Review of Lectures 9 to 16 AOSC 433/633 & CHEM 433. Ross Salawitch

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Review of Lectures 9 to 16 AOSC 433/633 & CHEM 433 Ross Salawitch Class Web Site: http://www.atmos.umd.edu/~rjs/class/spr2015 Review of Problem Set #4 will be held Mon, 13 April 6:30 pm Unfortunately the last day to withdraw is Mon, 13 April apologies for scheduling exam one day after this important deadline ELMS gradebook current: please let us know of any inconsistencies 9 April 2015 1

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Importance of Radicals With a few exceptions, the only reactions between molecules that proceed at appreciable rates are those involving at least one radical Radicals require significant energy to form: a bond must be broken Radical formation is tied to absorption of photons that photodissociate a compound, leading to radical formation Initiation O 2 + photon O + O Propagation O + O 2 + M O 3 + M O 3 + photon O( 1 D) +O 2 O( 1 D) + H 2 O OH +OH OH + O 3 HO 2 + O 2 HO 2 + O OH + O 2 Termination HO 2 + HO 2 H 2 O 2 + O 2 3

Atmospheric Radiation Solar irradiance (downwelling) at top of atmosphere occurs at wavelengths between ~200 and 2000 nm (~5750 K black body temperature) Panel (a) : Curves of black-body energy versus wavelength for 5750 K (Sun s approximate temperature) and for 245 K (Earth s mean temperature). The curves are drawn with equal area since, integrated over the entire Earth at the top of the atmosphere, the solar (downwelling) and terrestrial (upwelling) fluxes must be equal. Panel (b): absorption by atmospheric gases for a clear vertical column of the atmosphere (1.0 represents complete absorption). From Houghton, Physics of Atmospheres, 1991 Absorption and photodissociation in the UV occurs due to changes in the electronic state (orbital configuration) of molecules 4

Absorption Cross Section of O 2 From Brasseur & Solomon, Aeronomy of the Middle Atmosphere, 1986 O 2 can not dissociate longward of ~250 nm All absorption shown above is dissociative (e.g., leads to production of two O atoms) Structure in the O 2 cross section is related to whether the initial transition involves an unbound electronic state (smooth) or involves a specific vibrational level of an electronic state (banded, due to requirement of specific quanta of energy) 5

Recall the Beer-Lambert Law: F(z,λ) = F TOA (λ) e τ(z, λ) (TOA Optical Depth of O 2 Absorption : Top of Atmosphere) Also: 0 where: [O τ(z, λ) = m z σ λ [C] dz 24 2 2] dz 4 10 molecules/ cm (τ: optical depth) Schumann-Runge Continuum Schumann-Runge Bands Herzberg Continuum O 2 Optical Depth for θ = 0, z = 0 km σ max (cm 2 ) τ (0 km) e τ ( 0 km) 10 17 4 10 7 0. 10 20 4 10 4 0. 3 10 23 120 7.6 10 53 10 23 40 4.2 10 18 6

Optical Depth of O 3 Absorption A typical mid-latitude column abundance for O 3 is 300 Dobson units (DU): 1 DU = 2.687 10 16 molecules/cm 2 ; 300 DU = 8 10 18 molecules/cm 2 Aside: Column O Column Air 8 10 2 10 18 3 = = 0.4 parts per million 25 Ozone is a trace species! Hartley (~220 to 280 nm) Huggins (~310 to 330 nm) Chappuis (~500 to 700 nm) O 3 Optical Depth for θ = 0, z = 0 km σ max (cm 2 ) τ (0 km) e τ ( 0 km) O 3 Column, τ = 1.0 10 17 80 1.8 10 35 3.7 DU 10 19 0.8 0.45 372 DU 3 10 21 0.024 ~1.0 12,400 DU 7

Solar Spectral Actinic Flux O 3 Huggins & Chappuis Huggins: from ~310 to ~330 nm, τ = 1 @ Ground Chappuis: from 450 to 800 nm, optically thin O 2 Schumann-Runge τ = 1 @ 38 to 140 km FIGURE 6. Solar spectral actinic flux (photons cm 2 s 1 nm 1 ) at the top of Earth s atmosphere. O 2 Herzberg & O 3 Hartley O 2 : σ λ peak @ 200 nm, τ = 1 @ ~29 km O 3 : σ λ peak @ 250 nm, τ = 1 @ ~40 km From DeMore et al., Chemical Kinetics and Photochemical Data for Use in Stratospheric Modeling, Evaluation No. 11, 1994. From Seinfeld and Pandis, Atmospheric Chemistry and Physics, 1998. 8

Photolysis Frequency For a specific spectral interval, the photolysis frequency (partial J value) of a gas is given by the product of its absorption cross section and the solar irradiance: J gas (z,λ) = Quantum_Yield(λ) σ gas (λ,t) F(z,λ) Units: s 1 nm 1 The total photolysis frequency (J value) is found by integrating J gas (z,λ) over all wavelengths for which the gas photodissociates: J gas (z) = λ λ max min do J gas (z, λ) dλ Units: s 1 3 1 Rate of Reaction = = J [O 3] ; Units of J are s dt More precisely, calculations of photolysis frequencies consider the spectral actinic flux, which represents the amount of available photons integrated over all angles, rather than solar irradiance. These two quantities differ because of scattering of solar radiation by gases and aerosols, and reflection of radiation by clouds and the surface. 9

NO 2 Photolysis SZA = 85º Alt = 20 km SZA = 0º 40 km 20 km 0 km 10

O 3 O( 1 D) Photolysis SZA = 85º Alt = 20 km SZA = 0º 40 km 40 km 20 km 20 km 0 km 0 km 11

Bimolecular Gas Phase Reactions 8.9 kcal/mole 35.1 kcal/mole 17.8 kcal/mole 57.8 kcal/mole OH + CH 4 CH 3 + H 2 O dch dt 4 Rate of Reaction = = k [OH][CH 4] Arrhenius Expression for rate constant: Enthalpy = 13.8 kcal/mole Exothermic! E A / R Activation Energy / Gas Constant k e c k A factor S / R Entropy Term = 2.45 10 e cm sec 12 1775 / T 3 1 Energy Term R = 8.3143 10 7 erg / (K mole) = 2.87 10 6 erg / ( K gm) for air Yung and DeMore, Photochemistry of Planetary Atmospheres, Oxford, 1999. 12

Tropospheric Ozone Production versus NO Production of Tropospheric O 3 limited by:? As NO x rises: [HO 2 ] falls faster than [NO] rises, leading to a decrease in the value and hence the production rate of O 3. Illustrative calculation of the dependence of O 3 production on [NO] This curve has key policy implications! 13

Tropospheric Ozone Production versus NO x and VOCs Ridge: local maximum for O 3 that separates the NOx-limited regime from and VOC limited regime NO x Emission Rate (10 12 molec cm -2 s -1 ) VOC limited regime NOx limited regime Jacob, Chapter 12, Introduction to Atmospheric Chemistry, 1999 VOC Emission Rate (10 12 molec cm -2 s -1 ) Figure: http://www-personal.umich.edu/~sillman/ozone.htm 14

Day-to-day meteorology (weather!) affects severity and duration of pollution episodes Maryland has worst air quality during a particular time of year when a certain air circulation system develops H http://www.mde.state.md.us/assets/document/bjh%20-%20basics%20on%20ozone%20transport.ppt 15

Dramatic Improvements Local Air Quality, Past 4 Decades Days BWI T MAX > 90 F 16

Stratospheric Ozone: Chapman Chemistry Production of O 3 initiated when O 2 is photodissociated by UV sunlight O 3 formed when resulting O atom reacts with O 2 : hν + O 2 O + O (1) O + O 2 + M O 3 + M (2) O 3 removed by photodissociation (UV sunlight) or by reaction with O : hν + O 3 O + O 2 (3) O + O 3 O 2 + O 2 (4) This reaction sequence was first worked out in the 1930s by Sidney Chapman, an English mathematician and geophysicist 17

Chapman Chemistry The cycling between O and O 2 (rxns 2 and 3) occurs much more rapidly than leakage into (rxn 1) or out of the system (rxn 4) The sum O + O 3 is commonly called odd oxygen (1) (2) (3) (4) (4) Rxn (1) produces two odd oxygen molecules Rxn (4) consumes two odd oxygen molecules and reactions 2 and 3 recycle odd oxygen molecules 18

Stratospheric Photochemistry: Odd Oxygen Loss By Families Calculated fraction of odd oxygen loss due to various families of radicals After Osterman et al., GRL, 24, 1107, 1997; Sen et al., JGR, 103, 3571. 1998; Sen et al., JGR, 104, 26653, 1999. 19

One Atmosphere One Photochemistry Stratosphere HO 2 formation: OH + O 3 HO 2 + O 2 HO 2 loss: HO 2 + O 3 OH + 2 O 2 Net: O 3 + O 3 3 O 2 Troposphere HO 2 formation: O 2 OH + CO HO 2 + CO 2 HO 2 loss: HO 2 + NO OH + NO 2 Followed by: NO 2 + hν NO +O O+ O 2 + M O 3 + M Tropopause Net: CO + 2 O 2 CO 2 + O 3 Above Tropopause: Lots of O 3, little CO Below Tropopause: Lots of CO, little O 3 Courtesy of Laura Pan, NCAR 20

Tropospheric Chlorine Loading Total Organic Chlorine (CCl y ): Peaked at ~3.6 ppb around 1993 Slowly declining Montreal Protocol and Amendments have banned production of CFCs Table 5A-2, WMO/UNEP (2014) CFCs: long lived (50 to 100 yr lifetime) decompose in the stratosphere lose memory of emission location when enter stratosphere 21

Chlorine Abundance, Mid-Latitude Stratosphere Northern Hemisphere Mid-Latitudes November 1994 ClO 48.8 43.0 37.5 HCl 32.3 ClNO 3 Cl TOT Books 27.2 Balance CCl y 22.3 17.5 0 1.0 2.0 3.0 4.0 APPROX. ALTITUDE (km) ABUNDANCE (parts per billion) Note: Below ~30 km, ClO << ClNO 3 and HCl Zander et al., GRL, 1996 22

Chlorine Source Gases 23

Bromine Source Gases Halons: fire extinguishing agents production in developed world halted by Montreal Protocol present emissions primarily from banks CH 3 Br: fumigant; released by biomass burning production halted by Montreal Protocol significant natural & human sources VSL Gases (e.g., CHBr 3, CH 2 Br 2 ): emitted mainly by ocean biology not considered in most ozone calcs chemistry of decomposition products subject of active research 24

Ozone Depletion at Mid-Latitudes (55 S to 55 N) Column Ozone Anomaly (DU) Ozone data from http://acdb-ext.gsfc.nasa.gov/data_services/merged TSI (DU) Halogens (DU) Sulfate Surface Area (DU) QBO (DU) Predictor Variables Regression Coefficient Column Ozone Anomaly (DU) = 19.5 DU + 2.68 DU / W m 2 TSI + 12.4 DU / ppb Halogens + 0.98 DU ln (SSA) + 0.20 DU / m s 1 QBO where TSI = total solar irradiance Halogens=stratospheric chlorine & bromine loading SSA = Sulfate Surface Area QBO = Quasi-biennial oscillation of the direction of winds in the tropical lower strat 25

BrO x : BrO and Br BrO is central to stratospheric photochemistry, at mid-latitudes and polar regions Production : CH 3 Br + hν Inorganic bromine Halons+ hν Inorganic bromine CHBr 3 + hν Inorganic bromine CH 2 Br 2 + hν Inorganic bromine } } Considered in global models Generally neglected in global models O 3 Br NO BrO HO 2, H 2 CO O, ClO HBr Final sink : HBr solubility & rainout (lowermost stratosphere) 26

BrO x : BrO and Br BrO is central to stratospheric photochemistry, at mid-latitudes and polar regions: Rapid inner cycle: BrO loss step (2): BrO formation: Br + O 3 BrO+ O 2 (1) BrO loss: BrO + NO Br + NO 2 (2) or BrO + O Br + O 2 (3) or BrO + ClO BrCl + O 2 ClOO + Br OClO + Br (4a) (4b) (4c) Followed by: Br + O 3 BrO + O 2 BrO + NO Br + NO 2 Net: O 3 + NO NO 2 + O 2 BrO loss step (3): NO 2 + hν NO + O Final net: O 3 + hν O + O 2 Br + O 3 BrO + O 2 BrO + O Br + O 2 Can show: do3 do d ( Odd Oxygen) + = = 2 k dt dt dt 3 Net: O 3 + O 2 O 2 [BrO][O] As a convenient short hand, we consider BrO to be odd oxygen 27

Bromine Overview Bromine is more efficient, per molecule, than chlorine at removing ozone because: Organic bromine compounds degrade faster than CFCs lifetime of CH 3 Br much shorter than lifetime of CFCs Therefore Br y liberated more easily from CBr y than Cl y liberated from CCl y BrO/Br y >> ClO/Cl y Br + CH 4 HBr + CH 3 is endothermic and has rate constant of zero Cl + CH 4 HCl + CH 3 is exoothermic and proceeds at reasonable rate Also, J BrONO2 > J ClONO2 Loss due to BrO+ClO reaction generally counted as bromine loss, even though loss of ozone by this cycle depends on Br y and Cl y 28

Heterogeneous Chemistry Ozone responds to: a) rise and fall of chlorine b) volcanic perturbations to aerosol loading c) amount of bromine in lowermost stratosphere Low bromine High bromine Salawitch et al., GRL, 2004 29

Heterogeneous Chemistry, Mid-Latitude vs Polar Regions In all cases, γ must be measured in the laboratory Reaction probabilities given for various surface types, with formulations of various degrees of complexity, in Section 5 of the JPL Data Evaluation. Atmospheric Chemistry and Physics by Seinfeld and Pandis provides extensive treatment of aqueous phase chemistry, properties of atmospheric aerosol, organic aerosols, etc. Lecture 11, Slide 19 30

POLAR OZONE LOSS COLD TEMPERATURES POLAR STRATOSPHERIC CLOUDS (PSCs) REACTIONS ON PSC SURFACES LEAD TO ELEVATED ClO HCl + ClNO 3 Cl 2 (gas) + HNO 3 (solid) ClNO 3 + H 2 O HOCl + HNO 3 Cl 2 + SUNLIGHT + O 3 ClO HOCl + SUNLIGHT + O 3 ClO HNO 3 SEDIMENTS (PSCs fall due to gravity) ELEVATED ClO + SUNLIGHT DESTROYS O 3 BrO : REACTION PARTNER FOR ClO ADDITIONAL O 3 LOSS 31

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Arctic Ozone 2011 in Context of Prior Years based on average vortex size 33

Arctic Temperature POLAR STRATOS. CLOUD http://www.cpc.ncep.noaa.gov/products/stratosphere/temperature/archive/50mbnhlo_2011.gif 34

Arctic Temperature: Mar 2015 POLAR STRATOS. CLOUD Last Week http://www.cpc.ncep.noaa.gov/products/stratosphere/temperature/50mbnhlo.gif 35

EXCESS SKIN CANCER CASES 140,000 112,000 84,000 56,000 28,000 EXCESS SKIN CANCER CASES IN THE UNITED STATES, PER YEAR, DUE TO OZONE DEPLETION FOR VARIOUS CFC EMISSION SCENARIOS 0 No Protocol Montreal 1997 Montreal 1987 Longstreth et al., J. of Photochemistry and Photobiology B, 46, 20 39, 1998. London 1990 Copenhagen 1992 1980 2000 2020 2040 2060 2080 2100 YEAR See also Slaper et al., Estimates of ozone depletion and skin cancer incidence to examine the Vienna Convention achievements, Nature, 384, 256 258, 1996, who state: The no-restrictions and Montreal Protocol scenarios produce a runaway increase in skin cancer incidence, up to a quadrupling and doubling, respectively, by year 2100. 36

Second Exam Tuesday, 14 April, 2:00 pm to 3:15 pm CSS 2416 Closed book, no notes Focus mainly on Lectures 9 to 17 Mix of conceptual questions and simple calculations Please bring a calculator (we ll have extras if you forget) use of ipad, iphone or any other device able to go on the web or store notes is not allowed Backbone of course is the lectures and material from readings highlighted in class We ll be present: please let us know if a question requires clarification Exam for 633 will differ somewhat from exam for 433 Copyright 2013 University of Maryland. 37