JPS5848023B2 - Manufacturing method of wear-resistant iron-based sintered alloy - Google Patents
Manufacturing method of wear-resistant iron-based sintered alloyInfo
- Publication number
- JPS5848023B2 JPS5848023B2 JP51013056A JP1305676A JPS5848023B2 JP S5848023 B2 JPS5848023 B2 JP S5848023B2 JP 51013056 A JP51013056 A JP 51013056A JP 1305676 A JP1305676 A JP 1305676A JP S5848023 B2 JPS5848023 B2 JP S5848023B2
- Authority
- JP
- Japan
- Prior art keywords
- wear
- sintered alloy
- manufacturing
- sintered
- based sintered
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 229910045601 alloy Inorganic materials 0.000 title claims description 16
- 239000000956 alloy Substances 0.000 title claims description 16
- 238000004519 manufacturing process Methods 0.000 title claims description 8
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 title description 9
- 229910052742 iron Inorganic materials 0.000 title description 3
- 229910052710 silicon Inorganic materials 0.000 claims description 14
- 238000000034 method Methods 0.000 claims description 8
- 239000000843 powder Substances 0.000 claims description 8
- 239000002994 raw material Substances 0.000 claims description 6
- 229910000519 Ferrosilicon Inorganic materials 0.000 claims description 4
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 4
- 239000010703 silicon Substances 0.000 claims description 4
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 claims description 2
- 239000000463 material Substances 0.000 description 12
- 238000012360 testing method Methods 0.000 description 10
- 238000005245 sintering Methods 0.000 description 7
- 229910001018 Cast iron Inorganic materials 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 4
- 229910052802 copper Inorganic materials 0.000 description 4
- 239000010949 copper Substances 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 230000007423 decrease Effects 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 239000011856 silicon-based particle Substances 0.000 description 3
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 2
- 239000010953 base metal Substances 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 238000009792 diffusion process Methods 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 239000007769 metal material Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 229910001651 emery Inorganic materials 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 230000001050 lubricating effect Effects 0.000 description 1
- 239000010687 lubricating oil Substances 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 239000011812 mixed powder Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 229910021382 natural graphite Inorganic materials 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 1
Landscapes
- Powder Metallurgy (AREA)
Description
【発明の詳細な説明】
本発明は初期なじみが良好で耐摩耗性の改善された鉄系
焼結合金の製造方法に係る。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing a ferrous sintered alloy with good initial break-in and improved wear resistance.
摺動部品の耐摩耗性を高めるため潤滑油を摺動面に供給
してやること、或いは該部品の金属材料の硬度を高める
こと、または金属材料組織中に黒鉛の如き潤滑性を有す
る成分を分散させること等が一般に行なわれているが、
高温高速で摺動ずる部品の摺動面においては油膜が切れ
易く、摩耗が大きくなったり、或いは焼着きを生ずるこ
とが屡屡ある。In order to increase the wear resistance of sliding parts, supplying lubricating oil to the sliding surfaces, increasing the hardness of the metal material of the parts, or dispersing lubricating components such as graphite in the metal material structure. This is commonly done, but
Oil films on the sliding surfaces of parts that slide at high temperatures and high speeds tend to break off, often resulting in increased wear or seizure.
出願人は先に、このような厳しい条件下で使用される保
油性に富み、摩耗量の少ない焼結合金の製造方広として
シリコン含有量が1〜2%になるように200メッシュ
下のフエロシリコンを原料粉中に混合した圧粉体を、シ
リコンを拡散させずに粒状のまま残留させるように焼結
する耐摩耗性鉄系焼結合金の製造方法を提示した(特願
昭48−89556号(特開昭50−38611号公報
)、発明の名称、耐摩耗性焼結合金並びにその製造方法
。The applicant previously proposed a method for producing a sintered alloy with high oil retention and low wear that can be used under such severe conditions, and developed a 200-mesh or lower sintered alloy with a silicon content of 1 to 2%. We have proposed a method for producing wear-resistant iron-based sintered alloys in which a green compact containing erosilicon mixed in raw material powder is sintered so that the silicon remains in granular form without being diffused. No. 89556 (Japanese Unexamined Patent Publication No. 50-38611), title of the invention, wear-resistant sintered alloy and method for producing the same.
以下先願発明という)。本発明は先願発明の製造方法の
改良に係り、初期なじみが一層良好で耐摩耗性が更に改
善された鉄系焼結合金の製造方法を提供することを目的
とし、シリコン含有量が3〜10%になるように原料粉
に配合するほかは上記の方法と同様な方法によって圧粉
体を作り、かつこれを焼結して焼結体を得る方法に係る
。(hereinafter referred to as the "prior invention"). The present invention relates to an improvement of the manufacturing method of the prior invention, and aims to provide a method for manufacturing iron-based sintered alloys with even better initial fitting and further improved wear resistance. This relates to a method in which a green compact is produced by a method similar to the above method except that the powder is blended into the raw material powder so that the powder becomes 10%, and the green compact is sintered to obtain a sintered compact.
次に実施例について説明する。Next, an example will be described.
100メッシュ下の噴霧鉄粉、200メッシュ下のフエ
ロシリコン(Si品位50%)、325メッシュ下の電
解銅粉、10ミクロンの天然黒鉛、同じく10ミクロン
のステアリン酸亜鉛(Zn−stで示す)を用いて次の
二種類の配合割合で原料粉を配合した。Sprayed iron powder under 100 mesh, ferrosilicon (Si grade 50%) under 200 mesh, electrolytic copper powder under 325 mesh, natural graphite under 10 microns, zinc stearate (indicated by Zn-st) under 10 microns. Raw material powders were blended using the following two types of blending ratios.
試料A:1、2%C, 3%Si,3%Cu,0.7
5%Zn−st,残部Fe
試料B:1.2%C1 10%Si,7%Cu,067
5%Zn−st1残部Fe
それぞれを混合したのち、5t/Ciの圧力で呼び径7
3.Oi4幅2. O ynm,厚さ3.0關の自由形
状用の金型を用いてプレスし、得られた圧粉体を700
℃×20分予備焼結したのち、吸熱型ガス(24%Co
,31%H2、0.30〜0.32%CO2、N2残)
中で1120℃×50分の焼結を行なった。Sample A: 1, 2% C, 3% Si, 3% Cu, 0.7
5% Zn-st, balance Fe Sample B: 1.2% C1 10% Si, 7% Cu, 067
After mixing 5% Zn-st1 and balance Fe, the nominal diameter was 7 at a pressure of 5t/Ci.
3. Oi4 width 2. Pressed using a free-form mold with a thickness of 3.0 mm and a thickness of about 700 mm.
After pre-sintering for 20 minutes at ℃, an endothermic gas (24%Co
, 31% H2, 0.30-0.32% CO2, N2 remaining)
Sintering was carried out at 1120° C. for 50 minutes.
このようにして得た焼結体を呼び径73.0ii,幅2
. 0 mm,厚さ3. 0 mmのピストンリングに
加工して、ニッサンA−12エンジン、1 1 7 1
cc,最高出力68PS/6,00O r.p.mに
取付けて実機試験を行なった。The sintered body thus obtained has a nominal diameter of 73.0ii and a width of 2
.. 0 mm, thickness 3. Processed into 0 mm piston ring, Nissan A-12 engine, 1 1 7 1
cc, maximum output 68PS/6,00O r. p. An actual machine test was conducted by installing it on the M.
比較材としては鋳鉄製ピストンリングにクロムめっきを
ほどこしたものを用いた(試料Cで示す)。As a comparison material, a cast iron piston ring plated with chrome was used (shown as sample C).
試験条件は次の通りである。The test conditions are as follows.
6.00O r.p.m,4/4Load油、水温 :
900C
ガソリン : 無鉛ガソリン
試験結果を第1図に示す。6.00O r. p. m, 4/4Load oil, water temperature:
900C gasoline: Unleaded gasoline test results are shown in Figure 1.
横軸には運転時間、縦軸には外周摩耗量(ミクロン)を
とってあり、曲線A,B,Cは夫々試料A,B,Cの成
績を示している。The horizontal axis shows the operating time, and the vertical axis shows the outer circumferential wear amount (microns), and curves A, B, and C show the results of samples A, B, and C, respectively.
なお比較のため前記特願昭4889556に示した1.
05%Si,1.4%C, 3%Cuのピストンリン
グの同様な試験結果(曲線Dで示す)を載せてある。For comparison, 1. shown in the aforementioned Japanese Patent Application No. 4889556
Similar test results (shown as curve D) for a piston ring with 0.5% Si, 1.4% C, and 3% Cu are shown.
この図の曲線CおよびDから判るように、先願発明の1
.05%Siになるようにフエ口シリコンを配合したも
のDは運転初期にはクロムめっき材Cに比して摩耗量が
太きいが、運転時間が進むにつれて次第に摩耗量の増加
は減じ、約260〜270時間で両者は同じになり、そ
れ以上運転を続けると逆に1.05%Siの試験片の方
がクロムめっき鋳鉄材よりも摩耗量が少なくなって行き
、初期なじみがよく、一たんなじんでしまえば摩耗速度
が小さくなって優れた耐摩耗性を示すようになるのであ
るが、本発明に係る焼結合金においては曲線AおよびB
で示すようになお一層初期なじみ性が良く、3%Siの
もので約50時間、10%Siのもので約100時間で
クロムめっき材よりも摩耗量が少なくなって、先願発明
に係る焼結合金に比して初期なじみが一層改善されてい
る上に、その後の摩耗量も少なく、耐摩耗性が更に優れ
ていることが判る。As can be seen from curves C and D in this figure, 1 of the prior invention
.. 0.05% Si, material D has a greater amount of wear than chrome-plated material C at the beginning of operation, but as the operation time progresses, the increase in wear amount gradually decreases, and the amount of wear decreases to about 260% Si. After ~270 hours, the two become the same, and as the operation continues beyond that, the 1.05% Si test piece shows less wear than the chromium-plated cast iron, and the initial fit is better, and once the operation is continued, the amount of wear becomes smaller. Once the material is blended in, the wear rate decreases and it exhibits excellent wear resistance, but in the sintered alloy according to the present invention, curves A and B
As shown in , the initial conformability is even better, and the amount of wear is less than that of the chromium-plated material after about 50 hours for the 3% Si material and about 100 hours for the 10% Si material. It can be seen that the initial fit is much improved compared to the alloy, and the amount of subsequent wear is also small, indicating that the wear resistance is even more excellent.
このように本発明の焼結合金が耐摩耗性の点で優れてい
るのは、200メッシュ下のフエロシリコンをS i
含有Mが3〜10%になるように原料粉に配合してあり
、これを用いた圧粉体を本出願人の前記先願発明の方法
と同様に1120℃に加熱焼結してあるので、配合した
フエ口シリコン粒子が焼結中にまわりの地鉄中へ拡散す
ることがなく、該方法によるものと同様に粒状で残留し
ている上に、硬質のフエ口シリコン粒子と基地との面積
比が初期摩耗およびその後の摩耗量を少なくするのに一
層好適な値となっていることに依るものであろうと考え
られる。The reason why the sintered alloy of the present invention is excellent in terms of wear resistance is that the sintered alloy of the present invention is superior in terms of wear resistance.
The M content is blended into the raw material powder to be 3 to 10%, and the green compact using this is heated and sintered at 1120°C in the same manner as the method of the applicant's earlier invention. In addition, the blended Huekou silicon particles do not diffuse into the surrounding base metal during sintering, and remain in granular form as in the case of the method, and the hard Huekou silicon particles and the base do not diffuse into the surrounding base metal. It is thought that this is due to the fact that the area ratio is a value more suitable for reducing initial wear and subsequent wear.
このように本発明の焼結合金においては配合したフエ口
シリコン粒子がそのまま残留するように焼結するため焼
結温度は1150℃以下とする。As described above, in the sintered alloy of the present invention, the sintering temperature is set to 1150° C. or lower in order to sinter the blended silicon particles so as to remain as they are.
この温度が高くなると焼結時間を短くしてもSrの拡散
を押えることが困難になり、未拡散のSiの量のばらつ
きが大きくなる。When this temperature increases, it becomes difficult to suppress the diffusion of Sr even if the sintering time is shortened, and the variation in the amount of undiffused Si increases.
第2図は葉山式試験機による耐摩耗試験の結果を示して
おり、試料A,Bは前記配合と同じで、試料Eは次の配
合としたものである。FIG. 2 shows the results of an abrasion resistance test using a Hayama tester, in which samples A and B had the same formulation as above, and sample E had the following formulation.
試料E:1.2%C1 12%Si,7%Cu、0.7
5%Z n−s t
これらの各配合粉をそれぞれ混合したのち5t/ffl
の圧力で10X10X70mmに成形し、前記同様に焼
結したのち、5X5X301!jl!に加工し、エメリ
ー紙0.2まで研摩して試験に供した。Sample E: 1.2%C1 12%Si, 7%Cu, 0.7
5% Z n-s t After mixing each of these mixed powders, 5t/ffl
After molding to 10 x 10 x 70 mm under pressure and sintering in the same manner as above, 5 x 5 x 301! jl! The sample was polished to 0.2 emery paper and used for testing.
比較材(試料F)はピストンリング用鋳鉄である。The comparative material (sample F) is cast iron for piston rings.
図によればs i3%含有の試料Aは比較材に比して明
らかに摩耗量が少なく、耐摩耗性に優れているが、Si
lo%の試料Bは比較材に大よそ同等であり、8112
%の試料Eは比較材よりも摩耗量が多くなっている。According to the figure, sample A containing 3% Si has clearly less wear than the comparative material and has excellent wear resistance, but
lo% of sample B is roughly equivalent to the comparative material, 8112
% sample E has a greater amount of wear than the comparative material.
この試験結果からSi含有量の上限は10%とするのが
よいと考えられる。From this test result, it is considered that the upper limit of the Si content is preferably 10%.
以上説明したように、本発明の焼結合金は200メッシ
ュ以下のフエロシリコンをSi含有量が3〜10%にな
るように原料粉中に混合し、拡散しないように焼結して
あるので、硬質粒子と基地との面積比が改善された結果
苛酷な摺動条件においても初期なじみがよく、その後の
摩耗量が従来品のクロムめっき材に比べてはもとより、
前記先願発明の方法による焼結合金よりも顕著に僅少で
あうで、優れた耐摩耗性を示すものである。As explained above, the sintered alloy of the present invention is made by mixing ferrosilicon of 200 mesh or less into raw material powder so that the Si content is 3 to 10%, and sintering it to prevent diffusion. As a result of the improved area ratio of the hard particles to the matrix, the initial fit is good even under harsh sliding conditions, and the amount of subsequent wear is lower than that of conventional chrome-plated materials.
The amount is significantly smaller than that of the sintered alloy produced by the method of the prior invention, and exhibits excellent wear resistance.
第1図はエンジン実機試験結果を示すグラフ、第2図は
葉山式摩耗試験機による耐摩耗試験結果を示す棒グラフ
である。
曲線A,B・・・・・・本発明に係る焼結合金の戒績、
曲線C・・・・・・鋳鉄製ピストンリングにクロムめっ
きをほどこしたものの成績、曲線D・・・・・・Si含
有量が1.05%となるようにフエロシリコンを配合し
た試料の成績、曲線E・・・・・・Si含有量が12%
となるようにフエ口シリコンを配合した試料の成績、曲
線F・・・・・・ピストンリング用鋳鉄の戒績。FIG. 1 is a graph showing the results of an actual engine test, and FIG. 2 is a bar graph showing the results of a wear resistance test using a Hayama wear tester. Curves A, B...The merits of the sintered alloy according to the present invention,
Curve C: Performance of a cast iron piston ring plated with chrome, Curve D: Performance of a sample containing ferrosilicon with a Si content of 1.05% , Curve E...Si content is 12%
The results of the sample containing Hueguchi silicon so that the result, curve F... The merits of cast iron for piston rings.
Claims (1)
ッシュ以下のフエロシリコンを原料粉に混合、成形した
のち、還元性雰囲気中で1150℃以下に加熱して焼結
することを特徴とする初期なじみが良好で、耐摩耗性が
改善された鉄系焼結合金の製造方法。1. Ferrosilicon of 200 mesh or less is mixed with raw material powder so that the silicon content is 3 to 10%, molded, and then heated to 1150°C or less in a reducing atmosphere and sintered. A method for manufacturing a ferrous sintered alloy that has good initial fitting and improved wear resistance.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP51013056A JPS5848023B2 (en) | 1976-02-09 | 1976-02-09 | Manufacturing method of wear-resistant iron-based sintered alloy |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP51013056A JPS5848023B2 (en) | 1976-02-09 | 1976-02-09 | Manufacturing method of wear-resistant iron-based sintered alloy |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5295508A JPS5295508A (en) | 1977-08-11 |
| JPS5848023B2 true JPS5848023B2 (en) | 1983-10-26 |
Family
ID=11822459
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP51013056A Expired JPS5848023B2 (en) | 1976-02-09 | 1976-02-09 | Manufacturing method of wear-resistant iron-based sintered alloy |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5848023B2 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN108655389A (en) * | 2018-04-04 | 2018-10-16 | 扬州汇峰新材料有限公司 | A kind of piston one-piece forming technique |
-
1976
- 1976-02-09 JP JP51013056A patent/JPS5848023B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5295508A (en) | 1977-08-11 |
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