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US2989449A - Electrodeposition of zinc - Google Patents

Electrodeposition of zinc Download PDF

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US2989449A
US2989449A US20259A US2025960A US2989449A US 2989449 A US2989449 A US 2989449A US 20259 A US20259 A US 20259A US 2025960 A US2025960 A US 2025960A US 2989449 A US2989449 A US 2989449A
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water
zinc
alicyclic
anisaldehyde
polyvinyl alcohol
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US20259A
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Robert W Mackey
Donald A Swalheim
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EIDP Inc
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EI Du Pont de Nemours and Co
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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
    • C25D3/22Electroplating: Baths therefor from solutions of zinc
    • C25D3/24Electroplating: Baths therefor from solutions of zinc from cyanide baths

Definitions

  • Zinc electroplated onto base metals from a cyanidezinc electrolyte is usually dull and dark in appearance.
  • the use of brightening additives is necessary to obtain desirable zinc plates that have high luster and a bluewhite color.
  • an additive may con- .tain one or more extender or booster brighteners to prolong the life of the bath and to impart superior brightening effects to the plates.
  • Most of these high quality additives are available in the form of solids or slurries. Measuring and handling such additives is undesirable because they must be initially dissolved and otherwise manipulated before being added to the bath.
  • Such an additive can be added directly to aqueous cyanide-zinc plating baths without any of the ingredients separating. It has been found that when certain amounts of water and an alkali metal thiocyanate are added to a combination of conventional brighteners and a protective colloid, a single-phase liquid can be prepared.
  • Typical single-phase liquid additives can be prepared from the below-listed ingredients or their equivalents which additives include 20-70% water and 10-20% of an alkali metal thiocyanate.
  • Anisaldehyde is a suitable brightener, but other and related brighteners are equivalents thereof in the present invention. Among the equivalents are: veratralldehyde, piperonal, hydroxybenzaldehyde and the like. Hydroxybenzaldehyde is not quite as effective as anisaldehyde, but it and the abovelisted equivalents can be used either alone or in combination wtih one another. Anisaldehyde is preferred and it produces high luster deposits, but the use of extender or booster brighteners is necessary for optimum results.
  • An alicyclic alcohol or'ketone and a small amount of polyvinyl alcohol function as extender or booster brighteners in combination with substituted aromatic aldehydes.
  • the alicyclic compounds also assist to broaden the bright plating current density range.
  • the alicyclic compounds particularly useful as booster and extender brighteners in the presently described additive include those alicyclic alcohols and ketones having five to seven, preferably six, ring members.
  • the best alicyclic alcohols are cyclohexanol, Z-methyl cyclohexanol and trimethyl cyclohexanol; cyclohexanol is preferred.
  • the alicyclic ketones includecyclohexanone, Z-methyl cyclohexanone, 4-methyl cyclohexanone and trirnethyl cyclohexanone. Of these alicyclic ketones, cyclohexanone is preferred.
  • Additional alicyclic compounds include cyclopentanol, cycloheptanol, alicyclic glycols or alicyclic diols, alicyclic mono and di ethers such as tetrahydrofuran and 2,4-dioxane; other equivalents include the ketones disclosed in US. Patent No. 2,600,352, and the cyanhydrins of these ketones.
  • Both the aldehyde and alicyclic compound require solubilizing in aqueous cyanide-zinc plating baths, and these compounds should be solubilized before adding them to the plating bath.
  • Both of the above compounds are known to be soluble in alcohols, and 6-18% of a lower aliphatic alcohol that is miscible with water will satisfactorily solubilize both the aromatic aldehyde and the alicyclic alcohol or ketone.
  • Those alcohols having 1-6 carbon atoms such as methanol, ethanol, propanol, tertiary butanol and the like, are satisfactory, with isopropanol being preferred.
  • Other equivalents such as tetramethlethylenediamine, can be used as a solubilizer for the aromatic aldehyde and the alicyclic compound.
  • Polyvinyl alcohol is described in the prior art as being useful in cyanide-zinc baths and functions as a booster or extender brightener in combination with cyclohexanone.
  • Polyvinyl alcohols 'in general are suitable for use in the present invention and they may vary widely in characteristics. Where or more of the acetate groups are hydrolyzed to hydroxyl groups, the resulting polyvinyl alcohol is generally referred to as a completely hydrolyzed grade. Where fewer than 90% of the acetate groups are so hydrolyzed (or alcoholized), such an alcohol is usually denoted as partially hydrolyzed.
  • the molecular weight of the polyvinyl alcohol is likewise not critical, since most commercial polyvinyl alcohols are water soluble.
  • the average molecular weight may vary from about 10,000 to 200,000 or more.
  • the examples herein refer to completely hydrolyzed polyvinyl alcohols having average molecular weights of about 100,000 to 150,000, and such alcohols comprise about by weight of an aqueous solution. On a dry weight basis, the amount of-the polyvinyl alcohol should be 0.05 to 1.0% by weight of the single-phase liquid additive. Carboxymethylcellulose can be used as an equivalent of polyvinyl alcohol, although the latter is preferred.
  • the combination of ingredients that form a singlephase liquid additive includes a protective colloid that serves to improve coverage under barrel plating conditions at low current densities and facilitates the initial formation of zinc deposit.
  • Protective colloids are often used in cyanide-zinc plating baths and gelatin is preferred, although gum arabic, gum tragacanth, agaragar, peptone soluble starch and other colloids well known in the art are suitable.
  • the protective colloid will precipitate in the presence of water and alicyclic alcohol or ketone when the alcohol is added to solubilize the alicyclic compound.
  • additional water is added, together with polyvinyl alcohol, the mixture separates into three layers with the middle layer being an emulsion of the upper organic layer and the lower aqueous layer. The precipitate will slowly redissolve in the aqueous layer.
  • Example 1 An incomplete brightener formulation was prepared containing:
  • Example 1 Percent Anisaldehyde 10 Cyclohexanone 13 Gelatin 3 Polyvinyl alcohol (10% solution) 3 Sodium thiocyanate 15 Water 56 ingredients of Example 1 present in approximately the same amounts as indicated in that example. A pale yellow liquid was produced which separated into oily droplets when added to an aqueous solution, indicating that a protective colloid is necessary to retain the substituted aromatic aldehyde in solution.
  • an aliphatic alcohol and protective colloid must be present in the particular combination of ingredients disclosed herein that form superior additives.
  • Example 2 On addition of the isopropyl alcohol, part of the gelatin precipitated. After adding the remaining ingredients, the mixture separated into three layers with the middle layer being an emulsion of the other two liquid layers. After standing several days, the gelatin appeared to slowly redissolve in the lower (aqueous) layer. This example illustrates the elfect of omitting the alkali metal thiocyanate.
  • Example 3 A brightener formulation was prepared by mixing ingredients in the proportions shown below:
  • Example 4 Repeated plating tests of the brightener of Example 3 were made continuously in a 2-gallon laboratory barrel plating unit over a period of several days to determine the rate at which the brightener was consumed. These tests indicated that brightener additions of ca. 6 ml./gal. were required to maintain full brightness of the zinc plate for an 8-hour day, or 0.08 gram of anisaldehyde per hour. In similar tests of an additive containing anisaldehyde and gelatin, but no other brighteners, the anisaldehyde was consumed at the rate of 0.14 gram per hour. This illustrates the efiectiveness of the other components in the formulation of Example 3 in reducing the anisaldehyde consumption. Potassium and other alkali metal thiocyanates are substituted for the sodium compound in like amounts with the same results.
  • Example 5 A brightener formulation was prepared containing the following ingredients:
  • the resulting solution was a single-phase liquid having a clear amber color.
  • Deposits from a zinc plating bath to which two ml. of this brightener per gallon of plating solution had been added were brilliant and had a bluewhite color.
  • Example 6 A brightener formulation was prepared containing the following ingredients:
  • the resulting solution was a single phase liquid having a clear amber color.
  • a high luster zinc plate is produced.
  • a small amount of acetic acid was added to decompose inorganic impurities in the technical grade of gelatin used. It can be omitted if desired.
  • Example 7 A brightener formulation was prepared containing the following ingredients:
  • Example 8 A brightener formulation was prepared containing the following ingredients: a Percent Sodium thiocyanate 14.2 Gelatin 7.5 Isopropyl alcohol 5.7 Cyclohexanol 21.2 Polyvinyl alcohol (dry weight basis) 0.3 Acetic acid 0.6 Anisaidehyde 14.2 Water 36.3
  • the resulting product was a clear amber single phase solution which promotes the formation of high luster zinc plates.
  • the alicyclic alcohol or ketone and the polyvinyl alcohol function as booster or extender brighteners. Less anisaldehyde per ampere hour is thereby required. Of greater significance is the fact that the brightness does not decrease rapidly as the anisaldehyde becomes depleted. For example, the plating bath maintained with the liquid brightener containing these constituents will produce fair quality deposits upon resuming operation even after standing 16 hours or over a week-end. In contrast, other brighteners are largely decomposed under these conditions and plates deposited from solutions containing these additives are relatively dull. Larger additions are then required to restore the bath to full-bright plating performance. I
  • a single-phase liquid additive for an aqueous alkaline cyanide-zinc plating bath comprising by weight, 10- 20% of an alkali metal thio'cyanate, 5-25% of an alicyclic compound selected from the group consisting of alicyclic alcohols and alicyclic ketones, 210% of a protective colloid, 620% of a Water miscible aliphatic alcohol having 1-6 carbon atoms, 0.50-1.0% polyvinyl aloohol; 5-25% of a substituted aromatic aldehyde selected from the group consisting of anisaldehyde, vera-traldehyde, hydroxybenzaldehyde, piperonal and mixtures thereof and 20-70% water.
  • a single-phase liquid additive for an aqueous alkaline cyanide-zinc plating bath comprising by weight, 10-- 20% of an alkali metal thiocyanate, 525% cyclohexauol, 2-1 0% of a protective colloid, 6-20% of a water miscible aliphatic alcohol having l-6 carbon atoms, ODS-1.0% polyvinyl alcohol; 525% of a substituted aromatic aldehyde selected from the group consisting of anisaldehyde, veratraldehyde, hydroxybenzaldehyde, piperonal and mixtures thereof and 20-70% water.
  • a single-phase liquid additive for an aqueous alkaline cyanide-zinc plating bath comprising by weight, 10- 20% of an alkali metal thiocyanate, 5-25% cyclohexanone, 210% of a protective colloid, 620% of a water miscible aliphatic alcohol having 1-6 carbon atoms, 0.5- 1.0% polyvinyl alcohol; 5-25% of a substituted aromatic aldehyde selected from the group consisting of anisaldehyde, veratraldehyde, hydroxybenzaldehyde, piperonal and mixtures thereof and 20-70% water.
  • a single-phase liquid additive for an aqueous alkaline cyanide-zinc plating bath comprising by weight, 10- 20% of an alkali metal thiocyanate, 5-25% of an alicyclic compound selected from the group consisting of alicyclic alcohols and alicy ol-ic ketones, 2-10% of a protective colloid, 6-20% of a water miscible aliphatic alcohol having 1-6 carbon atoms, 0.05l.0% polyvinyl alcohol; 525% anisaldehyde and 2070% water.
  • a single-phase liquid additive for an aqueous alkaline cyanide-zinc plating bath comprising by weight, 10-- 20% of an alkali metal thiocyanate, 5-25% cyclohexauol, 2-10% of a protective colloid, 6-20% of a water miscible aliphatic alcohol having 1-6 carbon atoms, 0.05- 20% sodium thiocyanate, 5-25% cyclohexanol, 2-10% 1.70% polyvinyl alcohol; 525% anisaldehyde and 20- gelatin, 6-20% isopropanol, 0.05-1.0% polyvinyl alcohol,
  • a single-phase liquid additive for an aqueous alkaline cyanide-zinc plating bath comprising by weight, 10- 5 References Cited in the file of this patent 2 0% of an alkali metal thiocyanate, 5-25 cyclohexanol,

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Description

' in small amounts.
United States Patent 2,989,449 ELECTRODEPOSITION 0F ZINC Robert W. Mackey, Wilmington, and Donald A. Swalheim, Hockessin, Del., assignors to I. du Pont de Nemours and Company, Wilmington, Del., :1 corporation of Delaware No Drawing. Filed Apr. 6, 1960, Ser. No. 20,259 7 Claims. (Cl. 204-55) This invention relates to an improvement in the electrodeposition of zinc and, more particularly, this inven tion is concerned with depositing bright zinc plates from aqueous alkaline cyanide-zinc solutions containing a novel brightening additive.
Zinc electroplated onto base metals from a cyanidezinc electrolyte is usually dull and dark in appearance. The use of brightening additives is necessary to obtain desirable zinc plates that have high luster and a bluewhite color.
The problem of finding a combination of ingredients that will function correctly as brightening agents in aqueous alkaline plating solutions is complicated because of solubility, discoloration, stability and other factors, and to date these difficulties have only been partially overcome. Accordingly, past efforts have developed brightening agents that are unsatisfactory because of their inferior performance over a wide current density range due principally to the difiiculties encountered in maintaining an effective combination of ingredients in the bath. The plating bath cannot be controlled because of these difficulties and the continuous use of the bath will not deposit bright zinc plates.
Many of the additives now being employed in cyanidezinc plating baths contain several brighteners. In addition to the principal brighteners, an additive may con- .tain one or more extender or booster brighteners to prolong the life of the bath and to impart superior brightening effects to the plates. Most of these high quality additives are available in the form of solids or slurries. Measuring and handling such additives is undesirable because they must be initially dissolved and otherwise manipulated before being added to the bath.
Many of the desirable ingredients used in cyanide-zinc plating baths are organic and immiscible in Water, even For example, some of the aromatic aldehydes are excellent brighteners but require solubilizing. The use of additional organic ingredients as extender or booster brighteners requires a unique combination of ingredients if zinc plates of superior brightness are to be produced.
A single-phase liquid additive containing water and the necessary organic ingredients that are normally immiscible in water oflfers distinct and obvious advantages. Such an additive can be added directly to aqueous cyanide-zinc plating baths without any of the ingredients separating. It has been found that when certain amounts of water and an alkali metal thiocyanate are added to a combination of conventional brighteners and a protective colloid, a single-phase liquid can be prepared.
It is an object of the present invention to provide a single-phase liquid additive that will demonstrate high brightening activity in cyanide-zinc plating processes.
It is another object of the present invention to provide a single-phase liquid additive that may be readily added to an aqueous alkaline cyanide-zinc plating bath and remain in solution.
It is a further object of the present invention to provide a single-phase liquid additive that may be effectively used in an aqueous alkaline cyanide-zinc plating bath over a relatively broad current density range.
These and other objects are accomplished by employing 10-20% of an alkali metal thiocyanate and 20-70% Patented June 20, 1961 water in combination with several organic brighteners, solvents and a protective colloid.
Typical single-phase liquid additives can be prepared from the below-listed ingredients or their equivalents which additives include 20-70% water and 10-20% of an alkali metal thiocyanate.
5-25 of an alicyclic alcohol orketone 210% of a protective colloid 6-20% of a water miscible lower (1-6 carbon atoms) aliphatic alcohol vODS-1.0% polyvinyl alcohol 5-25% of a substituted aromatic aldehyde Percentages in the above typical formulations and throughout the specification are by weight.
As noted above, most superior brighteners contain a substituted aromatic aldehyde. Anisaldehyde is a suitable brightener, but other and related brighteners are equivalents thereof in the present invention. Among the equivalents are: veratralldehyde, piperonal, hydroxybenzaldehyde and the like. Hydroxybenzaldehyde is not quite as effective as anisaldehyde, but it and the abovelisted equivalents can be used either alone or in combination wtih one another. Anisaldehyde is preferred and it produces high luster deposits, but the use of extender or booster brighteners is necessary for optimum results. An alicyclic alcohol or'ketone and a small amount of polyvinyl alcohol function as extender or booster brighteners in combination with substituted aromatic aldehydes. The alicyclic compounds also assist to broaden the bright plating current density range. V p
The alicyclic compounds particularly useful as booster and extender brighteners in the presently described additive include those alicyclic alcohols and ketones having five to seven, preferably six, ring members. The best alicyclic alcohols are cyclohexanol, Z-methyl cyclohexanol and trimethyl cyclohexanol; cyclohexanol is preferred. The alicyclic ketones includecyclohexanone, Z-methyl cyclohexanone, 4-methyl cyclohexanone and trirnethyl cyclohexanone. Of these alicyclic ketones, cyclohexanone is preferred. Additional alicyclic compounds include cyclopentanol, cycloheptanol, alicyclic glycols or alicyclic diols, alicyclic mono and di ethers such as tetrahydrofuran and 2,4-dioxane; other equivalents include the ketones disclosed in US. Patent No. 2,600,352, and the cyanhydrins of these ketones.
Both the aldehyde and alicyclic compound require solubilizing in aqueous cyanide-zinc plating baths, and these compounds should be solubilized before adding them to the plating bath.
Both of the above compounds are known to be soluble in alcohols, and 6-18% of a lower aliphatic alcohol that is miscible with water will satisfactorily solubilize both the aromatic aldehyde and the alicyclic alcohol or ketone. Those alcohols having 1-6 carbon atoms, such as methanol, ethanol, propanol, tertiary butanol and the like, are satisfactory, with isopropanol being preferred. Other equivalents, such as tetramethlethylenediamine, can be used as a solubilizer for the aromatic aldehyde and the alicyclic compound.
Polyvinyl alcohol is described in the prior art as being useful in cyanide-zinc baths and functions as a booster or extender brightener in combination with cyclohexanone. Polyvinyl alcohols 'in general are suitable for use in the present invention and they may vary widely in characteristics. Where or more of the acetate groups are hydrolyzed to hydroxyl groups, the resulting polyvinyl alcohol is generally referred to as a completely hydrolyzed grade. Where fewer than 90% of the acetate groups are so hydrolyzed (or alcoholized), such an alcohol is usually denoted as partially hydrolyzed.
In addition, the molecular weight of the polyvinyl alcohol is likewise not critical, since most commercial polyvinyl alcohols are water soluble. The average molecular weight may vary from about 10,000 to 200,000 or more.
The examples herein refer to completely hydrolyzed polyvinyl alcohols having average molecular weights of about 100,000 to 150,000, and such alcohols comprise about by weight of an aqueous solution. On a dry weight basis, the amount of-the polyvinyl alcohol should be 0.05 to 1.0% by weight of the single-phase liquid additive. Carboxymethylcellulose can be used as an equivalent of polyvinyl alcohol, although the latter is preferred.
The combination of ingredients that form a singlephase liquid additive includes a protective colloid that serves to improve coverage under barrel plating conditions at low current densities and facilitates the initial formation of zinc deposit. Protective colloids are often used in cyanide-zinc plating baths and gelatin is preferred, although gum arabic, gum tragacanth, agaragar, peptone soluble starch and other colloids well known in the art are suitable.
In the past, it has been particularly difiicult to solubilize the protective colloid in the presence of the brighteners and other constituents. The combination of an alkali metal thiocyanate and water has a unique action in this respect and a single-phase liquid additive containing the above-listed combination of ingredients can be prepared only if water and the thiocyanate compound are used. In particular, the protective colloid will precipitate in the presence of water and alicyclic alcohol or ketone when the alcohol is added to solubilize the alicyclic compound. When additional water is added, together with polyvinyl alcohol, the mixture separates into three layers with the middle layer being an emulsion of the upper organic layer and the lower aqueous layer. The precipitate will slowly redissolve in the aqueous layer.
It the aliphatic alcohol is omitted from the above typical brightening solutions, two layers are formed, with the upper layer being largely organic and the lower layer being predominantly water with dissolved thiocyanate and polyvinyl alcohol.
An appreciable amount of water (20-70% by weight) must be present with the alkali metal thiocyanate in additives that contain conventional organic brighteners and a protective colloid. As noted above, there are numerous equivalents for the brighteners and protective colloid. The essential feature of the present invention is the formation of a single-phase liquid additive through the use of 10-20% of an alkali metal thiocyanate together with 20-70% water. The remainder of the additive can be the combination of organic brightening agents and protective colloids suggested by the above formulations. These formulations give excellent results, but other formulations that include organic brighteners and protective colloids will be benefited through the use of water and alkali metal thiocyanate.
Example 1 An incomplete brightener formulation was prepared containing:
Percent Anisaldehyde 10 Cyclohexanone 13 Gelatin 3 Polyvinyl alcohol (10% solution) 3 Sodium thiocyanate 15 Water 56 ingredients of Example 1 present in approximately the same amounts as indicated in that example. A pale yellow liquid was produced which separated into oily droplets when added to an aqueous solution, indicating that a protective colloid is necessary to retain the substituted aromatic aldehyde in solution.
As indicated above, an aliphatic alcohol and protective colloid must be present in the particular combination of ingredients disclosed herein that form superior additives.
Example 2 On addition of the isopropyl alcohol, part of the gelatin precipitated. After adding the remaining ingredients, the mixture separated into three layers with the middle layer being an emulsion of the other two liquid layers. After standing several days, the gelatin appeared to slowly redissolve in the lower (aqueous) layer. This example illustrates the elfect of omitting the alkali metal thiocyanate.
The importance of developing a single-phase liquid additive cannot be overemphasized. If an incorrectly balanced combination of brighteners and solubilizing agents is added to an aqueous zinc cyanide bath, a precipitate or separate oily phase will appear and inferior zinc plates will result, since the full activity of the brightening agents has been restricted.
Example 3 A brightener formulation was prepared by mixing ingredients in the proportions shown below:
This was a clear, amber single-phase liquid having a rather pleasant odor. A clear solution was obtained on mixing up to 1 volume of water in 2.5 volumes of brightener. The white precipitate resulting from further additions of water redissolved when the brightener concentration had been reduced to approximately 75 ml. of brightener per gallon of water. No oily droplets were visible when the brightener was added to water or to zinc plating solution in concentrations up to approximately ml./ ga
Additions of this brightener to cyanide-zinc plating solutions may be readily made. For instance, the above addi tive was added to a typical cyanide-zinc solution containing:
Oz./gal. Zinc cyanide 8.0 Sodium cyanide 6.4 Sodium hydroxide 10.4 Sodium carbonate 4.0
Example 4 Repeated plating tests of the brightener of Example 3 were made continuously in a 2-gallon laboratory barrel plating unit over a period of several days to determine the rate at which the brightener was consumed. These tests indicated that brightener additions of ca. 6 ml./gal. were required to maintain full brightness of the zinc plate for an 8-hour day, or 0.08 gram of anisaldehyde per hour. In similar tests of an additive containing anisaldehyde and gelatin, but no other brighteners, the anisaldehyde was consumed at the rate of 0.14 gram per hour. This illustrates the efiectiveness of the other components in the formulation of Example 3 in reducing the anisaldehyde consumption. Potassium and other alkali metal thiocyanates are substituted for the sodium compound in like amounts with the same results.
Example 5 A brightener formulation was prepared containing the following ingredients:
Percent Sodium thiocyanate 15.0 Gelatin 8.0 Isopropyl alcohol 13.0 Cyclohexanone 15.0 Polyvinyl alcohol (dry weight basis) 0.2 Anisaldehyde 10.0 Water 38.8
The resulting solution was a single-phase liquid having a clear amber color. Deposits from a zinc plating bath to which two ml. of this brightener per gallon of plating solution had been added were brilliant and had a bluewhite color.
Example 6 A brightener formulation was prepared containing the following ingredients:
Percent Sodium thiocyanate 15.0 Gelatin 8.0 Cyclohexanol 5:0 Isopropyl alcohol 17.5 Polyvinyl alcohol (dry weight basis) 0.3 Acetic acid 0.6 Anisaldehyde 15.0 Water 38.6
The resulting solution was a single phase liquid having a clear amber color. When added to the cyanide-zinc plating bath, a high luster zinc plate is produced. A small amount of acetic acid was added to decompose inorganic impurities in the technical grade of gelatin used. It can be omitted if desired.
Example 7 A brightener formulation was prepared containing the following ingredients:
Percent Sodium thiocyanate 15.0 Gelatin 8.0 Isopropyl alcohol 12.5 Cyclohexanol 10.0 Polyvinyl alcohol (dry weight basis) 0.3 Acetic acid 0.6 Anisaldehyde 15.0 Water 38.6
6 Example 8 A brightener formulation was prepared containing the following ingredients: a Percent Sodium thiocyanate 14.2 Gelatin 7.5 Isopropyl alcohol 5.7 Cyclohexanol 21.2 Polyvinyl alcohol (dry weight basis) 0.3 Acetic acid 0.6 Anisaidehyde 14.2 Water 36.3
The resulting product was a clear amber single phase solution which promotes the formation of high luster zinc plates.
The alicyclic alcohol or ketone and the polyvinyl alcohol function as booster or extender brighteners. Less anisaldehyde per ampere hour is thereby required. Of greater significance is the fact that the brightness does not decrease rapidly as the anisaldehyde becomes depleted. For example, the plating bath maintained with the liquid brightener containing these constituents will produce fair quality deposits upon resuming operation even after standing 16 hours or over a week-end. In contrast, other brighteners are largely decomposed under these conditions and plates deposited from solutions containing these additives are relatively dull. Larger additions are then required to restore the bath to full-bright plating performance. I
This application is a continuation-in-part of our application Serial No. 771,195, filed November 3, 1958, now abandoned.
We claim:
1. A single-phase liquid additive for an aqueous alkaline cyanide-zinc plating bath comprising by weight, 10- 20% of an alkali metal thio'cyanate, 5-25% of an alicyclic compound selected from the group consisting of alicyclic alcohols and alicyclic ketones, 210% of a protective colloid, 620% of a Water miscible aliphatic alcohol having 1-6 carbon atoms, 0.50-1.0% polyvinyl aloohol; 5-25% of a substituted aromatic aldehyde selected from the group consisting of anisaldehyde, vera-traldehyde, hydroxybenzaldehyde, piperonal and mixtures thereof and 20-70% water.
2. A single-phase liquid additive for an aqueous alkaline cyanide-zinc plating bath comprising by weight, 10-- 20% of an alkali metal thiocyanate, 525% cyclohexauol, 2-1 0% of a protective colloid, 6-20% of a water miscible aliphatic alcohol having l-6 carbon atoms, ODS-1.0% polyvinyl alcohol; 525% of a substituted aromatic aldehyde selected from the group consisting of anisaldehyde, veratraldehyde, hydroxybenzaldehyde, piperonal and mixtures thereof and 20-70% water.
3. A single-phase liquid additive for an aqueous alkaline cyanide-zinc plating bath comprising by weight, 10- 20% of an alkali metal thiocyanate, 5-25% cyclohexanone, 210% of a protective colloid, 620% of a water miscible aliphatic alcohol having 1-6 carbon atoms, 0.5- 1.0% polyvinyl alcohol; 5-25% of a substituted aromatic aldehyde selected from the group consisting of anisaldehyde, veratraldehyde, hydroxybenzaldehyde, piperonal and mixtures thereof and 20-70% water.
4. A single-phase liquid additive for an aqueous alkaline cyanide-zinc plating bath comprising by weight, 10- 20% of an alkali metal thiocyanate, 5-25% of an alicyclic compound selected from the group consisting of alicyclic alcohols and alicy ol-ic ketones, 2-10% of a protective colloid, 6-20% of a water miscible aliphatic alcohol having 1-6 carbon atoms, 0.05l.0% polyvinyl alcohol; 525% anisaldehyde and 2070% water.
5. A single-phase liquid additive for an aqueous alkaline cyanide-zinc plating bath comprising by weight, 10-- 20% of an alkali metal thiocyanate, 5-25% cyclohexauol, 2-10% of a protective colloid, 6-20% of a water miscible aliphatic alcohol having 1-6 carbon atoms, 0.05- 20% sodium thiocyanate, 5-25% cyclohexanol, 2-10% 1.70% polyvinyl alcohol; 525% anisaldehyde and 20- gelatin, 6-20% isopropanol, 0.05-1.0% polyvinyl alcohol,
70% water. 525% 'anisaldehyde and 2070% water.
6. A single-phase liquid additive for an aqueous alkaline cyanide-zinc plating bath comprising by weight, 10- 5 References Cited in the file of this patent 2 0% of an alkali metal thiocyanate, 5-25 cyclohexanol,
2-10% of a protective colloid, 6-20% isopropanol, 0.05- UNITED STATES PATENTS 1.0% polyvinyl alcohol; 5-25% anisaldehyde and 20- 2,101,580 Henricks Dec. 7, 1937 70% water. 2,621,152 Hoffman Dec. 9, 1952 7. A single-phase liquid additive for an aqueous alka- 10 2,740,754 Hoifman Apr. 3, 1956 line cyanide-zinc plating bath comprising by weight, 10- 2,860,089 Jackson Nov. 11, 1958 V UNITED STATES PATENT OFFICE CERTIFICATE OF CORRECTION Patent No, 2,989,449 June 20, 1961 Robert W. ,Mackey et a1.
It is hereby certified that error appears in the above numbered patent requiring correction and that the said Letters Patent should read as corrected below.
Column 6, line 41, for "0.50-1.0%" read 0.05-1.0% lines 59 and 60 for "O51.,O%" read 0.05-1.0%
Signed and sealed this 141th day of November 1961.
(SEAL) Attest:
ERNEST W. SWIDER DAVID L. LADD Commissioner of Patents Attesting Officer USCOM M- DC

Claims (1)

1. A SINGLE-PHASE LIQUID ADDITIVE FOR AN AQUEOUS ALKALINE CYANIDE-ZINC PLATING BATH COMPRISING BY WEIGHT, 1020% OF AN ALKALI METAL THIOCYANATE, 5-25% OF AN ALICYCLIC COMPOUND SELECTED FROM THE GROUP CONSISTING OF ALICYCLIC ALCOHOLS AND ALICYCLIC KETONES, 2-10% OF A PROTECTIVE COLLOID, 6-20% OF A WATER MISCIBLE ALIPHATIC ALCOHOL HAVING 1-6 CARBON ATOMS, 0.50-1.0% POLYVINYL ALCOHOL, 5-25% OF A SUBSTITUTED AROMATIC ALDEHYDE SELECTED FROM THE GROUP CONSISTING OF ANISALDEHYDE, VERATRALDEHYDE, HYDROXYBENZALDEHYDE, PIPERONAL AND MIXTURES THEREOF AND 20-70% WATER.
US20259A 1960-04-06 1960-04-06 Electrodeposition of zinc Expired - Lifetime US2989449A (en)

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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3274080A (en) * 1962-05-25 1966-09-20 Cowles Chem Co Brighteners and process for cyanide zinc electrodeposition
US3454475A (en) * 1965-07-13 1969-07-08 Du Pont Electroplating bath and process
US3945894A (en) * 1975-04-11 1976-03-23 Oxy Metal Industries Corporation Bath composition and method of electrodepositing utilizing the same

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2101580A (en) * 1936-05-02 1937-12-07 Udylite Company Process for obtaining bright zinc coating
US2621152A (en) * 1950-03-30 1952-12-09 Allied Res Products Inc Zinc cyanide plating bath
US2740754A (en) * 1952-11-07 1956-04-03 Allied Res Products Inc Zinc plating brightener
US2860089A (en) * 1956-08-09 1958-11-11 R O Hull & Company Inc Method of electro depositing zinc

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2101580A (en) * 1936-05-02 1937-12-07 Udylite Company Process for obtaining bright zinc coating
US2621152A (en) * 1950-03-30 1952-12-09 Allied Res Products Inc Zinc cyanide plating bath
US2740754A (en) * 1952-11-07 1956-04-03 Allied Res Products Inc Zinc plating brightener
US2860089A (en) * 1956-08-09 1958-11-11 R O Hull & Company Inc Method of electro depositing zinc

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3274080A (en) * 1962-05-25 1966-09-20 Cowles Chem Co Brighteners and process for cyanide zinc electrodeposition
US3454475A (en) * 1965-07-13 1969-07-08 Du Pont Electroplating bath and process
US3945894A (en) * 1975-04-11 1976-03-23 Oxy Metal Industries Corporation Bath composition and method of electrodepositing utilizing the same

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