JP5823697B2 - Ferrous sintered alloy valve seat - Google Patents
Ferrous sintered alloy valve seat Download PDFInfo
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- JP5823697B2 JP5823697B2 JP2011009719A JP2011009719A JP5823697B2 JP 5823697 B2 JP5823697 B2 JP 5823697B2 JP 2011009719 A JP2011009719 A JP 2011009719A JP 2011009719 A JP2011009719 A JP 2011009719A JP 5823697 B2 JP5823697 B2 JP 5823697B2
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F01—MACHINES OR ENGINES IN GENERAL; ENGINE PLANTS IN GENERAL; STEAM ENGINES
- F01L—CYCLICALLY OPERATING VALVES FOR MACHINES OR ENGINES
- F01L3/00—Lift-valve, i.e. cut-off apparatus with closure members having at least a component of their opening and closing motion perpendicular to the closing faces; Parts or accessories thereof
- F01L3/02—Selecting particular materials for valve-members or valve-seats; Valve-members or valve-seats composed of two or more materials
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F5/00—Manufacture of workpieces or articles from metallic powder characterised by the special shape of the product
- B22F5/008—Manufacture of workpieces or articles from metallic powder characterised by the special shape of the product of engine cylinder parts or of piston parts other than piston rings
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C27/00—Alloys based on rhenium or a refractory metal not mentioned in groups C22C14/00 or C22C16/00
- C22C27/04—Alloys based on tungsten or molybdenum
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C33/00—Making ferrous alloys
- C22C33/02—Making ferrous alloys by powder metallurgy
- C22C33/0207—Using a mixture of pre-alloyed powders or a master alloy
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C33/00—Making ferrous alloys
- C22C33/02—Making ferrous alloys by powder metallurgy
- C22C33/0207—Using a mixture of pre-alloyed powders or a master alloy
- C22C33/0221—Using a mixture of pre-alloyed powders or a master alloy comprising S or a sulfur compound
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C33/00—Making ferrous alloys
- C22C33/02—Making ferrous alloys by powder metallurgy
- C22C33/0207—Using a mixture of pre-alloyed powders or a master alloy
- C22C33/0228—Using a mixture of pre-alloyed powders or a master alloy comprising other non-metallic compounds or more than 5% of graphite
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/02—Ferrous alloys, e.g. steel alloys containing silicon
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/08—Ferrous alloys, e.g. steel alloys containing nickel
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/12—Ferrous alloys, e.g. steel alloys containing tungsten, tantalum, molybdenum, vanadium, or niobium
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
- C22C38/22—Ferrous alloys, e.g. steel alloys containing chromium with molybdenum or tungsten
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
- C22C38/24—Ferrous alloys, e.g. steel alloys containing chromium with vanadium
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F01—MACHINES OR ENGINES IN GENERAL; ENGINE PLANTS IN GENERAL; STEAM ENGINES
- F01L—CYCLICALLY OPERATING VALVES FOR MACHINES OR ENGINES
- F01L1/00—Valve-gear or valve arrangements, e.g. lift-valve gear
- F01L1/02—Valve drive
- F01L1/04—Valve drive by means of cams, camshafts, cam discs, eccentrics or the like
- F01L1/047—Camshafts
- F01L1/053—Camshafts overhead type
- F01L1/0532—Camshafts overhead type the cams being directly in contact with the driven valve
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F01—MACHINES OR ENGINES IN GENERAL; ENGINE PLANTS IN GENERAL; STEAM ENGINES
- F01L—CYCLICALLY OPERATING VALVES FOR MACHINES OR ENGINES
- F01L1/00—Valve-gear or valve arrangements, e.g. lift-valve gear
- F01L1/12—Transmitting gear between valve drive and valve
- F01L1/14—Tappets; Push rods
- F01L1/143—Tappets; Push rods for use with overhead camshafts
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F01—MACHINES OR ENGINES IN GENERAL; ENGINE PLANTS IN GENERAL; STEAM ENGINES
- F01L—CYCLICALLY OPERATING VALVES FOR MACHINES OR ENGINES
- F01L2303/00—Manufacturing of components used in valve arrangements
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F01—MACHINES OR ENGINES IN GENERAL; ENGINE PLANTS IN GENERAL; STEAM ENGINES
- F01L—CYCLICALLY OPERATING VALVES FOR MACHINES OR ENGINES
- F01L2800/00—Methods of operation using a variable valve timing mechanism
- F01L2800/18—Testing or simulation
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F01—MACHINES OR ENGINES IN GENERAL; ENGINE PLANTS IN GENERAL; STEAM ENGINES
- F01L—CYCLICALLY OPERATING VALVES FOR MACHINES OR ENGINES
- F01L2810/00—Arrangements solving specific problems in relation with valve gears
- F01L2810/02—Lubrication
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F01—MACHINES OR ENGINES IN GENERAL; ENGINE PLANTS IN GENERAL; STEAM ENGINES
- F01L—CYCLICALLY OPERATING VALVES FOR MACHINES OR ENGINES
- F01L2820/00—Details on specific features characterising valve gear arrangements
- F01L2820/01—Absolute values
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- General Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Powder Metallurgy (AREA)
Description
本発明は、内燃機関のバルブシートに関し、特に気筒内燃料噴射により潤滑状態の希薄な条件で使用される鉄基焼結合金製バルブシートに関する。 The present invention relates to a valve seat for an internal combustion engine, and more particularly, to a valve seat made of an iron-based sintered alloy that is used under lean conditions of lubrication by in-cylinder fuel injection.
内燃機関においては、環境対応のため、燃費の向上、低エミッション化、高出力化が図られ、燃焼状態の高負荷化、エンジン仕様の高負荷化により、燃焼室を構成する部品は、幅広い使用温度においてさらなる耐摩耗性の向上が要求されている。吸気バルブ、排気バルブの弁座であって燃焼室の機密を保つ機能を有するバルブシートも、燃焼時の燃焼圧に曝され、さらにバルブの往復運動により強い衝撃を繰り返し受ける。また、バルブは往復運動と同時にバルブ軸を中心として回転自在であり、バルブと接触するバルブシートの摺動面は耐摩耗性を必要とする。特に、気筒内に燃料が直接噴射されるDI(Direct Injection)型内燃機関では、バルブとバルブシートの摺動面に燃料による潤滑作用の無い無潤滑下での摺動となり、バルブシートには従来にも増す耐摩耗性の向上が求められる。このため、例えば特許文献1に開示されているように、フッ化カルシウム等の固体潤滑材を基地中に多量に分散させて自己潤滑性を高めることで、無潤滑下における耐摩耗性を向上させた鉄系焼結合金がバルブシートに用いられてきた。
In the internal combustion engine, in order to respond to the environment, the fuel consumption is improved, the emission is reduced, and the output is increased, and the components that make up the combustion chamber are widely used due to the increased load of the combustion state and the increased load of the engine specifications. There is a demand for further improvement in wear resistance at temperatures. The valve seats that are the seats of the intake and exhaust valves and have the function of keeping the combustion chamber secret are also exposed to the combustion pressure during combustion and are repeatedly subjected to strong impacts due to the reciprocating motion of the valves. Further, the valve is rotatable around the valve shaft at the same time as the reciprocating motion, and the sliding surface of the valve seat that contacts the valve requires wear resistance. In particular, in DI (Direct Injection) internal combustion engines, where fuel is directly injected into the cylinder, the sliding surface of the valve and valve seat slides without lubrication by the fuel without lubrication. In addition, there is a need for improved wear resistance. For this reason, as disclosed in
しかしながら、固体潤滑材としてフッ化カルシウムを基地中に多量に分散した従来の鉄系焼結合金によるバルブシートでは、焼結体の強度が低くなり、低温域での耐摩耗性が十分ではなく、幅広い使用温度域においての適用には問題があった。また、硬質粒子としてフェロモリブデンのみ含有させた従来の鉄系焼結合金製バルブシートも、幅広い使用温度域において耐摩耗性が十分ではなかった。 However, in the valve seat of the conventional iron-based sintered alloy in which calcium fluoride is dispersed in a large amount in the base as a solid lubricant, the strength of the sintered body is low, and the wear resistance in the low temperature range is not sufficient, There was a problem in application in a wide operating temperature range. Further, the conventional iron-based sintered alloy valve seat containing only ferromolybdenum as hard particles also has insufficient wear resistance in a wide operating temperature range.
上記問題に鑑み、本発明は、燃費の向上、低エミッション化、高出力化に対応したDI型内燃機関に使用することが可能な、幅広い温度域で高い耐摩耗性を有する鉄基焼結合金製バルブシートを提供することを課題とする。 In view of the above problems, the present invention is an iron-based sintered alloy having high wear resistance in a wide temperature range that can be used for a DI-type internal combustion engine corresponding to improvement in fuel consumption, low emission, and high output. It is an object to provide a valve seat made by the manufacturer.
本発明者達は、鋭意研究の結果、鉄基焼結合金製バルブシートの基地中に分散させる固体潤滑材の添加量を限定し、かつ硬さの異なる少なくとも二種類の硬質粒子を基地中に分散させることによって、高強度と自己潤滑性を同時に付与することができ、無潤滑下においても幅広い温度域において耐摩耗性を著しく向上することができることに想到した。 As a result of diligent research, the inventors of the present invention limited the amount of solid lubricant added to the base of the iron-based sintered alloy valve seat and contained at least two types of hard particles having different hardness in the base. By dispersing, it was conceived that high strength and self-lubricating properties can be simultaneously imparted, and wear resistance can be remarkably improved in a wide temperature range even under non-lubrication.
すなわち本発明のバルブシートは、固体潤滑材と硬さの異なる少なくとも二種類の硬質粒子を分散させた鉄基焼結合金製バルブシートであって、前記固体潤滑材は質量%で0.2〜0.8%分散させ、前記二種類の硬質粒子は第一硬質粒子と第二硬質粒子からなり、前記第一硬質粒子として平均粒径50〜150μm、ビッカース硬さHv800〜1200の硬質粒子を質量%で2〜8%、前記第二硬質粒子として平均粒径10〜150μm、ビッカース硬さHv400〜490の硬質粒子を質量%で5〜15%を分散させたことを特徴とする。
That is, the valve seat of the present invention is a valve seat made of an iron-based sintered alloy in which at least two kinds of hard particles different in hardness from a solid lubricant are dispersed, and the solid lubricant is 0.2 to 0.8% by mass%. The two kinds of hard particles are made up of first hard particles and second hard particles, and hard particles having an average particle size of 50 to 150 μm and Vickers hardness Hv 800 to 1200 as the first hard particles are 2 to 2% by mass. 8%, hard particles having an average particle diameter of 10 to 150 μm and Vickers hardness Hv of 400 to 490 are dispersed as 5% to 15% by mass% as the second hard particles .
前記硬質粒子としては、Fe-Mo系合金粒子、Fe-Cr-Mo-V系合金粒子、Co-Mo-Cr系合金粒子を用いることができる。特に、第一硬質粒子が、質量%で、Mo:40〜70%、Si:0.1〜2.0%、残部がFe及び不可避的不純物からなるFe-Mo-Si合金粒子、第二硬質粒子が、C:0.2〜0.5%、Cr:0.5〜5%、Mo:1〜5%、V:2〜5%、残部がFe及び不可避不純物からなるFe-C-Cr-Mo-V合金粒子であることが望ましい。
As the hard particles, Fe—Mo alloy particles, Fe—Cr—Mo—V alloy particles, and Co—Mo—Cr alloy particles can be used. In particular, the first hard particles are in mass%, Mo: 40-70%, Si: 0.1-2.0%, the balance is Fe-Mo-Si alloy particles consisting of Fe and inevitable impurities, the second hard particles are C : 0.2-0.5%, Cr: 0.5-5%, Mo: 1-5%, V: 2-5%, the balance being Fe-C-Cr-Mo-V alloy particles consisting of Fe and inevitable impurities desirable.
さらに、硬さの異なる少なくとも二種類の前記硬質粒子と固体潤滑材が分散する基地部の組成が、質量%で、C:0.5〜2.5%、Si:0.4〜2%、Mo:0.5〜5%、Ni:1〜5%、残部がFe及び不可避不純物からなることが好ましく、また、前記基地相が焼き戻しマルテンサイト相及びパーライト相を含むことが望ましい。 Furthermore, the composition of the base part in which at least two kinds of the hard particles having different hardness and the solid lubricant are dispersed is in mass%, C: 0.5 to 2.5%, Si: 0.4 to 2%, Mo: 0.5 to 5% Ni: 1 to 5%, the balance is preferably made of Fe and inevitable impurities, and the matrix phase preferably contains a tempered martensite phase and a pearlite phase.
さらに、固体潤滑材としては、MnSやMoS2などの硫化物、BNなどの窒化物から選択された1種以上の粉末が好ましく、その平均粒径が2〜50μmであることが好ましい。 Furthermore, as the solid lubricant, one or more powders selected from sulfides such as MnS and MoS 2 and nitrides such as BN are preferable, and the average particle diameter is preferably 2 to 50 μm.
本発明の鉄基焼結合金製バルブシートは、固体潤滑材を質量%で0.2〜0.8%分散し、かつ硬さの異なる少なくとも二種類の硬質粒子を基地中に分散させることで、高強度と自己潤滑性を同時に付与することができ、無潤滑下においても幅広い温度域において耐摩耗性を著しく向上することができる。二種類の硬質粒子は、一方の硬質粒子を構成する元素の一部が基材中に固溶又は基地中の元素と化合物を形成して基地を強化するとともに他方の硬質粒子を構成する元素の基材への固溶を抑制し、軟化抵抗を高めることにより、高温及び低温における耐摩耗性の向上に寄与する。これにより、気筒内に燃料が直接噴射されるDI型内燃機関に使用されるバルブシートとして、潤滑状態の希薄な条件下及びおよそ150〜350℃における低温度域から高温度域までの幅広い温度域での使用においても優れた耐摩耗性を示す。本発明の鉄基焼結合金製バルブシートは、特に、吸気用バルブシートとしてより好ましく適用できる。 The valve seat made of an iron-based sintered alloy according to the present invention has a high strength and high dispersion by dispersing 0.2 to 0.8% by mass% of the solid lubricant and dispersing at least two kinds of hard particles having different hardness in the base. Self-lubricating properties can be imparted simultaneously, and wear resistance can be significantly improved in a wide temperature range even without lubrication. Two types of hard particles are composed of a part of the elements constituting one hard particle, forming a solid solution or a compound with the element in the matrix to strengthen the matrix and the element constituting the other hard particle. By suppressing solid solution in the substrate and increasing softening resistance, it contributes to improvement of wear resistance at high and low temperatures. As a result, as a valve seat used in DI type internal combustion engines in which fuel is directly injected into the cylinder, a wide temperature range from low temperature range to high temperature range at about 150 to 350 ° C under lean conditions of lubrication Excellent wear resistance even when used in The iron-based sintered alloy valve seat of the present invention is particularly preferably applicable as an intake valve seat.
本発明の鉄基焼結合金製バルブシートは、基地と、基地中に分散した硬さの異なる少なくとも二種類の硬質粒子及び固体潤滑材で構成されている。基地中に分散される固体潤滑材は、質量%で0.2〜0.8%とする。固体潤滑材を0.8%を超えて分散させた場合、粉末圧縮成形時に粉末接合強度を低下させ、焼結体の強度が低下し、十分な耐摩耗性が得られない。一方、0.2%未満では被削性が低下する。固体潤滑材の平均粒径は2〜50μmであることが好ましく、基地中に均一に分散させることによって、耐摩耗性とともに自己潤滑性、被削性も向上させる。 The valve seat made of an iron-based sintered alloy according to the present invention is composed of a base, at least two kinds of hard particles having different hardness dispersed in the base, and a solid lubricant. The solid lubricant dispersed in the base is 0.2 to 0.8% by mass%. When the solid lubricant is dispersed in excess of 0.8%, the powder bonding strength is reduced during powder compression molding, the strength of the sintered body is reduced, and sufficient wear resistance cannot be obtained. On the other hand, if it is less than 0.2%, the machinability decreases. The average particle size of the solid lubricant is preferably 2 to 50 μm, and by dispersing uniformly in the matrix, the self-lubricating property and the machinability are improved as well as the wear resistance.
固体潤滑材には、MnS、MoS2などの硫化物、BN(窒化硼素)などの窒化物から選択された一種または二種以上を使用することが好ましい。固体潤滑材を二種以上使用するときは、少なくとも一種について平均粒径を2〜10μmとし、他種については平均粒径を10〜50μmとして均一に分散させることがより好ましい。平均粒径2〜10μmの固体潤滑材は、微細に分散することにより被削性を向上し、粒径範囲10〜50μmの固体潤滑材は、比較的粗大に介在することにより自己潤滑性を向上させ、耐摩耗性が向上する。 The solid lubricant is preferably one or more selected from sulfides such as MnS and MoS 2 and nitrides such as BN (boron nitride). When two or more kinds of solid lubricants are used, it is more preferable that at least one kind is uniformly dispersed with an average particle diameter of 2 to 10 μm and other kinds with an average particle diameter of 10 to 50 μm. Solid lubricants with an average particle size of 2 to 10 μm improve machinability by being finely dispersed, and solid lubricants with a particle size range of 10 to 50 μm improve self-lubricating properties by being relatively coarse. And wear resistance is improved.
基地中に分散させる硬質粒子に関し、第一硬質粒子は第二硬質粒子よりも硬く、第二硬質粒子は基地相よりも硬いものとする。中間の硬さの硬質粒子が存在することによって、基地相と硬質粒子の硬さのバランスが取れ、耐摩耗性を維持しつつ、相手材攻撃性を抑えることができる。 Regarding the hard particles dispersed in the matrix, the first hard particles are harder than the second hard particles, and the second hard particles are harder than the matrix phase. Due to the presence of the intermediate hardness hard particles, the hardness of the base phase and the hard particles can be balanced, and the attack of the mating material can be suppressed while maintaining the wear resistance.
第一硬質粒子は、平均粒径が50〜150μmでHv800〜1200のビッカース硬さを有し、質量%で2〜8%分散されているものとする。特に、質量%で、Mo:40〜70%、Si:0.1〜2.0%、残部がFe及び不可避的不純物からなる金属間化合物のFe-Mo-Si合金粒子を使用することが好ましい。後述する第二硬質粒子とともに用いることにより合金元素の基地中への拡散が抑制され、基地組織が変質することなく、軟化抵抗を高め、相手材への攻撃を抑えることができるとともに自己の耐摩耗性を向上することが可能となる。
The first hard particles have an average particle size has a Vickers hardness of Hv800~1200 at 50 to 150 [mu] m, is assumed to be distributed 2% to 8% in mass%. In particular, it is preferable to use Fe-Mo-Si alloy particles of an intermetallic compound consisting of Mo: 40 to 70%, Si: 0.1 to 2.0%, and the balance of Fe and inevitable impurities in mass%. By using it together with the second hard particles described later, diffusion of the alloy element into the matrix is suppressed, the matrix structure is not altered, softening resistance can be increased, attack on the counterpart material can be suppressed, and self wear resistance It becomes possible to improve the property.
第二硬質粒子は基地よりも硬く、平均粒径が10〜150μmでHv400〜490のビッカース硬さを有し、質量%で5〜15%分散されているものとする。平均粒径が20〜130μmであれば、さらに好ましい。特に、質量%で、C:0.2〜0.5%、Cr:0.5〜5%、Mo:1〜5%、V:2〜5%、残部がFe及び不可避的不純物からなるFe-C-Cr-Mo-V合金粒子を使用することが好ましい。比較的細かい第二硬質粒子を基地中に分散させることで、合金元素の一部(例えば、CrやV)が基地中に固溶、又は炭化物を形成して基地を強化するとともに第一硬質粒子の合金元素の基材への拡散を抑制する。これにより、相手材への攻撃を抑えることができるとともに自己の耐摩耗性を向上することが可能となる。
The second hard particles harder than the base, the average particle size has a Vickers hardness of Hv400~ 490 at 10 to 150 m, is assumed to be distributed 5-15% in mass%. More preferably, the average particle size is 20 to 130 μm. In particular, Fe-C-Cr-Mo consisting of mass%, C: 0.2-0.5%, Cr: 0.5-5%, Mo: 1-5%, V: 2-5%, the balance being Fe and inevitable impurities It is preferable to use -V alloy particles. By dispersing relatively fine second hard particles in the matrix, some of the alloy elements (for example, Cr and V) form solid solutions or carbides in the matrix to strengthen the matrix and the first hard particles Suppresses diffusion of the alloy element into the base material. As a result, it is possible to suppress attacks on the counterpart material and to improve the self wear resistance.
基地部は、質量%でC:0.5〜2.5%、Si:0.4〜2%、Mo:0.5〜5%、Ni:1〜5%、残部がFe及び不可避的不純物からなる組成を有するのが好ましい。Cは基地に固溶して基地を強化するとともに、他の合金元素と結合して炭化物を形成し、耐摩耗性を向上させる。また、Siは酸化膜の形成により耐摩耗性を向上させ、Moは優れた焼き入れ性及び基地強度の向上のほかバルブシートの酸化開始温度を下げ、耐摩耗性を向上させる。Niは基地の強度及び硬さの向上により耐摩耗性を向上させる。顕微鏡組織としては、焼戻しマルテンサイトとパーライトの混合組織を含むことが好ましく、その場合、適度な靱性を備えるとともに優れた耐摩耗性を示す。もちろん、前記混合組織には微細な炭化物が分散している。 The base portion preferably has a composition of C: 0.5 to 2.5%, Si: 0.4 to 2%, Mo: 0.5 to 5%, Ni: 1 to 5%, and the balance of Fe and inevitable impurities in mass%. . C dissolves in the base and strengthens the base, and combines with other alloy elements to form carbides, improving wear resistance. In addition, Si improves the wear resistance by forming an oxide film, and Mo improves the wear resistance by lowering the oxidation start temperature of the valve seat as well as improving the hardenability and base strength. Ni improves wear resistance by improving the strength and hardness of the base. The microscopic structure preferably includes a mixed structure of tempered martensite and pearlite. In this case, the microstructural structure has appropriate toughness and excellent wear resistance. Of course, fine carbides are dispersed in the mixed structure.
本発明の鉄基焼結合金製バルブシートの製造において、基地相の原料としては、鉄粉に各合金元素の金属粉末、黒鉛粉末等を加えても良く、予め所定の組成に合金化した合金粉末(プレアロイ合金粉末)を用いてもよい。基地相を構成する鉄粉及び/又はプレアロイ合金粉末と合金元素粉末に、硬さの異なる少なくとも二種類の硬質粒子粉末及び固体潤滑材粉末を配合し、混合した混合粉を原料粉とする。原料粉、すなわち、鉄粉、プレアロイ合金粉末、合金元素粉末、硬質粒子、固体潤滑材粉末の混合粉末の合計量に対して、ステアリン酸塩等を0.5〜2%、離型材として配合しても良い。混合粉末は成形プレス等により圧縮・成形して圧粉体に成形され、前記圧粉体は真空又は非酸化性(又は還元性)雰囲気中で1050〜1200℃の温度範囲で焼結され、さらに500〜700℃の温度範囲で焼き戻し処理される。焼き戻し後の焼結体には、樹脂等により封孔処理を実施してもよい。 In the production of the iron-based sintered alloy valve seat of the present invention, as a raw material of the base phase, metal powder of each alloy element, graphite powder, etc. may be added to iron powder, and an alloy alloyed in advance with a predetermined composition Powder (pre-alloy alloy powder) may be used. At least two types of hard particle powders and solid lubricant powders having different hardnesses are blended into the iron powder and / or prealloy alloy powder and alloy element powder constituting the matrix phase, and the mixed powder is used as raw material powder. Stearate, etc. may be blended as a mold release material in an amount of 0.5 to 2%, based on the total amount of raw material powder, that is, iron powder, pre-alloy alloy powder, alloy element powder, hard particles, and solid lubricant powder. good. The mixed powder is compressed and molded by a molding press or the like to form a green compact, and the green compact is sintered in a temperature range of 1050 to 1200 ° C. in a vacuum or a non-oxidizing (or reducing) atmosphere. It is tempered in the temperature range of 500-700 ° C. The sintered body after tempering may be sealed with a resin or the like.
焼結温度は1050℃未満では、拡散結合が不足し所定の強度が得られない。一方、1200℃を超える温度で焼結すると、硬質粒子と基地との間に異常拡散が生じ、耐摩耗性の劣化がおこる。非酸化性(又は還元性)雰囲気としては、具体的にはNH3ガスやN2とH2の混合ガス等を用いた雰囲気とすることが望ましい。 When the sintering temperature is less than 1050 ° C., diffusion bonding is insufficient and a predetermined strength cannot be obtained. On the other hand, if sintering is performed at a temperature exceeding 1200 ° C., abnormal diffusion occurs between the hard particles and the matrix, resulting in deterioration of wear resistance. Specifically, the non-oxidizing (or reducing) atmosphere is preferably an atmosphere using NH 3 gas or a mixed gas of N 2 and H 2 .
実施例1〜2(J1〜J2)、参考例1〜3(R1〜R3)及び比較例1〜6(C1〜C6)
粒度分布が150〜200メッシュにピークを有する純鉄粉及び/又はMo:2.5%、Si:1%、C:0.02%、残部が鉄(不可避的不純物を含む)からなるプレアロイ合金粉末に、表1に示す基地部A〜Kの配合量になるようなMo粉末、Si粉末、Ni粉末、黒鉛粉の所定量と、表2に示すFe-Mo-Si合金のL〜Rの第一硬質粒子及び表3に示すFe-C-Cr-Mo-V合金のS〜Yの第二硬質粒子、並びに表4に示す固体潤滑材粉末を、それぞれ表4に示す比率(質量%)で配合し、混合機で混練して混合粉を作製した。
Examples 1-2 (J1-J2), Reference Examples 1-3 (R1-R3) and Comparative Examples 1-6 (C1-C6)
Pure iron powder with a particle size distribution having a peak at 150 to 200 mesh and / or prealloy alloy powder consisting of Mo: 2.5%, Si: 1%, C: 0.02%, the balance being iron (including inevitable impurities) Predetermined amounts of Mo powder, Si powder, Ni powder, and graphite powder as shown in Table 1 and the first hard particles L to R of the Fe-Mo-Si alloy shown in Table 2 And the second hard particles of S to Y of the Fe—C—Cr—Mo—V alloy shown in Table 3 and the solid lubricant powder shown in Table 4 were blended in the ratios (mass%) shown in Table 4, respectively. A mixed powder was prepared by kneading with a mixer.
これらの混合粉を成形金型に充填し、成形プレスにより面圧6.5t/cm2で圧縮・成形した後、1120℃の真空雰囲気にて焼結し、外径37.6mmφ、内径26mmφ、厚さ8mmのリング状焼結体を作製した。その後、650℃にて焼き戻し処理を行った。このようにして、焼き戻しマルテンサイト相及びパーライト相を含む基地部と、基地中に硬さの異なる二種類の硬質粒子(Fe−Mo−Si合金とFe-C-Cr-Mo-V合金)と、固体潤滑材(MnS及び/又はBN)を分散した実施例1〜2(J1〜J2)及び参考例1〜3(R1〜R3)のリング状の焼結体を得た。比較例としては、固体潤滑材の総量が1%以上のもの(比較例1(C1)、2(C2)、4-6(C4-C6))、硬質粒子粉末を一種類のみとしたもの(比較例3、4(C3、C4))の混合粉を用い、実施例1〜2(J1〜J2)及び参考例1〜3(R1〜R3)と同様な工程で比較例1〜6(C1〜C6)のリング状の焼結体を得た。得られた焼結体の基地部、硬質粒子についてマイクロビッカース硬度計により、荷重50〜100gにてビッカース硬さを測定した。その結果を表4に併せて示す。
These mixed powders are filled into a molding die, compressed and molded with a molding press at a surface pressure of 6.5 t / cm 2 , and then sintered in a vacuum atmosphere at 1120 ° C., outer diameter 37.6 mmφ, inner diameter 26 mmφ, thickness An 8 mm ring-shaped sintered body was produced. Thereafter, a tempering treatment was performed at 650 ° C. Thus, the base part containing the tempered martensite phase and the pearlite phase, and two types of hard particles having different hardness in the base (Fe-Mo-Si alloy and Fe-C-Cr-Mo-V alloy) And the ring-shaped sintered compact of Examples 1-2 (J1-J2) and Reference Examples 1-3 (R1-R3) which disperse | distributed solid lubricant (MnS and / or BN) was obtained. As comparative examples, the total amount of solid lubricant is 1% or more (Comparative Examples 1 (C1), 2 (C2), 4-6 (C4-C6)), and only one type of hard particle powder ( Comparative Examples 3 and 4 (C3, C4)) were used in the same steps as in Examples 1 to 2 (J1 to J2) and Reference Examples 1 to 3 (R1 to R3) using
得られたリング状焼結体をバルブシートに加工し、図1に示した単体摩耗試験機を用いて耐摩耗性を評価した。バルブシート4はシリンダヘッド相当材のバルブシートホルダ2に圧入して試験機にセットされ、摩耗試験は、バーナー1によりバルブ3及びバルブシート4を加熱しながら、カム7の回転に連動してバルブ3を上下させることによって行われる。なお、バルブシート4には熱電対5, 6を埋め込み、バルブシートの当たり面が所定の温度になるようにバーナー1の火力を調節する。バルブシート4はバルブ3よって繰り返し叩かれることにより摩耗し、その摩耗量は試験前後のバルブシート及びバルブの形状を測定することにより、当たり面の後退量として算出した。ここで、バルブは上記バルブシートに適合するサイズのSUH合金(JIS規格:JIS G 4311)製のものを使用した。試験条件としては、温度150℃及び250℃、カム回転数2500 rpm、試験時間5時間とした。試験結果を表5、図2((a)試験温度150℃、(b)試験温度250℃)に示す。
The obtained ring-shaped sintered body was processed into a valve seat, and the wear resistance was evaluated using a single wear tester shown in FIG. The valve seat 4 is press-fitted into a
バルブシートの摩耗量は、硬質粒子にFe−Mo−Si合金のみを添加し分散した比較例3(C3)の摩耗量を1としたときの相対比率で示している。本発明による実施例1〜2(J1〜J2)及び参考例1〜3(R1〜R3)は、試験温度150℃及び250℃において、バルブシート摩耗量が比較例3(C3)に対していずれも低減し、相手材のバルブ摩耗量も低減しており、低温域及び高温域のいずれにおいても優れた耐摩耗性と比較的穏やかな相手材攻撃性を示していた。また、バルブシートとバルブの総摩耗量についても、本発明による実施例1〜2(J1〜J2)及び参考例1〜3(R1〜R3)は150℃及び250℃において比較例3の半分以下であり、低温度域から高温度域までの幅広い温度域で耐摩耗性が顕著に向上している。一方、固体潤滑材の総量が1%以上のもの(比較例1(C1), 2(C2), 4-6(C4-C6))、硬質粒子粉末を1種類のみとしたもの(比較例3, 4(C3, C4))は、試験温度150℃及び250℃の一方で耐摩耗性が向上するものもあるが、低温度域から高温度域までの幅広い温度域で顕著な耐摩耗性の向上をえることができなかった。本発明の実施例は、比較例に比べて低温度域から高温度域までの幅広い温度域でバルブシート摩耗量及び相手材の摩耗量が少なく、耐摩耗性が向上しかつ相手材の攻撃性も低下している。
The amount of wear of the valve seat is shown as a relative ratio when the amount of wear in Comparative Example 3 (C3) in which only the Fe—Mo—Si alloy is added and dispersed in the hard particles is 1. In Examples 1 to 2 (J1 to J2) and Reference Examples 1 to 3 (R1 to R3) according to the present invention, the valve seat wear amount at any of test temperatures 150 ° C. and 250 ° C. is different from that of Comparative Example 3 (C3). The valve wear amount of the counterpart material was also reduced, and excellent wear resistance and relatively gentle attack of the counterpart material were exhibited in both the low temperature range and the high temperature range. Moreover, also about the total amount of wear of a valve seat and a valve, Examples 1-2 (J1-J2) by this invention and Reference Examples 1-3 (R1-R3) are below half of comparative example 3 in 150 ° C and 250 ° C. The wear resistance is remarkably improved in a wide temperature range from a low temperature range to a high temperature range. On the other hand, the total amount of solid lubricant is 1% or more (Comparative Example 1 (C1), 2 (C2), 4-6 (C4-C6)), and only one type of hard particle powder (Comparative Example 3) , 4 (C3, C4)) have improved wear resistance at the test temperatures of 150 ° C and 250 ° C, but have a remarkable wear resistance in a wide temperature range from low to high temperatures. I couldn't improve. In the embodiment of the present invention, the valve seat wear amount and the wear amount of the counterpart material are small in a wide temperature range from the low temperature range to the high temperature range as compared with the comparative example, the wear resistance is improved, and the aggressiveness of the counterpart material is improved. Has also declined.
1 バーナー
2 バルブシートホルダ
3 バルブ
4 バルブシート
5 熱電対(高温側)
6 熱電対(低温側)
7 カム
1 Burner
2 Valve seat holder
3 Valve
4 Valve seat
5 Thermocouple (high temperature side)
6 Thermocouple (low temperature side)
7 cams
Claims (5)
5. The iron-based firing according to claim 1, wherein the solid lubricant is at least one selected from sulfides and nitrides, and has an average particle size of 2 to 50 μm. Bonded valve seat.
Priority Applications (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2011009719A JP5823697B2 (en) | 2011-01-20 | 2011-01-20 | Ferrous sintered alloy valve seat |
| MX2013008435A MX2013008435A (en) | 2011-01-20 | 2012-01-20 | VALVE SEAT FORMED OF IRON BASED SINTERED ALLOY. |
| PCT/JP2012/051191 WO2012099239A1 (en) | 2011-01-20 | 2012-01-20 | Iron-based sintered alloy valve seat |
| US13/980,612 US20130291822A1 (en) | 2011-01-20 | 2012-01-20 | Valve seat made of iron-based sintered alloy |
| CN2012800059983A CN103328776A (en) | 2011-01-20 | 2012-01-20 | Iron-based sintered alloy valve seat |
| EP12736573.2A EP2666981A4 (en) | 2011-01-20 | 2012-01-20 | FRITTED ALLOY VALVE SEAT BASED ON IRON |
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| JP2011009719A JP5823697B2 (en) | 2011-01-20 | 2011-01-20 | Ferrous sintered alloy valve seat |
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| JP2012149584A JP2012149584A (en) | 2012-08-09 |
| JP2012149584A5 JP2012149584A5 (en) | 2013-08-29 |
| JP5823697B2 true JP5823697B2 (en) | 2015-11-25 |
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| JP2011009719A Expired - Fee Related JP5823697B2 (en) | 2011-01-20 | 2011-01-20 | Ferrous sintered alloy valve seat |
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| US (1) | US20130291822A1 (en) |
| EP (1) | EP2666981A4 (en) |
| JP (1) | JP5823697B2 (en) |
| CN (1) | CN103328776A (en) |
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| WO (1) | WO2012099239A1 (en) |
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| JP6305811B2 (en) * | 2014-03-31 | 2018-04-04 | 日本ピストンリング株式会社 | Ferrous sintered alloy material for valve seat and method for producing the same |
| JP6427442B2 (en) * | 2015-03-09 | 2018-11-21 | 山陽特殊製鋼株式会社 | Hard powder for Fe-based sintering and Fe-based sintered body excellent in wear resistance using the same |
| JP6392796B2 (en) * | 2016-01-25 | 2018-09-19 | トヨタ自動車株式会社 | Method for producing wear-resistant iron-based sintered alloy, compact for sintered alloy, and wear-resistant iron-based sintered alloy |
| JP6352959B2 (en) * | 2016-02-04 | 2018-07-04 | トヨタ自動車株式会社 | Method for producing wear-resistant iron-based sintered alloy, compact for sintered alloy, and wear-resistant iron-based sintered alloy |
| WO2018179590A1 (en) * | 2017-03-28 | 2018-10-04 | 株式会社リケン | Sintered valve seat |
| JP6842345B2 (en) * | 2017-04-04 | 2021-03-17 | トヨタ自動車株式会社 | Abrasion-resistant iron-based sintered alloy manufacturing method |
| DE102018209682A1 (en) * | 2018-06-15 | 2019-12-19 | Mahle International Gmbh | Process for the manufacture of a powder metallurgical product |
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| JPS5620143A (en) * | 1979-07-24 | 1981-02-25 | Mazda Motor Corp | Sintered alloy for valve seat |
| JPH0593241A (en) * | 1991-09-30 | 1993-04-16 | Riken Corp | Production of iron-base sintered alloy for valve seat |
| EP0604773B2 (en) * | 1992-11-27 | 2000-08-30 | Toyota Jidosha Kabushiki Kaisha | Fe-based alloy powder adapted for sintering, Fe-based sintered alloy having wear resistance, and process for producing the same |
| JP3952344B2 (en) * | 1998-12-28 | 2007-08-01 | 日本ピストンリング株式会社 | Wear-resistant iron-based sintered alloy material for valve seat and valve seat made of iron-based sintered alloy |
| JP2001050020A (en) * | 1999-05-31 | 2001-02-23 | Nippon Piston Ring Co Ltd | Valve device for internal combustion engine |
| JP4001450B2 (en) * | 2000-05-02 | 2007-10-31 | 日立粉末冶金株式会社 | Valve seat for internal combustion engine and manufacturing method thereof |
| JP2002129296A (en) * | 2000-10-27 | 2002-05-09 | Nippon Piston Ring Co Ltd | Iron-base sintered alloy material for valve seat, and valve seat made of iron-base sintered alloy |
| JP3809944B2 (en) * | 2001-11-29 | 2006-08-16 | 株式会社リケン | Hard particle dispersed sintered alloy and method for producing the same |
| JP3970060B2 (en) * | 2002-03-12 | 2007-09-05 | 株式会社リケン | Ferrous sintered alloy for valve seat |
| JP3928782B2 (en) * | 2002-03-15 | 2007-06-13 | 帝国ピストンリング株式会社 | Method for producing sintered alloy for valve seat |
| JP3926320B2 (en) * | 2003-01-10 | 2007-06-06 | 日本ピストンリング株式会社 | Iron-based sintered alloy valve seat and method for manufacturing the same |
| JP4213060B2 (en) * | 2004-03-03 | 2009-01-21 | 日本ピストンリング株式会社 | Ferrous sintered alloy material for valve seats |
| CN100422376C (en) * | 2005-03-23 | 2008-10-01 | 日本活塞环株式会社 | Iron-based sintered alloy valve seat material for internal combustion engines |
| JP4584158B2 (en) * | 2005-03-23 | 2010-11-17 | 日本ピストンリング株式会社 | Valve seat material made of iron-based sintered alloy for internal combustion engines |
| JP2006193831A (en) * | 2006-01-23 | 2006-07-27 | Nippon Piston Ring Co Ltd | Abrasion resistance iron-based sintered alloy material for valve seat and valve seat made of iron-based sintered alloy |
| JP5484899B2 (en) * | 2008-03-31 | 2014-05-07 | 日本ピストンリング株式会社 | Ferrous sintered alloy for valve seat and valve seat for internal combustion engine |
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- 2011-01-20 JP JP2011009719A patent/JP5823697B2/en not_active Expired - Fee Related
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2012
- 2012-01-20 US US13/980,612 patent/US20130291822A1/en not_active Abandoned
- 2012-01-20 WO PCT/JP2012/051191 patent/WO2012099239A1/en not_active Ceased
- 2012-01-20 EP EP12736573.2A patent/EP2666981A4/en not_active Withdrawn
- 2012-01-20 MX MX2013008435A patent/MX2013008435A/en unknown
- 2012-01-20 CN CN2012800059983A patent/CN103328776A/en active Pending
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| WO2012099239A1 (en) | 2012-07-26 |
| CN103328776A (en) | 2013-09-25 |
| EP2666981A4 (en) | 2015-04-01 |
| EP2666981A1 (en) | 2013-11-27 |
| JP2012149584A (en) | 2012-08-09 |
| US20130291822A1 (en) | 2013-11-07 |
| MX2013008435A (en) | 2013-12-16 |
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