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

• This invention relates to electrolytic tin plating baths which embody improved addition agents.
• the strip In electrolytic processes for plating tin on steel strip, the strip is immersed in a plating bath from which a tin coating is electrolytically deposited on its surface.
• a plating bath Ordinarily consist of an aqueous solution of a tin salt, various acids or alkalies and various addition agents.
• Those with which the present invention is concerned consist of an acid, such as phenolsulfonic acid, benzene meta-disulfonic acid or sulphuric acid, and the corresponding stannous salt, besides the improved addition agent.
• Many substances have been used or tried as addition agents, perhaps the most common being glue, beta naphthol or sulfones, such as dihydroxy diphenyl sulfone. Their action is not fully understood, but satisfactory tin coatings cannot be produced in their absence.
• An object of the present invention is to provide tin plating baths which embody improved addition agents and which are capable of depositing on strip ductile and coherent coatings that are lustrous even though not melted.
• the addition agents of the present invention consist of complex condensation products formed by reacting aromatic amines with formaldehyde in an acid-medium.
• the aromatic amines can be those having a primary amino group attached either to an unsubstituted benzene ring (aniline) or to a benzene ring substituted by one or more alkyl or halo groups in any of the ortho, meta or para positions with respect to the amino group (6. g. ortho, meta or para toluidine or chloraniline or xylidine).
• My present preference is para toluidine, which also contains the ortho and meta isomers to some extent.
• the amine is used in an amount of 2 to 6 grams per liter of bath solution.
• the formaldehyde can be either an aqueous formaldehyde solution or solid paraformaldehyde, and is used in an amount to form a ratio of 1 to 3 mols of formaldehyde to each mol of amine. Larger concentrations of formaldehyde seem harmless but of no benefit.
• the usual sulphate, benzene meta-disulfonic or phenolsulfonic tin plating bath has a total free acid content expressed as the H2804 equivalent of 20 to 50 grams per liter. It contains 10 to grams per liter of tin in the form of the corresponding stannous salt.
• benzene meta-disulfonic acid baths and phenolsulfonic acid baths can contain sulphate radicals from an effective amount to about 35 grams per liter and phenolsulfonic acid baths often contain phenol as an impurity in amount up to about 5 grams per liter.
• the baths are capable of depositing bright, ductile and coherent coatings directly with a current density range of about to 600 amperes per square foot, within a temperature range of about 90 F. to F. and at strip speeds of about 50 to 600 feet per minute.
• the optimum current density, temperature, and strip speed must be determined individually for each plating line, as known in the art.
• these variables normally are within the foregoing ranges, they cannot necessarily be varied at will within these ranges and still produce satisfactory coatings. Instead any significant variation in one ordinarily must be compensated by variations in others, also as known in the art.
• the current density range widens as the strip speed increases, with the upper limit increasing more rapidly than the lower.
• the effect of raising the temperature is to shift the current density range upward, which effect becomes more pronounced at strip speeds greater than 300 feet per minute.
• baths compounded in ac- 3 cordance with the present invention are as follows:
• Example I The bath was an aqueous solution containing the following ingredients:
• Phenolsulfonic acid 130 Tin Tin 35 Total sulphate radical 35 Toluidine 3
• Formaldehyde sufficient to form a ratio of 3 mols per mol of toluidine.
• Phenolsulfonic' acid 50 Starinous phenolsulfonate 13'? Total sulphate radical 10 Toluidine 3 Formaldehyde 'sufilcient to form a ratio of 1 mol per mol of toluidine.
• Example III The bath was an aqueous solution containing the following ingredients:
• Example IV The bath was an aqueous solution containing the following ingredients:
• Example VI The bath was an aqueous solution containing the following ingredients:
• This bath likewise deposited bright tin coatings at about the same operating conditions as the bath in Example I.
• Example VII The bath was an aqueous solution containing the following ingredients:
• Phenolsulfonic acid 50 Stannous phenolsulfonate 137 Total sulphate radical 10
• Xylidine 4 Formaldehyde sufiicient to form a ratio of 1 mol per mol of xylidine.
• This bath also deposited bright tin coatings at about the same operating conditions as the bath in Example I.
• Example VIII The bath was an aqueous solution containing the following ingredients:
• This bath again deposited bright tin coatings at about the same operating conditions as the bath of Example I.
• An electrolytic tin plating bath consisting of an aqueous acid solution of 10 to 80 grams per liter of tin in the form of a stannous salt of an acid of the group consisting of phenolsulfonic acid, benzene meta-disulfonic acid and sulphuric acid, and the reaction ,product formed by dissolving an amine in saidsolution and gradually adding formaldehyde thereto at a temperature of 40 to C., the amine being present in a concentration .of 2 to 6 grams per liter and being of the group consisting of aniline, toluidine, xylidine'an'd chloraniline, the formaldehyde being present inan amount of 1 to 3 mols of formaldehyde.per mol of amine, said solution having a total free acid content expressed as the H2304 equivalent of 20, to 50 grams per liter.
• An electrolytic tin plating bath consisting of an aqueous acid solution of 10 to grams per liter of tin in the form of stannous phenolsulfonate and the reaction product formed by dissolving an amine in said solution and gradually adding formaldehyde thereto at a temperature of 40 to 60 C., the amine being present in a concentration of 2 to 6 grams per liter and being of the group consisting of aniline, toluidine, xylidine and chloraniline, the formaldehyde being present in an amount of 1 to 3 mols of formaldehyde per mol of amine, said solution having a total free acid content expressed as the H2804 equivalent of 20 to 50 grams per liter.
• An electrolytic tin plating bath as defined in claim 2 containing in addition sulphuric acid sufiicient to furnish sulphate radicals in an amount up to about 35 grams per liter.
• An electrolytic tin plating bath consisting of an aqueous acid solution of to 80 grams per liter of tin in the form of a stannous salt of an acid of the group consisting of phenolsulfonic acid, benzene meta-disulfonic acid and sulphuric acid, and the reaction product formed by dissolving in said solution 2 to 6 grams per liter of toluidine and gradually adding formaldehyde at a temperature of 40 to 60 C. in an amount of 1 to 3 mols of formaldehyde per mol of toluidine, said solution having a total free acid content expressed as the H2SO4 equivalent of to 50 grams per liter.
• An electrolytic tin plating bath consisting of an aqueous acid solution of 10 to 80 grams per liter of tin in the form of a stannous phenolsulfonate, and the reaction product formed by dissolving in said solution 2 to 6 grams per liter of toluidine and gradually adding formaldehyde at a temperature of 40 to 60 C. in an amount of 1 to 3 mols of formaldehyde per mol of toluidine, said solution having a total free acid content expressed as the H2804 equivalent of 20 to 50 grams per liter.
• An electrolytic tin plating bath consisting of an aqueous acid solution of 10 to 80 grams per liter of tin in the form of stannous sulphate and the reaction product formed by dissolving in said solution 2 to 6 grams per liter of an amine of the group consisting of aniline, toluidine, xylidine, and chloraniline and gradually adding formaldehyde at a temperature of 40 to 60 C. in an amount of 1 to 3 mols of formaldehyde per mol of amine, said solution having a total free acid content of 20 to 50 grams per liter H2804.
• An electrolytic tin plating bath consisting of an aqueous acid solution of 10 to 80 grams per liter of tin in the form of stannous sulphate and the reaction product formed by dissolving in said solution 2 to 6 grams per liter of toluidine and gradually adding formaldehyde at a temperature of 40 to 60 C. in an amount of 1 to 3 mols of formaldehyde per mol of toluidine, said solution having a total free acid content of 20 to 50 grams per liter H2SO4.
• An electrolytic tin plating bath consisting of an aqueous acid solution of 10 to 80 grams per liter of tin in the form of a stannous salt of an acid of the group consisting of phenolsulfonic acid, benzene meta-disulfonic acid and sulphuric acid, and the reaction product formed by dissolving in said solution 2 to 6 grams per liter of aniline and gradually adding formaldehyde at a temperature of 40 to 60 C. in an amount of 1 to 3 mols of formaldehyde per mol of aniline, said solution having a total free acid content expressed as the H2804 equivalent of 20 to 50 grams per liter.
• An electrolytic tin plating bath consisting of an aqueous acid solution of 10 to grams per liter of tin in the form of a stannous salt of an acid of the group consisting of phenolsulfonic acid, benzene meta-disulfonic acid and sulphuric acid, and the reaction product of 2 to 6 grams per liter formed by dissolving in said solution xylidine and gradually adding formaldehyde at a temperature of 40 to 60 C. in an amount of 1 to 3 mols of formaldehyde per mol of xylidine, said solution having a total free acid content expressed as the H2804 equivalent of 20 to 50 grams per liter.
• An electrolytic tin plating bath consisting of an aqueous acid solution of 10 to 80 grams per liter of tin in the form of a stannous salt of an acid of the group consisting of phenolsulfonic acid, benzene meta-disulfonic acid and sulphuric acid, and the reaction product formed by dissolving in said solution 2 to 6 grams per liter of chloraniline and gradually adding formaldehyde at a temperature of 40 to 60 C in an amount of 1 to 3 mols of formaldehyde per mol of chloraniline. said solution having a total free acid content expressed as the H2804 equivalent of 20 to 50 grams per liter.
• An electrolytic tin plating bath consisting per liter of tin in the form of a stannous salt of an acid of the group consisting of phenolsulfonic acid, benzene meta-disulfonic acid and sulphuric acid, and the reaction product formed by dissolving an amine in said solution and gradually adding formaldehyde thereto at a temperature of 40 to 60 C., the amine being present in a concentration of 2 to 6 grams per liter and being a primary aromatic amine having an amino group attached to one position on a benzene ring and groups of the class consisting of hydrogen, halogens, and alkyls attached to the other positions, the formaldehyde being present in an amount of 1 to 3 mols per mol of amine, said solution having a total free acid content expressed as the H2804 equivalent of 20 to 50 grams per liter.
• An electrolytic tin plating bath consisting C. in an amount of 1 to 3 mols of formaldehyde per mol of para toluidine, said solution having a total free acid content expressed as the H2804 equivalent of 20 to 50 grams per liter.

Landscapes

• 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)

Priority Applications (3)

Applications Claiming Priority (1)

Publications (1)

Family

ID=22763783

Family Applications (1)

Country Status (3)

Cited By (7)

Citations (2)

• 0
  • BE BE508197D patent/BE508197A/xx unknown
• 1951
  • 1951-01-12 US US205823A patent/US2598486A/en not_active Expired - Lifetime
  • 1951-07-24 GB GB17521/51A patent/GB684468A/en not_active Expired

Patent Citations (2)

Also Published As

Similar Documents