US3472743A - Zinc plating baths and additives therefor - Google Patents

Zinc plating baths and additives therefor Download PDF

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US3472743A
US3472743A US602522A US3472743DA US3472743A US 3472743 A US3472743 A US 3472743A US 602522 A US602522 A US 602522A US 3472743D A US3472743D A US 3472743DA US 3472743 A US3472743 A US 3472743A
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bath
hydroxybenzylidene
zinc
azomethine
plating
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John Derek Rushmere
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EIDP Inc
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EI Du Pont de Nemours and Co
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D213/44—Radicals substituted by doubly-bound oxygen, sulfur, or nitrogen atoms, or by two such atoms singly-bound to the same carbon atom
    • C07D213/53—Nitrogen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/72—Nitrogen atoms
    • C07D213/74—Amino or imino radicals substituted by hydrocarbon or substituted hydrocarbon radicals
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D217/00—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
    • C07D217/02—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with only hydrogen atoms or radicals containing only carbon and hydrogen atoms, directly attached to carbon atoms of the nitrogen-containing ring; Alkylene-bis-isoquinolines
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
    • C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D307/38—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D307/52—Radicals substituted by nitrogen atoms not forming part of a nitro radical
    • C—CHEMISTRY; METALLURGY
    • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25D—PROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
    • C25D3/00—Electroplating: Baths therefor
    • C25D3/02—Electroplating: Baths therefor from solutions
    • C25D3/22—Electroplating: Baths therefor from solutions of zinc
    • C25D3/24—Electroplating: Baths therefor from solutions of zinc from cyanide baths

Definitions

  • another part of the invention comprises adding to the plating baths organic polymers such as polyvinyl alcohol along with the defined azomethines to further improve the brightness and luster of the deposited zinc.
  • azomethines are efiective brightening agents for use in an aqueous zinc cyanide plating bath and that they have a much higher stability, with lower use cost than the aromatic aldehydes presently used. It has also been discovered that the brightness of the deposited zinc can be further improved by adding an organic polymer such as polyvinyl alcohol to the plating bath.
  • One way to prepare the azomethines used in this invention is to condense an aldehyde with a primray amine:
  • R and X may be either aryl or alkyl
  • the R and X can be substituted or unsubstituted with various substituents to be described more fully later herein.
  • R be aryl while X may be either aryl or alkyl.
  • the condensation reaction may be effected by mixing the aldehyde and amine together in a suitable solvent such as methyl alcohol, the azomethine crystallizing out on standing.
  • a suitable solvent such as methyl alcohol
  • azomethine which is chosen to practice the invention should be soluble in the plating bath.
  • soluble it is meant having a solubility of at least about 0.1 gram per liter at a temperature of about 25 C. in an alkaline cyanide zinc plating bath.
  • Azomethines which do not have the re quired solubility but which might otherwise be anticipated as being effective zinc brighteners, such as benzylidene aniline.
  • benzylidene aniline can be rendered useful by incorporating an alkali solubilizing group such as OH, COOH, or 4O H into the molecule.
  • an alkali solubilizing group such as OH, COOH, or 4O H
  • One way of adding the alkali solubilizing group to the azomethine molecule is to start with the appropriately substituted aldehyde or amine.
  • the invention comprises an aqueous cyanide zinc electroplating bath containing a brightening agent therefor an azomethine, the azomethine being soluble in the bath.
  • a sufiicient amount of azomethine present in the bath to yield a zinc electrodeposit of improved-brightness.
  • the azomethine used have at least one aromatic group as part of the molecule, and be present in the bath in an amount from about 0.1 to 10 grams per liter.
  • R be aryl and X be either aryl or alkyl.
  • Some of the aryl groups that are satisfactory for use in the R and X positions are phenyl, pyridyl, napthyl, quinolyl, and isoquinolyl. It is usually preferred that the alkyl group contain from about 1 to 6 carbon atoms. It is also possible to use certain heterocyclic groups having a partial aromatic nature such as pyrrole and furan in one or both of the R and X positions.
  • Organic polymers may be added to the plating bath along with aromatic azomethines to further improve brightness and luster of deposited zinc.
  • Polyvinyl alcohols natural polymers such as gelatin, peptone, gum tragacanth and agar-agar, as well as other synthetic polymers such as polyethyleneimine and the glyceryl ethers of polyvinyl alcohols are satisfactory for this purpose.
  • Polyvinyl alcohols having molecular weights from about 5,000 to 20,000 work well as additives to improve brightness and in addition exhibit outstanding tolerance to sodium carbonate which builds up in the plating bath and which tends to salt out polyvinyl alcohols of higher molecular weight.
  • a preferred polymer is polyvinyl alcohol which has a molecular weight of about 16,800 and which has been found to improve zinc brightness and exhibit excellent resistance to carbonate.
  • the optimum amount of the azomethine brightening agent will depend upon the specific compound used, the current density employed, and the type of plate desired. This optimum amount will generally range from about 0.1 to 10 g./l. of bath.
  • the polymer concentration should be from about 0.01 to 10 grams per liter of bath, preferably about 0.05 to 0.5 gram per liter of bath.
  • the azomethine and organic polymer may be added separately but are preferably added together in the form of a concentrated aqueous brightener additive solution. This solution may contain from 1:1 to 50:1 parts
  • Example I The zinc plating bath used in tests 1-5 was prepared in 4 liter batches having the following composition:
  • the brightening agent used was 3-(4-hydroxybenzylidene)3-aminopyridine 3-(4-hydroxybenzylidene) 3-am1nopyridine which was prepared by the condensation of 3-aminopyridine and p-hydroxybenzaldehyde.
  • Test 1 This test demonstrates that an improvement in brightness can be obtained over a wide range of current densities.
  • a steel Hull cell panel was plated at 2 amps for minutes in a bath as prepared above containing 0.8 g./l. of 3 (4-hydroxybenzylidene)3-aminopyridine. After washing in water and dipping in 0.5 wt. percent HNO to remove stains, the panel had the following appearance:
  • Test 2 This test demonstrates the utility of 3-(4-hydroxybenzylidene)3-aminopyridine as a brightening agent in practical still plating.
  • a steel automobile crank hole cover (the crank -hole cover which was used in the electroplating tests has an outer surface comprises of a series of convex surfaces and an inner surface comprised of a series of concave surfaces) was plated at 3.5 amps for minutes in a cyanide plating bath, as prepared above, containing 1.5 g./l. of 3-(4-hydroxybenzylidene)3-aminopyridine. After washing and dipping in 0.5 wt. percent HNO a very bright and shining plate was obtained on all surfaces except those of very low current density, which were somewhat duller. However, the plate on all surfaces was considerably improved over that obtained in the absence of any brightening agent.
  • Test 3 This test demonstrates the co-use of polyvinyl alcohol with 3-(4-hydroxybenzylidene)3-aminopyridine in practical still plating.
  • a steel crank hole cover was plated for 3.5 amps for 15 minutes in a cyanide plating bath, as prepared above, to which has been added 3.0 g./l. of 3-(4-hydroxybenzylidene)3-aminopyridine and 0.09 g./l. of Elvanol polyvinyl alcohol 51-03 (trademark for Du Ponts water-soluble polyvinyl alcohol having an average molecular weight of about 16,800).
  • After Washing and dipping in 0.5 wt. percent HNO a very bright plate was obtained on all surfaces, including those of low current density. The product was judged to be equal or superior to that obtained with the best commercial cyanide zinc brighteners.
  • Test 4 This 'test demonstrates the co-use of polyvinyl alcohol with 3-(4-hydroxybenzylidene)3-arninopyridine in practical barrel plating.
  • One hundred grns. of steel screws were barrel plated at 5 amps for 18 minutes in the bath from test 3.
  • the screws produced were bright, but were somewhat stained.
  • the stains were readily removed by dipping the screws in 0.5 wt. percent HNO
  • the result ing product had an overall quality equivalent to similar products available commercially.
  • Test 5 This test demonstrates the excellent stability of the 3 (4 hydroxybenzylidene)3 aminopyridine Elvanol 51-03 system in the cyanide plating bath.
  • the bath from test 4 was stored for two weeks and then used to plate an automobile crank hole cover at 3.5 amps for 15 minutes. The cover was then washed and dipped in 0.5 wt. percent HNO The result was a uniformly bright plate only slightly inferior to that produced from test 3.
  • the stability of the system used here is even more striking when compared with those using aromatic aldehydes, which lose their activity in a twenty-four hour idle period.
  • Example II The plating bath used in tests 1 and 2 was the same as that in Example I, i.e., it was prepared in 4 liter batches and had the following composition:
  • Example III In Examples 1-22 in the table which follows are listed a variety of azomethines which were prepared by the condensation of selected anldehydes and amines and tested for activity as cyanide zinc plating agents. The principal test used was "the still plating of automobile crank hole covers; the various brightening agents being The primary advantage of the brightening agents of added to the plating bath of Example I in amounts varythis invention is the excellent quality of bright zinc plate ing between about 0.1 and 10 -g./l. All azomethines obtained. Also, the compositions of this invention are listed in the Table gave an improved electroplate which stable both in storage and in the plating bath during was brighter and smoother than that obtained without a 5 use and periods of non-use. Their rate of consumption brightening agent.
  • azomethine brightening agents was rated as follows: particular importance is the fact that a brightener composition containing an azomethine is usually equally brighter"- fiii's fiv lfi l ifii ieiiiiifiZLZFFZLEEZ 1 l e l Enema-1t? g to the performance of the best range of current densities and also the fact that bright mercla pro ucts zinc deposits obtained from their use are responsive to Examples 23-42 in the table are other azomethines treatment with protective agents such as chromate conwhich are active brighteners for cyanide zinc plating 15 version coating preparations.
  • Examples 23-42 Source Example N o. Aldehyde Amine Resulting Azomethine Methylamine..- l-(d-hydroxybenzylidene)methylamine. Ethylemame. 1-(4-hydroxybenzylidene)ethylamine.
  • a bath-soluble organic polymer selected from the group consisting of polyvinyl alcohol, polyethyleneimine, gelatin and peptone is present in an amount from about 0.01 to 10 grams per liter of bath.
  • organic polymer is a polyvinyl alcohol having a molecular weight from about 5,000 to 20,000.
  • said brightening agent comprises 3- (4-hydroxybenzylidene) 3-aminopyridine.
  • said brightening agent comprises 1- (4-hydroxybenzylidene aniline.
  • said azomethine comprises 3-(4-hydroxybenzylidene)3-aminopyridine or 1-(4- hydroxybenzylidene)aniline and said organic polymer comprises polyvinyl alcohol having a molecular weight from about 5,000 to 20,000, said polyvinyl alcohol being present in an amount from about 0.05 to 0.5 gram per liter of bath.
  • composition of claim 8 wherein said azomethine is 3-(4-hydroxybenzylidene)3-aminopyridine or 1-(4- hydroxybenzylidene)aniline and said organic polymer is polyvinyl alcohol having a molecular weight of about 16,800.

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Description

United States Patent US. Cl. 20455 9 Claims ABSTRACT OF THE DISCLOSURE This invention relates to novel method of improving the brightness of zinc which is electrodeposited from aqueous zinc cyanide plating baths. More particularly, the invention comprises adding to the plating baths to improve the brightness of zinc deposited therefrom, an azomethine of the general formula RCH=NX wherein R and X are selected from the group consisting of phenyl, naphthyl and pyridyl and at least one of the groups R and X has substituted therein at least one substitutent selected from the group consisting of NH COOH, OH, SO H and alkoxy. In addition, another part of the invention comprises adding to the plating baths organic polymers such as polyvinyl alcohol along with the defined azomethines to further improve the brightness and luster of the deposited zinc.
BACKGROUND OF THE INVENTION The use of brightening agents in the eleetrodeposition of zinc from alkaline cyanide plating baths is well known. Aromatic aldehydes, usually in the form of an aldehyde bisulfite addition compound, have been used extensively as brightening agents in commercial zinc plating. The use of the bisulfite addition compounds is necessary to effect sufiicient solubility of the aromatic aldehyde in the plating bath to achieve beneficial plating results. Other brightening agents are also employed, with the type of brightening agent used generally depending on whether the plating bath is acid, containing zinc sulfate, chloride, or fluoroborate; or alkaline, containing zinc cyanide. This invention is concerned with alkaline zinc cyanide plating baths and improved brightening agents therefor.
One of the principal brightening agents used in zinc cyanide plating baths has ben aromatic aldehydes. The problem with the use of these compounds is their instability in the cyanide plating bath, causing rapid decomposition during use and storage, and resulting in a high use cost. Consequently, efforts have been made to discover compositions which are more stable in the plating bath than aromatic aldehydes and which have equivalent or better brightening activity.
DESCRIPTION OF THE INVENTION It has been discovered that azomethines are efiective brightening agents for use in an aqueous zinc cyanide plating bath and that they have a much higher stability, with lower use cost than the aromatic aldehydes presently used. It has also been discovered that the brightness of the deposited zinc can be further improved by adding an organic polymer such as polyvinyl alcohol to the plating bath.
One way to prepare the azomethines used in this invention is to condense an aldehyde with a primray amine:
where both R and X may be either aryl or alkyl, The R and X can be substituted or unsubstituted with various substituents to be described more fully later herein. For the purpose of practicing this invention it is preferred that R be aryl while X may be either aryl or alkyl. The condensation reaction may be effected by mixing the aldehyde and amine together in a suitable solvent such as methyl alcohol, the azomethine crystallizing out on standing. Of course, it may be more desirable from an economic viewpoint in practicing this invention to use a commercially available azomethine rather than preparing the azomethine as shown above.
From a practical standpoint the particular azomethine which is chosen to practice the invention should be soluble in the plating bath. (By the term soluble it is meant having a solubility of at least about 0.1 gram per liter at a temperature of about 25 C. in an alkaline cyanide zinc plating bath.) Azomethines which do not have the re quired solubility but which might otherwise be anticipated as being effective zinc brighteners, such as benzylidene aniline.
benzylidene aniline can be rendered useful by incorporating an alkali solubilizing group such as OH, COOH, or 4O H into the molecule. One way of adding the alkali solubilizing group to the azomethine molecule is to start with the appropriately substituted aldehyde or amine.
Specifically the invention comprises an aqueous cyanide zinc electroplating bath containing a brightening agent therefor an azomethine, the azomethine being soluble in the bath. There should be a sufiicient amount of azomethine present in the bath to yield a zinc electrodeposit of improved-brightness. It is preferred that the azomethine used have at least one aromatic group as part of the molecule, and be present in the bath in an amount from about 0.1 to 10 grams per liter.
In the azomethine molecule, having the general formula RCH=NX, it is preferred that R be aryl and X be either aryl or alkyl. Some of the aryl groups that are satisfactory for use in the R and X positions are phenyl, pyridyl, napthyl, quinolyl, and isoquinolyl. It is usually preferred that the alkyl group contain from about 1 to 6 carbon atoms. It is also possible to use certain heterocyclic groups having a partial aromatic nature such as pyrrole and furan in one or both of the R and X positions.
Organic polymers may be added to the plating bath along with aromatic azomethines to further improve brightness and luster of deposited zinc. Polyvinyl alcohols, natural polymers such as gelatin, peptone, gum tragacanth and agar-agar, as well as other synthetic polymers such as polyethyleneimine and the glyceryl ethers of polyvinyl alcohols are satisfactory for this purpose. Polyvinyl alcohols having molecular weights from about 5,000 to 20,000 work well as additives to improve brightness and in addition exhibit outstanding tolerance to sodium carbonate which builds up in the plating bath and which tends to salt out polyvinyl alcohols of higher molecular weight. A preferred polymer is polyvinyl alcohol which has a molecular weight of about 16,800 and which has been found to improve zinc brightness and exhibit excellent resistance to carbonate.
The optimum amount of the azomethine brightening agent will depend upon the specific compound used, the current density employed, and the type of plate desired. This optimum amount will generally range from about 0.1 to 10 g./l. of bath. When the azomethine is used in combination with an organic polymer, the polymer concentration should be from about 0.01 to 10 grams per liter of bath, preferably about 0.05 to 0.5 gram per liter of bath. The azomethine and organic polymer may be added separately but are preferably added together in the form of a concentrated aqueous brightener additive solution. This solution may contain from 1:1 to 50:1 parts Example I The zinc plating bath used in tests 1-5 was prepared in 4 liter batches having the following composition:
Grams per liter Sodium cyanide 40 Sodium hydroxide 90 Zinc cyanide 60 Sodium carbonate 80 Sodium sulfide 1 Plating operations were conducted at room temperature, i.e., 25-30 C.
The brightening agent used was 3-(4-hydroxybenzylidene)3-aminopyridine 3-(4-hydroxybenzylidene) 3-am1nopyridine which was prepared by the condensation of 3-aminopyridine and p-hydroxybenzaldehyde.
Test 1.-This test demonstrates that an improvement in brightness can be obtained over a wide range of current densities. A steel Hull cell panel was plated at 2 amps for minutes in a bath as prepared above containing 0.8 g./l. of 3 (4-hydroxybenzylidene)3-aminopyridine. After washing in water and dipping in 0.5 wt. percent HNO to remove stains, the panel had the following appearance:
Amp/sq. ft. Bright plate with slight haze 1-10 Bright plate -50 Semi-bright plate 50-120 In a control experiment conducted in the absence of any brightening agent, a uniformly dull plate was obtained over the entire face of the panel where densities varied from l-120 amp/sq. ft. This dull plate was considerably inferior to even the semibright plate obtained in the presence of the brightening agent.
Test 2.--This test demonstrates the utility of 3-(4-hydroxybenzylidene)3-aminopyridine as a brightening agent in practical still plating. A steel automobile crank hole cover (the crank -hole cover which was used in the electroplating tests has an outer surface comprises of a series of convex surfaces and an inner surface comprised of a series of concave surfaces) was plated at 3.5 amps for minutes in a cyanide plating bath, as prepared above, containing 1.5 g./l. of 3-(4-hydroxybenzylidene)3-aminopyridine. After washing and dipping in 0.5 wt. percent HNO a very bright and shining plate was obtained on all surfaces except those of very low current density, which were somewhat duller. However, the plate on all surfaces was considerably improved over that obtained in the absence of any brightening agent.
Test 3.This test demonstrates the co-use of polyvinyl alcohol with 3-(4-hydroxybenzylidene)3-aminopyridine in practical still plating. A steel crank hole cover was plated for 3.5 amps for 15 minutes in a cyanide plating bath, as prepared above, to which has been added 3.0 g./l. of 3-(4-hydroxybenzylidene)3-aminopyridine and 0.09 g./l. of Elvanol polyvinyl alcohol 51-03 (trademark for Du Ponts water-soluble polyvinyl alcohol having an average molecular weight of about 16,800). After Washing and dipping in 0.5 wt. percent HNO a very bright plate was obtained on all surfaces, including those of low current density. The product was judged to be equal or superior to that obtained with the best commercial cyanide zinc brighteners.
Test 4.This 'test demonstrates the co-use of polyvinyl alcohol with 3-(4-hydroxybenzylidene)3-arninopyridine in practical barrel plating. One hundred grns. of steel screws were barrel plated at 5 amps for 18 minutes in the bath from test 3. The screws produced were bright, but were somewhat stained. The stains were readily removed by dipping the screws in 0.5 wt. percent HNO The result ing product had an overall quality equivalent to similar products available commercially.
Test 5.This test demonstrates the excellent stability of the 3 (4 hydroxybenzylidene)3 aminopyridine Elvanol 51-03 system in the cyanide plating bath. The bath from test 4 was stored for two weeks and then used to plate an automobile crank hole cover at 3.5 amps for 15 minutes. The cover was then washed and dipped in 0.5 wt. percent HNO The result was a uniformly bright plate only slightly inferior to that produced from test 3. The stability of the system used here is even more striking when compared with those using aromatic aldehydes, which lose their activity in a twenty-four hour idle period.
Example II The plating bath used in tests 1 and 2 was the same as that in Example I, i.e., it was prepared in 4 liter batches and had the following composition:
Grams per liter Sodium cyanide 40 Sodium hydroxide 90 Zinc cyanide 60 Sodium carbonate Sodium sulfide 1 1.5 g./l. of brightener addedThe coating was somewhat brighter than that on a blank.
3.0 g./l. brightener added-Significant improvement in brightness on all surfaces, equal to that obtained using many commercial brighteners.
6.0 gal. brightener added-No further improvement note Test 2.In this test, demonstrating the co-use of 1- (4-hydroxybenzylidene)aniline and polyvinyl alcohol in practical still plating, 0.18 g. of Elvanol polyvinyl alcohol 51-03 was added to the plating bath of test 1 after the last addition of 1-(4-hydroxybenzylidene)aniline. A crank hole cover plated in this bath showed a significant improvement on all surfaces over the best sample in test 1, giving a shining bright zinc plated product.
Example III In Examples 1-22 in the table which follows are listed a variety of azomethines which were prepared by the condensation of selected anldehydes and amines and tested for activity as cyanide zinc plating agents. The principal test used was "the still plating of automobile crank hole covers; the various brightening agents being The primary advantage of the brightening agents of added to the plating bath of Example I in amounts varythis invention is the excellent quality of bright zinc plate ing between about 0.1 and 10 -g./l. All azomethines obtained. Also, the compositions of this invention are listed in the Table gave an improved electroplate which stable both in storage and in the plating bath during was brighter and smoother than that obtained without a 5 use and periods of non-use. Their rate of consumption brightening agent. The performance of the various is low, thus, making them economically attractive. f azomethine brightening agents was rated as follows: particular importance is the fact that a brightener composition containing an azomethine is usually equally brighter"- fiii's fiv lfi l ifii ieiiiiifiZLZFFZLEEZ 1 l e l Enema-1t? g to the performance of the best range of current densities and also the fact that bright mercla pro ucts zinc deposits obtained from their use are responsive to Examples 23-42 in the table are other azomethines treatment with protective agents such as chromate conwhich are active brighteners for cyanide zinc plating 15 version coating preparations.
baths. Since many different embodiments of this invention TABLE.AZOMETHINES AS ZINC BRIGHTENERS Examples 1-22 Source Example No. Aldehyde Amine Resulting Azomethine Performance 1 p-Hydroxybenzaldehyde Aniline 1-(4-hydroxybenzylidene)aniline Good. 2 do p-Amlnophenol 4-(4-hydroxybenzylidene)4-aminophenoL. Fair. 3 p-Hydroxybenzaldehyde (2 mols)... m-Phenylene diamine l,3bis(4-hydroxybenzylidene)-1,3phenyl- Fair to good.
ene iamme. 4 p-Hydroxybenzaldehyde o-Aminobenzoic acid 2-(4-l21ydr0xybenzylidene)2-aminobenzoic Do.
aci 5 .do m-Aminobenzoic acid 3-(thiydroxybenzylidene)3-aminobenzoic Fair.
8.01 6 d0 3-amin0pyrldine 3-(4-hydroxybenzylidene)3-aminopyridine. Excellent.
do 4-amin0pyr1dine.. 4-(4-hydroxybenzylidene)4-aminopyridine. Fair to Good. p-Hydroxybenzaldehyde (2 mols)-.- Ethylene diamine Lfihis-(4-hydroxybcnzylidene)-ethy1ene Good.
iamme. 9 do Diethylene triamine 1,1-1;is-( t-hydroxybenzylidene)-diethylene Fair to Good.
riamine. 10 do Tetraethylene pentamine 1,13-bis-(-hydroxybenzylidene)tetraeth- Do.
' ylpentamine. 11 do 1:2 propane diamme 1%bis-(4-hydroxybel1zylidene)propane Do.
iamine- 2. 12 do Hexamethylene diamlne 1,8-bis-(4-hydroxybenzylidene)hexemeth- Do.
ylene diamine. 13 p-Hydroxybenzaldehyde cyclehexylamine 1-(et-hydroxybenzylidene)cyclohexylamine. Fair. 14 m-Hydroxybenzaldehyde (2 mols).-. Ethylene diamlne 1,tipis-(IS-hydroxybenzylidene)ethylene Do.
iamine. 15 m-Hydroxybenzaldehyde., Aniline 1-(3-hydroxybenzylidene)aniline Fair to Good. 16. Benzaldehyde m-Aminophenol B-benzylidene 3-aminophenol Fair 17- do p-AminophenoL- 3-benzy1ideue B-aminophenol Do. 18 p-Methoxybenzaldehyde o-Aminobenzoic acid 2-(4-rgethoxybenzylidene)Z-aminobenzoio Do.
aci 19 Furiural m-Aminophenol 3-furfurylidene 3-aminophenol Do. 20. do o-Aminobenzoic acid. 2-iurfurylidene 2aminobenzoic a Do. do Cyclohexylaminem inriurylidene cyclohexylamine. D0 22 Pyridine 3-carboxaldehyde p-Aminobenzoic acid 4-(3-pyridylideue)4-aminobenzoic aci Do.
Examples 23-42 Source Example N o. Aldehyde Amine Resulting Azomethine Methylamine..- l-(d-hydroxybenzylidene)methylamine. Ethylemame. 1-(4-hydroxybenzylidene)ethylamine.
Propylamin l-(-hydroxybenzylidene)propylamine.
utylamine l-(-hydroxybenzylidene)butylamine. Pentylamin 1-(4-hydroxybenzylidene)pentylamine. exylamine 1-(4-hydroxybenzylidene)hexylamine).
. 4-methoxypen o-Aminobenzoic acid 5-amino-1-naphthelene sulfonic 2-amino benzoic acid 3-aminoqninoline... 5-aminoisoquinoline Aniline 1-(4-hydroxybenzylidene)4-methoxypentylamine. 2-(1-hexylidene)2-aminobenzoic acid.
5-benzylidene 5-amino-1-naphthalene sulfonic acid.
2-(2naphthylidene)Z-aminobenzoic acid.
. 3-(4-hydroxybenzylidene)3amino quinoline.
5-(benzylidene 2-snlfonic acid) 5-aminoisoquinoline.
1-(3-carboxybenzylidenc) aniline.
3-iormyl benzoic acid Benzaldehyde Amino acetic acid Benzylidene aminoacetic acid. m-Hydroxybenzaldehy Ethylene diamine.. 3-hydroxybcnzylidene ethylene diamine. Glycolic acid m-Phenylene diamine l-glycolidine 1,3-phenylene diamine.
3-formylbenzoic acid 4-hydroxybenzaldehyde- -do Anisaldehydm..
4-amide aniline p-Tol id 0 p-Aminoethylbenzoate. 4ethoxy 2-aminobenzoic acid 4-(3-carboxybenzylidene)4-amidoaniline.
4-(4-hydroxybenzylidene)4-toluidine.
4-(4-hydroxybenzylidenc)4-aminocthylbenzoate. 2-(4-methoxybenzylidcne)2-aminokethoxybenzoic aeid.
In addition to the azomethine compounds previously may be made without departing from the spirit and cited as having utility in the present inventionpsimilar scope thereof, it is to be understood that the invention compounds containing additional substituent groups on is not limited to the specific illustrations except to the the R and X groups in the molecule having ageneral extent defined in the following claims. formula RCH=NX, such as -NH -CO0H --COO What is claimed is: alkyl, alkyl, alkoxy, OH, and SO H may be used. The 1. An aqueous cyanide zinc electroplating bath conplating baths exemplified may, of course, be modified taining as a brightening agent an aromatic azomethine to substitute for the sodium salts, other salts, e.g., potasof the general formula RCH=NX wherein R and X are sium and lithium compounds, which behave similarly selected from the group consisting of phenyl, naphthyl in the bath. Also zinc oxide rather than zinc cyanide may and pyridyl and at least one of the groups R and X has be used. Details for preparing and using the baths are, substituted therein at least one substituent selected from of course, well known to those skilled in the art. the group consisting of NH COOH, OH, SO H and alkoxy, said azomethine being soluble in said bath and being present in said bath in an amount suflicient to yield a zinc electrodeposit of improved brightness.
2. The bath of claim 1 wherein said azomethine is present in said bath in an amount from about 0.1 to 10 grams per liter of bath.
3. The bath of claim 2 wherein a bath-soluble organic polymer selected from the group consisting of polyvinyl alcohol, polyethyleneimine, gelatin and peptone is present in an amount from about 0.01 to 10 grams per liter of bath.
4. The bath of claim 3 wherein said organic polymer is a polyvinyl alcohol having a molecular weight from about 5,000 to 20,000.
5. The bath of claim 1 wherein said brightening agent comprises 3- (4-hydroxybenzylidene) 3-aminopyridine.
6. The bath of claim 1 wherein said brightening agent comprises 1- (4-hydroxybenzylidene aniline.
7. The bath of claim 3 wherein said azomethine comprises 3-(4-hydroxybenzylidene)3-aminopyridine or 1-(4- hydroxybenzylidene)aniline and said organic polymer comprises polyvinyl alcohol having a molecular weight from about 5,000 to 20,000, said polyvinyl alcohol being present in an amount from about 0.05 to 0.5 gram per liter of bath.
8. An additive for an aqueous cyanide zinc electroplating bath consisting essentially of from about 1:1 to 50:1 parts by weight of an aromatic azomethine of the general formula RCH=NX wherein R and X are selected from the group consisting of phenyl, naphthyl and pyn'dyl and at least one of the groups R and X has substituted therein at least one substituent selected from the group consisting of NH COOH, OH, -SO H and alkoxy and a bath-soluble organic polymer selected from the group consisting of polyvinyl alcohol, polyethyleneimine, gelatin, and pept'one, said additive being soluble in said bath.
9. The composition of claim 8 wherein said azomethine is 3-(4-hydroxybenzylidene)3-aminopyridine or 1-(4- hydroxybenzylidene)aniline and said organic polymer is polyvinyl alcohol having a molecular weight of about 16,800.
References Cited UNITED STATES PATENTS 2,680,712 6/1954 Diggin et al. 204-55 2,860,089 11/1958 Jackson 204-55 3,088,884 5/1963 Passal 204-55 3,296,105 1/ 1967 Rushmere 204-55 3,317,412 5/1967 Dahlmann 204-55 DANIEL E. WYMAN, Primary Examiner C. F. DEES, Assistant Examiner U.S. Cl. X.R. 106-1; 204-114
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Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3620938A (en) * 1968-12-11 1971-11-16 Stauffer Chemical Co Method for obtaining a bright zinc coating by electrodeposition and the bath used therefor
FR2154685A1 (en) * 1971-09-30 1973-05-11 Du Pont
FR2168931A1 (en) * 1972-01-27 1973-09-07 Cortial
US3883405A (en) * 1972-07-10 1975-05-13 Gerald H Grossblatt Zinc plating baths
US3915815A (en) * 1972-11-15 1975-10-28 Reinhard Koch Alkaline zinc electroplating bath
FR2288798A1 (en) * 1974-10-24 1976-05-21 Popescu Francine Bright zinc electroplating bath - contg pyridine deriv and soluble organic polymer
US4101387A (en) * 1974-04-22 1978-07-18 Oxy Metal Industries Corporation Composition for electrodeposition of metal deposits, its method of preparation and uses thereof
EP0015628A1 (en) * 1979-03-13 1980-09-17 Shell Internationale Researchmaatschappij B.V. Use as fungicides of pyridyliminomethylbenzene derivatives and acid-addition salts thereof; pyridyliminomethylbenzene derivatives and their acid-addition salts; a process for preparing such compounds and intermediates for use in such process; and fungicidal compositions comprising such compounds
US4355035A (en) * 1980-03-17 1982-10-19 Shell Oil Company Derivatives of certain pyridyliminomethylbenzenes
US4404213A (en) * 1981-01-26 1983-09-13 Shell Oil Company Derivatives of certain pyridyliminomethyl-benzenes
FR2559481A2 (en) * 1984-02-10 1985-08-16 Rhone Poulenc Agrochimie New 3-(phenyliminomethyl)pyridine derivatives, their preparation and their employment in the preparation of pyridylacetonitrile derivatives which can be used as fungicides
US4675050A (en) * 1984-09-06 1987-06-23 Schering Ag Sulfate and sulfonate beta-naphthol polyglycol ethers
USRE49987E1 (en) 2013-11-22 2024-05-28 Invensas Llc Multiple plated via arrays of different wire heights on a same substrate

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2680712A (en) * 1951-08-07 1954-06-08 Hanson Van Winkle Munning Co Alkaline zinc plating baths
US2860089A (en) * 1956-08-09 1958-11-11 R O Hull & Company Inc Method of electro depositing zinc
US3088884A (en) * 1960-11-07 1963-05-07 Metal & Thermit Corp Electrodeposition
US3296105A (en) * 1964-04-03 1967-01-03 Du Pont Zinc cyanide electroplating bath and process
US3317412A (en) * 1961-07-06 1967-05-02 Schering Ag Method for obtaining a bright zinc coating by electrodeposition and the bath used therefor

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2680712A (en) * 1951-08-07 1954-06-08 Hanson Van Winkle Munning Co Alkaline zinc plating baths
US2860089A (en) * 1956-08-09 1958-11-11 R O Hull & Company Inc Method of electro depositing zinc
US3088884A (en) * 1960-11-07 1963-05-07 Metal & Thermit Corp Electrodeposition
US3317412A (en) * 1961-07-06 1967-05-02 Schering Ag Method for obtaining a bright zinc coating by electrodeposition and the bath used therefor
US3296105A (en) * 1964-04-03 1967-01-03 Du Pont Zinc cyanide electroplating bath and process

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3620938A (en) * 1968-12-11 1971-11-16 Stauffer Chemical Co Method for obtaining a bright zinc coating by electrodeposition and the bath used therefor
FR2154685A1 (en) * 1971-09-30 1973-05-11 Du Pont
FR2168931A1 (en) * 1972-01-27 1973-09-07 Cortial
US3883405A (en) * 1972-07-10 1975-05-13 Gerald H Grossblatt Zinc plating baths
US3915815A (en) * 1972-11-15 1975-10-28 Reinhard Koch Alkaline zinc electroplating bath
US4101387A (en) * 1974-04-22 1978-07-18 Oxy Metal Industries Corporation Composition for electrodeposition of metal deposits, its method of preparation and uses thereof
FR2288798A1 (en) * 1974-10-24 1976-05-21 Popescu Francine Bright zinc electroplating bath - contg pyridine deriv and soluble organic polymer
EP0015628A1 (en) * 1979-03-13 1980-09-17 Shell Internationale Researchmaatschappij B.V. Use as fungicides of pyridyliminomethylbenzene derivatives and acid-addition salts thereof; pyridyliminomethylbenzene derivatives and their acid-addition salts; a process for preparing such compounds and intermediates for use in such process; and fungicidal compositions comprising such compounds
US4355035A (en) * 1980-03-17 1982-10-19 Shell Oil Company Derivatives of certain pyridyliminomethylbenzenes
US4404213A (en) * 1981-01-26 1983-09-13 Shell Oil Company Derivatives of certain pyridyliminomethyl-benzenes
FR2559481A2 (en) * 1984-02-10 1985-08-16 Rhone Poulenc Agrochimie New 3-(phenyliminomethyl)pyridine derivatives, their preparation and their employment in the preparation of pyridylacetonitrile derivatives which can be used as fungicides
US4675050A (en) * 1984-09-06 1987-06-23 Schering Ag Sulfate and sulfonate beta-naphthol polyglycol ethers
USRE49987E1 (en) 2013-11-22 2024-05-28 Invensas Llc Multiple plated via arrays of different wire heights on a same substrate

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