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Electrodeposition of copper from acidic baths

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US3267010A
US3267010A US18792662A US3267010A US 3267010 A US3267010 A US 3267010A US 18792662 A US18792662 A US 18792662A US 3267010 A US3267010 A US 3267010A
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copper
liter
bath
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baths
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Creutz Hans-Gerhard
Richard M Stevenson
Edward A Romanowski
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OMI International Corp
Udylite Corp
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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
    • C25D3/38Electroplating: Baths therefor from solutions of copper

Description

United States Patent 3,267,010 ELECTRODEPOSITION OF COPPER FROM ACIDIC BATHS Hans-Gerhard Creutz, Wayne, Richard M. Stevenson, Grosse Pointe Woods, and Edward A. Romanowslii, Troy, Mich., assignors, by mesne assignments, to The Udylite Corporation, Warren, Mich., a corporation of Delaware No Drawing. Filed Apr. 16, 1962, Ser. No. 187,926 26 Claims. (Cl. 20452) This invention relates to the electrodeposition of copper from aqueous acidic baths, especially from acidic copper sulfate and fl-uoborate baths. More particularly it relates to the use of certain organic compounds in the baths in new relationships which make possible bright, highly ductible, low stress, good leveling copper deposits.

While a rather large number of organic compounds have been proposed and used to decrease the grain size and increase the luster of the copper deposits from acidic baths, nevertheless, much remains to be desired from the standpoint of obtaining lustrous leveling copper plate without striations and ribbing and without substantially decreasing the very high ductibility of the copper plate from the acidic baths.

It has now been found that bath-soluble polymers of 1,3-dioxolane,

which have molecular weights greater than 296 and at least up to about 30,000, make possible smooth, low stress, ductile semi-bright copper plate that is free from striations, from acidic copper sulfate or acidic copper fluoborate baths. For example, it about 0.1 gram/liter of a poly-1,3-dioxolane of average molecular weight of about 5,000 is added to an acid copper hath made up of 150 to 275 grams/ liter of blue vitriol and containing about 3 to 70 grams/liter of sulfuric acid, a very smooth semihr-ight copper plate is obtained within a current density range from the very lowest to the burning point or limiting current density, which with ordinary agitation is around 100 to 150 amps./ sq. ft., but is higher withvery rapid solution agitation. In the acidic fluoborate bath containing about 150 to at least 450 grams/liter of copper fluoborate and about 0.5 to at least 30 grams/ liter of fluoboric acid, even higher current densities can be used at the same bath temperatures and the same excellent copper plate can be obtained with the addition of about 0.1 gram/liter of the poly-dioxolane of average molecular weight of about 5,000. With lower molecular weight polymers, for example about 400 to 1,000, larger concentrations up to at least 5 grams/liter should be used. With the higher molecular weight polymers, i.e., about 5,000 and higher, concentrations as low as about 0.01 gram/liter can be used with good results, especially when used in conjunction with other organic additives.

In contrast with other high molecular weight polymers, no striations or ribbing of the plate occurs from the use of these poly-dioxolanes, and it is not essential to have present in the bath concentrations of chloride or bromide ion of at least about 0.02 to 0.1 gram/ liter.

It was further found that the 1,3-dioxolane polymers when used together in the acidic copper baths with very low concentrations of certain organic sulfide (thiols, thioethers, etc.) compounds carrying sulfonic groups such as those of Table I, enable the electrode'position of smooth bright copper plate without decreasing appreciably the ductility of the copper deposits. The organic sulfide compounds carrying sulfonic groups illustrated in Table I when used alone in the baths in the low concentrations 3,267,010 Patented August 16, 1966 "ice of 0.0005 to 0.04 gram/liter or even up to 0.1 gram/liter do not produce any noticeable or significant brightness and require a concentration of at least 1 gram/liter to produce brightness when used alone, though even then they do not produce the highest brightness. For example, the sulfonated organic sulfides first described for use in acidic copper baths by Henricks US. Patent 2,424,- 887, July 29, 1947, such as th-ianthrene sulfonic acids, Example 4, Table I, and the phenyl disulfide sulfonic acids, Example 5, Table I, used in as low concentrations as 0.0005 to 0.01 gram/liter with about 0.05 to 0.2 gram/liter of the high molecular weight 1,3-dioxolane polymers cooperate to give bright ductile copper deposits. However, when sulfonated thianthrene, for example, is used alone, or with a similar sul-fonated organic sulfide, in an acidic copper bath as shown in Example 8 of US. 2,424,887, it is necessary to use 1 to 2 grams/liter for brightness. In otherwords, when used in conjunction with the high molecular weight polymers of 1,3-dioxolane less than one hundredth of the concentration of thianthrene sulfonic acid is required than when it is used alone, and besides much better brightness is obtained. The same relationship of concentration holds true for the sulfonated phenyl dl-Sll'l'fidCS, and other sulfonated organic sulfides illustrated in Table I.

The effectiveness of the extremely small quantity of the organic sulfide compounds of this invention when used in conjunction with the high molecular weight polymers of 1,3-dioxolane, or other polyether polymers described in greater detail hereinafter, has the unexpected important advantage that no harmtul breakdown products are formed which tend to reduce the brightness, especially in the low current density area, even from extensive use of the baths. When, however, the concentration of the organic sulfide sulfonic acid compound is greater than about 0.04 gram/liter, then harmful breakdown products do form on extended electrolysis.

The 1,3-dioxolane though a 5-membered ring, can be converted into high molecular weight polymers in accordance with well-known polymerization procedures, namely by heating the dioxolane in the presence of an acidic catalyst until a polymer of the desired molecular weight has been obtained, which for this application is about 5,000. The best acidic catalyst for the polymerization of the dioxolane is the boron tri-fluoride type. The polymers of 1,3-dioxolane are polyethers consisting of alternating methylene and ethylene groups interrupted by oxygen atoms. The polymers of 1,3-dioxolane can be fiurther reacted with many organic compounds having a reactive hydrogen atom, such as alcohols, iglycols, sugars, aryl amines, chlorohydrins, amides, thiol compounds, .alkanol SllllfOHiC acids, nitriles, thio-aryl, and thioand thiol-alkane sulfonic acids, alkanolamines, etc., and such bath soluble polymers which can be formed in which the portion of poly-1,3-dioxolane predominates, that is, constitutes over 50% of the molecular weight of the polymer, usually produce beneficial efiects on the copper plate, and often improved results are obtained.

It was also found that the sulfonated organic sulfide compounds, that is the compounds of Table I, in the very low concentrations of 0.0005 to 0.01 gram/liter, below the concentration where brightness is discernible from these compounds, prevent the harmful striations and ribbing effects that polyethers such as the high molecular weight polyethylene ethanols and glycols (average molecular weight of 220 to at least 30,000) cause in the absence of at least 0.02 to 0.1 gram/liter of chloride or bromide ion. Not only are the striations and ribbing effects eliminated without the need of chloride or bromide ions, but just as had occurred with the poly-dioxolanes, a very bright deposit was also obtained. This was an unexpected result, because with either material used alone in the bath, there is no indication of the remarkable enhancement of brightness which occurs when the two materials are used together. It will be appreciated that the elimination of the ribbing or striations eifect is, in itself, an unexpected and important result, and this result is obtained with all of the compounds of Table I, though in the matter of obtaining the highest brightness, not all of the compounds of Table I are equally effective. Furthermore, polyethers such as polypropylene propanols and especially glycols of average molecular weight of about 290 to 1,000 Which cause very severe striations especially with the higher molecular weight species, when used in concentrations of about 0.1 to 0.5 gram/liter were found to give no striations and even brighter plate than the high molecular weight polyethylene ethanols and glycols, when used similarly with the very low concentrations of the compounds of Table I. In general, with the low concentrations of the compounds of Table I," a large class of bathsoluble derivatives of polyethylene oxide or polypropylene oxide, or mixtures, can be used. Terminal groups other than the hydroXy group may be present on the polyether polymers of this invention, such as amino, chloride, bromide, sulfonic, mercapto, methoxy to heptoxy, naphthoxy, phenoxy, and chloro, bromo, nitro, methoxy and ethoxy substituted phenoxy groups, as well as small chain alkyl phenoxy groups where the alkyl group is less than 6 carbon atoms.

Otherwise stated, the class of polymers which are useful for the purposes of this invention, includes the polyether compounds containing at least six ether oxygen atoms and which are free from alkyl chains having more than 6 carbon atoms. It has been found that compounds containing alkyl chains of more than 6 carbon atoms tend to overfoam with air agitation but more importantly de crease the luster of the deposit, especially in the low current density areas.

In Table II are listed representative examples of the bath soluble polyether derivatives which can be used with the low concentrations of the compounds of Table I to give bright, ductile copper plate. The preferred compounds of Table II, besides the poly-dioxolane, from the standpoint of best cooperation with the compounds of Table I, to give smooth, striation-free, bright, ductile copper are the polypropylene propanols and glycols of average molecular weight of about 360 to about 1,000.

It was further found that if low concentrations (0.001 to 0.0 gram/liter) of the dye Janus Green B (see US. Patent 2,707,166, April 26, 1955) are used in conjunction with both of the above described additives of Tables I and II, the brightness and leveling is further improved and a very brilliant, high leveling, ductile copper plate is obtained over a much Wider plating range, including the very low current density areas. This type of brilliance and extremely wide bright plate range is not obtained 7 when the Janus Green B is used just with the organic sulfide compounds carrying sulfonic groups (the compounds of Table I), or when used just with the compounds of Table II. Also, the brilliance and ductility far exceed that obtained with Janus Green B type dyes used together with thiourea or such thiourea derivatives as acetyl or propionyl thioureas. (US. Patent 2,738,318, March 13, 1956.)

The dyes of the phenaziine class (the Safranine type) and more especially the phenazine azo dyes (the Janus Green B type) which make possible the greatly improved leveling and extended b-right plating range can be represented by the following formula.

SH, and N=N-Z where Z=a coupling group, such as dimethyl aniline, aniline, phenylene diam-inc, and substituted anilines and phenylene diamines, naphthols and substituted naphthols, phenols and substituted phenols, thiazoles, benzothiazoles and aminobenzothiazoles, coupled to the azo linkage N=N.

The preferred phenazine 'dyes are the Janus Green B type (Diethyl Safranine Azo Dimethyl Aniline or Dimethyl Safranine Azo Dimethyl Aniline, C. I. Nos. 11045, 11050), or the Janus Black R type, also C. I. 11975 (Colour Index, Second Edition, vol. 3, 1956-57), as these compounds make possible the highest leveling and the widest bright plate range. The anions of these cat-ionic dyes are in general not important for its maximum activity, though there is evidence for ion pairing and small anions that are not surface-active in wetting are desirable, but surface-active anions such as dodecyl sulfonic are not desirable and tend to precipitate the phenazine dyes.

When acid copper baths are used for plating steel or ferrous articles, such as automobile bumper bars, hub caps, printing rollers, etc., a preliminary copper or brass strike from a cyanide bath or a nickel strike from an acidic, pH of about 0.5 to 5, nickel plating bath, is first used to avoid poorly adherent immersion deposits. The acidic nickel strike (low chloride, high sulfate type to minimize drag-in of chloride ions into the copper bath) is often preferred because it is easier to control and easier to rinse and easier for waste disposal. The inorganic composition of the acid copper plating baths such as the acidic sulfate or acidic fluoborate may vary over rather wide limits, an actually much lower acid content may be used with the unique combination of additives of this invention than is present in the usual standard compositions. However, when very low acid contents are used, higher tank voltages are needed. In the examples listed below as illustrations of lustrous copper plating baths, the standard types of acidic copper sulfate and fluoborate baths are used for the inorganic compositions. However, other acidic copper plating baths such as copper methane sulfonates, copper methane disulfonates, copper ethane sulfonates, copper ethane disulfonates, copper propane sulfonates with excess acidity supplied by the free sulfonic acids, can be used with the combinations of additives of this invention to give highly lustrous plate.

With high, unlike with low concentrations of these su'l fonate anions, the solubility of the phenazine dyes is greatly decreased, due to ion pairing.

Many inorganic cations which do not plate out from the normal acidic copper plating baths, may be present in concentrations as high .as at least 25 grams/liter with out detrimental eifects, for example, ferrous, nickel, cobalt, zinc and cadmium cations. Chloride and/or bromide anions should in general be kept below about 0.1 gram/liter, and preferably below about 0.02 gram/liter. Air agitation or cathode-rod agitation, or solution agitation and cathode-rod agitation is desirable for highest speed plating and optimum results. The best bath temperatures are 25-30 C., though lower or higher (even up to 50 C. in some cases) temperatures can be used.

In Table I, the various organic sulfide sulfon-ic compounds may have various substituting groups such as methyl, chloro, bromo, methoxy, ethoxy, car-boxy and hyd oxy on the molecules especially on the aromatic and heterocyclic sulfide sulfonic acids without iundamental changes in brightness. The organic sulfide sulfonic acids of Table I can be added to the baths as the free acids, or the alkali metal salts, or the organic amine salts such as the triethanolamine, guanidine, aminoguanidine, phenylguanidine, ethylene diamine and pyridine salts. In most cases it is preferred to use the free acids.

With the use of the combination of additives from Tables I and II and the combinations with the phenazine dyes, especially the Janus Green B types, it is preferred not to use surface-active agents, even though such anionic types as sodium octyl sulfate, sulfonated non-ionic types 6 such as Triton 720 (US. Patent 2,489,538, November 29, 1949), and similar materials, or polyoxy non-ionic wetting agents, have often been previously used in acidic copper plating baths with good results, they are not needed in the present type baths.

Below is a list of a number of acid copper plating baths for producing highly ductile, lustrous copper deposits. Baths A and B do not give as bright plate as the rest of the baths which employ combinations of addition agents. The highest brilliance, widest bright plate range, and best leveling is obtained with the baths using Janus Green as one of the brighteners.

TABLE I.-SULFONATED ORGANIC SULFIDES [Concentration range 0.0005 to 0.04 grams/liter when used with the compounds of Table II] C) I s SH, CHaCNH sO-sn O-S-S-QSMH. HOhQ-S-S-Qsgfl NHCOCH3 SH D) HOsS 503K 7) CzH5O C2H4(O (HEM-300E 1: S S SOaH 1;; HO (C3HBO)QZOHE N s NC3H(O C HOMoOI-I I1 113 H O (C 2H40) 6-100 C2H4N S C N-C 2H4 (O C2114) s-moO H (20) ([3113 (EH; H 2 40)51oo aH4Ofi3CECi3C-O C2H4(OC2I'I4)B1000H CH3 CH;

(21) (13113 1 H0 (C2 4O)510oC1 4O- fCE C2H4(O C2H4)a-i0oO (NH-C1H -NH-CzH u(C2 4O C2H4O) b a,=15, b=l0-100 (23) (-NH-CzH -NHC2H =(C3Ho0 CaHe0-) c a=12, 0 13-15 Example A 25 Example 7, Table I ()()1 ()2 Concentration, Janus Green B 0 grams/ liter Tem v p. 20-35 C. CuSO4'5H2O 150425 Av. cathode current density, amp3/ q 1 H 50 30-75 1,3-dioxolane polymer, av. mol. wt. 5,000 0.03-0.15 30 ExampleF Temp. -35 C. glrlgrergt/rfigon, Average cathode Cu n y, 5 P CuSO 5H O ISO-250 Example B 2 4 -75 Concentration, Polypropylene glycol, av. mol. Wt. 350-750 0.05-0.2 rams/liter Thianthrene sulfonic acid 0.001-0.02 Cu(BF I O-42 Dim hyl safranine azo dimethyl aniline 0 0 1 0 1 6 8'38 Tem 20-35 0.

3 3 A th (1 t 1,3-dioxo1ane polymer av. mol. wt. 1,000 to v ca 0 e current denslty 5 amps/Sq 10,000 0.01-1 Example G Temp. 20-35 C. Concentration, Av. cathode current density, 8 amps/sq. drn. grams/liter E l C CuSO .5H O 150-250 6 c 45 H 30-60 f l Example 12, Table II 5 0 5 g l Phenyl disulfide sulfonic acid (Example 5, cuSO4'5H2O Table I) 0 001 0 ()2 H2804 30-75 Janus Green T3 "I foo 0 0 1,3-dioxo1ane ypolymer av. mol. Wt. 5,000 01-0-2 T Diethyl safranine azo dimethyl aniline (Janus 50 mp. 2530 C.

Green B) 0.0O10.01 AV- e current density, 5 amps/sq, dm, Thiophene-Z-sulfonic acid (Example I,

Table 1) 0.0o1 0.01 Example H C t t' Temp. 20-3? 0. v, cathode current denslty, 5 P c s0 ,5H 0 150-250 Example D 2 4 30-60 Concentration, Polypropylene glycol, av. mol. Wt. 350-750 0.02-0.4 grams/lit r Example 3, Table I 0.0010.02 cuso,.sH o 2 Temp. 25-30 0. H25 A p p 1,3-dioxolane polymer, av. mol. Wt. 5,000 0.05-0.15 cathode current 1611810, 5 P q- Thianthrene sulfonic acid (Example 4, Example 1 Table 5 Concentration, Temp. 20-35 C. grams/liter Av, cathode current density, 5 amps/sq. dm. E; 150-425 HBF 10-30 ExampleE H BO 0 30 Concentration, 3 3

Example 12, Table II 0.02-0.3 grams/liter 50425 Example T ble I (1001-01)]. CHEF; Janus Black R 0 001-4) 01 10-30 H BO 0-30 Temp. 25-30 C.

1,3-dioxolane polymer, av. mol. wt. 5,000 0.1-0.3

Av. cathode current density, 5-10 amps/sq. dm.

13 Example I Concentration, grams/liter CUSO4-SH2O H 80 3060 Polypropylene glycol, av. mol. wt. 300-750 0.01-0.2 Janus Green B 0.001-0.02 Example 13, Table I .0010.02

Temp. 25-30 C. Av. cathode current density, 5 amps/sq. dm.

The addition agents of Tables I and II can be combined in the same molecule or combined with one of the phenazine dyes, or they may be used as individual molecules as listed in Tables I and II mixed together in the sa ine solution with or without the phenazine dyes because they all deplete from the solution at very nearly the same rate. The compounds of Table I used in the very low concentrations of 0.0005 to about 0.025 gram/liter deplete practically exactly at the same rate as the phenazine dyes used in the concentration range of 0.001 to 0.05 gram/liter.

The rate of depletion of the unique combiantion of additives of this invention is very closely the same in the acidic copper sulfate, copper fluoborate and copper methane sulfonate baths which are the preferred baths. In the case of the baths containing the small alkyl chain disulfonates the solubility of the cop-per salts of these compounds are much smaller than, for example, the copper methane, ethane or propane monosulfonates, and it is therefore necessary to use the d-isulfonates in much lower concentrations than the monosulfonates.

It is generally preferred to use phosp-horized copper anodes, especially when the additives in the acidic baths consist of combination of compounds selected from Tables I and II. In fact, if pure copper anodes are used, such as electrolytic copper or oxygen-free copper anodes, the anode corrosion is less smooth and also the brightness of the plate is less. Just why the plate is less bright is not clear. The phosphorized anodes contain from about 0.02 to about 0.2% phosphorous and the cathode copper plate obtained with the use of these phosphorized anodes also contains a very similar percent phosphorous, and it is the inclusion of this phosphorous in the plate that may aid in the brightening. The phosphorized copper anodes usually contain about 0.01 to 0.05% silver and smaller traces of nickel, iron, sulfur, arsenic, antimony, and bismuth. The cathode plate contains even less of these impurities. The silver seems to be precipitated out as the chloride, which probably explains its very much smaller concentration in the cathode plate.

However, when a phenazine dye such as Janus Green is also present in the acidic baths besides one or more of the compounds of Tables I and II, then the copper plate is about equally brilliant, independent of the type of the above-mentioned copper anodes used in the plating.

When the bright copper plates of this invention are heated to high temperatures in a hydrogen atmosphere, the plate from the fluoborate bath seems to be stronger than that from the sulfate bath.

What is claimed is:

1. A bath for electrodepositing ductile, lustrous copper comprising an aqueous acidic copper plating bath containing dissolved therein about 0.0005 to about 0.04 gram per liter of an organic sulfide compound carrying at least one sulfonic group, together with 0.01 to 5 grams/liter of a bath-soluble polyether compound containing at least 6 ether oxygen atoms and being free from alkyl chains having more than 6 carbon atoms.

2. A bath as claimed in claim 1 wherein said polyether is a polymer of 1,3-dioxolane having a molecular weight in the range of 296 to at least 30,000.

3. A bath as claimed in claim 1 wherein said polyether contains the group (-C H OC H O-) where x is an integer of magnitude of at least 3.

4. A bath as claimed in claim 1 wherein said polyether contains the group (C H OC H O--) Where y is an integer of magnitude of 3 to 10.

5. A bath as claimed in claim 1 wherein there is also present a bath-soluble phenazine dye in a concentration of 0.001 to 0.05 grams per liter.

6. A bath as claimed in claim 5 wherein said phenazine dye is diethyl safranine azo dimethyl aniline.

7. A bath as claimed in claim 5 wherein said phenazine dye is dimethyl safran-in azo dimethyl aniline.

8. A bath as claimed in claim 5 wherein said penazine dye is Janus Black.

9. A bath as claimed in claim 1 wherein said acid copper plating bath contains at least one copper salt selected from the group consisting of copper sulfate, copper fluoborate, copper methane sulfonates, copper methane disulfonates, copper ethane sulfonates, copper ethane disulfonates, copper propane sulfonates and copper propane d-isulfonates.

10. A method for electrodepositing ductile lustrous copper comprising the step of electrodepositing copper from an aqueous acidic copper plating bath containing dissolved therein about 0.0005 to about 0.04 gram/liter of an organic sulfide compound carrying at least one sulfonic group, together with 0.01 to 5 grams per liter of a bath-soluble polyether compound containing at least 6 ether oxygen atoms and being free from alkyl chains having more than 6 carbon atoms.

11. A method as claimed in claim 10 wherein said polyether in the said acidic copper baths is a polymer of 1,3-dioxolane having a molecular weight in the range of 296 to at least 30,000.

12. A method as claimed in claim 10 where-in said polyether in the said acidic copper baths contains the group (C H.;OC H O--) where x is an integer of magnitude of at least 3.

13. A method as claimed in claim 10 wherein said polyether in the said acidic copper baths contains the group (C H OC H O) where y is an integer of magnitude 3 to 10.

14. A method as claimed in claim 10 wherein said acid copper plating bath contains a bath-soluble phenazine dye in a concentration of 0.001 to 0.05 gram per liter.

15. A method as claimed in claim 14 wherein said phenazine dye is diethyl safranine azo dimethyl aniline.

16. A method as claimed in claim 14 wherein said phenazine dye is dimethyl safranine azo dimethyl aniline.

17. A method as claimed in claim 14 wherein said phenazine dye is Janus Black.

18. A method as claimed in claim 10 wherein said acid copper plating bath contains at least one copper salt selected from the class consisting of copper sulfate, copper fluoborate, copper methane sulfonates, copper methane disulfonates, copper ethane sulfonates, copper ethane disulfonates, copper propane sulfonates and copper propane disulfonates.

19. A bath as claimed in claim 1, wherein said organic sulfide compound is a thianthrene sulfonic acid and wherein said polyether contains the group (C H O) where x is an integer of magnitude of at least 6.

20. A bath as claimed in claim 1, wherein said organic sulfide compound is a disulfide sulfonic acid and wherein said polyether contains the group (C H O) wherein x is an integer of magnitude of at least 6.

21. A bath as claimed in claim 1, wherein said organic sulfide compound is a thianthrene sulfonic acid and wherein said polyether contains the group (C H O) where y is an integer of magnitude of about 620.

22. A bath as claimed in claim 1, wherein said organic sulfide compound is a disulfide sulfonic acid and wherein said polyether contains the group (C H O) where y is an integer of magnitude of about 6-20.

.23. A method as claimed in claim 10, wherein said organic sulfide is a thianthrene sulfonic acid and wherein said polyether contains the group (C I-I O) wherein at is an integer of magnitude of at least 6.

24. A method as claimed in claim 10, wherein said organic sulfide i s a disulfide sulfonic acid and wherein said polyether contains the group (C H O) wherein x is an integer of magnitude of at least 6.

25. A method as claimed in claim 10, wherein said organic sulfide is a disulfide sulfonic acid and wherein said polyether contains the group (C H O) wherein y is an integer of magnitude of about 620.

26. A method as claimed in claim 10, wherein said organic sulfide is a thianthrene sulfonic acid and wherein said polyether contains the group (C H O) where y is an integer of magnitude of about 6-20.

References Cited by the Examiner UNITED STATES PATENTS Brown et al. 204-52 Gundel et a1 20452 Kirstahiler et a1. 20452 Ostrow et a1 204 -52 Passal 20452 Strauss et al 20452 OTHER REFERENCES Nevers et a1., Plating, volume 41, No. 11, Nov. 1954, pages 1301-1306.

5 JOHN H. MACK, Primary Examiner.

JOSEPH REBOLD, Examiner.

G. KAPLAN, Assistant Examiner.

Claims (2)

1. A BATH FOR ELECTRODEPOSITING DUCTILE, LUSTROUS COPPER COMPRISING AN AQUEOUS ACIDIC COPPER PLATING BOTH CONTAINING DISSOLVED THEREIN ABOUT 0.0005 TO ABOUT 0.04 GRAM PER LITER OF AN ORGANIC SULFIDE COMPOUND CARRYING AT LEAST ONE SULFONIC GROUP, TOGETHER WITH 0.01 TO 5 GRAMS/LITER OF A BATH-SOLUBLE POLYETHER COMPOUND CONTAINING AT LEAST 6 ETHER OXYGEN ATOMS AND BEING FREE FROM ALKYL CHAINS HAVING MORE THAN 6 CARBON ATOMS.
5. A BATH AS CLAIMED IN CLAIM 1 WHEREIN THERE IS ALSO PRESENT A BATH-SOLUBLE PHENAZINE DYE IN A CONCENTRATION OF 0.001 TO 0.05 GRAMS PER LITER.
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Cited By (51)

* Cited by examiner, † Cited by third party
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US3373095A (en) * 1967-06-05 1968-03-12 Dayton Bright Copper Company Electroplating of copper
US3542655A (en) * 1968-04-29 1970-11-24 M & T Chemicals Inc Electrodeposition of copper
US3715289A (en) * 1971-02-08 1973-02-06 Stauffer Chemical Co Brightener composition for acid copper electroplating baths
US3743584A (en) * 1970-06-06 1973-07-03 Schering Ag Acid bright copper plating bath
US3770598A (en) * 1972-01-21 1973-11-06 Oxy Metal Finishing Corp Electrodeposition of copper from acid baths
US3940320A (en) * 1972-12-14 1976-02-24 M & T Chemicals Inc. Electrodeposition of copper
US3956078A (en) * 1972-12-14 1976-05-11 M & T Chemicals Inc. Electrodeposition of copper
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US3956120A (en) * 1972-12-14 1976-05-11 M & T Chemicals Inc. Electrodeposition of copper
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US3373095A (en) * 1967-06-05 1968-03-12 Dayton Bright Copper Company Electroplating of copper
US3542655A (en) * 1968-04-29 1970-11-24 M & T Chemicals Inc Electrodeposition of copper
US3743584A (en) * 1970-06-06 1973-07-03 Schering Ag Acid bright copper plating bath
US3715289A (en) * 1971-02-08 1973-02-06 Stauffer Chemical Co Brightener composition for acid copper electroplating baths
US3770598A (en) * 1972-01-21 1973-11-06 Oxy Metal Finishing Corp Electrodeposition of copper from acid baths
US3940320A (en) * 1972-12-14 1976-02-24 M & T Chemicals Inc. Electrodeposition of copper
US3956078A (en) * 1972-12-14 1976-05-11 M & T Chemicals Inc. Electrodeposition of copper
US3956079A (en) * 1972-12-14 1976-05-11 M & T Chemicals Inc. Electrodeposition of copper
US3956120A (en) * 1972-12-14 1976-05-11 M & T Chemicals Inc. Electrodeposition of copper
US3956084A (en) * 1972-12-14 1976-05-11 M & T Chemicals Inc. Electrodeposition of copper
US3966565A (en) * 1972-12-14 1976-06-29 M & T Chemicals Inc. Electrodeposition of copper
US4014760A (en) * 1974-11-21 1977-03-29 M & T Chemicals Inc. Electrodeposition of copper
US4036710A (en) * 1974-11-21 1977-07-19 M & T Chemicals Inc. Electrodeposition of copper
US4036711A (en) * 1975-12-18 1977-07-19 M & T Chemicals Inc. Electrodeposition of copper
US4316778A (en) * 1980-09-24 1982-02-23 Rca Corporation Method for the manufacture of recording substrates for capacitance electronic discs
US4336114A (en) * 1981-03-26 1982-06-22 Hooker Chemicals & Plastics Corp. Electrodeposition of bright copper
FR2502648A1 (en) * 1981-03-26 1982-10-01 Hooker Chemicals Plastics Corp Acid electrolyte for the electrolytic deposition of copper, in particular containing a phthalocyanine radical and an adduct of an alkylamine with a polyepichlorohydrin
US4376685A (en) * 1981-06-24 1983-03-15 M&T Chemicals Inc. Acid copper electroplating baths containing brightening and leveling additives
FR2547836A1 (en) * 1983-06-10 1984-12-28 Omi Int Corp Process for electrolytically depositing copper by means of an electrolyte containing such a compound of SUBSTITUTED phthalocyanine and a reaction product of polyethyleneimine alkyl
DE3421017A1 (en) * 1983-06-10 1984-12-13 Omi Int Corp Process for the electrochemical deposition of a technical kupferueberzugs
DE3420999A1 (en) * 1983-06-10 1984-12-13 Omi Int Corp The aqueous acidic galvanic copper bath and process for the galvanic deposition of a shiny leveled kupferueberzugs on a conductive substrate in this bath
GB2141141A (en) * 1983-06-10 1984-12-12 Omi Int Corp Electrodepositing copper
DE3518193A1 (en) * 1984-05-29 1985-12-05 Omi Int Corp Aqueous acidic copper-containing electrolyte and a process for the galvanic deposition of copper using this electrolyte
US4551212A (en) * 1985-03-11 1985-11-05 Rca Corporation Bath and process for the electrodeposition of micromachinable copper and additive for said bath
US4673467A (en) * 1986-09-02 1987-06-16 Cbs Inc. Method of manufacturing fine-grained copper substrate for optical information carrier
US5252196A (en) * 1991-12-05 1993-10-12 Shipley Company Inc. Copper electroplating solutions and processes
US5328589A (en) * 1992-12-23 1994-07-12 Enthone-Omi, Inc. Functional fluid additives for acid copper electroplating baths
DE4343946C2 (en) * 1992-12-23 1998-10-29 Enthone Omi Inc A galvanic copper bath and method for the galvanic deposition of copper
US6358388B1 (en) * 1996-07-15 2002-03-19 Semitool, Inc. Plating system workpiece support having workpiece-engaging electrodes with distal contact-part and dielectric cover
US5985126A (en) * 1996-07-15 1999-11-16 Semitool, Inc. Semiconductor plating system workpiece support having workpiece engaging electrodes with distal contact part and dielectric cover
US20050061675A1 (en) * 1996-07-15 2005-03-24 Bleck Martin C. Semiconductor plating system workpiece support having workpiece-engaging electrodes with distal contact part and dielectric cover
US20020194716A1 (en) * 1996-07-15 2002-12-26 Berner Robert W. Modular semiconductor workpiece processing tool
US7074246B2 (en) 1996-07-15 2006-07-11 Semitool, Inc. Modular semiconductor workpiece processing tool
US6663762B2 (en) 1996-07-15 2003-12-16 Semitool, Inc. Plating system workpiece support having workpiece engaging electrode
US6454926B1 (en) 1997-09-30 2002-09-24 Semitool Inc. Semiconductor plating system workpiece support having workpiece-engaging electrode with submerged conductive current transfer areas
US20030029732A1 (en) * 1997-09-30 2003-02-13 Ritzdorf Thomas L. Semiconductor plating system workpiece support having workpiece-engaging electrode with submerged conductive current transfer areas
US6936153B1 (en) 1997-09-30 2005-08-30 Semitool, Inc. Semiconductor plating system workpiece support having workpiece-engaging electrode with pre-conditioned contact face
US6776892B1 (en) 1997-09-30 2004-08-17 Semitool, Inc. Semiconductor plating system workpiece support having workpiece engaging electrode with pre-conditioned contact face
US6806186B2 (en) 1998-02-04 2004-10-19 Semitool, Inc. Submicron metallization using electrochemical deposition
US7144805B2 (en) 1998-02-04 2006-12-05 Semitool, Inc. Method of submicron metallization using electrochemical deposition of recesses including a first deposition at a first current density and a second deposition at an increased current density
US20040035708A1 (en) * 1998-03-20 2004-02-26 Semitool, Inc. Apparatus and method for electrolytically depositing copper on a semiconductor workpiece
US7332066B2 (en) 1998-03-20 2008-02-19 Semitool, Inc. Apparatus and method for electrochemically depositing metal on a semiconductor workpiece
US6565729B2 (en) 1998-03-20 2003-05-20 Semitool, Inc. Method for electrochemically depositing metal on a semiconductor workpiece
US20030141194A1 (en) * 1998-03-20 2003-07-31 Chen Linlin Apparatus and method for electrolytically depositing copper on a semiconductor workpiece
US6919013B2 (en) 1998-03-20 2005-07-19 Semitool, Inc. Apparatus and method for electrolytically depositing copper on a workpiece
US20040035710A1 (en) * 1998-03-20 2004-02-26 Semitool, Inc. Apparatus and method for electrolytically depositing copper on a semiconductor workpiece
US6638410B2 (en) 1998-03-20 2003-10-28 Semitool, Inc. Apparatus and method for electrolytically depositing copper on a semiconductor workpiece
US20040040857A1 (en) * 1998-03-20 2004-03-04 Semitool, Inc. Apparatus and method for electrolytically depositing copper on a semiconductor workpiece
US6632345B1 (en) 1998-03-20 2003-10-14 Semitool, Inc. Apparatus and method for electrolytically depositing a metal on a workpiece
US20040092065A1 (en) * 1998-03-20 2004-05-13 Semitool, Inc. Apparatus and method for electrolytically depositing copper on a semiconductor workpiece
US7115196B2 (en) 1998-03-20 2006-10-03 Semitool, Inc. Apparatus and method for electrochemically depositing metal on a semiconductor workpiece
US6932892B2 (en) 1998-03-20 2005-08-23 Semitool, Inc. Apparatus and method for electrolytically depositing copper on a semiconductor workpiece
US6811675B2 (en) 1998-03-20 2004-11-02 Semitool, Inc. Apparatus and method for electrolytically depositing copper on a semiconductor workpiece
US7247229B2 (en) * 1999-06-28 2007-07-24 Eltech Systems Corporation Coatings for the inhibition of undesirable oxidation in an electrochemical cell
US20040031692A1 (en) * 1999-06-28 2004-02-19 Kenneth Hardee Coatings for the inhibition of undesirable oxidation in an electrochemical cell
US20040187731A1 (en) * 1999-07-15 2004-09-30 Wang Qing Min Acid copper electroplating solutions
US6596148B1 (en) 1999-08-04 2003-07-22 Mykrolis Corporation Regeneration of plating baths and system therefore
US6391209B1 (en) 1999-08-04 2002-05-21 Mykrolis Corporation Regeneration of plating baths
US20020153254A1 (en) * 2000-05-25 2002-10-24 Mykrolis Corporation Method and system for regenerating of plating baths
US6942779B2 (en) 2000-05-25 2005-09-13 Mykrolis Corporation Method and system for regenerating of plating baths
EP1433544A1 (en) * 2000-08-18 2004-06-30 Ti Group Automotive Systems Limited A method for manufacturing a multiple walled tube
US6887364B2 (en) 2000-08-18 2005-05-03 Ti Group Automotive Systems Limited Method for manufacturing a multiple walled tube
US20030038161A1 (en) * 2000-08-18 2003-02-27 Ti Group Automotive Systems Ltd. Method for manufacturing a multiple walled tube
US20040074778A1 (en) * 2001-10-02 2004-04-22 Shipley Company, L.L.C. Plating bath and method for depositing a metal layer on a substrate
US20030221969A1 (en) * 2002-05-17 2003-12-04 Manabu Tomisaka Method for filling blind via holes
US7025866B2 (en) 2002-08-21 2006-04-11 Micron Technology, Inc. Microelectronic workpiece for electrochemical deposition processing and methods of manufacturing and using such microelectronic workpieces
US20060182879A1 (en) * 2002-08-21 2006-08-17 Collins Dale W Microelectronic workpiece for electrochemical deposition processing and methods of manufacturing and using such microelectronic workpieces
US20040038052A1 (en) * 2002-08-21 2004-02-26 Collins Dale W. Microelectronic workpiece for electrochemical deposition processing and methods of manufacturing and using such microelectronic workpieces
US7872130B2 (en) 2002-12-20 2011-01-18 Atotech Deutschland Gmbh Mixture of oligomeric phenazinium compounds and acid bath for electrolytically depositing a copper deposit
US20040211657A1 (en) * 2003-04-11 2004-10-28 Ingelbrecht Hugo Gerard Eduard Method of purifying 2,6-xylenol and method of producing poly(arylene ether) therefrom
US20080142370A1 (en) * 2003-08-08 2008-06-19 Wolfgang Dahms Aqueous, Acidic Solution and Method for Electrolytically Depositing Copper Coatings as Well as Use of Said Solution
US20050092611A1 (en) * 2003-11-03 2005-05-05 Semitool, Inc. Bath and method for high rate copper deposition
US7786303B2 (en) 2003-11-19 2010-08-31 Atotech Deutschland Gmbh Acidic bath for electrolytically depositing a copper deposit containing halogenated or pseudohalogenated monomeric phenazinium compounds
US20070108062A1 (en) * 2003-11-19 2007-05-17 Atotech Deutschland Gmbh Acidic bath for electrolytically depositing a copper deposit containing halogenated or pseudohalogenated monomeric phenazinium compounds
US20080087549A1 (en) * 2004-08-18 2008-04-17 Ebara-Udylite Co.,Ltd. Additive For Copper Plating And Process For Producing Electronic Circiut Substrate Therewith
US20100003399A1 (en) * 2008-07-01 2010-01-07 C. Uyemura & Co., Ltd. Electroless plating solution, method for electroless plating using the same and method for manufacturing circuit board
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US8580091B2 (en) 2010-10-08 2013-11-12 Water Star, Inc. Multi-layer mixed metal oxide electrode and method for making same
CN102523785A (en) * 2012-01-19 2012-07-04 南京农业大学 Application of safranine T in seed dye mark tracing aspect
CN102523785B (en) 2012-01-19 2013-10-02 南京农业大学 Application of safranine T in seed dye mark tracing aspect

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GB1034484A (en) 1966-06-29 application
DE1521062A1 (en) 1969-08-14 application
FR1361558A (en) 1964-05-22 grant
DE1521062B2 (en) 1971-11-18 application
NL291575A (en) application

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