JPH02213498A - Method for reforming metallic material surface - Google Patents
Method for reforming metallic material surfaceInfo
- Publication number
- JPH02213498A JPH02213498A JP3533789A JP3533789A JPH02213498A JP H02213498 A JPH02213498 A JP H02213498A JP 3533789 A JP3533789 A JP 3533789A JP 3533789 A JP3533789 A JP 3533789A JP H02213498 A JPH02213498 A JP H02213498A
- Authority
- JP
- Japan
- Prior art keywords
- fine particles
- hard
- particles
- wear resistance
- metallic
- 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
- 239000007769 metal material Substances 0.000 title claims abstract description 23
- 238000000034 method Methods 0.000 title claims description 20
- 238000002407 reforming Methods 0.000 title 1
- 239000002245 particle Substances 0.000 claims abstract description 48
- 238000007747 plating Methods 0.000 claims abstract description 43
- 239000010419 fine particle Substances 0.000 claims abstract description 23
- 239000002131 composite material Substances 0.000 claims abstract description 19
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 7
- 239000010439 graphite Substances 0.000 claims abstract description 7
- 229910002804 graphite Inorganic materials 0.000 claims abstract description 7
- 239000010445 mica Substances 0.000 claims abstract description 7
- 229910052618 mica group Inorganic materials 0.000 claims abstract description 7
- 229910018104 Ni-P Inorganic materials 0.000 claims abstract description 6
- 229910018536 Ni—P Inorganic materials 0.000 claims abstract description 6
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims abstract description 4
- 229910052804 chromium Inorganic materials 0.000 claims abstract description 3
- 239000011651 chromium Substances 0.000 claims abstract description 3
- 239000000843 powder Substances 0.000 claims description 37
- 239000002184 metal Substances 0.000 claims description 13
- 229910052751 metal Inorganic materials 0.000 claims description 13
- 238000012986 modification Methods 0.000 claims description 6
- 230000004048 modification Effects 0.000 claims description 6
- 239000000463 material Substances 0.000 abstract description 19
- 238000005097 cold rolling Methods 0.000 abstract description 3
- 238000005096 rolling process Methods 0.000 description 12
- 238000000576 coating method Methods 0.000 description 9
- 238000005461 lubrication Methods 0.000 description 9
- 239000011248 coating agent Substances 0.000 description 8
- 229910000831 Steel Inorganic materials 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 238000002715 modification method Methods 0.000 description 5
- 239000010959 steel Substances 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- 239000000314 lubricant Substances 0.000 description 4
- 239000010687 lubricating oil Substances 0.000 description 3
- 239000011159 matrix material Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 238000007751 thermal spraying Methods 0.000 description 3
- 238000005299 abrasion Methods 0.000 description 2
- 239000000919 ceramic Substances 0.000 description 2
- 238000005229 chemical vapour deposition Methods 0.000 description 2
- 238000012937 correction Methods 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 230000001050 lubricating effect Effects 0.000 description 2
- 230000013011 mating Effects 0.000 description 2
- 238000005240 physical vapour deposition Methods 0.000 description 2
- 230000003746 surface roughness Effects 0.000 description 2
- 229910021586 Nickel(II) chloride Inorganic materials 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 239000010953 base metal Substances 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 238000005255 carburizing Methods 0.000 description 1
- 239000011195 cermet Substances 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- QMMRZOWCJAIUJA-UHFFFAOYSA-L nickel dichloride Chemical compound Cl[Ni]Cl QMMRZOWCJAIUJA-UHFFFAOYSA-L 0.000 description 1
- KERTUBUCQCSNJU-UHFFFAOYSA-L nickel(2+);disulfamate Chemical compound [Ni+2].NS([O-])(=O)=O.NS([O-])(=O)=O KERTUBUCQCSNJU-UHFFFAOYSA-L 0.000 description 1
- 238000005121 nitriding Methods 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 238000010791 quenching Methods 0.000 description 1
- 230000000171 quenching effect Effects 0.000 description 1
- CVHZOJJKTDOEJC-UHFFFAOYSA-N saccharin Chemical compound C1=CC=C2C(=O)NS(=O)(=O)C2=C1 CVHZOJJKTDOEJC-UHFFFAOYSA-N 0.000 description 1
- 229940081974 saccharin Drugs 0.000 description 1
- 235000019204 saccharin Nutrition 0.000 description 1
- 239000000901 saccharin and its Na,K and Ca salt Substances 0.000 description 1
- 229910000679 solder Inorganic materials 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 238000005482 strain hardening Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000005496 tempering Methods 0.000 description 1
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
この発明は、金属材料の表面改質方法に関する。この発
明は、耐摩耗性および潤滑特性に優れた表面を必要とす
る材料に利用される。特に冷間圧延用ワークロールの耐
摩耗性および潤滑特性の向上に利用される。DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to a method for surface modification of metal materials. The invention finds application in materials requiring surfaces with excellent wear resistance and lubrication properties. It is especially used to improve the wear resistance and lubrication properties of work rolls for cold rolling.
(従来の技術)
摺動部の金属材料は使用時間の増加と共に摩擦によフて
摩耗が進行する。とりわけ、鋼板の圧延ワークロールの
表面の耐摩耗性は、板製品の表面性状の向上や圧延操業
の効率化をはかる上で、重要なロール特性の1つとなフ
ており、耐摩耗性の評価指標の1つである表面粗度を圧
延ワークロールの寿命の管理基準としている。(Prior Art) The metal materials of the sliding parts wear out due to friction as the usage time increases. In particular, the wear resistance of the surface of steel sheet rolling work rolls is one of the important roll characteristics in order to improve the surface quality of sheet products and improve the efficiency of rolling operations. Surface roughness, which is one of the indicators, is used as a control standard for the life of rolling work rolls.
また、圧延ロールのように大きな荷重のかかる環境で用
いられる材料は、通常の摺動材料よりも摩耗が激しく進
行する。耐摩耗性を高めるには材料自身の硬度を高めれ
ば良い。硬度を高める一般的な手法には、焼入れ・焼戻
し、浸炭法、窒化法、加工硬化させる方法などがあるが
、材料全体を処理するため、手間がかかる上にコストも
高くなりがちである。しかしながら、耐摩耗性を必要と
する部位は材料の摺動表面近傍だけでよく、そこで、摺
動表面近傍だけを固くする表面改質方法の適用が検討さ
れているのが現状である。Furthermore, materials used in environments where large loads are applied, such as rolling rolls, undergo more rapid wear than normal sliding materials. To increase wear resistance, it is sufficient to increase the hardness of the material itself. Common methods for increasing hardness include quenching/tempering, carburizing, nitriding, and work hardening, but since the entire material is treated, they are time-consuming and tend to be expensive. However, wear resistance is required only in the vicinity of the sliding surface of the material, and therefore, the application of surface modification methods that harden only the vicinity of the sliding surface is currently being considered.
表面改質方法には、溶射法゛、物理蒸着法、化学蒸着法
、メッキ法などの手法があり、要求する機能を満たすよ
うな金属材料もしくはセラミックを母材表面にコーティ
ングし、表面近傍だけに良好な耐摩耗性や耐熱性などの
特性を付与することが可能である0表面改質方法の一つ
として複合メッキ(例えば、特公昭5B−1808号公
報)が知られている。複合メッキは、共析微粒子を懸濁
したメッキ浴を用いて母材金属表面に複合メッキ皮膜を
形成させる表面改質方法である。複合メッキ皮膜は、共
析微粒子の物理的あるいは化学的性質に応じて耐摩耗性
、耐食性、潤滑性などに優れた性質を示す。Surface modification methods include thermal spraying, physical vapor deposition, chemical vapor deposition, and plating, in which the surface of the base material is coated with a metal material or ceramic that satisfies the required functionality, and the coating is applied only near the surface. Composite plating (for example, Japanese Patent Publication No. 5B-1808) is known as one of the surface modification methods capable of imparting properties such as good wear resistance and heat resistance. Composite plating is a surface modification method that forms a composite plating film on the surface of a base metal using a plating bath in which eutectoid fine particles are suspended. The composite plating film exhibits excellent properties such as wear resistance, corrosion resistance, and lubricity depending on the physical or chemical properties of the eutectoid fine particles.
一方、潤滑時゛性を高める手法としては、摺動部材の間
に潤滑油もしくは潤滑油に固体潤滑剤(グラファイト、
雲母など)を添加した潤滑剤を供給する方法が一般的で
あり、既に使用目的に応じた様々な種類の潤滑油があら
ゆるところで使用されている。On the other hand, as a method to improve lubrication properties, lubricating oil or solid lubricant (graphite,
A common method is to supply a lubricant containing mica (mica, etc.), and various types of lubricant oil are already used everywhere depending on the purpose of use.
(発明が解決しようとする課題)
しかしながら、金属材料に優れた耐摩耗性を付与するた
めに、上記のような溶射法、物理蒸着法、化学蒸着法な
どを用いて高硬度のセラミックもしくはサーメット皮膜
を金属材料に形成させた場合、皮膜と母材の諸性質(硬
度、弾性率など)が大きく異なるため、コーティング皮
膜の剥離が発生しやすく実用的ではない。金属もしくは
合金を溶射法やメッキ法などでコーティングした場合、
皮膜の剥離は上記の場合に比べて発生しにくいが、従来
材質よりも耐摩耗性を大きく向上させることは期待でき
ない、また、硬質粒子だけを分散させた複合メッキでは
耐摩耗性は向上するが潤滑特性は向上されず、自己潤滑
性の粉末だけを分散させた複合メッキ皮膜では、潤滑特
性は向上するが耐摩耗性は逆に悪くなる。一方、潤滑油
を用いると金属材料の表面の汚れなどが問題となってく
る場合あり、この様な材料には潤滑油以外の潤滑方法を
採用することが望ましく、金属材料自身に潤滑特性を備
えているような材料が期待されている0本発明は金属材
料に優れた耐摩耗性と優れた潤滑特性の両方を備えた表
面の改質方法を提供するものである。(Problem to be Solved by the Invention) However, in order to impart excellent wear resistance to metal materials, high hardness ceramic or cermet coatings are produced using the above thermal spraying method, physical vapor deposition method, chemical vapor deposition method, etc. When it is formed on a metal material, the properties of the coating and the base material (hardness, modulus of elasticity, etc.) are significantly different, so the coating is likely to peel off, making it impractical. When metals or alloys are coated by thermal spraying or plating,
Peeling of the film is less likely to occur compared to the above cases, but it cannot be expected to significantly improve wear resistance compared to conventional materials.Composite plating in which only hard particles are dispersed improves wear resistance, but The lubrication properties are not improved, and a composite plating film in which only self-lubricating powder is dispersed improves the lubrication properties but deteriorates the wear resistance. On the other hand, using lubricating oil may cause problems such as dirt on the surface of the metal material, so it is desirable to use a lubrication method other than lubricating oil for such materials. The present invention provides a method for modifying the surface of a metal material so that it has both excellent wear resistance and excellent lubrication properties.
(課題を解決するための手段および作用)本発明は、金
属メッキ皮膜中に粉末微粒子を分散させた複合メッキ皮
膜を金属材料表面に形成する方法において、Ni,Ni
−P,八−ドクロム或はCoの金属メッキ層中に、その
粒径が1から5μmであり硬度がビッカース硬度で90
0以上の微粒子と、粒径が1から5μIであるON、グ
ラフディトおよび雲母の1種または2種以上からなる微
粒子を、重量比で80:20〜50:50の割合で分散
させかつ、金属メッキ層中の前記微粒子の全含有量を1
0〜25wt%としたことを特徴とする金属材料の表面
改質方法に関するものである。(Means and effects for solving the problems) The present invention provides a method for forming a composite plating film on the surface of a metal material in which fine powder particles are dispersed in the metal plating film.
-P,octa-dochrome or Co metal plating layer has a particle size of 1 to 5 μm and a hardness of 90 on the Vickers scale.
0 or more fine particles and fine particles consisting of one or more types of ON, graphite, and mica having a particle size of 1 to 5 μI are dispersed in a weight ratio of 80:20 to 50:50, and metal plating is performed. The total content of the fine particles in the layer is 1
The present invention relates to a method for surface modification of a metal material, characterized in that the amount is 0 to 25 wt%.
第1図に複合メッキを施した金属材料の表面付近の断面
模式図を示す。この様な断面構造を持つ金属材料の表面
に別の相手材料が接触した場合、真実接触は金属材料の
最表面の粉末微粒子、1の部分で生じる0本発明の場合
、粉末微粒子は硬質粒子(例えばSIGのようなビッカ
ース硬度で900以上の粉末微粒子)と自己潤滑性に富
んだ粒子(BN、グラファイト、雲母)の混合粒子であ
る。金属マトリックスメッキよりも硬度が高い硬質粉末
微粒子により摺動時の面圧を支え耐摩耗性を向上させ、
自己潤滑性に富んだ粉末微粒子により潤滑特性を向上さ
せることができる。第2図に硬質粉末微粒子と自己潤滑
性に富んだ粉末微粒子の皮膜中における存在比と摩耗重
量の関係を示し、第3図に硬質粉末微粒子と自己潤滑性
に冨んだ粉末微粒子の皮膜中における存在比と摩擦係数
の関係を示す。硬質粉末微粒子と自己潤滑性に富んだ粉
末微粒子の皮膜中における存在比が50:50よりも自
己潤滑性に冨んだ粉末微粒子を多く存在させると、従来
材質(母材)よりも摩耗重量は大きくなり耐摩耗性は悪
くなる。硬質粉末微粒子と自己潤滑性に冨んだ粉末微粒
子の皮膜中における存在比が80:20よりも硬質粉末
粒子が多くなると、摩擦係数が従来材質よりも高くなり
潤滑特性が悪くなる。一方、メッキ皮膜中の粉末微粒子
の全分散量を10wt%未満にすると分散させた粉末微
粒子の効果が小さくなり、目的とする機能が発揮できな
い、また、メッキ皮膜中の粉末微粒子の全分散量を25
wt%以上とすると、粉末微粒子がメッキ皮膜の強度を
低下させ、メッキ皮膜の剥離が発生しやすくなる。第4
図に硬質粉末の平均粒径と摩耗重量の関係を示す。硬質
粉末の粒径が5μm以上ではマトリックスメッキが粒子
を支えきれず、粒子が皮膜から遊離してメッキ皮膜を引
っかき、逆に耐摩耗性は悪くなる。また、平均粒径1μ
m以下の粉末は実際入手が困難で、高価であり本発明の
効果を十分に発揮することができない。マトリックスメ
ッキに使用される金属は圧延ワークロールの使用環境条
件によりて任意に選択することが可能で有り、ワークロ
ール母材との密着力の優れたものを選択する必要が有る
ことから、現状では旧,Ni−P 、ハードクロム、G
oが最適と考えられる。FIG. 1 shows a schematic cross-sectional view near the surface of a metal material that has been subjected to composite plating. When another mating material comes into contact with the surface of a metal material having such a cross-sectional structure, the actual contact occurs at the outermost surface of the metal material, the powder particles (1).In the case of the present invention, the powder particles are hard particles ( For example, it is a mixed particle of fine powder particles such as SIG (with a Vickers hardness of 900 or more) and particles with high self-lubricating properties (BN, graphite, mica). Hard powder particles, which are harder than metal matrix plating, support surface pressure during sliding and improve wear resistance.
Lubricating properties can be improved by using fine powder particles that are highly self-lubricating. Figure 2 shows the relationship between the abundance ratio of hard powder particles and self-lubricating powder particles in the coating and the wear weight, and Figure 3 shows the relationship between the hard powder particles and self-lubricating powder particles in the coating. The relationship between the abundance ratio and the friction coefficient is shown. When the ratio of hard powder particles to powder particles rich in self-lubricating properties is 50:50 in the film, if more powder particles rich in self-lubricating properties are present, the wear weight will be lower than that of conventional materials (base materials). The larger the size, the worse the wear resistance. If the ratio of hard powder particles to self-lubricating powder particles in the film is greater than 80:20, the coefficient of friction will be higher than that of conventional materials and the lubricating properties will deteriorate. On the other hand, if the total amount of fine powder particles dispersed in the plating film is less than 10 wt%, the effect of the dispersed fine powder particles becomes small and the desired function cannot be achieved. 25
When the content is greater than wt%, the powder particles reduce the strength of the plating film, making it easy for the plating film to peel off. Fourth
The figure shows the relationship between the average particle diameter of hard powder and the wear weight. If the particle size of the hard powder is 5 μm or more, the matrix plating cannot support the particles, and the particles are released from the coating and scratch the plated coating, conversely worsening the wear resistance. Also, the average particle size is 1μ
Powders with a particle diameter of less than m are actually difficult to obtain and expensive, and cannot fully exhibit the effects of the present invention. The metal used for matrix plating can be arbitrarily selected depending on the operating environment conditions of the rolling work roll, and it is necessary to select a metal that has excellent adhesion to the work roll base material. Old, Ni-P, hard chrome, G
o is considered optimal.
本発明の目的であるところの金属材料の表面改質によっ
て金属材料の耐摩耗性及び潤滑特性を向上させることを
達成する複合メッキには電解法や無電解法がある。しか
し、本発明の目的を達成するに当たってその手法は本質
的でなく、本発明で特に限定する必要はない。Composite plating that achieves the object of the present invention, which is to improve the wear resistance and lubrication properties of metal materials by surface modification of the metal materials, includes electrolytic methods and electroless methods. However, this method is not essential to achieving the object of the present invention, and there is no need to specifically limit the method according to the present invention.
(実 施 例)
実施例−1
直径φ400mm 、バレル長100mg+のワークロ
ールに,Ni−P+ (SiC,BN)複合メッキを施
し、圧延実験を行った。ロール材質は通常の冷延ワーク
ロール用鍛鋼ロール材を用い,Ni−P + (Sin
、BN)分散メッキを膜厚10μmで施した。仕上げ表
面粗さはR1で0.05μIに調整した。メッキ浴には
スルファミン酸ニッケル60%液830 g/l、塩化
ニッケルL5g/l、ホウ酸45g/Ll、サッカリン
ソーダ3 g/l、 SiC(平均粒径2μm)150
g/文、BN(平均粒径3μm) 120g/、Qの混
合液を用い、不活性ガスによる気体攪はんによって固体
微粒子の凝集を防ぎながら複合メッキを行う、メッキ浴
の温度は57℃、pHは4.0、電流密度は20A/d
m’とした。複合メッキ皮膜中の硬質粉末微粒子と自己
潤滑性に富んだ粉末微粒子の存在割合は、87:33で
あった。こうして複合メッキしたワークロールを用いて
、試験用4 Hi冷間圧延機(バックアップロール:直
径φ480mm 、バレル長100mm1で、3%エマ
ルジョンを用いてステンレス鋼板(SUS430 、板
圧3.1oon)を圧下率30%で圧延したところ、従
来の圧延ロールを用いた圧延速度よりも1.6倍早い速
度で圧延で籾、ヒートストリーク発生も認められず、製
品の表面品質も良好であった。(Example) Example 1 A work roll with a diameter of 400 mm and a barrel length of 100 mg+ was plated with Ni-P+ (SiC, BN) composite plating, and a rolling experiment was conducted. The roll material used is ordinary forged steel roll material for cold-rolled work rolls, and Ni-P + (Sin
, BN) dispersion plating was applied to a film thickness of 10 μm. The finished surface roughness was adjusted to 0.05 μI with R1. The plating bath contained 830 g/l of 60% nickel sulfamate solution, 5 g/l of nickel chloride, 45 g/l of boric acid, 3 g/l of saccharin soda, and 150 g/l of SiC (average particle size 2 μm).
Composite plating is performed using a mixed solution of g/text, BN (average particle size 3 μm) 120 g/, Q, while preventing agglomeration of solid particles by gas agitation with an inert gas, the temperature of the plating bath is 57 ° C. pH is 4.0, current density is 20A/d
It was set as m'. The ratio of hard powder particles and highly self-lubricating powder particles in the composite plating film was 87:33. Using the thus composite plated work roll, a stainless steel plate (SUS430, plate thickness 3.1oon) was rolled using a 3% emulsion using a 4-Hi cold rolling machine for testing (backup roll: diameter φ480mm, barrel length 100mm1). When rolled at a rolling speed of 30%, which was 1.6 times faster than the rolling speed using conventional rolling rolls, no grains or heat streaks were observed, and the surface quality of the product was good.
実施例−2
圧延ロールを想定したリング状の試験片(サイズ:φ3
0X8m+o;鍛鋼)に、本発明である金属材料の表面
改質方法によって複合メッキ皮膜を形成させて、圧延材
に相当する相手片(サイズ:φ30 x 10 ff1
m;545G)を用いて転動摩擦試験を行フた(試験条
件二表1)。複合メッキ皮膜、固体潤滑剤と摩耗量、摩
擦係数を表2に示す。どの組合せも従来の鍛鋼よりも摩
耗量は小さく、摩擦係数も低いことが判明した。Example-2 Ring-shaped test piece assuming a rolling roll (size: φ3
0x8m+o; forged steel) is formed with a composite plating film by the method of surface modification of metal materials of the present invention, and a mating piece (size: φ30 x 10 ff1) corresponding to the rolled material is prepared.
A rolling friction test was conducted using a 545G (Test Conditions 2 Table 1). Table 2 shows the composite plating film, solid lubricant, wear amount, and friction coefficient. It was found that all combinations had less wear and a lower coefficient of friction than conventional forged steel.
表 1 試験条件
(発明の効果)
本発明であるところの金属メッキ皮膜中に粉末微粒子を
分散させた複合メッキ皮膜を金属材料表面に形成する方
法において、Nl,Ni−P,ハードクロム成はGoの
金属メッキ層中に、その粒径が1から5μIであり硬度
がビッカース硬度で900以上の硬質粉末微粒子と、粒
径が1から5μmであるBN、グラファイトおよび雲母
の1種または2種以上からなる微粒子を、重量比で80
:20〜50:50の割合で分散させかっ、金属メッキ
層中の前記微粒子の全含有量を10〜25宵t6Aとし
たことを特徴とする金属材料の表面改質方法により、耐
摩耗性に優れ、かつ潤滑特性に優れた表面改質が可能と
なり、製品コストの低減と生産性及び作業効率の向上を
はかることができる。この効果は特に圧延ワークロール
において著しい。Table 1 Test conditions (effects of the invention) In the method of the present invention for forming a composite plating film on the surface of a metal material in which fine powder particles are dispersed in a metal plating film, Nl, Ni-P, and hard chromium are The metal plating layer contains hard powder fine particles with a particle size of 1 to 5 μI and a hardness of 900 or more on the Vickers scale, and one or more of BN, graphite, and mica with a particle size of 1 to 5 μm. fine particles with a weight ratio of 80
Abrasion resistance can be improved by a surface modification method for a metal material, characterized in that the fine particles are dispersed in a ratio of 10 to 25:50 and the total content of the fine particles in the metal plating layer is 10 to 25 t6A. This enables surface modification with excellent lubrication properties, reducing product costs and improving productivity and work efficiency. This effect is particularly remarkable in rolling work rolls.
第1図は本発明の複合メッキを施したワークロール表面
付近の断面模式図、第2図は硬質粉末微粒子と自己潤滑
性に富んだ粉末微粒子の皮膜中における存在比と摩耗重
量の関係を示す図、第3図は硬質粉末微粒子と自己潤滑
性に富んだ粉末微粒子の皮膜中における存在比と摩擦係
数の関係を示す図、第4図は粉末の平均粒径と摩耗重量
の関係を示す図である。
1・・・粉末微粒子
第1図
第
図
他4名
wt”10B−−
A:硬質粉末微粒子
B:自己潤滑性に冨んだ粉末微粒子
第
図
策
図
f均粒径(メm)
A :、 @7ff;、W、7g−1んだ粉末微粒子本
願明細書中下記事項を補正致します。
記
第3頁11行目に
1゜
事件の表示
平成
@=4@/
年
特
許
願
第3夕8.37号
「特公昭5B−1808
号」
とあるを
「特公昭56−18080号」
と訂正する。
」
氏
名(名称)
新日本製鐵株式会社
4゜
代・
理
人
住
所
東京都千代色区丸の内2丁目6番2号丸の内へ重洲ビル
3305゜
補正命令の日付
す毛
7゜
補正の対象Figure 1 is a schematic cross-sectional view of the surface of a work roll coated with the composite plating of the present invention, and Figure 2 shows the relationship between the abundance ratio of hard powder particles and highly self-lubricating powder particles in the coating and the wear weight. Figure 3 is a diagram showing the relationship between the abundance ratio of hard powder particles and highly self-lubricating powder particles in the film and the coefficient of friction, and Figure 4 is a diagram showing the relationship between the average particle diameter of the powder and the abrasion weight. It is. 1... Powder fine particles Figure 1 Figure and 4 others wt"10B-- A: Hard powder fine particles B: Powder fine particles rich in self-lubricating properties Figure f Average particle size (m) A:, @7ff;, W, 7g-1 solder powder fine particles The following matters in the specification of this application are amended.Indication of 1° incident on page 3, line 11 Heisei @=4@/ Patent Application No. 3, 8 .37 ``Special Publication No. 5B-1808'' is corrected to ``Special Publication No. 56-18080.'' ” Name: Nippon Steel Corporation 4th Generation / DirectorAddress: 3305° Shigesu Building, 2-6-2 Marunouchi, Chiyoiro-ku, Tokyo Date of Correction Order: 7°Subject of Correction
Claims (1)
ッキ皮膜を金属材料表面に形成する方法において、Ni
,Ni−P,ハードクロム或はCoの金属メッキ層中に
、その粒径が1から5μmであり硬度がビッカース硬度
で900以上の硬質粉末微粒子と、粒径が1から5μm
であるBN、グラファイトおよび雲母の1種または2種
以上からなる微粒子を、重量比で 80:20〜50:50の割合で分散させかつ、金属メ
ッキ層中の前記微粒子の全含有量を10〜25wt%と
したことを特徴とする金属材料の表面改質方法。[Claims] 1. A method for forming a composite plating film on the surface of a metal material in which fine powder particles are dispersed in the metal plating film,
, Ni-P, hard chromium or Co metal plating layer contains hard powder fine particles with a particle size of 1 to 5 μm and a hardness of 900 or more on the Vickers scale, and a particle size of 1 to 5 μm.
Fine particles made of one or more of BN, graphite, and mica are dispersed in a weight ratio of 80:20 to 50:50, and the total content of the fine particles in the metal plating layer is 10 to 50:50. A method for surface modification of a metal material, characterized in that the content is 25 wt%.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3533789A JPH02213498A (en) | 1989-02-15 | 1989-02-15 | Method for reforming metallic material surface |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3533789A JPH02213498A (en) | 1989-02-15 | 1989-02-15 | Method for reforming metallic material surface |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH02213498A true JPH02213498A (en) | 1990-08-24 |
Family
ID=12439030
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP3533789A Pending JPH02213498A (en) | 1989-02-15 | 1989-02-15 | Method for reforming metallic material surface |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH02213498A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH04146291A (en) * | 1990-10-08 | 1992-05-20 | Yamauchi Corp | Press roll for paper making machine |
US5466359A (en) * | 1993-10-07 | 1995-11-14 | Nec Corporation | Method of manufacturing microwave tube collector |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS60196465A (en) * | 1984-03-15 | 1985-10-04 | Riken Corp | Piston ring |
-
1989
- 1989-02-15 JP JP3533789A patent/JPH02213498A/en active Pending
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS60196465A (en) * | 1984-03-15 | 1985-10-04 | Riken Corp | Piston ring |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH04146291A (en) * | 1990-10-08 | 1992-05-20 | Yamauchi Corp | Press roll for paper making machine |
US5466359A (en) * | 1993-10-07 | 1995-11-14 | Nec Corporation | Method of manufacturing microwave tube collector |
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