US3841404A - Subsidence control process for wells penetrating permafrost - Google Patents
Subsidence control process for wells penetrating permafrost Download PDFInfo
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- US3841404A US3841404A US00370124A US37012473A US3841404A US 3841404 A US3841404 A US 3841404A US 00370124 A US00370124 A US 00370124A US 37012473 A US37012473 A US 37012473A US 3841404 A US3841404 A US 3841404A
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- permafrost
- forming fluid
- hydrate forming
- well bore
- hydrate
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- 238000000034 method Methods 0.000 title claims abstract description 38
- 230000000149 penetrating effect Effects 0.000 title claims description 12
- 239000012530 fluid Substances 0.000 claims abstract description 55
- 239000007787 solid Substances 0.000 claims abstract description 22
- 150000004677 hydrates Chemical class 0.000 claims abstract description 21
- 239000000155 melt Substances 0.000 claims abstract description 13
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims description 32
- 239000000203 mixture Substances 0.000 claims description 21
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 claims description 18
- 230000005484 gravity Effects 0.000 claims description 13
- 238000002844 melting Methods 0.000 claims description 13
- 230000008018 melting Effects 0.000 claims description 13
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 claims description 12
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 claims description 12
- 239000003345 natural gas Substances 0.000 claims description 12
- 239000001294 propane Substances 0.000 claims description 9
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 claims description 7
- RGSFGYAAUTVSQA-UHFFFAOYSA-N Cyclopentane Chemical compound C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 claims description 6
- 239000004338 Dichlorodifluoromethane Substances 0.000 claims description 6
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 claims description 6
- GZUXJHMPEANEGY-UHFFFAOYSA-N bromomethane Chemical compound BrC GZUXJHMPEANEGY-UHFFFAOYSA-N 0.000 claims description 6
- 239000001569 carbon dioxide Substances 0.000 claims description 6
- 229910002092 carbon dioxide Inorganic materials 0.000 claims description 6
- PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 claims description 6
- 235000019404 dichlorodifluoromethane Nutrition 0.000 claims description 6
- 239000001282 iso-butane Substances 0.000 claims description 6
- 239000000460 chlorine Substances 0.000 claims description 5
- ZRNSSRODJSSVEJ-UHFFFAOYSA-N 2-methylpentacosane Chemical compound CCCCCCCCCCCCCCCCCCCCCCCC(C)C ZRNSSRODJSSVEJ-UHFFFAOYSA-N 0.000 claims description 3
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 3
- VOPWNXZWBYDODV-UHFFFAOYSA-N Chlorodifluoromethane Chemical compound FC(F)Cl VOPWNXZWBYDODV-UHFFFAOYSA-N 0.000 claims description 3
- XWCDCDSDNJVCLO-UHFFFAOYSA-N Chlorofluoromethane Chemical compound FCCl XWCDCDSDNJVCLO-UHFFFAOYSA-N 0.000 claims description 3
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 claims description 3
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 3
- 239000005977 Ethylene Substances 0.000 claims description 3
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 claims description 3
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 3
- 229910052794 bromium Inorganic materials 0.000 claims description 3
- 229910052801 chlorine Inorganic materials 0.000 claims description 3
- 229940042935 dichlorodifluoromethane Drugs 0.000 claims description 3
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 claims description 3
- DMEGYFMYUHOHGS-UHFFFAOYSA-N heptamethylene Natural products C1CCCCCC1 DMEGYFMYUHOHGS-UHFFFAOYSA-N 0.000 claims description 3
- 229910000037 hydrogen sulfide Inorganic materials 0.000 claims description 3
- 229940102396 methyl bromide Drugs 0.000 claims description 3
- NBVXSUQYWXRMNV-UHFFFAOYSA-N monofluoromethane Natural products FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 claims description 3
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 claims description 3
- CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 claims description 3
- 229940029284 trichlorofluoromethane Drugs 0.000 claims description 3
- SCYULBFZEHDVBN-UHFFFAOYSA-N 1,1-Dichloroethane Chemical compound CC(Cl)Cl SCYULBFZEHDVBN-UHFFFAOYSA-N 0.000 claims description 2
- FRCHKSNAZZFGCA-UHFFFAOYSA-N 1,1-dichloro-1-fluoroethane Chemical compound CC(F)(Cl)Cl FRCHKSNAZZFGCA-UHFFFAOYSA-N 0.000 claims description 2
- NEHMKBQYUWJMIP-NJFSPNSNSA-N chloro(114C)methane Chemical compound [14CH3]Cl NEHMKBQYUWJMIP-NJFSPNSNSA-N 0.000 claims description 2
- 239000003507 refrigerant Substances 0.000 claims 1
- 230000015572 biosynthetic process Effects 0.000 description 11
- 238000005755 formation reaction Methods 0.000 description 11
- 239000007789 gas Substances 0.000 description 7
- 238000004519 manufacturing process Methods 0.000 description 6
- 230000002706 hydrostatic effect Effects 0.000 description 4
- 238000012986 modification Methods 0.000 description 4
- 230000004048 modification Effects 0.000 description 4
- 238000005057 refrigeration Methods 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 238000005553 drilling Methods 0.000 description 3
- 238000002347 injection Methods 0.000 description 3
- 239000007924 injection Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000002689 soil Substances 0.000 description 3
- 238000012546 transfer Methods 0.000 description 3
- 241001647090 Ponca Species 0.000 description 2
- 238000009413 insulation Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000012423 maintenance Methods 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 238000011084 recovery Methods 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 1
- 239000004568 cement Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- UMNKXPULIDJLSU-UHFFFAOYSA-N dichlorofluoromethane Chemical compound FC(Cl)Cl UMNKXPULIDJLSU-UHFFFAOYSA-N 0.000 description 1
- 229940099364 dichlorofluoromethane Drugs 0.000 description 1
- 230000000887 hydrating effect Effects 0.000 description 1
- NMJORVOYSJLJGU-UHFFFAOYSA-N methane clathrate Chemical compound C.C.C.C.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O NMJORVOYSJLJGU-UHFFFAOYSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000012552 review Methods 0.000 description 1
Images
Classifications
-
- E—FIXED CONSTRUCTIONS
- E21—EARTH OR ROCK DRILLING; MINING
- E21B—EARTH OR ROCK DRILLING; OBTAINING OIL, GAS, WATER, SOLUBLE OR MELTABLE MATERIALS OR A SLURRY OF MINERALS FROM WELLS
- E21B36/00—Heating, cooling or insulating arrangements for boreholes or wells, e.g. for use in permafrost zones
- E21B36/003—Insulating arrangements
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K8/00—Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
- C09K8/60—Compositions for stimulating production by acting on the underground formation
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S166/00—Wells
- Y10S166/901—Wells in frozen terrain
Definitions
- This invention relates to a method for controlling subsidence of wells penetrating permafrost.
- This invention further relates to a method for controlling subsidence of wells penetrating permafrost by contacting the permafrost adjacent said wells with a hydrate forming fluid, thereby forming solid hydrates as the permafrost melts.
- Another method consists primarily of an attempt to insulate the well casing from the oil carrying pipe, thus preventing the transfer of heat from the oil to the permafrost.
- Such methods have enjoyed some success, but insulation does not prevent the transfer of heat but merely slows the transfer of heat, and, as a net result, the inevitable has merely been postponed and, after continued production from the well, the permafrost melts and instability in the permafrost zone occurs.
- a third method has been an attempt to refrigerate the well bore casings.
- the refrigerating fluid must be continually circulated and cooled, and, as a result, considerable extra equipment is required.
- the likelihood of the permafrost melting during equipment shutdowns, breakdowns, and the like, cannot be totally disregarded.
- FIGURE illustrates one embodiment of the present invention.
- a well bore 14 penetrates an overburden l2 and an oil bearing formation 11.
- the overburden consists in part of a permafrost layer 13.
- the well bore comprises a larger cased portion 16 and a smaller cased portion 17.
- An oilrecovery line 18 conveys oil from the oil bearing formation to the surface.
- cement 21 has been used to fill the space between the well bore casings and the well bore diameter.
- An inner casing 22 has been positioned inside the larger portion of the well bore casing.
- a second inner casing 23 also has been positioned inside the larger portion of the well bore casing as shown.
- the hydrate forming fluid is injected through injection line 24 and flows downwardly next to the portion of the casing adjacent the permafrost layer, beneath the lower end of the second inner casing and then upwardly and out through recovery line 25.
- a series of perforations 27 are positioned in a portion of the casing adjacent the permafrost layer so that the hydrate forming fluid is in contact with the permafrost zone and the overburden formation immediately beneath the permafrost zone.
- the maintenance of the hydrate forming fluid in contact with the permafrost zone results in the formation of solid hydrates as the permafrost melts.
- the permafrost will have a greater tendency to melt near the bottom of the permafrost zone and a typical configuration of a hydrate zone formed, 28, is shown.
- the well would be drilled and finished as shown.
- the production of oil typically involves the movement of warm fluids through the oil recovery line to the surface, thus resulting in melting the permafrost layer.
- the melting of the permafrost layer results in buckling of the well casing and numerous other difficulties associated with the melting of the permafrost zone.
- the embodiment of the present invention shown allows the use of refrigeration as well as the use of the hydrate forming fluid to form solid hydrates as the permafrost zone melts.
- the hydrate forming fluid can be cooled prior to injection through injection line 24 so that refrigeration is used to keep the outer casing cool, and any permafrost which melts is converted to a solid hydrate by the presence of a hydrate forming fluid.
- the second inner casing 23 could be omitted and the hydrates merely kept in contact with the permafrost zone.
- no real attempt at refrigeration is made, and the permafrost is allowed to melt and convert to the solid hydrate.
- many variations and modifications of the present invention are possible and may appear obvious or desirable to those skilled in the art. Such methods are suitable so long as the hydrating forming fluid is maintained continuously or intermittently in contact with the permafrost'zone.
- Hydrate forming fluids suitable for use in the process of the present invention are those fluids which form solid hydrates at temperatures greater than 32 F and preferably greater than about 40 F.
- Very desirable hydrate forming fluids are those which form solid hydrates at temperatures up to about 85 F and pressures from about 100 psi to about 900 psi.
- suitable hydrate forming materials are fluids and mixtures of fluids selected from the group consisting of: methane, ethane, propane, isobutane, n-butane, carbon dioxide, acetylene, ethylene, chlorine, sulfur dioxide, hydrogen sulfide, methyl chloride, bromine, cyclopentane, 1,1-dichloroethane, methyl fluoride, chlorodifluoromethane, chlorofluoromethane, methylbromide, trichlorofluoromethane, dichlorodifluoromethane, l, l dichloro-lfluoroethane, dichlorofluoromethane, mixtures of natural gases having specific gravities up to about 1.0, and the like.
- Preferred hydrate forming fluids are fluids and mixtures of fluids selected from the group consisting of: methane, ethane, propane, isobutane, carbon dioxide, dichlorodifluoromethane, and mixtures of natural gases having specific gravities up to about 1.0.
- Particularly preferred hydrate forming fluids are mixtures of natural gases having specific gravities up to about 1. These mixtures are preferred because of their ready availability and their desirable hydrate forming properties.
- the hydrate forming properties of such gases and mixtures of gases are shown in the Handbook of Natural Gas Engineering, pages 209 to 213. Ofthe natural gas mixtures, particularly preferred mixtures are those having a specific gravity from about 0.6 to about 0.9.
- the permafrost adjacent the well bore may be contacted with the hydrate forming fluid by a variety of methods.
- the hydrate forming fluid may be injected intermittently or preferably continuously maintained in contact with the permafrost adjacent the well bore.
- the hydrate forming fluid may be used in conjunction with known methods for maintaining the permafrost zone in a frozen condition, such as insulation and refrigeration.
- the essence of the present invention lies in the discovery that the permafrost zone adjacent well bores penetrating permafrost may be maintained in a solid condition by contacting the permafrost with a hydrate forming fluid so that when the ice in the permafrost zone melts, the water is immediately converted to solid hydrates, thus maintaining the permafrost zone in a solid state. It is believed that many variations and modifications within the scope of the present invention may be considered obvious or desirable to those skilled in the art upon a review of the foregoing description of the preferred embodiments and the following example.
- the soil At the base of the permafrost, the soil is frozen and has a temperature equal to its melting point. At shallower depths the permafrost exists at temperatures below its melting point. Therefore, the first melting of the permafrost due to heat losses from the oil will occur at the permafrost base.
- a mixture of 28.8 mole percent propane and 71.2 mole percent methane kept in contact with this permafrost at a pressure of psia will form a solid hydrate with liquid water from the melting permafrost.
- the hydrate will not decompose until its temperature exceeds 45 F.
- the pressure would be 120 psia at a depth of 243 feet.
- the normal hydrostatic pressure would be 170 psi at a depth of 358 feet.
- hydrate forming materials can be selected for use if higher temperatures are desired. For instance, ethane at 400 psia will form solid hydrates at temperatures up to 56 F. Increasing the gravity of natural gas will result in higher temperatures for hydrate formation. Pure methane at 500 psia will form a solid hydrate at 37 F or less. A 0.6 gravity gas will form hydrates at 51 F or less and 500 psia. A 0.9 gravity gas will form hydrates at 60 F or less and 500 psia. This pressure would correspond to a depth of 1,120 feet under normal hydrostatic gradient. Increasing the pressure up to a critical value for the material results in hydrate formation at higher temperatures as shown above with the methane/propane mixture. With a permafrost depth of 2,000 feet, the normal hydrostatic pressure will be 881 psi. Methane will form solid hydrates at this pressure and temperature up to 47 F.
- hydrate formation occurs I at higher temperatures as pressure is increased. In most instances the higher temperatures will be encountered at the lower portion of the permafrost zone.
- the hydrate forming fluid is, of course, under greater pressure in the lower portion of the permafrost zone due to the pressure gradient of the fluid. It is thus seen that the formation and maintenance of hydrates is ideally suited to maintaining the permafrost zone adjacent the well bore in a solid state.
- a process for controlling subsidence in well bore penetrating a permafrost region comprising contacting the permafrost adjacent the well bore with a hydrate forming fluid so that solid hydrates having a melting point above that of the ice in the permafrost are formed as the permafrost melts.
- said hydrate forming fluid is a fluid or mixture of fluids selected from the group consisting of: methane, ethane, propane, isobutane, n-butane, carbon dioxide, acetylene, ethylene, chlorine, sulfur dioxide, hydrogen sulfide, methyl chlo- 6 ride, bromine, cyclopentane, l,l-dichloroethane, methyl fluoride, chlorodifluoromethane, chlorofluoromethane, methylbromide, trichlorofluoromethane, dichlorodifluoromethane, 1,1-dichloro-1- fluoroethane, and mixtures of natural gases having specific gravities up to about 1.0.
- said hydrate forming fluid is selected from fluids and mixtures of fluids selected from the group consisting of: methane, ethane, propane, isobutane, carbon dioxide, dichlorodifluoromethane, and mixtures of natural gases having specific gravities up to about 1.0.
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Abstract
A method for controlling subsidence in wells completed through permafrost by contacting the permafrost adjacent the well bore with a hydrate forming fluid, thereby forming solid hydrates as the permafrost melts.
Description
Unite States Patent 1 Harmon [451 Oct. 15,1974
[ SUBSIDENCE CONTROL PROCESS FOR WELLS PENETRATING PERMAFROST [75] Inventor: Richard A. Harmon, Ponca City,
Okla.
[73] Assignee: Continental Oil Company, Ponca City, Okla.
[22] Filed: July 2, 1973 21 Appl. No.: 370,124
[52] US. Cl 166/292, 61/36 A, 166/DIG. l, -166/57 [51] Int. Cl ..E21b 33/13, E2lb 43/24 [58] Field of Search 61/36 A, 36 R, 46; 62/10,
62/260; 166/57, 292, 302, DIG. l
[56] References Cited UNITED STATES PATENTS 2,645,093 7/1953 Daxelhofer.....' 61/36 R 2,801,698 8/1957 Bond i 166/294 2,932,170 4/1960 Patterson et a1. 61/36 R 3,350,888 11/1967 Shrier 61/36 A 3,500,930 3/1970 Bradley 166/295 3,559,737 2/1971 Ralston et 166/302 3,581,513 6/1971 Cranmer et a1 62/260 3,627,047 Wilson et a1 [66/302 3,730,201 5/1973 3,760,876 9/1973 Blount ct a1. l66/DIG. 1 3,763,935 10/1973 Perkins 166/57 3,766,985 10/1973 Willhite l66/DIG. 1
OTHER PUBLICATIONS SPE 2881 Impermeation of Porous Media by lnSitu Gas Hydrate Formation," Journal of Pet. Tech., Sept, 1970, p. 1045.
Cross, Liquid Gas Freezes Bad Soil," Construction Methods and Equipment, July, 1964, p. 85.
Slope Operators Plan Subsidence Fight, Oil and Gas Journal, Dec. 2, 1969, pp. 69-72.
Primary Examiner-Stephen J Novosad Assistant Examiner-Jack E. Ebel Attorney, Agent, or FirmF. Lindsey Scott 5 7 ABSTRACT A method for controlling subsidence in wells completed through permafrost by contacting the permafrostadjacent the well bore with a hydrate forming fluid, thereby forming solid hydrates as the permafrost melts.
10 Claims, 1 Drawing Figure PAIEN'Itunm 1 51-214 SUBSIDENCE CONTROL PROCESS FOR WELLS 'PENETRATING PERMAFROST FIELD OF THE INVENTION This invention relates to a method for controlling subsidence of wells penetrating permafrost. This invention further relates to a method for controlling subsidence of wells penetrating permafrost by contacting the permafrost adjacent said wells with a hydrate forming fluid, thereby forming solid hydrates as the permafrost melts.
PRIOR ART As is well known, there have recently been discovered in many parts of the world petroleum reserves in areas which are covered with permafrost. Numerous new problems in drilling wells through the permafrost zones and recovering these petroleum reserves have been encountered. Many of these problems result from the unique nature of permafrost which is primarily frozen soil. As is well known, the permafrost remains frozen the year round and is often frozen to considerable depths. Problems have been encountered when oil is produced from oil bearing formations beneath the permafrost, as typically the oil produced is warmer than the melting point of the permafrost, and, as the oil is produced, the permafrost adjacent the well bore melts and ceases to provide support for the well bore casing and the like. As a result, the casing tends to buckle, distort, and otherwise fail to perform its assigned function, resulting in many difficulties in the production of the oil. Such problems are also encountered to 'a lesser degree in the drilling and completion of such wells-As a result, manyattempts have been made to stablilize the permafrost during drilling and production from wells penetrating permafrost zones.
One such attempt is the use of large concrete aprons surrounding the well bore. As will be obvious, a certain amount of stability is imparted by this method since the concrete apron rests upon a large area of the permafrost and substantial melting must occur over a wide area before the concrete apron shifts. No such limitations apply to the well bore casing, however, and as the permafrost adjacent the well bore casing melts, the casing is free to shift, buckle. and the like, beneath the concrete apron.
Another method consists primarily of an attempt to insulate the well casing from the oil carrying pipe, thus preventing the transfer of heat from the oil to the permafrost. Such methods have enjoyed some success, but insulation does not prevent the transfer of heat but merely slows the transfer of heat, and, as a net result, the inevitable has merely been postponed and, after continued production from the well, the permafrost melts and instability in the permafrost zone occurs.
A third method has been an attempt to refrigerate the well bore casings. Of course, the refrigerating fluid must be continually circulated and cooled, and, as a result, considerable extra equipment is required. In addition, the likelihood of the permafrost melting during equipment shutdowns, breakdowns, and the like, cannot be totally disregarded.
In some instances, the foregoing methods have been combined; however, each combination suffers some of the disadvantages of the methods combined, and, as a result, the search has continued for an inexpensive and 2 reliable method for controlling subsidence in wells penetrating permafrost.
OBJECTS OF THE INVENTION It is an objective of the present invention to provide a simple and reliable method for controlling subsidence in wells penetrating permafrost zones.
SUMMARY OF THE INVENTION BRIEF DESCRIPTION OF THE DRAWING The drawing discloses an embodiment of the invention.
DESCRIPTION OF PREFERRED EMBODIMENTS The FIGURE illustrates one embodiment of the present invention. In the FIGURE, a well bore 14 penetrates an overburden l2 and an oil bearing formation 11. The overburden consists in part of a permafrost layer 13. The well bore comprises a larger cased portion 16 and a smaller cased portion 17. An oilrecovery line 18 conveys oil from the oil bearing formation to the surface. It will be noted that cement 21 has been used to fill the space between the well bore casings and the well bore diameter. An inner casing 22 has been positioned inside the larger portion of the well bore casing. A second inner casing 23 also has been positioned inside the larger portion of the well bore casing as shown. The hydrate forming fluid is injected through injection line 24 and flows downwardly next to the portion of the casing adjacent the permafrost layer, beneath the lower end of the second inner casing and then upwardly and out through recovery line 25. A series of perforations 27 are positioned in a portion of the casing adjacent the permafrost layer so that the hydrate forming fluid is in contact with the permafrost zone and the overburden formation immediately beneath the permafrost zone. The maintenance of the hydrate forming fluid in contact with the permafrost zone results in the formation of solid hydrates as the permafrost melts. The permafrost will have a greater tendency to melt near the bottom of the permafrost zone and a typical configuration of a hydrate zone formed, 28, is shown. In the practice of the present invention, the well would be drilled and finished as shown. The production of oil typically involves the movement of warm fluids through the oil recovery line to the surface, thus resulting in melting the permafrost layer. The melting of the permafrost layer results in buckling of the well casing and numerous other difficulties associated with the melting of the permafrost zone. The embodiment of the present invention shown allows the use of refrigeration as well as the use of the hydrate forming fluid to form solid hydrates as the permafrost zone melts. In particular, the hydrate forming fluid can be cooled prior to injection through injection line 24 so that refrigeration is used to keep the outer casing cool, and any permafrost which melts is converted to a solid hydrate by the presence of a hydrate forming fluid.
Of course, many variations and modifications of the present invention are possible, and, for instance, the second inner casing 23 could be omitted and the hydrates merely kept in contact with the permafrost zone. In this embodiment of the invention, no real attempt at refrigeration is made, and the permafrost is allowed to melt and convert to the solid hydrate. As noted, many variations and modifications of the present invention are possible and may appear obvious or desirable to those skilled in the art. Such methods are suitable so long as the hydrating forming fluid is maintained continuously or intermittently in contact with the permafrost'zone.
It is readily seen that subsidence of the permafrost layer is effectively prevented since as the water melts solid hydrates are formed which have a higher melting point than the water. Thus, the permafrost zone adjacent the well bore may be maintained in a solid state, thus continuing to provide support and stability for the well bore casing during oil production.
Hydrate forming fluids suitable for use in the process of the present invention are those fluids which form solid hydrates at temperatures greater than 32 F and preferably greater than about 40 F. Very desirable hydrate forming fluids are those which form solid hydrates at temperatures up to about 85 F and pressures from about 100 psi to about 900 psi. Some examples of suitable hydrate forming materials are fluids and mixtures of fluids selected from the group consisting of: methane, ethane, propane, isobutane, n-butane, carbon dioxide, acetylene, ethylene, chlorine, sulfur dioxide, hydrogen sulfide, methyl chloride, bromine, cyclopentane, 1,1-dichloroethane, methyl fluoride, chlorodifluoromethane, chlorofluoromethane, methylbromide, trichlorofluoromethane, dichlorodifluoromethane, l, l dichloro-lfluoroethane, dichlorofluoromethane, mixtures of natural gases having specific gravities up to about 1.0, and the like. Preferred hydrate forming fluids are fluids and mixtures of fluids selected from the group consisting of: methane, ethane, propane, isobutane, carbon dioxide, dichlorodifluoromethane, and mixtures of natural gases having specific gravities up to about 1.0. Particularly preferred hydrate forming fluids are mixtures of natural gases having specific gravities up to about 1. These mixtures are preferred because of their ready availability and their desirable hydrate forming properties. The hydrate forming properties of such gases and mixtures of gases are shown in the Handbook of Natural Gas Engineering, pages 209 to 213. Ofthe natural gas mixtures, particularly preferred mixtures are those having a specific gravity from about 0.6 to about 0.9. As will be obvious to those skilled in the art, the permafrost adjacent the well bore may be contacted with the hydrate forming fluid by a variety of methods. For instance, the hydrate forming fluid may be injected intermittently or preferably continuously maintained in contact with the permafrost adjacent the well bore. The hydrate forming fluid may be used in conjunction with known methods for maintaining the permafrost zone in a frozen condition, such as insulation and refrigeration. Many such variations and modifications are possible within the scope of the present invention since the essence of the present invention lies in the discovery that the permafrost zone adjacent well bores penetrating permafrost may be maintained in a solid condition by contacting the permafrost with a hydrate forming fluid so that when the ice in the permafrost zone melts, the water is immediately converted to solid hydrates, thus maintaining the permafrost zone in a solid state. It is believed that many variations and modifications within the scope of the present invention may be considered obvious or desirable to those skilled in the art upon a review of the foregoing description of the preferred embodiments and the following example.
Example As oil at a 190 F flows from a production zone, heat will be transferred from the oil to the cooler formations (permafrost) surrounding the well. At the base of the permafrost, the soil is frozen and has a temperature equal to its melting point. At shallower depths the permafrost exists at temperatures below its melting point. Therefore, the first melting of the permafrost due to heat losses from the oil will occur at the permafrost base. A mixture of 28.8 mole percent propane and 71.2 mole percent methane kept in contact with this permafrost at a pressure of psia will form a solid hydrate with liquid water from the melting permafrost. At this pressure the hydrate will not decompose until its temperature exceeds 45 F. At a surface pressure of 14.7 psia and a hydrostatic pressure gradient of 0.433 psi/ feet, the pressure would be 120 psia at a depth of 243 feet. By increasing the pressure of the gas mixture to psi, it is possible to maintain a solid hydrate at temperatures up to 50 F. The normal hydrostatic pressure would be 170 psi at a depth of 358 feet.
Other hydrate forming materials can be selected for use if higher temperatures are desired. For instance, ethane at 400 psia will form solid hydrates at temperatures up to 56 F. Increasing the gravity of natural gas will result in higher temperatures for hydrate formation. Pure methane at 500 psia will form a solid hydrate at 37 F or less. A 0.6 gravity gas will form hydrates at 51 F or less and 500 psia. A 0.9 gravity gas will form hydrates at 60 F or less and 500 psia. This pressure would correspond to a depth of 1,120 feet under normal hydrostatic gradient. Increasing the pressure up to a critical value for the material results in hydrate formation at higher temperatures as shown above with the methane/propane mixture. With a permafrost depth of 2,000 feet, the normal hydrostatic pressure will be 881 psi. Methane will form solid hydrates at this pressure and temperature up to 47 F.
It is noted that in general hydrate formation occurs I at higher temperatures as pressure is increased. In most instances the higher temperatures will be encountered at the lower portion of the permafrost zone. The hydrate forming fluid is, of course, under greater pressure in the lower portion of the permafrost zone due to the pressure gradient of the fluid. It is thus seen that the formation and maintenance of hydrates is ideally suited to maintaining the permafrost zone adjacent the well bore in a solid state.
In the practice of the present invention wherein high casing are perforated. Such variations are well within the skill of those skilled in the art and need not be discussed further, since as has been shown, maintaining a hydrate forming fluid in contact with the permafrost zone adjacent the well bore affords a simple and reliable method for preventing and controlling well bore subsidence in well bores penetrating permafrost zones.
Having thus described the invention, 1 claim:
1. A process for controlling subsidence in well bore penetrating a permafrost region comprising contacting the permafrost adjacent the well bore with a hydrate forming fluid so that solid hydrates having a melting point above that of the ice in the permafrost are formed as the permafrost melts.
2. The process of claim 1 wherein said hydrate forming fluid is maintained substantially continuously in contact with said permafrost.
3. The process of claim 1 wherein said hydrate forming fluid forms stable hydrates at temperatures above about 40 F.
4. The process of claim 1 wherein said hydrate forming fluid forms stable hydrates at temperatures up to about 85 F.
5. The process of claim 1 wherein said hydrate forming fluid is a fluid or mixture of fluids selected from the group consisting of: methane, ethane, propane, isobutane, n-butane, carbon dioxide, acetylene, ethylene, chlorine, sulfur dioxide, hydrogen sulfide, methyl chlo- 6 ride, bromine, cyclopentane, l,l-dichloroethane, methyl fluoride, chlorodifluoromethane, chlorofluoromethane, methylbromide, trichlorofluoromethane, dichlorodifluoromethane, 1,1-dichloro-1- fluoroethane, and mixtures of natural gases having specific gravities up to about 1.0.
6. The process of claim 5 wherein said hydrate forming fluid is selected from fluids and mixtures of fluids selected from the group consisting of: methane, ethane, propane, isobutane, carbon dioxide, dichlorodifluoromethane, and mixtures of natural gases having specific gravities up to about 1.0.
7. The process of claim 6 wherein said hydrate forming fluid is a natural gas having a specific gravity from about 0.6 to about 0.9.
8. The process of claim 6 wherein said hydrate forming fluid is maintained in contact with said permafrost by injecting said hydrate forming fluid into a well bore casing having passageways in a portion of the casing adjacent to permafrost.
outer well bore casing.
Claims (10)
1. A PROCESS FOR CONTROLLING SUBSIDENCE IN WELL BORE PENETRATING A PERMAFROST REGION COMPRISING CONTACTING THE PERMAFROST ADJACENT THE WELL BORE WITH A HDYRATE FORMING FLUID SO THAT SOLID HYDRATES HAVING A MELTING POINT ABOVE THAT OF THE ICE IN THE PERMAFROST ARE FORMED AS THE PERMAFROST MELTS.
2. The prOcess of claim 1 wherein said hydrate forming fluid is maintained substantially continuously in contact with said permafrost.
3. The process of claim 1 wherein said hydrate forming fluid forms stable hydrates at temperatures above about 40* F.
4. The process of claim 1 wherein said hydrate forming fluid forms stable hydrates at temperatures up to about 85* F.
5. The process of claim 1 wherein said hydrate forming fluid is a fluid or mixture of fluids selected from the group consisting of: methane, ethane, propane, isobutane, n-butane, carbon dioxide, acetylene, ethylene, chlorine, sulfur dioxide, hydrogen sulfide, methyl chloride, bromine, cyclopentane, 1,1-dichloroethane, methyl fluoride, chlorodifluoromethane, chlorofluoromethane, methylbromide, trichlorofluoromethane, dichlorodifluoromethane, 1,1-dichloro-1-fluoroethane, and mixtures of natural gases having specific gravities up to about 1.0.
6. The process of claim 5 wherein said hydrate forming fluid is selected from fluids and mixtures of fluids selected from the group consisting of: methane, ethane, propane, isobutane, carbon dioxide, dichlorodifluoromethane, and mixtures of natural gases having specific gravities up to about 1.0.
7. The process of claim 6 wherein said hydrate forming fluid is a natural gas having a specific gravity from about 0.6 to about 0.9.
8. The process of claim 6 wherein said hydrate forming fluid is maintained in contact with said permafrost by injecting said hydrate forming fluid into a well bore casing having passageways in a portion of the casing adjacent to permafrost.
9. The process of claim 1 wherein a mixture comprising 28.8 mole percent propane and 71.2 mole percent methane is maintained in contact with said permafrost at a temperature lower than about 45* F and a pressure of about 120 psia.
10. The process of claim 8 wherein said hydrate forming fluid is also used as a refrigerant to cool the outer well bore casing.
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US00370124A US3841404A (en) | 1973-07-02 | 1973-07-02 | Subsidence control process for wells penetrating permafrost |
CA196,064A CA1018342A (en) | 1973-07-02 | 1974-03-26 | Subsidence control process for wells penetrating permafrost |
DK209374A DK209374A (en) | 1973-07-02 | 1974-04-17 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US00370124A US3841404A (en) | 1973-07-02 | 1973-07-02 | Subsidence control process for wells penetrating permafrost |
Publications (1)
Publication Number | Publication Date |
---|---|
US3841404A true US3841404A (en) | 1974-10-15 |
Family
ID=23458327
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US00370124A Expired - Lifetime US3841404A (en) | 1973-07-02 | 1973-07-02 | Subsidence control process for wells penetrating permafrost |
Country Status (3)
Country | Link |
---|---|
US (1) | US3841404A (en) |
CA (1) | CA1018342A (en) |
DK (1) | DK209374A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
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US3876004A (en) * | 1974-04-29 | 1975-04-08 | Atlantic Richfield Co | Method for completing wells |
US20190178046A1 (en) * | 2017-12-13 | 2019-06-13 | China University Of Petroleum (East China) | Anti-settling Apparatus and Method and Apparatus for Checking the Same, and Apparatus for Preventing Settlement of Well |
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1973
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- 1974-04-17 DK DK209374A patent/DK209374A/da unknown
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Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
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US3876004A (en) * | 1974-04-29 | 1975-04-08 | Atlantic Richfield Co | Method for completing wells |
US20190178046A1 (en) * | 2017-12-13 | 2019-06-13 | China University Of Petroleum (East China) | Anti-settling Apparatus and Method and Apparatus for Checking the Same, and Apparatus for Preventing Settlement of Well |
Also Published As
Publication number | Publication date |
---|---|
DK209374A (en) | 1975-02-10 |
CA1018342A (en) | 1977-10-04 |
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