JPH0359940B2 - - Google Patents

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Publication number
JPH0359940B2
JPH0359940B2 JP56171506A JP17150681A JPH0359940B2 JP H0359940 B2 JPH0359940 B2 JP H0359940B2 JP 56171506 A JP56171506 A JP 56171506A JP 17150681 A JP17150681 A JP 17150681A JP H0359940 B2 JPH0359940 B2 JP H0359940B2
Authority
JP
Japan
Prior art keywords
carbon fiber
resin
glycerin
weight
pps
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
JP56171506A
Other languages
Japanese (ja)
Other versions
JPS5874751A (en
Inventor
Haruo Watanabe
Motonobu Shibazaki
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.)
Toso Susteel Co Ltd
Original Assignee
Toso Susteel 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 Toso Susteel Co Ltd filed Critical Toso Susteel Co Ltd
Priority to JP17150681A priority Critical patent/JPS5874751A/en
Publication of JPS5874751A publication Critical patent/JPS5874751A/en
Publication of JPH0359940B2 publication Critical patent/JPH0359940B2/ja
Granted legal-status Critical Current

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  • Lubricants (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

本発明はポリフエニレンサルフアイド樹脂、炭
素繊維およびグリセリンの高級脂肪酸エステルの
混合樹脂組成物からなる磁気記録テープ用ポリエ
ステルフイルムとの接触用摺動部材に関するもの
である。 VTRやオーデイオ機器用のカセツトテープは
主にポリエステルフイルムが使用されており、音
質機能性向上化のためにテープ性能面の改良と、
軽量化やテープリール性能面からのケース改良と
が行なわれている。テープ面では特開昭50−
93103、52−73003、52−78953、53−78803、53−
106783、53−113868、53−139511、54−34207、
55−45118、特公昭55−15570等の明細書に見られ
るようにテープの表面粗さもCLA(粗面化された
フイルム粗さ曲線からその中心値の方向に測定長
さL(基準長2mm)の部分を抜き取り、この抜き
取り部分の中心線をX軸、縦倍率の方向をY軸と
して粗さ曲線をY=f(x)で表わしたとき、
CLA=1/L∫L 0|f(x)|dxの式で与えられた値
をμ単位で表わす。この測定を8個のサンプルに
ついて行ない、値の大きい方から3個除外し5個
の平均値で表わす。)値で0.02〜0.03μまで改良さ
れている。 一方、カセツトケースは、ケース内部でテープ
が回転走行するため、プラスチツク成型に際して
高精度の寸法安定性が要求される。通常ケース本
体部にはポリスチレン樹脂やポリメチルメタアク
リレート樹脂等が又、リール本体にはポリアセタ
ール樹脂等が使用されている。しかしながらケー
ス内部におけるテープ走行面との接触摺動部材で
あるガイドローラーピン、ガイドローラー(又は
サイドローラー)は表面仕上げ加工されたステン
レスが使用されているため、ポリエステルフイル
ムが走行接触した時の摩擦係数は0.2〜0.3と大き
くドロツプアウト現象や発音問題を起こす原因と
なつている。このため特殊なグリースを併用して
このドロツプアウト現象と摺動音の発生を防いで
いるのが現状である。 本発明らはポリエステルフイルムとの接触用摺
動部材を種々熱可塑性樹脂について検討した結
果、ポリフエニレンサルフアイド樹脂(以下PPS
と称す)を主成分とし炭素繊維および帯電防止剤
であるグリセリンの高級脂肪酸エステルを混合し
た樹脂組成物が摺動部材として好適であるとの知
見を得た。 ここで使用されるPPS樹脂とは
The present invention relates to a sliding member for contact with a polyester film for magnetic recording tape, which is made of a mixed resin composition of polyphenylene sulfide resin, carbon fiber, and higher fatty acid ester of glycerin. Cassette tapes for VTRs and audio equipment are mainly made of polyester film, and in order to improve sound quality and functionality, tape performance has been improved.
Improvements have been made to the case in terms of weight reduction and tape/reel performance. On the tape side, JP-A-1987-
93103, 52−73003, 52−78953, 53−78803, 53−
106783, 53−113868, 53−139511, 54−34207,
55-45118, Japanese Patent Publication No. 55-15570, etc., the surface roughness of the tape is also CLA (measured length L (reference length 2 mm) from the roughened film roughness curve in the direction of its center value). When the roughness curve is expressed as Y=f(x) with the center line of the extracted portion as the X axis and the vertical magnification direction as the Y axis,
The value given by the formula CLA=1/L∫ L 0 |f(x)|dx is expressed in μ units. This measurement was performed on 8 samples, the 3 samples with the largest values were excluded, and the average value of the 5 samples was expressed. ) value has been improved to 0.02~0.03μ. On the other hand, in the case of a cassette case, since the tape rotates inside the case, high precision dimensional stability is required during plastic molding. Usually, polystyrene resin, polymethyl methacrylate resin, etc. are used for the case body, and polyacetal resin, etc. are used for the reel body. However, the guide roller pins and guide rollers (or side rollers), which are the sliding members that come into contact with the tape running surface inside the case, are made of surface-finished stainless steel, so the friction coefficient when the polyester film comes into contact with the running surface is is 0.2 to 0.3, which is a large cause of drop-out phenomenon and pronunciation problems. For this reason, the current practice is to use special grease in combination to prevent this dropout phenomenon and the generation of sliding noise. The present inventors investigated various thermoplastic resins for sliding members for contact with polyester films, and found that polyphenylene sulfide resin (hereinafter referred to as PPS)
It has been found that a resin composition containing carbon fiber and a higher fatty acid ester of glycerin as an antistatic agent as a main component is suitable for a sliding member. What is the PPS resin used here?

【式】の分子構造を有する米国フイ リツプスペトロリアム社で開発された耐熱性樹脂
である。 PPS樹脂にガラス繊維を混入した樹脂組成物
は、機械部品として使用され、また、ポリテトラ
フツ化エチレン樹脂や炭素繊維、二硫化モリブデ
ン、グラフアイト等を混入した組成物は
USP3882030、4115283、特開昭51−28145の明細
書でみられるように、軸受部材としても使用され
ている。しかしながら、たとえば炭素繊維のみを
混入した場合は後に比較例1に示すように、摺動
部材として充分な性能を持つとは言えない。 本発明者らはPPS樹脂および炭素繊維からなる
樹脂組成物に種々の帯電防止剤等の添加剤を加え
摺動部材としての性能向上を検討した結果、グリ
セリンの高級脂肪酸エステルを加えることによ
り、次のような効果が具現されることを見い出し
た。すなわち、 内部潤滑効果により対摩擦、対摩耗特性が向
上する。 成型品表面の炭素繊維の浮きが少なくなる。 炭素繊維の導電的性質と相まつて、帯電性が
低下する。 以上3項目の総合効果により、テープ走行は非
常にスムーズに行なわれ、その結果、テープ走定
中の発音性がなく、ドロツプアウト現象も起きな
い理想的な摺動部材であるガイドローラーピンが
作成された。 本発明による摺動部材は、PPS樹脂40〜95重量
部、好ましくは60〜80重量部、炭素繊維5〜60重
量部、好ましくは20〜40重量部、グリセリンの高
級脂肪酸エステル0.1〜5重量部、好ましくは0.1
〜2重量部からなる。炭素繊維の添加量が多過ぎ
ると摺動部表面に繊維の浮きが多くなるため摩
擦、摩耗面で好ましい結果が得られない。又、グ
リセリンの高級脂肪酸エステルの添加量が多過ぎ
ると摺動部表面にブリード現象を起こす。なお、
本発明において使用されるグリセリンの高級脂肪
酸エステルは、例えばステアリン酸、オレイン
酸、パルミチン酸等とグリセリンとのエステルの
単体またはそれらの混合物であり、グリセリンに
対する高級脂肪酸のモル比は1ないし3のいずれ
でも良い。 以下実施例により本発明を詳細に説明する。 実施例 1 PPS樹脂(ライトンP−4、フイリツプスペト
ロリアム社製)6.9Kgと、乳鉢により微粉砕化し
たグリセロールトリステアレート(和光純薬工業
株社品)100gを46V型混合機に入れ毎分27回
転で15分間予備混合を行ない、そこに120℃3時
間乾燥した炭素繊維(クレハチヨツプKCF−100
−M107D、呉羽化学工業株社製)3.0Kgを入れさ
らに15分間混合した。これらの混合原料を65mmφ
押出成形機にダルメージ型スクリユーを装填し、
シリンダー温度をホツパー口より270℃から310℃
に勾配をつけ、ダイス温度を300℃に設定して押
出成形を行ない、ダスト部に取り付けたホツトカ
ツト装置により複合化ペレツトを得た。このペレ
ツト60gを射出成形機でシリンダー温度270〜310
℃、ノズル温度290℃、金型温度150℃に設定し、
射出圧1000Kg/cm2で、長さ120mm、巾30mm、厚さ
2mmのプレート、外径26.4mmφ、内径20.0mmφ、
高さ25.0mmの円筒および長さ22.0mm、2.4mmφのガ
イドポールを成形し、機械的性質、摩擦摩耗特
性、ビデオテープ走行性能としてのドロツプアウ
ト測定を行なつた。測定結果を比較例と共に表−
1に示したが、本発明の摺動部材用樹脂組成物は
他の樹脂組成物と較べて機械的性質、摩擦摩耗特
性およびテープ走行性にすぐれ、また従来の金属
性ガイドローラーピンと比較しても摩擦特性およ
びテープ走行性においてすぐれていることが明ら
かである。 以下実施例2、3、4および比較例1、2、
3、4を示すが、各例とも実施例1と同様の装置
および方法を用い、実施例1と同様の試験片
(120mm×30mm×2mmのプレート、外径26.4mmφ、
内径20.0mmφ、高さ25.0mmの円筒および22.0mm×
2.4mmφのガイドポール)を作成し、物性試験を
行つた。その結果は表−1および表−2に示す。 実施例 2 PPS(ライトンP−4) 4.9Kg グリセロールトリステアレート 100g 炭素繊維(クレハチヨツプKCF−100−
M107D) 5.0Kg ドロツプアウト数は0であり、摩擦特性も比較
例と較べて秀れていた。 実施例 3 PPS(ライトンP−4) 6.7Kg グリセロールトリステアレート 300g 炭素繊維(クレハチツプKCF−100−M107D)
3.0Kg ロツプアウト数は0であり、摩擦特性も比較
例と較べて秀れていた。 実施例 4 PPS(ライトンP−4) 6.9Kg グリセロールトリオレアート 100g 炭素繊維(クレハチツプKCF−100−M107D)
3.0Kg グリセロールトリステアレートを使用した場合
と同等の良い結果が得られた。 比較例 1 PPS(ライトンP−4) 7.0Kg 炭素繊維(クレハチツプKCF−100−M107D)
3.0Kg 摩擦特性は他の樹脂並である。ドロツプアウト
数は8であり、他の樹脂と比べればわずかに良い
が、グリセリンの高級脂肪酸エステルを入れた場
合と比べるとかなり性能低下がある。
It is a heat-resistant resin developed by Phillips Petroleum Company in the United States, which has the molecular structure of [Formula]. Resin compositions made by mixing PPS resin with glass fiber are used as mechanical parts, and compositions made by mixing polytetrafluoroethylene resin, carbon fiber, molybdenum disulfide, graphite, etc.
It is also used as a bearing member, as seen in the specifications of USP 3882030, 4115283, and Japanese Patent Application Laid-Open No. 51-28145. However, if only carbon fiber is mixed, for example, as will be shown later in Comparative Example 1, it cannot be said that it has sufficient performance as a sliding member. The present inventors investigated ways to improve the performance of sliding members by adding various additives such as antistatic agents to resin compositions made of PPS resin and carbon fibers, and found that by adding higher fatty acid esters of glycerin, the following results were obtained: We have found that the following effects can be realized. In other words, the internal lubrication effect improves anti-friction and anti-wear characteristics. The floating of carbon fibers on the surface of the molded product is reduced. Coupled with the electrically conductive properties of carbon fibers, charging properties are reduced. The overall effect of the above three items allows the tape to run very smoothly, and as a result, we have created a guide roller pin that is an ideal sliding member that does not cause any noise or drop-out phenomenon while the tape is running. Ta. The sliding member according to the present invention includes 40 to 95 parts by weight of PPS resin, preferably 60 to 80 parts by weight, 5 to 60 parts by weight of carbon fiber, preferably 20 to 40 parts by weight, and 0.1 to 5 parts by weight of higher fatty acid ester of glycerin. , preferably 0.1
~2 parts by weight. If the amount of carbon fiber added is too large, the fibers will float on the surface of the sliding part, making it impossible to obtain favorable results in terms of friction and wear. Furthermore, if the amount of higher fatty acid ester of glycerin added is too large, a bleed phenomenon will occur on the surface of the sliding part. In addition,
The higher fatty acid ester of glycerin used in the present invention is, for example, a single ester of stearic acid, oleic acid, palmitic acid, etc., and glycerin, or a mixture thereof, and the molar ratio of the higher fatty acid to glycerin is between 1 and 3. But it's okay. The present invention will be explained in detail below with reference to Examples. Example 1 6.9 kg of PPS resin (Ryton P-4, manufactured by Phillips Petroleum Co., Ltd.) and 100 g of glycerol tristearate (manufactured by Wako Pure Chemical Industries, Ltd.) finely pulverized in a mortar were placed in a 46V type mixer and the mixture was heated at 27 kg per minute. Premix by rotating for 15 minutes, then add carbon fiber (Kurehachiop KCF-100) dried at 120°C for 3 hours.
-M107D, manufactured by Kureha Chemical Industry Co., Ltd.) (3.0 kg) was added and mixed for an additional 15 minutes. These mixed raw materials are 65mmφ
Load the dalmage type screw into the extrusion molding machine,
Cylinder temperature from 270℃ to 310℃ from hopper mouth
Extrusion molding was carried out with a gradient of 300° C. and a die temperature of 300° C., and composite pellets were obtained using a hot cut device attached to the dust part. 60g of this pellet is put into an injection molding machine at a cylinder temperature of 270 to 310.
℃, nozzle temperature 290℃, mold temperature 150℃,
Injection pressure 1000Kg/ cm2 , plate length 120mm, width 30mm, thickness 2mm, outer diameter 26.4mmφ, inner diameter 20.0mmφ,
A cylinder with a height of 25.0 mm and a guide pole with a length of 22.0 mm and a diameter of 2.4 mm were molded, and dropout measurements were performed on mechanical properties, friction and wear characteristics, and videotape running performance. Table of measurement results along with comparative examples
As shown in 1, the resin composition for sliding members of the present invention has excellent mechanical properties, frictional wear characteristics, and tape running properties compared to other resin compositions, and also has superior properties compared to conventional metallic guide roller pins. It is clear that this material also has excellent friction properties and tape running properties. Examples 2, 3, 4 and comparative examples 1, 2,
3 and 4 are shown, but in each example, the same equipment and method as in Example 1 were used, and the same test pieces as in Example 1 (120 mm x 30 mm x 2 mm plate, outer diameter 26.4 mmφ,
Cylinder with inner diameter 20.0mmφ, height 25.0mm and 22.0mm×
A 2.4mmφ guide pole was created and physical property tests were conducted. The results are shown in Table-1 and Table-2. Example 2 PPS (Ryton P-4) 4.9Kg Glycerol tristearate 100g Carbon fiber (Kurehachiyopu KCF-100-
M107D) 5.0Kg The number of dropouts was 0, and the friction characteristics were also excellent compared to the comparative example. Example 3 PPS (Ryton P-4) 6.7Kg Glycerol tristearate 300g Carbon fiber (Kurehachipu KCF-100-M107D)
3.0Kg The number of dropouts was 0, and the friction properties were also excellent compared to the comparative example. Example 4 PPS (Ryton P-4) 6.9Kg Glycerol trioleate 100g Carbon fiber (Kurehachipu KCF-100-M107D)
Similar good results were obtained using 3.0Kg glycerol tristearate. Comparative example 1 PPS (Ryton P-4) 7.0Kg Carbon fiber (Kurehachipu KCF-100-M107D)
3.0Kg Friction properties are on par with other resins. The dropout number is 8, which is slightly better than other resins, but the performance is considerably lower than when higher fatty acid esters of glycerin are added.

【表】 比較例 2 PPS(ライトンP−4) 6.9Kg ステアリン酸 100g 炭素繊維 3Kg 摩擦特性は実施例2と同等であつたが、ドロツ
プアウト数は6と実施例に比べ劣る上に、機械強
度の低下も著しかつた。 比較例 3 PPS(ライトンP−4) 5.5Kg 二硫化モリブデン(日本モリブデン(株)Tパウダ
ー) 1.5Kg 炭素繊維 3.0Kg 摩擦特性が低下し、ドロツプアウト数も10と多
く改良の効果が認められなかつた。またテープ走
行面に若干擦り傷が認められた。 比較例 4 PPS(ライトンP−4) 6.9Kg ポリ四フツ化エチレンパウダー 1.5Kg 炭素繊維 3.0Kg 摩擦特性は実施例2と同等であつたが、ドロツ
プアウト数は9と多く改良の効果が認められなか
つた。
[Table] Comparative Example 2 PPS (Ryton P-4) 6.9Kg Stearic acid 100g Carbon fiber 3Kg The friction properties were the same as in Example 2, but the number of dropouts was 6, which was inferior to the Example, and the mechanical strength was The decline was also significant. Comparative Example 3 PPS (Ryton P-4) 5.5Kg Molybdenum disulfide (Nippon Molybdenum Co., Ltd. T Powder) 1.5Kg Carbon fiber 3.0Kg Friction characteristics decreased and the number of dropouts was as high as 10, so no improvement effect was recognized. . In addition, some scratches were observed on the tape running surface. Comparative Example 4 PPS (Ryton P-4) 6.9Kg Polytetrafluoroethylene powder 1.5Kg Carbon fiber 3.0Kg The friction characteristics were the same as in Example 2, but the number of dropouts was 9 and no improvement was observed. Ta.

【表】【table】

Claims (1)

【特許請求の範囲】[Claims] 1 ポリフエニレンサルフアイド樹脂40〜95重量
部、炭素繊維5〜60重量部、およびグリセリンの
ステアリン酸エステル、オレイン酸エステル、パ
ルミチン酸エステルの中から選ばれるグリセリン
の高級脂肪酸エステル0.1〜5重量部からなる、
磁気記録テープ用ポリエステルフイルムとの接触
用摺動部材。
1 40 to 95 parts by weight of polyphenylene sulfide resin, 5 to 60 parts by weight of carbon fiber, and 0.1 to 5 parts by weight of higher fatty acid ester of glycerin selected from stearate, oleate, and palmitate of glycerin. Consisting of
Sliding member for contact with polyester film for magnetic recording tape.
JP17150681A 1981-10-28 1981-10-28 Polyphenylene sulfide resin composition Granted JPS5874751A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP17150681A JPS5874751A (en) 1981-10-28 1981-10-28 Polyphenylene sulfide resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP17150681A JPS5874751A (en) 1981-10-28 1981-10-28 Polyphenylene sulfide resin composition

Publications (2)

Publication Number Publication Date
JPS5874751A JPS5874751A (en) 1983-05-06
JPH0359940B2 true JPH0359940B2 (en) 1991-09-12

Family

ID=15924368

Family Applications (1)

Application Number Title Priority Date Filing Date
JP17150681A Granted JPS5874751A (en) 1981-10-28 1981-10-28 Polyphenylene sulfide resin composition

Country Status (1)

Country Link
JP (1) JPS5874751A (en)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3607712A1 (en) * 1986-03-08 1987-09-10 Bayer Ag QUICK CRYSTALLIZING POLYPHENYLENE SULFIDES
JPS63289068A (en) * 1987-05-22 1988-11-25 Polyplastics Co Polyarylene sulfide resin composition
JPS6451463A (en) * 1987-08-22 1989-02-27 Matsushita Electric Works Ltd Polyphenylene sulfide resin composition
DE3728301A1 (en) * 1987-08-25 1989-03-09 Bayer Ag POLYPHENYLENE SULFIDE MOLDS WITH IMPROVED ELECTRICAL PROPERTIES
US5234984A (en) * 1987-08-25 1993-08-10 Bayer Aktiengesellschaft Polyphenylene sulphide moulding compounds with improved electrical properties
JP3159896B2 (en) * 1995-08-24 2001-04-23 ポリプラスチックス株式会社 Polyarylene sulfide resin composition
JP3508439B2 (en) * 1996-12-27 2004-03-22 ソニー株式会社 Magnetic recording tape cassette
WO2007001036A1 (en) * 2005-06-28 2007-01-04 Dainippon Ink And Chemicals, Inc. Polyphenylene sulfide resin structure
JP2007137996A (en) * 2005-11-17 2007-06-07 Polyplastics Co Polyarylene sulfide resin composition and molded product joined with epoxy adhesive

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5128145A (en) * 1974-09-04 1976-03-09 Hodogaya Chemical Co Ltd HORIFUENIRE NSARUFUAIDOJUSHISOSEIBUTSU
JPS54155300A (en) * 1978-05-30 1979-12-07 Asahi Glass Co Ltd Injection molding material of polyphenylene sulfide

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5128145A (en) * 1974-09-04 1976-03-09 Hodogaya Chemical Co Ltd HORIFUENIRE NSARUFUAIDOJUSHISOSEIBUTSU
JPS54155300A (en) * 1978-05-30 1979-12-07 Asahi Glass Co Ltd Injection molding material of polyphenylene sulfide

Also Published As

Publication number Publication date
JPS5874751A (en) 1983-05-06

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