JPS5961544A - Prehardened mold material for casting high melting metal - Google Patents

Prehardened mold material for casting high melting metal

Info

Publication number
JPS5961544A
JPS5961544A JP17258082A JP17258082A JPS5961544A JP S5961544 A JPS5961544 A JP S5961544A JP 17258082 A JP17258082 A JP 17258082A JP 17258082 A JP17258082 A JP 17258082A JP S5961544 A JPS5961544 A JP S5961544A
Authority
JP
Japan
Prior art keywords
balance
high melting
casting
cooling
melting point
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.)
Granted
Application number
JP17258082A
Other languages
Japanese (ja)
Other versions
JPS639575B2 (en
Inventor
Toshio Okuno
奥野 利夫
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 JP17258082A priority Critical patent/JPS5961544A/en
Publication of JPS5961544A publication Critical patent/JPS5961544A/en
Publication of JPS639575B2 publication Critical patent/JPS639575B2/ja
Granted legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C9/00Alloys based on copper
    • C22C9/06Alloys based on copper with nickel or cobalt as the next major constituent

Abstract

PURPOSE:To obtain a prehardened mold material for casting a high melting metal having 15-20HRC hardness by subjecting a casting alloy prepd. by adding Ni, Si and Zr to Cu to an age hardening treatment in a combination of an adequate component range and a heat treatment condition. CONSTITUTION:A casting alloy is composed, by weight %, of 2.5-8 Ni, 0.3-2 Si, 0.04-0.25 Zr and the balance Cu. Such casting alloy is hardened and cooled at the cooling rate higher than the cooling for 30min half cooling time from 850-950 deg.C and is then subjected to an age hardening treatment at 400-550 deg.C. The casting alloy may be composed of 3-6 Ni, 0.5-1.5 Si, 0.06-0.2 Zr and the balance Cu or 2.5-8 Ni, 0.3-2 Si, 0.2-1 Cr and the balance Cu.

Description

【発明の詳細な説明】 本発明は7e、 Ou金合金ど高融点金属鋳造用の金型
材料に適したOu  Ni  Si −Zr−1Or系
プリハードン金型利料に曲するものである。高温のFe
 、 Ou系合金の金型鋳造においては、大きな熱衝撃
による薄肉部を主体としたヒートクラック、突起部の溶
損、温度勾配による熱応力と強度とのバランスに関連し
た金型の反り、湯道部の溶損、温度勾配′による熱応力
と強度とのバランスに門連した金型の反り、湯道部の溶
損、へたり、型締めによるへたりなどが大きな問題点で
ある。
DETAILED DESCRIPTION OF THE INVENTION The present invention is directed to 7e, an OuNiSi-Zr-1Or based pre-hardened mold material suitable for a mold material for casting high melting point metals such as Ou gold alloys. High temperature Fe
, In mold casting of Ou-based alloys, heat cracks mainly in thin-walled parts due to large thermal shocks, melting of protrusions, mold warping related to the balance between thermal stress and strength due to temperature gradients, and runners. Major problems include mold warpage due to the balance between thermal stress and strength due to temperature gradients, melting loss and sagging of runners, and sagging due to mold clamping.

また、金型薄肉部、内部水冷を行ないにくい型訃分にお
ける昇温時の熱影響により型材が使用中に強度低下をま
ねき、漸次、へたり、ヒートクラック、溶損を生じる場
合がある。
In addition, the strength of the mold material may decrease during use due to the thermal effect of rising temperatures in thin-walled parts of the mold and parts of the mold that are difficult to cool internally with water, and may gradually become sagging, heat cracks, and melt damage.

一般の熱間工具鋼たとえはJIS SKD61(50r
−Mo−V@)を使用しても熱伝導率が小キく、局部的
な再焼入効果を受けた場合の過大な硬さ上昇による割れ
等のため要求される使用性能を満すことか困難な場合が
あった。
An example of general hot work tool steel is JIS SKD61 (50r
- Even if Mo-V@) is used, the thermal conductivity is low, and it satisfies the required usage performance because of cracks due to excessive increase in hardness when subjected to localized re-quenching effects. There were times when it was difficult.

一方熱伝導性のきわめて大きい純#il糸材料を使用す
れば熱応力の低減には役立つが、強度が元来低いため、
型締め圧力によるへたり、溶損等により要求寿命を満す
ことが困難であり、また金型の溶接補修が現実的には不
可能であり、金型材料としての適用が困難であった。
On the other hand, using pure #il yarn material with extremely high thermal conductivity will help reduce thermal stress, but its strength is inherently low.
It is difficult to meet the required lifespan due to wear and tear due to clamping pressure, and it is practically impossible to repair the mold by welding, making it difficult to use it as a mold material.

本発明はNi−3i析出硬化形合金として知られている
Ou −Ni −Si系合金にZr、 Orを添加し、
型材料として必要な昇温時の軟化抵抗を一層改善したも
ので、適切な成分範囲、熱処理状態の組合せで高融点金
属鋳造用型材料として適用し、使用時の昇温による軟化
をまねくことなく良好な型寿命をもたらすことを見出し
た結果によるもので新しい高融点金属鋳造用ブリハード
ン金型材料を提供するものである。
The present invention adds Zr and Or to an Ou-Ni-Si alloy known as a Ni-3i precipitation hardening alloy,
This material has further improved resistance to softening when the temperature rises, which is necessary for a mold material, and can be applied as a mold material for casting high-melting point metals by combining the appropriate composition range and heat treatment conditions, without causing softening due to temperature rise during use. This is based on the findings that it provides a good mold life, and provides a new brihardon mold material for casting high-melting point metals.

第1表に本願発明材料の成分例および焼入温度900U
より各種冷却速度で焼入後500CX2h時効硬化処理
した場合の硬さおよび900C空冷後高温の600Cで
2h過時効処理した板金の硬さを示す。
Table 1 shows an example of the composition of the invention material and a quenching temperature of 900U.
The hardness of sheet metals subjected to age hardening at 500C for 2 hours after quenching at various cooling rates and the hardness of sheet metals subjected to air cooling at 900C and overaging at a high temperature of 600C for 2 hours are shown.

焼入冷却速度の低重にしたがって時効硬さ値が相対的に
高く、かつ時効硬さの減少の程度が相対的に少なく、使
用時の昇温による強度低下に4える性質を備えているこ
とかわかる。
The aging hardness value is relatively high as the quenching cooling rate is low, the degree of decrease in aging hardness is relatively small, and the material has properties that prevent strength loss due to temperature rise during use. I understand.

第  1  表 本用途の金型材料として必要なl1RO15以上を解保
す2)ための焼入冷却速度は半冷時間約30m1nであ
る。
Table 1 The quenching cooling rate for releasing 11RO15 or more required for the mold material for this purpose2) is a half-cooling time of approximately 30 m1n.

第2表に本願発明材料の引張性質を示す。Table 2 shows the tensile properties of the materials of the present invention.

第2表 いずれも金型材料としての必要な延性を備えてしする。Table 2 Both have the necessary ductility as mold materials.

本願発明材料は高硬度が得られやすし)点も特徴の一つ
であるが、硬さの上昇は延性とのノ々ランスにより許容
限界がある。
One of the characteristics of the material of the present invention is that it is easy to obtain high hardness, but the increase in hardness has a permissible limit depending on the balance with ductility.

第3表に本願発明材料の熱伝導率を示す。Table 3 shows the thermal conductivity of the materials of the present invention.

第  3  表 本願発明材料は純銅よりも熱伝導率は低pzが熱間工具
鋼SKD 61の0.07と比較して明らかに高いレベ
ルレこある。
Table 3 The materials of the present invention have a thermal conductivity lower than that of pure copper, and the pz is clearly higher than that of hot work tool steel SKD 61, which is 0.07.

第4表に本願発明材料の耐ヒートクラ・ンク試験結果を
示す。
Table 4 shows the heat crank resistance test results of the materials of the present invention.

試験片は30闘φ×20−で、30mmφ面をノ々−リ
ーー加熱(本発明材料Aの表面温度を500Cに管理)
後水冷する操作を2000回繰返えしクラック発生状況
(30闘φの中央15朋表面部に沿うクラックの状況)
を断面観察した。
The test piece is 30mmφ x 20mm, and the 30mmφ surface is heated by Nono Lee (the surface temperature of the material A of the present invention is controlled at 500C).
After repeating the water cooling operation 2,000 times, cracks appeared (crack along the center 15mm surface of 30 mm diameter)
A cross-section was observed.

第  4  表 本発明材料は表面凹凸を生ぜず、またヒートクラックも
生じなかった。
Table 4 The materials of the present invention did not cause surface irregularities or heat cracks.

比較材料L(純銅)はヒートクラックを生じなかったが
強度か低いためやや凹凸を生じた。
Comparative material L (pure copper) did not cause heat cracks, but it did have some unevenness due to its low strength.

第5表に本願発明材料の耐溶損性試験結果を示す。Table 5 shows the results of the erosion resistance test for the materials of the present invention.

第5表 試験片は30闘φ(14翻φ)X’lO鰭tの円筒状試
験で1650Cの18−8ステンレス網の溶湯を繰返え
し500回高速で円筒内面を通過させた場合の内面の最
大溶損深さを測定した結果を示す。
The test pieces in Table 5 are the results of a cylindrical test with a diameter of 30 mm (14 mm) and a 18-8 stainless steel mesh made of 1650 C and passed through the inner surface of the cylinder at high speed 500 times. The results of measuring the maximum depth of erosion on the inner surface are shown.

本願発明材料よりも溶損寸法が相対的に小さい。The melting damage size is relatively smaller than that of the material of the present invention.

性 これは熱伝導率と強度、昇温における軟化抵抗とを兼備
しているためである。
This is because it has a combination of thermal conductivity, strength, and resistance to softening at elevated temperatures.

比較材L(純銅)は強度が低いため溶炉作用を相対的に
大きく受けたものである。
Comparative material L (pure copper) has low strength and has been subjected to relatively large blast furnace action.

第6表は本IA−発明材料の溶接性を示す。Table 6 shows the weldability of the present IA-invention materials.

溶接方法は110CsφX20鰭す試験片ブロックに1
5t+mφ×lo朋深さのくぼみをつけ、450Cに予
熱後Tig溶接により各々とも材溶接を行なったもので
ある。
The welding method is 1 to 110CsφX20 fin test piece block.
A recess with a depth of 5t+mφ×lo was made, and each material was welded by TIG welding after preheating to 450C.

第  6  表 本発明材料は溶接肉盛可能であり、断面観察でも内部欠
陥等はみられなかった。比較林料L(純銅)については
溶接肉盛が不能であった。
Table 6 The materials of the present invention can be overlaid by welding, and no internal defects were observed when cross-sectionally observed. Comparative forest material L (pure copper) could not be overlaid by welding.

これは熱伝導性が大きいため溶接部の昇温か行なわれに
<<、正常な肉盛が困難となったものである0 つぎに本発明材料の族1分限定理由について述べる。
This is because the heat conductivity of the welded part is high, and normal build-up is difficult.Next, the reason for the Group 1 minute limit for the material of the present invention will be described.

Ni、Siは固溶化処理により基地に固溶し、時効処理
によりNi−81,金鵜間化合物を形成、析出し)本願
発明材料としての必要な基礎的強度を与える。
Ni and Si are dissolved in the matrix by solid solution treatment, and are formed and precipitated by aging treatment to form Ni-81, a gold-coated compound (Ni-81, which is precipitated) to provide the necessary basic strength as the material of the present invention.

また適度の熱伝導性、これに関連して耐ヒートクラツク
性、耐溶損性、溶接性、耐型締めへたり性を付与するた
めに添加する。
It is also added to provide appropriate thermal conductivity and related properties such as heat crack resistance, erosion resistance, weldability, and mold clamping resistance.

多すぎると熱伝導性を過度に低下させ、低すぎると上記
添加の効果が得られないのでzr、 Or伊との関係に
おいてN1は25 M、OO%とし、Slはo3o−J
2.00% トする。
If it is too high, the thermal conductivity will be excessively reduced, and if it is too low, the effect of the above addition cannot be obtained.
2.00%.

N1、Slのより好ましい範囲はN13.00〜600
%、Si0.50〜1.50%である。
A more preferable range of N1 and Sl is N13.00 to 600.
%, and Si 0.50 to 1.50%.

Zr、 Orは時効処理時析出硬化性を高め、また過時
効温度域における硬さ低下を防ぎ、使用時の昇温による
強度低下を防止し、型寿命を向上させるために添加を行
なう。
Zr and Or are added to improve precipitation hardenability during aging treatment, prevent hardness from decreasing in the overaging temperature range, prevent strength from decreasing due to temperature rise during use, and improve mold life.

多すぎると熱伝導性、靭性の低下をまねき、低すぎると
上記添加の効果が1M・られないのでZrは0.0¥−
0,25%、Orは0.20−1.O0%とする。時効
硬さの上昇にはOrが安価で有利であるが過時効におけ
る軟化防止をとくに重視する場合にはZrの添加がより
有効であり、目的、用途により、Zr、orを単独また
は複合添加する。単独添加の場合のzrのより好ましい
範囲は0.06−0.20%、Orのより好ましい範囲
はα30−0.70%である。
If it is too high, it will cause a decrease in thermal conductivity and toughness, and if it is too low, the effect of the above addition will not be achieved by 1M, so Zr is 0.0 yen-
0.25%, Or is 0.20-1. 0%. Or is cheap and advantageous for increasing aging hardness, but when prevention of softening during overaging is particularly important, addition of Zr is more effective. Depending on the purpose and use, Zr and or may be added alone or in combination. . When added alone, the more preferable range for zr is 0.06-0.20%, and the more preferable range for Or is α30-0.70%.

熱処理は固溶化処理温度として850−950pの範囲
とし、結晶粒の粗大化、溶融相の生成を防き、焼入冷却
速度は必要な硬さを確保しっつ遂大な残留応力の生成を
防ぐため半冷時間30m1nの冷却よりはやい冷却速度
範囲内にコントロールする。
The heat treatment is carried out at a solution treatment temperature in the range of 850-950p to prevent coarsening of crystal grains and the formation of molten phase, and the quenching cooling rate is set to ensure the necessary hardness while preventing the generation of extremely large residual stress. In order to prevent this, the cooling rate is controlled within a range that is faster than the half-cooling time of 30mln.

これより遅い冷却速度では必要な弱・度HRO15以上
がかならずしも得られなくなり、また一方硬芒が高すぎ
ると被切削性、物性の減少をともなうのてHRO35以
下とする。
If the cooling rate is slower than this, it will not necessarily be possible to obtain the required weak degree HRO of 15 or more, and on the other hand, if the awn is too high, machinability and physical properties will decrease, so the HRO should be 35 or less.

以」二に記述のとおり、本願発明材料はNi−8i金金
属化合物の析出強化を利用した0u−Ni−8i系材料
にZr、 Orを添加し、高融点金属鋳造用金型材料と
して必要tj耐ヒートクラック性、強度、延性、高温へ
の昇温に対する軟化抵抗、耐溶損性、溶接性を何与する
ための成分バランス、熱処理の適正な組合ゼを検討しン
こ結果得られたプリハードン金型材料で、被切削性も良
好で金型に加工後そのまま使用され良好な金弗寿命と成
形号イクルRN’=Jの短縮による成形能率向上に寄与
するものである。
As described in Section 2 below, the material of the present invention is a 0u-Ni-8i material that utilizes precipitation strengthening of a Ni-8i gold metal compound, with the addition of Zr and Or, and is used as a mold material for casting high-melting point metals. The pre-hardened gold obtained by examining the proper combination of component balance and heat treatment to provide heat crack resistance, strength, ductility, softening resistance to high temperatures, erosion resistance, and weldability. It is a mold material that has good machinability, and can be used as is after being processed into a mold, contributing to good mold life and improved molding efficiency by shortening the molding cycle RN'=J.

Claims (1)

【特許請求の範囲】 L  Ni2−50〜8.00%、Si0.30〜2.
OO%、Zr0.04w O,25%、残部Ouよりな
る鍛造あるいは鋳造合金を850−950cより半冷時
間30 minの冷却よりもはやい冷却速用で焼入冷却
ののち、400−550Cの温度で時効硬化処理してH
RO15〜35の硬さにした高融点金属鋳造用プリノ1
−トン型材料。 2、  Ni3.OO〜6.00%、S10.50−1
.50%、Zr0.06間、20%、残部Ouよりなる
第1項記載の高融点金属鋳造用ブリノ・−トン型材料。 3、  N12=50〜&00%、Si0.30〜ZO
O% 、Oro、20〜l、00% 、残部Ouよりな
る鋳造あるいは@造合金を850−9501:l’より
半冷時間8φm1℃の冷却よりはやい冷却速度で焼入冷
却ののち、400−550fCの温度で時効硬化処理し
てHRO゛15〜35の硬さとした高融点金属鋳造用ブ
リノ・−トン型材料。 4 Ni3.OO〜6.00%、Si0.50〜1.5
0%、Oro、30〜0.70%、残部0uよりなる第
3項記載の高融点金属鋳造用プリノ・−トン型材料。 5、  Ni2−50−400%、Siα50〜1.5
0%、Zr0.04〜0.25%、〇九20〜1.00
%、残部Ouよりなる鍛造あるいは鋳造合金を85 M
 50′Cより半冷時間30m1nの冷却よりはやい冷
却速度で焼入冷却ののち、40o−55oCの温度で時
効硬化してHRO15〜35の硬さにした高融点金Jl
造用プリハードン型材料。
[Claims] L Ni2-50-8.00%, Si0.30-2.
A forged or cast alloy consisting of OO%, Zr0.04w O, 25%, and the balance O is quenched and cooled at a temperature of 400-550C from 850-950C with a cooling rate faster than half-cooling time of 30 min. H after age hardening treatment
Purino 1 for high melting point metal casting with hardness of RO15-35
-Ton type material. 2. Ni3. OO~6.00%, S10.50-1
.. 2. The Blino-ton type material for casting high melting point metals according to claim 1, comprising 50% Zr, 0.06% Zr, 20% O and the balance O. 3. N12=50~&00%, Si0.30~ZO
O%, Oro, 20~l, 00%, the balance O is a cast or @cast alloy made from 850-9501:l', and is quenched and cooled at a cooling rate faster than the half-cooling time of 8φm1℃, and then heated to 400-550fC. A Blino-ton type material for casting high melting point metals which has been age hardened at a temperature of 15 to 35 HRO. 4 Ni3. OO~6.00%, Si0.50~1.5
4. The Prino-ton type material for casting high melting point metals according to claim 3, comprising 0%, Oro, 30 to 0.70%, and the balance Ou. 5, Ni2-50-400%, Siα50-1.5
0%, Zr0.04~0.25%, 〇920~1.00
%, the balance O for forged or cast alloy 85 M
After quenching and cooling at a faster cooling rate than 50'C with a half-cooling time of 30ml, high melting point gold Jl was age-hardened at a temperature of 40o-55oC to a hardness of HRO 15 to 35.
Pre-hardened material for construction.
JP17258082A 1982-10-01 1982-10-01 Prehardened mold material for casting high melting metal Granted JPS5961544A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP17258082A JPS5961544A (en) 1982-10-01 1982-10-01 Prehardened mold material for casting high melting metal

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP17258082A JPS5961544A (en) 1982-10-01 1982-10-01 Prehardened mold material for casting high melting metal

Publications (2)

Publication Number Publication Date
JPS5961544A true JPS5961544A (en) 1984-04-07
JPS639575B2 JPS639575B2 (en) 1988-02-29

Family

ID=15944472

Family Applications (1)

Application Number Title Priority Date Filing Date
JP17258082A Granted JPS5961544A (en) 1982-10-01 1982-10-01 Prehardened mold material for casting high melting metal

Country Status (1)

Country Link
JP (1) JPS5961544A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2011036919A (en) * 2002-05-17 2011-02-24 Metglas Inc Copper-nickel-silicon two phase quench substrate

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5443121A (en) * 1977-09-12 1979-04-05 Hitachi Zosen Corp Ingot case material for continuous casting equipment
JPS58107460A (en) * 1981-12-21 1983-06-27 Chuetsu Gokin Chuko Kk Mold material for precipitation hardening type continuous casting

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5443121A (en) * 1977-09-12 1979-04-05 Hitachi Zosen Corp Ingot case material for continuous casting equipment
JPS58107460A (en) * 1981-12-21 1983-06-27 Chuetsu Gokin Chuko Kk Mold material for precipitation hardening type continuous casting

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2011036919A (en) * 2002-05-17 2011-02-24 Metglas Inc Copper-nickel-silicon two phase quench substrate

Also Published As

Publication number Publication date
JPS639575B2 (en) 1988-02-29

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