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JPS6140260B2 - - Google Patents

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Publication number
JPS6140260B2
JPS6140260B2 JP58010336A JP1033683A JPS6140260B2 JP S6140260 B2 JPS6140260 B2 JP S6140260B2 JP 58010336 A JP58010336 A JP 58010336A JP 1033683 A JP1033683 A JP 1033683A JP S6140260 B2 JPS6140260 B2 JP S6140260B2
Authority
JP
Japan
Prior art keywords
thermoplastic polyurethane
lubricating oil
polyurethane resin
parts
resin
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
Application number
JP58010336A
Other languages
Japanese (ja)
Other versions
JPS59135250A (en
Inventor
Koichi Iwata
Hideo Takahashi
Akihiko Isomura
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 Electric Industries Ltd
Original Assignee
Sumitomo Electric Industries 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 Electric Industries Ltd filed Critical Sumitomo Electric Industries Ltd
Priority to JP58010336A priority Critical patent/JPS59135250A/en
Publication of JPS59135250A publication Critical patent/JPS59135250A/en
Publication of JPS6140260B2 publication Critical patent/JPS6140260B2/ja
Granted legal-status Critical Current

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  • Polyurethanes Or Polyureas (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Description

【発明の詳細な説明】 3―1 技術分野 本発明は、摺動特性に優れた熱可塑性ポリウレ
タン樹脂組成物に関するものである。 3―2 背景 従来、熱可塑性ポリウレタンはゴム弾性を持つ
と同時に熱可塑性であることから、安価でかつ、
複雑形状の部品に適した射出・押出成形が可能な
ことから、自動車用部品、精密工業部品あるいは
家電機器部品等幅広い分野で実用化されている。 しかし、軸受あるいはスライダーといつた摺動
用機構部品として用いる場合は、その耐摩耐性は
十分ではなく、摺動界面への注油あるいはグリー
ス塗布を必要としていた。この場合、摺動界面で
の油切れを防ぐには、別途潤滑油補給機構を設け
ねばならず、部品の複雑化、コスト高等の問題が
あつた。 熱可塑性ポリウレタン自身の耐摩性を向上させ
るには、四フツ化樹脂パウダーあるいは二硫化モ
リブデンあるいはグラフアイト等の固体潤滑剤を
添加混合する方法があるが、これら固体潤滑剤の
効果は十分ではなく、過酷な摺動条件下では、や
はり給油を行なう必要があつた。 3―3 発明の構成 本発明者らはかかる熱可塑性ポリウレタン樹脂
の欠点を改善し、耐摩性、低摩擦係数といつた摺
動特性に優れた熱可塑性ポリウレタン樹脂組成物
を見い出すことに成功したものである。 即ち、特許請求範囲第1項記載のように、比表
面積1m2/g以上の油保持担体と潤滑油を、その
容積比が1/10〜1/1(担体/油)となるように
し、かつ、潤滑油の容積比率が全組成物に対して
3〜15%となるように熱可塑性ポリウレタン樹脂
に添加混合するのである。 ここで用いる熱可塑性ポリウレタン樹脂とは、
その分子が部分的に架橋したウレタン基を有する
ゴム状弾性高分子であり、例えば、商品名エラス
トラン(日本エラストラン株式会社製)が市販さ
れている。 油保持担体としては、1m2/g以上の比表面積
を有する活性炭が用いられ、その目的は、加工時
の油分離、成形品内部の潤滑油のブリードを防止
することにある。 潤滑油としては、母材樹脂に対する浸蝕・膨潤
性がなく、かつ、射出・押出成形時に揮発分の少
ないことが必要である。 望ましい潤滑油としては、炭化水素油が挙げら
れるが特に限定されるものではない。 添加する潤滑油量は、3〜15容積%でなければ
ならない。3容積%より少ないと、十分な潤滑効
果が得られず、又15容積%を越えると油分離によ
る成形障害が起こりやすくなりかつ、ポリウレタ
ン自体の物性を損なう。 油保持担体の添加量は潤滑油との容積比率が
0.1〜1(担体/油)でなければならない。比率
が0.1より小さいと油保持効果が十分ではなく油
分離による成形障害が起こる。比率が1を越える
と、潤滑油が完全に担体に吸着され、摺動界面へ
の浸出が妨げられる為、十分な潤滑効果が得られ
ない。 このようにして得られる特許請求範囲第1項記
載の熱可塑性ポリウレタン樹脂組成物は、優れた
摺動特性を持ち、摺動用部品としての実用に供す
ることが出来る。しかし射出成形法による加工に
おいては、スクリユーへの喰い込み時間が長くな
り、成形所要時間が増大するきらいがあつた。 本発明者らは、さらに射出成形におけるスクリ
ユーへの喰い込み時間短縮を鋭意検討した結果、
特許請求範囲第二項記載の組成物をみい出したも
のである。 即ち、特許請求範囲第一項記載の組成物に対
し、母材樹脂である熱可塑性ポリウレタン100重
量部に対し、融点200℃以下のポリアミド樹脂5
〜40重量部を添加混合するのである。 熱可塑性ポリウレタンと一般樹脂、例えば
PVC樹脂ABS樹脂、アセタール樹脂、アクリル
樹脂等とを自由に混合出来ることは従来知られて
いるが、本発明らによつてポリアミド樹脂と混合
することにより、スクリユーへの喰い込み時間が
大巾に短縮出来ることが初めて見い出された。 本発明に用いるポリアミド樹脂としては、200
℃以下の融点を持つポリアミドであればよく例え
ばナイロン11あるいはナイロン12が挙げられる。
ポリウレタンのゴム状弾性を維持するためには、
ポリアミドの弾性率は低い程良く、エラストマー
タイプのポリアミドが最も望ましい。 3―4 実施例 本発明の実施例を以下に示す。 (実施例 1) 熱可塑性ポリウレタン樹脂に対し、分解温度
350℃の鉱物系パラフイン油を10Vol%、比表面
積1000m2/gの活性炭を5Vol%となるように混
合し、これをスクリユー式押出練で溶融混練りに
してペレツト化を行なつた。このものをスクリユ
ー径32mmの射出成形機にて所定の形状に成形し
た。 (実施例 2) 熱可塑性ポリウレタン樹脂100重量部に対し、
融点160℃のポリアミドエラストマー20重量部
を、かつ全体の組成物に対して、実施例1記載の
鉱物系パラフイン油を10Vol%、活性炭を5Vol%
となるように添加混合し、このものスクリユー径
32mmの射出成形機にて所定の形状に成形した。 3―5 効果 本発明の実施例1及び実施例2の摩擦特性、反
ぱつ弾性率及び射出成形における可塑化時間を第
1表に示す。第1表には比較の為に、添加剤を含
まない熱可塑性ポリウレタン樹脂及び四フツ化樹
脂ワツクスを5重量%添加した熱可塑性ポリウレ
タン樹脂の物性を同時に示す。 第1表で明らかなように本発明の実施例のもの
は、著しく耐摩性が改善され、かつ摩擦係数も低
下する。又、実施例2の組成物は射出成形での可
塑化時間が、無添加の熱可塑性ポリウレタン樹脂
と同等以下になり、成形所要時間を短縮すること
が出来る。 【表】
Detailed Description of the Invention 3-1 Technical Field The present invention relates to a thermoplastic polyurethane resin composition with excellent sliding properties. 3-2 Background Conventionally, thermoplastic polyurethane has rubber elasticity and is thermoplastic, so it is inexpensive and
Because injection and extrusion molding is suitable for parts with complex shapes, it has been put into practical use in a wide range of fields such as automobile parts, precision industrial parts, and home appliance parts. However, when used as a sliding mechanical component such as a bearing or a slider, its wear resistance is not sufficient and the sliding interface needs to be lubricated or greased. In this case, in order to prevent oil from running out at the sliding interface, a separate lubricating oil replenishment mechanism must be provided, resulting in problems of complicated parts and high costs. To improve the wear resistance of thermoplastic polyurethane itself, there is a method of adding and mixing solid lubricants such as tetrafluoride resin powder, molybdenum disulfide, or graphite, but the effects of these solid lubricants are not sufficient; Under harsh sliding conditions, it was still necessary to lubricate. 3-3 Structure of the Invention The present inventors have succeeded in improving the drawbacks of such thermoplastic polyurethane resins and found a thermoplastic polyurethane resin composition that has excellent sliding properties such as wear resistance and low coefficient of friction. It is. That is, as described in claim 1, an oil holding carrier having a specific surface area of 1 m 2 /g or more and a lubricating oil are mixed in a volume ratio of 1/10 to 1/1 (carrier/oil), The lubricating oil is added to the thermoplastic polyurethane resin and mixed so that the volume ratio of the lubricating oil is 3 to 15% based on the total composition. The thermoplastic polyurethane resin used here is
It is a rubber-like elastic polymer whose molecule has a partially crosslinked urethane group, and is commercially available, for example, under the trade name Elastran (manufactured by Nippon Elastran Co., Ltd.). Activated carbon having a specific surface area of 1 m 2 /g or more is used as the oil-holding carrier, and its purpose is to prevent oil separation during processing and bleeding of lubricating oil inside the molded product. The lubricating oil must not corrode or swell the base resin, and must have a low volatile content during injection/extrusion molding. Desirable lubricating oils include, but are not limited to, hydrocarbon oils. The amount of lubricating oil added should be between 3 and 15% by volume. If it is less than 3% by volume, a sufficient lubricating effect cannot be obtained, and if it exceeds 15% by volume, molding failures due to oil separation are likely to occur and the physical properties of the polyurethane itself are impaired. The amount of oil holding carrier added depends on the volume ratio with the lubricating oil.
Must be 0.1-1 (carrier/oil). If the ratio is less than 0.1, the oil retention effect will not be sufficient and molding problems will occur due to oil separation. If the ratio exceeds 1, the lubricating oil will be completely adsorbed on the carrier and will be prevented from leaching to the sliding interface, making it impossible to obtain a sufficient lubricating effect. The thermoplastic polyurethane resin composition as described in claim 1 thus obtained has excellent sliding properties and can be put to practical use as sliding parts. However, when processing by injection molding, the time required for biting into the screw becomes long, which tends to increase the time required for molding. The inventors of the present invention further investigated how to shorten the time required for biting into the screw in injection molding, and found that
The composition described in claim 2 has been discovered. That is, for the composition described in claim 1, 5 parts by weight of a polyamide resin with a melting point of 200°C or less is added to 100 parts by weight of thermoplastic polyurethane as a base material resin.
~40 parts by weight are added and mixed. Thermoplastic polyurethane and general resins, e.g.
It has been known in the past that PVC resin, ABS resin, acetal resin, acrylic resin, etc. can be mixed freely, but by mixing it with polyamide resin by the present inventors, the time required to feed the screw into the screw can be greatly increased. It was discovered for the first time that it could be shortened. As the polyamide resin used in the present invention, 200
Any polyamide having a melting point of 0.degree. C. or less may be used, such as nylon 11 or nylon 12.
In order to maintain the rubber-like elasticity of polyurethane,
The lower the elastic modulus of polyamide, the better, and elastomer type polyamide is most desirable. 3-4 Examples Examples of the present invention are shown below. (Example 1) Decomposition temperature for thermoplastic polyurethane resin
Mineral paraffin oil at 350°C was mixed at 10 vol% and activated carbon having a specific surface area of 1000 m 2 /g was mixed at 5 vol%, and the mixture was melt-kneaded using a screw extrusion kneader to form pellets. This product was molded into a predetermined shape using an injection molding machine with a screw diameter of 32 mm. (Example 2) For 100 parts by weight of thermoplastic polyurethane resin,
20 parts by weight of a polyamide elastomer with a melting point of 160°C, and 10 Vol% of the mineral paraffin oil described in Example 1 and 5 Vol% of activated carbon based on the entire composition.
Add and mix so that the screw diameter of this
It was molded into the specified shape using a 32 mm injection molding machine. 3-5 Effects Table 1 shows the friction characteristics, rebound modulus, and plasticization time in injection molding of Examples 1 and 2 of the present invention. For comparison, Table 1 also shows the physical properties of a thermoplastic polyurethane resin containing no additives and a thermoplastic polyurethane resin to which 5% by weight of tetrafluoride resin wax was added. As is clear from Table 1, the examples of the present invention have significantly improved wear resistance and a reduced coefficient of friction. Furthermore, the plasticization time of the composition of Example 2 during injection molding is equal to or less than that of an additive-free thermoplastic polyurethane resin, and the time required for molding can be shortened. 【table】

Claims (1)

【特許請求の範囲】 1 熱可塑性ポリウレタン樹脂に比表面積1m2
g以上の活性炭と潤滑油とを含み、活性炭と潤滑
油との容積比が1:10〜1:1で、かつ潤滑油の
全組成物に対する容積比率が3〜15%であること
を特徴とする熱可塑性ポリウレタン樹脂組成物。 2 熱可塑性ポリウレタン樹脂100重量部に対し
融点200℃以下のポリアミド樹脂5〜40重量部混
合した樹脂組成物に比表面積1m2/g以上の活性
炭と潤滑油とを含み、活性炭と潤滑油との容積比
が1:10〜1:1で、かつ潤滑油の全組成物に対
する容積比率が3〜15%であることを特徴とする
熱可塑性ポリウレタン樹脂組成物。
[Claims] 1. Thermoplastic polyurethane resin has a specific surface area of 1 m 2 /
g or more of activated carbon and lubricating oil, the volume ratio of activated carbon to lubricating oil is 1:10 to 1:1, and the volume ratio of lubricating oil to the total composition is 3 to 15%. A thermoplastic polyurethane resin composition. 2 A resin composition in which 100 parts by weight of thermoplastic polyurethane resin is mixed with 5 to 40 parts by weight of polyamide resin having a melting point of 200°C or less, contains activated carbon with a specific surface area of 1 m 2 /g or more and lubricating oil, and the activated carbon and lubricating oil are mixed together. A thermoplastic polyurethane resin composition characterized in that the volume ratio is 1:10 to 1:1, and the volume ratio of lubricating oil to the total composition is 3 to 15%.
JP58010336A 1983-01-24 1983-01-24 Thermoplastic polyurethane resin composition Granted JPS59135250A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP58010336A JPS59135250A (en) 1983-01-24 1983-01-24 Thermoplastic polyurethane resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58010336A JPS59135250A (en) 1983-01-24 1983-01-24 Thermoplastic polyurethane resin composition

Publications (2)

Publication Number Publication Date
JPS59135250A JPS59135250A (en) 1984-08-03
JPS6140260B2 true JPS6140260B2 (en) 1986-09-08

Family

ID=11747350

Family Applications (1)

Application Number Title Priority Date Filing Date
JP58010336A Granted JPS59135250A (en) 1983-01-24 1983-01-24 Thermoplastic polyurethane resin composition

Country Status (1)

Country Link
JP (1) JPS59135250A (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0791454B2 (en) * 1987-05-20 1995-10-04 エヌオーケー株式会社 Method for producing oil-containing polyurethane elastomer composition
KR100372801B1 (en) * 1994-04-05 2003-05-01 도요 보세키 가부시키가이샤 Polyamide Resin Compositions and Molded Articles
JP5465459B2 (en) * 2008-05-15 2014-04-09 大日精化工業株式会社 Thermoplastic polyurethane resin composition

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5134536A (en) * 1974-09-17 1976-03-24 Kubota Ltd YUATSUSEISUIHINIOKERUHITAIHOJISOCHI
JPS538734A (en) * 1976-07-12 1978-01-26 Yuasa Battery Co Ltd Button silver peroxide battery

Also Published As

Publication number Publication date
JPS59135250A (en) 1984-08-03

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