US1722358A - Alloy and method of making alloys - Google Patents

Alloy and method of making alloys Download PDF

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US1722358A
US1722358A US203722A US20372227A US1722358A US 1722358 A US1722358 A US 1722358A US 203722 A US203722 A US 203722A US 20372227 A US20372227 A US 20372227A US 1722358 A US1722358 A US 1722358A
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antimony
lead
alloy
arsenic
alloys
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Seljesaeter Kaare Svaar
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AT&T Corp
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Western Electric Co Inc
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    • 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
    • H01M4/685Lead alloys
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22FCHANGING THE PHYSICAL STRUCTURE OF NON-FERROUS METALS AND NON-FERROUS ALLOYS
    • C22F1/00Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working
    • C22F1/12Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working of lead or alloys based thereon
    • 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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  • This invention relates generally to alloys and methods of making alloys, and more particularly to improved ternaryl alloys having lead and antimony as their principal constituents and methods of making such alloys.
  • Objects vof the invention are to provide improved alloys containing lead and antimony and having increased hardness and tensile strength as compared with pure lead or b1- nary alloys of lead and antimony, and to provide an improved method of making such alloys.
  • antimony and a small amount oi anothei' material such as arsenic, are alloyed with lead and the alloy allowed to solidify.
  • Fig. 1 is a graph showing the relationship between the Brinell hardness of a 'ternary alloy produced in accordance with the invention after being age-hardened at Q5 to 300 C. for various periods of time and the llrinell hardness of a binary alloy of lead and antimony age-hardened under like conditions
  • Fig. 2 is a similar graph illustrating a like relationship between the same alloys agehardened for various periods at 48 to 50O C.;
  • lTig. 3 is a graph showing the Brinell hardness of a ternary alloy of another composition age-hardened at to 30 C. for various periods, and
  • Fig. 4 is a graph similar to that shown in llig. l showing a like relationship between still vanother ternary alloy and another binary alloy age-hardened at 25 to 300 C.
  • lead, antimony and arsenic are melted together in the proportions of not more than 21/2% antimony, not more than 1% arsenic, and the iemainder lead, and the resulting alloy is allowed to solidify.
  • the alloy is then heated at a temperature of approximately 240 C. for a period of time sufficient to cause the antimony to form a homogeneous solid solution in the lead.
  • the material is then quenched or suddenly cooled F or lead-antimony alloys, theto room temperature to produce a supersaturated solid solution of the antimony in the lead, and the alloy is then aged at a temperature below 100 C. in order to permit the alloy to assume a substantially stable condition.
  • Fig. 1 of the drawing the curve A indicates the variation in Brinell hardness of a ternary alloy comprising 2% antimony, .05% arsenic, and the remainder lead, which has been subjected to the heating and quencing steps outlined above, with variation intime of. aging, at a temperature of 25 to 30 C.
  • curve B indicates the variation in Brinell hardness of a binary alloy containing 2% antimony and the remainder lead, which has been subjected to a similar treatment, with variation in time of aging at the same temperature.
  • Fig. 1 of the drawing the curve A indicates the variation in Brinell hardness of a ternary alloy comprising 2% antimony, .05% arsenic, and the remainder lead, which has been subjected to the heating and quencing steps outlined above, with variation intime of. aging, at a temperature of 25 to 30 C.
  • curve B indicates the variation in Brinell hardness of a binary alloy containing 2% antimony and the remainder lead, which has been subjected to
  • the curve C indicates the variation in Brinell hardness of the same alloy as indicated in curve A with time of aging at a temperature of 48 to 50 C.
  • curve D indicates the Brinell hardness of the alloy indicated in curve B when subjected to the same treatment as the alloy indicated in curve C.
  • the curve E in Fig. 3 indicates variations in Brinell hardness of a ternary alloy containing 2% antimony, 1% arsenate, and the remainder lead with time of age-hardening at a temperature of 25 to 30 C. after having been heated and quenched as described above.
  • curves F and G show the relationship between the Brinell hardness of a ternary alloy comprising 1% antimony, .15% arsenic, and the remainder lead, and a binary alloy composed of 1% antimony and the remainder lead when subjected to a similar heating and quenching treatment and age-hardened at a temperature of 25 to 30 C.
  • the improved properties of the alloy are believed to be due primarily to the presence of nely divided, dispersed particles of antimony in a matrix of lead.
  • the improvements resulting from employing the above outlined treatment upon ternary alloys of the class described seem to result from the fact that the antimony which Aseparates out in finely dividf ed particles throughout the lead when the supersaturated solution of antimony in lead is aged is prevented by the third ingredient which is present. from agglomerating or forming large particles and thereby rendering the material unsatisfactory.
  • the resulting product consists of a matrix of lead throughout which finely divided .particles which separate out from the supersaturated'soluton produced by the quenching step arenwidely dispersed and throughout which matrix are also dispersed larger particles of antimony or antimony combined with the third ingredient.
  • a material of the type produced by practicing this invention is especially useful in the production of articles which are usually made of lead or lead alloys and in which increased hardness and tensile strength are desirable.
  • articles which are usually made of lead or lead alloys and in which increased hardness and tensile strength are desirable.
  • articles are battery ⁇ grids, bearings and sheaths for electrical cables. Since a desirable metal for use in bearings is one in which there is a hard ingredient dispersed throughout a matrix of a softer ⁇ material, it is evident that alloys of the type produced by practicing this invention which comprise a matrix of lead throughout which the antimony and the third ingredient are dispersed are especially applicable to the manufacture of bearings.
  • lhat is claimed is: l.
  • Aprocess for making an improved ternaryl alloy which consists in alloylng with a cor'istituent thereof a constituent which has a varying solid solubility in said constituent and another constituent which is substantialternary alloy, which consists in alloying with lead and antimony a small amount of another material which is substantially in soluble in lead and which combines with antimony, forming the resultingv alloy into a substantially homogeneous solid solution, reducing the alloy to a super-saturated solid solution, and aging the alloy.
  • a process for making an improved ter- -nary lead-antimony containing alloy which consistsin alloying therewith a small amount of a third ingredient which is soluble in antimony and'substantially insoluble'in lead, reducing the resultingalloy to a supersaturated solid solution, and allowing the'alloy to assume a more stable state.
  • a process for making an improved ternary alloy which consists'in alloying with lead not more than 4% antimony and a small amount of another material which is soluble in antimony and substantially insoluble in lead, reducing the resulting alloy to a supersaturated solid solution, and allowing the alloyto assume a more stable state.
  • a process for making an improved ternary alloy which consists in alloyingwith lead antimony and not more than 1% of an- ⁇ other lmaterial which is soluble in antimony and substantially insoluble in'lead, reducing the resulting alloy to a supersaturated solid -solution, and allowing the alloy to assume 'a more stable state.
  • a process for making an improved ternary alloy which consists.. in alloying with lead not more than 2.5% antimony and not more than 14% of' another material which is solublin antimony and substantially insoluble in lead, reducing the resulting alloy to a supersaturated solid solution, and allowing the alloy to assume a more stable state.
  • a process for making an improved ternary lead-antimony alloy which consists in alloying a small amount of arsenic therewith, reducing-the resulting alloy to a supersaturated solid solution, said solution containing the major portion of the antimony and substantially all of the arsenic, and allowing the alloy to assume a more stable state.
  • a process for making an improved .ternary alloy which consists 'in alloying not more than 4% antimony and a small amount of arsenic with lead, reducing the resulting alloy to a supersaturated solid solution, said solution containing the major portion of the antimony and substantially all of the arsenic, and allowing the alloy to asusme a more stable state.
  • An improved'ternary allo)v comprising lead ⁇ antimony and a small amount ot a third nulterial which is substantially insoluble in lead and which combines with antimony, and characterized by the presence of minute particles of the antimony and the third ingredient dispersed substantailly uniformly throughout the lead.
  • An improved ternary alloy comprising lead. antimony and a third ingredient in which minute particles ot' the antimony and the third ingredient are dispersed substantially uniform throughout the lead.
  • An improved ternary alloy comprising lead. antin'iony anda small amountoi" a third material chararterized by the presence of minute particles of the antimony and the third ingredient Idispersed substantially uniformly throughoutthe lead.
  • lo. .- ⁇ n improved ternary alloy comprising not more, than 2.5% antimony, a. small amount of another material and the remainder lead, and characterized by the presence ot the minute particles of the antimony and the third ingredient dispersed substantially uniformly throughout the lead.
  • An limproved ternary alloy comprising lead, antixnony and not more than 1% of another material, and characterized by the presence of the minute particles of the antimony and the third ingredient dispersed substantiallyl uniformly throughout the lead.
  • An improved ternary alloy comprising not more than 4% antimony, not more than 1% of another material, and the remainder lead, and characterized by the presence of the minute particles of the antimony and lthe third ingredient dispersed substantially'uniformly throughoutthe lead.
  • An improved ternary alloy comprising lead .ant.in1on v and a small amount of arsenic, characterized by the presence of minute particles of antimony and arsenic dispersed substantially uniformly throughout the lead.
  • An improved terna-ry alloy comprising not. more than 4% antimony, a smallpamount ot' arsenic, and the remainder lead, and'characterized by the presence of minute particles of ant-imony and arsenic dispersed substantially uniformly throughout the lead.
  • a process for improving the properties of a ternary alloy composed of not more than 4% antimo'ny, not more than 1% arsenic and the remainder lead which consists in forming the alloy into a substantially homogeneous solid solution, quenching the alloy to produce a super-saturated solid solution, and aging the alloy to cause the separation f minute particles of antimony and arsenic substantially uniformly throughout the lead.
  • An in'iproved ternary alloy comprising not more than 2.5% ant-imony, not more than 1% arsenic, and the. remainder lead.
  • An improved ternary alloy comprising not more. than 4% antimony, not more than 1% arsenic, and the remainder lead.

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Description

Patented July 30, 19,29.
.uNiTED STATES PATENT oFFicE.
MARE SVAAR SELJESAETER, OF CHICAGO, ILLINOIS, ASSIGNOR T WESTERN ELEC- TRIO COMPANY, INCORPORATED, OF NEW YORK, N'. Y., A CORPORATION 0F NEW YORK.
Application led July 6,
This invention relates generally to alloys and methods of making alloys, and more particularly to improved ternaryl alloys having lead and antimony as their principal constituents and methods of making such alloys.
Objects vof the invention are to provide improved alloys containing lead and antimony and having increased hardness and tensile strength as compared with pure lead or b1- nary alloys of lead and antimony, and to provide an improved method of making such alloys. n
` In accomplishing the objects of the invention, antimony and a small amount oi anothei' material, such as arsenic, are alloyed with lead and the alloy allowed to solidify., The
solidified material is then treated in a manner similar to that described in Patents Nos.
1,674,954 and 1,674,958, issued J une 26, 1928 2O to R. S. Dean and W. E. Hudson, for treating binary alloys. Briefly stated, the treatment consists in heating the alloy to producea saturated solid solution of the antimony in the lead (quenching the alloy to produce a supersaturatedsolid solution, and then aging the allo @ther features and objects of the invention will be apparent from the following detailed description taken in connectionwith the attached drawing and will be particularly indi-- cated in the appended claims.
lin the drawing,
Fig. 1 is a graph showing the relationship between the Brinell hardness of a 'ternary alloy produced in accordance with the invention after being age-hardened at Q5 to 300 C. for various periods of time and the llrinell hardness of a binary alloy of lead and antimony age-hardened under like conditions Fig. 2 is a similar graph illustrating a like relationship between the same alloys agehardened for various periods at 48 to 50O C.;
lTig. 3 is a graph showing the Brinell hardness of a ternary alloy of another composition age-hardened at to 30 C. for various periods, and
Fig. 4 is a graph similar to that shown in llig. l showing a like relationship between still vanother ternary alloy and another binary alloy age-hardened at 25 to 300 C.
rlhe aforementioned patents disclose a method whereby binary alloys composed of' materials, such as lead and antimony, one of ALLOY AND METHOD .OF MAKING ALLOYS.
i927.' serial No. 203,722.
which has a solid solubility in the other which varies with temperature, may be treated to produce improvements, such as increased hardness and tensile strength, in such alloys. Alloys so treated not only have properties superior to those of pure lead but also superior to similar alloys which had not been subjected to the treatment outlined therein. Those patents?? also disclose the fact that the optimum percentage of the material alloyed with the major ingredient in order to produce improvement in the binary alloy is the ina-X- imum amount which will form a solid solution with the major constituent at any temperature. maximum percentage ofantimony soluble in solid lead is approximately 2.5%.
Experiments have shown that if a small amount of a third ingredient which. is substantially insoluble in lead, but which combines with antimony, is alloyed with a binary lead-antimony alloy of the type disclosed in the aforementioned application and the resulting ternary alloy is subjected to a treatment consisting of heating, quenching and aging, the resulting alloy will have enhanced properties superior to those of similar binary alloys. Among the materials which have been found to have the above described characteristics and to produce a noticeable improvement when alloyed with lead and antimony and subjected to proper treatment are cadmium, sulphur, arsenic, tellurium, thalliuui and bismuth. ln order to enable a person skilled in the art to practice the invention, the process embodying the invention will be described as employed with ternary alloys consisting of lead, antimony and arsenic. llt is to be understood, oi' course, that the invention may bepracticed with alloys containing lead, antimony and another material, such as one of those listed above, and satisfactory results be obtained.
ln practicing the invention, in one specific embodiment thereof, lead, antimony and arsenic are melted together in the proportions of not more than 21/2% antimony, not more than 1% arsenic, and the iemainder lead, and the resulting alloy is allowed to solidify. The alloy is then heated at a temperature of approximately 240 C. for a period of time sufficient to cause the antimony to form a homogeneous solid solution in the lead. The material is then quenched or suddenly cooled F or lead-antimony alloys, theto room temperature to produce a supersaturated solid solution of the antimony in the lead, and the alloy is then aged at a temperature below 100 C. in order to permit the alloy to assume a substantially stable condition.
The beneficial results obtained by makin lead-antimony-arsenic alloys of the above described constituents and subjecting them to the above outlined treatment are apparent from the graphs shown in the accompanying drawing. In Fig. 1 of the drawing, the curve A indicates the variation in Brinell hardness of a ternary alloy comprising 2% antimony, .05% arsenic, and the remainder lead, which has been subjected to the heating and quencing steps outlined above, with variation intime of. aging, at a temperature of 25 to 30 C., While curve B indicates the variation in Brinell hardness of a binary alloy containing 2% antimony and the remainder lead, which has been subjected to a similar treatment, with variation in time of aging at the same temperature. In Fig. 2 the curve C indicates the variation in Brinell hardness of the same alloy as indicated in curve A with time of aging at a temperature of 48 to 50 C., While curve D indicates the Brinell hardness of the alloy indicated in curve B when subjected to the same treatment as the alloy indicated in curve C. The curve E in Fig. 3 indicates variations in Brinell hardness of a ternary alloy containing 2% antimony, 1% arsenate, and the remainder lead with time of age-hardening at a temperature of 25 to 30 C. after having been heated and quenched as described above. lIn Fig. 4, curves F and G show the relationship between the Brinell hardness of a ternary alloy comprising 1% antimony, .15% arsenic, and the remainder lead, and a binary alloy composed of 1% antimony and the remainder lead when subjected to a similar heating and quenching treatment and age-hardened at a temperature of 25 to 30 C.
An examination of the above described curves Will show that in every instance a tenary alloy containing a small amount of arsenic has superior hardness to a similar alloy in which the arsenic is absent and when the age-hardening step is carried out at a suiiiciently low temperature. For example, after aging for thirty days at 25 to 30 C. an alloy containing 2% antimony and .05% arsenic had a Brinell hardness of approximately 24, while an alloy containing2% antimony and no arsenic which had aged at the same temperature for thirty days had a Brinell hardness of approximately 17. The hardness curves for the other alloys illustnated show similar results. It has been found by experiments, however, that when the aging ste is performed at a temperature above 100 substantially no beneficial results are obtained and consequently the aging at a temperature g in hardness and tensile strength result when materials other than arsenic, such as those listed hereinbefore, are alloyed with lead and antimony.
The improved properties of the alloy are believed to be due primarily to the presence of nely divided, dispersed particles of antimony in a matrix of lead. The improvements resulting from employing the above outlined treatment upon ternary alloys of the class described seem to result from the fact that the antimony which Aseparates out in finely dividf ed particles throughout the lead when the supersaturated solution of antimony in lead is aged is prevented by the third ingredient which is present. from agglomerating or forming large particles and thereby rendering the material unsatisfactory. It is believed that the explanation of this phenomenon lies in the fact that the third ingredient alloyed with the lead and antimony vis practically insoluble or only slightly soluble in solid lead While it combines with the antimony to form either a true solid solution or else a compound there- C. Experiments indicate l with. When a supersaturated solution of f antimony in lead is permitted to age, the antimony tends to slowly separate out of the lead in minute particles and the third constituent, Which is dispersed throughout the lead since it is insoluble therein, either by forming a protective film around the finely divided, Widely dispersed particles of antimony, or by some other means, prevents agglomerationof the antimony particles.
It has also been found by experiment that enhanced properties result when percentages of antimony greater than 2.5%, the maximum percentage which enters solid solution in lead. are employed and that an improvement resuits when a third constituent of the type described above is alloyed with a lead-antimony7 alloy of any composition up to 4% antimony. It is believed that when alloys containing more than 2.5% antimony are heated at a temperature'of approximately 240 C. only 2.5% of the antimony enters solid solution in the lead and the remainder of the antimony is present in the form of dispersed particles. lVhen this material is quenched and aged, the small antimony particles which separate out of the resulting' supersaturated solid solution are prevented, as in the case of alloys containing 2.5% antimony or less, by the third ingredient from agglomerating with the undissolved dispersed particles and with each other to form large particles. It seems then that in lead alloys containing from 2.5 to 4% antimony and a small amount of a third ingredient which is substantially insoluble in lead,
but which combines withA antimony, which have. been heated, quenched and aged in the manner outlined above the resulting product consists of a matrix of lead throughout which finely divided .particles which separate out from the supersaturated'soluton produced by the quenching step arenwidely dispersed and throughout which matrix are also dispersed larger particles of antimony or antimony combined with the third ingredient.
Experiments conducted upon alloys of compositions other than those hereinbefore described showed an alloy containing approximately 2.5% antimony, about .13% arsenic and the remainder lead, after heat treatment and aging, to haveA a Brincll lhardness of 27,
'while a binary lead alloy containing approximately-2.5% antimony and no arsenic had a Brinell hardness of 21.6. Also an alloy comprising approximately 4% antimony, about .12% arsenic and the remainder lead after being subjected to the above described treatment exhibited a Brinell hardness of 29, while a` lead alloy containing approximately 4% antimony and no arsenic exhibited auBrinell hardness of 21.6. One 4% antimony alloy containing a small amount of arsenic had a Brinell hardness of 33.5. Experiments also show that no appreciable improvements result when more than 1% of the third ingredient is alloyed with lead and antimony alloys of any composition up to.4^% antimony and consequently the use of more than 1% of the -third ingredient is unnecessary in order to obtain the desired results.
A material of the type produced by practicing this invention is especially useful in the production of articles which are usually made of lead or lead alloys and in which increased hardness and tensile strength are desirable. Among such articles are battery` grids, bearings and sheaths for electrical cables. Since a desirable metal for use in bearings is one in which there is a hard ingredient dispersed throughout a matrix of a softer` material, it is evident that alloys of the type produced by practicing this invention which comprise a matrix of lead throughout which the antimony and the third ingredient are dispersed are especially applicable to the manufacture of bearings.
lhat is claimed is: l. A process for improving the properties of an alloy composed of a plurality of con- -stituents with which is alloyed another constituent which is substantially insoluble in one of the first mentioned constituents and Y which combines with another one ofsaid constituents, consisting in reducing the alloy to a super-saturated'solid solution, and causing the alloy to-assume a more stable state.
2. Aprocess for making an improved ternaryl alloy, which consists in alloylng with a cor'istituent thereof a constituent which has a varying solid solubility in said constituent and another constituent which is substantialternary alloy, which consists in alloying with lead and antimony a small amount of another material which is substantially in soluble in lead and which combines with antimony, forming the resultingv alloy into a substantially homogeneous solid solution, reducing the alloy to a super-saturated solid solution, and aging the alloy.
4. A process for making an improved ter- -nary lead-antimony containing alloy, which consistsin alloying therewith a small amount of a third ingredient which is soluble in antimony and'substantially insoluble'in lead, reducing the resultingalloy to a supersaturated solid solution, and allowing the'alloy to assume a more stable state.
5. A process for making an improved ternary alloy, which consists'in alloying with lead not more than 4% antimony and a small amount of another material which is soluble in antimony and substantially insoluble in lead, reducing the resulting alloy to a supersaturated solid solution, and allowing the alloyto assume a more stable state.
6. A process for making an improved ternary alloy, which consists in alloyingwith lead antimony and not more than 1% of an-` other lmaterial which is soluble in antimony and substantially insoluble in'lead, reducing the resulting alloy to a supersaturated solid -solution, and allowing the alloy to assume 'a more stable state.
7. A process for making an improved ternary alloy, which consists.. in alloying with lead not more than 2.5% antimony and not more than 14% of' another material which is solublin antimony and substantially insoluble in lead, reducing the resulting alloy to a supersaturated solid solution, and allowing the alloy to assume a more stable state.
8. A process for making an improved ternary lead-antimony alloy, which consists in alloying a small amount of arsenic therewith, reducing-the resulting alloy to a supersaturated solid solution, said solution containing the major portion of the antimony and substantially all of the arsenic, and allowing the alloy to assume a more stable state.
9. A process for making an improved .ternary alloy, which consists 'in alloying not more than 4% antimony and a small amount of arsenic with lead, reducing the resulting alloy to a supersaturated solid solution, said solution containing the major portion of the antimony and substantially all of the arsenic, and allowing the alloy to asusme a more stable state.
lll
solution is formed, said solution Containing the major portion ot the antimony and substantially all ofthe arsenic," quenching 'the alloy. and aging.v
1:2. A. process for making an improved ternary alloy` which consists in alloying not more than 4% antimony and not more than lft ot' arsenic with lead. reducing the resulting alloy to a supersaturatcd solid solution,
and allowing the alloy to assume a more stable state.
13. An improved'ternary allo)v comprising lead` antimony and a small amount ot a third nulterial which is substantially insoluble in lead and which combines with antimony, and characterized by the presence of minute particles of the antimony and the third ingredient dispersed substantailly uniformly throughout the lead.
14. An improved ternary alloy comprising lead. antimony and a third ingredient in which minute particles ot' the antimony and the third ingredient are dispersed substantially uniform throughout the lead.
15. An improved ternary alloy comprising lead. antin'iony anda small amountoi" a third material chararterized by the presence of minute particles of the antimony and the third ingredient Idispersed substantially uniformly throughoutthe lead.
lo. .-\n improved ternary alloy comprising not more, than 2.5% antimony, a. small amount of another material and the remainder lead, and characterized by the presence ot the minute particles of the antimony and the third ingredient dispersed substantially uniformly throughout the lead.
17. An limproved ternary alloy comprising lead, antixnony and not more than 1% of another material, and characterized by the presence of the minute particles of the antimony and the third ingredient dispersed substantiallyl uniformly throughout the lead.
18. An improved ternary alloy comprising not more than 4% antimony, not more than 1% of another material, and the remainder lead, and characterized by the presence of the minute particles of the antimony and lthe third ingredient dispersed substantially'uniformly throughoutthe lead.
19.' An improved ternary alloy comprising lead .ant.in1on v and a small amount of arsenic, characterized by the presence of minute particles of antimony and arsenic dispersed substantially uniformly throughout the lead.
20. An improved terna-ry alloy comprising not. more than 4% antimony, a smallpamount ot' arsenic, and the remainder lead, and'characterized by the presence of minute particles of ant-imony and arsenic dispersed substantially uniformly throughout the lead.
21. A process for improving the properties of a ternary alloy composed of not more than 4% antimo'ny, not more than 1% arsenic and the remainder lead, which consists in forming the alloy into a substantially homogeneous solid solution, quenching the alloy to produce a super-saturated solid solution, and aging the alloy to cause the separation f minute particles of antimony and arsenic substantially uniformly throughout the lead.
22. A process for improving the properties ot` a ternary alloyrl composed of not more than 2.5% antin1on \f,notmore than 1% arsenic and the remainder lead, which consists in reducin g the alloy to a super-saturated solid solut ion. and -ausing the alloy to assume a more stable state.
23. An in'iproved ternary alloy comprising not more than 2.5% ant-imony, not more than 1% arsenic, and the. remainder lead.
24. An improved ternary alloy comprising not more. than 4% antimony, not more than 1% arsenic, and the remainder lead.
Inwitness whereof, I hereunto subscribe my name this 23d dav of June A. D., 1927.
KAARE SVAR SELJESAETER.
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Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE747964C (en) * 1939-05-13 1944-10-23 Comp Generale Electricite Production of electrode grids for lead collectors with improved module breaking load / unit elongation
US2588095A (en) * 1949-12-24 1952-03-04 Gen Electric Lead cable sheath alloy
US2678341A (en) * 1953-11-05 1954-05-11 Electric Storage Battery Co Storage battery and grid therefor
US2695845A (en) * 1950-02-15 1954-11-30 American Smelting Refining Antimonial lead alloys
US2715151A (en) * 1953-07-14 1955-08-09 Electro Acid Corp Electric storage battery and method
US3859084A (en) * 1971-09-30 1975-01-07 Gould Inc Cadmium-antimony-lead alloy
US3888703A (en) * 1974-05-22 1975-06-10 Us Interior Method of producing creep resistance of pb-sb alloys
US5464487A (en) * 1993-10-26 1995-11-07 Bull-X, Inc. Method of making a hardened bullet

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE747964C (en) * 1939-05-13 1944-10-23 Comp Generale Electricite Production of electrode grids for lead collectors with improved module breaking load / unit elongation
US2588095A (en) * 1949-12-24 1952-03-04 Gen Electric Lead cable sheath alloy
US2695845A (en) * 1950-02-15 1954-11-30 American Smelting Refining Antimonial lead alloys
US2715151A (en) * 1953-07-14 1955-08-09 Electro Acid Corp Electric storage battery and method
US2678341A (en) * 1953-11-05 1954-05-11 Electric Storage Battery Co Storage battery and grid therefor
US3859084A (en) * 1971-09-30 1975-01-07 Gould Inc Cadmium-antimony-lead alloy
US3888703A (en) * 1974-05-22 1975-06-10 Us Interior Method of producing creep resistance of pb-sb alloys
US5464487A (en) * 1993-10-26 1995-11-07 Bull-X, Inc. Method of making a hardened bullet

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