US20100000873A1 - Electrolytic tin plating solution and electrolytic tin plating method - Google Patents

Electrolytic tin plating solution and electrolytic tin plating method Download PDF

Info

Publication number
US20100000873A1
US20100000873A1 US12/456,077 US45607709A US2010000873A1 US 20100000873 A1 US20100000873 A1 US 20100000873A1 US 45607709 A US45607709 A US 45607709A US 2010000873 A1 US2010000873 A1 US 2010000873A1
Authority
US
United States
Prior art keywords
plating
tin plating
plating solution
chip components
acid
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
US12/456,077
Other languages
English (en)
Inventor
Masaaki Imanari
Fai Lung Ting
Motoya Shimazu
Yasuo Ohta
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Rohm and Haas Electronic Materials LLC
Original Assignee
Rohm and Haas Electronic Materials LLC
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Rohm and Haas Electronic Materials LLC filed Critical Rohm and Haas Electronic Materials LLC
Publication of US20100000873A1 publication Critical patent/US20100000873A1/en
Abandoned legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25DPROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
    • C25D3/00Electroplating: Baths therefor
    • C25D3/02Electroplating: Baths therefor from solutions
    • C25D3/30Electroplating: Baths therefor from solutions of tin
    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25DPROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
    • C25D17/00Constructional parts, or assemblies thereof, of cells for electrolytic coating
    • C25D17/16Apparatus for electrolytic coating of small objects in bulk

Definitions

  • the present invention relates to a tin plating solution and an electrolytic tin plating method; and in further detail relates to an electrolytic tin plating solution and plating method for plating chip components such as ceramic capacitors.
  • Chip components are metal plated with tin, copper, silver, gold, nickel, palladium, or an alloy thereof, or the like, using a plating method such as barrel plating, plating with a flow-through plater, or the like, depending on the shape of the chip and the construction of the regions to be plated.
  • a plating method such as barrel plating, plating with a flow-through plater, or the like, depending on the shape of the chip and the construction of the regions to be plated.
  • the purpose for tin plating is to provide solderability to the electrode parts of the chip component.
  • the chip components will stick to each other (hereinafter also referred to as aggregation, sticking, and coupling). Chips that stick together become defective products, and reduce the yield of the product.
  • the ratio of chip components that stick together from the total number of chip components is referred to as the coupling rate, and in severe cases, the coupling rate can exceed 90%.
  • a tin plating bath with excellent solder wetting properties is important for tin plating to provide solderability to the chip components, or the like.
  • the present inventors have previously improved on this point, and have discovered that specific naphthol compounds are useful as an additive for electrolytic tin plating that can form a tin film with uniform appearance, and the deposited tin film will have favorable solder wetting properties, and have also discovered that the solderability can be improved using specific naphthol compounds.
  • an objective present invention is to provide a plating solution for chip components and a plating method for chip components, which does not use a complexing agent, and which provides favorable solder wetting properties and an extremely low coupling rate when electrolytic tin plating is performed, and particularly when electrolytic tin plating is performed using a barrel plating method.
  • a smooth tin plating film with higher film surface hardness than a conventional film and which can minimize sticking between plated substrates can be achieved by using specific compounds in a strongly acidic (pH of 1 or lower) tin plating bath, and particularly in a barrel tin plating bath that does not contain a complexing agent.
  • one aspect of the present invention provides an electrolytic tin plating solution for chip components, comprising (A) stannous ions, (B) acid, (C) N,N-dipolyoxyalkylene-N-alkyl amine, amine oxide, or blend thereof, and (D) an anti-sticking agent; wherein the pH is 1 or lower.
  • one aspect of the present invention provides an electrolytic tin plating solution for chip components, further containing (E) a plating uniformity improver in addition to the components (A) through (D).
  • one aspect of the present invention provides an electrolytic tin plating solution for chip components, further containing (F) an acrylic acid or acrylic acid derivative expressed by the following General Formula (1) and (G) an antioxidant, in addition to the components of (A) through (E).
  • R represents a hydrogen atom or an alkyl group containing between 1 and 3 carbon atoms.
  • one aspect of the present invention provides an electrolytic tin plating solution for chip components, wherein the aforementioned N,N-dipolyoxyalkylene-N-alkyl amine is one or more compounds expressed by the following General Formula (2).
  • R represents an alkyl group with between 6 and 28 carbon atoms
  • w, x, y, and z each represent an integer between 0 and 30.
  • the sum of w, x, y, and z is not 0.
  • one aspect of the present invention provides an electrolytic tin plating solution for chip components, wherein the aforementioned amine oxide is one or more compound expressed by the following General Formula (3).
  • R represents an alkyl group, cycloalkyl group, or aryl group
  • R′ represents a hydrogen atom, alkyl group, or cycloalkyl group
  • one aspect of the present invention provides an electrolytic tin plating solution for chip components, wherein the aforementioned (D) anti-sticking agent is one or more compound selected from a group consisting of aromatic aldehydes and aromatic ketones.
  • one aspect of the present invention provides a method of plating chip components, comprising electrolytically tin plating chip components using an electrolytic tin plating solution comprising (A) stannous ions, (B) acid, (C) N,N-dipolyoxyalkylene-N-alkyl amine, amine oxide, or blend thereof, and (D) an anti-sticking agent; wherein the pH is 1 or lower.
  • the plating solution of the present invention is very effective at preventing substrates from sticking together and can minimize plating defects so the product yield increases when a plurality of substrates such as chip components, or the like, are electrolytically tin plated, and particularly when electrolytically tin plated using a barrel plating method.
  • making the tin plating film smooth can reduce the sticking phenomenon that occurs when substrates come in contact with each other, where substrates lock together and physically cannot be peeled apart, similar to mat plating.
  • increasing the film surface hardness can prevent tin plating films from deforming when substrates come in mutual contact, caused by the film surface being soft such as with mat plating, and can minimize the occurrence of tin plating films sticking together.
  • the plating solution of the present invention does not include a complexing agent, so wastewater treatment is easier than with a convention plating solution for barrel plating.
  • the terms “plating solution” and “plating bath” used in this specification have exactly the same meaning and are used interchangeably.
  • the electrolytic tin plating solution of the present invention is an electrolytic tin plating solution for chip components, containing: (A) stannous ions, (B) acid, (C) N,N-dipolyoxyalkylene-N-alkyl amine, amine oxide, or blend thereof, and (D) an anti-sticking agent; wherein the pH is 1 or lower.
  • the components are described below in order.
  • the plating bath of the present invention contains stannous ions as an essential component.
  • Stannous ions are bivalent tin ions. Any compound that can provide stannous ions to the plating bath can be used. Generally, the tin salt of an inorganic acid or an organic acid is preferable.
  • tin salts of inorganic acids include the stannous salt of sulfuric acid or hydrochloric acid
  • examples of tin salts of organic acids include the stannous salt of substituted or unsubstituted alkanesulfonic acids or alkanolsulfonic acids, such as methanesulfonic acid, ethane-sulfonic acid, propanesulfonic acid, 2-hydroxyethane-1-sulfonic acid, 2-hydroxypro-pane-1-sulfonic acid, and 1-hydroxypropane-2-sulfonic acid, and the like.
  • stannous ions are stannous sulfate for salts of inorganic acids and stannous methane-sulfonate for salts of organic acids.
  • the compounds which can provide these ions can be used individually, or as a blend of 2 or more types.
  • the amount of stannous ion added to the plating bath is, for example, between 1 g/L and 150 g/L, preferably between 5 g/L and 50 g/L, and more preferably between 8 g/L and 20 g/L.
  • the acid can be any arbitrary acid that can adjust the pH to 1 or lower and can provide conductivity to the plating bath.
  • the acid can be any inorganic or organic acid.
  • organic acids include substituted or unsubstituted alkanesulfonic acids or alkanolsulfonic acids, such as methanesulfonic acid, ethanesulfonic acid, propanesulfonic acid, 2-hydroxyethane-1-sulfonic acid, 2-hydroxypropane-1-sulfonic acid, and 1-hydroxypropane-2-sulfonic acid. Methanesulfonic acid is preferable.
  • examples of inorganic acids include sulfuric acid and hydrochloric acid, and sulfuric acid is preferable. These acids that can adjust the pH to 1 or lower and can provide conductivity to the plating bath can be used individually, or as a blend of 2 or more types.
  • the amount of acid in the plating bath solution is preferably at least stoichiometically equivalent to the amount of bivalent tin ions in the plating bath.
  • the amount of free acid in the plating bath is, for example, between 10 g/L and 500 g/L, preferably between 30 g/L and 300 g/L, and more preferably between 50 g/L and 200 g/L.
  • the plating bath of the present invention contains N,N-dipolyoxyalkylene-N-alkyl amine, amine oxide, or blend thereof as an essential component.
  • the present inventors have evaluated various nonionic surfactants, and have discovered that uniform plating at the required plating film thickness can be achieved by using N,N-dipolyoxyalkylene-N-alkyl amine or amine oxides which are specific anionic surfactants.
  • N,N-dipolyoxyalkylene-N-alkyl amine is preferably a polyoxypropylene polyoxyethylenealkylamine expressed by the following General Formula (2).
  • R represents a straight or branched alkyl group with between 6 and 26 carbon atoms, and w, x, y, and z each represent an integer between 0 and 30. However, the sum of w, x, y, and z is not 0. Preferably, R represents a straight chain alkyl group with between 8 and 18 carbon atoms, and the sum of w, x, y, and z is between 10 and 20.
  • the amine oxide is one or more compound expressed by the following General Formula (4).
  • R 1 , R 2 , and R 3 each represent an alkyl group, a cycloalkyl group, or an aryl group, which may have a substitution group. Examples include a methyl group, ethyl group, propyl group, butyl group, pentyl group, hexyl group, phenyl group, tolyl group xylyl group and naphthyl group, and the like.
  • the amine oxide of the present invention is preferably one or more amine oxides with a structure as expressed by General Formula (3).
  • R represents an alkyl group, cycloalkyl group or aryl group
  • R′ represents an alkyl group or a cycloalkyl group
  • N,N-dipolyoxyalkylene-N-alkyl amine or amine oxide can act as a film modifying agent in the plating bath of the present invention.
  • smoothing the plating film with N,N-dipolyoxyalkylene-N-alkyl amine or amine oxide can minimize the sticking phenomenon where substrates lock together and physically cannot be peeled apart, similar to mat plating, which occurs when substrates come in contact with each other.
  • the aforementioned preferable anti-sticking agents are particular effective when used in combination with the aforementioned (C) N,N-dipolyoxyalkylene-N-alkyl amine or amine oxide.
  • concentration of anti-sticking agent in the plating bath is suitably between 1 mg/L and 50 g/L, preferably between 5 mg/L and 10 g/L, and more preferably between 10 mg/L and 5 g/L.
  • the plating bath of the present invention preferably contains a plating uniformity improver as an arbitrary component in addition to the aforementioned components (A) through (D).
  • the plating uniformity improver of the present invention is a compound that improves the plating uniformity particularly in areas of low current density.
  • barrel plating in particular, the object to be plated is placed in a barrel and electroplating is performed while rotating the barrel with the parts immersed in the plating solution, and therefore variation in the current density will occur, the current density range of the object to be plated will vary widely from a high current density region to a low current density region, and in the low current density region, there will be problems with lower plating uniformity, and therefore the plating film will have variation.
  • the plating uniformity improver By adding a plating uniformity improver, the plating can be uniformly performed even in the low current density regions.
  • Examples of plating uniformity improvers include 2-naphthol-7-sulfonic acid and compounds (I) with the structural formula shown below.
  • 2-naphthol-7-sulfonic acid can be either in the form of a free acid or as a salt.
  • Suitable salts of 2-naphthol-7-sulfonic acid include water soluble salts such as potassium, sodium, ammonium, and tin, or the like, but potassium and sodium salts are preferable, and sodium 2-naphthol-7-sulfonate is even more preferable. These salts can be used individually, or as a blend of two or more types.
  • the amount of 2-naphthol-7-sulfonic acid or salt thereof added to the plating bath is between 0.01 g/L and 20 g/L, preferably between 0.1 g/L and 10 g/L, and more preferably between 0.2 g/L and 5 g/L.
  • the plating bath of the present invention preferably contains one or more acrylic acid or acrylic acid derivative expressed by the following General Formula (1) as an arbitrary component.
  • acrylic acid and methacrylic acid are preferable.
  • R represents a hydrogen atom or an alkyl group containing between 1 and 3 carbon atoms.
  • the methacrylic acid or acrylic acid is preferably added to the plating solution of the present invention as an auxiliary anti-sticking agent that supports the aforementioned (D) anti-sticking agent.
  • the methacrylic acid or acrylic acid can further increase the component anti-sticking effect of the (D) anti-sticking agent, and in particular has the effect of increasing the film surface hardness, and can increase the sustainability of the anti-sticking effect, by being used in combination with the (D) anti-sticking agent.
  • An antioxidant can arbitrarily be used in the plating solution of the present invention.
  • the antioxidant is used to prevent oxidation of the bivalent tin ions to tetravalent tin ions, and examples include hydroquinone, catechol, resorcin, phloroglucin, pyrogallol, hydroquinonesulfonic acid, and salts thereof.
  • the concentration of antioxidant in the plating bath is suitably between 10 mg/L and 100 g/L, preferably between 100 mg/L and 50 g/L, more preferably between 0.5 g/L and 5 g/L.
  • additives can be added to the plating bath of the present invention, if necessary, such as glossing agents, smoothing agents, conductivity agents, and anode dissolving agents, and the like.
  • Examples of the chip components that can be plated using the plating solution of the present invention include electronic components such as resistors, capacitors, inductors, variable resistors, variable capacitors, and other passive components, quartz oscillator, LC filter, ceramic filter, delay lines, SAW filters, and other functional components, switches, connectors, relay fuses, optical components, and other contact components.
  • electronic components such as resistors, capacitors, inductors, variable resistors, variable capacitors, and other passive components, quartz oscillator, LC filter, ceramic filter, delay lines, SAW filters, and other functional components, switches, connectors, relay fuses, optical components, and other contact components.
  • the electroplating method that is used with the plating solution of the present invention can be a commonly known plating method such as barrel plating, and plating using a flow-through plater, or the like.
  • the concentration of the various components (A) through (F) in the plating solution can be arbitrarily selected based on the forgoing descriptions for each of the components.
  • the electroplating method that is used with the plating solution of the present invention can be performed at a bath temperature between 10° C. and 50° C., preferably between 15° C. and 30° C.
  • the cathode current density is suitably selected within a range between 0.01 and 5 A/dm 2 , preferably between 0.05 and 3 A/dm 2 .
  • the plating bath may be left without stirring, or can be stirred using a stirrer, or the like, or re-circulated using a pump, or the like.
  • a bath was formed using the tin plating solution with the following composition.
  • Barrel tin plating was performed on chip resistors that had been nickel plated using a 1 L tin plating solution at the conditions shown below, and then various evaluations were performed. The results are shown in Table 1.
  • Object for plating chip resistor, barrel: Yamamoto minibarrel (volume: 140 mL) Rotational speed: 20 rpm Nickel plating: 2.4 A—60 minutes Tin plating: 2 A—90 minutes Chip R resistor (size 1608): 4.7 k ⁇ 15 mL/barrel Steel ball: 1 mm ⁇ 30 mL/barrel
  • the plating thickness on the front surface, back surface, and on the left and right sides was measured using a fluorescent light x-ray film thickness meter, and the thickness and the plating thickness various between each point were evaluated.
  • the barrel-plated chip components were sorted into chips which were stuck together and chips that were not stuck together, and the coupling rate was calculated as a ratio (%) with the weight of chips that stuck together in the numerator and the weight of all of the chips in the denominator (stuck chips/(stuck chips+unstuck chips) ⁇ 100).
  • the zero cross time was measured and a value of 3.0 seconds or less was considered a PASS.
  • the pass rate was calculated as a percentage using the number of samples with a zero cross time of 3 seconds or less in the numerator, and the total number of samples measured (10 samples) in the denominator.
  • Tin plating baths were created at the ratios shown in Table 1 and Table 2 in a similar manner to Example 1, and the various tests were performed similar to Example 1. The results are also shown in Table 1 and Table 2. Note, the symbols related to the evaluation of the plating thickness are as shown below.
  • Plating thickness is uniform on the front surface, back surface, and on the left and right sides: O
  • Plating is not uniform: ⁇ Plating is not formed: X

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)
  • Electroplating Methods And Accessories (AREA)
US12/456,077 2008-06-12 2009-06-11 Electrolytic tin plating solution and electrolytic tin plating method Abandoned US20100000873A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2008-154461 2008-06-12
JP2008154461A JP5583894B2 (ja) 2008-06-12 2008-06-12 電気錫めっき液および電気錫めっき方法

Publications (1)

Publication Number Publication Date
US20100000873A1 true US20100000873A1 (en) 2010-01-07

Family

ID=41334608

Family Applications (1)

Application Number Title Priority Date Filing Date
US12/456,077 Abandoned US20100000873A1 (en) 2008-06-12 2009-06-11 Electrolytic tin plating solution and electrolytic tin plating method

Country Status (6)

Country Link
US (1) US20100000873A1 (de)
EP (1) EP2141261B1 (de)
JP (1) JP5583894B2 (de)
KR (1) KR101593475B1 (de)
CN (1) CN101619470B (de)
TW (1) TWI468554B (de)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20130206602A1 (en) * 2012-02-09 2013-08-15 Rohm And Haas Electronic Materials Llc Plating bath and method
US20150122662A1 (en) * 2013-11-05 2015-05-07 Rohm And Haas Electronic Materials Llc Plating bath and method
US20150122661A1 (en) * 2013-11-05 2015-05-07 Rohm And Haas Electronic Materials Llc Plating bath and method
US9080247B2 (en) 2009-07-31 2015-07-14 Shinji Dewaki Tin-containing alloy plating bath, electroplating method using same, and substrate with the electroplating deposited thereon
JP2017504715A (ja) * 2013-12-05 2017-02-09 ハネウェル・インターナショナル・インコーポレーテッド 調節されたpHを有するメタンスルホン酸第一スズ溶液
US9574281B2 (en) 2009-02-06 2017-02-21 M-Tech Japan Co., Ltd. Silver-containing alloy plating bath and method for electrolytic plating using same
US9926637B2 (en) 2012-12-27 2018-03-27 Rohm And Haas Electronic Materials Llc Tin or tin alloy plating liquid
US11268203B2 (en) * 2017-10-24 2022-03-08 Mitsubishi Materials Corporation Tin or tin alloy plating solution

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2012021224A (ja) * 2010-06-15 2012-02-02 Mitsubishi Shindoh Co Ltd 錫めっき液中のスラッジ発生防止方法
EP2740820A1 (de) 2012-12-04 2014-06-11 Dr.Ing. Max Schlötter GmbH & Co. KG Elektrolyt und Verfahren zur Abscheidung von lötbaren Schichten
CN105755513A (zh) * 2016-04-28 2016-07-13 四川昊吉科技有限公司 一种镀锡防腐剂
JP6818520B2 (ja) 2016-11-11 2021-01-20 ローム・アンド・ハース電子材料株式会社 中性スズめっき液を用いたバレルめっきまたは高速回転めっき方法
JP6620858B2 (ja) * 2017-10-24 2019-12-18 三菱マテリアル株式会社 錫又は錫合金めっき堆積層の形成方法
JP2021508359A (ja) 2017-12-20 2021-03-04 ビーエイエスエフ・ソシエタス・エウロパエアBasf Se 抑制剤を含むスズまたはスズ合金電気めっき用組成物
SG11202009106XA (en) 2018-04-20 2020-11-27 Basf Se Composition for tin or tin alloy electroplating comprising suppressing agent
CN109518233B (zh) * 2018-11-27 2020-07-14 东莞美坚化工原料有限公司 一种防止微型电子元器件粘片的导电溶液及其制备方法

Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2846381A (en) * 1956-01-16 1958-08-05 Max Schlotter Dr Ing Method of electrolytically depositing smooth layers of tin
US3616306A (en) * 1969-11-19 1971-10-26 Conversion Chem Corp Tin plating bath and method
US4000047A (en) * 1972-11-17 1976-12-28 Lea-Ronal, Inc. Electrodeposition of tin, lead and tin-lead alloys
US4135991A (en) * 1977-08-12 1979-01-23 R. O. Hull & Company, Inc. Bath and method for electroplating tin and/or lead
US4582576A (en) * 1985-03-26 1986-04-15 Mcgean-Rohco, Inc. Plating bath and method for electroplating tin and/or lead
US4717460A (en) * 1983-12-22 1988-01-05 Learonal, Inc. Tin lead electroplating solutions
US4871429A (en) * 1981-09-11 1989-10-03 Learonal, Inc Limiting tin sludge formation in tin or tin/lead electroplating solutions
US4885064A (en) * 1989-05-22 1989-12-05 Mcgean-Rohco, Inc. Additive composition, plating bath and method for electroplating tin and/or lead
US20060051610A1 (en) * 2001-05-24 2006-03-09 Shipley Company, L.L.C. Tin plating
US20070068823A1 (en) * 2005-08-19 2007-03-29 Rohm And Haas Electronic Materials Llc Tin electroplating solution and tin electroplating method

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2856857B2 (ja) * 1990-07-27 1999-02-10 石原薬品株式会社 錫、鉛または錫―鉛合金めっき浴
JP2001040498A (ja) * 1999-07-27 2001-02-13 Ne Chemcat Corp 錫−銅合金めっき皮膜で被覆された電子部品
JP2001234387A (ja) * 2000-02-17 2001-08-31 Yuken Industry Co Ltd 錫系電気めっきのウィスカー発生防止剤および防止方法
JP3910028B2 (ja) 2001-09-13 2007-04-25 株式会社村田製作所 チップ型セラミックス電子部品の電極形成法
EP1948852B1 (de) * 2005-11-18 2018-08-29 Luxembourg Institute of Science and Technology (LIST) Master-elektrode und herstellungsverfahren dafür

Patent Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2846381A (en) * 1956-01-16 1958-08-05 Max Schlotter Dr Ing Method of electrolytically depositing smooth layers of tin
US3616306A (en) * 1969-11-19 1971-10-26 Conversion Chem Corp Tin plating bath and method
US4000047A (en) * 1972-11-17 1976-12-28 Lea-Ronal, Inc. Electrodeposition of tin, lead and tin-lead alloys
US4135991A (en) * 1977-08-12 1979-01-23 R. O. Hull & Company, Inc. Bath and method for electroplating tin and/or lead
US4871429A (en) * 1981-09-11 1989-10-03 Learonal, Inc Limiting tin sludge formation in tin or tin/lead electroplating solutions
US4717460A (en) * 1983-12-22 1988-01-05 Learonal, Inc. Tin lead electroplating solutions
US4582576A (en) * 1985-03-26 1986-04-15 Mcgean-Rohco, Inc. Plating bath and method for electroplating tin and/or lead
US4885064A (en) * 1989-05-22 1989-12-05 Mcgean-Rohco, Inc. Additive composition, plating bath and method for electroplating tin and/or lead
US20060051610A1 (en) * 2001-05-24 2006-03-09 Shipley Company, L.L.C. Tin plating
US20070068823A1 (en) * 2005-08-19 2007-03-29 Rohm And Haas Electronic Materials Llc Tin electroplating solution and tin electroplating method

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9574281B2 (en) 2009-02-06 2017-02-21 M-Tech Japan Co., Ltd. Silver-containing alloy plating bath and method for electrolytic plating using same
US9080247B2 (en) 2009-07-31 2015-07-14 Shinji Dewaki Tin-containing alloy plating bath, electroplating method using same, and substrate with the electroplating deposited thereon
EP2626449A3 (de) * 2012-02-09 2017-08-16 Rohm and Haas Electronic Materials LLC Plattierbad und -verfahren
TWI467066B (zh) * 2012-02-09 2015-01-01 羅門哈斯電子材料有限公司 電鍍浴及方法
US8888984B2 (en) * 2012-02-09 2014-11-18 Rohm And Haas Electronic Materials Llc Plating bath and method
US20130206602A1 (en) * 2012-02-09 2013-08-15 Rohm And Haas Electronic Materials Llc Plating bath and method
US9926637B2 (en) 2012-12-27 2018-03-27 Rohm And Haas Electronic Materials Llc Tin or tin alloy plating liquid
US20150122662A1 (en) * 2013-11-05 2015-05-07 Rohm And Haas Electronic Materials Llc Plating bath and method
US20150122661A1 (en) * 2013-11-05 2015-05-07 Rohm And Haas Electronic Materials Llc Plating bath and method
KR20150051927A (ko) * 2013-11-05 2015-05-13 롬 앤드 하스 일렉트로닉 머트어리얼즈 엘엘씨 도금조 및 방법
KR102454558B1 (ko) * 2013-11-05 2022-10-13 롬 앤드 하스 일렉트로닉 머트어리얼즈 엘엘씨 도금조 및 방법
JP2017504715A (ja) * 2013-12-05 2017-02-09 ハネウェル・インターナショナル・インコーポレーテッド 調節されたpHを有するメタンスルホン酸第一スズ溶液
US11268203B2 (en) * 2017-10-24 2022-03-08 Mitsubishi Materials Corporation Tin or tin alloy plating solution

Also Published As

Publication number Publication date
CN101619470B (zh) 2012-03-28
KR101593475B1 (ko) 2016-02-12
KR20090129373A (ko) 2009-12-16
EP2141261A2 (de) 2010-01-06
TWI468554B (zh) 2015-01-11
EP2141261B1 (de) 2017-03-01
TW201006966A (en) 2010-02-16
JP2009299123A (ja) 2009-12-24
EP2141261A3 (de) 2010-07-28
CN101619470A (zh) 2010-01-06
JP5583894B2 (ja) 2014-09-03

Similar Documents

Publication Publication Date Title
US20100000873A1 (en) Electrolytic tin plating solution and electrolytic tin plating method
US7150781B2 (en) Pyrophosphoric acid bath for use in copper-tin alloy plating
EP1754805B1 (de) Zinn galvanisches Bad und Zinn galvanisches Abscheidungsverfahren
JP4162246B2 (ja) シアン化物非含有銀系メッキ浴、メッキ体及びメッキ方法
JP3301707B2 (ja) 錫−銀合金酸性電気めっき浴
US7931793B2 (en) Tin or tin alloy electroplating solution
EP3002350B1 (de) Cyanidfreie galvanische bäder für weisse bronze basierend auf kupfer (i) ionen
CN101243210A (zh) 具有最小化锡晶须生长性能或特性的锡电沉积物
TWI548782B (zh) 無氰化物之酸性消光銀電鍍組成物及方法
EP3321396B1 (de) Trommelplattierung oder hochgeschwindigkeitsdrehplattierung mit einer neutralen zinnplattierungslösung
US8277630B2 (en) Tin electroplating solution and a method for tin electroplating
TWI623654B (zh) 鉍電鍍浴及將鉍電鍍於基板上的方法
US20040149587A1 (en) Electroplating solution containing organic acid complexing agent
US6458264B1 (en) Sn-Cu alloy plating bath
TW201700797A (zh) 使用銨鹽之鍍敷液
JP2009191335A (ja) めっき液及び電子部品
TW201704546A (zh) 使用鋶鹽之鍍敷液
TW202233897A (zh) 錫合金鍍液

Legal Events

Date Code Title Description
STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION