US2636009A - Conditioning of metal surfaces - Google Patents

Conditioning of metal surfaces Download PDF

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US2636009A
US2636009A US694424A US69442446A US2636009A US 2636009 A US2636009 A US 2636009A US 694424 A US694424 A US 694424A US 69442446 A US69442446 A US 69442446A US 2636009 A US2636009 A US 2636009A
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metal
bath
sulfur
acid
scale
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Joseph T Irwin
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    • 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
    • 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
    • C23G1/08Iron or steel
    • C23G1/081Iron or steel solutions containing H2SO4

Definitions

  • This invention relates to the conditioning of metal surfaces.
  • Metallurgical operations involve various types of handling a metallic base.
  • the preparation or cleaning desirably has to do with exposing uniformly the metal texture thruout. Expeditiously and reliably to achieve this end means that the stock is in most acceptable condition for direct use in its true state, as well as for receiving a coating, plating, or a wide range of surface applications thereto or thereon.
  • This invention has utility in accelerating bath treatment of the metal, say as ferrous sheets thru pickling for enameling thereof.
  • the hindering factor from normal exposure to the air or weathering conditions, is corrosion, or more seriously, scale.
  • the problem to be solved has to do with the removal from the iron or steel, any and all objectionable substances or material thereon. This may arise from substances used in manufacture, such as oils, soaps and the like. More especilaly, the treatment is efiective on scale, so snugly adhering from its oxidation bonding upon the metal.
  • An acid pickling bath in which the materials are submerged, under an instance for use of the invention herein, has the attack materially expedited as well as efiects advantages in a resulting superior product.
  • An instance under the invention herein may be taken of the treatment of sheet iron of say 20 gauge and of a character usually suitable for tin plating, galvanizing, electroplating or enameling.
  • This sheet iron is submerged in a vat or tank of sulfuric acid of strength in the range of 7% acid by weight to 93% water.
  • a course taken, to have the temperature somewhat above normal atmospheric, is helpful in establishing a reliable practice for holding to uniform operating conditions. While the operation may be acceptably carried thru at F., or even lower, instances illustrative of performance efiiciency herein have been taken at F.
  • Sulfuric acid is adapted for its dissolving or penetrating action upon scales or oxide coatings.
  • the acid eats its way thru the undesirable surface to the base, where the metal itself is more readily attacked.
  • the sulfuric acid develops fissures or crack-like courses in the scale to reach the iron. The longer the interval of the bath,
  • Hydrogen gas generated by the chemical reaction of the sulfuric acid upon the iron, may be trapped under the scale surface about the crack or fissure to blast off scale particles.
  • the seeming nature of this hydrogen is that it has responded to reaction and now has a trait of spreading out or locating as an inert film coating over the metal and the residual scale on the metal.
  • the adsorbed film of gas is too thin to have buoyancy to rise as a bubble and thus to escape from the bath.
  • compound may be taken which will produce finely divided sulfur in suspension, when added to an acid solution.
  • a polysulfide, as well as micronized sulfur, selenium and tellurium, will answer.
  • sodiumthiosulfate NazSzOa
  • this salt cppper, brass, zinc, oralumirfum.
  • the proportion of this sodium thiosulfate may be one part in seven hundred by weight as to the weight of 7% sulfuric acid (H2804) in the bath, which would produce one part of reactive sulfur in five thousand, approximately, by weight as to the twetirglht of the 7% sulfuric acid (H2804) in the In a ten minute interval, the attacking rate upon iron was speeded up from .07% to .19%. Increase in this nascent, colloidal-characteristic sulfur, in the experience hereunder, does not proportionally accelerate the pickling bath operation. Doubling, or for two parts of sodium thiosulfate (NazSzOs-5Hz0) in seven hundred,
  • Dispersion of the agent at the attack region upon the metal is effectively achieved in the form of fines, say of sulfur resulting from the addition of sodium polysulfide to an acid solution.
  • fines of sulfur provide a maximum of exposure area in the micron dimension range, and this seems to fit in very helpfully in working thru for the desired acceleration sought herein.
  • the handling may be in batches, or thru continuous operation. The importance, in the latter instance, is quite noticeable in considering the material handled may have bath transit from 100 per minute set up to 300' per minute, and depending upon the physical dimensions of the solution tanks, acid concentration and temperature of the bath.
  • the saving due to the acceleration may be not only in time, as in the continuous process, but in equipment, say as to bath dimension curtailment; in supplies, in reduced quantity of acid required, not offset by the relatively negligible quantity of accelerator of the general types herein disclosed, which may be selectively taken upon the conditions which, marketwise, seems more appropriate.
  • a superior product with practical elimination of any objectionable etching is had under the accelerator treatment herein disclosed, as for the undesired coating removal, whether from iron, steel, alloys,
  • the higher temperatures ingredients disclosed herein for incorporation therewith are minimal in proportion.
  • a complementally reactive agent say the dispersed nascent, crystalloidal or colloidal characteristic of micron fineness sulfur, possesses reactive properties of sufficient hydrogen pick-up efficiency to clear the surface being treated of the seemingly relatively inert hydrogen film.
  • This film is so tenuously thin as not readily to gather into droplet masses, and thus, of itself, does not tend to rise in the solution to be clear of the metal. It is thus seen that the great surface area of the sulfur, as to its real mass or quantity, imparts under the treatment as herein disclosed, an eflicient dispersion of reactant particles of penetratingly minute effectiveness to get to the film and form hydrogen sulfide.
  • the dis ersed sulfur is haii i ibita z ka F C ?B, P2ES? e resent lemma" P ica'sid i'fzhhseh.
  • the a at c ina fi n f genaaaeniaaasnmah gr g e efiifi aiiiiabetnmmeatly are: 1.;
  • the purpose of the trea ment is to keep exposed the oxide or sulface portions to be removed.
  • the course adopted hereunder is to eliminate the hydrogen film on said portions.
  • the fines of the sulfur provide a maximum of area to react on the film.
  • the sulfuric acid is not spent in any way against the celerator treatment herein disclosed.
  • there be not occasion in any euiowdissipetefil pickling a ky ileiiii sulf ThTfiiiiitsiin'EFp'rofirtion relationship of the accelerator to the entire bath leaves the way open for the reactive agent and the accelerator each to pursue its reaction course, one not to the detriment of the other. In the more low ranges, the more wide seems to be the per-unit sulfur value.
  • a process of improving the surface condition of a metal in an acid pickling bath which consists in treating the surface of the metal to be pickled with a bath consisting of a pickling acid which is predominantly sulfuric acid and one t eight parts of sodium thiosulfate per seven hundred parts of 7% H2SO4.

Description

Patented Apr. 21, 1953 UNITED EXAMm STATES PATENT OFFICE No Drawing. Application August 31, 1948, Serial No. 694,424
1 Claim.
This invention relates to the conditioning of metal surfaces. Metallurgical operations involve various types of handling a metallic base. The preparation or cleaning desirably has to do with exposing uniformly the metal texture thruout. Expeditiously and reliably to achieve this end means that the stock is in most acceptable condition for direct use in its true state, as well as for receiving a coating, plating, or a wide range of surface applications thereto or thereon.
This invention has utility in accelerating bath treatment of the metal, say as ferrous sheets thru pickling for enameling thereof. The hindering factor, from normal exposure to the air or weathering conditions, is corrosion, or more seriously, scale. The problem to be solved has to do with the removal from the iron or steel, any and all objectionable substances or material thereon. This may arise from substances used in manufacture, such as oils, soaps and the like. More especilaly, the treatment is efiective on scale, so snugly adhering from its oxidation bonding upon the metal. An acid pickling bath in which the materials are submerged, under an instance for use of the invention herein, has the attack materially expedited as well as efiects advantages in a resulting superior product. This achievement is due to the introduction into the bath of an agent which, in itself, need not necessarily have traits to attack the iron or steel. The bath, into which the metal to be treated is immersed, serves as a menstruum or carrier. The fact that the invention treatment, with the substances or ingredients, brings about definite acceleration, establishes that the functioning of applicants invention is contrary to any slowing down on the metal cleaning operation or reaction. Actually, the way is cleared for efficient pickling performance by the bath, with no detractive results from applicant's taking advantage of the liquid state of the bath to adapt it as a carrier for generally exposing the surface or surfaces open to pickling attack. At the surface or surfaces, the bath carrier for the relatively minimal quantity for the invention treatment agent is efficient in major scavenger-like performance.
Manufacturing processes have to do with various special handling operations. With metals, more particularly with iron and steel, there may be various heat treatments, annealing and forging. Various pickling baths are adapted to remove the oxide or scale. The baths, usually of acid, may predominantly be sulfuric acid, altho hydrochloric, hydrofluoric and nitric acids, as well as various combinations thereof, and even alkalis have place. Pickling baths of caustic soda and caustic potash have more value in the treatment of aluminum and magnesium articles. Phosphates are in other baths. 1
An instance under the invention herein may be taken of the treatment of sheet iron of say 20 gauge and of a character usually suitable for tin plating, galvanizing, electroplating or enameling. This sheet iron is submerged in a vat or tank of sulfuric acid of strength in the range of 7% acid by weight to 93% water. A course taken, to have the temperature somewhat above normal atmospheric, is helpful in establishing a reliable practice for holding to uniform operating conditions. While the operation may be acceptably carried thru at F., or even lower, instances illustrative of performance efiiciency herein have been taken at F.
Sulfuric acid is adapted for its dissolving or penetrating action upon scales or oxide coatings. The acid eats its way thru the undesirable surface to the base, where the metal itself is more readily attacked. The sulfuric acid develops fissures or crack-like courses in the scale to reach the iron. The longer the interval of the bath,
the deeper such eating is directly into the metal to etch it away. Hydrogen gas, generated by the chemical reaction of the sulfuric acid upon the iron, may be trapped under the scale surface about the crack or fissure to blast off scale particles. The seeming nature of this hydrogen is that it has responded to reaction and now has a trait of spreading out or locating as an inert film coating over the metal and the residual scale on the metal. The adsorbed film of gas is too thin to have buoyancy to rise as a bubble and thus to escape from the bath.
Applicant has realized that taking away of this deterrent hydrogen film by an oxygen agent may not be quite as promotive in clearing of oxide or permitting more rapid attack of the base metal, as may be desired, asproceeding therefrom along the periodic chart scale in the general sulfur. selenium, tellurium direction. Accordingly, the course adopted is to introduce a substance to react with this released hydrogen and get it away from the iron as a hydride, say as in hydrogen sulfide, hydrogen selenide, and hydrogen telluride.
In accordance with the practice of the invention, compound may be taken which will produce finely divided sulfur in suspension, when added to an acid solution. A polysulfide, as well as micronized sulfur, selenium and tellurium, will answer. For a specific instance, sodiumthiosulfate (NazSzOa) may be taken. Considering this salt as cppper, brass, zinc, oralumirfum.
carrying five molecules of water (NazSzOa-SHzO). and that but one of the sulfur atoms be released for the accelerating response herein, the proportion of this sodium thiosulfate may be one part in seven hundred by weight as to the weight of 7% sulfuric acid (H2804) in the bath, which would produce one part of reactive sulfur in five thousand, approximately, by weight as to the twetirglht of the 7% sulfuric acid (H2804) in the In a ten minute interval, the attacking rate upon iron was speeded up from .07% to .19%. Increase in this nascent, colloidal-characteristic sulfur, in the experience hereunder, does not proportionally accelerate the pickling bath operation. Doubling, or for two parts of sodium thiosulfate (NazSzOs-5Hz0) in seven hundred,
instead of one part as above, or two parts available of finely divided sulfur per five thousand parts sulfuric acid (H2804) in the 7% by weight acid bath, resulting from the breakdown of the two parts of sodium thiosulfate (NazSzOa-SHzO) per seven hundred Darts sulfuric acid (H2804), seems to make no difference.
By the use of four parts in seven hundred, the attack rate is run up to the range of .3%, and when up to eight parts, the showing is only around .4%. This latter rate condition does not seem to be materially improved by further increase, even up to sixty-four parts in seven hundred of the sulfur carrying agent as to the acid. This prompts the applicant to reach the conclusion that an optimum condition is developed in the low proportion ranges as set forth.
Performance checkings with other substances of the periodic chart, more remote from oxygen than sulfur, seem to show about half the speedup rate attributable to sulfur, when the metal acted upon approached cleanness at starting. However, when there was a heavy scale, and the treatment was continued thru to complete or full removal of such scale, then the results seem to bring the selenium and tellurium agents more closely to approximate that developed under like circumstances from sulfur treating agents.
Dispersion of the agent at the attack region upon the metal is effectively achieved in the form of fines, say of sulfur resulting from the addition of sodium polysulfide to an acid solution. These fines of sulfur provide a maximum of exposure area in the micron dimension range, and this seems to fit in very helpfully in working thru for the desired acceleration sought herein. The handling may be in batches, or thru continuous operation. The importance, in the latter instance, is quite noticeable in considering the material handled may have bath transit from 100 per minute set up to 300' per minute, and depending upon the physical dimensions of the solution tanks, acid concentration and temperature of the bath. The saving due to the acceleration may be not only in time, as in the continuous process, but in equipment, say as to bath dimension curtailment; in supplies, in reduced quantity of acid required, not offset by the relatively negligible quantity of accelerator of the general types herein disclosed, which may be selectively taken upon the conditions which, marketwise, seems more appropriate. A superior product with practical elimination of any objectionable etching is had under the accelerator treatment herein disclosed, as for the undesired coating removal, whether from iron, steel, alloys,
In pickling practice, the higher temperatures ingredients disclosed herein for incorporation therewith are minimal in proportion. As a complementally reactive agent, say the dispersed nascent, crystalloidal or colloidal characteristic of micron fineness sulfur, possesses reactive properties of sufficient hydrogen pick-up efficiency to clear the surface being treated of the seemingly relatively inert hydrogen film. This film is so tenuously thin as not readily to gather into droplet masses, and thus, of itself, does not tend to rise in the solution to be clear of the metal. It is thus seen that the great surface area of the sulfur, as to its real mass or quantity, imparts under the treatment as herein disclosed, an eflicient dispersion of reactant particles of penetratingly minute effectiveness to get to the film and form hydrogen sulfide. The dis ersed sulfur is haii i ibita z ka F C ?B, P2ES? e resent lemma" P ica'sid i'fzhhseh. IL The a at c ina fi n f genaaaeniaaasnmah gr g e efiifi aiiiiabetnmmeatly are: 1.;
as, 1' The purpose of the trea ment is to keep exposed the oxide or sulface portions to be removed. The course adopted hereunder is to eliminate the hydrogen film on said portions. The fines of the sulfur provide a maximum of area to react on the film. Generally the sulfuric acid is not spent in any way against the celerator treatment herein disclosed. Furthermore hereunder, there be not occasion in any euiowdissipetefil pickling a ky ileiiii sulf ThTfiiiiiitsiin'EFp'rofirtion relationship of the accelerator to the entire bath leaves the way open for the reactive agent and the accelerator each to pursue its reaction course, one not to the detriment of the other. In the more low ranges, the more wide seems to be the per-unit sulfur value.
The more heavy the scale, the longer the time interval which is normally required for complete removal, say in pickling of ferrous metal. Specifically in operating to such end, 7% H2804 solution has been operated to clear the metal of scale in 3 min. Checking of this character of metal by the addition to the bath of accelerator, to the total weight of the acid, eight parts in seven hundred NazSzOa shortened the operating time for complete de-scaling to 2%; min. There seems to be an attack factor relevant to the accelerator that it does not increase the mass of the material removed directly relatively to the acid, but as to the metal area or surface exposed. Even here it may show some buildup, but not directly in proportion to the acid attack total. Importance resides in the fact that it does not accelerate the root attack upon the metal base itself. Per unit period of time, the extent of attack is greater with the heavy scale; or to carry thru a definite operation, the total time lapse therefor may be increased. The specific instance above approximates 30% time saving.
Supplementing the foregoing is the resultant surface condition of the treated stock. The surface grain fineness approaches that of new stock so closely as to be almost indistinguishable therefrom. Absence of accelerator, under the disclosure herein, shows a most marked degree of roughness or pebbled face efiect. In experiences for subsequent coating operations, such roughness or pebbling, as revealed in macrophotographs, involve many difficulties for establishing adequate surface anchoring, as well as failing to provide bases to carry attractive plating, coating, enameling and the like. There may be required less precision in performance to deliver a high grade merchantable output in applying the finishing coating upon the superior grade base, than when the character of the base be not so helpful. Accordingly the pre-treatment before coating, in which the accelerator of this invention be used, has worth in carrying thru for high grade finished products.
i h t is claigfl and it is desired to secure by Letters Patent is:
A process of improving the surface condition of a metal in an acid pickling bath which consists in treating the surface of the metal to be pickled with a bath consisting of a pickling acid which is predominantly sulfuric acid and one t eight parts of sodium thiosulfate per seven hundred parts of 7% H2SO4.
JOSEPH T. IRWIN.
References Cited in the file of this patent UNITED STATES PATENTS Number Name Date 2,071,989 Thomas Feb. 23, 1937 2,249,383 Hilty July 15, 1941 OTHER REFERENCES Mellor, Modern Inorganic Chemistry," 1939,
page 475, Longmans, Green and Co., New York. (Copy in Div. 27.)
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Cited By (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2831814A (en) * 1951-12-19 1958-04-22 Poor & Co Acid pickling of metals and compositions therefor
DE1033481B (en) * 1954-06-10 1958-07-03 Poor & Co Acid baths for pickling metals
US2868680A (en) * 1952-03-03 1959-01-13 Devex Corp Method of pickling and coating stainless steel in the same bath
DE1062518B (en) * 1954-06-09 1959-07-30 Poor & Co Acid pickling bath for pickling metals, especially steel
US2903384A (en) * 1956-03-05 1959-09-08 United States Steel Corp Method of preparing stainless-steel wire for drawing and forming
DE1123176B (en) * 1957-09-17 1962-02-01 Poor & Co Aqueous solution for the bright pickling of objects made of iron and steel
US3223649A (en) * 1962-11-06 1965-12-14 Monsanto Co Corrosion-inhibited phosphate solutions and compositions useful for manufacturing them
US3226180A (en) * 1964-03-06 1965-12-28 Cowles Chem Co Process of conditioning metal surfaces and compositions therefor
US3275566A (en) * 1965-09-16 1966-09-27 Monsanto Co Corrosion-inhibited phosphate solutions
US3293189A (en) * 1962-11-06 1966-12-20 Monsanto Co Corrosion-inhibited phosphate solutions and compositions useful for manufacturing them
DE1261370B (en) * 1958-04-25 1968-02-15 Inst Francais Du Petrol Process for protecting metal surfaces against corrosion by aqueous acidic solutions
DE1289719B (en) * 1965-11-04 1969-02-20 Cowles Chem Co Acid pickling solution and process for pickling ferrous metal
US4132568A (en) * 1977-12-16 1979-01-02 Irwin David W Process and composition for pickling metal surfaces
US6352967B1 (en) 1999-07-19 2002-03-05 David W. Irwin Additives for improving acid reactivity and method for controlling acid reactions

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2071989A (en) * 1934-02-16 1937-02-23 Du Pont Inhibitor for pickling and cleaning solutions
US2249383A (en) * 1937-12-29 1941-07-15 Hilty Donald Cleve Pickling of steel

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2071989A (en) * 1934-02-16 1937-02-23 Du Pont Inhibitor for pickling and cleaning solutions
US2249383A (en) * 1937-12-29 1941-07-15 Hilty Donald Cleve Pickling of steel

Cited By (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2831814A (en) * 1951-12-19 1958-04-22 Poor & Co Acid pickling of metals and compositions therefor
US2868680A (en) * 1952-03-03 1959-01-13 Devex Corp Method of pickling and coating stainless steel in the same bath
DE1062518B (en) * 1954-06-09 1959-07-30 Poor & Co Acid pickling bath for pickling metals, especially steel
DE1033481B (en) * 1954-06-10 1958-07-03 Poor & Co Acid baths for pickling metals
US2903384A (en) * 1956-03-05 1959-09-08 United States Steel Corp Method of preparing stainless-steel wire for drawing and forming
DE1123176B (en) * 1957-09-17 1962-02-01 Poor & Co Aqueous solution for the bright pickling of objects made of iron and steel
DE1261370B (en) * 1958-04-25 1968-02-15 Inst Francais Du Petrol Process for protecting metal surfaces against corrosion by aqueous acidic solutions
US3223649A (en) * 1962-11-06 1965-12-14 Monsanto Co Corrosion-inhibited phosphate solutions and compositions useful for manufacturing them
US3293189A (en) * 1962-11-06 1966-12-20 Monsanto Co Corrosion-inhibited phosphate solutions and compositions useful for manufacturing them
US3226180A (en) * 1964-03-06 1965-12-28 Cowles Chem Co Process of conditioning metal surfaces and compositions therefor
US3275566A (en) * 1965-09-16 1966-09-27 Monsanto Co Corrosion-inhibited phosphate solutions
DE1289719B (en) * 1965-11-04 1969-02-20 Cowles Chem Co Acid pickling solution and process for pickling ferrous metal
US4132568A (en) * 1977-12-16 1979-01-02 Irwin David W Process and composition for pickling metal surfaces
US6352967B1 (en) 1999-07-19 2002-03-05 David W. Irwin Additives for improving acid reactivity and method for controlling acid reactions

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