US3483100A - Tin plating baths - Google Patents
Tin plating baths Download PDFInfo
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- US3483100A US3483100A US666983A US3483100DA US3483100A US 3483100 A US3483100 A US 3483100A US 666983 A US666983 A US 666983A US 3483100D A US3483100D A US 3483100DA US 3483100 A US3483100 A US 3483100A
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- United States
- Prior art keywords
- tin
- group
- brightener
- baths
- bath
- Prior art date
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- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 title description 13
- 238000007747 plating Methods 0.000 title description 12
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 12
- 150000001875 compounds Chemical class 0.000 description 11
- 239000003792 electrolyte Substances 0.000 description 9
- 239000001257 hydrogen Substances 0.000 description 9
- 229910052739 hydrogen Inorganic materials 0.000 description 9
- 125000000217 alkyl group Chemical group 0.000 description 8
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 7
- 239000002253 acid Substances 0.000 description 6
- 150000002431 hydrogen Chemical group 0.000 description 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 4
- -1 aliphatic aldehyde Chemical class 0.000 description 4
- HYBBIBNJHNGZAN-UHFFFAOYSA-N furfural Chemical compound O=CC1=CC=CO1 HYBBIBNJHNGZAN-UHFFFAOYSA-N 0.000 description 4
- LEQAOMBKQFMDFZ-UHFFFAOYSA-N glyoxal Chemical compound O=CC=O LEQAOMBKQFMDFZ-UHFFFAOYSA-N 0.000 description 4
- 150000002894 organic compounds Chemical class 0.000 description 4
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 239000004094 surface-active agent Substances 0.000 description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- 150000001450 anions Chemical class 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 150000001728 carbonyl compounds Chemical class 0.000 description 3
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 125000000623 heterocyclic group Chemical group 0.000 description 3
- 150000002500 ions Chemical class 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 description 2
- BWHOZHOGCMHOBV-UHFFFAOYSA-N Benzalacetone Natural products CC(=O)C=CC1=CC=CC=C1 BWHOZHOGCMHOBV-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- 150000001299 aldehydes Chemical class 0.000 description 2
- 125000003282 alkyl amino group Chemical group 0.000 description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
- 239000007859 condensation product Substances 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 238000000151 deposition Methods 0.000 description 2
- 229940015043 glyoxal Drugs 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
- KKFHAJHLJHVUDM-UHFFFAOYSA-N n-vinylcarbazole Chemical compound C1=CC=C2N(C=C)C3=CC=CC=C3C2=C1 KKFHAJHLJHVUDM-UHFFFAOYSA-N 0.000 description 2
- RNVCVTLRINQCPJ-UHFFFAOYSA-N o-toluidine Chemical compound CC1=CC=CC=C1N RNVCVTLRINQCPJ-UHFFFAOYSA-N 0.000 description 2
- 229910052697 platinum Inorganic materials 0.000 description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- 229910021653 sulphate ion Inorganic materials 0.000 description 2
- 229910001432 tin ion Inorganic materials 0.000 description 2
- BWHOZHOGCMHOBV-BQYQJAHWSA-N trans-benzylideneacetone Chemical compound CC(=O)\C=C\C1=CC=CC=C1 BWHOZHOGCMHOBV-BQYQJAHWSA-N 0.000 description 2
- 229940117958 vinyl acetate Drugs 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- JKNCOURZONDCGV-UHFFFAOYSA-N 2-(dimethylamino)ethyl 2-methylprop-2-enoate Chemical compound CN(C)CCOC(=O)C(C)=C JKNCOURZONDCGV-UHFFFAOYSA-N 0.000 description 1
- KGIGUEBEKRSTEW-UHFFFAOYSA-N 2-vinylpyridine Chemical compound C=CC1=CC=CC=N1 KGIGUEBEKRSTEW-UHFFFAOYSA-N 0.000 description 1
- MNFZZNNFORDXSV-UHFFFAOYSA-N 4-(diethylamino)benzaldehyde Chemical compound CCN(CC)C1=CC=C(C=O)C=C1 MNFZZNNFORDXSV-UHFFFAOYSA-N 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 1
- SXRSQZLOMIGNAQ-UHFFFAOYSA-N Glutaraldehyde Chemical compound O=CCCCC=O SXRSQZLOMIGNAQ-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 239000011260 aqueous acid Substances 0.000 description 1
- JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 description 1
- WRUAHXANJKHFIL-UHFFFAOYSA-N benzene-1,3-disulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC(S(O)(=O)=O)=C1 WRUAHXANJKHFIL-UHFFFAOYSA-N 0.000 description 1
- 238000005282 brightening Methods 0.000 description 1
- 229940075397 calomel Drugs 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- ZOMNIUBKTOKEHS-UHFFFAOYSA-L dimercury dichloride Chemical compound Cl[Hg][Hg]Cl ZOMNIUBKTOKEHS-UHFFFAOYSA-L 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000002659 electrodeposit Substances 0.000 description 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 description 1
- 229960000587 glutaral Drugs 0.000 description 1
- MTNDZQHUAFNZQY-UHFFFAOYSA-N imidazoline Chemical compound C1CN=CN1 MTNDZQHUAFNZQY-UHFFFAOYSA-N 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 235000019645 odor Nutrition 0.000 description 1
- RPQRDASANLAFCM-UHFFFAOYSA-N oxiran-2-ylmethyl prop-2-enoate Chemical compound C=CC(=O)OCC1CO1 RPQRDASANLAFCM-UHFFFAOYSA-N 0.000 description 1
- AYEFIAVHMUFQPZ-UHFFFAOYSA-N propane-1,2-diol;prop-2-enoic acid Chemical compound CC(O)CO.OC(=O)C=C AYEFIAVHMUFQPZ-UHFFFAOYSA-N 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- FAKFSJNVVCGEEI-UHFFFAOYSA-J tin(4+);disulfate Chemical compound [Sn+4].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O FAKFSJNVVCGEEI-UHFFFAOYSA-J 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25D—PROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
- C25D3/00—Electroplating: Baths therefor
- C25D3/02—Electroplating: Baths therefor from solutions
- C25D3/30—Electroplating: Baths therefor from solutions of tin
- C25D3/32—Electroplating: Baths therefor from solutions of tin characterised by the organic bath constituents used
Definitions
- R and R being hydrogen, alkyl or phenyl or 0R wherein R is alkyl where at least one hydrogen has been replaced by amino, alkylamino or hydroxyl groups or a secondary brightener of the formula n being 0-5 and possibly one or more hydrogen atoms in the CH group being replaced by hydroxyl groups.
- these secondary brighteners are glyoxal, vinylacetate and N-vinyl carbazole.
- the invention relates to an acid tin-plating bath containing sulphate, sulphonate or fluoborate anions and brighteners by means of which bright tin deposits can be obtained.
- Acid tin-plating baths which contain as brightener a condensation product of an aliphatic aldehyde and an organic compound having a basic nitrogen-containing group, for example a reaction product of acetaldehyde and o-toluidine. These brighteners become resinous very soon, however, so that the bath has only a short stability.
- acid tin-plating baths which contain as brightener an aromatic or heterocyclic aldehyde. These baths have the disadvantage, however, that they produce bright deposits only in a very limited current density range, only between about 5 and 20 A/sq. dm. This means that strongly profiled workpieces having sharp edges and small perforations, the electrolytic coating of which involves current density variations of a factor of even as low as 100, cannot be coated with a thin layer of uniform thickness and brightness. The current density variations are considerably larger if the electrolytic coating process is carried out in a drum.
- CHO, -COOH, -CH OH, --R or OR is a corresponding nonsaturated ketone.
- These baths moreover contain formalin, imidazolin or derivatives and mixtures thereof.
- a number of organic compounds have been found which, when added instead of formalin together with a brightener to an electrolyte tin-plating bath, have the advantage that they have a larger brightening effect on the tin obtained and that they do not have disagreeable odors.
- the usable com pounds can be found in a few chemical classes which are chemically not at all related to each other. However, the applicant has found a common electrochemical criterion which the said compounds must satisfy.
- a non-ionic surface-active substance to a solution of sulfuric acid, an aryl sulphonate or a fluo borate, the overvoltage for the separation of hydrogen at a cathode of tin is raised.
- the cell containing a platinum anode and a tin cathode; the EMF is measured between the tin cathode and the platinum anode or an auxiliary calomel electrode provided in the cell, a small quantity of the substance to be tested being added to the electrolyte liquid. If the EMF decreases after addition of X the substance, the latter suits the purpose of the invention.
- R reprsents a hydrogen atom, an alkyl group or a phenyl group and R OH
- n a value 0, 1, 2, 3, 4 or 5, while in the CH groups one or more hydrogen atoms are allowed to be replaced by OH groups.
- each of the symbols R R and R represents a hydrogen atom, an aromatic, heterocyclic or aliphatic group or a similar group which may be entirely or partly hydrated and which may have substituents which cannot be ionized or cannot be reduced in this medium
- R represents hydrogen, an alkyl group or an esterified carboxyl group, or where the combination represents a ring system, on the understanding that the group C:C-- has a purely non-saturated character.
- a further improvement is obtained by the use of the last-mentioned baths, i.e. a larger brightness and an even larger current density range if instead of formalin such a compound which is capable of reducing the overvoltage for the evolution of hydrogen at a tin cathode, is added to the tin-plating bath.
- Lissapol N is a non-ionic wetting agent which consists of a condensation product of polyoxyethylene and alkylphenol.
- tin ion anions selected from the group consisting of sulfate, organic sulfonate and fluoborate ions, at non-ionic surface active agent and an olefinically unsaturated organic carbonyl primary brightener and as a secondary brightener a polymerizable organic compound capable of reducing the overvoltage for the evolution of hydrogen at a tin cathode
- said polymerizable organic compound is selected from the group consisting of a compound of the formula wherein R is a member of the group consisting of hydrogen, alkyl and phenyl, R is a member selected from the group consisting of 011 and N R3 and R4 being selected from the group consisting of phenyl, hydrogen, alkyl and 0R wherein R is alkyl wherein at least one hydrogen atom has been replaced by a member selected from the group consisting of amino
- a carbonyl compound selected from the group consisting of aromatic and heterocyclic ring containing aldehydes wherein the carbonyl group is directly attached to one of said rings and a, B olefinically unsaturated carbonyl compounds; said carbonyl compounds being free of ionizable and reducible substituents, nitrogen containing substituents and compounds hydrolyzable in said bath to said carbonyl com- References Cited pound.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Electroplating And Plating Baths Therefor (AREA)
Description
United States Patent U.S. Cl. 204-54 4 Claims ABSTRACT OF THE DISCLOSURE Acid electrolyte bath for obtaining bright tin deposit containing sulfate, sulfonates or fluoroborate ions; an unsaturated aldehyde or ketone bn'ghtener, for example, furfural; and as a secondary brightener a polymerizable compound of the formula wherein R is hydrogen, alkyl or phenyl and R is OH,
R and R being hydrogen, alkyl or phenyl or 0R wherein R is alkyl where at least one hydrogen has been replaced by amino, alkylamino or hydroxyl groups or a secondary brightener of the formula n being 0-5 and possibly one or more hydrogen atoms in the CH group being replaced by hydroxyl groups. Examples of these secondary brighteners are glyoxal, vinylacetate and N-vinyl carbazole.
The invention relates to an acid tin-plating bath containing sulphate, sulphonate or fluoborate anions and brighteners by means of which bright tin deposits can be obtained.
Acid tin-plating baths are known which contain as brightener a condensation product of an aliphatic aldehyde and an organic compound having a basic nitrogen-containing group, for example a reaction product of acetaldehyde and o-toluidine. These brighteners become resinous very soon, however, so that the bath has only a short stability.
Furthermore, acid tin-plating baths are known which contain as brightener an aromatic or heterocyclic aldehyde. These baths have the disadvantage, however, that they produce bright deposits only in a very limited current density range, only between about 5 and 20 A/sq. dm. This means that strongly profiled workpieces having sharp edges and small perforations, the electrolytic coating of which involves current density variations of a factor of even as low as 100, cannot be coated with a thin layer of uniform thickness and brightness. The current density variations are considerably larger if the electrolytic coating process is carried out in a drum.
Further, electrolyte tin-plating baths have become known recently which contain a brightener consisting of a compound of the general formula XCH=:CHY in which X represents an isocyclic or heterocyclic ring that may be substituted and Y is one of the groups H,
"ice
CHO, -COOH, -CH OH, --R or OR is a corresponding nonsaturated ketone. These baths moreover contain formalin, imidazolin or derivatives and mixtures thereof.
According to the invention, a number of organic compounds have been found which, when added instead of formalin together with a brightener to an electrolyte tin-plating bath, have the advantage that they have a larger brightening effect on the tin obtained and that they do not have disagreeable odors. The usable com pounds can be found in a few chemical classes which are chemically not at all related to each other. However, the applicant has found a common electrochemical criterion which the said compounds must satisfy. By the addition of a non-ionic surface-active substance to a solution of sulfuric acid, an aryl sulphonate or a fluo borate, the overvoltage for the separation of hydrogen at a cathode of tin is raised. Those compounds have proved usable which, when added to these solutions, are capable of reducing this overvoltage. This criterion can be easily applied. By means of a simple test it can be determined for each individual case whether a given compound is usable. For this purpose, an electrolytic cell is utilized the electrolyte of which only consists of dilute sulfuric acid and a non-ionic surface-active substance, while this cell is operated at a constant current density, for example, of 2 A./ sq. dm., the cell containing a platinum anode and a tin cathode; the EMF is measured between the tin cathode and the platinum anode or an auxiliary calomel electrode provided in the cell, a small quantity of the substance to be tested being added to the electrolyte liquid. If the EMF decreases after addition of X the substance, the latter suits the purpose of the invention. If n reprsents the said EMF in millivolts and c the concentration of the substance to be added in millimol/litre, this requirement can be briefly represented by Ac Ac 0 A class of chemical compounds which are capable of considerably reducing the said EMF and hence provide a considerable increase in brightness and exhibit a larger current density range than formalin-containing tin-plating baths, may be represented by the general formula:
where R, reprsents a hydrogen atom, an alkyl group or a phenyl group and R OH,
a,4ss, 100
than formalin-containing tin-plating baths may be represented by the general formula:
II II where n a value 0, 1, 2, 3, 4 or 5, while in the CH groups one or more hydrogen atoms are allowed to be replaced by OH groups.
In applicants copending application, Ser. No. 521,803, filed Jan. 20, 1966, an acid tin-plating bath has been described which contains bivalent tin ions, an anions sulphate-, sulphonateor fiuoborate ions a surface-active compound of non-ionic nature and as brightener a sufiiciently soluble compound corresponding with the general formula:
where each of the symbols R R and R represents a hydrogen atom, an aromatic, heterocyclic or aliphatic group or a similar group which may be entirely or partly hydrated and which may have substituents which cannot be ionized or cannot be reduced in this medium, R represents hydrogen, an alkyl group or an esterified carboxyl group, or where the combination represents a ring system, on the understanding that the group C:C-- has a purely non-saturated character. With the aid of these baths which contain beside the aforementioned constituents also formalin, bright tin deposits can be obtained without difficulty, even on workpieces which are strongly profiled, have sharp edges or small perforations, and even if the electrolytic coating process is carried out in a drum. During operation of this bath, current density variations of a factor 1000 are unobjectionable. Moreover, these tin-plating baths have an extremely high stability.
In a preferred embodiment of the method according to the invention, a further improvement is obtained by the use of the last-mentioned baths, i.e. a larger brightness and an even larger current density range if instead of formalin such a compound which is capable of reducing the overvoltage for the evolution of hydrogen at a tin cathode, is added to the tin-plating bath.
A number of baths will now be described by way of example, in which workpieces, having sharp edges which had been punched out of conventional sheet iron, were tin-plated at a bath temperature of approximately 20 C. and at average current densities lying between 0.5 and A./sq. drn. The articles thus tin-plated all had a uniform brightness of excellent quality throughout their surface.
For this purpose, there was added to one of the three following known tin-plating baths containing per litre of liquid the following dissolved constitutents:
(a): G. Stannous sulphate 40 Sulfuric acid (d=1.84) 120 Lissapol N" S Tin finoborate Sn(BF 30 Fluobroic acid 200 Lissapol N 5 Tin sulphate 40 m-Benzene disulphonic acid 170 Lissapol N 3 4 one of the following brighteners in the indicated quantities:
G./l. Dihydrotolylaldehyde 0.12 Benzalacetone 0.16
Furfural 1.20
Moreover, one of the following constituents was added to these baths in the indicated quantities.
G./l. Acrylic acid 0.3 Methacrylic acid 2.0 Acrylicamide 0.2 Methacrylicamide 0.2 Glycidylacrylate 0.2 Propylene glycolacrylate 0.1 Dimethylaminoethylmethacrylate 3.0 Glyoxal 4.0 Glutaric dialdehyde 0.2 u-Hydroxyadipicaldehyde 0.2 N-vinylpyroolidone 1.0 p-Diethylaminobenzaldehyde O. 1 N-vinylcarbazole 1.0 2-vinylpyridine 0.5 Tetrahydrofuran 2.3 Vinylacetate 1.0 Alkylglycidyl ether 1.5
These baths had an extremely high stability. Lissapol N is a non-ionic wetting agent which consists of a condensation product of polyoxyethylene and alkylphenol.
What we claim is:
1. In an aqueous acid electrolyte bath for the electrolytic deposition of bright tin said bath containing bivalent tin ion anions selected from the group consisting of sulfate, organic sulfonate and fluoborate ions, at non-ionic surface active agent and an olefinically unsaturated organic carbonyl primary brightener and as a secondary brightener a polymerizable organic compound capable of reducing the overvoltage for the evolution of hydrogen at a tin cathode, the improvement wherein said polymerizable organic compound is selected from the group consisting of a compound of the formula wherein R is a member of the group consisting of hydrogen, alkyl and phenyl, R is a member selected from the group consisting of 011 and N R3 and R4 being selected from the group consisting of phenyl, hydrogen, alkyl and 0R wherein R is alkyl wherein at least one hydrogen atom has been replaced by a member selected from the group consisting of amino, alkylamino and hydroxyl and a compound of the formula n being an integer ranging from 0 to 5 and the hydroxy substituted derivatives thereof, said primary and secondary brighteners being present in an amount sufficient to provide a bright tin electrodeposit.
2. The electrolyte bath for depositing tin of claim 1 wherein it contains as the primary brightener a carbonyl compound selected from the group consisting of aromatic and heterocyclic ring containing aldehydes wherein the carbonyl group is directly attached to one of said rings and a, B olefinically unsaturated carbonyl compounds; said carbonyl compounds being free of ionizable and reducible substituents, nitrogen containing substituents and compounds hydrolyzable in said bath to said carbonyl com- References Cited pound.
3. The electrolyte bath of claim 2 wherein the primary UNITED STATES PATENTS brightener is present in a quantity lying between 25 and 3,361,652 1/1968 'p et a1 204-54 300 mg. and the secondary brightener is present in a 5 quantity lying between 0.01 and 10 g. per litre of bath FOREIGN PATENTS liquid. 6501841 8/1966 Netherlands.
4. The electrolyte bath of claim 1 wherein said primary brightener is benzalacetone and said secondary brightener JOHN H. MACK, Primary Examiner is acrylic acid 10 G. L. KAPLAN, Assistant Examiner UNITED STATES PATENT OFFICE CERTIFICATE OF CORRECTION Patent No. 3,483,100 Dated D m r 9, 6
Inventor(s) JAN JOHANNES ENGELSMAN ET AL It is certified that error appears in the above-identified patent and that said Letters Patent are hereby corrected as shown below:
Column 2, line 34, "reprsents" should read represents 3R R3 Column 2, lines 56-60, "-N/ should read -N Colwnn 4, line 20, "N-vinylpyroolidone" should read N-vinylpyrrolidone Signed and sealed this 25 day of August 1970.
VIII-LIN! ll. JR. oomnsllomzof Patents
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NL666612936A NL151449B (en) | 1966-09-14 | 1966-09-14 | PROCESS FOR THE PREPARATION OF AN ACID BATH FOR THE ELECTROLYTIC DEPOSITION OF TIN. |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3483100A true US3483100A (en) | 1969-12-09 |
Family
ID=19797659
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US666983A Expired - Lifetime US3483100A (en) | 1966-09-14 | 1967-09-11 | Tin plating baths |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US3483100A (en) |
| AT (1) | AT278462B (en) |
| BE (1) | BE703841A (en) |
| CH (1) | CH519581A (en) |
| FR (1) | FR1536736A (en) |
| GB (1) | GB1199634A (en) |
| NL (1) | NL151449B (en) |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3755096A (en) * | 1971-07-01 | 1973-08-28 | M & T Chemicals Inc | Bright acid tin plating |
| FR2428686A1 (en) * | 1978-06-16 | 1980-01-11 | M & T Chemicals Inc | NEW ELECTROLYTIC DEPOSIT BATH OF BRILLIANT TIN |
| US5814202A (en) * | 1997-10-14 | 1998-09-29 | Usx Corporation | Electrolytic tin plating process with reduced sludge production |
| US20090098398A1 (en) * | 2006-04-14 | 2009-04-16 | C. Uyemura & Co., Ltd. | Tin electroplating bath, tin plating film, tin electroplating method, and electronic device component |
| US8440065B1 (en) * | 2009-06-07 | 2013-05-14 | Technic, Inc. | Electrolyte composition, method, and improved apparatus for high speed tin-silver electroplating |
| US20150122661A1 (en) * | 2013-11-05 | 2015-05-07 | Rohm And Haas Electronic Materials Llc | Plating bath and method |
| CN106222710A (en) * | 2016-08-29 | 2016-12-14 | 昆明理工大学 | A kind of acid half bright tin plating solution and preparation method thereof |
| CN115058762A (en) * | 2022-08-11 | 2022-09-16 | 深圳市板明科技股份有限公司 | Tin settling agent for electrotinning process and use method thereof |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL6501841A (en) * | 1965-02-13 | 1966-08-15 | ||
| US3361652A (en) * | 1963-08-28 | 1968-01-02 | Max Schlotter Dr Ing | Electrodeposition of bright tin |
-
1966
- 1966-09-14 NL NL666612936A patent/NL151449B/en not_active IP Right Cessation
-
1967
- 1967-09-11 AT AT828767A patent/AT278462B/en not_active IP Right Cessation
- 1967-09-11 US US666983A patent/US3483100A/en not_active Expired - Lifetime
- 1967-09-11 CH CH1263867A patent/CH519581A/en not_active IP Right Cessation
- 1967-09-13 BE BE703841D patent/BE703841A/xx not_active IP Right Cessation
- 1967-09-13 FR FR120832A patent/FR1536736A/en not_active Expired
- 1967-09-14 GB GB42001/67A patent/GB1199634A/en not_active Expired
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3361652A (en) * | 1963-08-28 | 1968-01-02 | Max Schlotter Dr Ing | Electrodeposition of bright tin |
| NL6501841A (en) * | 1965-02-13 | 1966-08-15 |
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3755096A (en) * | 1971-07-01 | 1973-08-28 | M & T Chemicals Inc | Bright acid tin plating |
| FR2428686A1 (en) * | 1978-06-16 | 1980-01-11 | M & T Chemicals Inc | NEW ELECTROLYTIC DEPOSIT BATH OF BRILLIANT TIN |
| US5814202A (en) * | 1997-10-14 | 1998-09-29 | Usx Corporation | Electrolytic tin plating process with reduced sludge production |
| US20090098398A1 (en) * | 2006-04-14 | 2009-04-16 | C. Uyemura & Co., Ltd. | Tin electroplating bath, tin plating film, tin electroplating method, and electronic device component |
| US8440066B2 (en) * | 2006-04-14 | 2013-05-14 | C. Uyemura & Co., Ltd. | Tin electroplating bath, tin plating film, tin electroplating method, and electronic device component |
| US8440065B1 (en) * | 2009-06-07 | 2013-05-14 | Technic, Inc. | Electrolyte composition, method, and improved apparatus for high speed tin-silver electroplating |
| US20150122661A1 (en) * | 2013-11-05 | 2015-05-07 | Rohm And Haas Electronic Materials Llc | Plating bath and method |
| CN106222710A (en) * | 2016-08-29 | 2016-12-14 | 昆明理工大学 | A kind of acid half bright tin plating solution and preparation method thereof |
| CN115058762A (en) * | 2022-08-11 | 2022-09-16 | 深圳市板明科技股份有限公司 | Tin settling agent for electrotinning process and use method thereof |
| CN115058762B (en) * | 2022-08-11 | 2022-11-08 | 深圳市板明科技股份有限公司 | Tin settling agent for electrotinning process and use method thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| CH519581A (en) | 1972-02-29 |
| NL151449B (en) | 1976-11-15 |
| GB1199634A (en) | 1970-07-22 |
| DE1621127A1 (en) | 1971-05-13 |
| AT278462B (en) | 1970-02-10 |
| BE703841A (en) | 1968-03-13 |
| DE1621127B2 (en) | 1972-11-09 |
| FR1536736A (en) | 1968-08-16 |
| NL6612936A (en) | 1968-03-15 |
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