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GB1575811A - Lead alloys - Google Patents

Lead alloys Download PDF

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Publication number
GB1575811A
GB1575811A GB9011/76A GB901176A GB1575811A GB 1575811 A GB1575811 A GB 1575811A GB 9011/76 A GB9011/76 A GB 9011/76A GB 901176 A GB901176 A GB 901176A GB 1575811 A GB1575811 A GB 1575811A
Authority
GB
United Kingdom
Prior art keywords
tin
calcium
weight
aluminium
electrode structure
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
Application number
GB9011/76A
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.)
Chloride Group Ltd
Original Assignee
Chloride Group 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 Chloride Group Ltd filed Critical Chloride Group Ltd
Priority to GB9011/76A priority Critical patent/GB1575811A/en
Priority to SE7702395A priority patent/SE7702395L/en
Priority to NL7702309A priority patent/NL7702309A/en
Priority to US05/774,030 priority patent/US4125690A/en
Priority to FR7706279A priority patent/FR2343336A1/en
Priority to DK97577A priority patent/DK97577A/en
Priority to NZ183497A priority patent/NZ183497A/en
Priority to IN323/CAL/77A priority patent/IN147403B/en
Priority to DE19772709483 priority patent/DE2709483A1/en
Priority to ZA00771319A priority patent/ZA771319B/en
Priority to AU22955/77A priority patent/AU512823B2/en
Priority to ES77456524A priority patent/ES456524A1/en
Publication of GB1575811A publication Critical patent/GB1575811A/en
Expired legal-status Critical Current

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Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M4/64Carriers or collectors
    • H01M4/66Selection of materials
    • H01M4/68Selection of materials for use in lead-acid accumulators
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C11/00Alloys based on lead
    • C22C11/02Alloys based on lead with an alkali or an alkaline earth metal as the next major constituent
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C11/00Alloys based on lead
    • C22C11/06Alloys based on lead with tin as the next major constituent
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/10Energy storage using batteries

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Cell Electrode Carriers And Collectors (AREA)

Description

(54) LEAD ALLOYS (71) We, CHLORIDE GROUP LIMITED, a Company registered under the laws of England, of 52 Grosvenor Gardens, London SW1W OAU, do hereby declare the invention, for which we pray that a patent may be granted to us, and the method by which it is to be performed to be particularly described in and by the following statement-: The present invention relates to lead alloys for use in electric storge batteries in particular for use in the production of cast grids or other support structures for the active material of the electrodes.
The specification of British Patent No.
712798 discloses lead calcium and lead tin calcium alloys containing aluminium as an antidrossing agent. The presence of aluminium reduced the oxidation rate of the bulk of the molten metal and minimizes the loss of alloying elements.
This earlier specification discloses an alloy containing 0.08% by weight calcium, 1.5% by weight tin, 0.05% by weight aluminium and 98.37% by weight lead. It also teaches that alloys having 0.03% to 0.1% calcium, 1 % to 2% by weight tin, 0.01% to 0.1% aluminium, balance lead have superior properties.
The specification of British Patent No.
1338823 teaches the use of a lead-calcium alloy containing 0.02 to 0.1% calcium, and 0.3 to 3.0% tin the ratio of tin to calcium being in the range 150:1 to 5:1.
We have found however that at calcium contents below 0.075% the material is insufficiently hard within acceptable periods of time to be mechanically trimmed and in addition the corrosion of the alloy is greater as the tin content increases above 1%.
We have found that greatly improved results are obtained if one works with alloys having a selected combination of calcium, tin and aluminium contents.
Thus according to the present invention a lead-calcium tin alloy comprises 0.075% to 0.13% by weight calcium, preferably 0.8 to 0.10% and more preferably 0.08% to 0.09% calcium, 0.005to up to less than 1.0% by weight tin, preferably 0.005% to 0.99% by weight and more preferably 0.1% to 0.8% and especially 0.4 to 0.7% tin, aluminium in an amount of 0.0001% to 0.lWo e.g. 0.001 % to 0.1 % the balance being lead, the alloy when cast having an initial Brinell hardness measured within 15 minutes of casting of at least 7.5 and desirably at least 10.
The invention also extends to a lead calcium-tin alloy comprising 0.081% (vo to 0.099% calcium and more preferably 0.085% to 0.09% calcium, 0.35% to 0.99% tin and more preferably 0.37% to 0.8% tin and especially 0.4% to 0.7% tin, aluminium in an amount effective in the production of the alloy to diminish oxide inclusions and preferably in an amount of 0.0001% to less than 0.1%, more preferably 0.0005% to less than 0.01% aluminium, especially 0.003 to 0.009% e.g.
0.003 to 0.006% the balance being lead, the alloy preferably containing at least 98.5% lead, the alloy when cast having an initial Brinell hardness measured within 15 minutes of casting of at least 10.
Alloys of this defined composition are very suitable for casting into the shape of current conducting grids for lead acid electric storage batteries.
The invention also extends to a finished TABLE 1 Pot alloy composition Grid analysis by % weight Example Ca .. Sn Ca Sn - Al Content Content Content Content Content 1 0.08 0.4 0.06 0.4 0.003 2 0.08 0.7 0.06 0.7 0.003 3 0.095 0.4 0.075 0.4 0.003 4 0.095 0.7 0.075 0.7 0.003 5 O.11 0.4 0.09 0.4 0.006 6 0.11 0.7 0.09 0.7 0.006 shape cast product, e.g. a battery grid, or other cast structure or a thin sheet from which the grid will be produced by cool temperature mechanical shaping e.g.
punching or slitting and expanding.
Thus the invention also extends to an apertured shaped product for example a battery electrode structure such as a cast grid comprising a lead-calcium-tin alloy comprising 0.075 to 0.13% preferably 0.081% to 0.099% by weight calcium, more preferably 0.085 to 0.099% and especially 0.085% to 0.09 10 calcium, 0.005 up to 0.99%, preferably 0.35 10 up to 0.99 70 by weight tin, more preferably 0.35 70 to 0.9 70 by weight and especially 0.37% to 0.8 70 and especially 0.4 70 to 0.7% tin, and aluminium in an amount up to less than 0.01who and preferably in an amount of 0.000loo to less than 0.01%, more preferably 0.003% to 0.009% aluminium.
Another preferred composition is 0.081% to 0.095% calcium, 0.005% to 0.01% aluminium, 0.35% to 0.9% tin, balance lead.
The invention may be put into practice in various ways and a number of specific embodiments will be described to illustrate the invention with reference to the following Examples, and the drawing accompanying the provisional specifications.
Examples 1 and 2 are comparison examples.
Examples 1-6 The compositions for these examples are given in Table 1. Each alloy was made up by the addition of a solid lead, 2% calcium, 0.2% aluminium alloy to molten lead held at 375-4000C. Tin was added as the pure solid metal to the molten alloy after it had been cooled to 3500C.
The alloy was cast on a water cooled grid casting machine having an enclosed delivery system of the type conventionally used for casting 6% antimony lead grids.
The pot was held at 400"C and the metal delivery pipe at 5200C so that the metal is kept out of contact with air until it issues from the outlet orifices. The aluminium content of the pot was arranged always to be at least 0.01% by weight.
The mould face was spray coated with a thermal insulation layer of cork composition to a thickness of about 0.005 inches. Conventional automotive battery grids of the shape and size shown in the Figure were cast satisfactorily and a convenient casting rate was 11 grids per minute. The thickness of the frame 12 was 1.85 mm for the positive and 1.68 mm for the negative and the cross-sectional area of the lozenge 13 was 0.009 sq cm for the positive and 0.008 sq cm for the negative, the cross sectional area of the wires 14, being 0.014 sq cm for the positive and 0.012 sq cm for the negative.
The alloys given in Table 1 were cast at rates of between 7 and 11 castings per minute using cooling water at 4 gallons per hour and at 7 gallons per hour, and with the inlet water temperature at 25 0C or at 15"C. Analysis of the tensile strength results indicated that the use of high rates of cooling and casting with the higher calcium level of 0.09% in the grid resulted in the strongest grids.
Table 2 shows the result of age hardening tests. These were carried out on the lug 10 of the grids (see the Figure) using a 1 mm diameter ball indentor with a 1 kg load applied to it. The higher the value in Table 2 the harder is the material; a value -of at least 12 is desirable to enable the grid to be automatically trimmed and handled.
It is thus desirable that a value of 12 should be achieved as soon as possible after casting.
Table 3 shows the results of corrosion tests. These were carried out on complete battery grids which were cleaned, dried and weighed before assembly into test cells as the anode. Sheet lead cathodes were used with 1.250 specific gravity sulphuric acid as the electrolyte.
The test cells were connected in series and the grids were corroded at a constant TABLE 2 Number of days since casting 0 1 2 5 10 25 100 Calcium Tin Example content content o7o 1 0.06 0.4 6.6 6.8 6.9 7.1 7.3 9.2 10.1 2 0.06 0.7 6.7 7.3 7.7 8.5 9.5 12.6 13.6 3 0.075 0.4 7.6 8.6 9.2 10.6 12.1 13.0 14.5 4 0.075 0.7 7.7 9.4 10.3 11.8 13.0 13.9 14.8 5 0.09 0.4 10.8 12.8 13.0 13.0 13.0 14.2 14.4 6 0.09 0.7 11.1 12.5 13.3 14.0 14.4 14.8 15.9 TABLE 3 Calcium Tin Mean Range of Example Content Content Weight Range of Loss 1 0.06 0.4 3.43 3.23-3.73 2 0.06 0.7 3.17 2.96-3.44 3 0.075 0.4 3.44 3.29-3.61 4 0.075 0.7 3.33 3.08-3.45 5 0.09 0.4 3.83 3.71-3.97 6 0.09 0.7 3.82 3.40-4.11 current density of 0.84mA/sq cm of surface area exposed to the electrolyte at room temperature, 200 C, for six weeks.
The current and electrolyte specific gravity were maintained at these levels regularly throughout the test.
The grids were then washed and immersed in a stripping solution to remove the corrosion products. The stripping solution was made up of 300 g ammonium acetate, 200 g hydrazine dihydrochloride, 40 ml glacial acetic acid, and 2 litres of water.
The stripped grids were then washed, dried and weighed and the Wo weight loss calculated.
The samples were also examined microscopically. Sections of the grid were mounted and the surface ground and polished and then etched in citric acid/ammonium molybdate to show up the grain structure.
The microscopic metallographic analysis revealed that as the calcium content increases the grain size is reduced whilst as the tin content increases the grain size tends to increase.
Careful analysis of tensile strength tests indicates that whilst the tensile strength values range between 260 and 525 kg/sq cm the higher the calcium level and the more rapid the cooling of the cast grid the higher the strength tends to be. It is clear that with both the tin and the calcium being expensive ingredients, one will wish to keep their presence to the minimum value compatible with satisfactory grid properties.
Moreover at tin levels in the grid above 0.9% the resistance of the grids to corrosion as indicated both by the weight loss tests and by metallographic examination is reduced at the higher levels of calcium which it is desirable to use on the grounds of rapidity of age hardening and increased tensile strength.
A particularly preferred alloy composition comprises 0.085 to 0.099% e.g.
0.088 to 0.099% by weight calcium, 0.401 to 0.499% by weight tin, the ratio of tin to calcium being less than 5 to 1, there being 0.001 to less than 0.01, e.g. 0.002 to 0.009 70 aluminium, the balance being substantially lead.
Specific examples of such preferred alloys are given in Table 4 overleaf.
As mentioned above, the alloy of this invention can be converted into supports TABLE 4 Calcium Tin Aluminium Example Content Content Content 7 0.090 0.42 0.006 8 0.095 0.42 0.007 9 0.095 0.45 0.007 10 0.097 0.48 0.008 for the electrodes of lead acid cells either by casting in a mould defining a grid or by cold wrought procedures. When these latter procedures are to be used, the alloy may be continuously cast as a sheet and is then preferably immediately rolled to a sheet once it has solidified or it may be given additional cooling so that it is rolled at about ambient temperature. The rolling can conveniently be carried out continuously, e.g. on the output from a chilled roll continuous sheet casting machine. Thus the rolling may be carried out within less than one minute, or less than ten minutes and certainly less than one hour, from the moment the metal has solidified. This procedure has a desirable effect on the age hardening and strength properties of the alloy.
The sheet may be rolled so as to reduce its thickness by an amount of at least from an original thickness of 2 down to a rolled thickness of 1, i.e. a reduction ratio of at least 2, and preferably at least 4, e.g. in the range 2 to 20 or 4 to 10.
The rolled sheet can then be punched out to the desired shape or preferably slit in rows of short spaced apart slits and then pulled either lengthwise or preferably across the length of the strip continuously to form an expanded metal mesh, in this case the rows of slits being along the length of the strip. This expanded mesh is then used as the electrode support and may be pasted with active material in conventional manner.
WHAT WE CLAIM IS: 1. A battery electrode structure made of a lead-calcium-tin alloy comprising 0.075 to 0.13% by weight calcium, 0.005 to 0.99 70 by weight tin and 0.0001% to 0.1% by weight aluminium, the balance being substantially lead.
2. A battery electrode structure as claimed in claim 1 containing 0.08 to 0.10% calcium and 0.1% to 0.8% tin.
3. A battery electrode structure as claimed in claim 1 and claim 2 containing 0.4 to 0.7% tin.
4. A battery electrode structure as claimed in claim 1 or claim 2 or claim 3 containing 0.003 to 0.006% aluminium.
5. A battery electrode structure as claimed in claim 1 or claim 2 comprising 0.081 to 0.099% by weight calcium and 0.35 to 0.99% by weight tin and aluminium in an amount of 0.0001% up to less than 0.01% by weight, the balance being substantially lead.
6. A battery electrode structure as claimed in claim 5 containing 0.003 to 0.009% aluminium.
7. A battery electrode structure as claimed in claim 5 or claim 6 comprising 0.085% to 0.099% by weight calcium, 0.401 to 0.499% by weight tin, the ratio of tin to calcium being less than 5:1 and 0.001 to less than 0.01% aluminium, the balance being substantially lead.
8. A battery electrode structure made of an alloy as described with reference to any one of Examples 3 to 10.
**WARNING** end of DESC field may overlap start of CLMS **.

Claims (1)

  1. **WARNING** start of CLMS field may overlap end of DESC **.
    TABLE 4 Calcium Tin Aluminium Example Content Content Content
    7 0.090 0.42 0.006
    8 0.095 0.42 0.007
    9 0.095 0.45 0.007
    10 0.097 0.48 0.008 for the electrodes of lead acid cells either by casting in a mould defining a grid or by cold wrought procedures. When these latter procedures are to be used, the alloy may be continuously cast as a sheet and is then preferably immediately rolled to a sheet once it has solidified or it may be given additional cooling so that it is rolled at about ambient temperature. The rolling can conveniently be carried out continuously, e.g. on the output from a chilled roll continuous sheet casting machine. Thus the rolling may be carried out within less than one minute, or less than ten minutes and certainly less than one hour, from the moment the metal has solidified. This procedure has a desirable effect on the age hardening and strength properties of the alloy.
    The sheet may be rolled so as to reduce its thickness by an amount of at least from an original thickness of 2 down to a rolled thickness of 1, i.e. a reduction ratio of at least 2, and preferably at least 4, e.g. in the range 2 to 20 or 4 to 10.
    The rolled sheet can then be punched out to the desired shape or preferably slit in rows of short spaced apart slits and then pulled either lengthwise or preferably across the length of the strip continuously to form an expanded metal mesh, in this case the rows of slits being along the length of the strip. This expanded mesh is then used as the electrode support and may be pasted with active material in conventional manner.
    WHAT WE CLAIM IS: 1. A battery electrode structure made of a lead-calcium-tin alloy comprising 0.075 to 0.13% by weight calcium, 0.005 to 0.99 70 by weight tin and 0.0001% to 0.1% by weight aluminium, the balance being substantially lead.
    2. A battery electrode structure as claimed in claim 1 containing 0.08 to 0.10% calcium and 0.1% to 0.8% tin.
    3. A battery electrode structure as claimed in claim 1 and claim 2 containing 0.4 to 0.7% tin.
    4. A battery electrode structure as claimed in claim 1 or claim 2 or claim 3 containing 0.003 to 0.006% aluminium.
    5. A battery electrode structure as claimed in claim 1 or claim 2 comprising 0.081 to 0.099% by weight calcium and 0.35 to 0.99% by weight tin and aluminium in an amount of 0.0001% up to less than 0.01% by weight, the balance being substantially lead.
    6. A battery electrode structure as claimed in claim 5 containing 0.003 to 0.009% aluminium.
    7. A battery electrode structure as claimed in claim 5 or claim 6 comprising 0.085% to 0.099% by weight calcium, 0.401 to 0.499% by weight tin, the ratio of tin to calcium being less than 5:1 and 0.001 to less than 0.01% aluminium, the balance being substantially lead.
    8. A battery electrode structure made of an alloy as described with reference to any one of Examples 3 to 10.
GB9011/76A 1976-03-05 1976-03-05 Lead alloys Expired GB1575811A (en)

Priority Applications (12)

Application Number Priority Date Filing Date Title
GB9011/76A GB1575811A (en) 1976-03-05 1976-03-05 Lead alloys
SE7702395A SE7702395L (en) 1976-03-05 1977-03-03 LEAD ALLOYS
NL7702309A NL7702309A (en) 1976-03-05 1977-03-03 ACCUMULATOR ELECTRODE CONSTRUCTION.
US05/774,030 US4125690A (en) 1976-03-05 1977-03-03 Battery electrode structure
FR7706279A FR2343336A1 (en) 1976-03-05 1977-03-03 LEAD ALLOYS FOR ELECTRIC ACCUMULATORS
DK97577A DK97577A (en) 1976-03-05 1977-03-04 LEAD ALLOY
NZ183497A NZ183497A (en) 1976-03-05 1977-03-04 Battery electrode structure made of lead-calcium-tinlead alloy
IN323/CAL/77A IN147403B (en) 1976-03-05 1977-03-04
DE19772709483 DE2709483A1 (en) 1976-03-05 1977-03-04 LEAD ALLOY AND BATTERY ELECTRODE CARRIER FRAME INSIDE
ZA00771319A ZA771319B (en) 1976-03-05 1977-03-04 Lead alloys
AU22955/77A AU512823B2 (en) 1976-03-05 1977-03-04 Lead alloy
ES77456524A ES456524A1 (en) 1976-03-05 1977-09-21 Improvements in the manufacture of electrode structures for batteries. (Machine-translation by Google Translate, not legally binding)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB9011/76A GB1575811A (en) 1976-03-05 1976-03-05 Lead alloys

Publications (1)

Publication Number Publication Date
GB1575811A true GB1575811A (en) 1980-10-01

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GB9011/76A Expired GB1575811A (en) 1976-03-05 1976-03-05 Lead alloys

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GB (1) GB1575811A (en)
ZA (1) ZA771319B (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS58157933A (en) * 1982-03-12 1983-09-20 Furukawa Battery Co Ltd:The Lead-based alloy for lead-acid batteries
EP0959509A1 (en) * 1998-05-23 1999-11-24 VB Autobatterie GmbH Electrode grid for lead-acid battery

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS58157933A (en) * 1982-03-12 1983-09-20 Furukawa Battery Co Ltd:The Lead-based alloy for lead-acid batteries
EP0959509A1 (en) * 1998-05-23 1999-11-24 VB Autobatterie GmbH Electrode grid for lead-acid battery

Also Published As

Publication number Publication date
ZA771319B (en) 1978-10-25

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