US3855085A - Acid zinc electroplating electrolyte, process and additive - Google Patents

Acid zinc electroplating electrolyte, process and additive Download PDF

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Publication number
US3855085A
US3855085A US00369815A US36981573A US3855085A US 3855085 A US3855085 A US 3855085A US 00369815 A US00369815 A US 00369815A US 36981573 A US36981573 A US 36981573A US 3855085 A US3855085 A US 3855085A
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United States
Prior art keywords
zinc
range
ketone
chloride
composition according
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Expired - Lifetime
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US00369815A
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English (en)
Inventor
J Rushmere
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EIDP Inc
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EI Du Pont de Nemours and Co
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Application filed by EI Du Pont de Nemours and Co filed Critical EI Du Pont de Nemours and Co
Priority to US00369815A priority Critical patent/US3855085A/en
Priority to NL7407297A priority patent/NL7407297A/xx
Priority to IT23956/74A priority patent/IT1015050B/it
Priority to DE19742428499 priority patent/DE2428499A1/de
Priority to FR7420504A priority patent/FR2233419B3/fr
Priority to JP49067262A priority patent/JPS5035037A/ja
Priority to BE145469A priority patent/BE816384A/xx
Application granted granted Critical
Publication of US3855085A publication Critical patent/US3855085A/en
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Classifications

    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25DPROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
    • C25D3/00Electroplating: Baths therefor
    • C25D3/02Electroplating: Baths therefor from solutions
    • C25D3/22Electroplating: Baths therefor from solutions of zinc

Definitions

  • Certain polyoxyethylene compounds and certain ketone compounds have been proposed for. use in bright acid zinc electroplating, usually in combination with other additives.
  • US. Pat. No. 3,594,291 Todt et al. describes the use of certain ketones with N-polyvinyl pyrrolidone as brighteners in such baths, although the plate produced is not truly bright at high current densities.
  • US. Pat. No. 3,694,330 Korpiun et al. and generally corresponding British Pat. No. 1,149,106 disclose the use, along with an aromatic carbonyl compound and ammonium chloride, of a nonionogenic, surface active polyoxyethylene compound.
  • Suitable aromatic carbonyl compounds are said to include carboxylic acids, carboxylic acid esters, aldehydes and ketones. However, the disclosures do not teach the combined use of both carboxylic acids and ketones but rather the use of them individually as equivalents.
  • the bright plating range is also limited to l to 50 a./ft. although the range below 10 a./ft. is particularly desirable for commercial barrel plating operations.
  • Harbulak teaches bright acid zinc electroplating using as additives polyethers and at least one nonaromatic a,B-unsaturated carbonyl compound. Harbulak also discloses the use of citric acid as a bath component in addition to the polyoxyethylene compound and a ketone. However, the function of the citric acid is that of a complexing agent rather than that of a brightener. The citric acid maintains the zinc in solution at pHs above 5.5, preventing the precipitation of insoluble zinc salts.
  • the present invention in certain of its embodiments, provides compositions for acid zinc electrolytic plating baths and additives for such baths, as well as methods for using such baths.
  • the plating bath compositions of the invention comprise an aqueous bath composition containing at least one zinc compound providing zinc ions for electroplating zinc, a source of chloride ion, at least one nonionic polyoxyethylene compound, at least one ketone, and at least one carboxylic acid, wherein said polyoxyethylene compound is selected from compounds of the formula wherein n m 2 10, x l or 2, derived from a reaction of oxyethylene with a polyol selected from the group consisting of 2,4,7,9-tetramethyl-5-decyne-4,7 diol, v polyoxypropylene glycol of molecular weight at least about 900, and I N,N QIQN-tetrakis(polyoxypropylene glycol) ethylene diamine of molecular weight at least about and wherein R is defined by the selected polyol;
  • said ketone is selected from the group consisting of 4-phenyl-3'buten-2-one (benzalacetone),
  • said carboxylic acid is selected from the group consisting of benzoic acid,
  • the polyoxyethylene 2,4,7,9-tetramethyl-5-decyne- 4,7 diol is sold under the name Surfynol" by Air Products and Chemicals, lnc., of Wayne, Pa.
  • the polyoxyethylene polyoxypropylene glycol is sold under the name Pluronic by BASF Wyandotte Corp. of Wyandotte, Michigan.
  • the polyoxyethylene-N,N,N',N'- tetrakis(polyoxypropylene glycol) ethylene diamine is sold under the name Tetronic by BASF Wyandotte Corp.
  • the bath is preferably operated at a pH between 3.5 and 6.1.
  • the preferred pH range for optimum brightness and operability is 5 to 6.
  • Zinc deposits of acceptable commercial quality can be obtained over the temperature range of 15 to 40C., and the preferred operating temperature range is 20 to 35C.
  • the preferred range of zinc metal content in the bath is 30 to 60 g./l., preferably added as zinc chloride.
  • the bath should have a total chloride ion content of to g./l., with the major portion (over 50% by weight) of the chloride, other than that derived from zinc chloride, added in the form of ammonium chloride.
  • concentration ranges of the brightening additives in the bath are as follows: polyoxyethylene compounds 0.05 to 20 g./l., preferably 2 to 10 g./l., ketone: 0.05 to 2 g./l., preferably 0.1 to 0.5 g./l.; carboxylic acid: 0.05 to 20 g./l., preferably 1 to 6 g./l.
  • the concentration ranges of the brightening additives are: polyoxyethylene compounds: 10 to 400 g./l., preferably 20 to 50 g./l.; ketone: l0 to 200 g./l., preferably 20 to 50 g./l.; carboxylic acid: ID to 200 g./l., preferably 20 to-SO g./l.
  • the polyethylene compounds of the invention are used at the same time to obtain the most beneficial results and widest bright plating range.
  • the operating pH of the bath is established at about 3.5 to 6.1 because at a pH much below 3.5 undesirable dissolution of zinc anodes occurs even without electrolysis, and at a pH much above 6.1 precipitation of insoluble zinc salts commences.
  • the bath tends to seek its own pH level of about 5.8 to 6.1, and lower pH levels can be maintained only by periodic additions of acid.
  • the higher pH is also desirable in that it minimizes corrosion effects on plated parts due to poor rinsing.
  • baths can be operated with the zinc metal content outside the preferred range of 30 to 60 g./I., such conditions are less preferred due to decreasing cathode efficiencies at lower zinc concentrations and increasing low current density dullness at higher concentrations.
  • the preferred range for total chloride ion content of 150 to I90 g./I. is arrived at from a recognition of the fact that baths containing lower concentrations of chloride, while operable, have the disadvantages of poorer low current density operation, poorer anode corrosion, and a tendency to precipitate insoluble zinc salts at pH's much above 5.5.
  • bath formulations may also contain other metal salts such as, for example, potassium sulfate or sodium sulfamate. However, there appears to be little practical advantage to using such materials. Bath formulations may also contain mixtures of zinc salts such as zinc sulfate along with the zinc chloride. Again, there appears to be little or no practical advantage to this, and the preferred range of chloride content of the bath should still be met. If no zinc chloride is used. this chloride should come primarily from ammonium chloride.
  • Alternative sources of zinc include zinc oxide dissolved in common industrial acids such as hydrochloric, sulfuric, acetic, fluoboric, and sulfamic acids. Alternatively, aqueous solutions of commercial zinc salts themselves may be employed, and, as mentioned above, zinc chloride is preferred.
  • the pH of the bath is adjusted to the desired level by means of addition of ammonium hydroxide, sodium hydroxide or equivalent materials.
  • the zinc electrode deposits obtained from such acid baths are typically coarse and dull in appearance and have little commercial value until other additives are used.
  • the additive of the invention including certain nonionic polyoxyethylene compounds, certain ketones, and certain carboxylic acids, each component added to the bath in suitable amounts, permits the production of a bright, shiny zinc electrodeposit of a high decorative quality over a wide range of operating current densities and in a higher pH range than taught by the prior art.
  • Brightener chemicals are preferably added to the bath as two types of additives in order to obtain the correct balance of components for initial start up and subsequent continued maintenance of the bath under optimum conditions of performance.
  • a starter additive is usually used only once at the start as a new bath is made up. It comprises an aqueous solution containing: polyoxyethylene compounds: I00 to 500 g./l., preferably 200 to 350 g./l.; and carboxylic acid (added as sodium, potassium, ammonium or similar salts) 50 to 250 g./l., preferably to 200 g./I.
  • a maintenance additive is added initially to the bath and then on demand to maintain performance. It comprises an organoaqueous solution containing: polyoxyethylene compounds 10-400 g./l. preferably 20 to 50 g./l.; carboxylic acid (as sodium, potassium, ammonium or similar salt) 10-200 g./l. preferably 20 to 50 g./l.; and ketone 10 to 200 g./I., preferably 20 to 50 g./l.
  • methanol is used to solubilize the sparingly soluble ketones of the invention. The amount of methanol required varies depending on the concentration of ketone used in the formulation, but typically may comprise 30 to 50 percent by weight of the formulation. In place of methanol other inexpensive organic solvents such as ethanol, acetone and the like may be employed.
  • the desired amount of starter additive typically l0 to 40 cc. per liter of bath
  • the desired amount of maintenance additive typically 10 to 40 cc. per liter of bath is added to the bath and well mixed. The bath is now ready for operation.
  • EXAMPLE I poclyoxyethyleneh tetramethyl ecyn diol (Surfynol 465") (polyoxyethyleneh tetramethyl decyn diol (Surfynol 485") benzalacetone mac (n 267 ml. of this solution were transferred to a Hull cell and a steel cathode panel plated at 2 amps for 10 minutes. The panel showed the followingplate characteristics:
  • EXAMPLE 2 (polyoxyethylenem tetramethyl decyn diol 2.0 g. (polyoxyethylene M tetramethyl decyn diol 2.0 g. benzoic acid (as sodium salt) 2.0 g.
  • EXAMPLE 8 A liter zinc chloride/ammonium chloride bath at pH 5.9 was prepared. To it as brightener were added:
  • a variety of parts including nuts, bolts, washers, safety harness clamps were barrel plated in a horizontal barrel for 20-30 minutes. Loading varied from 900-1,800 grams and plating current from 20-45 amps. Bright, shiny, well-adherent zinc with good coverage in recesses was obtained on all parts.
  • a composition for providing bright zinc electrode deposits which comprises an aqueous acidic electrolyte composition containing at least one zinc compound providing zinc ions for electroplating zinc, a source of chloride ion, 0.05 to 20 g./l. of at least one nonionic wherein n m I 10, x l or 2, derived from a reaction of oxyethylene with a polyol selected from the group consisting of 2,4,7,9-tetramethyl-5-decyne-4,7 diol,
  • polyoxypropylene glycol of molecular weight at least about 900
  • said ketone being selected from the group consisting of 4-phenyl-3-buten-2-one, 4-(4-methoxyphenyl)-3-buten-2-one, 4-(3,4-dimethoxyphenyl)-3-buten-2-one, 4-(3,4-methylenedioxyphenyl)-3-buten-2-one, and 4-(2-furyl)-3-buten-2-one; and
  • said carboxylic acid being selected from the group consisting of benzoic acid,
  • a composition according to claim 1 having a zinc metal content within the range of about 30 to 60 g./l. with the zinc added as zinc chloride, a total chloride ion content of about 150 to I90 g./l. with the chloride other than zinc chloride being added in the form of ammonium chloride, a pH in the range of about 3.5 to 6.1, the polyoxyethylene compounds being present in the range of about 0.05 to 20 g./l., the ketone being present in the range of about 0.05 to 2 g./l., and the carboxylic acid being present in the range of about 0.05 to 20 g./l.
  • a composition according to claim 2 having a pH in the range of about 5 to 6, a content of polyoxyethylene compounds in the range of about 2 to 10 g./l., a ketone content of about 0.1 to 0.5 g./l., and a carboxylic acid content of about 1 to 6 g./l. wherein said polyoxyethylene compounds are polyoxyethylene 2,4,7,9- tetramethyl-5-decyne-4,7 diol and said ketone is 4-phenyl-3-buten-2-one.
  • composition according to claim 1 wherein the polyol is 2,4,7,9-tetramethyl-5-decyne-4,7 diol.
  • composition according to claim 1 wherein the polyol is polyoxypropylene glycol of molecular weight of at least 900.
  • composition according to claim 1 wherein the polyol is N,N,N,N'-tetrakis(polyoxypropylene glycol) ethylene diamine of molecular weight at least about 500.
  • composition according to claim 1 wherein said ketone is 4-phenyl-3-buten-2-one.
  • composition according to claim 1 wherein said ketone is 4-(4-methoxyphenyl)-3-buten-2-one.
  • composition according to claim 1 wherein said ketone is 4-(3,4-dimethoxyphenyl)-3-buten-2-one.
  • composition according to claim 1 wherein said ketone is 4-(3,4-methylenedioxyphenyl)-3-buten- 2-one.
  • a composition according to claim I wherein said ketone is 4-(2-furyl)-3-buten-2-one.
  • composition according to claim 1 wherein said carboxylic acid is benzoic acid.
  • a composition according to claim 1 wherein the zinc concentration measured as metal is in the range of about 30 to 60 g./I., and the zinc is provided as zinc chloride.
  • a composition according to claim 1 wherein the bath has a total chloride ion concentration of about 150 to l g./l., with the major portion of the chloride being provided as zinc chloride and ammonium chloride.
  • composition according to claim 1 wherein the carboxylic acid is present in a concentration range of about 1 to 6 g./l.
  • a method of producing bright zinc electrodeposits which comprises passing current from an anode to a cathode at a temperature about in the range of 15 to 40C. through an aqueous acidic electrolyte composition containing at least one zinc compound providing zinc ions for electroplating zinc, a source of chloride ion, 0.05 to 20 g./l. of at least one nonionic polyoxyethylene compound, 0.05 to 2 g./l. of at least one ketone, and 0.05 to 20 g./l. of at least one carboxylic acid,
  • polyoxyethylene compound being selected from compounds of the formula wherein n m 10, x l or 2, derived from a reaction of oxyethylene with a polyol selected from the group consisting of 2,4,7,9-tetramethyl-5-decyne-4,7 diol,
  • polyoxypropylene glycol of molecular weight at least about 900
  • said ketone being selected from the group consisting of 4-phenyl-3-buten-2-one,
  • said carboxylic acid being selected from the group consisting of benzoic acid,
  • a method of claim 19 operated at temperatures in the range of to 40C. with a zinc metal content within the range of about 30 to 60 g./l., the zinc being added as zinc chloride, a total chloride ion content of about 150 to 190 g./l. with the chloride other than zinc chloride being added in the form of ammonium chloride, a pH in the range of about 3.5 to 6.1, the polyoxy ethylene compounds being present in the range of about 0.05 to g./l., the ketone being present in the range of about 0.05 to 2 g./l., and the carboxylic acid being present in the range of about 0.05 to 20 g./l.
  • a method of claim 20 having a pH in the range of about 5 to 6, a content of polyoxyethylene compounds in the range of about 2 to 10 g./l., a ketone content of about 0.1 to 0.5 g./l., and a carboxylic acid content of about 1 to 6 g./l. wherein said polyoxyethylene compounds are polyoxyethylene 2,4,7,9-tetramethyl-5- decyne-4,7 diol and said ketone is 4-phenyl-3-buten- 2-one.
  • An organoaqueous-addition agent for use in preparing an acid zinc electroplating bath composition comprising:
  • polyoxypropylene glycol of molecular weight at least about 900
  • N,N,N',N-tetrakis(polyoxypropylene glycol) ethylthe polyoxyethylene compounds are polyoxyethylene- 2,4,7,9-tetramethyl-5-decyne-4,7 diols, the ketone is 4-phenyl-3-buten-2-one, and the carboxylic acid is benzoic acid.
  • An addition agent according to claim 29 contain- I ing 20 to 50 g./l. of the polyoxyethylene compounds, 20 to 50 g./l. of the ketone, and 20 to 50 g./l. of the carboxylic acid.

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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)
US00369815A 1973-06-14 1973-06-14 Acid zinc electroplating electrolyte, process and additive Expired - Lifetime US3855085A (en)

Priority Applications (7)

Application Number Priority Date Filing Date Title
US00369815A US3855085A (en) 1973-06-14 1973-06-14 Acid zinc electroplating electrolyte, process and additive
NL7407297A NL7407297A (enrdf_load_stackoverflow) 1973-06-14 1974-05-30
IT23956/74A IT1015050B (it) 1973-06-14 1974-06-12 Zincatura galvanica con bagno acido
DE19742428499 DE2428499A1 (de) 1973-06-14 1974-06-12 Glanzverzinkung
FR7420504A FR2233419B3 (enrdf_load_stackoverflow) 1973-06-14 1974-06-13
JP49067262A JPS5035037A (enrdf_load_stackoverflow) 1973-06-14 1974-06-14
BE145469A BE816384A (fr) 1973-06-14 1974-06-14 Depot electrolytique de zinc a partir de bains acides

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US00369815A US3855085A (en) 1973-06-14 1973-06-14 Acid zinc electroplating electrolyte, process and additive

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JP (1) JPS5035037A (enrdf_load_stackoverflow)
BE (1) BE816384A (enrdf_load_stackoverflow)
DE (1) DE2428499A1 (enrdf_load_stackoverflow)
FR (1) FR2233419B3 (enrdf_load_stackoverflow)
IT (1) IT1015050B (enrdf_load_stackoverflow)
NL (1) NL7407297A (enrdf_load_stackoverflow)

Cited By (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3945894A (en) * 1975-04-11 1976-03-23 Oxy Metal Industries Corporation Bath composition and method of electrodepositing utilizing the same
US4075066A (en) * 1977-01-27 1978-02-21 R. O. Hull & Company, Inc. Electroplating zinc, ammonia-free acid zinc plating bath therefor and additive composition therefor
US4089755A (en) * 1977-07-11 1978-05-16 The Richardson Company Acid bright zinc plating
US4119502A (en) * 1977-08-17 1978-10-10 M&T Chemicals Inc. Acid zinc electroplating process and composition
US4137133A (en) * 1977-12-15 1979-01-30 M&T Chemicals Inc. Acid zinc electroplating process and composition
US4138294A (en) * 1977-12-06 1979-02-06 M&T Chemicals Inc. Acid zinc electroplating process and composition
US4162947A (en) * 1978-05-22 1979-07-31 R. O. Hull & Company, Inc. Acid zinc plating baths and methods for electrodepositing bright zinc deposits
US4270990A (en) * 1979-06-07 1981-06-02 Minnesota Mining And Manufacturing Company Acidic electroplating baths with novel surfactants
US4422908A (en) * 1981-11-23 1983-12-27 E. I. Du Pont De Nemours & Co. Zinc plating
US4444630A (en) * 1977-07-11 1984-04-24 Richardson Chemical Company Acid bright zinc plating
US4981730A (en) * 1989-05-19 1991-01-01 Man-Gill Chemical Company Low VOC aqueous coating compositions and coated substrates
US4981729A (en) * 1989-05-25 1991-01-01 Man-Gill Chemical Company Electroconductive aqueous coating compositions, process, and coated substrates
US5326516A (en) * 1989-10-03 1994-07-05 Plasticolors, Inc. Method of preparing a cured pigmented thermosetting polymer composition exhibiting improved color values and reduced haze
US5443775A (en) * 1992-05-08 1995-08-22 Plasticolors, Inc. Process for preparing pigmented thermoplastic polymer compositions and low shrinking thermosetting resin molding composition
EP0774534A1 (en) 1995-11-15 1997-05-21 McGean-Rohco Inc. Aqueous electroless plating solutions
US6017872A (en) * 1998-06-08 2000-01-25 Ecolab Inc. Compositions and process for cleaning and finishing hard surfaces
WO2006057873A1 (en) * 2004-11-29 2006-06-01 Technic, Inc. Near neutral ph tin electroplating solution
US7905994B2 (en) 2007-10-03 2011-03-15 Moses Lake Industries, Inc. Substrate holder and electroplating system
US8262894B2 (en) 2009-04-30 2012-09-11 Moses Lake Industries, Inc. High speed copper plating bath
US9604316B2 (en) 2014-09-23 2017-03-28 Globalfoundries Inc. Tin-based solder composition with low void characteristic

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4070256A (en) * 1975-06-16 1978-01-24 Minnesota Mining And Manufacturing Company Acid zinc electroplating bath and process
JPS53131976A (en) * 1977-04-23 1978-11-17 Matsushita Electric Ind Co Ltd Catalyst reactor
JPH064899Y2 (ja) * 1989-01-06 1994-02-09 エヌデーシー株式会社 触媒等の保持構造物

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3594291A (en) * 1968-08-10 1971-07-20 Schering Ag Bright zinc plating from an acid electrolyte
US3669854A (en) * 1970-08-03 1972-06-13 M & T Chemicals Inc Zinc electroplating electrolyte and process
US3694330A (en) * 1967-05-23 1972-09-26 Joachim Korpium Electroplating bath for depositing bright zinc plates
US3758386A (en) * 1966-11-02 1973-09-11 M & T Chemicals Inc Novel zinc plating process

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3758386A (en) * 1966-11-02 1973-09-11 M & T Chemicals Inc Novel zinc plating process
US3694330A (en) * 1967-05-23 1972-09-26 Joachim Korpium Electroplating bath for depositing bright zinc plates
US3594291A (en) * 1968-08-10 1971-07-20 Schering Ag Bright zinc plating from an acid electrolyte
US3669854A (en) * 1970-08-03 1972-06-13 M & T Chemicals Inc Zinc electroplating electrolyte and process

Cited By (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3945894A (en) * 1975-04-11 1976-03-23 Oxy Metal Industries Corporation Bath composition and method of electrodepositing utilizing the same
US4075066A (en) * 1977-01-27 1978-02-21 R. O. Hull & Company, Inc. Electroplating zinc, ammonia-free acid zinc plating bath therefor and additive composition therefor
US4089755A (en) * 1977-07-11 1978-05-16 The Richardson Company Acid bright zinc plating
US4444630A (en) * 1977-07-11 1984-04-24 Richardson Chemical Company Acid bright zinc plating
US4119502A (en) * 1977-08-17 1978-10-10 M&T Chemicals Inc. Acid zinc electroplating process and composition
US4138294A (en) * 1977-12-06 1979-02-06 M&T Chemicals Inc. Acid zinc electroplating process and composition
US4137133A (en) * 1977-12-15 1979-01-30 M&T Chemicals Inc. Acid zinc electroplating process and composition
US4162947A (en) * 1978-05-22 1979-07-31 R. O. Hull & Company, Inc. Acid zinc plating baths and methods for electrodepositing bright zinc deposits
US4270990A (en) * 1979-06-07 1981-06-02 Minnesota Mining And Manufacturing Company Acidic electroplating baths with novel surfactants
US4422908A (en) * 1981-11-23 1983-12-27 E. I. Du Pont De Nemours & Co. Zinc plating
US4981730A (en) * 1989-05-19 1991-01-01 Man-Gill Chemical Company Low VOC aqueous coating compositions and coated substrates
US4981729A (en) * 1989-05-25 1991-01-01 Man-Gill Chemical Company Electroconductive aqueous coating compositions, process, and coated substrates
US5326516A (en) * 1989-10-03 1994-07-05 Plasticolors, Inc. Method of preparing a cured pigmented thermosetting polymer composition exhibiting improved color values and reduced haze
US5443775A (en) * 1992-05-08 1995-08-22 Plasticolors, Inc. Process for preparing pigmented thermoplastic polymer compositions and low shrinking thermosetting resin molding composition
EP0774534A1 (en) 1995-11-15 1997-05-21 McGean-Rohco Inc. Aqueous electroless plating solutions
US6017872A (en) * 1998-06-08 2000-01-25 Ecolab Inc. Compositions and process for cleaning and finishing hard surfaces
WO2006057873A1 (en) * 2004-11-29 2006-06-01 Technic, Inc. Near neutral ph tin electroplating solution
US20060113195A1 (en) * 2004-11-29 2006-06-01 George Hradil Near neutral pH tin electroplating solution
US7905994B2 (en) 2007-10-03 2011-03-15 Moses Lake Industries, Inc. Substrate holder and electroplating system
US8262894B2 (en) 2009-04-30 2012-09-11 Moses Lake Industries, Inc. High speed copper plating bath
US9604316B2 (en) 2014-09-23 2017-03-28 Globalfoundries Inc. Tin-based solder composition with low void characteristic

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Publication number Publication date
JPS5035037A (enrdf_load_stackoverflow) 1975-04-03
FR2233419A1 (enrdf_load_stackoverflow) 1975-01-10
DE2428499A1 (de) 1975-01-16
FR2233419B3 (enrdf_load_stackoverflow) 1977-04-08
IT1015050B (it) 1977-05-10
NL7407297A (enrdf_load_stackoverflow) 1974-12-17
BE816384A (fr) 1974-12-16

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