US20240263277A1 - Lead-free free-cutting beryllium copper alloy - Google Patents
Lead-free free-cutting beryllium copper alloy Download PDFInfo
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- US20240263277A1 US20240263277A1 US18/609,350 US202418609350A US2024263277A1 US 20240263277 A1 US20240263277 A1 US 20240263277A1 US 202418609350 A US202418609350 A US 202418609350A US 2024263277 A1 US2024263277 A1 US 2024263277A1
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- 229910000881 Cu alloy Inorganic materials 0.000 title claims abstract description 137
- DMFGNRRURHSENX-UHFFFAOYSA-N beryllium copper Chemical compound [Be].[Cu] DMFGNRRURHSENX-UHFFFAOYSA-N 0.000 title claims abstract description 78
- 238000005520 cutting process Methods 0.000 title claims abstract description 72
- 229910000765 intermetallic Inorganic materials 0.000 claims abstract description 47
- 239000011159 matrix material Substances 0.000 claims abstract description 16
- 239000010949 copper Substances 0.000 claims abstract description 12
- 229910052710 silicon Inorganic materials 0.000 claims abstract description 12
- 229910052790 beryllium Inorganic materials 0.000 claims abstract description 10
- 239000012535 impurity Substances 0.000 claims abstract description 9
- 238000012360 testing method Methods 0.000 claims description 8
- 238000004458 analytical method Methods 0.000 claims description 3
- 238000010894 electron beam technology Methods 0.000 claims description 3
- 239000000463 material Substances 0.000 description 34
- 238000001878 scanning electron micrograph Methods 0.000 description 27
- 239000000523 sample Substances 0.000 description 25
- 235000019589 hardness Nutrition 0.000 description 16
- 238000010438 heat treatment Methods 0.000 description 12
- 238000005259 measurement Methods 0.000 description 10
- 238000000137 annealing Methods 0.000 description 9
- 239000000203 mixture Substances 0.000 description 9
- 230000032683 aging Effects 0.000 description 8
- 238000000265 homogenisation Methods 0.000 description 8
- 238000005482 strain hardening Methods 0.000 description 8
- 238000009826 distribution Methods 0.000 description 7
- 238000004453 electron probe microanalysis Methods 0.000 description 7
- 238000013507 mapping Methods 0.000 description 7
- 239000002994 raw material Substances 0.000 description 7
- 238000011156 evaluation Methods 0.000 description 6
- 229910052759 nickel Inorganic materials 0.000 description 6
- 238000000921 elemental analysis Methods 0.000 description 5
- 229910052742 iron Inorganic materials 0.000 description 5
- 229910001369 Brass Inorganic materials 0.000 description 4
- 239000010951 brass Substances 0.000 description 4
- 239000000470 constituent Substances 0.000 description 4
- 239000013078 crystal Substances 0.000 description 4
- 238000005430 electron energy loss spectroscopy Methods 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 238000000851 scanning transmission electron micrograph Methods 0.000 description 4
- 229910045601 alloy Inorganic materials 0.000 description 3
- 239000000956 alloy Substances 0.000 description 3
- 238000005266 casting Methods 0.000 description 3
- 238000010586 diagram Methods 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 238000000550 scanning electron microscopy energy dispersive X-ray spectroscopy Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 230000002411 adverse Effects 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 230000001419 dependent effect Effects 0.000 description 2
- 238000000635 electron micrograph Methods 0.000 description 2
- 230000001747 exhibiting effect Effects 0.000 description 2
- 238000010884 ion-beam technique Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 241000252073 Anguilliformes Species 0.000 description 1
- 229910020630 Co Ni Inorganic materials 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 101000993059 Homo sapiens Hereditary hemochromatosis protein Proteins 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- ATBAMAFKBVZNFJ-UHFFFAOYSA-N beryllium atom Chemical group [Be] ATBAMAFKBVZNFJ-UHFFFAOYSA-N 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 229910052797 bismuth Inorganic materials 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 235000019646 color tone Nutrition 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000009749 continuous casting Methods 0.000 description 1
- 238000012937 correction Methods 0.000 description 1
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- 238000013480 data collection Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 238000000445 field-emission scanning electron microscopy Methods 0.000 description 1
- 238000005242 forging Methods 0.000 description 1
- 229910052745 lead Inorganic materials 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 229910052761 rare earth metal Inorganic materials 0.000 description 1
- 238000000992 sputter etching Methods 0.000 description 1
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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
-
- 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
- C22C9/10—Alloys based on copper with silicon as the next major constituent
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22F—CHANGING THE PHYSICAL STRUCTURE OF NON-FERROUS METALS AND NON-FERROUS ALLOYS
- C22F1/00—Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working
- C22F1/08—Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working of copper or alloys based thereon
Definitions
- the present invention relates to a lead-free free-cutting beryllium copper alloy.
- Patent Literature 1 JPS50-139017A discloses a quaternary copper alloy for spring materials, composed of from 0.5% to 1.5% of Be, from 0.2% to 3.0% of Sn, from 0.5% to 2.0% of Si, and the balance being Cu and inevitable impurities as an example of beryllium copper alloys.
- a free-cutting beryllium copper alloy (UNS No.: C17300) is generally known as a beryllium copper alloy with superior machinability. This alloy is improved in machinability by allowing beryllium copper to contain from about 0.2% to 0.6% by weight of lead (Pb).
- Patent Literature 2 JPS54-30369B discloses a free-cutting beryllium copper alloy as such a copper alloy, in which a copper alloy containing 0.5% to 4% by weight of Be is allowed to contain from 0.01% to 3% by weight of one selected from Pb, Te, and Bi, from 0.01% to 5% by weight of rare earth elements, and from 0.1% to 5% by weight of Al or Si.
- Patent Literature 3 JP2000-119775A discloses a leadless free-cutting copper alloy defined by an alloy composition composed of from 69% to 79% by weight of Cu, from 2.0% to 4.0% by weight of Si, and the balance consisting of Zn.
- Patent Literature 4 JP2021-42459A discloses a free-cutting copper alloy containing from 58.5 mass % to 63.5 mass % of Cu, from more than 0.4 mass % to 1.0 mass % of Si, from 0.003 mass % to 0.25 mass % of Pb, from 0.005 mass % to 0.19 mass % of P, and the balance composed of Zn and inevitable impurities.
- Lead-containing copper alloys including free-cutting beryllium copper alloys as disclosed in Patent Literature 2 are superior in machinability, as described above, and accordingly have been conventionally used as a constituent material of various products.
- lead is a harmful substance that adversely affects the human body and environment, and its use has tended to be greatly restricted in recent years.
- lead-free free-cutting brass has been developed, as disclosed in Patent Literatures 3 and 4.
- beryllium copper alloys however, there is no practical free-cutting material free from lead, and lead-free free-cutting beryllium copper alloys have been long awaited to be developed.
- the present inventors have recently found that a specific microstructure formed by allowing a beryllium copper alloy containing from 1.80% to 2.10% by weight of Be to contain from 0.10% to 3.00% by weight of Si can provide a lead-free beryllium copper alloy exhibiting superior machinability.
- an object of the present invention is to provide a lead-free free-cutting beryllium copper alloy that is superior in machinability.
- the present invention provides the following aspects:
- a lead-free free-cutting beryllium copper alloy consisting of:
- the lead-free free-cutting beryllium copper alloy according to any one of aspects 1 to 3, wherein when a cross section of the lead-free free-cutting beryllium copper alloy is observed, the Co—Be—Si intermetallic compound grains have a cross-sectional area from 0.3 to 70 ⁇ m 2 per grain.
- the lead-free free-cutting beryllium copper alloy according to any one of aspects 1 to 4, wherein when a cross section of swarf generated by cutting the lead-free free-cutting beryllium copper alloy is observed along a longitudinal direction, the cross section of the swarf has a sheared profile with zigzag-shaped unevenness that satisfies a relationship 1.10 ⁇ h 2 /h 1 ⁇ 6.60, wherein h 1 represents the average of distances between recesses in the zigzag-shaped unevenness, and h 2 represents the average of heights of protrusions in the unevenness.
- the lead-free free-cutting beryllium copper alloy according to any one of aspects 1 to 5, wherein in a phase map of 75 ⁇ m ⁇ 75 ⁇ m field of view obtained by electron beam backscatter diffraction (EBSD) analysis of a cross section of the lead-free free-cutting beryllium copper alloy, the percentage of area S BCC of BCC regions identified as body-centered cubic (BCC) lattices relative to the sum of area S FCC of FCC regions identified as face-centered cubic (FCC) lattices and area S BCC , that is, 100 ⁇ S BCC /(S FCC +S BCC ), is 5% or more.
- EBSD electron beam backscatter diffraction
- FIG. 1 depicts sectional SEM images and SEM-EDX results of copper alloy samples of Examples 4, 6, and 7.
- FIG. 2 A depicts sectional SEM images of the copper alloy sample (Si: 1.09% by weight) of Example 6 at varying magnifications.
- FIG. 2 B depicts EPMA mapping images of Example 6 measured in the region corresponding to the SEM image in the lower right of FIG. 2 A .
- FIG. 3 A depicts sectional SEM images of the copper alloy sample (Si: 2.98% by weight) of Example 7 at varying magnifications.
- FIG. 3 B depicts EPMA mapping images of Example 7 measured in the region corresponding to the SEM image in the lower right of FIG. 3 A .
- FIG. 3 C depicts EPMA mapping images of Example 7 measured in the region corresponding to the SEM image in the lower right of FIG. 3 A .
- FIG. 4 A depicts sectional STEM images of the copper alloy sample (Si: 1.09% by weight) of Example 6 at varying magnifications.
- FIG. 5 A depicts a CCD image of the copper alloy sample (Si: 0.29% by weight) of Example 4 and the hardness distribution in the rectangular region of the CCD image.
- FIG. 5 B depicts a histogram of the hardness distribution of intermetallic compound grains measured for the copper alloy sample (Si: 0.29% by weight) of Example 4.
- FIG. 6 depicts a sectional SEM image of the copper alloy sample (Si: 2.98% by weight) of Example 7.
- FIG. 7 depicts schematic diagrams illustrating the method of cutting a copper alloy sample in machinability evaluation 1 for the Examples.
- FIG. 8 A depicts SEM images in observing cross sections of swarf from copper alloy samples in Examples 2 to 4.
- FIG. 8 B depicts SEM images in observing cross sections of swarf from copper alloy samples in Examples 5 to 7.
- FIG. 9 depicts a schematic diagram illustrating distance h 1 between recesses and the largest height h 2 of the protrusions in the unevenness at a cross section of swarf in machinability evaluation 1 for the Examples.
- FIG. 10 depicts a schematic diagram illustrating the method of cutting a copper alloy sample in machinability evaluation 2 for the Examples.
- FIG. 11 depicts Table 2 presenting sectional SEM images of copper alloy samples of Examples 1 and 5 to 7 and EBSD phase maps of the regions corresponding to the respective sectional SEM images, each together with the area percentage of the BCC region and the cutting resistance (thrust force).
- the lead-free free-cutting beryllium copper alloy according to the present invention consists of from 1.80% to 2.10% by weight of Be, from 0.10% to 3.00% by weight of Si, from 0.20% to 0.40% by weight of Co, from 0% to 0.10% by weight of Fe, from 0% to 0.10% by weight of Ni, and the balance being Cu and inevitable impurities.
- lead-free free-cutting beryllium copper alloy contains no lead (Pb).
- This copper alloy has a matrix phase being an ⁇ phase, a Si-rich phase being a ⁇ phase rich in Si, and Co—Be—Si intermetallic compound grains.
- the Co—Be—Si intermetallic compound grains contain Co, Be, and Si, and optionally Fe and/or Ni.
- a specific microstructure formed by allowing a beryllium copper alloy containing from 1.80% to 2.10% by weight of Be to contain from 0.10% to 3.00% by weight of Si can provide a lead-free beryllium copper alloy exhibiting superior machinability.
- Lead-containing copper alloys including free-cutting beryllium copper alloys, are superior in machinability, as described above, and accordingly have been conventionally used as a constituent material of various products.
- lead is a harmful substance that adversely affects the human body and environment, and its use has tended to be greatly restricted in recent years.
- the lead-free free-cutting beryllium copper alloy of the present invention can solve the above issue favorably. More specifically, allowing a beryllium copper alloy to contain Si reduces the cutting resistance of the beryllium copper alloy.
- the swarf produced by cutting beryllium copper alloys containing Si is easy to shear into chips and unlikely to wind around the tool.
- the beryllium copper alloy of the present invention exhibits superior machinability not only in terms of reducing cutting resistance but also in terms of improving the shapes of the swarf.
- “lead-free” in the lead-free free-cutting beryllium copper alloy means that the lead content is lower than or equal to the detection limit in the elemental analysis of the copper alloy.
- Si-rich phases and Co—Be—Si intermetallic compound grains containing Si probably serve as a stress concentration origin of shear failure to facilitate the braking of the swarf into smaller pieces.
- Be imparts superior fundamental performance (strength, workability, fatigue properties, heat resistance, corrosion resistance, etc.) as beryllium copper alloy to copper alloy.
- the Be content of the copper alloy of the present invention is from 1.80% to 2.10% by weight and is preferably from 1.80% to 2.00% by weight. A Be content in such a range can lead to the above-mentioned fundamental performance effectively and prevent excess Be from reducing electric conductivity.
- Si forms Si-rich phases and Co—Be—Si intermetallic compound grains to impart superior machinability to beryllium copper alloy.
- the Si content of the copper alloy of the present invention is from 0.10% to 3.00% by weight, preferably from 0.30% to 2.50% by weight, more preferably from 0.45% to 2.50% by weight, still more preferably from 0.50% to 2.20% by weight, particularly preferably from 0.80% to 2.00% by weight and is, for example, from 1.00% to 2.00% by weight.
- a Si content in such a range can improve machinability effectively and prevent excess Si from reducing productivity (causing cracking during forging) in actual operations.
- the Si content of the copper alloy can be preferably from 0.45% to 3.00% by weight, more preferably from 0.50% to 3.00% by weight, particularly preferably from 1.00% to 3.00% by weight, for example, from 2.00% to 3.00% by weight.
- Co forms Co—Be—Si intermetallic compound grains to impart superior machinability to beryllium copper alloy.
- the Co content of the copper alloy of the present invention is from 0.20% to 0.40% by weight, preferably from 0.20% to 0.35% by weight, more preferably from 0.22% to 0.30% by weight, and particularly preferably from 0.22% to 0.28% by weight.
- a Co content in such a range enables effective crystal refinement and the improvement of copper alloy properties and can prevent excess Co from reducing productivity in actual operations.
- Fe and Ni are optional elements that may be considered as impurities in the copper alloy of the present invention, and desired to be as little as possible because high Fe and Ni contents degrade mechanical properties. Accordingly, the Fe and Ni contents of the copper alloy of the present invention are each from 0% to 0.10% by weight, preferably from 0% to 0.005% by weight.
- the copper alloy of the present invention has a microstructure including a matrix phase, Si-rich phases, and Co—Be—Si intermetallic compound grains.
- the Si-rich phases are present in the matrix phase
- the Co—Be—Si intermetallic compound grains are present at the interfaces between the Si-rich phases and the matrix phase.
- the matrix phase is defined by an ⁇ phase and contributes to the superior fundamental performance (strength, workability, fatigue properties, heat resistance, corrosion resistance, etc.) as beryllium copper alloy.
- a Si-rich phase is defined by a ⁇ phase rich in Si and contributes to improving the machinability.
- the presence of Si in the matrix phase improves shearability and facilitates breaking the swarf into smaller pieces.
- the expression “rich in Si” means that Si is detected in a higher concentration in the elemental analysis than in the matrix phase (a phase) and not necessarily in a higher concentration than in Co—Be—Si intermetallic compound grains.
- the matrix phase has a face-centered cubic (FCC) lattice crystal structure
- the Si-rich phase has a body-centered cubic (BCC) lattice crystal structure.
- the BCC structure is unlikely to deform and more shearable than the FCC structure. This means that Si-rich phases having a BCC structure can also contribute to improving the machinability.
- the percentage of area S BCC of BCC regions identified as body-centered cubic (BCC) lattices relative to the sum of area S FCC of FCC regions identified as face-centered cubic (FCC) lattices and area S BCC of BCC regions is preferably 5% or more, more preferably from 5 to 40%, still more preferably from 10 to 30%, particularly preferably from 15 to 30%, and most preferably from 15 to 25%.
- the EBSD measurement can be conducted according to the procedure and conditions described in the Examples below.
- Co—Be—Si intermetallic compound grains also contribute to improving the machinability.
- the Co—Be—Si intermetallic compound grains contain Co, Be, and Si, and optionally Fe and/or Ni.
- Co—Be—Si intermetallic compound grains contain Co, Be, and Si as essential elements, and these elements are dominant.
- Fe and Ni are optional elements or trace elements that can be considered impurities, as mentioned above and are, therefore, not considered dominant in the Co—Be—Si intermetallic compound grains.
- the Co—Be—Si intermetallic compound grains preferably have a hardness from 1.0 to 12.0 GPa, more preferably from 1.5 to 7.5 GPa, and still more preferably from 2.0 to 6.0 GPa as measured by a nanoindentation test in accordance with ISO14577. Having a hardness in such a range achieves machinability effectively.
- the nanoindentation test measures hardness in a small region at many points, and the resulting hardnesses have a wide distribution. Therefore, 100% of the measured points of the Co—Be—Si intermetallic compound grains need not be within the above ranges as long as the majority (for example, 90% or more) is within the above ranges. Hence, it is acceptable that the distribution of measured hardnesses includes hardnesses less than 1.0 GPa or higher than 12.0 GPa to a small extent (for example, less than 10%).
- the number of Co—Be—Si intermetallic compound grains is not limited, provided that the machinability of the beryllium copper alloy can be improved without impairing the above-described fundamental performance. From the viewpoint of improving machinability more effectively, the number of Co—Be—Si intermetallic compound grains at a cross section of the copper alloy is preferably 320 or less per unit area of 1 mm 2 , more preferably from 50 to 300, and still more preferably from 80 to 200.
- the shape of Co—Be—Si intermetallic compound grains is not limited to spherical and may be plate-like, rod-shaped, needle-shaped, or in variant shapes without limitation. Accordingly, the size of the Co—Be—Si intermetallic compound grains is preferably specified by cross-sectional area rather than by diameter.
- the Co—Be—Si intermetallic compound grains have a cross-sectional area preferably from 0.3 to 70 ⁇ m 2 per grain, more preferably from 1.0 to 65 ⁇ m 2 , and still more preferably from 5.0 to 60 ⁇ m 2 .
- the copper alloy of the present invention has superior machinability, as described above, and when a cross section of the swarf generated by cutting the copper alloy is observed along a longitudinal direction, the cross section of the swarf has a sheared profile with zigzag-shaped unevenness.
- the zigzag-shaped unevenness preferably satisfies the relationship 1.10 ⁇ h 2 /h 1 ⁇ 6.60, more preferably 2.0 ⁇ h 2 /h 1 ⁇ 6.6, and still more preferably 2.5 ⁇ h 2 /h 1 ⁇ 6.6, wherein as depicted in FIGS.
- h 1 represents the average of distances between recesses in the zigzag-shaped unevenness
- h 2 represents the average of heights of the protrusions in the unevenness.
- the lead-free free-cutting beryllium copper alloy of the present invention can be preferably produced by, but not limited to, (a) melting and casting of raw materials for the above-described composition; (b) homogenization heat treatment; (c) hot working; (d) cold working; (e) solution annealing; and (f) aging treatment, in this order.
- the preferred aspects of copper alloys have been described above, and thus descriptions will be omitted here.
- one or more raw materials whose constituents are adjusted to result in the above-described composition are melted into a copper alloy molten metal. If a given element is added, the element alone, a master alloy, or the like can be added to the raw material. Alternatively, a raw material containing such additive elements may be melted together with a copper raw material.
- the copper alloy molten metal whose constituents are adjusted to result in the above-described composition is poured into a mold to form an ingot.
- continuous casting is preferred.
- a (cylindrical, for example) ingot (billet) can be produced.
- the resulting ingot is subjected to homogenization heat treatment. That is, the ingot is homogenized by heating.
- the heating temperature of the ingot is preferably in the range of 500 to 900° C., and the temperature is preferably held in this range for a period from 1 to 24 hours.
- the resulting hot-worked material is cold-worked into a cold-worked material with a predetermined diameter.
- the cold working percentage is preferably from 0.5 to 95%.
- the hot-worked material may be optionally annealed for softening to improve workability.
- annealing conditions are not limited, the heating temperature is preferably in the range from 500 to 900° C., and the temperature is preferably held in this range for a period from 0.2 to 6 hours.
- the resulting cold-worked material is subjected to solution annealing to uniformly dissolve the elements in the material, yielding a solution-annealed material.
- the solution annealing temperature is preferably in the range from 600 to 900° C., and the temperature is preferably held in this range for a period from 0.2 to 3 hours.
- the resulting solution-annealed material is subjected to aging treatment to obtain the beryllium copper alloy of the present invention.
- the aging temperature is preferably in the range from 200 to 500° C., and the temperature is preferably held in this range for a period from 0.2 to 3 hours.
- the solution-annealed material may be optionally subjected to cold working or oxide coating removal. At this time, the cold working conditions are not limited, but the working percentage is preferably from 0.5 to 95%.
- the lead-free beryllium copper alloy with superior machinability can be favorably produced through the above steps (a) to (f).
- Beryllium copper alloys were produced according to the following procedure and evaluated.
- a copper alloy raw material that can provide the compositions presented in Table 1 was prepared.
- the copper alloy raw material was melted, and the resulting molten metal was poured into a mold to form a cylindrical ingot (billet).
- the resulting ingot was held at 800° C. for 4 hours for homogenization heat treatment.
- the ingot subjected to homogenization heat treatment was annealed at 800° C. for 1 hour and then hot-worked into a cylindrical hot-worked material with a diameter of 1.8 cm.
- the material Before hot-working into a hot-worked material, the material was annealed at 800° C. for 1 hour and then subjected to cold-working at a working percentage of 40% into a cylindrical cold-worked material with a diameter of 1.4 cm.
- the resulting cold-worked material was subjected to solution annealing at 800° C. for 1 hour to yield a solution-annealed material.
- the solution-annealed material was cold-worked at a working percentage of 38%.
- the resulting solution-annealed material was subjected to aging treatment at 320° C. for 2 hours to yield a cylindrical beryllium copper alloy sample with a diameter of 1.1 cm and a length of 100 cm.
- the resulting beryllium copper alloy sample (hereinafter referred to as a copper alloy sample) was evaluated in terms of the following.
- the copper alloy sample was cut into a cross section and sliced with a focused ion beam (FIB).
- the resulting cross section was observed under an SEM (scanning electron microscope), and the cross section was subjected to elemental analysis under the measurement condition of an accelerating voltage of 15 kV with an energy dispersive X-ray analyzer (EDX, model name: JXA-8530FPlus, manufactured by JEOL Ltd.) attached to the SEM.
- EDX energy dispersive X-ray analyzer
- JXA-8530FPlus manufactured by JEOL Ltd.
- the same cross section was also subjected to elemental analysis under the measurement condition of an accelerating voltage of 15 kV with an electron probe microanalyzer (EPMA, model name: JXA-8530FPlus, manufactured by JEOL Ltd.)
- FIG. 1 depicts SEM images of the samples of Examples 4, 6, and 7 and their SEM-EDX results at individual measurement locations.
- FIG. 2 A depicts sectional SEM images of the copper alloy sample (Si: 1.09% by weight) of Example 6 at varying magnifications.
- the three SEM images on the left are secondary electron micrographs, clearly showing fine structures at a surface of the sample, and the three SEM images on the right are backscattered electron composition images (COMPO images), showing contrasts dependent on the atomic numbers. Any of these six SEM images are obtained by observing the same face of the sample.
- FIG. 2 B depicts EPMA mapping images of Example 6 measured in the region corresponding to the SEM image in the lower right of FIG. 2 A .
- FIG. 3 A depicts sectional SEM images of the copper alloy sample (Si: 2.98% by weight) of Example 7 at varying magnifications.
- the three SEM images on the left are secondary electron micrographs, clearly showing fine structures at a surface of the sample, and the three SEM images on the right are backscattered electron composition images (COMPO images), showing contrasts dependent on the atomic numbers. Any of these six SEM images are obtained by observing the same face of the sample.
- FIGS. 3 B and 3 C depict EPMA mapping images of Example 7 measured in the region corresponding to the SEM image in the lower right of FIG. 3 A .
- the copper alloy sample was cut into a cross section and sliced with a focused ion beam (FIB).
- the resulting cross section was observed under the measurement condition at an accelerating voltage of 200 kV under a scanning transmission electron microscope with a spherical aberration correction function (STEM, model name: HD-2700, manufactured by Hitachi High-Tech Corporation).
- STEM spherical aberration correction function
- elemental analysis was performed on the vicinity of interfaces between the matrix phase and the intermetallic compound grains under the measurement condition of 200 kV voltage with an electron energy loss spectrometer (EELS, trade name: Syndicium, manufactured by Gatan Inc.)/energy dispersive X-ray analyzer (EDX, model name: XMAXN 100TLE, manufactured by Oxford Instruments plc) attached to the STEM.
- EELS electron energy loss spectrometer
- EDX energy dispersive X-ray analyzer
- FIG. 4 A depicts sectional STEM images of the copper alloy sample (Si: 1.09% by weight) of Example 6 at varying magnifications
- FIG. 4 B depicts STEM-EELS mapping images of Example 6 measured in the region corresponding to the STEM image in the right end of FIG. 4 A .
- the hardness (GPa) of Co—Be—Si intermetallic compound grains at the cross section of beryllium copper alloys was measured at each microregion by a nanoindentation test. This test was performed in accordance with ISO14577 on samples with a Poisson's ratio of 0.3 under the conditions of 0.25 mN maximum load, 60 ⁇ m (X axis) ⁇ 60 ⁇ m (Y axis) measurement region, and 60 (X axis) ⁇ 60 (Y axis) measurement points using a nanoindenter (trade name: iMicro nanoindenter, manufactured by KLA Corporation). The hardness distribution of the Co—Be—Si intermetallic compound grains thus measured were represented by histograms.
- FIG. 5 A depicts a CCD image of the copper alloy sample (Si: 0.29% by weight) of Example 4 and the hardness distribution in the rectangular region of the CCD image
- FIG. 5 B depicts a histogram of the hardness distribution thus obtained.
- FIG. 6 depicts a sectional SEM image (area of field of view: 48118.52 ⁇ m 2 ) of the copper alloy sample (Si: 2.98% by weight) of Example 7.
- black dots represent Co—Be—Si intermetallic compound grains, and the number of the dots was 15.
- the number of Co—Be—Si intermetallic compound grains present at a cross section was identified as 311 per unit area of 1 mm 2 .
- Copper alloy samples were used as work materials to be cut, and the swarf produced when the work materials were cut with a tool (tool bit) was examined. More specifically, as illustrated in FIG. 7 , a work material 2 was moved in a straight line, and the surface layer at the top of the work material was cut with a tool 4 (as in planing). At this time, the copper alloy was cut under the conditions of 150 m/min cutting speed, a cutting position at a depth of 0.10 mm from the copper alloy surface and 2 mm cutting width, and 5° rake angle. The profile of the cross section of swarf was identified by observing the copper alloy sample at a magnification of 200 times by SEM. The results are presented in Table 1. FIGS.
- the cross section of the swarf desirably has a sheared profile with zigzag-shaped unevenness. This is because when the swarf produced by cutting the copper alloy has such a sheared profile, the swarf is easy to shear into chips and unlikely to wind around the tool. In contrast, when the swarf has an undulatory profile (smoothly uneven profile) rather than a sheared profile, the swarf easily forms strings of cut pieces, which are likely to wind around the tool, reducing productivity.
- FIGS. 8 A and 8 B retain auxiliary lines drawn at this time by hand to calculate the distances.
- the resulting average h 2 was divided by average h 1 to obtain ratio h 2 /h 1 (degree of unevenness). The results are presented in Table 1.
- Copper alloy samples were used as work materials, and the cutting resistance (N) of the work materials when cut with a tool (tool bit) was examined. More specifically, a work material 2 was lowered while being rotated to be spirally cut with a tool 4 , as depicted in FIG. 10 under the test environment and cutting conditions below. At this time, the cutting resistance of the work material was measured with a multi-component force dynamometer (9129AA, manufactured by Kistler Group). The results are presented in Table 1.
- BBT40-HMC25S-75 (manufactured by BIG Daishowa Seiki Co., Ltd.)
- Lubricant YUSHIROKEN FGE 234 (manufactured by Yushiro Chemical Industry Co., Ltd., from 5 to 10% concentration)
- Copper alloy samples of Examples 1 and 5 to 7 were cut and subjected to Ar ion milling to obtain cross sections to be measured.
- the area percentage of BCC phases was measured by EBSD with a scanning electron microscope (FE-SEM, JSM-7800F manufactured by JEOL Ltd.) and an OIM crystal orientation analyzer (OIM Data Collection/OIM, manufactured by TSL Solutions K. K.). This EBSD measurement was conducted under the conditions of 15 kV accelerating voltage and 0.2 ⁇ m step size.
- FIG. 11 presents EBSD phase maps in the region surrounded by the frame in each SEM image.
- FCC face-centered cubic
- BCC body-centered cubic
- the percentage of area S BCC of the BCC regions to the total area of area S FCC of the FCC regions and area S BCC of the BCC regions was calculated to obtain the values presented in Table 2 (see FIG. 11 ).
- Table 2 (see FIG. 11 ) also presents cutting resistances (thrust forces).
- the results presented in Table 2 reveal that the area percentage of BCC phases (that is, Si-rich phases) increases with increasing amount of Si added and that the cutting resistance (particularly thrust force) decreases (that is, machinability improves) with increasing BCC phase area percentage.
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JPS63143247A (ja) * | 1986-12-06 | 1988-06-15 | Ngk Insulators Ltd | 鋳造方法 |
JP3378430B2 (ja) * | 1996-03-28 | 2003-02-17 | 日本碍子株式会社 | 耐熱性および曲げ部の美観に優れる高強度ベリリウム銅合金 |
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