NATS 101

Lecture 23
Air Pollution Meteorology

AMS Glossary of Meteorology
air pollution—The presence of substances in the atmosphere, particularly those that do not occur naturally.
These substances are generally contaminants that substantially alter or degrade the quality of the atmosphere.
The term is often used to identify undesirable substances produced by human activity, that is, anthropogenic air pollution.
Air pollution usually designates the collection of substances that adversely affects human health, animals, and plants; deteriorates structures; interferes with commerce; or interferes with the enjoyment of life.

Major Air Pollution Episodes       of Historic Significance
Some of the worst events in the last two centuries occurred in London
Key ingredients: calm winds, fog, smoke particles from coal burning
1873 - 700 deaths
1911- 1150 deaths
1952 - 12,000 deaths (Dec 5 - 9)
Last event led to the Parliament passing a Clean Air Act in 1956

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Major U.S. Air Pollution Episodes       of Historic Significance
U.S. air quality degraded shortly after the beginning of the industrial revolution
Coal burning in Central and Midwest U.S.
1939 St. Louis Smog Nov 28
1948 Donora, PA in the Monongahela River Valley
20 deaths, 1000Õs took ill in 5 days Oct 27
Prompted Air Pollution Control Act of 1955
Ignored automobiles

Major U.S. Air Pollution Episodes       of Historic Significance
1960s - NYC had several severe smog episodes
1950s onward – LA had many smog alerts from an increase in industry and motor vehicle use
Led to passage of the Clean Air Act of 1970 (updated 1977 and 1990)
Empowered Federal Government to set emission standards that each state had to meet

U.S. Air Pollution Examples
Air Pollution in Grand Canyon
Even remote areas are affected by pollution
Canyon on a clear day
Canyon on a smog day

Primary Pollutants
Injected directly into atmosphere
Carbon Monoxide (CO)
odorless, colorless, poisonous gas
byproduct of burning fossil fuels
body acts as if CO is O2 in blood, can result in death
Nitrogen Oxides (NOx, NO)
NO - nitric oxide
emitted directly by autos, industry

Primary Pollutants
Sulfur Oxides (SOx)
SO2 - sulfur dioxide
produced largely through coal burning
responsible for acid rain problem
Volatile Organic Compounds (VOCs)
highly reactive organic compounds
released through incomplete combustion and industrial sources
Particulate Matter (dust, ash, smoke, salt)
10 um particles (PM10) stay lodged in your lungs
2.5 um particles (PM2.5) can enter blood stream

Secondary Pollutants
Form in atmosphere from chemical-photochemical reactions that involve primary pollutants
Sulfuric Acid H2SO4
major cause of acid rain
Nitrogen Dioxide NO2
brownish hue

Secondary Pollutants
Ozone O3
colorless gas
has an acrid, sweet smell
oxidizing agent
Primary and secondary pollutants are found in the two types of smog:
London-type smog
LA-type photochemical smog (LA AQMD)
SMOG = SMOKE + FOG

Human Response to One Hour Pollutant Exposure (Turco, p194)
Physiology of Exposure to CO
Human Response to One Hour Pollutant Exposure (Turco, p194)
Human Response to One Hour Pollutant Exposure (Turco, p194)
Human Response to One Hour Pollutant Exposure (Turco, p194)
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Beijing Air Pollution
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U.S. Pollutant Trends
1940-1995
Most pollutants decreased after the 1970 Clean Air Act
Lead
Particulates
SO2
VOCÕs
CO
NO2 is Leveling Off

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Air Pollution Weather
Strong low-level inversion
Subsidence inversion that diurnal heating does not break or weaken significantly
Weak surface winds
Persistent surface anticyclone
Sunny weather for photochemical smog
Hot weather to accelerate O3 production

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Air Pollution Dispersion
Air pollution dispersion is often studied with simple models, termed Box Models.  How is a box defined for the LA basin?
Box Model Boundaries for the LA Basin
Ventilation factor is a simple way of relating concentrations of pollutants to parameters that modulate the dispersion of pollutants in a local environments.
An increase in either the mixing height or the wind speed increases the effective volume in which pollutants are allowed to mix.
The larger the volume, the lower the pollution concentration.
How does a box model work?

 Ventilation Factor (VF)
Acid Rain and Deposition
Sulfur dioxide (SO2) and oxides of nitrogen (NOx) within clouds (including fog) form acidic particles when they react with water:
SO2 + H2O Þ H2SO4 (sulfuric acid)
NOx + H2O Þ HNO3 (nitric acid)
Acid Rain is worse downstream of the point sources of pollution
Acid Rain affects Trees, Lakes, Structures
Acid Deposition is a world-wide problem

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Impact on Aquatic Organisms
Sandstone Figure in Germany
Summary
Air Pollutants – Long History
Primary: CO, NOx, SOx, VOC, PM
Secondary: H2SO4, NO2, O3
Global Problem - Knows No Boundaries!
Serious Health Consequences
US Air Improving - Clean Air Act
But It is Degrading in Emerging Economies
Air Pollution Weather and Air Dispersion
Acid Rain

NATS 101

Lecture
Ozone Depletion

Supplemental References for TodayÕs Lecture
Danielson, E. W., J. Levin and E. Abrams, 1998: Meteorology. 462 pp. McGraw-Hill. (ISBN 0-697-21711-6)
Moran, J. M., and M. D. Morgan, 1997: Meteorology, The Atmosphere and the Science of Weather, 5th Ed. 530 pp. Prentice Hall.          (ISBN 0-13-266701-0)

Review:          Ultraviolet (UV) Absorption
O2 and O3 absorb UV (shorter than 0.3 mm)
Therefore, reductions in the level of O3 would increase the amount of UV radiation that penetrates to the surface

Hazards of Increased UV
Increase number of cases of skin cancers
Increase in eye cataracts and sun burning
Suppression of human immune system
Damage to crops and animals
Reduction in ocean phytoplankton

Natural Balance of Ozone
Disassociation of O2 absorbs UV < 0.2 mm
O2 + UV ¨ O + O
O3 forms when O2 and O molecules collide
O2 + O ¨ O3
Disassociation of O3 absorbs 0.2-0.3 mm UV
O3 + UV ¨ O2 + O
Balance exists between O3 creation-destruction
CFCÕs disrupts balance

Sources of CFCÕs
CFCÕs make up many important products
Refrigerants
Insulation Materials
Aerosol Propellants
Cleaning Solvents

Commonly Used CFCÕs
Name Formula Primary Use     Residence Time
      (50% decrease)
CFC-11 CCl3F Propellant ~55 years
CFC-12 CCl2F2 Refrigerant ~100 years
CFC-113 C2Cl3F3 Cleaning Solvent ~65 years
It would take 10-20 years for CFC levels to start falling if all production ended today due to leakage of CFCÕs from old appliances, etc.

Chronology of Ozone Depletion
1881 Discovery of ozone layer in stratosphere
1928 Synthesis of CFCÕs for use as a refrigerant
1950s Rapid increase in use of CFCÕs
1974 Description of ozone loss chemical reactions
1979 Ban of CFC use in most aerosol cans in U.S.
1980s Growth of CFC use worldwide
1985 Discovery of Antarctic ozone hole
1987 Adoption of Montreal Protocol calling for a 50% reduction in use of CFCÕs by 1998

Chronology of Ozone Depletion
1989 Confirmation of ozone declines in mid-latitudes of Northern Hemisphere and in the Arctic
1990 Montreal Protocol amended to require a complete phase out of all ozone depleting chemicals by 2000
1990 U.S. requirement for recycling of CFCÕs
1992 Discovery of high levels of ClO over middle and high latitudes of Northern Hemisphere
1992 Further amendment of Montreal Protocol calling for an accelerated phase out by ozone depleting chemicals
2100 Time needed for ozone layer to heal completely?

How O3 is Measured: Dobson Unit
Ozone can be measured by the depth of ozone if all ozone in a column of atmosphere is brought to sea-level temperature and pressure.
One Dobson unit corresponds to a 0.01 mm depth at sea-level temperature and pressure
The ozone layer is very thin in Dobson units.
There are only a few millimeters (few hundred Dobsons) of total ozone in a column of air.

Mean Monthly Total Ozone
Setting the Stage
Conditions over Antarctica promote ozone loss.
Circumpolar vortex keeps air over Antarctica from mixing with warmer air from middle latitudes.
Temperatures drop to below    -85oC in stratosphere.
Chemical reactions unique to extreme cold occur in air isolated inside vortex.

How Ozone is Destroyed
June: Winter begins.
Polar vortex strengthens and temperatures begin to fall.
July-August: The temperatures fall to below -85oC.
Ice clouds form from water vapor and nitric acid.
Chemical reactions that can occur on ice crystals, but not in air, free chlorine atoms from the CFC.

How Ozone is Destroyed
Sept: As sunlight returns in early Spring, stratospheric temperatures begin to rise.
Clouds then evaporate, releasing chlorine atoms into air that were ice locked.
Free chlorine atoms begin destroying ozone.
Oct: Lowest levels of ozone are detected in early spring.
Nov: Vortex weakens and breaks down, allowing ozone poor air to spread.

Chemistry of the Ozone Hole
Chlorine atoms can be freed from CFCÕs by UV reaction
CCl3F + UV ¨ CCl2F + Cl
CCl2F2 + UV ¨ CClF2 + Cl
C2Cl3F3 + UV ¨ C2Cl2F3 + Cl
Once a chlorine atom is freed, it can destroy thousands of ozone molecules before being removed from the air
  Cl + O3 ¨ O2 + ClO
  ClO + O ¨ O2 + Cl

Annual Cycle of Ozone over SP
Mean Monthly Total Ozone
Ozone Hole Statistics
Key Points: Ozone Hole
Chlorofluorocarbons (CFCs) disrupt the natural balance of O3 in S.H. stratosphere
CFCs responsible for the ozone hole over SP!
Responsible for lesser reductions worldwide.
Special conditions exist in stratosphere over Antarctica that promote ozone destruction:
Air trapped inside circumpolar vortex
Cold temperatures fall to below -85oC

Key Points: Ozone Hole
CFCs stay in atmosphere for ~100 years
One freed chlorine atom destroys thousands of O3 molecules before leaving stratosphere
Montreal Protocol mandated total phase out of ozone depleting substances by 2000.
Even with a complete phase out, O3 levels
Would not increase for another 10-20 years
Would not completely recover for ~100 years