US2523190A - Electrodeposition of nickel from an acid bath - Google Patents

Electrodeposition of nickel from an acid bath Download PDF

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Publication number
US2523190A
US2523190A US603753A US60375345A US2523190A US 2523190 A US2523190 A US 2523190A US 603753 A US603753 A US 603753A US 60375345 A US60375345 A US 60375345A US 2523190 A US2523190 A US 2523190A
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US
United States
Prior art keywords
nickel
mixture
bath
acid
chloride
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
US603753A
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English (en)
Inventor
Brown Henry
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.)
Udylite Corp
Original Assignee
Udylite 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 FR955898D priority Critical patent/FR955898A/fr
Application filed by Udylite Corp filed Critical Udylite Corp
Priority to US603753A priority patent/US2523190A/en
Priority to GB13288/46A priority patent/GB611483A/en
Priority to US22489A priority patent/US2523191A/en
Application granted granted Critical
Publication of US2523190A publication Critical patent/US2523190A/en
Priority to DEU622A priority patent/DE845732C/de
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25DPROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
    • C25D3/00Electroplating: Baths therefor
    • C25D3/02Electroplating: Baths therefor from solutions
    • C25D3/12Electroplating: Baths therefor from solutions of nickel or cobalt

Definitions

  • This invention relates to the electrodepositlon of'nickel from aqueous acidic nickel baths.
  • the object of this invention is to decrease the grain size and increase the luster and brightncss of the nickel deposit without decreasing appreciably the ductility of the plate or the current density range of the nickel bath.
  • Table I are listed a number of alpha and beta unsaturated aliphatic sulfonic acids and their optimum concentrations in the nickel baths. Actually they all can be used up to saturation in the baths, that is, they do not have critical upper concentration limits.
  • Th brighteners listed in Table I can be used in any type of operating acidic nickel baths with beneficial effects.
  • Table II are listed by way of illustration a number of such acidic nickel baths.
  • the nickel plate obtained with the alpha and beta unsaturated sulfonic acids present in the acidic baths is very fine-grained, of good color and ductile, and remarkably free from pitting. On bufied surfaces the plate obtained is as good in reflectivity and brightness as the base.
  • nickel brighteners such as, for example, zinc or cadmium in a concentration of about 0.1-0.5 g./l.
  • the plate obtained is brighter than with either material alone in the bath.
  • the bath can tolerate larger concentrations of the zinc and cadmium than the plain bath without getting brittle, darkish, poorly adherent plate. This is also true with respect to thallous and mercuric salts in about the same concentrations.
  • the impurity, copper which does not produce any appreciable brightness when present in small concentrations, but tends, instead to very readily produce dark deposits, first appearing at the lowest current densities and extending upward as the concentration or copper is increased.
  • the vinyl and allyl sulfonic acids ar extremely good. That is, they are very effective for the very low current density values while at the same time being very efiective for the middle and high current density values.
  • beta unsaturated aliphatic sulfonic acids e. g., allyl sulfonic acid
  • alpha unsaturated sulfonic acids e. g., vinyl sulfonic acid
  • the vinyl sulionic acid makes possibl a toleration of somewhat larger concentrations of materials (both inorganic and organic) which plate out preferentially to nickel and which when alone in the bath cause brittle and easily stained plate of poor color.
  • the beta olefinic double bond as present in allyl sulfonic acid does exert an eilect on, or transmits an eilect to, the sulfonic group and increases its reactivity, but not as strongly as does an alpha unsaturated bond.
  • the sulfonic group affects the active unsaturation characteristics of the alpha carbon double bonds more strongly than the more distant beta, that is, the beta double bonds are more strongly olefinic in character, and thus allyl sulfonic acid also exerts a brightening effect in a somewhat similar manner as does allyl alcohol, allyl amine, allyl urea, arsonic acid, and acrylic acid. The latter, however, do not increase the toleration of impurities,
  • the alpha and beta unsaturated sulfonic acids can be used with beneficial effects in other acidic nickel baths, besides those listed in Table II, for example, in baths made up with nickel sulfamate allyl the naphthalene sulfonic acids, the benzene sulfonic acids, the benzene sulfonamides, the diphenyl sulfone sulfonic acids, in that the ductility of the plate and the brightness in the recesses .(low current density areas) is improved. This is especially true'if-ithe chloride concentration of such nickel baths'is above '75 g./l. NiClaGHzO.
  • Mixtures of compounds of Table I can be used with beneficial eifects (improved brightness of plate) as, for example, allyl sulfonic acid with vinyl sulfonic.
  • beneficial eifects improved brightness of plate
  • mixtures of the compounds of Table I with aryl sulfonates, aryl sulfonamides, aryl sulfimides, aryl sulfone sulfonic acids enhance or improve the brightness of the plate.
  • 0.1-.2 g./l. of o-benzoyl sulfimide with 0.1- 3 g./l. of vinyl and allyl sulfonic acids In general the nickel salts of the alpha or beta unsaturated aliphatic sulfonic acids are preferred for additions instead of the free acids in order not to alter the pH of the baths very much.
  • a method for electrodepositing fine-grained, lustrous nickel comprising the step of electrodepositing fine-grained, lustrous nickel from an aqueous acid solution consisting essentially of a material selected from the group consisting of nickel chloride, nickel sulfate, a mixture of nickel sulfate and nickel chloride, a mixture of nickel REFERENCES CITED fiuoborate and nickel chloride, a mixture of nickel
  • aqueous acid solution consisting essentially of a material selected from the group consisting of nickel chloride, nickel sulfate, a mixture of nickel sulfate and nickel chloride, a mixture of nickel REFERENCES CITED fiuoborate and nickel chloride, a mixture of nickel
  • the following references are of record in the fiuoborate and nickel sulfate, a mixture of nickel me of this patent:

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Electroplating And Plating Baths Therefor (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
US603753A 1945-07-07 1945-07-07 Electrodeposition of nickel from an acid bath Expired - Lifetime US2523190A (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
FR955898D FR955898A (ja) 1945-07-07
US603753A US2523190A (en) 1945-07-07 1945-07-07 Electrodeposition of nickel from an acid bath
GB13288/46A GB611483A (en) 1945-07-07 1946-05-02 Improvements in the electrodeposition of nickel from aqueous acidic nickel baths
US22489A US2523191A (en) 1945-07-07 1948-04-21 Electrodeposition of nickel from an acid bath
DEU622A DE845732C (de) 1945-07-07 1950-09-24 Bad fuer die galvanische Vernickelung

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US603753A US2523190A (en) 1945-07-07 1945-07-07 Electrodeposition of nickel from an acid bath

Publications (1)

Publication Number Publication Date
US2523190A true US2523190A (en) 1950-09-19

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Family Applications (1)

Application Number Title Priority Date Filing Date
US603753A Expired - Lifetime US2523190A (en) 1945-07-07 1945-07-07 Electrodeposition of nickel from an acid bath

Country Status (4)

Country Link
US (1) US2523190A (ja)
DE (1) DE845732C (ja)
FR (1) FR955898A (ja)
GB (1) GB611483A (ja)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2550449A (en) * 1946-04-20 1951-04-24 Udylite Corp Electrodeposition of nickel from an acid bath
DE1001078B (de) * 1953-08-13 1957-01-17 Dehydag Gmbh Galvanische Baeder zur Herstellung von Metallueberzuegen
US3095362A (en) * 1960-11-21 1963-06-25 Incar Inc Zinc plating composition and process
US3109784A (en) * 1960-11-21 1963-11-05 Incar Inc Copper plating composition and process
US3152975A (en) * 1961-02-07 1964-10-13 Hanson Van Winkle Munning Co Electrodeposition of nickel
US3417005A (en) * 1965-12-27 1968-12-17 Gen Motors Corp Neutral nickel-plating process and bath therefor
US6045682A (en) * 1998-03-24 2000-04-04 Enthone-Omi, Inc. Ductility agents for nickel-tungsten alloys

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL238490A (ja) * 1958-04-26
GB2171114A (en) * 1985-02-06 1986-08-20 Canning W Materials Ltd Trivalent chromium electroplating baths and rejuvenation thereof
DE4221970C2 (de) * 1992-06-30 1996-01-18 Atotech Deutschland Gmbh Verfahren zur Vermeidung der Halogengasentwicklung in Metallabscheidungsbädern mit mindestens zwei Elektrolyträumen

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1818229A (en) * 1928-02-23 1931-08-11 Grasselli Chemical Co Electroplating
US2029387A (en) * 1934-03-14 1936-02-04 Harshaw Chem Corp Method and means of electrodeposition
US2112818A (en) * 1934-08-15 1938-03-29 Mcgean Chem Co Inc Electrodeposition of metals
US2125229A (en) * 1936-04-14 1938-07-26 Harshaw Chem Corp Electrodeposition of metals
US2171842A (en) * 1936-07-13 1939-09-05 Du Pont Electroplating
US2198267A (en) * 1939-12-14 1940-04-23 Harshaw Chem Corp Electrodeposition of metals

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1818229A (en) * 1928-02-23 1931-08-11 Grasselli Chemical Co Electroplating
US2029387A (en) * 1934-03-14 1936-02-04 Harshaw Chem Corp Method and means of electrodeposition
US2112818A (en) * 1934-08-15 1938-03-29 Mcgean Chem Co Inc Electrodeposition of metals
US2125229A (en) * 1936-04-14 1938-07-26 Harshaw Chem Corp Electrodeposition of metals
US2171842A (en) * 1936-07-13 1939-09-05 Du Pont Electroplating
US2198267A (en) * 1939-12-14 1940-04-23 Harshaw Chem Corp Electrodeposition of metals

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2550449A (en) * 1946-04-20 1951-04-24 Udylite Corp Electrodeposition of nickel from an acid bath
DE1001078B (de) * 1953-08-13 1957-01-17 Dehydag Gmbh Galvanische Baeder zur Herstellung von Metallueberzuegen
US3095362A (en) * 1960-11-21 1963-06-25 Incar Inc Zinc plating composition and process
US3109784A (en) * 1960-11-21 1963-11-05 Incar Inc Copper plating composition and process
US3152975A (en) * 1961-02-07 1964-10-13 Hanson Van Winkle Munning Co Electrodeposition of nickel
US3417005A (en) * 1965-12-27 1968-12-17 Gen Motors Corp Neutral nickel-plating process and bath therefor
US6045682A (en) * 1998-03-24 2000-04-04 Enthone-Omi, Inc. Ductility agents for nickel-tungsten alloys

Also Published As

Publication number Publication date
DE845732C (de) 1952-08-04
GB611483A (en) 1948-10-29
FR955898A (ja) 1950-01-20

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