JPH05306371A - Resin composition for gear - Google Patents

Resin composition for gear

Info

Publication number
JPH05306371A
JPH05306371A JP11129692A JP11129692A JPH05306371A JP H05306371 A JPH05306371 A JP H05306371A JP 11129692 A JP11129692 A JP 11129692A JP 11129692 A JP11129692 A JP 11129692A JP H05306371 A JPH05306371 A JP H05306371A
Authority
JP
Japan
Prior art keywords
resin
gear
weight
melt viscosity
polyphenylene sulfide
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.)
Pending
Application number
JP11129692A
Other languages
Japanese (ja)
Inventor
Tadashi Kosuge
匡志 小菅
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.)
NTN Corp
Original Assignee
NTN Corp
NTN Toyo Bearing 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 NTN Corp, NTN Toyo Bearing Co Ltd filed Critical NTN Corp
Priority to JP11129692A priority Critical patent/JPH05306371A/en
Publication of JPH05306371A publication Critical patent/JPH05306371A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To provide a resin composition for a gear with required molding accuracy, heat distortion resistance, mechanical strength and injection moldability and enable the molding of the gear having abrasion resistance without damaging the opposite gear made of a synthetic resin. CONSTITUTION:The resin composition for a gear is obtained by blending 100 pts.wt. cross-linked polyphenylene sulfide resin, having 1400-15000P melt viscosity and prepared by cross-linking an uncross-linked polyphenylene sulfide having 350-3000P as polymerized melt viscosity with 10-50 pts.wt. unsintered polytetrafluoroethylene resin having >=10000 number-average molecular weight, 10-30 pts.wt. aromatic polyamide pulp and 30-80 pts.wt. zinc oxide whisker.

Description

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

【0001】[0001]

【産業上の利用分野】この発明は樹脂製歯車の成形用材
料として用いる歯車用樹脂組成物に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a resin composition for gears used as a molding material for resin gears.

【0002】[0002]

【従来の技術】一般に、音響機器、複写機、自動車用部
品等の様々な分野で合成樹脂製の歯車が用いられている
が、そのような歯車の成形用材料として、寸法安定性や
成形体に優れたポリアセタールやナイロンが知られてい
る。これらポリアセタールやナイロンは、耐熱性および
機械的強度が充分ではなく、この点で優るエンジニアリ
ングプラスチックとしては、ポリフェニレンサルファイ
ド樹脂(以下、PPS樹脂と略記する)も知られてい
る。
2. Description of the Related Art Generally, gears made of synthetic resin are used in various fields such as audio equipment, copying machines, automobile parts, etc. Excellent polyacetal and nylon are known. These polyacetals and nylons are not sufficient in heat resistance and mechanical strength, and polyphenylene sulfide resin (hereinafter abbreviated as PPS resin) is also known as an engineering plastic excellent in this respect.

【0003】このようなPPS樹脂は、ガラス転移点が
88℃と低いが、ガラス繊維や炭素繊維等の補強材を配
合する事により、機械的強度の低下を防ぐことができ、
またこれらの補強材を配合した組成物は、250℃を越
える耐熱性を有する。
Such a PPS resin has a low glass transition point of 88 ° C., but by adding a reinforcing material such as glass fiber or carbon fiber, it is possible to prevent the mechanical strength from decreasing.
The composition containing these reinforcing materials has a heat resistance of more than 250 ° C.

【0004】[0004]

【発明が解決しようとする課題】しかし、前記したガラ
ス繊維や炭素繊維は高硬度であるため、このような繊維
補強材を配合したPPS樹脂で歯車を形成すると、この
歯車は、これと噛み合う相手歯車の歯面を削り、著しい
摩耗を起こすという問題点がある。
However, since the above-mentioned glass fiber and carbon fiber have a high hardness, when a gear is formed from PPS resin containing such a fiber reinforcing material, the gear is a partner with which it meshes. There is a problem that the tooth surface of the gear is scraped off, resulting in remarkable wear.

【0005】一方、比較的軟質の繊維補強材として、芳
香族ポリアミド繊維(以下、アラミド繊維という)、チ
タン酸カリウムウィスカまたは酸化亜鉛ウィスカがあ
り、前記高硬度の繊維補強材に代えてこれらを用いるこ
とも考えられる。
On the other hand, there are aromatic polyamide fibers (hereinafter referred to as aramid fibers), potassium titanate whiskers or zinc oxide whiskers as relatively soft fiber reinforcing materials, which are used in place of the high hardness fiber reinforcing materials. It is also possible.

【0006】しかし、このような繊維補強材を配合した
PPS樹脂では、成形された歯車に耐摩耗性が充分に備
わらず、しかも相手歯車(合成樹脂製)を削る、即ち攻
撃性があるという問題点がある。また、上記の繊維補強
材に代えて、アラミドパウダー等の粉末状充填材を配合
したPPS樹脂で歯車を形成すれば、相手歯車に対する
損傷性の点では優れるが、耐摩耗性に劣るという問題点
がある。
However, with a PPS resin containing such a fiber reinforcing material, the molded gear does not have sufficient wear resistance, and the mating gear (made of synthetic resin) is scraped, that is, it has an attacking property. There is a problem. Further, if a gear is formed of a PPS resin containing a powdered filler such as aramid powder instead of the above fiber reinforcement, it is excellent in terms of damage to the mating gear but poor in wear resistance. There is.

【0007】この発明は上記した問題点を解決し、歯車
用樹脂組成物を、所要の成形精度、耐熱変形性、機械的
強度および射出成形性を備えると共に、合成樹脂製の相
手歯車を損傷させることなく、しかも耐摩耗性があり、
安定してトルク伝達を行ない得る歯車を成形できるもの
とすることを課題としている。
The present invention solves the above-mentioned problems and provides a resin composition for gears with required molding accuracy, heat distortion resistance, mechanical strength and injection moldability, and damages a mating gear made of synthetic resin. Without wear and wear resistance,
An object of the present invention is to make it possible to form a gear that can stably transmit torque.

【0008】[0008]

【課題を解決するための手段】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100重量部に対し、ポリテトラフルオロエチレン樹
脂10〜50重量部、芳香族ポリアミドパルプ10〜3
0重量部および酸化亜鉛ウィスカ30〜80重量部を配
合して成る構成を採用したのである。
In order to solve the above problems, in the present invention, 10 to 50 parts by weight of polytetrafluoroethylene resin and 10 to 3 parts of aromatic polyamide pulp are used with respect to 100 parts by weight of polyphenylene sulfide resin.
The composition of 0 parts by weight and 30 to 80 parts by weight of zinc oxide whiskers is used.

【0009】また、上記ポリフェニレンサルファイド樹
脂が、重合上がりの溶融粘度350〜3000ポイズの
未架橋ポリフェニレンサルファイド樹脂を架橋して得ら
れる溶融粘度1400〜15000ポイズの架橋性ポリ
フェニレンサルファイド樹脂であってよく、上記ポリテ
トラフルオロエチレン樹脂が数平均分子量10000以
上の未焼成ポリテトラフルオロエチレン樹脂であってよ
い。以下、その詳細を述べる。
The polyphenylene sulfide resin may be a crosslinkable polyphenylene sulfide resin having a melt viscosity of 1400 to 15000 poise obtained by crosslinking an uncrosslinked polyphenylene sulfide resin having a melt viscosity of 350 to 3000 poise just after polymerization. The polytetrafluoroethylene resin may be an unsintered polytetrafluoroethylene resin having a number average molecular weight of 10,000 or more. The details will be described below.

【0010】まず、この発明におけるPPS樹脂は、下
記式〔化1〕で示されるものである。
First, the PPS resin in the present invention is represented by the following formula [Chemical formula 1].

【0011】[0011]

【化1】 [Chemical 1]

【0012】上記のPPS樹脂の代表例としては下記式
〔化2〕で示される重合体が挙げられる。
As a typical example of the above PPS resin, there is a polymer represented by the following formula [Chemical formula 2].

【0013】[0013]

【化2】 [Chemical 2]

【0014】この重合体は、Na2 Sとp−ジクロロベ
ンゼンを、n−メチルピロリドンやジメチルアセトアミ
ド等のアミド系溶媒、もしくはスルホラン等のスルホン
系溶媒中で縮合させて得られ、この段階をPPS樹脂の
重合上がりとしている。この重合上がりの低分子量PP
S樹脂を熱処理等の工程にかけると、樹脂中に交差結合
の全くないものから部分的交差結合を有するものに至る
まで、任意の重合度のものを自由に製造することができ
る。すなわち、溶融ブレンドに最適な溶融粘度特性を有
する樹脂を、任意に選択使用できる。
This polymer is obtained by condensing Na 2 S and p-dichlorobenzene in an amide solvent such as n-methylpyrrolidone or dimethylacetamide or a sulfone solvent such as sulfolane. It is supposed to be the polymerization of resin. This polymerized low molecular weight PP
By subjecting the S resin to a step such as heat treatment, it is possible to freely produce resins having any degree of polymerization, from those having no cross-linking in the resin to those having partial cross-linking. That is, a resin having the optimum melt viscosity characteristic for melt blending can be arbitrarily selected and used.

【0015】また重合上がりの溶融粘度については、3
50〜3000ポイズのものが好適である。例えば、3
50ポイズ未満のPPS樹脂を架橋させた、架橋性PP
S樹脂は、機械的強度、特に柔軟性に劣るため、衝撃強
度や靭性を要求される部位での使用は適さず、また、3
000ポイズを越える場合には高温雰囲気下での耐クリ
ープ性に劣るため、PPS樹脂の耐熱性を生かした高温
での使用性が阻害されるからである。
The melt viscosity after polymerization is 3
It is preferably 50 to 3000 poise. For example, 3
Crosslinkable PP obtained by crosslinking PPS resin of less than 50 poise
Since S resin is inferior in mechanical strength, especially in flexibility, it is not suitable for use in a site where impact strength and toughness are required.
If it exceeds 000 poise, the creep resistance in a high temperature atmosphere is poor, and the heat resistance of the PPS resin is hindered from being used at high temperatures.

【0016】一方、直鎖状のPPS樹脂を使用すると、
添加したポリテトラフルオロエチレン樹脂(以下、PT
FE樹脂と略記する)が繊維化されず、また、充填材の
アラミドパルプも解砕されないので、潤滑性、耐摩耗性
が低下する。
On the other hand, when a linear PPS resin is used,
Added polytetrafluoroethylene resin (hereinafter PT
(FE resin) is not fiberized and the filler aramid pulp is not crushed, so that the lubricity and wear resistance are reduced.

【0017】重合上がりのPPS樹脂を架橋するために
は、既述の架橋方法と同様に熱処理等により処理する。
具体的には酸素存在下における融点以下の加熱、もしく
は架橋剤、分岐剤の添加により行われる。このようにし
て得られた架橋性PPS樹脂で好ましいものは、溶融粘
度が1400〜15000ポイズのものである。なぜな
ら、溶融粘度が1400ポイズ未満の架橋性PPS樹脂
は、150℃以上の高温領域で耐クリープ性が低下し、
塑性変形しやすくなる。また、20000ポイズを越え
る架橋性PPS樹脂は、重合上がりの溶融粘度が350
〜3000ポイズであっても成形性が著しく劣り、柔軟
性においても劣るので好ましくない。
In order to crosslink the PPS resin after polymerization, it is treated by heat treatment or the like as in the above-mentioned crosslinking method.
Specifically, it is carried out by heating below the melting point in the presence of oxygen, or by adding a crosslinking agent or a branching agent. The preferable crosslinkable PPS resin thus obtained has a melt viscosity of 1400 to 15000 poise. This is because the crosslinkable PPS resin having a melt viscosity of less than 1400 poise has a low creep resistance in a high temperature range of 150 ° C. or higher,
Easier to plastically deform. Further, a crosslinkable PPS resin having a viscosity of more than 20,000 poise has a melt viscosity of 350 after polymerization.
Even when the porosity is up to 3000 poise, the moldability is remarkably inferior and the flexibility is also inferior, which is not preferable.

【0018】この発明で用いるPTFE樹脂は、特にそ
の分子量を限定することなく用いることも可能である
が、数平均分子量が10000以上で未焼成のものが好
ましい。なぜなら、低分子量のPTFE樹脂を用いた場
合、溶融粘度が過度に低くなり、さらにPPS樹脂との
界面エネルギーの差が大きくなって、溶融ブレンドやイ
ンジェクションに際して層分離を起こす事があるからで
ある。
The PTFE resin used in the present invention may be used without any particular limitation on its molecular weight, but it is preferable that it has a number average molecular weight of 10,000 or more and is unbaked. This is because when a low-molecular weight PTFE resin is used, the melt viscosity becomes excessively low, and the difference in interfacial energy with the PPS resin becomes large, which may cause layer separation during melt blending or injection.

【0019】一方、分子量10000以上のものは、溶
融粘度が高いため、溶融ブレンド時やインジェクション
時に層分離しにくく、好ましいものである。また未焼成
PTFE樹脂を用いると、インジェクション時のせん断
応力により、PTFE樹脂の繊維化を促す。このように
繊維化したPTFE樹脂は、均一にマトリックス中に分
散して後述するアラミドパルプと強固に絡み合うので、
良好な摩擦・摩耗特性を得ることができる。
On the other hand, those having a molecular weight of 10,000 or more are preferable because they have a high melt viscosity and are unlikely to separate into layers during melt blending or injection. If unsintered PTFE resin is used, shear stress during injection promotes fiberization of the PTFE resin. Since the PTFE resin thus fiberized is uniformly dispersed in the matrix and strongly entangled with the aramid pulp described later,
Good friction and wear characteristics can be obtained.

【0020】この発明に用いる芳香族ポリアミドパルプ
(以下、アラミドパルプと記す)は、パルプ状であれば
特に限定するものではないが、例えば、繊維長6mm、繊
維径12μmのアラミド繊維を擦り潰し、羽毛状にした
ものである。このものは、マトリックスであるPPS樹
脂によく濡れて親和性を示し、パルプの羽毛状の3次元
的な微細繊維がPPS樹脂を取り込み、さらにテトラポ
ット状の酸化亜鉛ウィスカおよびPTFE樹脂と絡み合
って、3次元網目構造を形成する。またパルプ中の繊維
は微細であるために、摺動時における相手歯車に対する
攻撃性は、殆ど無い。
The aromatic polyamide pulp (hereinafter referred to as aramid pulp) used in the present invention is not particularly limited as long as it is in a pulp form. For example, aramid fibers having a fiber length of 6 mm and a fiber diameter of 12 μm are crushed, It is feathered. This product is well wetted with the matrix PPS resin and shows an affinity, and the feather-like three-dimensional fine fibers of the pulp take up the PPS resin, and are further entangled with the tetrapot-shaped zinc oxide whiskers and the PTFE resin, Form a three-dimensional mesh structure. Further, since the fibers in the pulp are fine, there is almost no attack on the mating gear during sliding.

【0021】この様な羽毛状の3次元的な微細繊維が充
分に形成されているアラミドパルプは、その比表面積が
大きく、具体的には3m2 /g以上のものが好ましく、
特に5m2 /g以上のものが好ましい。
The aramid pulp on which such feather-like three-dimensional fine fibers are sufficiently formed has a large specific surface area, and specifically, one having a specific surface area of 3 m 2 / g or more is preferable.
It is particularly preferably 5 m 2 / g or more.

【0022】この発明の用いる酸化亜鉛ウィスカは、結
晶1単位当りがテトラポット型の針状結晶であるゆえ
に、微細なマトリックスの欠落を防ぐ事が出来る。また
針状ウィスカでは、インジェクション時に樹脂の流動に
より異方性が生ずるが、3次元ウィスカであるがゆえ
に、異方性が緩和された状態になって寸法精度が良い。
また酸化亜鉛ウィスカは制振特性を持つので、駆動時に
発生するノイズが抑制できる。
Since the zinc oxide whiskers used in the present invention are tetrapod-type needle-shaped crystals per unit of crystal, it is possible to prevent the loss of fine matrix. Further, in the needle-shaped whiskers, anisotropy occurs due to the flow of the resin at the time of injection, but since it is a three-dimensional whisker, the anisotropy is relaxed and the dimensional accuracy is good.
Further, since the zinc oxide whiskers have vibration damping characteristics, noise generated during driving can be suppressed.

【0023】上記した原材料の配合割合をそれぞれ所定
範囲内とするのは、以下の理由による。すなわち、固体
潤滑材のPTFE樹脂が、PPS樹脂100重量部に対
して10重量未満の場合、摩耗係数が大きくなり、トル
ク伝達に支障を来す。また逆に50重量部を越す場合
は、強度が低下し高荷重に耐えかねる。
The mixing ratios of the above raw materials are set within the predetermined ranges for the following reasons. That is, when the PTFE resin as the solid lubricant is less than 10 parts by weight with respect to 100 parts by weight of the PPS resin, the wear coefficient becomes large, and the torque transmission is hindered. On the other hand, when it exceeds 50 parts by weight, the strength is lowered and it cannot withstand a high load.

【0024】補強充填剤の1つであるアラミドパルプ
が、PPS樹脂100重量部に対して10重量部未満の
場合、耐摩耗性が著しく低下する。また、50重量部を
越えると溶融ブレンドやインジェクションに際し、流動
性が悪く、成形出来ない。
When the amount of aramid pulp, which is one of the reinforcing fillers, is less than 10 parts by weight with respect to 100 parts by weight of PPS resin, the abrasion resistance is significantly reduced. On the other hand, if the amount exceeds 50 parts by weight, fluidity is poor during melt blending or injection, and molding cannot be performed.

【0025】もう一つの補強充填材酸化亜鉛ウィスカ
が、PPS樹脂100重量部に対して30重量部未満の
場合には特に強度が劣り、歯車が歯こぼれを起こし易く
なる。70重量部を越えると、プラスチックや軟質金属
相手にアブレーシブな摩耗を引き起こす。
If the amount of the other reinforcing filler zinc oxide whiskers is less than 30 parts by weight with respect to 100 parts by weight of the PPS resin, the strength is particularly poor and the gears are apt to cause tooth spillage. If it exceeds 70 parts by weight, it causes abrasive wear on a plastic or soft metal partner.

【0026】ここで、前述の原材料を混合する方法は、
特に限定するものではなく、通常広く用いられている方
法、例えば主成分となる樹脂その他の諸原料をそれぞれ
個別に、またはヘンシェルミキサー、ボールミル、タン
ブラーミキサー等の混合機によって適宜に乾式混合した
後、溶融混合性のよい射出成形機もしくは溶融押出成形
機に供給するか、または、予め熱ロール、ニーダ、バン
バリーミキサー、溶融押出機などで溶融混合するなどの
方法を利用すればよい。さらに、この発明の歯車用樹脂
組成物は、その成形方法を限定するものではなく、射出
成形その他汎用の方法を採用できる。
Here, the method of mixing the above-mentioned raw materials is as follows.
It is not particularly limited, and a method which is generally widely used, for example, a resin as a main component and other various raw materials are individually or after appropriately dry mixed by a mixer such as a Henschel mixer, a ball mill, a tumbler mixer, A method of supplying to an injection molding machine or a melt extrusion molding machine having a good melt mixing property, or performing melt mixing with a hot roll, a kneader, a Banbury mixer, a melt extruder or the like in advance may be used. Further, the molding method of the resin composition for gears of the present invention is not limited, and injection molding or other general-purpose methods can be adopted.

【0027】なお、この発明のPPS樹脂を主成分とす
る組成物に対して、潤滑性、耐摩耗性、および非攻撃性
等の所期の目的とする特性を悪化させない範囲内におい
て、酸化防止剤、熱安定剤、紫外線吸収剤、着色剤、難
燃剤、帯電防止剤、結晶化促進剤等の、各種の添加剤を
配合することもできる。
With respect to the composition containing the PPS resin as a main component of the present invention, oxidation prevention is provided within a range that does not deteriorate desired properties such as lubricity, abrasion resistance, and non-aggressiveness. Various additives such as an agent, a heat stabilizer, an ultraviolet absorber, a colorant, a flame retardant, an antistatic agent, and a crystallization accelerator can be blended.

【0028】[0028]

【作用】この発明に係る歯車用樹脂組成物は、PPS樹
脂本来の耐熱性、耐候性、射出成形性と、PTFE樹脂
の良好な潤滑性とを有すると共に、アラミドパルプの羽
毛状で3次元的な微細繊維塊が親和性よくPPS樹脂を
取り込み、さらにテトラポット状の酸化亜鉛ウィスカと
絡み合って、3次元網目構造を形成するので、耐摩耗性
があり、かつ相手歯車を損傷させない。また、繊維充填
材の配向に起因する強度のばらつきがないので、安定し
た機械的強度が備わる。
The resin composition for gears according to the present invention has the inherent heat resistance, weather resistance and injection moldability of the PPS resin, and the good lubricity of the PTFE resin, and the feather-like three-dimensional shape of aramid pulp. Since such fine fiber lumps incorporate PPS resin with good affinity and further entangle with tetrapod-shaped zinc oxide whiskers to form a three-dimensional network structure, they have wear resistance and do not damage the mating gear. Further, since there is no variation in strength due to the orientation of the fiber filler, stable mechanical strength is provided.

【0029】[0029]

【実施例】実施例および比較例に使用した原材料を一括
して示すと次のとおりである。なお、P1 は重合上がり
の溶融粘度、P2 は架橋後の溶融粘度、Mは数平均分子
量を示す。
EXAMPLES The raw materials used in Examples and Comparative Examples are collectively shown below. In addition, P 1 is a melt viscosity after polymerization, P 2 is a melt viscosity after crosslinking, and M is a number average molecular weight.

【0030】(1) 直鎖状PPS樹脂(呉羽化学工業社
製:KPS−#214、P1 =1400ポイズ) (2) 架橋性PPS樹脂(トープレン社製:T−4(2) 、
1 =700ポイズ、P2 =1840ポイズ) (3) 架橋性PPS樹脂(トープレン社製:K−4、P1
=100ポイズ、P2 =2000ポイズ) (4) PTFE樹脂(ダイキン工業社製:M−12、M=
7000000) (5) PTFE樹脂(ダイキン工業社製:ルブロンL−
2、M=30000) (6) 酸化亜鉛ウィスカ(松下電器工業社製) (7) アラミドパルプ(日本アラミド社製:トワロン−A
R−1097pulp) (8) チタン酸カリウム繊維(大塚化学社製:ティスモD
101) (9) 炭素繊維(東レ社製:トレカMLD−100) (10) アラミドファイバー(帝人社製:コーネックスカ
ットファイバー1mm) 上記の諸原材料(1) 〜(7) を表1に示す割合で配合し、
ヘンシェルミキサーで乾式混合した後、溶融押出機(池
貝社製:PCM45)に供給し、シリンダー温度290
℃、スクリュー回転数100rpmにて溶融ブレンドし
た。その後、シリンダー温度325℃射出圧力1000
kg/cm2 の条件で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、摩擦係数、比摩
耗量、相手材損傷性、歯先摩耗、相手歯車損傷度を以下
に示す試験方法によって求めた。
(1) Linear PPS resin (Kureha Chemical Industry Co., Ltd .: KPS- # 214, P 1 = 1400 poise) (2) Crosslinkable PPS resin (Topren Co .: T-4 (2),
P 1 = 700 poise, P 2 = 1840 poise) (3) Crosslinkable PPS resin (K-4, P 1 manufactured by Topren Co., Ltd.)
= 100 poise, P 2 = 2000 poise) (4) PTFE resin (manufactured by Daikin Industries, Ltd.: M-12, M =
7000000) (5) PTFE resin (manufactured by Daikin Industries, Ltd .: Lubron L-
2, M = 30000) (6) Zinc oxide whiskers (manufactured by Matsushita Electric Industrial Co., Ltd.) (7) Aramid pulp (manufactured by Nippon Aramid Co .: Twaron-A)
R-1097pulp) (8) Potassium titanate fiber (Otsuka Chemical Co., Ltd .: Tismo D)
101) (9) Carbon fiber (manufactured by Toray Industries: trading card MLD-100) (10) Aramid fiber (manufactured by Teijin Ltd .: Conex Cut Fiber 1 mm) The ratios of the above raw materials (1) to (7) shown in Table 1. Blended with
After dry-mixing with a Henschel mixer, it is supplied to a melt extruder (PCM45 manufactured by Ikegai Co., Ltd.), and a cylinder temperature is 290.
Melt blending was carried out at a temperature of ℃ and a screw rotation speed of 100 rpm. After that, the cylinder temperature is 325 ° C and the injection pressure is 1000.
A predetermined test piece was prepared by applying an injection molding machine under the condition of kg / cm 2 , and the bending strength, friction coefficient, specific wear amount, mating material damage property, tooth tip wear, mating gear damage degree of the obtained test piece were as follows. It was determined by the test method shown in.

【0031】曲げ試験 ASTM−D790による曲げ強度(10g/cm2
の測定を行なった。曲げ強度の単位は、kgf/cm2
とした。
Bending test Bending strength according to ASTM-D790 (10 g / cm 2 ).
Was measured. The unit of bending strength is kgf / cm 2
And

【0032】摩砕摩耗試験 摩擦係数、比摩耗量、相手材損傷性について、NTN式
スラスト型摩擦摩耗試験機により測定を行なった。
Grinding wear test The friction coefficient, the specific wear amount, and the damage to the mating material were measured with an NTN thrust type friction wear tester.

【0033】摺動条件 周速 :128m/min 面圧 :3.9kg/cm2 雰囲気:R.Tドライ 相手材:SUS303鋼 なお、上述の試験結果の単位について、摩擦係数は無次
元数、比摩耗量は×10-10 cm3 /kg・mで表し
た。相手材損傷性については、相手材SUS303鋼の
摺動痕の深さにより以下に示す基準で4段階評価を行な
った。
Sliding conditions Peripheral speed: 128 m / min Surface pressure: 3.9 kg / cm 2 Atmosphere: R.S. T dry mating material: SUS303 steel With respect to the unit of the above test results, the friction coefficient was expressed by a dimensionless number, and the specific wear amount was expressed by × 10 -10 cm 3 / kg · m. As for the mating material damage property, four-level evaluation was performed based on the following criteria according to the depth of sliding marks of the mating material SUS303 steel.

【0034】評価基準 ◎:摩耗深さ≦1μm 〇:1μm<摩耗深さ≦5μm △:5μm<摩耗深さ≦10μm ×:10μm<摩耗深さ ギヤ実機耐久試験 試験片から成形した歯車について、NTN精密樹脂製歯
車強度試験機により、耐久試験を行なった。
Evaluation Criteria ⊚: Wear depth ≦ 1 μm ◯: 1 μm <wear depth ≦ 5 μm Δ: 5 μm <wear depth ≦ 10 μm ×: 10 μm <wear depth Gear actual machine durability test A durability test was conducted using a precision resin gear strength tester.

【0035】試験条件 試験時間:200hr 回転数 :470rpm 350rpm トルク :4.5〜5.5kgf・cm 雰囲気 :R.T. 駆動歯車:各PPS系歯車(NTN精密樹脂社製:PC
D47) 相手歯車:ポリアセタール歯車(ポリプラスチック社
製:PCD35) 試験結果における歯先摩耗および相手歯車損傷度は、下
記の基準により評価した。
Test conditions Test time: 200 hr Revolution: 470 rpm 350 rpm Torque: 4.5 to 5.5 kgf · cm Atmosphere: R.S. T. Drive gear: Each PPS gear (NTN Precision Resins Co .: PC
D47) Counter gear: polyacetal gear (PCD35 manufactured by Polyplastics Co., Ltd.) The tooth tip wear and the counter gear damage degree in the test results were evaluated according to the following criteria.

【0036】評価基準 ◎:摩耗深さ≦10μm 〇:10μm<摩耗深さ≦50μm △:50μm<摩耗深さ≦100μm ×:100μm<摩耗深さEvaluation criteria ⊚: wear depth ≦ 10 μm ◯: 10 μm <wear depth ≦ 50 μm Δ: 50 μm <wear depth ≦ 100 μm ×: 100 μm <wear depth

【0037】[0037]

【表1】 [Table 1]

【0038】〔比較例1〜8〕前記した諸原料(1) 、
(4) 、(6) 〜(10)を表4に示す割合で配合した以外は実
施例1〜10と全く同様にして試験片を作製し、また前
記した試験方法と全く同様にして評価し、この結果を表
2中に併記した。
[Comparative Examples 1 to 8] The various raw materials (1) described above,
(4) Test pieces were prepared in exactly the same manner as in Examples 1 to 10 except that (6) to (10) were mixed in the proportions shown in Table 4, and evaluated in the same manner as in the above-mentioned test method. The results are also shown in Table 2.

【0039】[0039]

【表2】 [Table 2]

【0040】表1および表2の結果から明らかなよう
に、酸化亜鉛ウィスカを使用しても、アラミドパルプを
使わなかった比較例2、3、酸化亜鉛ウィスカを用いて
もアラミドパルプ以外のアラミド繊維を用いた比較例
4、アラミドパルプを用いても酸化亜鉛ウィスカを使用
しなかった比較例5、これらはいずれも耐摩耗性に劣
り、また相手損傷性が大きい。
As is clear from the results shown in Tables 1 and 2, Comparative Examples 2 and 3 in which aramid pulp was not used even if zinc oxide whiskers were used, and aramid fibers other than aramid pulp were used even when zinc oxide whiskers were used. Comparative Example 4 using No. 3, Comparative Example 5 using zinc oxide whiskers even if using aramid pulp, and all of them are inferior in abrasion resistance and have high damage to the other party.

【0041】また、酸化亜鉛ウィスカおよびアラミドパ
ルプを用いてもPTFE樹脂を使用しなかった比較例6
は、摩擦係数が大きく、耐摩耗性に劣る。さらにまた、
この発明における4つの必須成分が配合されていても、
酸化亜鉛ウィスカの配合量が少量の比較例7は耐摩耗性
に劣り、添加量が過量の比較例8は、相手損傷性に劣っ
ていた。
Comparative Example 6 in which PTFE resin was not used even with zinc oxide whiskers and aramid pulp
Has a large friction coefficient and is poor in wear resistance. Furthermore,
Even if the four essential components in this invention are blended,
Comparative Example 7 containing a small amount of zinc oxide whiskers was inferior in abrasion resistance, and Comparative Example 8 containing an excessive amount of zinc oxide was inferior in damage to the other party.

【0042】一方、4つの必須成分が所定の割合で配合
された実施例1〜10は、優れた物性を示し、特に、架
橋性PPS樹脂で所定溶融粘度のものを用い、数平均分
子量が7000000の高分子量のPTFE配合した実
施例2のものが、耐摩耗性に最も優れていた。また、実
施例2と実施例4を比較すると、高分子量のPTFE樹
脂を用いた組成物の方が低摩擦係数であり、かつ耐摩耗
性に優れることが判明した。
On the other hand, Examples 1 to 10 in which the four essential components were blended in a predetermined ratio exhibited excellent physical properties. In particular, a crosslinkable PPS resin having a predetermined melt viscosity was used and the number average molecular weight was 7,000,000. The example 2 in which the high-molecular-weight PTFE was mixed was the most excellent in abrasion resistance. Further, comparing Example 2 and Example 4, it was found that the composition using the high-molecular weight PTFE resin has a lower friction coefficient and is excellent in wear resistance.

【0043】[0043]

【効果】この発明は、以上説明したように、PPS樹脂
およびPTFE樹脂を主要材料として、所定量のアラミ
ドパルプおよび酸化亜鉛ウィスカといったそれぞれ特性
ある3次元構造の補強材を所定量配合したので、繊維状
補強材の配向に起因した強度のばらつきがなく、成形に
よる寸法精度、耐熱変形性、機械的強度および射出成形
性を満足すると共に、相手歯車を損傷させることなく、
耐摩耗性がある。したがって、安定してトルク伝達を行
ない得る歯車成形用の成形用材料として最適のものであ
るといえる。
As described above, according to the present invention, the PPS resin and the PTFE resin are used as the main materials, and the predetermined amount of the reinforcing material having a three-dimensional structure such as aramid pulp and zinc oxide whiskers is mixed. There is no variation in strength due to the orientation of the reinforcing material, dimensional accuracy by molding, heat distortion resistance, mechanical strength and injection moldability are satisfied, and the mating gear is not damaged,
Has wear resistance. Therefore, it can be said that it is the most suitable as a molding material for gear molding capable of stable torque transmission.

フロントページの続き (51)Int.Cl.5 識別記号 庁内整理番号 FI 技術表示箇所 C08L 27:18 77:00) Continuation of front page (51) Int.Cl. 5 Identification code Office reference number FI technical display area C08L 27:18 77:00)

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】 ポリフェニレンサルファイド樹脂100
重量部に対し、ポリテトラフルオロエチレン樹脂10〜
50重量部、芳香族ポリアミドパルプ10〜30重量部
および酸化亜鉛ウィスカ30〜80重量部を配合して成
る歯車用樹脂組成物。
1. A polyphenylene sulfide resin 100.
10 parts by weight of polytetrafluoroethylene resin
A resin composition for gears, which comprises 50 parts by weight, 10 to 30 parts by weight of aromatic polyamide pulp and 30 to 80 parts by weight of zinc oxide whiskers.
【請求項2】 上記ポリフェニレンサルファイド樹脂
が、重合上がりの溶融粘度350〜3000ポイズの未
架橋ポリフェニレンサルファイド樹脂を架橋して得られ
る溶融粘度1400〜15000ポイズの架橋性ポリフ
ェニレンサルファイド樹脂である請求項1記載の歯車用
樹脂組成物。
2. The crosslinkable polyphenylene sulfide resin having a melt viscosity of 1400 to 15000 poise, which is obtained by crosslinking an uncrosslinked polyphenylene sulfide resin having a melt viscosity of 350 to 3000 poise just after polymerization, in the polyphenylene sulfide resin. Resin composition for gears.
【請求項3】 上記ポリテトラフルオロエチレン樹脂が
数平均分子量10000以上の未焼成ポリテトラフルオ
ロエチレン樹脂である請求項1記載の歯車用樹脂組成
物。
3. The resin composition for gears according to claim 1, wherein the polytetrafluoroethylene resin is an unsintered polytetrafluoroethylene resin having a number average molecular weight of 10,000 or more.
JP11129692A 1992-04-30 1992-04-30 Resin composition for gear Pending JPH05306371A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP11129692A JPH05306371A (en) 1992-04-30 1992-04-30 Resin composition for gear

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP11129692A JPH05306371A (en) 1992-04-30 1992-04-30 Resin composition for gear

Publications (1)

Publication Number Publication Date
JPH05306371A true JPH05306371A (en) 1993-11-19

Family

ID=14557629

Family Applications (1)

Application Number Title Priority Date Filing Date
JP11129692A Pending JPH05306371A (en) 1992-04-30 1992-04-30 Resin composition for gear

Country Status (1)

Country Link
JP (1) JPH05306371A (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH08151497A (en) * 1994-11-29 1996-06-11 Nichias Corp Sliding resin composition
US5962376A (en) * 1997-02-25 1999-10-05 Ntn Corporation Resin composition for sliding member and resin gear
JP2003055550A (en) * 2001-08-10 2003-02-26 Mitsubishi Gas Chem Co Inc Resin for gear wheel and gear wheel using the same
WO2004060995A1 (en) * 2002-12-27 2004-07-22 Du Pont-Mitsui Fluorochemicals Co., Ltd. Fluororesin composition
CN104231607A (en) * 2013-06-07 2014-12-24 上海杰事杰新材料(集团)股份有限公司 Nylon/polyphenylene sulfide blend material used for selective laser sintering, and preparation method thereof
CN104231626A (en) * 2013-06-07 2014-12-24 上海杰事杰新材料(集团)股份有限公司 Polyphenylene sulfide powder material used for selective laser sintering, and preparation method thereof
JP2019089922A (en) * 2017-11-14 2019-06-13 大塚化学株式会社 Resin composition, molded body, sliding member, and sliding method

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH08151497A (en) * 1994-11-29 1996-06-11 Nichias Corp Sliding resin composition
US5962376A (en) * 1997-02-25 1999-10-05 Ntn Corporation Resin composition for sliding member and resin gear
JP2003055550A (en) * 2001-08-10 2003-02-26 Mitsubishi Gas Chem Co Inc Resin for gear wheel and gear wheel using the same
WO2004060995A1 (en) * 2002-12-27 2004-07-22 Du Pont-Mitsui Fluorochemicals Co., Ltd. Fluororesin composition
CN104231607A (en) * 2013-06-07 2014-12-24 上海杰事杰新材料(集团)股份有限公司 Nylon/polyphenylene sulfide blend material used for selective laser sintering, and preparation method thereof
CN104231626A (en) * 2013-06-07 2014-12-24 上海杰事杰新材料(集团)股份有限公司 Polyphenylene sulfide powder material used for selective laser sintering, and preparation method thereof
JP2019089922A (en) * 2017-11-14 2019-06-13 大塚化学株式会社 Resin composition, molded body, sliding member, and sliding method

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