US3189989A - Dispersion hardening of lead - Google Patents

Dispersion hardening of lead Download PDF

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US3189989A
US3189989A US281754A US28175463A US3189989A US 3189989 A US3189989 A US 3189989A US 281754 A US281754 A US 281754A US 28175463 A US28175463 A US 28175463A US 3189989 A US3189989 A US 3189989A
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lead
metal
particles
extruded
dispersion
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US281754A
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Ebdon Denis Keith
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Associated Electrical Industries Ltd
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Associated Electrical Industries Ltd
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    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C32/00Non-ferrous alloys containing at least 5% by weight but less than 50% by weight of oxides, carbides, borides, nitrides, silicides or other metal compounds, e.g. oxynitrides, sulfides, whether added as such or formed in situ
    • C22C32/001Non-ferrous alloys containing at least 5% by weight but less than 50% by weight of oxides, carbides, borides, nitrides, silicides or other metal compounds, e.g. oxynitrides, sulfides, whether added as such or formed in situ with only oxides
    • C22C32/0015Non-ferrous alloys containing at least 5% by weight but less than 50% by weight of oxides, carbides, borides, nitrides, silicides or other metal compounds, e.g. oxynitrides, sulfides, whether added as such or formed in situ with only oxides with only single oxides as main non-metallic constituents
    • C22C32/0042Matrix based on low melting metals, Pb, Sn, In, Zn, Cd or alloys thereof

Definitions

  • This invention is concerned with the manufacture of lead sheeting, and extruded lead sections, and is particularly concerned with a method of producing a sheet material consisting of lead or lead alloy which has been specially strengthened for certain industrial purposes.
  • Dispersion-hardened metal particles of hard material which are inert to the matrix are well dispersed throughout the body of the metal. Dispersion-hardened metal objects are therefore commonly made by powder metallurgy techniques according to which a uniform mixture of the powdered metal and hardening component in appropriate proportions are compacted to the required shape and then sintered.
  • the hardening component may be in the form of the oxide of the same or another metal and is very finely divided, the size range being typically from 0.1 to microns.
  • the oxide films and fragments are further broken up and dispersed throughout the metal and further recrystallisation of the metal occurs with the fragments of oxide located within and between the metal crystals.
  • recrystallisation has occurred is evidenced by the 3,139,989 Patented June 22, 1965 ICC ductility of the rolled sheet.
  • the oxide fragments being situated inside the leadcrystals and in the grain boundaries, inhibit slip thus increasing the tensile strength, creep strength and hardness of the metal, and its resistance to gram growth.
  • the rigidity of the dispersion-hardened lead is increased and an increase of tensile strength up to two-to-three times that of normal lead can be obtained.
  • Grain growth can be described in general terms as follows:
  • a body of metal may be regarded as being composed of grains (i.e. crystals) very strongly bonded together, and it is generally accepted that the grain boundary regions are stronger than the grains themselves. Neglecting the influence of other factors such as Work hardening etc., the hardness and strength of a metal will depend upon the grain size. The larger the grain size the softer and weaker the metal and conversely. Thus, when the temperature of a piece of metal is raised sufficiently high it commonly happens that the metal grains coalesce (i.e. grain growth occurs) so that, after cooling, the said piece of metal is composed of a smaller number of larger grains and is accordingly softer and weaker than it was before. Most metals have to be heated to well above room temperature to cause grain growth; 250 C. for copper for example and 400-450 C. for iron. In the case of ordinary lead, however, grain growth occurs at room temperature.
  • dispersion-strengthened lead the dispersed particles and, in particular, those particles located at or near the grain boundaries, prevent grain boundary movement and thus inhibit grain growth.
  • the preferred size range of the initial lead particles is determined by such considerations as thickness of oxide, packing density of the particles and the. final grain size required, but the range would normally be from 1 to microns.
  • the method is not necessarily limited to pure lead particles, but may be applied to lead alloy particles. Particles of lead containing, for instance, 1% tin to improve the corrosion resistance of the finished product, might be used.
  • Example I Lead powder with a maximum particle size of about 104 microns was taken as received, with its natural lead oxide coating, and compacted into a 2 inches diameter billet. This was extruded to a cross-section of 1 /2 inches x 0.375 inch at room temperature (about 20 C.) and the resultant strip was then rolled firstly in the direction of the extrusion to reduce the 0.375 inch dimension to 0.175 inch, and then crosswise to reduce this dimension to 0.075 inch. The tensile strength of pieces of lead so prepared was found to be between 3220 and 3360 pounds per square inch, namely approaching twice that of ordinary lead (18002000 pounds per square inch).
  • Example 11 Lead powder with a maximum particle size of about a 53 microns, again taken as received with its natural lead oxide coating, was compacted and extruded as in Example I and then rolled lengthwise and crosswise to reduce the 0.375 inch dimension to 0.005 inch.
  • the tensile strength of pieces of lead so prepared from this finer powder was found to be in the region of 5700 pounds per square inch. This is about three times the strength of ordinary lead.
  • Example III A specimen of ordinary cast pure lead was extruded and found to have a coarse grain size of less than 1 grain per square inch at 500 diameters magnification.
  • a sample of lead made by extruding and rolling lead powder as in Example I was found to have a grain size of about 200 grains per square inch at 500 diameters magnification in the well crystallised skin.
  • a specimen of the latter material when heated to 200 C. for half an hour was found still to have a grain size of about 200 grains per square inch at 500 diameters magnification, that is the grain growth was negligible.
  • a method of producing strengthened lead which comprises extruding lead oxide coated lead particles through a die and then rolling the extruded lead along and across the direction of extrusion.
  • a method of producing strengthened lead which comprises compacting lead oxide coated lead particles into a billet, extruding this billet into a thin sheet, then rolling the sheet lengthwise and crosswise relative to the direction of extrusion.

Description

United States Patent 3,139,989 DISPERSION HARDENING F LEAD Denis Keith Ebdon, Harlow, Essex, England, assignor to Associated Electrical Industries Limited, London, England, a British company No Drawing. Filed May 20, 196B, Ser. No. 281,754
3 Claims. (Cl. 29-4205) This application is a continuation-in-part of my patent application Serial No. 71,410 filed November 25, 1960, and now US. Patent 3,098,293.
This invention is concerned with the manufacture of lead sheeting, and extruded lead sections, and is particularly concerned with a method of producing a sheet material consisting of lead or lead alloy which has been specially strengthened for certain industrial purposes.
The rather low tensile strength and softness of unalloyed lead often present major difliculties in the use of lead for constructional purposes, e.g. in the construction of accumulators. Some method of strengthening the metal is therefore desirable, and a method based on the technique called dispersion-hardening has been found to give the desired result.
In a dispersion-hardened metal, particles of hard material which are inert to the matrix are well dispersed throughout the body of the metal. Dispersion-hardened metal objects are therefore commonly made by powder metallurgy techniques according to which a uniform mixture of the powdered metal and hardening component in appropriate proportions are compacted to the required shape and then sintered. The hardening component may be in the form of the oxide of the same or another metal and is very finely divided, the size range being typically from 0.1 to microns. However conventional powder metallurgy methods are not suitable for dispersion-hardening of lead, principally because the natural oxide film with which lead particles are normally covered is not broken down during the normal compacting process, and there is therefore no metal-to-metal con-tact to permit the particles to be sintered. Sintering in a reducing atmosphere will not effectively remove the oxide coating from the surfaces of the particles.
As a result of experiments in the cold working of lead, it has been found that by cold extrusion of lead oxide coated lead particles through a die of circular or other cross-section and followed by rolling the extruded lead along and across the direction of extrusion, a polycrustalline piece of lead can be obtained with the lead oxide distributed uniformly throughout it-the lead being thus dispersion-hardened The process of extrusion breaks up the oxide film on some of the particles into fragments which become embedded in the lead particles. The lead particles then bond to each other and recrystallise as a result of the deformation to which they are subjected. If a crosssection through a piece of lead extruded in the manner described above is examined under a microscope, it will be seen that the oxide films on the original particles have been most effectively broken up near the surface of the extruded piece, i.e. in the region subjected to the greatest deformation whilst the lead was being forced through the die. Towards the centre of the extruded piece the break up of the oxide films into discrete fragments becomes progressively less pronounced until finally no break up can be seen.
When the extruded piece is rolled down to a thin sheet the oxide films and fragments are further broken up and dispersed throughout the metal and further recrystallisation of the metal occurs with the fragments of oxide located within and between the metal crystals. The fact that recrystallisation has occurred is evidenced by the 3,139,989 Patented June 22, 1965 ICC ductility of the rolled sheet. The oxide fragments, being situated inside the leadcrystals and in the grain boundaries, inhibit slip thus increasing the tensile strength, creep strength and hardness of the metal, and its resistance to gram growth. The rigidity of the dispersion-hardened lead is increased and an increase of tensile strength up to two-to-three times that of normal lead can be obtained.
Grain growth can be described in general terms as follows:
A body of metal may be regarded as being composed of grains (i.e. crystals) very strongly bonded together, and it is generally accepted that the grain boundary regions are stronger than the grains themselves. Neglecting the influence of other factors such as Work hardening etc., the hardness and strength of a metal will depend upon the grain size. The larger the grain size the softer and weaker the metal and conversely. Thus, when the temperature of a piece of metal is raised sufficiently high it commonly happens that the metal grains coalesce (i.e. grain growth occurs) so that, after cooling, the said piece of metal is composed of a smaller number of larger grains and is accordingly softer and weaker than it was before. Most metals have to be heated to well above room temperature to cause grain growth; 250 C. for copper for example and 400-450 C. for iron. In the case of ordinary lead, however, grain growth occurs at room temperature.
Cold, plastic deformation (i.e. deformation without cracking) of a piece of metal, distorts and Work hardens the crystals so that the piece of metal as a whole is workhardened. Heating a,work-hardened piece of metal to a sufiiciently high temperature results in recrystallisation (i.e. the growth of new small crystals) and further heating to higher temperatures results in grain growth as described above. It is a peculiarity of ordinary lead that such recrystallisation and grain growth will occur at temperatures not much above room temperature.
In dispersion-strengthened lead the dispersed particles and, in particular, those particles located at or near the grain boundaries, prevent grain boundary movement and thus inhibit grain growth.
The preferred size range of the initial lead particles is determined by such considerations as thickness of oxide, packing density of the particles and the. final grain size required, but the range would normally be from 1 to microns.
The method is not necessarily limited to pure lead particles, but may be applied to lead alloy particles. Particles of lead containing, for instance, 1% tin to improve the corrosion resistance of the finished product, might be used.
To demonstrate the remarkable improvement in the strength of lead treated in accordance with the invention the following examples are given.
Example I Lead powder with a maximum particle size of about 104 microns was taken as received, with its natural lead oxide coating, and compacted into a 2 inches diameter billet. This was extruded to a cross-section of 1 /2 inches x 0.375 inch at room temperature (about 20 C.) and the resultant strip was then rolled firstly in the direction of the extrusion to reduce the 0.375 inch dimension to 0.175 inch, and then crosswise to reduce this dimension to 0.075 inch. The tensile strength of pieces of lead so prepared was found to be between 3220 and 3360 pounds per square inch, namely approaching twice that of ordinary lead (18002000 pounds per square inch).
Example 11 Lead powder with a maximum particle size of about a 53 microns, again taken as received with its natural lead oxide coating, was compacted and extruded as in Example I and then rolled lengthwise and crosswise to reduce the 0.375 inch dimension to 0.005 inch. The tensile strength of pieces of lead so prepared from this finer powder was found to be in the region of 5700 pounds per square inch. This is about three times the strength of ordinary lead.
The reduction of grain size and improved resistance to grain growth is demonstrated by the following example:
7 Example III A specimen of ordinary cast pure lead was extruded and found to have a coarse grain size of less than 1 grain per square inch at 500 diameters magnification. A sample of lead made by extruding and rolling lead powder as in Example I was found to have a grain size of about 200 grains per square inch at 500 diameters magnification in the well crystallised skin. Moreover a specimen of the latter material when heated to 200 C. for half an hour was found still to have a grain size of about 200 grains per square inch at 500 diameters magnification, that is the grain growth was negligible.
What I claim is:
1. A method of producing strengthened lead which comprises extruding lead oxide coated lead particles through a die and then rolling the extruded lead along and across the direction of extrusion.
2. The production of strengthened lead by cold extrusion of lead oxide coated lead particles followed by rolling of the extruded lead.
3. A method of producing strengthened lead which comprises compacting lead oxide coated lead particles into a billet, extruding this billet into a thin sheet, then rolling the sheet lengthwise and crosswise relative to the direction of extrusion.
References (Ii'ted by the Examiner Powder Metallurgy, 1962 No. 10, Preparation and Selection Properties of Certain Dispersion-Strengthened Lead-Base Alloys, Lenel, pp. 120421.
"Dispersion-Strengthened Lead and Its Applications, Roberts et al., pp. 132-157.
WHlTMORE A. NILTZ, Primary Examiner.

Claims (1)

1. A METHOD OF PRODUCING STRENGTHENED LEAD WHICH COMPRISES EXTRUDING LEAD OXIDE COATED LEAD PARTICLES THROUGH A DIE AND THEN ROLLING THE EXTRUDED LEAD ALONG AND ACROSS THE DIRECTION OF EXTRUSION.
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Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3315342A (en) * 1962-05-21 1967-04-25 St Joseph Lead Co Dispersion strengthening of lead
US3320664A (en) * 1962-04-26 1967-05-23 St Joseph Lead Co Process for the production of dispersion strengthened lead
US3377143A (en) * 1964-09-28 1968-04-09 Du Pont Dispersion-strengthened, low melting point metals
US3393069A (en) * 1964-11-10 1968-07-16 St Joseph Lead Co Manufacture of dispersion strengthened lead by screw extrusion of oxide-coated particles
US3440042A (en) * 1965-01-28 1969-04-22 Whittaker Corp Method of producing dispersion hardened metals
US3472709A (en) * 1966-03-25 1969-10-14 Nasa Method of producing refractory composites containing tantalum carbide,hafnium carbide,and hafnium boride
US3483046A (en) * 1966-02-10 1969-12-09 St Joseph Lead Co Stabilized non-bubbling dispersion strengthened lead
US3694536A (en) * 1970-02-06 1972-09-26 Dow Chemical Co Method of preparing lead article
US20020157743A1 (en) * 2001-02-26 2002-10-31 Clark Douglas G. Continuous extruded lead alloy strip for battery electrodes
US20050145960A1 (en) * 2003-12-16 2005-07-07 Habboosh Samir W. EMF sensor with protective sheath

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
None *

Cited By (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3320664A (en) * 1962-04-26 1967-05-23 St Joseph Lead Co Process for the production of dispersion strengthened lead
US3315342A (en) * 1962-05-21 1967-04-25 St Joseph Lead Co Dispersion strengthening of lead
US3377143A (en) * 1964-09-28 1968-04-09 Du Pont Dispersion-strengthened, low melting point metals
US3393069A (en) * 1964-11-10 1968-07-16 St Joseph Lead Co Manufacture of dispersion strengthened lead by screw extrusion of oxide-coated particles
US3440042A (en) * 1965-01-28 1969-04-22 Whittaker Corp Method of producing dispersion hardened metals
US3483046A (en) * 1966-02-10 1969-12-09 St Joseph Lead Co Stabilized non-bubbling dispersion strengthened lead
US3484305A (en) * 1966-02-10 1969-12-16 St Joseph Lead Co Nonbubbling dispersion strengthened lead
US3499800A (en) * 1966-02-10 1970-03-10 St Joseph Lead Co Method of making lead particles for non-bubbling dispersion strengthened lead
US3472709A (en) * 1966-03-25 1969-10-14 Nasa Method of producing refractory composites containing tantalum carbide,hafnium carbide,and hafnium boride
US3694536A (en) * 1970-02-06 1972-09-26 Dow Chemical Co Method of preparing lead article
US20020157743A1 (en) * 2001-02-26 2002-10-31 Clark Douglas G. Continuous extruded lead alloy strip for battery electrodes
US6797403B2 (en) * 2001-02-26 2004-09-28 Teck Cominco Metals Ltd. Continuous extruded lead alloy strip for battery electrodes
US20050145960A1 (en) * 2003-12-16 2005-07-07 Habboosh Samir W. EMF sensor with protective sheath
US7611280B2 (en) * 2003-12-16 2009-11-03 Harco Laboratories, Inc. EMF sensor with protective sheath

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