JPH01289667A - Manufacture of electrodeposition type grinding element - Google Patents
Manufacture of electrodeposition type grinding elementInfo
- Publication number
- JPH01289667A JPH01289667A JP11249388A JP11249388A JPH01289667A JP H01289667 A JPH01289667 A JP H01289667A JP 11249388 A JP11249388 A JP 11249388A JP 11249388 A JP11249388 A JP 11249388A JP H01289667 A JPH01289667 A JP H01289667A
- Authority
- JP
- Japan
- Prior art keywords
- acid
- plating film
- plating
- abrasive grains
- bath
- 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
- 238000004519 manufacturing process Methods 0.000 title claims description 7
- 238000000227 grinding Methods 0.000 title description 6
- 238000004070 electrodeposition Methods 0.000 title description 4
- 238000007747 plating Methods 0.000 claims abstract description 73
- 239000006061 abrasive grain Substances 0.000 claims abstract description 24
- 239000010953 base metal Substances 0.000 claims abstract description 22
- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 claims abstract description 9
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims abstract description 8
- ACVYVLVWPXVTIT-UHFFFAOYSA-N phosphinic acid Chemical compound O[PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-N 0.000 claims abstract description 5
- 238000000034 method Methods 0.000 claims description 11
- LNOPIUAQISRISI-UHFFFAOYSA-N n'-hydroxy-2-propan-2-ylsulfonylethanimidamide Chemical compound CC(C)S(=O)(=O)CC(N)=NO LNOPIUAQISRISI-UHFFFAOYSA-N 0.000 claims description 9
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 8
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 6
- 230000001376 precipitating effect Effects 0.000 claims 1
- 239000002253 acid Substances 0.000 abstract 2
- 230000006835 compression Effects 0.000 abstract 2
- 238000007906 compression Methods 0.000 abstract 2
- 238000004299 exfoliation Methods 0.000 abstract 2
- XTEGARKTQYYJKE-UHFFFAOYSA-N chloric acid Chemical compound OCl(=O)=O XTEGARKTQYYJKE-UHFFFAOYSA-N 0.000 abstract 1
- 229940005991 chloric acid Drugs 0.000 abstract 1
- 150000001805 chlorine compounds Chemical class 0.000 abstract 1
- 239000003002 pH adjusting agent Substances 0.000 abstract 1
- 238000005520 cutting process Methods 0.000 description 14
- 239000000203 mixture Substances 0.000 description 8
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 6
- 239000004327 boric acid Substances 0.000 description 6
- KERTUBUCQCSNJU-UHFFFAOYSA-L nickel(2+);disulfamate Chemical compound [Ni+2].NS([O-])(=O)=O.NS([O-])(=O)=O KERTUBUCQCSNJU-UHFFFAOYSA-L 0.000 description 6
- 229910021586 Nickel(II) chloride Inorganic materials 0.000 description 5
- QMMRZOWCJAIUJA-UHFFFAOYSA-L nickel dichloride Chemical compound Cl[Ni]Cl QMMRZOWCJAIUJA-UHFFFAOYSA-L 0.000 description 5
- 229910003460 diamond Inorganic materials 0.000 description 4
- 239000010432 diamond Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 3
- 238000009864 tensile test Methods 0.000 description 3
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 239000011148 porous material Substances 0.000 description 2
- IIACRCGMVDHOTQ-UHFFFAOYSA-M sulfamate Chemical compound NS([O-])(=O)=O IIACRCGMVDHOTQ-UHFFFAOYSA-M 0.000 description 2
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- 244000194101 Ginkgo biloba Species 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000005238 degreasing Methods 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000009713 electroplating Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 229910021421 monocrystalline silicon Inorganic materials 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229910000008 nickel(II) carbonate Inorganic materials 0.000 description 1
- ZULUUIKRFGGGTL-UHFFFAOYSA-L nickel(ii) carbonate Chemical compound [Ni+2].[O-]C([O-])=O ZULUUIKRFGGGTL-UHFFFAOYSA-L 0.000 description 1
- 238000005554 pickling Methods 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 229910000859 α-Fe Inorganic materials 0.000 description 1
Landscapes
- Polishing Bodies And Polishing Tools (AREA)
Abstract
Description
【発明の詳細な説明】 [産業上の利用分野] 本発明は電着式砥石の製造方法に関する。[Detailed description of the invention] [Industrial application field] The present invention relates to a method for manufacturing an electrodeposited grindstone.
[従来の技術]
従来の電着式砥石の製造方法は例えば特開昭58−45
871号公報に示されるように塩化物含有スルファミン
酸浴を用いて、または特開昭58−66668号公報に
示されるようにワット浴を用いて、電気ニッケルめっき
によって台金にダイヤモンド、立方晶窒化ホウ素などの
砥粒を電着させるようにしたものである。[Prior art] A conventional method for manufacturing an electrodeposited grindstone is disclosed in, for example, Japanese Patent Application Laid-Open No. 58-45.
Diamond and cubic nitridation are applied to the base metal by electronickel plating using a chloride-containing sulfamic acid bath as shown in Japanese Patent Application No. 871, or using a Watts bath as shown in Japanese Patent Application Laid-Open No. 58-66668. This is made by electrodepositing abrasive grains such as boron.
[発明が解決しようとする課題]
シリコン、水晶、フェライトなどの硬くて脆い材料を薄
片に切断する内周刃方式、マルチブレード方式などのス
ライシングマシンに用いられる切断刃(砥石)の場合に
は、切断代を少なくするために切断刃の厚さをできる限
り薄くする。このため、切断刃の単位面積当たりの切断
抵抗が大きくなるが、これに耐えられるように切断刃に
は切断方向に直交する方向に予備引張応力を与える(い
わゆる、張り上げ)、すなわち、台金に引張方向の塑性
変形を与える。[Problems to be solved by the invention] In the case of cutting blades (grinding wheels) used in slicing machines such as internal blade type and multi-blade type that cut hard and brittle materials such as silicon, crystal, and ferrite into thin pieces, The thickness of the cutting blade should be made as thin as possible to reduce the cutting allowance. For this reason, the cutting resistance per unit area of the cutting blade increases, but in order to withstand this, a preliminary tensile stress is applied to the cutting blade in the direction perpendicular to the cutting direction (so-called tensioning). Gives plastic deformation in the tensile direction.
しかし、上記のような従来方法によって得られるめっき
皮膜には最初から引張応力が残留する。However, tensile stress remains in the plating film obtained by the conventional method as described above from the beginning.
塩化物浴からのニッケルめっきは特に引張応力が大きい
、(「表面技術総覧−めっき・陽[i酸化績−」広信社
、昭和58年6月15日発行の第310頁及び第313
頁参照)、このため、めっきによる残留引張応力に加え
て切断刃の張り上げによる引張応力がめつき皮膜に加え
られるため、必要以上に大きな引張応力が作用すること
になり、台金からめっき皮膜が剥離したり、めっき皮膜
から砥粒が脱落したりし易くなる。また、切断中には切
断による引張応力が付加されるためめっき皮膜が早期に
疲労破壊し、ここに応力が集中し、台金も破断される場
合がある。Nickel plating from a chloride bath has particularly high tensile stress.
For this reason, in addition to the residual tensile stress caused by the plating, tensile stress due to tensioning of the cutting blade is applied to the plating film, resulting in a tensile stress that is larger than necessary and causing the plating film to peel off from the base metal. or the abrasive grains may easily fall off from the plating film. Furthermore, since tensile stress is applied during cutting, the plating film may undergo fatigue failure at an early stage, stress may be concentrated there, and the base metal may also break.
従って、本発明はこのような問題点を解決することを目
的としている。Therefore, the present invention aims to solve these problems.
[課題を解決するための手段]
即ち、本発明は台金上に砥粒を電着させた電着式砥石の
製造方法におい゛C1塩化物含有スルファミン酸浴に亜
リン酸及び次亜リン酸のいずれか一方または両方を添加
したものをめっき浴として用い、該めっき浴のpHをス
ルファミン酸、塩酸及び硫酸よりなる群から選択された
1fIまたは2種以上のpH調整剤により0.8〜1.
2の範囲内に維持しながら台金表面上に圧縮応力が残存
するめつき皮膜を析出させることを特徴とする電着式砥
石の製造方法に係る。[Means for Solving the Problems] That is, the present invention provides a method for manufacturing an electrodeposition type grindstone in which abrasive grains are electrodeposited on a base metal, in which phosphorous acid and hypophosphorous acid are added to a C1 chloride-containing sulfamic acid bath. The pH of the plating bath is adjusted to 0.8 to 1 using 1fI or two or more pH adjusters selected from the group consisting of sulfamic acid, hydrochloric acid, and sulfuric acid. ..
The present invention relates to a method for producing an electrodeposited grindstone characterized by depositing a plating film in which compressive stress remains on the surface of the base metal while maintaining the stress within the range of 2.
[作 用]
本発明はめっき皮膜に圧縮応力を残留されるめっき浴条
件下で砥粒を含有するめっき浴にて電着を行うことによ
り得られるめっき皮膜に圧縮応力を付導することができ
る。[Function] The present invention can impart compressive stress to a plating film obtained by electrodeposition in a plating bath containing abrasive grains under plating bath conditions that leave compressive stress in the plating film. .
以下、本発明方法を詳述する。The method of the present invention will be explained in detail below.
本発明で使用するめっき浴は塩化物含有スルファミン酸
塩めっき浴を主体とするものである。The plating bath used in the present invention is mainly a chloride-containing sulfamate plating bath.
塩化物含有スルファミン酸塩めっき浴はスルファミン酸
ニッケル、塩化ニッケル及びホウ酸よりなる。The chloride-containing sulfamate plating bath consists of nickel sulfamate, nickel chloride, and boric acid.
スルファミン酸ニッケルの添加配合1は300〜650
y/1、好ましくは35ON450g#の範囲内である
。該添加配合量が300g/1未満では電流効率が低く
、生産性が悪化するために好ましくない、更に、得られ
るめっき皮膜に圧縮応力を残留させることができない、
また、該添加配合量が650g/lを超えるとめっき皮
膜中に空孔が生じ、良質なめっき皮膜が得られず、更に
、めっき浴が高価となるために好ましくない。Additive formulation 1 of nickel sulfamate is 300 to 650
y/1, preferably within the range of 35ON450g#. If the amount added is less than 300 g/1, the current efficiency will be low and productivity will deteriorate, which is undesirable.Furthermore, compressive stress cannot remain in the resulting plating film.
Moreover, if the amount added exceeds 650 g/l, pores will be generated in the plating film, making it impossible to obtain a high-quality plating film, and furthermore, the plating bath will become expensive, which is not preferable.
塩化ニッケルの添加配合量は5〜15g/l、好ましく
は8〜12g/lの範囲内である。該添加配合量が59
/l未溝であると、陽極の溶解が悪くなり、浴電圧が上
昇して最後には陽極が不動態化するなめに好ましくない
、また、該添加配合量が159/i’を超えるとめつき
皮膜に大きな引張応が残留するために好ましくない。The amount of nickel chloride added is in the range of 5 to 15 g/l, preferably 8 to 12 g/l. The added amount is 59
/l If there is no groove, the dissolution of the anode will be poor, the bath voltage will increase, and the anode will eventually become passivated, which is undesirable. Also, if the amount added exceeds 159/i', it will be difficult to dissolve the anode. This is not preferable because a large tensile stress remains in the film.
ホウ酸の添加配合量は30〜50y/j!、好ましくは
35〜45tt/1の範囲内である。該添加配合量が3
0g、#未満であると、めっき浴の急激なpH変化を防
止することができないために好ましくない、また、該添
加配合量が50y/1を超えると均一な色調のめつき皮
膜が得られず、コゲや密着不良が生ずるために好ましく
ない。The amount of boric acid added is 30-50y/j! , preferably within the range of 35 to 45 tt/1. The added amount is 3
If it is less than 0g, #, it is not preferable because it will not be possible to prevent a sudden pH change in the plating bath, and if the amount added exceeds 50y/1, a plated film with a uniform color tone will not be obtained. , which is undesirable because it causes burnt spots and poor adhesion.
本発明に使用するめつき浴は上述のような組成をもつ塩
化物含有スルファミン酸浴に更に亜リン酸及び次亜リン
酸のいずれか一方または両方を添加する。亜リン酸及び
/または次亜リン酸の添加配合量は5〜5oy/1、好
ましくは8〜30g/lの範囲内である。該添加配合量
が5g/1未満ではpHの変化によってめっき皮膜に生
ずる残留応力の制御が困難になるために好ましくない、
iな、該添加配合量が50fI/Nを超えると電流効率
が低下して生産性が悪くなり、また、めっき皮膜の品質
も低下するために好ましくない。The plating bath used in the present invention is prepared by adding either or both of phosphorous acid and hypophosphorous acid to a chloride-containing sulfamic acid bath having the composition described above. The amount of phosphorous acid and/or hypophosphorous acid added is in the range of 5 to 5 oy/l, preferably 8 to 30 g/l. If the amount added is less than 5 g/1, it is not preferable because it becomes difficult to control the residual stress generated in the plating film due to pH changes.
However, if the added amount exceeds 50 fI/N, the current efficiency decreases, productivity deteriorates, and the quality of the plating film also deteriorates, which is not preferable.
上述の組成を有するめっき浴にpHFJu剤を添加して
めっき浴のpHを0.8〜1.2の範囲内に調整する。A pHFJu agent is added to the plating bath having the above composition to adjust the pH of the plating bath to within the range of 0.8 to 1.2.
使用できるpH調整剤としてはスルファミン酸、塩酸、
硫酸等を挙げることができる。なお、これらのpH調整
剤は2種以上を併用することもできる。Usable pH adjusters include sulfamic acid, hydrochloric acid,
Examples include sulfuric acid. In addition, two or more types of these pH adjusters can also be used in combination.
家な、台金への砥粒の付着方法を特に限定されるもので
はなく、例えばめっき浴中に砥粒を懸濁さぜる懸濁法、
めっき開始時に浴の撹拌を停止して台金を受皿として砥
粒を沈降させる沈降法、予め砥粒を台金に付着させる仮
付は法等を使用することができる。However, the method of attaching the abrasive grains to the base metal is not particularly limited, and examples include a suspension method in which the abrasive grains are suspended in a plating bath,
A sedimentation method in which stirring of the bath is stopped at the start of plating and the abrasive grains are allowed to settle using the base metal as a receiving plate, a tacking method in which the abrasive grains are attached to the base metal in advance, etc. can be used.
本発明方法を行う際のめつき浴温度は40〜60°C1
好ましくは45〜55℃の範囲内である。The plating bath temperature when carrying out the method of the present invention is 40 to 60°C1
Preferably it is within the range of 45 to 55°C.
該温度が40℃未満であると、電流効率が低下して生産
性が悪化するために好ましくない、また、該温度が60
℃を超えるとめっき浴が不安定になり、分解し易くなり
、操作性が悪くなるために好ましくない。If the temperature is less than 40°C, the current efficiency will decrease and productivity will deteriorate, which is undesirable.
If the temperature exceeds .degree. C., the plating bath becomes unstable, easily decomposed, and operability deteriorates, which is not preferable.
また、電流密度は3〜30 A / dwa”、好まし
くは5〜15A/dm2の範囲内である。電流密度が3
A/dm2未満では電流効率が低くなり生産性が悪くな
るために好ましくない、また、電流密度が30 A /
’dm”を超えるとめっき皮膜中に空孔が生じ、良質な
めっき皮膜が得られないために好ましくない。In addition, the current density is within the range of 3 to 30 A/dwa'', preferably 5 to 15 A/dm2.
If the current density is less than 30 A/dm2, the current efficiency will be low and the productivity will be poor, so it is not preferable.
If it exceeds 'dm', pores will occur in the plating film, making it impossible to obtain a good quality plating film, which is not preferable.
上記のようなめっき浴組成及びめっき条件下で電着を行
うことにより、砥粒を台金に固着するめっき皮膜に圧縮
応力が残留する。めっき皮膜に圧縮応力が残留している
ので張り上げによって生ずる引張応力が軽減される。こ
れにより砥粒の脱落、めっき皮膜の剥離、疲労破壊など
を防止することができる。By performing electrodeposition under the above plating bath composition and plating conditions, compressive stress remains in the plating film that fixes the abrasive grains to the base metal. Since compressive stress remains in the plating film, the tensile stress caused by tensioning is reduced. This can prevent the abrasive grains from falling off, the plating film from peeling off, and fatigue failure from occurring.
[実 施 例]
以下に実施例(以下、特記しない限り単に「例」と記載
する)を挙げ、本発明を更に説明する。[Examples] The present invention will be further explained by giving examples (hereinafter simply referred to as "examples" unless otherwise specified) below.
第1図に電着式砥石の部分断面図を示す0台金(10)
に対してめっき皮膜(12)が設けられ、このめっき皮
III (12)によって例えばダイヤモンドなどの砥
粒(14)が保持される。このための電気めっきは例え
ば次のような条件で行われる。Figure 1 shows a partial cross-sectional view of an electrodeposited grindstone (0 base metal (10))
A plating film (12) is provided on the plating film III (12), and abrasive grains (14) such as diamond are held by this plating film III (12). Electroplating for this purpose is performed, for example, under the following conditions.
燵−1
厚さ0.21m、幅61、長さ420III111の台
金(素材5K5)を脱脂、酸洗などの前処理工程を行っ
た後、次のような組成のめっき浴で電気めっきを行った
。Tatsu-1 A base metal (material 5K5) with a thickness of 0.21m, a width of 61m, and a length of 420III111 was subjected to pretreatment processes such as degreasing and pickling, and then electroplated in a plating bath with the following composition. Ta.
咋コ」」先■裁2
スルファミン酸ニッケル 450g/l塩化ニッ
ゲル 10y/j!ホウ酸
40y/1亜リン酸
10g/l’スルファミン酸
30g/ll糺灸先
浴温 50℃pH1,1
電流帯度 10A/d輪2めっ
き厚さ 40μmなお、40〜
60μ晴の大きさのダイヤモンド砥粒を台金に仮付けし
、余分なものを除去し、その後最終的に固着する方式と
した。``Kuiko'''' previous ■ trial 2 Nickel sulfamate 450g/l Nigel chloride 10y/j! Boric acid
40y/1 phosphorous acid
10g/l'sulfamic acid
30g/ll moxibustion tip bath temperature 50℃ pH 1.1 Current band 10A/d 2-wheel plating thickness 40μm Note that 40~
Diamond abrasive grains with a size of 60 μm were temporarily attached to the base metal, the excess was removed, and then the diamond abrasive grains were finally fixed.
得られためっき皮膜の残留圧縮応力はO,,8ky/a
m2であった。こうして得られた砥石を引張試験機に取
付け、引張力を作用させて台金を塑性変形させ、200
kFIまで張り上げを行った。その結果、めっき皮膜の
剥離及び砥粒の脱落は発生しなかった。また、この砥石
をマルチブレード型スライシングマシンに取付け、単結
晶シリコンを切断速度2.5mm/時間の条件で切断を
行った。切断後もめっき皮膜の剥離及び砥粒の脱落は発
生しなかった。The residual compressive stress of the resulting plating film was O, 8ky/a.
It was m2. The grindstone obtained in this way was attached to a tensile testing machine, and tensile force was applied to plastically deform the base metal.
I tensioned it up to kFI. As a result, peeling of the plating film and falling off of the abrasive grains did not occur. Further, this grindstone was attached to a multi-blade type slicing machine, and single crystal silicon was cut at a cutting speed of 2.5 mm/hour. Even after cutting, peeling of the plating film and falling off of the abrasive grains did not occur.
鮮−J工
例1に記載する台金と同じ台金を使用して次のようなめ
っき浴組成及び電解条件でめっきを行った。Using the same base metal as that described in Sen-J Example 1, plating was carried out under the following plating bath composition and electrolytic conditions.
吟こ」し潅JLt
スルファミン酸ニッケル 4!50g/l塩化ニ
ッケル 10g/lホウ酸
40g/l亜リン酸
10g/lスルファミン酸
60y/Ili1
浴温 50℃pHO,8
電流帯度 10A/d輸2めっ
き厚さ 40μ蒙こうして得ら
れた電着式砥石のめっき皮膜の残留圧縮応力は12 k
g/ am2であった。この電着式砥石についても20
0ktまでの張り上げを行ったが、めっき皮膜の剥離及
び砥粒の脱落は発生しなかった。また、例1と同様の条
件下で実際の切断を行ったところ、めっき皮膜の剥離及
び脱落は発生しなかった。Ginko Shikan JLt Nickel sulfamate 4.50g/l Nickel chloride 10g/l Boric acid
40g/l phosphorous acid
10g/l sulfamic acid
60y/Ili1 Bath temperature: 50°C pHO, 8 Current band: 10A/d 2 Plating thickness: 40 μm The residual compressive stress of the electroplated coating on the electrodeposited grinding wheel thus obtained was 12 k
g/am2. Regarding this electrodeposited whetstone, 20
Although tensioning was carried out to 0 kt, no peeling of the plating film or falling off of the abrasive grains occurred. Furthermore, when actual cutting was performed under the same conditions as in Example 1, no peeling or falling off of the plating film occurred.
L艷漣Y
上述の例1及び2(実施例)と比較するために同様の素
材を台金として用い、次のようなめつき浴組成及び電解
粂件でめっきを行った。For comparison with Examples 1 and 2 (Example) described above, plating was performed using the same material as the base metal and the following plating bath composition and electrolytic conditions.
へユニ童IJL
スルファミン酸ニッケル 450g/l塩化ニッ
ケル 10i/1ホウ酸
40g/l亜リン酸
10y/1電Jli丘−
浴温 50℃pH1,4
電流密度 10A/d@”めっ
き厚さ 40μ醜こうして得ら
れた電着式砥石のめつき皮膜には、圧縮応力ではなく、
逆に30 kg/ sn”の引張応力が残留した。この
電着式砥石を引張試験機に取り付けて張り上げを行った
結果、張り上げカフ0kgで砥粒が脱落を開始し、張り
上げ力120kgでめっき皮膜が剥離を開始した。Heunido IJL Nickel sulfamate 450g/l Nickel chloride 10i/1 boric acid
40g/l phosphorous acid
10y/1 electric Jli hill - Bath temperature 50℃pH 1.4 Current density 10A/d@" Plating thickness 40μ Ugly The plating film of the electrodeposited grinding wheel obtained in this way has not compressive stress, but
On the contrary, a tensile stress of 30 kg/sn" remained. When this electrodeposited grindstone was attached to a tensile testing machine and tensioned, the abrasive grains began to fall off at a tensioning cuff of 0 kg, and the plating film failed at a tensioning force of 120 kg. started peeling off.
L欺」1
比較例1と同様の台金を用いて次のようなめっき浴組成
及び電解粂件でめっきを行った。Plating was carried out using the same base metal as in Comparative Example 1 with the following plating bath composition and electrolytic conditions.
ΔIL直糺え
スルファミン酸ニッケル 450f/i’塩化ニ
ツケル 10y/lホウ酸
40g/l亜リン酸
10y/l炭酸ニツケル
30g/l(1東1
浴温 50℃pH1,6
電流密度 10A/dm2めっ
き厚さ 40μ−こうして得ら
れた電着式砥石のめっき皮膜の残留引張応力は40 k
g/ +em”であった、この電着式砥石を引張試験機
に取り付けて張り上げを行った結果、張り上げ力60k
gで砥粒の脱落が始まり、張り上げ力110kgでめっ
き皮膜が剥離を開始した。ΔIL direct sulfamate nickel 450f/i' nickel chloride 10y/l boric acid
40g/l phosphorous acid
10y/l nickel carbonate
30 g/l (1 East 1 Bath temperature 50℃ pH 1.6 Current density 10 A/dm2 Plating thickness 40 μ - The residual tensile stress of the electroplated grinding wheel thus obtained is 40 k
g/ +em". When this electrodeposited grindstone was attached to a tensile testing machine and tensioned, the tensioning force was 60k.
The abrasive grains began to fall off at a pressure of 110 kg, and the plating film began to peel off at a tensioning force of 110 kg.
[発明の効果]
以上説明してきたように、本発明によると、台金に砥粒
を固着するめつき皮膜に圧縮応力を残留させるようにし
たので、砥石の張り上げ時におけるめっき皮膜の剥離及
び砥石の脱落を防止することができ、また、切断時の疲
労による砥石の破断も防止することができる。また、張
り上げ力を増大することができるので、切断速度を増大
することができ生産性を向上することができる。[Effects of the Invention] As explained above, according to the present invention, compressive stress is left in the plating film that fixes the abrasive grains to the base metal, which prevents peeling of the plating film when tensioning the whetstone and preventing the grinding wheel from peeling off. It is possible to prevent the grindstone from falling off, and also to prevent the grindstone from breaking due to fatigue during cutting. Furthermore, since the tensioning force can be increased, the cutting speed can be increased and productivity can be improved.
第1図は電着式砥石の部分断面図である8図中、10・
・・台金、12・・・めっき皮膜、14・・・砥粒。
特許出願人 株式会社 日本製鋼所Figure 1 is a partial cross-sectional view of an electrodeposited grindstone.
... Base metal, 12... Plating film, 14... Abrasive grain. Patent applicant: Japan Steel Works, Ltd.
Claims (1)
いて、塩化物含有スルファミン酸浴に亜リン酸及び次亜
リン酸のいずれか一方または両方を添加したものをめっ
き浴として用い、該めっき浴のpHをスルファミン酸、
塩酸及び硫酸よりなる群から選択された1種または2種
以上のpH調整剤により0.8〜1.2の範囲内に維持
しながら台金表面上に圧縮応力が残存するめっき皮膜を
析出させることを特徴とする電着式砥石の製造方法。In a method for manufacturing an electrodeposited grindstone in which abrasive grains are electrodeposited on a base metal, a plating bath in which one or both of phosphorous acid and hypophosphorous acid is added to a chloride-containing sulfamic acid bath is used. , the pH of the plating bath is adjusted to sulfamic acid,
Precipitating a plating film with residual compressive stress on the surface of the base metal while maintaining the pH within the range of 0.8 to 1.2 using one or more pH adjusters selected from the group consisting of hydrochloric acid and sulfuric acid. A method for manufacturing an electrodeposited grindstone characterized by the following.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11249388A JPH01289667A (en) | 1988-05-11 | 1988-05-11 | Manufacture of electrodeposition type grinding element |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11249388A JPH01289667A (en) | 1988-05-11 | 1988-05-11 | Manufacture of electrodeposition type grinding element |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH01289667A true JPH01289667A (en) | 1989-11-21 |
Family
ID=14588026
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP11249388A Pending JPH01289667A (en) | 1988-05-11 | 1988-05-11 | Manufacture of electrodeposition type grinding element |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH01289667A (en) |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS56152582A (en) * | 1980-04-25 | 1981-11-26 | Matsushita Electric Ind Co Ltd | Electrodeposited grindstone |
-
1988
- 1988-05-11 JP JP11249388A patent/JPH01289667A/en active Pending
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS56152582A (en) * | 1980-04-25 | 1981-11-26 | Matsushita Electric Ind Co Ltd | Electrodeposited grindstone |
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