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Controls on halogen concentrations in sedimentary formation waters

Published online by Cambridge University Press:  05 July 2018

Richard H. Worden*
Affiliation:
BP Exploration Limited, Research and Engineering Centre, Chertsey Road, Sunbury on Thames, Middlesex, TW16 7LN, UK

Abstract

Chlorine is the most abundant halogen in sedimentary formation waters with concentrations from <100 to >250000 mg/l. Bromine is the second most abundant halogen at <1 mg/l to >6000 mg/l with iodine from <0.1 mg/l to >100 mg/l and fluorine from <0.1 mg/l to 30 mg/l. Chlorine and bromine show a strong systematic covariation suggesting that they are subject to the same controlling mechanisms. Fluorine only shows relatively high concentrations at elevated chlorine and bromine concentrations showing that fluorine, chlorine and bromine are possibly controlled by the same processes. Iodine does not correlate with any of the other halogens indicating that unique processes control iodine.

Key geological parameters that influence chlorine and bromine (and possibly fluorine) concentrations are the presence of salt in a basin, the age of the reservoir unit and the kerogen-type within the main hydrocarbon source rock in a basin. The presence of salt in a basin shows that sea water was evaporated to halite saturation producing connate waters with high concentrations of chlorine and bromine. The presence of salt also leads to high salinity waters through water-salt interaction during burial and diagenesis. Tertiary reservoirs typically have much lower chlorine and bromine concentrations than Mesozoic or Palaeozoic reservoirs. The age of the reservoir unit may simply reflect the different amounts of time available for formation water to interact with salt. The dominance of type II marine kerogen in a basin leads to higher bromine concentrations. This may reflect the dominance of a marine influence in a basin which is more likely to lead to salt deposition than terrestrial depositional environments. Iodine concentrations are independent of all these parameters. Other geological parameters such as depth of burial, temperature, basin forming mechanism and reservoir lithology have no influence upon halogen concentrations.

Key processes that affect halogen concentrations are sea water evaporation and dilution, water—salt interaction and input from organic sources. Chlorine and bromine data lie close to the experimentally-derived sea water evaporation trend showing that sea water evaporation may be an important general control on halogens. Sea water dilution is probably responsible for most low salinity formation water chlorine and bromine concentrations for the same reason. Sea water dilution can occur either by meteoric invasion during burial, or following uplift and erosion, or by diagenetic dehydration reactions. Water can interact with salt in a variety of ways: halite dissolution by congruent processes, halite recrystallization by incongruent processes, sylvite dissolution or recrystallization and halite fluid inclusion rupture. Halite dissolution will lead to high chlorine and relatively low bromine waters because halite contains little bromine. In contrast, halite recrystallization will lead to bromine-enhanced waters because NaBr dissolves preferentially to NaCl. The occurrence of dissolution or recrystallization will depend on the water rock ratio, greater volumes of water will lead to more dissolution and waters with higher Cl/Br ratios. Sylvite is usually rich in bromine so dissolution will lead to bromine-enhanced waters. Primary aqueous inclusions in halite contain high bromine concentrations so that rupture, during deformation or recrystallization, will lead to bromine-enhanced formation water. A combination of these processes are responsible for the very limited range of Cl/Br ratios although congruent halite dissolution must have a limited role due to the absence of waters with high Cl/Br ratios.

Iodine is strongly concentrated in organic materials in the marine environment; oils and organic rich-source rocks have high I/Cl and I/Br ratios relative to sea water or evaporated sea water. All formation waters are enriched in iodine relative to sea water implying that there has been input from organic matter or interaction with oil. However, hydrocarbon source rock type in a basin has no discernible effect upon iodine concentrations.

Type
Halogen Mineralogy and Geochemistry
Copyright
Copyright © The Mineralogical Society of Great Britain and Ireland 1996

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Footnotes

*

Present address: School of Geosciences, Queen’s University of Belfast, Belfast, Northern Ireland, BT7 INN, UK

References

Bennett, D.G. and Barker, A.J. (1992) High salinity fluids: the result of retrograde metamorphism in thrust zones. Geochim. Cosmochim. Acta, 56, 81-95.CrossRefGoogle Scholar
Bethke, C.M. (1985) A numerical model of compaction driven groundwater flow and heat transfer and its application to the palaeohydrology of intracratonic sedimentary basins. J. Geophys. Res., 90(B8), 6817–28.CrossRefGoogle Scholar
Bjørlykke, K. (1994) Fluid flow processes and diagenesis in sedimentary basins. In Geofluids: origin, migration and evolution of fluids in sedimentary basins. (Parnell, J., ed.). Geol. Soc. Spec. Publ. 78, 127–40.Google Scholar
Carpenter, A.B. (1978) Origin and chemical evolution of brines in sedimentary basins. Oklahoma Geol. Surv. Circ., 79, 589606.Google Scholar
Carpenter, A.B. and Miller, J.C. (1969) Geochemistry of saline subsurface water, Saline County, (Missouri). Chem. Geol., 4, 135—67.CrossRefGoogle Scholar
Carpenter, A.B., Trout, M.L. and Pickett, E.E. (1974) Preliminary report on the origin and chemical evolution of lead- and zinc-rich oil field brines in Central Mississippi. Econ, Geol, 69, 1191—206.CrossRefGoogle Scholar
Collins, A.G. (1969) Chemistry of some Anadarko Basin brines containing high concentrations of iodine. Chem. Geol., 4, 169—87.CrossRefGoogle Scholar
Collins, A.G. (1975) Geochemistry of oilfield waters. Elsevier, 496 pp.Google Scholar
Collins, A.G. (1987) Properties of produced waters. Ch. 24 in Petroleum Engineering Handbook. (Bradley, H.B., ed.) Soc. Petrol. Eng., Richardson, Texas, U.S.A.Google Scholar
Collins, A.G., Bennett, J.H. and Manuel, O.K. (1971) Iodine and algae in sedimentary rocks associated with iodine-rich brines. Geol. Soc. Amer. Bull., 82, 2607–10.CrossRefGoogle Scholar
Connolly, C.A., Walter, L.M., Baadsgaard, H. and Longstaffe, F.J. (1990) Origin and evolution of formation waters, Alberta basin, Western Canada sedimentary basin. I. Chemistry. AppL Geochem., 5, 375–95.CrossRefGoogle Scholar
Cosgrove, M.E. (1970) Iodine in the bituminous Kimmeridge shales of the Dorset coast, England. Geochim. Cosmochim. Acta, 34, 830—6.CrossRefGoogle Scholar
Crossey, L.J., Surdam, R.C. and Lahann, R. (1986) Application of organic/inorganic diagenesis to porosity prediction. In Roles of organic matter in sediment diagenesis(Gautier, D.L., ed.), Soc. Econ. Paleo. Mineral., Spec. Publ. 38, 147—55.Google Scholar
Dickey, P.A. (1966) Increasing concentration of subsurface brines with depth. Chem. Geol. 4, 361—70.Google Scholar
Edmunds, W.M., Bath A.H. and Miles, M.L. (1982) Pore fluid of the Bridport (Lower Jurassic) and the Sherwood sandstone (Triassic) intervals of the Winterborne Kingston borehole, Dorset. In The Winterborne Kingston borehole, Dorset.(G.H. Rhys, G.K. Lott and M.A. Calver, eds.). Rep. Inst. Geol. Sci. No 81/3, 149–63.Google Scholar
Egeberg, P.K. and Aargaard, P. (1989) Origin and evolution of formation waters from oilfields on the Norwegian shelf. Appl Geochem., 4, 131–42.CrossRefGoogle Scholar
Ellrich, J., Hirner, A. and Stark, H. (1985) Distribution of trace elements in crude oils from Southern Germany. Chem. Geol., 48, 313–23.CrossRefGoogle Scholar
Eugster, H.P. and Jones, B.F. (1979) Behaviour of major solutes during closed-basin brine evolution. Amer. J. ScL, 279, 609–31.CrossRefGoogle Scholar
Ferguson, J., Etminan, H. and Ghassemi, F. (1993) Geochemistry of deep formation waters in the Canning basin, Western Australia, and their relationship to Zn-Pb mineralization. Austral. J. Earth Sci., 40, 471–83.CrossRefGoogle Scholar
Fisher, J.B. and Boles, J.R. (1990) Water-rock interaction in Tertiary sandstones, San Joaquin basin, California, U.S.A.: Diagenetic controls on water composition. Chem. Geol.y 82, 83—101.Google Scholar
Fisher, R.S. and Kreitler, C.W. (1987) Geochemistry and hydrodynamics of deep basin brines, Palo Duro basin, Texas, U.S.A. Appl. Geochem., 2, 459–76.CrossRefGoogle Scholar
Fontes, J.Ch. and Matray, J.M. (1993a) Geochemistry and origin of formation brines from the Paris basin, France 1. Brines associated with Triassic salts. Chem. GeoL, 109, 149–75.CrossRefGoogle Scholar
Fontes, J.Ch. and Matray, J.M. (1993^) Geochemistry and origin of formation brines from the Paris basin, France 2. Saline solutions associated with oil fields. Chem. GeoL, 109, 177200.CrossRefGoogle Scholar
Fournier, R.O. and Rowe, J.J. (1977) The solubility of amorphous silica in water at high temperatures and pressures. Amer. Mineral, 64, 1052–6.Google Scholar
Graf, D.L. (1982) Chemical osmosis, reverse chemical osmosis, and the origin of subsurface brines. Geochim. Cosmochim. Acta, 46, 1431–48.CrossRefGoogle Scholar
Hanor, J.S. (1994a) Physical and chemical controls on the composition of waters in sedimentary basins. Mar. Petrol. Geol 11, 31—45.Google Scholar
Hanor, J.S. (1994b) Origin of saline fluids in sedimentary basins. In Geofluids: origin, migration and evolution of fluids in sedimentary basins. (Parnell, J., ed.), Geol. Soc. Spec. Publ. 78, 151–74.Google Scholar
Hardie, L.A. (1984) Evaporites, marine or non-marine? Amer. J. Sci., 284, 193 —204.CrossRefGoogle Scholar
Herut, B., Starinsky, A., Katz, A. and Bein, A. (1990) The role of sea water freezing in the formation of subsurface brines. Geochim. Cosmochim. Acta, 54, 1321.CrossRefGoogle Scholar
Hitchon, B., Billings, G.K. and Klovam, J.E. (1971) Geochemistry and origin of formation waters in the Western Canada basin -III. Factors controlling chemical composition. Geochim. Cosmochim. Acta, 35, 567–98.CrossRefGoogle Scholar
Holser, W.T. (1919a) Mineralogy of evaporites. In Marine minerals (R.G. Burns, ed.), Reviews in Mineralogy, 6, Mineral Soc. Amer., Washington D. C., 211-94.Google Scholar
Holser, W.T. (1979^?) Trace elements and isotopes in evaporites. In Marine Minerals (Bums, R.G., ed.), Reviews in Mineralogy, 6 Mineral Soc. Amer., Washington D. C., 295346.Google Scholar
Kharaka, Y.K. and Berry, F.A.F. (1973) Simultaneous flow of water and solutes through geological membranes, I. Experimental investigations. Geochim. Cosmochim. Acta, 37, 2577–603.CrossRefGoogle Scholar
Kharaka, Y.K. and Carothers, W.W. (1988) Geochemistry of oil-field waters from the North Slope. US Geol. Survey Prof. Paper, 1399, 551–61.Google Scholar
Kharaka, Y.K., Law, L.M., Carothers, W.W. and Goerlitz, D.F. (1986) Role of organic species dissolved in formation waters from sedimentary basins in mineral diagenesis. In Roles of organic matter in sediment diagenesis(D.L. Gautier, ed.), Soc. Econ. Paleo. Mineral., Spec. Publ. 38, 111—22.Google Scholar
Kharaka, Y.K., Maest, A.S., Carothers, W.W., Law, L.M., Lamothe, P.J. and Fries, T.L. (1987) Chemistry of metal-rich brines from Central Mississippi salt dome basin, U.S.A. Appl. Geochem, 2, 543–61.CrossRefGoogle Scholar
Klemme, H.D. and Ulmishek, G.F. (1991) Effective petroleum source rocks of the world: stratigraphic distribution and controlling depositional factors. Amer. Assoc. Petrol. Geol. Bull., 75, 1809–51.Google Scholar
Land, L.S. and MacPherson, G.L. (1989) Geochemistry of formation water, Plio-Pleistocene reservoirs, offshore Louisiana. Gulf Coast Geol Soc. Trans., 39, 421–30.Google Scholar
Land, L.S. and Prezbindowski, D.R. (1981) The origin and evolution of saline formation water, Lower Cretaceous carbonates, south-central Texas, U.S.A., J. HydroL, 54, 5174.CrossRefGoogle Scholar
Land, L.S., Kupecz, J.A. and Mack, L.E. (1988) Louann salt geochemistry (Gulf of Mexico sedimentary basin, U.S.A.): a preliminary synthesis. Chem.. Geol., 74, 2535.CrossRefGoogle Scholar
Lundegaard, P.D. and Trevena, A.S. (1990) Sandstone diagenesis in the Pattani basin (Gulf of Thailand): history of water rock interaction and comparison with the Gulf of Mexico. Appl. Geochem., 5, 669-85.Google Scholar
MacPherson, G.L. (1989) Bromide in Gulf basin formation waters: organics as an additional source. Geol. Soc. Amer. 1989 meeting abstracts A316.Google Scholar
MacPherson, G.L. (1992) Regional variations in formation water chemistry: Major and minor elements, Frio formation fluids, Texas. Amer. Assoc. Petrol. Geol. Bull., 76, 14Q-57.Google Scholar
Marsden, S.S. and Kawai, K. (1965) “Suiyosei- Ten’Nengasu,”; a special type of Japanese natural gas deposit. Amer. Assoc. Petrol Geol. Bull., 49, 286–95.Google Scholar
Martin, J.B., Gieskes, J.M., Torres, M. and Kastner, M. (1993) Bromine and iodine in Peru margin sediments and pore fluids: implications for fluid origin. Geochim. Cosmochim. Acta, 57, 4377–89.CrossRefGoogle Scholar
McCaffrey, M.A., Lazar, B. and Holland, H.D. (1987) The evaporation path of sea water and coprecipitation of Br’ and K+ with halite. J. Sed. Petrol., 57, 928–37.Google Scholar
Merino, E. (1975) Diagenesis in Tertiary sandstones from Kettleman North Dome, California - II. Interstitial solutions: distribution of aqueous species at 100°C and chemical relation to the diagenetic mineralogy. Geochim. Cosmochim. Acta, 39, 1629–45.CrossRefGoogle Scholar
Moldovanyi, E.P. and Walter, L.M. (1992) Regional trends in water chemistry, Smackover formation, Southwest Arkansas: Geochemical and physical controls. Amer. Assoc. Petrol. Geol. Bull., 76, 864–94.Google Scholar
Morad, S., Bergan, M., Knarud, R. and Nystuen, J.P. (1990) Albitization of detrital plagioclase in Triassic reservoir sandstone from the Snorre Field, Norwegian sector. J. Sed. Petrol., 60, 411–25.Google Scholar
Morad, S., Ben Ismail, H.N., De Ros, L.F., Al-Aasm, I.S. and Serrhini, N.-E. (1994) Diagenesis and formation water chemistry of Triassic reservoir sandstones from Southern Tunisia. Sedimentology, 41, 1253–72.CrossRefGoogle Scholar
Morton, R.A. and Land, L.S. (1987) Regional variations in formation water chemistry, Frio Formation (Oligocene), Texas Gulf coast. Amer. Assoc. Petrol. Geol. Bull., 71, 191206.Google Scholar
Posey, H.H. and Kyle, J.R. (1988) Fluid-rock interactions in the salt dome environment: an introduction and review. Chem. Geol.y 74, 1—24.Google Scholar
Price, N.B., Calvert, S.E. and Jones, P.G.W. (1970) The distribution of iodine and bromine in the sediments of the south-western Barents Sea. J. Mar. Res., 28, 2234.Google Scholar
Roedder, E. (1984) Fluid inclusions. Reviews in Mineralogy 12, Mineral Soc. Amer., Washington D. C., 644 pp.CrossRefGoogle Scholar
Sanders, L.L. (1991) Geochemistry of formation waters from the Lower Silurian Clinton Formation (Albion sandstone), Eastern Ohio. Amer. Assoc. Petrol Geol Bull, 75, 1593–608.Google Scholar
Sanford, W.E. and Wood, W.W. (1991) Brine evolution and mineral deposition in hydrologically open evaporite basins. Amer. J. Sci., 291, 687710.CrossRefGoogle Scholar
Smirnova, A.Y. (1969) Genesis of boron, bromine and iodine in ground waters of western Ciscaucasian Cretaceous deposits, Geol. Kev., 12, 703—10.Google Scholar
Stoessel, R.K. and Carpenter, A.B. (1986) Stoichiometric saturation tests of NaCl1-xBrx and NaCli_rBrx. Geochim. Cosmochim. Acta, 50, 1465–74.CrossRefGoogle Scholar
Stueber, A.M. and Walter, L.M. (1991) Origin and chemical evolution of formation waters from Silurian-Devonian strata in the Illinois basin, U.S.A.. Geochim. Cosmochim. Acta, 55, 309–25.CrossRefGoogle Scholar
Stueber, A.M., Walter, L.M., Huston, T.J. and Pushkar, P. (1993) Formation waters from Mississippian- Pennsylvanian reservoirs, Illinois basin, U.S.A: Chemical and isotopic constraints on evolution and migration. Geochim. Cosmochim. Acta, 57, 763–84.CrossRefGoogle Scholar
Sverjensky, D.A. (1984) Oil field brines as ore-forming solutions. Econ. Geol., 79, 2337.CrossRefGoogle Scholar
Wilson, T.P. and Long, D.T. (1993a) Geochemistry and isotope chemistry of Michegan basin brines: Devonian formations. Appi Geochem., 8, 81 — 100.Google Scholar
Wilson, T.P. and Long, D.T. (1993b) Geochemistry and isotope chemistry of Ca-Na-Cl brines in Silurian strata, Michegan basin, U.S.A. Appl. Geochem., 8, 507524.CrossRefGoogle Scholar
Worden, R.H. and Matray, J.M. (1995) Cross forma- tional flow in the Paris Basin. Basin Res., 7, 5366.CrossRefGoogle Scholar
Worden, R.H. and Smalley, P.C. (1993) Making water in sour gas deep carbonate reservoirs. In Geofluids ‘93: Contributions to an international conference on fluid evolution, migration and interaction in rocks (Parnell, J., Ruffell, A.H., Moles, N.R., eds.) 21—5.Google Scholar
Zherebtsova, I.K. and Volkova, N.N. (1966) Experimental study of behaviour of trace elements in the process of natural solar evaporation of Black Sea and Sasyk-Sivash brine. Geochem Int., 3, 656–70.Google Scholar