[go: up one dir, main page]

US3793161A - Methods for electroplating solder - Google Patents

Methods for electroplating solder Download PDF

Info

Publication number
US3793161A
US3793161A US00279933A US3793161DA US3793161A US 3793161 A US3793161 A US 3793161A US 00279933 A US00279933 A US 00279933A US 3793161D A US3793161D A US 3793161DA US 3793161 A US3793161 A US 3793161A
Authority
US
United States
Prior art keywords
solder
anode
consumable
necking
percent
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.)
Expired - Lifetime
Application number
US00279933A
Inventor
H Manko
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.)
Alpha Metals Ltd
Original Assignee
Alpha Metals Ltd
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 Alpha Metals Ltd filed Critical Alpha Metals Ltd
Application granted granted Critical
Publication of US3793161A publication Critical patent/US3793161A/en
Anticipated expiration legal-status Critical
Expired - Lifetime 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
    • C25D17/00Constructional parts, or assemblies thereof, of cells for electrolytic coating
    • C25D17/10Electrodes, e.g. composition, counter electrode

Definitions

  • ABSTRACT A consumable solder anode being an anode shaped body composed of an alloy of 5 to 100 percent high purity tin and 0 to 95 percent high purity lead with approximately 50 p.p.m. of a grain refiner such as calcium, phosphorous, tellurium, sulfur.
  • This invention relates generally to consumable solder anodes, and particularly to consumable solder anodes which display a high degree of resistance to intergranular corrosion in electrolytes of either low or high pH, which do not proliferate surface accumulations of insoluble reaction products, and which are capable of sustaining high current density for fast plating, without the aforementioned surface accumulations, corrosion or necking.
  • the anode When necking occurs, the anode cannot support high current density throughout its entire structure without heating at the neck, so that the process of deterioration becomes even more rapidly progressive. Finally, the main body of the anode is deprived totally of support, when the neck ruptures and the body separates from its hook and falls into the electrolyte. This may cause serious difficulties, such as a short circuit, or the dissolving of the anode in the electrolyte, causing a vast chemical imbalance. Obviating the problem of necking is therefore a very necessary and pressing one.
  • a consumable solder anode may be prepared which, when subjected to high current density for fast plating, when subjected to high and low pH electrolytes, nevertheless is highly resistant to necking, is highly resistant to intergranular corrosion, and is relatively free of surface accumulations of insoluble reaction products.
  • An anode is prepared by any of the well-known methods such as extruding, rolling, drawing, extending, casting, forming, chill-casting or clading.
  • the anode is composed of relatively pure tin and up to approximately percent lead. Not less than 20 p.p.m. calcium is added as a grain reducing material. As an alternative to calcium, phosphorus, tellurium and sulfur or combinations thereof may be substituted.
  • This anode is highly resistant to necking and has a much lesser degree, regardless of whether the electrolyte is of high or low pH and of very aggressive chemical character.
  • the anode may be used at a high current density for faster solder plating because surface accumulations of insoluble reaction products are eliminated to a high degree.
  • the constant checking of the composition of the electrolyte is no longer necessary, its frequent replenishment is not necessary, filtration need not be resorted to to remove the impurities that may appear in the electrolyte and impair its proper functioning.
  • the plating accomplished is of a high degree of uniformity, and the ratio of tin and lead which characterizes the composition of the anode is reproduced on the work piece.
  • the presence of the grain reducers accomplishes a vast reduction of the size of the crystal structure of the anode, so that the aggressive electrolytes do not succeed in rapidly undermining large crystals and introducing impurities into the electrolyte. Likewise, the refinement of crystal structure inhibits the necking of the electrode.
  • the method of solder plating with a consumable solder anode subjected to necking, intergranular corrosion by high or low pH electrolytes, surface accumulation of insoluble reaction products, or high current density comprising:
  • solder anode consisting essentially of 20 to 100 ppm calcium and the remainder about 60 percent tin and about 40 percent lead, and
  • solder anode consisting essentially of 20 to 100 ppm sulfur and the remainder about 5 percent tin and about percent lead
  • solder anode consisting essentially of 20 ppm of material selected from the group consisting of calcium, phosphorous, sulfur, or tellurium, and the remainder about 5 100 percent tin and about 0 95 percent lead, and

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)

Abstract

A consumable solder anode being an anode shaped body composed of an alloy of 5 to 100 percent high purity tin and 0 to 95 percent high purity lead with approximately 50 p.p.m. of a grain refiner such as calcium, phosphorous, tellurium, sulfur.

Description

United States Patent [191 Manko 1 Feb. 19, 1974 METHODS FOR ELECTROPLATING SOLDER [52] US. Cl 204/43 S, 75/166 D, 75/175 R,
204/54 R, 204/293 [51] Int. Cl. C23b 5/14, C23b 5/38, C23b 5/40 [58] Field of Search... 204/293, 43 S, 54; 75/175 R,
[56] References Cited FOREIGN PATENTS OR APPLICATIONS 718,982 11/1954 Great Britain 75/175 R OTHER PUBLICATIONS Equilibrium Data for Tin Alloys, Tin Research Insti tute, (1949), p. 16.
Primary ExaminerG. L. Kaplan Attorney, Agent, or Firm-Popper, Bain, Bobis, Gilfillan & Rhodes [5 7 ABSTRACT A consumable solder anode being an anode shaped body composed of an alloy of 5 to 100 percent high purity tin and 0 to 95 percent high purity lead with approximately 50 p.p.m. of a grain refiner such as calcium, phosphorous, tellurium, sulfur.
4 Claims, No Drawings BACKGROUND OF THE INVENTION 1. Field of Invention This invention relates generally to consumable solder anodes, and particularly to consumable solder anodes which display a high degree of resistance to intergranular corrosion in electrolytes of either low or high pH, which do not proliferate surface accumulations of insoluble reaction products, and which are capable of sustaining high current density for fast plating, without the aforementioned surface accumulations, corrosion or necking.
2. Description of the Prior Art Cast solder anodes are in wide general use. In casting anodes, an intergranular structure is achieved which is particularly subject to chemical attack by aggressive electrolytes which may be of either high or low pH. The anodes rapidly deteriorate because whole grains are eaten around until they are physically unsupported and become discharged from the surface of the anode. Also, the anode is said to be necked, i.e., it is more rapidly eaten away at its upper end at the level of the surface of the electrolyte, until the main body portion of the anode is only supported by a thin connecting neck; hence the term necked.
When necking occurs, the anode cannot support high current density throughout its entire structure without heating at the neck, so that the process of deterioration becomes even more rapidly progressive. Finally, the main body of the anode is deprived totally of support, when the neck ruptures and the body separates from its hook and falls into the electrolyte. This may cause serious difficulties, such as a short circuit, or the dissolving of the anode in the electrolyte, causing a vast chemical imbalance. Obviating the problem of necking is therefore a very necessary and pressing one. Likewise the intergranular corrosion resulting from the attack by the electrolyte upon portions of the anode, resulting in the discharge of large crystal structures from the anode, may cause these crystals to fall into the electrolyte and be dissolved with equal chemical imbalance in the electrolyte. There is also the possibility of a pile-up of crystals and a shorting.
In order to counteract the deleterious effects of the rapid dissolution of portions of the anode creating sludge, constant filtrationof the electrolyte is usually resorted to in order to maintain a high degree of perfection of the electrodeposit. Such remedies are not entirely successful so the problem still remains of the continuing rapid pollution of the electrolyte. The pollution of the electrolyte also requires not only filtration, but analysis of the content of the bath to determine its composition and need for replenishment, thereby raising the cost of maintaining electrodeposition to accomplish plating of the desired degree of perfection. Efforts to reduce these problems by lowering the current density serve merely to prolong the plating process but, do not,
substantially improve the quality of the plate. There is still corrosion and sludging. The neck of the anode still deteriorates dimensionally.
Extruding of a consumable solder anode has been found to definitely produce a more suitable grain structure which is compatable to a degree with a longer life somewhat less necking, and less intergranular corrosion. But still, the problems persist in a lesser degree.
SUMMARY OF THE INVENTION It has been found that a consumable solder anode may be prepared which, when subjected to high current density for fast plating, when subjected to high and low pH electrolytes, nevertheless is highly resistant to necking, is highly resistant to intergranular corrosion, and is relatively free of surface accumulations of insoluble reaction products. An anode is prepared by any of the well-known methods such as extruding, rolling, drawing, extending, casting, forming, chill-casting or clading. The anode is composed of relatively pure tin and up to approximately percent lead. Not less than 20 p.p.m. calcium is added as a grain reducing material. As an alternative to calcium, phosphorus, tellurium and sulfur or combinations thereof may be substituted.
This anode is highly resistant to necking and has a much lesser degree, regardless of whether the electrolyte is of high or low pH and of very aggressive chemical character. The anode may be used at a high current density for faster solder plating because surface accumulations of insoluble reaction products are eliminated to a high degree. Thus, the constant checking of the composition of the electrolyte is no longer necessary, its frequent replenishment is not necessary, filtration need not be resorted to to remove the impurities that may appear in the electrolyte and impair its proper functioning. The plating accomplished is of a high degree of uniformity, and the ratio of tin and lead which characterizes the composition of the anode is reproduced on the work piece. The presence of the grain reducers accomplishes a vast reduction of the size of the crystal structure of the anode, so that the aggressive electrolytes do not succeed in rapidly undermining large crystals and introducing impurities into the electrolyte. Likewise, the refinement of crystal structure inhibits the necking of the electrode.
PREFERRED EMBODIMENTS Numerous compositions in accordance with the present inventions are possible.
EXAMPLE I Tin 5-lOO% Lead 0-95% Calcium, phosphorus, Sulfur,
Tellurium Not less than 20 p.p.m.
of any one or combination thereof EXAMPLE ll Tin Calcium Not less than 20 p.p.m.
EXAMPLE lll Tin 60% Lead 40% Calcium Not less than 20 p.p.m.
EXAMPLE IV Tin 5%" Lead 95% Sulfur Not less than 20 p.p.m.
In each of these examples, while 20 has been set forth as a minimum, it is preferable to use 50 to 100 p.p.m.
What is claimed is:
l. The method of solder plating with a consumable solder anode subjected to necking, intergranular corrosion by high or low pH electrolytes, surface accumulation of insoluble reaction products, or high current density, comprising:
a. preparing a solder anode consisting essentially of to 100 ppm calcium, and the remainder tin, and
b. electrodepositing solder from the anode on a work piece.
2. The method of solder plating with a consumable solder anode subjected to necking, intergranular corrosion by high or low pH electrolytes, surface accumulation of insoluble reaction products, or high current density, comprising:
a. preparing a solder anode consisting essentially of 20 to 100 ppm calcium and the remainder about 60 percent tin and about 40 percent lead, and
b. electrodepositing solder from the anode on a work piece.
3. The method of solder plating with a consumable solder anode subjected to necking, intergranular corrosion by high or low pH electrolytes, surface accumulation of insoluble reaction products, or high current density, comprising:
a. preparing a solder anode consisting essentially of 20 to 100 ppm sulfur and the remainder about 5 percent tin and about percent lead, and
b. electrodepositing solder from the anode on a work piece.
4. The method of solder plating with a consumable solder anode subjected to necking, intergranular corrosion by high or pH electrolytes, surface accumulation of insoluble reaction products, or high current density, comprising:
a. preparing a solder anode consisting essentially of 20 ppm of material selected from the group consisting of calcium, phosphorous, sulfur, or tellurium, and the remainder about 5 100 percent tin and about 0 95 percent lead, and
b. electrodepositing'solder from the anode on a work piece.

Claims (3)

  1. 2. The method of solder plating with a consumable solder anode subjected to necking, intergranular corrosion by high or low pH electrolytes, surface accumulation of insoluble rEaction products, or high current density, comprising: a. preparing a solder anode consisting essentially of 20 to 100 ppm calcium and the remainder about 60 percent tin and about 40 percent lead, and b. electrodepositing solder from the anode on a work piece.
  2. 3. The method of solder plating with a consumable solder anode subjected to necking, intergranular corrosion by high or low pH electrolytes, surface accumulation of insoluble reaction products, or high current density, comprising: a. preparing a solder anode consisting essentially of 20 to 100 ppm sulfur and the remainder about 5 percent tin and about 95 percent lead, and b. electrodepositing solder from the anode on a work piece.
  3. 4. The method of solder plating with a consumable solder anode subjected to necking, intergranular corrosion by high or pH electrolytes, surface accumulation of insoluble reaction products, or high current density, comprising: a. preparing a solder anode consisting essentially of 20 - 100 ppm of material selected from the group consisting of calcium, phosphorous, sulfur, or tellurium, and the remainder about 5 -100 percent tin and about 0 - 95 percent lead, and b. electrodepositing solder from the anode on a work piece.
US00279933A 1972-08-11 1972-08-11 Methods for electroplating solder Expired - Lifetime US3793161A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US27993372A 1972-08-11 1972-08-11

Publications (1)

Publication Number Publication Date
US3793161A true US3793161A (en) 1974-02-19

Family

ID=23070963

Family Applications (1)

Application Number Title Priority Date Filing Date
US00279933A Expired - Lifetime US3793161A (en) 1972-08-11 1972-08-11 Methods for electroplating solder

Country Status (1)

Country Link
US (1) US3793161A (en)

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4053372A (en) * 1975-10-09 1977-10-11 Amp Incorporated Tin-lead acidic plating bath
US4192923A (en) * 1978-10-27 1980-03-11 Allied Chemical Corporation Amino resin foam, one-phase solution foam precursor and method of producing foam
US4323393A (en) * 1978-06-09 1982-04-06 Teiji Nagahori Hot dipping lead base coating material
US4588657A (en) * 1984-11-01 1986-05-13 Rca Corporation Solder composition
US4734256A (en) * 1986-04-21 1988-03-29 Allied-Signal Inc. Wetting of low melting temperature solders by surface active additions
US5487868A (en) * 1994-03-09 1996-01-30 Nihon Superior Co., Ltd. Tin based solder alloy containing lead, antimony, and tellurium
WO2003076087A1 (en) * 2002-03-05 2003-09-18 Erik Orwoll Electro-chemical cleaning process for electrical connectors
US20070205017A1 (en) * 2005-01-31 2007-09-06 Sanyo Electric Co., Ltd. Circuit device and method of manufacturing the same
US20150004427A1 (en) * 2011-08-17 2015-01-01 Honeywell International Inc. Lead-free solder compositions
US10955439B2 (en) * 2019-03-12 2021-03-23 International Business Machines Corporation Electrochemical cleaning of test probes

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB718982A (en) * 1952-02-20 1954-11-24 British Insulated Callenders Improvements in the tinning of aluminium and aluminium alloys

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB718982A (en) * 1952-02-20 1954-11-24 British Insulated Callenders Improvements in the tinning of aluminium and aluminium alloys

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
Equilibrium Data for Tin Alloys , Tin Research Institute, (1949), p. 16. *

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4053372A (en) * 1975-10-09 1977-10-11 Amp Incorporated Tin-lead acidic plating bath
US4323393A (en) * 1978-06-09 1982-04-06 Teiji Nagahori Hot dipping lead base coating material
US4192923A (en) * 1978-10-27 1980-03-11 Allied Chemical Corporation Amino resin foam, one-phase solution foam precursor and method of producing foam
US4588657A (en) * 1984-11-01 1986-05-13 Rca Corporation Solder composition
US4734256A (en) * 1986-04-21 1988-03-29 Allied-Signal Inc. Wetting of low melting temperature solders by surface active additions
US5487868A (en) * 1994-03-09 1996-01-30 Nihon Superior Co., Ltd. Tin based solder alloy containing lead, antimony, and tellurium
WO2003076087A1 (en) * 2002-03-05 2003-09-18 Erik Orwoll Electro-chemical cleaning process for electrical connectors
US20070205017A1 (en) * 2005-01-31 2007-09-06 Sanyo Electric Co., Ltd. Circuit device and method of manufacturing the same
US7936569B2 (en) * 2005-01-31 2011-05-03 Sanyo Electric Co., Ltd. Circuit device and method of manufacturing the same
US20150004427A1 (en) * 2011-08-17 2015-01-01 Honeywell International Inc. Lead-free solder compositions
US10955439B2 (en) * 2019-03-12 2021-03-23 International Business Machines Corporation Electrochemical cleaning of test probes

Similar Documents

Publication Publication Date Title
US3793161A (en) Methods for electroplating solder
WO2003071001A1 (en) Electroplating solution containing organic acid complexing agent
Petrova et al. Investigation of the processes of obtaining plastic treatment and electrochemical behaviour of lead alloys in their capacity as anodes during the electroextraction of zinc I. Behaviour of Pb Ag, Pb Ca and PB Ag Ca alloys
US2484068A (en) Electrodeposition apparatus
US4364807A (en) Method of electrolytically recovering zinc
US2541721A (en) Process for replenishing nickel plating electrolyte
US2923671A (en) Copper electrodeposition process and anode for use in same
US3547789A (en) Electrodeposition of thick coatings of palladium
US2649409A (en) Electrodeposition of selenium
US6875324B2 (en) Sputtering target material
US3488264A (en) High speed electrodeposition of nickel
US4525327A (en) Lead-antimony-magnesium alloys for storage cell supports and method of manufacturing said alloys
JPH0867932A (en) Copper anode for high current density plating
US2854389A (en) Bright copper plating process
US3721618A (en) Aluminum sacrifical anode
JPH0625882A (en) Copper electrolytic refining method
US2458827A (en) Electrodeposition of lead-tin-antimony alloys
US4189359A (en) Process for the electrodeposition of ferro-nickel alloys
US2831803A (en) Electro-deposition of alloys
JP2000054181A (en) Copper electrolytic refining method
CA1265470A (en) Manufacture of self supporting members of copper containing phosphorus
US3753874A (en) Method and electrolyte for electrodepositing a gold-arsenic alloy
US2356897A (en) Process for electrodeposition of metal
US2654705A (en) Nickel plating
US3794570A (en) Electroplating chromium with a nonconsumable chrome plating anode