Microbial enhanced treatment of carbonate reservoirs for in situ hydrocarbon recovery
a carbonate reservoir and in situ hydrocarbon technology, applied in the field of in situ hydrocarbon recovery, can solve the problems of difficult hydrocarbon recovery efficiency of carbonate reservoirs, complex bitumen production from this formation, and difficult recovery of heavy hydrocarbons from carbonate reservoirs, so as to promote the dissolution of carbonate compounds, enhance hydrocarbon recovery, and increase the porosity and permeability of carbonate reservoirs
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Example 1
Production of Acetic Acid from Carbon Dioxide and Hydrogen Diffusing Through Oil
[0183]Samples were obtained from the Medicine Hat Glauconitic C (MHGC) field near Medicine Hat, Alberta. This is a shallow (850 m), low temperature (30° C.) field that produces heavy oil (API of 16°) from pre dominantly sandstone reservoir rock by water injection (Voordouw, G., et al. (2009) Environmental Science and Technology, Vol. 43, pp. 9512-9518; Agrawal, A. et al. (2012) Environmental Science and Technology, Vol. 46, pp. 1285-1292, 2012). Produced waters from producing wells 5 and 16 (5-PW and 16-PW) were collected in a 1 L Nalgene bottle that was filled to the brim to exclude air. Upon arrival in the lab these samples were stored in a Coy anaerobic hood with an atmosphere of 90% N2 and 10% CO2. To 159 mL serum bottles, 5 mL of sample (5-PW or 16-PW) and 45 mL of acetogen medium were added. A layer of 10 mL of heavy oil (HO, 2300 cP at 20° C.) or light oil (LO, 3.5 cP at 20° C.) was then ...
example 2
Dissolution of Carbonate Minerals with Acetic Acid
[0185]In order to demonstrate dissolution of carbonate minerals with acetic acid, a sample of calcium carbonate and a sample of oilfield core material were incubated with acetic acid. The experiment was performed by adding 100 μl amounts of 4 or 17.5 M acetic acid to a mixture of 10 mL deionized water and 0.50 g of calcium carbonate (CaCO3; 500 mM) and sample crushed core in a glass vial under stirring. The chemical reaction was monitored by measuring pH as a function of time. Following completion of the reaction, vacuum filtration was used to collect undissolved CaCO3 on an 0.2 μm Millipore filter. The resulting solid was dried at 100° C. for 2 hours, allowed to cool down to room temperature and then weighed.
[0186]The results of the experiment with CaCO3 are shown in FIG. 12. The suspension of CaCO3 in water had a pH of 10, decreasing to 9.2 over 102 minutes of monitoring. The pH decreased to 5.8 following addition 40 mM acetic acid...
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