JP6133711B2 - Method for forming chromium carbide layer - Google Patents
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- JP6133711B2 JP6133711B2 JP2013139719A JP2013139719A JP6133711B2 JP 6133711 B2 JP6133711 B2 JP 6133711B2 JP 2013139719 A JP2013139719 A JP 2013139719A JP 2013139719 A JP2013139719 A JP 2013139719A JP 6133711 B2 JP6133711 B2 JP 6133711B2
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- 229910003470 tongbaite Inorganic materials 0.000 title claims description 51
- 238000000034 method Methods 0.000 title claims description 37
- UFGZSIPAQKLCGR-UHFFFAOYSA-N chromium carbide Chemical compound [Cr]#C[Cr]C#[Cr] UFGZSIPAQKLCGR-UHFFFAOYSA-N 0.000 title claims 8
- 239000000843 powder Substances 0.000 claims description 28
- 239000000243 solution Substances 0.000 claims description 24
- 238000001746 injection moulding Methods 0.000 claims description 14
- 229910052751 metal Inorganic materials 0.000 claims description 14
- 239000002184 metal Substances 0.000 claims description 14
- 229910001220 stainless steel Inorganic materials 0.000 claims description 12
- 239000011230 binding agent Substances 0.000 claims description 11
- 238000002347 injection Methods 0.000 claims description 11
- 239000007924 injection Substances 0.000 claims description 11
- 239000010935 stainless steel Substances 0.000 claims description 11
- 239000000203 mixture Substances 0.000 claims description 10
- 239000000463 material Substances 0.000 claims description 9
- 229910000963 austenitic stainless steel Inorganic materials 0.000 claims description 8
- 238000010304 firing Methods 0.000 claims description 8
- 239000011347 resin Substances 0.000 claims description 7
- 229920005989 resin Polymers 0.000 claims description 7
- -1 The machine parts Substances 0.000 claims description 2
- 239000004925 Acrylic resin Substances 0.000 claims description 2
- 229920000178 Acrylic resin Polymers 0.000 claims description 2
- 229920005990 polystyrene resin Polymers 0.000 claims description 2
- GVEHJMMRQRRJPM-UHFFFAOYSA-N chromium(2+);methanidylidynechromium Chemical compound [Cr+2].[Cr]#[C-].[Cr]#[C-] GVEHJMMRQRRJPM-UHFFFAOYSA-N 0.000 description 43
- 239000011651 chromium Substances 0.000 description 24
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 23
- 229910052804 chromium Inorganic materials 0.000 description 23
- 238000004458 analytical method Methods 0.000 description 11
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 8
- 229910052799 carbon Inorganic materials 0.000 description 8
- 238000009826 distribution Methods 0.000 description 8
- 230000015572 biosynthetic process Effects 0.000 description 6
- 238000010586 diagram Methods 0.000 description 6
- 238000002149 energy-dispersive X-ray emission spectroscopy Methods 0.000 description 6
- 238000000921 elemental analysis Methods 0.000 description 5
- 238000010438 heat treatment Methods 0.000 description 5
- 230000003287 optical effect Effects 0.000 description 5
- 238000000879 optical micrograph Methods 0.000 description 5
- 238000010894 electron beam technology Methods 0.000 description 4
- 238000005238 degreasing Methods 0.000 description 3
- 238000000465 moulding Methods 0.000 description 3
- 238000005254 chromizing Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000005530 etching Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000005498 polishing Methods 0.000 description 2
- 238000005245 sintering Methods 0.000 description 2
- 239000006104 solid solution Substances 0.000 description 2
- 239000001993 wax Substances 0.000 description 2
- 229910000604 Ferrochrome Inorganic materials 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 238000004512 die casting Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 238000005495 investment casting Methods 0.000 description 1
- 238000003754 machining Methods 0.000 description 1
- 229910001105 martensitic stainless steel Inorganic materials 0.000 description 1
- 239000011812 mixed powder Substances 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920005553 polystyrene-acrylate Polymers 0.000 description 1
- 238000004663 powder metallurgy Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
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- Powder Metallurgy (AREA)
Description
本発明は、ステンレス鋼からなる機械部品の表面にクロム炭化物層を形成するためのクロム炭化物層の形成方法に関する。 The present invention relates to a method of forming chromium carbide layer to form a chromium carbide layer on the surface of machine parts made of stainless steel.
過給機におけるタービンにはステンレス鋼からなるタービン部品(機械部品の一例)が用いられており、また、タービン部品の耐熱性、耐摩耗性等を向上させるために、タービン部品の表面に対してクロマイズ処理を施してタービン部品の表面にクロム炭化物層を形成することがよく行われている(特許文献1及び特許文献2参照)。 The turbine in the turbocharger uses a stainless steel turbine part (an example of a mechanical part). In order to improve the heat resistance, wear resistance, etc. of the turbine part, A chromium carbide layer is often formed on the surface of a turbine component by performing a chromization treatment (see Patent Document 1 and Patent Document 2).
一方、近年、高寸法精度及び高強度の成形体の製造を可能にした金属粉末射出成形(MIM工法)が機械加工、ダイキャスト、粉末冶金、精密鋳造に次ぐ第5世代の精密加工技術として注目されている。それに伴い、ステンレス鋼の粉末とバインダの混合物を射出材料とし、タービン部品の成形(製造)に金属粉末射出成形を適用する試みがなされている。 On the other hand, in recent years, metal powder injection molding (MIM method), which enables the production of compacts with high dimensional accuracy and high strength, has attracted attention as the fifth-generation precision processing technology after machining, die casting, powder metallurgy, and precision casting. Has been. Accordingly, attempts have been made to apply metal powder injection molding to the molding (manufacturing) of turbine parts using a mixture of stainless steel powder and binder as an injection material.
しかしながら、ステンレス鋼の粉末とバインダの混合物を射出材料として金属粉末射出成形によって実際に成形体を成形して焼成し、焼結済みの成形体の表面及び断面について電子線マイクロアナライザー(EPMA)による元素分析を行うと、成形体の表面及び断面にクロム(Cr)の濃度の高い箇所が存在することが確認された(後述の実施例参照)。また、クロムの濃度の高い箇所についてエネルギー分散型X線分析(EDX)による点分析すると、クロム炭化物が存在していることが確認された。つまり、成形体を成形して焼成すると、成形体の表面及び内部にクロム炭化物が生成され、成形体の表面及び内部における、クロム炭化物の周辺の炭素(C)が少なくなり、クロマイズ処理によってクロムと結合するための炭素の絶対量が減ることになる。そのため、焼結済みの成形体の表面に対してクロマイズ処理を施しても、焼結済みの成形体の表面に形成されたクロム炭化物層の厚みが薄かったり、クロム炭化物層の厚みのばらつきが生じたりして(後述の実施例参照)、焼結済みの成形体により構成されるタービン部品の耐熱性、耐摩耗性等を十分に向上させることが困難であるという問題がある。 However, by using a mixture of stainless steel powder and binder as an injection material, the molded body is actually molded and fired by metal powder injection molding, and the surface and cross section of the sintered molded body are measured with an electron beam microanalyzer (EPMA). When the analysis was performed, it was confirmed that there were locations with high chromium (Cr) concentration on the surface and cross-section of the molded body (see Examples described later). Further, when point analysis by energy dispersive X-ray analysis (EDX) was performed on a portion having a high chromium concentration, it was confirmed that chromium carbide was present. In other words, when the molded body is molded and fired, chromium carbide is generated on the surface and inside of the molded body, and the carbon (C) around the chromium carbide on the surface and inside of the molded body is reduced. The absolute amount of carbon for bonding is reduced. Therefore, even if chromization treatment is applied to the surface of the sintered compact, the thickness of the chromium carbide layer formed on the surface of the sintered compact is thin or the thickness of the chromium carbide layer varies. However, there is a problem that it is difficult to sufficiently improve the heat resistance, wear resistance, and the like of the turbine component constituted by the sintered compact (see the examples described later).
そこで、本発明は、前述の問題を解決することができる、新規な構成のクロム炭化物層の形成方法を提供することを目的とする。 Then, this invention aims at providing the formation method of the chromium carbide layer of a novel structure which can solve the above-mentioned problem.
本発明の発明者は、前述の課題を解決するために、試行錯誤を繰り返した結果、ステンレス鋼の粉末を用いて金属粉末射出成形によって成形して焼成した焼結済みの成形体に対して溶体化処理(固溶化処理)を施すと、焼成時に成形体の表面及び内部に生成されたクロム炭化物をほぼ消滅させることができるという、新規な知見を得ることができ、本発明を完成するに至った。これは、成形体の表面及び内部に含まれるクロム炭化物が溶体化処理によって炭素とクロムに分離したことによるものと考えられる。 The inventor of the present invention, as a result of repeated trial and error to solve the above-mentioned problems, resulted in a solution to a sintered compact that was molded and fired by metal powder injection molding using stainless steel powder. When the heat treatment (solid solution treatment) is performed, a new finding that the chromium carbide generated on the surface and inside of the molded body during firing can be almost eliminated can be obtained, and the present invention has been completed. It was. This is considered due to the fact that chromium carbide contained in the surface and inside of the compact was separated into carbon and chromium by solution treatment.
本発明の態様は、ステンレス鋼からなる機械部品の表面にクロム炭化物層を形成するためのクロム炭化物層の形成方法において、
前記機械部品は、ステンレス鋼の粉末と、ポリスチレン系樹脂及びアクリル系樹脂の複数種の樹脂とワックスとからなるバインダとの混合物を射出材料として金属粉末射出成形(MIM工法)によって成形して焼成した焼結済みの成形体により構成され、前記機械部品に対して溶体化処理(固溶化処理)を施す溶体化工程と、前記溶体化工程の終了後に、前記機械部品の表面に対してクロマイズ処理を施すことにより、前記機械部品の表面に前記クロム炭化物層を形成するクロマイズ工程と、を具備したことである。
An aspect of the present invention is a method for forming a chromium carbide layer for forming a chromium carbide layer on the surface of a mechanical component made of stainless steel.
The mechanical components, a powder of stainless steel, and fired by molding by a metal powder injection molding a mixture as an injection material for a binder consisting of a plurality of kinds of resin and wax polystyrene resin and an acrylic resin (MIM method) A solution forming step that is formed of a sintered compact and that is subjected to a solution treatment (solid solution treatment) on the machine component, and after the solution treatment step, the surface of the machine component is subjected to chromization treatment. by applying a Kuromaizu forming the chromium carbide layer on the mechanical parts of the surface, Ru der that provided with the.
ここで、「機械部品」とは、過給機におけるタービンに用いられるタービン部品の他、種々の機械に用いられる部品を含む意である。 Here, the “mechanical part” means a part used for various machines in addition to a turbine part used for a turbine in a supercharger.
本発明の態様によると、前記機械部品はステンレス鋼の粉末とバインダの混合物を射出材料として金属粉末射出成形によって成形された焼結済みの前記成形体により構成され、前記機械部品に対して溶体化処理を施しているため、前述の新規な知見を適用すると、焼成時に前記機械部品の表面及び内部に生成されたクロム炭化物を消滅させることができる。これにより、前記機械部品の表面に対してクロマイズ処理を施す前に、前記機械部品の表面及び内部における、クロマイズ処理によってクロムと結合するための炭素の絶対量を増やすことができる。 According to an aspect of the present invention, the mechanical part is constituted by the sintered compact that is molded by metal powder injection molding using a mixture of stainless steel powder and binder as an injection material, and is formed into a solution with respect to the mechanical part. Since the treatment is applied, when the above-described novel knowledge is applied, chromium carbides generated on the surface and inside of the mechanical part at the time of firing can be eliminated. Thereby, before performing a chromization process with respect to the surface of the said machine component, the absolute amount of the carbon for couple | bonding with a chromium by the chromization process in the surface and the inside of the said machine part can be increased.
本発明によれば、前記機械部品の表面に対してクロマイズ処理を施す前に、前記機械部品の表面及び内部における、クロマイズ処理によってクロムと結合するための炭素の絶対量を増やすことができるため、前記機械部品が金属粉末射出成形によって成形して焼成した焼結済みの前記成形体により構成される場合でも、前記クロム炭化物層の厚みの均一性を高めつつ、前記クロム炭化物層の厚みを厚くして、前記機械部品の耐熱性、耐摩耗性等を十分に向上させることができる。 According to the present invention, before performing the chromization treatment on the surface of the mechanical component, the absolute amount of carbon to be combined with chromium by the chromization treatment on the surface and inside of the mechanical component can be increased. Even when the mechanical part is constituted by the sintered compact that is molded and fired by metal powder injection molding, the thickness of the chromium carbide layer is increased while increasing the uniformity of the thickness of the chromium carbide layer. Thus, the heat resistance, wear resistance, etc. of the mechanical part can be sufficiently improved.
以下、本発明の実施形態に係るクロム炭化物層の形成方法の形成対象であるノズルリンク、及び本発明の実施形態に係るクロム炭化物層の形成方法等について順次説明する。 Hereinafter, a nozzle link which is a formation target of a method for forming a chromium carbide layer according to an embodiment of the present invention, a method for forming a chromium carbide layer according to an embodiment of the present invention, and the like will be sequentially described.
図1(a)に示すように、本発明の実施形態に係るクロム炭化物層の形成方法の形成対象であるノズルリンク1は、特開2012−163083号公報、特開2008−75635号公報、及び特開2007−40251号公報等に示すように、可変容量型過給機におけるタービンの可変ノズル機構(図示省略)に用いられるタービン部品の1つであって、可変ノズル機構の駆動リング(図示省略)の回転力を可変ノズル機構のノズル翼(図示省略)に伝達するものである。また、ノズルリンク1の基部には、貫通穴2が形成されており、ノズルリンク1の基部は、ノズル翼の翼軸をノズルリンク1の貫通穴2に挿通させた状態で、ノズル翼の翼軸の先端部をかしめることによってノズル翼の翼軸に一体的に連結されるものである。更に、ノズルリンク1は、先端側に、対向した一対のアーム部3を有しており、ノズルリンク1の一対のアーム部3は、駆動リングに設けられた矩形のジョイント部材4を挟むように係合するものである。なお、ノズルリンク1の一対のアーム部3の対向面3fは、ジョイント部材4の側面との摺動面になっている。 As shown in FIG. 1 (a), a nozzle link 1 that is a formation target of a method for forming a chromium carbide layer according to an embodiment of the present invention is disclosed in JP 2012-163083 A, JP 2008-75635 A, and As disclosed in Japanese Patent Application Laid-Open No. 2007-40251 and the like, it is one of turbine parts used for a variable nozzle mechanism (not shown) of a turbine in a variable capacity supercharger, and is a drive ring (not shown) of the variable nozzle mechanism. ) Is transmitted to the nozzle blades (not shown) of the variable nozzle mechanism. Further, a through hole 2 is formed in the base portion of the nozzle link 1, and the base portion of the nozzle link 1 is a blade blade of the nozzle blade in a state where the blade shaft of the nozzle blade is inserted into the through hole 2 of the nozzle link 1. It is integrally connected to the blade shaft of the nozzle blade by caulking the tip of the shaft. Further, the nozzle link 1 has a pair of opposed arm portions 3 on the distal end side, and the pair of arm portions 3 of the nozzle link 1 sandwich a rectangular joint member 4 provided on the drive ring. To engage. The opposing surfaces 3 f of the pair of arm portions 3 of the nozzle link 1 are sliding surfaces with the side surfaces of the joint member 4.
ノズルリンク1は、オーステナイト系ステンレス鋼からなり、具体的には、オーステナイト系ステンレス鋼の粉末とバインダの混合物を射出材料として金属粉末射出成形(MIM工法)によって成形して焼成した焼結済みの成形体により構成されている。ここで、金属粉末射出成形は、射出成形金型のキャビティ(図示省略)に混合物を射出して、ノズルリンク1の最終形状と相似形の成形体を成形する射出工程と、射出工程の終了後に、成形体に含まれるバインダを脱脂する脱脂工程と、脱脂工程の終了後に、成形体を焼成して焼結させて、最終形状まで熱収縮させる焼成工程とを具備している。また、バインダとは、ポリスチレン,ポリメチルメタアクリレート等の複数種の樹脂とパラフィンワックス等のワックスとからなるものである。なお、ノズルリンク1がオーステナイト系ステンレス鋼からなる代わりに、フェライト系ステンレス鋼又はマルテンサイト系ステンレス鋼からなるものであっても構わない。 The nozzle link 1 is made of austenitic stainless steel, and specifically, a sintered molded product that is formed by metal powder injection molding (MIM method) using a mixture of austenitic stainless steel powder and binder as an injection material and fired. It is composed of the body. Here, the metal powder injection molding is performed by injecting a mixture into a cavity (not shown) of an injection mold to form a molded body having a shape similar to the final shape of the nozzle link 1, and after completion of the injection process. And a degreasing step for degreasing the binder contained in the molded body, and a firing step for firing and sintering the molded body after the degreasing process to heat shrink to the final shape. The binder is composed of a plurality of types of resins such as polystyrene and polymethyl methacrylate and waxes such as paraffin wax. The nozzle link 1 may be made of ferritic stainless steel or martensitic stainless steel instead of austenitic stainless steel.
続いて、本発明の実施形態に係るクロム炭化物層の形成方法について説明する。 Then, the formation method of the chromium carbide layer which concerns on embodiment of this invention is demonstrated.
本発明の実施形態に係るクロム炭化物層の形成方法は、オーステナイトステンレス系ステンレス鋼からなるノズルリンク1の表面にクロム炭化物層Cを形成するための方法であって、溶体化工程と、クロマイズ工程とを具備している。そして、本発明の実施形態に係るクロム炭化物層の形成方法における各工程の具体的な内容は、次のようになる。 A method for forming a chromium carbide layer according to an embodiment of the present invention is a method for forming a chromium carbide layer C on the surface of a nozzle link 1 made of austenitic stainless steel, which includes a solution treatment step, a chromization step, It has. And the specific content of each process in the formation method of the chromium carbide layer which concerns on embodiment of this invention is as follows.
(i)溶体化工程
溶体化処理炉(図示省略)を用いて、ノズルリンク1に対して溶体化処理を施す。具体的には、ノズルリンク1を溶体化処理炉内の所定位置にセットして、溶体化処理炉内の温度(溶体化温度)を1050〜1150℃の温度域に0.1〜5時間保持する。ここで、溶体化温度を1050〜1150℃の温度域に設定したのは、ノズルリンク1の表面及び内部に含まれるクロム炭化物を炭素とクロムに十分に分離させるためである。また、保持時間(溶体化時間)を0.1時間以上に設定したのは、ノズルリンク1の表面及び内部に含まれるクロム炭化物を炭素とクロムに十分に分離させるためであり、保持時間を5時間以下に設定したのは、溶体化処理炉の稼働時間の短縮を図るためである。
(I) Solution Treatment Step A solution treatment is performed on the nozzle link 1 using a solution treatment furnace (not shown). Specifically, the nozzle link 1 is set at a predetermined position in the solution treatment furnace, and the temperature (solution temperature) in the solution treatment furnace is maintained in a temperature range of 1050 to 1150 ° C. for 0.1 to 5 hours. To do. Here, the solution temperature was set to a temperature range of 1050 to 1150 ° C. in order to sufficiently separate the chromium carbide contained in the surface and the inside of the nozzle link 1 into carbon and chromium. The reason why the holding time (solution time) is set to 0.1 hour or more is to sufficiently separate the chromium carbide contained in the surface and inside of the nozzle link 1 into carbon and chromium, and the holding time is set to 5 hours. The reason for setting the time below is to shorten the operation time of the solution treatment furnace.
(ii)クロマイズ処理
溶体化工程の終了後に、加熱炉(図示省略)を用いて、ノズルリンク1の表面全体に対して粉末パック法によるクロマイズ処理を施す。具体的には、クロム源としてのクロム粉末又はフェロクロム粉末と焼結防止剤としてのアルミナ粉末との混合粉末と共にノズルリンク1を容器(図示省略)に封入する。そして、容器を加熱炉の所定位置にセットして、加熱炉内を真空雰囲気中又は不活性ガス雰囲気中に保ちつつ、加熱炉内の温度を900〜1400℃、好ましくは900〜1200℃の温度域で3〜10時間保持する。これにより、図1(b)に示すように、ノズルリンク1の表面全体にクロム炭化物層Cを形成することができる。
(Ii) Chromizing treatment After the solution treatment step, the entire surface of the nozzle link 1 is subjected to a chromizing treatment by a powder pack method using a heating furnace (not shown). Specifically, the nozzle link 1 is enclosed in a container (not shown) together with a mixed powder of chromium powder or ferrochrome powder as a chromium source and alumina powder as a sintering inhibitor. And a container is set in the predetermined position of a heating furnace, The temperature in a heating furnace is 900-1400 degreeC, Preferably it is the temperature of 900-1200 degreeC, keeping the inside of a heating furnace in a vacuum atmosphere or an inert gas atmosphere. Hold in zone for 3-10 hours. Thereby, as shown in FIG.1 (b), the chromium carbide layer C can be formed in the whole surface of the nozzle link 1. FIG.
なお、ノズルリンク1の表面全体に対してクロマイズ処理を施す代わりに、ノズルリンク1の表面の一部である一対のアーム部3の対向面(摺動面)3fのみに対してクロマイズ処理を施しても構わない。また、ノズルリンク1の表面に粉末パック法によるクロマイズ処理を施す代わりに、気体法又は塩浴法によるクロマイズ処理を施しても構わない。 Instead of performing the chromization process on the entire surface of the nozzle link 1, the chromization process is performed only on the opposing surfaces (sliding surfaces) 3f of the pair of arm portions 3 that are part of the surface of the nozzle link 1. It doesn't matter. Further, instead of subjecting the surface of the nozzle link 1 to the chromization treatment by the powder pack method, the chromization treatment by the gas method or the salt bath method may be performed.
続いて、本発明の実施形態の作用及び効果について説明する。 Then, the effect | action and effect of embodiment of this invention are demonstrated.
ノズルリンク1はオーステナイト系ステンレス鋼の粉末とバインダの混合物を射出材料として金属粉末射出成形によって成形して焼成した焼結済みの成形体により構成され、ノズルリンク1に対して溶体化処理を施しているため、前述の新規な知見を適用すると、焼成時にノズルリンク1の表面及び内部に生成されたクロム炭化物を消滅させることができる。これにより、ノズルリンク1の表面に対してクロマイズ処理を施す前に、ノズルリンク1の表面及び内部における、クロマイズ処理によってクロムと結合するための炭素の絶対量を増やすことができる。 The nozzle link 1 is composed of a sintered compact that is formed by metal powder injection molding using a mixture of austenitic stainless steel powder and binder as an injection material and fired. The nozzle link 1 is subjected to a solution treatment. Therefore, when the above-described new knowledge is applied, the chromium carbide generated on the surface and inside of the nozzle link 1 during firing can be eliminated. Thereby, before performing a chromization process with respect to the surface of the nozzle link 1, the absolute amount of the carbon for couple | bonding with chromium by the chromization process in the surface and the inside of the nozzle link 1 can be increased.
従って、本発明の実施形態によれば、ノズルリンク1が金属粉末射出成形によって成形して焼成した成形体により構成される場合でも、クロム炭化物層Cの厚みの均一性を高めつつ、クロム炭化物層Cの厚みを厚くして、ノズルリンク1の耐熱性、耐摩耗性等を十分に向上させることができる。 Therefore, according to the embodiment of the present invention, even when the nozzle link 1 is composed of a molded body that is molded and fired by metal powder injection molding, the chromium carbide layer is improved in uniformity of the thickness of the chromium carbide layer C. By increasing the thickness of C, the heat resistance and wear resistance of the nozzle link 1 can be sufficiently improved.
なお、本発明は、前述の実施形態の説明に限られるものではなく、例えば、クロム炭化物層の形成方法の形成対象をノズルリンク1以外のタービン部品又はタービン部品以外の機械部品に変更する等、その他、種々の態様で実施可能である。また、本発明に包含される権利範囲は、表面に本発明の実施形態に係るクロム炭化物層の形成方法によってクロム炭化物層Cが形成されたノズルリンク1等の機械部品にも及ぶものである。 The present invention is not limited to the description of the above-described embodiment. For example, the formation target of the chromium carbide layer forming method is changed to a turbine part other than the nozzle link 1 or a machine part other than the turbine part. In addition, various embodiments can be implemented. The scope of rights encompassed by the present invention also extends to mechanical parts such as the nozzle link 1 having the chromium carbide layer C formed on the surface thereof by the chromium carbide layer forming method according to the embodiment of the present invention.
次に、本発明の実施例について説明する。 Next, examples of the present invention will be described.
(クロマイズ処理前の試験片の表面観察)
オーステナイト系ステンレス鋼の粉末とバインダの混合物を射出材料として金属粉末射出成形によって成形して焼成することにより、焼結済みの成形体により構成される試験片1を製作した。そして、倍率500倍で走査型電子顕微鏡(SEM)により試験片1の表面の観察を行い、図2A(a)に示すような観察結果を得て、図2A(a)に示された部分を電子線マイクロアナライザー(EPMA)によって元素分析を行い、図2A(b)に示すような分析結果を得た。これによると、試験片1の表面にクロムの濃度の高い箇所(薄くなっている箇所)が存在することが確認された。なお、エネルギー分散型X線分析(EDX)による点分析によってクロムの濃度の高い箇所にクロム炭化物が存在していることが確認された。
(Surface observation of specimen before chromization treatment)
A test piece 1 constituted of a sintered compact was manufactured by molding and firing a mixture of austenitic stainless steel powder and binder as an injection material by metal powder injection molding. Then, the surface of the test piece 1 was observed with a scanning electron microscope (SEM) at a magnification of 500 times to obtain an observation result as shown in FIG. 2A (a), and the portion shown in FIG. 2A (a) was obtained. Elemental analysis was performed with an electron beam microanalyzer (EPMA) to obtain an analysis result as shown in FIG. 2A (b). According to this, it was confirmed that the location where the density | concentration of chromium is high (the location which is thin) exists in the surface of the test piece 1. FIG. In addition, it was confirmed by the point analysis by energy dispersive X-ray analysis (EDX) that chromium carbide is present in a portion having a high chromium concentration.
オーステナイト系ステンレス鋼の粉末とバインダの混合物を射出材料として金属粉末射出成形によって成形して焼成し、焼結済みの成形体に固溶化処理を施すことにより、試験片2を製作した。そして、倍率500倍で走査型電子顕微鏡により試験片2の表面の観察を行い、図2B(a)に示すような観察結果を得て、図2B(a)に示された部分を電子線マイクロアナライザーによって元素分析を行い、図2B(b)に示すような分析結果を得た。これによると、試験片2の表面にクロムの濃度の高い箇所がなくなって、試験片2の表面からクロム炭化物が略消滅したことが確認された。 A test piece 2 was manufactured by forming a mixture of austenitic stainless steel powder and a binder as an injection material by metal powder injection molding and firing, and subjecting the sintered compact to a solution treatment. Then, the surface of the test piece 2 was observed with a scanning electron microscope at a magnification of 500 times to obtain an observation result as shown in FIG. 2B (a). The portion shown in FIG. Elemental analysis was performed with an analyzer to obtain an analysis result as shown in FIG. 2B (b). According to this, it was confirmed that the location where the chromium concentration was high disappeared on the surface of the test piece 2, and chromium carbide was almost disappeared from the surface of the test piece 2.
(クロマイズ処理前の試験片の断面観察)
試験片1を切断して、試験片1を埋込樹脂に埋め込んだ状態で、試験片1の切断面に対して研磨処理及びエッチング処理を順次行った。そして、倍率500倍で走査型電子顕微鏡により試験片1の断面端部(断面における表面側)及び断面中央部の観察を行い、図3A(a)及び図4A(a)に示すような観察結果を得て、図3A(a)及び図4A(a)に示された部分を電子線マイクロアナライザーによって元素分析を行い、図3A(b)及び図4A(b)に示すような分析結果を得た。これによると、試験片1の断面端部及び断面中央部、換言すれば、試験片1の内部にクロムの濃度の高い箇所が存在することが確認された。また、倍率20倍で光学顕微鏡により試験片1の断面端部及び断面中央部の観察を行い、図5A(a)及び図5A(b)に示すような観察結果を得た。なお、エネルギー分散型X線分析(EDX)による点分析によって、図5A(a)及び図5A(b)に示された部分にクロム炭化物が存在することが確認された。
(Cross-section observation of specimen before chromization treatment)
With the test piece 1 cut and the test piece 1 embedded in the embedded resin, the cut surface of the test piece 1 was sequentially subjected to polishing treatment and etching treatment. And the cross-sectional end part (surface side in a cross section) and cross-sectional center part of the test piece 1 are observed with a scanning electron microscope at a magnification of 500 times, and the observation results as shown in FIGS. 3A (a) and 4A (a). 3A (a) and 4A (a) are subjected to elemental analysis by an electron beam microanalyzer, and the analysis results as shown in FIGS. 3A (b) and 4A (b) are obtained. It was. According to this, it was confirmed that the cross-sectional end part and the cross-sectional center part of the test piece 1, in other words, a location with a high chromium concentration exists in the test piece 1. Moreover, the cross-sectional edge part and cross-sectional center part of the test piece 1 were observed with the optical microscope at 20 times magnification, and the observation result as shown to FIG. 5A (a) and FIG. 5A (b) was obtained. In addition, it was confirmed by the point analysis by energy dispersive X-ray analysis (EDX) that chromium carbide exists in the portion shown in FIG. 5A (a) and FIG. 5A (b).
試験片2を切断して、試験片2を埋込樹脂に埋め込んだ状態で、試験片2の切断面に対して研磨処理及びエッチング処理を順次行った。そして、倍率500倍で走査型電子顕微鏡により試験片2の断面端部及び断面中央部の観察を行い、図3B(a)及び図4B(a)に示すような観察結果を得て、図3B(a)及び図4B(a)に示された部分を電子線マイクロアナライザーによって元素分析を行い、図3B(b)及び図4B(b)に示すような分析結果を得た。これによると、試験片2の断面端部及び断面中央部、換言すれば、試験片2の内部にクロムの濃度の高い箇所がなくなって、試験片2の内部からクロム炭化物が略消滅したことが確認された。また、倍率20倍で光学顕微鏡により試験片2の断面端部及び断面中央部の観察を行い、図5B(a)及び図5B(b)に示すような観察結果を得た。 With the test piece 2 cut and the test piece 2 embedded in the embedded resin, the cut surface of the test piece 2 was sequentially subjected to polishing treatment and etching treatment. Then, the cross-sectional end and the central cross-section of the test piece 2 were observed with a scanning electron microscope at a magnification of 500 times to obtain observation results as shown in FIGS. 3B (a) and 4B (a). Element analysis was performed on the portion shown in (a) and FIG. 4B (a) using an electron beam microanalyzer, and analysis results as shown in FIG. 3B (b) and FIG. 4B (b) were obtained. According to this, the cross-sectional end part and the central part of the cross section of the test piece 2, in other words, the location where the chromium concentration is high in the test piece 2 disappears, and the chromium carbide has almost disappeared from the inside of the test piece 2. confirmed. Moreover, the cross-sectional edge part and cross-sectional center part of the test piece 2 were observed with the optical microscope at 20 times magnification, and the observation result as shown to FIG. 5B (a) and FIG. 5B (b) was obtained.
(クロマイズ処理後の試験片の断面観察)
試験片1の表面全体にクロマイズ処理を施した後に、試験片1を切断して、試験片1を埋込樹脂に埋め込んだ状態で、試験片1の切断面に対して研磨処理及びエッチング処理を順次行った。そして、倍率500倍で走査型電子顕微鏡により試験片1の断面端部の観察を行い、図6A(a)に示すような観察結果を得て、図6A(a)に示された部分を電子線マイクロアナライザーによって元素分析を行い、図6A(b)に示すような分析結果を得た。また、倍率20倍で光学顕微鏡により試験片1の断面端部の異なる箇所の観察を行い、図7A(a)(b)に示すような観察結果を得た。これによると、試験片1の表面に形成されたクロム炭化物層の厚みが薄く、クロム炭化物層の厚みにばらつきがあることが確認された。
(Cross section observation of the specimen after chromization treatment)
After the entire surface of the test piece 1 is chromized, the test piece 1 is cut, and the cut surface of the test piece 1 is polished and etched in a state where the test piece 1 is embedded in the embedded resin. We went sequentially. Then, the cross-sectional end of the test piece 1 was observed with a scanning electron microscope at a magnification of 500 times to obtain an observation result as shown in FIG. 6A (a), and the part shown in FIG. Elemental analysis was performed with a line microanalyzer, and analysis results as shown in FIG. 6A (b) were obtained. Moreover, the different location of the cross-sectional edge part of the test piece 1 was observed with the optical microscope at 20 times magnification, and the observation result as shown to FIG. 7A (a) (b) was obtained. According to this, it was confirmed that the thickness of the chromium carbide layer formed on the surface of the test piece 1 is thin and the thickness of the chromium carbide layer varies.
試験片2の表面全体にクロマイズ処理を施した後に、試験片2を切断して、試験片2を埋込樹脂に埋め込んだ状態で、試験片2の切断面に対して研磨処理及びエッチング処理を順次行った。そして、倍率500倍で走査型電子顕微鏡により試験片1の断面端部の観察を行い、図6B(a)に示すような観察結果を得て、図6B(a)に示された部分を電子線マイクロアナライザーによって元素分析を行い、図6B(b)に示すような分析結果を得た。また、倍率20倍で光学顕微鏡により試験片2の断面端部の異なる箇所の観察を行い、図7B(a)(b)に示すような観察結果を得た。これによると、試験片2の表面に形成されたクロム炭化物層の厚みが厚くなって、クロム炭化物層の厚みのばらつきが小さくなったことが確認された。 After the entire surface of the test piece 2 is chromized, the test piece 2 is cut and the cut surface of the test piece 2 is polished and etched in a state where the test piece 2 is embedded in the embedded resin. We went sequentially. Then, the cross-sectional end portion of the test piece 1 was observed with a scanning electron microscope at a magnification of 500 times to obtain an observation result as shown in FIG. 6B (a), and the portion shown in FIG. Elemental analysis was performed with a line microanalyzer, and analysis results as shown in FIG. 6B (b) were obtained. Moreover, the different location of the cross-sectional edge part of the test piece 2 was observed with the optical microscope at 20 times magnification, and the observation result as shown to FIG. 7B (a) (b) was obtained. According to this, it was confirmed that the thickness of the chromium carbide layer formed on the surface of the test piece 2 was increased, and the variation in the thickness of the chromium carbide layer was reduced.
1:ノズルリンク(タービン部品、機械部品)、2:貫通穴、3:アーム部、4:ジョイント部材、C:クロム炭化物層 1: Nozzle link (turbine part, machine part) 2: Through hole 3: Arm part 4: Joint member C: Chromium carbide layer
Claims (4)
前記機械部品は、ステンレス鋼の粉末と、ポリスチレン系樹脂及びアクリル系樹脂の複数種の樹脂とワックスとからなるバインダとの混合物を射出材料として金属粉末射出成形によって成形して焼成した焼結済みの成形体により構成され、
前記機械部品に対して溶体化処理を施す溶体化工程と、
前記溶体化工程の終了後に、前記機械部品の表面に対してクロマイズ処理を施すことにより、前記機械部品の表面に前記クロム炭化物層を形成するクロマイズ工程と、を具備した、クロム炭化物層の形成方法。 In a chromium carbide layer forming method for forming a chromium carbide layer on the surface of a mechanical part made of stainless steel,
The machine parts, stainless steel powder and, a plurality of kinds of polystyrene resin and an acrylic resin resin and a mixture of a binder consisting of a wax as an injection material metal powder injection molding sintered for firing molded by Consists of molded bodies,
A solution treatment step for applying a solution treatment to the mechanical parts;
After completion of the solution process, by performing Kuromaizu processing on the mechanical parts of the surface, and Kuromaizu forming the chromium carbide layer on the mechanical parts of the surface, equipped with a method of forming chromium carbide layer .
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