JPS6333988B2 - - Google Patents
Info
- Publication number
- JPS6333988B2 JPS6333988B2 JP5596980A JP5596980A JPS6333988B2 JP S6333988 B2 JPS6333988 B2 JP S6333988B2 JP 5596980 A JP5596980 A JP 5596980A JP 5596980 A JP5596980 A JP 5596980A JP S6333988 B2 JPS6333988 B2 JP S6333988B2
- Authority
- JP
- Japan
- Prior art keywords
- plating
- diamond
- abrasive grains
- bath
- nickel
- 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
- 229910003460 diamond Inorganic materials 0.000 claims description 25
- 239000010432 diamond Substances 0.000 claims description 25
- 239000006061 abrasive grain Substances 0.000 claims description 21
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 12
- 239000003093 cationic surfactant Substances 0.000 claims description 9
- 238000009713 electroplating Methods 0.000 claims description 7
- 229910052759 nickel Inorganic materials 0.000 claims description 6
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 5
- 239000010953 base metal Substances 0.000 claims description 5
- 229910052802 copper Inorganic materials 0.000 claims description 5
- 239000010949 copper Substances 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 5
- 229910052582 BN Inorganic materials 0.000 claims description 3
- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 claims description 3
- 238000000151 deposition Methods 0.000 claims 1
- 239000002184 metal Substances 0.000 claims 1
- 229910052751 metal Inorganic materials 0.000 claims 1
- 238000007747 plating Methods 0.000 description 29
- 238000000034 method Methods 0.000 description 9
- 239000000203 mixture Substances 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- 238000003756 stirring Methods 0.000 description 6
- 239000000126 substance Substances 0.000 description 5
- 239000002585 base Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 238000000227 grinding Methods 0.000 description 4
- 229910021586 Nickel(II) chloride Inorganic materials 0.000 description 3
- 239000000853 adhesive Substances 0.000 description 3
- 230000001070 adhesive effect Effects 0.000 description 3
- QMMRZOWCJAIUJA-UHFFFAOYSA-L nickel dichloride Chemical compound Cl[Ni]Cl QMMRZOWCJAIUJA-UHFFFAOYSA-L 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- -1 Nickel sulfate Nickel chloride Borate Chemical compound 0.000 description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- RIIFPDUMQWZISY-UHFFFAOYSA-L [H][Cl][Ni](Cl)Cl Chemical compound [H][Cl][Ni](Cl)Cl RIIFPDUMQWZISY-UHFFFAOYSA-L 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 238000005554 pickling Methods 0.000 description 2
- 229910052938 sodium sulfate Inorganic materials 0.000 description 2
- 235000011152 sodium sulphate Nutrition 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 229910000881 Cu alloy Inorganic materials 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- XLVAVZLFABUPKX-UHFFFAOYSA-J S(=O)(=O)([O-])[O-].[Cu+4].S(=O)(=O)([O-])[O-] Chemical compound S(=O)(=O)([O-])[O-].[Cu+4].S(=O)(=O)([O-])[O-] XLVAVZLFABUPKX-UHFFFAOYSA-J 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000005238 degreasing Methods 0.000 description 1
- 238000004070 electrodeposition Methods 0.000 description 1
- 238000001962 electrophoresis Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- LGQLOGILCSXPEA-UHFFFAOYSA-L nickel sulfate Chemical compound [Ni+2].[O-]S([O-])(=O)=O LGQLOGILCSXPEA-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
- 229910000363 nickel(II) sulfate Inorganic materials 0.000 description 1
- DITXJPASYXFQAS-UHFFFAOYSA-N nickel;sulfamic acid Chemical compound [Ni].NS(O)(=O)=O DITXJPASYXFQAS-UHFFFAOYSA-N 0.000 description 1
- 238000001259 photo etching Methods 0.000 description 1
- 125000002924 primary amino group Chemical class [H]N([H])* 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 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
- 238000007650 screen-printing Methods 0.000 description 1
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Landscapes
- Polishing Bodies And Polishing Tools (AREA)
Description
【発明の詳細な説明】
本発明は電着砥石の改良に係り、電着砥石を製
作する上でダイヤモンド、立方晶窒化ホウ素等の
砥粒にカチオン系界面活性済により親水基を付加
させ電気めつき浴における分散を良くすること
で、めつき金属に対する砥粒の共析量を一定量に
制御し、研削性能に合わせた電着砥石を製作する
ことを目的とする。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to the improvement of electrodeposited grindstones, and in producing the electrodeposition grindstones, hydrophilic groups are added to abrasive grains such as diamond or cubic boron nitride through cationic surface activation. The aim is to control the amount of eutectoid abrasive grains to a fixed amount by improving the dispersion in the plating bath, and to manufacture an electrodeposited grindstone that matches the grinding performance.
従来の電着砥石の製法としては、1ダイヤモン
ド等の砥粒をただ単にめつき浴に攪拌しながら懸
濁させ、めつき浴の下方に置いた台金上に砥粒を
沈積させ、その後に電解めつきで結合し、余分な
砥粒は払い落す方法がある。この方法ではダイヤ
モンド等の砥粒の配合比の調整が不可能である。
2ダイヤモンド等の砥粒に予め化学銅めつき又は
化学ニツケルめつきを施し、それを電気めつき浴
に攪拌しながら懸濁させて電解めつきを行う方法
もあるが、この方法では第一段階での化学めつき
の砥粒に対する密着性が良いとは言えず、結合力
が良くない。3砥粒を周知の接着剤で台金に接着
し、先ず化学めつきを下地めつきとして処理した
後で、電解めつきを行つて固定する方法がある。
しかし接着剤の耐熱性がなく、研削時に発生する
熱によつて接着強度が弱まること。又砥粒面に化
学めつき及び電気めつきを施すため、研削面を出
す必要性から必ずドレツシングの後加工が必要で
ある。 The conventional manufacturing method for electrodeposited grindstones is to simply suspend abrasive grains such as 1 diamond in a plating bath while stirring, deposit the abrasive grains on a base metal placed below the plating bath, and then There is a method of bonding using electrolytic plating and removing excess abrasive grains. With this method, it is impossible to adjust the blending ratio of abrasive grains such as diamond.
2. There is also a method of performing electrolytic plating by applying chemical copper plating or chemical nickel plating to abrasive grains such as diamond in advance and suspending it in an electroplating bath while stirring, but in this method, the first step is It cannot be said that the adhesion of chemical plating to the abrasive grains is good, and the bonding strength is poor. There is a method of bonding three abrasive grains to a base metal using a well-known adhesive, first applying chemical plating as a base plating, and then performing electrolytic plating to fix the abrasive grains.
However, the adhesive does not have heat resistance, and the adhesive strength weakens due to the heat generated during grinding. In addition, since chemical plating and electroplating are applied to the abrasive grain surface, post-dressing processing is always required to expose the ground surface.
以上従来の電着砥石の製作法では欠点が多くあ
るに加え、最適の工法がまだ固まつていない問題
があつた。 In addition to the many drawbacks of the conventional method of manufacturing electrodeposited grindstones, there is also the problem that the optimal method has not yet been established.
本発明はダイヤモンド等の砥粒を親水化して、
めつき浴に均一に分散させることにある。又電解
めつき浴中で陰極上に析出させるためには陰極へ
の電気泳動が良くてはならない。以上の条件を満
すものとしてカチオン系界面活性剤が適してい
る。これは、カチオン系の界面活性剤分子が水溶
液において陽イオンを生じることに基づくもので
ある。以下の各実施例においては、いずれもカチ
オン系界面活性剤として、第一級アミン誘導体や
第四級アンモニウム塩等を用いて実施し、いずれ
も同様の効果が得られることを確認している。ダ
イヤモンド等の砥粒、粒径3〜30μのもの約1g
を約50c.c.のカチオン系界面活性剤中で数時間撹拌
して、砥粒表面を界面活性剤で包んで親水化し
た。めつき浴に添加する場合には前述の溶液状の
もので行つた。 The present invention makes abrasive grains such as diamond hydrophilic,
The purpose is to uniformly disperse it in the plating bath. In addition, in order to deposit on the cathode in an electrolytic plating bath, electrophoresis to the cathode must be good. Cationic surfactants are suitable as those that satisfy the above conditions. This is based on the fact that cationic surfactant molecules generate cations in aqueous solution. In each of the following Examples, a primary amine derivative, a quaternary ammonium salt, or the like was used as the cationic surfactant, and it was confirmed that similar effects could be obtained in each case. Approximately 1g of abrasive grains such as diamond, particle size 3-30μ
was stirred in about 50 c.c. of a cationic surfactant for several hours to wrap the surface of the abrasive grains in the surfactant and make them hydrophilic. When adding to the plating bath, the above-mentioned solution was used.
以下実施例について述べる。 Examples will be described below.
実施例 1
台金の材質が鉄、銅、銅合金の場合には通常の
前処理工程を行つた後で下記のめつき浴でダイヤ
モンド砥石を製作した。Example 1 When the material of the base metal was iron, copper, or copper alloy, a diamond whetstone was manufactured using the following plating bath after performing the usual pretreatment process.
浴組成硫酸ニツケル
塩化ニツケル
硼酸
ラウリン硫酸ソーダ
ダイヤモンド砥粒液※240g/
45g/
30g/
0.5g/
10〜50c.c./
※ダイヤモンド/カチオン界面活性剤=1g/
50c.c.
条件 PH:2〜4
温度:40〜50℃
電流密度:1〜5A/dm2
撹拌:マグネツトスターラー
台金がステンレスの場合には上記めつき浴で、
めつきを行う前に下記の塩化ニツケル浴で下地め
つきを施した後で実施した。Bath composition Nickel sulfate Nickel chloride Borate Lauric Sodium sulfate Diamond abrasive solution *240g/ 45g/ 30g/ 0.5g/ 10~50c.c./ *Diamond/cationic surfactant = 1g/
50c.c. Conditions PH: 2~4 Temperature: 40~50℃ Current density: 1~5A/dm 2 Stirring: Magnetic stirrer If the base metal is stainless steel, use the above plating bath.
Before plating, a base plating was performed using the following nickel chloride bath.
浴組成塩化ニツケル
塩酸240g/
120g/
条件 PH:2.0
温度:20〜30℃
電流密度:3〜5A/dm2
時間:1分
その時のダイヤモンドの添加量及び電流密度に
対するダイヤモンドの析出量の関係を第1図に示
す。但し通常ダイヤモンド砥石の場合ダイヤモン
ド4.4カラツト/cm3の時を集中度100として示すの
でそれに従つて表示した。又めつき浴を撹拌した
時としない時の違いを第2図に示す。第1図から
ダイヤモンドの析出量はダイヤモンドの添加量及
び電流密度の増加に従つて増加する傾向にある。
第2図から撹拌の有無の差はほとんどなくカチオ
ン系界面活性剤の分散効果が著るしいことを示
す。Bath composition Nickel chloride hydrochloric acid 240g/120g/ Conditions PH: 2.0 Temperature: 20~30℃ Current density: 3~5A/dm 2 hours: 1 minute The relationship between the amount of diamond added and the amount of diamond deposited against the current density was Shown in Figure 1. However, in the case of diamond whetstones, the concentration level is usually 100 when the diamond weight is 4.4 carats/cm 3 , so the values are shown accordingly. Figure 2 shows the difference between when the plating bath is stirred and when it is not stirred. As can be seen from FIG. 1, the amount of diamond deposited tends to increase as the amount of diamond added and the current density increase.
FIG. 2 shows that there is almost no difference between the presence and absence of stirring, and the dispersion effect of the cationic surfactant is remarkable.
実施例 2
実施例1では一般にワツト浴と言われるニツケ
ルめつき浴について示したが、スルフアミン酸ニ
ツケルめつき浴においてもダイヤモンド砥石の製
作が可能である。その条件を下記に示す。Example 2 In Example 1, a nickel plating bath generally called a Watt bath was shown, but a diamond grindstone can also be manufactured using a sulfamic acid nickel plating bath. The conditions are shown below.
浴組成スルフアミン酸ニツケル
塩化ニツケル
硼酸
サツカリンソーダ
ダイヤモンド砥粒液450g/
10g/
30g/
1g/
10〜50c.c./
条件 PH:1〜4
温度:50〜60℃
電流密度:1〜10A/dm2
撹拌:マグネツトスターラー
結果はワツト浴とほぼ同じものを得ることがで
きた。Bath composition: Nickel sulfamate, nickel chloride, saccharin borate, soda diamond abrasive solution 450g/10g/30g/1g/10~50c.c./Conditions PH: 1~4 Temperature: 50~60℃ Current density: 1~10A/dm 2 Stirring: Magnetic stirrer The results were almost the same as in the Watt bath.
実施例 3
実施例1、2ではニツケルめつきに関して示し
たが銅めつきでも実施可能である。Example 3 In Examples 1 and 2, nickel plating was shown, but copper plating is also possible.
浴組成硫酸銅
硫酸
ダイヤモンド砥粒液200g/
100g/
10〜50c.c./
条件 温度:25〜30℃
電流密度:1〜5A/dm2
実施例 4
ステンレス等の剛性を有する薄板材料の内外
径をバリ及びソリが出ないように第3図に示す通
りフオトエツチング加工で先ず打抜く。砥石の
パターンを設計し、スクリーン印刷版を製作す
る。第4図a及びbに示すような形状にめつき
レジストインクをスクリーン印刷する。但しこの
時使用するインクは耐アルカリ性、耐酸性を有す
るめつきレジストインクを使用し、印刷後充分に
熱硬化させる。続いて通常のめつき前処理と同
様に電解脱脂、酸洗いを行う。次の条件で下地
ニツケルめつきを行う。Bath composition Copper sulfate sulfate diamond abrasive grain liquid 200g/ 100g/ 10~50c.c./ Conditions Temperature: 25~30℃ Current density: 1~5A/dm 2 Examples 4 Inner and outer diameters of rigid thin plate materials such as stainless steel First, punch out by photo etching process as shown in Fig. 3 to prevent burrs and warpage. Design the whetstone pattern and produce the screen printing plate. Plating resist ink is screen printed in the shape shown in FIGS. 4a and 4b. However, the ink used at this time is a plating resist ink having alkali resistance and acid resistance, and is sufficiently cured with heat after printing. Next, electrolytic degreasing and pickling are performed in the same way as normal plating pretreatment. Perform base nickel plating under the following conditions.
浴組成塩化ニツケル
塩酸240g/
120g/
条件 PH:2.0
温度:20〜30℃
電流密度:3〜5A/dm2
時間:1分
直ちに酸洗いを行う。下記に示す条件で複
合めつきを行う。但しこの時予めダイヤモンド等
の砥粒、粒径3〜30μのもの約1gを約50c.c.のカ
チオン系界面活性剤中に入れて数時間撹拌して親
水化しておく必要がある。この溶液をダイヤモン
ド砥粒液とする。Bath composition Nickel chloride hydrochloric acid 240g/120g/Conditions PH: 2.0 Temperature: 20-30°C Current density: 3-5A/dm 2 hours: 1 minute Pickling is performed immediately. Composite plating is performed under the conditions shown below. However, at this time, it is necessary to add about 1 g of abrasive grains such as diamond, with a particle size of 3 to 30 μm, into about 50 c.c. of a cationic surfactant and stir it for several hours to make it hydrophilic. This solution is referred to as a diamond abrasive grain solution.
浴組成硫酸ニツケル
塩化ニツケル
硼酸
ラウリン硫酸ソーダ
ダイヤモンド砥粒液240〜360g/
45〜70g/
30〜40g/
0.5〜2g/
10〜50c.c./
条件 PH:2〜4
温度:40〜50℃
電流密度:1〜5A/dm2
以上実施例に記述しなかつたがこの方法はニツ
ケル、銅以外にクロム、亜鉛等のめつきについて
も可能であり、砥粒としてはダイヤモンド以外の
立方晶窒化ホウ素、炭化ケイ素等についても応用
可能である。Bath composition: Nickel sulfate, Nickel chloride, Borate, Lauric acid, Sodium sulfate, Diamond abrasive grain solution 240-360g/ 45-70g/ 30-40g/ 0.5-2g/ 10-50c.c./ Conditions PH: 2-4 Temperature: 40-50℃ Current Density: 1 to 5 A/dm 2 or more Although not described in the examples, this method is also possible for plating chromium, zinc, etc. in addition to nickel and copper, and as the abrasive grains, cubic boron nitride, other than diamond, It is also applicable to silicon carbide and the like.
上記各実施例により示した本発明は、下記のよ
うな顕著な効果を奏する。 The present invention shown in each of the above embodiments has the following remarkable effects.
1 ダイヤモンド等の砥粒の析出量の制御可能。1. The amount of abrasive grains such as diamond deposited can be controlled.
2 金属イオンとの共析めつきで密着力が良い。2 Good adhesion due to eutectoid plating with metal ions.
3 厚付けめつきが可能。3 Thick plating is possible.
4 種々のタイプの砥石の製作が可能。4 Various types of whetstones can be manufactured.
5 研削性能の良い形状の製作が可能。5. It is possible to manufacture shapes with good grinding performance.
第1図はダイヤモンド析出量を示す図、第2図
はカチオン系界面活性剤の効果を示す図、第3図
は電着砥石台金を示す断面図、第4図a,bは電
着砥石複合めつき部を示す断面図である。
Figure 1 shows the amount of diamond deposited, Figure 2 shows the effect of the cationic surfactant, Figure 3 is a cross-sectional view of the electrodeposited grinding wheel base, and Figures 4 a and b show the electrodeposited grindstone. It is a sectional view showing a compound plating part.
Claims (1)
粒をカチオン系界面活性剤により親水性を帯びさ
せて、ニツケル、銅等の電気めつき浴に分散さ
せ、電解することによつて陰極上の台金上に金属
と砥粒とを同時に析出させて製作することを特徴
とする電着砥石の製造方法。1. Microabrasive grains such as diamond or cubic boron nitride are made hydrophilic with a cationic surfactant, dispersed in an electroplating bath of nickel or copper, and electrolyzed to form a base metal on the cathode. A method for producing an electroplated grindstone, which is characterized in that it is produced by simultaneously depositing metal and abrasive grains on top.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5596980A JPS56152582A (en) | 1980-04-25 | 1980-04-25 | Electrodeposited grindstone |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5596980A JPS56152582A (en) | 1980-04-25 | 1980-04-25 | Electrodeposited grindstone |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS56152582A JPS56152582A (en) | 1981-11-26 |
JPS6333988B2 true JPS6333988B2 (en) | 1988-07-07 |
Family
ID=13013893
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP5596980A Granted JPS56152582A (en) | 1980-04-25 | 1980-04-25 | Electrodeposited grindstone |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS56152582A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2003146637A (en) * | 2001-08-30 | 2003-05-21 | Tadamasa Fujimura | Diamond-containing aqueous suspension having excellent dispersive stability, metallic film containing the diamond, and product thereof |
US9042454B2 (en) | 2007-01-12 | 2015-05-26 | Activevideo Networks, Inc. | Interactive encoded content system including object models for viewing on a remote device |
US9077860B2 (en) | 2005-07-26 | 2015-07-07 | Activevideo Networks, Inc. | System and method for providing video content associated with a source image to a television in a communication network |
US9123084B2 (en) | 2012-04-12 | 2015-09-01 | Activevideo Networks, Inc. | Graphical application integration with MPEG objects |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6386963U (en) * | 1986-11-27 | 1988-06-06 | ||
JPH01289667A (en) * | 1988-05-11 | 1989-11-21 | Japan Steel Works Ltd:The | Manufacture of electrodeposition type grinding element |
JPH0918182A (en) * | 1995-06-27 | 1997-01-17 | Nec Shizuoka Ltd | Electromagnetic shielding method |
-
1980
- 1980-04-25 JP JP5596980A patent/JPS56152582A/en active Granted
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2003146637A (en) * | 2001-08-30 | 2003-05-21 | Tadamasa Fujimura | Diamond-containing aqueous suspension having excellent dispersive stability, metallic film containing the diamond, and product thereof |
US9077860B2 (en) | 2005-07-26 | 2015-07-07 | Activevideo Networks, Inc. | System and method for providing video content associated with a source image to a television in a communication network |
US9042454B2 (en) | 2007-01-12 | 2015-05-26 | Activevideo Networks, Inc. | Interactive encoded content system including object models for viewing on a remote device |
US9123084B2 (en) | 2012-04-12 | 2015-09-01 | Activevideo Networks, Inc. | Graphical application integration with MPEG objects |
Also Published As
Publication number | Publication date |
---|---|
JPS56152582A (en) | 1981-11-26 |
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