US3072516A - Solution and method for brightening cadmium - Google Patents

Solution and method for brightening cadmium Download PDF

Info

Publication number
US3072516A
US3072516A US97164A US9716461A US3072516A US 3072516 A US3072516 A US 3072516A US 97164 A US97164 A US 97164A US 9716461 A US9716461 A US 9716461A US 3072516 A US3072516 A US 3072516A
Authority
US
United States
Prior art keywords
cadmium
per liter
ions
bath
brightening
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
Application number
US97164A
Inventor
Kenneth P Bellinger
Eugene G Chapdelaine
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Conversion Chemical Corp
Original Assignee
Conversion Chemical Corp
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Priority to US26130D priority Critical patent/USRE26130E/en
Application filed by Conversion Chemical Corp filed Critical Conversion Chemical Corp
Priority to US97164A priority patent/US3072516A/en
Priority to GB6904/62A priority patent/GB952255A/en
Priority to DEC26543A priority patent/DE1207182B/en
Priority to FR909316A priority patent/FR1333493A/en
Application granted granted Critical
Publication of US3072516A publication Critical patent/US3072516A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

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
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C22/00Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
    • C23C22/05Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions
    • C23C22/06Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using aqueous acidic solutions with pH less than 6
    • C23C22/34Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using aqueous acidic solutions with pH less than 6 containing fluorides or complex fluorides
    • 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
    • C23FNON-MECHANICAL REMOVAL OF METALLIC MATERIAL FROM SURFACE; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL; MULTI-STEP PROCESSES FOR SURFACE TREATMENT OF METALLIC MATERIAL INVOLVING AT LEAST ONE PROCESS PROVIDED FOR IN CLASS C23 AND AT LEAST ONE PROCESS COVERED BY SUBCLASS C21D OR C22F OR CLASS C25
    • C23F3/00Brightening metals by chemical means
    • C23F3/04Heavy metals
    • C23F3/06Heavy metals with acidic solutions
    • 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
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C2222/00Aspects relating to chemical surface treatment of metallic material by reaction of the surface with a reactive medium
    • C23C2222/10Use of solutions containing trivalent chromium but free of hexavalent chromium

Definitions

  • the present invention relates to a novel solution and method for the chemical brightening of cadmium surfaces.
  • cadmium surfaces refers to the surfaces of cadmium and cadmium base alloy articles and other metallic articles having a coating of cadmium such as produced by electroplating.
  • -It is an aim of the present invention to provide a method for the brightening of cadmium surfaces which is rapid and relatively non-critical so as to enable greater uniformity of operation and appearance.
  • Another aim is to provide a method for brightening cadmium surfaces wherein the rinsing of the workpiece subsequent to the action of the brightening bath is relatively non-critical so as to provide attractive, uniformly brightened workpieces with minimal rejection.
  • a further aim is to provide an easily transported and handled dry powder composition for addition to an aqueous acid bath in relatively small amounts for the production of a dilute cadmium brightening solution to attain the foregoing aims.
  • the foregoing and related aims can be obtained by a method in which the cadmium workpieces are immersed in an acid bath consisting essentially of dilute aqueous solution of trivalent chromium ions, nirtate ions, and ions selected from the group consisting of fluoride, sulfate, and combinations thereof.
  • the pH of the bath should be maintained between about 10-35, and preferably in the range of 1.5-2.0 for short dips of up to 10 seconds, and in the range of 1.8-3.5 for dips up to one minute or longer.
  • Hexavalent chromium ions have been found to produce a dulling effect upon the cadmium surfaces so that the presence of hexavalent chromium is to be avoided.
  • a concentration of as little as 0.02 gram per liter of hexavalent chromium constitutes the upper limit of tolerance, and a dulling surface effect is noticeable.
  • a greater concentration of hexavalent chromium can be tolerated, although the amount is still relatively small and less than 0.3 gram per liter.
  • the bath itself is non-oxidizing with respect to the trivalent chromium so that only impurities in the components or impurities carried into the bath upon the workpieces need be considered.
  • the baths of the present invention are thus essentially characterized as substantially free from hexavalent chromium ions.
  • the bath should contain trivalent chromium ions in the range of 0.08-l.0 gram per liter, nitrate ions in the range of about 0.l-l8.0 grams per liter, and ions selected from the group consisting of fluoride, sulfate, and the combination thereof, in the range of 0.4-5.2 grams per liter.
  • the preferred solutions in accordance with the present invention contain both sulfate and fluoride ions since 'of any unessential ions.
  • the fluoride ion concentration in such solutions should be about one-third that of the sulfate ion and be in the range of about 0.1-1.2 grams per liter, and the. sulfate ion concentration about 0.25-4.0 grams per liter.
  • the bath of the present invention is preferably utilized at ambient temperatures on the order of 60-90 F. for optimum operation. However, elevated temperatures of 45-150 F. may be employed depending upon the concentration of the bath and the time of treatment. Generally, the more dilute the bath, the higher the temperature that may be employed so as to provide a satisfactory treatment time and brightening action.
  • the time of treatment will vary with the temperature, pH and concentration of the bath. Generally, the period of immersion will vary between about 2 seconds and 10 minutes depending upon these three factors. The optimum time of treatment for a given bath concentration, temperature and pH is best determined by visual observation of a specimen workpiece. Generally, the preferred baths of the presentinvention operated at am-v bient temperatures require an immersion period of only about 5-45 seconds.
  • the cadmium workpieces are rinsed in cold water and then rinsed in hot water for drying.
  • the preferred baths of the present invention are those containing about 0.2-0.3 gram per liter of trivalent chromium ions, 3.75-5.0 grams per liter of nitrate ions, 0.2-0.4 gram per liter of fluoride ions and 0.75-1.5 grams per liter of sulfate ions, the bath having a pH of about 1.5-2.0 and being substantially free from hexavalent chromium ions. Additionally, 0.5-1.0 gram per liter of zinc or cadmium ions is desirable for control and optimum brightening action during initial use. Such a bath composition produces a highly desirable luster and mild protection upon the cadmium surface at ambient temperatures in 5-45 seconds immersion.
  • the bath is prepared by addition to water of nitric acid and suitable salts of the various other ions.
  • suitable salts of the various other ions As can readily be appreciated, the introduction of unnecessary ions is desirably avoided since interference may be provided thereby.
  • Complex fluoride salts can also be employed such as the fluoroborates and fluosilicates.
  • a specific dry powder composition which is readily transported and utilized for the production of cadmium brightening baths of the present invention is one containing the following salts in the indicated proportions;
  • This composition is then best utilized by an admixture of 1-4 pounds of the above, .100 gallons of water Patented Jan. 8, 1963 3 and 0.1-4.0 quarts of 42 Baum nitric acid, and prefera'bly 1.0-3.0 quarts of nitric acid for a bath requiring a relatively short immersion time of about 5 to seconds.
  • suitable tanks should be employed to avoid contamination such as rigid polyvinyl chloride, steel lined with polyvinyl chloride or resinbonded glass fibers or polyethylene.
  • the bath will have to be replenished by the addition of the several components as the contentration is reduced by carry-out and reaction. This can generally be determined by visual observation of lesser brightening of the workpieces. Generally, addition of one-half the original make-up amounts is conveniently employed when such visual reduction is observed.
  • the bath can be titrated with 1 N sodium hydroxide using phenolphthalein as an indicator. For example, when using the formulation set forth with respect to the dry powder composition, the following test is conveniently employed. For a 100 cc. sample, 10 cc. sodium hydroxide is required for optimum bath concentration.
  • Example 1 A cadmium brightening bath was prepared by adding to water 42 Baum nitric acid and a dry powder mix containing 7.12 percent by weight sodium acid fluoride, 21.25 percent by weight chromium fluoride, and 71.63 percent by weight zinc sulfate. The nitric acid and dry powder mix were added in a ratio of two quarts and two pounds, respectively, per 100 gallons of water. The resulting bath had a pH of about 1.8 and was maintained at a temperature of about 75 F.
  • Test panels of steel plated with cadmium to a thickness of about 0.0002 inch and measuring 1 /2 inches by 1% inches were immersed in the bath for ten seconds, rinsed in cold water for three seconds, rinsed in hot water (180 F.) for three seconds and air dried.
  • the treated panels were observed to have a lustrous finish of uniform brightness and were observed to be much brighter than an untreated control panel specimen.
  • specimens were subjected to a humidity test in which they were exposed to 100 percent humidity at a temperature of 100 F. for forty-eight hours. At the end of this exposure, there was no evidence of spotting out or formation of dark blemishes, which is indicative of the mild protection afforded by the treatment of the present invention.
  • Example 2 A bath was prepared in accordance with Example 1 and maintained at a temperature of about 80 F. Test specimens similar to those employed in Example 1 were immersed in the bath for about eight seconds, rinsed in cold water, rinsed in hot water and air dried. The resultant panels had a uniform luster much brighter than an untreated control panel.
  • One of the tests utilized in the industry to evaluate protection is that of placing a drop of 1.0 percent by weight lead acetate solution on the treated part and determining the time in which the spot turns black. An untreated specimen will turn black immediately. When the treated panels were tested, the spot turned grey in about fi e t ten seconds and continued darkening until completely black at the end of about fifty to sixty seconds. The treatment is thus seen to have provided mild protection for the cadmium surface in addition to high brightness.
  • An acid bath for the brightening of cadmium surfaces comprising a dilute aqueous solution containing essentially 0.08-1.0 gram per liter of trivalent chromium ions, 0.1-18.0 grams per liter of nitrate ions and 0.4-5.2 grams per liter of ions selected from the group consisting of fluoride, sulfate and the combination thereof, said solution having a pH of about 1.0-3.5 and containing less than about 0.3 gram per liter of hexavalent chromium 2.
  • the bath in accordance with claim 1 containing 0.25-4.0 grams per liter of sulfate ion and 0.1-1.2 grams per liter of fluoride ion, with the fluoride ion being about one-third the concentration of the sulfate ion.
  • An acid bath for the brightening of cadmium surfaces and providing a mild protection therefor comprising a dilute aqueous solution containing essentially 0.2-0.3 gram per liter of trivalent chromium ions, 375-5 .0 grams per liter of nitrate ions, 0.2-0.4 gram per liter of fluoride ions, 0.75-1.5 grams per liter of sulfate ions and 0.5-1.0 gram per liter of ions selected from the group consisting of zinc, cadmium and the combination thereof, said solution having a pH of about 1.5-2.0 and containing less than about 0.02 gram per liter of hexavalent chromium ions.
  • chromium fluoride 20-22 percent by weight chromium fluoride, and 70-72 percent by weight of the sulfate salt of a metal selected from the group consisting of Zinc and cadmium.
  • the method of brightening cadmium surfaces comprisingproviding a dilute aqueous solution containing essentially 0.08-1.0 gram per liter of trivalent chromium ions, 0.1-18.0 grams per liter of nitrate ions and 0.4-5.2 grams per liter of ions selected from the group consisting of fluoride, sulfate, and the combination thereof, said solution having a pH of about 1.0-3.5 and containing less than about 0.3 gram per liter of hexavalent chromium ions; maintaining said solution at a temperature of about 45-150 F.; immersing a cadmium workpiece in said solution for a period of time suflicient to brighten the surface thereof; and rinsing said workpiece in cold water.
  • the method of brightening cadmium surfaces comprising providing a dilute aqueous solution containing essentially 0.2-0.3 gram per liter of trivalent chromium ions, 3.75-5 .0 grams per liter of nitrate ions, 0.1-0.4 gram per liter of fluoride ions, 0.75-1.5 grams per liter of sulfate ions and 0.5-1.0 gram per liter of ions selected from the group consisting of zinc, cadmium, and the combination thereof, said solution having a pH of about 1.5-2.0 and containing less than about 0.02 gram per liter of hexavalent chromium ions; maintaining said solution at ambient temperature; immersing a cadmium workpiece in said solution for a period of about 5-45 seconds sufficient to brighten the surface thereof; and rinsing said workpiece in cold water.

Landscapes

  • 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)
  • Chemical Treatment Of Metals (AREA)

Description

United States Patent Ofilice 3,072,516 SOLUTION AND METHDD FOR BRIGHTENING CADMIUM Kenneth P. Bellinger, Ellington, and Eugene G. Chapdelaine, Hazardville, Comm, assignors to Conversion Chemical Corporation, Rockville, Conn., a corporation or Connecticut No Drawing. Filed Mar. 21, 1961, Ser. No. 97,164
., 6 Claims. (Cl. 15620) The present invention relates to a novel solution and method for the chemical brightening of cadmium surfaces. 1
The term cadmium surfaces as used herein refers to the surfaces of cadmium and cadmium base alloy articles and other metallic articles having a coating of cadmium such as produced by electroplating.
-It is an aim of the present invention to provide a method for the brightening of cadmium surfaces which is rapid and relatively non-critical so as to enable greater uniformity of operation and appearance.
It is also an aim of the present invention to provide a method for brightening cadmium surfaces by a simple and inexpensive one-step treatment which further provides mild corrosion and tarnish protection for the cadmium surface.
. Another aim is to provide a method for brightening cadmium surfaces wherein the rinsing of the workpiece subsequent to the action of the brightening bath is relatively non-critical so as to provide attractive, uniformly brightened workpieces with minimal rejection.
A further aim is to provide an easily transported and handled dry powder composition for addition to an aqueous acid bath in relatively small amounts for the production of a dilute cadmium brightening solution to attain the foregoing aims Other advantages will be readily apparent from the following detailed specification and claims.
It has now been found that the foregoing and related aims can be obtained by a method in which the cadmium workpieces are immersed in an acid bath consisting essentially of dilute aqueous solution of trivalent chromium ions, nirtate ions, and ions selected from the group consisting of fluoride, sulfate, and combinations thereof. The pH of the bath should be maintained between about 10-35, and preferably in the range of 1.5-2.0 for short dips of up to 10 seconds, and in the range of 1.8-3.5 for dips up to one minute or longer.
Hexavalent chromium ions have been found to produce a dulling effect upon the cadmium surfaces so that the presence of hexavalent chromium is to be avoided. In baths having a pH of about 1.0-2.0, a concentration of as little as 0.02 gram per liter of hexavalent chromium constitutes the upper limit of tolerance, and a dulling surface effect is noticeable. With baths of higher pH on the order of 2.0-3.5, a greater concentration of hexavalent chromium can be tolerated, although the amount is still relatively small and less than 0.3 gram per liter. The bath itself is non-oxidizing with respect to the trivalent chromium so that only impurities in the components or impurities carried into the bath upon the workpieces need be considered. The baths of the present invention are thus essentially characterized as substantially free from hexavalent chromium ions.
Generally, the bath should contain trivalent chromium ions in the range of 0.08-l.0 gram per liter, nitrate ions in the range of about 0.l-l8.0 grams per liter, and ions selected from the group consisting of fluoride, sulfate, and the combination thereof, in the range of 0.4-5.2 grams per liter.
The preferred solutions in accordance with the present invention contain both sulfate and fluoride ions since 'of any unessential ions.
solutions containing both ions have been found to pro. vide the cadmium surface with an appreciable degree. of protection to corrosion by fume and moisture. Generally, the fluoride ion concentration in such solutions should be about one-third that of the sulfate ion and be in the range of about 0.1-1.2 grams per liter, and the. sulfate ion concentration about 0.25-4.0 grams per liter.
The initial presence of zinc and/or cadmium ions in the bath has also been found desirable in controlling the action of the bath upon the cadmium surface and in providing uniform brightness. These metallic ions are preferably added as the sulfate salt so as to provide the desired pH by the nitric acid and limit the introduction Generally, when such ions are to be incorporated, they should be presented in the amount of about 0.1-3.0 grams per liter.
The bath of the present invention is preferably utilized at ambient temperatures on the order of 60-90 F. for optimum operation. However, elevated temperatures of 45-150 F. may be employed depending upon the concentration of the bath and the time of treatment. Generally, the more dilute the bath, the higher the temperature that may be employed so as to provide a satisfactory treatment time and brightening action.
The time of treatment will vary with the temperature, pH and concentration of the bath. Generally, the period of immersion will vary between about 2 seconds and 10 minutes depending upon these three factors. The optimum time of treatment for a given bath concentration, temperature and pH is best determined by visual observation of a specimen workpiece. Generally, the preferred baths of the presentinvention operated at am-v bient temperatures require an immersion period of only about 5-45 seconds.
Subsequent to immersion in the bath of the present invention, the cadmium workpieces are rinsed in cold water and then rinsed in hot water for drying.
The preferred baths of the present invention are those containing about 0.2-0.3 gram per liter of trivalent chromium ions, 3.75-5.0 grams per liter of nitrate ions, 0.2-0.4 gram per liter of fluoride ions and 0.75-1.5 grams per liter of sulfate ions, the bath having a pH of about 1.5-2.0 and being substantially free from hexavalent chromium ions. Additionally, 0.5-1.0 gram per liter of zinc or cadmium ions is desirable for control and optimum brightening action during initial use. Such a bath composition produces a highly desirable luster and mild protection upon the cadmium surface at ambient temperatures in 5-45 seconds immersion.
Generally, the bath is prepared by addition to water of nitric acid and suitable salts of the various other ions. As can readily be appreciated, the introduction of unnecessary ions is desirably avoided since interference may be provided thereby. Thus, it has been found that the use of a dry powder composition containing chromium fluoride, sodium acid fluoride, and zinc or cadmium sulfate has been economical for the consumer while providing highly desirable results and enabling easy ships ment. Complex fluoride salts can also be employed such as the fluoroborates and fluosilicates.
A specific dry powder composition which is readily transported and utilized for the production of cadmium brightening baths of the present invention is one containing the following salts in the indicated proportions;
Percent by weight This composition is then best utilized by an admixture of 1-4 pounds of the above, .100 gallons of water Patented Jan. 8, 1963 3 and 0.1-4.0 quarts of 42 Baum nitric acid, and prefera'bly 1.0-3.0 quarts of nitric acid for a bath requiring a relatively short immersion time of about 5 to seconds.
Because of the acidity and corrosive nature of the baths of the present invention, suitable tanks should be employed to avoid contamination such as rigid polyvinyl chloride, steel lined with polyvinyl chloride or resinbonded glass fibers or polyethylene.
From time to time, the bath will have to be replenished by the addition of the several components as the contentration is reduced by carry-out and reaction. This can generally be determined by visual observation of lesser brightening of the workpieces. Generally, addition of one-half the original make-up amounts is conveniently employed when such visual reduction is observed. Analytically, the bath can be titrated with 1 N sodium hydroxide using phenolphthalein as an indicator. For example, when using the formulation set forth with respect to the dry powder composition, the following test is conveniently employed. For a 100 cc. sample, 10 cc. sodium hydroxide is required for optimum bath concentration. For every cubic centimeter of sodium hydroxide less than 10 cc., 3% ounces of the dry powder composition and 6 /1 fluid ounces of 42 Baurn nitric acid are added per 100 gallons of bath. Of course, the pH should be maintained within the described limits during operation.
Indicative of the efiicacy of the present invention are the following specific examples wherein cadmium-plated workpieces were treated.
Example 1 A cadmium brightening bath was prepared by adding to water 42 Baum nitric acid and a dry powder mix containing 7.12 percent by weight sodium acid fluoride, 21.25 percent by weight chromium fluoride, and 71.63 percent by weight zinc sulfate. The nitric acid and dry powder mix were added in a ratio of two quarts and two pounds, respectively, per 100 gallons of water. The resulting bath had a pH of about 1.8 and was maintained at a temperature of about 75 F.
Test panels of steel plated with cadmium to a thickness of about 0.0002 inch and measuring 1 /2 inches by 1% inches were immersed in the bath for ten seconds, rinsed in cold water for three seconds, rinsed in hot water (180 F.) for three seconds and air dried. The treated panels were observed to have a lustrous finish of uniform brightness and were observed to be much brighter than an untreated control panel specimen.
To measure the protection afforded by the treatment, specimens were subjected to a humidity test in which they were exposed to 100 percent humidity at a temperature of 100 F. for forty-eight hours. At the end of this exposure, there was no evidence of spotting out or formation of dark blemishes, which is indicative of the mild protection afforded by the treatment of the present invention.
Example 2 A bath was prepared in accordance with Example 1 and maintained at a temperature of about 80 F. Test specimens similar to those employed in Example 1 were immersed in the bath for about eight seconds, rinsed in cold water, rinsed in hot water and air dried. The resultant panels had a uniform luster much brighter than an untreated control panel.
One of the tests utilized in the industry to evaluate protection is that of placing a drop of 1.0 percent by weight lead acetate solution on the treated part and determining the time in which the spot turns black. An untreated specimen will turn black immediately. When the treated panels were tested, the spot turned grey in about fi e t ten seconds and continued darkening until completely black at the end of about fifty to sixty seconds. The treatment is thus seen to have provided mild protection for the cadmium surface in addition to high brightness.
We claim:
1. An acid bath for the brightening of cadmium surfaces comprising a dilute aqueous solution containing essentially 0.08-1.0 gram per liter of trivalent chromium ions, 0.1-18.0 grams per liter of nitrate ions and 0.4-5.2 grams per liter of ions selected from the group consisting of fluoride, sulfate and the combination thereof, said solution having a pH of about 1.0-3.5 and containing less than about 0.3 gram per liter of hexavalent chromium 2. The bath in accordance with claim 1 containing 0.25-4.0 grams per liter of sulfate ion and 0.1-1.2 grams per liter of fluoride ion, with the fluoride ion being about one-third the concentration of the sulfate ion.
3. An acid bath for the brightening of cadmium surfaces and providing a mild protection therefor comprising a dilute aqueous solution containing essentially 0.2-0.3 gram per liter of trivalent chromium ions, 375-5 .0 grams per liter of nitrate ions, 0.2-0.4 gram per liter of fluoride ions, 0.75-1.5 grams per liter of sulfate ions and 0.5-1.0 gram per liter of ions selected from the group consisting of zinc, cadmium and the combination thereof, said solution having a pH of about 1.5-2.0 and containing less than about 0.02 gram per liter of hexavalent chromium ions.
4. As a dry powder additive for dilute solutions of nitric acid to provide an acid bath for the brightening of cadmium surfaces, a mixture containing essentially about 6-8 percent by weight of sodium acid fluoride,
20-22 percent by weight chromium fluoride, and 70-72 percent by weight of the sulfate salt of a metal selected from the group consisting of Zinc and cadmium.
5. The method of brightening cadmium surfaces comprisingproviding a dilute aqueous solution containing essentially 0.08-1.0 gram per liter of trivalent chromium ions, 0.1-18.0 grams per liter of nitrate ions and 0.4-5.2 grams per liter of ions selected from the group consisting of fluoride, sulfate, and the combination thereof, said solution having a pH of about 1.0-3.5 and containing less than about 0.3 gram per liter of hexavalent chromium ions; maintaining said solution at a temperature of about 45-150 F.; immersing a cadmium workpiece in said solution for a period of time suflicient to brighten the surface thereof; and rinsing said workpiece in cold water.
6. The method of brightening cadmium surfaces comprising providing a dilute aqueous solution containing essentially 0.2-0.3 gram per liter of trivalent chromium ions, 3.75-5 .0 grams per liter of nitrate ions, 0.1-0.4 gram per liter of fluoride ions, 0.75-1.5 grams per liter of sulfate ions and 0.5-1.0 gram per liter of ions selected from the group consisting of zinc, cadmium, and the combination thereof, said solution having a pH of about 1.5-2.0 and containing less than about 0.02 gram per liter of hexavalent chromium ions; maintaining said solution at ambient temperature; immersing a cadmium workpiece in said solution for a period of about 5-45 seconds sufficient to brighten the surface thereof; and rinsing said workpiece in cold water.
References Cited in the file of this patent UNITED STATES PATENTS 2,194,498 Dupernell et al. Mar. 26, 1940 2,904,413 Hampel Sept. 15, 1959 2,904,414 Ostrander et al Sept. 15, 1959 2,955,027 Newell et al. Oct. 4, 1960 FOREIGN PATENTS 481,183 Canada Feb. 19, 1952

Claims (1)

  1. 5. THE METHOD OF BRIGHTENING CADMIUM SURFACES COMPRISING PROVIDING A DILUTE AQUEOUS SOLUTION CONTAINING ESSENTIALLY 0.08-1.0 GRAM PER LITER OF TRIVALENT CHROMIUM IONS, 0.1-18.0 GRAMS PER LITER OF NITRATE IONS AND 0.4-5.2 GRAMS PER LITER OF IONS SELECTED FROM THE GROUP CONSISTING OF FLUORIDE, SULFATE, AND THE COMBINATION THEREOF, SAID SOLUTION HAVING A PH OF ABOUT 1.0-3.5 AND CONTAINING LESS THAN ABOUT 0.3 GRAM PER LITER OF HEXAVALENT CHROMIUM IONS; MAINTAINING SAID SOLUTION AT A TEMPERATURE OF ABOUT 45-150*F., IMMERSING A CADMIUM WORKPIECE IN SAID SOLUTION FOR A PERIODD OF TIME SUFFICIENT TO BRIGHTEN THE SURFACE THEREOF; AND RINSING SAID WORKPIECE IN COLD WATER.
US97164A 1961-03-21 1961-03-21 Solution and method for brightening cadmium Expired - Lifetime US3072516A (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
US26130D USRE26130E (en) 1961-03-21 Solution and method for brightening cadmium
US97164A US3072516A (en) 1961-03-21 1961-03-21 Solution and method for brightening cadmium
GB6904/62A GB952255A (en) 1961-03-21 1962-02-22 Solution and method for brightening cadmium
DEC26543A DE1207182B (en) 1961-03-21 1962-03-21 Bath and process for chemical glazing of cadmium surfaces
FR909316A FR1333493A (en) 1961-03-21 1962-09-13 Cadmium brightening process and solution used for this purpose

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US97164A US3072516A (en) 1961-03-21 1961-03-21 Solution and method for brightening cadmium

Publications (1)

Publication Number Publication Date
US3072516A true US3072516A (en) 1963-01-08

Family

ID=22261642

Family Applications (2)

Application Number Title Priority Date Filing Date
US26130D Expired USRE26130E (en) 1961-03-21 Solution and method for brightening cadmium
US97164A Expired - Lifetime US3072516A (en) 1961-03-21 1961-03-21 Solution and method for brightening cadmium

Family Applications Before (1)

Application Number Title Priority Date Filing Date
US26130D Expired USRE26130E (en) 1961-03-21 Solution and method for brightening cadmium

Country Status (3)

Country Link
US (2) US3072516A (en)
DE (1) DE1207182B (en)
GB (1) GB952255A (en)

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3171765A (en) * 1962-10-04 1965-03-02 Conversion Chem Corp Powder composition for bright dipping zinc and cadmium
US3171766A (en) * 1962-10-04 1965-03-02 Conversion Chem Corp Bright polishing of cadmium and zinc
US3171767A (en) * 1963-09-30 1965-03-02 Conversion Chem Corp Composition and method for brightening cadmium and zinc
US4002489A (en) * 1973-06-21 1977-01-11 Nyby Bruk Ab Method of pickling metallic material
US6287704B1 (en) 1996-04-19 2001-09-11 Surtec Produkte Und System Fur Die Oberflachenbehandlung Gmbh Chromate-free conversion layer and process for producing the same
EP1318212A1 (en) * 2001-11-07 2003-06-11 Henkel Kommanditgesellschaft auf Aktien Agents and methods for the surface treatment of zinc-based coatings
US7314671B1 (en) 1996-04-19 2008-01-01 Surtec International Gmbh Chromium(VI)-free conversion layer and method for producing it
US20110070429A1 (en) * 2009-09-18 2011-03-24 Thomas H. Rochester Corrosion-resistant coating for active metals
US11230674B2 (en) 2019-09-23 2022-01-25 China University Of Petroleum-Beijing Integrated method and apparatus for catalytic cracking of heavy oil and production of syngas

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3423990A1 (en) * 1983-07-19 1985-01-31 Omi International Corp., Warren, Mich. PEROXIDE-FREE CHROME (III) PASSIVATION SOLUTION AND METHOD FOR PASSIVATING SUBSTRATES WITH THIS SOLUTION
JP4446230B2 (en) * 2003-12-09 2010-04-07 ディップソール株式会社 Trivalent chromate solution for aluminum or aluminum alloy and method for forming corrosion-resistant film on aluminum or aluminum alloy surface using the same

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2194498A (en) * 1936-10-26 1940-03-26 Udylite Corp Method of brightening metals electronegative to iron
CA481183A (en) * 1952-02-19 Aluminum Company Of America Surface treatment of magnesium and magnesium alloy articles
US2904414A (en) * 1954-08-04 1959-09-15 Allied Res Products Inc Formulation for producing a protective bright chemically polished surface on zinc and cadmium
US2904413A (en) * 1954-06-23 1959-09-15 Jervis Corp Process of bright dipping zinc base alloys
US2955027A (en) * 1957-08-07 1960-10-04 Isaac L Newell Method for the deburring of zinc-base die castings

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB357887A (en) * 1930-12-23 1931-10-01 Chester T Neal Method of treating cadmium plated goods

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA481183A (en) * 1952-02-19 Aluminum Company Of America Surface treatment of magnesium and magnesium alloy articles
US2194498A (en) * 1936-10-26 1940-03-26 Udylite Corp Method of brightening metals electronegative to iron
US2904413A (en) * 1954-06-23 1959-09-15 Jervis Corp Process of bright dipping zinc base alloys
US2904414A (en) * 1954-08-04 1959-09-15 Allied Res Products Inc Formulation for producing a protective bright chemically polished surface on zinc and cadmium
US2955027A (en) * 1957-08-07 1960-10-04 Isaac L Newell Method for the deburring of zinc-base die castings

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3171765A (en) * 1962-10-04 1965-03-02 Conversion Chem Corp Powder composition for bright dipping zinc and cadmium
US3171766A (en) * 1962-10-04 1965-03-02 Conversion Chem Corp Bright polishing of cadmium and zinc
US3171767A (en) * 1963-09-30 1965-03-02 Conversion Chem Corp Composition and method for brightening cadmium and zinc
US4002489A (en) * 1973-06-21 1977-01-11 Nyby Bruk Ab Method of pickling metallic material
US6287704B1 (en) 1996-04-19 2001-09-11 Surtec Produkte Und System Fur Die Oberflachenbehandlung Gmbh Chromate-free conversion layer and process for producing the same
US6946201B2 (en) 1996-04-19 2005-09-20 Surtec International Gmbh Chromium (VI)-free conversion layer and method for producing it
US7314671B1 (en) 1996-04-19 2008-01-01 Surtec International Gmbh Chromium(VI)-free conversion layer and method for producing it
EP1318212A1 (en) * 2001-11-07 2003-06-11 Henkel Kommanditgesellschaft auf Aktien Agents and methods for the surface treatment of zinc-based coatings
US20110070429A1 (en) * 2009-09-18 2011-03-24 Thomas H. Rochester Corrosion-resistant coating for active metals
US11230674B2 (en) 2019-09-23 2022-01-25 China University Of Petroleum-Beijing Integrated method and apparatus for catalytic cracking of heavy oil and production of syngas

Also Published As

Publication number Publication date
USRE26130E (en) 1966-12-27
DE1207182B (en) 1965-12-16
GB952255A (en) 1964-03-11

Similar Documents

Publication Publication Date Title
US2312855A (en) Method of coating aluminum
US2035380A (en) Method of coating zinc or cadmium base metals
US3919000A (en) Preanneal rinse process for inhibiting rust on steel strip
US2106904A (en) Coating malleable non-noble heavy metals
US3072516A (en) Solution and method for brightening cadmium
US2577887A (en) Activation of oxalate metal coating compositions
SE8006172L (en) PASSIVATION OF CHROME FREE OR LOW CHROME SURFACE
US3929514A (en) Composition and method for forming a protective coating on a zinc metal surface
US2976193A (en) Process and compositions for producing aluminum surface conversion coatings
US2904414A (en) Formulation for producing a protective bright chemically polished surface on zinc and cadmium
US4451304A (en) Method of improving the corrosion resistance of chemical conversion coated aluminum
US3843430A (en) Chromate-free bright dip for zinc and cadmium surfaces
US3032435A (en) Process for improving the corrosion resistance of pieces of light metals and light metal alloys
US4897129A (en) Corrosion resistant coating
US3895969A (en) Composition and process for inhibiting corrosion of non-ferrous metal surfaced articles and providing surface for synthetic resin coating compositions
US3171767A (en) Composition and method for brightening cadmium and zinc
US2502476A (en) Producing transparent protective films on zinc or cadmium
US4749417A (en) Corrosion resistant coating
US2431728A (en) Treatment of ferrous metals to improve resistance to rusting
US2314887A (en) Method of coating metal and material
US3090710A (en) Method and solution for producing chromate coatings on zinc and zinc alloys
US2617749A (en) Activation of oxalate metal coating compositions
US2514149A (en) Coating of metal surfaces
US3171765A (en) Powder composition for bright dipping zinc and cadmium
US3121033A (en) Composition and method for coating stainless metal articles