US3888703A - Method of producing creep resistance of pb-sb alloys - Google Patents

Method of producing creep resistance of pb-sb alloys Download PDF

Info

Publication number
US3888703A
US3888703A US472388A US47238874A US3888703A US 3888703 A US3888703 A US 3888703A US 472388 A US472388 A US 472388A US 47238874 A US47238874 A US 47238874A US 3888703 A US3888703 A US 3888703A
Authority
US
United States
Prior art keywords
percent
alloys
per pass
finish
deformation
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 - Lifetime
Application number
US472388A
Inventor
Milton M Tilman
Robert L Crosby
Leander A Neumeier
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.)
US Department of the Interior
Original Assignee
US Department of the Interior
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 US Department of the Interior filed Critical US Department of the Interior
Priority to US472388A priority Critical patent/US3888703A/en
Application granted granted Critical
Publication of US3888703A publication Critical patent/US3888703A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • 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

Definitions

  • creep resistance of Pb-Sb alloys containing up to about percent Sb may be substantially improved by the use of a processing procedure comprising breakdown deformation, cold or hot, with greater than about percent reduction per pass for about 67 percent, or greater, reduction of original thickness, followed by finish deformation of less than 10 percent per pass, and preferably about 5 percent per pass or less, at a temperature of about 100 to 200C.
  • the alloys of the invention consist essentially of lead and up to about 5 percent of antimony.
  • the process of the invention has been found to be particularly beneficial in treatment of alloys containing about 0.25 to 2.0 percent antimony.
  • Deformation will generally be by means of rolling, but other means such as press forming may also be used. These procedures, and the equipment employed, are conventional in the art of metal working. Rolling speed and lubricants are also conventional, and are not critical. Reheating between passes need be only long enough to restore the elevated temperature, and the workpiece is normally air cooled after the last rolling pass.
  • slabs were cut in half, each half measuring 0.69 inch X 4 inches X 3 inches to 3.5 inches.
  • the slabs were preheated at either 125 or 175C for 1 hour. Re duction per pass was 20 percent based on the thickness obtained after the preceding pass. Kerosene was used as a lubricant.
  • the slabs were reheated for 10 to minutes between each pass. Five passes at 125 or 175C were sufficient to reduce the slabs to 0.225 inch to 0.227 inch X 4 inches X 9 inches to 9.5 inches. These slabs were cut in half to 0.225 inch to 0.227 inch X 4 inches X 4.5 inches to 4.75 inches long and used as starting stock for finish rolling.
  • the final 26 percent reduction (based on original thickness of 0.69 inch) was made at either room temperature, 125 or 175C at consecutive reductions of either 5 percent per pass or 20 percent per pass based on the thickness obtained after each preceding pass.
  • the plate When rolling at 125 or 175C, the plate was preheated for 1 hour at the selected temperature and reheated for 10 to 15 minutes between each pass. Final dimensions were approximately 4.125 inches X 18 inches X 0.0625 inch. Standard 8 inches sheet tensile and creep speciments were cut longitudinally from the finished sheet.
  • Table 1 gives creep data for Pb-Sb alloys that were finish rolled at 5 to 20 percent reduction per pass at 125C. The marked improvement in creep rates for the 5 percent reductions is apparent. Furthermore, the im- 700-psi stress, tests at :3F
  • Table 2 lists creep data, in percent per year, for Pb-Sb alloys containing up to 5 percent Sb, that were processed in various ways including the process of the invention, after breakdown rolling in the range-of to C.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Heat Treatment Of Steel (AREA)

Abstract

Lead-antimony alloys of improved creep resistance are prepared by means of a process comprising finish deformation at elevated temperature with light, i.e., less than 10 percent reductions.

Description

United States Patent [191 Tilman et al.
METHOD OF PRODUCING CREEP RESISTANCE OF PB-SB ALLOYS Inventors: Milton M. Tilman; Robert L.
Crosby; Leander A. Neumeier, all of Rolla, M0.
The United States of America as represented by the Secretary of the Interior, Washington, DC.
Filed: May 22, 1974 Appl. No.: 472,388
Assignee:
US. Cl 148/11.5 R Int. Cl. C22c 11/00 Field of Search 148/1 1.5 R; 75/166 B References Cited UNITED STATES PATENTS 1l/1902 Lloyd 75/168 B Primary ExaminerW. Stallard Attorney, Agent, or FirmWilliam S. Brown ABSTRACT Lead-antimony alloys of improved creep resistance are prepared by means of a process comprising finish deformation at elevated temperature with light, i.e., less than 10 percent reductions.
5 Claims, No Drawings METHOD OF PRODUCING CREEP RESISTANCE OF PB-SB ALLOYS Lead-antimony alloys containing about 1 to 9 percent antimony are in common usage for a variety of applications such as chemical processing equipment, sound barriers, radiation shielding, roofing and flashing. Conventional processing procedures commonly produce usable, although not high, tensile strength in these alloys. Such procedures generally do not produce desirably high creep resistance. It has now been found, according to the invention, that creep resistance of Pb-Sb alloys containing up to about percent Sb may be substantially improved by the use of a processing procedure comprising breakdown deformation, cold or hot, with greater than about percent reduction per pass for about 67 percent, or greater, reduction of original thickness, followed by finish deformation of less than 10 percent per pass, and preferably about 5 percent per pass or less, at a temperature of about 100 to 200C.
The alloys of the invention consist essentially of lead and up to about 5 percent of antimony. The process of the invention has been found to be particularly beneficial in treatment of alloys containing about 0.25 to 2.0 percent antimony. Deformation will generally be by means of rolling, but other means such as press forming may also be used. These procedures, and the equipment employed, are conventional in the art of metal working. Rolling speed and lubricants are also conventional, and are not critical. Reheating between passes need be only long enough to restore the elevated temperature, and the workpiece is normally air cooled after the last rolling pass.
The following examples will serve to more particularly illustrate the invention and the advantages achieved thereby.
EXAMPLES Samples were initially prepared by means of the following procedure:
Sixteen pound heats of lead-antimony alloys consisting of corroding grade lead and antimony of 99.99 percent purity were melted in an induction furnace using MgO crucibles. The lead was brought to the molten condition and a ZnCl flux cover added. The required amount of antimony was added through the flux cover at approximately 420C. After cooling to approximately 400C, NaCl was added to the flux cover to thicken the flux and facilitate removal. The flux was skimmed and the molten alloy was cast at approximately 400C into two preheated (about 300C) steel slab molds. Upon removal from the molds, the slabs measured 0.69 inch X 4 inches approximately 7 inches and weighed approximately 8 lbs. each. A inch slice was cut from the riser end of each slab and discarded. Samples for chemical analysis were then filed from both riser and butt ends of each slab and each sample analyzed separately for antimony content.
By rolling, slabs were cut in half, each half measuring 0.69 inch X 4 inches X 3 inches to 3.5 inches. The slabs were preheated at either 125 or 175C for 1 hour. Re duction per pass was 20 percent based on the thickness obtained after the preceding pass. Kerosene was used as a lubricant. The slabs were reheated for 10 to minutes between each pass. Five passes at 125 or 175C were sufficient to reduce the slabs to 0.225 inch to 0.227 inch X 4 inches X 9 inches to 9.5 inches. These slabs were cut in half to 0.225 inch to 0.227 inch X 4 inches X 4.5 inches to 4.75 inches long and used as starting stock for finish rolling.
The final 26 percent reduction (based on original thickness of 0.69 inch) was made at either room temperature, 125 or 175C at consecutive reductions of either 5 percent per pass or 20 percent per pass based on the thickness obtained after each preceding pass. When rolling at 125 or 175C, the plate was preheated for 1 hour at the selected temperature and reheated for 10 to 15 minutes between each pass. Final dimensions were approximately 4.125 inches X 18 inches X 0.0625 inch. Standard 8 inches sheet tensile and creep speciments were cut longitudinally from the finished sheet.
Table 1 gives creep data for Pb-Sb alloys that were finish rolled at 5 to 20 percent reduction per pass at 125C. The marked improvement in creep rates for the 5 percent reductions is apparent. Furthermore, the im- 700-psi stress, tests at :3F
Table 2 lists creep data, in percent per year, for Pb-Sb alloys containing up to 5 percent Sb, that were processed in various ways including the process of the invention, after breakdown rolling in the range-of to C.
Column II of the table gives data for alloys finish rolled cold, i.e., near room temperature, for 26 percent reduction based on starting thickness. This procedure is similar to commercial practice, which is done at various reductions per pass.
Columns Ill and VI give data for alloys finish rolled at 175C for 26 percent reduction based on starting thickness, for 5 and 20 percent reduction per pass, respectively.
Column IV gives data for alloys finish rolled at room temperature at 20 percent reduction per pass prior to annealing at 220C, and with a final pass at 175C and 5 percent reduction.
Column V gives data for alloys finish rolled at room temperature at 20 percent reduction per pass prior to solution treatment at 235C and aging 10 to 12 days at 90F.
As seen from the data of table 2, there is a vast difference in creep rates between alloys finish rolled cold and those finish rolled hot with light passes. The data of column 111, where repeated light passes were given at elevated temperature, shows very low creep rates, i.e., high creep resistance, and creep rates about the same for alloys containing 0.5 to 5.0 percent Sb. In contrast, rolling at 175C with 20 percent reduction per pass does not result in low creep rate, as shown in column V1.
The data in column 1V show that a single pass at 175C and 5 percent reduction does not provide maximum benefits, although the Pb-l.0 Sb alloy is approaching the rate for repeated passes (column Ill).
thickness and (2) finish deformation of the alloy at a temperature of about 100 to 200C and with reduction per pass less than percent.
2. The method of claim 1 in which the alloy contains about 0.5 to 2.0 percent antimony.
3. The method of claim 1 in which the deformation is accomplished by rolling.
At room temperature. Last 26 pct total reduction at 5 pct per pass. "Finish rolled at 175C. Last 26 pct total reduction at 5 pct per pass.
TABLE 2 I II III IV V VI Sb, Finish rolled Finish rolled Annealed Solution Finish rolled wt pct cold, at 175C, 220C. 7 treated at 175C,
Reduction per pass 5 pct reduction last pass at 235C,
5 pct 20 pct. per pass at 175C. aged 10 to 12 20 pct reduction 5 pct reduction days F per pass Rolled at 10 pct reduction per pass to avoid cracking.
TABLE 3 1.0 pct Sb 2.0 pct Sb 5.0 pct Sb Finish Finish Finish Property rolled Invention rolled Invention" rolled Invention cold cold cold Tensile strength, psi 2890 3310 3180 3940 3630 4930 Yield strength, psi 1470 2160 1920 2920 2320 4080 (0.2% offset) Elongation in 2 inches, pct 47 44 47 37 62 34 4. The method of claim 1 in which the finish deformation is accomplished at a temperature of about 125", to C.
5. The method of claim 1 in which the finish deformation is accomplished at a reductions per pass of about 5 percent.

Claims (5)

1. A METHOD FOR TREATMENT OF LEAD-ANTIMONY ALLOYS, CONTAINING UP TO ABOUT 5 PERCENT ANTIMONY, COMPRISING (1) BREAKDOWN DEFORMATION OF THE ALLOY WITH REDUCTIONS PER PASS GREATER THAN ABOUT 10 PERCENT FOR A TOTAL REDUCTION OF AT LEAST ABOUT 67 PERCENT OF THE ORIGINAL THICKNESS AND (2) FINISH DEFORMATION OF THE ALLOY AT A TEMPERATURE OF ABOUT 100* TO 200*C AND WITH REDUCTION PER PASS LESS THAN 10 PERCENT.
2. The method of claim 1 in which the alloy contains about 0.5 to 2.0 percent antimony.
3. The method of claim 1 in which the deformation is accomplished by rolling.
4. The method of claim 1 in which the finish deformation is accomplished at a temperature of about 125* to 175*C.
5. The method of claim 1 in which the finish deformation is accomplished at a reductions per pass of about 5 percent.
US472388A 1974-05-22 1974-05-22 Method of producing creep resistance of pb-sb alloys Expired - Lifetime US3888703A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US472388A US3888703A (en) 1974-05-22 1974-05-22 Method of producing creep resistance of pb-sb alloys

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US472388A US3888703A (en) 1974-05-22 1974-05-22 Method of producing creep resistance of pb-sb alloys

Publications (1)

Publication Number Publication Date
US3888703A true US3888703A (en) 1975-06-10

Family

ID=23875322

Family Applications (1)

Application Number Title Priority Date Filing Date
US472388A Expired - Lifetime US3888703A (en) 1974-05-22 1974-05-22 Method of producing creep resistance of pb-sb alloys

Country Status (1)

Country Link
US (1) US3888703A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4332629A (en) * 1979-06-29 1982-06-01 Chloride Group Limited Method of making extended strip of lead-antimony alloys for battery electrodes
US5283459A (en) * 1989-11-15 1994-02-01 Kabushiki Kaisha Toshiba Semiconductor sensor including an aperture having a funnel shaped section intersecting a second section
US6342110B1 (en) * 1996-03-01 2002-01-29 Integran Technologies Inc. Lead and lead alloys with enhanced creep and/or intergranular corrosion resistance, especially for lead-acid batteries and electrodes therefor
US20040112486A1 (en) * 1996-03-01 2004-06-17 Aust Karl T. Thermo-mechanical treated lead and lead alloys especially for current collectors and connectors in lead-acid batteries
US6802917B1 (en) * 2000-05-26 2004-10-12 Integran Technologies Inc. Perforated current collectors for storage batteries and electrochemical cells, having improved resistance to corrosion

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US713568A (en) * 1900-06-29 1902-11-11 Electric Storage Battery Co Non-active metal for use in storage batteries.
US1029152A (en) * 1911-07-01 1912-06-11 Hoyt Metal Company Composite metal.
US1722358A (en) * 1927-07-06 1929-07-30 Western Electric Co Alloy and method of making alloys
US2060534A (en) * 1931-11-19 1936-11-10 Goodlass Wall And Lead Ind Ltd Lead alloy
US3637440A (en) * 1970-04-24 1972-01-25 Dow Chemical Co Method of making a creep resistant lead alloy

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US713568A (en) * 1900-06-29 1902-11-11 Electric Storage Battery Co Non-active metal for use in storage batteries.
US1029152A (en) * 1911-07-01 1912-06-11 Hoyt Metal Company Composite metal.
US1722358A (en) * 1927-07-06 1929-07-30 Western Electric Co Alloy and method of making alloys
US2060534A (en) * 1931-11-19 1936-11-10 Goodlass Wall And Lead Ind Ltd Lead alloy
US3637440A (en) * 1970-04-24 1972-01-25 Dow Chemical Co Method of making a creep resistant lead alloy

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4332629A (en) * 1979-06-29 1982-06-01 Chloride Group Limited Method of making extended strip of lead-antimony alloys for battery electrodes
US5283459A (en) * 1989-11-15 1994-02-01 Kabushiki Kaisha Toshiba Semiconductor sensor including an aperture having a funnel shaped section intersecting a second section
US6342110B1 (en) * 1996-03-01 2002-01-29 Integran Technologies Inc. Lead and lead alloys with enhanced creep and/or intergranular corrosion resistance, especially for lead-acid batteries and electrodes therefor
US20040112486A1 (en) * 1996-03-01 2004-06-17 Aust Karl T. Thermo-mechanical treated lead and lead alloys especially for current collectors and connectors in lead-acid batteries
AU767992B2 (en) * 1999-10-06 2003-11-27 Integran Technologies Inc. Lead and lead alloys, with enhanced creep and/or intergranular corrosion resistance, especially for lead-acid batteries and electrodes therefor
US6802917B1 (en) * 2000-05-26 2004-10-12 Integran Technologies Inc. Perforated current collectors for storage batteries and electrochemical cells, having improved resistance to corrosion

Similar Documents

Publication Publication Date Title
US3512221A (en) Aluminum alloy wire
US3614816A (en) Method of making cartridge cases
DE1966231C3 (en) Process for the production of transformer sheets
US3346370A (en) Aluminum base alloy
ES475808A1 (en) Al-Mn Alloy and process of manufacturing semifinished products having improved strength properties
US3888703A (en) Method of producing creep resistance of pb-sb alloys
GB1566776A (en) Processing chromium-containing precipitation hardenable copper base alloys
US3670401A (en) Method of fabricating aluminum alloy rod
US2506788A (en) Method of enhancing physical properties of aluminum base alloys containing zinc and magnesium
US3333989A (en) Aluminum base alloy plate
US5223055A (en) Method of making a sheet or strip of zircaloy with good formability and the strips obtained
US3346371A (en) Aluminum base alloy
US2596485A (en) Titanium base alloy
US3966506A (en) Aluminum alloy sheet and process therefor
US2826518A (en) Aluminum base alloy article
US2589881A (en) Method of producing steel products and articles
US2670309A (en) Metal-working process and product
US3366476A (en) Aluminum base alloy
US3346372A (en) Aluminum base alloy
DE2536167B2 (en) Process for the production of bubble-free copper alloys
US3556872A (en) Process for preparing aluminum base alloys
US3862863A (en) Heat treatment for wrought zinc-aluminum alloys
EP0026941B1 (en) Chromium modified silicon-tin containing copper base alloys, process of treating same and uses of same
US3346374A (en) Aluminum base alloy
DE602004010138T2 (en) METHOD FOR PRODUCING PARTS FROM TITANIUM OR A TITANIUM ALLOY