US2719085A - Silver-silicon alloys - Google Patents

Silver-silicon alloys Download PDF

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US2719085A
US2719085A US262337A US26233751A US2719085A US 2719085 A US2719085 A US 2719085A US 262337 A US262337 A US 262337A US 26233751 A US26233751 A US 26233751A US 2719085 A US2719085 A US 2719085A
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alloys
silicon
silver
phosphorus
binary
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US262337A
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Schatz Johannes
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Evonik Operations GmbH
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Degussa GmbH
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    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C5/00Alloys based on noble metals
    • C22C5/06Alloys based on silver

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  • the silicon in the eutectic mixture usually is in the form of platelets or long needle-like structures which cannot be uniformly and finely distributed in the silver ground mass even during subsequent working of the alloy. Consequently, such alloys are diflicult to work and numerous intermediate annealings are required. The relatively large sized silicon inclusions render it impossible to impart a high polish to the surface of such alloys. These drawbacks of the alloys have been found extremely disadvantageous for many uses of the alloys.
  • the alloys, in accordance with the invention, containing from 0.15% of silicon and 0.0010.l% of phosphorus not only avoid the above-mentioned drawbacks, but also possess improved mechanical properties while still maintaining the same chemical properties as the binary alloys devoid of phosphorus or arsenic. It has been found that the presence of phosphorus in the quantities specified cause the silicon to crystallize in a finegrained form in the eutectic mass. Comparative tests have shown that the silicon grains in the eutectic mass of cast alloys according to the invention are only about /5 to as large as those in the binary silver silicon alloys devoid of phosphorus or arsenic.
  • the copper content can be between 0.01 and 0.5% and the nickel content can be between 0.01 and 0.2%. It is also possible to add both copper and nickel within the ranges given, as long as their total does not exceed 0.5%.
  • the alloys according to the invention are not only more workable because of the fine-grained crystals of silicon, but they also have substantially improved mechanical properties over the binary silver silicon alloys. While a cast binary 97% silver 3% silicon alloy can only be cold worked about -20% before annealing, the same alloy with a 0.03% phosphorus addition can be cold rolled 40-50% before annealing. In view of the good 2,719,085 Patented Sept. 27., 195.5
  • the alloys according to the invention are well suited as plating metals on base metal alloys while the binary alloys are uneconomical to use for plating purposes in view of their comparatively low workability.
  • The'fine-grained structure of the alloys according to the invention also improves their hardness, as well as their tensile strength.
  • the following table compares the tensile strength (TS) and the Brinell hardness (HB) of binary silver silicon alloys of various silicon contents with silver silicon alloys containing 0.05% of phosphorus.
  • the alloys according to the invention have tensile strengths and Brinell hardnesses which are 10% and more higher than those of the binary alloys.
  • the excellent workability of the phosphorus containing silver-silicon alloys according to the invention renders it possible to utilize more fully the improvements in mechanical properties which are engendered by cold working.
  • the following table shows the tensile strength (TS), elongation at break (E) and the Brinell hardness (HB) of a 96.97% by 3% silicon 0.03% phosphorus alloy at various stages of cold working.
  • the alloys in accordance with the invention have an unexpectedly high corrosion resistance which is substantially the same as that of pure silver.
  • an alloy consisting of 96.97% Ag, 3% silicon and 0.03% phosphorus has a yearly loss of thickness when exposed to acetic acid at C. of 1.3 microns. Because of the known influence of phosphorus upon silver, it was rather to be expected that the corrosion resistance of the alloys according to the invention would be considerably below that of pure silver.

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
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Description

United States Patent SILVER-SILICON ALLOYS Johannes Schatz, Frankfurt am Main, Germany, assignor to Deutsche Goldund Silber-Scheideanstalt vormals Roessler, Frankfurt am Main, Germany, a corporation of Germany No Drawing. Application December 18, 1951, Serial No. 262,337
Claims priority, application Germany December 22, 1950 5 Claims. (Cl... 75-473) silver or silicon and both components in eutectic mixture.
The silicon in the eutectic mixture usually is in the form of platelets or long needle-like structures which cannot be uniformly and finely distributed in the silver ground mass even during subsequent working of the alloy. Consequently, such alloys are diflicult to work and numerous intermediate annealings are required. The relatively large sized silicon inclusions render it impossible to impart a high polish to the surface of such alloys. These drawbacks of the alloys have been found extremely disadvantageous for many uses of the alloys.
It has now been found, according to the invention, that the alloys, in accordance with the invention, containing from 0.15% of silicon and 0.0010.l% of phosphorus not only avoid the above-mentioned drawbacks, but also possess improved mechanical properties while still maintaining the same chemical properties as the binary alloys devoid of phosphorus or arsenic. It has been found that the presence of phosphorus in the quantities specified cause the silicon to crystallize in a finegrained form in the eutectic mass. Comparative tests have shown that the silicon grains in the eutectic mass of cast alloys according to the invention are only about /5 to as large as those in the binary silver silicon alloys devoid of phosphorus or arsenic. This produces a more uniform distribution of the silicon in the silver containing matrix so that a much more uniform and finer distribution of the silicon takes place upon working than occurs with the binary alloys devoid of phosphorus. The finest silicon distribution is achieved in alloys containing 14% of silicon and 0.01 to 0.05% of phosphorus or arsenic.
Further advantageous properties can be obtained by the addition of small quantities of copper or nickel. The copper content can be between 0.01 and 0.5% and the nickel content can be between 0.01 and 0.2%. It is also possible to add both copper and nickel within the ranges given, as long as their total does not exceed 0.5%.
The alloys according to the invention are not only more workable because of the fine-grained crystals of silicon, but they also have substantially improved mechanical properties over the binary silver silicon alloys. While a cast binary 97% silver 3% silicon alloy can only be cold worked about -20% before annealing, the same alloy with a 0.03% phosphorus addition can be cold rolled 40-50% before annealing. In view of the good 2,719,085 Patented Sept. 27., 195.5
workability of the alloys according to the invention, they are well suited as plating metals on base metal alloys while the binary alloys are uneconomical to use for plating purposes in view of their comparatively low workability.
The'fine-grained structure of the alloys according to the invention also improves their hardness, as well as their tensile strength. The following table compares the tensile strength (TS) and the Brinell hardness (HB) of binary silver silicon alloys of various silicon contents with silver silicon alloys containing 0.05% of phosphorus.
Ag.-Si Ag-Si 0.05% P Silicon, Percent TS (kg./ HB (kg./ TS .(kg./ HB (kg./ mm?) mm?) mm?) mm!) As may be seen from the table, the alloys according to the invention have tensile strengths and Brinell hardnesses which are 10% and more higher than those of the binary alloys.
The excellent workability of the phosphorus containing silver-silicon alloys according to the invention renders it possible to utilize more fully the improvements in mechanical properties which are engendered by cold working.
The following table shows the tensile strength (TS), elongation at break (E) and the Brinell hardness (HB) of a 96.97% by 3% silicon 0.03% phosphorus alloy at various stages of cold working.
. TS, kg./ E, Per- HB, kg/ Cold Working, Percent cent m Corrosion tests have shown that the alloys in accordance with the invention have an unexpectedly high corrosion resistance which is substantially the same as that of pure silver. For example, an alloy consisting of 96.97% Ag, 3% silicon and 0.03% phosphorus has a yearly loss of thickness when exposed to acetic acid at C. of 1.3 microns. Because of the known influence of phosphorus upon silver, it was rather to be expected that the corrosion resistance of the alloys according to the invention would be considerably below that of pure silver. Also, it was to be expected that the inclusion of phosphorus in the alloys according to the invention would have an unfavorable effect on such alloys in view of their normal embrittling action. Consequently, it was entirely unexpected that the addition of phosphorus to the binary silver-silicon alloys would result in such improved mechanical properties that they would be suitable for uses for which the binary alloys were not practical. The excellent polishing characteristics of the alloys according to this invention is of special importance, as it ensures good resistance to chemical and mechanical attacks. The addition of copper and nickel facilitates the inclusion of the easily volatilizable phosphorus because the compounds CusP or NiaP are selected as carriers of the phosphorus to be added to the silver-silicon alloy, Contrary to elementary phosphorus these compounds do not show a significant phosphorus vapor pressure even at a temperature of about 1100" C. Furthermore, the addition of these small quantities of copper and/ or nickel have no disadvantageous influence on the corrosion resistance of the alloys.
The following are further examples of alloys according to the invention which have been found to have substantially improved properties over the corresponding binary silver-silicon alloys.
Grain size of silicon in the cast alloy in comparison with alloys without addi tion of P Composition Additions, percent Si, percent Ag, percent - $60 to $60. lo to $60.
addition at least one of the following metals; nickel in a quantity between 0.01 and 0.2% and copper in a quantity between 0.01 and 0.5%, the total quantity of such addition being up to 0.5
4. A11 alloy in accordance with claim 1, containing in addition 0.01 to 0.2% of nickel.
5. An alloy in accordance with claim 1, containing in addition 0.01 to 0.5 of copper.
References Cited in the file of this patent UNITED STATES PATENTS 1,643,304 Korunsky Sept. 27, 1927 1,720,894 Gray et a1. July 16, 1929 1,863,645 Assman June 21, 1932 2,202,054 Hensel et a1 May 28, 1940 2,221,949 Kinzel et al Nov. 19, 1940 2,241,816 Hensel et a1 May 13, 1941 2,353,254 McCandless July 11, 1944 2,450,340 Hensel et al Sept. 28, 1948 FOREIGN PATENTS 877,647 France Dec. 11, 1942 OTHER REFERENCES Addicks: Silver Industry, published by Reinhold Publishing Corp. New York, New York, 1940; pages 105-108 and 164.

Claims (1)

1. A SILVER-SILICON ALLOY CONSISTING OF 0.1 TO 5% OF SILICON, 0.001 TO 0.1% OF PHOSPHORUS AND THE BALANCE SILVER.
US262337A 1950-12-22 1951-12-18 Silver-silicon alloys Expired - Lifetime US2719085A (en)

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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6413649B2 (en) * 1998-03-06 2002-07-02 The Morgan Crucible Company Plc Silver-copper-nickel infiltration brazing filler metal and composites made therefrom
US20070128456A1 (en) * 2003-10-16 2007-06-07 Koichi Hasegawa Sputtering target material
US9194024B1 (en) 2010-05-17 2015-11-24 Stuller, Inc. Jewelry article of white precious metals and methods for making the same
US9217190B2 (en) 2011-09-01 2015-12-22 Stuller, Inc. Sterling silver alloy and articles made from same

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1643304A (en) * 1924-05-16 1927-09-27 Electro Metallurg Co Silver-silicon alloy and process of making the same
US1720894A (en) * 1924-04-03 1929-07-16 Oneida Community Ltd Tarnish-resisting silver alloy, etc., and process for producing the same
US1863645A (en) * 1926-06-19 1932-06-21 Ig Farbenindustrie Ag Chemically resistant silver alloy
US2202054A (en) * 1939-05-02 1940-05-28 Mallory & Co Inc P R Electric contact element
US2221949A (en) * 1939-06-13 1940-11-19 Electro Metallurg Co Handling hot aqueous solutions of phosphoric acid
US2241816A (en) * 1940-01-16 1941-05-13 Mallory & Co Inc P R Silver electric contact
FR877647A (en) * 1940-12-20 1942-12-11 Fr Kammerer Ag Silver and copper alloy for electrical contacts
US2353254A (en) * 1941-10-28 1944-07-11 Linde Air Prod Co Bursting disk
US2450340A (en) * 1944-02-03 1948-09-28 Mallory & Co Inc P R Silver base alloy for metal evaporation

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1720894A (en) * 1924-04-03 1929-07-16 Oneida Community Ltd Tarnish-resisting silver alloy, etc., and process for producing the same
US1643304A (en) * 1924-05-16 1927-09-27 Electro Metallurg Co Silver-silicon alloy and process of making the same
US1863645A (en) * 1926-06-19 1932-06-21 Ig Farbenindustrie Ag Chemically resistant silver alloy
US2202054A (en) * 1939-05-02 1940-05-28 Mallory & Co Inc P R Electric contact element
US2221949A (en) * 1939-06-13 1940-11-19 Electro Metallurg Co Handling hot aqueous solutions of phosphoric acid
US2241816A (en) * 1940-01-16 1941-05-13 Mallory & Co Inc P R Silver electric contact
FR877647A (en) * 1940-12-20 1942-12-11 Fr Kammerer Ag Silver and copper alloy for electrical contacts
US2353254A (en) * 1941-10-28 1944-07-11 Linde Air Prod Co Bursting disk
US2450340A (en) * 1944-02-03 1948-09-28 Mallory & Co Inc P R Silver base alloy for metal evaporation

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6413649B2 (en) * 1998-03-06 2002-07-02 The Morgan Crucible Company Plc Silver-copper-nickel infiltration brazing filler metal and composites made therefrom
US20070128456A1 (en) * 2003-10-16 2007-06-07 Koichi Hasegawa Sputtering target material
US7959746B2 (en) * 2003-10-16 2011-06-14 Ishifuku Metal Industry Co., Ltd. Sputtering target material
US20110211988A1 (en) * 2003-10-16 2011-09-01 Koichi Hasegawa Sputtering target material
US8252127B2 (en) 2003-10-16 2012-08-28 Ishifuku Metal Industry Co., Ltd. Sputtering target material
US20130094990A1 (en) * 2003-10-16 2013-04-18 Ishifuku Metal Industry Co., Ltd. Sputtering target material
US8858877B2 (en) * 2003-10-16 2014-10-14 Ishifuku Metal Industry Co., Ltd. Sputtering target material
US9127346B2 (en) 2003-10-16 2015-09-08 Ishifuku Metal Industry Co., Ltd. Sputtering target material
US9194024B1 (en) 2010-05-17 2015-11-24 Stuller, Inc. Jewelry article of white precious metals and methods for making the same
US9217190B2 (en) 2011-09-01 2015-12-22 Stuller, Inc. Sterling silver alloy and articles made from same
US10697044B1 (en) 2011-09-01 2020-06-30 Stuller, Inc. Sterling silver alloy and articles made from the same

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