US2493462A - Inhibiting corrosion in wells - Google Patents
Inhibiting corrosion in wells Download PDFInfo
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- US2493462A US2493462A US719117A US71911746A US2493462A US 2493462 A US2493462 A US 2493462A US 719117 A US719117 A US 719117A US 71911746 A US71911746 A US 71911746A US 2493462 A US2493462 A US 2493462A
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- well
- corrosion
- bone oil
- fluids
- wells
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- 230000002401 inhibitory effect Effects 0.000 title claims description 19
- 238000005260 corrosion Methods 0.000 title description 35
- 230000007797 corrosion Effects 0.000 title description 35
- 210000000988 bone and bone Anatomy 0.000 claims description 38
- 150000007524 organic acids Chemical class 0.000 claims description 21
- 238000000034 method Methods 0.000 claims description 20
- 235000005985 organic acids Nutrition 0.000 claims description 19
- 229910052751 metal Inorganic materials 0.000 claims description 16
- 239000002184 metal Substances 0.000 claims description 16
- 238000009835 boiling Methods 0.000 claims description 2
- 239000012530 fluid Substances 0.000 description 46
- 239000003921 oil Substances 0.000 description 41
- 239000003795 chemical substances by application Substances 0.000 description 13
- 230000002378 acidificating effect Effects 0.000 description 12
- 239000002253 acid Substances 0.000 description 11
- 239000000243 solution Substances 0.000 description 11
- 239000012267 brine Substances 0.000 description 9
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 9
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 8
- 150000007513 acids Chemical class 0.000 description 8
- 239000003112 inhibitor Substances 0.000 description 8
- -1 alkaline earth metal sulfide Chemical class 0.000 description 7
- 239000000284 extract Substances 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- 229930195733 hydrocarbon Natural products 0.000 description 6
- 150000002430 hydrocarbons Chemical class 0.000 description 6
- 239000004215 Carbon black (E152) Substances 0.000 description 5
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 4
- 239000002585 base Substances 0.000 description 4
- 239000011575 calcium Substances 0.000 description 4
- 239000000470 constituent Substances 0.000 description 4
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 4
- 229910052742 iron Inorganic materials 0.000 description 4
- 239000002244 precipitate Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 235000020681 well water Nutrition 0.000 description 4
- 239000002349 well water Substances 0.000 description 4
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 229910052791 calcium Inorganic materials 0.000 description 3
- 150000003568 thioethers Chemical class 0.000 description 3
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 229910001209 Low-carbon steel Inorganic materials 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- 241000364021 Tulsa Species 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 239000008398 formation water Substances 0.000 description 2
- 230000005764 inhibitory process Effects 0.000 description 2
- 239000003350 kerosene Substances 0.000 description 2
- 238000006386 neutralization reaction Methods 0.000 description 2
- 235000019260 propionic acid Nutrition 0.000 description 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 241000272194 Ciconiiformes Species 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 239000000908 ammonium hydroxide Substances 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 238000004891 communication Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000013270 controlled release Methods 0.000 description 1
- 239000010779 crude oil Substances 0.000 description 1
- 239000010432 diamond Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 235000019441 ethanol Nutrition 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 229910000037 hydrogen sulfide Inorganic materials 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 108010080511 serum sodium transport inhibitor Proteins 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 230000003442 weekly effect Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23F—NON-MECHANICAL REMOVAL OF METALLIC MATERIAL FROM SURFACE; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL; MULTI-STEP PROCESSES FOR SURFACE TREATMENT OF METALLIC MATERIAL INVOLVING AT LEAST ONE PROCESS PROVIDED FOR IN CLASS C23 AND AT LEAST ONE PROCESS COVERED BY SUBCLASS C21D OR C22F OR CLASS C25
- C23F11/00—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent
- C23F11/08—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids
- C23F11/10—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids using organic inhibitors
-
- 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
- Y10S507/00—Earth boring, well treating, and oil field chemistry
- Y10S507/939—Corrosion inhibitor
Definitions
- This invention relates to a method of inhibiting corrosion and more particularly to a method of, and a corrosion inhibitor for, preventing or reducing corrosion of metal parts, such as flow lines, wellhead equipment, rods, tubing, etc., used in connection with petroleum wells.
- Rapid corrosion also occurs when crude oil containing soluble sulfides is produced and the corrosion of oil field equipment is especially severe in areas where brines are associated with the. sour crudes.
- These corrosive sulfide brines are believed to include alkali sulfides, alkaline earth metal sulfide, and acid sulfide such as hydrogen sulfide. It has been found that sulfide corrosion occurs in both acidic sulfide brines and in alkaline sulfide brines with a pH below 9. Neutralization of acidic component does not inhibit corrosion because the salts are readily hydrolyzed to bases and volatile acids which may condense on the cold metal parts.
- an object of this invention to provide a method for inhibiting corrosion in wells due, for example, to organic acids or sulfides. It is a further object of this invention to provide an inhibitor for such corrosion and a method by which it may be introduced into the well in such a manner that it will inhibit corrosion by the produced well fluids for a substantial period of time. A further object to provide such an inhibitor that will not form harmful solid reaction products or corrosive compounds when dispersed in the well fluids. Other objects and advantages will be apparent from the following description of examples of my process and inhibitor.
- Organic acids which I have identified are acids of aliphatic hydrocarbons, such as formic, acetic, propionic, butyric, valeric, etc. In one sample of well water they were found to be in a concentration of about 250 parts per million. The actual concentration was probably higher because of the difliculty in quantitatively recovering these acids from such dilute solutions. In order to ascertain the possible corrosive eflects of these acids, a liter of solution of acids (0.5%) which were extracted from well fluids was compared with a similar solution of propionic acid and one of caproic. The solution of well acids had a pH of 4.9 while the other solutions were 4.5. The following table will indicate the relative corrosion of mild steel panels at 150 F. when exposed to the above-mentioned synthetic and actual solutions:
- Propionio acid 0. l 383 Acids extracted from well water 0. 1 320 5
- Known treating agents have been introduced into the distillate wells and in some cases favorable results were obtained from the point of inhibiting corrosion but serious scale formation has resulted from the treating agent or from a reaction product of the treating agent, and the dissolved contents of the well fluids. As a consequence of such scale formation production is reduced and shutdowns result.
- it has been found that the injection of ammonium l5 hydroxide in the corrosive condensate wells will 3 prevent corrosion.
- True condensate production contains no appreciable amount of calcium or scale forming elements and the neutralization with ammonium hydroxide does not produce a scale.
- some wells classed as corrosive condensate wells also produce a formation water which is very acidic and high in calcium content.
- Bone oil is a by-product of the manufacture of bone charcoal and is a complex mixture including pyridine and quinoline, together with a tar fraction which is insoluble in well fluids. If the entire bone oil fraction were employed as the corrosion inhibiting agent. the insoluble tar fraction tends to form an amorphous precipitate in the bottom of the well and this precipitate would adversely affect production by tending to plug the well pores.
- a very useful corrosion inhibitor can be obtained by extractin a quantity of bone oil with at least an equal quantity of a hydrocarbon such as kerosene to produce an extract of the soluble constituents.
- Ethyl alcohol is not a suitable extractant because bone oil is completely soluble therein.
- a particularly desirable way to produce the precipitate-free inhibitor is to first dissolve the bone oil in a portion of the produced well fluids, thereby introducing into the well only that portion of the bone oil which is soluble in the particular well fluids to be encountered.
- the extent of corrosion is indicated by the concentration of iron in the well eiiluent or produced water. It has been found that the corrosion can be materially reduced or inhibited by adding to the well an extract of about 1 gallon of bone oil to about ten barrels of acidic brine produced. For example, in one well producing about twenty barrels of oil per day and twenty barrels of water per day having a pH of approximately 5.7, the introduction of an extract of about one gallon of bone oil per day was adequate to inhibit corrosion completely. It is contemplated, however, that in general an extract of between about 0.25 gallon and about 1.5 gallons of bone oil per day will effectively inhibit corrosion and maintain the iron content of the produced well fluids below about twenty-five parts per million.
- the segregated or confined quantity of the material can be disposed in the well for the controlled release of the treating agent over a substantial period of time, thus continually preventing corrwion of the metal parts with which the well fluids come into contact.
- I may introduce into the well hole a receptacle for the treating agent which may be positionedand retrieved from the base of the well by the customary running and retrievin tool.
- This receptacle if the treating agent is a liquid, for example bone oil, may comprise a metal bottle having an automatically operated valve means in the opening thereof and a pressure-equalizing tube for permitting the well fluids to flow in behind the treating agent which flows from the bottle against the pressure within the well when the valve is open.
- the treating agent will be discharged at a continuous rate into the well fluids over a period of time determined by the quantity of material that the bottle will contain.
- the vapors of the treating agent may, however, be then absorbed by the well fluids.
- I claim: 1. The method inhibiting the tendency of corrosive brines containing low-boiling organic acids to attack metal surfaces which comprises the stepofmixingwithsaidbrinesasmallamount of bone oil.
- the method of protecting ferrous metals from attack by aqueous fluids having organic acids dissolved therein which comprises the step of dispersing a small amount of bone oil in the aqueous fluids.
- the method of treating organic acid-containing well fluids to inhibit its tendency to cause corrosion which includes the stepof mixing with the well fluids being produced a small amount of bone oil.
- the method of inhibiting corrosion of metals in wells due to acidic brine containing organic acids produced from the well comprising the step of commingling bone oil with the well fluids in the ratio of about one gallon of bone oil to ten barrels of acidic brine produced.
- the method of inhibiting corrosion of ferrous metals by well fluids containing organic acids and brine which comprises supplying to well fluids in a lower region of a producing well a minor quantity of bone oil said quantity being substantially proportional to the volume of brine produced.
- the method of inhibiting the tendency of corrosive hydrocarbon well fluids containing organic acids to attack metal surfaces which comprises the steps of introducing a small amount of bone oil near the base of the well at spaced intervals of time while producing said well, said amount being substantially proportional to the volume of brine produced.
- the method of treating organic acid-containing well fluids to inhibit their tendency to cause corrosion which includes the step of dispersing in said well fluids a small amount of bone oil soluble in hydrocarbons.
- a corrosion inhibitor for wells producing mixtures of aqueous and non-aqueous well fluids containing organic acidic materials comprising a light hydrocarbon fraction having dissolved therein an extract of commercial bone oil obtained by treating said bone oil with a portion REFERENCES crran
- the following references are of record in the file of this patent:
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Preventing Corrosion Or Incrustation Of Metals (AREA)
Description
Patented Jan. 3, 1950 INHIBITING CORROSION IN WELLS Paul L. Menaul, Tulsa, Okla., assignor to Stanolind Oil and Gas Company, Tulsa, Okla., a corporation of Delaware No Drawing. Application December 28, 1946, Serial No. 719,117
Claims. (Cl. 252-855) This invention relates to a method of inhibiting corrosion and more particularly to a method of, and a corrosion inhibitor for, preventing or reducing corrosion of metal parts, such as flow lines, wellhead equipment, rods, tubing, etc., used in connection with petroleum wells.
The well corrosion encountered in producing wells presents a major problem in maintenance of equipment. The inspection and replacementof tubing and wellhead equipment, including the cost of work-over jobs is an important factor in the economy evaluation of fields which produce corrosive well fluids. Therefore, much work has been and is being done to remedy the particularly vicious corrosion encountered in high pressure wells of the gas-condensate type.
I have discovered that there are organic acids present in many highly corrosive well fluids, particularly in the well water or brine withdrawn from high-pressure distillate wells. While the origin of these organic acids is not known, it is probably in the buried vegetation of past geologic ages. Their presence in distillate well production is assumed to be due to the fact that the corrosive organic acids are volatile at temperatures encountered in deep distillate wells plus the fact that they are highly soluble in the water. At lower temperatures such as are encountered near the wellhead these acids may precipitate or coprecipitate with water on the cold metal parts causing the severe corrosion.
Rapid corrosion also occurs when crude oil containing soluble sulfides is produced and the corrosion of oil field equipment is especially severe in areas where brines are associated with the. sour crudes. These corrosive sulfide brines are believed to include alkali sulfides, alkaline earth metal sulfide, and acid sulfide such as hydrogen sulfide. It has been found that sulfide corrosion occurs in both acidic sulfide brines and in alkaline sulfide brines with a pH below 9. Neutralization of acidic component does not inhibit corrosion because the salts are readily hydrolyzed to bases and volatile acids which may condense on the cold metal parts.
It is, therefore, an object of this invention to provide a method for inhibiting corrosion in wells due, for example, to organic acids or sulfides. It is a further object of this invention to provide an inhibitor for such corrosion and a method by which it may be introduced into the well in such a manner that it will inhibit corrosion by the produced well fluids for a substantial period of time. A further object to provide such an inhibitor that will not form harmful solid reaction products or corrosive compounds when dispersed in the well fluids. Other objects and advantages will be apparent from the following description of examples of my process and inhibitor.
Organic acids which I have identified are acids of aliphatic hydrocarbons, such as formic, acetic, propionic, butyric, valeric, etc. In one sample of well water they were found to be in a concentration of about 250 parts per million. The actual concentration was probably higher because of the difliculty in quantitatively recovering these acids from such dilute solutions. In order to ascertain the possible corrosive eflects of these acids, a liter of solution of acids (0.5%) which were extracted from well fluids was compared with a similar solution of propionic acid and one of caproic. The solution of well acids had a pH of 4.9 while the other solutions were 4.5. The following table will indicate the relative corrosion of mild steel panels at 150 F. when exposed to the above-mentioned synthetic and actual solutions:
Loss in Solution pH- mumlday Propionic acid 4. 6 12 1 Ca roic acid 4. 5 9. 9 Ac ds extracted from well water 4.9 7.4
on o 11 Solution Percent in mm! (P. P. M.)
Propionio acid 0. l 383 Acids extracted from well water 0. 1 320 5 Known treating agents have been introduced into the distillate wells and in some cases favorable results were obtained from the point of inhibiting corrosion but serious scale formation has resulted from the treating agent or from a reaction product of the treating agent, and the dissolved contents of the well fluids. As a consequence of such scale formation production is reduced and shutdowns result. For example, it has been found that the injection of ammonium l5 hydroxide in the corrosive condensate wells will 3 prevent corrosion. True condensate production contains no appreciable amount of calcium or scale forming elements and the neutralization with ammonium hydroxide does not produce a scale. However, some wells classed as corrosive condensate wells also produce a formation water which is very acidic and high in calcium content.
Thus, by treating well fluids containing these organic acids to reduce the acidity of the solution or neutralize them, the corrosive properties of the well fluids are substantially reduced but if formation water high in calcium content is also produced there is a scale formation.
Bone oil is a by-product of the manufacture of bone charcoal and is a complex mixture including pyridine and quinoline, together with a tar fraction which is insoluble in well fluids. If the entire bone oil fraction were employed as the corrosion inhibiting agent. the insoluble tar fraction tends to form an amorphous precipitate in the bottom of the well and this precipitate would adversely affect production by tending to plug the well pores. I have found that a very useful corrosion inhibitor can be obtained by extractin a quantity of bone oil with at least an equal quantity of a hydrocarbon such as kerosene to produce an extract of the soluble constituents. Ethyl alcohol is not a suitable extractant because bone oil is completely soluble therein. Some residue is obtained with carbon tetrachloride and with benzene but extraction with heptane produced the largest amount of an insoluble precipitate. A particularly desirable way to produce the precipitate-free inhibitor is to first dissolve the bone oil in a portion of the produced well fluids, thereby introducing into the well only that portion of the bone oil which is soluble in the particular well fluids to be encountered.
The extent of corrosion is indicated by the concentration of iron in the well eiiluent or produced water. It has been found that the corrosion can be materially reduced or inhibited by adding to the well an extract of about 1 gallon of bone oil to about ten barrels of acidic brine produced. For example, in one well producing about twenty barrels of oil per day and twenty barrels of water per day having a pH of approximately 5.7, the introduction of an extract of about one gallon of bone oil per day was adequate to inhibit corrosion completely. It is contemplated, however, that in general an extract of between about 0.25 gallon and about 1.5 gallons of bone oil per day will effectively inhibit corrosion and maintain the iron content of the produced well fluids below about twenty-five parts per million.
A comparison of the inhibiting power of bone oil compared with the same concentrations of selected constituents of commercial bone oil under the same conditions has clearly demonstrated that the known constituents of commercial bone oil including acetonitrile, quinoline, pyridine, triethylamine and aniline, do not have an inhibiting power which even approaches that of commercial bone oil or extracts of bone oil. To demonstrate this fact a series of tests were conducted which consisted in exposing a mild steel panel of 2 square inches surface area, to 5 liters of deaerated solution of acetic acid in a concentration of 600 P. P. M. acetic acid to which the inhibitor was added in a concentration of 500 a P. P. M., the panels were immersed in the solutions for three days (73 hrs.) at 180 1". Nearly complete inhibition was obtained with bone oil whereas the percent inhibition with the separate constituents ranged as low as zero and averaged less than percent as effective as the bone oil.
The mechanism by which this complex mixture of bone oil, or an extract from which the insoluble tar has been removed, eifectively inhibits corrosion is not entirely understood. Nevertheless, I have found that great advantage can be obtained by the addition of my inhibitin agent to acidic brines before they contact the metal parts associated with a well. This treatment counteracts almost completely the normal corrosive tendency of acidic brines even under elevated temperature conditions.
In practicing my improved method, as for example, in inhibiting the corrosion in a high pressure distillate well wherein organic acids are found in the well fluids, I introduce into the well, preferably at the bottom of the well below the mouth of the tubing from which the well fluids are withdrawn, 9. quantity of the treating material sufllcient to inhibit the corrosive action of the organic acids produced. If desired, the segregated or confined quantity of the material can be disposed in the well for the controlled release of the treating agent over a substantial period of time, thus continually preventing corrwion of the metal parts with which the well fluids come into contact.
To effect the introduction of a treating agent at the base of the well in my preferred manner, and particularly where the well is producing and a packer set between the tubing and the casing prevents a communication from the surface with the bottom of the well, I may introduce into the well hole a receptacle for the treating agent which may be positionedand retrieved from the base of the well by the customary running and retrievin tool. This receptacle, if the treating agent is a liquid, for example bone oil, may comprise a metal bottle having an automatically operated valve means in the opening thereof and a pressure-equalizing tube for permitting the well fluids to flow in behind the treating agent which flows from the bottle against the pressure within the well when the valve is open. By selecting the proper size of orifice on the bottle, the flow of treatin agent can be controlled.
Where the temperatures of the well are sufliciently high to vaporize the contents of the bottle, the treating agent will be discharged at a continuous rate into the well fluids over a period of time determined by the quantity of material that the bottle will contain. The vapors of the treating agent may, however, be then absorbed by the well fluids.
The preferred embodiment of my invention described herein is for the purpose of illustra tion only and is not intended to limit the scope of the invention deflned by the appended claims, since it is apparent that the principles of my invention may be applied generally by thoseskilled in the art in view of the foregoing description.
I claim: 1. The method inhibiting the tendency of corrosive brines containing low-boiling organic acids to attack metal surfaces which comprises the stepofmixingwithsaidbrinesasmallamount of bone oil.
2.. The method of protecting ferrous metals from attack by aqueous fluids having organic acids dissolved therein which comprises the step of dispersing a small amount of bone oil in the aqueous fluids.
3. The method of treating organic acid-containing well fluids to inhibit its tendency to cause corrosion which includes the stepof mixing with the well fluids being produced a small amount of bone oil.
4. The method of inhibiting corrosion in wells wherein well fluids containing organic acids are produced, the step which comprises treating the well fluids with bone oil.
5. The method of inhibiting corrosion of metals in wells due to acidic brine containing organic acids produced from the well, comprising the step of commingling bone oil with the well fluids in the ratio of about one gallon of bone oil to ten barrels of acidic brine produced.
6. The method of inhibiting corrosion of ferrous metals by well fluids containing organic acids and brine which comprises supplying to well fluids in a lower region of a producing well a minor quantity of bone oil said quantity being substantially proportional to the volume of brine produced.
7. The method of inhibiting the tendency of corrosive hydrocarbon well fluids containing organic acids to attack metal surfaces which comprises the steps of introducing a small amount of bone oil near the base of the well at spaced intervals of time while producing said well, said amount being substantially proportional to the volume of brine produced.
8. The method of inhibiting the normal tendency of organic acids in a corrosive mixture of dissimilar fluids to attack metal surfaces which comprises the step of adding to said mixture a small amount of bone oil which is dispersed in at least one of said dissimilar fluids.
9. The method of treating organic acid-containing well fluids to inhibit their tendency to cause corrosion which includes the step of dispersing in said well fluids a small amount of bone oil soluble in hydrocarbons.
10. The method of inhibiting corrosion of ferrous metals in distillate wells due to water-soluble organic acids, the steps which comprise dissolving bone oil in a kerosene fraction and dispersing the dissolved bone oil in the well fluids at a low point in the well from which they are produced.
11. The method of inhibiting the attack of ferrous metals by normally corrosive aqueous fluids containing water-soluble organic acids and pro: duced with a major proportion of hydrocarbon fluids which comprises dispersing in the fluids a small amount of bone oil soluble in said hydrocarbon fluids.
12. The method of producing a distillate well fluid which is normally corrosive due to acidic brine containing organic acids, the steps which comprise segregating a small quantity of distfllate well fluid, dissolving a small amount of bone oil in said well fluid, and dispersing said dissolved bone oil in a lower region of said well, said small amount of bone oil being proportioned to the quantity of acidic brine produced.
13. In the method of inhibiting the attack of ferrous metals by normally corrosive, nonaqueous and aqueous well fluids containing watersoluble organic acidic material wherein corrosion is evidenced at the surface by the iron content of the aqueous well fluids produced, the steps which comprise dispersing in the well fluids a small amount of a bone oil fraction soluble in the nonaqueous well fluids produced by said well, said small amount being sufficient to maintain the iron content of the aqueous well fluids below about parts per million.
14. A corrosion inhibitor for wells producing mixtures of aqueous and non-aqueous well fluids containing organic acidic materials comprising a light hydrocarbon fraction having dissolved therein an extract of commercial bone oil obtained by treating said bone oil with a portion REFERENCES crran The following references are of record in the file of this patent:
UNITED STATES PATENTS Number Date Name 1,248,302 Foster Nov. 27, 1917 1,678,775 Gravell July 31, 1928 1,873,084 Walker Aug. 23, 1932 1,877,504 Grebe et a1 Sept. 13, 1932 1,988,823 Winning et a1 Jan. 22, 1935 2,225,695 Henderson Dec. 24, 1940 2,357,559 Smith Sept. 5, 1944' 2,441,848 Sexton May 18, 1948 2,441,849 Sexton et a1 May 18, 1948 OTHER. REFERENCES Bannister et al.: An X-Ray Study of Diamonds, article in Mineralogical Magazine. vol. 26, 1943. pages 315-321.
Condensate Corrosion, article in The Oil Weekly, May 6, 1946, page 32.
Claims (1)
1. THE METHOD INHIBITING THE TENDENCY OF CORROSIVE BRINES CONTAINING LOW-BOILING ORGANIC ACIDS TO ATTACK METAL SURFACE WHICH COMPRISES THE STEP OF MIXING WITH SAID BRINES A SMALL AMOUNT OF BONE OIL.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US719117A US2493462A (en) | 1946-12-28 | 1946-12-28 | Inhibiting corrosion in wells |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US719117A US2493462A (en) | 1946-12-28 | 1946-12-28 | Inhibiting corrosion in wells |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2493462A true US2493462A (en) | 1950-01-03 |
Family
ID=24888817
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US719117A Expired - Lifetime US2493462A (en) | 1946-12-28 | 1946-12-28 | Inhibiting corrosion in wells |
Country Status (1)
| Country | Link |
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| US (1) | US2493462A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2698295A (en) * | 1952-06-04 | 1954-12-28 | Dow Chemical Co | Combating ferrous metal corrosion |
| US2706714A (en) * | 1952-06-13 | 1955-04-19 | Cities Service Res & Dev Co | Method of inhibiting corrosion of metals |
| US2955083A (en) * | 1956-08-13 | 1960-10-04 | Bj Service Inc | Corrosion inhibitors in well treating compositions |
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| US1248302A (en) * | 1917-11-27 | John P Foster | Liquid fuel for internal-combustion engines. | |
| US1678775A (en) * | 1928-07-31 | Stobage and transportation of acid hixtttbes in steel dhotis | ||
| US1873084A (en) * | 1928-07-19 | 1932-08-23 | Empire Oil And Refining Compan | Method of preventing corrosion in oil wells |
| US1877504A (en) * | 1932-06-30 | 1932-09-13 | Dow Chemical Co | Treatment of deep wells |
| US1988823A (en) * | 1932-01-26 | 1935-01-22 | Stanco Inc | Rust remover |
| US2225695A (en) * | 1936-11-30 | 1940-12-24 | Pure Oil Co | Method for increasing flow of deep wells |
| US2357559A (en) * | 1942-08-24 | 1944-09-05 | Odessa Chemical And Equipment | Method of sweetening sour gas and preventing corrosion of oil producing wells |
| US2441849A (en) * | 1945-08-06 | 1948-05-18 | Dow Chemical Co | Stabilization of alkylene glycols |
| US2441848A (en) * | 1945-08-06 | 1948-05-18 | Dow Chemical Co | Stabilizing alkylene glycols |
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1946
- 1946-12-28 US US719117A patent/US2493462A/en not_active Expired - Lifetime
Patent Citations (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1248302A (en) * | 1917-11-27 | John P Foster | Liquid fuel for internal-combustion engines. | |
| US1678775A (en) * | 1928-07-31 | Stobage and transportation of acid hixtttbes in steel dhotis | ||
| US1873084A (en) * | 1928-07-19 | 1932-08-23 | Empire Oil And Refining Compan | Method of preventing corrosion in oil wells |
| US1988823A (en) * | 1932-01-26 | 1935-01-22 | Stanco Inc | Rust remover |
| US1877504A (en) * | 1932-06-30 | 1932-09-13 | Dow Chemical Co | Treatment of deep wells |
| US2225695A (en) * | 1936-11-30 | 1940-12-24 | Pure Oil Co | Method for increasing flow of deep wells |
| US2357559A (en) * | 1942-08-24 | 1944-09-05 | Odessa Chemical And Equipment | Method of sweetening sour gas and preventing corrosion of oil producing wells |
| US2441849A (en) * | 1945-08-06 | 1948-05-18 | Dow Chemical Co | Stabilization of alkylene glycols |
| US2441848A (en) * | 1945-08-06 | 1948-05-18 | Dow Chemical Co | Stabilizing alkylene glycols |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2698295A (en) * | 1952-06-04 | 1954-12-28 | Dow Chemical Co | Combating ferrous metal corrosion |
| US2706714A (en) * | 1952-06-13 | 1955-04-19 | Cities Service Res & Dev Co | Method of inhibiting corrosion of metals |
| US2955083A (en) * | 1956-08-13 | 1960-10-04 | Bj Service Inc | Corrosion inhibitors in well treating compositions |
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