JP2008542548A - Aluminum sliding bearing alloy - Google Patents
Aluminum sliding bearing alloy Download PDFInfo
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- JP2008542548A JP2008542548A JP2008515049A JP2008515049A JP2008542548A JP 2008542548 A JP2008542548 A JP 2008542548A JP 2008515049 A JP2008515049 A JP 2008515049A JP 2008515049 A JP2008515049 A JP 2008515049A JP 2008542548 A JP2008542548 A JP 2008542548A
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- 229910052782 aluminium Inorganic materials 0.000 title claims abstract description 31
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 title claims abstract description 30
- 239000001996 bearing alloy Substances 0.000 title claims abstract description 18
- 229910052797 bismuth Inorganic materials 0.000 claims abstract description 36
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 claims abstract description 36
- 238000005096 rolling process Methods 0.000 claims abstract description 19
- 238000010438 heat treatment Methods 0.000 claims abstract description 18
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims abstract description 14
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims abstract description 14
- 229910052802 copper Inorganic materials 0.000 claims abstract description 14
- 239000010949 copper Substances 0.000 claims abstract description 14
- 238000004519 manufacturing process Methods 0.000 claims abstract description 13
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims abstract description 12
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims abstract description 12
- 229910052725 zinc Inorganic materials 0.000 claims abstract description 12
- 239000011701 zinc Substances 0.000 claims abstract description 12
- 238000005266 casting Methods 0.000 claims abstract description 10
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims abstract description 7
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims abstract description 7
- 229910052787 antimony Inorganic materials 0.000 claims abstract description 7
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 claims abstract description 7
- 229910052804 chromium Inorganic materials 0.000 claims abstract description 7
- 239000011651 chromium Substances 0.000 claims abstract description 7
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 claims abstract description 7
- 229910052759 nickel Inorganic materials 0.000 claims abstract description 7
- 229910052726 zirconium Inorganic materials 0.000 claims abstract description 7
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims abstract description 6
- 229910052742 iron Inorganic materials 0.000 claims abstract description 6
- 229910052719 titanium Inorganic materials 0.000 claims abstract description 6
- 239000010936 titanium Substances 0.000 claims abstract description 6
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 claims abstract description 5
- 229910052796 boron Inorganic materials 0.000 claims abstract description 5
- 229910017052 cobalt Inorganic materials 0.000 claims abstract description 5
- 239000010941 cobalt Substances 0.000 claims abstract description 5
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims abstract description 5
- 229910052750 molybdenum Inorganic materials 0.000 claims abstract description 5
- 239000011733 molybdenum Substances 0.000 claims abstract description 5
- 229910052758 niobium Inorganic materials 0.000 claims abstract description 5
- 239000010955 niobium Substances 0.000 claims abstract description 5
- GUCVJGMIXFAOAE-UHFFFAOYSA-N niobium atom Chemical compound [Nb] GUCVJGMIXFAOAE-UHFFFAOYSA-N 0.000 claims abstract description 5
- 229910052720 vanadium Inorganic materials 0.000 claims abstract description 5
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims abstract description 4
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims abstract description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 4
- 229910052684 Cerium Inorganic materials 0.000 claims abstract description 4
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims abstract description 4
- 229910052790 beryllium Inorganic materials 0.000 claims abstract description 4
- ATBAMAFKBVZNFJ-UHFFFAOYSA-N beryllium atom Chemical compound [Be] ATBAMAFKBVZNFJ-UHFFFAOYSA-N 0.000 claims abstract description 4
- 229910052791 calcium Inorganic materials 0.000 claims abstract description 4
- 239000011575 calcium Substances 0.000 claims abstract description 4
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 4
- 229910052706 scandium Inorganic materials 0.000 claims abstract description 4
- SIXSYDAISGFNSX-UHFFFAOYSA-N scandium atom Chemical compound [Sc] SIXSYDAISGFNSX-UHFFFAOYSA-N 0.000 claims abstract description 4
- 229910052709 silver Inorganic materials 0.000 claims abstract description 4
- 239000004332 silver Substances 0.000 claims abstract description 4
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 claims abstract description 4
- 229910052721 tungsten Inorganic materials 0.000 claims abstract description 4
- 239000010937 tungsten Substances 0.000 claims abstract description 4
- GWXLDORMOJMVQZ-UHFFFAOYSA-N cerium Chemical compound [Ce] GWXLDORMOJMVQZ-UHFFFAOYSA-N 0.000 claims abstract 2
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 claims abstract 2
- 229910045601 alloy Inorganic materials 0.000 claims description 38
- 239000000956 alloy Substances 0.000 claims description 38
- 239000000463 material Substances 0.000 claims description 14
- 238000000034 method Methods 0.000 claims description 13
- 238000000576 coating method Methods 0.000 claims description 11
- 239000011248 coating agent Substances 0.000 claims description 10
- 238000009749 continuous casting Methods 0.000 claims description 9
- 238000001816 cooling Methods 0.000 claims description 7
- 239000013078 crystal Substances 0.000 claims description 7
- 238000005275 alloying Methods 0.000 claims description 3
- 239000000203 mixture Substances 0.000 claims description 3
- 239000003795 chemical substances by application Substances 0.000 claims description 2
- 238000002360 preparation method Methods 0.000 claims description 2
- 238000007670 refining Methods 0.000 claims description 2
- 239000011265 semifinished product Substances 0.000 claims description 2
- 239000002245 particle Substances 0.000 abstract description 3
- 239000011135 tin Substances 0.000 description 15
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 14
- 229910052718 tin Inorganic materials 0.000 description 14
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 12
- 239000011133 lead Substances 0.000 description 12
- 229910052710 silicon Inorganic materials 0.000 description 12
- 239000010703 silicon Substances 0.000 description 12
- 238000009826 distribution Methods 0.000 description 10
- 230000000694 effects Effects 0.000 description 8
- 239000011777 magnesium Substances 0.000 description 8
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 7
- 239000010410 layer Substances 0.000 description 7
- 229910052749 magnesium Inorganic materials 0.000 description 7
- 239000011159 matrix material Substances 0.000 description 7
- 229910000831 Steel Inorganic materials 0.000 description 6
- 239000010959 steel Substances 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 5
- 239000002244 precipitate Substances 0.000 description 5
- 229910000838 Al alloy Inorganic materials 0.000 description 4
- 239000000654 additive Substances 0.000 description 3
- 238000000137 annealing Methods 0.000 description 3
- 229910052738 indium Inorganic materials 0.000 description 3
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 description 3
- 239000000155 melt Substances 0.000 description 3
- 239000012791 sliding layer Substances 0.000 description 3
- 238000007711 solidification Methods 0.000 description 3
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 3
- 229910001152 Bi alloy Inorganic materials 0.000 description 2
- YVIMHTIMVIIXBQ-UHFFFAOYSA-N [SnH3][Al] Chemical compound [SnH3][Al] YVIMHTIMVIIXBQ-UHFFFAOYSA-N 0.000 description 2
- -1 aluminum silicon-bismuth Chemical compound 0.000 description 2
- ZMIGMASIKSOYAM-UHFFFAOYSA-N cerium Chemical compound [Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce] ZMIGMASIKSOYAM-UHFFFAOYSA-N 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 241000446313 Lamella Species 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- 229910001128 Sn alloy Inorganic materials 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 239000002318 adhesion promoter Substances 0.000 description 1
- 238000005253 cladding Methods 0.000 description 1
- 238000005345 coagulation Methods 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 230000005672 electromagnetic field Effects 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 238000009830 intercalation Methods 0.000 description 1
- 230000002687 intercalation Effects 0.000 description 1
- 229910000765 intermetallic Inorganic materials 0.000 description 1
- 230000002045 lasting effect Effects 0.000 description 1
- 239000002346 layers by function Substances 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 238000010791 quenching Methods 0.000 description 1
- 230000000171 quenching effect Effects 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000001172 regenerating effect Effects 0.000 description 1
- 238000009991 scouring Methods 0.000 description 1
- 238000005204 segregation Methods 0.000 description 1
- 238000010583 slow cooling Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
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Classifications
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C21/00—Alloys based on aluminium
- C22C21/10—Alloys based on aluminium with zinc as the next major constituent
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22D—CASTING OF METALS; CASTING OF OTHER SUBSTANCES BY THE SAME PROCESSES OR DEVICES
- B22D11/00—Continuous casting of metals, i.e. casting in indefinite lengths
- B22D11/001—Continuous casting of metals, i.e. casting in indefinite lengths of specific alloys
- B22D11/003—Aluminium alloys
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D9/00—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor
- C21D9/40—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor for rings; for bearing races
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C21/00—Alloys based on aluminium
-
- 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
- C22F1/04—Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working of aluminium or alloys based thereon
-
- 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
- C22F1/04—Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working of aluminium or alloys based thereon
- C22F1/053—Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working of aluminium or alloys based thereon of alloys with zinc as the next major constituent
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- Sliding-Contact Bearings (AREA)
Abstract
本発明は、5ないし20重量%のビスマスと、3ないし20重量%の亜鉛と、1ないし4重量%の銅と、さらにマンガン、バナジウム、ニオブ、ニッケル、モリブデン、コバルト、鉄、タングステン、クロム、銀、カルシウム、スカンジウム、セリウム、ベリリウム、アンチモン、ホウ素、チタン、炭素およびジルコニウムのいくつかの成分を合計で5重量%以下と、100重量%にするアルミニウムとを含み、ストリップ鋳造で作られ、後の滑り軸受の製造工程の間、圧延または圧延結合の後に、およそ270ないし400℃の熱処理を受けた偏晶アルミニウム滑り軸受合金に関する。圧延または圧延結合によって作られた長いビスマス粒子またはシートは再凝固して、20μm以下のサイズをもつ微細分布した球状溶滴を与えることができる。
【選択図】 図3The present invention relates to 5 to 20% by weight of bismuth, 3 to 20% by weight of zinc, 1 to 4% by weight of copper, manganese, vanadium, niobium, nickel, molybdenum, cobalt, iron, tungsten, chromium, Made by strip casting, including 5% by weight total of several components of silver, calcium, scandium, cerium, beryllium, antimony, boron, titanium, carbon and zirconium and 100% by weight aluminum, and later The invention relates to a monoclinic aluminum slide bearing alloy that has been subjected to a heat treatment of approximately 270 to 400 ° C. after rolling or roll bonding during the manufacturing process of the present invention. Long bismuth particles or sheets made by rolling or roll bonding can be re-solidified to give finely distributed spherical droplets with a size of 20 μm or less.
[Selection] Figure 3
Description
本発明は高耐久性のアルミニウム軸受合金(特に多層軸受)、その製造方法ならびに関連する滑り軸受シェルおよび滑り軸受に関する。 The present invention relates to a highly durable aluminum bearing alloy (especially a multi-layer bearing), a method of manufacturing the same, and related sliding bearing shells and sliding bearings.
高耐久性滑り軸受は、軸受に必要とされる種々の要求を満たし、かつある程度相容れない、いくつかの層から作られる。主に鋼−アルミニウム複合材料が使用される。鋼の支持シェルは、機械的負荷を吸収し、強固な適合を保証するが、滑り軸受の材料は種々の摩擦負荷および疲労に耐えなければならない。この要求を満たすために、アルミニウムマトリクス中の滑り軸受の材料は、一方で例えばケイ素および金属間析出物のような硬質相と、他方で例えば鉛やスズのような軟質相を含む。高耐久性多層軸受は、しばしば、さらに機能層上に電解被覆された高い鉛含有量の滑り層をもつ。この軟質滑り層は、軸受の良好な緊急動作特性を与える。これは磨耗粒子を埋め込んで、滑り表面からそれらを離脱させることができる。 High durability sliding bearings are made of several layers that meet the various requirements of the bearing and are somewhat incompatible. Mainly steel-aluminum composite material is used. Steel support shells absorb mechanical loads and ensure a tight fit, but the plain bearing material must withstand various friction loads and fatigue. To meet this requirement, the material of the sliding bearing in the aluminum matrix contains on the one hand a hard phase such as silicon and intermetallic precipitates and on the other hand a soft phase such as lead and tin. High durability multilayer bearings often have a high lead content sliding layer that is further electrolytically coated on the functional layer. This soft sliding layer provides good emergency operating characteristics of the bearing. This can embed the wear particles and release them from the sliding surface.
鉛を含んだアルミニウム滑り軸受合金に対する環境に優しい代替物は、アルミニウムスズ−ベースの滑り軸受であり、これは追加の滑り層なしに用いられる。しかしながら、これらの合金の機械的特性、例えば疲労耐性および耐熱性には限界がある。比較的高いスズ含有量は、鋳造の間に粒界にて互いに結合したスズのネットワークの形成をもたらす。これは、特に比較的高温において、これらの合金の耐荷重能力をかなり損なう。 An environmentally friendly alternative to lead-containing aluminum sliding bearing alloys is aluminum tin-based sliding bearings, which are used without an additional sliding layer. However, the mechanical properties of these alloys, such as fatigue resistance and heat resistance, are limited. The relatively high tin content results in the formation of tin networks that are bonded together at grain boundaries during casting. This significantly impairs the load carrying capacity of these alloys, especially at relatively high temperatures.
スズと対比して、ビスマスはアルミニウムマトリクス中の軟質相としていくつかの利点をもつ。例えば、ビスマスは高い融点を持ち、より高い温度で使用することができる。加えて、特別な鋳造および熱処理手段によって、滑り軸受合金の粒界におけるビスマスの塊状濃縮を避け、微細構造中のビスマス溶滴の十分に均質かつ微細な分布を得ることが可能である。これは、アルミニウムスズ合金と比較して、耐荷重能力および摩擦特性の向上を最終的にはもたらす。 In contrast to tin, bismuth has several advantages as a soft phase in the aluminum matrix. For example, bismuth has a high melting point and can be used at higher temperatures. In addition, by special casting and heat treatment means, it is possible to avoid mass concentration of bismuth at the grain boundaries of the sliding bearing alloy and to obtain a sufficiently homogeneous and fine distribution of bismuth droplets in the microstructure. This ultimately results in improved load carrying capacity and friction properties compared to aluminum tin alloys.
そこで、DE 4003018 A1においては、アルミニウム合金は、1ないし50重量%、好ましくは5ないし30重量%の鉛と、3ないし50重量%、好ましくは5ないし30重量%のビスマスと、15ないし50重量%のインジウムのうちの1つ以上の成分と、さらに0.1ないし20重量%のケイ素、0.1ないし20重量%のスズ、0.1ないし10重量%の亜鉛、0.1ないし5重量%のマグネシウム、0.1ないし20重量%の銅、0.05ないし3重量%の鉄、0.05ないし3重量%のマンガン、0.05ないし3重量%のニッケルおよび0.001ないし0.30重量%チタンのうちの1つ以上の成分を含んでもよいことが提案されている。DE 4003018 A1によって知られるこの合金は、連続鋳造によって垂直に鋳造され、厚さまたは直径で5ないし20mmのストリップまたはワイヤーにされ、溶融物は300ないし1500K/sの冷却速度で鋳造される。急冷速度は、マイナー相の大容量析出物が、偏析温度以下への温度降下とマトリクス金属の完全な凝固との間の時間に形成されるのを回避することを意図している。しかしながら、アルミニウム合金の連続鋳造における実際的経験から、非常に速い冷却速度はクラック形成のかなりのリスクがあり、大量生産に要求される加工安定性がかろうじて保証されるにすぎないという結果を与えることがわかっている。 Thus, in DE 4003018 A1, the aluminum alloy is 1 to 50 wt.%, Preferably 5 to 30 wt.% Lead, 3 to 50 wt.%, Preferably 5 to 30 wt.% Bismuth, and 15 to 50 wt. % One or more components of indium and 0.1 to 20% by weight silicon, 0.1 to 20% by weight tin, 0.1 to 10% by weight zinc, 0.1 to 5% by weight % Magnesium, 0.1-20% copper, 0.05-3% iron, 0.05-3% manganese, 0.05-3% nickel and 0.001-0. It has been proposed that one or more components of 30 wt% titanium may be included. This alloy, known from DE 4003018 A1, is cast vertically by continuous casting into strips or wires with a thickness or diameter of 5 to 20 mm, and the melt is cast at a cooling rate of 300 to 1500 K / s. The quenching rate is intended to avoid the formation of large volume precipitates of minor phase at a time between the temperature drop below the segregation temperature and the complete solidification of the matrix metal. However, practical experience in continuous casting of aluminum alloys gives the result that very fast cooling rates are a significant risk of crack formation and only guarantee the processing stability required for mass production. I know.
EP 0940474 A1に記載されている方法は、15重量%以下のビスマスと、ケイ素、スズ、および亜鉛を含む群からの少なくとも1つの成分を合計で0.5ないし15重量%と、銅、マンガン、マグネシウム、ニッケル、クロム、亜鉛およびアンチモンを含む群からの可能な添加物を合計3重量%以下の程度までとを含む、鋳造が困難な偏晶アルミニウム滑り軸受合金を、ストリップ鋳造によって再現可能な品質で鋳造できるようにする。マイナー相の均質な分布は、この場合、電磁場中で溶融物を強く攪拌することによって達成される。結晶微細化剤を加えることによって、この合金の微細構造はさらに微細化される。これがもつ効果の中には、鋳造状態において最大40μmの直径をもつ溶滴の形状のビスマス析出物のサイズへの有利な効果もある。結晶微細化剤の添加量は、EP 0940474 A1によれば、溶融物中のビスマス含有量を考慮した式によって計算される。この発明は、特許に記載されている結果を得るために使用される結晶微細化添加物の類の指示を全く含んでいない。 The method described in EP 0940474 A1 comprises a total of 0.5 to 15% by weight of at least one component from the group comprising 15% by weight of bismuth and silicon, tin and zinc, copper, manganese, Reproducible quality by strip casting of difficult-to-cast hard aluminum alloy bearings containing up to 3% by weight of possible additives from the group including magnesium, nickel, chromium, zinc and antimony So that it can be cast in. A homogeneous distribution of the minor phase is in this case achieved by vigorously stirring the melt in an electromagnetic field. By adding a crystal refiner, the microstructure of this alloy is further refined. Among the effects this has is also an advantageous effect on the size of bismuth precipitates in the form of droplets with a diameter of up to 40 μm in the cast state. According to EP 0940474 A1, the addition amount of the crystal refining agent is calculated by a formula that takes into account the bismuth content in the melt. This invention does not include any indication of the type of refinement additive used to obtain the results described in the patent.
EP 0190691は、4ないし7重量%のビスマスと、1ないし4.5重量%のケイ素と、0ないし1.7重量%の銅と、0ないし2.5重量%の鉛と、ニッケル、マンガンおよびクロムを含む群からの少なくとも1つの元素を合計1重量%以下の程度までと、さらにスズ、亜鉛およびアンチモンを含む群からの少なくとも1つの元素を合計5重量%以下とを含んだ合金を開示している。高いケイ素含有量はアルミニウムマトリクスを強化するが、それらはマイナー相のサイズに不利な影響を及ぼし、ストランド中の溶滴分布を明らかに悪くする。このような鋳造構造を圧延する間、元来は球状の鉛またはビスマス相が非常に太いフィラメントに変形する。このことは、材料の機械的な耐荷重能力および摩擦特性をかなり減じてしまう。 EP 090691 describes 4 to 7% by weight of bismuth, 1 to 4.5% by weight of silicon, 0 to 1.7% by weight of copper, 0 to 2.5% by weight of lead, nickel, manganese and Disclosed is an alloy comprising at least one element from the group comprising chromium to a total extent of less than 1% by weight, and further comprising at least one element from the group comprising tin, zinc and antimony to a total of less than 5% by weight. ing. High silicon contents strengthen the aluminum matrix, but they have a detrimental effect on the size of the minor phase and clearly impair the droplet distribution in the strands. While rolling such a cast structure, the originally spherical lead or bismuth phase is transformed into a very thick filament. This significantly reduces the mechanical load carrying capacity and frictional properties of the material.
所望の材料特性を設定するために可能な1つの解決策は、マイナー相の細長い析出物を引き続いての熱処理によって密な構造の形状に変形させることである。例えばDE 4014430 A1によれば、偏晶アルミニウムケイ素−ビスマス合金を575〜585℃で熱処理してビスマス相の微細分布を達成し、圧延後にラメラの形態に延伸される。 One possible solution for setting the desired material properties is to transform the minor phase elongated precipitates into a dense structure by subsequent heat treatment. For example, according to DE 4014430 A1, a twin crystal aluminum silicon-bismuth alloy is heat-treated at 575-585 ° C. to achieve a fine distribution of the bismuth phase and is drawn into a lamellar form after rolling.
さらなる利点として、熱処理は硬化効果によってアルミニウム滑り軸受の強度値を向上させる可能性を提供する。可能な硬化効果の達成に好適な元素は、例えばケイ素、マグネシウム、亜鉛およびジルコニウムである。銅の添加は硬化速度を増大させ、これらの元素と組み合わせて使用することができる。 As a further advantage, the heat treatment offers the possibility of improving the strength value of the aluminum plain bearing by a hardening effect. Suitable elements for achieving possible hardening effects are, for example, silicon, magnesium, zinc and zirconium. The addition of copper increases the cure rate and can be used in combination with these elements.
US 5,286,445は、2〜15重量%の含有量のビスマスと、0.05ないし1重量%の含有量のジルコニウムと、1.5重量%以下の含有量の銅および/またはマグネシウムをもつアルミニウム滑り軸受合金を開示している。加えてこの合金は、スズ、鉛およびインジウムを含む群からの少なくとも1つの元素を合計で0.05ないし2重量%、またはケイ素、マンガン、バナジウム、アンチモン、ニオブ、モリブデン、コバルト、鉄、チタンおよびクロムを含む群からの少なくとも1つの元素を合計で0.05ないし5重量%含む。スズ、鉛およびインジウムの添加は、200〜350℃の温度で、延伸されたビスマス溶滴のより微細な析出物への再凝固を助ける。元素ジルコニウム、ケイ素およびマグネシウムは、480ないし525℃の温度範囲におけるアニール後に、実際の硬化効果をもたらす。これはUS 5,286,445によれば、圧延被覆の少し前に実施される。遷移元素は、材料の機械的な耐荷重能力のさらなる増大を確保することを意図している。 US 5,286,445 contains bismuth with a content of 2 to 15% by weight, zirconium with a content of 0.05 to 1% by weight and copper and / or magnesium with a content of 1.5% by weight or less. An aluminum slide bearing alloy is disclosed. In addition, this alloy has a total of 0.05 to 2% by weight of at least one element from the group comprising tin, lead and indium, or silicon, manganese, vanadium, antimony, niobium, molybdenum, cobalt, iron, titanium and A total of 0.05 to 5% by weight of at least one element from the group comprising chromium. The addition of tin, lead and indium assists in re-solidification of the stretched bismuth droplets into finer precipitates at temperatures of 200-350 ° C. The elements zirconium, silicon and magnesium provide an actual hardening effect after annealing in the temperature range of 480 to 525 ° C. This is carried out according to US 5,286,445 shortly before the rolling coating. The transition elements are intended to ensure a further increase in the mechanical load bearing capacity of the material.
マイナー相のサイズおよび分布へのケイ素の好ましくない効果は既に報告されている。マグネシウムの添加は、さらに、マグネシウムが優先的にビスマスとともに金属間化合物Mg3Bi2を形成するという不都合を伴う。これはビスマス溶滴間に挿入され、磨耗粒子を埋め込むビスマス溶滴の能力を明らかに減じる。スズを添加することは、高温での滑り軸受材料の機械的な耐荷重能力をかなり損なう。さらに、DE 40144 30 A1およびUS 5,286,445において提案されている480℃を超える熱処理の温度は、鋼の支持シェルとアルミニウムとの間の脆い金属間相の形成に関して非常に不利に選択されている。先行技術によれば、アルミニウムを鋼で被覆するのに許容できる温度範囲は400℃未満である。 The undesirable effects of silicon on minor phase size and distribution have already been reported. The addition of magnesium is further accompanied by the disadvantage that magnesium preferentially forms the intermetallic compound Mg 3 Bi 2 with bismuth. This is inserted between the bismuth droplets and clearly reduces the ability of the bismuth droplets to embed the wear particles. Adding tin significantly impairs the mechanical load bearing capacity of the sliding bearing material at high temperatures. Furthermore, the temperature of the heat treatment above 480 ° C. proposed in DE 40144 30 A1 and US Pat. No. 5,286,445 is very disadvantageously selected for the formation of a brittle intermetallic phase between the steel support shell and aluminum. ing. According to the prior art, the acceptable temperature range for coating aluminum with steel is less than 400 ° C.
上述したビスマスを含んだ合金のうち、これまでにいかなる実用的な重要性も獲得したものはない。なぜならば、連続鋳造および滑り軸受シェルを形成するための後のさらなる加工によるそれらの製造の間に生じる、複雑な過程を適切に克服することは未だ不可能だからである。鋳造状態におけるマイナー相の微細分布のほかに、アルミニウム滑り軸受合金の最適な特性のための必要条件は、特に、必要な成形および圧延被覆操作の後でさえ、マイナー相の微細分布を確立できる可能性である。他の要求は、高い強度、機械的な耐荷重能力(高温時も含む)、アルミニウムマトリクスの耐磨耗性および良好な成形性である。 None of the above-described alloys containing bismuth has gained any practical significance. This is because it is still impossible to adequately overcome the complex processes that occur during continuous casting and their production by subsequent further processing to form sliding bearing shells. In addition to the minor phase fine distribution in the cast state, the requirements for optimal properties of the aluminum plain bearing alloy can establish a minor phase fine distribution, especially even after the necessary forming and rolling coating operations. It is sex. Other requirements are high strength, mechanical load capacity (including high temperatures), aluminum matrix wear resistance and good formability.
したがって、本発明は、高耐久性のアルミニウム滑り軸受合金を提供する目的に基づいており、これは先行技術の不都合を回避し、かつビスマス相の均質かつ微細な分布を達成し、および滑り軸受シェルを形成する加工段階における後のさらなるストリップの加工の間これを維持し、可能ならば向上させることを可能にする。 The present invention is therefore based on the object of providing a highly durable aluminum sliding bearing alloy, which avoids the disadvantages of the prior art and achieves a homogeneous and fine distribution of the bismuth phase, and a sliding bearing shell. This can be maintained during further processing of subsequent strips in the processing stage to form and improve if possible.
この目的は、以下の成分を含むアルミニウム滑り軸受合金によって達成される。およそ5ないし20重量%のビスマスと、およそ3ないし20重量%の亜鉛と、およそ1ないし4重量%の銅と、さらにマンガン、バナジウム、ニオブ、ニッケル、モリブデン、コバルト、鉄、タングステン、クロム、銀、カルシウム、スカンジウム、セリウム、アンチモン、ホウ素、ベリリウム、チタン、炭素およびジルコニウムのうち1以上の成分を合計で5重量%以下と、残りのアルミニウムであるが、スズ、鉛およびケイ素は精練に由来する不純物によって生じる量のほかに含まず、すなわち各々多くとも1重量%以下の量である。これは、原則的に、本発明による合金は合金成分としてスズおよびケイ素を含んではならないことが意図されていることを意味する。しかしながら、スズ(Sn)だけでなく鉛(Pb)およびケイ素(Si)は、およそ0.3重量%以下の不純物によって生じる量で、あるいはおよそ1重量%以下の少量であるが、より良好にはおよそ0.5重量%以下で存在していてもよく、本発明の利点を過剰に損なうことがない。本発明による滑り軸受合金は、好ましくは連続鋳造され、ビスマス相の微細分布によって鋳造状態において既に区別され、これは引き抜き速度および冷却速度に大きく依存しない。圧延および圧延被覆時のさらなる処理の途中で作られる長いビスマスのラメラは、その後に270〜400℃の温度で熱処理によって完全に再凝固して、微細に分布した球状溶滴を形成し、これらは工程が適切に行われた場合には20μmより小さい。 This object is achieved by an aluminum plain bearing alloy comprising the following components: Approximately 5 to 20% by weight bismuth, approximately 3 to 20% by weight zinc, approximately 1 to 4% by weight copper, and manganese, vanadium, niobium, nickel, molybdenum, cobalt, iron, tungsten, chromium, silver , Calcium, scandium, cerium, antimony, boron, beryllium, titanium, carbon and zirconium, and the remaining aluminum is a total of 5% by weight or less, but tin, lead and silicon are derived from scouring In addition to the amount produced by the impurities, it is not more than 1% by weight. This means in principle that the alloys according to the invention are intended not to contain tin and silicon as alloying components. However, not only tin (Sn) but also lead (Pb) and silicon (Si) are produced by impurities of about 0.3 wt% or less, or in small amounts of about 1 wt% or less, but better It may be present at about 0.5% by weight or less and does not excessively detract from the advantages of the present invention. The plain bearing alloy according to the invention is preferably continuously cast and is already distinguished in the cast state by the fine distribution of the bismuth phase, which does not depend greatly on the drawing and cooling rates. Long bismuth lamellae produced during further processing during rolling and roll coating are then completely re-solidified by heat treatment at temperatures of 270-400 ° C. to form finely distributed spherical droplets, which are If the process is properly performed, it is smaller than 20 μm.
合金は好ましくはおよそ7〜12重量%のビスマスを含む。亜鉛含有量は好ましくはおよそ3〜6重量%であり、銅含有量はおよそ2〜4重量%、特に2〜3重量%である。種々の元素の含有量は、与えられた範囲内で互いに独立に可変である。 The alloy preferably contains approximately 7-12% by weight of bismuth. The zinc content is preferably approximately 3 to 6% by weight and the copper content is approximately 2 to 4% by weight, in particular 2-3% by weight. The content of the various elements can be varied independently of each other within a given range.
本発明による合金は、単一の軟質相形成剤としてのビスマスの使用によって、既知の合金と異なる。すなわち、ビスマスと鉛および/またはスズとの組み合わせがなく、亜鉛の含有量は最大20重量%以下に増大し、銅の含有量は最大4重量%以下に増大する。記載した量の添加した亜鉛および銅は、二元Al−Bi合金と比較して、鋳造状態におけるビスマス溶滴のサイズにわずかな悪化をもたらすが、それらは、被覆パスの後に高度に延伸されたビスマスフィラメントの完全な再凝固を可能にし、サイズで20μm以下の微細な球状溶滴を形成する。アニール時間は化学組成に依存する。加えて、増大した銅の含有量はアルミニウムマトリクスの強度増大をもたらし、我々の経験では、ビスマス含有滑り軸受材料の腐食耐性を向上させる。 The alloys according to the invention differ from known alloys by the use of bismuth as a single soft phase former. That is, there is no combination of bismuth and lead and / or tin, the zinc content increases to a maximum of 20 wt% or less, and the copper content increases to a maximum of 4 wt% or less. The stated amounts of added zinc and copper cause a slight deterioration in the size of the bismuth droplets in the cast state compared to the binary Al-Bi alloy, but they were highly stretched after the coating pass. Enables complete re-coagulation of the bismuth filament and forms fine spherical droplets of 20 μm or less in size. The annealing time depends on the chemical composition. In addition, the increased copper content results in increased strength of the aluminum matrix, and our experience improves the corrosion resistance of bismuth-containing plain bearing materials.
およそ0.3ないし2重量%の添加量で加える商業的に入手できる結晶微細化剤AlTi5B1またはAlTi3CO、15を使用することは、本発明による合金に優れた結晶微細化効果があり、様々な冷却速度で連続鋳造の間に確実にヒートクラックの形成を防ぐことがわかっている。言及した結晶微細化剤の添加は、マイナー相のサイズを明らかに減じるさらなる効果をもつ。結晶微細化添加物の使用によって、比較的遅いおよそ5K/sの冷却速度でさえも、鋳造状態におけるビスマス溶滴の最大直径を30μm未満に減じることが可能となっている。 The use of the commercially available crystal refiner AlTi5B1 or AlTi3CO, 15 added in an addition amount of approximately 0.3 to 2% by weight has an excellent crystal refinement effect in the alloys according to the invention, and various cooling It has been found to reliably prevent the formation of heat cracks during continuous casting at speed. The addition of the mentioned crystal refiner has the further effect of clearly reducing the size of the minor phase. The use of grain refiner additives makes it possible to reduce the maximum diameter of bismuth droplets in the cast state to less than 30 μm, even at a relatively slow cooling rate of approximately 5 K / s.
元素マンガン、バナジウム、ニオブ、ニッケル、モリブデン、コバルト、鉄、タングステン、クロム、銀、カルシウム、スカンジウム、セリウム、ベリリウム、アンチモン、ホウ素、チタン、ジルコニウムおよび炭素の助けにより、本発明による合金の特性を特にそれぞれの意図された用途に適合させることが可能である。 With the help of the elements manganese, vanadium, niobium, nickel, molybdenum, cobalt, iron, tungsten, chromium, silver, calcium, scandium, cerium, beryllium, antimony, boron, titanium, zirconium and carbon, the properties of the alloys according to the invention are particularly It can be adapted to each intended use.
本発明はさらに、上述した本発明による組成物を使用したアルミニウム滑り軸受合金を製造する方法を含む。好ましくは、5ないし1000K/sの冷却速度の鋳造工程で合金化成分を結合させ、合金を形成する。あるいは、合金を他の通常の製造方法によって、特に他の鋳造方法によって製造することもできる。連続鋳造による製造が今のところ好ましい。したがって条件は、好ましくは溶滴形状のビスマスインターカレーションが形成されるように適合させる。連続鋳造の間、引き抜き速度は好ましくは2ないし15mm/sである。 The present invention further includes a method of producing an aluminum plain bearing alloy using the composition according to the present invention described above. Preferably, the alloying components are combined in a casting process with a cooling rate of 5 to 1000 K / s to form an alloy. Alternatively, the alloy can be manufactured by other conventional manufacturing methods, in particular by other casting methods. Production by continuous casting is currently preferred. The conditions are therefore preferably adapted so that a droplet-shaped bismuth intercalation is formed. During continuous casting, the drawing speed is preferably 2 to 15 mm / s.
この発明の好ましい実施態様によれば、鋳造によって得られる合金は、後の形成工程の途中でおよそ270〜400℃の温度で少なくとも1つの熱処理を受ける。このような熱処理は、好ましくは圧延および/または圧延被覆の後になされ、いくつかの圧延および/または被覆操作を、合金の鋳造と最終製品との間の製造工程内で実施することができ、かつ少なくとも1つの熱処理を最終的な圧延および/または圧延被覆操作の後またはこれらの操作のいくつかまたは全ての後に実施することができる。 According to a preferred embodiment of the invention, the alloy obtained by casting is subjected to at least one heat treatment at a temperature of approximately 270 to 400 ° C. during the subsequent forming step. Such heat treatment is preferably done after rolling and / or roll coating, several rolling and / or coating operations can be carried out in the manufacturing process between the casting of the alloy and the final product, and At least one heat treatment can be performed after the final rolling and / or roll coating operations or after some or all of these operations.
半完成品の調製のため、または例えば滑り軸受のような製品の製造の途中で、鋳造合金は少なくとも1つの支持層を備えていてもよい。支持層は特に鋼の層でもよい。さらなる層、例えば粘着促進層または被膜を追加してもよい。 For the preparation of a semi-finished product or in the course of the manufacture of a product such as a sliding bearing, the cast alloy may be provided with at least one support layer. The support layer may in particular be a steel layer. Additional layers, such as adhesion promoting layers or coatings may be added.
本発明はさらに、本発明による合金をそれに用いられる材料の1つとして含むかまたはこの合金からなる滑り軸受シェルを含む。 The invention further includes a plain bearing shell comprising the alloy according to the invention as one of the materials used therein or consisting of this alloy.
最後に、本発明はこのような滑り軸受シェルを備えた滑り軸受、または滑り軸受における本発明による滑り軸受シェルの使用を含む。 Finally, the invention includes a sliding bearing with such a sliding bearing shell, or the use of a sliding bearing shell according to the invention in a sliding bearing.
本発明を、例示的な実施態様に基づいて、以下により詳細に説明する。 The invention is explained in more detail below on the basis of exemplary embodiments.
滑り軸受材料を製造するために、この例においては10mm×100mmの断面をもつ鋳造ストリップを、先行技術において知られているように垂直連続鋳造装置で、0.6重量%のAlTi5B1を添加して作る。ストリップの製造において、引き抜き速度は8mm/sであり、冷却速度は600K/sである。ストランドを最初に広い面に水平に圧延して、およそ8mmの厚さにする。 In order to produce a plain bearing material, a cast strip having a cross section of 10 mm × 100 mm in this example is added in a vertical continuous casting apparatus as known in the prior art with 0.6 wt% AlTi5B1. create. In the production of the strip, the drawing speed is 8 mm / s and the cooling rate is 600 K / s. The strand is first rolled horizontally on a wide surface to a thickness of approximately 8 mm.
続いて、つや消し、脱脂されたアルミニウム合金の粘着促進剤を、圧延スタンドにおける最初の圧延パスにより、同様につや消し、脱脂されたAlZn5Cu3Bi7合金に被覆する。被覆された原材料ストリップの厚さは4mmである。これを、引き続いていくつかの圧延パスで1.3mmに圧延する。これには5つの圧延パスが必要である。アルミニウム軸受材料ストリップの被覆特性を向上させるために、これは370℃で3時間以下の再生アニール操作を受ける。次の加工工程において、鋼ストリップとアルミニウム滑り軸受材料ストリップを被覆圧延機で互いに結合させる。 Subsequently, the matte and degreased AlZn5Cu3Bi7 alloy is similarly coated with the matte and degreased aluminum alloy adhesion promoter in the first rolling pass in the rolling stand. The thickness of the coated raw material strip is 4 mm. This is subsequently rolled to 1.3 mm in several rolling passes. This requires five rolling passes. In order to improve the coating properties of the aluminum bearing material strip, it is subjected to a regenerative annealing operation at 370 ° C. for up to 3 hours. In the next processing step, the steel strip and the aluminum plain bearing material strip are bonded together in a coated rolling mill.
続いて、作られた材料の組み合わせに360℃の温度で3時間続く熱処理を施し、鋼とアルミニウム滑り軸受材料との間の結合を拡散過程によって増大させ、クラッディング後のアルミニウム−亜鉛−銅マトリクス中で高度に延伸されたビスマスフィラメントを完全に改質して、サイズが20μm以下の微細な球状溶滴にする。同様に熱処理から生じる少なくとも43 HB 2.5/62.5/30の高度な硬さも有利である。この熱処理後に、被覆ストリップを細分して軸受シェルに成形してもよい。 The resulting material combination is then subjected to a heat treatment lasting 3 hours at a temperature of 360 ° C. to increase the bond between the steel and the aluminum plain bearing material by a diffusion process, and the aluminum-zinc-copper matrix after cladding. The bismuth filaments that are highly stretched therein are completely modified to form fine spherical droplets having a size of 20 μm or less. Similarly, a high hardness of at least 43 HB 2.5 / 62.5 / 30 resulting from heat treatment is advantageous. After this heat treatment, the coated strip may be subdivided and formed into a bearing shell.
図1ないし図3は、本発明による合金(ここではAlZn5Cu3Bi7合金)が加工の間にその微細構造においてどのように変化するかを一例として示す。図1は、連続鋳造による製造後の合金の微細構造を示す。溶滴の形状のビスマス相は暗い部分として示される。 1 to 3 show by way of example how an alloy according to the invention (here AlZn5Cu3Bi7 alloy) changes in its microstructure during processing. FIG. 1 shows the microstructure of the alloy after production by continuous casting. The droplet-shaped bismuth phase is shown as dark.
図2は、圧延後の合金の微細構造を示す。圧延によって延伸されたビスマスのラメラが圧延構造中に見える。 FIG. 2 shows the microstructure of the alloy after rolling. Bismuth lamellae stretched by rolling are visible in the rolled structure.
図3は360℃で3時間の熱処理後の圧延構造を示す。延伸されたBiラメラを、熱処理によって有効に再凝固することが可能になっている。大きな溶滴(その孤立した例が図1には未だ見られる)は、延伸および再凝固されることによって破壊されるので、処理によって全体の微細分布の程度は増大する。 FIG. 3 shows the rolled structure after heat treatment at 360 ° C. for 3 hours. The stretched Bi lamella can be effectively re-solidified by heat treatment. Because large droplets (an isolated example of which is still seen in FIG. 1) are destroyed by stretching and re-solidification, the process increases the degree of overall fine distribution.
例は単に説明のために役立つだけであり、本発明を限定しないことが言及されるべきである。当業者は、滑り軸受および軸受シェルがどのようにして製造されるか、ならびに本発明による合金の製造が結果として通常の軸受製造工程にどのようにして組み込まれるかがわかる。 It should be mentioned that the examples are merely illustrative and do not limit the invention. The person skilled in the art knows how slide bearings and bearing shells are manufactured and how the manufacture of the alloy according to the invention is consequently incorporated into the normal bearing manufacturing process.
Claims (13)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PCT/EP2005/006091 WO2006131129A1 (en) | 2005-06-07 | 2005-06-07 | Aluminium plain bearing alloy |
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| Publication Number | Publication Date |
|---|---|
| JP2008542548A true JP2008542548A (en) | 2008-11-27 |
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| Application Number | Title | Priority Date | Filing Date |
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| JP2008515049A Pending JP2008542548A (en) | 2005-06-07 | 2005-06-07 | Aluminum sliding bearing alloy |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US20100221141A1 (en) |
| EP (1) | EP1888798B1 (en) |
| JP (1) | JP2008542548A (en) |
| AT (1) | ATE417132T1 (en) |
| DE (1) | DE502005006241D1 (en) |
| WO (1) | WO2006131129A1 (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103031459A (en) * | 2012-12-05 | 2013-04-10 | 安徽徽铝铝业有限公司 | Preparation method of refining agent for smelting fly ash doped aluminum alloy |
| JP2014218743A (en) * | 2013-05-07 | 2014-11-20 | 現代自動車株式会社 | Abrasion resistant alloy having composite microstructure |
| JP2020523475A (en) * | 2017-06-15 | 2020-08-06 | ツォレルン・ベーハーベー・グライトラガー・ゲーエムベーハー・ウント・コンパニー・カーゲーZollern BHW Gleitlager GmbH & Co. KG | Monoclinic aluminum plain bearing alloy, method of making the same, and plain bearing made thereby |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8403027B2 (en) * | 2007-04-11 | 2013-03-26 | Alcoa Inc. | Strip casting of immiscible metals |
| ES2330713B2 (en) * | 2008-06-11 | 2010-04-19 | Abinash Banerji | ALUMINUM BASED GRAIN TUNER. |
| CN101838783B (en) * | 2010-02-05 | 2012-01-04 | 新星化工冶金材料(深圳)有限公司 | Method for controlling variable quantity of grain refinement capability of TiAl carbon alloy by compression ratio control |
| US9963770B2 (en) | 2015-07-09 | 2018-05-08 | Ut-Battelle, Llc | Castable high-temperature Ce-modified Al alloys |
| DE102015112550B3 (en) * | 2015-07-30 | 2016-12-08 | Zollern Bhw Gleitlager Gmbh & Co. Kg | Process for the preparation of a monotectic alloy |
| JP7249105B2 (en) * | 2018-03-22 | 2023-03-30 | 大同メタル工業株式会社 | sliding member |
| CN110157935B (en) * | 2019-06-28 | 2021-05-07 | 上海大学 | Al-V-B refiner for casting aluminum-silicon alloy, its preparation method and application |
| CN110578075A (en) * | 2019-10-24 | 2019-12-17 | 沈阳航空航天大学 | A kind of high-performance homogeneous aluminum-bismuth immiscible alloy and preparation method thereof |
| CN111057911A (en) * | 2020-01-06 | 2020-04-24 | 高品质特殊钢冶金与制备国家重点实验室张家港产业中心 | Al-Bi monotectic alloy and preparation method thereof |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0947260A1 (en) * | 1998-02-04 | 1999-10-06 | Deutsches Zentrum für Luft- und Raumfahrt e.V. | Sliding bearing made of monotectic alloys |
-
2005
- 2005-06-07 US US11/916,413 patent/US20100221141A1/en not_active Abandoned
- 2005-06-07 DE DE502005006241T patent/DE502005006241D1/en not_active Expired - Lifetime
- 2005-06-07 JP JP2008515049A patent/JP2008542548A/en active Pending
- 2005-06-07 AT AT05756177T patent/ATE417132T1/en active
- 2005-06-07 EP EP05756177A patent/EP1888798B1/en not_active Expired - Lifetime
- 2005-06-07 WO PCT/EP2005/006091 patent/WO2006131129A1/en not_active Ceased
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103031459A (en) * | 2012-12-05 | 2013-04-10 | 安徽徽铝铝业有限公司 | Preparation method of refining agent for smelting fly ash doped aluminum alloy |
| CN103031459B (en) * | 2012-12-05 | 2015-03-04 | 安徽徽铝铝业有限公司 | Preparation method of refining agent for smelting fly ash doped aluminum alloy |
| JP2014218743A (en) * | 2013-05-07 | 2014-11-20 | 現代自動車株式会社 | Abrasion resistant alloy having composite microstructure |
| JP2020523475A (en) * | 2017-06-15 | 2020-08-06 | ツォレルン・ベーハーベー・グライトラガー・ゲーエムベーハー・ウント・コンパニー・カーゲーZollern BHW Gleitlager GmbH & Co. KG | Monoclinic aluminum plain bearing alloy, method of making the same, and plain bearing made thereby |
Also Published As
| Publication number | Publication date |
|---|---|
| ATE417132T1 (en) | 2008-12-15 |
| DE502005006241D1 (en) | 2009-01-22 |
| EP1888798A1 (en) | 2008-02-20 |
| WO2006131129A1 (en) | 2006-12-14 |
| EP1888798B1 (en) | 2008-12-10 |
| US20100221141A1 (en) | 2010-09-02 |
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