First Comprehensive Measurements of Emission Rates of Greenhouse Gases, Volatile Organic Compounds and Reduced Sulfur Compounds from a Tailings Pond in the Alberta Oil Sands

Author(s):  
Ralf Staebler ◽  
Samar Moussa ◽  
Yuan You ◽  
Hayley Hung ◽  
Maryam Moradi ◽  
...  

<p>Canada’s Oil Sands Region in northern Alberta contains the world’s largest deposits of commercially exploited bitumen. Extraction of synthetic crude oil from these deposits is a water intensive process, requiring large ponds for water recycling and/or final storage of tailings, already covering a total of over 100 km<sup>2</sup> of liquid surface area in the Athabasca Oil sands. The primary extraction tailings ponds primarily contain sand, silt, clay and unrecovered bitumen, while a few secondary extraction ponds also receive solvents and inorganic and organic by-products of the extraction process. Fugitive emissions of pollutants from these ponds to the atmosphere may therefore be a concern, but until recently, data on emission rates for many pollutants, other than a few reported under regulatory compliance monitoring, were sparse. We present here the results from a comprehensive field campaign to quantify the emissions from a secondary extraction pond to the atmosphere of 68 volatile organic compounds (VOCs), 22 polycyclic aromatic compounds (PACs), 8 reduced sulfur compounds as well as methane, carbon dioxide and ammonia. Three micrometeorological flux methods (eddy covariance, vertical gradients and inverse dispersion modeling) were evaluated for methane fluxes to ensure their mutual comparability. Methane and carbon dioxide fluxes were similar to previous results based on flux chamber measurements. Emission rates for 12 PACs, alkanes and aromatic VOCs, several sulfur species, and ammonia were found to be significant. PACs were dominated by methyl naphthalenes and phenanthrenes, while diethylsulfide and  and n-heptane were the dominant reduced sulfur and VOC species, respectively. The role of these previously unavailable emission rates in regional pollutant budgets will be discussed.</p>

2021 ◽  
Vol 7 (6) ◽  
pp. 465
Author(s):  
Takahito Toyotome ◽  
Masahiko Takino ◽  
Masahiro Takaya ◽  
Maki Yahiro ◽  
Katsuhiko Kamei

Schizophyllum commune is a causative agent of allergic bronchopulmonary mycosis, allergic fungal rhinosinusitis, and basidiomycosis. Diagnosis of these diseases remains difficult because no commercially available tool exists to identify the pathogen. Unique volatile organic compounds produced by a pathogen might be useful for non-invasive diagnosis. Here, we explored microbial volatile organic compounds produced by S. commune. Volatile sulfur compounds, dimethyl disulfide (48 of 49 strains) and methyl ethyl disulfide (49 of 49 strains), diethyl disulfide (34 of 49 strains), dimethyl trisulfide (40 of 49 strains), and dimethyl tetrasulfide (32 of 49 strains) were detected from headspace air in S. commune cultured vials. Every S. commune strain produced at least one volatile sulfur compound analyzed in this study. Those volatile sulfur compounds were not detected from the cultures of Aspergillus spp. (A. fumigatus, A. flavus, A. niger, and A. terreus), which are other major causative agents of allergic bronchopulmonary mycosis. The last, we examined H2S detection using lead acetate paper. Headspace air from S. commune rapidly turned the lead acetate paper black. These results suggest that those volatile sulfur compounds are potent targets for the diagnosis of S. commune and infectious diseases.


1996 ◽  
Vol 5 (4) ◽  
pp. 232-235
Author(s):  
Stefan Willers ◽  
Sven Andersson ◽  
Rolf Andersson ◽  
Jörgen Grantén ◽  
Christina Sverdrup ◽  
...  

2010 ◽  
Vol 10 (17) ◽  
pp. 8391-8412 ◽  
Author(s):  
B. Langford ◽  
P. K. Misztal ◽  
E. Nemitz ◽  
B. Davison ◽  
C. Helfter ◽  
...  

Abstract. As part of the OP3 field study of rainforest atmospheric chemistry, above-canopy fluxes of isoprene, monoterpenes and oxygenated volatile organic compounds were made by virtual disjunct eddy covariance from a South-East Asian tropical rainforest in Malaysia. Approximately 500 hours of flux data were collected over 48 days in April–May and June–July 2008. Isoprene was the dominant non-methane hydrocarbon emitted from the forest, accounting for 80% (as carbon) of the measured emission of reactive carbon fluxes. Total monoterpene emissions accounted for 18% of the measured reactive carbon flux. There was no evidence for nocturnal monoterpene emissions and during the day their flux rate was dependent on both light and temperature. The oxygenated compounds, including methanol, acetone and acetaldehyde, contributed less than 2% of the total measured reactive carbon flux. The sum of the VOC fluxes measured represents a 0.4% loss of daytime assimilated carbon by the canopy, but atmospheric chemistry box modelling suggests that most (90%) of this reactive carbon is returned back to the canopy by wet and dry deposition following chemical transformation. The emission rates of isoprene and monoterpenes, normalised to 30 °C and 1000 μmol m−2 s−1 PAR, were 1.6 mg m−2 h−1 and 0.46mg m−2 h−1 respectively, which was 4 and 1.8 times lower respectively than the default value for tropical forests in the widely-used MEGAN model of biogenic VOC emissions. This highlights the need for more direct canopy-scale flux measurements of VOCs from the world's tropical forests.


Sign in / Sign up

Export Citation Format

Share Document