JPS61152373A - Synthetic resinous abrasive - Google Patents

Synthetic resinous abrasive

Info

Publication number
JPS61152373A
JPS61152373A JP27197484A JP27197484A JPS61152373A JP S61152373 A JPS61152373 A JP S61152373A JP 27197484 A JP27197484 A JP 27197484A JP 27197484 A JP27197484 A JP 27197484A JP S61152373 A JPS61152373 A JP S61152373A
Authority
JP
Japan
Prior art keywords
synthetic resin
abrasive
parts
synthetic resinous
powder
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
Application number
JP27197484A
Other languages
Japanese (ja)
Inventor
Kazunori Tsujinaga
和徳 辻永
Motoyuki Torikai
基之 鳥飼
Yasuo Okita
泰郎 大喜多
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.)
Mitsui Toatsu Chemicals Inc
Original Assignee
Mitsui Toatsu Chemicals Inc
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Mitsui Toatsu Chemicals Inc filed Critical Mitsui Toatsu Chemicals Inc
Priority to JP27197484A priority Critical patent/JPS61152373A/en
Publication of JPS61152373A publication Critical patent/JPS61152373A/en
Pending legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B24GRINDING; POLISHING
    • B24DTOOLS FOR GRINDING, BUFFING OR SHARPENING
    • B24D3/00Physical features of abrasive bodies, or sheets, e.g. abrasive surfaces of special nature; Abrasive bodies or sheets characterised by their constituents
    • B24D3/02Physical features of abrasive bodies, or sheets, e.g. abrasive surfaces of special nature; Abrasive bodies or sheets characterised by their constituents the constituent being used as bonding agent
    • B24D3/20Physical features of abrasive bodies, or sheets, e.g. abrasive surfaces of special nature; Abrasive bodies or sheets characterised by their constituents the constituent being used as bonding agent and being essentially organic
    • B24D3/28Resins or natural or synthetic macromolecular compounds
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B24GRINDING; POLISHING
    • B24DTOOLS FOR GRINDING, BUFFING OR SHARPENING
    • B24D3/00Physical features of abrasive bodies, or sheets, e.g. abrasive surfaces of special nature; Abrasive bodies or sheets characterised by their constituents
    • B24D3/34Physical features of abrasive bodies, or sheets, e.g. abrasive surfaces of special nature; Abrasive bodies or sheets characterised by their constituents characterised by additives enhancing special physical properties, e.g. wear resistance, electric conductivity, self-cleaning properties
    • B24D3/342Physical features of abrasive bodies, or sheets, e.g. abrasive surfaces of special nature; Abrasive bodies or sheets characterised by their constituents characterised by additives enhancing special physical properties, e.g. wear resistance, electric conductivity, self-cleaning properties incorporated in the bonding agent
    • B24D3/344Physical features of abrasive bodies, or sheets, e.g. abrasive surfaces of special nature; Abrasive bodies or sheets characterised by their constituents characterised by additives enhancing special physical properties, e.g. wear resistance, electric conductivity, self-cleaning properties incorporated in the bonding agent the bonding agent being organic

Landscapes

  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Polishing Bodies And Polishing Tools (AREA)
  • Finish Polishing, Edge Sharpening, And Grinding By Specific Grinding Devices (AREA)

Abstract

PURPOSE:To prevent minute powder of an abrasive from sticking to a synthetic resinous product so as to make the product look neat by mixing a specified useful substance with synthetic resin and regulating peculiar surface resistance of the abrasice below 10<10>OMEGA/cm. CONSTITUTION:One or more than two sorts of useful substances out of an antistatic agent (such as alkyl phosphoric acid, diethanol amino acid or the like) a surface active agent (such as dodecyl benzene sulfon acid or the like,) or a conductive filler (such as carbon black) are mixed with synthetic resin (such as non-saturated polyester resin). Then, synthetic resinous abrasive with peculiar surface resistance below 10<10>OMEGA/cm is obtained.

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は、乾式ブラスト法、バレル法、インペラー法等
の静電気の発生をともなう研磨方法に使用される合成樹
脂研磨材に関する。
DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to a synthetic resin abrasive material used in polishing methods that involve the generation of static electricity, such as dry blasting, barrel methods, and impeller methods.

(従来技術とその問題点) 従来より合成樹脂成形品のパリ取り方法としては上記し
た方法が用いられ、この除研磨材としては、カーボラン
ダム、アランダム、珪石、硅砂。
(Prior art and its problems) Conventionally, the above-mentioned method has been used to remove burrs from synthetic resin molded products, and the abrasive materials used include carborundum, alundum, silica stone, and silica sand.

ガラスピーズ、鉄粉等の硬質研磨材および合成樹脂、ク
ルミ粉等の軟質研磨材が使用されてきた。
Hard abrasives such as glass peas and iron powder and soft abrasives such as synthetic resin and walnut powder have been used.

上記のうち合成樹脂研磨材を使用する場合は。When using synthetic resin abrasives among the above.

研磨材と空気および成形品との摩擦のために、作業中に
著しい静電気が発生し、このため粒径の小さな研磨材は
成形物に付着し、外観不良の問題を惹起していた。
Due to the friction between the abrasive and the air and the molded product, significant static electricity is generated during operation, and as a result, the abrasive with small particle size adheres to the molded product, causing problems in appearance.

この問題は、従来用いられていたナイロンやポリカーボ
ネートの様なカットワイヤー型のものでは認められず、
最近用いられ始めた成形物を粉砕して得られる合成樹脂
研磨材に特有のものである。
This problem is not observed in conventionally used cut wire type materials such as nylon and polycarbonate.
This is unique to synthetic resin abrasives obtained by crushing molded products, which have recently begun to be used.

而してこれらの合成樹脂研磨材としてはポリアセタール
樹脂等の熱可塑性樹脂、不飽和ポリエステル樹脂、フェ
ノール樹脂、メラミン樹脂等の熱硬化性樹脂研磨、材が
挙げられ、その製造方法に基因して各粒子の形状は不定
形であり表面積が大きく、通常、各用途ごとに適当な粒
度分布になるよう分級により分別使用されている。
These synthetic resin abrasives include thermoplastic resins such as polyacetal resin, thermosetting resins such as unsaturated polyester resins, phenolic resins, and melamine resins. The particles are irregular in shape and have a large surface area, and are usually used by classification to obtain an appropriate particle size distribution for each application.

しかし乍ら分級方法として篩分は等を採用する一般的方
法では当然静電気が発生し、そのため大粒子に微粒子が
不着し分離できずに製品研磨材中に混入し前記の問題を
派生する。
However, in the general classification method that employs sieving, etc., static electricity is naturally generated, and as a result, fine particles adhere to large particles and cannot be separated, leading to the above-mentioned problem.

上記の如く粉砕して得られる研磨材は、粒度分布が自由
に設定でき、従来の研磨材に比してはるかに小さい粒子
を製造できるので、従来使用されなかったICやLSI
等の精密加工品のパリ取りに利用可能であるにも拘わら
ず、上記の問題を派生して充分な実用化には至っていな
い。
The particle size distribution of the abrasive obtained by pulverization as described above can be set freely, and particles much smaller than conventional abrasives can be produced, so it is possible to manufacture ICs and LSIs that have not been used in the past.
Despite the fact that it can be used to remove burrs from precision processed products such as, it has not been fully put into practical use due to the above-mentioned problems.

(問題点を解決するための手段) 本発明者らは上記した問題の解決について鋭意検討した
結果。
(Means for Solving the Problems) The present inventors have made extensive studies to solve the above problems.

1)通常の帯電防止剤を合成樹脂研磨材に添加するかコ
ーティングする、 2)界面活性剤を合成樹脂研磨材に添加するかコーティ
ングする。
1) Adding or coating a conventional antistatic agent to the synthetic resin abrasive; 2) Adding or coating a surfactant to the synthetic resin abrasive.

3)導電性フィラーを使用する合成樹脂に添加する。3) Adding a conductive filler to the synthetic resin used.

ことにより合成樹脂研磨材の電気抵抗を表面固有抵抗と
して1010Ω/国以下に下げることが有効であること
を見出して本発明に到達した。
As a result, the inventors have discovered that it is effective to lower the electrical resistance of a synthetic resin abrasive to a surface resistivity of 1010 Ω/country or less, and have arrived at the present invention.

即ち本発明は、合成樹脂に帯電防止剤、界面活性剤およ
び導電性フィラーからなる群から選ばれた1種または2
種以上の物質を配合することにより表面固有抵抗を10
10Ω/備以下に調整したことを特徴とする合成樹脂研
磨材である。
That is, the present invention provides synthetic resin with one or two selected from the group consisting of antistatic agents, surfactants, and conductive fillers.
By blending more than one substance, the surface resistivity can be increased to 10
This is a synthetic resin abrasive material that is characterized by being adjusted to 10 Ω/min or less.

本発明の合成樹脂研磨材においては、帯電防止剤、界面
活性剤および導電性フィラーのうちの有用物質を夫々単
独で用いることも可能であるが。
In the synthetic resin abrasive material of the present invention, useful substances among antistatic agents, surfactants, and conductive fillers can be used alone.

それらを共用することによって定められた表面固有抵抗
値に調整することが好ましい方法として挙げられる。
A preferred method is to adjust to a predetermined surface resistivity value by sharing them.

本発明の合成樹脂研磨材の製造に用いられる合成樹脂と
しては、ポリアセタール等の熱可塑性樹脂、不飽和ポリ
エステル樹脂、フェノール樹脂、メラミン樹脂等の熱硬
化性樹脂があげられるが。
Examples of the synthetic resin used for producing the synthetic resin abrasive material of the present invention include thermoplastic resins such as polyacetal, thermosetting resins such as unsaturated polyester resins, phenolic resins, and melamine resins.

なかでも不飽和ポリエステル樹脂の使用が好ましい。Among them, it is preferable to use unsaturated polyester resin.

本発明に用いられる帯電防止剤としては、アルキルリン
酸ジェタノールアミン塩、アルキルリン酸カリウム塩の
、様なアルキルリン酸エステル塩類、ポリオキシエチレ
ンオレイルエーテルの様なポリオキシエチレンアルキル
エーテル類、ポリオキシエチレンステアレート、ポリオ
キシエチレングリコールモノステアレートの様なポリオ
キシエチレン脂肪酸エステル類、ラウリルトリメチルア
ンモニウムクロライドの様な第四級アミン塩類、N。
The antistatic agents used in the present invention include alkyl phosphate ester salts such as alkyl phosphate jetanolamine salt and alkyl phosphate potassium salt, polyoxyethylene alkyl ethers such as polyoxyethylene oleyl ether, and polyoxyethylene alkyl ethers such as polyoxyethylene oleyl ether. Polyoxyethylene fatty acid esters such as oxyethylene stearate and polyoxyethylene glycol monostearate, quaternary amine salts such as lauryl trimethylammonium chloride, N.

Nジメチルエタノールアミンの様なポリオキシエチレン
アルキルアミン類、ラウリルベタインの様なアルキルベ
タイン類等の帯電防止効果を有する物質の中から選ばれ
単独又は混合して使用される。
The material is selected from substances having an antistatic effect, such as polyoxyethylene alkylamines such as N-dimethylethanolamine, and alkyl betaines such as lauryl betaine, and is used alone or in combination.

而してこれらを粉砕した合成樹脂研磨材にコーティング
する場合には、必要によっては適当な溶剤で帯電防止剤
を溶解または稀釈して添加もしくは浸漬処理し、その後
乾燥させる方法が採用される。
When coating these on a pulverized synthetic resin abrasive material, a method may be employed in which the antistatic agent is dissolved or diluted with an appropriate solvent, added or immersed, and then dried.

また、界面活性剤としては、ドデシルベンゼンスルホン
酸の様なアルキルベンゼンスルホン酸類、ドデシルベン
ゼンスルホン酸ナトリウムの様なアルキルベンゼンスル
ホン酸塩類、ラウリル硫酸ナトリウムの様なアルキル硫
酸エステル塩類、β−ナフタレンスルホン酸ホルマリン
縮合物のナトリウム塩の様なナフタレンスルホン酸ホル
マリン縮合物類の様な界面活性機能を有する物質の中か
ら選ばれ、単独又は混合して使用される。粉砕した研磨
材にコーティングする場合には帯電防止剤の場合と同様
忙行なえば良い。
In addition, as surfactants, alkylbenzenesulfonic acids such as dodecylbenzenesulfonic acid, alkylbenzenesulfonates such as sodium dodecylbenzenesulfonate, alkylsulfate ester salts such as sodium lauryl sulfate, β-naphthalenesulfonic acid formalin condensation The material is selected from substances having a surface-active function such as naphthalene sulfonic acid formalin condensates such as sodium salts of Naphthalene, and is used alone or in combination. When coating pulverized abrasive material, it is sufficient to apply the coating in the same manner as in the case of antistatic agents.

更に、導電性フィラーとしてはカーボンブランク、黒鉛
等の炭素の他アルミ粉、鉄粉、銀粉、銅粉、ニッケル粉
、すず粉、鉛粉、亜鉛粉等の金属粉が使用できる。これ
らフィラーの分散時に必要に応じて各種分散改良剤、カ
ップリング剤、沈降防止剤を添加しても良い。これらの
フィラーは単独又は混合して使用される。
Further, as the conductive filler, in addition to carbon such as carbon blank and graphite, metal powder such as aluminum powder, iron powder, silver powder, copper powder, nickel powder, tin powder, lead powder, and zinc powder can be used. When dispersing these fillers, various dispersion improvers, coupling agents, and antisettling agents may be added as necessary. These fillers may be used alone or in combination.

以上挙げた各種帯電防止剤、界面活性剤および導電性フ
ィラーの有効配合量は、用いる材料によってそれぞれ異
なるので、例えば後述する実施例、比較例を参考にして
実験的に表面固有抵抗が10′。
The effective blending amounts of the various antistatic agents, surfactants, and conductive fillers listed above vary depending on the materials used, so for example, based on the Examples and Comparative Examples described later, we have experimentally determined that the surface resistivity is 10'.

Ω/c11以下になる様決定しなければならない。It must be determined to be Ω/c11 or less.

しかし乍ら一般的には合成樹脂研磨材100重量部当り
帯電防止剤として0.05〜2重量部、界面活性剤とし
て2〜10重量部、導電性フィラーとして例えば炭素系
の場合は0.5〜5重量部、金属粉系の場合100〜2
00重量部の範囲である。
However, in general, per 100 parts by weight of the synthetic resin abrasive material, the antistatic agent is 0.05 to 2 parts by weight, the surfactant is 2 to 10 parts by weight, and the conductive filler is 0.5 parts by weight, for example in the case of carbon-based filler. ~5 parts by weight, 100~2 in case of metal powder type
00 parts by weight.

本発明において各種物質の配合とは、前記した物質を、
合成樹脂研豪材の製造工程において添加混合する方法、
得られる研磨材にコーティングする方法等如何なる方法
を採用しても差支えない。
In the present invention, the blending of various substances refers to the above-mentioned substances,
A method of adding and mixing in the manufacturing process of synthetic resin abrasive materials,
Any method may be used to coat the resulting abrasive material.

またこれらの物質は単独で用いても良いが、併用するこ
とによって更に効果を高めることができる。
Further, these substances may be used alone, but the effect can be further enhanced by using them in combination.

即ち、例えば導電性フィラーを合成樹脂中に分散させた
のち帯電防止剤および/又は界面活性剤を添加或は混合
しても良い。
That is, for example, after a conductive filler is dispersed in a synthetic resin, an antistatic agent and/or a surfactant may be added or mixed.

本発明において定められる表面固有抵抗は1合成樹脂1
clI当たりの電気抵抗であり、成形板を作製し後述す
る通常の方法で測定すれば良い。猶、粉砕後に帯電防止
剤および/または界面活性剤で表面にコーディングした
ものについては、通常325メツシュパス程度の微粉を
分級し、5 Q kg/ciでプレスした成形板を作成
し測定に供した。
The surface resistivity defined in the present invention is 1 synthetic resin 1
It is the electrical resistance per clI, and it can be measured by preparing a molded plate and using the usual method described below. For those whose surfaces were coated with an antistatic agent and/or surfactant after pulverization, the fine powder was usually classified to about 325 mesh passes, and a molded plate was prepared by pressing at 5 Q kg/ci and used for measurement.

(実施例) 次に実施例により詳細に本発明を説明する。(Example) Next, the present invention will be explained in detail with reference to Examples.

表面固有抵抗はULTRA MEGOHMMETERM
ODEL  5M−10にて20部湿度70%の条件で
測定した。測定用サンプルは4 clIX 4 cMX
 3 mのものを使用した。又1合成樹脂成形品に対し
て乾式プラスト加工を行ない、プラスト後にどの程度研
磨材が付着しているかを目視にて評価した。
Surface resistivity is ULTRA MEGOHMMETERM
Measurement was carried out using ODEL 5M-10 under conditions of 20 parts and 70% humidity. The sample for measurement is 4 clIX 4 cMX
A 3 m long one was used. Further, one synthetic resin molded article was subjected to dry blasting, and the extent to which the abrasive was attached after blasting was visually evaluated.

比較例 イソフタル酸1,5モル、マレイン酸無水物3.0モル
、フロピレンゲリコール4.95モルを加工、180〜
210℃、に保ち、酸価が35になるまで反応させた。
Comparative Example Processing 1.5 mol of isophthalic acid, 3.0 mol of maleic anhydride, and 4.95 mol of furopylene gellicol, 180~
The temperature was maintained at 210°C, and the reaction was allowed to occur until the acid value reached 35.

これを不飽和ポリエステル■とする。This is referred to as unsaturated polyester (■).

次いで、この生成物100部に対しスチレンを43部、
6%ナフテン酸コバルト0.5部、メチルエチルケトン
パーオキサイド1部を加え混合後常温にて20時間放置
し、その後80℃にて3時間加熱した。得られた硬化物
を粉砕した後分級により60メツシユパス、100メン
シユオンを分取し、研磨材Iを得た。
Then, 43 parts of styrene was added to 100 parts of this product.
After adding 0.5 part of 6% cobalt naphthenate and 1 part of methyl ethyl ketone peroxide and mixing, the mixture was left at room temperature for 20 hours, and then heated at 80° C. for 3 hours. The obtained cured product was pulverized and then classified into 60 mesh passes and 100 mesh passes to obtain abrasive material I.

実施例1 帯電防止剤を硬化前に添加した例を示す。Example 1 An example in which an antistatic agent was added before curing is shown.

不飽和ポリエステルIの100部にラウリルトリメチル
アンモニウムクロライドをそれぞれ0.1部、0.5部
および1部添加し、比較例と同様にして研磨材2.3お
よび4を得た。
Abrasives 2.3 and 4 were obtained in the same manner as in Comparative Example by adding 0.1 part, 0.5 part and 1 part of lauryltrimethylammonium chloride to 100 parts of unsaturated polyester I, respectively.

実施例2 帯電防止剤をコーティングした例を示す。Example 2 An example coated with an antistatic agent is shown.

研磨材Iの100部にラウリルトリメチルアンモニウム
クロライドのイングロビルアルコール溶液をそれぞれ0
.1部、0.5部および1部附着するようにコーティン
グし、研磨材5,6および7を得た。
Inglobil alcohol solution of lauryltrimethylammonium chloride was added to 100 parts of Abrasive I, respectively.
.. Abrasive materials 5, 6 and 7 were obtained by coating in amounts of 1 part, 0.5 part and 1 part.

実施例3 界面活性剤を硬化前に添加した例を示す。Example 3 An example in which a surfactant was added before curing is shown.

不飽和ポリエステルlの100部にドデシルベンゼンス
ルホン酸をそれぞれ1部、5部および1゜部を添加し、
比較例と同様にして研磨材8,9および10を得た。
Adding 1 part, 5 parts and 1 part of dodecylbenzenesulfonic acid to 100 parts of unsaturated polyester l, respectively,
Abrasive materials 8, 9 and 10 were obtained in the same manner as in the comparative example.

実施例4 界面活性剤をコーティングした例を示す。Example 4 An example coated with a surfactant is shown.

研磨材Iの100部にドデシルベンゼンスルホン酸をそ
れぞれ1部、5部および1部部を実施例3と同様にして
コーティングし、研磨材11.12および13を得た。
Abrasive materials 11, 12 and 13 were obtained by coating 1 part, 5 parts and 1 part of dodecylbenzenesulfonic acid on 100 parts of abrasive material I in the same manner as in Example 3.

実施例5 導電性フィラーを硬化前に添加した例を示す。Example 5 An example is shown in which a conductive filler is added before curing.

不飽和ポリエステルエの100部に、アセチレンブラッ
クとして旭電化■製、デンカブラックを0.5部、1部
、1.5部、2部および2.5部添加し、比較例と同様
にして研磨1材14.15.16.17および18を得
た。
0.5 parts, 1 part, 1.5 parts, 2 parts, and 2.5 parts of Denka Black (manufactured by Asahi Denka ■) as acetylene black were added to 100 parts of unsaturated polyester, and polished in the same manner as in the comparative example. 1 materials 14, 15, 16, 17 and 18 were obtained.

実施例6 導電性フィラーと帯電防止剤とを併用した例を示す。Example 6 An example in which a conductive filler and an antistatic agent are used together will be shown.

不飽和ポリエステル■の100部にアセチレンブラック
として旭電化■製、デンカブラックを1.0部を帯電防
止剤としてラウリルトリメチルアンモニウムクロライド
を0.1部を添加し比較例と同様にして研真材19を得
た。
To 100 parts of unsaturated polyester ■, acetylene black made by Asahi Denka ■, 1.0 part of Denka black and antistatic agent, 0.1 part of lauryl trimethyl ammonium chloride was added, and the same procedure as in the comparative example was made to prepare abrasive material 19. I got it.

実施例7 導電性フィラーと界面活性剤とを併用した例を示す。Example 7 An example in which a conductive filler and a surfactant are used in combination will be shown.

不飽和ポリエステル■の100部に上記のアセチレンブ
ランク1.0部を界面活性剤としてドデシルベンゼンス
ルホン酸を1部添加し比較例と同様にして研磨材20を
得た。
Abrasive material 20 was obtained in the same manner as in Comparative Example by adding 1 part of dodecylbenzenesulfonic acid to 100 parts of unsaturated polyester (1), using 1.0 part of the above acetylene blank as a surfactant.

評価方法および評価結果 第1表に前記各研磨材1〜19の評価結果を示す。Evaluation method and results Table 1 shows the evaluation results for each of the abrasives 1 to 19.

合成樹脂成形品に対して乾式プラスト加工を行ない、プ
ラスト後に対象物表面にどの程度研磨剤微粉が付着して
いるかを目視にて判定した。
Dry blasting was performed on a synthetic resin molded article, and the extent to which abrasive fine powder adhered to the surface of the object after blasting was visually determined.

(発明の効果) 比較例および実施例からも理解される様に1本発明によ
る合成樹脂研磨材を使用すれば1合成樹脂成形品に研磨
材の做粉が付着する事による外観不良等の問題は完全に
解消される。
(Effects of the Invention) As can be understood from the comparative examples and examples, if the synthetic resin abrasive material of the present invention is used, problems such as poor appearance due to adhesion of abrasive powder to the synthetic resin molded product will be avoided. is completely eliminated.

Claims (1)

【特許請求の範囲】[Claims] (1)合成樹脂に帯電防止剤、界面活性剤および導電性
フィラーからなる群から選ばれた1種または2種以上の
物質を配合することにより表面固有抵抗を10^1^0
Ω・cm以下に調整したことを特徴とする合成樹脂研磨
材。
(1) Surface resistivity can be reduced to 10^1^0 by blending one or more substances selected from the group consisting of antistatic agents, surfactants, and conductive fillers with synthetic resin.
A synthetic resin abrasive material characterized by being adjusted to Ω・cm or less.
JP27197484A 1984-12-25 1984-12-25 Synthetic resinous abrasive Pending JPS61152373A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP27197484A JPS61152373A (en) 1984-12-25 1984-12-25 Synthetic resinous abrasive

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP27197484A JPS61152373A (en) 1984-12-25 1984-12-25 Synthetic resinous abrasive

Publications (1)

Publication Number Publication Date
JPS61152373A true JPS61152373A (en) 1986-07-11

Family

ID=17507392

Family Applications (1)

Application Number Title Priority Date Filing Date
JP27197484A Pending JPS61152373A (en) 1984-12-25 1984-12-25 Synthetic resinous abrasive

Country Status (1)

Country Link
JP (1) JPS61152373A (en)

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63169270A (en) * 1986-12-27 1988-07-13 Dainippon Printing Co Ltd Abrasive tape
JPH02106275A (en) * 1988-10-15 1990-04-18 Hitachi Maxell Ltd Polishing tape
JPH02172666A (en) * 1988-12-23 1990-07-04 Yamau Sangyo Kk Abrasive grain
EP0414494A2 (en) * 1989-08-21 1991-02-27 Minnesota Mining And Manufacturing Company Conductive coated abrasives
US5137542A (en) * 1990-08-08 1992-08-11 Minnesota Mining And Manufacturing Company Abrasive printed with an electrically conductive ink
US5203884A (en) * 1992-06-04 1993-04-20 Minnesota Mining And Manufacturing Company Abrasive article having vanadium oxide incorporated therein
US5328716A (en) * 1992-08-11 1994-07-12 Minnesota Mining And Manufacturing Company Method of making a coated abrasive article containing a conductive backing
US5560753A (en) * 1992-02-12 1996-10-01 Minnesota Mining And Manufacturing Company Coated abrasive article containing an electrically conductive backing
US6352471B1 (en) 1995-11-16 2002-03-05 3M Innovative Properties Company Abrasive brush with filaments having plastic abrasive particles therein
US7294667B2 (en) 2001-02-08 2007-11-13 3M Innovative Properties Company Coated abrasive articles containing graphite
KR20220168648A (en) * 2021-06-17 2022-12-26 배진범 Anti-Static Abrasive Media

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63169270A (en) * 1986-12-27 1988-07-13 Dainippon Printing Co Ltd Abrasive tape
JPH02106275A (en) * 1988-10-15 1990-04-18 Hitachi Maxell Ltd Polishing tape
JPH02172666A (en) * 1988-12-23 1990-07-04 Yamau Sangyo Kk Abrasive grain
AU633956B2 (en) * 1989-08-21 1993-02-11 Minnesota Mining And Manufacturing Company Conductive coated abrasives
US5108463A (en) * 1989-08-21 1992-04-28 Minnesota Mining And Manufacturing Company Conductive coated abrasives
EP0414494A2 (en) * 1989-08-21 1991-02-27 Minnesota Mining And Manufacturing Company Conductive coated abrasives
US5137542A (en) * 1990-08-08 1992-08-11 Minnesota Mining And Manufacturing Company Abrasive printed with an electrically conductive ink
US5560753A (en) * 1992-02-12 1996-10-01 Minnesota Mining And Manufacturing Company Coated abrasive article containing an electrically conductive backing
US5203884A (en) * 1992-06-04 1993-04-20 Minnesota Mining And Manufacturing Company Abrasive article having vanadium oxide incorporated therein
US5328716A (en) * 1992-08-11 1994-07-12 Minnesota Mining And Manufacturing Company Method of making a coated abrasive article containing a conductive backing
US6352471B1 (en) 1995-11-16 2002-03-05 3M Innovative Properties Company Abrasive brush with filaments having plastic abrasive particles therein
US7294667B2 (en) 2001-02-08 2007-11-13 3M Innovative Properties Company Coated abrasive articles containing graphite
KR20220168648A (en) * 2021-06-17 2022-12-26 배진범 Anti-Static Abrasive Media

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