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US3100170A - Pickling magnesium articles - Google Patents

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US3100170A
US3100170A US83A US8360A US3100170A US 3100170 A US3100170 A US 3100170A US 83 A US83 A US 83A US 8360 A US8360 A US 8360A US 3100170 A US3100170 A US 3100170A
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magnesium
article
pickling
halogen
composition
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Levy Donald Jack
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Dow Chemical Co
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Dow Chemical Co
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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
    • C23G1/12—Light metals

Definitions

  • the invention pertains to cleaning or pickling metal articles composed of at least about 75 percent magnesium, hereinafter sometimes referred to as magnesium articles.
  • Such magnesium articles usually contain contaminants on the surface thereof which stimulate corrosion thereof following working, shaping, or fabrication. Corrosion of the surface contaminated magnesium articles manifests itself by the formation of a tarnish and/ or tenaciously adhering scale during storage and use at a rate which is deteriorating and destructive to the metal unless such contaminants are removed.
  • a chemical composition usually consisting of dipping or otherwise applying the composition as an aqueous solution followed by water-rinsing, and usually, thereafter, by drying.
  • the chemical treating solution usually being acidic, is commonly called a pickle bath and the treatment therein, pickling.
  • Pickling of magnesium articles has been successful to some extent to remove the contaminants from the surface of the article thus treated to lessen subsequent corrosion and is widely practiced.
  • a number of pickling compositions have been employed in attempts to attain this purpose, some of which have been found useful to attain such contaminant removal from magnesium articles and provide improved resistance against corrosion to magnesium articles.
  • a bright lustrous surface having high corrosion resistance can be obtained by subjecting a magnesium-base alloy article containing not more than 2.0 percent zinc to the action of an aqueous composition 3,100,170 Patented Aug. 6, 1963 "ice 2 prepared by admixing with an aqueous sulfuric acid solution, of at least 20 N but not over 25 N, one or more of a halogen ionor nitrate ion-yielding compound wherein the halogen is chlorine or iodine.
  • HNO a soluble nitrate salt, HCl, a soloble chloride salt, a soluble iodide salt, HI, an oxychloride salt, an oxyiodide salt, or a halogen-substituted ionizable organic compound such as monochloroacetic acid, for a time sufficient to remove the contaminants or scale therefrom, waterarinsing, and preferably drying the magnesium article so treated.
  • reaction rate is undesirably fast and the extent of corrosion resistance imparted to the article is unsatisfactory even though an excessive amount of metal is removed from the magnesiarticle during treatment.
  • acid normality is greater than 25 N, the reaction rate is undesirably slow and more of the halide ionor nitrate ion-yielding additament is required to attain satisfactory cleaning and corrosion protection.
  • the halide ionor nitrate ion-yielding compound is admixed with the sulfuric acid solution in an amount sufficient to yield a weight of between 5 and 250 grams of the (N0 or halogen fraction or portion of the compound per liter of the sulfuric acid-treating composition so made.
  • the practice of the invention is applicable to brightening and providing corrosion resistance to any magnesium or magnesium-base alloy article including those containing zinc alloyed therein up to 2 percent thereof. Articles thus treated are free from undesirable blotches or streaks which form on certain extensively used magnesium-base alloy articles when sulfuric acid alone is used.
  • the composition containing any of the above named acids or salts as an adjuvant to sulfuric acid of the required normality for pickling magnesium articles exerts a minimum attack on the magnesium article being pickled and is relatively low in cost.
  • the article so pickled shows a particularly high resistance to corrosion in relation to the depth of the layer of metal removed during pickling.
  • the improved composition employed in the invention requires no sequestering or buffering agent as do most compositions presently employed in pickling magnesium-base alloys. Such sequestering or buffering agents are relatively expensive and sometimes prevent a satisfactory removal of the tarnish or scale during the pickling operation.
  • the preferred mode of treating the article to be cleaned and given protection against corrosion 'in accordance with the invention is to employ a bath of the aqueous acid or salt and sulfuric acid of a suitable normality and immerse the article to be treated therein.
  • the temperature of the bath may be any temperature less than the boiling point thereof but it is preferred that it be between and F.
  • the period of immersion of the article being treated in the bath depends upon the concentration and the temperature of the bath, the composition of magnesium alloy being treated, and the severity of tarnish or "scale on the article. Immersion in the bath should be sufiiciently long to provide the necessary corrosion re sistance desired.
  • the treating bath therefore, less contaminated, but the bright lustrous surface attained on the metal is equally as good when only enough metal the period of exposure to air is 2 minutes. The duration of the test was 7 days. The thus treated article is cleaned,
  • Table I sets out pickling compositions illustrative of the practice of the invention wherein the recommend a nitrate, chloride, or iodide portion or fraction of a nitrate ion-, chloride ionor iodide ion-yielding compound is added to (the sulfuric acid solution having the normality shown.
  • the pickling composition employed in the practice of the invention may be revivified conveniently as required. Periodic tests thereof show when the acid normality and/ or the concentration of the halide ion or nitrate ion concentration thereof require adjustment. Such adjustment is readily done by adding suflicient sulfuric acid and/or the thalide ionor nitrate ion-yielding material to bring the concentration thereof within the ranges thereof set out hercinabove.
  • the bath may be separated therefrom by merely filtering, decanting, siphoning, or otherwise drawing oil the supernatant liquid pickling composition therefrom.
  • the corrosion rate of a magnesium or magnesiumbase alloy article is commonly measured by "a standard alternate brine immersion and air exposure test and, therefore, such test is applicable for determining the effectiveness of pickling compositions and methods.
  • a test was employed to ascertain corrosion rates of magnesium or magnesium-base alloys when treated according to the invention and when not so treated for purposes of comparison.
  • the test employed herein is designated A.S.T.M. B192.44T as described in American Society for Testing Materials Standards, 1958, page 243.
  • the test broadly consists of alternately immersing a previously weighed magnesium article in a sodium chloride brine and exposing it to the air at fixed intervals for a specified testing period at a temperature of 80 F.
  • the sodium chloride brine was a 3 percent by weight solution.
  • each immersion period is 0.5 minute and produce a from 3 to 10 minutes at from to 200 F. to remove oil, grease, and other organic substances therefrom.
  • a common aqueous alkaline cleaner employed is one prepared by dissolving 3 ounces of Na CO -l0H O and 2 ounces of NaOH in sufl'icient Thereafter the magnesium article is subjected to the action of the pickle bath in accordance with the method of the invention.
  • Convenient size magnesium alloy sheet panels of between 0.05 and 0.06 inch thick were deg-reased by immersion in an alkaline degreasing bath for about 5 minutes at about F., removed therefrom, and rinsed.
  • Solutions of aqueous sulfuric acid were prepared having a normality of either 25 or 23. Pickle baths were then prepared by admixing with portions of such normality sulfuric acid, sufficient weights of a nitrate ion-, chloride ion, or iodide ion-yielding compound, to provide the desired weight of N0 C1, or I fraction thereof per liter of the aqueous sulfuric acid solutions.
  • the degreased panels were then immersed in the pickling bath thus prepared and agitated moderately therein until 0.5 mil thickness of metal had been removed per side of the panel being pickled.
  • the thus treated panels were then removed, water-rinsed promptly, and air-dried.
  • the articles treated were composed of either an extensively-used magnesiumexamples are illustrative :of the practice the normality of the H 80 solution and the grams of N0 C1, or I present per liter of H 80 solution, and the compounds added to yield the N0 Cl, or I ions.
  • Table II also sets out the temperature of the bath, the length of immersion, and the corrosion rate as determined by subjecting 'both unpickled panels and panels pickled according to the invention to A.S.T.M. test Bl92-44T.
  • Each of the magnesium alloy panels tested showed a very bright lustrous surface after treatment in accordance with the invention whereas those not treated had a dull tarnished surface due to unremoved contaminants thereon.
  • the practice of the invention offers a number of advantages heretofore not attained by the employment of known methods of pickling magnesiumbase alloy articles. It has been noted particularly that the zinc content does not result in a discolored surface after pickling. It is also to be noted that the Zirconium-thorium magnesium-base alloy, which has a particularly high corrosion rate when it is not pickled, had 'a particularly low corrosion rate when pickled in accordance with the practice of the invention.
  • the advantages of the invention are the consistently and outstandingly good resistance to corrosion and bright finish obtained at room temperature at a relatively fast but easily controlled pickling rate accompanied by unusually low metal loss.
  • the method of pickling a magneslum article containing at least about 75 percent magnesium and not over 2 percent Zinc to remove contaminating tarnish and scale therefrom and to improve the corrosion resistance thereof which consists of subjecting the article to the action of an aqueous composition pickle composition consisting essentially of H 80 having an acid normality of at least but not over and having dissolved therein a compound selected from the class consisting of soluble nitrates, halides, oxyhalides, halogen-substituted organic acids, and mixtures thereof, capable of yielding nitrate and halogen-containing ions in solution, wherein the halogen is chlorine or iodine, in sufiicient amount to provide between 5 and 250 grams of the nitrate and halogen fractions of said compounds per liter of said aqueous composition.
  • ble nitrate ion-yielding compound is nitric acid.

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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)

Description

United States Patent 3,100,170 PICKLING MAGNESIUM AdRTICLES Donald Jack Levy, Olivette, Mm, assignor to The Dow Chemical Company, Midland, Mich, a corporation of Delaware No Drawing. Filed Jan. 4, 1960, Ser. No. 83
11 Claims.
The invention pertains to cleaning or pickling metal articles composed of at least about 75 percent magnesium, hereinafter sometimes referred to as magnesium articles.
Such magnesium articles, usually contain contaminants on the surface thereof which stimulate corrosion thereof following working, shaping, or fabrication. Corrosion of the surface contaminated magnesium articles manifests itself by the formation of a tarnish and/ or tenaciously adhering scale during storage and use at a rate which is deteriorating and destructive to the metal unless such contaminants are removed.
A number of attempts have been made to remove such contaminants and thereby lessen the corrosion of magnesium articles. Among such attempts are scalping away the contaminated outer layer and by subjecting the contaminated article to the action of a chemical composition usually consisting of dipping or otherwise applying the composition as an aqueous solution followed by water-rinsing, and usually, thereafter, by drying. The chemical treating solution, usually being acidic, is commonly called a pickle bath and the treatment therein, pickling. Pickling of magnesium articles has been successful to some extent to remove the contaminants from the surface of the article thus treated to lessen subsequent corrosion and is widely practiced. A number of pickling compositions have been employed in attempts to attain this purpose, some of which have been found useful to attain such contaminant removal from magnesium articles and provide improved resistance against corrosion to magnesium articles. There are nevertheless one or more difficulties attendant upon the use thereof. Among such difliculties are: excessive attack of the composition on a magnesium article resulting in uneconomical loss of magnesium metal; relatively short life of the composition and/ or impracticality or impossibility of revivifying the composition periodically for continued use; the failure of the composition to remove adequately the contaminating tarnish and scale; the tendency of the composition to form on the treated magnesium article mottled or streaked blemishes often due to the presence of heavy metal com ounds such as those of iron, copper or zinc; expense or unavailability of the ingredients of the composition; and ineffectiveness in improving the corrosion resistance of the article so treated.
Relatively concentrated solutions of sulfuric acid, having a normality of at least about 20 N have recently been found to be especially effective for removing tarnish and scale from some magnesium-base alloy articles. However, when such articles are composed of certain magnesium-base alloys, and especially magnesium-base alloys containing over 0.5 percent Zinc, a black discoloration appears upon such sulfuric acid-treated magnesium-zinc articles. Since a large percent of magnesium-base alloys contain between 0.5 and 1.5 percent zinc, there is clearly a desideratum in the art of treating magnesium-base alloy articles to provide a method of treatment by which to obtain a bright surface thereon as well as impart thereto good resistance to corrosion when such articles contain more than 0.5 percent zinc.
I have now found that a bright lustrous surface having high corrosion resistance can be obtained by subjecting a magnesium-base alloy article containing not more than 2.0 percent zinc to the action of an aqueous composition 3,100,170 Patented Aug. 6, 1963 "ice 2 prepared by admixing with an aqueous sulfuric acid solution, of at least 20 N but not over 25 N, one or more of a halogen ionor nitrate ion-yielding compound wherein the halogen is chlorine or iodine. Illustrative of such compounds are: HNO a soluble nitrate salt, HCl, a soloble chloride salt, a soluble iodide salt, HI, an oxychloride salt, an oxyiodide salt, or a halogen-substituted ionizable organic compound such as monochloroacetic acid, for a time sufficient to remove the contaminants or scale therefrom, waterarinsing, and preferably drying the magnesium article so treated.
When aqueous sulfuric acid of less than 20 N is employed, in the practice of the invention, the reaction rate is undesirably fast and the extent of corrosion resistance imparted to the article is unsatisfactory even though an excessive amount of metal is removed from the magnesiarticle during treatment. When the acid normality is greater than 25 N, the reaction rate is undesirably slow and more of the halide ionor nitrate ion-yielding additament is required to attain satisfactory cleaning and corrosion protection.
In the practice of the invention the halide ionor nitrate ion-yielding compound is admixed with the sulfuric acid solution in an amount sufficient to yield a weight of between 5 and 250 grams of the (N0 or halogen fraction or portion of the compound per liter of the sulfuric acid-treating composition so made.
The practice of the invention is applicable to brightening and providing corrosion resistance to any magnesium or magnesium-base alloy article including those containing zinc alloyed therein up to 2 percent thereof. Articles thus treated are free from undesirable blotches or streaks which form on certain extensively used magnesium-base alloy articles when sulfuric acid alone is used. The composition containing any of the above named acids or salts as an adjuvant to sulfuric acid of the required normality for pickling magnesium articles exerts a minimum attack on the magnesium article being pickled and is relatively low in cost. The article so pickled shows a particularly high resistance to corrosion in relation to the depth of the layer of metal removed during pickling. The improved composition employed in the invention requires no sequestering or buffering agent as do most compositions presently employed in pickling magnesium-base alloys. Such sequestering or buffering agents are relatively expensive and sometimes prevent a satisfactory removal of the tarnish or scale during the pickling operation.
The preferred mode of treating the article to be cleaned and given protection against corrosion 'in accordance with the invention is to employ a bath of the aqueous acid or salt and sulfuric acid of a suitable normality and immerse the article to be treated therein. The temperature of the bath may be any temperature less than the boiling point thereof but it is preferred that it be between and F. The period of immersion of the article being treated in the bath depends upon the concentration and the temperature of the bath, the composition of magnesium alloy being treated, and the severity of tarnish or "scale on the article. Immersion in the bath should be sufiiciently long to provide the necessary corrosion re sistance desired. A minimum of 0.1 mil of metal should be removed per side and generally 0.2 to 0.3 mil is usually removed per side from the commercial coil-rolled magnesium alloy strip metal to remove, substantially, the surface contamination in accordance with the invention. Not only are there extensive material savings by removing a lesser amount of metal than heretofore has been commonly required, and the treating bath, therefore, less contaminated, but the bright lustrous surface attained on the metal is equally as good when only enough metal the period of exposure to air is 2 minutes. The duration of the test was 7 days. The thus treated article is cleaned,
Water, and thereafter reweighed and the metal loss calculated.
Table I below sets out pickling compositions illustrative of the practice of the invention wherein the recommend a nitrate, chloride, or iodide portion or fraction of a nitrate ion-, chloride ionor iodide ion-yielding compound is added to (the sulfuric acid solution having the normality shown.
Table I Minimum recommended weight of N01, OLtor I fraction of compound added in grams per 1i er Normality of H 280, Weight of N 03 added as- Weight of 01 added as- Weight of I added asa HNO; K01 H0104 MOA 1 NM I K103 NaNOg NH4NO3 HCl NaCl l Monocholoroacetic acid. nesium alloy preferentially to the metal itself and as one of the concomitant elfects thereof, it is unnecessary to undercut the contaminants to the extent necessary when employing known methods of cleaning, brightening, and providing protection against corrosion to magnesiumbase alloy articles.
When the magnesium article is removed from the treating bath lit has a liquid film of the bath adhering thereto. Best results are attained in the practice of the invention when the film of bath is water-rinsed oif shortly after such removal, e.g., within and preferably within 5 seconds. It is recommended that the water he applied during the rinsing operation generously to flush the adhering acid from the entire surface of the anticle rather rapidly. The temperature of the rinse water is unimportant, water at room temperature commonly being em ploycd. The article thus treated is preferably thereafter dried, as in a forced-air drier.
The pickling composition employed in the practice of the invention may be revivified conveniently as required. Periodic tests thereof show when the acid normality and/ or the concentration of the halide ion or nitrate ion concentration thereof require adjustment. Such adjustment is readily done by adding suflicient sulfuric acid and/or the thalide ionor nitrate ion-yielding material to bring the concentration thereof within the ranges thereof set out hercinabove. Since some magnesium sulfate and other salts are formed during the pickling operation in accordance with the invention, and such salts largely settle to the bottom of the bath as a precipitate, the bath may be separated therefrom by merely filtering, decanting, siphoning, or otherwise drawing oil the supernatant liquid pickling composition therefrom.
The corrosion rate of a magnesium or magnesiumbase alloy article is commonly measured by "a standard alternate brine immersion and air exposure test and, therefore, such test is applicable for determining the effectiveness of pickling compositions and methods. Such a test was employed to ascertain corrosion rates of magnesium or magnesium-base alloys when treated according to the invention and when not so treated for purposes of comparison. The test employed herein is designated A.S.T.M. B192.44T as described in American Society for Testing Materials Standards, 1958, page 243. The test broadly consists of alternately immersing a previously weighed magnesium article in a sodium chloride brine and exposing it to the air at fixed intervals for a specified testing period at a temperature of 80 F. The sodium chloride brine was a 3 percent by weight solution. The length of each immersion period is 0.5 minute and produce a from 3 to 10 minutes at from to 200 F. to remove oil, grease, and other organic substances therefrom. A common aqueous alkaline cleaner employed is one prepared by dissolving 3 ounces of Na CO -l0H O and 2 ounces of NaOH in sufl'icient Thereafter the magnesium article is subjected to the action of the pickle bath in accordance with the method of the invention.
The following of the invention:
Convenient size magnesium alloy sheet panels of between 0.05 and 0.06 inch thick were deg-reased by immersion in an alkaline degreasing bath for about 5 minutes at about F., removed therefrom, and rinsed. Solutions of aqueous sulfuric acid were prepared having a normality of either 25 or 23. Pickle baths were then prepared by admixing with portions of such normality sulfuric acid, sufficient weights of a nitrate ion-, chloride ion, or iodide ion-yielding compound, to provide the desired weight of N0 C1, or I fraction thereof per liter of the aqueous sulfuric acid solutions. The degreased panels were then immersed in the pickling bath thus prepared and agitated moderately therein until 0.5 mil thickness of metal had been removed per side of the panel being pickled. The thus treated panels were then removed, water-rinsed promptly, and air-dried. The articles treated were composed of either an extensively-used magnesiumexamples are illustrative :of the practice the normality of the H 80 solution and the grams of N0 C1, or I present per liter of H 80 solution, and the compounds added to yield the N0 Cl, or I ions. Table II also sets out the temperature of the bath, the length of immersion, and the corrosion rate as determined by subjecting 'both unpickled panels and panels pickled according to the invention to A.S.T.M. test Bl92-44T. Each of the magnesium alloy panels tested showed a very bright lustrous surface after treatment in accordance with the invention whereas those not treated had a dull tarnished surface due to unremoved contaminants thereon.
T ble II Normality Grams of Magnesium alloy, percent by weight of H280; N
o 0.7 Zr, 3.0 Th, and balance Mg *Monoehloroacctic acid.
An examination of the results of Table the corrosion resistance of the magnesium panels treated according to the invention, wherein 0.5 mil thickness of metal was removed per side, had a corrosion rate which was markedly less than the corrosion rate of the panels which were not treated.
It is obvious that the practice of the invention offers a number of advantages heretofore not attained by the employment of known methods of pickling magnesiumbase alloy articles. It has been noted particularly that the zinc content does not result in a discolored surface after pickling. It is also to be noted that the Zirconium-thorium magnesium-base alloy, which has a particularly high corrosion rate when it is not pickled, had 'a particularly low corrosion rate when pickled in accordance with the practice of the invention. Among the advantages of the invention are the consistently and outstandingly good resistance to corrosion and bright finish obtained at room temperature at a relatively fast but easily controlled pickling rate accompanied by unusually low metal loss.
Having described the invention, what is claimed and desired to be protected by Letters Patent is:
l. The method of pickling a magneslum article containing at least about 75 percent magnesium and not over 2 percent Zinc to remove contaminating tarnish and scale therefrom and to improve the corrosion resistance thereof which consists of subjecting the article to the action of an aqueous composition pickle composition consisting essentially of H 80 having an acid normality of at least but not over and having dissolved therein a compound selected from the class consisting of soluble nitrates, halides, oxyhalides, halogen-substituted organic acids, and mixtures thereof, capable of yielding nitrate and halogen-containing ions in solution, wherein the halogen is chlorine or iodine, in sufiicient amount to provide between 5 and 250 grams of the nitrate and halogen fractions of said compounds per liter of said aqueous composition.
2. The method according to claim 1 wherein the length II shows that solution ions present] liter of the immersion of said article in said aqueous pickle composition is between 0.1 and 90 minutes.
3. The method according to claim 1 wherein the article being pickled is immersed in the aqueous pickle composition for a time sufficient to remove substantially all foreign contaminating materials from the surface thereof, removed therefrom, and water-rinsed.
4. The method according to claim 3 wherein the magnesium alloy article being treated is immersed in the aqueous pickle composition for a time suflicient to remove metal to a depth of at least 0.1 mil per side.
5. The method according to claim 3 wherein the magnesium metal article being treated is water-rinsed within 15' seconds after its removal from the aqueous pickle composition.
6. The method according to claim 3 wherein the aqueous pickle composition and the magnesium alloy article immersed therein are maintained in motion relative to each other.
7. The method according to claim 3 wherein the temperature of the aqueous pickle bath is between about F. and 300 F.
8. The method according to claim 3 wherein the soluble halogen-containing ion is chlorine.
9. The method according to claim 3 wherein the soluble halogen-containing ion is iodine.
10. The method according to claim 3 wherein ble nitrate ion-yielding compound is nitric acid.
11. The method according to claim 3 wherein the soluble nitrate ion-yielding compound is a nitrate salt.
References Cited in the file of this patent UNITED STATES PATENTS the solu- 1,918,545 Hoy July 18, 1933 2,287,050 Miller June 23, 1942 2,411,532 Escoffery Nov. 26, 1946 2,511,988 Myers et al June 20, 1950 I 2,574,049 Mayhew Nov. 6, 1951 2,751,342 Guggenberger June 19, 1956 2,762,728 Hahn Sept. 11, 1956 2,864,730 Kinder et a1 Dec. 16, 1958 2,894,883 Walker et a1. July 14, 1959 2,967,136 Cybriwsky et a1. Ian. 3, 1961

Claims (1)

1. THE METHOD OF PICKLING A MAGNESIUM ARTICLE CONTAINING AT LEAST ABOUT 75 PERCENT MAGNESIUM AND NOT OVER 2 PERCENT ZINC TO REMOVE CONTAMINATING TARNISH AND SCALE THEREFROM AND TO IMPROVE THE CORROSION RESISTANCE THEREOF WHICH CONSISTS OF SUBJECTING THE ARTICLE TO THE ACTION OF AN AQUEOUS COMPOSITION PICKLE COMPOSITION CONSISTING ESSENTIALLY OF H2SO4 HAVING AN ACID NORMALITY OF AT LEAST 20 BUT NOT OVER 25 AND HAVING DISSOLVED THEREIN A COMPOUND SELECTED FROM THE CLASS CONSISTING OF SOLUBLE NITRATES, HALIDES, OXYHALIDES, HALOGEN-SUBDTITUTED ORGANIC ACIDS, AND MIXTURES THEREOF CAPABLE OF YIELDING NITRATE AND HALOGEN-CONTAINING IONS IN SOLUTION, WHEREIN THE HALOGEN IS CHLORINE OR IODINE, IN SUFFICIENT AMOUNT TO PROVIDE BETWEEN 5 AND 250 GRAMS OF THE NITRATE AND HALOGEN FRACTIONS OF SAID COMPOUNDS PER LITER OF SAID AQUEOUS COMPOSITION.
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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3322673A (en) * 1964-04-01 1967-05-30 Macdermid Inc Composition for and method of dissolving copper and copper alloys by chemical action
US3399143A (en) * 1967-08-02 1968-08-27 Macdermid Inc Method of stripping nickel from articles and the composition used therein
US3654001A (en) * 1968-06-25 1972-04-04 North American Rockwell Process for etching beryllium
US3726930A (en) * 1970-10-29 1973-04-10 United States Borax Chem Preparation of 3,5-dinitrobenzotrifluoride compounds

Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1918545A (en) * 1930-06-03 1933-07-18 Dow Chemical Co Method of fabricating metal parts of magnesium or magnesium alloys
US2287050A (en) * 1942-06-23 mummert
US2411532A (en) * 1945-02-16 1946-11-26 Standard Telephones Cables Ltd Method of roughening steel
US2511988A (en) * 1945-05-09 1950-06-20 Columbia Steel Company Pickling process
US2574049A (en) * 1948-11-12 1951-11-06 Nat Steel Corp Pickling
US2751342A (en) * 1953-05-12 1956-06-19 Fromson Orban Co Inc Polishing of aluminum and aluminum base alloys
US2762728A (en) * 1953-10-02 1956-09-11 Lyon Inc Steel pickling process
US2864730A (en) * 1953-12-17 1958-12-16 Allied Res Products Inc Method for protecting magnesium and magnesium alloys from corrosion
US2894883A (en) * 1949-07-18 1959-07-14 David E Walker Method of electropolishing uranium
US2967136A (en) * 1954-03-01 1961-01-03 Reynolds Metals Co Chemical brightening and electrolytic polishing of aluminum

Patent Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2287050A (en) * 1942-06-23 mummert
US1918545A (en) * 1930-06-03 1933-07-18 Dow Chemical Co Method of fabricating metal parts of magnesium or magnesium alloys
US2411532A (en) * 1945-02-16 1946-11-26 Standard Telephones Cables Ltd Method of roughening steel
US2511988A (en) * 1945-05-09 1950-06-20 Columbia Steel Company Pickling process
US2574049A (en) * 1948-11-12 1951-11-06 Nat Steel Corp Pickling
US2894883A (en) * 1949-07-18 1959-07-14 David E Walker Method of electropolishing uranium
US2751342A (en) * 1953-05-12 1956-06-19 Fromson Orban Co Inc Polishing of aluminum and aluminum base alloys
US2762728A (en) * 1953-10-02 1956-09-11 Lyon Inc Steel pickling process
US2864730A (en) * 1953-12-17 1958-12-16 Allied Res Products Inc Method for protecting magnesium and magnesium alloys from corrosion
US2967136A (en) * 1954-03-01 1961-01-03 Reynolds Metals Co Chemical brightening and electrolytic polishing of aluminum

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3322673A (en) * 1964-04-01 1967-05-30 Macdermid Inc Composition for and method of dissolving copper and copper alloys by chemical action
US3399143A (en) * 1967-08-02 1968-08-27 Macdermid Inc Method of stripping nickel from articles and the composition used therein
US3654001A (en) * 1968-06-25 1972-04-04 North American Rockwell Process for etching beryllium
US3726930A (en) * 1970-10-29 1973-04-10 United States Borax Chem Preparation of 3,5-dinitrobenzotrifluoride compounds

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