US2128122A - Process for increasing the electric conductivity of tin bronzes - Google Patents
Process for increasing the electric conductivity of tin bronzes Download PDFInfo
- Publication number
- US2128122A US2128122A US110648A US11064836A US2128122A US 2128122 A US2128122 A US 2128122A US 110648 A US110648 A US 110648A US 11064836 A US11064836 A US 11064836A US 2128122 A US2128122 A US 2128122A
- Authority
- US
- United States
- Prior art keywords
- tin
- alloys
- increasing
- tempering
- bronzes
- 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
Links
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 title description 22
- 238000000034 method Methods 0.000 title description 11
- 230000008569 process Effects 0.000 title description 10
- 229910045601 alloy Inorganic materials 0.000 description 22
- 239000000956 alloy Substances 0.000 description 22
- 238000005496 tempering Methods 0.000 description 16
- 230000009467 reduction Effects 0.000 description 11
- 238000010586 diagram Methods 0.000 description 6
- 239000013078 crystal Substances 0.000 description 5
- 238000001953 recrystallisation Methods 0.000 description 5
- 238000005482 strain hardening Methods 0.000 description 5
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
- 238000007792 addition Methods 0.000 description 4
- 229910052802 copper Inorganic materials 0.000 description 4
- 239000010949 copper Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 3
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 229910052749 magnesium Inorganic materials 0.000 description 2
- 239000011777 magnesium Substances 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- 238000011084 recovery Methods 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- 239000010703 silicon Substances 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- 229910002056 binary alloy Inorganic materials 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005242 forging Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 235000000396 iron Nutrition 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910052752 metalloid Inorganic materials 0.000 description 1
- 150000002738 metalloids Chemical class 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- -1 phosaraama phorus Chemical compound 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 229920000136 polysorbate Polymers 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 238000005476 soldering Methods 0.000 description 1
- 238000005728 strengthening Methods 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C9/00—Alloys based on copper
- C22C9/02—Alloys based on copper with tin as the next major constituent
Definitions
- lo'o 200 300 400 500' DRAWING TEMPERATURE.
- the alloys In carrying out the improved process the alloys, after any desired heat treatment, are first shaped by. forging, rolling or drawing in the cold state and then tempered at temperatures be- 0 tween about 150 and 400 C.
- Fig. 1 is a diagram illustrating the relation between the tin content and the specific resistance in Slrnm of the binary alloys
- Fig. 2 is a diagram illustrating the relation between specific resistance percentage deformation and drawing temperature
- Figs. 3 and 4 are diagrams illustrating the relation between specific resistance and time of tempering.
- Fig. 2 shows in the left hand portion the eilect of the cold working on the electrical resistance.
- the right hand portion of the diagram shows the recovery of the single alloys from the resistance increase efiected through subsequent tempering.
- the resistance drops, owing to the one hour tempering at 300- 350 C., below the value of the samples not cold worked. This drop can be further increased and more particularly it can be extended to alloys of lower percentage by increasing the duration of thetempering.
- Fig. 3. In this figure, for temperatures of 250 and 300 C. the variation of the electrical resistance is in connection with certain alloys in Figs. 2 and 3.
- Fig. 4 shows that the cold strengthened state is a requirement for this reduction of the electrical resistance.
- the efiect of tempering at 300 C. is indicated for increasing degree of deformation. No change is eflected in the period of tempering employed in connection ,0
- any increasein the electrical conductivity of tin bronzes is particularly desirable since such alloys are employed in great quantities as current conducting springs.
- the bronzes serve simultaneously as constructive material and as current conducting members for instance as electrodes for welding machines, soldering irons, current collector rollers, etc.
- the strengthening by tempering below the recrystallization interval i. e. tempering without any reduction of the cold-hardening, is to be particularly recommended.
- the addition of one or several of the above-mentioned third and fourth constituent parts is also generally to be recommended, because thereby, the conductivity is still further increased, particularly in connection with the alloys having low contents of tin, down to about 1%.
Description
Aug. 23, 1938.
O. DAHL ET AL PROCESS FOR INCREASING THE ELECTRIC CONDUGTIVITY OF TIN BRONZES SPECIFIC ELECTRIC RESISTANCE.
OJOO- Filed Fi cgI.
SPECIFIC ELECTRIC RESISTANCE.
-+ TIN CONTENT OFALLOY.
SPECIFIC ELECTRIC RESISTANCE. 2 Q s 2 WITH 250' REHEATZ TIME OFiTEMPERING.
Nov 15, 1936 DEF'ORMATION.
lo'o" 200 300 400 500' DRAWING TEMPERATURE.
IOOO
I0 I00 I000 TIME OF EHPERING.
Inventors: Otto Dal-1| Carl Haase,
Their Attorney.
Patented Aug. 23, 1938 UNITED STATES PROCESS FOR INCREASING THE ELECTRIC CONDUCTIVITY F TIN BRONZES Dtto Dahl, Berlin-Wilmersdorf, and Carl Mahlsdorf/Sud, Germany, assignors to General Electric Company, a corporation of New York Application November 13, 1936, Serial No. 110,648 In Germany December 9, i935 4Claims.
sion resistance. A disadvantage of such alloys is.
5 their relatively low electrical conductivity due to the addition of tin to the copper.
Extensive investigations relating to the influence on the physical and mechanical properties of the alloy by cold deformation and the recovery of the materials from the alterations which have occurred, by subsequent tempering, have resulted in an improved process, by means of which a considerable increase of the conductivity of tin bronzes of the a mixed crystal range can be attained.
In carrying out the improved process the alloys, after any desired heat treatment, are first shaped by. forging, rolling or drawing in the cold state and then tempered at temperatures be- 0 tween about 150 and 400 C.
The novel features which are characteristic of our invention are set forth with particularity in the appended claims. Our invention however will best be understood from reference to the 1'01- lowing specification when considered in connection with the accompanying drawing in which Fig. 1 is a diagram illustrating the relation between the tin content and the specific resistance in Slrnm of the binary alloys; Fig. 2 is a diagram illustrating the relation between specific resistance percentage deformation and drawing temperature; while Figs. 3 and 4 are diagrams illustrating the relation between specific resistance and time of tempering. l
The 'eifect of our improved proces is disclosed 40 Fig. 2 shows in the left hand portion the eilect of the cold working on the electrical resistance. The right hand portion of the diagram shows the recovery of the single alloys from the resistance increase efiected through subsequent tempering. As will be seen, not only is the previously eiiected resistance increase cancelled but the resistance drops, owing to the one hour tempering at 300- 350 C., below the value of the samples not cold worked. This drop can be further increased and more particularly it can be extended to alloys of lower percentage by increasing the duration of thetempering. This will be evident from Fig. 3. In this figure, for temperatures of 250 and 300 C. the variation of the electrical resistance is in connection with certain alloys in Figs. 2 and 3.
(Cl. 148ll1.5)
plotted for alloys containing 10.5 and 13.5% tin in dependence on the duration of the tempering period. As in Fig. 2 the alloys were shaped in a cold state before tempering to the extent of reduction in the thickness. As will be seen, a very great reduction of the electric resistance occurs. This takes place at 250 withoutany reduction whatever of the strength as shown by the diagrams of, the Brinell hardness. This condition is of particular importance because in this way high conductivity can be attained with great strength, i. e. those properties can be produced, which are required for current conducting springs or for current conducting electrodes or contacts for the electrode technique. A slight drop in the hardness occurs at 300 but'here also the greatest part of the cold work hardness is maintained.
In the reversed case, Fig. 4 shows that the cold strengthened state is a requirement for this reduction of the electrical resistance. In this figure, for the alloys shown in Fig. 3, the efiect of tempering at 300 C. is indicated for increasing degree of deformation. No change is eflected in the period of tempering employed in connection ,0
with the non-hardened alloys. The drop becomes noticeable with a reduction in thiclmess of more than 10% reduction and increases continther acceleratedand increased by small additions either alone or mixed of other metals or .metalloids such as phosphorus, magnesium, silicon, nickel, iron, aluminum and zinc in quantities of about 0.1 to 2%. The conductivity attained is greater the higher the content of tin.
For the binary bronzes containing only tin and copper the possibility of improvement extends downwardly to about 3% tin. On introducing additions, asmentioned above, this limit drops to below 1%; As far as the metallurgical basis of the process described is concerned, it is to be assumed, based on the knowledge of other systerns of alloys, that it is a question of decreasing the solubility of tin in copper, i. e. ofadecrease in the power of copper for dissolving tin at a low temperature. This decrease of solubility evidently cannot be brought about with the non work-hardened alloys owing to the low temperature and the low power of diffusion consequent thereon and its effect has therefore never been observed hitherto. It is only by means of cold deformation that this phenomenon is effected within technically practicable tempering periods. As is proved by the diagrams shown in this case also the period of tempering employed to develop this result necessarily is greater than that normally required for recrystallization which takes place only at higher temperatures.
Any increasein the electrical conductivity of tin bronzes is particularly desirable since such alloys are employed in great quantities as current conducting springs. This is also the case where the bronzes serve simultaneously as constructive material and as current conducting members for instance as electrodes for welding machines, soldering irons, current collector rollers, etc., For this purpose the strengthening by tempering below the recrystallization interval, i. e. tempering without any reduction of the cold-hardening, is to be particularly recommended. Besides this, in these cases, the addition of one or several of the above-mentioned third and fourth constituent parts is also generally to be recommended, because thereby, the conductivity is still further increased, particularly in connection with the alloys having low contents of tin, down to about 1%.
What we claim as new and desire to secure by Letters Patent of the United States, is:
1. The process for increasing the electrical conductivity of tin bronzes of the a mixed crystal range having upwards of 1% tin which contain an appreciable quantity and up to 2% of material from the group silicon, aluminum, iron, phosaraama phorus, nickel, zinc and magnesium, which comprises cold working said alloys to eifect a reduction in thickness greater than 50% and thereafter tempering said alloys between 150 and 400 C. for a period greater than that normally required for recrystallization which takes place only at higher temperatures.
2. The process for increasing the electrical conductivity of tin bronzes of the a mixed crystal range having upwards of 3% tin which comprises cold working said alloys to efiect a reduction of about 90% in thickness and thereafter tempering said alloys at a temperature in the neighborhood of 300 C. for a period greater than that normally required for recrystallization which takes place only at higher temperatures.
3. The process for increasing the electrical conductivity of tin bronzes of the a mixed crystal range having upwards of 3% tin which comprises cold working said alloys to eifect a reduction in thickness greater than 50% and thereafter tempering the alloys at a temperature in the neighborhood of 300 C. for a period greater than that normally required for recrystallization which takes place only at higher temperatures.
4. The process for increasing the electrical conductivity of tin bronzes of the a mixed crystal range having upwards of 3% tin which comprises cold working said alloys to efiect a reduction of about 90% in thickness and thereafter tempering said alloys at a temperature in the neighborhood of 300 C. for a period of .time greater than ten hours. v
OI'IO DAHL. CARL HAASE.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE2128122X | 1935-12-09 |
Publications (1)
Publication Number | Publication Date |
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US2128122A true US2128122A (en) | 1938-08-23 |
Family
ID=7986278
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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US110648A Expired - Lifetime US2128122A (en) | 1935-12-09 | 1936-11-13 | Process for increasing the electric conductivity of tin bronzes |
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US (1) | US2128122A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4012240A (en) * | 1975-10-08 | 1977-03-15 | Bell Telephone Laboratories, Incorporated | Cu-Ni-Sn alloy processing |
US4090890A (en) * | 1972-10-10 | 1978-05-23 | Bell Telephone Laboratories, Incorporated | Method for making copper-nickel-tin strip material |
US20110229367A1 (en) * | 2010-03-17 | 2011-09-22 | Shau-Kuan Chiu | Copper nickel aluminum alloy |
-
1936
- 1936-11-13 US US110648A patent/US2128122A/en not_active Expired - Lifetime
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4090890A (en) * | 1972-10-10 | 1978-05-23 | Bell Telephone Laboratories, Incorporated | Method for making copper-nickel-tin strip material |
US4012240A (en) * | 1975-10-08 | 1977-03-15 | Bell Telephone Laboratories, Incorporated | Cu-Ni-Sn alloy processing |
US20110229367A1 (en) * | 2010-03-17 | 2011-09-22 | Shau-Kuan Chiu | Copper nickel aluminum alloy |
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