US1807788A - Paul kemp - Google Patents

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US1807788A
US1807788A US1807788DA US1807788A US 1807788 A US1807788 A US 1807788A US 1807788D A US1807788D A US 1807788DA US 1807788 A US1807788 A US 1807788A
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antimony
tin
arsenic
lead
hardness
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    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C11/00Alloys based on lead
    • C22C11/08Alloys based on lead with antimony or bismuth as the next major constituent

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  • My invention relates to an alloy of lead and antimony and to the process of producing the same.
  • the principal object of the invention is the production of an alloy of this kind of greater than normal hardness and having an antimony content higher than was heretofore deemed permissible. I attain this object by adding suitable quantities of arsenic and tin to the lead and antimony alloy.
  • Lead and antimony alloys of greater than normal hardness are Well known.
  • the increase in hardness beyond normal is usually achieved by the following sequence of steps (a) tempering the alloy at a temperature closely below the eutectic temperature, (1)) quenching and (c) seasoning.
  • the improvement thus efi'ected is ascribable to the intermediate formation of a saturated solid solution of antimony in the lead, the saturation concentration of such solution being at approximately 2.5% of antimony.
  • any excess of antimony beyond approximately 2.5% counteracted increase of hardness of the alloy see Western Electric Company British Patent 248,458), it was customary heretofore to subject to this hardness increasing action only such-lead-antimony alloys whose antimony content did not exceed approximately 2.5%.
  • arsenic and tin are particularly eifective. Not only does the use of these substances prevent the reduction in hardness which occurs upon the tempering, quenching and seasoning of an antimony-lead alloy containing over 2.5% antimony, but surprisingly enough the presence of arsenic and tin will cause the excess of antimony to enhance the hardness of such alloy containing over 2.5% antimony and will thus greatly increase the Serial No. 396,403, and in Austria July 27, 1829.
  • arsenic and tin in the case of arsenic it extends from about 0.2 to about 2% and in the case of tin it is such that its optimum effectiveness is present when the tin content is about one-fifth that of the antimony content.
  • the antimony content itself is preferably between approximately 1% and 10%.
  • a special advantage of the use of arsenic and tin as contemplated by the present invention is that by their presence, the temperature duration as Well as the seasoning duration may be materially curtailed.
  • a leadantimony alloy of greater than normal hardness comprising a maximum of 10% antimony, from approximately 0.2% to approximately 2% arsenic and from approximately 0.1% to approximately 2% tin, the tin content being substantially one fifth of the antimony content.

Description

Patented June 2, 1931 UNITED STATES PAUL KEMP, or VIENNA, AUSTRIA .ALLOY OF LEAD AND ANTIMONY No Drawing. Application filed September 30, 1929,
My invention relates to an alloy of lead and antimony and to the process of producing the same. I
The principal object of the invention is the production of an alloy of this kind of greater than normal hardness and having an antimony content higher than was heretofore deemed permissible. I attain this object by adding suitable quantities of arsenic and tin to the lead and antimony alloy.
Lead and antimony alloys of greater than normal hardness are Well known. The increase in hardness beyond normal is usually achieved by the following sequence of steps (a) tempering the alloy at a temperature closely below the eutectic temperature, (1)) quenching and (c) seasoning. The improvement thus efi'ected is ascribable to the intermediate formation of a saturated solid solution of antimony in the lead, the saturation concentration of such solution being at approximately 2.5% of antimony. Inasmuch as any excess of antimony beyond approximately 2.5% counteracted increase of hardness of the alloy (see Western Electric Company British Patent 248,458), it was customary heretofore to subject to this hardness increasing action only such-lead-antimony alloys whose antimony content did not exceed approximately 2.5%.
By means of the present invention I am onabled to obtain improved alloys of lead and antimony in whichthe antimony content may be substantially greater than 2.5% which is at present deemed the permissible maximum. In accordance with my invention I add suitable quantities of arsenic and tin to the lead and antimony alloys, which are subjected to the usual steps of tempering, quenching and seasoning.
I find that arsenic and tin are particularly eifective. Not only does the use of these substances prevent the reduction in hardness which occurs upon the tempering, quenching and seasoning of an antimony-lead alloy containing over 2.5% antimony, but surprisingly enough the presence of arsenic and tin will cause the excess of antimony to enhance the hardness of such alloy containing over 2.5% antimony and will thus greatly increase the Serial No. 396,403, and in Austria July 27, 1829.
beneficial efl'ect. For example, with an anti-, mony content of 4.- to 8% Sb (the balance lead), in the absence of arsenic or tin the hardness decreased from the maximum of 28 Brinell when Sb content is approximately 2.5% to 25 to 20 Brinell, whilev in the presence of say 0.4% arsenic the conditions were reversed to the extent that with increasing antimony content there was a parallel increase in hardness until the latter had attained 28 to 30 Brinell.
The eifect just described is peculiar to arsenic and tin; in the case of arsenic it extends from about 0.2 to about 2% and in the case of tin it is such that its optimum effectiveness is present when the tin content is about one-fifth that of the antimony content. The antimony content itself is preferably between approximately 1% and 10%. A special advantage of the use of arsenic and tin as contemplated by the present invention is that by their presence, the temperature duration as Well as the seasoning duration may be materially curtailed.
I claim: As a new article of manufacture, a leadantimony alloy of greater than normal hardness, comprising a maximum of 10% antimony, from approximately 0.2% to approximately 2% arsenic and from approximately 0.1% to approximately 2% tin, the tin content being substantially one fifth of the antimony content.
In testimony whereof I afiix my signature.
PAUL KEMP.
US1807788D Paul kemp Expired - Lifetime US1807788A (en)

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Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2678341A (en) * 1953-11-05 1954-05-11 Electric Storage Battery Co Storage battery and grid therefor
US2791619A (en) * 1955-11-22 1957-05-07 Accumulatorenfabrik Ag Lead alloy for accumulator grid
US2821565A (en) * 1955-10-19 1958-01-28 John J Lander Battery grid and plate
US3144356A (en) * 1960-08-11 1964-08-11 Electric Storage Battery Co Battery grid alloy
US3819406A (en) * 1968-02-16 1974-06-25 Mitsui Mining & Smelting Co Hot-dip lead coating
US3923501A (en) * 1974-01-09 1975-12-02 Asarco Inc Filler solder
US4112141A (en) * 1976-05-06 1978-09-05 Nissan Motor Company, Limited Method of using filling solder for automobile body
EP0207236A2 (en) * 1985-04-11 1987-01-07 The Furukawa Electric Co., Ltd. Lead alloy foil and lead laminated tape using the foil, both designed for covering cables

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2678341A (en) * 1953-11-05 1954-05-11 Electric Storage Battery Co Storage battery and grid therefor
US2821565A (en) * 1955-10-19 1958-01-28 John J Lander Battery grid and plate
US2791619A (en) * 1955-11-22 1957-05-07 Accumulatorenfabrik Ag Lead alloy for accumulator grid
US3144356A (en) * 1960-08-11 1964-08-11 Electric Storage Battery Co Battery grid alloy
US3819406A (en) * 1968-02-16 1974-06-25 Mitsui Mining & Smelting Co Hot-dip lead coating
US3923501A (en) * 1974-01-09 1975-12-02 Asarco Inc Filler solder
US4112141A (en) * 1976-05-06 1978-09-05 Nissan Motor Company, Limited Method of using filling solder for automobile body
EP0207236A2 (en) * 1985-04-11 1987-01-07 The Furukawa Electric Co., Ltd. Lead alloy foil and lead laminated tape using the foil, both designed for covering cables
EP0207236A3 (en) * 1985-04-11 1987-01-21 The Furukawa Electric Co., Ltd. Lead alloy foil and lead laminated tape using the foil, both designed for covering cables
US4769514A (en) * 1985-04-11 1988-09-06 The Furukawa Electric Co., Ltd. Lead alloy foil for laminated tape

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