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

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, or concentrated animal feeding operations, as well as natural sources such as volcanoes. Various jurisdictions have or plan to establish Air Ambient Quality Objectives/Guidelines/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, particle sulfate, hydrogen sulfide (H₂S) and the sum of all remaining reduced sulfur compounds (non-H₂S 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 SO₂ 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 low by 20% on average. Based on this new method, Sulfur dioxide (SO₂) was observed to be responsible for about 40% of the TS mass in Fort McKay, while TRS and particulate sulfate made up 50% and 10%, respectively. TRS dominated the distribution during winter months when SO₂ plumes emitted from stacks tended to remain elevated due to diminished vertical mixing. During periods with TS below 5 ppb, which was 84% of the time, TRS (with H₂S) accounted for 55% of the sulfur mass observed in Fort McKay.