JPH07331011A - Sliding composition - Google Patents

Sliding composition

Info

Publication number
JPH07331011A
JPH07331011A JP14226594A JP14226594A JPH07331011A JP H07331011 A JPH07331011 A JP H07331011A JP 14226594 A JP14226594 A JP 14226594A JP 14226594 A JP14226594 A JP 14226594A JP H07331011 A JPH07331011 A JP H07331011A
Authority
JP
Japan
Prior art keywords
composition
wear
filler
test
base 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.)
Granted
Application number
JP14226594A
Other languages
Japanese (ja)
Other versions
JP2851532B2 (en
Inventor
Norio Tanaka
功雄 田中
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.)
Nippon Pillar Packing Co Ltd
Original Assignee
Nippon Pillar Packing 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 Nippon Pillar Packing Co Ltd filed Critical Nippon Pillar Packing Co Ltd
Priority to JP6142265A priority Critical patent/JP2851532B2/en
Publication of JPH07331011A publication Critical patent/JPH07331011A/en
Application granted granted Critical
Publication of JP2851532B2 publication Critical patent/JP2851532B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Abstract

PURPOSE:To obtain a sliding composition small in abrasion coefficient, excellent in mechanical strength and sealability, and useful for piston rings, etc., by compounding a specific base resin, a lubricating filler such as carbon, and an abrasion-resistant filler such as potassium titanate in a specific ratio. CONSTITUTION:This sliding composition is produced by compounding (A) 50-85wt.% of ethylene tetrafluoride resin and 5-50wt.% of a polyethersulfone, and further compounding (B) 2-15wt.% of a lubricating filler comprising one or more kinds of carbon, graphite and molybdenum disulfide and (C) either one kind of potassium titanate, wollastonite, zonotolite and aramid fibers.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】この発明は、例えば、ピストンリ
ング、ロッドパッキン、ベアリング等の摺動性及び耐摩
耗性が要求される部分に用いられる摺動性組成物に関す
る。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a slidable composition which is used in parts such as piston rings, rod packings, bearings, etc., which require slidability and wear resistance.

【0002】[0002]

【従来の技術】従来、上述例のような部分に用いられる
摺動性組成物としては、例えば、ベースレジンとなる四
フッ化エチレン樹脂に、全芳香族ポリエステル、ポリイ
ミド、ポリフェニレンサルファイド等の耐熱性樹脂を適
宜量配合し、さらに、ガラス繊維、カーボン繊維、炭酸
カルシウム、タルク、ガラス粉、銅、雲母等の充填材を
適宜量配合してなる組成物がある。
2. Description of the Related Art Conventionally, as a slidable composition used for a portion such as the above example, for example, tetrafluoroethylene resin serving as a base resin, heat resistance of wholly aromatic polyester, polyimide, polyphenylene sulfide, etc. There is a composition in which a resin is blended in an appropriate amount, and further, a filler such as glass fiber, carbon fiber, calcium carbonate, talc, glass powder, copper, mica is blended in an appropriate amount.

【0003】[0003]

【発明が解決しようとする課題】しかし、上述のような
充填材を添加した組成物は、表2に示すように、摩擦係
数及び摩耗係数が大きい。また、相手材を損傷しやす
く、攻撃性が大きいという特性を有している。その組成
物を適宜部分に用いた場合、相手材に生じる摩耗量が大
きく、損傷や破損等が起きることがあるため、長期間に
於いて良好なシール性を確保することができない。且
つ、図3に示すように、PV値が高くなると組成物の摩
耗係数が急激に大きくなり、組成物及び相手材に異常摩
耗が生じるという問題点を有している。
However, the composition to which the above-mentioned filler is added has a large coefficient of friction and a large coefficient of wear as shown in Table 2. In addition, it has the characteristics that it easily damages the mating material and is highly aggressive. When the composition is used in an appropriate portion, the amount of wear generated in the mating material is large and damage or breakage may occur, so that it is not possible to secure good sealing properties for a long period of time. In addition, as shown in FIG. 3, when the PV value becomes high, the wear coefficient of the composition rapidly increases, and there is a problem that abnormal wear occurs in the composition and the mating material.

【0004】また、組成物及び相手材が短期間で摩耗す
るため、定期的に交換する必要性があるが、例えば、ポ
リエーテルケトン(PEK)を使用する組成物(特開平
2−212539号公報)は、ポリエーテルスルホン
(PES)を使用する本発明の組成物に比べて高価であ
り、製品化したときの価格が約4倍〜約5倍となるた
め、交換時期が短くなると、必然的に交換回数も多くな
り、コストアップとなる問題点を有している。
Further, since the composition and the mating material are worn out in a short period of time, it is necessary to replace them regularly. For example, a composition using polyether ketone (PEK) (Japanese Patent Laid-Open No. 212539/1990). ) Is more expensive than the composition of the present invention using polyether sulfone (PES), and the price when commercialized is about 4 times to about 5 times, so it is inevitable that the replacement time becomes short. In addition, the number of times of replacement increases, which causes a problem of cost increase.

【0005】この発明は上記問題に鑑み、組成物のベー
スレジンに四フッ化エチレン樹脂とポリエーテルスルホ
ンとを配合し、そのベースレジンに潤滑性充填材と耐摩
耗性充填材とを配合することにより、耐摩耗性及び機械
的強度が格段に向上し、長期間に於いて優れたシール性
が得られると共に、交換回数を削減して、コストの低減
を図ることができる摺動性組成物の提供を目的とする。
In view of the above problems, the present invention comprises blending a tetrafluoroethylene resin and polyether sulfone in a base resin of a composition, and blending a lubricating filler and an abrasion resistant filler in the base resin. As a result, the wear resistance and the mechanical strength are remarkably improved, excellent sealing properties can be obtained for a long period of time, and the number of replacements can be reduced to reduce the cost. For the purpose of provision.

【0006】[0006]

【課題を解決するための手段】この発明の摺動性組成物
は、組成物を構成するベースレジンとして四フッ化エチ
レン樹脂を50wt%〜85wt%配合し、ポリエーテルス
ルホンを5wt%〜50wt%配合すると共に、上記ベース
レジンに充填される潤滑性充填材として、カーボン、グ
ラファイト、二硫化モリブデンの何れか一種又は複数種
を2wt%〜15wt%配合し、上記ベースレジンに充填さ
れる耐摩耗性充填材として、チタン酸カリウム、ウォレ
ストナイト、ゾノトライト、アラミド繊維の何れか一種
を5wt%〜30wt%配合した摺動性組成物であることを
特徴とする。
The slidable composition of the present invention comprises a tetrafluoroethylene resin as a base resin constituting the composition in an amount of 50 wt% to 85 wt% and a polyether sulfone in an amount of 5 wt% to 50 wt%. As a lubricating filler to be filled in the base resin, one or more of carbon, graphite and molybdenum disulfide are blended in an amount of 2 wt% to 15 wt% and the wear resistance filled in the base resin is It is characterized in that it is a slidable composition containing 5 wt% to 30 wt% of any one of potassium titanate, wallostite, xonotlite and aramid fiber as a filler.

【0007】[0007]

【発明の効果】この発明によれば、組成物のベースレジ
ンとして四フッ化エチレン樹脂とポリエーテルスルホン
とを配合し、潤滑性充填材としてカーボン、グラファイ
ト、二硫化モリブデンの一種又は複数種を配合し、耐摩
耗性充填材としてチタン酸カリウム、ウォレストナイ
ト、ゾノトライト、アラミド繊維の一種を配合している
ので、表2に示すように、従来例の組成物に比べて、本
発明を構成する組成物の方が摩擦係数及び摩耗係数が小
さく、摺動性が安定しているため、耐摩耗性及び機械的
強度が格段に向上し、長期間に於いて優れたシール性を
得ることができる。しかも、相手材に与える損傷が少な
く、耐摩耗性に優れているため、寿命が大幅に延長され
ると共に、交換回数を削減して、コストの低減を図るこ
とができる。
According to the present invention, tetrafluoroethylene resin and polyether sulfone are blended as the base resin of the composition, and one or more of carbon, graphite and molybdenum disulfide are blended as the lubricating filler. However, since one kind of potassium titanate, wallostite, xonotlite, and aramid fiber is blended as the wear-resistant filler, as shown in Table 2, as compared with the composition of the conventional example, the composition that constitutes the present invention. Since the product has a smaller friction coefficient and wear coefficient and more stable slidability, wear resistance and mechanical strength are remarkably improved, and excellent sealability can be obtained for a long period of time. Moreover, since the damage to the mating material is small and the wear resistance is excellent, the life is greatly extended, the number of times of replacement can be reduced, and the cost can be reduced.

【0008】[0008]

【実施例】この発明の一実施例を以下図面に基づいて詳
述する。図面は摺動性及び耐摩耗性が要求される部分に
用いられる摺動性組成物を示し、この摺動性組成物は、
組成物を構成するベースレジンに潤滑性充填材と耐摩耗
性充填材とを適宜量配合して成形する。つまり、ベース
レジンとして四フッ化エチレン樹脂(PTFE)とポリ
エーテルスルホン(PES)とを適宜量配合し、ベース
レジンに充填される潤滑性充填材として、カーボン粉末
(C)、グラファイト(Gr)、二硫化モリブデン(M
oS2 )の何れか一種又は複数種を適宜量配合し、ベー
スレジンに充填される耐摩耗性充填材として、板状のチ
タン酸カリウム(PTW)、ウォレストナイト(W
n)、ゾノトライト、アラミド繊維(Af)の何れか一
種を適宜量配合して、後述するフリーベーキング成形法
(予備成形後、電気炉中で焼成)により適宜形状寸法に
成形した組成物である。
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS An embodiment of the present invention will be described in detail below with reference to the drawings. The drawing shows a slidable composition used in a portion where slidability and wear resistance are required.
An appropriate amount of a lubricating filler and an abrasion resistant filler is mixed with the base resin constituting the composition, and the composition is molded. That is, an appropriate amount of tetrafluoroethylene resin (PTFE) and polyether sulfone (PES) are blended as a base resin, and carbon powder (C), graphite (Gr), as a lubricating filler filled in the base resin, Molybdenum disulfide (M
oS2) is appropriately mixed in an appropriate amount, and as a wear-resistant filler to be filled in the base resin, plate-like potassium titanate (PTW), wallstone (WW) is used.
n), xonotlite, and aramid fiber (Af) are mixed in an appropriate amount, and the composition is formed into an appropriate shape by a free baking forming method (preliminary forming and firing in an electric furnace) described later.

【0009】上述した摺動性組成物を成形する場合、例
えば、ベースレジンとして四フッ化エチレン樹脂を50
wt%〜85wt%配合し、ポリエーテルスルホンを5wt%
〜50wt%配合すると共に、潤滑性充填材としてカーボ
ン粉末、グラファイト、二硫化モリブデンの何れか一種
又は複数種を2wt%〜15wt%配合し、耐摩耗性充填材
として板状のチタン酸カリウム(直径=10μ〜30
μ、長さ=80μ〜350μ)、ウォレストナイト、ゾ
ノトライト、アラミド繊維の何れか一種を5wt%〜30
wt%配合した後、組成原料をドライブレンド(乾式混
合)する。フリーベーキング成形法(予備成形後、電気
炉中で焼成)により組成原料を適宜形状寸法に圧縮成形
した後、焼成処理を行い、その後、適宜形状寸法に切削
加工する。
When molding the above-mentioned slidable composition, for example, a tetrafluoroethylene resin is used as a base resin in an amount of 50.
wt% -85wt% blended, polyethersulfone 5wt%
In addition to 50 wt%, 2 wt% to 15 wt% of carbon powder, graphite, or molybdenum disulfide is added as a lubricating filler, and plate-like potassium titanate (diameter is used as a wear-resistant filler). = 10μ-30
μ, length = 80μ to 350μ), 5 wt% to 30% of any one of Wallacenite, zonotolite and aramid fiber
After blending wt%, the composition raw materials are dry blended (dry mixed). The composition raw material is compression-molded into an appropriate shape and dimension by a free-baking forming method (preliminary forming and then fired in an electric furnace), followed by firing treatment, and then cutting into an appropriate shape and dimension.

【0010】上述した四フッ化エチレン樹脂は、50wt
%〜85wt%の配合範囲で使用されるが、50wt%以下
に配合量を減量すると組成物の伸び率(弾性)が小さく
なり、成形性が悪くなる。一方、85wt%以上に配合量
を増量すると十分な摩耗特性が得られず、長期使用に必
要な耐久性が得られない。且つ、耐コールドフロー性が
著しく低下するので、好ましくは、60wt%〜80wt%
の配合範囲で使用するのが最適である。
The above-mentioned tetrafluoroethylene resin is 50 wt.
% To 85 wt%, but if the blending amount is reduced to 50 wt% or less, the elongation (elasticity) of the composition becomes small and the moldability deteriorates. On the other hand, if the compounding amount is increased to 85 wt% or more, sufficient wear characteristics cannot be obtained and the durability required for long-term use cannot be obtained. In addition, since cold flow resistance is significantly reduced, it is preferably 60 wt% to 80 wt%.
It is most suitable to use in the compounding range of.

【0011】ポリエーテルスルホンは、5wt%〜50wt
%の配合範囲で使用されるが、5wt%以下に配合量を減
量すると十分な摩耗特性が得られなくなり、添加による
改善効果が無い。一方、50wt%以上に配合量を増量す
ると成形性が悪くなり、切削加工及び製造上の点で問題
が生じるため、好ましくは、10wt%〜30wt%の配合
範囲で使用するのが最適である。
Polyethersulfone is 5 wt% to 50 wt%
%, But if the compounding amount is reduced to 5 wt% or less, sufficient wear characteristics cannot be obtained, and there is no improvement effect by the addition. On the other hand, if the compounding amount is increased to 50 wt% or more, the formability is deteriorated and problems occur in cutting and manufacturing. Therefore, it is optimal to use the compounding range of 10 wt% to 30 wt%.

【0012】潤滑性充填材として使用されるカーボン粉
末、グラファイト、二硫化モリブデンは、2wt%〜15
wt%の配合範囲で使用するのが最適である。2wt%以下
に配合量を減量すると添加効果(磨耗係数を低くし、発
熱温度を抑え、摩耗性能の向上)が顕著に現れなくな
る。一方、15wt%以上に配合量を増加すると分散性が
低下し、変形や歪み等が生じるため、成形性が悪くな
る。且つ、成形品に配合された充填材に脱落や剥離が起
きる。
The carbon powder, graphite and molybdenum disulfide used as the lubricating filler are 2 wt% to 15%.
It is optimal to use it in the blending range of wt%. If the compounding amount is reduced to 2 wt% or less, the effect of addition (reduction of wear coefficient, suppression of heat generation temperature, improvement of wear performance) does not appear remarkably. On the other hand, if the compounding amount is increased to 15 wt% or more, the dispersibility decreases, deformation and distortion occur, and the moldability deteriorates. In addition, the filler compounded in the molded product may fall off or peel off.

【0013】耐摩耗性充填材として使用される板状のチ
タン酸カリウム、ウォレストナイト、ゾノトライト、ア
ラミド繊維は、5wt%〜30wt%の配合範囲で使用する
のが最適である。5wt%以下に配合量を減量すると強度
的な強化効果が現れず、摩耗特性の向上が悪くなる。一
方、30wt%以上に配合量を増量すると充填材の分散性
が低下し、変形や歪み等が生じるため、成形性が悪くな
る。且つ、成形品に配合された充填材に脱落や剥離が起
きるため、良好な成形品を得ることができない。
The plate-like potassium titanate, wallestonite, xonotlite and aramid fiber used as the wear resistant filler are optimally used in the range of 5 wt% to 30 wt%. If the compounding amount is reduced to 5 wt% or less, the strengthening effect in strength does not appear, and the improvement of wear characteristics deteriorates. On the other hand, if the compounding amount is increased to 30 wt% or more, the dispersibility of the filler decreases and deformation or distortion occurs, resulting in poor moldability. Moreover, since the filler compounded in the molded product may fall off or peel off, a good molded product cannot be obtained.

【0014】また、チタン酸カリウム、ウォレストナイ
ト、ゾノライトをチタネート系カップリング剤又はシラ
ン系カップリング剤で表面処理してから添加すること
で、これら充填材とポリエーテルスルホンとの密着性が
良くなり、四フッ化エチレン樹脂とポリエーテルスルホ
ンとの分子鎖の絡み合いにより、チタン酸カリウム、ウ
ォレストナイト、ゾノライトの滑りが抑えられ、機械的
強度及び耐コールドフロー性が向上する。
Further, by adding potassium titanate, wallestonite and zonolite after surface-treating them with a titanate coupling agent or a silane coupling agent, the adhesion between these fillers and polyether sulfone is improved. The entanglement of the molecular chains of the tetrafluoroethylene resin and the polyethersulfone suppresses the slippage of potassium titanate, wallestonite, and zonolite, and improves the mechanical strength and cold flow resistance.

【0015】図1及び図2は鈴木式摩擦摩耗スラスト試
験機2による摺動性組成物1の試験方法を示し、このス
ラスト試験機2は、同機を構成する回転台3の上面側に
摺動性組成物1を固定し、金属製の相手材4を摺動性組
成物1の上面側に圧接した後、回転台3を回転させなが
ら相手材4で加圧して、相手材4の摺動部分に生じる発
熱温度と摩擦係数とを測定する。
FIGS. 1 and 2 show a method for testing a slidable composition 1 by means of a Suzuki type friction and wear thrust tester 2, which thrust tester 2 slides on the upper surface side of a rotary table 3 which constitutes the same. Of the mating material 4 is fixed, the mating material 4 made of metal is pressed against the upper surface of the slidable composition 1, and then the mating material 4 is pressed while rotating the turntable 3 to slide the mating material 4. The exothermic temperature generated in the part and the coefficient of friction are measured.

【0016】つまり、発熱温度を測定する場合、相手材
4の摺動部分から約3mm離れた位置に熱電対5を差込
み、同熱電対5の接続点に生じる熱起電力を発熱温度に
変換してペンレコーダー(図示省略)で記録する。且
つ、摩擦係数を測定する場合、摺動時に於ける摩擦抵抗
をロードセル(図示省略)で検知し、その抵抗値をペン
レコーダーで記録する。
That is, when measuring the exothermic temperature, the thermocouple 5 is inserted at a position about 3 mm away from the sliding portion of the mating member 4, and the thermoelectromotive force generated at the connection point of the thermocouple 5 is converted into the exothermic temperature. Record with a pen recorder (not shown). Moreover, when measuring the friction coefficient, the friction resistance during sliding is detected by a load cell (not shown), and the resistance value is recorded by a pen recorder.

【0017】上述した摺動性組成物1の比較例として、
例えば、四フッ化エチレン樹脂(PTFE)、ポリエー
テルスルホン(PES)、カーボン粉末(C)、グラフ
ァイト(Gr)、二硫化モリブデン(MoS2 )、板状
のチタン酸カリウム(PTW)、ウォレストナイト(W
n)、ゾノトライト、アラミド繊維(Af)を適宜量配
合してなる本発明の各試験片A,B,C,D,E,F,
G,H,Iと、四フッ化エチレン樹脂(PTFE)、全
芳香族ポリエステル(LCP)、ポリフェニレンサルフ
ァイド(PPS)、ガラス繊維(GF)、グラファイト
(Gr)、二硫化モリブデン(MoS2 )を適宜量配合
してなる従来品の各試験片J,K,L,Mとを、上述し
た鈴木式摩擦摩耗スラスト試験機2により同一の試験条
件で試験する。
As a comparative example of the above-mentioned sliding composition 1,
For example, tetrafluoroethylene resin (PTFE), polyether sulfone (PES), carbon powder (C), graphite (Gr), molybdenum disulfide (MoS2), plate-like potassium titanate (PTW), wallestnite (W).
n), xonotlite, and aramid fiber (Af) are mixed in appropriate amounts. Each test piece A, B, C, D, E, F of the present invention,
G, H, I and tetrafluoroethylene resin (PTFE), wholly aromatic polyester (LCP), polyphenylene sulfide (PPS), glass fiber (GF), graphite (Gr), molybdenum disulfide (MoS2) in appropriate amounts. Each of the conventional test pieces J, K, L, and M prepared by blending is tested under the same test conditions by the above-mentioned Suzuki type friction and wear thrust tester 2.

【0018】下記の表1は、本発明の各試験片A〜I
と、従来品の各試験片J〜Mとの配合量を示す。
Table 1 below shows the test pieces A to I of the present invention.
And the amount of each conventional test piece J to M mixed.

【0019】[0019]

【表1】 [Table 1]

【0020】上述した各試験片A〜Mを同一条件で試験
する場合、空気中に於いて、試験温度を室温(約25
℃)に設定し、相手材質をS45Cに設定し、試験時間
を初期摺動0Hr〜4Hrに設定し、常時摺動4Hr〜20Hr
に設定し、且つ、試験面圧Pと、試験速度Vと、PV値
とを後述する試験条件に設定して各試験片A〜Mを夫々
試験する。
When the above-mentioned test pieces A to M are tested under the same conditions, the test temperature in air is room temperature (about 25
℃), the mating material is set to S45C, the test time is set to initial sliding 0Hr to 4Hr, and normal sliding 4Hr to 20Hr
And the test surface pressure P, the test speed V, and the PV value are set to the test conditions described later, and each of the test pieces A to M is tested.

【0021】第1の試験条件として、試験面圧Pを0.
29MPa.m/sec (3kgf/cm2 )に設定し、試験速度Vを
1m/sec (100cm/sec)に設定し、PV値を0.29
MPa.m/sec (300kgf/cm2 ・cm/sec)に設定する。第
2の試験条件として、試験面圧Pを0.59MPa.m/sec
(6kgf/cm2 )に設定し、試験速度Vを1m/sec (10
0cm/sec)に設定し、PV値を0.59MPa.m/sec (6
00kgf/cm2 ・cm/sec)に設定する。
As a first test condition, a test surface pressure P of 0.
29MPa.m / sec (3kgf / cm 2 ), test speed V 1m / sec (100cm / sec), PV value 0.29
Set to MPa.m / sec (300 kgf / cm 2 · cm / sec). As the second test condition, the test surface pressure P is 0.59 MPa.m / sec
(6 kgf / cm 2 ) and the test speed V is 1 m / sec (10
0cm / sec) and PV value is 0.59MPa.m / sec (6
00kgf / cm 2 · cm / sec).

【0022】第3の試験条件として、試験面圧Pを0.
98MPa.m/sec (10kgf/cm2 )に設定し、試験速度V
を1m/sec (100cm/sec)に設定し、PV値を0.9
8MPa.m/sec (1000kgf/cm2 ・cm/sec)に設定す
る。下記の表2は、上記条件で本発明の各試験片A〜I
と、従来品の各試験片J〜Mとを試験した結果を示す。
As the third test condition, the test surface pressure P is 0.
Set to 98MPa.m / sec (10kgf / cm 2 ) and test speed V
Is set to 1 m / sec (100 cm / sec) and PV value is set to 0.9
Set to 8MPa.m / sec (1000kgf / cm 2 · cm / sec). Table 2 below shows the test pieces A to I of the present invention under the above conditions.
And the test results of the conventional test pieces J to M are shown.

【0023】[0023]

【表2】 [Table 2]

【0024】上記の表2に記述した摩耗係数Kを測定す
る場合、試験開始前と試験終了後とに於いて各試験片A
〜Mの重量を化学天秤で計量し、その摩耗重量Mから摩
耗高さWを下記の数1で求める。
When measuring the wear coefficient K described in Table 2 above, each test piece A was measured before the start of the test and after the end of the test.
The weights up to M are weighed with an analytical balance, and the wear height W is calculated from the wear weight M by the following formula 1.

【0025】[0025]

【数1】 [Equation 1]

【0026】さらに、ここで求めた摩耗高さWと、試験
面圧Pと、試験速度Vと、試験時間Hとから摩耗係数K
を下記の数2で求める。
Further, the wear coefficient K is calculated from the wear height W, the test surface pressure P, the test speed V, and the test time H obtained here.
Is calculated by the following formula 2.

【0027】[0027]

【数2】 [Equation 2]

【0028】上記の試験結果で明らかなように、本発明
の各試験片A〜Iと、従来品の各試験片J〜Mとの摩擦
係数には大きな差が認められないが、図3に示すよう
に、従来品の各試験片J〜Mに比べて、本発明の各試験
片A〜Iの方が摩耗係数が小さく、PV値が高くなるほ
ど本発明の各試験片A〜Iと従来品の各試験片J〜Mと
の差が大きくなるため、耐摩耗性に優れていることが証
明される。且つ、摩耗係数が安定しているため、機械的
強度にも優れている。
As is clear from the above test results, there is no significant difference in the friction coefficient between the test pieces A to I of the present invention and the test pieces J to M of the conventional product. As shown, as compared with the conventional test pieces J to M, the test pieces A to I of the present invention have a smaller wear coefficient and the higher the PV value, the test pieces A to I of the present invention and the conventional test pieces A to I. Since the difference between each of the test pieces J to M of the product becomes large, it is proved that the wear resistance is excellent. Moreover, since the wear coefficient is stable, the mechanical strength is also excellent.

【0029】以上のように、摺動性組成物1を構成する
ベースレジンとして四フッ化エチレン樹脂とポリエーテ
ルスルホンとを適宜量配合し、そのベースレジンに充填
される潤滑性充填材としてカーボン粉末、グラファイ
ト、二硫化モリブデンの一種又は複数種を適宜量配合
し、耐摩耗性充填材としてチタン酸カリウム、ウォレス
トナイト、ゾノトライト、アラミド繊維の一種を適宜量
配合しているので、表2に示すように、従来品の各試験
片J〜Mに比べて、本発明の各試験片A〜Iの方が摩擦
係数及び摩耗係数が小さく、摺動性が安定しているた
め、耐摩耗性及び機械的強度が格段に向上し、長期間に
於いて優れたシール性を得ることができる。しかも、相
手材4に与える損傷が少なく、耐摩耗性に優れているた
め、寿命が大幅に延長されると共に、交換回数を削減し
て、コストの低減を図ることができる。
As described above, tetrafluoroethylene resin and polyether sulfone are appropriately mixed as the base resin constituting the slidable composition 1, and carbon powder is used as the lubricating filler to be filled in the base resin. , Graphite, and molybdenum disulfide are mixed in appropriate amounts, and as the wear-resistant filler, potassium titanate, wallestonite, zonotolite, and aramid fiber are appropriately mixed in appropriate amounts. In comparison with the conventional test pieces J to M, each of the test pieces A to I of the present invention has a smaller friction coefficient and wear coefficient and more stable slidability. The mechanical strength is remarkably improved, and excellent sealability can be obtained for a long period of time. Moreover, since the damage to the mating member 4 is small and the wear resistance is excellent, the life can be greatly extended, the number of replacements can be reduced, and the cost can be reduced.

【0030】なお、この発明は、上述の実施例の構成の
みに限定されるものではない。上述した四フッ化エチレ
ン樹脂、ポリエーテルスルホン、カーボン粉末、グラフ
ァイト、二硫化モリブデン、板状のチタン酸カリウム、
ウォレストナイト、ゾノトライト、アラミド繊維とを予
め設定した範囲内で増量配合及び減量配合し、その使用
目的及び使用条件に応じた各配合量に増減調整して上述
した摺動性組成物1を成形するもよい。
The present invention is not limited to the configuration of the above embodiment. The above-mentioned tetrafluoroethylene resin, polyether sulfone, carbon powder, graphite, molybdenum disulfide, plate-like potassium titanate,
Walletite, xonotlite, and aramid fiber are compounded in an increasing amount and a decreasing amount within a preset range, and the above-mentioned slidable composition 1 is molded by increasing or decreasing each compounding amount according to the purpose of use and use conditions. Good.

【図面の簡単な説明】[Brief description of drawings]

【図1】摺動性組成物の試験形状を示す斜視図。FIG. 1 is a perspective view showing a test shape of a slidable composition.

【図2】鈴木式摩擦摩耗スラスト試験機による摺動性組
成物の試験方法を示す側面図。
FIG. 2 is a side view showing a method for testing a slidable composition by a Suzuki type friction and wear thrust tester.

【図3】試験片のPV値と摩耗係数との関係を示す特性
図。
FIG. 3 is a characteristic diagram showing a relationship between a PV value of a test piece and a wear coefficient.

【符号の説明】[Explanation of symbols]

1…摺動性組成物 2…スラスト試験機 3…回転台 4…相手材 5…熱電対 1 ... Sliding composition 2 ... Thrust tester 3 ... Rotating table 4 ... Counterpart material 5 ... Thermocouple

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 庁内整理番号 FI 技術表示箇所 C08K 7/02 KJN C08L 81/06 LRF F16C 33/24 A 7123−3J F16J 9/28 ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 6 Identification code Internal reference number FI Technical display area C08K 7/02 KJN C08L 81/06 LRF F16C 33/24 A 7123-3J F16J 9/28

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】組成物を構成するベースレジンとして四フ
ッ化エチレン樹脂を50wt%〜85wt%配合し、ポリエ
ーテルスルホンを5wt%〜50wt%配合すると共に、上
記ベースレジンに充填される潤滑性充填材として、カー
ボン、グラファイト、二硫化モリブデンの何れか一種又
は複数種を2wt%〜15wt%配合し、上記ベースレジン
に充填される耐摩耗性充填材として、チタン酸カリウ
ム、ウォレストナイト、ゾノトライト、アラミド繊維の
何れか一種を5wt%〜30wt%配合した摺動性組成物。
1. A base resin constituting a composition, which is blended with 50 wt% to 85 wt% of tetrafluoroethylene resin and 5 wt% to 50 wt% of polyether sulfone, and which is a lubricating filler to be filled in the base resin. 2 wt% to 15 wt% of carbon, graphite, or molybdenum disulfide is blended as a material, and potassium titanate, wallestonite, xonotlite, aramid is used as an abrasion resistant filler to be filled in the base resin. A slidable composition containing 5 wt% to 30 wt% of any one of the fibers.
JP6142265A 1994-05-31 1994-05-31 Sliding composition Expired - Fee Related JP2851532B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP6142265A JP2851532B2 (en) 1994-05-31 1994-05-31 Sliding composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP6142265A JP2851532B2 (en) 1994-05-31 1994-05-31 Sliding composition

Publications (2)

Publication Number Publication Date
JPH07331011A true JPH07331011A (en) 1995-12-19
JP2851532B2 JP2851532B2 (en) 1999-01-27

Family

ID=15311329

Family Applications (1)

Application Number Title Priority Date Filing Date
JP6142265A Expired - Fee Related JP2851532B2 (en) 1994-05-31 1994-05-31 Sliding composition

Country Status (1)

Country Link
JP (1) JP2851532B2 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007032800A (en) * 2005-07-29 2007-02-08 Tenryu Kagaku Kogyo Kk Plunger for viscous fluid container and auxiliary tool for fitting it
WO2014192947A1 (en) * 2013-05-31 2014-12-04 三菱電線工業株式会社 Resin composition and seal member using same

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6038465A (en) * 1983-08-11 1985-02-28 Sumitomo Chem Co Ltd Resin composition
JPS62146944A (en) * 1985-12-20 1987-06-30 Taiho Kogyo Co Ltd Sliding material
JPS6449716A (en) * 1987-08-18 1989-02-27 Nat Aerospace Lab Retainer for roller bearing
JPH03239756A (en) * 1990-02-19 1991-10-25 Sutaaraito Kogyo Kk Composition for sliding member

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6038465A (en) * 1983-08-11 1985-02-28 Sumitomo Chem Co Ltd Resin composition
JPS62146944A (en) * 1985-12-20 1987-06-30 Taiho Kogyo Co Ltd Sliding material
JPS6449716A (en) * 1987-08-18 1989-02-27 Nat Aerospace Lab Retainer for roller bearing
JPH03239756A (en) * 1990-02-19 1991-10-25 Sutaaraito Kogyo Kk Composition for sliding member

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007032800A (en) * 2005-07-29 2007-02-08 Tenryu Kagaku Kogyo Kk Plunger for viscous fluid container and auxiliary tool for fitting it
WO2014192947A1 (en) * 2013-05-31 2014-12-04 三菱電線工業株式会社 Resin composition and seal member using same
JP2014234442A (en) * 2013-05-31 2014-12-15 三菱電線工業株式会社 Resin composition and seal member using the same
US10189992B2 (en) 2013-05-31 2019-01-29 Mitsubishi Cable Industries, Ltd. Resin composition and seal member using same

Also Published As

Publication number Publication date
JP2851532B2 (en) 1999-01-27

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