US1749443A - Electrodeposition of chromium - Google Patents

Electrodeposition of chromium Download PDF

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Publication number
US1749443A
US1749443A US345888A US34588829A US1749443A US 1749443 A US1749443 A US 1749443A US 345888 A US345888 A US 345888A US 34588829 A US34588829 A US 34588829A US 1749443 A US1749443 A US 1749443A
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United States
Prior art keywords
chromium
baths
chromic acid
electrodeposition
chrome
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Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
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US345888A
Inventor
Proctor Charles 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.)
Roessler and Hasslacher Chemical Co
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Roessler and Hasslacher Chemical Co
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Publication date
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Priority to US345888A priority Critical patent/US1749443A/en
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Publication of US1749443A publication Critical patent/US1749443A/en
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    • 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
    • C25D3/04Electroplating: Baths therefor from solutions of chromium

Definitions

  • This invention relates to improvements in the electrodeposition of chromium.
  • the electrolytic baths commonly usedfor plating articles with chromium contain chromic acid and usually include small amounts of sulphate ions.
  • a great variety of addition agents, such as inorganic salts, have been dissolved with the chromic acid in the prior art baths.
  • a limitation of these baths is that they do not throw a deposit into the recesses of irregularly shaped articles which are being chromium plated.
  • My invention also increases thethrowing power of chromic acid baths, shortens the time in which good deposits will begin to appear, and the internal resistance .of the baths is less than that of the previously known chromic acid baths.
  • Chrome-iron ores are known to contain in general the following oxides in approximately the proportions given:
  • Anodes of sheet steel orlead may be used and the bath temperature maintained at 95- 120 F. with current densities of 100-125 amps. per sq. ft.
  • Ghromic acid (CrO 8 to 48 ozs. Chrome-iron ore (commercial) to 1 ozs. Sulfuric acid to ozs.
  • Chrome oxide C130 48-50% Iron oxide (Fe O 20-25% Silicon oxide (SiO 4- 7% Magnesium oxide (MgO) 12-14% Aluminum oxide (A1 0 740% Signed at New York city, N. Y., in the county of New York and State of New York this 16th day of February, A. D. 1929.

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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)

Description

Patented Mar. 4, 1930 UNITED STATES- PATENT OFFICE CHARLES HENRY PROCTOR, OF ARLINGTON, NEW JERSEY, ASSIGNOR TO THE ROESSLER & HASSLACHER CHEMICAL COMIBANY, OF NEW YORK, N. Y., A CORPORATION OF NEW YORK ELECTRODEPOSITION OF CHROMIUM N0 Drawing.
This invention relates to improvements in the electrodeposition of chromium.
The electrolytic baths commonly usedfor plating articles with chromium contain chromic acid and usually include small amounts of sulphate ions. A great variety of addition agents, such as inorganic salts, have been dissolved with the chromic acid in the prior art baths. However, a limitation of these baths is that they do not throw a deposit into the recesses of irregularly shaped articles which are being chromium plated.
I have now found that the presence of a naturally occurring chrome-iron ore, such as chromite, in electrolytic solutions containing chromic acid shortens the time in which deposits can be plated out. The resulting deposits are also whiter and more evenly distributed over the object to be plated than those which have been obtained by the chromic acid baths previously known. 7
My invention also increases thethrowing power of chromic acid baths, shortens the time in which good deposits will begin to appear, and the internal resistance .of the baths is less than that of the previously known chromic acid baths.
Chrome-iron ores are known to contain in general the following oxides in approximately the proportions given:
Chromic oxide (Gr O -65% Iron oxides .(Fe O 20-35% Magnesium oxide (MgO) 4-16% Aluminumoxide AI O 7-20% Silicon dioxide iO 4- 7% The naturally occurringchrome-iron ore, which I prefer to dissolve in my baths, can be obtained commercially in the form of a fine powder, the empiricalformula of which -shows essentially the following oxides or their equivalents in about the proportions given:
Aluminum oxide (A1 0 7-10% Application filed March 9, 1929. Serial No. 345,888.
One example of my successful chromicacid baths is as follows:
lVater 1 gallon Chromic acid 8-48 02. Chrome-iron ore to 1% oz.
(as described above) H Sulphuric acid (60%) to oz.
Anodes of sheet steel orlead may be used and the bath temperature maintained at 95- 120 F. with current densities of 100-125 amps. per sq. ft.
What I claim is:
1. As a new composition, a chromic acid electroplating solution containing chromeiron ore.
2. As a new composition a chromic acid electroplating solution containing, for each gallon of Water, the following ingredients in about the proportions given:
Ghromic acid (CrO 8 to 48 ozs. Chrome-iron ore (commercial) to 1 ozs. Sulfuric acid to ozs.
the chrome-iron ore having essentially the following analysis;
By weight Chrome oxide (C130 48-50% Iron oxide (Fe O 20-25% Silicon oxide (SiO 4- 7% Magnesium oxide (MgO) 12-14% Aluminum oxide (A1 0 740% Signed at New York city, N. Y., in the county of New York and State of New York this 16th day of February, A. D. 1929.
CHARLES HENRY PROCTOR.
US345888A 1929-03-09 1929-03-09 Electrodeposition of chromium Expired - Lifetime US1749443A (en)

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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2601306A (en) * 1948-02-24 1952-06-24 Rex R Lloyd Method for dissolution of chromium from chromite ores
US2841541A (en) * 1955-10-28 1958-07-01 Diamond Alkali Co Chemical composition for chromium plating
US2992171A (en) * 1957-06-27 1961-07-11 Gen Dev Corp Method and composition for chromium plating
US4406756A (en) * 1981-07-13 1983-09-27 Canadian Corporate Management Company Limited Hard chromium plating from hexavalent plating bath

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2601306A (en) * 1948-02-24 1952-06-24 Rex R Lloyd Method for dissolution of chromium from chromite ores
US2841541A (en) * 1955-10-28 1958-07-01 Diamond Alkali Co Chemical composition for chromium plating
US2992171A (en) * 1957-06-27 1961-07-11 Gen Dev Corp Method and composition for chromium plating
US4406756A (en) * 1981-07-13 1983-09-27 Canadian Corporate Management Company Limited Hard chromium plating from hexavalent plating bath

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