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JPS6234828B2 - - Google Patents
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JPS6234828B2 - - Google Patents

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Publication number
JPS6234828B2
JPS6234828B2 JP2859184A JP2859184A JPS6234828B2 JP S6234828 B2 JPS6234828 B2 JP S6234828B2 JP 2859184 A JP2859184 A JP 2859184A JP 2859184 A JP2859184 A JP 2859184A JP S6234828 B2 JPS6234828 B2 JP S6234828B2
Authority
JP
Japan
Prior art keywords
steel
machinability
sulfides
zrn
sulfide
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
Application number
JP2859184A
Other languages
Japanese (ja)
Other versions
JPS60174854A (en
Inventor
Setsuo Mishima
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Proterial Ltd
Original Assignee
Hitachi Metals Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Hitachi Metals Ltd filed Critical Hitachi Metals Ltd
Priority to JP2859184A priority Critical patent/JPS60174854A/en
Publication of JPS60174854A publication Critical patent/JPS60174854A/en
Priority to JP18413386A priority patent/JPS62167863A/en
Publication of JPS6234828B2 publication Critical patent/JPS6234828B2/ja
Granted legal-status Critical Current

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Description

【発明の詳細な説明】[Detailed description of the invention]

本発明は切削加工における仕上面粗度が小さく
優れた鏡面仕上性を有することを最大の特徴と
し、併せて優れたシボ加工性および強靭性を兼備
したプリハードンタイプのプラスチツク成形金型
用鋼に関するものである。 プラスチツク成形金型用鋼としては、 (1) 被切削性が良いこと。 (2) 鏡面仕上性がよく、ピンホールやその他微細
ピツトが発生しないこと。 (3) シボ加工性が良いこと。 (4) 耐食、耐発錆性が良いこと。 (5) 強度、耐摩耗性が大きいこと。 等の特性が要求されている。 (2),(5)の点では高硬度であること。(2),(4)の点
では鋼質が本質的に清浄になりやすい成分のもの
であること。(3)の点では焼入性が十分大きいこと
などが要求される。この場合ユーザーでの熱処理
が不要なプリハードン鋼で上記諸要求を満たすこ
とが金型精度、納期、コスト面で特に有利であ
る。 従来、高硬度のプリハードン鋼には切削加工に
よる型彫りに長時間を要すと共に、切削工具の寿
命も短く工具交換の回数が増大する等の問題があ
り、これを改善するためにプリハードン鋼に快削
元素を添加することによつて被削性を向上させる
方法が採られている。そして快削元素としては
S,Se,Te,Pb,Ag等が一般に用いられる。し
かしながら十分な被削性を得るに必要な量の快削
元素を添加すると、この添加によつて上記(2),
(3),(4),(5)の特性が少なからず劣化する問題が生
起していた。 本発明鋼は、重量比でC0.04〜0.30%、Si0.1〜
1.5%、Mn0.2〜2.0%、Cr0.1〜3.5%、Mo0.1〜
3.0%、Cu0.2〜3.0%、S0.05〜0.20%にAl0.05〜
0.50%の添加を行い、(O+N)を0.007〜0.012%
に低く制御したのち、Zrを0.005〜0.20%添加す
ることにより、硫化物に有効な接種作用を有する
微細なZrO2およびZrNが多数生成して、これが硫
化物を著しく微細にさせるとともに均一に分布さ
せることにより、硫黄快削鋼で従来問題となつて
いた被削性の不均一、大きな仕上面あらさ及び機
械的性質の異方性を著しく改善するとともに、C
量を抑え熱処理により均一なベーナイト組織基地
にCu―Fe金属間化合物およびMo,Cr等の炭化
物を微細に析出させ強度と硬度を付与したことに
より、鏡面仕上性、シボ加工性を有することを最
大の特色とする。また被削性、機械的性質の異方
性を改善するため必要に応じ、Se0.05〜0.15%、
Te0.05〜0.15%、Ca0.001〜0.010%、Mg0.001〜
0.010%の添加を実施することができるものであ
る。 次に成分範囲の限定理由について説明する。 Cは本発明鋼の焼入組織を被削性、鏡面仕上性
およびシボ加工性に優れるベーナイト組織にする
ための、さらにMo,Cr炭化物による析出硬化を
もたらすための基本的添加元素である。しかして
Cは多過ぎると基地マルテンサイト組織化して被
削性、鏡面仕上性を減ずること、また研削工数を
著しく増大させるため0.30%以下とし、低すぎる
とフエライト生成を招き十分な焼もどし硬さが得
がたくなるので0.04%以上とする。 Siは脱酸剤として含有され、また耐酸化性、焼
入性に有効である。しかし0.1%未満では製鋼上
脱酸効果が得られず、1.5%を超えると耐酸化性
向上の効果が少なくなり被削性も劣化し実用的で
ない。 Mnは焼入性を高めまた要求かたさレベルに応
じてベーナイトかたさを調整し、フエライト生成
を防ぎ、またSとの間にMnS系介在物を形成し
て高度の被削性を付与するための不可欠の含有元
素である。多すぎると被削性を低下させるので
2.0%以下とし、低すぎると上記の効果が得られ
ずまた熱間加工性を害するため0.2%以上とす
る。 Crは耐食性、焼入性を高め、また焼戻し時、
微細な炭化物析出をもたらし、析出硬化における
かたさ値を適度に調整する。多すぎるとフエライ
ト生成をまねくので3.5%以下とし、低すぎると
上記効果が得られないので0.1%以上とする。 Moは500℃以上の高温焼戻し処理において微細
炭化物を析出し、析出硬化をもたらし、強度を形
成するための、また使用時の雰囲気に対する耐食
性を高めるための含有元素である。多すぎると被
削性、靭性低下を招くので3.0%以下とし、低す
ぎると上記効果が得られないので0.1%以上とす
る。 Cuは500℃以上の高温焼戻し処理において析出
硬化をもたらし所要のかたさを得るための不可欠
の含有元素であり、耐食性を高め、またフエライ
ト生成を抑制する効果を有するのである。多すぎ
ると被削性を低下させるので3.0%以下とし、低
すぎると上記効果が得られないので0.2%以上と
する。 Sは被削性向上のための不可欠な元素である。
多すぎると強靭性、納間加工性を害するので0.2
%以下とし、低すぎると上記効果が得られないの
で0.05%以上とする。 AlはZrの硫化物に対する接種作用を増大さ
せ、硫化物を微細にすることにより、被削性およ
び鏡面仕上性を改善するための元素である。しか
し0.05%未満では上記効果が少なく、また多すぎ
るとZrO2生成量が不十分になるとともに、鋳造
時の再酸化および吸窒による被削性に有害な硬質
の非金属介在物Al2O3およびAlNが生成しやすく
なるため0.5%以下とする。 Zrは被削性および鏡面仕上性を改善するための
必須元素である。添加Zrは硫化物に対して有効な
接種作用を有するZrO2又はZrNとなる。この接種
作用により硫化物の形状、寸度および分布に極め
て良好な均一性が生ずる。そしてこの均一性が被
削性、鏡面仕上性を著しく改善する。さらに
ZrO2およびZrNの夫々70%以上を硫化物と共存さ
せることにより切削加工における工具寿命の低下
を抑えることができる。しかしZrが多すぎると上
記効果が飽和するとともに硫化物と共存せず基地
に独立して存在するZrO2およびZrNが増大し、工
具の機械的摩耗を促進させ被削性を低下させると
共に、研摩時のピツト発生による鏡面仕上性を劣
化させるので0.20%以下とする。低すぎると上記
効果が得られないので0.005%以上とする。 O,NはZrO2およびZrNの構成元素であり、本
発明鋼の特色であるZr化合物ZrO2,ZrNによる硫
化物に対する接種作用にとつて必須の元素であ
る。良好な被削性を得るにはZrO2およびZrNの
夫々70%以上が硫化物と共存することが必要であ
り、さらに硫化物を微細化するためにはZr0.005
〜0.20%のときに(O+N)も0.007〜0.012%と
低く厳密に制御しなければならない。(O+N)
が0.007%未満では接種作用が十分でなく硫化物
の形状分布の不均一および硫化物の粗大化が生
じ、また粗大なZrの炭化物が基地に独立して生成
し工具寿命を短くする。(O+N)が0.012%を超
えると硫化物と共存せずに基地に独立して存在す
る酸化物あるいは窒化物が増大し、被削性および
機械的性質を劣化させるおそれがある。 Seは被削性および耐食性を向上させる。0.15%
を超えると靭性の低下が著しく、0.03%未満では
上記効果が小さい。 TeはSe同様に被削性および耐食性を向上させ
る。0.15%を超えると靭性の低下が著しく、0.05
%未満では上記効果が小さい。 Ca,Mgの効果はZr化合物のS′deに対する接種
作用を助け、S′deの形状、分布を均一にするとと
もにCaS,MgSの生成により圧延加工時における
硫化物の延伸性を抑えることにより、機械的異方
性を改善するものである。多すぎるとCa,Mgに
よる脱酸が過度に進行するため接種効果が得られ
なくなるので夫々0.010%以下とする。低すぎる
と上記効果が得られないので夫々0.001%以上と
する。 Se,Te,Ca,Mgは、いずれも蒸気圧が高い
ので、添加にあたつてはインジエクシヨン、合金
弾、出鋼時添加等の方法によるとともに、Ca,
Mgは活性でもあるため、事前の脱酸も重要であ
り、添加前の溶鋼中の酸素含有量を60ppmいか
に規制する。 以下に本発明鋼の実施例を示す。 表1に供試材の化学組成(すべてFe Bal)を
示す。また硫化物と共存するZr化合物の割合を表
2に示す。
The present invention relates to a pre-hardened steel for plastic molds, which has the greatest feature of having a small surface roughness during cutting and excellent mirror finish, and also has excellent texturability and toughness. It is. Steel for plastic molds should: (1) have good machinability; (2) Good mirror finish and no pinholes or other minute pits. (3) Good texturing properties. (4) Good corrosion resistance and rust resistance. (5) High strength and wear resistance. The following characteristics are required. High hardness in terms of (2) and (5). Regarding (2) and (4), the steel must be of a composition that is essentially easy to clean. Regarding (3), it is required that the hardenability is sufficiently high. In this case, it is particularly advantageous in terms of mold accuracy, delivery time, and cost to meet the above requirements with prehardened steel that does not require heat treatment by the user. Conventionally, high-hardness pre-hardened steel has problems such as requiring a long time to carve the die by cutting, and the life of the cutting tool is short, increasing the number of tool changes. A method has been adopted to improve machinability by adding free-cutting elements. S, Se, Te, Pb, Ag, etc. are generally used as free-cutting elements. However, if the amount of free-cutting elements necessary to obtain sufficient machinability is added, this addition will result in the above (2).
A problem occurred in which the characteristics (3), (4), and (5) deteriorated to some extent. The steel of the present invention has a weight ratio of C0.04 to 0.30% and Si0.1 to
1.5%, Mn0.2~2.0%, Cr0.1~3.5%, Mo0.1~
3.0%, Cu0.2~3.0%, S0.05~0.20%, Al0.05~
Addition of 0.50% and (O+N) of 0.007 to 0.012%
By adding 0.005 to 0.20% Zr after controlling the sulfide to a low level, a large number of fine ZrO 2 and ZrN, which have an effective inoculation effect on sulfides, are generated, which makes the sulfides extremely fine and uniformly distributed. This significantly improves the uneven machinability, large surface roughness, and anisotropy of mechanical properties that have traditionally been a problem with sulfur free-cutting steel.
By suppressing the amount and heat-treating, Cu-Fe intermetallic compounds and carbides such as Mo and Cr are finely precipitated on a uniform bainite structure base, giving it strength and hardness, resulting in maximum mirror finish and grain workability. Features: In addition, to improve machinability and anisotropy of mechanical properties, Se0.05~0.15%,
Te0.05~0.15%, Ca0.001~0.010%, Mg0.001~
It is possible to add 0.010%. Next, the reason for limiting the component range will be explained. C is a basic additive element for making the quenched structure of the steel of the present invention into a bainitic structure with excellent machinability, mirror finish, and graining workability, and further for bringing about precipitation hardening due to Mo and Cr carbides. However, if the C content is too high, it will form a matrix martensite structure, reducing machinability and mirror finish, and will significantly increase the number of grinding steps, so it should be 0.30% or less, and if it is too low, it will lead to the formation of ferrite, resulting in insufficient tempering hardness. Since it will be difficult to obtain a profit, it should be set at 0.04% or more. Si is contained as a deoxidizing agent and is effective in improving oxidation resistance and hardenability. However, if it is less than 0.1%, no deoxidizing effect can be obtained in steel manufacturing, and if it exceeds 1.5%, the effect of improving oxidation resistance will be reduced and machinability will deteriorate, making it impractical. Mn is essential for improving hardenability, adjusting bainite hardness according to the required hardness level, preventing ferrite formation, and forming MnS-based inclusions between S and imparting high machinability. It is a containing element. Too much will reduce machinability, so
The content should be 2.0% or less, and if it is too low, the above effects will not be obtained and hot workability will be impaired, so the content should be 0.2% or more. Cr increases corrosion resistance and hardenability, and during tempering,
Produces fine carbide precipitation and appropriately adjusts the hardness value during precipitation hardening. If it is too high, it will lead to the formation of ferrite, so it should be set at 3.5% or less, and if it is too low, the above effects cannot be obtained, so it should be set at 0.1% or more. Mo is an element that precipitates fine carbides during high-temperature tempering treatment at 500° C. or higher, brings precipitation hardening, builds strength, and improves corrosion resistance against the atmosphere during use. If it is too high, machinability and toughness will deteriorate, so the content should be 3.0% or less, and if it is too low, the above effects cannot be obtained, so the content should be 0.1% or more. Cu is an essential element for precipitation hardening and obtaining the required hardness during high-temperature tempering treatment at temperatures above 500°C, and has the effect of increasing corrosion resistance and suppressing ferrite formation. If it is too high, machinability will deteriorate, so the content should be 3.0% or less, and if it is too low, the above effects cannot be obtained, so the content should be 0.2% or more. S is an essential element for improving machinability.
Too much will impair toughness and workability during delivery, so 0.2
% or less, and if it is too low, the above effects cannot be obtained, so it should be 0.05% or more. Al is an element that increases the inoculation effect of Zr on sulfides and makes the sulfides finer, thereby improving machinability and mirror finish. However, if it is less than 0.05%, the above effect will be small, and if it is too much, the amount of ZrO 2 produced will be insufficient, and hard non-metallic inclusions Al 2 O 3 that are harmful to machinability due to reoxidation and nitrification during casting will be produced. It is set to 0.5% or less because it facilitates the generation of AlN and AlN. Zr is an essential element for improving machinability and mirror finish. The added Zr becomes ZrO 2 or ZrN, which has an effective inoculation effect against sulfides. This inoculation effect results in very good uniformity in the shape, size and distribution of the sulphides. This uniformity significantly improves machinability and mirror finish. moreover
By allowing 70% or more of each of ZrO 2 and ZrN to coexist with sulfide, it is possible to suppress the decrease in tool life during cutting. However, if there is too much Zr, the above effect will be saturated, and ZrO 2 and ZrN, which do not coexist with sulfides and exist independently in the matrix, will increase, which will accelerate mechanical wear of the tool and reduce machinability, as well as reduce the polishing ability. It should be kept at 0.20% or less since it deteriorates the mirror finish due to the occurrence of pits. If the content is too low, the above effects cannot be obtained, so the content should be 0.005% or more. O and N are constituent elements of ZrO 2 and ZrN, and are essential elements for the inoculating action against sulfides by the Zr compounds ZrO 2 and ZrN, which is a feature of the steel of the present invention. In order to obtain good machinability, it is necessary for 70% or more of each of ZrO 2 and ZrN to coexist with sulfide, and to further refine the sulfide, Zr0.005
-0.20%, (O+N) must also be kept as low as 0.007-0.012% and must be strictly controlled. (O+N)
If Zr is less than 0.007%, the inoculation effect is insufficient, resulting in uneven sulfide shape distribution and coarsening of the sulfide, and coarse Zr carbides are formed independently on the matrix, shortening tool life. If (O+N) exceeds 0.012%, oxides or nitrides that do not coexist with sulfides and exist independently in the matrix increase, which may deteriorate machinability and mechanical properties. Se improves machinability and corrosion resistance. 0.15%
If it exceeds 0.03%, the toughness will be significantly reduced, and if it is less than 0.03%, the above effect will be small. Like Se, Te improves machinability and corrosion resistance. If it exceeds 0.15%, the toughness decreases significantly;
If it is less than %, the above effect will be small. The effects of Ca and Mg help the inoculation effect of Zr compounds on S′de, making the shape and distribution of S′de uniform, and suppressing the elongation of sulfide during rolling processing by producing CaS and MgS. This improves mechanical anisotropy. If the amount is too high, deoxidation by Ca and Mg will proceed excessively, making it impossible to obtain the inoculation effect, so each should be kept at 0.010% or less. If the content is too low, the above effects cannot be obtained, so each content should be 0.001% or more. Se, Te, Ca, and Mg all have high vapor pressures, so when adding them, use methods such as injection injection, alloy bullets, or addition at the time of tapping.
Since Mg is active, it is also important to deoxidize it in advance, and the oxygen content in molten steel is controlled to 60 ppm before Mg is added. Examples of the steel of the present invention are shown below. Table 1 shows the chemical composition of the test materials (all Fe Bal). Table 2 also shows the proportion of Zr compounds coexisting with sulfides.

【表】【table】

【表】【table】

【表】 第1,2図(本発明鋼C)、第3,4図(従来
鋼A)は本発明鋼、従来鋼の鋳造組織を示す顕微
鏡写真である。 図より本発明鋼および従来鋼ともに硫化物の分
布はほぼ一様でありかつZr化合物が硫化物と共存
していることがわかる。しかし硫化物の寸度につ
いては本発明鋼の方が従来鋼に比べ著しく微細に
なつていることがわかる。これは、Alを添加す
ることによつて得られたZrの硫化物に対する接種
効果の増大によるものである。 第5図および第6図は各々本発明鋼Cと従来鋼
Aの鍛造比20の材料における硫化物の形態を示す
顕微鏡写真である。 本発明鋼では硫化物が極めて小さく、形状、分
布も均一で被削性、鏡面仕上性に好ましい硫化物
形態となつている。 表3に本発明鋼および従来鋼の焼入焼戻し(H
RC32)における被切削性を、従来鋼Aの被削性
を100として指数で示したものである。しかして
指数が大きいほぼ被削性が良いことを示すもので
ある。 本発明鋼は被切削性に関し、従来鋼よりも明ら
かに優れていることがわかる。 第7図および第8図イ,ロ,ハ,ニ、は、それ
ぞれ従来鋼Aおよびと本発明鋼C,D,E、の切
削試験の仕上面あらさを示すグラフである。第
7,8図より本発明鋼の仕上面あらさは著しく改
善されていることがわかる。これらは、Alおよ
びZrの添加と(O+N)%の制御により硫化物の
分布形状が均一であるだけでなく硫化物が著しく
微細になつたことに帰因している。
[Table] Figures 1 and 2 (invention steel C) and Figures 3 and 4 (conventional steel A) are micrographs showing the casting structures of the invention steel and conventional steel. The figure shows that the distribution of sulfides is almost uniform in both the steel of the present invention and the conventional steel, and that Zr compounds coexist with sulfides. However, it can be seen that the size of sulfides is significantly finer in the steel of the present invention than in the conventional steel. This is due to the increase in the inoculating effect of Zr on sulfides obtained by adding Al. FIGS. 5 and 6 are micrographs showing the morphology of sulfides in inventive steel C and conventional steel A with a forging ratio of 20, respectively. In the steel of the present invention, the sulfide content is extremely small, the shape and distribution are uniform, and the sulfide form is favorable for machinability and mirror finish. Table 3 shows the quenching and tempering (H
The machinability in R C32) is expressed as an index with the machinability of conventional steel A as 100. Therefore, a large index indicates good machinability. It can be seen that the steel of the present invention is clearly superior to the conventional steel in terms of machinability. 7 and 8 are graphs showing the finished surface roughness of conventional steel A and steels C, D, and E of the present invention in cutting tests, respectively. It can be seen from Figures 7 and 8 that the finished surface roughness of the steel of the present invention is significantly improved. These results are attributable to the addition of Al and Zr and the control of (O+N)%, which not only made the sulfide distribution uniform but also made the sulfide extremely fine.

【表】【table】

【表】 表4は、本発明鋼の鏡面仕上性(耐ピツト性)
を従来鋼と対比したものである。試料は50mm□で
RC32に焼入焼戻しし時効処理後グラインダー
→ペーパー→ダイヤモンドコンパウンド方式にて
鏡面仕上を行い、10倍の拡大鏡を用いて微細なピ
ツト発生個数をカウントしたものである。
[Table] Table 4 shows the mirror finish (pit resistance) of the steel of the present invention.
compared with conventional steel. The sample was quenched and tempered to H R C32 with a size of 50 mm square, and after aging treatment, a mirror finish was applied using a grinder → paper → diamond compound method, and the number of minute pits was counted using a 10x magnifying glass.

【表】 本発明鋼は極めて優れた鏡面仕上性を備えてい
ることがわかる。これは、Alを添加することに
より(O+N)濃度を下げ非金属介在物の絶対量
を低減したことと、先に述べたAl添加により硫
化物に対する接種剤ZrO2およびZrNが微細化する
とともに硫化物も微細化したことによるものであ
る。 以上に詳述したように本発明鋼は切削加工にお
いて極めて優れた仕上面を有し、鏡面仕上性に優
れることを最大の特色とするものであり、また被
削性の向上によりユーザーでの金型作成の効率化
を図ることができるとともに、内外均一な硫化物
の微細分布によつてシボ加工性、機械的性質の改
善がなされ、発錆等の懸念を要せず、強靭性で長
寿命を有する快削性プラスチツク成型プリハード
ン金型用鋼である。
[Table] It can be seen that the steel of the present invention has extremely excellent mirror finish properties. This is because the addition of Al lowered the (O+N) concentration and reduced the absolute amount of nonmetallic inclusions, and the addition of Al, which was mentioned earlier, made the inoculants ZrO 2 and ZrN for sulfides finer and reduced the amount of sulfide. This is due to the miniaturization of objects. As detailed above, the steel of the present invention has an extremely excellent finished surface in cutting processing, and its greatest feature is that it has excellent mirror finish properties. In addition to improving the efficiency of mold creation, the uniform fine distribution of sulfide inside and outside improves grain workability and mechanical properties, eliminating the need for concerns such as rust, making it tough and long lasting. This is a free-cutting steel for pre-hardened molds for plastic molding.

【図面の簡単な説明】[Brief explanation of the drawing]

第1,2図は本発明鋼Cの、第3,4図は従来
鋼Aの鋳造組織を夫々示す金属組織の顕微鏡写
真、第5図は本発明鋼Cの、第6図は従来鋼Aの
鍛造比20の場合の硫化物の形態を夫々示す金属組
織の顕微鏡写真、第7図は従来鋼Aの、第8図イ
〜ハは本発明鋼C,D,Eの仕上面あらさを夫々
表わすグラフである。
Figures 1 and 2 are micrographs of the metallographic structures of the invention steel C, and Figures 3 and 4 are micrographs of the metal structure of the conventional steel A. Figure 5 is the metal structure of the invention steel C, and Figure 6 is the conventional steel A. Micrographs of metal structures showing the morphology of sulfides at a forging ratio of 20, Figure 7 shows the finished surface roughness of conventional steel A, and Figures 8 A to C show the finished surface roughness of inventive steels C, D, and E, respectively. This is a graph representing

Claims (1)

【特許請求の範囲】 1 重量比でC0.04〜0.30%、Si0.1〜1.5%、
Mn0.2〜2.0%、Cr0.1〜3.5%、Mo0.1〜3.0%、
Cu0.2〜3.0%、S0.05〜0.20%、Al0.05〜0.50%、
Zr0.005〜0.20%、(O+N)0.007〜0.012%を含
み、さらにZrの化合物ZrO2およびZrNの夫々70%
以上が硫化物と共存し、残部不可避的不純物およ
びFeよりなることを特徴とする被削性に優れた
プラスチツク成形プリハードン金型用鋼。 2 重量比でC0.04〜0.30%、Si0.1〜1.5%、
Mn0.2〜2.0%、Cr0.1〜3.5%、Mo0.1〜3.0%、
Cu0.2〜3.0%、S0.05〜0.20%、Al0.05〜0.50%、
Zr0.005〜0.20%、(O+N)0.007〜0.012%およ
びSe0.05〜0.15%、Te0.05〜0.15%の1種または
2種を含有し、さらにZrの化合物ZrO2およびZrN
の夫々70%以上が硫化物と共存し、残部不可避的
不純物およびFeよりなることを特徴とする被削
性に優れたプラスチツク成形プリハードン金型用
鋼。 3 重量比でC0.04〜0.30%、Si0.1〜1.5%、
Mn0.2〜2.0%、Cr0.1〜3.5%、Mo0.1〜3.0%、
Cu0.2〜3.0%、S0.05〜0.20%、Al0.05〜0.50%、
Zr0.005〜0.20%、(O+N)0.007〜0.012%およ
びCa0.001〜0.010%、Mg0.001〜0.010%の1種ま
たは2種を含有し、さらにZrの化合物ZrO2およ
びZrNの夫々70%以上が硫化物と共存し、残部不
可避的不純物およびFeよりなることを特徴とす
る被削性に優れたプラスチツク成形プリハードン
金型用鋼。
[Claims] 1. C0.04~0.30%, Si0.1~1.5% by weight,
Mn0.2~2.0%, Cr0.1~3.5%, Mo0.1~3.0%,
Cu0.2~3.0%, S0.05~0.20%, Al0.05~0.50%,
Contains Zr0.005~0.20%, (O+N)0.007~0.012%, and further contains 70% each of Zr compounds ZrO 2 and ZrN
A steel for plastic forming pre-hardened molds having excellent machinability, characterized in that the above coexists with sulfides, and the remainder consists of inevitable impurities and Fe. 2 C0.04~0.30%, Si0.1~1.5% by weight,
Mn0.2~2.0%, Cr0.1~3.5%, Mo0.1~3.0%,
Cu0.2~3.0%, S0.05~0.20%, Al0.05~0.50%,
Contains one or two of Zr0.005-0.20%, (O + N) 0.007-0.012%, Se0.05-0.15%, Te 0.05-0.15%, and further contains Zr compounds ZrO 2 and ZrN
A steel for plastic forming pre-hardened molds with excellent machinability, characterized in that 70% or more of each coexists with sulfides, and the remainder consists of unavoidable impurities and Fe. 3 C0.04~0.30%, Si0.1~1.5% by weight,
Mn0.2~2.0%, Cr0.1~3.5%, Mo0.1~3.0%,
Cu0.2~3.0%, S0.05~0.20%, Al0.05~0.50%,
Contains one or two of Zr0.005-0.20%, (O+N) 0.007-0.012%, Ca0.001-0.010%, Mg0.001-0.010%, and further contains 70% each of Zr compounds ZrO 2 and ZrN A steel for plastic forming pre-hardened molds having excellent machinability, characterized in that the above coexists with sulfides, and the remainder consists of inevitable impurities and Fe.
JP2859184A 1984-02-20 1984-02-20 Free-cutting steel for prehardened metallic mold for molding plastic Granted JPS60174854A (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
JP2859184A JPS60174854A (en) 1984-02-20 1984-02-20 Free-cutting steel for prehardened metallic mold for molding plastic
JP18413386A JPS62167863A (en) 1984-02-20 1986-08-07 Free-cutting steel for prehardened metallic mold for molding plastic

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2859184A JPS60174854A (en) 1984-02-20 1984-02-20 Free-cutting steel for prehardened metallic mold for molding plastic

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP18413386A Division JPS62167863A (en) 1984-02-20 1986-08-07 Free-cutting steel for prehardened metallic mold for molding plastic

Publications (2)

Publication Number Publication Date
JPS60174854A JPS60174854A (en) 1985-09-09
JPS6234828B2 true JPS6234828B2 (en) 1987-07-29

Family

ID=12252834

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2859184A Granted JPS60174854A (en) 1984-02-20 1984-02-20 Free-cutting steel for prehardened metallic mold for molding plastic

Country Status (1)

Country Link
JP (1) JPS60174854A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2686075B2 (en) * 1986-11-04 1997-12-08 日立金属株式会社 Plastic forming pre-hardened steel for mold

Also Published As

Publication number Publication date
JPS60174854A (en) 1985-09-09

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