JP2766703B2 - Seal part material for scroll compressor - Google Patents

Seal part material for scroll compressor

Info

Publication number
JP2766703B2
JP2766703B2 JP2075170A JP7517090A JP2766703B2 JP 2766703 B2 JP2766703 B2 JP 2766703B2 JP 2075170 A JP2075170 A JP 2075170A JP 7517090 A JP7517090 A JP 7517090A JP 2766703 B2 JP2766703 B2 JP 2766703B2
Authority
JP
Japan
Prior art keywords
weight
resin
pps
scroll
organic 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.)
Expired - Lifetime
Application number
JP2075170A
Other languages
Japanese (ja)
Other versions
JPH03273083A (en
Inventor
雅史 渡辺
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.)
ENU TEI ENU KK
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ENU TEI ENU KK
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Filing date
Publication date
Application filed by ENU TEI ENU KK filed Critical ENU TEI ENU KK
Priority to JP2075170A priority Critical patent/JP2766703B2/en
Publication of JPH03273083A publication Critical patent/JPH03273083A/en
Application granted granted Critical
Publication of JP2766703B2 publication Critical patent/JP2766703B2/en
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Expired - Lifetime legal-status Critical Current

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Classifications

    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F04POSITIVE - DISPLACEMENT MACHINES FOR LIQUIDS; PUMPS FOR LIQUIDS OR ELASTIC FLUIDS
    • F04CROTARY-PISTON, OR OSCILLATING-PISTON, POSITIVE-DISPLACEMENT MACHINES FOR LIQUIDS; ROTARY-PISTON, OR OSCILLATING-PISTON, POSITIVE-DISPLACEMENT PUMPS
    • F04C27/00Sealing arrangements in rotary-piston pumps specially adapted for elastic fluids
    • F04C27/005Axial sealings for working fluid

Landscapes

  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • General Engineering & Computer Science (AREA)
  • Rotary Pumps (AREA)
  • Sealing Devices (AREA)
  • Sealing Material Composition (AREA)

Description

【発明の詳細な説明】 〔産業上の利用分野〕 この発明はスクロール型コンプレッサー用のシール部
材料に関する。
The present invention relates to a seal material for a scroll compressor.

〔従来の技術〕[Conventional technology]

一般に、スクロール型コンプレッサーは、基板の片面
にうず巻壁を形成した一対のスクロール部材を設け、各
スクロール部材のうず巻壁相互を偏心状態にかみ合わ
せ、相対的な公転運動を行なわせることによって、うず
巻壁間の密閉空間を中心方向に移動させながら流体を圧
縮し、これを中心部から吐出するようにしたものであ
り、たとえば特開昭50−32512号公報、同55−81296号公
報等によって既によく知られているものである。
Generally, a scroll-type compressor is provided with a pair of scroll members each having a spiral wall formed on one surface of a substrate, and by engaging the spiral walls of each scroll member with each other in an eccentric state to perform a relative orbital motion. The fluid is compressed while moving the closed space between the winding walls in the center direction, and the fluid is discharged from the central portion. For example, Japanese Patent Application Laid-Open Nos. 50-32512 and 55-81296 disclose the method. It is already well known.

第1図および第2図は従来公知のスクロール部材1を
示すものであり、そのうず巻壁2の先端部には溝3が形
成され、その溝3にシール部材料4が装着されている。
また第3図は上記スクロール部材1を可動側とし、固定
スクロール部材1′と偏心させてかみ合わせた状態を示
しており、両方のうず巻壁2の各シール部材料4を相互
に他のスクロール部材1、1′のうず巻溝の底に摺接さ
せ、相互にシールを図るようになっている。
FIG. 1 and FIG. 2 show a conventional scroll member 1 in which a groove 3 is formed at the tip of a spiral wall 2 and a seal material 4 is mounted in the groove 3.
FIG. 3 shows a state in which the scroll member 1 is movable and the fixed scroll member 1 'is eccentrically engaged with each other. 1, 1 'are brought into sliding contact with the bottom of the spiral groove to seal each other.

上記のようなスクロール型コンプレッサーにおいて
は、最近その軽量化を図るためにスクロール部材1をア
ルミニウムまたはアルミニウム合金のような軽金属類で
製作するようになり、また、コンプレッサー本体を一層
小型化するために、スクロール部材1、1′のうず巻溝
の幅および溝深さも精密に成形するようになってきた。
In the scroll type compressor as described above, the scroll member 1 has recently been made of a light metal such as aluminum or an aluminum alloy in order to reduce its weight, and in order to further reduce the size of the compressor body, The width and depth of the spiral grooves of the scroll members 1, 1 'have also been precisely formed.

シール部材料4としては、従来、四フッ化エチレン樹
脂(以下、PTFEと略称する)が用いられており、この材
料は、耐熱性、耐薬品性、難燃性、自己潤滑性、非粘着
性、低摩擦係数など優れた性能を有するが、耐摩耗性、
耐クリープ性は必ずしも満足できるものではなかった。
Conventionally, a tetrafluoroethylene resin (hereinafter abbreviated as PTFE) has been used as the seal material 4, and this material is heat-resistant, chemical-resistant, flame-retardant, self-lubricating, and non-adhesive. , Has excellent performance such as low friction coefficient,
Creep resistance was not always satisfactory.

そこで、この出願人らは、特願昭60−254481号におい
てPTFEに有機系充填剤(たとえばポリフェニレンサルフ
ァイド、ポリイミド、芳香族系ポリエステル、芳香族系
ポリアミド、ポリアミド、ポリエーテルケトン等)およ
び射出成形可能なフッ素樹脂粉末を添加混合したシール
部材料を開示した。
Thus, the applicants have disclosed in Japanese Patent Application No. 60-254481 that PTFE and an organic filler (eg, polyphenylene sulfide, polyimide, aromatic polyester, aromatic polyamide, polyamide, polyether ketone, etc.) and injection molding can be used. A material for a seal portion in which a suitable fluororesin powder is added and mixed is disclosed.

しかし、上記組成物からなるシール部材料は、射出成
形が不可能であって生産性が劣り、当然のことながら製
品コストも高くなって好ましくないという問題を有する
ものであった。
However, the seal material made of the above composition has a problem that injection molding is not possible, productivity is poor, and of course, the product cost is high, which is not preferable.

上記の問題を解決するため、この出願人は、特願昭61
−305064号において、芳香族ポリエーテルケトン樹脂に
フルオロカーボン重合体、炭素繊維および金属粉末を添
加したシール部材料を開示した。
In order to solve the above problem, the applicant has filed Japanese Patent Application No.
Japanese Patent No. -305064 discloses a seal material in which a fluorocarbon polymer, carbon fiber and metal powder are added to an aromatic polyetherketone resin.

しかし、このシール部材料においても、高荷重下にお
ける摺動特性、機械的強度が劣り、相手材に傷を付けた
り、長時間摺動したとき耐摩耗性が低下し、かつ、コン
プレッサーの小型化に伴う精密な射出成形を対応できな
いという問題点を有するものであった。
However, even with this seal material, the sliding characteristics and mechanical strength under high load are inferior, the mating material is damaged, the abrasion resistance is reduced when sliding for a long time, and the compressor is downsized. However, there is a problem that precise injection molding cannot be dealt with.

〔発明が解決しようとする課題〕[Problems to be solved by the invention]

この発明の課題は、上記したように従来のシール部材
の高荷重下の摺動特性や機械的強度が劣る点、相手材に
傷を付け易く、摺動時の耐摩耗性および射出成形性が劣
る点を改善し、高荷重下でも摺動特性が良く、機械的強
度に優れ、相手材に損傷を与えず摺動時の耐摩耗性およ
び精密な射出成形がし易いシール部材料とすることにあ
る。
The object of the present invention is that the conventional sealing member has poor sliding characteristics under high load and poor mechanical strength as described above, easily damages a mating material, and has abrasion resistance and injection moldability during sliding. Improve the inferior point, and have good sliding characteristics even under high load, excellent mechanical strength, abrasion resistance during sliding without damaging the mating material, and a seal material that is easy to perform precise injection molding. It is in.

〔課題を解決するための手段〕[Means for solving the problem]

上記の課題を解決するため、この発明においては、ポ
リフェニレンサルファイド樹脂35〜80重量%に、フルオ
ロカーボン重合体10〜35重量%、ピッチ系炭素繊維5〜
15重量%および前記ポリフェニレサルファイド樹脂の溶
融成形温度で固体状を保つ有機粉末5〜15重量%を添加
した手段を採用したものである。以下その詳細を述べ
る。
In order to solve the above problems, in the present invention, the polyphenylene sulfide resin is 35 to 80% by weight, the fluorocarbon polymer 10 to 35% by weight, the pitch-based carbon fiber 5 to 5%.
A means is employed in which 15% by weight and 5 to 15% by weight of an organic powder which maintains a solid state at the melt molding temperature of the polyphenylene sulfide resin are added. The details are described below.

まず、この発明に使用されるポリフェニレンサルファ
イド樹脂(以下、PPSと略称する)は、一般式 Ph−S で示される合成樹脂である。ここで式中−Ph−は、 QはF、Cl、BrのハロゲンもしくはCH3であり、mは1
〜4の整数を示す。これらのうち、特に典型的なものは で示されるものであり、米国フィリップス・ペトローリ
アム社から「ライトン」の商標で市販され、その製造方
法は、米国特許第3,354,129号(対応特許公昭45−3368
号)に開示されている。それによると、ライトンは、N
−メチルピロリドン溶媒中、160〜250℃、加圧条件下に
P−ジクロルベンゼンと、二硫化ソーダと反応させるこ
とによって製造され、樹脂中に交差結合が全くないもの
から部分的な交差結合を有するものに至るまで、各種重
合度のものを後熱処理工程にかけて自由に製造すること
ができるので、目的の溶媒ブレンドに適正な溶媒粘度特
性を有するものを任意に選択使用することが可能であ
る。また、架橋構造をとらず直鎖状のものも使用でき
る。
First, polyphenylene sulfide resin used in the present invention (hereinafter abbreviated as PPS) is a synthetic resin represented by the general formula Ph-S n. Where -Ph- is Q is a halogen of F, Cl, Br or CH 3 , and m is 1
Shows an integer of ~ 4. Of these, the most typical ones are Which is commercially available from Philips Petroleum Corp. under the trademark "Ryton" and is manufactured according to U.S. Pat. No. 3,354,129 (corresponding to Japanese Patent Publication No. 45-3368).
No.). Ryton states that N
It is produced by reacting P-dichlorobenzene with sodium disulfide in a methylpyrrolidone solvent at 160 to 250 ° C. under a pressurized condition, and partially cross-links from those having no cross-links in the resin. Since it is possible to freely produce those having various degrees of polymerization through post-heat treatment steps, it is possible to arbitrarily select and use those having a proper solvent viscosity characteristic for the target solvent blend. In addition, a linear one without a crosslinked structure can be used.

つぎに、この発明におけるフルオロカーボン重合体は
ポリテトラフルオロエチレン、ポリテトラフルオロエチ
レン・ヘキサフルオロプロピレン共重合体、ポリトリク
ロロフルオロエチレン、テトラフルオロエチレン・パー
フルオロアルキルビニルエーテル共重合体などを含む
が、特に前記のPTFEが好ましい。また、PTFEでも平均粒
系20μm未満の滑剤級の粉末が好ましく、市販されてい
るものの例としては、米国アイ・シー・アイ社のフルオ
ン(商標)L169、L170、同L171、ダイキン工業社のルブ
ロン(商標)L−2、同L−5、同L−D−1、米国デ
ュポン社のテフロン(商標)TLP−10、同TLP−10F−1
などが挙げることができる。
Next, the fluorocarbon polymer in the present invention includes polytetrafluoroethylene, polytetrafluoroethylene / hexafluoropropylene copolymer, polytrichlorofluoroethylene, tetrafluoroethylene / perfluoroalkylvinyl ether copolymer, and the like. PTFE is preferred. Lubricant-grade powder having an average particle size of less than 20 μm is also preferable for PTFE. Examples of commercially available powders include Fluon (trademark) L169, L170, L171, and L171 from ICI, USA, and Lubron from Daikin Industries, Ltd. (Trademark) L-2, L-5, LD-1, Teflon (trademark) TLP-10, TLP-10F-1 of DuPont, USA
And the like.

さらに、この発明で使用する炭素繊維としてはピッチ
系のものを用いる。なぜなら、ピッチ系の炭素繊維を用
いると、摺動相手材の摩耗を少なくすることができるか
らであり、PAN系の炭素繊維を用いるとシール特性や流
れ性に劣ることが判明している。さらに溶融成形時の流
動性を保つために、ピッチ系炭素繊維の長さは1mm以下
が望ましい。この炭素繊維は表面をたとえばエポキシ樹
脂、ポリアミド樹脂、ポリカーボネート樹脂、ポリアセ
タール樹脂等の処理剤で処理したものを用いることが好
ましいが、これらに限定されるものではない。このよう
な炭素繊維としては、呉羽化学工業社製クレカM、クレ
カCなどを挙げることができる。
Further, pitch-based carbon fibers are used as the carbon fibers used in the present invention. This is because the use of pitch-based carbon fibers can reduce the wear of a sliding partner material, and it has been found that the use of PAN-based carbon fibers is inferior in sealing properties and flowability. Further, in order to maintain fluidity during melt molding, the length of the pitch-based carbon fiber is desirably 1 mm or less. It is preferable to use a carbon fiber whose surface is treated with a treating agent such as an epoxy resin, a polyamide resin, a polycarbonate resin, and a polyacetal resin, but the carbon fiber is not limited to these. Examples of such carbon fibers include Kureka M and Kureka C manufactured by Kureha Chemical Industry Co., Ltd.

また、この発明で使用する前記PPSの溶融成形温度で
固体状を保つ有機粉末とは、芳香族ポリエステル、芳香
族ポリアミド、ポリイミド、ポリアミドイミド、ポリエ
ーテルエーテルケトン、熱不融性粒状フェノールなどか
ら選ばれた単独または2種以上の混合物からなる有機粉
末であって、たとえば一般的なPPSの溶融成形の温度で
ある300〜350℃で固体状を保つ有機粉末である。
Further, the organic powder that maintains a solid state at the melt molding temperature of the PPS used in the present invention is selected from aromatic polyesters, aromatic polyamides, polyimides, polyamideimides, polyetheretherketones, heat-infusible granular phenols, and the like. Organic powder comprising a single or a mixture of two or more of them, for example, an organic powder that maintains a solid state at a general PPS melt molding temperature of 300 to 350 ° C.

以上のPPS、フルオロカーボン重合体、ピッチ系炭素
繊維および前記PPSの溶融成形温度で固体状を保つ有機
粉末を配合するには、PPS35〜80重量%、フルオロカー
ボン重合体10〜35重量%、ピッチ系炭素繊維5〜15重量
%、有機粉末5〜15重量%とする。なぜならPPSの量が3
5重量%未満の少量のときは、樹脂組成物の流動性が失
われ、たとえ射出成形によって、成形品が得られてもそ
の機械的強度は非常に低く脆いものとなり、フルオロカ
ーボン重合体が10重量%未満の少量では潤滑性が不充分
であり、逆に35重量%を越える多量では機械的強度が低
下するからである。ピッチ系炭素繊維は、5重量%未満
の少量では機械的強度が不充分であり、逆に15重量%を
越える多量では軟質の相手剤を損耗して良好なシール特
性が得られず、かつ流れ性も悪くなる。PPSの溶融成形
温度で固体状を保つ単独または2種以上の混合物からな
る有機粉末においては、5重量%未満の少量のときは、
溶融成形時に良好な流れ性がなく、逆に15重量%を越え
る多量でも前記流れ性は悪くなる。
To mix the PPS, fluorocarbon polymer, pitch-based carbon fiber, and organic powder that maintains a solid state at the melting temperature of the PPS, 35 to 80% by weight of PPS, 10 to 35% by weight of fluorocarbon polymer, 5 to 15% by weight of fiber and 5 to 15% by weight of organic powder. Because the amount of PPS is 3
When the amount is less than 5% by weight, the fluidity of the resin composition is lost, and even if a molded article is obtained by injection molding, its mechanical strength becomes very low and brittle, and the fluorocarbon polymer becomes 10% by weight. If the amount is less than 35% by weight, the lubricating property is insufficient, and if the amount exceeds 35% by weight, the mechanical strength decreases. If the pitch-based carbon fiber is less than 5% by weight, the mechanical strength is insufficient. On the other hand, if it is more than 15% by weight, the soft mating agent is worn away, and good sealing properties cannot be obtained. Also worse. In the case of an organic powder consisting of a single or a mixture of two or more kinds that maintains a solid state at the melt molding temperature of PPS, when the amount is less than 5% by weight,
There is no good flowability at the time of melt molding, and conversely, even at a large amount exceeding 15% by weight, the flowability deteriorates.

これらの諸原料の混合は、ヘンシェルミキサーなどを
用いたドライブレンドやブラベンダ、押出機を用いた溶
融混合など公知の手段で行なうことができる。
Mixing of these various materials can be performed by known means such as dry blending using a Henschel mixer or the like, melt mixing using a brabender, or an extruder.

〔実施例〕〔Example〕

樹脂および比較例に使用した原材料を一括して示すと
つぎのとおりである。すなわち、 PPS(米国フィリプスペトローリアム社製:ライトン
P−4) フルオロカーボン重合体(ダイキン工業社製:ルブロ
ンL−5)[PTFEと称する] ピッチ系炭素繊維(呉羽化学社製:クレハM207S繊維
長12〜13μm) PAN系炭素繊維(東邦レーヨン社製:ベスファイトHTA
−C6−E,繊維長7〜8μm) オキシベンゾイルポリエステル(住友化学社製:エコ
ノールE101M) 二硫化モリブデン(ダウ・コーニング社製:モリコー
トZ) ポリエチレン(三井石油化学社製:ハイゼックスミリ
オン240S) ポリイミド(宇部興産社製:ポリイミド粉末Rタイ
プ) ポリエーテルエーテルケトン(英国アイ・シー・アイ
社製:Udel−PEEK 150P)[PEEK] ポリアミド(米国アモコ社製:TORON4000[PAI] ポリエーテルイミド(米国ゼネラルエレクトリック社
製:ULTEM1000[PEI] 実施例1〜9 上記の諸原材料〜を第1表に示す割合で配合し、
ヘンシェルミキサーで充分混合した後、二軸溶融押出機
(池具鉄工社製:PCM−30型)に供給し、温度320℃、ス
クリュー回転数50rpm、径2mm孔7個のストランドダイか
ら押出してペレット状に造粒した。このペレットをバレ
ル温度300〜330℃で金型温度140℃、射出圧力1000kg/cm
2の射出成形機にかけて所定の試験片を作製し、得られ
た試験片の曲げ強度kg/cm2はASTM−D790にまたアイゾッ
ト衝撃強度kg・cm/cmはASTM−D256に基づき、また摩擦
係数は鈴木・松原式摩擦摩耗試験機を用いた内径17mm、
外径21mm、長さ10mmのリング試片の圧力10kg/cm2、速度
毎分10mの条件下における値を、さらに限界PV値kg/cm2
・m/分は前記鈴木・松原式摩擦摩耗試験機および同寸法
のリング試片を用い速度Vを毎分308mに一定とし、スニ
ソ4GSオイル中において圧力PをPVが5000、6000、7000
……kg/cm2・m/分と5分間に1000ずつ増加するように上
昇させながら、試片が溶融を伴った異常摩耗を起こし始
めるか、または摩擦係数が急激に不安定となるときのPV
値を、そして実機耐熱性は第1図に示すシール部材料4
(半径2mmの円の伸開曲線で幅1.5m、厚さ1.5mm、展開長
さ300mm)を成形し、回転数毎分5500回転、雰囲気フレ
オンガス5容量%+オイル95容量%、温度300℃以上、
運転時間10時間の条件下の試験中にシール部材料4が溶
融を伴った異常摩耗を起こすか摩耗係数が急激に不安定
になった時間をもってそれぞれ評価した。
The raw materials used for the resin and the comparative examples are collectively shown as follows. That is, PPS (manufactured by Phillips Petroleum Corporation, USA: Ryton P-4) fluorocarbon polymer (manufactured by Daikin Industries, Ltd .: Lubron L-5) [referred to as PTFE] Pitch-based carbon fiber (manufactured by Kureha Chemical Company: Kureha M207S fiber length) PAN-based carbon fiber (Toho Rayon Co., Ltd .: Vesfight HTA)
-C6-E, fiber length 7 to 8 µm) Oxybenzoyl polyester (Sumitomo Chemical Co., Ltd .: Econol E101M) Molybdenum disulfide (Dow Corning Co., Ltd .: Molycoat Z) Polyethylene (Mitsui Petrochemical Co., Ltd .: Hi-Zex Million 240S) Polyimide ( Ube Industries, Ltd .: Polyimide powder R type Polyetheretherketone (ICI, UK: Udel-PEEK 150P) [PEEK] Polyamide (Amoco, USA: TORON4000 [PAI] Polyetherimide (General Electric, USA) Company: ULTEM1000 [PEI] Examples 1 to 9 The above various raw materials are blended in the proportions shown in Table 1,
After thoroughly mixing with a Henschel mixer, the mixture is fed to a twin-screw extruder (PCM-30, manufactured by Ikegi Tekko Co., Ltd.), and is extruded from a strand die having a temperature of 320 ° C., a screw rotation speed of 50 rpm, and 7 holes of 2 mm in diameter and pellets. And granulated. The pellets are heated at a barrel temperature of 300 to 330 ° C, a mold temperature of 140 ° C, and an injection pressure of 1000 kg / cm.
A predetermined test piece was produced by using an injection molding machine of No. 2 and the bending strength kg / cm 2 of the obtained test piece was based on ASTM-D790 and the Izod impact strength kg / cm / cm was based on ASTM-D256, and the coefficient of friction was Is 17mm inside diameter using Suzuki / Matsubara friction and wear tester,
The value under the conditions of an outer diameter of 21 mm, a ring specimen having a length of 10 mm, a pressure of 10 kg / cm 2 , and a speed of 10 m per minute is further increased to a limit PV value kg / cm 2
・ The m / min was set at a constant speed V of 308 m / min using the Suzuki-Matsubara friction wear tester and a ring specimen of the same size, and the pressure P was adjusted to 5000, 6000, and 7000 in Suniso 4GS oil.
…… When the specimen starts to undergo abnormal wear accompanied by melting or the coefficient of friction becomes suddenly unstable while increasing in increments of 1000 kg / cm 2 · m / min in 5 minutes. PV
Values and the actual heat resistance are shown in FIG.
(The expansion curve of a circle with a radius of 2 mm is 1.5 m in width, 1.5 mm in thickness, and deployment length is 300 mm). ,
During the test under the conditions of the operation time of 10 hours, the evaluation was made based on the time when the seal portion material 4 caused abnormal wear accompanied by melting or the wear coefficient became rapidly unstable.

次に、相手材損傷度は、上記実機耐熱性試験におい
て、運転時間10時間後の相手摺動部(アルミニウム製)
の損傷深さが0〜5μmのとき◎印、5〜10μmのとき
○印、10〜15μmのとき△印、15μmを越えるとき×印
として四段階に評価した。また、射出成形性は、第1図
に示すシール部材料の形状(半径mmの円の伸開曲線)で
幅1.5mm、厚さ1.5mm展開長さ400mmの射出成形用金型を
作成し、その樹脂注入口(ゲート口)を外側末端部に設
け、バレル温度300〜330℃、金型温度140℃、射出圧力1
000kg/cm2の射出条件で整形した時、樹脂の流れ得る長
さが200〜250mmのとき×印、250〜300mmのとき△印、30
0〜350mmのとき○印、350〜400mmのとき◎印として四段
階に評価した。得られた各測定値を第2表にまとめた。
Next, in the above-mentioned heat resistance test of the actual machine, the degree of damage of the mating material was determined by the mating sliding portion (made of aluminum) after an operation time of 10 hours.
When the damage depth was 0 to 5 μm, it was evaluated as ◎, when 5 to 10 μm, 10, when 10 to 15 μm, Δ, and when more than 15 μm, ×. Injection moldability was determined by creating an injection mold having a width of 1.5 mm, a thickness of 1.5 mm and a development length of 400 mm in the shape of the seal part material (expansion curve of a circle with a radius of mm) shown in FIG. The resin injection port (gate port) is provided at the outer end, the barrel temperature is 300-330 ° C, the mold temperature is 140 ° C, and the injection pressure is 1
When shaped under injection conditions of 000 kg / cm 2 , the cross mark indicates that the flowable length of the resin is 200 to 250 mm, and the cross mark indicates that the length is 250 to 300 mm.
When 0 to 350 mm, it was evaluated as a circle, and when it was 350 to 400 mm, it was evaluated as a double circle. Table 2 summarizes the obtained measured values.

比較例1〜12: 前記諸原材料〜を第3表に示す割合で配合した以
外は実施例1〜9と全く同様の操作を行なって試験片を
作製しその曲げ強度、アイゾット衝撃強度、摩擦係数、
限界PV値、実機耐久性、相手材損傷度、射出成形性を測
定した。得られた結果は第4表にまとめた。
Comparative Examples 1 to 12: Except that the above-mentioned raw materials were blended in the proportions shown in Table 3, the same operation as in Examples 1 to 9 was carried out to prepare test pieces, and their bending strength, Izod impact strength, and coefficient of friction were prepared. ,
The critical PV value, the durability of the actual machine, the degree of damage to the partner material, and the injection moldability were measured. The results obtained are summarized in Table 4.

第4表中、実機耐久性の欄と相手材損傷度の欄で−表
示のものは、成形性が悪く、所要のチップシールが得ら
れなかったため試験不能を意味する。
In Table 4, those indicated by "-" in the column of the actual machine durability and the column of the damage degree of the mating member mean that the test was impossible because the moldability was poor and a required chip seal was not obtained.

ここで、実施例1〜9と比較例1〜12とを比べると、
実施例1〜9の配合比についてはすべて望ましいと思わ
れる範囲内にあるため機械的特性、潤滑特性、限界PV
値、実機耐久試験、相手材損傷度、射出成形性のすべて
の面において優れている。
Here, comparing Examples 1 to 9 and Comparative Examples 1 to 12,
Since the compounding ratios of Examples 1 to 9 are all within the range considered to be desirable, mechanical properties, lubricating properties, and critical PV
It is excellent in all aspects such as value, actual machine durability test, damage degree of mating material, and injection moldability.

しかし、比較的1〜12については、PPS、フルオロカ
ーボン重合体、ピッチ系炭素繊維、有機粉末の配合比が
一つでも望ましい範囲からはずれることによって、また
炭素繊維がPAN系の場合、あるいはPPSの溶融温度で固体
状を保たない有機粉末または無機物では、実施例で述べ
た特性をすべて満足することは不可能である。たとえ
ば、比較例1、2において有機粉末が15重量%を越える
かまたは5重量%未満の場合は、射出成形性が悪い。比
較例3の場合は、PTFEが10重量%未満であるため摩擦係
数が悪く、比較例4、5は炭素繊維の配合割合が望まし
い範囲外であるため機械的強度や限界PV値は低い。ま
た、比較例7、8では、有機粉末を配合していないため
射出成形性が非常に悪い。比較例6、9は、炭素繊維が
PAN系であると共に、有機粉末の配合割合が15重量%で
あり、相手材の損傷度が悪いか、または流れ性が著しく
劣っていた。さらに、比較例10、11は無機物の二硫化モ
リブデンおよびPPSの溶融成形温度で固体状態を保たな
いポリエチレンを添加したもので流れ性が悪かった。し
たがって、有機粉末はPPSの溶融成形温度で固体状に保
つことが必要で、オキシベンゾイルポリエステルが好ま
しことが明らかとなった。なお、比較例12は、有機粉末
としてポリイミドを用いているが、その配合割合が15重
量%を越えているため、比較例9と同様に流れ性が悪
い。
However, for relatively 1 to 12, the mixing ratio of PPS, fluorocarbon polymer, pitch-based carbon fiber, and organic powder is deviated from the desired range, and if the carbon fiber is PAN-based, or PPS is melted. An organic powder or inorganic substance that does not maintain a solid state at a temperature cannot satisfy all the characteristics described in the examples. For example, in Comparative Examples 1 and 2, when the organic powder exceeds 15% by weight or less than 5% by weight, the injection moldability is poor. In the case of Comparative Example 3, the coefficient of friction was poor because PTFE was less than 10% by weight, and in Comparative Examples 4 and 5, the mechanical strength and the critical PV value were low because the compounding ratio of the carbon fibers was outside the desired range. In Comparative Examples 7 and 8, the injection moldability was very poor because no organic powder was blended. In Comparative Examples 6 and 9, the carbon fibers
In addition to being a PAN type, the compounding ratio of the organic powder was 15% by weight, and the mating material had a poor degree of damage or was extremely poor in flowability. Furthermore, Comparative Examples 10 and 11 were obtained by adding molybdenum disulfide as an inorganic substance and polyethylene which did not maintain a solid state at the melt molding temperature of PPS, and had poor flowability. Therefore, it was necessary to keep the organic powder in a solid state at the melting temperature of PPS, and it became clear that oxybenzoyl polyester was preferred. In Comparative Example 12, polyimide was used as the organic powder, but the mixing ratio exceeded 15% by weight, so that the flowability was poor as in Comparative Example 9.

比較例13〜15: 前記諸原材料〜を第5表に示す割合で配合
した以外は実施例1〜9と全く同様の操作を行なって試
験片を作製し、その射出成形性を調べた。この結果を比
較例〜と全く同様にして評価し、第5表中に併記し
た。
Comparative Examples 13 to 15: Specimens were prepared by exactly the same operations as in Examples 1 to 9 except that the above-mentioned raw materials were blended in the proportions shown in Table 5, and the injection moldability was examined. The results were evaluated in exactly the same manner as in Comparative Examples 1 to 3, and are also shown in Table 5.

第5表の測定結果からも明らかなように、主原料がPP
S以外の樹脂では、他の配合成分及びその割合が適当で
あっても射出成形性に改善がみられなかった。
As is clear from the measurement results in Table 5, the main raw material is PP
For resins other than S, no improvement was observed in injection moldability even when the other components and their proportions were appropriate.

〔効果〕〔effect〕

以上のことから明らかなように、この発明のシール部
材料は、高荷重下における摺動特性、機械的強度、相手
材損傷度などに優れ、かつスクロール型コンプレッサー
の小型化に伴なう精密な射出成形が可能となる流れ性良
好な材料であり、今後のスクロール型コンプレッサーの
仕様に大いに貢献することになる。したがって、この発
明の意義はきわめて大きいということができる。
As is clear from the above, the seal material of the present invention is excellent in sliding characteristics under high load, mechanical strength, damage degree of a mating material, etc., and is precise with the downsizing of the scroll compressor. It is a material with good flowability that enables injection molding, and will greatly contribute to the specifications of future scroll compressors. Therefore, it can be said that the significance of the present invention is extremely large.

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

第1図はスクロール部材の斜視図、第2図は第1図の要
部断面図、第3図はスクロール部材をかみ合わせたコン
プレッサーの内部構造を例示する断面図である。 1、1′……スクロール部材、2……うず巻壁、3……
溝、4……シール部材料。
1 is a perspective view of a scroll member, FIG. 2 is a cross-sectional view of a main part of FIG. 1, and FIG. 3 is a cross-sectional view illustrating an internal structure of a compressor in which a scroll member is engaged. 1, 1 '... scroll member, 2 ... spiral wall, 3 ...
Groove, 4 ... Seal material.

Claims (1)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】ポリフェニレンサルファイド樹脂35〜80重
量%に、フルオロカーボン重合体10〜35重量%、ピッチ
系炭素繊維5〜15重量%および前記ポリフェニレンサル
ファイド樹脂の溶融成形温度で固体状を保つ有機粉末5
〜15重量%を添加したことを特徴とするスクロール型コ
ンプレッサー用シール部材料。
1. A polyphenylene sulfide resin of 35 to 80% by weight, a fluorocarbon polymer of 10 to 35% by weight, a pitch-based carbon fiber of 5 to 15% by weight, and an organic powder 5 which is solid at the melt molding temperature of the polyphenylene sulfide resin.
A scroll material for a scroll type compressor, characterized by adding up to 15% by weight.
JP2075170A 1990-03-22 1990-03-22 Seal part material for scroll compressor Expired - Lifetime JP2766703B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2075170A JP2766703B2 (en) 1990-03-22 1990-03-22 Seal part material for scroll compressor

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2075170A JP2766703B2 (en) 1990-03-22 1990-03-22 Seal part material for scroll compressor

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP6986997A Division JP2942514B2 (en) 1997-03-24 1997-03-24 Method of manufacturing seal for scroll compressor

Publications (2)

Publication Number Publication Date
JPH03273083A JPH03273083A (en) 1991-12-04
JP2766703B2 true JP2766703B2 (en) 1998-06-18

Family

ID=13568459

Family Applications (1)

Application Number Title Priority Date Filing Date
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Country Status (1)

Country Link
JP (1) JP2766703B2 (en)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2866781B2 (en) * 1993-05-31 1999-03-08 大同メタル工業株式会社 Seal part material
JP2835575B2 (en) * 1994-10-25 1998-12-14 大同メタル工業株式会社 Sealing material for scroll compressor
JP3281752B2 (en) * 1995-03-30 2002-05-13 三菱重工業株式会社 Scroll type fluid machine
WO2007082111A1 (en) 2006-01-05 2007-07-19 Saint-Gobain Performance Plastics Corporation Annular seal and pump including same
WO2007082110A1 (en) 2006-01-05 2007-07-19 Saint-Gobain Performance Plastics Corporation Composite material and seals formed thereof
CN102245943A (en) 2008-12-24 2011-11-16 美国圣戈班性能塑料公司 Polymer material and seals formed thereof for high pressure pump applications

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0730747B2 (en) * 1986-03-22 1995-04-10 株式会社豊田自動織機製作所 Scroll type compressor seal member
JPH0769015B2 (en) * 1986-12-18 1995-07-26 エヌティエヌ株式会社 Material of seal part for scroll type compressor

Also Published As

Publication number Publication date
JPH03273083A (en) 1991-12-04

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