JPH0349931B2 - - Google Patents
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- Publication number
- JPH0349931B2 JPH0349931B2 JP57042150A JP4215082A JPH0349931B2 JP H0349931 B2 JPH0349931 B2 JP H0349931B2 JP 57042150 A JP57042150 A JP 57042150A JP 4215082 A JP4215082 A JP 4215082A JP H0349931 B2 JPH0349931 B2 JP H0349931B2
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- Prior art keywords
- rubber
- parts
- lubricating agent
- weight
- porous particles
- Prior art date
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Description
【発明の詳細な説明】
本発明は、低摩擦摺動面を有する加硫ゴムに関
する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a vulcanized rubber having a low friction sliding surface.
伝動Vベルトの使用時の騒音とアラインメント
性は、ベルトの摺動面の表面摩擦抵抗に関係し、
摩擦係数を小さくすることにより、騒音を低下さ
せることができ、また、アラインメント性を改善
することができる。このため、例えば、ベルトを
その使用に先立つて、シリコン油のような滑性化
剤に浸漬することも試みられているが、この処理
によれば、ベルトの使用によつて、ベルト表面に
付着しているシリコン油が速やかに飛散するの
で、ベルト摺動面の摩擦係数を減じる効果は、速
やかに消失し、長期間にわたつて維持されない。 Noise and alignment when using a transmission V-belt are related to the surface friction resistance of the belt's sliding surface.
By reducing the coefficient of friction, noise can be reduced and alignment properties can be improved. For this reason, for example, attempts have been made to soak the belt in a lubricating agent such as silicone oil prior to its use, but this treatment prevents the particles from sticking to the belt surface as a result of use of the belt. Since the silicone oil containing the belt quickly scatters, the effect of reducing the friction coefficient of the belt sliding surface quickly disappears and is not maintained over a long period of time.
一方、シリコン油は、ゴムとの相溶性に劣るた
めに、一般に、直接に未加硫ゴムと混練し得る量
は限られており、ゴム100重量部について、3重
量部以上に混練すると、ゴム表面へのブリーデイ
ングが著しく、ベルト表面がべたつきを生じ、ベ
ルトの機能や製品価値を却つて低めることとな
る。 On the other hand, since silicone oil has poor compatibility with rubber, the amount that can be directly kneaded with unvulcanized rubber is generally limited. Bleeding to the surface is significant, causing the belt surface to become sticky, which in turn reduces the belt's functionality and product value.
更に、ゴムとの相溶性に劣るシリコン油を直接
にゴムに混練することは容易ではなく、特に、ゴ
ムへの配合量が増えるにつれて、例えば、最も一
般的なロールによる混練の場合、ゴムがロール上
で滑り、或いはロールからはずれる等、ロール操
作性が著しく悪くなり、ゴムに均一に分散させる
ことができない。この結果、このような未加硫ゴ
ム組成物から得られる加硫ゴムは、品質の安定性
に欠けると共に、シリコン油の激しいブリーデイ
ングのために、ベルト摺動面の摩擦係数を小さく
する効果は短期間に消失する。 Furthermore, it is not easy to directly knead silicone oil, which has poor compatibility with rubber, into rubber, and especially as the amount of silicone oil added to rubber increases, for example, in the most common kneading process using rolls, rubber The roll operability becomes extremely poor, such as slipping on the top or coming off the roll, and it is not possible to uniformly disperse the rubber into the rubber. As a result, the vulcanized rubber obtained from such an unvulcanized rubber composition lacks stability in quality, and due to severe bleeding of silicone oil, it is not effective in reducing the coefficient of friction of the belt sliding surface. Disappears in a short period of time.
本発明は、上記した種々の問題を解決するため
になされたものであつて、本来、ゴムとの相溶性
に劣る滑性化剤が多孔性粒子に吸着されて、ゴム
内に均一に分散されていると共に、その滑性化剤
が長期にわたつて実質的に一定した小さい速度で
ゴム表面にブリーデイングし、かくして、ゴム表
面が長期にわたつて実質的に一定した小さい摩擦
係数を有する加硫ゴム、即ち、底摩擦摺動面を有
する加硫ゴムを提供することを目的とする。 The present invention has been made to solve the various problems described above, and the lubricating agent, which originally has poor compatibility with rubber, is adsorbed to porous particles and dispersed uniformly within the rubber. vulcanization, in which the lubricating agent bleeds into the rubber surface at a small, substantially constant rate over time, such that the rubber surface has a small, substantially constant coefficient of friction over time. An object of the present invention is to provide a rubber, that is, a vulcanized rubber having a bottom friction sliding surface.
本発明による低摩擦摺動面を有する加硫ゴム
は、ゴム100重量部について、シリコン油及びフ
ツ素化合物から選ばれる滑性化剤1〜10重量部が
多孔性粒子に吸着されて、ゴムに配合されてなる
ゴム組成物の加硫ゴムからなることを特徴とす
る。 The vulcanized rubber having a low-friction sliding surface according to the present invention is produced by adsorbing 1 to 10 parts by weight of a lubricating agent selected from silicone oil and fluorine compounds on porous particles per 100 parts by weight of rubber. It is characterized by being made of a vulcanized rubber compounded rubber composition.
本発明による加硫ゴムにおいて、滑性化剤と
は、ゴムとの相溶性が劣るために、ゴム表面に移
行して、その摩擦抵抗を減じ、表面を滑性化する
配合物を意味し、好ましくはシリコン油が用いら
れるが、これ以外に、フツ素化合物も滑性化剤と
して用いることができ、このような滑性化剤は、
適宜の有機溶剤に溶解した溶液とし、又は水性エ
マルジヨンとして、多孔性粒子に吸着させて、ゴ
ムに配合される。 In the vulcanized rubber according to the present invention, the lubricating agent refers to a compound that migrates to the rubber surface due to its poor compatibility with the rubber, reduces its frictional resistance, and makes the surface lubricated; Preferably, silicone oil is used, but in addition to this, fluorine compounds can also be used as a lubricating agent, and such lubricating agents include:
It is blended into rubber either as a solution dissolved in an appropriate organic solvent or as an aqueous emulsion and adsorbed onto porous particles.
ゴム工業においては、鉱物油をプロセス油や軟
化剤としてゴムに配合することが一般的に行なわ
れている。しかしながら、プロセス油や軟化剤
は、本来、ゴムとの相溶性が良好であつて、ゴム
に均一に分散し、ゴムを軟化させて、その加工性
を改善するために用いられるものであり、ゴム表
面へ移行してはならない。これに対して、本発明
において用いる滑性化剤は、ゴムに配合された場
合、ロール操作性等の加工性を悪化させると共
に、ゴム表面に移行しやすい。 In the rubber industry, it is common practice to blend mineral oil into rubber as a process oil or softener. However, process oils and softeners inherently have good compatibility with rubber, and are used to uniformly disperse in rubber and soften the rubber to improve its processability. Do not migrate to the surface. On the other hand, when the lubricating agent used in the present invention is blended with rubber, it deteriorates processability such as roll operability and is likely to migrate to the rubber surface.
本発明によれば、ゴムとの相溶性に劣る滑性化
剤を多孔性粒子に吸着させることにより、ゴムと
の混練において、その作業性を悪化させず、一方
において、加硫後は、そのゴム表面への移行を制
御して、いわば徐放させる。従つて、本発明にお
ける滑性化剤は、プロセス油や軟化剤とはその目
的、機能を異にしており、これらとは区別される
べきである。 According to the present invention, by adsorbing a lubricating agent with poor compatibility with rubber into porous particles, the workability of the lubricating agent when kneading with rubber is not deteriorated. The transfer to the rubber surface is controlled, so to speak, for sustained release. Therefore, the lubricating agent in the present invention has a different purpose and function from a process oil or a softening agent, and should be distinguished from these.
本発明において、上述したような滑性化剤を吸
着させるための多孔性粒子としては、平均粒径が
1μm〜30μm、好ましくは10μm〜25μmの範囲に
ある無機質多孔性粒子が好ましく用いられる。こ
のような無機質多孔性粒子の好ましい具体例とし
て、例えば、活性炭、ケイソウ土及び合成水和カ
ルシウムシリケート等を挙げることができる。本
発明においては、特に、平均粒径が1〜100mμの
活性炭、平均粒径が10〜30μmのケイソウ土及び
平均粒径が1〜5μmの合成水和カルシウムシリ
ケートが好ましく用いられる。 In the present invention, the porous particles for adsorbing the lubricating agent as described above have an average particle size of
Inorganic porous particles in the range of 1 μm to 30 μm, preferably 10 μm to 25 μm are preferably used. Preferred specific examples of such inorganic porous particles include activated carbon, diatomaceous earth, and synthetic hydrated calcium silicate. In the present invention, activated carbon having an average particle size of 1 to 100 μm, diatomaceous earth having an average particle size of 10 to 30 μm, and synthetic hydrated calcium silicate having an average particle size of 1 to 5 μm are particularly preferably used.
このような多孔性粒子に滑性化剤を吸着させる
には、通常の方法、例えば、密閉式ブレンダーを
用いる方法によつて両者を混合すればよい。滑性
化剤が前記したフツ素化合物の場合には、これら
の溶液又はエマルジヨンと多孔性粒子を混合した
後、乾燥して溶剤を除去する。 In order to make such porous particles adsorb a lubricating agent, both may be mixed by a conventional method, for example, a method using an internal blender. When the lubricating agent is the above-mentioned fluorine compound, the solution or emulsion is mixed with the porous particles and then dried to remove the solvent.
多孔性粒子への滑性化剤の吸着量は、用いる多
孔性粒子と滑性化剤の種類にもよるが、通常、多
孔性粒子100重量部について、100〜1000重量部、
好ましくは200〜500重量部である。 The amount of the lubricating agent adsorbed onto the porous particles depends on the type of porous particles and lubricating agent used, but is usually 100 to 1000 parts by weight per 100 parts by weight of the porous particles.
Preferably it is 200 to 500 parts by weight.
このようにして滑性化剤を吸着させた多孔性粒
子を未加硫ゴムに混練するには、練りロール、バ
ンバリーミキサー、インターミキサー、スパーミ
キサー等、従来の通常の混練手段によることがで
きる。 The porous particles on which the lubricating agent has been adsorbed in this manner can be kneaded into unvulcanized rubber by conventional kneading means such as kneading rolls, Banbury mixers, intermixers, and spar mixers.
ゴムとしては、天然ゴム、スチレン−ブタジエ
ンゴム、ブタジエンゴム、クロロプレンゴム、エ
チレン−プロピレン−ジエンゴム、ブチルゴム、
イソブチレンゴム、ニトリルゴム、クロルスルホ
ン化ポリエチレンゴム、ポリサルフアイドゴム、
シリコンゴム、ウレタンゴム、アクリルゴム等が
用いられる。 Rubbers include natural rubber, styrene-butadiene rubber, butadiene rubber, chloroprene rubber, ethylene-propylene-diene rubber, butyl rubber,
Isobutylene rubber, nitrile rubber, chlorosulfonated polyethylene rubber, polysulfide rubber,
Silicone rubber, urethane rubber, acrylic rubber, etc. are used.
未加硫ゴムへの滑性化剤の配合量は、未加硫ゴ
ム100重量部について、1〜10重量部の範囲にわ
たつてよいが、好ましくは2〜8重量部、特に好
ましくは3〜6重量部である。滑性化剤の配合量
が少なすぎるときは、得られる加硫ゴム表面の滑
性化が不十分であつて、表面摩擦抵抗の低減に効
果がなく、一方、多すぎるきは、ゴムとの相溶性
に劣る滑性化剤がゴム表面に過多にブリーデイン
グして、好ましくないからである。 The amount of the lubricant added to the unvulcanized rubber may range from 1 to 10 parts by weight per 100 parts by weight of the unvulcanized rubber, preferably from 2 to 8 parts by weight, particularly preferably from 3 to 8 parts by weight. 6 parts by weight. If the amount of the lubricant is too small, the resulting vulcanized rubber surface will be insufficiently lubricated and will not be effective in reducing surface frictional resistance. This is because a lubricating agent with poor compatibility may bleed excessively onto the rubber surface, which is undesirable.
本発明において、未加硫ゴム組成物は、通常、
ゴムに配合される加硫剤、加硫促進剤、老化防止
剤、補強剤、充填剤、滑剤等を含有していてもよ
い。滑性化剤を吸着させた多孔性粒子の未加硫ゴ
ムへの配合は、これらの配合薬品や補強剤と共
に、未加硫ゴムに混練してもよく、また、予め未
加硫ゴムに配合薬品や補強剤、充填剤等を配合し
た後に、滑性化剤を吸着させた多孔性粒子を混練
してもよい。 In the present invention, the unvulcanized rubber composition is usually
It may contain a vulcanizing agent, a vulcanization accelerator, an anti-aging agent, a reinforcing agent, a filler, a lubricant, etc. that are mixed into the rubber. Porous particles adsorbed with a lubricating agent may be mixed into the unvulcanized rubber together with these compounded chemicals and reinforcing agents, or they may be mixed into the unvulcanized rubber in advance. After blending chemicals, reinforcing agents, fillers, etc., porous particles adsorbed with a lubricant may be kneaded.
本発明による加硫ゴムは、このような未加硫ゴ
ム組成物を常法に従つて加硫することによつて得
ることができる。 The vulcanized rubber according to the present invention can be obtained by vulcanizing such an unvulcanized rubber composition according to a conventional method.
本発明による加硫ゴムは、本来、ゴムとの相溶
性に劣る滑性化剤を多孔性粒子に吸着させ、これ
をゴム内に均一に分散させ、かかる未加硫ゴムを
加硫することによつて得られるものである。従つ
て、かかる加硫ゴムにおいては、その表面への滑
性化剤のブリーデイングが実質的に一定した小さ
い速度で長期にわたつて行なわれ、この結果、加
硫ゴム表面は、長期にわたつて、実質的に一定し
た小さい摩擦係数を有する。 The vulcanized rubber according to the present invention is produced by adsorbing a lubricating agent, which originally has poor compatibility with rubber, into porous particles, uniformly dispersing it within the rubber, and vulcanizing the unvulcanized rubber. This is what you get. Therefore, in such vulcanized rubber, bleeding of the lubricating agent onto the surface occurs at a substantially constant and small rate over a long period of time, and as a result, the vulcanized rubber surface remains lubricant over a long period of time. , has a substantially constant and small coefficient of friction.
従つて、本発明による加硫ゴムは、伝動Vベル
ト等に好適であり、このような伝動Vベルトは、
使用時の騒音が抑えられると共に、アラインメン
ト性が向上する。また、ゴムとの相溶性に劣るシ
リコン油のような液状薬品は、ゴムに直接に混練
することが困難であるが、本発明によれば、多孔
性粒子に吸着されているので、混練は、通常の方
法によつて容易に行なうことができ、且つ、多量
に配合することができる。 Therefore, the vulcanized rubber according to the present invention is suitable for power transmission V-belts, etc., and such power transmission V-belts are
Noise during use is suppressed and alignment is improved. In addition, it is difficult to directly knead liquid chemicals such as silicone oil with poor compatibility with rubber, but according to the present invention, since they are adsorbed on porous particles, kneading can be done easily. It can be easily carried out by a conventional method and can be blended in large amounts.
以下に実施例を挙げて本発明を説明するが、本
発明はこれら実施例により何ら限定されるもので
はない。尚、以下において、部は重量部を示す。 The present invention will be explained below with reference to Examples, but the present invention is not limited to these Examples in any way. In addition, in the following, parts indicate parts by weight.
実施例 1
平均粒径2.7μmの合成水和カルシウムシリケー
ト(John Manville社製Micro−Cel)10部をシ
リコン油(東芝シリコン(株)製KM722)30部と混
合し、少し湿りを帯びた粉末を得た。Example 1 10 parts of synthetic hydrated calcium silicate (Micro-Cel, manufactured by John Manville) with an average particle size of 2.7 μm was mixed with 30 parts of silicone oil (KM722, manufactured by Toshiba Silicon Co., Ltd.), and a slightly moist powder was prepared. Obtained.
別に、ネオプレンGRT(昭和ネオプレン(株)製)
500部、ステアリン酸5部、マグネシア20部、亜
鉛華3号25部、オクチル化ジフエニルアミン5部
及びカーボンFEF250部をロールで混練し、この
練ゴムに上で得た粉末を添加し、ロールで混練し
て、未加硫ゴム組成物を得た。 Separately, neoprene GRT (manufactured by Showa Neoprene Co., Ltd.)
500 parts of stearic acid, 5 parts of magnesia, 25 parts of zinc white No. 3, 5 parts of octylated diphenylamine, and 250 parts of carbon FEF were kneaded with a roll, and the powder obtained above was added to this kneaded rubber, and kneaded with a roll. An unvulcanized rubber composition was obtained.
この未加硫ゴム組成物を所定の寸法に裁断後、
ウイリアムス摩耗試験用金型に装着し、148℃の
温度で3分間加硫し、加硫ゴム試験片を得た。こ
の試験片をウイリアムス摩耗試験機にて2.6Kg荷
重で摩耗させた後、研磨面を鉄片に換え、4.1Kg
荷重で表面摩耗抵抗を測定した。図面に研磨面の
回転数と試験片の摩擦抵抗との関係を示す。 After cutting this unvulcanized rubber composition into predetermined dimensions,
It was mounted in a Williams abrasion test mold and vulcanized for 3 minutes at a temperature of 148°C to obtain a vulcanized rubber test piece. After abrading this test piece with a Williams abrasion tester under a load of 2.6 kg, the polished surface was replaced with an iron piece, and the test piece weighed 4.1 kg.
Surface abrasion resistance was measured under load. The figure shows the relationship between the rotation speed of the polished surface and the frictional resistance of the test piece.
比較例として、上記練ゴム500部とシリコン油
30部を直接ロールで混練した後、同様にして、加
硫ゴム試験片を得た。但し、混練は、非常に困難
を伴ない、ゴムがロールからはずれる等の不都合
があつて、上記の1.5倍の時間を要した。この試
験片についても、上記と同様にして加硫後、研磨
面の回転数と試験片の摩擦抵抗との関係を図面に
示す。 As a comparative example, 500 parts of the above kneaded rubber and silicone oil were used.
After directly kneading 30 parts with a roll, a vulcanized rubber test piece was obtained in the same manner. However, kneading was extremely difficult and required 1.5 times the time as described above due to inconveniences such as the rubber coming off the rolls. This test piece was also vulcanized in the same manner as above, and the relationship between the number of rotations of the polished surface and the frictional resistance of the test piece is shown in the drawing.
図示した結果から明らかなように、本発明によ
る加硫ゴムは、表面摩擦抵抗が長期にわたつて実
質的に一定して小さい値を維持している。これに
対して、比較例による加硫ゴムは、表面にシリコ
ン油がブリーデイングしており、且つ、表面摩擦
抵抗は、速やかに増大した。 As is clear from the results shown, the surface frictional resistance of the vulcanized rubber according to the present invention maintains a substantially constant and small value over a long period of time. On the other hand, the vulcanized rubber according to the comparative example had silicone oil bleeding on the surface, and the surface friction resistance rapidly increased.
実施例 2
フツ素化合物の水エマルジヨン((株)ネオス製フ
リリース20)を平均粒径50mμの活性炭10部に混
合し、活性炭にフツ素化合物20部を吸着させた湿
り気のある粉末を得た。これを100℃の乾燥機内
で4時間乾燥させた後、実施例1と同じネオプレ
ンゴムの練ゴムに加え、ロール練りして、未加硫
ゴム組成物を得た。Example 2 A water emulsion of a fluorine compound (Freely 20 manufactured by Neos Co., Ltd.) was mixed with 10 parts of activated carbon with an average particle size of 50 mμ to obtain a moist powder in which 20 parts of a fluorine compound was adsorbed to the activated carbon. . After drying this in a dryer at 100° C. for 4 hours, it was added to the same neoprene rubber kneading as in Example 1 and kneaded with rolls to obtain an unvulcanized rubber composition.
この未加硫ゴム組成物を実施例1と同様にして
加硫して、加硫ゴム試験片を得た。この試験片に
ついて、実施例1と同様にして、表面摩耗抵抗を
測定したところ、実施例1の加硫ゴムと同じく、
長期にわたつて、ほぼ一定した摩擦係数を有して
いた。 This unvulcanized rubber composition was vulcanized in the same manner as in Example 1 to obtain a vulcanized rubber test piece. Regarding this test piece, the surface abrasion resistance was measured in the same manner as in Example 1. As with the vulcanized rubber of Example 1,
It had a nearly constant coefficient of friction over a long period of time.
図面は本発明のゴム組成物から得た加硫ゴムの
ウイリアムス摩耗試験機による研摩面回転数と表
面摩擦抵抗との関係を比較例と共に示すグラフで
ある。
The drawing is a graph showing the relationship between the number of rotations of the polished surface measured by a Williams abrasion tester and the surface friction resistance of vulcanized rubber obtained from the rubber composition of the present invention, together with comparative examples.
Claims (1)
ツ素化合物から選ばれる滑性化剤1〜10重量部が
多孔性粒子に吸着されて、ゴムに配合されてなる
ゴム組成物の加硫ゴムからなり、表面に実質的に
一定した小さい速度で上記滑性化剤をブリーデイ
ングさせることを特徴とする低摩擦摺動面を有す
る加硫ゴム。 2 多孔性粒子100重量部について、滑性化剤100
〜1000重量部が吸着されていることを特徴とする
特許請求の範囲第1項記載の低摩擦摺動面を有す
る加硫ゴム。[Scope of Claims] 1. A rubber composition in which 1 to 10 parts by weight of a lubricating agent selected from silicone oil and fluorine compounds is adsorbed to porous particles and blended into rubber, based on 100 parts by weight of rubber. A vulcanized rubber comprising a low-friction sliding surface, characterized in that the lubricating agent bleeds onto the surface at a substantially constant and small rate. 2 For 100 parts by weight of porous particles, 100 parts by weight of lubricating agent
The vulcanized rubber having a low-friction sliding surface according to claim 1, wherein ~1000 parts by weight is adsorbed.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP4215082A JPS58157836A (en) | 1982-03-16 | 1982-03-16 | rubber composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP4215082A JPS58157836A (en) | 1982-03-16 | 1982-03-16 | rubber composition |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP4108233A Division JPH0649804B2 (en) | 1992-04-28 | 1992-04-28 | Transmission belt |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS58157836A JPS58157836A (en) | 1983-09-20 |
| JPH0349931B2 true JPH0349931B2 (en) | 1991-07-31 |
Family
ID=12627906
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP4215082A Granted JPS58157836A (en) | 1982-03-16 | 1982-03-16 | rubber composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS58157836A (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS63179942A (en) * | 1987-01-21 | 1988-07-23 | Tokai Rubber Ind Ltd | Slide-type vibration damping rubber |
| US5599868A (en) * | 1994-04-19 | 1997-02-04 | Bridgestone Corporation | Process for compounding filler materials and polymers and products therefrom |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5040139A (en) * | 1973-08-17 | 1975-04-12 | ||
| JPS5222650B2 (en) * | 1973-11-05 | 1977-06-18 |
-
1982
- 1982-03-16 JP JP4215082A patent/JPS58157836A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS58157836A (en) | 1983-09-20 |
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