Lecture #13 - Atmospheric and Oceanic Science

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LECTURE 13

Atmospheric Aerosols

AOSC 434

AIR POLLUTION

RUSSELL R. DICKERSON

Atmospheric Aerosols

Bibliography

Seinfeld & Pandis, Atmospheric Chemistry and Physics, Chapt. 7-13

Finlayson-Pitts & Pitts, Chemistry of the Upper and Lower Atmosphere ,

Chapt. 9.

Classic papers:

Prospero et al. Rev. Geophys. Space Phys., 1607, 1983; Charlson et al. Nature

1987; Charlson et al., Science, 1992.

Recent Papers:

Ramanathan et al., Science , 2001; Andreae and Crutzen, Science , 1997;

Dickerson et al., Science 1997; Jickells et al., Global Iron Connections Between

Desert Dust, Ocean Biogeochemistry and Climate, Science, 308 67-71, 2005.

EPA REGIONAL HAZE RULE: FEDERAL CLASS I AREAS

TO RETURN TO “ NATURAL ” VISIBILITY LEVELS BY 2064

…will require essentially total elimination of anthropogenic aerosols!

• clean day moderately polluted day

Acadia National Park http://www.hazecam.net/

INTRODUCTION:

Particles are one of the most important and certainly the most visible aspects of air pollution. The effects span the areas of health (1% increase in mortality per 10 μg m -3 ); acid rain, visibility degradation, radiation and photochemistry and cloud microphysics changes

(and thus climate changes), and the Antarctic ozone hole. For a view into the "bad old days" see Killer Smog by William Wise.

NOMENCLATURE:

Particle refers to a solid or liquid, larger than a molecule, diameter > 0.01

μ m, but small enough to remain in the atmosphere for a reasonable time, diameter < 100

μ m.

Particulate is an adjective, in spite of what EPA tries to say.

Aerosol is a suspension of particles in a gas.

Particles, like gases, are characterized by chemical content, usually expressed in m g m -3 , but unlike gases, particles also have a characteristic size. We may want to start discussion the characteristics of atmospheric aerosols by addressing the question "What is the mean diameter of the particles?" The answer to this question changes with your point of view.

A. Size Number Distribution

If your concern is the mass of some pollutant that is being transported through the air for biogeochemical cycles, then you want to know the mean diameter of the particles with the mass or volume . In other words, "What size particles carry the most mass?

If your concern loss of visibility then you want to know the diameter of the particles that have the largest cross section or surface area . In other words, "What size particles cover the largest surface area?"

If your concern is cloud formation or microphysics then you want to know the range of diameters with the largest number of particles. In other words, "What is the size of the most abundant particles?"

If your concern is human health then you need to know about both the mass and number of the particles, because only a certain size particle can enter the lungs.

Here we define the number distribution function , f n

(D p

), and the number of particles with diameter between D p and D p

+ dD p in a cm 3 of air as follows: f n

(D p

) dD p

(particles cm -3 / m m)

The total number of particles, N , is given by the following integral (everywhere we integrate from 0 to infinite diameters):

N =

f

n

(D p

) dD p

(particles cm -3 )

We can define a surface area distribution function, f s

(D p

), for spherical particles as follows: f s

(D p

)dD p

= p

D p

2 f n

(D p

) ( m m 2 m m -1 cm -3 )

This gives the surface area of particles in a size range per cm 3 of air. The total surface area of the particles, S , is given by the integral over all diameters:

S

=

 f s

(D p

) dD p

= p

D p

2 f n

(D p

) dD p

( m m 2 cm -3 )

Likewise the volume distribution function and the total volume: f v

(D p

) dD p

= { p

/6} D p

3 f n

(D p

) ( m m 3 m m -1 cm -3 )

V

=

 f v

(D p

) dD p

=

 p

/6 D p

3 f n

(D p

) dD p

( m m 3 cm -3 )

The distributions based on log D p n(log D p

)dlogD p can be defined in a similar manner, where is the number of particles in one cm 3 with diameter from D p

The total number is:

N =

 n(log D p

) d(logD p

) (particles cm -3 ) to D p

+ log D p.

The normalized distribution functions based on log D p for surface area and volume are similar. For the differential number of particles between D p and D p

+ dD p we use the notation dN, and likewise dS and dV, we can represent the size distribution functions as n (log D p

) = {dN} / {N dlogD p n n v s

(log D p

) = {dS} / {S dlogD p

(log D p

) = {dV} / {V dlogD p

}

}

}

This is the common notation for expressing the variation in particle number, surface area or volume with the log of the diameter.

B. Chemical Composition

The bimodal nature of the size-number distribution of atmospheric particles suggests at least two distinct mechanisms of formation, and the chemical composition of the particles reflects their origins.

Fine particles have a diameter smaller than about 2.5 m m, and are produced by the condensation of vapors, accumulation, and coagulation. They have a chemical composition that reflects the condensable trace gases in the atmosphere: SO

2

, NH

3

, HNO

3

,

VOC ’ s, and H

2

O. The chemical composition is water with SO

4

-2 , NO

C(soot), and organic matter; where biomass burning is prevalent, K + .

3

, NH

4

+ , Pb, Cl , Br ,

Coarse Particles have a diameter greater than about 2.5 m m, are produced by mechanical weathering of surface materials. Their lifetimes, controlled by fallout and washout, are generally short. The composition of particles in this size range reflects that of the earth's surface - silicate (SiO

2

), iron and aluminum oxides, CaCO

3 oceans , NaCl.

and MgCO

3; over the

ORIGIN OF THE ATMOSPHERIC AEROSOL

Aerosol: dispersed condensed matter suspended in a gas

Size range: 0.001 m m (molecular cluster) to 100 m m (small raindrop)

Soil dust

Sea salt

Environmental importance: health (respiration), visibility, radiative balance, cloud formation, heterogeneous reactions, delivery of nutrients…

AEROSOL NUCLEATION

# molecules 1 2 3 4

Surface tension effect

D

G

Thermo driving force

Critical cluster size cluster size

Atmospheric Aerosols

Number

• cloud formation

Surface

• visibility

Volume

• mass

Mass & Number

• human health

Aerosol Distributions

TYPICAL U.S. AEROSOL SIZE DISTRIBUTIONS

Fresh urban

Aged urban rural remote

Warneck [1999]

SAMPLE AEROSOL SIZE DISTRIBUTION (MARINE AIR)

Sea salt

Sulfate

(natural)

From USEPA (Neil Frank)

C. Optical Properties and Visibility

The optics of aerosol science follow the most rigorous physics. Traditionally defined visibility is the distance at which a large dark object, such as a hill or a barn can just be seen.

A more quantitative definition can be obtained by considering the change in intensity of light reflecting off an object as a function of the scattering of light by the atmosphere.

D

I/I = e (-b

D

X)

Where I is the intensity of light, b (or b ext

) is the extinction coefficient with units of m -1 , and

X is the distance in m. The limit to visibility for the human eye is a 2% change in intensity relative to the background or:

D

I/I = 0.02

Radiation and fine particles

Atmospheric Visibility

(absorption & scattering)

1.Residual

2.Scattered away

3.Scattered into

4.Airlight

The extinction coefficient represents the sum of the extinctions from gases and particles, each of which can in turn be divided into extinction due to absorption or scattering.

b ext b ext

= b gas

+ b particles

= b abs

+ b scatt b abs

(gases) = Beer's Law absorption b abs b scatt b scatt

(gases) = Rayleigh Scattering

(particles) = Usually < 10% of extinction

(particles) = Mie Scattering = (b sp

)

The ultimate limit to visibility in a very clean atmosphere is Rayleigh scattering, but

Mie scattering usually dominates. The range of b sp is 10 -5 m -1 to 10 -3 m -1 .

Single scattering albedo, w

, is a measure of the fraction of aerosol extinction caused by scattering: w

= b sp

/ (b sp

+ b ap

)

Optical Properties of Small Particles

m = n + i k

m = complex index of refraction n = scattering (real part) k = absorption (imaginary part)

The real part of the index of refraction is only a weak function of wavelength, while the imaginary part, i k, depends strongly on wavelength.

Refractive indices of aerosol particles at

= 589 nm

m = n + ik

Substance

Water n

1.333

Ice

NaCl

1.309

1.544

H

2

SO

4

NH

4

HSO

4

(NH

4

)

2

SO4

SiO

2

1.426

1.473

1.521

1.55

Black Carbon (soot) 1.96

Mineral dust ~1.53

k

10 -8

10 -8

0

0

0

0

0

0.66

~0.006

The scattering cross section is the product of the mass loading, and the surface area per unit mass; note the ln of 0.02 is about -3.9, thus:

Visibility ≈ 3.9(b sp

) -1 b sp

= S

 m

Where b sp is the scattering coefficient in units of m -1 m is the mass loading in units of g m -3

S is the surface area per unit mass in units of m 2 g -1

For sulfate particles, S is about 3.2 m 2 g -1 where the humidity is less than about 70%; for other materials it can be greater.

Visibility = 3.9/(3.2 m )

= 1.2 /( m )

Example: Visibility improvement during the 2003 North

American Blackout

Normal conditions over Eastern US during an air pollution episode: b sp

≈ 120 Mm -1 = 1.2 x 10 -4 m -1 at 550 nm b ap

= 0.8 x 10 -5 m -1 b ext

= 1.28 x 10 -4 m -1

Visual Range ≈ 3.9/b ext

= 30 km

During blackout b sp

= 40 Mm -1 = 4.0 x 10 -5 m -1 b ap

= 1.2 x 10 -5 m -1 b ext

= 0.52 x 10 -4 m -1

Visual Range = 3.9/b ext

= 75 km

Example: Visibility improvement during the 2003 North

American Blackout

Single scattering albedo, w

, normal = 1.20/1.28 = 0.94

Blackout = 0.4/0.52 = 0.77

With the sulfate from power plants missing, and the soot from diesel engines remaining the visual range is up, but the single scattering albedo is down. Ozone production inhibited.

See: Marufu et al., Geophys Res. Lett., 2004.

Extinction Coefficient

as a PM2.5 Surrogate

PM

2.5

= 7.6 m g/m 3

PM

2.5

= 21.7 m g/m 3

PM

2.5

= 65.3 m g/m 3

Glacier National Park images are adapted from Malm, An Introduction to

Visibility (1999) http://webcam.srs.fs.fed.us/intropdf.htm

ANNUAL MEAN PARTICULATE MATTER (PM)

CONCENTRATIONS AT U.S. SITES, 1995-2000

NARSTO PM Assessment, 2003

PM10 (particles > 10 m m) PM2.5 (particles > 2.5 m m)

Red circles indicate violations of national air quality standard:

50 m g m -3 for PM10 15 m g m -3 for PM2.5

AEROSOL OPTICAL DEPTH (GLOBAL MODEL)

Annual mean

AEROSOL OBSERVATIONS FROM SPACE

Biomass fire haze in central America (4/30/03)

Fire locations in red

Modis.gsfc.nasa.gov

BLACK CARBON EMISSIONS

DIESEL

DOMESTIC

COAL BURNING

BIOMASS

BURNING

Chin et al. [2000]

ASIAN DUST INFLUENCE IN UNITED STATES

Dust observations from U.S. IMPROVE network

April 16, 2001

Asian dust in western U.S.

April 22, 2001

Asian dust in southeastern U.S.

Glen

Canyon,

AZ

0 2 4 6 8 m g m -3

Clear day

April 16, 2001: Asian dust!

TRANSPACIFIC TRANSPORT OF ASIAN DUST PLUMES

GEOS-CHEM Longitude cross-section at 40N, 16 April, 2001

10

Source region

(inner Asia)

Asian plumes over Pacific

Subsidence over western U.S.

5

0

100E

ASIA

150E

LONGITUDE

150W 100W

UNITED STATES

T.D. Fairlie, Harvard

The future is hard to predict.

What really happened?

National Emission Trends

Courtesy of Dr. Hao He http://www.epa.gov/ttn/chief/trends/index.html

Aerosols in the Atmosphere

Abundance and size

• Aerosol concentration is highly variable in space and time. Concentrations are usually highest near the ground and near sources.

• A concentration of 10 5 cm -3 is typical of polluted air near the ground, but values may range from 2 orders of magnitude higher in very polluted regions to several lower in very clean air.

• Radii range from ~ 10 -7 cm for the for small ions to more than 10 µm (10 -3 cm) for the largest salt and dust particles.

• Small ions play almost no role in atmospheric condensation because of the very high supersaturations required for condensation.

• The largest particles, however, are only able to remain airborne for a limited time

Aerosol Size Naming Convention

Usually divided into three size groups ( D - diameter)

1.

Aitken Nuclei

2 x 10 -3 µm < D  2 µm

2.

Large Nuclei

 

2 µm < D  2.5 µm

(also called the accumulation mode)

3. Giant Nuclei

 D > 2.5 µm

Other Naming Convention

• Nucleation mode

 D ≤ 0.1 µm

• Accumulation or coagulation mode

 0.1 µm < D ~ 1 µm

Thought to be most important in natural cloud formation

• Coarse Particle Mode

 D ~ 1 µm

Origins of Atmospheric Aerosols

1.

Condensation and sublimation of of vapors and the formation of smokes in natural and man-made combustion.

2.

Reactions between trace gases in the atmosphere through the action of heat, radiation, or humidity.

3.

The mechanical disruption and dispersal of matter at the earth ’ s surface, either as sea spray over the oceans, or as mineral dusts over the continents.

4.

Coagulation of nuclei which tends to produce larger particles of mixed constitution

Aerosol Makeup

• Typical substances formed in large quantities by condensation following combustion include ashes, soot, tar products, oils as well as sulfuric acid and sulfates. These particles are primarily within the range of Aitken nuclei.

• Mechanical disintegration, by wind and water, of rocks and soil produces particles with diameters > 0.2 µm. These fall primarily in the large nuclei range.

• According to Jaenicke ( Science, 308 p. 73, 2005) about 25% of the number of particles with diameter greater than 0.2 µm are biogenic. (remains to be verified).

Aerosol Makeup - continued

• Chemical reactions between nitrogen, oxygen, water vapor and various trace gases (e.g., sulfur dioxide, chlorine, ammonia, ozone, and oxides of nitrogen) primarily produce particles in the Aitken and Large range.

Examples

Formation of ammonium chloride from NH

3 and HCl

Oxidation of SO

2 to H

2

SO

4

Reaction of sulfur dioxide, ammonia, and water to produce ammonium sulfate particles.

Production of higher oxides of nitrogen through the action of heat, ozone or ultraviolet radiation

Cloud Condensation Nuclei - CCN

• Comprises a small fraction of the total aerosol population

• Sea salt is the predominant constituent of CCN with D > 1µm

• For 0.1 µm < D < 1 µm, the main component is thought to be sulfate, which may be present as sulfuric acid, ammonium sulfate, or from phytoplankton produced dimethyl sulfide (see Charlson et al.,

Nature , 326 , 655-661).

Activity Spectrum

Let N c be the number of particles per unit volume that are activated to become cloud droplets.

Data from cloud chamber measurements are often parameterized as

N c

= C (S-1) k where C and k are parameters that depend on air mass type.

Rogers gives:

Maritime air: 30 < C < 300 cm -3 ; 0.3 < k < 1

Continental air: 300 < C < 3000 cm -3 ; 0.2 < k < 2

Thus, for the same saturation ratio, one would expect to find small numbers of CCN per unit volume in maritime air and large numbers per unit volume in continental air.

How aerosols affect the radiative properties of clouds.By nucleating a larger number of smaller cloud drops, aerosols affect cloud radiative forcing in various ways.

D Rosenfeld et al. Science 2014;343:379-380

Published by AAAS

Summary

1. Aerosols are the most visible of air pollution classes.

2. The PM2.5 standard to protect health is 15 m g/m 3 .

3. Number, surface and volume (mass) all play a role.

4. Log-normal distributions.

5. Single scattering albedo w = bsp/(bsp + bap)

6. Composition reflects sources and sinks.

7. Large and still uncertain impact on climate, but Z Li et al. showed that aerosols inhibit gentle rains but exacerbate severe storms.

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