US2175223A - Copper alloy - Google Patents

Copper alloy Download PDF

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Publication number
US2175223A
US2175223A US216891A US21689138A US2175223A US 2175223 A US2175223 A US 2175223A US 216891 A US216891 A US 216891A US 21689138 A US21689138 A US 21689138A US 2175223 A US2175223 A US 2175223A
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United States
Prior art keywords
boron
alloys
copper
alloy
silicon
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US216891A
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Horace F Silliman
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American Brass Co
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American Brass Co
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Priority to US216891A priority Critical patent/US2175223A/en
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    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C9/00Alloys based on copper
    • C22C9/10Alloys based on copper with silicon as the next major constituent

Definitions

  • My invention relates to the alloys of copper and more particularly to the copper-base alloys' are added to impart certain properties.
  • boron added to the copper-silicon alloys improves them.
  • the addition of boron to copper-silicon alloys permits a close control of the grain size.
  • the addition of boron has a fluxing effect so that the alloys flow more readily in casting and welding;
  • a further advantage gained from the pres ence of boron in the composition that the scale formed on the surface of the alloy annealed in an oxygen-bearing atmosphere is reduced in quantity and modified in composition so that it can be removed more easily.
  • the boron has the added value of improving the resistance of the alloys to mechanical wear.
  • the boric anhydride is a mobile, non-volatile liquid at the casting, brazing, and welding temperatures employed, and has a great solvent power for other oxides.
  • boron itself is so active chemically that it actually reduces the oxides of many metals such as iron, tin, manganese, zinc, copper, and others, thus producing cleaner and more ductile alloys.
  • Phosphorus is an efficient deoxidizer for copper alloys but it has the disadvantage as compared to boron) that the phosphoric acid anhydride produced beginsto sublime at 347 C. so that the protective liquid covering and oxidesolvent jefi'ect is not obtained with the phosphorus as it is with boron.
  • the scale has a different coefiicient of expansion than the metal, and cracks into small pieces on cooling, and partly due to the fact that the scale is made up of more easily soluble boron-bearing compounds.
  • boron present in the silicon-copper alloys increases their wear resistance.
  • the boron in amounts up to 2% and higher forms numerous, vsmall, hard particles of an intermetallic compound uniformly distributed throughout the alloy, but the matrix of the alloy is comparatively soft. This structure is similar to that of the white alloys commonly used for bearing materials, and its greater hardness results in a greatly superior wear resistance.
  • I melt and alloy the copper-silicon, and other metals in the customary manner. I then add to the melt a boron alloy such as cupro-boron, ferro-boron, manganose boron, or boron itself. It is. a difficult matter to introduce boron into copper alloys with most of the available boron alloys and compounds, but I have obtained excellent results with an alloy of boron 2% to balance copper. I may also add the boron by one of the methods of my copending application for a process for producing boron-copper alloys, Serial No. 188,471, filed February 3,1938.
  • the ,quantity of boron introduced may vary from .005% up to about 4.5%. Usually I prefer to keep the quantity as low as possible to save expense, the preferred range being up to about 0.5% as this is suflicient for most applications.
  • the range of silicon may be from 0.1% to 5%, the preferred range being 1% to 4% as this is the range of alloys which are the more easily workable and have the better properties.
  • the castings may be used as castings, or they'may be rolled, drawn, forged, extruded, or worked hot or cold in any way into any desired form, such as sheet, rod, wire, tubes, profiles, and shapes.
  • silicon-copper alloys and silicon-copper alloys containing one or more of the metals manganese (up to 4%), tin- (up to 5%), iron (up to 3%), zinc (up to 20%), or selenium (up to 4%). These are the ones which appear to be of the most commercial value at present.-
  • a copper-base alloy comprising 0.1% to 5.0% silicon, 0.005% to 4.5% boron, and balance sub- 1 stantially all copper.
  • a copper-base alloy comprising 1% to 4% silicon, 0.005% to 0.5% boron, and balance substantially all copper.
  • a copper alloy comprising 0.1% to 5.0% silicon, 0.005% to 4.5% boron, and balance principally copper and at least 90.5% or over, and

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Sliding-Contact Bearings (AREA)

Description

Patented a. 10, 1939 UNITED STATES PATENT OFFICE COPPER. ALLOY Horace F. Sillimau, Waterbury, Conm, assignor to The American Brass Company,
Waterbury,
Oonn., a corporation or Connecticut No Drawing. Application July Serial No. 210,891
3 Claims. (01. 75-160) My invention relates to the alloys of copper and more particularly to the copper-base alloys' are added to impart certain properties.
I have discovered that boron added to the copper-silicon alloys improves them. For example, the addition of boron to copper-silicon alloys permits a close control of the grain size. Also, the addition of boron has a fluxing effect so that the alloys flow more readily in casting and welding; A further advantage gained from the pres ence of boron in the composition that the scale formed on the surface of the alloy annealed in an oxygen-bearing atmosphere is reduced in quantity and modified in composition so that it can be removed more easily. In relatively larger amounts the boron has the added value of improving the resistance of the alloys to mechanical wear.
To illustrate the grain refining efiect of boron, there is given below a table showing the grain size of three copper-siliconsmanganese alloys, two of which contained boron. The compositions by chemical analysis were:
hot forged, and then coldrolled to .040" ga. strip with anneals at 750 0., as required. The final reduction in thickness by cold rolling was 37.5%. Specimens were cut, annealed for 30 minutes at the temperatures noted and'examined microscopically to determine the grain size. The following table shows that for any given annealing temperature, the boron is present.
- Diameter of, average grain-mm.
grain size will be smaller when Alloy Annealing temperature O.
Testsof the copper-silicon-manganese alloys with and without boron additions show that the tensile strength is increased somewhat by the boron. For example, the hard-rolled samples of Allo'y #771 without boron had a tensile strength of 100,000 lb./sq. in. while Alloy #775 with 0.58% boron and in the same gauge andtemper had a tensile strength of 112,000 lb./sq. in.-
It is well known that boigax and boric acid anhydrid'eare an important constituent of practically all welding and brazing fluxes. I have found that when boron is present in the siliconcopper alloys, some of it oxidizes to boric acid anhydride when the alloys are melted, and has a fiuxing eifect. The boric anhydride is a mobile, non-volatile liquid at the casting, brazing, and welding temperatures employed, and has a great solvent power for other oxides. Furthermore, boron itself is so active chemically that it actually reduces the oxides of many metals such as iron, tin, manganese, zinc, copper, and others, thus producing cleaner and more ductile alloys.
Boron renders the alloy very free flowing as compared to the alloy without the boron. All these things result in sounder metal with better surfaces whenever theboron-bearing alloys are cast. or welded. Because of this fluxing efiect and the grain refining effect as well as the increased fluidity these alloys make very good solders and welding rods. 7
Phosphorus is an efficient deoxidizer for copper alloys but it has the disadvantage as compared to boron) that the phosphoric acid anhydride produced beginsto sublime at 347 C. so that the protective liquid covering and oxidesolvent jefi'ect is not obtained with the phosphorus as it is with boron.
One of the mosttroublesomeieatures in the production of silicon-copper alloys in wrought forms is the pickling operation necessary for removing the film of oxide formed when the alloy is annealed in atmospheres containing oxygen. This scale resists attack by acids such as those used in pickling brass, for example. When stronger or hotter acid is used the surfaces of the silicon-copper alloys become roughened by the etching before the scale has been removed. I have found that when a small amount of boron is present in the silicon-copper alloy, the pickling operation is much easier and quicker. The presence of boron modifies the scale so that it can be removed by acids which do not etch the underlying metal.
This may be due partly to the fact that the scale has a different coefiicient of expansion than the metal, and cracks into small pieces on cooling, and partly due to the fact that the scale is made up of more easily soluble boron-bearing compounds.
One further advantage of having boron present in the silicon-copper alloys is that it increases their wear resistance. The boron in amounts up to 2% and higher forms numerous, vsmall, hard particles of an intermetallic compound uniformly distributed throughout the alloy, but the matrix of the alloy is comparatively soft. This structure is similar to that of the white alloys commonly used for bearing materials, and its greater hardness results in a greatly superior wear resistance.
In producing my new alloys, I melt and alloy the copper-silicon, and other metals in the customary manner. I then add to the melt a boron alloy such as cupro-boron, ferro-boron, manganose boron, or boron itself. It is. a difficult matter to introduce boron into copper alloys with most of the available boron alloys and compounds, but I have obtained excellent results with an alloy of boron 2% to balance copper. I may also add the boron by one of the methods of my copending application for a process for producing boron-copper alloys, Serial No. 188,471, filed February 3,1938.
The ,quantity of boron introduced may vary from .005% up to about 4.5%. Usually I prefer to keep the quantity as low as possible to save expense, the preferred range being up to about 0.5% as this is suflicient for most applications. The range of silicon may be from 0.1% to 5%, the preferred range being 1% to 4% as this is the range of alloys which are the more easily workable and have the better properties.
After the boron has been added, I bring the melt to the proper pouring temperature and cast it in suitable molds. Thereafter the castings may be used as castings, or they'may be rolled, drawn, forged, extruded, or worked hot or cold in any way into any desired form, such as sheet, rod, wire, tubes, profiles, and shapes.
I have mentioned silicon-copper alloys and silicon-copper alloys containing one or more of the metals manganese (up to 4%), tin- (up to 5%), iron (up to 3%), zinc (up to 20%), or selenium (up to 4%). These are the ones which appear to be of the most commercial value at present.-
Other elements may also be present such for example as cadmium (up to about 3%) lead (up to about 5%), aluminum (up to and magneslum (up to 2%) It is at once obvious to those skilled in the art that the advantagesresultingfrom the presence of boron are due to the boron alone, and not to the presence of other elements. Therefore, I consider that any of the numerous possible copperbase alloys of silicon and boron fall within the scope of this invention.
Having thus set forth the nature of my invention, what I claim is:
1. A copper-base alloy comprising 0.1% to 5.0% silicon, 0.005% to 4.5% boron, and balance sub- 1 stantially all copper.
2. A copper-base alloy comprising 1% to 4% silicon, 0.005% to 0.5% boron, and balance substantially all copper.
3. A copper alloy comprising 0.1% to 5.0% silicon, 0.005% to 4.5% boron, and balance principally copper and at least 90.5% or over, and
US216891A 1938-07-01 1938-07-01 Copper alloy Expired - Lifetime US2175223A (en)

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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3293029A (en) * 1963-08-05 1966-12-20 Eutectic Welding Alloys Wear-facing alloy
US3496682A (en) * 1964-05-05 1970-02-24 Eutectic Welding Alloys Composition for producing cutting and/or wearing surfaces
DE4404406A1 (en) * 1994-02-11 1995-08-17 Degussa Hard solder on the basis of copper@ for soldering porous sinter steels
US20040261913A1 (en) * 2003-04-30 2004-12-30 Kiyohito Ishida Copper alloy

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3293029A (en) * 1963-08-05 1966-12-20 Eutectic Welding Alloys Wear-facing alloy
US3496682A (en) * 1964-05-05 1970-02-24 Eutectic Welding Alloys Composition for producing cutting and/or wearing surfaces
DE4404406A1 (en) * 1994-02-11 1995-08-17 Degussa Hard solder on the basis of copper@ for soldering porous sinter steels
US20040261913A1 (en) * 2003-04-30 2004-12-30 Kiyohito Ishida Copper alloy

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