US2472400A - Method of protecting metal surfaces against hydrogen sulfide corrosion - Google Patents
Method of protecting metal surfaces against hydrogen sulfide corrosion Download PDFInfo
- Publication number
- US2472400A US2472400A US711804A US71180446A US2472400A US 2472400 A US2472400 A US 2472400A US 711804 A US711804 A US 711804A US 71180446 A US71180446 A US 71180446A US 2472400 A US2472400 A US 2472400A
- Authority
- US
- United States
- Prior art keywords
- hydrogen sulfide
- well
- corrosion
- oil
- brine
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
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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
- C23F11/14—Nitrogen-containing compounds
- C23F11/149—Heterocyclic compounds containing nitrogen as hetero atom
-
- 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 o pr .”ifing underground metal equipment against-cor- ;r 0sion by hydrogen sulfide, and relates particuq 1 larly to the prevention of hydrogen sulfide corrosion of the metal parts buried in oil wells drawj ing sour crudes.
- the method of protecting metal surfaces in the oil well comprises injecting into the annual space between the casing and the tubing of the well a solution of a particular compound to contact the casing wall and tubing and pumping it from the well together with crude 1 oil and brine, thereby efiectively contacting those surfaces of the well which not only are contacted by fluids drawn from the well, but are exposed to'vapors of water, hydrogen sulfide and other.
- the injection of the protective compound is accomplished from the surface in a manner such that the casing of the well is contacted with the compound as it descends to the bottom.
- the invention involves the discovery that cyclic for protecting metal surfaces against corrosive "action of hydrogen sulfide in wells.
- pyridine bases such as pyridine
- a typical composition applied to an oil well according to our invention for protecting against hydrogen sulfide corrosion involves injecting into an oil well 1 quart of pyridine per 100 barrels of brine. By so doing, the pyridine can be applied to the well in aliquot portions during a day to maintain an eifective concentration in the well.
- Example I In an experimental test run in which the protective value of the inhibiting solution for steel exposed to corrosive conditions essentially duplicating those found in a well was measured, the following procedure was carried out: A high-carbon steel rod inch in diameter and 4 inches long was cleaned, sandblasted, weighed, and placed in a large test tube. To the tube there were then added 3 cc. of oil well brine and 20 cc. crude oil, after which 2 cc. of a solution made up of 0.5 gram of pyridine in 50 cc. of benzene was added. The system was freed of air by freezing the liquid contents of the tube and evacuating, after which the contents were thawed and saturated with hydrogen sulfide.
- the tube was sealed and allowed to remain at room temperature for a period of 64 days, after which it was opened and the specimen cleaned by washing with acetone and water, and dipping in acid to remove surface sulfides.
- a determination of Weight loss was made as a measure of the protective value of the pyridine as a corrosion inhibitor.
- the pyridine in the ratio of 1 part of the inhibitor per 1,000 parts of brine and oil held the corrosion down to a weight loss of about 0.0012 gram in 64 days.
- Example I A similar test was carried out with 2 cc. of a quinoline solution made up of 0.5 gram of quinoline in 50 cc. of benzene in which the inhibitor was present in the system in a quantity of 1 part to 1,000 parts of oil and brine, and it was found that after a period of 64 days the Weight loss was only 0.0012 gram.
- Example III Quinoline in per cent ethyl alcohol solution was added to a test tube containing a steel sample and oil well brine in amount suflicient to establish a ratio of 1 part of quinoline to 1,000 parts of brine by weight.
- the tube contents were '4 saturated with hydrogen sulfide, the tube sealed and allowed to stand for 31 days. Upon expiration of the period, the tube was opened and the sample cleaned as indicated above. The wei ht loss determined was only 0.004 gram.
- Example 11 Example V Similar tests weer carried out with pyridine and quinoline hydrochlorides and it was found that corrosion was materially reduced by amounts comparable to those cases where the tertiary bases were used, when the inhibitor was present in the system in the amount of about 1 part per 1,000.
- Example VI Denaturing grade pyridine was tested for its efiicacy as an inhibitor according to the procedure outlined. It was found that 1 part of the pyridine in 1,000 parts of the hydrogen sulfidebrine system reduced the corrosion rate of the steel sample to the point where a weight loss of only 0.0016 gram in 30 days occurred.
- Denaturing pyridine is a technical grade commonly used for denaturing alcohol.
- Example VII Blank tests were conducted under conditions duplicating those of the previous specific examples with the inhibiting material left out of the system. In each case it was found that the rate of corrosion of the steel by hydrogen sulfide exceeded 0.05. to 0.1 gram in 30 days.
- the experimental tests and the results are duplicated by injecting periodically an amount of the protective material or solution thereof to supply the inhibitor in a ratio of about 1 part per 1,000 to 10,000 of brine produced from the well.
- the protective material can be injected into the well as an aqueous alkaline, alcoholic, or alkaline alcoholic solution in concentrations which make for convenience in handling and economy in the quantity of material used. In general, it will be found advantageous to use the inhibitor in about 5jto 15 or 20 per cent solution in the solvent carer.
Landscapes
- 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
v 2,412,400 -1'ur:'rnon or PROTECTING METAL sua- 'FACES' AGAINST CORROSION ROGEN SULFIDE Donald C. Bond,'Nort hbrook,iaiid Michael Savoy,
' Chicago, 111., assignors to The Pure Oil Com- "pany, Chicago, Ill.,:a corporation of Ohio *No-Drawingr Application November 22, 1946, l Serial No. 711,804
5 Claims. ('01. 2 52+s.5s)
This'inventionrelates to a method o pr ."ifing underground metal equipment against-cor- ;r 0sion by hydrogen sulfide, and relates particuq 1 larly to the prevention of hydrogen sulfide corrosion of the metal parts buried in oil wells drawj ing sour crudes.
' Itfis an object of theinvention to protect oil well casings and tubing against hydrogen sulfide corrosion. J
It is a second object of the invention'to protect the suckerrods and pumping machinery of an oil well against corrosion by hydrogen sulfide.
It is a thirdobject' of theinvention to improve upon the eiiiciency and economy of oil well drilling and operation by reducing the extent of hydrogen'su'lfide corrosion occurring in the easing, tubes, and machinery in the well.
Other objects and advantages of the invention will in part be obvious, and in part appear hereinafter. I
We have discovered that hydrogen sulfide corrosion of the metal parts buried in anoil well can be prevented to a substantial degree by depositing on those metal parts protective films of certain related chemical compounds and ma- 'terials which are either adsorbed on the metal surfaces or react with the metal surfaces to lay thereon a protective coating impermeable to hydrogen sulfide, or resistant to its corrosive action. In brief, the method of protecting metal surfaces in the oil well comprises injecting into the annual space between the casing and the tubing of the well a solution of a particular compound to contact the casing wall and tubing and pumping it from the well together with crude 1 oil and brine, thereby efiectively contacting those surfaces of the well which not only are contacted by fluids drawn from the well, but are exposed to'vapors of water, hydrogen sulfide and other.
corrosive media occurring in wells. The injection of the protective compound is accomplished from the surface in a manner such that the casing of the well is contacted with the compound as it descends to the bottom.
The invention involves the discovery that cyclic for protecting metal surfaces against corrosive "action of hydrogen sulfide in wells.
Many oil fields, for example fields found in west Texas, some in Michigan, Kansas, and Oklahoma, are characterized by the fact that they produce very sour crudes which contain a relatively high proportion of sulfur compoundmand,
nitrogen compounds containing a tertiary nitrogen in which the nitrogen is present in the ring, v
typified by pyridine bases,- such as pyridine,
.. quinoline, isoquinoline,- alkyl derivatives thereof, and mineral acid salts thereof, are effective media accordingly, the pumping of the wellis accompanied by the evolution of considerable quantities of hydrogen sulfide with its consequent corrosive effect on the'well tubing, casing and machinery. The corrosion by hydrogen sulfide is greatly accentuated in the presence of moisture, and inasmuch as moisture is practically always present in an oil well,the corrosion conditions-become ideal -for the destruction of the metal parts. In many cases experience has shown that, the tubing and V the sucker rods in the well can beso badly weakened in a period of about thirty daysasto break off and require "fishing in order 1 to remove broken parts for replacement.
As the flow of oil from a well diminishes; the
quantity of brine drawn therefrom increases. Since the well will usually give hydrogen sulfide in addition to other sulfur compounds, together with crude oil, the increasing quantity of brine in combination with the hydrogen sulfide aggravates the corrosion problem in the well. In
due course, as the flow of brine increases, the aggravation of the corrosion attributable to the hydrogen sulfide in the well and enhanced by an increased quantity of brine can hasten the time when it become uneconomical to pump the well to strip it further of oil. I
' In the journal of Petroleum Technology for January, 1946, the American Institute of Mining and Metallurgical Engineers, Technical, Publica tion 1970, there appears a good summary and description of the problem of hydrogen sulfide pounds which are very effective protective agents against hydrogen sulfide corrosion and include such compounds as pyridine, quinoline, methyl pyridines, methyl quinolines, and their salts, which, when placed in alkaline solution and used in the well in the ratio of about 1 gallon of 25 per cent aqueous or alcoholic solution per 100 barrels of brine, are effective in substantially completely arresting hydrogen sulfide corrosion of the metal parts in the well. Use of the solution in the quantity indicated represents a ratio of about 1 part of active inhibiting agent to 10,000 parts of brine. Related materials such as hydrochlorides, sulfates, and other salts of the bases are generally about as effectlve as the tertiary bases themselves in preventing the oil well corrosion.
A typical composition applied to an oil well according to our invention for protecting against hydrogen sulfide corrosion, involves injecting into an oil well 1 quart of pyridine per 100 barrels of brine. By so doing, the pyridine can be applied to the well in aliquot portions during a day to maintain an eifective concentration in the well. The compositions and method of practicing the invention and the possibilities for its application will be more readily understood by consideration of the following examples giving some experimental data:
Example I In an experimental test run in which the protective value of the inhibiting solution for steel exposed to corrosive conditions essentially duplicating those found in a well was measured, the following procedure was carried out: A high-carbon steel rod inch in diameter and 4 inches long was cleaned, sandblasted, weighed, and placed in a large test tube. To the tube there were then added 3 cc. of oil well brine and 20 cc. crude oil, after which 2 cc. of a solution made up of 0.5 gram of pyridine in 50 cc. of benzene was added. The system was freed of air by freezing the liquid contents of the tube and evacuating, after which the contents were thawed and saturated with hydrogen sulfide. The tube was sealed and allowed to remain at room temperature for a period of 64 days, after which it was opened and the specimen cleaned by washing with acetone and water, and dipping in acid to remove surface sulfides. A determination of Weight loss was made as a measure of the protective value of the pyridine as a corrosion inhibitor. The pyridine in the ratio of 1 part of the inhibitor per 1,000 parts of brine and oil held the corrosion down to a weight loss of about 0.0012 gram in 64 days.
Example I! A similar test was carried out with 2 cc. of a quinoline solution made up of 0.5 gram of quinoline in 50 cc. of benzene in which the inhibitor was present in the system in a quantity of 1 part to 1,000 parts of oil and brine, and it was found that after a period of 64 days the Weight loss was only 0.0012 gram.
Example III Quinoline in per cent ethyl alcohol solution was added to a test tube containing a steel sample and oil well brine in amount suflicient to establish a ratio of 1 part of quinoline to 1,000 parts of brine by weight. The tube contents were '4 saturated with hydrogen sulfide, the tube sealed and allowed to stand for 31 days. Upon expiration of the period, the tube was opened and the sample cleaned as indicated above. The wei ht loss determined was only 0.004 gram.
Example 11! Example V Similar tests weer carried out with pyridine and quinoline hydrochlorides and it was found that corrosion was materially reduced by amounts comparable to those cases where the tertiary bases were used, when the inhibitor was present in the system in the amount of about 1 part per 1,000.
Example VI Denaturing grade pyridine was tested for its efiicacy as an inhibitor according to the procedure outlined. It was found that 1 part of the pyridine in 1,000 parts of the hydrogen sulfidebrine system reduced the corrosion rate of the steel sample to the point where a weight loss of only 0.0016 gram in 30 days occurred.
Denaturing pyridine is a technical grade commonly used for denaturing alcohol.
Example VII Blank tests were conducted under conditions duplicating those of the previous specific examples with the inhibiting material left out of the system. In each case it Was found that the rate of corrosion of the steel by hydrogen sulfide exceeded 0.05. to 0.1 gram in 30 days.
When the protective materials are employed to reduce the rate of corrosion of the parts of a well under actual producting conditions, the experimental tests and the results are duplicated by injecting periodically an amount of the protective material or solution thereof to supply the inhibitor in a ratio of about 1 part per 1,000 to 10,000 of brine produced from the well. The protective material can be injected into the well as an aqueous alkaline, alcoholic, or alkaline alcoholic solution in concentrations which make for convenience in handling and economy in the quantity of material used. In general, it will be found advantageous to use the inhibitor in about 5jto 15 or 20 per cent solution in the solvent carer.
It has been found that when the inhibitor is injected into the well in the recommended proportions, that shutdowns of the well normally necessitated by corrosion of the parts within the well structure are materially reduced with the consequent improvement in the economy and efficiency of operation of the well.
Since certain changes may be made in carrying out the method described without departing in oil wellsagainst hydrogen sulfide and brine corrosion comprising continually introducing into said wells during. production of oil and brine therefrom compounds selected from the group consisting of pyridine, quincline, their methyl derivatives and their mineral acid salts, in an amount ofabout 1 part of said compoundsper the compound is quincline.
5, Method in accordance with claim 1 m which the compound is quincline hydrochloride.
DONALD c. BOND. MICHAEL savor.
6 I R ENCES crrEn The following re erences are of'record in the file of this patent:
UNITED STATES PATENT Name Number Date Bolton et a1 Dec. 1'7, 1940 Henderson et a1. Dec. 24, 1940 Smith Sept. 5, 1944 OTHER REFERENCES Formaldehyde vs. Sulfide Corrosion, article in Industrial and Engineering Chemistry, vol. 38, pages 0 and 14, Jan. 16, 1946. 4
Menaul et a1.--Formaldehyde as an Inhibitor of Corrosion Caused by Hydrogen Sulfide, article in The Oil and Gas Journal, Oct. 13, 1945, pages 20 93 and 94.
Grebe et a1 Sept. 13, 1932 Lawton et al June 11," 1940 v
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US711804A US2472400A (en) | 1946-11-22 | 1946-11-22 | Method of protecting metal surfaces against hydrogen sulfide corrosion |
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US711804A US2472400A (en) | 1946-11-22 | 1946-11-22 | Method of protecting metal surfaces against hydrogen sulfide corrosion |
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Cited By (32)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2593057A (en) * | 1949-12-29 | 1952-04-15 | Pure Oil Co | Inhibitors against hydrogen sulfide and brine corrosion |
US2602779A (en) * | 1947-09-11 | 1952-07-08 | Cities Service Oil Co | Method of inhibiting hydrogen sulfide corrosion of metals |
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 |
DE946003C (en) * | 1956-01-26 | 1956-07-19 | Siegfried Peter Dipl Chem Dr | Anti-rust and primer |
US2761839A (en) * | 1954-11-18 | 1956-09-04 | Gulf Research Development Co | Treatment of clays |
US2761840A (en) * | 1954-11-18 | 1956-09-04 | Gulf Research Development Co | Treatment of clays |
US2761836A (en) * | 1954-11-18 | 1956-09-04 | Gulf Research Development Co | Treatment of clays |
US2761838A (en) * | 1954-11-18 | 1956-09-04 | Gulf Research Development Co | Treatment of clays |
US2761841A (en) * | 1954-11-18 | 1956-09-04 | Gulf Research Development Co | Treatment of clays |
US2761842A (en) * | 1954-11-18 | 1956-09-04 | Gulf Research Development Co | Treatment of clays |
US2761837A (en) * | 1954-11-18 | 1956-09-04 | Gulf Research Development Co | Treatment of clays |
US2761835A (en) * | 1954-11-18 | 1956-09-04 | Gulf Research Development Co | Treatment of clays |
US2761843A (en) * | 1954-11-18 | 1956-09-04 | Gulf Research Development Co | Treatment of clays |
US2814593A (en) * | 1953-12-18 | 1957-11-26 | Gen Aniline & Film Corp | Corrosion inhibition |
US2869978A (en) * | 1955-09-26 | 1959-01-20 | Union Oil Co | Method of gas purification utilizing an amine solution and an anti-corrosion agent |
US2955087A (en) * | 1957-04-08 | 1960-10-04 | Arthur D Berryman | Compositions and methods for treating metal surfaces |
US2955083A (en) * | 1956-08-13 | 1960-10-04 | Bj Service Inc | Corrosion inhibitors in well treating compositions |
DE1097068B (en) * | 1957-08-16 | 1961-01-12 | Iashellia Res Ltd | Lubricants and heat transfer agents based on mineral or synthetic oils |
US2972861A (en) * | 1953-03-11 | 1961-02-28 | Midland Tar Distillers Ltd | Method of reducing the corrosive attack of combustion gases on metal |
US2999811A (en) * | 1957-08-07 | 1961-09-12 | Amchem Prod | Inhibitor composition |
US3017355A (en) * | 1958-04-18 | 1962-01-16 | Dow Chemical Co | Corrosion inhibitor composition |
US3033784A (en) * | 1959-05-13 | 1962-05-08 | Pan American Petroleum Corp | Water soluble corrosion inhibitor and bactericide |
US3066097A (en) * | 1960-06-09 | 1962-11-27 | Pan American Petroleum Corp | Polyalkyl pyridines for corrosion inhibiting |
US3077453A (en) * | 1961-09-01 | 1963-02-12 | Dow Chemical Co | Corrosion inhibition |
US3107221A (en) * | 1958-04-18 | 1963-10-15 | Dow Chemical Co | Corrosion inhibitor composition |
US3432527A (en) * | 1964-11-05 | 1969-03-11 | Armour Ind Chem Co | Corrosion inhibitor composition and method |
US3885913A (en) * | 1972-10-26 | 1975-05-27 | Petrolite Corp | Method of inhibiting the corrosion of metals in an acidic environment using quaternary ammonium salts of polyepihalohydrin |
US4276185A (en) * | 1980-02-04 | 1981-06-30 | Halliburton Company | Methods and compositions for removing deposits containing iron sulfide from surfaces comprising basic aqueous solutions of particular chelating agents |
US4554090A (en) * | 1984-03-09 | 1985-11-19 | Jones L W | Combination corrosion/scale inhibitor |
US5084210A (en) * | 1990-02-07 | 1992-01-28 | Chemlink Incorporated | Corrosion inhibitor |
US5089226A (en) * | 1986-01-20 | 1992-02-18 | Nippon Mining Co., Ltd. | Method for protecting austenitic stainless steel-made equipment from occurrence of stress-corrosion cracking |
Citations (5)
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US1877504A (en) * | 1932-06-30 | 1932-09-13 | Dow Chemical Co | Treatment of deep wells |
US2204223A (en) * | 1939-01-30 | 1940-06-11 | Shell Dev | Method of treating oil and gas wells |
US2225294A (en) * | 1938-02-05 | 1940-12-17 | Du Pont | Cleaning process |
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 |
-
1946
- 1946-11-22 US US711804A patent/US2472400A/en not_active Expired - Lifetime
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
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 |
US2225294A (en) * | 1938-02-05 | 1940-12-17 | Du Pont | Cleaning process |
US2204223A (en) * | 1939-01-30 | 1940-06-11 | Shell Dev | Method of treating oil and gas 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 |
Cited By (32)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2602779A (en) * | 1947-09-11 | 1952-07-08 | Cities Service Oil Co | Method of inhibiting hydrogen sulfide corrosion of metals |
US2593057A (en) * | 1949-12-29 | 1952-04-15 | Pure Oil Co | Inhibitors against hydrogen sulfide and brine corrosion |
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 |
US2972861A (en) * | 1953-03-11 | 1961-02-28 | Midland Tar Distillers Ltd | Method of reducing the corrosive attack of combustion gases on metal |
US2814593A (en) * | 1953-12-18 | 1957-11-26 | Gen Aniline & Film Corp | Corrosion inhibition |
US2761835A (en) * | 1954-11-18 | 1956-09-04 | Gulf Research Development Co | Treatment of clays |
US2761836A (en) * | 1954-11-18 | 1956-09-04 | Gulf Research Development Co | Treatment of clays |
US2761838A (en) * | 1954-11-18 | 1956-09-04 | Gulf Research Development Co | Treatment of clays |
US2761841A (en) * | 1954-11-18 | 1956-09-04 | Gulf Research Development Co | Treatment of clays |
US2761842A (en) * | 1954-11-18 | 1956-09-04 | Gulf Research Development Co | Treatment of clays |
US2761837A (en) * | 1954-11-18 | 1956-09-04 | Gulf Research Development Co | Treatment of clays |
US2761840A (en) * | 1954-11-18 | 1956-09-04 | Gulf Research Development Co | Treatment of clays |
US2761843A (en) * | 1954-11-18 | 1956-09-04 | Gulf Research Development Co | Treatment of clays |
US2761839A (en) * | 1954-11-18 | 1956-09-04 | Gulf Research Development Co | Treatment of clays |
US2869978A (en) * | 1955-09-26 | 1959-01-20 | Union Oil Co | Method of gas purification utilizing an amine solution and an anti-corrosion agent |
DE946003C (en) * | 1956-01-26 | 1956-07-19 | Siegfried Peter Dipl Chem Dr | Anti-rust and primer |
US2955083A (en) * | 1956-08-13 | 1960-10-04 | Bj Service Inc | Corrosion inhibitors in well treating compositions |
US2955087A (en) * | 1957-04-08 | 1960-10-04 | Arthur D Berryman | Compositions and methods for treating metal surfaces |
US2999811A (en) * | 1957-08-07 | 1961-09-12 | Amchem Prod | Inhibitor composition |
DE1097068B (en) * | 1957-08-16 | 1961-01-12 | Iashellia Res Ltd | Lubricants and heat transfer agents based on mineral or synthetic oils |
US3107221A (en) * | 1958-04-18 | 1963-10-15 | Dow Chemical Co | Corrosion inhibitor composition |
US3017355A (en) * | 1958-04-18 | 1962-01-16 | Dow Chemical Co | Corrosion inhibitor composition |
US3033784A (en) * | 1959-05-13 | 1962-05-08 | Pan American Petroleum Corp | Water soluble corrosion inhibitor and bactericide |
US3066097A (en) * | 1960-06-09 | 1962-11-27 | Pan American Petroleum Corp | Polyalkyl pyridines for corrosion inhibiting |
US3077453A (en) * | 1961-09-01 | 1963-02-12 | Dow Chemical Co | Corrosion inhibition |
US3432527A (en) * | 1964-11-05 | 1969-03-11 | Armour Ind Chem Co | Corrosion inhibitor composition and method |
US3885913A (en) * | 1972-10-26 | 1975-05-27 | Petrolite Corp | Method of inhibiting the corrosion of metals in an acidic environment using quaternary ammonium salts of polyepihalohydrin |
US4276185A (en) * | 1980-02-04 | 1981-06-30 | Halliburton Company | Methods and compositions for removing deposits containing iron sulfide from surfaces comprising basic aqueous solutions of particular chelating agents |
US4554090A (en) * | 1984-03-09 | 1985-11-19 | Jones L W | Combination corrosion/scale inhibitor |
US5089226A (en) * | 1986-01-20 | 1992-02-18 | Nippon Mining Co., Ltd. | Method for protecting austenitic stainless steel-made equipment from occurrence of stress-corrosion cracking |
US5084210A (en) * | 1990-02-07 | 1992-01-28 | Chemlink Incorporated | Corrosion inhibitor |
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