JP3247964B2 - Surface treatment method for metal parts - Google Patents

Surface treatment method for metal parts

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Publication number
JP3247964B2
JP3247964B2 JP03145793A JP3145793A JP3247964B2 JP 3247964 B2 JP3247964 B2 JP 3247964B2 JP 03145793 A JP03145793 A JP 03145793A JP 3145793 A JP3145793 A JP 3145793A JP 3247964 B2 JP3247964 B2 JP 3247964B2
Authority
JP
Japan
Prior art keywords
electrolysis
treated
treatment method
surface treatment
present
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 - Fee Related
Application number
JP03145793A
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Japanese (ja)
Other versions
JPH06220689A (en
Inventor
利彦 岩野
久男 中野
俊史 丹治
勝 桜井
マス ピエール
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.)
Dowa Holdings Co Ltd
Original Assignee
Dowa Holdings Co Ltd
Dowa Mining Co Ltd
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Filing date
Publication date
Application filed by Dowa Holdings Co Ltd, Dowa Mining Co Ltd filed Critical Dowa Holdings Co Ltd
Priority to JP03145793A priority Critical patent/JP3247964B2/en
Publication of JPH06220689A publication Critical patent/JPH06220689A/en
Application granted granted Critical
Publication of JP3247964B2 publication Critical patent/JP3247964B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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  • Other Surface Treatments For Metallic Materials (AREA)
  • Electroplating Methods And Accessories (AREA)

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【産業上の利用分野】本発明は、自動車、その他の輸送
機器、産業機器、事務用機器等を構成する金属部品の耐
焼付き、かじり性、初期なじみ性、耐摩耗性、耐疲労性
等の向上を目的した表面処理法に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to the use of metal parts constituting automobiles, other transportation equipment, industrial equipment, office equipment, etc., such as seizure resistance, galling, initial conformability, abrasion resistance, and fatigue resistance. It relates to a surface treatment method for the purpose of improvement.

【0002】[0002]

【従来の技術】金属部品の表面に硫化鉄及び硫黄化合物
からなる生成層(以下、浸硫層という。)を生成させる
表面処理法として、いわゆる低温浸硫処理法が提案され
ている(例えば、特公昭44−1809号公報参照)。
該方法は溶融塩浴中に被処理材を浸漬し、被処理材を陽
極、塩浴槽を陰極として一定の電流密度のもとで連続的
に直流電解を行い、被処理材の表面に1〜10μm程度
の浸硫層を生成させるものである。
2. Description of the Related Art A so-called low-temperature sulfurizing treatment method has been proposed as a surface treatment method for forming a formation layer (hereinafter referred to as a "sulfurized layer") composed of iron sulfide and a sulfur compound on the surface of a metal component (for example, see, for example, Japanese Patent Application Laid-Open Publication No. H11-163873). See Japanese Patent Publication No. 44-1809).
In this method, the material to be treated is immersed in a molten salt bath, the material to be treated is used as an anode, the salt bath is used as a cathode, and DC electrolysis is continuously performed under a constant current density. It forms a sulfurized layer of about 10 μm.

【0003】前記低温浸硫処理法において、浸硫層の厚
み(以下、膜厚という。)は、電流密度と電解時間の積
である負荷電気量により支配され、平衡状態に達するま
では、負荷電気量の増加に伴い膜厚も増加する傾向にあ
るが、被処理材の面荒れ、変寸量等の精度変化も負荷電
気量にほぼ比例して増加するものであった。
In the low-temperature sulfurizing treatment, the thickness of the sulfurized layer (hereinafter referred to as the film thickness) is governed by the load electric quantity, which is the product of the current density and the electrolysis time. Although the film thickness tends to increase with an increase in the amount of electricity, the accuracy changes such as the surface roughness of the material to be processed and the amount of change in size also increase almost in proportion to the amount of load electricity.

【0004】浸硫層の生成メカニズムは、電解初期には
数μm程度のピット状の層とは言いがたい硫化鉄及び硫
黄化合物(以下、硫化物という。)が被処理材の表面に
生成され、その後さらに電解を連続的に継続すると、前
記ピット状の核を起点に被処理材の表面及び深さ方向に
硫化物が拡大され、電解終了時点では硫化物の層、すな
わち、浸硫層が生成されるものであり、浸炭処理、焼入
れ処理、窒化処理を施した金属部品にも有効である。
[0004] The mechanism of formation of the sulfurized layer is such that iron sulfide and sulfur compounds (hereinafter referred to as sulfides), which cannot be called a pit-like layer of about several μm, are formed on the surface of the material to be treated in the early stage of electrolysis. Then, when the electrolysis is further continued continuously, the sulfide is expanded in the surface and depth direction of the material to be processed starting from the pit-like nucleus, and at the time of the end of the electrolysis, the sulfide layer, that is, the sulfurized layer is formed. It is produced and is also effective for carburized, quenched, and nitrided metal parts.

【0005】[0005]

【発明が解決しようとする課題】しかしながら、前記の
ごとき反応形態により生成された浸硫層の膜厚は、非常
に不均一で、また処理前の被処理材が研削加工等を施し
た平滑な表面の場合には浸硫層の表面ならびに浸硫層と
被処理材との境界の粗さが荒れる傾向にあった。また、
被処理材の形状によっては、被処理材各部での表面粗
さ、浸硫層の膜厚及び変寸量にばらつきが生じることが
多々あった。
However, the thickness of the sulfurized layer formed by the above-described reaction mode is very uneven, and the material to be treated before the treatment is smooth and has been subjected to grinding or the like. In the case of the surface, the roughness of the surface of the sulfurized layer and the boundary between the sulfurized layer and the material to be treated tended to be rough. Also,
Depending on the shape of the material to be processed, the surface roughness, the thickness of the sulfurized layer, and the amount of change in the size of the vulcanized layer often vary.

【0006】そこで、従来精度の要求される被処理材で
は、処理後に超仕上げ加工等により修正したり、修正の
困難な被処理材の場合には負荷電気量を下げて処理を行
い、精度変化を抑える等の方法が採用されていた。
[0006] Therefore, in the case of a conventionally required material to be processed with accuracy, the material is corrected by superfinishing after processing, or in the case of a material which is difficult to correct, processing is performed by lowering the amount of load electricity to change the accuracy. And other methods have been adopted.

【0007】しかしながら、被処理材の精度変化を極力
抑えるために負荷電気量を下げて処理すると、浸硫層の
膜厚が不均一であるため、局部的に浸硫層が生成されず
に素地が残存して、耐摩耗性に欠ける等の問題が残され
ていた。
[0007] However, if the treatment is performed with a reduced amount of load electricity in order to minimize the change in precision of the material to be treated, the thickness of the sulfurized layer is not uniform, so that the substrate is not locally formed without the formation of the sulfurized layer. Remain, and problems such as lack of wear resistance remain.

【0008】そこで、本発明は、均一な膜厚の生成と、
表面粗さが小さく、変寸量のばらつきが少なく、処理後
の修正を不要とし、従来精度上適用することが困難とさ
れていた金属部品に対しても適用できる処理法を提供す
ることを目的とする。
Accordingly, the present invention provides a method for forming a uniform film thickness,
The object of the present invention is to provide a processing method that can be applied to metal parts that have a small surface roughness, a small variation in the amount of size change, do not require correction after processing, and are conventionally difficult to be applied due to accuracy. And

【0009】[0009]

【課題を解決するための手段】すなわち、本発明は、被
処理材の金属部品を摂氏160〜240度に保持した溶
融塩浴中に浸漬し、溶融塩電解により被処理材の表面に
硫化鉄及び硫黄化合物からなる生成層を得る表面処理法
において、その電解の際に供給する直流電流を矩形波の
断続波形としたものであり、あるいは前記矩形波の断続
波形に、連続的な直流電解を組み合わせたものである。
That is, according to the present invention, a metal part of a material to be treated is immersed in a molten salt bath maintained at 160 to 240 degrees Celsius, and iron sulfide is applied to the surface of the material by molten salt electrolysis. And a surface treatment method for obtaining a generation layer composed of a sulfur compound, wherein the DC current supplied during the electrolysis is an intermittent waveform of a rectangular wave, or the intermittent waveform of the rectangular It is a combination.

【0010】[0010]

【作用】前記塩浴電解は、摂氏160〜240度に保持
したロダンナトリウム(NaSCN)、ロダンカリウム
(KSCN)を主剤とした溶融塩浴中に、脱脂、酸洗浄
等の前処理、さらには浸炭処理、焼入れ処理、窒化処理
等を行った被処理材を浸漬し、被処理材を陽極、塩浴槽
を陰極として直流電解として行われる。
In the salt bath electrolysis, pretreatment such as degreasing, acid washing, etc., and carburizing are carried out in a molten salt bath mainly containing rhodan sodium (NaSCN) and rhodan potassium (KSCN) maintained at 160 to 240 degrees Celsius. The material to be treated, which has been subjected to treatment, quenching, nitriding, etc., is immersed, and the material to be treated is used as an anode, and the salt bath is used as a cathode to perform DC electrolysis.

【0011】その結果、陽極では下記1式のごとく、鉄
イオンの生成行われ、陰極では下記2式の硫黄イオンの
生成反応が行われ、被処理材の表面近傍で行われる下記
3式の硫化反応により、被処理材の表面に浸硫層が生成
される。
As a result, iron ions are generated at the anode as shown in the following equation (1), and sulfur ions are generated at the cathode as shown in the following equation (2). By the reaction, a sulfurized layer is generated on the surface of the material to be treated.

【0012】 Fe → Fe2+ +2e (1) SCN + 2e → S2− + CN (2) Fe2+ + S2− → FeS (3) 本発明においても前記同様の化学反応により浸硫層が生
成される。しかしながら、本発明においては、電解初期
に従来法(図4参照)と異なり、被処理材の表面に従来
法より小さな、多数のピット状の硫化物の反応核が密に
しかも均等に生成される(図3参照)ため、それらを起
点に硫化反応が進み、その結果として均一な膜厚を得る
ことができ、さらに表面粗さが小さく、変寸量にばらつ
きが少ない等の効果が得られるものであり、処理後の修
正が不要で、従来精度上適用が困難とされていた金属部
品に対して適用が可能となったものである。
[0012] Fe → Fe 2+ + 2e (1 ) SCN - + 2e → S 2+ CN - (2) Fe 2+ + S 2- → FeS (3)硫層immersion by the same chemical reaction in the present invention Generated. However, in the present invention, unlike the conventional method (see FIG. 4), a large number of pit-like sulfide reaction nuclei smaller than the conventional method are formed densely and uniformly on the surface of the material to be treated unlike the conventional method (see FIG. 4) in the initial stage of electrolysis. (See FIG. 3) Therefore, the sulfuration reaction proceeds from these starting points, and as a result, a uniform film thickness can be obtained, and further, effects such as a small surface roughness and a small variation in the size change can be obtained. This eliminates the need for correction after processing and makes it possible to apply the method to metal parts that have been conventionally difficult to apply due to accuracy.

【0013】[0013]

【実施例】以下に本発明の一実施例を詳細に説明する。
被処理材として、所定の成分を有するJIS SCM4
15材を摂氏930度にて6時間、浸炭、拡散を行い、
摂氏840度に降温して油焼入れし、さらに摂氏180
度にて2時間焼戻しを行った後、研削加工により1.6
sに調整したものを用いた。
DESCRIPTION OF THE PREFERRED EMBODIMENTS One embodiment of the present invention will be described below in detail.
JIS SCM4 having predetermined components as a material to be treated
Carburizing and diffusing 15 materials at 930 degrees Celsius for 6 hours,
The temperature was lowered to 840 degrees Celsius and oil quenching was performed.
After tempering for 2 hours at a temperature, 1.6 g by grinding.
Those adjusted to s were used.

【0014】溶融塩浴として、ロダンカリウム(KSC
N)75%、ロダンナトリウム(NaSCN)25%か
らなり、摂氏190度に保持したものを用いた。前記被
処理材を、前記塩浴中に浸漬し、被処理材を陽極、塩浴
槽を陰極として直流電解を行った。
[0014] As a molten salt bath, rodan potassium (KSC
N) 75% and rhodane sodium (NaSCN) 25% were used, which was maintained at 190 degrees Celsius. The material to be treated was immersed in the salt bath, and DC electrolysis was performed using the material to be treated as an anode and the salt bath as a cathode.

【0015】本発明では、電解時の通電パタ−ンが図1
に示されるように制御される。すなわち、所定の電流密
度(ip)を所定の電流印加時間(t−on)と所定の
電流休止時間(t−off)をnサイクル繰り返し行う
矩形波の断続波形とするものである。なお、前記電流密
度(ip)、電流印加時間(t−on)、電流休止時間
(t−off)、サイクル数(n)は、ある所定の範囲
内で被処理材の材質、形状、要求精度等に応じて選択さ
れる。
In the present invention, the energization pattern during electrolysis is shown in FIG.
Is controlled as shown in FIG. That is, the predetermined current density (ip) is a rectangular wave intermittent waveform in which a predetermined current application time (t-on) and a predetermined current pause time (t-off) are repeated n cycles. The current density (ip), the current application time (t-on), the current pause time (t-off), and the number of cycles (n) are within a certain predetermined range, and the material, shape, and required accuracy of the material to be processed are specified. It is selected according to the above.

【0016】なお、従来の電解時の通電パタ−ンは、図
2に示すごとく、所定の電流密度(id)を一定に保
ち、連続的に所定の時間(Td)電流を連続的に供給す
るものであった。
As shown in FIG. 2, in the conventional energization pattern during electrolysis, a predetermined current density (id) is kept constant and a current is continuously supplied for a predetermined time (Td). Was something.

【0017】実施例1.前記被処理材を前記溶融塩浴に
より、本発明の通電パタ−ン、具体的には、 電流密度(ip)=32.0(A/dm ) 電流印加時間(t−on)=0.01(s) 電流休止時間(t−off)=0.03(s) サイクル(n)=6000 により処理した。ト−タル負荷電気量は1920A/d
である。
Embodiment 1 FIG. The material to be treated is supplied to the molten salt bath using the current-carrying pattern of the present invention, specifically, current density (ip) = 32.0 (A / dm 2 ), current application time (t-on) = 0. 01 (s) Current pause time (t-off) = 0.03 (s) Cycle (n) = 6000 Total load electric quantity is 1920 A / d
a m 2.

【0018】実施例2.前記被処理材を前記溶融塩浴に
より、前記従来の通電パタ−ン及び前記本発明の通電パ
タ−ンを組み合わせて処理した。すなわち、第1段階を
従来と同様の連続的直流電解、具体的には、 電流密度(ip)=3.2(A/dm ) 電流印加時間(Td)=150(s) サイクル(n)=1 により処理した後、第2段階として、本発明の通電パタ
−ン、具体的には、 電流密度(ip)=64.0(A/dm ) 電流印加時間(t−on)=0.1(s) 電流休止時間(t−off)=0.9(s) サイクル(n)=225 で処理した。なお、ト−タル負荷電気量は前記実施例1
と同じく1920A/dm である。
Embodiment 2 FIG. The material to be treated was treated with the molten salt bath in combination with the conventional energizing pattern and the energizing pattern of the present invention. That is, the first step is a continuous DC electrolysis similar to the conventional one, specifically, current density (ip) = 3.2 (A / dm 2 ), current application time (Td) = 150 (s) cycle (n) = 1, as a second step, the current-carrying pattern of the present invention, specifically, current density (ip) = 64.0 (A / dm 2 ), current application time (t-on) = 0 .1 (s) Current pause time (t-off) = 0.9 (s) Cycle (n) = 225 Note that the total load electric quantity is the same as in the first embodiment.
It is 1920 A / dm 2 similarly to.

【0019】実施例3.前記被処理材を前記溶融塩浴に
より、前記従来の通電パタ−ン、すなわち、従来と同様
の連続的直流電解、具体的には、 電流密度(ip)=3.2(A/dm ) 電流印加時間(Td)=600(s) サイクル(n)=1 で処理した。なお、ト−タル負荷電気量は前記実施例1
及び2と同じく1920A/dm である。
Embodiment 3 FIG. The material to be treated is treated by the molten salt bath in the conventional energizing pattern, that is, continuous DC electrolysis similar to the conventional one, specifically, current density (ip) = 3.2 (A / dm 2 ). Current application time (Td) = 600 (s) Cycle (n) = 1 Note that the total load electric quantity is the same as in the first embodiment.
And 2, as in 1920 A / dm 2 .

【0020】図3及び図4は、前記実施例1及び3にお
ける電解初期の被処理材の表面を撮影した顕微鏡写真を
模式的に表したもので、図4に示した従来法(実施例
3)では、比較的大きく、さらに大きさの異なるピット
状の硫化物の反応核が相互に比較的距離をおいて生成さ
れているのに対して、図3に示した本発明の方法(実施
例1及び2)では、多数の小さなピット状の硫化物の反
応核が密にしかも均等に生成されている。
FIGS. 3 and 4 schematically show micrographs of the surface of the material to be treated in the initial stage of the electrolysis in Examples 1 and 3, and show the conventional method shown in FIG. 4 (Example 3). 3), pit-like sulfide reaction nuclei having relatively large sizes and different sizes are generated at a relatively large distance from each other, whereas the method of the present invention shown in FIG. In 1) and 2), many small pit-like sulfide reaction nuclei are densely and uniformly generated.

【0021】図5は、前記実施例1乃至3の処理後にお
ける表面粗さの測定結果と断面組織の顕微鏡写真を模式
的に表したものである。それらを観察すると、同じ負荷
電気量のもとで生成される浸硫層の膜厚は同等である
が、本願発明の方法の方が従来法に比べて膜厚の均一性
が極めて高く、さらに表面粗さが小さいことが確認され
る。
FIG. 5 schematically shows a measurement result of the surface roughness after the treatment of the above-mentioned Examples 1 to 3 and a micrograph of the cross-sectional structure. When observing them, the thickness of the sulfurized layer generated under the same load electricity is the same, but the method of the present invention has a much higher uniformity of the film thickness than the conventional method, and furthermore, It is confirmed that the surface roughness is small.

【0022】さらに、被処理材の各部における変寸量の
ばらつきを小さく抑えることができ、高精度要求部品に
も処理後の修正加工手数を必要とせずに適用が可能であ
ることが確認された。
Furthermore, it has been confirmed that the variation in the amount of change in the size of each part of the material to be processed can be suppressed to a small value, and it can be applied to parts requiring high precision without requiring the number of corrections after processing. .

【0023】図6は、実施例1の本願発明の方法による
処理物と、実施例3の従来法による処理物の耐焼付き試
験結果であり、負荷荷重毎での摩擦係数の推移と試験終
了までの耐久荷重を示し、曲線aが本発明の方法による
処理物の試験結果を示し、曲線bが従来法による処理物
の試験結果を示す。なお、曲線cは未処理物、すなわ
ち、前記浸炭、研削加工済の被処理材の試験結果であ
る。
FIG. 6 shows the seizure resistance test results of the processed product of the present invention of Example 1 and the processed product of the conventional method of Example 3, showing the transition of the coefficient of friction for each applied load and the end of the test. , The curve a shows the test result of the processed material by the method of the present invention, and the curve b shows the test result of the processed material by the conventional method. Note that a curve c is a test result of an untreated material, that is, the material to be treated that has been carburized and ground.

【0024】試験条件は下記の通りである。The test conditions are as follows.

【0025】 試験機 ;FAVILLE試験機 (図7参照) 固定片 ;Vブロック SCM415浸炭・研削材 試験環境 ;非潤滑(大気中) 負荷荷重 ;初期荷重150kgfからの連続増加 荷重増加率;20〜25(kgf/s) すべり速度;0.1(m/s) 図6を観察すると、曲線cで示された未処理品は、摩擦
係数0.2〜0.3前後を推移し、負荷荷重600kg
f前後で焼付きにより試験終了に至った。これに対し、
本願発明の方法及び従来法の処理を施した試験片は、い
ずれも摩擦係数0.1〜0.05前後を推移し、負荷荷
重1200kgf前後で摩擦熱による塑性変形から荷重
低下を起こし試験終了に至ったものであり、未処理品と
の差には著しいものが確認された。
Test machine: FAVILLE test machine (see FIG. 7) Fixed piece: V block SCM415 carburized / ground material Test environment: Non-lubricated (in air) Load: Continuous increase from initial load 150 kgf Load increase rate: 20 to 25 (Kgf / s) Sliding speed; 0.1 (m / s) Observing FIG. 6, the untreated product indicated by the curve c changes the friction coefficient around 0.2 to 0.3, and the applied load is 600 kg.
The test was completed at about f due to seizure. In contrast,
Each of the test pieces subjected to the method of the present invention and the conventional method has a coefficient of friction of about 0.1 to 0.05, and the load decreases from plastic deformation due to frictional heat at a load of about 1200 kgf, and the test ends. The difference between the untreated product and the untreated product was confirmed.

【0026】[0026]

【発明の効果】本発明によれば、均一な膜厚を得ること
ができ、さらに表面粗さが小さく、変寸量にばらつきが
少なく、したがって、処理後の修正が不要で、従来精度
上適用が困難とされていた金属部品に対しても適用でき
る効果が得られる。
According to the present invention, a uniform film thickness can be obtained, the surface roughness is small, and the variation in the amount of change is small. An effect that can be applied to a metal component that has been considered difficult to obtain is obtained.

【図面の簡単な説明】[Brief description of the drawings]

【図1】本発明の方法を実施する通電パタ−ンを示す波
形図である。
FIG. 1 is a waveform diagram showing an energization pattern for implementing a method of the present invention.

【図2】従来法の通電パタ−ンを示す波形図である。FIG. 2 is a waveform diagram showing an energization pattern according to a conventional method.

【図3】本発明における電解初期の被処理材の表面を模
式的に表した図である。
FIG. 3 is a diagram schematically showing the surface of a material to be treated in the initial stage of electrolysis according to the present invention.

【図4】従来法における電解初期の被処理材の表面を模
式的に表した図である。
FIG. 4 is a diagram schematically showing the surface of a material to be treated at the initial stage of electrolysis in a conventional method.

【図5】各実施例における処理品の表面粗さの測定結果
及び断面組織を模式的に表した図である。
FIG. 5 is a diagram schematically showing a measurement result of surface roughness and a cross-sectional structure of a processed product in each example.

【図6】各実施例における処理品の耐焼付き試験結果を
示す線図である。
FIG. 6 is a diagram showing a seizure resistance test result of a treated product in each example.

【図7】試験機の構成を示す説明図である。FIG. 7 is an explanatory diagram showing a configuration of a tester.

───────────────────────────────────────────────────── フロントページの続き (72)発明者 桜井 勝 栃木県真岡市鬼怒ケ丘17 同和鉱業株式 会社真岡工場内 (72)発明者 ピエール マス フランス国 42100 サン・エテイ エ ンヌ・リュー・ラセーニュ8 (56)参考文献 特開 昭51−54041(JP,A) 特開 昭59−89793(JP,A) 特開 昭64−65295(JP,A) 特開 平1−133794(JP,A) 特開 平2−228483(JP,A) (58)調査した分野(Int.Cl.7,DB名) C25D 11/00 - 11/34 C23C 8/40 ────────────────────────────────────────────────── ─── Continuing on the front page (72) Inventor Masaru Sakurai 17 Kinuokaoka, Moka-shi, Tochigi Dowa Mining Co., Ltd. Moka Plant (72) Inventor Pierre-Mas France 42100 Saint-Etienne-en-Leu-Lasagne 8 ( 56) References JP-A-51-54041 (JP, A) JP-A-59-89793 (JP, A) JP-A-64-65295 (JP, A) JP-A-1-133794 (JP, A) Hei 2-228483 (JP, A) (58) Fields investigated (Int. Cl. 7 , DB name) C25D 11/00-11/34 C23C 8/40

Claims (2)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 被処理材の金属部品を摂氏160〜24
0度に保持した溶融塩浴中に浸漬し、溶融塩電解により
被処理材の表面に硫化鉄及び硫黄化合物からなる生成層
を得る表面処理法において、その電解の際に供給する直
流電流を矩形波の断続波形としたことを特徴とする金属
部品の表面処理法。
1. A metal part as a material to be treated is heated to 160 to 24 degrees Celsius.
In a surface treatment method of immersing in a molten salt bath maintained at 0 ° and obtaining a product layer composed of iron sulfide and a sulfur compound on the surface of the material to be treated by molten salt electrolysis, the DC current supplied during the electrolysis is rectangular. A surface treatment method for a metal part, characterized in that the wave has an intermittent waveform.
【請求項2】 矩形波の断続波形による直流電解に、連
続的な直流電解を組み合わせた請求項1記載の金属部品
の表面処理法。
2. The surface treatment method for a metal part according to claim 1, wherein continuous DC electrolysis is combined with DC electrolysis using a rectangular intermittent waveform.
JP03145793A 1993-01-27 1993-01-27 Surface treatment method for metal parts Expired - Fee Related JP3247964B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP03145793A JP3247964B2 (en) 1993-01-27 1993-01-27 Surface treatment method for metal parts

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP03145793A JP3247964B2 (en) 1993-01-27 1993-01-27 Surface treatment method for metal parts

Publications (2)

Publication Number Publication Date
JPH06220689A JPH06220689A (en) 1994-08-09
JP3247964B2 true JP3247964B2 (en) 2002-01-21

Family

ID=12331791

Family Applications (1)

Application Number Title Priority Date Filing Date
JP03145793A Expired - Fee Related JP3247964B2 (en) 1993-01-27 1993-01-27 Surface treatment method for metal parts

Country Status (1)

Country Link
JP (1) JP3247964B2 (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3382108B2 (en) * 1997-01-13 2003-03-04 同和鉱業株式会社 Sulfurization treatment method for iron-based articles
CN1119432C (en) * 1997-08-26 2003-08-27 张志乾 Salt-bath low-temp. electrolytic sulfurizing for steel-iron components
JP4126346B2 (en) 1999-10-20 2008-07-30 Dowaサーモテック株式会社 Sliding member with excellent seizure resistance and method for producing the same
CN107419314A (en) * 2017-08-08 2017-12-01 肥西县通力机械有限公司 A kind of processing method for reducing stamping parts of automobile plucking phenomenon

Also Published As

Publication number Publication date
JPH06220689A (en) 1994-08-09

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