US20100226815A1 - Lead-Free Brass Alloy - Google Patents
Lead-Free Brass Alloy Download PDFInfo
- Publication number
- US20100226815A1 US20100226815A1 US12/400,283 US40028309A US2010226815A1 US 20100226815 A1 US20100226815 A1 US 20100226815A1 US 40028309 A US40028309 A US 40028309A US 2010226815 A1 US2010226815 A1 US 2010226815A1
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- United States
- Prior art keywords
- alloy
- lead
- mpa
- alloys
- tellurium
- 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.)
- Abandoned
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- 229910045601 alloy Inorganic materials 0.000 title claims abstract description 81
- 239000000956 alloy Substances 0.000 title claims abstract description 81
- 229910001369 Brass Inorganic materials 0.000 title claims abstract description 15
- 239000010951 brass Substances 0.000 title claims abstract description 15
- 229910052714 tellurium Inorganic materials 0.000 claims abstract description 19
- PORWMNRCUJJQNO-UHFFFAOYSA-N tellurium atom Chemical group [Te] PORWMNRCUJJQNO-UHFFFAOYSA-N 0.000 claims abstract description 19
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 15
- 239000010949 copper Substances 0.000 claims description 15
- 229910052802 copper Inorganic materials 0.000 claims description 15
- 239000011701 zinc Substances 0.000 claims description 13
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 12
- 229910052725 zinc Inorganic materials 0.000 claims description 12
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 claims description 4
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 3
- 229910052710 silicon Inorganic materials 0.000 claims description 3
- 239000010703 silicon Substances 0.000 claims description 3
- UQBKQFMSHMLFJK-UHFFFAOYSA-N copper;zinc Chemical compound [Cu+2].[Zn+2] UQBKQFMSHMLFJK-UHFFFAOYSA-N 0.000 claims 1
- 239000000203 mixture Substances 0.000 description 13
- 238000000034 method Methods 0.000 description 11
- 239000000047 product Substances 0.000 description 8
- 230000008901 benefit Effects 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 6
- 230000009467 reduction Effects 0.000 description 5
- 239000007795 chemical reaction product Substances 0.000 description 4
- 230000008569 process Effects 0.000 description 4
- 238000001125 extrusion Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000009428 plumbing Methods 0.000 description 3
- WGACMNAUEGCUHG-VYBOCCTBSA-N (2s)-2-[[(2s)-2-[[(2s)-2-acetamidopropanoyl]amino]propanoyl]amino]-n-[(2s)-6-amino-1-[[(2s)-1-[(2s)-2-[[(2s)-1-[[(2s)-5-amino-1-[[(2s)-1-[[(2s)-1-[[(2s)-6-amino-1-[[(2s)-1-amino-3-(4-hydroxyphenyl)-1-oxopropan-2-yl]amino]-1-oxohexan-2-yl]amino]-3-hydroxy- Chemical compound CC(=O)N[C@@H](C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CO)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CO)C(=O)N[C@@H](CCCCN)C(=O)N[C@H](C(N)=O)CC1=CC=C(O)C=C1 WGACMNAUEGCUHG-VYBOCCTBSA-N 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 238000002386 leaching Methods 0.000 description 2
- 108010074544 myelin peptide amide-12 Proteins 0.000 description 2
- 238000004663 powder metallurgy Methods 0.000 description 2
- 238000004064 recycling Methods 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229910001340 Leaded brass Inorganic materials 0.000 description 1
- 229910000978 Pb alloy Inorganic materials 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- 229910052785 arsenic Inorganic materials 0.000 description 1
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910052797 bismuth Inorganic materials 0.000 description 1
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 238000010622 cold drawing Methods 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 238000003754 machining Methods 0.000 description 1
- 230000007257 malfunction Effects 0.000 description 1
- ZAUUZASCMSWKGX-UHFFFAOYSA-N manganese nickel Chemical compound [Mn].[Ni] ZAUUZASCMSWKGX-UHFFFAOYSA-N 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 230000008520 organization Effects 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 238000005554 pickling Methods 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 231100000167 toxic agent Toxicity 0.000 description 1
- 239000003440 toxic substance Substances 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
- C22C9/04—Alloys based on copper with zinc as the next major constituent
Definitions
- the present invention relates to brass compositions with extremely low to no lead content.
- the compositions exhibit good machinability and strength similar to that of conventional leaded brass alloy free machining brass.
- the lead phase in copper lead alloys can be affected by corrosive attacks with hot organic or mineral oil.
- hot organic or mineral oil For example, when temperature of such an alloy rises, it has been known that the oil can break down to form peroxides and organic gases which effect a degree of leaching on the lead phase within the alloy. If this leaching progresses to any appreciable extent, the component, if it is a bearing or structural component, may eventually malfunction or fail.
- the present invention comprises a brass alloy containing from about 0.20% to 1.5% tellurium as a substitute for lead, typically added to the brass composition.
- the tellurium ranges from about 0.4% to about 1.0%.
- the resulting alloy typically has a lead content of from less than about 0.025% to less than about 0.001% which is considered “lead-free.”
- Brass alloys of the invention typically have a copper content of from about 98% to about 57%, a zinc content of from about 43% to about 2%, a tellurium content of from about 1.0% to about 0.02%, a lead content of from about 0.025% to about 0.001%, and a maximum phosphorous content of about 0.05%.
- the resulting alloys exhibit excellent machinability and conductivity.
- the tensile strength will vary between 240 MPa and 530 MPa and yield strength will vary from about 200 to about 450 MPa.
- Conductivity will range from about 28% to about 49% IACS.
- the machinability of the novel alloys of the invention is similar to that for lead containing compositions. This eliminates or reduces the amount of retooling needed to use the novel alloys to produce finished products such as plumbing fixtures.
- composition of the novel alloys also allows the end product manufacturers to recycle the scrap from the manufacturing process itself. This eliminates the need to return the scrap to the alloy manufacturer for recycling.
- alloys containing less than about 15% zinc exhibit excellent dezincification resistance.
- FIG. 1 is a photomicrograph of the alloy used in Sample C1 after draw.
- FIG. 2 is a photomicrograph of the alloy used in Sample C2 after draw.
- FIG. 3 is a photomicrograph of the alloy used in Sample C3 after draw.
- the brass alloys of the present invention are prepared by first melting copper at a temperature of about 1050° C. Zinc and tellurium are then added to the molten copper. Brass alloy is then cast into billets utilizing horizontal or vertical casting methods.
- the copper used to make the alloys is typically copper cathode or high grade uncontaminated and pure copper scrap comprising 99.95% minimum copper and to 0.05% impurities.
- Lead is a typical impurity, comprising less than 0.025% of the copper used.
- copper comprises from about 57.00 to about 98.00% of the alloy.
- Zinc is the next major component comprising from about 2.00% to about 43.00% of the alloy.
- Tellurium is used as a replacement for lead. Like lead, tellurium is added to improve machinability of the alloy without the negative contribution of lead. Tellurium is added in an amount ranging from about 0.20% to about 1.5% of the alloy. In one series of embodiments, the tellurium ranges from about 0.4 to about 1.0%. In one embodiment, tellurium comprises about 0.5% of the alloy. The amount of tellurium used will depend, in part, on the amount of copper used in the alloy, as copper levels increase the amount of tellurium used with decrease. Like lead, the addition of tellurium to the alloy creates discontinuities in the copper and zinc phases of the alloy like those shown in FIGS. 1-3 . The good dispersion of these discontinuities leads to the improved machinability of the alloys.
- One advantage of the present invention is that the alloys exhibit machinability similar to that of lead containing alloys while using significantly lower amounts of tellurium.
- brass alloys include arsenic, nickel manganese, silicon, and phosphorous. When phosphorous is used, the amount present will typically be less than 0.05% of the alloy.
- the resulting alloys will generally exhibit excellent machinability and conductivity as indicated by Ultimate Tensile Strength (UTS) ranging from about 240 to about 530 MPa and a yield strength of from about 200 MPa to about 450 MPa as determined using ASTM method B 140 .
- UTS Ultimate Tensile Strength
- the actual Tensile strength and Yield strength will depend, in part, on the actual composition of the alloy.
- Conductivity of the alloys will range from about 28 to about 45% IACS.
- the billets were then changed into an extrusion press at a temperature ranging from about 780° C. to about 860° C.
- the billets were then hot extruded through a variety of dies and at different pressures to produce numerous sizes. Each shot was lubricated prior to extrusion and the extrusion dies were preheated. The results are shown in Table 2.
- Conductivity tests were then conducted on various samples. Conductivity diminishes as the ratio of zinc content increases. The results ranged from at least about 28% to about 49% maximum.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Conductive Materials (AREA)
- Contacts (AREA)
- Adornments (AREA)
Abstract
The invention relates to brass alloys that are substantially lead-free. In the alloys of the invention, lead is replaced with tellurium resulting in alloys that exhibit excellent machinability and conductivity.
Description
- The present invention relates to brass compositions with extremely low to no lead content. The compositions exhibit good machinability and strength similar to that of conventional leaded brass alloy free machining brass.
- It has been common practice to add up to 4.5% lead to brass compositions to improve the machinability of the resulting product. Lead, however, is a toxic substance and its use in the production of alloys is surrounded by legislation and expensive control procedures. For example, California adopted legislation which limits the amount of lead in plumbing fixtures to 0.25% or less beginning in 2010.
- Furthermore, the lead phase in copper lead alloys can be affected by corrosive attacks with hot organic or mineral oil. For example, when temperature of such an alloy rises, it has been known that the oil can break down to form peroxides and organic gases which effect a degree of leaching on the lead phase within the alloy. If this leaching progresses to any appreciable extent, the component, if it is a bearing or structural component, may eventually malfunction or fail.
- There is, therefore, considerable advantage in reducing, or if possible, eliminating the contents of lead within powder metallurgy compositions. Various proposals have been put forward for doing this. The considerable proportions of lead incorporated in powder metallurgy materials in the past has resulted in ease of machinability and durability of the resulting product component. Replacement of part of the lead by bismuth has been proposed in International Application published under No. WO91/14012. This results in successful replacement of part of the lead without significant reduction in the machinability. It is, however, accompanied by some reduction of transverse strength of the material. For many purposes this reduction in transverse strength is not a significant problem.
- Another approach has been described in U.S. Pat. No. 5,445,665. In this product 0.1 to 1.5% graphite is added to the alloy allowing for reduction of lead to 2% of the alloy or less.
- While the alloys described above yield substantially lead-free alloys, they do not possess the same machinability as the lead containing alloys. This results in the need for substantial retooling of the equipment used to produce end product, such as plumbing equipment and the like. In addition, the scrap produced during the manufacturing of the lead products often cannot be readily recycled by the end product manufacturer. Recycling typically can only be done by the manufacturer of the alloys. The cost of shipping the scrap back to the initial foundry increases the overall product cost of the end product.
- Thus, there remains a need for a lead-free brass alloy which exhibits machinability similar to that of lead containing products and that can be recycled by the customer.
- The present invention comprises a brass alloy containing from about 0.20% to 1.5% tellurium as a substitute for lead, typically added to the brass composition. In one series of embodiments the tellurium ranges from about 0.4% to about 1.0%. The resulting alloy typically has a lead content of from less than about 0.025% to less than about 0.001% which is considered “lead-free.”
- Brass alloys of the invention typically have a copper content of from about 98% to about 57%, a zinc content of from about 43% to about 2%, a tellurium content of from about 1.0% to about 0.02%, a lead content of from about 0.025% to about 0.001%, and a maximum phosphorous content of about 0.05%.
- The resulting alloys exhibit excellent machinability and conductivity. Depending on the composition of the alloy, the tensile strength will vary between 240 MPa and 530 MPa and yield strength will vary from about 200 to about 450 MPa. Conductivity will range from about 28% to about 49% IACS. The machinability of the novel alloys of the invention is similar to that for lead containing compositions. This eliminates or reduces the amount of retooling needed to use the novel alloys to produce finished products such as plumbing fixtures.
- The composition of the novel alloys also allows the end product manufacturers to recycle the scrap from the manufacturing process itself. This eliminates the need to return the scrap to the alloy manufacturer for recycling. Yet another key feature of the present invention is that the alloys containing less than about 15% zinc exhibit excellent dezincification resistance.
- The foregoing has outlined rather broadly the features and technical advantages of the present invention in order that the detailed description of the invention that follows may be better understood. Additional features and advantages of the invention will be described hereinafter which form the subject of the claims of the invention. It should be appreciated by those skilled in the art that the conception and specific embodiment disclosed may be readily utilized as a basis for modifying or designing other structures for carrying out the same purposes of the present invention. It should also be realized by those skilled in the art that such equivalent constructions do not depart from the spirit and scope of the invention as set forth in the appended claims. The novel features which are believed to be characteristic of the invention, both as to its organization and method of operation, together with further objects and advantages will be better understood from the following description when considered in connection with the accompanying figures. It is to be expressly understood, however, that each of the figures is provided for the purpose of illustration and description only and is not intended as a definition of the limits of the present invention.
-
FIG. 1 is a photomicrograph of the alloy used in Sample C1 after draw. -
FIG. 2 is a photomicrograph of the alloy used in Sample C2 after draw. -
FIG. 3 is a photomicrograph of the alloy used in Sample C3 after draw. - The brass alloys of the present invention are prepared by first melting copper at a temperature of about 1050° C. Zinc and tellurium are then added to the molten copper. Brass alloy is then cast into billets utilizing horizontal or vertical casting methods.
- The copper used to make the alloys is typically copper cathode or high grade uncontaminated and pure copper scrap comprising 99.95% minimum copper and to 0.05% impurities. Lead is a typical impurity, comprising less than 0.025% of the copper used. In the formation of the alloys of the invention, copper comprises from about 57.00 to about 98.00% of the alloy.
- Zinc is the next major component comprising from about 2.00% to about 43.00% of the alloy.
- Tellurium is used as a replacement for lead. Like lead, tellurium is added to improve machinability of the alloy without the negative contribution of lead. Tellurium is added in an amount ranging from about 0.20% to about 1.5% of the alloy. In one series of embodiments, the tellurium ranges from about 0.4 to about 1.0%. In one embodiment, tellurium comprises about 0.5% of the alloy. The amount of tellurium used will depend, in part, on the amount of copper used in the alloy, as copper levels increase the amount of tellurium used with decrease. Like lead, the addition of tellurium to the alloy creates discontinuities in the copper and zinc phases of the alloy like those shown in
FIGS. 1-3 . The good dispersion of these discontinuities leads to the improved machinability of the alloys. - One advantage of the present invention is that the alloys exhibit machinability similar to that of lead containing alloys while using significantly lower amounts of tellurium.
- Other materials which may be added to the brass alloys include arsenic, nickel manganese, silicon, and phosphorous. When phosphorous is used, the amount present will typically be less than 0.05% of the alloy.
- The resulting alloys will generally exhibit excellent machinability and conductivity as indicated by Ultimate Tensile Strength (UTS) ranging from about 240 to about 530 MPa and a yield strength of from about 200 MPa to about 450 MPa as determined using ASTM method B140. The actual Tensile strength and Yield strength will depend, in part, on the actual composition of the alloy. Conductivity of the alloys will range from about 28 to about 45% IACS.
- A series of brass alloys were prepared where the added lead (typically about 2%) was replaced with approximately 0.5% tellurium. The composition of each alloy is shown in Table 1.
-
TABLE 1 Sample Cu Pb Zn Te P Sn A Balance <0.01 5.10 0.5 0.011 — B Balance 0.00 8.82 0.57 .001 — C 83.03 0.06 Balance .052 0.05 0.11 D 59.41 0.02 Balance 0.17 0.05 — - The billets were then changed into an extrusion press at a temperature ranging from about 780° C. to about 860° C. The billets were then hot extruded through a variety of dies and at different pressures to produce numerous sizes. Each shot was lubricated prior to extrusion and the extrusion dies were preheated. The results are shown in Table 2.
-
TABLE 2 Sample Final Draw Size Shot Temp Pressure Length A1 31.75 mm 808° C. 234 MPa 12 m A2 75.40 mm 822° C. 268 MPa 18.5 m A3 19.05 mm 803° C. 305 MPa 34 m B1 31.75 mm 794° C. 267 MPa 12 m B2 25.40 mm 800° C. 289 MPa 18.5 m B3 19.05 mm 806° C. 304 MPa 34 m B4 12.70 mm 870° C. 265 MPa 67 m C1a 25.40 mm 830° C. 298 MPa 18.4 m C1b 25.40 mm 867° C. 280 MPa 18.4 m C2a 50.80 mm 750° C. 230 MPa 21.5 m C3a 22.23 mm AF 830° C. 312 MPa 21.5 m Hex C3b 22.23 mm AF 837° C. 324 MPa 21.5 m Hex D1a 50.8 mm 640° C. 128 MPa 4.6 m D1b 50.80 mm 637° C. 142 MPa 4.6 m D2a 25.4 mm 650° C. 234 MPa 18.4 m D2b 25.4 mm 660° C. 214 MPa 18.4 m D3a 22.23 mm AF 648° C. 235 MPa 21.5 m Hex D3b 22.23 mm 621° C. 276 MPa 21.5 m - The bars were then passed through a bath of sulfuric pickling acid and then cold drawn so as to induce the correct mechanical properties and grain size requirements. Also this process ensures that the correct size tolerances are met. The cold drawing operation was accomplished effortlessly. The products were then tested for tensile strength, hardness, conductivity, and machinability. The results are shown in Table 3.
-
TABLE 3 Ultimate Reduction Tensile Yield Sam- in Area Strength Strength HARDNESS ple (%) (MPa) (MPa) ELONGATION (Rb) A1 11.24 267.9 210.3 30% 56 A2 12.8 296.5 341.3 24% 57 A3 1_.71 322 279.2 16% 60 B1 11.24 302.7 241.3 26% 59 B2 12.8 322 259.2 24% 63 B3 17.71 322.7 268.9 21% 64 B4 28.32 393.7 393 12% 69 C1 12.8 350.2 291.9 20% 51 C2 11.13 354.9 295.8 20% 52 C3 13 358.8 294.1 22% 53 D1 14.10 487.8 378.2 29% 75 D2 14.10 531.6 443 20% 78 D3 14.44 485.3 407.8 19% 76 - Conductivity tests were then conducted on various samples. Conductivity diminishes as the ratio of zinc content increases. The results ranged from at least about 28% to about 49% maximum.
- Photomicrographs of Samples C1, C2 and C3 were taken after draw and are shown in FIGS. 1-3. The micro structure in the alloys were uniform indicating good dispersion of the tellurium throughout the alloy.
- Although the present invention and its advantages have been described in detail, it should be understood that various changes, substitutions and alterations can be made herein without departing from the spirit and scope of the invention as defined by the appended claims. Moreover, the scope of the present application is not intended to be limited to the particular embodiments of the process, machine, manufacture, composition of matter, means, methods and steps described in the specification. As one of ordinary skill in the art will readily appreciate from the disclosure of the present invention, processes, machines, manufacture, compositions of matter, means, methods, or steps, presently existing or later to be developed that perform substantially the same function or achieve substantially the same result as the corresponding embodiments described herein may be utilized according to the present invention. Accordingly, the appended claims are intended to include within their scope such processes, machines, manufacture, compositions of matter, means, methods, or steps.
Claims (19)
1. A brass alloy comprising:
Copper;
Zinc;
Tellurium; and
Lead
wherein lead comprises less than 0.25% of the alloy and the tellurium comprises from about 0.025% to about 1% of the alloy, and
wherein the alloy has a tensile strength of from about 240 MPa to about 530 MPa, and
wherein the alloy is silicon free.
2. The alloy of claim 1 wherein the copper comprises from about 57% to about 98% of the alloy.
3. The alloy of claim 1 wherein the zinc comprises from about 2.0% to about 43% of the alloy.
4. The alloy of claim 1 further comprising less than about 0.02% phosphorous.
5. A brass alloy comprising:
about 57% to about 98% copper;
about 2% to about 43% zinc; and
about 0.025% to about 1.0% tellurium
wherein the alloy has a tensile strength of from about 240 MPa to about 530 MPa, and
wherein the alloy is silicon free.
6. The alloy of claim 5 further comprising less than about 0.025% lead.
7. (canceled)
8. The alloy of claim 1 having a yield strength of from about 200 MPa to about 450 MPa.
9. The alloy of claim 1 having a conductivity of from about 28% to about 49% IACS.
10. The alloy of claim 1 wherein the zinc comprises about 5% of the alloy.
11. The alloy of claim 1 wherein the zinc comprises about 10% of the alloy.
12. The alloy of claim 1 wherein the zinc comprises about 15% of the alloy.
13. The alloy of claim 1 when the zinc comprises about 40% of the alloy.
14. (canceled)
15. The alloy of claim 5 having a lead content of less than about 0.5%.
16. The alloy of claim 5 having a lead content of less than about 0.01%.
17. The alloy of claim 5 having a tensile strength of from about 240 MPa to about 530 MPa.
18. The alloy of claim 5 having a yield strength of from about 200 MPa to about 450 MPa.
19. The alloy of claim 5 having a conductivity of from about 28% to about 49% IACS.
Priority Applications (20)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US12/400,283 US20100226815A1 (en) | 2009-03-09 | 2009-03-09 | Lead-Free Brass Alloy |
KR1020117023686A KR20110131272A (en) | 2009-03-09 | 2009-08-12 | Lead-free brass alloy |
SG2011065042A SG174312A1 (en) | 2009-03-09 | 2009-08-12 | Lead-free brass alloy |
AU2009341842A AU2009341842A1 (en) | 2009-03-09 | 2009-08-12 | Lead-free brass alloy |
ES09841636.5T ES2655893T3 (en) | 2009-03-09 | 2009-08-12 | Lead-free brass alloy |
MX2011009526A MX2011009526A (en) | 2009-03-09 | 2009-08-12 | Lead-free brass alloy. |
JP2011554028A JP2012519781A (en) | 2009-03-09 | 2009-08-12 | Lead-free brass alloy |
CN2009801588751A CN102414337A (en) | 2009-03-09 | 2009-08-12 | Lead-free brass alloy |
PL09841636T PL2406406T3 (en) | 2009-03-09 | 2009-08-12 | Lead-free brass alloy |
RU2011140852/02A RU2011140852A (en) | 2009-03-09 | 2009-08-12 | Lead Free Brass Alloy |
BRPI0924388-7A BRPI0924388B1 (en) | 2009-03-09 | 2009-08-12 | LEAD FREE BRASS ALLOY |
CA2754813A CA2754813A1 (en) | 2009-03-09 | 2009-08-12 | Lead-free brass alloy |
PCT/US2009/053505 WO2010104527A1 (en) | 2009-03-09 | 2009-08-12 | Lead-free brass alloy |
EP09841636.5A EP2406406B1 (en) | 2009-03-09 | 2009-08-12 | Lead-free brass alloy |
US12/759,402 US20100303667A1 (en) | 2009-03-09 | 2010-04-13 | Novel lead-free brass alloy |
IL215077A IL215077A0 (en) | 2009-03-09 | 2011-09-11 | Lead-free brass alloy |
ZA2011/06652A ZA201106652B (en) | 2009-03-09 | 2011-09-12 | Lead-free brass alloy |
CO11131873A CO6450681A2 (en) | 2009-03-09 | 2011-10-06 | LEAD FREE BRONZE ALLOY |
US15/289,580 US20170145544A1 (en) | 2009-03-09 | 2016-10-10 | Lead-Free Brass Alloy |
US18/149,139 US20230151457A1 (en) | 2009-03-09 | 2023-01-02 | Lead-Free Brass Alloy |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US12/400,283 US20100226815A1 (en) | 2009-03-09 | 2009-03-09 | Lead-Free Brass Alloy |
Related Child Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US12/759,402 Continuation-In-Part US20100303667A1 (en) | 2009-03-09 | 2010-04-13 | Novel lead-free brass alloy |
US15/289,580 Continuation US20170145544A1 (en) | 2009-03-09 | 2016-10-10 | Lead-Free Brass Alloy |
Publications (1)
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US20100226815A1 true US20100226815A1 (en) | 2010-09-09 |
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Family Applications (3)
Application Number | Title | Priority Date | Filing Date |
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US12/400,283 Abandoned US20100226815A1 (en) | 2009-03-09 | 2009-03-09 | Lead-Free Brass Alloy |
US15/289,580 Abandoned US20170145544A1 (en) | 2009-03-09 | 2016-10-10 | Lead-Free Brass Alloy |
US18/149,139 Pending US20230151457A1 (en) | 2009-03-09 | 2023-01-02 | Lead-Free Brass Alloy |
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Application Number | Title | Priority Date | Filing Date |
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US15/289,580 Abandoned US20170145544A1 (en) | 2009-03-09 | 2016-10-10 | Lead-Free Brass Alloy |
US18/149,139 Pending US20230151457A1 (en) | 2009-03-09 | 2023-01-02 | Lead-Free Brass Alloy |
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US (3) | US20100226815A1 (en) |
EP (1) | EP2406406B1 (en) |
JP (1) | JP2012519781A (en) |
KR (1) | KR20110131272A (en) |
CN (1) | CN102414337A (en) |
AU (1) | AU2009341842A1 (en) |
BR (1) | BRPI0924388B1 (en) |
CA (1) | CA2754813A1 (en) |
CO (1) | CO6450681A2 (en) |
ES (1) | ES2655893T3 (en) |
IL (1) | IL215077A0 (en) |
MX (1) | MX2011009526A (en) |
PL (1) | PL2406406T3 (en) |
RU (1) | RU2011140852A (en) |
SG (1) | SG174312A1 (en) |
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CN109266900A (en) * | 2018-12-07 | 2019-01-25 | 宁波艾维洁具有限公司 | A kind of Anti-dezincificationyellow yellow brass alloy of lead-free corrosion resistant and preparation method thereof |
US11427891B2 (en) | 2019-07-24 | 2022-08-30 | Nibco Inc. | Low silicon copper alloy piping components and articles |
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- 2009-08-12 EP EP09841636.5A patent/EP2406406B1/en active Active
- 2009-08-12 BR BRPI0924388-7A patent/BRPI0924388B1/en active IP Right Grant
- 2009-08-12 RU RU2011140852/02A patent/RU2011140852A/en unknown
- 2009-08-12 CN CN2009801588751A patent/CN102414337A/en active Pending
- 2009-08-12 ES ES09841636.5T patent/ES2655893T3/en active Active
- 2009-08-12 WO PCT/US2009/053505 patent/WO2010104527A1/en active Application Filing
- 2009-08-12 CA CA2754813A patent/CA2754813A1/en not_active Abandoned
- 2009-08-12 KR KR1020117023686A patent/KR20110131272A/en not_active Application Discontinuation
- 2009-08-12 AU AU2009341842A patent/AU2009341842A1/en not_active Abandoned
- 2009-08-12 MX MX2011009526A patent/MX2011009526A/en not_active Application Discontinuation
- 2009-08-12 JP JP2011554028A patent/JP2012519781A/en active Pending
- 2009-08-12 PL PL09841636T patent/PL2406406T3/en unknown
- 2009-08-12 SG SG2011065042A patent/SG174312A1/en unknown
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2011
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Also Published As
Publication number | Publication date |
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EP2406406A1 (en) | 2012-01-18 |
WO2010104527A1 (en) | 2010-09-16 |
KR20110131272A (en) | 2011-12-06 |
EP2406406A4 (en) | 2015-09-02 |
IL215077A0 (en) | 2011-12-01 |
ES2655893T3 (en) | 2018-02-22 |
SG174312A1 (en) | 2011-10-28 |
US20230151457A1 (en) | 2023-05-18 |
PL2406406T3 (en) | 2018-05-30 |
CN102414337A (en) | 2012-04-11 |
BRPI0924388A2 (en) | 2017-06-06 |
ZA201106652B (en) | 2012-05-30 |
RU2011140852A (en) | 2013-04-20 |
CA2754813A1 (en) | 2010-09-16 |
MX2011009526A (en) | 2011-12-16 |
AU2009341842A1 (en) | 2011-10-06 |
EP2406406B1 (en) | 2017-11-22 |
BRPI0924388B1 (en) | 2021-05-04 |
CO6450681A2 (en) | 2012-05-31 |
US20170145544A1 (en) | 2017-05-25 |
JP2012519781A (en) | 2012-08-30 |
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