US3329619A - Pickling ferrous metal - Google Patents

Pickling ferrous metal Download PDF

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Publication number
US3329619A
US3329619A US476708A US47670865A US3329619A US 3329619 A US3329619 A US 3329619A US 476708 A US476708 A US 476708A US 47670865 A US47670865 A US 47670865A US 3329619 A US3329619 A US 3329619A
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United States
Prior art keywords
pickling
acid
ferrous metal
hydrogen
inhibitors
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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US476708A
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English (en)
Inventor
Robert M Hudson
Clair J Warning
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United States Steel Corp
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United States Steel Corp
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Publication date
Application filed by United States Steel Corp filed Critical United States Steel Corp
Priority to US476708A priority Critical patent/US3329619A/en
Priority to GB29741/66A priority patent/GB1140955A/en
Priority to FR70636A priority patent/FR1487656A/fr
Priority to ES0329707A priority patent/ES329707A1/es
Application granted granted Critical
Publication of US3329619A publication Critical patent/US3329619A/en
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Classifications

    • CCHEMISTRY; METALLURGY
    • C23COATING 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
    • C23GCLEANING OR DE-GREASING OF METALLIC MATERIAL BY CHEMICAL METHODS OTHER THAN ELECTROLYSIS
    • C23G1/00Cleaning or pickling metallic material with solutions or molten salts
    • C23G1/02Cleaning or pickling metallic material with solutions or molten salts with acid solutions
    • C23G1/04Cleaning or pickling metallic material with solutions or molten salts with acid solutions using inhibitors
    • C23G1/06Cleaning or pickling metallic material with solutions or molten salts with acid solutions using inhibitors organic inhibitors
    • C23G1/063Cleaning or pickling metallic material with solutions or molten salts with acid solutions using inhibitors organic inhibitors heterocyclic compounds

Definitions

  • This invention relates to pickling. More particularly, the invention is directed to a pickling composition and to a method of pickling ferrous metal.
  • ferrous metal refers to iron, iron alloys and steel.
  • oxide coating (Samples hydrogen concentration, uninhibited acid) oxide coating, formed during manufacturing, from the surface.
  • oxide coating referred to as scale is objectionable when the material is to undergo subsequent processing.
  • oxide scale must be removed and a clean surface provided if satisfactory results are to be obtained from hot rolled sheet and strip in any operation involving deformation of the product.
  • steel prepared for drawing must possess a clean surface and removal of the oxide scale therefrom is essential since the scale tends to shorten drawing-die life as well as destroy the surface smoothness of the finished product.
  • Oxide removal from sheet or strip is also necessary prior to coating operations to permit proper alloying or adherence of the coating to the ferrous metal strip or sheet. Prior to cold reduction, it is necessary that the oxide formed during hot rolling be completely removed to preclude surface irregularities and enable uniform reduction of the work.
  • pickling The chemical process used to remove oxide from metal surfaces is referred to as pickling."
  • Typical pickling processes involve the use of aqueous acid solutions, usually inorganic acids, into which the metal article is immersed.
  • the acid solution reacts with the oxides to form hydrogen and a salt of the acid.
  • a common problem in this process is overpickling which is a condition resulting when the ferrous metal remains in the pickling solution after the oxide scale is removed from the surface and the pickling solution reacts with the ferrous metal base.
  • An additional difficulty in pickling results from the liberated hydrogen being absorbed by the metal base and causing hydrogen embrittlement.
  • To overcome the aforementioned problems in pickling it has been customary to add inhibitors to the pickling solution. Although most inhibitors in present use are effective in preventing of overpicklin-g, many do not prevent hydrogen absorption and consequent hydrogen embrittlement. A number of known inhibitors such as some organic compounds containing sulfur have been found to actualy promote hydrogen embrittlement.
  • the present invention avoids the above-described problems in pickling ferrous metal articles and provides a pickling composition which minimizes both overpickling and hydrogen embrittlement.
  • the pickling inhibitors described herein not only prevent excessive dissolution of the ferrous metal base but effectively limit the amount of hydrogen absorption thereby during pickling.
  • a pickling composition for ferrous metal which comprises a pickling acid such as sulfuric or hydrochloric acid and a small but effective amount of a pyrrole ring compound from the group consisting of pyrrole, pyrrolidine, l-methylpyrrole, 2,5-dimet-hylpyrrole, indole, indoline, and Z-methylindole, 2,5-dimethylindole or 3-pyrroline to inhibit both metal dissolution and hydrogen embrittlement.
  • Ferrous metal articles are pickled with inhibitor)] with inhibitor) 1
  • the above equations give an indication of the percent inhibition (1) and percent limitation of hydrogen absorption (L).
  • the samples weight change in the uninhibited acid refers to the change in the samples weight due to dissolution by the acid.
  • the samples weight change with 'the inhibitor refers to change in weight of the sample in an acid solution containing the specified pickling inhibitor. All measurements are made after lapse of the same time period and in the data provided herein a standard 4-hour period was used.
  • the samples hydrogen concentration, uninhibited acid refers to the amount of hydrogen that is driven off by warm extraction of the sample, i.e. heating at 160-1 65 C. for 16 hours. The value used in this equation is in cc. of hydrogen/ grams sample.
  • the samples hydrogen concentration, with inhibitor refers to the amount of hydrogen obtained in the same manner (i.e. by warm extraction) from the sample contacted with pickling acid composition containing a specified pickling inhbitor; also in both these cases for the same unit time, e.g. 4 hours.
  • the results of a number of tests of various pickling inhibitors including those within the purview of the invention are presented in Tables I and II below.
  • the samples used were of commercially available normalized and temper-rolled low-carbon sheet steel of the following composition: 0.022% carbon, 0.14% manganese, 0.007% phosphorus, 0.017% sulfur, 0.004% silicon, 0.015% copper, 0.002% nickel, 0.010% chromium, 0.002% aluminum, the balance being essentially iron.
  • the samples were 2 x and 0.036" thick and were vapor degreased with trichloroethylene before use. All the samples were pickled at 100 F.
  • Tables I and II below indicate the relative effectiveness of inhibitors present in difierent concentrations. For some, increasing the quantity of inhibitors does not provide a proportional increase in effectiveness, for others increasing the amount of inhibitors increases their eifectiveness.
  • pickling inhibitors differ greatly in their effectiveness, that is, the I and L values associated with the inhibitor. Moreover, the data illustrate the unpredictability of inhibitor effectiveness since, as shown, some pyrrole ring compounds would not be commercially useful while others are.
  • the inhibitors exhibiting I values of 80 or above may be preferred.
  • the residence time of steel in the pickling bath is relatively short and inhibitors exhibiting lower I values, eg [:40 may be considered useful.
  • inhibitor concentration on the order of 0.1 volume or weight percent in acid solution would be used.
  • many inhibitors can be used at 0.05 volume or weight percent. It is generally desirable to use the least amount of inhibitor which provides the desired results.
  • the quantity of inhibitors used is related to the pickling acid strength. For example, if 0.1 volume or weight percent inhibitor concentration is effective for a 2 N acid solution, then 0.05 volume or weight percent inhibitor concentration should be adequate for 1 N acid solution. In the same Way, 0.2 volume or weight percent inhibitor should be adequate for a 4 N acid solution.
  • a pickling composition for ferrous metal consisting essentially of a pickling acid from the group consisting of sulfuric acid and hydrochloric acid and a small but effective amount of a pyrrole ring compound from the group consisting of pyrrole, pyrrolidine, l-methylpyrrole, 2,5-dimethylpyrrole, indole, indoline, and Z-methylindole, 2,5-dimethylindole and 3-pyrroline to inhibit both dissolution and hydrogen embrittlement of said ferrous metal by said pickling acid.
  • a method of pickling a ferrous metal surface comprising contacting said surface with a composition comprising a pickling acid from the group consisting of sulfuric acid and hydrochloric acid and a pyrrole ring compound from the group consisting of pyrrole, pyrrolidine, l-methylpyrrole, 2,5-dimethylpyrrole, indole, indoline, and Z-methylindole, 2.,5-dimethylindole and 3-pyrroline, said pickling composition being effective to remove oxides from said ferrous metal surface with minimum dissolution and hydrogen embrittlement thereof, and washing said ferrous metal to remove said pickling composition.
  • said pickling acid is ulfuric acid and said pyrrole ring compound is a member from the group consisting of pyrrole, pyrrolidine, l-methylpyrrole, 2,5-dimethylpyrrole, indole, indoline and Z-methylindole.

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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)
US476708A 1965-08-02 1965-08-02 Pickling ferrous metal Expired - Lifetime US3329619A (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
US476708A US3329619A (en) 1965-08-02 1965-08-02 Pickling ferrous metal
GB29741/66A GB1140955A (en) 1965-08-02 1966-07-01 Pickling ferrous metal
FR70636A FR1487656A (fr) 1965-08-02 1966-07-25 Procédé et composition de décapage des métaux ferreux
ES0329707A ES329707A1 (es) 1965-08-02 1966-07-30 Procedimiento para el decapado de superficies ferrosas.

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US476708A US3329619A (en) 1965-08-02 1965-08-02 Pickling ferrous metal

Publications (1)

Publication Number Publication Date
US3329619A true US3329619A (en) 1967-07-04

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US476708A Expired - Lifetime US3329619A (en) 1965-08-02 1965-08-02 Pickling ferrous metal

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US (1) US3329619A (fr)
ES (1) ES329707A1 (fr)
FR (1) FR1487656A (fr)
GB (1) GB1140955A (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4210590A (en) * 1978-01-06 1980-07-01 Mcneil Laboratories, Incorporated Reduction of indole compounds to indoline compounds

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB8608797D0 (en) * 1986-04-11 1986-05-14 Pyrene Chemical Services Ltd Compositions for abrasive blast cleaning

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1719650A (en) * 1929-07-02 George b
US1746679A (en) * 1929-07-18 1930-02-11 Fred H Rhodes Chemical reagent
US2043257A (en) * 1933-10-09 1936-06-09 Stauffer Chemical Co Preservation of chlorinated hydrocarbons
GB765522A (en) * 1954-02-16 1957-01-09 Diamond Alkali Co Improvements in or relating to the stabilization of chlorohydrocarbons
US3056746A (en) * 1959-02-24 1962-10-02 Jr Frederick C Brightly Acid pickling composition with inhibitor
US3214433A (en) * 1964-03-23 1965-10-26 Upjohn Co Novel pyrido[3, 4-b]indoles

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1719650A (en) * 1929-07-02 George b
US1746679A (en) * 1929-07-18 1930-02-11 Fred H Rhodes Chemical reagent
US2043257A (en) * 1933-10-09 1936-06-09 Stauffer Chemical Co Preservation of chlorinated hydrocarbons
GB765522A (en) * 1954-02-16 1957-01-09 Diamond Alkali Co Improvements in or relating to the stabilization of chlorohydrocarbons
US3056746A (en) * 1959-02-24 1962-10-02 Jr Frederick C Brightly Acid pickling composition with inhibitor
US3214433A (en) * 1964-03-23 1965-10-26 Upjohn Co Novel pyrido[3, 4-b]indoles

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4210590A (en) * 1978-01-06 1980-07-01 Mcneil Laboratories, Incorporated Reduction of indole compounds to indoline compounds

Also Published As

Publication number Publication date
FR1487656A (fr) 1967-07-07
GB1140955A (en) 1969-01-22
ES329707A1 (es) 1967-06-01

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