scholarly journals Emissions Preparation and Analysis for Multiscale Air Quality Modelling over the Athabasca Oil Sands Region of Alberta, Canada

Author(s):  
Junhua Zhang ◽  
Michael D. Moran ◽  
Qiong Zheng ◽  
Paul A. Makar ◽  
Pegah Baratzadeh ◽  
...  

Abstract. The oil sands of Alberta, Canada are classified as unconventional oil, but they are also the third-largest oil reserves in the world, behind only Venezuela and Saudi Arabia. We describe here a six-year effort to improve the emissions data used for air quality (AQ) modelling of the roughly 100 km x 100 km oil extraction and processing industrial complex operating in the Athabasca Oil Sands Region (AOSR) of north-eastern Alberta. The objective of this work was to review the available emissions data, provide information for comparison with observation-based emissions estimates, and generate model-ready emissions files for the Global Environmental Multiscale–Modelling Air-quality and CHemistry (GEM-MACH) AQ modelling system for application to the AOSR. GEM-MACH was used to produce nested AQ forecasts during an AQ field study carried out in the AOSR in summer 2013 as well as ongoing experimental forecasts since then and retrospective model simulations and analyses for the field-study period. This paper discusses the generation of GEM-MACH emissions input files, in particular for a high-resolution model domain with 2.5-km grid spacing covering much of western Canada and centred over the AOSR. Prior to the field study, ten pre-2013 national, provincial, or sub-provincial emissions inventories for up to seven criteria-air-contaminant species (NOx, VOC, SO2, NH3, CO, PM2.5, and PM10) that covered the AOSR study area and that had been compiled for various purposes were reviewed, and then a detailed hybrid emissions inventory was created by combining the best available emissions data from some of these ten inventories. After the field study, additional sources of emissions-related data became available, including 2013 hourly SO2 and NOx emissions and stack characteristics for large point sources measured by Continuous Emission Monitoring Systems, 2013-specific national inventories, daily reports of SO2 emissions from one AOSR facility for a one-week period during the field campaign when that facility experienced upset conditions, aircraft measurements of VOC and PM2.5 concentrations from the 2013 field campaign and derived estimates of their emissions, and measurements of chemical composition of dust collected from various AOSR sites. These new data were used to generate updated emissions input files for various post-campaign GEM-MACH sensitivity studies. Their inclusion resulted in some significant emissions revisions, including a reduction in total VOC and SO2 emissions from surface mining facilities of about 40 % and 20 %, respectively, and a ten-fold increase in PM2.5 emissions based on aircraft observations. In addition, standard emissions processing approaches could not provide an accurate representation of emissions from such large, unconventional emissions sources as AOSR surface mines. In order to generate more accurate high-resolution, model-ready emissions files, AOSR-specific improvements were made to the emissions processing methodology. To account for the urban-scale spatial extent of the AOSR mining facilities and the high-resolution 2.5-km model grid, novel facility-specific gridded spatial surrogate fields were generated using spatial information from GIS (geographic information system) shapefiles and satellite images to allocate emissions spatially within each mining facility. Facility- and process-specific temporal profiles and VOC speciation profiles were also developed. The pre-2013 vegetation and land-use data bases normally used to estimate biogenic emissions and meteorological surface properties were modified to account for the rapid change of land use in the study area due to marked, year-by-year changes in surface mining activities, including the 2013 opening of a new mine. Lastly, mercury emissions data were also processed to support AOSR mercury modelling activities. The combination of emissions inventory updates and methodological improvements to emissions processing has resulted in a more representative and more accurate set of emissions input files to support AQ modelling to predict the ecosystem impacts of AOSR air pollutant emissions. Seven other papers in this special issue used some of these new sets of emissions input files.

2018 ◽  
Vol 18 (10) ◽  
pp. 7361-7378 ◽  
Author(s):  
Sabour Baray ◽  
Andrea Darlington ◽  
Mark Gordon ◽  
Katherine L. Hayden ◽  
Amy Leithead ◽  
...  

Abstract. Aircraft-based measurements of methane (CH4) and other air pollutants in the Athabasca Oil Sands Region (AOSR) were made during a summer intensive field campaign between 13 August and 7 September 2013 in support of the Joint Canada–Alberta Implementation Plan for Oil Sands Monitoring. Chemical signatures were used to identify CH4 sources from tailings ponds (BTEX VOCs), open pit surface mines (NOy and rBC) and elevated plumes from bitumen upgrading facilities (SO2 and NOy). Emission rates of CH4 were determined for the five primary surface mining facilities in the region using two mass-balance methods. Emission rates from source categories within each facility were estimated when plumes from the sources were spatially separable. Tailings ponds accounted for 45 % of total CH4 emissions measured from the major surface mining facilities in the region, while emissions from operations in the open pit mines accounted for ∼ 50 %. The average open pit surface mining emission rates ranged from 1.2 to 2.8 t of CH4 h−1 for different facilities in the AOSR. Amongst the 19 tailings ponds, Mildred Lake Settling Basin, the oldest pond in the region, was found to be responsible for the majority of tailings ponds emissions of CH4 (> 70 %). The sum of measured emission rates of CH4 from the five major facilities, 19.2 ± 1.1 t CH4 h−1, was similar to a single mass-balance determination of CH4 from all major sources in the AOSR determined from a single flight downwind of the facilities, 23.7 ± 3.7 t CH4 h−1. The measured hourly CH4 emission rate from all facilities in the AOSR is 48 ± 8 % higher than that extracted for 2013 from the Canadian Greenhouse Gas Reporting Program, a legislated facility-reported emissions inventory, converted to hourly units. The measured emissions correspond to an emissions rate of 0.17 ± 0.01 Tg CH4 yr−1 if the emissions are assumed as temporally constant, which is an uncertain assumption. The emission rates reported here are relevant for the summer season. In the future, effort should be devoted to measurements in different seasons to further our understanding of the seasonal parameters impacting fugitive emissions of CH4 and to allow for better estimates of annual emissions and year-to-year variability.


2012 ◽  
Vol 12 (8) ◽  
pp. 3677-3685 ◽  
Author(s):  
A. Maurizi ◽  
F. Russo ◽  
M. D'Isidoro ◽  
F. Tampieri

Abstract. The interaction between air quality and climate involves dynamical scales that cover a very wide range. Bridging these scales in numerical simulations is fundamental in studies devoted to megacity/hot-spot impacts on larger scales. A technique based on nudging is proposed as a bridging method that can couple different models at different scales. Here, nudging is used to force low resolution chemical composition models with a run of a high resolution model on a critical area. A one-year numerical experiment focused on the Po Valley hot spot is performed using the BOLCHEM model to asses the method. The results show that the model response is stable to perturbation induced by the nudging and that, taking the high resolution run as a reference, performances of the nudged run increase with respect to the non-forced run. The effect outside the forcing area depends on transport and is significant in a relevant number of events although it becomes weak on seasonal or yearly basis.


2018 ◽  
Vol 18 (14) ◽  
pp. 10459-10481 ◽  
Author(s):  
Junhua Zhang ◽  
Michael D. Moran ◽  
Qiong Zheng ◽  
Paul A. Makar ◽  
Pegah Baratzadeh ◽  
...  

Abstract. The oil sands (OS) of Alberta, Canada, which are classified as unconventional oil, are the third-largest oil reserves in the world. We describe here a 6-year effort to improve the emissions data used for air quality (AQ) modeling of the roughly 100 km × 100 km oil extraction and processing industrial complex operating in the Athabasca Oil Sands Region (AOSR) of northeastern Alberta. This paper reviews the national, provincial, and sub-provincial emissions inventories that were available during the three phases of the study, supplemented by hourly SO2 and NOx emissions and stack characteristics for larger point sources measured by a continuous emission monitoring system (CEMS), as well as daily reports of SO2 from one AOSR facility for a 1-week period during a 2013 field campaign when the facility experienced upset conditions. Next it describes the creation of several detailed hybrid emissions inventories and the generation of model-ready emissions input files for the Global Environmental Multiscale–Modelling Air quality and CHemistry (GEM-MACH) AQ modeling system that were used during the 2013 field study and for various post-campaign GEM-MACH sensitivity studies, in particular for a high-resolution model domain with 2.5 km grid spacing covering much of western Canada and centered over the AOSR. Lastly, it compares inventory-based bottom-up emissions with aircraft-observation-based top-down emissions estimates. Results show that emissions values obtained from different data sources can differ significantly, such as a possible 10-fold difference in PM2.5 emissions and approximately 40 and 20 % differences for total VOC (volatile organic compound) and SO2 emissions. A novel emissions-processing approach was also employed to allocate emissions spatially within six large AOSR mining facilities in order to address the urban-scale spatial extent of the facilities and the high-resolution 2.5 km model grid. Gridded facility- and process-specific spatial surrogate fields that were generated using spatial information from GIS (geographic information system) shapefiles and satellite images were used to allocate non-smokestack emissions for each facility to multiple grid cells instead of treating these emissions as point sources and allocating them to a single grid cell as is normally done. Facility- and process-specific temporal profiles and VOC speciation profiles were also developed. The pre-2013 vegetation and land-use databases normally used to estimate biogenic emissions and meteorological surface properties were modified to account for the rapid change in land use in the study area due to marked, year-by-year changes in surface mining activities, including the 2013 opening of a new mine. Lastly, mercury emissions data were also processed in addition to the seven criteria-air-contaminant (CAC) species (NOx, VOC, SO2, NH3, CO, PM2.5, and PM10) to support AOSR mercury modeling activities. Six GEM-MACH modeling papers in this special issue used some of these new sets of emissions and land-use input files.


2017 ◽  
Author(s):  
Sabour Baray ◽  
Andrea Darlington ◽  
Mark Gordon ◽  
Katherine L. Hayden ◽  
Amy Leithead ◽  
...  

Abstract. Aircraft-based measurements of methane (CH4) and other air pollutants in the Athabasca Oil Sands Region (AOSR) were made during a summer intensive field campaign between August 13 and September 7 2013, in support of the Joint Canada–Alberta Implementation Plan for Oil Sands Monitoring. Chemical signatures were used to identify CH4 sources from tailings ponds (BTEX VOC's), open-pit surface mines (NOy and rBC) and elevated plumes from bitumen upgrading facilities (SO2 and NOy). Emission rates of CH4 were determined for the five primary surface mining facilities in the region using two mass balance methods. Emission rates from source categories within each facility were estimated when plumes from the sources were spatially separable. Tailings ponds accounted for 45 % of total CH4 emissions measured from the major surface mining facilities in the region while emissions from operations in the open pit mines accounted for ~ 50 %. The average open pit surface mining emission rates ranged from 1.2 to 2.8 tonnes of CH4 hr−1 for different facilities in the AOSR. Amongst the 19 tailings ponds, Mildred Lake Settling Basin, the oldest pond in the region, was found to be responsible for the majority of tailings ponds emissions of CH4 (> 70 %). The sum of measured emission rates of CH4 from the five major facilities, 19.2 ± 1.1 tonnes CH4 hr−1, was similar to a single mass balance determination of CH4 from all major sources in the AOSR determined from a single flight downwind of the facilities, 23.7 ± 3.7 tonnes CH4 hr−1. The measured hourly CH4 emission rate from all facilities in the AOSR is 48 ± 8 % higher than that extracted for 2013 from the Canadian Green House Gas Reporting Program, a legislated facility-reported Emissions Inventory, converted to hourly units. The measured emissions correspond to an emissions rate of 0.17 ± 0.01 Tg CH4 yr−1, if the emissions are assumed temporally constant, an uncertain assumption. The emission rates reported here are relevant for the summer season. In future, effort should be devoted to measurements in different seasons to further our understanding of seasonal parameters impacting fugitive emissions of CH4 and to allow better estimates of annual emissions and year to year variability.


2013 ◽  
Vol 140 (681) ◽  
pp. 1189-1197 ◽  
Author(s):  
J. A. Waller ◽  
S. L. Dance ◽  
A. S. Lawless ◽  
N. K. Nichols ◽  
J. R. Eyre

2002 ◽  
Vol 5 (3) ◽  
pp. 212-212 ◽  
Author(s):  
U. Tiede ◽  
A. Pommert ◽  
B. Pflesser ◽  
E. Richter ◽  
M. Riemer ◽  
...  

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