US3654101A - Novel chromium plating compositions and processes - Google Patents
Novel chromium plating compositions and processes Download PDFInfo
- Publication number
- US3654101A US3654101A US1874A US3654101DA US3654101A US 3654101 A US3654101 A US 3654101A US 1874 A US1874 A US 1874A US 3654101D A US3654101D A US 3654101DA US 3654101 A US3654101 A US 3654101A
- Authority
- US
- United States
- Prior art keywords
- chromium
- bromate
- electroplating
- bath
- chromium plating
- 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
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- 239000011651 chromium Substances 0.000 title abstract description 66
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 title abstract description 65
- 229910052804 chromium Inorganic materials 0.000 title abstract description 65
- 239000000203 mixture Substances 0.000 title abstract description 42
- 238000007747 plating Methods 0.000 title abstract description 30
- 238000000034 method Methods 0.000 title abstract description 17
- -1 BROMATE ION Chemical class 0.000 abstract description 33
- SXDBWCPKPHAZSM-UHFFFAOYSA-M bromate Inorganic materials [O-]Br(=O)=O SXDBWCPKPHAZSM-UHFFFAOYSA-M 0.000 abstract description 30
- 238000009713 electroplating Methods 0.000 abstract description 17
- 230000002378 acidificating effect Effects 0.000 abstract description 14
- 229910052751 metal Inorganic materials 0.000 abstract description 14
- 239000002184 metal Substances 0.000 abstract description 14
- JOPOVCBBYLSVDA-UHFFFAOYSA-N chromium(6+) Chemical compound [Cr+6] JOPOVCBBYLSVDA-UHFFFAOYSA-N 0.000 abstract description 5
- 239000000654 additive Substances 0.000 abstract description 4
- 230000000996 additive effect Effects 0.000 abstract description 4
- 150000001845 chromium compounds Chemical class 0.000 abstract description 4
- 229910001430 chromium ion Inorganic materials 0.000 abstract description 3
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 16
- KRVSOGSZCMJSLX-UHFFFAOYSA-L chromic acid Substances O[Cr](O)(=O)=O KRVSOGSZCMJSLX-UHFFFAOYSA-L 0.000 description 14
- AWJWCTOOIBYHON-UHFFFAOYSA-N furo[3,4-b]pyrazine-5,7-dione Chemical compound C1=CN=C2C(=O)OC(=O)C2=N1 AWJWCTOOIBYHON-UHFFFAOYSA-N 0.000 description 14
- 239000003054 catalyst Substances 0.000 description 11
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 9
- 239000000463 material Substances 0.000 description 8
- 229910052759 nickel Inorganic materials 0.000 description 8
- BEOODBYKENEKIC-UHFFFAOYSA-N azanium;bromate Chemical compound [NH4+].[O-]Br(=O)=O BEOODBYKENEKIC-UHFFFAOYSA-N 0.000 description 6
- SXDBWCPKPHAZSM-UHFFFAOYSA-N bromic acid Chemical compound OBr(=O)=O SXDBWCPKPHAZSM-UHFFFAOYSA-N 0.000 description 6
- 239000002659 electrodeposit Substances 0.000 description 5
- 229910001369 Brass Inorganic materials 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- 229910052783 alkali metal Inorganic materials 0.000 description 4
- 239000010951 brass Substances 0.000 description 4
- 150000002222 fluorine compounds Chemical class 0.000 description 4
- CRWJEUDFKNYSBX-UHFFFAOYSA-N sodium;hypobromite Chemical compound [Na+].Br[O-] CRWJEUDFKNYSBX-UHFFFAOYSA-N 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 150000001450 anions Chemical class 0.000 description 3
- 239000000872 buffer Substances 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 229910000906 Bronze Inorganic materials 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000010974 bronze Substances 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- KUNSUQLRTQLHQQ-UHFFFAOYSA-N copper tin Chemical compound [Cu].[Sn] KUNSUQLRTQLHQQ-UHFFFAOYSA-N 0.000 description 2
- 229910052749 magnesium Inorganic materials 0.000 description 2
- 239000011777 magnesium Substances 0.000 description 2
- 235000021317 phosphate Nutrition 0.000 description 2
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- KMUONIBRACKNSN-UHFFFAOYSA-N potassium dichromate Chemical compound [K+].[K+].[O-][Cr](=O)(=O)O[Cr]([O-])(=O)=O KMUONIBRACKNSN-UHFFFAOYSA-N 0.000 description 2
- NROKBHXJSPEDAR-UHFFFAOYSA-M potassium fluoride Chemical compound [F-].[K+] NROKBHXJSPEDAR-UHFFFAOYSA-M 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- PUZPDOWCWNUUKD-UHFFFAOYSA-M sodium fluoride Chemical compound [F-].[Na+] PUZPDOWCWNUUKD-UHFFFAOYSA-M 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- UBXAKNTVXQMEAG-UHFFFAOYSA-L strontium sulfate Chemical compound [Sr+2].[O-]S([O-])(=O)=O UBXAKNTVXQMEAG-UHFFFAOYSA-L 0.000 description 2
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- QLOKJRIVRGCVIM-UHFFFAOYSA-N 1-[(4-methylsulfanylphenyl)methyl]piperazine Chemical compound C1=CC(SC)=CC=C1CN1CCNCC1 QLOKJRIVRGCVIM-UHFFFAOYSA-N 0.000 description 1
- JHWIEAWILPSRMU-UHFFFAOYSA-N 2-methyl-3-pyrimidin-4-ylpropanoic acid Chemical compound OC(=O)C(C)CC1=CC=NC=N1 JHWIEAWILPSRMU-UHFFFAOYSA-N 0.000 description 1
- 101150111246 BIO3-BIO1 gene Proteins 0.000 description 1
- PYKPNBZBSSKTDP-UHFFFAOYSA-K Br(=O)(=O)[O-].[Cr+3].Br(=O)(=O)[O-].Br(=O)(=O)[O-] Chemical compound Br(=O)(=O)[O-].[Cr+3].Br(=O)(=O)[O-].Br(=O)(=O)[O-] PYKPNBZBSSKTDP-UHFFFAOYSA-K 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 229910000978 Pb alloy Inorganic materials 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical class OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 101100493963 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) BIO3 gene Proteins 0.000 description 1
- 150000001241 acetals Chemical class 0.000 description 1
- 229920006397 acrylic thermoplastic Polymers 0.000 description 1
- XECAHXYUAAWDEL-UHFFFAOYSA-N acrylonitrile butadiene styrene Chemical compound C=CC=C.C=CC#N.C=CC1=CC=CC=C1 XECAHXYUAAWDEL-UHFFFAOYSA-N 0.000 description 1
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 1
- 239000004676 acrylonitrile butadiene styrene Substances 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- WPAPFUDMJMTAQF-UHFFFAOYSA-K aluminum;tribromate Chemical compound [Al+3].[O-]Br(=O)=O.[O-]Br(=O)=O.[O-]Br(=O)=O WPAPFUDMJMTAQF-UHFFFAOYSA-K 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 229940070337 ammonium silicofluoride Drugs 0.000 description 1
- 239000011260 aqueous acid Substances 0.000 description 1
- ZUHFXGOGKYCXSS-UHFFFAOYSA-L azanium calcium hydrogen sulfate sulfate Chemical compound S(=O)(=O)([O-])[O-].[NH4+].S(=O)(=O)([O-])O.[Ca+2] ZUHFXGOGKYCXSS-UHFFFAOYSA-L 0.000 description 1
- 150000001642 boronic acid derivatives Chemical class 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- WUKWITHWXAAZEY-UHFFFAOYSA-L calcium difluoride Chemical compound [F-].[F-].[Ca+2] WUKWITHWXAAZEY-UHFFFAOYSA-L 0.000 description 1
- 229910001634 calcium fluoride Inorganic materials 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- XHKOOTFZHJHDTI-UHFFFAOYSA-K cerium(3+);tribromate Chemical compound [Ce+3].[O-]Br(=O)=O.[O-]Br(=O)=O.[O-]Br(=O)=O XHKOOTFZHJHDTI-UHFFFAOYSA-K 0.000 description 1
- QCCDYNYSHILRDG-UHFFFAOYSA-K cerium(3+);trifluoride Chemical compound [F-].[F-].[F-].[Ce+3] QCCDYNYSHILRDG-UHFFFAOYSA-K 0.000 description 1
- 230000002301 combined effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- DTDCCPMQHXRFFI-UHFFFAOYSA-N dioxido(dioxo)chromium lanthanum(3+) Chemical compound [La+3].[La+3].[O-][Cr]([O-])(=O)=O.[O-][Cr]([O-])(=O)=O.[O-][Cr]([O-])(=O)=O DTDCCPMQHXRFFI-UHFFFAOYSA-N 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000004070 electrodeposition Methods 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- 150000002240 furans Chemical class 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 229910001506 inorganic fluoride Inorganic materials 0.000 description 1
- 229910052920 inorganic sulfate Inorganic materials 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- RLWQGQQQYGASQR-UHFFFAOYSA-N lanthanum(3+) oxido-(oxido(dioxo)chromio)oxy-dioxochromium Chemical compound [Cr](=O)(=O)([O-])O[Cr](=O)(=O)[O-].[La+3].[Cr](=O)(=O)([O-])O[Cr](=O)(=O)[O-].[Cr](=O)(=O)([O-])O[Cr](=O)(=O)[O-].[La+3] RLWQGQQQYGASQR-UHFFFAOYSA-N 0.000 description 1
- INHCSSUBVCNVSK-UHFFFAOYSA-L lithium sulfate Inorganic materials [Li+].[Li+].[O-]S([O-])(=O)=O INHCSSUBVCNVSK-UHFFFAOYSA-L 0.000 description 1
- RNUHOKZSYYKPPI-UHFFFAOYSA-L magnesium;dibromate Chemical compound [Mg+2].[O-]Br(=O)=O.[O-]Br(=O)=O RNUHOKZSYYKPPI-UHFFFAOYSA-L 0.000 description 1
- GIOZLVMCHDGNNZ-UHFFFAOYSA-N magnesium;oxido-(oxido(dioxo)chromio)oxy-dioxochromium Chemical compound [Mg+2].[O-][Cr](=O)(=O)O[Cr]([O-])(=O)=O GIOZLVMCHDGNNZ-UHFFFAOYSA-N 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- VHQJZYCGDGGQCN-UHFFFAOYSA-N methyl bromate Chemical compound COBr(=O)=O VHQJZYCGDGGQCN-UHFFFAOYSA-N 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 235000013824 polyphenols Nutrition 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- OCATYIAKPYKMPG-UHFFFAOYSA-M potassium bromate Chemical compound [K+].[O-]Br(=O)=O OCATYIAKPYKMPG-UHFFFAOYSA-M 0.000 description 1
- 235000003270 potassium fluoride Nutrition 0.000 description 1
- 239000011698 potassium fluoride Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- XUXNAKZDHHEHPC-UHFFFAOYSA-M sodium bromate Chemical compound [Na+].[O-]Br(=O)=O XUXNAKZDHHEHPC-UHFFFAOYSA-M 0.000 description 1
- PXLIDIMHPNPGMH-UHFFFAOYSA-N sodium chromate Chemical compound [Na+].[Na+].[O-][Cr]([O-])(=O)=O PXLIDIMHPNPGMH-UHFFFAOYSA-N 0.000 description 1
- 235000013024 sodium fluoride Nutrition 0.000 description 1
- 239000011775 sodium fluoride Substances 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 1
- NAMOWWYAIVZKKA-UHFFFAOYSA-L strontium bromate Chemical compound [Sr+2].[O-]Br(=O)=O.[O-]Br(=O)=O NAMOWWYAIVZKKA-UHFFFAOYSA-L 0.000 description 1
- NVKTUNLPFJHLCG-UHFFFAOYSA-N strontium chromate Chemical compound [Sr+2].[O-][Cr]([O-])(=O)=O NVKTUNLPFJHLCG-UHFFFAOYSA-N 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- RBTVSNLYYIMMKS-UHFFFAOYSA-N tert-butyl 3-aminoazetidine-1-carboxylate;hydrochloride Chemical compound Cl.CC(C)(C)OC(=O)N1CC(N)C1 RBTVSNLYYIMMKS-UHFFFAOYSA-N 0.000 description 1
- ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 1
- SWURHZJFFJEBEE-UHFFFAOYSA-J tetrafluorocerium Chemical compound F[Ce](F)(F)F SWURHZJFFJEBEE-UHFFFAOYSA-J 0.000 description 1
- NAWVCYVCEVTDBQ-UHFFFAOYSA-M tetramethylazanium;bromate Chemical compound [O-]Br(=O)=O.C[N+](C)(C)C NAWVCYVCEVTDBQ-UHFFFAOYSA-M 0.000 description 1
- 150000003673 urethanes Chemical class 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25D—PROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
- C25D3/00—Electroplating: Baths therefor
- C25D3/02—Electroplating: Baths therefor from solutions
- C25D3/04—Electroplating: Baths therefor from solutions of chromium
Definitions
- this invention relates to novel compositions and to a process for electroplating chromium plate onto a basis metal which comprises passing current from an anode to a cathode at least a portion of which contains a conductive metal layer through an aqueous acidic chromium plating bath composition containing 1) At least one chromium compound providing hexavalent chromium ions for electroplating chromium; and
- This invention relates to novel compositions and to novel processes for the electrodeposition of chromium from an aqueous acidic chromium plating bath.
- chromium may be plated onto various basis metals from aqueous bath solutions.
- aqueous bath solutions it has been found that the use of certain catalysts such as silicofluoride ions and sulfate ions provide improved chromium electrodeposits especially in so-called low current density areas.
- catalysts such as silicofluoride ions and sulfate ions provide improved chromium electrodeposits especially in so-called low current density areas.
- the effect of such catalyst systems has been found to vary with the concentration of the chromic acid and the ratio of the catalysts to the total chromic acid content.
- the concentration of the chromium plating bath continually varies during operation due to the removal of chromium in the form of deposited metal and due to the addition of impurities arising from the electrodes as well as decomposition products, it has been diflicult to control and maintain the proper catalyst and chromic acid concentrations throughout the life of a typical aqueous acidic chromium electroplating bath.
- chromium electroplating composition which is stable over the life of the bath and provides a chromium electroplate of improved coverage.
- the bath compositions of the invention ar further characterized by increased throwing power (i.e. the ability to provide satisfactory chromium electrodeposits in recessed areas and areas of non-uniform shape).
- 'It is an object of this invention to provide improved electroplating compositions and processes.
- a further object of th invention is to provide chromium plating bath compositions which have good throwing power, excellent coverage, and extended useful life.
- this invention relates to novel compositions and to a process for electroplating chromium plate onto a basis metal which comprises passing current from an anode to a cathode at least a portion of which contains a conductive metal layer through an aqueous acidic chromium plating bath composition containing:
- At least one chromium compound providing hexavalent chromium ions for electroplating chromium
- the chromium electroplating bath compositions of the invention may contain about 50-600 g./l. of chromic acid expressed as 010 (preferably about 200-300 g./l. of chromic acid) and may be prepared from commercial chromic acid solutions.
- a portion of the chromic acid used in the bath composition may be furnished by a salt of hexavalent chromium such as sodium chromate, sodium dichromate, potassium chromate, potassium dichromate, strontium chromate, magnesium dichromate, lanthanum chromate, lanthanum dichromate, etc.
- a salt of hexavalent chromium such as sodium chromate, sodium dichromate, potassium chromate, potassium dichromate, strontium chromate, magnesium dichromate, lanthanum chromate, lanthanum dichromate, etc.
- Catalyst anions may also be included in the aqueous chromium plating bath to regulate the concentrations of the active ingredients during electroplating.
- sulfate, fluoride, and complex fluorides may be used.
- fluosilicates, fluoborates, fluoaluminates, fluotitanates, and fluozirconates may be included in the aqueous chromium plating bath composition without adversely affecting the properties of the novel chromium electroplate which is produced according to the invention.
- the fluoride ions may be added to the chromium electroplating bath in the form of compounds such as sodium silicofluoride (Na SiF fluosilicic acid (H2 F6), strontium silicofluoride (SrSiF ammonium silicofluoride [(NTH SEF magnesium silicofluoride (MgSiF calcium silicofluoride (CaSiF etc.
- Other fluoride compounds which may be used in the bath according to the invention include sodium fluoride, potassium fluoride, calcium fluoride, hydrofluoric acid, ceric fluoride, cerous fluoride, etc.
- fluoride ions including complex fluoride ions
- fluoaluminates include, for example, fluoroborates, fluotitanates, and fiuozirconates.
- Sulfate ions may also be added to the chromium electroplating bath in the form of suitable sulfate compounds such as strontium sulfate (SrSO sulfuric acid (H lithium sulfate (M 80 ammonium sulfate calcium sulfate (CaSO etc.
- suitable sulfate compounds such as strontium sulfate (SrSO sulfuric acid (H lithium sulfate (M 80 ammonium sulfate calcium sulfate (CaSO etc.
- the total amount of combined catalysts may be present in the chromium plating bath composition in catalytic amounts (such as 0.015.0 g./l.) or in amounts of 0.01- g./l.
- the chromium electroplating process may use temperatures of 30-70" C. with a chromic acid bath containing l00-600 g./l. of chromic acid (as CrO When using sulfate, the ratio of chromic acid to sulfate ion (CF03 Z 804 may be maintained at 100-550: I, typically ISO-300:1 and preferably about 200: 1.
- Suitable neutralizers and/or buffers may also be employed in the bath composition of the invention.
- neutralizers or buffers may include phosphates, borates, sulfonates, and carboxylates.
- catalyst anions as heretofore recited may also be used in amounts suflicient to act as buffers or neutralizers in combined effect with their catalyst properties.
- Bromate ions may be added to the bath compositions of the invention in the form of salts such as alkali metal bromates (NaBrO KBrO 'LiBrO CsBrO alkaline earth metal bromates [Ca(BrO Sr(BrO etc.]; ammonium bromate, (including alkyl-substituted ammonium bromates such as tetramethylammonium bromate, etc.), chromium bromate, cerium bromate, aluminum bromate, magnesium bromate, etc. Any bath compatible source of bromate ion may be used (including organic bromates such as methyl bromate, etc.). Alkali metal and ammonium bromates (especially NH BrO and are preferred.
- alkali metal bromates NaBrO KBrO 'LiBrO CsBrO alkaline earth metal bromates [Ca(BrO Sr(BrO etc.]
- ammonium bromate (including alkyl-substituted ammoni
- the bromate ion may be used in a chromium plating bath composition (containing about 100-600 g./l. of CrO in eifective amounts of about 0.01-10 g./l., preferably 0.05-5.0 g./l. of bromate (.BrO anion. Larger amounts of bromate ion may be used, but no additional improvement is obtained thereby and the use of excessive amounts of bromate ion serves to increase the cost factors of the novel chromium plating bath compositions and processes based thereon.
- the basis material which may be treated according to this invention to produce an improved chromium deposit may include a basis material such as iron, steel, brass, bronze, copper, zinc, aluminum, magnesium, nickel, etc. either pure or in the form of an alloy or as multilayer deposits.
- the preferred basis metal to be plated in accordance with this invention may be steel, zinc, or brass which has first been plated with a conductive deposit such as a plate of bright nickel, typically preceded by a first plate of copper, bronze, or semi-bright nickel.
- basis materials to be treated by the process of this invention may include plastics and resins including acrylonitrile-butadiene-styrene, acetals, acrylics, alkyds, alkyls, amines, cellulosics, chlorinated polyethers, epoxies, furanes, fluorocarbons, isocyanates (urethanes), polyamides (nylons), phenoxides, phenolics, polycarbonates, polyesters, polyethylenes, silicones, polystyrenes, polyvinyls, and copolymers, etc. of these materials.
- the basis material to be treated by the process of this invention is a plastic or resin, the surface thereof will be pre-treated by deposition thereon of a conductive deposit, such as a nickel deposit.
- the basis material bearing a conductive surface may be immediately treated after disposition of such plate or it may be water rinsed; or it may be rinsed, dipped in aqueous acid solution such as 0.5 %-10%, say 2%, by weight of sulfuric acid prior to further treatment.
- aqueous acid solution such as 0.5 %-10%, say 2%, by weight of sulfuric acid prior to further treatment.
- the so-treated material may be dried or it may be further treated as is. If drying has been permitted, the conductive surface may be cleaned as by cathodically treating in alkaline cleaner followed by rinsing .in water or dipping in an acid solution before further treatment.
- the aqueous acidic chromium plating bath compositions which contain an effective amount of bromate ion may be employed at temperatures of about 30-7 C. to prepare improved chromium plated articles by passing current from an anode to a basis metal cathode through said aqueous acidic chromium plating solution at a temperature of 30-70 C. for a time sufiicient to deposit a chromium electroplate having a thickness of at least 1x 10- mm.
- Current densities which may be employed may be 1.0-90 amperes per square decimeter (a.s.d.) and preferably about 3-50 a.s.d. Especially good results may be obtained using pulsed or intermittent direct current.
- the bath compositions of the invention may be used with lead anodes and/ or lead alloy anodes.
- a typical bath composition which may be used in the invention to produce an improved chromium electrodeposit may comprise chromic acid in the amount of 50- 600 g./l. as CrO in combination with 0.01- g./l. of bromate ion.
- Other bath compatible materials may be incorporated in the bath.
- inorganic sulfates and fluorides or complex fluorides and phosphates may be incorporated into the bath.
- the improved chromium deposit may be obtained using plating currents of 2-30 amperes per square decimeter (a.s.d.) at temperatures of 10-80' C. using plating times of one-half minute to one hour (typically 2-30 minutes).
- EXAMPLE 1 An aqueous chromium plating bath composition containing the following ingredients in the indicated amounts (all amounts in grams per liter, g./l., unless otherwise specified) was prepared:
- a panel of buffed brass containing a 45 bend measuring 75 x x 0.45 millimeters was cleaned and plated with a bright nickel deposit.
- the nickel plated panel was immersed in a Standard Hull Cell and the panel was connected as cathode.
- a total current of 8 amperes was passed through the solution for a time period of five minutes while maintaining the bath solution at about 35-45".
- C. The resulting chromium electrodeposit was satisfactory, but showed the usual minute defects in recessed areas of the bent portions of the test panel.
- EXAMPLE 2 The aqueous chromium plating bath composition of Example 1 was used with a mixture of 1.0 g./l. of NaBrO and 1.0 g./l. of KBrO A buffed brass panel plated with a nickel strike was chromium plated using the time, temperature, and plating current of Example 1 to produce an excellent chromium plate over the bent surfaces of the test panel.
- a process for electroplating chromium plate onto a basis metal which comprises passing current from an anode to a cathode at least a portion of which contains a cient to deposit a chromium electroplate having a' thickness of at least 1X 10- mm.) 7
- aqueous acidic chromium plating bath composition contains:
- a composition for electroplating chromium plate on a basis metal which comprises an aqueous acidic chromium plating bath composition containing:
- At least one chromium compound providing hexavalent chromium for electroplating chromium, sulfate ions such that the ratio of chromic acid to sulfate ion is between 100:1 and 550:1;
- a composition as claimed in claim 7 wherein a portion of the bromate ion is provided by an alkali metal bromate or NH BrO 10.
- a composition as claimed in claim 7 wherein a portion of the bromate ion is provided by at least one member selected from the group consisting of KBrO NaBrO and NH BrO 11.
- the aqueous acidic chromium plating bath composition contains 600 g./l. of CrO and 0.01-10 g./l. of bromate anion BIO 12.
- the aqueous acidic chromium plating bath composition contains:
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Abstract
IN ACCORDANCE WITH CERTAIN OF ITS ASPECTS, THIS INVENTION RELATES TO NOVEL COMPOSITIONS AND TO A PROCESS FOR ELECTROPLATING CHROMIUM PLATE ONTO A BASIS METAL WHICH COMPRISES PASSING CURRENT FROM AN ANODE TO A CATHODE AT LEAST A PORTION OF WHICH CONTAINS A CONDUCTIVE METAL LAYER THROUGH AN AQUEOUS ACIDIC CHROMIUM PLATING BATH COMPOSITION CONTAINING (1) AT LEAST ONE CHROMIUM COMPOUND PROVIDING HEXAVALENT CHROMIUM IONS FOR ELECTROPLATING CHROMIUM; AND (2) BROMATE ION AS COOPERATING ADDITIVE TO PROVIDE INCREASED CHROMIUM THROWING POWER; FOR A TIME SUFFICIENT TO DEPOSIT A CHROMIUM ELECTROPLATE HAVING A THICKNESS OF AT LEAST 1X10**-5 MM.
Description
United States Patent 3,654,101 NOVEL CHROMIUM PLATING COMPOSITIONS AND PROCESSES Fred Aoun, Madison Heights, Mich., assignor to M & T Chemicals Inc., New York, N.Y. No Drawing. Filed Jan. 9, 1070, Ser. No. 1,874
Int. Cl. C23b /06 US. Cl. 204--51 12 Claims ABSTRACT OF THE DISCLOSURE In accordance with certain of its aspects, this invention relates to novel compositions and to a process for electroplating chromium plate onto a basis metal which comprises passing current from an anode to a cathode at least a portion of which contains a conductive metal layer through an aqueous acidic chromium plating bath composition containing 1) At least one chromium compound providing hexavalent chromium ions for electroplating chromium; and
(2) Bromate ion as cooperating additive to provide increased chromium throwing power; for a time sufficient to deposit a chromium electroplate having a thickness of at least 1X10 mm.
This invention relates to novel compositions and to novel processes for the electrodeposition of chromium from an aqueous acidic chromium plating bath.
It is known that chromium may be plated onto various basis metals from aqueous bath solutions. During chromium plating using such bath compositions it has been found that the use of certain catalysts such as silicofluoride ions and sulfate ions provide improved chromium electrodeposits especially in so-called low current density areas. The effect of such catalyst systems, however, has been found to vary with the concentration of the chromic acid and the ratio of the catalysts to the total chromic acid content. Since the concentration of the chromium plating bath continually varies during operation due to the removal of chromium in the form of deposited metal and due to the addition of impurities arising from the electrodes as well as decomposition products, it has been diflicult to control and maintain the proper catalyst and chromic acid concentrations throughout the life of a typical aqueous acidic chromium electroplating bath.
It has now been found that the addition of bromate ions in combination with an aqueous acidic bath containing chromic acid results in a chromium electroplating composition which is stable over the life of the bath and provides a chromium electroplate of improved coverage. The bath compositions of the invention ar further characterized by increased throwing power (i.e. the ability to provide satisfactory chromium electrodeposits in recessed areas and areas of non-uniform shape).
'It is an object of this invention to provide improved electroplating compositions and processes. A further object of th invention is to provide chromium plating bath compositions which have good throwing power, excellent coverage, and extended useful life. Other objects of the invention will be apparent to those skilled in the art upon inspection of the following detailed description of the invention.
In accordance with certain of its aspects, this invention relates to novel compositions and to a process for electroplating chromium plate onto a basis metal which comprises passing current from an anode to a cathode at least a portion of which contains a conductive metal layer through an aqueous acidic chromium plating bath composition containing:
1) At least one chromium compound providing hexavalent chromium ions for electroplating chromium; and
(2) Bromate ion as cooperating additive to provide increased chromium throwing power; for a time suflicient to deposit a chromium electroplate having a thickness of at least 1x10" mm.
The chromium electroplating bath compositions of the invention may contain about 50-600 g./l. of chromic acid expressed as 010 (preferably about 200-300 g./l. of chromic acid) and may be prepared from commercial chromic acid solutions. Preferably, a portion of the chromic acid used in the bath composition may be furnished by a salt of hexavalent chromium such as sodium chromate, sodium dichromate, potassium chromate, potassium dichromate, strontium chromate, magnesium dichromate, lanthanum chromate, lanthanum dichromate, etc. In many cases it may be advantageous to employ one or more of such salts in order to provide for a means of control of the composition or of the acidity of the aqueous chromium plating bath.
Catalyst anions may also be included in the aqueous chromium plating bath to regulate the concentrations of the active ingredients during electroplating. For example, sulfate, fluoride, and complex fluorides may be used. Typically, fluosilicates, fluoborates, fluoaluminates, fluotitanates, and fluozirconates may be included in the aqueous chromium plating bath composition without adversely affecting the properties of the novel chromium electroplate which is produced according to the invention. The fluoride ions may be added to the chromium electroplating bath in the form of compounds such as sodium silicofluoride (Na SiF fluosilicic acid (H2 F6), strontium silicofluoride (SrSiF ammonium silicofluoride [(NTH SEF magnesium silicofluoride (MgSiF calcium silicofluoride (CaSiF etc. Other fluoride compounds which may be used in the bath according to the invention include sodium fluoride, potassium fluoride, calcium fluoride, hydrofluoric acid, ceric fluoride, cerous fluoride, etc.
Other fluoride ions (including complex fluoride ions) which may be employed include, for example, fluoaluminates, fluoroborates, fluotitanates, and fiuozirconates.
Sulfate ions may also be added to the chromium electroplating bath in the form of suitable sulfate compounds such as strontium sulfate (SrSO sulfuric acid (H lithium sulfate (M 80 ammonium sulfate calcium sulfate (CaSO etc.
The total amount of combined catalysts may be present in the chromium plating bath composition in catalytic amounts (such as 0.015.0 g./l.) or in amounts of 0.01- g./l.
The chromium electroplating process may use temperatures of 30-70" C. with a chromic acid bath containing l00-600 g./l. of chromic acid (as CrO When using sulfate, the ratio of chromic acid to sulfate ion (CF03 Z 804 may be maintained at 100-550: I, typically ISO-300:1 and preferably about 200: 1.
Suitable neutralizers and/or buffers may also be employed in the bath composition of the invention. Examples of such neutralizers or buffers may include phosphates, borates, sulfonates, and carboxylates. In addition, catalyst anions as heretofore recited may also be used in amounts suflicient to act as buffers or neutralizers in combined effect with their catalyst properties.
Bromate ions may be added to the bath compositions of the invention in the form of salts such as alkali metal bromates (NaBrO KBrO 'LiBrO CsBrO alkaline earth metal bromates [Ca(BrO Sr(BrO etc.]; ammonium bromate, (including alkyl-substituted ammonium bromates such as tetramethylammonium bromate, etc.), chromium bromate, cerium bromate, aluminum bromate, magnesium bromate, etc. Any bath compatible source of bromate ion may be used (including organic bromates such as methyl bromate, etc.). Alkali metal and ammonium bromates (especially NH BrO and are preferred.
The bromate ion may be used in a chromium plating bath composition (containing about 100-600 g./l. of CrO in eifective amounts of about 0.01-10 g./l., preferably 0.05-5.0 g./l. of bromate (.BrO anion. Larger amounts of bromate ion may be used, but no additional improvement is obtained thereby and the use of excessive amounts of bromate ion serves to increase the cost factors of the novel chromium plating bath compositions and processes based thereon.
The basis material which may be treated according to this invention to produce an improved chromium deposit may include a basis material such as iron, steel, brass, bronze, copper, zinc, aluminum, magnesium, nickel, etc. either pure or in the form of an alloy or as multilayer deposits. The preferred basis metal to be plated in accordance with this invention may be steel, zinc, or brass which has first been plated with a conductive deposit such as a plate of bright nickel, typically preceded by a first plate of copper, bronze, or semi-bright nickel.
Other basis materials to be treated by the process of this invention may include plastics and resins including acrylonitrile-butadiene-styrene, acetals, acrylics, alkyds, alkyls, amines, cellulosics, chlorinated polyethers, epoxies, furanes, fluorocarbons, isocyanates (urethanes), polyamides (nylons), phenoxides, phenolics, polycarbonates, polyesters, polyethylenes, silicones, polystyrenes, polyvinyls, and copolymers, etc. of these materials. When the basis material to be treated by the process of this invention is a plastic or resin, the surface thereof will be pre-treated by deposition thereon of a conductive deposit, such as a nickel deposit.
The basis material bearing a conductive surface, preferably a bright nickel plate, may be immediately treated after disposition of such plate or it may be water rinsed; or it may be rinsed, dipped in aqueous acid solution such as 0.5 %-10%, say 2%, by weight of sulfuric acid prior to further treatment. The so-treated material may be dried or it may be further treated as is. If drying has been permitted, the conductive surface may be cleaned as by cathodically treating in alkaline cleaner followed by rinsing .in water or dipping in an acid solution before further treatment.
According to this invention, the aqueous acidic chromium plating bath compositions which contain an effective amount of bromate ion may be employed at temperatures of about 30-7 C. to prepare improved chromium plated articles by passing current from an anode to a basis metal cathode through said aqueous acidic chromium plating solution at a temperature of 30-70 C. for a time sufiicient to deposit a chromium electroplate having a thickness of at least 1x 10- mm. Current densities which may be employed may be 1.0-90 amperes per square decimeter (a.s.d.) and preferably about 3-50 a.s.d. Especially good results may be obtained using pulsed or intermittent direct current. The bath compositions of the invention may be used with lead anodes and/ or lead alloy anodes.
A typical bath composition which may be used in the invention to produce an improved chromium electrodeposit may comprise chromic acid in the amount of 50- 600 g./l. as CrO in combination with 0.01- g./l. of bromate ion. Other bath compatible materials may be incorporated in the bath. For example, inorganic sulfates and fluorides or complex fluorides and phosphates may be incorporated into the bath.
ingredients in the amounts indicated:
All amounts in grams per liter (g./1.) Chromic acid (CrO 50-600 Sulfate (SO 0.6-6 Bromate (1BrO 0.5-6 Acetic acid 10-25 The improved chromium deposit may be obtained using plating currents of 2-30 amperes per square decimeter (a.s.d.) at temperatures of 10-80' C. using plating times of one-half minute to one hour (typically 2-30 minutes).
The following examples are submitted for the purpose of illustration only and are not to be construed as limiting the scope of the invention in any way.
EXAMPLE 1 An aqueous chromium plating bath composition containing the following ingredients in the indicated amounts (all amounts in grams per liter, g./l., unless otherwise specified) was prepared:
Ingredient: Concentration (g./l.) CrO 200 SO 3.5 SiF 2.0
A panel of buffed brass containing a 45 bend measuring 75 x x 0.45 millimeters was cleaned and plated with a bright nickel deposit. The nickel plated panel was immersed in a Standard Hull Cell and the panel was connected as cathode. A total current of 8 amperes was passed through the solution for a time period of five minutes while maintaining the bath solution at about 35-45". C. The resulting chromium electrodeposit was satisfactory, but showed the usual minute defects in recessed areas of the bent portions of the test panel. I
To the above solution was added 1.0-1.5 g./l. of bromate ion (added as potassium bromate salt) and an identical test panel was chromium plated in the Standard Hull Cell under the same conditions of temperature, plating current and time. The resulting chromium electrodeposit showed improved coverage and the bath composition provided improved throwing power.
Similar improved results are obtained using sodium bromate, ammonium bromate, strontium bromate etc. either with or without suitable catalysts such as sulfates, silicofluorides, etc. I
EXAMPLE 2 The aqueous chromium plating bath composition of Example 1 was used with a mixture of 1.0 g./l. of NaBrO and 1.0 g./l. of KBrO A buffed brass panel plated with a nickel strike was chromium plated using the time, temperature, and plating current of Example 1 to produce an excellent chromium plate over the bent surfaces of the test panel.
Although this invention has been illustrated by reference to specific embodiments, modifications thereof which are clearly within the scope of the invention will be apparent to those skilled in the art.
I claim:
1. A process for electroplating chromium plate onto a basis metal which comprises passing current from an anode to a cathode at least a portion of which contains a cient to deposit a chromium electroplate having a' thickness of at least 1X 10- mm.) 7
2. A process as claimed in claim 1 wherein a portion of the bromate ion is provided by a bath compatible metal bromate or an ammonium bromate.
3. A process as claimed in claim 1 wherein a portion of the bromate ion is provided by an alkali metal bromate or NH BrO 4. A process as claimed in claim 1 wherein a portion of the bromate ion is provided by at least one member selected from the group consisting of KBrO NaBrO and NH BrO 5. A process as claimed in claim 1 wherein the aqueous acidic chromium plating bath composition contains 50- 600 g./l. of Cr and 0.01- g./l. of bromate anion BIO3.
6. A process as claimed in claim 1 wherein the aqueous acidic chromium plating bath composition contains:
(a) 50-600 g./l. of CrO (b) 0.01-100 g./l. of combined catalyst selected from the group consisting of sulfate ions and fluoride ions; and
(c) 0.01-10 g./l. of bromate anion BrO and wherein the aqueous acidic chromium plating bath composition is maintained at temperatures of -7 0 C.
7. A composition for electroplating chromium plate on a basis metal which comprises an aqueous acidic chromium plating bath composition containing:
(1) at least one chromium compound providing hexavalent chromium for electroplating chromium, sulfate ions such that the ratio of chromic acid to sulfate ion is between 100:1 and 550:1; and
,(2) bromate as cooperating additive to provide increased chromium throwing power.
8. A composition as claimed in claim 7 wherein a portion of the bromate ion is provided by a bath compatible metal bromate or an ammonium bromate.
9. A composition as claimed in claim 7 wherein a portion of the bromate ion is provided by an alkali metal bromate or NH BrO 10. A composition as claimed in claim 7 wherein a portion of the bromate ion is provided by at least one member selected from the group consisting of KBrO NaBrO and NH BrO 11. A composition as claimed in claim 7 wherein the aqueous acidic chromium plating bath composition contains 600 g./l. of CrO and 0.01-10 g./l. of bromate anion BIO 12. A composition as claimed in claim 7 wherein the aqueous acidic chromium plating bath composition contains:
(a) 50-600 g./l. of CrO (b) 0.01- g./l. of combined catalyst; and
(0) 001-10 g./l. of bromate anion BrOy.
References Cited UNITED STATES PATENTS 3,288,691 11/1966 Yonezaki et al. 204-56 3,341,434 9/1967 Passal 20451 3,505,183 4/1970 Seyb et al. 204-51 OTHER REFERENCES John L. Grifiin, Plating, pp. l96-203, February 1966.
GERALD L. KAPLAN, Primary Examiner
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US187470A | 1970-01-09 | 1970-01-09 |
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Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4093522A (en) * | 1975-01-10 | 1978-06-06 | Horst Dillenberg | Electrolytic chromic acid bath for chrome plating |
DE2909697A1 (en) * | 1978-03-14 | 1979-09-20 | Centre Rech Metallurgique | METAL STRIP SURFACE TREATMENT METHOD |
EP0073568A1 (en) * | 1981-08-24 | 1983-03-09 | M & T Chemicals, Inc. | Bright chromium plating baths |
GB2158100A (en) * | 1984-05-01 | 1985-11-06 | Nat Res Dev | Chromium electroplating bath |
DE3514673A1 (en) * | 1984-05-01 | 1985-11-07 | National Research Development Corp., London | GALVANIC CHROME BATH AND CHROME METHOD |
US4680099A (en) * | 1986-04-07 | 1987-07-14 | Raymund Singleton | Electroplating apparatus |
US5243320A (en) * | 1988-02-26 | 1993-09-07 | Gould Inc. | Resistive metal layers and method for making same |
US6197183B1 (en) * | 2000-02-18 | 2001-03-06 | Richard C. Iosso | Electrodeposition bath for wear-resistant zinc articles |
-
1970
- 1970-01-09 US US1874A patent/US3654101A/en not_active Expired - Lifetime
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4093522A (en) * | 1975-01-10 | 1978-06-06 | Horst Dillenberg | Electrolytic chromic acid bath for chrome plating |
DE2909697A1 (en) * | 1978-03-14 | 1979-09-20 | Centre Rech Metallurgique | METAL STRIP SURFACE TREATMENT METHOD |
EP0073568A1 (en) * | 1981-08-24 | 1983-03-09 | M & T Chemicals, Inc. | Bright chromium plating baths |
US4472249A (en) * | 1981-08-24 | 1984-09-18 | M&T Chemicals Inc. | Bright chromium plating baths and process |
GB2158100A (en) * | 1984-05-01 | 1985-11-06 | Nat Res Dev | Chromium electroplating bath |
DE3514673A1 (en) * | 1984-05-01 | 1985-11-07 | National Research Development Corp., London | GALVANIC CHROME BATH AND CHROME METHOD |
US4648947A (en) * | 1984-05-01 | 1987-03-10 | National Research Development Corp. | Chromium electroplating and bath therefor |
US4680099A (en) * | 1986-04-07 | 1987-07-14 | Raymund Singleton | Electroplating apparatus |
US5243320A (en) * | 1988-02-26 | 1993-09-07 | Gould Inc. | Resistive metal layers and method for making same |
US6197183B1 (en) * | 2000-02-18 | 2001-03-06 | Richard C. Iosso | Electrodeposition bath for wear-resistant zinc articles |
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