JPS592741B2 - Boronitriding method - Google Patents
Boronitriding methodInfo
- Publication number
- JPS592741B2 JPS592741B2 JP6326376A JP6326376A JPS592741B2 JP S592741 B2 JPS592741 B2 JP S592741B2 JP 6326376 A JP6326376 A JP 6326376A JP 6326376 A JP6326376 A JP 6326376A JP S592741 B2 JPS592741 B2 JP S592741B2
- Authority
- JP
- Japan
- Prior art keywords
- steel
- nitriding
- treatment
- boronitriding
- case
- 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
- 238000000034 method Methods 0.000 title claims description 16
- 238000005121 nitriding Methods 0.000 claims description 22
- 229910000831 Steel Inorganic materials 0.000 claims description 16
- 239000010959 steel Substances 0.000 claims description 16
- 239000007787 solid Substances 0.000 claims description 7
- 229910000851 Alloy steel Inorganic materials 0.000 claims description 6
- 229910000975 Carbon steel Inorganic materials 0.000 claims description 6
- 239000010962 carbon steel Substances 0.000 claims description 6
- 239000003795 chemical substances by application Substances 0.000 claims description 6
- 239000007789 gas Substances 0.000 claims description 6
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 4
- 229910052757 nitrogen Inorganic materials 0.000 claims description 2
- 239000012299 nitrogen atmosphere Substances 0.000 claims description 2
- 238000001816 cooling Methods 0.000 claims 1
- 239000000463 material Substances 0.000 description 17
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 5
- 238000004381 surface treatment Methods 0.000 description 5
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 2
- 239000012298 atmosphere Substances 0.000 description 2
- 238000005452 bending Methods 0.000 description 2
- 229910021538 borax Inorganic materials 0.000 description 2
- 229910052796 boron Inorganic materials 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000010791 quenching Methods 0.000 description 2
- 230000000171 quenching effect Effects 0.000 description 2
- 239000004328 sodium tetraborate Substances 0.000 description 2
- 235000010339 sodium tetraborate Nutrition 0.000 description 2
- 101150105594 SCM3 gene Proteins 0.000 description 1
- INAHAJYZKVIDIZ-UHFFFAOYSA-N boron carbide Chemical compound B12B3B4C32B41 INAHAJYZKVIDIZ-UHFFFAOYSA-N 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 150000004767 nitrides Chemical class 0.000 description 1
- 238000003303 reheating Methods 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
Landscapes
- Solid-Phase Diffusion Into Metallic Material Surfaces (AREA)
Description
【発明の詳細な説明】
本発明は、固体浸硼剤で覆われた鉄鋼を窒化処理条件で
熱処理する方法に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for heat treating steel coated with a solid borening agent under nitriding conditions.
従来より各種摺動部材の耐摩耗性、耐食性の向上さらに
カジリ、焼付の問題を解決するための表面処理方法とし
て、窒化処理が広範囲に実施されて成果を上げている。BACKGROUND ART Nitriding has been widely used and achieved results as a surface treatment method for improving the wear resistance and corrosion resistance of various sliding members and solving the problems of galling and seizure.
しかしながら、窒化処理法によつて炭素鋼および低合金
鋼(窒化鋼を除く)を窒化処理した場合に、高硬度の硬
化層が得られず硬化層も浅く窒化処理による表面処理の
効果はあまりなかつた。However, when carbon steel and low alloy steel (excluding nitrided steel) are nitrided using the nitriding method, a hardened layer with high hardness cannot be obtained and the hardened layer is shallow, so the surface treatment effect by nitriding is not very effective. Ta.
また最近、表面処理として浸硼処理法が実施されている
。浸硼処理法は、短時間で高硬度の硬化層が得られる等
の利点はあるが、As変態点以上の高温度で処理するた
め、同処理後の素材の変形、特に長軸部品に著しい変形
が起り、内部硬度が低くなる傾向にあつた。このために
、内部硬度を高めるため浸硼処理後直接焼入あるいは再
加熱焼入した場合には、さらに素材の変形が大きくなり
、後工程における加工を困難なものとしていた。本発明
は、窒化処理および浸硼処理のこれらの欠点を除去する
ため、炭素鋼および低合金鋼(窒化鋼を除く)に対して
所要の十分な硬化層を得ると共に素材の曲りを微小とし
た表面処理法を提供することにある。すなわち、本発明
は炭素鋼および低合金鋼(窒化鋼を除く)を固体浸硼剤
に埋設し、窒化処理条件で表面処理することによつて炭
素鋼および低合10金鋼(窒化用鋼を除く)等の鉄鋼に
対しても変形が小さく高硬度で十分な深さの硬化層を得
られるようにしたものである。Also, recently, a boronic treatment method has been implemented as a surface treatment. The borening treatment method has the advantage of being able to obtain a hardened layer with high hardness in a short time, but since it is treated at a high temperature above the As transformation point, the deformation of the material after the treatment, especially in long-axis parts, is significant. Deformation occurred and the internal hardness tended to decrease. For this reason, when direct quenching or reheating quenching is performed after the borening treatment to increase the internal hardness, the deformation of the material becomes even greater, making processing in subsequent steps difficult. In order to eliminate these drawbacks of nitriding and borening, the present invention provides a method for obtaining a sufficient hardening layer for carbon steel and low alloy steel (excluding nitriding steel) and minimizing bending of the material. The object of the present invention is to provide a surface treatment method. That is, the present invention provides carbon steel and low-alloy steel (excluding nitriding steel) by embedding carbon steel and low-alloy steel (excluding nitriding steel) in a solid boring agent and surface-treating the material under nitriding treatment conditions. This makes it possible to obtain a hardened layer with small deformation, high hardness, and sufficient depth even for steels such as steel (excluding steel).
以下実施例を基に本発明を説明する。The present invention will be explained below based on Examples.
第1図は、ガス窒化処理炉の断面構造を示す。FIG. 1 shows a cross-sectional structure of a gas nitriding furnace.
151は表面処理される鉄鋼素材、2は固体浸硼剤で、
硼素供給剤としての炭化硼素(B4C)に浸硼促進剤と
しての硼砂(Na。151 is a steel material to be surface treated, 2 is a solid borourant,
Boron carbide (B4C) is used as a boron supplying agent, and borax (Na) is used as a borizing accelerator.
B4O7)を8:2の割合で混合している。3は固体浸
硼剤2に埋設した鉄鋼素材1を収納するケース、4はケ
ース3を20窒化雰囲気とする窒化ケース、5は窒化ケ
ース4の一側部に設けたアンモニアガス入口、6は窒化
ケース4の一側部に設けたアンモニアガス出口、Tは窒
化ケース4の全体を覆う炉、8は炉7内部を加熱するヒ
ーターである。B4O7) are mixed at a ratio of 8:2. 3 is a case for storing the steel material 1 embedded in solid borizing agent 2, 4 is a nitriding case that makes case 3 a 20 nitriding atmosphere, 5 is an ammonia gas inlet provided on one side of the nitriding case 4, and 6 is a nitriding case. An ammonia gas outlet is provided on one side of the case 4, T is a furnace that covers the entire nitriding case 4, and 8 is a heater that heats the inside of the furnace 7.
25固体浸硼剤2で覆われた鉄鋼材料1をアンモニアガ
スによる窒素雰囲気中でヒーター8によつて500〜5
80℃に加熱し、10時間以上保持することによつて、
鉄鋼素材1の表面に窒素および硼素が拡散して高硬度の
窒化物および硼化物が生30成し、所要の硬度で十分な
硬化層を得ることができることを見出した。25 The steel material 1 covered with the solid boring agent 2 is heated to 500 to 500 ml by the heater 8 in a nitrogen atmosphere using ammonia gas.
By heating to 80°C and holding for 10 hours or more,
It has been found that nitrogen and boron diffuse into the surface of the steel material 1, forming highly hard nitrides and borides, and that a sufficient hardened layer with the required hardness can be obtained.
材料SCM3材直径50φ長さ1000mmに対して(
1)ガス窒化処理した場合(処理条件;510℃、50
時間保持)、(2)浸硼処理した場合(処理35条件:
900℃、5時間保持)、(3)浸硼窒化処理した場合
(処理条件:第1図に示す装置を用いて510℃、50
時間保持)について、素材表面かiハクーらの距離と硬
度の関係を第2図に、素材一端面からの距離とその変形
量の関係を第3図に示す。For material SCM3 material diameter 50φ length 1000mm (
1) In the case of gas nitriding treatment (processing conditions: 510°C, 50°C
(2) In the case of borosilication treatment (treatment 35 conditions:
900°C, 5 hours), (3) Boronitriding treatment (processing conditions: 510°C, 50°C using the equipment shown in Figure 1)
Regarding the time retention), FIG. 2 shows the relationship between the distance from the surface of the material and the hardness, and FIG. 3 shows the relationship between the distance from one end of the material and the amount of deformation thereof.
第2図において、素材表面より0.31mmの範囲で硬
度を比較した場合、浸硼処理した場合が一番高く、次に
浸硼窒化処理、ガス窒化処理の順になつている。硬度が
高けれは、耐摩耗性に対しては望ましいことであるけれ
ども、逆に浸硼処理のように高温度で熱処理するので素
材の変形も大きく、また素材そのものの内部硬度も低く
なる。In FIG. 2, when comparing the hardness within a range of 0.31 mm from the surface of the material, the hardness is highest in the case of borening treatment, followed by boronitriding treatment and gas nitriding treatment. Although high hardness is desirable for wear resistance, on the other hand, heat treatment at high temperatures such as boring treatment causes large deformation of the material and also reduces the internal hardness of the material itself.
本発明の浸硼窒化法による場合は、ガス窒化法と温度条
件および保持時間は同じであるにもかかわらず、浸硼雰
囲気の差によつて表面から0.3mm内では約300H
vほど高くなつている。In the case of the boronitriding method of the present invention, although the temperature conditions and holding time are the same as those of the gas nitriding method, the temperature within 0.3 mm from the surface is approximately 300 H due to the difference in the borizing atmosphere.
It is as high as v.
第3図は、前記SCM3に対する各表面処理終了後にお
ける曲り変形量を示す。FIG. 3 shows the amount of bending deformation of the SCM 3 after each surface treatment is completed.
(変形量は素材を平担な面上に置いて回転させた場合の
最大変化量をいう。)本発明による浸硼窒化法および窒
化法によるものはほとんど変形がなく、浸硼法によるも
のは最大0.8mmという大きな変形を生じた。本実施
例において、浸硼剤に浸硼促進剤として硼砂を用いたが
これ以外に炭酸塩、ハロゲン化物等を適宜加えることに
よつて浸硼窒化処理に要する時間を短縮することが可能
となる。以上述べたごとく、浸硼窒化法は、浸硼法程に
硬度が上らないが安定した所要の硬度を有し、なおかつ
変形量が少なく、従来のガス窒化法では、十分な硬度と
硬化層を得ることかできなかつた炭素鋼または低合金鋼
(窒化鋼を除く)等の鉄鋼についても満足な結果を得る
ことができた。(The amount of deformation refers to the maximum amount of change when the material is placed on a flat surface and rotated.) There is almost no deformation in the boronitriding and nitriding methods of the present invention, and in the case of the boronitriding method according to the present invention, A large deformation of up to 0.8 mm occurred. In this example, borax was used as a borons accelerator, but the time required for the boronitriding process can be shortened by appropriately adding carbonates, halides, etc. . As mentioned above, the boronitriding method does not increase the hardness as much as the boronic method, but it has the required stable hardness and the amount of deformation is small. Satisfactory results were also obtained for steels such as carbon steel or low alloy steel (excluding nitrided steel), which had previously been difficult to obtain.
第1図はガス窒化処理炉の断面図。
1;鉄鋼素材、2:固体浸硼剤、3:ケース、4;窒化
ケース、5;アンモニアガス入口、6:アンモニアガス
出口、7:炉、8:ヒータ。FIG. 1 is a cross-sectional view of a gas nitriding furnace. 1: Steel material, 2: Solid borourant, 3: Case, 4: Nitriding case, 5: Ammonia gas inlet, 6: Ammonia gas outlet, 7: Furnace, 8: Heater.
Claims (1)
素鋼を除く)をガス窒化処理炉内に設置し、同炉内を窒
素雰囲気とし温度500〜580℃の範囲で10時間以
上加熱保持した後、空冷することを特徴とする浸硼窒化
法。1. Place carbon steel or low alloy steel (excluding nitrogen steel) embedded in a solid boring agent in a gas nitriding furnace, and heat the furnace in a nitrogen atmosphere at a temperature of 500 to 580°C for 10 hours or more. A boronitriding method characterized by air cooling after holding.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP6326376A JPS592741B2 (en) | 1976-05-31 | 1976-05-31 | Boronitriding method |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP6326376A JPS592741B2 (en) | 1976-05-31 | 1976-05-31 | Boronitriding method |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS52145345A JPS52145345A (en) | 1977-12-03 |
| JPS592741B2 true JPS592741B2 (en) | 1984-01-20 |
Family
ID=13224211
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP6326376A Expired JPS592741B2 (en) | 1976-05-31 | 1976-05-31 | Boronitriding method |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS592741B2 (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2441276C (en) * | 2001-03-21 | 2009-10-06 | Honda Giken Kogyo Kabushiki Kaisha | Steel material and method for preparation thereof |
| JP3745971B2 (en) | 2001-03-21 | 2006-02-15 | 本田技研工業株式会社 | Steel material |
-
1976
- 1976-05-31 JP JP6326376A patent/JPS592741B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS52145345A (en) | 1977-12-03 |
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