can result in salinization of the rivers and
groundwater
E 7.1 Discuss salinization, nutrient depletion and soil pollution as causes of soil
degradation. Nutrient depletion: agriculture disrupts the normal cycling of
nutrients through the soil food web when crops are harvested This removes all nutrients & minerals absorbed from soil while
growing Practices leading to amelioration of nutrient depletion may further
contribute to environmental pollution Solutions: rotation, using legumes (nitrogen), compost (organic waste),
ploughing (air, oxygen)
E 7.1 Discuss salinization, nutrient depletion and soil pollution as causes of soil
degradation. Soil pollution: this is the consequence of the use of chemicals such
as pesticides and fertilizers These chemicals can disrupt the soil food web (plants & animals),
reduce soil’s biodiversity and ultimately ruin the soil Chemicals also run off the soil into the surface waters and move
through the soil, polluting the groundwater Other sources of soil pollution: mining, improper disposal of toxic
waste … or Poo Poo Beach, Lagos Problems do not occur directly in the soil but in waterways where the
pollutants are leached out of the soil
E 7.2 Describe the relevance of the soil organic matter (SOM) in preventing soil degradation, and
outline its physical and biological functions. SOM: organic constituents in the soil,
such as undecayed plant and animal tissues, their partial decomposition products and the soil biomass.
SOM only constitutes about 5% of soil
SOM includes: Identifiable, high molecular mass
organic materials (polysaccharides & proteins)
Simpler substances (sugars, amino acids, other small molecules)
Humic substances
E 7.2 Describe the relevance of the soil organic matter (SOM) in preventing soil degradation, and
outline its physical and biological functions.
The functions of SOM can be classified into:
Biological: provides source of nutrients (PNS) and contributes to the resilience of the soil / plant system
Physical: improves structural stability (organic matter loosens the soil, increasing the amount of pore space → air, water), influences water-retention properties and alters the soil thermal properties
E 7.3 List common soil pollutants and their sources.
organic pollutant source
petroleum hydrocarbonstransport, solvents, industrial
processes
agrichemicals pesticides, herbicides, fungicides
volatile organic compounds (VOCs)
solvents, especially paints and protective coatings, dry cleaning
and industry
solvents industry
polyaromatic hydrocarbons (PAHs)
incomplete combustion of coal, oil, gas, wood, garbage
organic pollutant source
polychlorinated biphenyls
(PCBs)
coolant, insulator in electrical
equipment (transformers and
generators)
organotin compounds bactericides, fungicides used in
paper, wood, textile
semi-volatile organic
compounds (SVOCs)
solvents, industrial processes
E 7.3 List common soil pollutants and their sources.
E8 WasteE8 Waste E 8.1 Outline and compare the various methods
for waste disposal.
E 8.2 Describe the recycling of metal, glass, plastic and paper products, and outline its benefits.
E 8.3 Describe the characteristics and sources of different types of radioactive waste.
E 8.4 Compare the storage and disposal methods for different types of radioactive waste.
E 8.1 Outline and compare the various methods for waste disposal.
Method Advantages Disadvantages
Landfill
(the land must be
isolated from
groundwater)
Efficient method to deal
with large volumes. Filled
land can be used for
building
•Local residents may object•Land needs time to settle and
may require maintenance
(methane), non-biodegradable
plastics
Open dumping Convenient, inexpensive
•Causes air and ground water
pollution•Health hazard (rodents)
Incineration
•Reduces volume.•Requires minimum space.
Produces stable, odorless
residue•A source of energy
•Expensive to build and run
•Can cause pollutants (CO2,
CO, HCl, dioxin)•Requires energy
Method Advantages Disadvantages
Ocean dumping
•Source of nutrients
•Convenient
•Inexpensive
•Danger to marine
animals
•Sea pollution
RecyclingProvides a sustainable
environment
•Expensive
•Difficulty in
separating different
materials
E 8.2 Describe the recycling of metal, glass, plastic and paper products, and outline its benefits.
Metal: Mainly aluminium, steel Sorted (steel by magnet), melted, used for
purification (saving energy aluminium) Saves reserves, reduces energy costs Aluminium is resistant to corrosion, high cost
of the initial extraction process
E 8.2 Describe the recycling of metal, glass, plastic and paper products, and outline its benefits.
Glass: Sorted by colour, washed, crushed, melted,
and moulded into new products Non-degradable, can be recycled many times Reduces energy costs, the need for sandstone
and limestone quarries
E 8.2 Describe the recycling of metal, glass, plastic and paper products, and outline its benefits.
Plastic: • Sorted, degraded into monomers (in the
absence of air, pyrolysis) then repolymerized• Less pollutants, less energy than producing
new plastics• Sorting can be problematic
E 8.2 Describe the recycling of metal, glass, plastic and paper products, and outline its benefits.
Paper: sorted, washed (ink, additives are removed),
slurry (by adding water then repulping), formation of new types of paper (reduced strength, low-grade products, cellulose fibers are damaged)
Energy required to transport, compost more efficient
E 8.3 Describe the characteristics and sources of different types of radioactive waste.
Nature of waste Source Characteristics
Low Level:Lab equipment,
protective clothing
Power stations, hospitals & research
establishments
1. 0.001% of waste radioactivity2. Compressed into steel
containers & buried or incineration
3. High volume
Intermediate Level: Cladding around nuclear fuel elements, ‘sludge’
from treatment
Power stations 1. 1% of waste radioactivity2. Cemented inside steel drums
and stored in secure repository under layers of clay
High Level: Waste nuclear fuel
Able to generate heat
Power stations 1. 99% of waste radioactivity2. ‘Vitrified’, i.e. changed to a
dense glass block and stored in secure repository, underground
3. Low volume
E 8.4 Compare the storage and disposal methods for different types of radioactive waste.
Low level
Decay process produces heat, waste is stored in water till activity level is low. Water is passed through an ion exchange resin, diluted, released into the sea. Other method: keeping the waste in steel containers inside concrete-lined vaults.
E 8.4 Compare the storage and disposal methods for different types of radioactive waste.
High level
The spent rods removed from the reactor, transfered to deep pools cooled by water containing neutron absorber. Cased in ceramic, packed in metal containers, buried deep in the Earth (granite rock, unused mine). The site must prevent the material from entering the underground water supply. The waste is buried in remote places that are geologically stable (earthquake).