scholarly journals Three-dimensional model evaluation of the Ozone Depletion Potentials for n-propyl bromide, trichloroethylene and perchloroethylene

2010 ◽  
Vol 10 (7) ◽  
pp. 17889-17910 ◽  
Author(s):  
D. J. Wuebbles ◽  
K. O. Patten ◽  
D. Wang ◽  
D. Youn ◽  
M. Martínez-Avilés ◽  
...  
Keyword(s):  
Ozone Depletion ◽  
Transport Model ◽  
Stratospheric Ozone ◽  
Three Dimensional ◽  
Three Dimensional Model ◽  
Chemistry Transport Model ◽  
Atmospheric Lifetime ◽  
Land Surfaces ◽  
Simplified Modeling ◽  
First Time

Abstract. The existing solvents trichloroethylene (TCE) and perchloroethylene (PCE) and proposed solvent n-propyl bromide (nPB) have atmospheric lifetimes from days to a few months, but contain chlorine or bromine that could affect stratospheric ozone. Several previous studies estimated the Ozone Depletion Potentials (ODPs) for various assumptions for location of nPB emissions, but these studies used simplified modeling treatments. The primary purpose of this study is to reevaluate the ODP for nPB using a current-generation chemistry-transport model of the troposphere and stratosphere. For the first time, ODPs for TCE and PCE are also evaluated. Emissions representing industrial use of each compound are incorporated on land surfaces from 30° N to 60° N. The atmospheric chemical lifetime obtained for nPB is 24.7 days, similar to past literature, but the ODP is 0.0049, lower than in past studies. The derived atmospheric lifetime for TCE is 13.0 days and for PCE is 111 days. The corresponding ODPs are 0.00035 and 0.0060, respectively.

scholarly journals Three-dimensional model evaluation of the Ozone Depletion Potentials for n-propyl bromide, trichloroethylene and perchloroethylene

2011 ◽  
Vol 11 (5) ◽  
pp. 2371-2380 ◽  
Author(s):  
D. J. Wuebbles ◽  
K. O. Patten ◽  
D. Wang ◽  
D. Youn ◽  
M. Martínez-Avilés ◽  
...  
Keyword(s):  
Atmospheric Chemistry ◽  
Ozone Depletion ◽  
Transport Model ◽  
Stratospheric Ozone ◽  
Three Dimensional ◽  
Past Study ◽  
Three Dimensional Model ◽  
Chemistry Transport Model ◽  
Land Surfaces ◽  
Simplified Modeling

Abstract. The existing solvents trichloroethylene (TCE) and perchloroethylene (PCE) and proposed solvent n-propyl bromide (nPB) have atmospheric lifetimes from days to a few months, but contain chlorine or bromine that could affect stratospheric ozone. Several previous studies estimated the Ozone Depletion Potentials (ODPs) for various assumptions of nPB emissions location, but these studies used simplified modeling treatments. The primary purpose of this study is to reevaluate the ODP for n-propyl bromide (nPB) using a current-generation chemistry-transport model of the troposphere and stratosphere. For the first time, ODPs for TCE and PCE are also evaluated in a three-dimensional, global atmospheric chemistry-transport model. Emissions representing industrial use of each compound are incorporated on land surfaces from 30° N to 60° N. The atmospheric chemical lifetime obtained for nPB is 24.7 days, similar to past literature, but the ODP is 0.0049, lower than in our past study of nPB. The derived atmospheric lifetime for TCE is 13.0 days and for PCE is 111 days. The corresponding ODPs are 0.00037 and 0.0050, respectively.

scholarly journals Atmospheric lifetimes and Ozone Depletion Potentials of trans-1-chloro-3,3,3-trifluoropropylene and trans-1,2-dichloroethylene in a three-dimensional model

2010 ◽  
Vol 10 (22) ◽  
pp. 10867-10874 ◽  
Author(s):  
K. O. Patten ◽  
D. J. Wuebbles
Keyword(s):  
Environmental Effects ◽  
Atmospheric Chemistry ◽  
Ozone Depletion ◽  
Stratospheric Ozone ◽  
Three Dimensional ◽  
Dimensional Model ◽  
Three Dimensional Model ◽  
Atmospheric Lifetime ◽  
Ozone Loss ◽  
Land Surfaces

Abstract. The chloroalkenes trans-1-chloro-3,3,3-trifluoropropylene (tCFP) and trans-1,2-dichloroethylene (tDCE) have been proposed as candidate replacements for other compounds in current use that cause concerns regarding potential environmental effects including destruction of stratospheric ozone. Because tCFP and tDCE contain chlorine atoms, the effects of these short-lived compounds on stratospheric ozone must be established. In this study, we derive the atmospheric lifetimes and Ozone Depletion Potentials (ODPs) for tCFP and for tDCE assuming emissions from land surfaces at latitudes 30° N to 60° N using the MOZART 3 three-dimensional model of atmospheric chemistry and physics. 53% of the ozone loss due to tCFP and 98% of the ozone loss due to tDCE take place in the troposphere, rather than in the stratosphere as generally expected from longer-lived chlorocarbons. The atmospheric lifetime of tCFP against chemical reaction is 40.4 days, and its ODP is quite small at 0.00034. The tDCE atmospheric lifetime is 12.7 days, and its ODP is 0.00024, which is the lowest ODP found for any chlorocarbon we have studied. Our study suggests that chlorine from tCFP and tDCE are unlikely to affect ozone at quantities likely to be emitted to the atmosphere.

scholarly journals Atmospheric lifetimes and ozone depletion potentials of trans-1-chloro-3,3,3-trifluoropropylene and trans-1,2-dichloroethylene in a three-dimensional model

2010 ◽  
Vol 10 (7) ◽  
pp. 16637-16657 ◽  
Author(s):  
K. O. Patten ◽  
D. J. Wuebbles
Keyword(s):  
Chemical Reaction ◽  
Environmental Effects ◽  
Atmospheric Chemistry ◽  
Ozone Depletion ◽  
Stratospheric Ozone ◽  
Three Dimensional ◽  
Dimensional Model ◽  
Three Dimensional Model ◽  
Atmospheric Lifetime ◽  
Land Surfaces

Abstract. The chloroalkenes trans-1-chloro-3,3,3-trifluoropropylene (tCFP) and trans-1,2-dichloroethylene (tDCE) have been proposed as candidate replacements for other compounds in current use that cause concerns regarding potential environmental effects including destruction of stratospheric ozone. Because tCFP and tDCE contain chlorine atoms, the effects of these short-lived compounds on stratospheric ozone must be established. In this study, we derive the atmospheric lifetimes and Ozone Depletion Potentials (ODPs) for tCFP and for tDCE assuming emissions from land surfaces at latitudes 30° N to 60° N using the MOZART 3 three-dimensional model of atmospheric chemistry and physics. Both tCFP and tDCE are shown to primarily affect ozone in the troposphere, rather than in the stratosphere as generally expected from longer-lived chlorocarbons. The atmospheric lifetime of tCFP against chemical reaction is 40.4 days, and its ODP is quite small at 0.00034. The tDCE atmospheric lifetime is 12.7 days, and its ODP is 0.00024, which is the lowest ODP found for any chlorocarbon we have studied. Our study suggests that chlorine from tCFP and tDCE are unlikely to significantly affect ozone at quantities likely to be emitted to the atmosphere.

scholarly journals Potential impact of iodinated replacement compounds CF<sub>3</sub>I and CH<sub>3</sub>I on atmospheric ozone: a three-dimensional modeling study

2010 ◽  
Vol 10 (7) ◽  
pp. 16659-16690
Author(s):  
◽  
K. O. Patten ◽  
D. J. Wuebbles ◽  
◽  
Keyword(s):  
Transport Model ◽  
Stratospheric Ozone ◽  
Three Dimensional ◽  
Atmospheric Ozone ◽  
Dimensional Model ◽  
Three Dimensional Model ◽  
Model Calculations ◽  
Three Dimensional Modeling ◽  
Land Surfaces ◽  
The Tropics

Abstract. The concept of Ozone Depletion Potentials (ODPs) is extensively used in policy considerations related to concerns about the effects of various halocarbons and other gases on stratospheric ozone. Many of the recent candidate replacement compounds have atmospheric lifetimes shorter than one year in order to limit their environmental effects, especially on stratospheric ozone. Using a three-dimensional global chemistry-transport model (CTM) of the troposphere and the stratosphere, the purpose of this study is to evaluate the potential effects of several very short-lived iodinated substances, namely iodotrifluoromethane (CF3I) and methyl iodide (CH3I), on atmospheric ozone. Like other chemicals with extremely short lifetimes, the stratospheric halogen loading and resulting ozone effects from these compounds are strongly dependent on the location of emissions. For CF3I, a possible replacement candidate for bromotrifluoromethane (CF3Br), ODPs derived by the three-dimensional model are 0.008 with chemical lifetime of 5.03 days and 0.016 with a lifetime of 1.13 days for emissions assumed to be evenly distributed over land surfaces at mid-latitudes and the tropics, respectively. While this is the first time the ODPs have been evaluated with a three-dimensional model, these values are in good agreement with those derived previously. The model calculations suggest that tropical convection could deliver a larger portion of the gas and their breakdown products to the upper troposphere and lower stratosphere if emission source is located in the tropics. The resulting ODP for CH3I, emitted from mid-latitudes, is 0.017 with lifetime of 13.59 days. The validity of our model iodine chemistry to evaluate ODPs of the iodine species is guaranteed with good qualitative agreement between the model derived distribution of background CH3I, based on global source emission fluxes from previous studies, and available observations especially in vertical profiles.

scholarly journals Stratospheric ozone depletion during the 1995–1996 Arctic winter: 3-D simulations on the potential role of different PSC types

2001 ◽  
Vol 19 (9) ◽  
pp. 1163-1181 ◽  
Author(s):  
J. Hendricks ◽  
F. Baier ◽  
G. Günther ◽  
B. C. Krüger ◽  
A. Ebel
Keyword(s):  
Ozone Depletion ◽  
Middle Atmosphere ◽  
Spatial Scales ◽  
Stratospheric Ozone ◽  
Three Dimensional ◽  
Particle Growth ◽  
Atmospheric Composition ◽  
Formation Mechanisms ◽  
Three Dimensional Model ◽  
Type Ia

Abstract. The sensitivity of modelled ozone depletion in the winter Arctic stratosphere to different assumptions of prevalent PSC types and PSC formation mechanisms is investigated. Three-dimensional simulations of the winter 1995/96 are performed with the COlogne Model of the Middle Atmosphere (COMMA) by applying different PSC microphysical schemes. Model runs are carried out considering either liquid or solid PSC particles or a combined microphysical scheme. These simulations are then compared to a model run which only takes into account binary sulfate aerosols. The results obtained with the three-dimensional model agree with trajectory-box simulations performed in previous studies. The simulations suggest that conditions appropriate for type Ia PSC existence (T < TNAT ) occur over longer periods and cover larger areas when compared to conditions of potential type Ib PSC existence. Significant differences in chlorine activation and ozone depletion occur between the simulations including only either liquid or solid PSC particles. The largest differences, occurring over large spatial scales and during prolonged time periods, are modelled first, when the stratospheric temperatures stay below TNAT , but above the threshold of effective liquid particle growth and second, in the case of the stratospheric temperatures remaining below this threshold, but not falling below the ice frost point. It can be generally concluded from the present study that differences in PSC microphysical schemes can cause significant fluctuations in ozone depletion modelled for the winter Arctic stratosphere.Key words. Atmospheric composition and structure (aerosols and particles; cloud physics and chemistry; middle atmosphere composition and chemistry)

scholarly journals Potential impact of iodinated replacement compounds CF<sub>3</sub>I and CH<sub>3</sub>I on atmospheric ozone: a three-dimensional modeling study

2010 ◽  
Vol 10 (20) ◽  
pp. 10129-10144 ◽  
Author(s):  
D. Youn ◽  
K. O. Patten ◽  
D. J. Wuebbles ◽  
H. Lee ◽  
C.-W. So
Keyword(s):  
Transport Model ◽  
Stratospheric Ozone ◽  
Vertical Mixing ◽  
Three Dimensional ◽  
Convective Transport ◽  
Atmospheric Ozone ◽  
Dimensional Model ◽  
Three Dimensional Model ◽  
Model Calculations ◽  
The Tropics

Abstract. The concept of Ozone Depletion Potentials (ODPs) is extensively used in policy considerations related to concerns about the effects of various halocarbons and other gases on stratospheric ozone. Many of the recent candidate replacement compounds have atmospheric lifetimes shorter than one year in order to limit their environmental effects, especially on stratospheric ozone. Using a three-dimensional global chemistry-transport model (CTM) of the troposphere and the stratosphere, the purpose of this study is to evaluate the potential effects of several very short-lived iodinated substances, namely iodotrifluoromethane (CF3I) and methyl iodide (CH3I), on atmospheric ozone. Like other chemicals with extremely short lifetimes, the stratospheric halogen loading and resulting ozone effects from these compounds are strongly dependent on the location of emissions. For CF3I, a possible replacement candidate for bromotrifluoromethane (CF3Br), ODPs derived by the three-dimensional model are 0.008 with chemical lifetime of 5.03 days and 0.016 with a lifetime of 1.13 days for emissions assumed to be evenly distributed over land surfaces at mid-latitudes and the tropics, respectively. While this is the first time the ODPs have been evaluated with a three-dimensional model, these values are in good agreement with those derived previously. The model calculations suggest that tropical convection could deliver a larger portion of the gas and their breakdown products to the upper troposphere and lower stratosphere if emission source is located in the tropics. The resulting ODP for CH3I, emitted from mid-latitudes, is 0.017 with lifetime of 13.59 days. Valid simulations of convective transport, vertical mixing and degradation chemistry of CH3I are shown that have good qualitative agreement between the model derived distribution of background CH3I, based on global source emission fluxes from previous studies, and available observations especially in vertical profiles.

scholarly journals Assimilation of stratospheric ozone in the chemical transport model STRATAQ

2004 ◽  
Vol 22 (8) ◽  
pp. 2669-2678 ◽  
Author(s):  
B. Grassi ◽  
G. Redaelli ◽  
G. Visconti
Keyword(s):  
Total Ozone ◽  
Transport Model ◽  
Stratospheric Ozone ◽  
Three Dimensional ◽  
Chemical Transport ◽  
Numerical Code ◽  
Chemical Transport Model ◽  
Three Dimensional Model ◽  
Simultaneous Evaluation ◽  
Analysis Errors

Abstract. We describe a sequential assimilation approach useful for assimilating tracer measurements into a three-dimensional chemical transport model (CTM) of the stratosphere. The numerical code, developed largely according to Kha00, uses parameterizations and simplifications allowing assimilation of sparse observations and the simultaneous evaluation of analysis errors, with reasonable computational requirements. Assimilation parameters are set by using χ2 and OmF (Observation minus Forecast) statistics. The CTM used here is a high resolution three-dimensional model. It includes a detailed chemical package and is driven by UKMO (United Kingdom Meteorological Office) analyses. We illustrate the method using assimilation of Upper Atmosphere Research Satellite/Microwave Limb Sounder (UARS/MLS) ozone observations for three weeks during the 1996 antarctic spring. The comparison of results from the simulations with TOMS (Total Ozone Mapping Spectrometer) measurements shows improved total ozone fields due to assimilation of MLS observations. Moreover, the assimilation gives indications on a possible model weakness in reproducing polar ozone values during springtime.

Record springtime stratospheric ozone depletion at 80°N in 2020

2021 ◽  
Author(s):  
Ramina Alwarda ◽  
Kristof Bognar ◽  
Kimberly Strong ◽  
Martyn Chipperfield ◽  
Sandip Dhomse ◽  
...  
Keyword(s):  
Ozone Depletion ◽  
Transport Model ◽  
Stratospheric Ozone ◽  
Polar Vortex ◽  
The Arctic ◽  
Optical Absorption Spectroscopy ◽  
Chemical Transport Model ◽  
Polar Stratospheric Clouds ◽  
Ozone Loss ◽  
Stratospheric Clouds

&lt;p&gt;The Arctic winter of 2019-2020 was characterized by an unusually persistent polar vortex and temperatures in the lower stratosphere that were consistently below the threshold for the formation of polar stratospheric clouds (PSCs). These conditions led to ozone loss that is comparable to the Antarctic ozone hole. Ground-based measurements from a suite of instruments at the Polar Environment Atmospheric Research Laboratory (PEARL) in Eureka, Canada (80.05&amp;#176;N, 86.42&amp;#176;W) were used to investigate chemical ozone depletion. The vortex was located above Eureka longer than in any previous year in the 20-year dataset and lidar measurements provided evidence of polar stratospheric clouds (PSCs) above Eureka. Additionally, UV-visible zenith-sky Differential Optical Absorption Spectroscopy (DOAS) measurements showed record ozone loss in the 20-year dataset, evidence of denitrification along with the slowest increase of NO&lt;sub&gt;2&lt;/sub&gt; during spring, as well as enhanced reactive halogen species (OClO and BrO). Complementary measurements of HCl and ClONO&lt;sub&gt;2&lt;/sub&gt; (chlorine reservoir species) from a Fourier transform infrared (FTIR) spectrometer showed unusually low columns that were comparable to 2011, the previous year with significant chemical ozone depletion. Record low values of HNO&lt;sub&gt;3&lt;/sub&gt; in the FTIR dataset are in accordance with the evidence of PSCs and a denitrified atmosphere. Estimates of chemical ozone loss were derived using passive ozone from the SLIMCAT offline chemical transport model to account for dynamical contributions to the stratospheric ozone budget.&lt;/p&gt;

scholarly journals Analysis of a rapid increase of stratospheric ozone during late austral summer 2008 over Kerguelen (49.4° S, 70.3° E)

2011 ◽  
Vol 11 (1) ◽  
pp. 363-373 ◽  
Author(s):  
H. Bencherif ◽  
L. El Amraoui ◽  
G. Kirgis ◽  
J. Leclair De Bellevue ◽  
A. Hauchecorne ◽  
...  
Keyword(s):  
Potential Vorticity ◽  
Large Scale ◽  
Lower Stratosphere ◽  
Transport Model ◽  
Stratospheric Ozone ◽  
Three Dimensional ◽  
Austral Summer ◽  
Air Masses ◽  
Global Mapping ◽  
The Tropics

Abstract. This paper reports on an increase of ozone event observed over Kerguelen (49.4° S, 70.3° E) in relationship with large-scale isentropic transport. This is evidenced by ground-based observations (co-localised radiosonde and SAOZ experiments) together with satellite global observations (Aura/MLS) assimilated into MOCAGE, a Méteo-France model. The study is based on the analyses of the first ozonesonde experiment never recorded at the Kerguelen site within the framework of a French campaign called ROCK that took place from April to August 2008. Comparisons and interpretations of the observed event are supported by co-localised SAOZ observations, by global mapping of tracers (O3, N2O and columns of O3) from Aura/MLS and Aura/OMI experiments, and by model simulations of Ertel Potential Vorticity initialised by the ECMWF (European Centre for Medium-Range Weather Forecasts) data reanalyses. Satellite and ground-based observational data revealed a consistent increase of ozone in the local stratosphere by mid-April 2008. Additionally, Ozone (O3) and nitrous oxide (N2O) profiles obtained during January–May 2008 using the Microwave Limb Sounder (MLS) aboard the Aura satellite are assimilated into MOCAGE (MOdèle de Chimie Atmosphérique à Grande Echelle), a global three-dimensional chemistry transport model of Météo-France. The assimilated total O3 values are consistent with SAOZ ground observations (within ±5%), and isentropic distributions of O3 match well with maps of advected potential vorticity (APV) derived from the MIMOSA model, a high-resolution advection transport model, and from the ECMWF reanalysis. The event studied seems to be related to the isentropic transport of air masses that took place simultaneously in the lower- and middle-stratosphere, respectively from the polar region and from the tropics to the mid-latitudes. In fact, the ozone increase observed by mid April 2008 resulted simultaneously: (1) from an equator-ward departure of polar air masses characterised with a high-ozone layer in the lower stratosphere (near the 475 K isentropic level), and (2) from a reverse isentropic transport from the tropics to mid- and high-latitudes in the upper stratosphere (nearby the 700 K level). The increase of ozone observed over Kerguelen from the 16-April ozonesonde profile is thus attributed to a concomitant isentropic transport of ozone in two stratospheric layers: the tropical air moving southward and reaching over Kerguelen in the upper stratosphere, and the polar air passing over the same area but in the lower stratosphere.

scholarly journals A three-dimensional model study of long-term mid-high latitude lower stratosphere ozone changes

2003 ◽  
Vol 3 (1) ◽  
pp. 1081-1107 ◽  
Author(s):  
M. P. Chipperfield
Keyword(s):  
High Latitude ◽  
Lower Stratosphere ◽  
Transport Model ◽  
Three Dimensional ◽  
Horizontal Resolution ◽  
Chemical Transport Model ◽  
Three Dimensional Model ◽  
Detailed Chemistry ◽  
Basic Model ◽  
Column Ozone

Abstract. We have used a 3D off-line chemical transport model (CTM) to study the causes of the observed changes in ozone in the mid-high latitude lower stratosphere from 1979–1998. The model was forced by European Centre for Medium Range Weather Forecasts (ECMWF) analyses and contains a detailed chemistry scheme. A series of model runs were performed at a horizontal resolution of 7.5°×7.5° and covered the domain from about 12 km to 30 km. The basic model performs well in reproducing the decadal evolution of the springtime depletion in the northern hemisphere (NH) and southern hemisphere (SH) high latitudes in the 1980s and early 1990s. After about 1994 the modelled interannual variability does not match the observations as well, which is probably due in part to changes in the operational ECMWF analyses – which places limits on using this dataset to diagnose dynamical trends. For mid-latitudes (35°–60°) the basic model reproduces the observed column ozone decreases from 1980 until the early 1990s. Model experiments show that the halogen trends appear to dominate this modelled decrease and of this around 30–50% is due to high-latitude processing on polar stratospheric clouds (PSCs). Dynamically induced ozone variations in the model correlate with observations over the timescale of a few years. Large discrepancies between the modelled and observed variations in the mid 1980s and mid 1990s can be largely resolved by assuming that the 11-year solar cycle (not explicitly included in the 3D model) causes a 2% (min-max) change in mid-latitude column ozone.

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