GB2058144A - Solder flux composition - Google Patents

Solder flux composition Download PDF

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Publication number
GB2058144A
GB2058144A GB8006718A GB8006718A GB2058144A GB 2058144 A GB2058144 A GB 2058144A GB 8006718 A GB8006718 A GB 8006718A GB 8006718 A GB8006718 A GB 8006718A GB 2058144 A GB2058144 A GB 2058144A
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GB
United Kingdom
Prior art keywords
flux composition
acid
flux
water
composition
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.)
Granted
Application number
GB8006718A
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GB2058144B (en
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.)
STC PLC
Original Assignee
Standard Telephone and Cables PLC
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
Priority claimed from GB7921338A external-priority patent/GB2051137B/en
Application filed by Standard Telephone and Cables PLC filed Critical Standard Telephone and Cables PLC
Priority to GB8006718A priority Critical patent/GB2058144B/en
Publication of GB2058144A publication Critical patent/GB2058144A/en
Application granted granted Critical
Publication of GB2058144B publication Critical patent/GB2058144B/en
Expired legal-status Critical Current

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Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B23MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
    • B23KSOLDERING OR UNSOLDERING; WELDING; CLADDING OR PLATING BY SOLDERING OR WELDING; CUTTING BY APPLYING HEAT LOCALLY, e.g. FLAME CUTTING; WORKING BY LASER BEAM
    • B23K35/00Rods, electrodes, materials, or media, for use in soldering, welding, or cutting
    • B23K35/22Rods, electrodes, materials, or media, for use in soldering, welding, or cutting characterised by the composition or nature of the material
    • B23K35/36Selection of non-metallic compositions, e.g. coatings, fluxes; Selection of soldering or welding materials, conjoint with selection of non-metallic compositions, both selections being of interest
    • B23K35/3612Selection of non-metallic compositions, e.g. coatings, fluxes; Selection of soldering or welding materials, conjoint with selection of non-metallic compositions, both selections being of interest with organic compounds as principal constituents
    • B23K35/3618Carboxylic acids or salts

Landscapes

  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Electric Connection Of Electric Components To Printed Circuits (AREA)

Abstract

A solder flux comprises a mixture of sarcosine and tartronic or tartaric acid dissolved in water or water and an aliphatic alcohol, the acid-sarcosine weight ratio being 90:10 to 30:70 and the solution containing phenol and/or alicyclic acid lead carbonate. The flux is employed for tin/lead soldering of a range of metals and alloys including copper, nickel, nickel-cobalt- iron and nickel-iron. Biodegradation of the flux is inhibited by the inclusion of 0.001 to 1.0 weight percent of, phenol or salicylic acid 0.002-0.005 lead carbonate.

Description

SPECIFICATION Solder flux composition This invention relates to solder flux composition and in particular to flux compositions of the amino acid type for use with tin-lead type solders.
According to the invention there is provided a solder-flux composition, including sarcosine together with tartronic acid or tartaric acid, a solvent comprising water or a miscible mixture of water and one or more aliphatic alcohols, and a biologically effective proportion of an antibiodegradation agent comprising phenol or salicylic acid, or mixtures thereof, or lead carbonate, and wherein the weight ratio of acid to sarcosine is from 90:10 to 30:70.
Tartronic acid which has the structural formula
and tartaric acid which has the structural formula
rapidly remove oxide surface films from metals such as copper, nickel, nickel-iron alloys and nickel-cobalt-iron alloys. Tartronic acid decomposes on melting to form an inert compound with substantially no fluxing power.
Tartaric acid partly decomposes when melted and more so at soldering temperatures.
When these acids are used for soldering their high acidity causes rapid initial solder wetting even on aged and tarnished metal surfaces.
However the decomposition reaction results in subsequent de-wetting of the solder coat at temperatures in the region of 2300 C, i.e. at temperatures comparable with the tin-lead soldering temperature.
Sarcosine, which is an amino acid having the structural formula CH2 NH CH2 CO0H has a good fluxing activity, but initial wetting by soldering is relatively slow. The compound melts at 2080C with some decomposition or polymerisation although this does not substantially affect its fluxing action. The compound itself and its decomposition products are biodegradable and are only slightly corrosive to metals at temperatures below 700C. The flux may be employed e.g. for soldering applications on printed circuit boards.
We have found that mixtures of tartronic acid or tartaric acid and sarcosine are particularly effective as solder fluxes when used with solders of the tin-lead type. Advantageously the two compounds are employed in a solution which is applied to a metal surface which is to be soldered.
Typically the materials are dissolved in water or a miscible mixture of water and one or more aliphatic alcohols. In particular a 40:60 volume mixture of water and isopropyl alcohol may be used for this purpose when tartronic acid is used.
Less isopropyl alcohol may be used (under 30:70) with tartaric acid mixtures. The sarcosine is insoluble in isopropyl alcohol and excess alcohol addition results in partition into two immiscible liquids. Such a solution wets metal surfaces evenly thus ensuring an even coverage of flux prior to soldering.
If water is employed as the solvent a wetting agent, for example TRITON X-1 00, should be added to the solution to ensure even wetting of a metal surface, to which the solution is applied.
Advantageously the wetting agent comprises between 0.005% and 0.02% by weight of the solution, when TRITON is used.
The flux mixture must contain a sufficient proportion of sarcosine to suppress the de-wetting effect of the tartronic or tartaric acid decomposition products, this proportion varying from metal to metal. Advantageously the acidsarcosine ratio should not exceed 90:10 parts by weight and should not be less than 30:70 parts by weight. A 50:5Q mixture is suitable for most purposes.
A problem encountered with this organic flux composition is that of biodegradation by microorganisms during storage before use.
Biodegradation after use is a desirable feature. We have found that such biodegradation during storage is substantially prevented in the flux composition described herein by the addition of 0.002 to 0.005 weight percent, based on the weight of the flux of a suitable biocidal material. In particular we have found that the inclusion of lead carbonate in the flux composition strongly inhibits biodegradation, although more than 0.005% is insoluble in the flux.
In some circumstances however lead compounds are unsuitable owing to their poisonous nature, especially the danger of absorption through the skin. Where lead salts cannot be used a similar biocidal function can be provided by adding 0.001 to 1% by weight of phenol or salicylic acid or mixtures thereof to the flux composition, 0.1% being found adequate and without effect on subsequent flux residue removal.
The concentration of the solid flux in the solution must be adequate to ensure rapid solder coating of a metal surface to which the flux is applied. Clean copper is readily soldered with a 5 weight % solution, but for general purposes soldering of aged (room temperature oxidised) substrates a 10 to 20 weight % solution should be employed, and preferably 15%.
The residue remaining after soldering with the flux composition described herein is readily soluble in water. Thus, brushing the work whilst rinsing with clean water removes the residue together with any undecomposed flux. Brushing is not necessary if hot (70or) water be used, with agitation such as jetting the water or mechanically shaking the soldered components.
It is found that, particularly when employing a 50:50 mixture of tartaric acid and sarcosine, the residue remaining after hot water rinsing and a subsequent rinse in cold distilled or de-ionised water is virtually nil. Exposure to damp heat such as is specified in BS 2011 tests C or D subsequent to washing discloses no corrosive residue remaining on part soldered copper test coupons.
The flux composition may be applied to an article to be soldered, e.g. a printed circuit board, by any conventional method. In particular the flux may be applied to a circuit board as a preferably non-stable foam, the board thereafter being subjected to a flow or wave soldering process.
Following soldering the board is washed in water to remove any residual flux.

Claims (14)

1. A solder flux composition, including sarcosine together with tartronic acid or tartaric acid, a solvent comprising water or a miscible mixture of water and one or more aliphatic alcohols, and a biologically effective proportion of an antibiodegradation agent comprising phenol or salicylic acid or mixtures thereof, on lead carbonate, and wherein the weight ratio of acid to sarcosine is from 90:10 to 30:70.
2. A solder flux composition as claimed in claim 1, wherein the antibiodegradation agent comprises 0.002 to 0.005 weight percent, based on the weight of the flux, of lead carbonate.
3. A solder flux composition as claimed in claim 1, wherein the antibiodegradation agent comprises 0.01 to 1.0 weight percent of phenol or salicylic acid or mixtures thereof.
4. A flux composition as claimed in any one of claims 1 to 3, and wherein the solvent comprises a mixture of equal volumes of water and isopropyl alcohol.
5. A film composition as claimed in any one of claims 1 to 4 and in which the solution concentration is between 5 and 20 weight percent of solids.
6. A flux composition as claimed in any one of claims 1 to 5, and wherein the weight concentrations of sarcosine and acid are substantially equal.
7. A flux composition as claimed in any one of claims 1 to 6, and which includes from 0.01 to 0.1 weight percent of a wetting agent.
8. A solder flux composition substantially as hereinbefore described.
9. A method of preventing biodegradation of flux composition substantially as hereinbefore described.
10. A printed circuit board fluxed with a composition as claimed in any one of claims 1 to 8.
11. A method of soldering a printed circuit board, including applying to the board, a solder flux composition as claimed in any one of claims 1 to 8, applying a molten solder to the fluxed board, and washing the board in water to remove residual flux.
12. A method as claimed in claim 1 wherein the flux composition is applied as a non-stable foam.
13. A method of soldering substantially as described herein.
14. A printed circuit board soldered by a process as claimed in claim 1 1, 12 or 13.
GB8006718A 1979-06-19 1980-02-28 Solder flux composition Expired GB2058144B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB8006718A GB2058144B (en) 1979-06-19 1980-02-28 Solder flux composition

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB7921338A GB2051137B (en) 1979-06-19 1979-06-19 Solder flux composition
GB8006718A GB2058144B (en) 1979-06-19 1980-02-28 Solder flux composition

Publications (2)

Publication Number Publication Date
GB2058144A true GB2058144A (en) 1981-04-08
GB2058144B GB2058144B (en) 1983-05-25

Family

ID=26271897

Family Applications (1)

Application Number Title Priority Date Filing Date
GB8006718A Expired GB2058144B (en) 1979-06-19 1980-02-28 Solder flux composition

Country Status (1)

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GB (1) GB2058144B (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0710522A1 (en) * 1994-10-24 1996-05-08 Ford Motor Company Flux formulation

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0710522A1 (en) * 1994-10-24 1996-05-08 Ford Motor Company Flux formulation

Also Published As

Publication number Publication date
GB2058144B (en) 1983-05-25

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PCNP Patent ceased through non-payment of renewal fee