US3282850A - Corrosion inhibition with dipropargyl butylamine - Google Patents

Corrosion inhibition with dipropargyl butylamine Download PDF

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US3282850A
US3282850A US360074A US36007464A US3282850A US 3282850 A US3282850 A US 3282850A US 360074 A US360074 A US 360074A US 36007464 A US36007464 A US 36007464A US 3282850 A US3282850 A US 3282850A
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dipropargyl
butylamine
corrosion
acid
inhibitor
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US360074A
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Davidowich George
Morton W Leeds
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Cumberland Chemical Corp
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Cumberland Chemical Corp
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    • 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
    • C23G—CLEANING OR DE-GREASING OF METALLIC MATERIAL BY CHEMICAL METHODS OTHER THAN ELECTROLYSIS
    • C23G1/00—Cleaning or pickling metallic material with solutions or molten salts
    • C23G1/02—Cleaning or pickling metallic material with solutions or molten salts with acid solutions
    • C23G1/04—Cleaning or pickling metallic material with solutions or molten salts with acid solutions using inhibitors
    • C23G1/06—Cleaning or pickling metallic material with solutions or molten salts with acid solutions using inhibitors organic inhibitors
    • C23G1/068—Cleaning or pickling metallic material with solutions or molten salts with acid solutions using inhibitors organic inhibitors compounds containing a C=C bond
    • 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
    • Y10S507/933—Acidizing or formation destroying
    • Y10S507/934—Acidizing or formation destroying with inhibitor

Definitions

  • This invention relates to the inhibition of metal corrosion in acidic solutions and is more particularly concerned with inhibited aqueous acid solutions suitable for the treatment of metals.
  • Metal cleaning baths and pickling baths generally comprise aqueous solutions of inorganic acids such as sulfuric acid, hydrochloric acid, and phosphoric acid and are useful in the cleaning and treatment of iron, zinc, ferrous alloys and the like.
  • inorganic acids such as sulfuric acid, hydrochloric acid, and phosphoric acid
  • aqueous acidic baths to treat metals
  • additives or inhibitors in the baths are desirable to prevent or inhibit corrosion or erosion of the metal surfaces. If no corrosion inhibitor is present in the acidic bath, excessive metal loss, production of undesirable metal surface properties, excessive consumption or less of acid, and like adverse results will be experienced. While it is wellknown to use corrosion inhibitors in such acidic baths, and many different types of inhibitors have been proposed, there has been a continuing search for inhibitors which can be effectively used even in very low concentrations.
  • Another object of this invention is to provide a novel inhibited aqueous acidic composition.
  • a further object of the invention is to provide improved metal treating baths containing an inhibitor which is effective to inhibit corrosion even when present in very low concentrations.
  • dipropargyl butylamine which has the formula CHaCECH (l aCfizoHaCHgN CHaCECH
  • Dipropargyl butylamine is readily prepared by interacting propargyl bromide of the formula BICHZCECH, and nbutylamine, e.g. by the procedure described by Von Braun et al. in Berichte der Deutschen Chemischentechnik, vol. 59 (1926), pp. 1081-1090, or the procedure described by Wolf in Annalen der Chemie, vol. 576 (1952), pp. 35-45.
  • the procedure described by Purcell and Pollard in the Journal of the American Chemical Society, vol. 72 (1950), pp. 3312-3313, can also be used.
  • dipropargyl butylamine in aqueous inorganic acid solutions has been found to have the desirable result of inhibiting or substantially preventing the corrosive action or attack of the acid upon metal surfaces with which it comes into contact.
  • the use of dipropargyl butylamine in acid cleaning and pickling baths does not hinder or interfere with the desired action of the acid on the oxide, rust, grease, scale, or other undesirable surface material or coating which is to be removed.
  • the inhibitor of this invention is useful, in general, in the inhibition of corrosion of metal surfaces in contact with aqueous mineral acid solutions, for example, in the acidizing of oil wells, electrolytic cleaning baths, and electrolytic refining of metals, as well as in metal cleaning and pickling baths.
  • dipropargyl butylamine as a corrosion inhibitor for metals in aqueous mineral acid solutions is advantageous in that dipropargyl butylamine can be employed as a corrosion inhibitor over a wide and useful concentration range.
  • a further advantage of this inhibitor is that it may be used even at elevated temperatures to provide good corrosion inhibition, even when in low concentration.
  • the most effective amount of dipropargyl butylamine to be used in accordance with this invention can vary, depending upon local operating conditions.
  • the temperature and other characteristics of the acid corrosive system may have a bearing upon the amount of inhibitor to be used.
  • a concentration of dipropargyl butylamine between 0.01% to 0.5% by weight of the aqueous acidic solution is an effective corrosion inhibiting concentration, with a concentration between 0.05% to 0.5% being particularly preferred, especially for corrosive systems at elevated temperatures, e.g. in the neighborhood of C.
  • the following specific examples are illustrative of the corrosion inhibiting properties of dipropargyl butylamine.
  • the inhibitor concentration is expresed as a percent by weight of the aqueous acidic solution in which it is incorporated and the acid concentration of the solution is expressed as percent by weight of the solution.
  • the method used to determine the inhibiting properties of dipropargyl butylamine as set forth in the following examples employed test specimens of low carbon 1020 steel. Coupons in. x 1% in. were cut from the steel sheet-stock and pickled in dilute HCl to remove scale and surface film. After pickling they were dipped in sodium bicarbonate solution, rinsed well in tap water while rubbing with a piece of cotton, rinsed in distilled water and finally dried with acetone.
  • the clean and dry specimens were then weighed to the nearest 0.1 mg., all handling being effected with forceps to keep the coupons free of oil or moisture from the hands.
  • the dipropargyl butylamine was weighed and placed in ml. of the acidic solution. Weighed and identified coupons in duplicate were supported on glass hooks in a 4 oz. glass jar, the solution being studied added, the jar covered and placed in a constant temperature oven at 80 C. for 3 hours. At the end of the exposure period, the jars were removed from the oven, samples removed, rinsed with tap water, sodium bicarbonate solution, tap water, distilled water and finally acetone. The dry coupons were weighed and the percent inhibition calculated by subtracting the loss in weight of the coupon from the original weight, dividing by the original weight and multiplying by 100. This is expressed by the following formula:
  • Example 1 Using the procedures described above, steel coupons cut from low-carbon 1020 steel of 16 gauge were immersed in 4.8 N hydrochloric acid containing varying concentrations of dipropargyl butylamine at 80 C. (176 F.) for 3
  • Example 2 In order to demonstrate further the outstanding effectiveness of dipropargyl butylamine as a corrosion in hibitor, the tests described in Example 1 where repeated but with a lower concentration of the inhibitor and with a more-corrosion-susceptible steel.
  • coupons cut from a low-carbon 1020 steel of 18 gauge were immersed in the same hydrochloric acid under the conditions described in Example 1, with the acid containing only 0.05%
  • Inhibitor concentration Immersion corrosion rate, percent .05% 96 None (control) 6
  • Example 3 Using the procedures described above, steel coupons were immersed in a solution of 4.8 N sulfuric acid at a temperature of 80 C. (175 F.). The inhibitor concentrations were those employed in Example 1. The following results were obtained.
  • Example4 In order to demonstrate further the outstanding efiectiveness of dipropargyl butylamine in sulfuric acid, coupons cut from the steel used in Example 2 were immersed in the sulfuric acid and under the conditions described in Example 3, with the acid containing only 0.05% of dipropargyl butylamine. The results of these tests are set forth below.

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Cleaning And De-Greasing Of Metallic Materials By Chemical Methods (AREA)
  • Detergent Compositions (AREA)

Description

3,282,850 CORROSION INHIBITION WITH DIPROPARGYL BUTYLAMINE George Davidowich, Bayonne, and Morton W. Leeds, Murray Hill, N.Ii., assignors, by mesne assignments, to Cumberland Chemical Corporation, New York, N.Y., a corporation of Delaware No Drawing. Filed Apr. 15, 1964, Ser. No. 360,074
4 Claims. (Cl. 252-448) This invention relates to the inhibition of metal corrosion in acidic solutions and is more particularly concerned with inhibited aqueous acid solutions suitable for the treatment of metals.
Metal cleaning baths and pickling baths generally comprise aqueous solutions of inorganic acids such as sulfuric acid, hydrochloric acid, and phosphoric acid and are useful in the cleaning and treatment of iron, zinc, ferrous alloys and the like.
In the use of aqueous acidic baths to treat metals, additives or inhibitors in the baths are desirable to prevent or inhibit corrosion or erosion of the metal surfaces. If no corrosion inhibitor is present in the acidic bath, excessive metal loss, production of undesirable metal surface properties, excessive consumption or less of acid, and like adverse results will be experienced. While it is wellknown to use corrosion inhibitors in such acidic baths, and many different types of inhibitors have been proposed, there has been a continuing search for inhibitors which can be effectively used even in very low concentrations.
It is accordingly an object of this invention to provide an improved means for the protection of metal surfaces against erosion or corrosion in aqueous acid solutions.
Another object of this invention is to provide a novel inhibited aqueous acidic composition.
A further object of the invention is to provide improved metal treating baths containing an inhibitor which is effective to inhibit corrosion even when present in very low concentrations.
These and other objects are achieved in accordance with the present invention by the incorporation in aqueous inorganic acid solutions of a small but effective inhibiting amount of dipropargyl butylamine, which has the formula CHaCECH (l aCfizoHaCHgN CHaCECH Dipropargyl butylamine is readily prepared by interacting propargyl bromide of the formula BICHZCECH, and nbutylamine, e.g. by the procedure described by Von Braun et al. in Berichte der Deutschen Chemischen Gesellschaft, vol. 59 (1926), pp. 1081-1090, or the procedure described by Wolf in Annalen der Chemie, vol. 576 (1952), pp. 35-45. The procedure described by Purcell and Pollard in the Journal of the American Chemical Society, vol. 72 (1950), pp. 3312-3313, can also be used.
The introduction of dipropargyl butylamine in aqueous inorganic acid solutions has been found to have the desirable result of inhibiting or substantially preventing the corrosive action or attack of the acid upon metal surfaces with which it comes into contact. The use of dipropargyl butylamine in acid cleaning and pickling baths does not hinder or interfere with the desired action of the acid on the oxide, rust, grease, scale, or other undesirable surface material or coating which is to be removed.
The inhibitor of this invention is useful, in general, in the inhibition of corrosion of metal surfaces in contact with aqueous mineral acid solutions, for example, in the acidizing of oil wells, electrolytic cleaning baths, and electrolytic refining of metals, as well as in metal cleaning and pickling baths.
States Patent 3,282,850 Patented Nov. 1, 1966 The use of dipropargyl butylamine as a corrosion inhibitor for metals in aqueous mineral acid solutions is advantageous in that dipropargyl butylamine can be employed as a corrosion inhibitor over a wide and useful concentration range. A further advantage of this inhibitor is that it may be used even at elevated temperatures to provide good corrosion inhibition, even when in low concentration.
The most effective amount of dipropargyl butylamine to be used in accordance with this invention can vary, depending upon local operating conditions. Thus, the temperature and other characteristics of the acid corrosive system may have a bearing upon the amount of inhibitor to be used.
In general, it has been found that a concentration of dipropargyl butylamine between 0.01% to 0.5% by weight of the aqueous acidic solution is an effective corrosion inhibiting concentration, with a concentration between 0.05% to 0.5% being particularly preferred, especially for corrosive systems at elevated temperatures, e.g. in the neighborhood of C.
The following specific examples are illustrative of the corrosion inhibiting properties of dipropargyl butylamine. In the examples, the inhibitor concentration is expresed as a percent by weight of the aqueous acidic solution in which it is incorporated and the acid concentration of the solution is expressed as percent by weight of the solution. The method used to determine the inhibiting properties of dipropargyl butylamine as set forth in the following examples employed test specimens of low carbon 1020 steel. Coupons in. x 1% in. were cut from the steel sheet-stock and pickled in dilute HCl to remove scale and surface film. After pickling they were dipped in sodium bicarbonate solution, rinsed well in tap water while rubbing with a piece of cotton, rinsed in distilled water and finally dried with acetone. The clean and dry specimens were then weighed to the nearest 0.1 mg., all handling being effected with forceps to keep the coupons free of oil or moisture from the hands. The dipropargyl butylamine was weighed and placed in ml. of the acidic solution. Weighed and identified coupons in duplicate were supported on glass hooks in a 4 oz. glass jar, the solution being studied added, the jar covered and placed in a constant temperature oven at 80 C. for 3 hours. At the end of the exposure period, the jars were removed from the oven, samples removed, rinsed with tap water, sodium bicarbonate solution, tap water, distilled water and finally acetone. The dry coupons were weighed and the percent inhibition calculated by subtracting the loss in weight of the coupon from the original weight, dividing by the original weight and multiplying by 100. This is expressed by the following formula:
Percent inhibition:
(original weight specimen-weight loss) X100 original weight specimen The results are expressed as percent inhibition and are the average of the duplicate samples.
Example 1 Using the procedures described above, steel coupons cut from low-carbon 1020 steel of 16 gauge were immersed in 4.8 N hydrochloric acid containing varying concentrations of dipropargyl butylamine at 80 C. (176 F.) for 3 Example 2 In order to demonstrate further the outstanding effectiveness of dipropargyl butylamine as a corrosion in hibitor, the tests described in Example 1 where repeated but with a lower concentration of the inhibitor and with a more-corrosion-susceptible steel. Thus, coupons cut from a low-carbon 1020 steel of 18 gauge were immersed in the same hydrochloric acid under the conditions described in Example 1, with the acid containing only 0.05%
dipropargyl butylamine. The results of these tests are set forth below.
Inhibitor concentration: Immersion corrosion rate, percent .05% 96 None (control) 6 Example 3 Using the procedures described above, steel coupons were immersed in a solution of 4.8 N sulfuric acid at a temperature of 80 C. (175 F.). The inhibitor concentrations were those employed in Example 1. The following results were obtained.
Immersion corrosion Inhibitor concentration:
- rate, percent None (control) 61 Example4 In order to demonstrate further the outstanding efiectiveness of dipropargyl butylamine in sulfuric acid, coupons cut from the steel used in Example 2 were immersed in the sulfuric acid and under the conditions described in Example 3, with the acid containing only 0.05% of dipropargyl butylamine. The results of these tests are set forth below.
Inhibitor concentration: Immersion corrosion rate, percent .05% 96 None (control) 14 It will be understood that various changes and modifications may be made in the foregoing description without parting from the scope of the invention, as defined in the appended claims and it is intended, therefore, that all matter contained in the foregoing description shall be interpreted as illustrative only and not as limitative of the References Cited by the Examiner UNITED STATES PATENTS 10/1963 Harrison et al. 252l46 XR OTHER REFERENCES Acetylenic Corrosion Inhibitors, Industrial and Engineering Chemistry, vol. 51, No. 7 (July 1959), pages 825-828.
Purcell et al.: JACS, vol. 72 (1950), pages 3312-3313.
LEON D. ROSDOL, Primary Examiner.
JULIUS GREENWALD, Examiner.
S. E. DARDEN, Assistant Examiner.

Claims (1)

1. AN AQUEOUS SOLUTION OF A MINERAL ACID CONTAINING A CORROSION-INHIBITING AMOUNT OF DIPROPARGYL BUTYLAMINE.
US360074A 1964-04-15 1964-04-15 Corrosion inhibition with dipropargyl butylamine Expired - Lifetime US3282850A (en)

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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4174269A (en) * 1978-06-21 1979-11-13 Ppg Industries, Inc. Method of treating electrodes
US4187277A (en) * 1975-03-07 1980-02-05 Petrolite Corporation Process of inhibiting corrosion with quaternaries of halogen derivatives of alkynoxymethyl amines
US5284593A (en) * 1990-04-26 1994-02-08 Roto-Finish Company, Inc. Nonchelating metal finishing compounds
US11034921B2 (en) 2018-05-16 2021-06-15 Adam Mason PRINCE Method, kit, and composition for corrosion removal

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3107221A (en) * 1958-04-18 1963-10-15 Dow Chemical Co Corrosion inhibitor composition

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3107221A (en) * 1958-04-18 1963-10-15 Dow Chemical Co Corrosion inhibitor composition

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4187277A (en) * 1975-03-07 1980-02-05 Petrolite Corporation Process of inhibiting corrosion with quaternaries of halogen derivatives of alkynoxymethyl amines
US4174269A (en) * 1978-06-21 1979-11-13 Ppg Industries, Inc. Method of treating electrodes
US5284593A (en) * 1990-04-26 1994-02-08 Roto-Finish Company, Inc. Nonchelating metal finishing compounds
US11034921B2 (en) 2018-05-16 2021-06-15 Adam Mason PRINCE Method, kit, and composition for corrosion removal

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