JPH0266152A - Surface hardening method for titanium or titanium alloy - Google Patents
Surface hardening method for titanium or titanium alloyInfo
- Publication number
- JPH0266152A JPH0266152A JP21362788A JP21362788A JPH0266152A JP H0266152 A JPH0266152 A JP H0266152A JP 21362788 A JP21362788 A JP 21362788A JP 21362788 A JP21362788 A JP 21362788A JP H0266152 A JPH0266152 A JP H0266152A
- Authority
- JP
- Japan
- Prior art keywords
- glass
- titanium
- alloy
- layer
- hardened layer
- 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.)
- Pending
Links
- 229910052719 titanium Inorganic materials 0.000 title claims abstract description 14
- 229910001069 Ti alloy Inorganic materials 0.000 title claims abstract description 11
- 238000000034 method Methods 0.000 title claims description 23
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 title claims description 12
- 239000010936 titanium Substances 0.000 title claims description 11
- 238000010438 heat treatment Methods 0.000 claims abstract description 20
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 14
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 12
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 11
- 239000011521 glass Substances 0.000 claims abstract description 9
- 238000009792 diffusion process Methods 0.000 claims abstract description 6
- 239000005388 borosilicate glass Substances 0.000 claims abstract description 4
- 210000003298 dental enamel Anatomy 0.000 claims abstract description 4
- 229910052788 barium Inorganic materials 0.000 claims abstract description 3
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 claims abstract description 3
- 238000005242 forging Methods 0.000 claims abstract description 3
- 238000005096 rolling process Methods 0.000 claims abstract description 3
- 239000005361 soda-lime glass Substances 0.000 claims abstract description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 18
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 11
- 239000001301 oxygen Substances 0.000 claims description 11
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 7
- 238000010304 firing Methods 0.000 claims description 4
- 239000007789 gas Substances 0.000 claims description 4
- 239000005354 aluminosilicate glass Substances 0.000 claims description 2
- 239000000203 mixture Substances 0.000 claims description 2
- 229910045601 alloy Inorganic materials 0.000 abstract 1
- 239000000956 alloy Substances 0.000 abstract 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 abstract 1
- 238000001354 calcination Methods 0.000 abstract 1
- 239000005368 silicate glass Substances 0.000 abstract 1
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- 238000005121 nitriding Methods 0.000 description 3
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 238000005336 cracking Methods 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 229910000765 intermetallic Inorganic materials 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000007781 pre-processing Methods 0.000 description 1
- 239000005297 pyrex Substances 0.000 description 1
- 238000003303 reheating Methods 0.000 description 1
- 239000006104 solid solution Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
チタン及びチタン合金を素材とし、表面が500Hv程
度の約0.1 tm以上の比較的厚い硬化層が必要な板
、部品の製造に利用可能なチタンまたはチタン合金の表
面硬化方法に関するものである。Detailed Description of the Invention (Industrial Application Field) It can be used to manufacture plates and parts that are made of titanium and titanium alloy and require a relatively thick hardened layer of about 0.1 tm or more on the surface of about 500 Hv. The present invention relates to a method for surface hardening titanium or titanium alloys.
(従来の技術)
従来のチタン及びチタン合金の表面硬化法は、成形済み
のものに対して行われており、硬化法としては、酸素、
窒素等の侵入型硬化法、金属及び金属間化合物を利用し
た硬化法、硬質粉末物質のチタン母材中への分散による
硬化法があり、これらは、加熱炉、電気メツキ、溶射、
イオンブレーティング、プラズマアーク、レーザー等を
用いて行なわれている。このうち、酸素、窒素、炭素ま
たは、これらの内2種以上の元素が、チタン及びチタン
合金の表面から拡散するような雰囲気ガスまたはシアン
含有塩溶融浴中で加熱することで、硬化層を形成する方
法は比較的低コストであり、−船釣に行なわれている。(Prior art) Conventional surface hardening methods for titanium and titanium alloys are performed on molded products, and hardening methods include oxygen,
There are interstitial hardening methods such as nitrogen, hardening methods using metals and intermetallic compounds, and hardening methods by dispersing hard powder materials into the titanium matrix.
This is done using ion blating, plasma arc, laser, etc. Among these, oxygen, nitrogen, carbon, or two or more of these elements are heated in an atmospheric gas or cyanide-containing salt molten bath that diffuses from the surface of titanium and titanium alloy to form a hardened layer. This method is relatively low cost and is commonly used in boat fishing.
例として、特開昭50−60437号公報、特開昭50
60438号公報、特開昭50−98451号公報、特
開昭5240442号公報、特開昭53−120642
号公報、特開昭53−138936号公報、特開昭56
−146875号公報、特開昭58−161771号公
報、特開昭62〜161947号公報、特開昭62−2
56956号公報記載の方法がある。しかしながら、こ
れらの方法は成形加工後に、硬化処理を行うため、形状
、材質を確保すべく、処理温度を約900”C以下とし
ており、厚く硬化層を形成させるにはかなりの長時間を
必要とする。For example, JP-A-50-60437, JP-A-50
60438, JP 50-98451, JP 5240442, JP 53-120642
No. 53-138936, Japanese Patent Application Laid-Open No. 1983
-146875, JP 58-161771, JP 62-161947, JP 62-2
There is a method described in No. 56956. However, since these methods perform hardening treatment after molding, the treatment temperature is kept at about 900"C or less to ensure the shape and material quality, and it takes a considerable amount of time to form a thick hardened layer. do.
(発明が解決しようとする課題)
従来の技術では、成形済みのものに対して表面硬化が行
なわれるために、加熱炉を用いて全体を高温にして処理
する方法では、材質や形状を確保するために、β域以上
の高温にすることが出来ない。一方、β域以下の温度で
硬化層を十分に厚くするには長時間が必要で、生産性が
低い。(Problem to be solved by the invention) In conventional technology, surface hardening is performed on the molded product, so the method of heating the entire product to a high temperature using a heating furnace makes it difficult to secure the material and shape. Therefore, it is not possible to raise the temperature to a temperature higher than the β range. On the other hand, it takes a long time to make the cured layer sufficiently thick at temperatures below the β range, resulting in low productivity.
(課題を解決するための手段)
本発明は、成形加工前に硬化処理を行うことを特徴とす
る表面硬化法であり、すなわち、酸素窒素、炭素または
これらの内2種以上の元素がチタン及びチタン合金の表
面から拡散するようす雰囲気のガスや溶融浴中で第1回
目の加熱を行い、短時間で厚く、侵入型元素の拡散によ
る硬化層を形成させたのち、特定の硬さ以上を有する加
工に不適切な層が発生する場合には、それを除去し、つ
づいて、第2回目の加熱を行い圧延、鍛造等の成形加工
を行うことを特徴とする表面硬化方法である。(Means for Solving the Problems) The present invention is a surface hardening method characterized by performing a hardening treatment before forming. That is, oxygen, nitrogen, carbon, or two or more of these elements are titanium and The first heating is performed in an atmosphere of gas or molten bath that diffuses from the surface of the titanium alloy to form a thick, hardened layer in a short time due to the diffusion of interstitial elements, and then it has a hardness of at least a certain level. If a layer unsuitable for processing is generated, this surface hardening method is characterized in that it is removed, followed by second heating and forming processing such as rolling or forging.
ここで、第1回目の加熱温度は1000〜1600℃で
あり、酸素、窒素、炭素を含む雰囲気、シアンを含有す
る塩浴などの窒化性溶融浴中または、ソーダ石灰ガラス
、ホウケイ酸ガラスなどの酸化性溶融浴中等で行う。1
000℃未満では硬化層を形成するには時間がかかり生
産性が悪く、1600℃を超えると炉の経済性が著しく
悪くなるためである。Here, the first heating temperature is 1000 to 1600°C, in an atmosphere containing oxygen, nitrogen, and carbon, in a nitriding melt bath such as a salt bath containing cyanide, or in an atmosphere containing oxygen, nitrogen, and carbon, or in a nitriding melt bath such as a salt bath containing cyanide, or in an atmosphere containing oxygen, nitrogen, and carbon, or in a nitriding melt bath such as a salt bath containing cyanide. Perform in an oxidizing molten bath, etc. 1
This is because if the temperature is less than 1,600°C, it takes time to form a hardened layer and productivity is poor, and if it exceeds 1,600°C, the economical efficiency of the furnace becomes extremely poor.
ここで例として第1図は、加熱温度と、加工に適する4
00〜5008νを有する層の厚さの関係を示した。こ
の様に、高温で加熱することにより短時間で厚い硬化層
をうろことが出来る。本発明では硬化処理の後に加工を
行う。Here, as an example, Fig. 1 shows the heating temperature and 4 suitable for processing.
The relationship between layer thicknesses with 00 to 5008 ν is shown. In this way, by heating at high temperatures, a thick hardened layer can be coated in a short time. In the present invention, processing is performed after hardening treatment.
ここで、特定の硬さ以上を有する加工に不適切な層とし
ては、ビッカース硬度600Hv以上のものであるが、
これは熱間加工時に割れが発生している硬度を調べ決定
した。尚加工に不適切な層を不必要に作らない方法とし
て、アルゴンガス中に適量の酸素等を含有させたり、シ
アン塩浴中で行なうのもよいが、経済的及び公害問題の
ない点からガラス等の溶融浴を用いると良い。Here, a layer having a hardness of more than a certain level and unsuitable for processing is a layer having a Vickers hardness of 600 Hv or more,
This was determined by examining the hardness at which cracks occur during hot working. In addition, as a method to avoid unnecessary formation of layers inappropriate for processing, it is also possible to include an appropriate amount of oxygen in argon gas or to perform the process in a cyanide salt bath, but from the viewpoint of economical and non-pollution problems, glass It is recommended to use a molten bath such as
ここでガラス等の溶融浴として、軟化点が650〜95
0℃であるソーダ石灰ガラス、バリウムガラス、ホウケ
イ酸ガラス、アルミノシリケイトガラス及び焼成温度が
750℃以上の琺瑯またはこれらの2種以上の混合物が
よい。軟化点650℃未満のガラスでは、大気中と同様
に加熱によりスケール等の加工に不適切な層が発生する
からであり、950 ”C超では十分に酸素固溶層を形
成しないからである。また焼成温度750℃未満の琺瑯
では、同様にスケール等の加工に不適切な層が発生する
からである。以上の内容を表11表2に示す。Here, as a molten bath of glass etc., the softening point is 650 to 95.
Soda lime glass, barium glass, borosilicate glass, aluminosilicate glass having a firing temperature of 0°C, enamel having a firing temperature of 750°C or higher, or a mixture of two or more of these are preferred. This is because glass with a softening point of less than 650°C will produce a layer unsuitable for processing, such as scale, due to heating as in the air, and a glass with a softening point of less than 950''C will not form a sufficient oxygen solid solution layer. In addition, if the firing temperature is lower than 750° C., a layer unsuitable for processing such as scale will similarly occur.The above contents are shown in Table 11 and Table 2.
表1
表2
尚溶融浴加熱後、水冷することにより、ガラス、琺瑯は
簡単に除去出来、かつ、組織的にも均一で、靭性が増す
ことが確認された。Table 1 Table 2 It was confirmed that by cooling with water after heating the molten bath, the glass and enamel could be easily removed, the structure was uniform, and the toughness was increased.
次に加工のための第2回目の加熱を行う。Next, a second heating for processing is performed.
ここで、第2回目の加熱温度は、700〜1600 ”
Cである。第2図に示す様に700℃未満では高温で軟
化する室温で600Hv未満の層といえども母材チタン
に比べて硬く、歪速度0.1〜100 /secの加工
が困難となり、割れが発生するからである。また160
0℃超では、炉の経済性が著しく悪くなるためである。Here, the second heating temperature is 700 to 1600"
It is C. As shown in Figure 2, even if the layer is less than 600 Hv at room temperature, which softens at high temperatures below 700°C, it is harder than the base material titanium, making it difficult to process at strain rates of 0.1 to 100/sec, and cracking occurs. Because it does. 160 again
This is because if the temperature exceeds 0° C., the economical efficiency of the furnace deteriorates significantly.
(実施例1)
JIS 2種相等の50 mm tのチタン板を大気中
で1200℃X17H加熱酸化後、ショットを行い、続
いて片面0.3mmはど溶剤した。この結果表面の硬さ
は約480Hvであった。この板を920 ”Cに再加
熱したのち、5 mm tまで圧延し空冷した。この板
の硬さ分布を第3図に示す。第1図から、圧延前の40
0〜50旧1vを有する硬化層の厚さは約211ffI
lであり、加工により厚さは1/10になるため0、2
mmの硬化層となるはずであるが、第3図では0、4
mmとなっている。これは加工による細粒化のために
硬化層厚さが増加したもので、硬化層が不均一に加工さ
れたものではない。(Example 1) A titanium plate of 50 mm t, such as a JIS type 2 phase, was heated and oxidized in the atmosphere at 1200° C. for 17 hours, shot, and then 0.3 mm thick on one side with a solvent. As a result, the surface hardness was approximately 480 Hv. After reheating this plate to 920"C, it was rolled to 5 mm t and air-cooled. The hardness distribution of this plate is shown in Figure 3. From Figure 1, it can be seen that
The thickness of the cured layer with 0-50 old 1v is about 211ffI
l, and the thickness becomes 1/10 due to processing, so 0,2
It should be a hardened layer of mm, but in Figure 3 it is 0,4 mm.
mm. This is because the thickness of the hardened layer has increased due to grain refinement due to processing, and the hardened layer is not processed unevenly.
(実施例2)
JIS 3種相等の25φのチタン棒をホウケイ酸ガラ
ス(商標パイレックス)溶融浴中に1300”CX 4
H保持後水冷し、ガラスを除去したのち長さ13nv
++に切断し、長さ方向を5mmまで高速鍛造加工した
。その時の加工前加熱温度と、割れの有無および形状の
結果を表3に示す。また900℃で鍛造したものの硬化
層形成状況を第4図に示す。(Example 2) A 25φ titanium rod of JIS 3 types, etc. was placed in a borosilicate glass (trademark Pyrex) melting bath in a 1300” CX 4
After holding H, cooled with water and removed the glass, the length was 13nv.
It was cut into ++ and forged at high speed to a length of 5 mm. Table 3 shows the pre-processing heating temperature and the presence/absence and shape of cracks. FIG. 4 shows the state of hardened layer formation in a product forged at 900°C.
表3
(発明の効果)
本発明においては、酸素、窒素等の拡散による侵入型硬
化処理を成形加工前に行うため、形状確保上問題となる
高温を用いることが出来、従って短時間の拡散処理で厚
い硬化層をうることが可能であり、また高温で軟化する
ビッカース硬度600Hv未満の表面にして成形加工す
るため、割れ等の問題がなく、以上の硬化処理を加熱炉
のみを用いて行うためコストが安く、また加工後の急冷
や熱処理により組織調整が可能である、等の数多くの利
点がある。Table 3 (Effects of the Invention) In the present invention, since the interstitial hardening treatment by diffusion of oxygen, nitrogen, etc. is performed before the molding process, it is possible to use high temperatures that pose a problem in securing the shape, and therefore the diffusion treatment can be performed in a short time. It is possible to obtain a thick hardened layer in the process, and since the surface is molded with a Vickers hardness of less than 600 Hv, which softens at high temperatures, there are no problems such as cracking, and the above hardening process is performed using only a heating furnace. It has many advantages, such as low cost and the ability to adjust the structure by rapid cooling or heat treatment after processing.
第1図は加熱温度と、400〜500Hvの硬化層厚さ
との関係を示す図、第2図は温度とビッカース硬さとの
関係を示す図、第3図は板表面からの深さと、ピンカー
ス硬さとの関係を示す図、第4図は円板部品の断面の硬
化分布を示す図である。
第1図
100゜
OO
1;’00 /300
温度(℃)
(室玉)
1屋(C)
<my+t)
半径力向長さ
第
図
板表力・うの深さ(筑m)
手
続
補
正
二tI:
(自発ン
昭(=[J 63年11月12Figure 1 shows the relationship between heating temperature and hardened layer thickness of 400 to 500 Hv, Figure 2 shows the relationship between temperature and Vickers hardness, and Figure 3 shows the depth from the plate surface and Pinkers hardness. FIG. 4 is a diagram showing the hardening distribution in the cross section of the disk component. Fig. 1 100゜OO 1;'00 /300 Temperature (°C) (Murotama) 1 house (C) <my+t) Radial force direction length Fig. Plate surface force/depth (Chikum) Procedure amendment 2 tI: (Shihansho (=[J November 12, 1963
Claims (2)
元素が、チタン及びチタン合金の表面から拡散するよう
な雰囲気のガスまたは溶融浴中で第1回目の加熱を10
00℃〜1600℃で行い、酸素、窒素、炭素の侵入型
元素の拡散による硬化層を形成させたのち、ビッカース
硬度600Hv以上の層が、発生する場合には、それを
除去し、つづいて、第2回目の加熱を700℃〜160
0℃で行い、圧延、鍛造等の成形加工を行うことを特徴
とするチタンまたはチタン合金の表面硬化方法。(1) The first heating is carried out in a gas or molten bath in an atmosphere where oxygen, nitrogen, carbon, or two or more of these elements diffuse from the surface of titanium and titanium alloy.
After forming a hardened layer by diffusion of interstitial elements such as oxygen, nitrogen, and carbon at 00°C to 1600°C, if a layer with a Vickers hardness of 600Hv or more is generated, it is removed, and then, Second heating to 700℃~160℃
A method for surface hardening titanium or titanium alloy, which is carried out at 0° C. and is characterized by performing forming processes such as rolling and forging.
ダ石灰ガラス、バリウムガラス、ホウケイ酸ガラス、ア
ルミノシリケイトガラス、もしくは焼成温度が750℃
以上の琺瑯またはこれらの2種以上の混合物である特許
請求の範囲第1項記載の表面硬化方法。(2) The molten bath is soda lime glass, barium glass, borosilicate glass, aluminosilicate glass with a softening point of 650°C to 950°C, or a firing temperature of 750°C.
The surface hardening method according to claim 1, which is the above enamel or a mixture of two or more thereof.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP21362788A JPH0266152A (en) | 1988-08-30 | 1988-08-30 | Surface hardening method for titanium or titanium alloy |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP21362788A JPH0266152A (en) | 1988-08-30 | 1988-08-30 | Surface hardening method for titanium or titanium alloy |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH0266152A true JPH0266152A (en) | 1990-03-06 |
Family
ID=16642288
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP21362788A Pending JPH0266152A (en) | 1988-08-30 | 1988-08-30 | Surface hardening method for titanium or titanium alloy |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0266152A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102703852A (en) * | 2012-06-15 | 2012-10-03 | 西北有色金属研究院 | Method for composite hydrogen-free oxygen-carburizing on surface of two-phase titanium alloy |
-
1988
- 1988-08-30 JP JP21362788A patent/JPH0266152A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102703852A (en) * | 2012-06-15 | 2012-10-03 | 西北有色金属研究院 | Method for composite hydrogen-free oxygen-carburizing on surface of two-phase titanium alloy |
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