JPS6120602B2 - - Google Patents
Info
- Publication number
- JPS6120602B2 JPS6120602B2 JP9976876A JP9976876A JPS6120602B2 JP S6120602 B2 JPS6120602 B2 JP S6120602B2 JP 9976876 A JP9976876 A JP 9976876A JP 9976876 A JP9976876 A JP 9976876A JP S6120602 B2 JPS6120602 B2 JP S6120602B2
- Authority
- JP
- Japan
- Prior art keywords
- forging
- preform
- forged
- metal article
- powder metal
- 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
- 238000005242 forging Methods 0.000 claims description 29
- 239000000843 powder Substances 0.000 claims description 26
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 23
- 238000000034 method Methods 0.000 claims description 20
- 229910052799 carbon Inorganic materials 0.000 claims description 19
- 229910052751 metal Inorganic materials 0.000 claims description 19
- 239000002184 metal Substances 0.000 claims description 19
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 18
- 238000005245 sintering Methods 0.000 claims description 18
- 238000010791 quenching Methods 0.000 claims description 17
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 16
- 230000000171 quenching effect Effects 0.000 claims description 13
- 229910000640 Fe alloy Inorganic materials 0.000 claims description 11
- 229910052742 iron Inorganic materials 0.000 claims description 9
- 238000004519 manufacturing process Methods 0.000 claims description 9
- 229910052759 nickel Inorganic materials 0.000 claims description 8
- 238000003754 machining Methods 0.000 claims description 6
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 claims description 5
- 229910052748 manganese Inorganic materials 0.000 claims description 5
- 239000011572 manganese Substances 0.000 claims description 5
- 230000000694 effects Effects 0.000 claims description 3
- 239000012256 powdered iron Substances 0.000 claims description 3
- 238000005255 carburizing Methods 0.000 claims description 2
- 238000005498 polishing Methods 0.000 claims description 2
- 239000000047 product Substances 0.000 description 13
- 239000000314 lubricant Substances 0.000 description 7
- 239000000203 mixture Substances 0.000 description 6
- 230000001681 protective effect Effects 0.000 description 6
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 5
- 238000007796 conventional method Methods 0.000 description 5
- 229910002804 graphite Inorganic materials 0.000 description 5
- 239000010439 graphite Substances 0.000 description 5
- 229910052750 molybdenum Inorganic materials 0.000 description 5
- 239000011733 molybdenum Substances 0.000 description 5
- 229910001566 austenite Inorganic materials 0.000 description 4
- 230000006835 compression Effects 0.000 description 4
- 238000007906 compression Methods 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- 238000012545 processing Methods 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 229910045601 alloy Inorganic materials 0.000 description 3
- 239000000956 alloy Substances 0.000 description 3
- 230000007547 defect Effects 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 230000001590 oxidative effect Effects 0.000 description 3
- 238000003672 processing method Methods 0.000 description 3
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000012467 final product Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 239000012255 powdered metal Substances 0.000 description 2
- 238000004381 surface treatment Methods 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 229910000754 Wrought iron Inorganic materials 0.000 description 1
- PCEXQRKSUSSDFT-UHFFFAOYSA-N [Mn].[Mo] Chemical compound [Mn].[Mo] PCEXQRKSUSSDFT-UHFFFAOYSA-N 0.000 description 1
- 238000005275 alloying Methods 0.000 description 1
- 150000001721 carbon Chemical class 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 238000009770 conventional sintering Methods 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000005485 electric heating Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 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 description 1
- 229910000734 martensite Inorganic materials 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000007769 metal material Substances 0.000 description 1
- 239000011812 mixed powder Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000012778 molding material Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 238000004663 powder metallurgy Methods 0.000 description 1
- 238000003303 reheating Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Powder Metallurgy (AREA)
Description
【発明の詳細な説明】
本発明は、焼入れ後に更に機械加工、表面処理
及び熱処理を必要としない高いRc硬度をもつ鍛
造された粉末金属物品の製造法に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing a forged powder metal article with high Rc hardness that does not require further machining, surface treatment and heat treatment after quenching.
比較的小さい鍛造鉄基金属物品は鍛練素材
(wroughf stock)又は粉末金属から製造でき、
粉末金属から製造は金属粉末を圧縮する比較的新
しい技術である。 Relatively small wrought iron-based metal articles can be manufactured from wrought stock or powdered metal;
Manufacturing from powdered metals is a relatively new technology for compacting metal powders.
一般にRc60程度の高いRc硬度(これは実質的
に高いマルテンサイト含量を意味する)を良好な
表面仕上及び寸法安定性と組合せて有するかかる
金属物品を製俗するには、鍛造後の加工品を少な
くとも冷却、機械加工及び再硬化の追加の工程に
供することが必要である。しかしながら、それぞ
れの後続工程はコスト高であるばかりでなく、次
の加工工程で考慮せねばならない種々の金属状態
を導くことになる。 To manufacture such metal articles having a high Rc hardness, typically around Rc60 (which means a substantially high martensite content) combined with good surface finish and dimensional stability, the workpiece after forging is It is necessary to subject it to at least the additional steps of cooling, machining and rehardening. However, each subsequent step is not only costly, but also introduces different metal conditions that must be taken into account in the next processing step.
粉末金属予備形成品の鍛造は結果として、鍛連
素材を用いるる場合に必要な機械加工操作を排除
する点でコスト安利点のために金属加工法として
許容されるに至つている。かかる加工法におい
て、予め合金化された金属粉末は黒鉛及び滑剤と
混合され、プリケツト(団鉱)に圧縮され、焼結
され、ついで鍛造される。この比較的新しい方法
は望ましいものであるが、その有益性はまだ充分
には実現されていない。 Forging of powder metal preforms has consequently become accepted as a metal processing method due to its cost advantages in eliminating the machining operations required when using forged continuous stock. In such processing methods, prealloyed metal powders are mixed with graphite and a lubricant, compressed into briquettes, sintered, and then forged. Although this relatively new method is desirable, its benefits have not yet been fully realized.
例えば、加工表面において約Re60の硬度をも
つ粉末鉄基金属物品を製造する場合には、
a 0.2〜0.3重量%の炭素含量を使用して加炭処
理し、ついで加工品を硬化させるか、あるいは
b 0.5〜0.7重量%の炭素含量を使用して物品を
オーステナイト化し、ついで急冷する、ことが
常に必要であると考えられてきた。それぞれの
加工法a及びbを実施する方法は種々あり、当
該分野で周知である。本発明を説明する目的に
は、それぞれの方法は所望の表面硬度及び表面
仕上を達成させるが、熱作用により物品それ自
体に望ましくない寸法変化を惹起する欠点を指
適すれば充分であろう。 For example, when producing a powdered iron-based metal article with a hardness of about Re60 at the worked surface, a carbon content of 0.2 to 0.3% by weight is used to carburize and then the workpiece is hardened, or b It has always been considered necessary to austenitize the article using a carbon content of 0.5 to 0.7% by weight, followed by rapid cooling. There are various ways to carry out each of processing methods a and b and are well known in the art. For purposes of describing the invention, it will suffice to point out that each method achieves the desired surface hardness and surface finish, but has the drawback of causing undesirable dimensional changes in the article itself due to thermal effects.
本発明の方法は粉末治金鍛造に伴なう前述の問
題を克服し、所望の密度及びより精密な寸法許容
差を有しかつ表面欠陥及び内部欠陥のない物品を
一段階鍛造で与えるものである。更に、本発明の
方法は浸炭により得られる如き単なる表面硬度で
はなく、全体に亘つて実質的に均一高いRc硬度
をもつ物品を製造せしめる。 The method of the present invention overcomes the aforementioned problems associated with powder metallurgy forging and provides articles with the desired density and tighter dimensional tolerances and free of surface and internal defects in a single step forging. be. Furthermore, the method of the present invention produces articles having substantially uniformly high Rc hardness throughout, rather than just surface hardness as obtained by carburization.
従つて本発明は、
従つて、本発明では、炭素含有量が0.2〜0.9重
量%の鉄合金粉末を圧縮してプリケツトとし;
該プリケツトを焼結して焼結予備形成品とし;
該予備形成品の温度をそれがオーステナイト状態
に保持される温度に調節し;
かく加熱した予備形成品をオーステナイト状態に
保持しつゝ一段階で鍛造して鍛造品とし;
該鍛造品をオーステナイト状態に保持しつゝ一段
階で鍛造して鍛造品とし;
該鍛造品をオーステナイト状態に保持しつゝ上記
鍛造工程の直後に油焼入浴中で焼入れし;
かく焼入れした鍛造品を焼入浴から取出し、この
鍛造品から応力を除去して、少くともRc40の表
面硬度を有しかつ表面研磨以外の機械加工を更に
必要としない表面仕上りと寸法を有する鍛造され
た粉末金属物品を製造する;
ことからなる、理論値の少なくとも約99.5%の密
度を有する。全体的に硬化されたスケールのない
鍛造粉末金属物品の製造法を提供するものであ
る。 Accordingly, the present invention comprises: compressing an iron alloy powder having a carbon content of 0.2 to 0.9% by weight into a pricket; sintering the pricket into a sintered preform; adjusting the temperature of the article to a temperature at which it remains in the austenitic state; forging the thus heated preform in one step into a forging while retaining it in the austenitic state; retaining the forging in the austenitic state; The forged product is forged in one step to produce a forged product; the forged product is kept in an austenitic state and quenched in an oil quenching bath immediately after the above forging process; the thus quenched forged product is taken out of the quenching bath and the forged product is relieving stress from the article to produce a forged powder metal article having a surface hardness of at least Rc40 and a surface finish and dimensions that require no further machining other than surface polishing; having a density of at least about 99.5% of the value. The present invention provides a method for manufacturing a wholly hardened scale-free forged powder metal article.
本発明の方法は一般に、添付図面に10として概
略される流れ図に従つて実施される。この流れ図
において、最初の工程には鉄合金粉末の予備成形
である、この粉末の組成は最終物品に所望される
性質に応じて広く変化するであろう。勿論鉄を主
成分とし、これにマンガン、モリブデン、ニツケ
ルの如き金属が種々の量で添加される。炭素は黒
鉛(グラフアイト)の形態でプリケツト化の前に
添加される。実施の際には、まず鉄と他の金属を
慣用法により合金化し、得られた合金を微粉化し
て鉄合金粉末を形成させる。ついでこの鉄合金粉
末を黒鉛及び滑剤と混合する。かかる滑剤として
は、後述の如く焼結炉で燃焼されるロウ状又は脂
肪物質が慣用される。合金化及び微粉化の方法は
当該分野で慣用のものである。 The method of the present invention is generally carried out according to the flowchart outlined at 10 in the accompanying drawings. In this flowchart, the first step is the preforming of an iron alloy powder, the composition of which will vary widely depending on the properties desired in the final article. Of course, iron is the main component, to which metals such as manganese, molybdenum, and nickel are added in various amounts. Carbon is added in the form of graphite before precketing. In practice, iron and other metals are first alloyed by conventional methods and the resulting alloy is pulverized to form an iron alloy powder. This iron alloy powder is then mixed with graphite and a lubricant. Such lubricants are commonly used as waxy or fatty substances which are burned in a sintering furnace as described below. Alloying and micronization methods are conventional in the art.
典形的な例として、鉄合金粉末は下記の組成を
有し得る:
重量%
マンガン 0.25−0.5
モリブデン 0.25−0.5
ニツケル 0.25−0.25
炭素 0.2−0.9
鉄 残部
本発明における原料混合粉末中における当初の
炭素含有量範囲を0.2〜0.9重量%とする理由、予
備成形品が焼結炉内で焼結される際にこの炭素含
有量が減少されるのを見込んで決定されるもので
ある。上記範囲の当初の炭素含有量でないと最終
製品に少なくともRc40の硬度が得られないため
である。 As a typical example, the iron alloy powder may have the following composition: wt% manganese 0.25-0.5 molybdenum 0.25-0.5 nickel 0.25-0.25 carbon 0.2-0.9 iron balance initial carbon in the raw mixed powder of the present invention The reason why the content range is 0.2 to 0.9% by weight is determined with the expectation that this carbon content will be reduced when the preform is sintered in a sintering furnace. This is because if the initial carbon content is not within the above range, the final product will not have a hardness of at least Rc40.
得られた粉末はついで金型中の加圧によりプリ
ケツト14に形成される。このプリケツト化は密
度、形状及び一般的な寸法許容差を調節するため
に行われる。通常プリケツト化は理論値の約85%
までの密度を達成できる。ここで使用される圧縮
の型も一般圧縮又は等圧(isostaie)圧縮の如く
変えることができる。 The resulting powder is then formed into prickets 14 by pressure in a mold. This pricketting is done to control density, shape, and general dimensional tolerances. Normally, pre-ketization is about 85% of the theoretical value.
It is possible to achieve a density of up to The type of compression used here can also vary, such as general compression or isostaie compression.
圧縮後プリケツト(予備成形品)は16で焼結
される。これは予備成形品を焼結炉中に導入する
ことによつて行われる。焼結炉には慣用的に、滑
剤燃焼用の予備帯域、焼結用の高温帯域及び冷却
帯域が設けられる。鉄金属材料の焼結は通常約
1121〜1149℃(2050〜2100〓)の温度で行われ
る。焼結は内部酸化及び予備形成品の表面上の酸
化性スケールの形成を防止するために保護雰囲
気、即ち酸素を含まない雰囲気中で行われる。焼
結炉内の雰囲気は予備成形品の所望の結合炭素レ
ベルを保持する炭素ポテンシヤルを有する。この
目的に慣用されている任意の保護雰囲気が適当で
ある。予備形成品の炭素含量を増加させ、かくし
てその表面に浸炭浄態をもたらす表面濃縮作用も
提供され得る。実際に、この工程は硬度を保持す
るばかりでなく。引続く急冷工程で起り得る一般
的な割れを排除することが認められた。 After compression, the preform is sintered at 16. This is done by introducing the preform into a sintering furnace. Sintering furnaces are conventionally provided with a preliminary zone for lubricant combustion, a hot zone for sintering, and a cooling zone. Sintering of ferrous metal materials usually takes about
It is carried out at a temperature of 1121-1149℃ (2050-2100〓). Sintering is carried out in a protective atmosphere, ie, an oxygen-free atmosphere, to prevent internal oxidation and the formation of oxidative scales on the surface of the preform. The atmosphere within the sintering furnace has a carbon potential that maintains the desired bonded carbon level in the preform. Any protective atmosphere customary for this purpose is suitable. A surface enrichment effect may also be provided which increases the carbon content of the preform and thus brings about a carburized condition on its surface. In fact, this process not only retains hardness; It has been found to eliminate common cracking that can occur during subsequent quenching steps.
焼結された予備形成品は鍛造前に工程18でそ
れがオーステナイト状態に保たれる温度に加熱さ
れる。慣用の焼結炉内で予備成形品は室温に冷却
されるので、ついで予備成形品はそのオーステナ
イト温度以上に再加熱されねばならない、選定さ
れるオーステナイト温度以上の個々の温度は主と
して予備形成品の形状及び断面の厚さに応じて変
化する。例えば、約850℃のオーステナイト温度
をもつ予備形成品は約870〜1040℃の予備鍛造温
度に調節できる。 Prior to forging, the sintered preform is heated in step 18 to a temperature that maintains it in its austenitic state. As the preform is cooled to room temperature in a conventional sintering furnace, the preform must then be reheated above its austenitic temperature; the particular temperature above the selected austenitic temperature is primarily the temperature of the preform. Varies depending on shape and cross-sectional thickness. For example, a preform having an austenite temperature of about 850°C can be adjusted to a preforging temperature of about 870-1040°C.
適当な温度に加熱した直後に予備形成品を保護
雰囲気中で鍛造操作20にかけるが、この工程で
は約60〜80トン/6452cm2の単−プロ−(一段階鍛
造)により予備成形品を所望の仕上品に成形す
る。 Immediately after heating to the appropriate temperature, the preform is subjected to a forging operation 20 in a protective atmosphere, in which the preform is formed into the desired shape by a single forging of approximately 60-80 tons/6452 cm2 . Formed into a finished product.
ついで鍛造品をそのオーステナイト温度近辺に
亘つて均一な温度に到達せしめて慣用の焼入浴2
2中ですばやく焼入れする。慣用の油焼入浴を用
いることが好ましいが、エチレングリコール含有
水の如き他の焼入浴を用いることもできる。 The forging is then allowed to reach a uniform temperature around its austenite temperature and subjected to a conventional quenching bath 2.
Quench quickly in 2. Although it is preferred to use a conventional oil quenching bath, other quenching baths such as water containing ethylene glycol can also be used.
鍛造及び急冷前の温度の注意深い調整は、成形
品全体に亘つて所望の許容差及び硬度を達成させ
るための引続く熱処理又は物品の加工の必要性を
回避せしめることが認められた。更に、焼結及び
鍛造を保護雰囲気中で行うことによつて酸化性ス
ケールの形成が回避される。物品26に急冷浴か
らの取出24後に仕上状態におかれる。 Careful control of the temperature prior to forging and quenching has been found to avoid the need for subsequent heat treatment or processing of the article to achieve the desired tolerances and hardness throughout the molded article. Furthermore, by performing the sintering and forging in a protective atmosphere, the formation of oxidizing scales is avoided. After removal 24 from the quench bath, the article 26 is placed in a finished condition.
硬度について、本発明の方法はRe40−62又は
それ以上の硬度を与える。より低い硬度が所望さ
れる場合には仕上品を更に熱処理できることは明
らかであろう。同様に、仕上品は所望ならば表面
硬化させることもできる。 Regarding hardness, the method of the invention gives a hardness of Re40-62 or higher. It will be clear that the finished product can be further heat treated if a lower hardness is desired. Similarly, the finished product can be surface hardened if desired.
次に本発明を実施により更に説明する。 Next, the present invention will be further explained by implementation.
実施例 1
下記の組成をもつ鉄合金粉末を調製した;
重量%
マンガン 0.25
モリブデン 0.5
ニツケル 1.8
炭素 0.6
鉄 96.85
100.00
鉄、マンガンモリブデン及びニツケルを常法に
より合金化し、得られた合金を微粉化して鉄合金
粉末を得た。この粉末を黒鉛と混合して炭素を供
給しかつ滑剤(融点94−97℃の硬質白色合成ロウ
であるAcrawax)と混合し、得られた粉末を標
準プリケツト成形プレスの金型キヤピテイ中に入
れて加圧し、粉末を後続工程で取扱うに充分な強
度をもつプリケツト(生圧縮体)に形成した。Example 1 An iron alloy powder having the following composition was prepared; wt% manganese 0.25 molybdenum 0.5 nickel 1.8 carbon 0.6 iron 96.85 100.00 Iron, manganese molybdenum and nickel were alloyed by a conventional method, and the resulting alloy was pulverized to produce iron. An alloy powder was obtained. This powder is mixed with graphite to provide carbon and a lubricant (Acrawax, a hard white synthetic wax with a melting point of 94-97°C), and the resulting powder is placed into the mold cap of a standard preket forming press. Pressure was applied to form the powder into prickets with sufficient strength for handling in subsequent steps.
ついでプリケツトを約1120%の焼結炉内で保護
雰囲気中において約30分間焼結した。用いた焼結
炉は、滑剤焼結用帯域、焼結用高温帯域及び冷却
帯域を設けた公知の型のものであつた。焼結した
予備形成品は焼結炉から取出した時に約94℃の温
度にあつた。この予備成形品をついで電熱コアー
内で保護雰囲気中において約900℃の温度に加熱
した。この温度は成形材料のオーステナイト温度
(843℃)より高い。 The prickets were then sintered in a sintering furnace at about 1120% in a protective atmosphere for about 30 minutes. The sintering furnace used was of a known type equipped with a lubricant sintering zone, a hot sintering zone and a cooling zone. The sintered preform was at a temperature of approximately 94°C when removed from the sintering furnace. This preform was then heated in a protective atmosphere in an electric heating core to a temperature of approximately 900°C. This temperature is higher than the austenite temperature (843°C) of the molding material.
かく加熱した予備成形品をすばやく鍛造用プレ
スに移し、約60トン/6.452cm2の打撃により平滑
なO,D及びスプラインI,D,をもつ鍛造され
た固定子クラツチレースに成形した。鍛造後、鍛
造品を安定化せしめ、約843℃のオーステナイト
温度に冷却し、慣用の油焼中で焼入れした。 The heated preform was quickly transferred to a forging press and formed into a forged stator clutch race with smooth O, D and splines I, D, by a blow of about 60 tons/6.452 cm 2 . After forging, the forging was stabilized, cooled to an austenite temperature of approximately 843°C, and quenched in a conventional oil quench.
油浴から取出して応力を除去した物品は表面に
酸化性スケールがなく、試験により7.82g/c.c.の
密度、即ち理論値の99.%の密度を有する(7.87
g/c.c.が許容される理論最大密度である)ことが
認められた。最も重要なことに、この製品は全体
に亘つてRc59−62の硬度を有していた。また重
要なことに、物品は所望の形状及び寸法を有し、
従つて製品の所望の硬度を得るのに更に加工を必
要としなかつた。 The article, removed from the oil bath and released from stress, has no oxidative scale on the surface and has a tested density of 7.82 g/cc, or 99.% of the theoretical value (7.87 g/cc).
g/cc is the theoretical maximum density allowed). Most importantly, the product had an overall hardness of Rc 59-62. Also importantly, the article has the desired shape and dimensions;
Therefore, no further processing was required to obtain the desired hardness of the product.
実施例 2
下記の組成を有する鉄合金粉末を実施例1と同
様に調製した:
重量%
ニツケル 0.5
マンガン 0.3
モリブデン 0.5
炭素 0.65
鉄 残 部
100.00
黒鉛及び滑剤を実施例1と同様に添加し混合物
を慣用のプリケツト成形プレスのダイセツトの金
型キヤビテイ中に入れてプリケツトに圧縮した。
このプリケツトをついで実施例1と同様に焼結し
加熱し、鍛造し、焼入れし、応力を除去した。か
くして製造された鍛造品は試験により、酸化スケ
ール及び他の表面欠陥のない優れた表面品質を有
し、更に処理することなくそのまま販売できるこ
とが認められた。その硬度は物品全体に亘つて良
好であり、すべての方向に亘つて同様の性質を有
していた。Example 2 An iron alloy powder having the following composition was prepared in the same manner as in Example 1: % by weight Nickel 0.5 Manganese 0.3 Molybdenum 0.5 Carbon 0.65 Iron balance 100.00 Graphite and lubricant were added as in Example 1 and the mixture was prepared in a conventional manner. The material was put into the mold cavity of the die set of a preket molding press and compressed into a pricket.
This pricket was then sintered, heated, forged, hardened, and stress relieved in the same manner as in Example 1. The forgings thus produced were found by testing to have excellent surface quality, free of oxide scale and other surface defects, and could be sold as is without further treatment. The hardness was good throughout the article, with similar properties in all directions.
実施例 3
下記の組成をもつニツケル含有鉄合金粉末を実
施例1と同様に調製した。Example 3 Nickel-containing iron alloy powder having the following composition was prepared in the same manner as in Example 1.
重量%
ニツケル 2.0
マンガン 0.25
モリブデン 0.3
炭素 0.5
鉄 残 部
100.00
実施例1の加工工程に従つて仕上鍛造品を製造
した。得られた鍛造品は試験により、酸化スケー
ル及び他の表面欠陥のない優れた表面品質を有
し、更に表面処理することなくそのまま販売でき
ることが認められた。物品の硬度は実施例1及び
2と同様に、物品全体に亘つて良好であり
(Rc55〜57)あらゆる方向に亘つて同様の性質を
有していた。 Weight% Nickel 2.0 Manganese 0.25 Molybdenum 0.3 Carbon 0.5 Iron balance 100.00 A finished forged product was manufactured according to the processing process of Example 1. The resulting forgings were tested and found to have excellent surface quality, free of oxide scale and other surface defects, and can be sold as is without further surface treatment. Similar to Examples 1 and 2, the hardness of the article was good throughout the article (Rc55-57) and had similar properties in all directions.
本発明方法の実施試験から、得られた製品は、
従来法の場合には生起した表面劣化を除くために
2万分の1ないし3万分の1×2.54cmを除去する
通常の機械加工の必要なく、鍛造されたままで販
売輸送できることが判明した。更に、本発明によ
る鍛造直後の最終製品の取得は、従来法の如く物
品の寸法が物品を鍛造後に浸炭処理した際に変化
した場合に必要とされる許容差を惹起する。従つ
て、本発明方法による鍛造直後の焼入れは、従来
法の場合に必要な引続く浸炭処理の如き再加熱中
に起る寸法変化により得られる余分の許容差の広
がりを排除する。 From the practical tests of the method of the present invention, the products obtained were:
It has been found that it is possible to sell and transport forged products without the need for the usual machining process that removes 1/20,000 to 1/30,000 x 2.54 cm to remove surface deterioration that occurs in the case of conventional methods. Furthermore, obtaining a final product immediately after forging according to the present invention introduces tolerances that are required if the dimensions of the article change when the article is carburized after forging, as in conventional methods. Therefore, quenching immediately after forging according to the method of the present invention eliminates the extra tolerance spread resulting from dimensional changes that occur during reheating, such as subsequent carburizing, required in conventional methods.
本発明による鍛造焼入れ法によつて達成される
高い硬度は、特に材料が機械加工できず粉砕され
得るにすぎないほど硬度が高い、即ちRe35以上
の場合に、操業中重い運転荷重を支えるのに必要
な機械部品にとつて実際に適合するものである。
例えば、減摩性軸受レースはRe57〜58近辺の硬
度をもたなければ急速に摩耗し、寿命は短くなる
であろう。 The high hardness achieved by the forge-quenching process according to the invention makes it difficult to support heavy operating loads during operation, especially when the material is so hard that it cannot be machined and can only be crushed, i.e. Re35 or higher. It is a practical match for the required mechanical parts.
For example, anti-friction bearing races must have a hardness around Re57-58 or they will wear quickly and have a short lifespan.
以上本発明で好ましい実施態様について説明し
たが、これは本発明を前記の特定の態様に限定す
るためのものではなく、本発明の本質及び範囲内
に包含され得るような別法、変更及び均等物の保
護を意図するものである。 Although the preferred embodiments of the present invention have been described above, this is not intended to limit the present invention to the specific embodiments described above, and any other methods, modifications and equivalents that may be included within the essence and scope of the present invention are It is intended to protect property.
図面は本発明方法を実施する際に採用される主
要工程を示す流れ図である。
The drawing is a flowchart showing the main steps taken in carrying out the method of the invention.
Claims (1)
圧縮してプリケツトとし; 該プリケツトを焼結して焼結予備形成品とし; 該予備形成品の温度をそれがオーステナイト状態
に保持される温度に調節し; かく加熱した予備形成品をオーステナイト状態に
保持しつゝ一段階で鍛造して鍛造品とし; 該鍛造品をオーステナイト状態に保持しつゝ上記
鍛造工程の直後に油焼入浴中で焼入れし; かく焼入れした鍛造品を焼入浴から取出し、この
鍛造品から応力を除去して、少くともRc40の表
面硬度を有しかつ表面研磨以外の機械加工を更に
必要としない表面仕上りと寸法を有する鍛造され
た粉末金属物品を製造する; ことからなる、理論値の少なくとも約9.95%の密
度を有する。全体的に硬化されたスケールのない
鍛造粉末金属物品の製造法。 2 粉末鉄合金が重量によりマンガン0.25〜0.5
%、ニツケル0.25〜0.5%、炭素0.2〜0.9%及び残
部鉄からなる特許請求の範囲第1項記載の鍛造粉
末金属物品の製造法。 3 プリケツトの焼結を炭素ポチンシヤルの高い
ガス状雰囲気中で行ない、この焼結により予備成
形品の表面に加炭作用が与えられる特許請求の範
囲第1項又は第2項記載の鍛造粉末金属物品の製
造法。 4 粉末鉄合金が0.5〜0.9%の炭素を含む特許請
求の範囲第2項又は第3項記載の鍛造粉末金属物
品の製造法。 5 鍛造前の予備形成品の温度調節を焼結直後に
行なつて、焼結予備形成品の残熱を該予備成形品
がオーステナイト状態に保持される範囲の温度に
到達させる目的で利用しかつ引続く加炭処理にお
ける消費熱の必要性を排除することによつて熱エ
ネルギーを保存して所望の硬度を達成させる特許
請求の範囲第1項記載の鍛造粉末金属物品の製造
法。 6 鍛造工程後かつ焼入れ工程前に鍛造品の温度
を実質的に安定化せしめる特許請求の範囲第1項
記載の鍛造粉末金属物品の製造法。[Claims] 1. Compressing an iron alloy powder with a carbon content of 0.2 to 0.9% by weight to form a pricket; sintering the pricket to form a sintered preform; adjusting the temperature to maintain the austenitic state; forging the thus heated preform in one step to form a forged product while maintaining the austenitic state; carrying out the above forging process while maintaining the forged product in the austenitic state; Immediately thereafter quenching in an oil quenching bath; the thus quenched forging is removed from the quenching bath, stress is removed from the forging and the forging has a surface hardness of at least Rc40 and requires no further machining other than surface polishing. producing a forged powder metal article having a surface finish and dimensions that are not equal to and having a density of at least about 9.95% of theoretical; A method of manufacturing a wholly hardened scale-free forged powder metal article. 2 Powdered iron alloy contains 0.25 to 0.5 manganese depending on weight.
%, 0.25-0.5% nickel, 0.2-0.9% carbon, and the balance iron. 3. The forged powder metal article according to claim 1 or 2, wherein the preket is sintered in a gaseous atmosphere with a high carbon potential, and this sintering imparts a carburizing effect to the surface of the preform. manufacturing method. 4. A method for manufacturing a forged powder metal article according to claim 2 or 3, wherein the powdered iron alloy contains 0.5 to 0.9% carbon. 5. Temperature control of the preform before forging is carried out immediately after sintering, so that the residual heat of the sintered preform is utilized for the purpose of reaching a temperature range at which the preform remains in the austenitic state; 2. A method of making a wrought powder metal article according to claim 1, which conserves thermal energy to achieve a desired hardness by eliminating the need for expended heat in subsequent carburization. 6. The method for producing a forged powder metal article according to claim 1, wherein the temperature of the forged product is substantially stabilized after the forging process and before the quenching process.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP9976876A JPS5326207A (en) | 1976-08-23 | 1976-08-23 | Process for production of casting product of powdered metal |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP9976876A JPS5326207A (en) | 1976-08-23 | 1976-08-23 | Process for production of casting product of powdered metal |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5326207A JPS5326207A (en) | 1978-03-10 |
| JPS6120602B2 true JPS6120602B2 (en) | 1986-05-23 |
Family
ID=14256137
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP9976876A Granted JPS5326207A (en) | 1976-08-23 | 1976-08-23 | Process for production of casting product of powdered metal |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5326207A (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5538983A (en) * | 1978-09-13 | 1980-03-18 | Sumitomo Electric Ind Ltd | Production of high density powder molding by powder hot forging process |
| US4251273A (en) * | 1979-03-02 | 1981-02-17 | Smith David T | Method of forming valve lifters |
| JPS57123902A (en) * | 1981-01-21 | 1982-08-02 | Uitetsuku Keiman Patentsu Ltd | Manufacture of bakes granular structure and crush compress formation |
-
1976
- 1976-08-23 JP JP9976876A patent/JPS5326207A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5326207A (en) | 1978-03-10 |
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