Skip To Content

Oil Sands Environmental Management Bibliography

The Cumulative Environmental Management Association (CEMA)partnered with the Oil Sands Research and Information Network (OSRIN) to create the new Oil Sands Environmental Management Bibliography, which includes documents relevant to the environmental management of oil sands development in Alberta. The majority of the documents focus on the mineable oil sands in the Athabasca deposit, though some documents relate to in-situ developments. This bibliography was last updated in November 2014.

Depositional history of sediment in Great Slave Lake: spatial and temporal patterns in geochronology, bulk parameters, PAHs and chlorinated contaminants

Year of Publication: 1996

Abstract:
This report presents the results of August 1993 and March 1994 sediment studies in the West Basin of Great Slave Lake. In August 1993, a series of 10 surficial sediment samples were collected in the vicinity of the Slave River mouth. PCB was the predominant organochlorine (OC) compound detected followed by chlorobenzene, total DDT, HCH, and dieldrin. Concentrations were low and comparable to values reported for other subarctic and arctic lakes. There was no apparent pattern in the distribution of these compounds relative to the Slave River outflow. PAHs were very abundant and were dominated by benzo(g,h,i)perylene, benzo(e)pyrene, and phenathrene: concentrations were slightly higher offshore the river mouth than elsewhere. PCDD and PCDF concentrations were exceedingly low. PCDDs were dominated by DiCDD and OCDD while PCDFs were dominated by DiCDF and TriCDF. The presence of the lower chlorinated forms may be suggestive of a pulp and paper mill influence. Similarly the presence of pentachloroanisole, trichloroveratrole, and tetrachloroveratrole may be suggestive of a pulp and paper mill influence. Two cores were collected in August 1993 on the shelf region immediately west of the Slave River. Station depths were less than 30 m. Both cores were in areas of high erosion and could not be assigned meaningful dates. In March 1994, a series of sediment cores was collected at five sites (Sites 12, 13, 16, 19, and 23) in the West Basin, to the west of the August 1993 surficial sediment and coring studies. A single core from each site was dated at the Freshwater Institute and two additional cores (one each from Sites 13 and 19) were dated at the National Water Research Institute. Cores from four of the sites were in depositional areas while the core collected offshore of the Slave River mouth (Site 23) was in an erosional area. However, sufficient sediment deposition had occurred at this site for the core to be dated. The two cores examined from Site 13, in the central region of the West Basin, gave similar dating estimates. However, the two cores examined from Site 19, further to the east, gave somewhat different estimates from each other. These two cores were collected in a less physically-stable region of the lake with some evidence of postdepositional erosion of older material on top of newer sediments. The core from Site 23 was in the least stable region o f the five sites examined. Sedimentation rate estimates were similar to those for Lake Athabasca and Lakes Ontario and Erie. They were higher than estimates for subarctic and arctic lakes and for Lake Superior. Based on estimates of the suspended sediment loading to Great Slave Lake, we conclude that our cores were not collected in the high-sedimentation regions of Great Slave Lake. The greatest sedimentation may occur offshore of the Slave River mouth. Analysis of cores collected in March 1995 should allow us to confirm this hypothesis. Two cores (Cores 12B and 19B) were analyzed for organochlorine compounds. Concentrations of OCs in Core 12B, collected offshore of Hay River, were relatively high and require verification. Thus, these data are not presented in this report. For Core 19B, there was some evidence of increasing PCB, chlorobenzene, and HCH concentrations over the 1949 - 1994 period investigated. Dieldrin showed a weaker time trend. Based on the analysis of sediment trap material collected in August 1994, we conclude that the Slave River is a significant source of organochlorine compounds to Great Slave Lake. Cores from Sites 12 and 19 were analyzed for PAHs. Although the same number of slices were examined for both cores, slices from Core 12B did not extend as far back in time: thus, the PAH record has not been determined for Core 12B prior to the mid 1960s. Both cores were dominated by naphthalene, 1-methylnaphthalene, and 2-methylnaphthalene suggesting a petrogenic source. Concentrations were higher at Site 19, closer to the Slave River, than Site 12. There was strong evidence that concentrations of these compounds increased since the 1960s suggesting an additional anthropogenic source of these PAHs: temporal patterns of increase differed for Core 12B and Core 19B. Fluorene, phenanthrene, anthracene, fluoranthene, pyrene, benzo(a)anthracene, and chrysene all occurred in higher concentrations in Core 12B than Core 19B. Concentrations varied little over time for Core 19B but showed some evidence of higher concentrations in Core 12B for two periods - the late 1970s and the late 1980s. This is suggestive of a localized input, possibly from Hay River. Higher molecular weight PAHs occurred in similar concentrations in Cores 12B and 19B. There was a suggestion of slightly higher concentrations of these compounds in Core 12B during the late 1970s than earlier and later times. PCCDs and PCDFs concentrations were determined in Cores 19D and 23A. Concentrations of PCDDs were substantially higher during the 1950s through the 1970s than in more recent times. Temporal patterns of increase differed for Core 19D and Core 23A. PCDDs were dominated by HpCDDs and OCDDs with only low concentrations of the lower chlorinated forms being detected. Total PCDFs were less abundant than PCDDs: this is in notable contrast to the surficial samples where PCDDs and PCDFs occurred in similar concentrations to one another. PCDFs (primarily TriCDF and TCDF) showed some evidence of increasing concentrations since the 1950s for Core 23A while this trend was less apparent for Core 19D. These increases in PCDD and PCDF concentrations may be related to increased atmospheric sources and/or paper and pulp mill activities. There was some evidence of a pulp and paper mill signature in Core 19B with pentachloroanisole increasing in concentration from 1949 to the early 1980s and then declining somewhat thereafter: trichloroveratrole and tetrachloroveratrole occurred in low concentrations in the 1950s and in increasing concentrations thereafter. Total organic carbon (TOC) and total organic nitrogen (TON) concentrations were determined in Cores 13C and 19D. Concentrations of both compounds have increased since the early 1900s with the greatest increase occurring since the 1950s. Moreover, the increase was more pronounced in Core 13C than Core 19D. This suggests that the West Basin of Great Slave Lake has undergone a slight increase in productivity, possibly due to land clearing and increased anthropogenic development in the Peace and Athabasca River watersheds. Localized activities, occurring at the towns of Hay River and Yellowknife, may also have been important. While Great Slave Lake is essentially a pristine system, it does show signs of recent anthropogenic contamination. A significant fraction of OCs, PAHs, PCCDs, and PCDFs probably entered the West Basin of Great Slave Lake with Slave River inflow. However, the primaiy source of these compounds is less certain, e.g., localized inputs from industries along the Peace and Athabasca Rivers and/or atmospheric deposition (wet and dry) over the broader watershed with the eventual transport of these compounds into the Peace, Athabasca, and Slave rivers and then into Great Slave Lake.

Depositional history of sediments in Lake Athabasca: Geochronology, bulk parameters, contaminants and biogeochemical markers

Year of Publication: 1996

Abstract:
The primary objective of this study was to collect and analyze high quality, well-described sediment cores for use in defining the depositional history of sediment-bound contaminants in Lake Athabasca, including those which have atmospheric or upstream sources.

Depositional history of sediments in Legend and Weekes Lakes: Geochronology and bulk parameters

Year of Publication: 1996

Abstract:
A key question addressed by this project is whether or not sediment cores from headwater lakes can be used to track naturally produced biomarkers and contaminants transported atmospherically. Specifically, this was assessed by dating sediment cores collected form Legend and Weekes lakes using the lead (Pb210) and cesium Cs137) methods. Geochronology results were used to determine sedimentation rates and time scales, and utility for interpreting the results for subsequent contaminant analyses. Cores were also analyzed for bulk parameters such as particle size and organic carbon and nitrogen species to give indications of the consistency of the depositional environment.

Description of two treatment methods for detoxifying oil sands tailings pond water

Year of Publication: 1986

Abstract:
Large quantities of toxic wastewater are produced in the processing of oil sands. The toxicity appears to be due primarily to polar organic carboxylic acids (naphthenic acids). These surfactants occur naturally in oil sands and are released during the caustic hot-water extraction process. Relatively high concentrations of suspended particulate matter, bitumen, and dissolved solids, as well as low dissolved oxygen levels, may also contribute to the toxicity of the water. Tailings pond water can be detoxified by rapid chemical treatments which involved coagulation at a pH between 4. 5-5. 0, followed by flocculation with an anionic polyelectrolyte. This method has been successfully scaled up to large batch and flowthrough systems under field conditions. A second treatment method involves the storage of tailings pond water in shallow, well aerated pits for 1 - 2 years, during which period natural processes result in a significant improvement in water quality.

Design and application of a transportable experimental stream system for assessing effluent impacts on riverine biota

Year of Publication: 1996

Abstract:
The objective of this project was to design and construct a transportable artificial stream for testing impacts of nutrients and contaminants from pulp mill effluents on aquatic ecosystems in rivers. This report describes the design of that artificial system, and its placement beside the Athabasca River at Hinton. The description also includes specific hydraulic characteristics, important details and procedures of installation, and results from initial start-up tests of the system

Design of performance improvement factors (PIFs) for sustainable development indicators (SDIs) metrics for oil sands projects with application to surface mining operations based on continual performance improvement (CPI)

Year of Publication: 2013

Abstract:
The sustainability assessment approach utilized in the development of the WA-PA-SU project sustainability rating system includes three distinctive areas of knowledge: sustainability, continuous performance improvement, and multi-criteria decision-making. Previously, the study of sustainability led to (1) concluding the need for the development of a rating system for industrial projects, with a particular application to oil sands and heavy oil projects; (2) defining the structure of the rating system; and (3) assisting in the pre-selection of sustainable development indicators (SDIs) for surface mining operations. Assessing the sustainability of projects at certain points in time required the application of a methodology selected by the interested groups and/or stakeholders; however, measuring the improvement of projects in sustainable development performance over time (i.e., continuous performance improvement) presents additional challenges. Certain industries (i.e., oil & gas), projects (i.e., oil sands or heavy oil), or specific operations (i.e., surface mining) require a rating system with a particular level of flexibility, offering the opportunity for developers to improve the performance of operations, and for stakeholders to understand the difficulties-and benefits-of implementing SDIs and perform up to levels of truly sustainable development. The present manuscript introduces the performance improvement factor (PIF), which can be determined using three different methodologies: relevance factor or subjective stakeholder valuation, comparative assessment methods, and links to metrics. Additionally, the continuous performance improvement (CPI) indicator measurement is suggested and discussed for a pre-selected set of SDIs for surface mining operations in oil sands projects. Finally, a brief preamble discusses the proposed integrated approach for sustainability assessment and the part it plays in continual performance improvement, offering a foreword to upcoming manuscripts that discuss the other complementary parts of the integrated approach.

Designer biochar-coke mixtures to remove naphthenic acids from oil sands process-affected water (OSPW)

Year of Publication: 2014

Abstract:
The objective of this 6-month pilot experimental study was to test the ability of biochars derived from Alberta biomass and an oil sands petroleum coke to remove selected organic acids from water. To this end, we selected one biochar produced from wheat straw and made by the Alberta Biochar Initiative, and an oil sands petroleum coke produced by Syncrude Canada Ltd. Both materials were extensively characterized for morphology, surface area, surface reactivity, porosity, and composition. Following this characterization, two model organic species, lauric acid and 1-methylcyclohexanecarboxylic acid, were adsorbed to the biochar, coke, and mixtures of the two, at varying ratios. Our results indicate that the biochar used in this study is a significantly more efficient sorbent for removal of both organic acids tested from water than is the petroleum coke. The petroleum coke was found to remove a lower but significant amount of each organic acid from solution. The use of petroleum coke as a sorbent will likely depend on environmental risks such as the leaching of sulphur, vanadium, and nickel from the material, and its cost relative to the production and delivery of biochar to oil sands facilities. Future studies should focus on assessing the total sorption capacity of each sorbent in flow-through reactor experiments, and determining whether combined biochar + petroleum coke systems may be efficient at removing both organic contaminants and metals from oil sands process-affected water.

Desulfurization of oil sands coke

Year of Publication: 1977

Abstract:
Research done on the development of a process to desulfurize oil sands coke is described. Solvent extraction, steam treatment alone, steam treatment in the presence of sodium compounds, treatment with steam and air mixtures, hydrodesulfurization and preoxidation followed by hydrodesulfurization have been investigated. It has been found that oxidative pretreatment of oil sands coke with air at low temperatures enhances the rate of sulfur removal during the subsequent hydrodesulfurization. Up to 75% of the sulfur present in the oil sands coke can be removed by preoxidizing the coke at 530°F for eight hours followed by hydrodesulfurization with hydrogen at 1200°F for eight hours using shallow fluidized beds of –20 mesh coke particles. Yields of purified coke of approximately 56% were obtained from this process.

Detailed linear characterization of selected townships located south of Fort McMurray, Alberta

Authors Nash, J. C.
Year of Publication: 2012

Abstract:
This document contains the results from a lineal characterization project conducted in the Regional Municipality of Wood Buffalo, Alberta. The lineal characterization is based on remotely sensed data; specifically, conventional 1:30,000 Black & White aerial photography digitized and viewed in 3-dimension using specialized computer software. All anthropogenic disturbances that occurred within the project area, up to the summers of 2008 and 2009 , were digitized and interpreted based on what was seen in the aerial photography. A number of attributes were collected for each anthropogenic disturbance, which ranged from disturbance-type (e.g. seismic line or pipeline) to vegetation and ecological information such as tree-species, vegetation height and ecosite, for example. A total of 12,313 kilometers (km) of anthropogenic features were surveyed. Over half of this total, 52% (6,415 km), was low-impact 3D-seismic lines. The second most common was the higher impact, 2D-seismic lines at 30% (3,628 km). The remaining 18% represented other anthropogenic disturbances with the two most common of these being Cut-trails (8% - 924km) and Pipelines (4% -544 km).

Detecting naphthenic acids in water using gas chromatography-mass spectrometry

Year of Publication: 2007

Abstract:
Naphthenic acids (general formula CnH2n+ZO2) are water-soluble, toxic compounds found in petroleum and bitumen. Some of the current methods for detecting these acids in waters depend on measuring the presence of the carboxylic acid functional group, and therefore many of these methods also detect naturally occurring carboxylic acids that are not naphthenic acids. We report a procedure that includes liquid–liquid extraction, cleanup, and derivatization to form t-butyldimethylsilyl esters prior to gas chromatography–mass spectrometry (GC–MS) analysis. Using low- and high-resolution MS to detect the ion C15H27O2Si+ (nominal m/z = 267) is an excellent indicator of the presence of naphthenic acids at concentrations ≥10 μg L−1.

Detecting oil sands process-affected waters in the Alberta oil sands region using synchronous fluorescence spectroscopy

Year of Publication: 2009

Abstract:
Large volumes of oil sands process-affected waters (OSPW) are produced during the extraction of bitumen from oil sand. There are approximately 109 m3 of OSPW currently being stored in settling basins on oil sands mining sites in Northern Alberta. Developers plan to create artificial lakes with OSPW and it is expected that this water may eventually enter the environment. This study was conducted in order to determine if synchronous fluorescence spectroscopy (SFS) could detect OSPW contamination in water systems. Water samples collected from ponds containing OSPW and selected sites in the Alberta oil sands region were evaluated using SFS with an offset value of 18 nm. OSPW ponds consistently displayed a minor peak at 282.5 nm and a broad major peak ranging between 320 and 340 nm. Water from reference sites within the oil sands region had little fluorescence at 282.5 nm but greater fluorescence beyond 345 nm. Naphthenic acids are the major toxic component of OSPW. Both a commercial naphthenic acid and a naphthenic acid extract prepared from OSPW had similar fluorescent spectra with peaks at 280 nm and 320 nm and minor shoulders at approximately 303 and 331 nm. The presence of aromatic acids closely associated with the naphthenic acids may be responsible for unique fluorescence at 320–340 nm. SFS is proposed to be a simple and fast method to monitor the release of OSPW into ground and surface waters in the oil sands region.

Detection of naphthenic acids in fish exposed to commercial naphthenic acids and oil sands process-affected water

Year of Publication: 2007

Abstract:
Naphthenic acids are a complex mixture of carboxylic acids that occur naturally in petroleum. During the extraction of bitumen from the oil sands in northeastern Alberta, Canada, naphthenic acids are released into the aqueous phase and these acids become the most toxic components in the process-affected water. Although previous studies have exposed fish to naphthenic acids or oil sands process-affected waters, there has been no analytical method to specifically detect naphthenic acids in fish. Here, we describe a qualitative method to specifically detect these acids. In 96-h static renewal tests, rainbow trout (Oncorhynchus mykiss) fingerlings were exposed to three different treatments: (1) fed pellets that contained commercial naphthenic acids (1.5 mg g−1 of food), (2) kept in tap water that contained commercial naphthenic acids (3 mg l−1) and (3) kept in an oil sands process-affected water that contained 15 mg naphthenic acids l−1. Five-gram samples of fish were homogenized and extracted, then the mixture of free fatty acids and naphthenic acids was isolated from the extract using strong anion exchange chromatography. The mixture was derivatized and analyzed by gas chromatography–mass spectrometry. Reconstructed ion chromatograms (m/z = 267) selectively detected naphthenic acids. These acids were present in each fish that was exposed to naphthenic acids, but absent in fish that were not exposed to naphthenic acids. The minimum detectable concentration was about 1 μg naphthenic acids g−1 of fish.

Enter keywords or search terms and press Search

Search this site


Subscribe to the site

Syndicate content

Bookmark and Share