The development and application of a new method for quantifying total atmospheric sulfur in the Alberta Oil Sands

Continuous ambient sulfur measurements are routinely conducted around the globe at numerous monitoring sites impacted by industrial sources, such as gas and oil processing facilities, pulp and paper mills, smelters, sewage treatment facilities, and concentrated animal feeding operations, as well as by natural sources, such as volcanoes. Various jurisdictions have or plan to establish air ambient quality objectives, guidelines, or standards for total reduced sulfur (TRS) based on odor perception and/or health effects. A conventional TRS monitoring technique is widely used, but few studies have looked at potential biases in the resulting TRS measurements. This paper presents a novel method to quantify total sulfur (TS) concentrations to investigate odor events caused by sulfur compounds and to construct the sulfur budget for sulfur dioxide (SO<sub>2</sub>), particle sulfate, hydrogen sulfide (H<sub>2</sub>S), and the sum of all remaining reduced sulfur compounds (non-H<sub>2</sub>S RSCs). This methodology was tested and improved through multi-year monitoring (2013–2017) at the Oski-ôtin site in the indigenous community of Fort McKay, in the Alberta Oil Sands Region (AOSR). Comparisons with SO<sub>2</sub> and conventional TRS data from two long-term monitoring sites located within five kilometers of Oski-ôtin suggest that the conventional approach for TRS is biased, being low by 20% on average. Based on this new method, SO<sub>2</sub> was observed to be responsible for about 40% of the TS mass in Fort McKay, whereas TRS and particle sulfate were 50% and 10%, respectively. During winter months, when SO<sub>2</sub> plumes emitted from stacks tend to remain elevated due to diminished vertical mixing, TRS dominated the distribution. During periods with TS below 5 ppb, which was 84% of the time, TRS (with H<sub>2</sub>S) accounted for 55% of the sulfur mass observed in Fort McKay. <i>Implications</i>: Reduced sulfur compounds have a significant impact on the air quality near various types of industrial emission sources, but their accurate quantification has been hindered by technical problems inherent in standard sulfur measurement methods. We have developed, evaluated and applied a new method for measuring total sulfur. Comparisons in the Alberta Oil Sands suggest that standard methods underestimate total sulfur by typically 20% at this location. Sulfur dioxide (SO<sub>2</sub>) was observed to be responsible for about 40% of the total sulfur mass in Fort McKay, while total reduced sulfur and particulate sulfate made up 50% and 10%, respectively.

Publication Details

Journal
Figshare
Published
2025-01-01
DOI
https://doi.org/10.6084/m9.figshare.28008487.v2
Primary Topic
Odor and Emission Control Technologies
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article
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article

The development and application of a new method for quantifying total atmospheric sulfur in the Alberta Oil Sands

Figshare
Odor and Emission Control Technologies
article

The development and application of a new method for quantifying total atmospheric sulfur in the Alberta Oil Sands

article en

Abstract

Continuous ambient sulfur measurements are routinely conducted around the globe at numerous monitoring sites impacted by industrial sources, such as gas and oil processing facilities, pulp and paper mills, smelters, sewage treatment facilities, and concentrated animal feeding operations, as well as by natural sources, such as volcanoes. Various jurisdictions have or plan to establish air ambient quality objectives, guidelines, or standards for total reduced sulfur (TRS) based on odor perception and/or health effects. A conventional TRS monitoring technique is widely used, but few studies have looked at potential biases in the resulting TRS measurements. This paper presents a novel method to quantify total sulfur (TS) concentrations to investigate odor events caused by sulfur compounds and to construct the sulfur budget for sulfur dioxide (SO<sub>2</sub>), particle sulfate, hydrogen sulfide (H<sub>2</sub>S), and the sum of all remaining reduced sulfur compounds (non-H<sub>2</sub>S RSCs). This methodology was tested and improved through multi-year monitoring (2013–2017) at the Oski-ôtin site in the indigenous community of Fort McKay, in the Alberta Oil Sands Region (AOSR). Comparisons with SO<sub>2</sub> and conventional TRS data from two long-term monitoring sites located within five kilometers of Oski-ôtin suggest that the conventional approach for TRS is biased, being low by 20% on average. Based on this new method, SO<sub>2</sub> was observed to be responsible for about 40% of the TS mass in Fort McKay, whereas TRS and particle sulfate were 50% and 10%, respectively. During winter months, when SO<sub>2</sub> plumes emitted from stacks tend to remain elevated due to diminished vertical mixing, TRS dominated the distribution. During periods with TS below 5 ppb, which was 84% of the time, TRS (with H<sub>2</sub>S) accounted for 55% of the sulfur mass observed in Fort McKay. <i>Implications</i>: Reduced sulfur compounds have a significant impact on the air quality near various types of industrial emission sources, but their accurate quantification has been hindered by technical problems inherent in standard sulfur measurement methods. We have developed, evaluated and applied a new method for measuring total sulfur. Comparisons in the Alberta Oil Sands suggest that standard methods underestimate total sulfur by typically 20% at this location. Sulfur dioxide (SO<sub>2</sub>) was observed to be responsible for about 40% of the total sulfur mass in Fort McKay, while total reduced sulfur and particulate sulfate made up 50% and 10%, respectively.

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Odor and Emission Control Technologies
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