Controlled Use of Downhole Calcium Carbonate Scaling for Sand Control: Laboratory and Field Results on Gullfaks
- Niall Fleming (Statoil ASA) | Eivind Berge (Statoil ASA) | Mohamed Ridene (Statoil ASA) | Terje Østvold (NTNU) | Leif Jøsang (NTNU) | Hans Christian Rohde (M-I Swaco)
- Document ID
- Society of Petroleum Engineers
- SPE Production & Operations
- Publication Date
- May 2012
- Document Type
- Journal Paper
- 223 - 232
- 2012. Society of Petroleum Engineers
- 3.2.5 Produced Sand / Solids Management and Control, 2.4.3 Sand/Solids Control, 4.1.2 Separation and Treating, 2.2.2 Perforating, 5.2.1 Phase Behavior and PVT Measurements, 1.8 Formation Damage, 4.1.5 Processing Equipment, 2 Well Completion
- calcium carbonate scaling, Gullfaks, sand control
- 1 in the last 30 days
- 748 since 2007
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Gullfaks has been in production since 1986 and produces approximately 11 500 std m3/d of oil from three Condeep platforms. The average water cut is approximately 75 to 80% and gas/oil ratio (GOR) is approximately 200 std m3/std m3. It has been estimated that between 50 and 100 t of sand is produced yearly per platform, with approximately 60 to 70% of the wells in active production (approximately 90) limited by sand production. The typical well completion is cased hole with selective production through perforated liners. Rock-mechanics studies have shown that sand will be produced irrespective of well inclination and perforation design.
On Gullfaks, the sand-management strategy used has been to produce wells at "maximum" or "acceptable" sand rates. This strategy has led to significant gains in production, although there are challenges with this approach that include choke erosion, sand removal from the separators, and oil-in-water quality associated with discharge to sea. In response to this, Statoil has investigated different methods of retaining sand downhole by chemical sand consolidation, of which in-situ calcium carbonate (CaCO3) precipitation will form the basis for this paper. This technology involves squeezing into the near-wellbore formation predefined concentrations of urea and calcium nitrate along with the enzyme urease. After application, the well is shut in, during which the enzyme catalyzes the decomposition of urea to bicarbonate that reacts with calcium to form calcium carbonate.
This paper will provide details of the laboratory evaluation and, in particular, will focus on the field results from the first-ever application of this type. A low-risk candidate well was selected that had a short perforated interval (19 m) and produced 88 std m3/d oil with a water cut of 94%. Results of the operation design and planning, logistics examination, thorough risk evaluation, and post-operation results with lessons learned will be presented.
|File Size||3 MB||Number of Pages||10|
Andrews, J.S., Kjorholt, H., and Joranson, H. 2005. Production enhancementfrom sand management philosophy. A Case Study from Statfjord and Gullfaks.Paper SPE 94511 presented at the SPE European Formation Damage Conference,Sheveningen, The Netherlands, 25-27 May. http://dx.doi.org/10.2118/94511-MS.
Blakeley, R.L. and Zerner, B. 1984. Jack bean urease: the first nickelenzyme. J. Mol. Catal. 23 (2-3): 263-292. http://dx.doi.org/10.1016/0304-5102(84)80014-0.
Blakeley, R.L., Hinds, J.A., Kunze, H.E., Webb, E.C., and Zerner, B.1969. Jack bean urease (EC 22.214.171.124). Demonstration of a carbamoyl-transferreaction and inhibition by hydroxamic acids. Biochemistry 8(5): 1991-2000.
Blakeley, R.L., Treston, A., Andrews, R.K., and Zerner, B. 1982.Nickel(II)-promoted ethanolysis and hydrolysis of N-(2-pyridylmethyl)urea. Amodel for urease. J. Am. Chem. Soc. 104 (2): 612-614. http://dx.doi.org/10.1021/ja00366a040.
Chierici, G.L. 1994. Principles of Petroleum Reservoir Engineering,Vol. 1. Berlin, Germany: Springer Verlag.
Daif, M.A. and El-Din, M.M. 1979. Studies on urea hydrolysis. Part 2.Effects of some heavy metals on urease activity. Beitr Trop LandwirtschVeterinarmed 17 (3): 261-266.
Estiu, G. and Merz, K.M. 2006. Catalyzed Decomposition of Urea. MolecularDynamics Simulations of the Binding of Urea to Urease. Biochemistry 45 (14): 4429-4443. http://dx.doi.org/10.1021/bi052020p.
Harris, R.E. and McKay, I.D. 2002. Methods for deposition of materials inunderground reservoirs. US Patent No. 6,401,819.
Kotlar, H.K., Moen, A., Haavind, F., and Strom, S. 2008. Field EperienceWith Chemical Sand Consolidation as a Remedial Sand Control Option. Paper SPE19417 presented at the Offshore Technology Conference, Houston, 5-8 May. http://dx.doi.org/10.4043/19417-MS.
Larsen, T. 2005. Sand stabilization with mineral precipitation. PhDthesis, Norwegian University of Science and Technology (NTSU), Trondheim,Norway.
Lioliou, M.G., Paraskeva, C.A., Koutsoukos, P.G., and Payatakes, A.C. 2007.Heterogeneous nucleation and growth of calcium carbonate on calcite and quartz.J. Colloid Interface Sci. 308 (2): 421-428. http://dx.doi.org/10.1016/j.jcis.2006.12.045.
Østvold, T. 2009. Method for Water Tightening of Water Bearing Zones andStabilization of Sand in Underground Constructions. International (PCT) PatentApplication No. 20093567 (A).
Østvold, T. 2010. Method for water tightening of water bearing zones andstabilization of sand in underground constructions. International (PCT)Application No. PCT/NO10/00479.
Østvold, T., Gustavsen, Ø., Larsen, T., et al. 2008. Method and Compositionfor Stabilizing Earth and Sand to Prevent Soil Erosion (Fremgangsmåte ogmiddel for stabilisering og tetting av underjordiske formasjoner ellerforhindring av jorderosjon). International (PCT) Application No.PCT/NO2006/004400, Application Priority Data No. (NO) 20050005255. (US PatentNo. 7,841,804 B2, 30 November 2010).
Østvold, T., Payatakes, A.C., Koutsoukos, P.G., and Read, P. 2000.Precipitation of Inorganic Salts in Porous Media. International (PCT)Application No. WO1999NO00341 19991112; Application Priority Data No.NO19980005505 19981126.
Shaw, W.H.R. 1954. The Inhibition of Urease by Various Metal Ions. J. Am.Chem. Soc. 76 (8): 2160-2163. http://dx.doi.org/10.1021/ja01637a034.
Sumner, J.B., Gralën, N., and Eriksson-Quensel, I.-B. 1938. TheMolecular Weights of Urease, Canavalin, Concanavalin A ond Concanavalin B.Science 87 (2261): 395-396. http://dx.doi.org/10.1126/science.87.2261.395.
Yoon, S.H., Park, S.H., and Lee, C.S. 2007. Experimental Investigation onthe Fuel Properties of Biodiesel and Its Blends at Various Temperatures.Energy Fuels 22 (1): 652-656. http://dx.doi.org/10.1021/ef7002156.
Zaborska, W., Krajewska, B., and Olech, Z. 2004. Heavy Metal IonsInhibition of Jack Bean Urease: Potential for Rapid Contaminant Probing. J.Enzyme Inhib. Med. Chem. 19 (1): 65-69. http://dx.doi.org/doi:10.1080/14756360310001650237.
Zaborska, W., Krajewska, B., Leszko, M., and Olech, Z. 2001. Inhibition ofurease by Ni2+ ions: Analysis of reaction progress curves. J. Mol. Catal. B:Enzym. 13 (4-6): 103-108. http://dx.doi.org/10.1016/s1381-1177(00)00234-4.