JPS62290732A - Production of low-hardness rubber abrasive - Google Patents

Production of low-hardness rubber abrasive

Info

Publication number
JPS62290732A
JPS62290732A JP13400286A JP13400286A JPS62290732A JP S62290732 A JPS62290732 A JP S62290732A JP 13400286 A JP13400286 A JP 13400286A JP 13400286 A JP13400286 A JP 13400286A JP S62290732 A JPS62290732 A JP S62290732A
Authority
JP
Japan
Prior art keywords
rubber
crosslinking agent
abrasive
crosslinking
crosslinked
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
JP13400286A
Other languages
Japanese (ja)
Inventor
Masashi Aoshima
正志 青嶋
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.)
Sumitomo Chemical Co Ltd
Original Assignee
Sumitomo Chemical Co Ltd
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 Sumitomo Chemical Co Ltd filed Critical Sumitomo Chemical Co Ltd
Priority to JP13400286A priority Critical patent/JPS62290732A/en
Publication of JPS62290732A publication Critical patent/JPS62290732A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To produce the title abrasive excellent in flexibility and elasticity, by incorporating a polymeric elastomer which does not crosslink with a crosslinking agent. CONSTITUTION:Abrasive grains (e.g., diamond dust), a crosslinking agent, 100pts. wt. binder rubber which can crosslink with the crosslinking agent (e.g., butadiene rubber), 20-100pts.wt. polymeric elastomer which does not crosslink with the crosslinking agent (e.g., ethylene/alpha-olefin copolymer) and, optionally, carbon black, a white pigment (e.g., clay), a crosslinking accelerator, a crosslinking aid, a process oil, a low-MW plasticizer, an antioxidant, etc., are mixed together and molded. The obtained molding is crosslinked.

Description

【発明の詳細な説明】 8、発明の詳細な説明 (産業上の利用分野) 本発明は砥粒の結合体としてゴムを用いたゴムPjl材
の製造方法に関する。
Detailed Description of the Invention 8. Detailed Description of the Invention (Field of Industrial Application) The present invention relates to a method for producing a rubber Pjl material using rubber as a bond of abrasive grains.

〔従来技術〕[Prior art]

研磨材の切削、研磨特性は、砥粒の含有率が高くなるほ
ど良くなることが知られている。ゴムを結合体として用
いたゴム研磨材においては砥粒が一般には体積分率で2
0%以上、多くの場合80%以上を占め、時には80%
以上を占めることもあり、このような場合、ゴム結合体
として用いるときの特徴である低硬度、柔軟性及び弾性
が失なわれ、被研磨物質の形状に適合しにくいといりた
問題がありた。
It is known that the cutting and polishing properties of an abrasive material improve as the content of abrasive grains increases. In rubber abrasives using rubber as a binder, the volume fraction of abrasive grains is generally 2.
More than 0%, often more than 80%, sometimes 80%
In such cases, the low hardness, flexibility, and elasticity that are characteristic when used as a rubber bond are lost, and there is a problem that it is difficult to conform to the shape of the material to be polished. .

〔発明が解決しようとする問題点〕[Problem that the invention seeks to solve]

上記の従来技術のもつ問題点を解決する目的でプロセス
オイルや低分子量液状可塑剤(例えば、ジオクチルフタ
レート、ジイソブチルフタレート)等を添加φ増量する
ことによりある程度低硬度化、柔軟性を付与できる。し
かし大量の砥粒がプロセスオイルや低分子量液状可塑剤
を吸収することにより、改良効果が損なわれたり、また
は吸収性が全くない場合には、プロセスオイルや低分子
ffi液状可塑剤が表面に移行することにより、効果が
時間とともに失なわれる一方、製品外観を損ねるのでこ
れらの使用は制限され、低硬度で柔軟性に富んだゴム研
磨材を、Plることは従来困難でありt二。
In order to solve the problems of the above-mentioned prior art, it is possible to reduce the hardness and give flexibility to some extent by adding process oil, a low molecular weight liquid plasticizer (for example, dioctyl phthalate, diisobutyl phthalate), etc. to increase the amount of φ. However, if a large amount of abrasive grains absorbs process oil or low molecular weight liquid plasticizer, the improvement effect is lost, or if there is no absorption at all, the process oil or low molecular weight liquid plasticizer migrates to the surface. As a result, their effectiveness is lost over time, and the appearance of the product is impaired, so their use is limited. Conventionally, it has been difficult to use rubber abrasives with low hardness and high flexibility.

〔問題点を解決するための手段〕[Means for solving problems]

本発明は、架橋剤を用いて砥粒の結合体であるゴムを架
橋せしめたゴム研磨材を低硬度化し、柔軟性、弾力性を
付与する新規な方法に関するものである。さらに具体的
には、当該架橋剤では架橋しない高分子弾性体を含有せ
しめることを特徴とするゴム研磨材の製造方法に関する
The present invention relates to a novel method for reducing the hardness and imparting flexibility and elasticity to a rubber abrasive material in which rubber, which is a bond of abrasive grains, is crosslinked using a crosslinking agent. More specifically, the present invention relates to a method for manufacturing a rubber abrasive material, which comprises containing an elastomer polymer that is not crosslinked with the crosslinking agent.

本発明でいうところの架橋剤と該架橋剤により架橋せし
める結合体たるゴムの組合わせとしては以下のものが例
示される。
Examples of the combination of a crosslinking agent and a rubber serving as a bond crosslinked by the crosslinking agent in the present invention include the following.

(1)硫黄系架橋剤により架橋されるもの天然ゴム、ブ
タジェンゴム、スチレン−ブタジェンゴム、ニトリルゴ
ム、エチレン−αオレフィン−非共役ジエン共重合体ゴ
ム、クロロブレンゴム、ハロゲン化エチレン−αオレフ
ィン−非共役ジエン共重合体ゴム等 (2)  金属酸化物系架橋剤により架橋されるものク
ロロブレンゴム、ハロゲン化エチレン−αオレフィン共
重合体、ハロゲン化エチレン−αオレフィン−非共役ジ
エン共重合体、クロロスルホン化ポリエチレン等 (3)  アミン系架橋剤により架橋されるものアクリ
ルゴム、フッ素ゴム等 他方、該架橋剤では架橋しないか、または架橋が著しく
低い高分子弾性体と架橋剤との組合わせ例は以下のよう
なものが挙げられる。
(1) Items that can be crosslinked with a sulfur-based crosslinking agent Natural rubber, butadiene rubber, styrene-butadiene rubber, nitrile rubber, ethylene-α-olefin-nonconjugated diene copolymer rubber, chloroprene rubber, halogenated ethylene-α-olefin-nonconjugated Diene copolymer rubber, etc. (2) Crosslinked with a metal oxide crosslinking agent Chloroprene rubber, halogenated ethylene-α-olefin copolymer, halogenated ethylene-α-olefin-nonconjugated diene copolymer, chlorosulfone Polyethylene, etc. (3) Items that can be crosslinked with an amine crosslinking agent Acrylic rubber, fluororubber, etc. On the other hand, the following are examples of combinations of polymeric elastomers that are not crosslinked with the crosslinking agent or have extremely low crosslinking and the crosslinking agent. Examples include things like.

(1)硫黄系架橋剤により架橋されないものエチレン−
αオレフィン共重合体、ハロゲン化エチレン−αオレフ
ィン共重合体、アクリルゴム、シリコンゴム、フッ素ゴ
ム等(2)金属酸化物系架橋剤、アミン系架橋剤により
架橋されないもの 天然ゴム、ブタジェンゴム、スチレン−ブタジェンゴム
、ニトリルゴム、エチレン−αオレフィン共重合体、エ
チレン−αオレフィン−非共役ジエン共重合体、シリコ
ンゴム等また、軟質エチレン−酢酸ビニル共重合体、軟
質ポリ塩化ビニル、アタクチックポリプロピレン類等も
必要に応じて、架橋剤との組合わせによっては架橋しな
い高分子弾性体として選択使用できる。
(1) Ethylene that cannot be crosslinked with a sulfur-based crosslinking agent
α-olefin copolymers, halogenated ethylene-α-olefin copolymers, acrylic rubber, silicone rubber, fluororubber, etc. (2) Materials that cannot be crosslinked with metal oxide crosslinking agents or amine crosslinking agents Natural rubber, butadiene rubber, styrene rubber, etc. Butadiene rubber, nitrile rubber, ethylene-α-olefin copolymer, ethylene-α-olefin-nonconjugated diene copolymer, silicone rubber, etc. Also, soft ethylene-vinyl acetate copolymer, soft polyvinyl chloride, atactic polypropylene, etc. Depending on the combination with a crosslinking agent, it can be selectively used as a non-crosslinked polymeric elastomer, if necessary.

架橋剤には他に過酸化物系架橋剤があるが、これは多く
の高分子弾性体を架橋するので、本発明の目的に用いる
場合は、天然ゴムのように過酸化物により架橋よりも分
解が進むような高分子弾性体を用いる場合に使用するこ
とができる。以上の他にもいくつかの架橋剤が公知であ
り、使用するゴム環に応じて適宜用いられる。
Other cross-linking agents include peroxide-based cross-linking agents, but since they cross-link many polymeric elastomers, when used for the purpose of the present invention, they are more effective than cross-linking with peroxides, such as natural rubber. It can be used when using an elastomer polymer that decomposes rapidly. In addition to the above, several other crosslinking agents are known and are appropriately used depending on the rubber ring used.

架橋剤で架橋しない高分子弾性体の使用量が多くなる程
ゴム研■剤は低硬度化され柔軟性に富むようになる。そ
の使用層は架橋剤により架橋する結合体としてのゴムの
使用量100M量部当りの20〜100重屋部であるが
、ときには10G¥jL量部を越して用いることもある
。  1該高分子弾性体の種類や分子念及び使用量は目
的とする硬度、柔軟性、ゴム研磨材の成形性、強度、耐
磨耗性等を考慮して決めることができる。
As the amount of the polymeric elastomer that is not crosslinked with a crosslinking agent increases, the rubber abrasive becomes less hard and more flexible. The layer used is 20 to 100 parts per 100 M parts of rubber as a bond crosslinked with a crosslinking agent, but sometimes more than 10 G\jL parts are used. 1. The type, molecular weight and amount of the elastomer to be used can be determined in consideration of the desired hardness, flexibility, moldability of the rubber abrasive, strength, abrasion resistance, etc.

本発明において用いる砥粒はとくに限定されないが、ダ
イヤモンド粒子、アルミナ、カーボランダム等が好適に
用いろnる。
The abrasive grains used in the present invention are not particularly limited, but diamond particles, alumina, carborundum, etc. are preferably used.

砥粒、架傭剤、架橋剤により架橋する結合休日’IMイ
t−kkノ!Il1mj:ll−ys14ノL’llτ
E1.jrL)%s#f−1)享しく架橋しにくい高分
子弾性体の他に、必要に応じてカーボンブラック、白色
充填剤(例えばクレー、タルク、炭酸カルシウム、シリ
カ等)、架橋促進剤、架橋助剤、プロセスオイル、低分
子量可塑剤、老化防止剤、各種安定剤、顔料及びゴムで
あることの特性を損なわない範囲での各種樹脂等をバン
バリー、ニーダ−、ロール等にて混合し、プレス、押出
機、ロール、オーブン等を用いて成形し、架橋して目的
のゴム研磨材を製造する。
Bonding holiday 'IM IT-KKNO! Cross-linked by abrasive grains, cross-linking agent, and cross-linking agent! Il1mj:ll-ys14ノL'llτ
E1. jrL)%s#f-1) In addition to the pleasant and difficult-to-crosslink polymeric elastomer, carbon black, white filler (e.g. clay, talc, calcium carbonate, silica, etc.), crosslinking accelerator, crosslinking Auxiliary agents, process oils, low molecular weight plasticizers, anti-aging agents, various stabilizers, pigments, and various resins within a range that does not impair the characteristics of rubber are mixed using a banbury, kneader, roll, etc., and then pressed. , molded using an extruder, roll, oven, etc., and crosslinked to produce the desired rubber abrasive material.

実施例〕 以下に本発明の実施例を示すが、本発明はこれらに限定
されるものではない。
Examples] Examples of the present invention are shown below, but the present invention is not limited thereto.

実施例1〜3、比較例1 砥粒としてアルミナ、硫黄架橋可能なニド!J ルーt
 ムとii架iしないエチレンプロピレン共重合体を用
いた例について示す。第1表に配合を、第2表に評価結
果を記した。
Examples 1 to 3, Comparative Example 1 Alumina and sulfur crosslinkable nide as abrasive grains! J route
An example using an ethylene-propylene copolymer that does not crosslink with the polymer will be shown. Table 1 shows the formulations, and Table 2 shows the evaluation results.

jI1表  (配合) 第1表の配合物をニーダーにて作成し、プレスを用いて
160℃にて16分間架橋処理た研磨材の硬度を測定す
るとともに、灯油を滑剤に用いて鉄板表面を手動にて研
磨し、研磨された鉄粉が灯油中に分散して黒く変色する
度合から研磨特性を評価した。
jI1 Table (Formulation) The hardness of the abrasive material was prepared using a kneader using the composition shown in Table 1, cross-linked for 16 minutes at 160°C using a press, and the surface of the iron plate was manually polished using kerosene as a lubricant. The polishing characteristics were evaluated based on the degree to which the polished iron powder dispersed in kerosene and turned black.

第2表  (評価結果) いずれの研磨材も鉄板表面上を手動にて研磨したとき、
50回の往復運動で灯油はかなり黒く変色し、優れた研
H特性を有していlコ。
Table 2 (Evaluation results) When each abrasive was manually polished on the surface of an iron plate,
After 50 reciprocations, the kerosene turns considerably black and has excellent abrasive properties.

WrLlRで架橋できないエチレン−プロピレン共重合
体を増量することにより研磨特性を損なわずに硬度を大
きく低下させることができ、柔軟性を付与することがで
きた結果、被研磨物との形状適合性が改良された。
By increasing the amount of ethylene-propylene copolymer that cannot be crosslinked with WrLlR, the hardness can be significantly reduced without impairing the polishing properties, and flexibility can be imparted, resulting in improved shape compatibility with the object to be polished. Improved.

実施例4〜6、比較例2 エチレン−プロピレン−エチリデンノルボルネン共重合
体(以下ENB系EPDMとする)系ゴム研磨材の例を
示す。
Examples 4 to 6, Comparative Example 2 Examples of ethylene-propylene-ethylidene norbornene copolymer (hereinafter referred to as ENB-based EPDM)-based rubber abrasives are shown below.

第8表  (配合) 上記配合物をニーダ−を用いて作成、プレスを用いて1
60℃にて20分間架橋処理を行ない、厚さ2襲の研磨
材を得た。第4表に結果を記した。砥粒としてダイヤモ
ンドを使用しているために、昇常に研磨特性1c @れ
、80回の往復研磨で灯油は黒く変色した。実施例のも
のは、低硬度であり良好な形状適合性を示した。
Table 8 (Composition) The above composition was prepared using a kneader, and 1
Crosslinking treatment was performed at 60° C. for 20 minutes to obtain a two-stroke thick abrasive material. The results are shown in Table 4. Because diamond was used as the abrasive grain, the polishing properties were 1c @, and the kerosene turned black after 80 reciprocating polishings. The examples had low hardness and good shape compatibility.

第4表  (評価結果) 実施例6〜7、比較例3 架橋剤として全脂酸化物を用いたクロロプレンゴム研磨
材の例を示す。
Table 4 (Evaluation Results) Examples 6 to 7, Comparative Example 3 An example of a chloroprene rubber abrasive material using full fat oxide as a crosslinking agent is shown.

第5表  (配合) クロロプレンゴムにスチレンブタジェンゴムやエチレン
プロピレン共重合体を併用することにより研磨材の硬度
を下げることができる。二次加熱処理により比較例では
硬度が7ポイント上昇するのに対し、実施例6では8ポ
イント、同7では2ポイントしか上昇せずクロロブレン
ゴムと併用されている スチレンブタジェンゴム及びエ
チレンプロピレン共重合体ゴムが架橋されていないこと
がわかる。
Table 5 (Blend) The hardness of the abrasive can be lowered by using styrene-butadiene rubber or ethylene-propylene copolymer in combination with chloroprene rubber. Although the hardness of the comparative example increases by 7 points due to secondary heat treatment, it increases by 8 points in Example 6 and only 2 points in Example 7, which is used in combination with chloroprene rubber.Styrene-butadiene rubber and ethylene propylene rubber It can be seen that the polymer rubber is not crosslinked.

〔発明の効果〕〔Effect of the invention〕

本発明を用いることにより、金属、ガラス、セラミック
ス等を切削、研磨することのできる低硬度ゴム研磨材を
得ることができる。
By using the present invention, a low hardness rubber abrasive material that can cut and polish metals, glass, ceramics, etc. can be obtained.

Claims (1)

【特許請求の範囲】[Claims]  架橋剤を用いて砥粒結合体であるゴムを架橋せしめて
ゴム研磨材を製造するに際して、該架橋剤では架橋し得
ない高分子弾性体を砥粒結合体として併用することを特
徴とする柔軟性に優れた低硬度ゴム研磨材の製造方法。
A flexible material characterized in that, when producing a rubber abrasive material by crosslinking rubber as an abrasive binder using a crosslinking agent, an elastic polymer material that cannot be crosslinked with the crosslinking agent is also used as an abrasive binder. A method for producing a low hardness rubber abrasive with excellent properties.
JP13400286A 1986-06-10 1986-06-10 Production of low-hardness rubber abrasive Pending JPS62290732A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP13400286A JPS62290732A (en) 1986-06-10 1986-06-10 Production of low-hardness rubber abrasive

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP13400286A JPS62290732A (en) 1986-06-10 1986-06-10 Production of low-hardness rubber abrasive

Publications (1)

Publication Number Publication Date
JPS62290732A true JPS62290732A (en) 1987-12-17

Family

ID=15118083

Family Applications (1)

Application Number Title Priority Date Filing Date
JP13400286A Pending JPS62290732A (en) 1986-06-10 1986-06-10 Production of low-hardness rubber abrasive

Country Status (1)

Country Link
JP (1) JPS62290732A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0197572A (en) * 1987-10-09 1989-04-17 Tadao Koyakata Plastic flexible grinding stone
EP0438671A2 (en) * 1990-01-22 1991-07-31 Somar Corporation Abrasive film and method for production thereof
EP0650807A1 (en) * 1993-10-29 1995-05-03 Minnesota Mining And Manufacturing Company Abrasive article, a process for its manufacture, and a method of using it
KR100581347B1 (en) 2004-03-10 2006-05-17 (주)에이알앤씨 Plant mix type color binder for color paving

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0197572A (en) * 1987-10-09 1989-04-17 Tadao Koyakata Plastic flexible grinding stone
JPH0411335B2 (en) * 1987-10-09 1992-02-28
EP0438671A2 (en) * 1990-01-22 1991-07-31 Somar Corporation Abrasive film and method for production thereof
EP0650807A1 (en) * 1993-10-29 1995-05-03 Minnesota Mining And Manufacturing Company Abrasive article, a process for its manufacture, and a method of using it
US5549961A (en) * 1993-10-29 1996-08-27 Minnesota Mining And Manufacturing Company Abrasive article, a process for its manufacture, and a method of using it to reduce a workpiece surface
CN1070754C (en) * 1993-10-29 2001-09-12 美国3M公司 Abrasive article, a process for its manufacture, and a method of using it to reduce a workpiece surface
KR100581347B1 (en) 2004-03-10 2006-05-17 (주)에이알앤씨 Plant mix type color binder for color paving

Similar Documents

Publication Publication Date Title
AU2002323878A1 (en) Polyolefin with improved scratch resistance and process for producing the same
JPS62290732A (en) Production of low-hardness rubber abrasive
US3756607A (en) Golf ball having improved physical properties
JPS648020B2 (en)
EP1417261B1 (en) Eraser
JP2000143884A (en) Thermoplastic olefin elastomer composition
JPH0545440B2 (en)
JP3035075B2 (en) grip
AU2002309928A1 (en) Eraser
US2384683A (en) Grinding wheels
JPS6279967A (en) Diamond contained rubber abrasive
US2384684A (en) Grinding wheels
US6503612B1 (en) Hand-held conformable sanding block
JP3210444B2 (en) Oil seal for power steering
JPS62153381A (en) Low-hardness rubber abrasive which can be highly hardened
US785231A (en) Composition for polishing and abrading tools.
JP2000198518A (en) Rubber composition excellent in breaking strength, elongation and wear resistance for conveyer belt cover
JPS58125726A (en) Production of crosslinked foamed production for footwear soles
JPH0753789A (en) Thermoplastic polyolefinic elastomer
JP2001161404A (en) Shoe sole
JPS6142551A (en) Halogenated polymer composition
JP3953640B2 (en) eraser
JP4050563B2 (en) Correction tape remover
JPS6140114A (en) Method for molding and vulcanizing rubber product
JPH10324855A (en) Resin composition and crosslinked resin composition for use in adhering, and laminated product