US3030283A - Process for the production of metal electrodeposits - Google Patents
Process for the production of metal electrodeposits Download PDFInfo
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- US3030283A US3030283A US735360A US73536058A US3030283A US 3030283 A US3030283 A US 3030283A US 735360 A US735360 A US 735360A US 73536058 A US73536058 A US 73536058A US 3030283 A US3030283 A US 3030283A
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- United States
- Prior art keywords
- copper
- electrodeposits
- impurities
- electroplating baths
- baths
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- 239000002659 electrodeposit Substances 0.000 title claims description 26
- 238000000034 method Methods 0.000 title claims description 16
- 230000008569 process Effects 0.000 title claims description 16
- 229910052751 metal Inorganic materials 0.000 title claims description 11
- 239000002184 metal Substances 0.000 title claims description 11
- 238000004519 manufacturing process Methods 0.000 title description 8
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 34
- 229910052802 copper Inorganic materials 0.000 claims description 34
- 239000010949 copper Substances 0.000 claims description 34
- 238000009713 electroplating Methods 0.000 claims description 34
- 239000012535 impurity Substances 0.000 claims description 31
- 238000005282 brightening Methods 0.000 claims description 21
- 239000003795 chemical substances by application Substances 0.000 claims description 19
- -1 AMINO COMPOUND Chemical class 0.000 claims description 16
- 239000002253 acid Substances 0.000 claims description 11
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims description 9
- 239000008233 hard water Substances 0.000 claims description 8
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 20
- 150000001875 compounds Chemical class 0.000 description 15
- 239000011734 sodium Substances 0.000 description 13
- 229910052708 sodium Inorganic materials 0.000 description 13
- 239000000654 additive Substances 0.000 description 12
- 230000002452 interceptive effect Effects 0.000 description 9
- 239000004215 Carbon black (E152) Substances 0.000 description 7
- 229930195733 hydrocarbon Natural products 0.000 description 7
- 229910052757 nitrogen Inorganic materials 0.000 description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- 229910000365 copper sulfate Inorganic materials 0.000 description 6
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 description 6
- 230000002411 adverse Effects 0.000 description 5
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 5
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- GEYOCULIXLDCMW-UHFFFAOYSA-N 1,2-phenylenediamine Chemical compound NC1=CC=CC=C1N GEYOCULIXLDCMW-UHFFFAOYSA-N 0.000 description 3
- RAXXELZNTBOGNW-UHFFFAOYSA-N 1H-imidazole Chemical compound C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 3
- LCZUOKDVTBMCMX-UHFFFAOYSA-N 2,5-Dimethylpyrazine Chemical compound CC1=CN=C(C)C=N1 LCZUOKDVTBMCMX-UHFFFAOYSA-N 0.000 description 3
- VARKIGWTYBUWNT-UHFFFAOYSA-N 2-[4-(2-hydroxyethyl)piperazin-1-yl]ethanol Chemical compound OCCN1CCN(CCO)CC1 VARKIGWTYBUWNT-UHFFFAOYSA-N 0.000 description 3
- FQYRLEXKXQRZDH-UHFFFAOYSA-N 4-aminoquinoline Chemical compound C1=CC=C2C(N)=CC=NC2=C1 FQYRLEXKXQRZDH-UHFFFAOYSA-N 0.000 description 3
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 3
- KWYHDKDOAIKMQN-UHFFFAOYSA-N N,N,N',N'-tetramethylethylenediamine Chemical compound CN(C)CCN(C)C KWYHDKDOAIKMQN-UHFFFAOYSA-N 0.000 description 3
- KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Chemical compound C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 3
- UDGSVBYJWHOHNN-UHFFFAOYSA-N n',n'-diethylethane-1,2-diamine Chemical compound CCN(CC)CCN UDGSVBYJWHOHNN-UHFFFAOYSA-N 0.000 description 3
- 125000004433 nitrogen atom Chemical group N* 0.000 description 3
- HKOOXMFOFWEVGF-UHFFFAOYSA-N phenylhydrazine Chemical compound NNC1=CC=CC=C1 HKOOXMFOFWEVGF-UHFFFAOYSA-N 0.000 description 3
- XSCHRSMBECNVNS-UHFFFAOYSA-N quinoxaline Chemical compound N1=CC=NC2=CC=CC=C21 XSCHRSMBECNVNS-UHFFFAOYSA-N 0.000 description 3
- 229910052717 sulfur Inorganic materials 0.000 description 3
- 239000011593 sulfur Substances 0.000 description 3
- XFNJVJPLKCPIBV-UHFFFAOYSA-N trimethylenediamine Chemical compound NCCCN XFNJVJPLKCPIBV-UHFFFAOYSA-N 0.000 description 3
- DDPRYTUJYNYJKV-UHFFFAOYSA-N 1,4-diethylpiperazine Chemical compound CCN1CCN(CC)CC1 DDPRYTUJYNYJKV-UHFFFAOYSA-N 0.000 description 2
- LLZRSOPHIGKISM-UHFFFAOYSA-N 1,4-diphenylpiperazine Chemical compound C1CN(C=2C=CC=CC=2)CCN1C1=CC=CC=C1 LLZRSOPHIGKISM-UHFFFAOYSA-N 0.000 description 2
- VEPOHXYIFQMVHW-XOZOLZJESA-N 2,3-dihydroxybutanedioic acid (2S,3S)-3,4-dimethyl-2-phenylmorpholine Chemical compound OC(C(O)C(O)=O)C(O)=O.C[C@H]1[C@@H](OCCN1C)c1ccccc1 VEPOHXYIFQMVHW-XOZOLZJESA-N 0.000 description 2
- NSMWYRLQHIXVAP-UHFFFAOYSA-N 2,5-dimethylpiperazine Chemical compound CC1CNC(C)CN1 NSMWYRLQHIXVAP-UHFFFAOYSA-N 0.000 description 2
- MSZQCNIEXFAWKV-UHFFFAOYSA-N 2,5-diphenylpyrazine Chemical compound C1=CC=CC=C1C1=CN=C(C=2C=CC=CC=2)C=N1 MSZQCNIEXFAWKV-UHFFFAOYSA-N 0.000 description 2
- MXDRPNGTQDRKQM-UHFFFAOYSA-N 3-methylpyridazine Chemical compound CC1=CC=CN=N1 MXDRPNGTQDRKQM-UHFFFAOYSA-N 0.000 description 2
- XWSSUYOEOWLFEI-UHFFFAOYSA-N 3-phenylpyridazine Chemical compound C1=CC=CC=C1C1=CC=CN=N1 XWSSUYOEOWLFEI-UHFFFAOYSA-N 0.000 description 2
- NUKYPUAOHBNCPY-UHFFFAOYSA-N 4-aminopyridine Chemical compound NC1=CC=NC=C1 NUKYPUAOHBNCPY-UHFFFAOYSA-N 0.000 description 2
- QZHXKQKKEBXYRG-UHFFFAOYSA-N 4-n-(4-aminophenyl)benzene-1,4-diamine Chemical compound C1=CC(N)=CC=C1NC1=CC=C(N)C=C1 QZHXKQKKEBXYRG-UHFFFAOYSA-N 0.000 description 2
- LRSYZHFYNDZXMU-UHFFFAOYSA-N 9h-carbazol-3-amine Chemical compound C1=CC=C2C3=CC(N)=CC=C3NC2=C1 LRSYZHFYNDZXMU-UHFFFAOYSA-N 0.000 description 2
- 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 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 2
- PCNDJXKNXGMECE-UHFFFAOYSA-N Phenazine Natural products C1=CC=CC2=NC3=CC=CC=C3N=C21 PCNDJXKNXGMECE-UHFFFAOYSA-N 0.000 description 2
- NQEQVKVMCQIFFB-UHFFFAOYSA-N [4-(hydroxymethyl)piperazin-1-yl]methanol Chemical compound OCN1CCN(CO)CC1 NQEQVKVMCQIFFB-UHFFFAOYSA-N 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 150000001879 copper Chemical class 0.000 description 2
- 125000005842 heteroatom Chemical group 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000011777 magnesium Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- NOUUUQMKVOUUNR-UHFFFAOYSA-N n,n'-diphenylethane-1,2-diamine Chemical compound C=1C=CC=CC=1NCCNC1=CC=CC=C1 NOUUUQMKVOUUNR-UHFFFAOYSA-N 0.000 description 2
- HUDSSSKDWYXKGP-UHFFFAOYSA-N n-phenylpyridin-2-amine Chemical compound C=1C=CC=NC=1NC1=CC=CC=C1 HUDSSSKDWYXKGP-UHFFFAOYSA-N 0.000 description 2
- OKBVMLGZPNDWJK-UHFFFAOYSA-N naphthalene-1,4-diamine Chemical compound C1=CC=C2C(N)=CC=C(N)C2=C1 OKBVMLGZPNDWJK-UHFFFAOYSA-N 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- ATGUVEKSASEFFO-UHFFFAOYSA-N p-aminodiphenylamine Chemical compound C1=CC(N)=CC=C1NC1=CC=CC=C1 ATGUVEKSASEFFO-UHFFFAOYSA-N 0.000 description 2
- BXRNXXXXHLBUKK-UHFFFAOYSA-N piperazine-2,5-dione Chemical compound O=C1CNC(=O)CN1 BXRNXXXXHLBUKK-UHFFFAOYSA-N 0.000 description 2
- 238000005498 polishing Methods 0.000 description 2
- KIDHWZJUCRJVML-UHFFFAOYSA-N putrescine Chemical compound NCCCCN KIDHWZJUCRJVML-UHFFFAOYSA-N 0.000 description 2
- PBMFSQRYOILNGV-UHFFFAOYSA-N pyridazine Chemical compound C1=CC=NN=C1 PBMFSQRYOILNGV-UHFFFAOYSA-N 0.000 description 2
- 150000003254 radicals Chemical class 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 1
- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 description 1
- 239000001934 2,5-dimethylpyrazine Substances 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- BHPQYMZQTOCNFJ-UHFFFAOYSA-N Calcium cation Chemical compound [Ca+2] BHPQYMZQTOCNFJ-UHFFFAOYSA-N 0.000 description 1
- 208000010228 Erectile Dysfunction Diseases 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- VTLYFUHAOXGGBS-UHFFFAOYSA-N Fe3+ Chemical compound [Fe+3] VTLYFUHAOXGGBS-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 1
- BGRDGMRNKXEXQD-UHFFFAOYSA-N Maleic hydrazide Chemical compound OC1=CC=C(O)N=N1 BGRDGMRNKXEXQD-UHFFFAOYSA-N 0.000 description 1
- 239000004902 Softening Agent Substances 0.000 description 1
- 241000272534 Struthio camelus Species 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Natural products NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 230000001464 adherent effect Effects 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- DMLAVOWQYNRWNQ-UHFFFAOYSA-N azobenzene Chemical compound C1=CC=CC=C1N=NC1=CC=CC=C1 DMLAVOWQYNRWNQ-UHFFFAOYSA-N 0.000 description 1
- HFACYLZERDEVSX-UHFFFAOYSA-N benzidine Chemical compound C1=CC(N)=CC=C1C1=CC=C(N)C=C1 HFACYLZERDEVSX-UHFFFAOYSA-N 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 229910001424 calcium ion Inorganic materials 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 125000001664 diethylamino group Chemical group [H]C([H])([H])C([H])([H])N(*)C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 229960004979 fampridine Drugs 0.000 description 1
- 229910001447 ferric ion Inorganic materials 0.000 description 1
- 150000002391 heterocyclic compounds Chemical class 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 229910001425 magnesium ion Inorganic materials 0.000 description 1
- 125000000250 methylamino group Chemical group [H]N(*)C([H])([H])[H] 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 229940067157 phenylhydrazine Drugs 0.000 description 1
- IJAPPYDYQCXOEF-UHFFFAOYSA-N phthalazin-1(2H)-one Chemical compound C1=CC=C2C(=O)NN=CC2=C1 IJAPPYDYQCXOEF-UHFFFAOYSA-N 0.000 description 1
- 238000007747 plating Methods 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 239000003352 sequestering agent Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 150000003458 sulfonic acid derivatives Chemical class 0.000 description 1
- 239000008399 tap water Substances 0.000 description 1
- 235000020679 tap water Nutrition 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
-
- 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
- C25D3/38—Electroplating: Baths therefor from solutions of copper
Definitions
- Still another objects of our invention is to provide additives for copper electroplating baths which will overcome the adverse effects of inorganic impurities contained in such baths on the brightness of the metal electrodeposited therefrom.
- Still other compounds which, when added to electroplating baths, will render inorganic impurities in the baths impotent as interfering substances in accordance with our invention are heterocyclic compounds which contain two nitrogen atoms in the molecule of a fiveor six-membered ring system, and their derivatives.
- the additives of our invention may be used with a number of sulfonic acid brightening compounds which have been completely described in my copending application Ser. No. 442,199, now Patent No. 2,849,351. A number of examples of these compounds are shown in Table 1. These are brighteners which produce copper electrodeposits of a brightness requiring no further polishing. These brightening compounds are generally used in the quantity of 0.01 to 20 grams per liter of electroplating bath.
- 2-arninopyridine (23) 4-aminopyridine (24) 2-anilino-pyridine (25) 4-amino-quinoline (26) 4-amino-lipidiue (27) 3-amino-carbazole (28) 3,7-dimethyl-3,G-diamino-acridine (29) Pyrazine (30) 2,5-dimethylpyrazine (31) 2,5-diphenylpyrazine (32) Quinoxaline (33) Phenazine (34) Piperazine (35) Z-methylpiperazine (36) 2,5-dimethylpiperazine (37) N,N'-diethylpiperazine (38) N,N'-dihydroxymethylpiperazine (39) N,N'-dihydroxyethylpiperazine (40) N,N'-diphenylpiperazine (41) 2,5-diketopiperazine (42) N,N-diethyl-2,S-diketopiperazine (43) N,N-dibenzylpiperazine (44) Pyrida
- the amounts in which the additives in accordance with our invention can be added to produce the desired eifect range from about 0.01 gm./liter of bath to about 20 gm./liter of bath, but the preferred amount is from 3 to 12 gm./ liter of bath.
- the precise amounts required vary from one additive to the other and are also dependent upon the type of brightening agent employed and the amount and kind of inorganic impurities present in the bath.
- objects can be electroplated in such baths at temperatures ranging from 30 C. to 60 C., and with current densities ranging from 0.5 to 15 amp./dm.
- the use of the additives in accordance with our invention does not require any change in the composition of the electroplating baths commonly used, nor does it require any change in the conditions under which objects are usually electroplated, particularly with respect to the temperature of the plating bath and the current densities usually employed.
- the additives we use are soluble in the usual acid copperplating baths containing the usual copper salts in an acid aqueous solution. The additives are not decomposed during the electroplating process.
- additives for electroplating baths in accordance with our invention can be used in con junction with any copper electroplating bath containing a sulfonic acid brightening agent and in which the quality of the metal electrodeposits produced therefrom are adversely affected by impurities of the type described.
- Various combinations of brightening agents and the additives of the invention may be made. Table 3 sets forth a number of specific examples of such combinations.
- Agent of Preferred Agent of Preferred Combination N 0. Table 1, Ooncen- Table 2, Concen- No. tration, No. tration,
- X is an organic radical selected from the group consisting of bivalent acyclic hydrocarbon radicals, bivalent cyclic hydrocarbon radicals, and heterocyclic hydrocarbon radicals which include at least one of the nitrogen'atoms, and R 'R R and R are selected from the group consisting of hydrogen, substituted hydrocarbon radicals and unsubstituted hydrocarbon radicals, whereby said impurities are prevented from interfering with the production of bright metal electrodeposits.
- step 2 which comprises adding to such electroplating baths 0.01 to 20 g./l. of l,3-bis-(diethylamino)- propanol-Z, whereby said impurities are prevented from interfering with the production of bright copper electrodeposits.
- step 3 which comprises adding to such electroplating baths 0.01 to 20 g./l. of 1,3-bis-(diethylamino)-propanol-2, whereby said impurities are prevented from interfering with the production of bright copper electrodeposits.
- step 4 which comprises adding to such electroplating baths 0.01 to 20 g./l. of 1,3-bis-(diethylamino)-propanol-2, whereby said impurities are prevented from interfering with the production of bright copper electrodeposits.
- step 5 which comprises adding to such electroplating baths 0.01 to 20 g./l. of l,3-bis-(diethylamino)- propanol 2, whereby said impurities are prevented from interfering with the production of bright copper electrodeposits.
- step 6 which comprises adding 0.01 to 20 g./l. of N,N-diethyl-ethylenediamine to such electroplating baths, whereby said impurities are prevented from interfering with the production of bright copper electrodeposits.
- step 7 which comprises adding to such electroplating baths 0.01 to 20 g./l. of N,N,N,N-tetraethanol-ethylenediamino, whereby said impurities are prevented from interfering with the production of bright copper electrodeposits.
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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
3,030,283 PROCESS FOR THE PRODUCTIUN F METAL ELECTRODEPOSITS Wennemar Strauss, Dusseldorf-Benrath, Wolfgang Gundel, Duseldorf-Oberkassel, Alfred Kirstahler, Dusseldorf, and Wolf-Dieter Willmund, Dusseldorf-Holthausen,-Germany, assignors to Dehydag, Deutsche Hydrierwerke G.m.b.H., Dusseldorf, Germany, a corporation of Germany No Drawing. Filed May 15, 1958, Ser. No. 735,360 Claims priority, application Germany Mar. 13, 1954 Claims. (Cl. 204-52) This invention relates to a process for producing metal electrodeposits, and more particularly to additives for copper electroplating baths which are capable of eliminating the adverse effects of impurities in such baths upon the quality of the metal deposits produced by means of such baths.
It is known that copper electroplates which exhibit a so-called semi-brightness can be produced with the aid of customary brightening agents, such as thiourea. As we have disclosed in our prior applications, namely Ser. No. 442,199, now Patent No. 2,849,351, and to a certain extent Ser. No. 464,638, now Patent No. 2,830,014, there are brightening agents which, in contrast to the known brightening gagents, produce electroplates which exhibit full brightness; that is, electroplates which can be further utilized directly without subsequent polishing. These brightening agents are the sulfonic acid derivatives of compounds containing sulfur, nitrogen or oxygen atoms. We have now found that this full brightness is achieved in its best form only if the copper baths are compounded with distilled water and if chemically pure copper salts are used, which is not customary in industry, especially since impurities are always introduced into these baths under conditions of industrial operation. If these highgrade brightening agents are used in electroplating baths which have been compounded with technical-grade tap water-that is, water which contains calcium and magnesium ions-and which contain the customary technicaltent as substances which reduce the qualities of electrodeposits produced from such baths.
Still another objects of our invention is to provide additives for copper electroplating baths which will overcome the adverse effects of inorganic impurities contained in such baths on the brightness of the metal electrodeposited therefrom.
Other objects and advantages will become apparent as the description of our invention proceeds.
We have found that the adverse efiect of inorganic impurities upon the qualities of electrodeposits produced 3,030,283 Patented Apr. 17, 1962 ICC from copper electroplating baths containing, in addition, sulfonic acid brighteners, can be eliminated by adding small amounts of amino compounds free from carboxyl groups to the electroplating bath. Compounds which are added according to our invention have the general structural formula wherein R R R and R are hydrogen or hydrocarbon radicals, and X is a bivalent acylic or cyclic hydrocarbon radical or a heterocyclic ring system which includes one or both of the nitrogen atoms. The hydrocarbon radicals above refer-red to may also include heteroatoms, such as oxygen, sulfur or nitrogen, as well as heteroatom groups derived therefrom. Furthermore, the above hydrocarbon radicals may also have substituents containing oxygen, sulfur or nitrogen atoms.
Other compounds which can be added to electroplating baths containing inorganic impurities of the types referred to above in order to render such impurities inettective as interfering substances are those which contain a =NN= or N=N group.
Still other compounds which, when added to electroplating baths, will render inorganic impurities in the baths impotent as interfering substances in accordance with our invention are heterocyclic compounds which contain two nitrogen atoms in the molecule of a fiveor six-membered ring system, and their derivatives.
The additives of our invention may be used with a number of sulfonic acid brightening compounds which have been completely described in my copending application Ser. No. 442,199, now Patent No. 2,849,351. A number of examples of these compounds are shown in Table 1. These are brighteners which produce copper electrodeposits of a brightness requiring no further polishing. These brightening compounds are generally used in the quantity of 0.01 to 20 grams per liter of electroplating bath.
Table 1 acid-n-propylester-w-sodi- (l1) N-hydroXyethyl-dithiocarbamic acid-n-propylesterw-sodium sulfonate (12) N,N-pentarnethylene-dithiocarbamic acid-n-propylester-w-sodium sulfonate (l3) N-piperazino-dithioformic acid-n-propylester-w-sdium sulfonate (14) 2-mercaptobenzothiazole-S-propane-w-sodium sulfonate (15 S-phenyl-trithiocarbonic acid-S-propane w sodium sulfonate (16) Isothiourea-S-butanew-sulfOnic acid (17) S-phenyl-l,3,4-oxdiazolyl 2 mercaptopropane-wpotassium sulfonate In place of the -n-propylester-w-sulfonic acid radicals, the above compounds may also contain the following:
radicals:
(a) -Ethylester-w-sodium sulfonate (b) -Butylester-w-sodium sulfonate (c) -2-hydroxypropylester-w-sodium sulfonate (d) -2-chloropropylester-w-sodium sulfonate (e) -Isopropylester-w-sodium sulfonate (f) -Benzylester sodium sulfonate Examples of the compounds which are added according to our invention to prevent the adverse efiects of impurities on bright copper electrodeposits are set forth in Table 2.
Table 2 (1) Ethylene diamine (2) N,N-diethyl-ethylenediamine (3) N,N,N,N'-tetraethyl-ethylenediamine (4) N,N'-diphenyl-ethylenediamine (5) N,N'-diethanol-ethylenedianiine (6) N,N,N',N'-tetraethanol-ethylenediamine (7) 1,3-propylenediamine (8) 1,4-tetramethylenediamine (9) 1,6-hexamethylenediamine (10) Diethylenetriarnine 1 l Triethlenetetramine 2.) Hydrazine (13) Phenylhydrazine (14) Azobenzene 15) 1,2-phenylenediamine (16) 1,4-phenylenediamine 17) 1,4-naphthylenediamine (18) 4-amino-diphenylamine (19) 4,4'-diamino-diphenylamine (20) 4,4-diamine-diphenylmethane (21) Benzidine (22). 2-arninopyridine (23) 4-aminopyridine (24) 2-anilino-pyridine (25) 4-amino-quinoline (26) 4-amino-lipidiue (27) 3-amino-carbazole (28) 3,7-dimethyl-3,G-diamino-acridine (29) Pyrazine (30) 2,5-dimethylpyrazine (31) 2,5-diphenylpyrazine (32) Quinoxaline (33) Phenazine (34) Piperazine (35) Z-methylpiperazine (36) 2,5-dimethylpiperazine (37) N,N'-diethylpiperazine (38) N,N'-dihydroxymethylpiperazine (39) N,N'-dihydroxyethylpiperazine (40) N,N'-diphenylpiperazine (41) 2,5-diketopiperazine (42) N,N-diethyl-2,S-diketopiperazine (43) N,N-dibenzylpiperazine (44) Pyridazine (45) 3-methylpyridazine (46) 3-phenylpyridazine (47) Diketotetrahydropyridazine (maleic acid hydrazide) 4 Phthalazine (4,5-benzopyridazine) Cinnoline (5,6-benzopyridazine) Phthalazone Pyrirnidine 2,4-dimethyl-6-aminopyrimidine 2,6-dihydroxypyrimidine (Uracil) 2,4,6-trihydroxypyrimidine 1,3-diphenylhexahydropyrimidine Quinazoline 3,4-dihydroquinazoline Tetrahydroquinazoline Pyrazole l-phenylpyrazole Glyoxaline Z-methylimidazole Benzimidazole Z-phenylbenzimidazole 1,3-bis-( diethylamino) -propanol-2 1,3-bis-(dipropylamino)-propano1-2 1,3-bis-(diisopropylamino)-propanol-2 1,3-bis-(dibutylamino)-propanol-2 1-diethylamino-2-methyl-dodecyl-amino-propanol-Z 1-diethylamino-3-dodecylamino-propanol-2 1-mcthylanilino-3-diethylamino-propanol-2 1-methylanilino-3-piperidino-propano1-2 1-methylanilino3-morpholino-propanol-2 1-cyc1ohexylarnino-3-diethylamino-propanol-2 1,3-bis-(cyclohexylamino)-propanol-2 (76) 1-dicyclohexyl-amino-3-diethylamino-propanol-2 (77 1 dicyclohexyl amino 3 cyclhexylamino propanol-2 (78) 1,3-bis- (dicycloheXyl-amino -propanol-2 (79) 1,3-bis-(methyl-ethyl-amino)-propanol-2 1,3-bisethylamino -propano1-2 (81) 1,3 -bis- (methylamino -propanol-2 (82) N,N'-bis bis (3-diethylanrino-Z-hydroxy-propyl)- piperazine When any of the compounds from- Table 2 or mixtures thereof are added to copper electroplating baths containing sulfonic acid brightening agents, electrodeposits produced thereby are bright and lustrous despite the fact that the bath contains impurities of the type described above, such as impurities which cause hardness, etc. Such bright deposits are obtained over the entire efiective range of current densities. In addition, these additives have the further advantage that they increase the ductility of the electrodeposits.
The amounts in which the additives in accordance with our invention can be added to produce the desired eifect range from about 0.01 gm./liter of bath to about 20 gm./liter of bath, but the preferred amount is from 3 to 12 gm./ liter of bath. The precise amounts required vary from one additive to the other and are also dependent upon the type of brightening agent employed and the amount and kind of inorganic impurities present in the bath. In general, objects can be electroplated in such baths at temperatures ranging from 30 C. to 60 C., and with current densities ranging from 0.5 to 15 amp./dm.
While the theory of the action of such additives in baths containing impurities of the nature described is not fully understood, it has been found that they do not function as softening agents in the usual sense and cannot be replaced by the typical water-softening substances such as sequestering agents and detergents. Nevertheless, they are capable of completely eliminating the disturbing effects of magnesium and calcium ions, introduced by the tap water, and of ferric ions, introduced by the technical grade metal salts used to prepare the electroplating baths, during the electroplating process. It is believed that their effectiveness comes into play on the metal surface of the objects being electroplated, which is indicated by the high concentrations which are required in some instances to produce the desired effect.
The use of the additives in accordance with our invention does not require any change in the composition of the electroplating baths commonly used, nor does it require any change in the conditions under which objects are usually electroplated, particularly with respect to the temperature of the plating bath and the current densities usually employed. In the form of amines the additives we use are soluble in the usual acid copperplating baths containing the usual copper salts in an acid aqueous solution. The additives are not decomposed during the electroplating process.
The above-described additives for electroplating baths in accordance with our invention can be used in con junction with any copper electroplating bath containing a sulfonic acid brightening agent and in which the quality of the metal electrodeposits produced therefrom are adversely affected by impurities of the type described. Various combinations of brightening agents and the additives of the invention may be made. Table 3 sets forth a number of specific examples of such combinations.
The examples of Table 3 will enable persons skilled in the art to understand our invention more completely. However, it will be understood that there is no intention on our part of limiting our invention to these examples.
Table 3 In an acid copper bath which contains 100-240 gm./ liter CuSO .5H O and 10-100 gm./liter H SO the following combinations of brightening agent and diamino compounds free from carboxyl groups are used to produce full bright copper electrodeposits:
Agent of Preferred Agent of Preferred Combination N 0. Table 1, Ooncen- Table 2, Concen- No. tration, No. tration,
gun/liter gmJliter 120 0.5 65 5.0 14 1. 5 2 6.0 4!) 0. 5 6 4. 1 0.8 39 7.0 16 2.0 10 5. 0 7b 0. 13 4. 0 1b 0.25 9 6.0 10 0.1 67 O. 25 0.25 65 0. 3 6f 0. 2 68 0. 2 46 0.1 75 0.1 111 0.05 80 0.6 1a 0.05 69 0. 1 17a 0 03 74 0.1 158 0.25 79 0.5
1a 0.05 82 0.05 1a 07 1 5s 0. 8e 0. 1 38 2.00 0.05 55 0.2 9 0.2 40 0.5 13 0. 25 65 0. 7 2a 0.05 72 0. 1 1e 0.05 81 1. 2
Objects electroplated according to the baths the examples over wide ranges of current densities were provided with a highly lustrous, very bright, adherent and ductile copper plate. These copper plates are much improved over those obtained with the use of the brightening compounds alone.
While we have disclosed certain specific embodiments of our invention, we wish it to be understood that various changes and modifications may be made without departing from the spirit of our invention or the scope of the appended claims.
This application is a cont-innation-in-part of our previous application Ser. No. 458,984, filed September 28, 1954, now abandoned.
We claim:
1. In a process of producing bright copper electrodeposits from acid copper electroplating baths containing impurities found in hard water and in technical grade metal salts, and containing a sulfonic acid brightening agent, the step which comprises adding to such electroplating baths 0.01 to 20 g./l. of an amino compound free 6 from carboxyl groups having the general structural formula wherein X is an organic radical selected from the group consisting of bivalent acyclic hydrocarbon radicals, bivalent cyclic hydrocarbon radicals, and heterocyclic hydrocarbon radicals which include at least one of the nitrogen'atoms, and R 'R R and R are selected from the group consisting of hydrogen, substituted hydrocarbon radicals and unsubstituted hydrocarbon radicals, whereby said impurities are prevented from interfering with the production of bright metal electrodeposits.
2. In a process of producing bright copper electrodeposits from acid copper electroplating baths containing impurities found in hard water and in technical grade copper sulfate, and containing a sulfonic acid brightening agent, the step which comprises adding to such electroplating baths 0.01 to 20 g./l. of l,3-bis-(diethylamino)- propanol-Z, whereby said impurities are prevented from interfering with the production of bright copper electrodeposits.
3. In a process of producing bright copper electrodeposits from acid copper electroplating baths containing impurities found in hard water and in technical grade copper sulfate and containing N,N'-pentarnethylene-dithiocarbamic acid-n-butylester-w-sodium sulfonate as a brightening agent, the step which comprises adding to such electroplating baths 0.01 to 20 g./l. of 1,3-bis-(diethylamino)-propanol-2, whereby said impurities are prevented from interfering with the production of bright copper electrodeposits.
4. In a process of producing bright copper electrodeposits from acid copper electroplating baths containing impurities found in hard water and in technical grade copper sulfate and containing Z-mercapto-benzothiazole- S-propane-w-sodium sulfonate as a brightening agent, the step which comprises adding to such electroplating baths 0.01 to 20 g./l. of 1,3-bis-(diethylamino)-propanol-2, whereby said impurities are prevented from interfering with the production of bright copper electrodeposits.
5. In a process of producing bright copper electrodeposits from acid copper electroplating baths containing impurities found in hard water and in technical grade copper sulfate and containing N,N-dimethyl-dithiocarbamic acid-n-butyl ester-w-sodium sulfonate as a brightening agent, the step which comprises adding to such electroplating baths 0.01 to 20 g./l. of l,3-bis-(diethylamino)- propanol 2, whereby said impurities are prevented from interfering with the production of bright copper electrodeposits.
6. In a process of producing bright copper electrodeposits from acid copper electroplating baths containing impurities found in hard water and technical grade copper sulfate and containing a sulfonic acid brightening agent, the step which comprises adding 0.01 to 20 g./l. of N,N-diethyl-ethylenediamine to such electroplating baths, whereby said impurities are prevented from interfering with the production of bright copper electrodeposits.
7. In a process of producing bright copper electrodeposits from acid copper electroplating baths containing impurities found in hard water and technical grade copper sulfate and containing a sulfonic acid brightening agent, the step which comprises adding to such electroplating baths 0.01 to 20 g./l. of N,N,N,N-tetraethanol-ethylenediamino, whereby said impurities are prevented from interfering with the production of bright copper electrodeposits.
8. The process of claim 1 wherein the compound added to counteract impurities in the electroplating bath is 1,6- hexamethylene diamine.
9. The process of claim 1 wherein the compound added to counteract impurities in the electroplating bath is 1,3- bis- (diethylamino) -prop ano1-2.
10. The process of claim 1 wherein the compound added to counteract impurities in the electroplating bath is N,N'-dihydroXyethyl-piperazine.
References Cited in the file of this patent UNITED STATES PATENTS 2,195,454- Greenspan Apr. 2, 1 940 2,355,070 Harford Aug. 8, 1944 8 Gundel June 3, 1958 Gundel Aug. 26, 1958 FOREIGN PATENTS I France Mar. 5, 1956 ermany Sept. 3, 1953 Great Britain Mar. 21, 1939 OTHER REFERENCES Transactions Electrochemical see, vol. 71 1937); pp;
Transactions Electrochemical sac, Vol 73 (1938), pp.-
Claims (1)
1. IN A PROCESS OF PRODUCING BRIGHT COPPER ELECTRODEPOSITS FROM ACID COPPER ELECTROPLATING BATHS CONTAINING IMPURITIES FOUND IN HARD WATER AND IN TECHNICAL GRADE METAL SALTS, AND CONTAINING A SULFONIC ACID BRIGHTENING AGENT, THE STEP WHICH COMPRISES ADDING TO SUCH ELECTROPLATING BATHS 0.01 TO 20 G/L. OF AN AMINO COMPOUND FREE FROM CARBOXYL GROUPS HAVING THE GENERAL STRUCTURAL FORMULA
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DED17304A DE1000204B (en) | 1954-03-13 | 1954-03-13 | Process for the production of galvanic copper coatings |
| DED24913A DE1030133B (en) | 1954-03-13 | 1957-02-13 | Process for the production of galvanic copper coatings |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3030283A true US3030283A (en) | 1962-04-17 |
Family
ID=25970685
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US714687A Expired - Lifetime US2986498A (en) | 1954-03-13 | 1958-02-12 | Process for the production of metal electrodeposits |
| US735360A Expired - Lifetime US3030283A (en) | 1954-03-13 | 1958-05-15 | Process for the production of metal electrodeposits |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US714687A Expired - Lifetime US2986498A (en) | 1954-03-13 | 1958-02-12 | Process for the production of metal electrodeposits |
Country Status (6)
| Country | Link |
|---|---|
| US (2) | US2986498A (en) |
| BE (2) | BE534101A (en) |
| CH (2) | CH340395A (en) |
| DE (1) | DE1030133B (en) |
| FR (1) | FR1118019A (en) |
| GB (2) | GB807574A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20130313119A1 (en) * | 2012-05-25 | 2013-11-28 | Trevor Pearson | Additives for Producing Copper Electrodeposits Having Low Oxygen Content |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE563647A (en) * | 1954-03-13 | |||
| DE1235101B (en) * | 1959-08-21 | 1967-02-23 | Langbein Pfanhauser Werke Ag | Electrolyte with gloss additive for galvanic deposition of mirror-glossy, leveled, ductile nickel deposits |
| US3787297A (en) * | 1971-10-26 | 1974-01-22 | Conversion Chem Corp | Zinc plating bath and method |
| DE2355581C3 (en) * | 1973-11-07 | 1979-07-12 | Deutsche Gold- Und Silber-Scheideanstalt Vormals Roessler, 6000 Frankfurt | Galvanic bright gold bath with high deposition rate |
| US4376685A (en) * | 1981-06-24 | 1983-03-15 | M&T Chemicals Inc. | Acid copper electroplating baths containing brightening and leveling additives |
| PL3502320T3 (en) * | 2017-12-22 | 2021-03-08 | Atotech Deutschland Gmbh | A method for increasing corrosion resistance of a substrate comprising an outermost chromium alloy layer |
| WO2025114220A1 (en) * | 2023-11-30 | 2025-06-05 | Basf Se | Non-acidic composition for copper electroplating comprising a defect reduction agent |
Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB503095A (en) * | 1937-10-04 | 1939-03-31 | Bruno Friedrich Schweig | Improvements in the production of electrodeposits of copper |
| US2195454A (en) * | 1939-01-07 | 1940-04-02 | Louis Weisberg Inc | Electrodeposition of copper |
| US2355070A (en) * | 1937-07-03 | 1944-08-08 | Little Inc A | Electrolytic deposition of metal |
| DE888493C (en) * | 1951-11-03 | 1953-09-03 | Hydrierwerke A G Deutsche | Process for the production of firmly adhering and shiny galvanic copper coatings |
| FR1118019A (en) * | 1954-03-13 | 1956-05-30 | Dehydag | Process for preparing galvanic metal coatings |
| US2837472A (en) * | 1953-09-19 | 1958-06-03 | Dehydag Gmbh | Brighteners for electroplating baths |
-
0
- BE BE563647D patent/BE563647A/xx unknown
- BE BE534101D patent/BE534101A/xx unknown
-
1954
- 1954-12-28 CH CH340395D patent/CH340395A/en unknown
-
1955
- 1955-01-20 FR FR1118019D patent/FR1118019A/en not_active Expired
- 1955-03-11 GB GB7161/55A patent/GB807574A/en not_active Expired
-
1957
- 1957-02-13 DE DED24913A patent/DE1030133B/en active Pending
-
1958
- 1958-01-07 CH CH5441958A patent/CH370612A/en unknown
- 1958-02-12 US US714687A patent/US2986498A/en not_active Expired - Lifetime
- 1958-02-12 GB GB4550/58A patent/GB884035A/en not_active Expired
- 1958-05-15 US US735360A patent/US3030283A/en not_active Expired - Lifetime
Patent Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2355070A (en) * | 1937-07-03 | 1944-08-08 | Little Inc A | Electrolytic deposition of metal |
| GB503095A (en) * | 1937-10-04 | 1939-03-31 | Bruno Friedrich Schweig | Improvements in the production of electrodeposits of copper |
| US2195454A (en) * | 1939-01-07 | 1940-04-02 | Louis Weisberg Inc | Electrodeposition of copper |
| DE888493C (en) * | 1951-11-03 | 1953-09-03 | Hydrierwerke A G Deutsche | Process for the production of firmly adhering and shiny galvanic copper coatings |
| US2837472A (en) * | 1953-09-19 | 1958-06-03 | Dehydag Gmbh | Brighteners for electroplating baths |
| US2849351A (en) * | 1953-09-19 | 1958-08-26 | Dehydag Gmbh | Electroplating process |
| FR1118019A (en) * | 1954-03-13 | 1956-05-30 | Dehydag | Process for preparing galvanic metal coatings |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20130313119A1 (en) * | 2012-05-25 | 2013-11-28 | Trevor Pearson | Additives for Producing Copper Electrodeposits Having Low Oxygen Content |
| JP2015521237A (en) * | 2012-05-25 | 2015-07-27 | マクダーミッド アキューメン インコーポレーテッド | Additives for producing copper electrodeposits with low oxygen content |
| US9243339B2 (en) * | 2012-05-25 | 2016-01-26 | Trevor Pearson | Additives for producing copper electrodeposits having low oxygen content |
Also Published As
| Publication number | Publication date |
|---|---|
| BE563647A (en) | |
| GB807574A (en) | 1959-01-21 |
| FR1118019A (en) | 1956-05-30 |
| GB884035A (en) | 1961-12-06 |
| CH340395A (en) | 1959-08-15 |
| BE534101A (en) | |
| US2986498A (en) | 1961-05-30 |
| DE1030133B (en) | 1958-05-14 |
| CH370612A (en) | 1963-07-15 |
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