JP2003201398A - Gear made of resin - Google Patents

Gear made of resin

Info

Publication number
JP2003201398A
JP2003201398A JP2001400474A JP2001400474A JP2003201398A JP 2003201398 A JP2003201398 A JP 2003201398A JP 2001400474 A JP2001400474 A JP 2001400474A JP 2001400474 A JP2001400474 A JP 2001400474A JP 2003201398 A JP2003201398 A JP 2003201398A
Authority
JP
Japan
Prior art keywords
resin
gear
component
weight
acid
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
JP2001400474A
Other languages
Japanese (ja)
Other versions
JP3664133B2 (en
Inventor
Tomohiko Tanaka
智彦 田中
Shoichi Ikeda
晶一 池田
Hiroki Nakahama
裕樹 中濱
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.)
Yuka Denshi Co Ltd
Mitsubishi Chemical Corp
Original Assignee
Yuka Denshi Co Ltd
Mitsubishi Chemical Corp
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 Yuka Denshi Co Ltd, Mitsubishi Chemical Corp filed Critical Yuka Denshi Co Ltd
Priority to JP2001400474A priority Critical patent/JP3664133B2/en
Publication of JP2003201398A publication Critical patent/JP2003201398A/en
Application granted granted Critical
Publication of JP3664133B2 publication Critical patent/JP3664133B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Abstract

<P>PROBLEM TO BE SOLVED: To provide a gear made of a resin which excels in dimensional accuracy and long-term strength. <P>SOLUTION: The gear is obtained by molding a resin composition to be obtained by compounding 10 pts.wt. resin component comprising (A) 80-96 wt.% polyamide obtained by polymerizing a diamine containing ≥70 mol% m- xylylenediamine and a carboxylic acid containing ≥70 mol% 6-12C α,ω-aliphatic dicarboxylic acid, (B) 2-10 wt.% unsaturated organic acid-modified polyolefin, and (C) 2-10 wt.% ultra-high-molecular-weight polyethylene with (D) 40-250 pts.wt. glass fibers. <P>COPYRIGHT: (C)2003,JPO

Description

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

【0001】[0001]

【発明の属する技術分野】本発明は、寸法精度に優れ、
機械的強度の長期持続性に優れた樹脂製歯車に関する。
TECHNICAL FIELD The present invention has excellent dimensional accuracy,
The present invention relates to a resin gear having excellent long-term durability of mechanical strength.

【0002】[0002]

【従来の技術】従来、樹脂を成形して得られる樹脂製歯
車の成形材料としては、比較的強度を要求されない用途
にはポリオキシメチレンを代表とする非強化樹脂が用い
られ、強度が要求される用途には繊維強化ポリアミド、
繊維強化ポリフェニレンスルフィド等の繊維強化樹脂が
用いられてきた。
2. Description of the Related Art Conventionally, as a molding material for a resin-made gear obtained by molding a resin, a non-reinforced resin represented by polyoxymethylene has been used for applications where relatively high strength is not required. Fiber-reinforced polyamide,
Fiber reinforced resins such as fiber reinforced polyphenylene sulfide have been used.

【0003】しかし、繊維強化樹脂で樹脂製歯車を成形
した場合、成形金型のゲート近傍とウエルド近傍とで繊
維の配向が異なるものとなり、この繊維の配向差のため
に、得られる歯車の真円度が悪くなり、寸法ないし形状
精度に優れた樹脂製歯車を得ることができないという問
題があった。また、ナイロン6、ナイロン66やナイロ
ン46等をベースにした繊維強化ナイロンの場合には、
成形後、吸湿により寸法変化が起こり、寸法精度をより
一層悪化させるという問題があった。
However, when a resin-made gear is molded with a fiber-reinforced resin, the fiber orientation differs between the gate and weld of the molding die, and due to this fiber orientation difference, the true gear of the resulting gear is obtained. There is a problem that the roundness becomes poor and a resin gear having excellent dimensional or shape accuracy cannot be obtained. In the case of fiber reinforced nylon based on nylon 6, nylon 66, nylon 46, etc.,
After molding, there is a problem that dimensional change occurs due to moisture absorption, which further deteriorates dimensional accuracy.

【0004】これに対して、メタキシリレンジアミンと
炭素数6〜12の脂肪族ジカルボン酸とを反応させて得
られたポリアミドは、吸湿による寸法変化が小さく、こ
れにガラス繊維を配合すると、ガラス繊維強化ナイロン
6やナイロン66に比較して化学的、熱的、機械的諸性
質に優れた成形材料となることが報告されている(特開
昭50−61449号公報)。
On the other hand, the polyamide obtained by reacting metaxylylenediamine with an aliphatic dicarboxylic acid having 6 to 12 carbon atoms has a small dimensional change due to moisture absorption. It has been reported that the molding material has excellent chemical, thermal and mechanical properties as compared with fiber reinforced nylon 6 and nylon 66 (Japanese Patent Laid-Open No. 61414/1975).

【0005】[0005]

【発明が解決しようとする課題】しかし、特開昭50−
61449号公報に記載される、メタキシリレンジアミ
ンと炭素数6〜12の脂肪族ジカルボン酸とを反応させ
て得られたポリアミドにガラス繊維を配合したガラス繊
維強化樹脂を成形して得られる樹脂製歯車は、長期強
度、即ち、機械的強度の長期持続性、耐久性が、ガラス
繊維で強化したナイロン6やナイロン66を成形して得
られた樹脂製歯車に比べて十分とは言えず、その改善が
望まれていた。
However, Japanese Patent Laid-Open No. Sho 50-
JP-A-61449 discloses a resin obtained by molding a glass fiber reinforced resin in which glass fiber is mixed with polyamide obtained by reacting metaxylylenediamine with an aliphatic dicarboxylic acid having 6 to 12 carbon atoms. It cannot be said that the gear has sufficient long-term strength, that is, long-term durability of mechanical strength and durability as compared with resin gears obtained by molding nylon 6 or nylon 66 reinforced with glass fiber. Improvement was desired.

【0006】本発明は、上記従来の問題点を解決し、寸
法精度、長期強度に優れた樹脂製歯車を提供することを
目的とする。
An object of the present invention is to solve the above-mentioned conventional problems and to provide a resin gear having excellent dimensional accuracy and long-term strength.

【0007】[0007]

【課題を解決するための手段】本発明の樹脂製歯車は、
(A)メタキシリレンジアミンを70モル%以上含むジ
アミンと、炭素数6〜12のα,ω−脂肪族ジカルボン
酸を70モル%以上含むカルボン酸とを重合して得られ
たポリアミド80〜96重量%と、(B)不飽和有機酸
変性ポリオレフィン2〜10重量%と、(C)超高分子
量ポリエチレン2〜10重量%とを含む樹脂成分100
重量部に対して、(D)ガラス繊維40〜250重量部
を配合して得られる樹脂組成物を成形してなることを特
徴とする。
The resin gear of the present invention comprises:
(A) Polyamides 80 to 96 obtained by polymerizing a diamine containing 70 mol% or more of metaxylylenediamine and a carboxylic acid containing 70 mol% or more of an α, ω-aliphatic dicarboxylic acid having 6 to 12 carbon atoms. 100% by weight, (B) 2 to 10% by weight of unsaturated organic acid-modified polyolefin, and (C) 2 to 10% by weight of ultrahigh molecular weight polyethylene.
It is characterized by being formed by molding a resin composition obtained by blending 40 to 250 parts by weight of glass fiber (D) with respect to parts by weight.

【0008】メタキシリレンジアミンを主体とするジア
ミンと炭素数6〜12のα,ω−脂肪族ジカルボン酸を
主体とするジカルボン酸とを重合させて得られるポリア
ミドに、有機酸変性ポリオレフィン、超高分子量ポリエ
チレン及びガラス繊維を所定の割合で配合してなる樹脂
組成物であれば、従来のガラス繊維強化ナイロン樹脂組
成物に比べて吸湿による寸法変化も小さく、良好な長期
強度を有する樹脂製歯車を成形することができる。
A polyamide obtained by polymerizing a diamine mainly containing metaxylylenediamine and a dicarboxylic acid mainly containing an α, ω-aliphatic dicarboxylic acid having 6 to 12 carbon atoms, is added to an organic acid-modified polyolefin, ultrahigh If the resin composition is a mixture of molecular weight polyethylene and glass fibers in a predetermined ratio, a resin gear having less dimensional change due to moisture absorption than a conventional glass fiber reinforced nylon resin composition and having good long-term strength can be obtained. It can be molded.

【0009】即ち、前述の如く、メタキシリレンジアミ
ンを主体とするジアミンと炭素数6〜12のα,ω−脂
肪族ジカルボン酸を主体とするジカルボン酸とを重合さ
せて得られるポリアミドは、吸湿による寸法変化が小さ
く、樹脂製歯車の寸法安定性に寄与する。また、化学
的、熱的、機械的強度の面においても良好な特性を示す
が、長期強度の面で問題があった。
That is, as described above, a polyamide obtained by polymerizing a diamine mainly containing metaxylylenediamine and a dicarboxylic acid mainly containing an α, ω-aliphatic dicarboxylic acid having 6 to 12 carbon atoms has a moisture absorption property. It contributes to the dimensional stability of resin gears due to small dimensional changes. Further, although it shows good characteristics in terms of chemical, thermal and mechanical strength, it has a problem in terms of long-term strength.

【0010】このようなポリアミドに超高分子量ポリエ
チレンを配合することにより、超高分子量ポリエチレン
がポリアミド中に島(ドメイン)状に分散し、得られる
樹脂製歯車の表面にも存在して滑り剤(潤滑剤)として
機能し、樹脂製歯車の摺動性、耐摩耗性の向上に寄与す
る。
By mixing ultra high molecular weight polyethylene with such a polyamide, the ultra high molecular weight polyethylene is dispersed in the polyamide in the form of islands (domains) and is also present on the surface of the resulting resin gear, and the slip agent ( It functions as a lubricant) and contributes to the improvement of the slidability and wear resistance of the resin gear.

【0011】また、不飽和有機酸変性ポリオレフィン
は、ポリアミドと超高分子量ポリエチレンとの親和性を
高め、超高分子量ポリエチレンの脱落を防止すると共
に、不飽和有機酸変性ポリオレフィン自体も樹脂製歯車
の耐摩耗性の向上に寄与する。
Further, the unsaturated organic acid-modified polyolefin enhances the affinity between the polyamide and the ultra-high molecular weight polyethylene to prevent the ultra-high-molecular-weight polyethylene from falling off, and the unsaturated organic acid-modified polyolefin itself is resistant to the resin gears. It contributes to the improvement of wear resistance.

【0012】このようなことから、ポリアミドに超高分
子量ポリエチレンと不飽和有機酸変性ポリオレフィンと
を配合することにより、樹脂製歯車の摺動性、耐摩耗性
が高められ、長期強度が改善される。
From the above, by blending polyamide with ultra-high molecular weight polyethylene and unsaturated organic acid-modified polyolefin, the slidability and wear resistance of the resin gear are increased and the long-term strength is improved. .

【0013】本発明において、強化繊維として用いるガ
ラス繊維は、特に、平均残存繊維長が80〜1000μ
mであることが好ましく、とりわけ、長さ方向に直角な
断面における長径と短径との比が1.5〜6:1の非円
形断面ガラス繊維であることが好ましい。
In the present invention, the glass fiber used as the reinforcing fiber particularly has an average residual fiber length of 80 to 1000 μm.
m is preferable, and in particular, non-circular cross-section glass fiber having a ratio of major axis to minor axis of 1.5 to 6: 1 in a cross section perpendicular to the length direction is preferable.

【0014】[0014]

【発明の実施の形態】以下に本発明の樹脂製歯車の実施
の形態を詳細に説明する。
BEST MODE FOR CARRYING OUT THE INVENTION Embodiments of the resin gear according to the present invention will be described in detail below.

【0015】本発明で用いる(A)成分のポリアミド
は、メタキシリレンジアミンを70モル%以上含むジア
ミンと炭素数6〜12のα,ω−脂肪族ジカルボン酸を
70モル%以上含むジカルボン酸を重合して得られる。
ジアミン成分としては、メタキシリレンジアミン単独又
はメタキシリレンジアミン70モル%以上とパラキシリ
レンジアミン30モル%以下のキシリレンジアミン混合
物を用いる。酸成分としては炭素数6〜12のα,ω−
脂肪族ジカルボン酸、例えばアジピン酸、セバシン酸、
スベリン酸、ドデカン二酸、エイコジオン酸等が挙げら
れ、これらは1種を単独で用いても良く、2種以上の混
合物として用いても良い。酸成分としては好ましくはア
ジピン酸が挙げられる。
The component (A) polyamide used in the present invention comprises a diamine containing 70 mol% or more of metaxylylenediamine and a dicarboxylic acid containing 70 or more mol% of an α, ω-aliphatic dicarboxylic acid having 6 to 12 carbon atoms. Obtained by polymerization.
As the diamine component, metaxylylenediamine alone or a mixture of xylylenediamine of 70 mol% or more and metaxylylenediamine of 30 mol% or less is used. As the acid component, α, ω- having 6 to 12 carbon atoms
Aliphatic dicarboxylic acids such as adipic acid, sebacic acid,
Examples thereof include suberic acid, dodecanedioic acid, and eicodioic acid. These may be used alone or as a mixture of two or more kinds. Adipic acid is preferably used as the acid component.

【0016】(A)成分のポリアミドは、この両成分の
重縮合反応によって製造されるものである。なお、この
ポリアミドは通常のナイロン6等と比較して結晶化が遅
いという難点があり、結晶核剤として特開昭50−61
449号公報に記載の少量のタルク、特開昭51−63
860号に記載の少量のナイロン66、特開平3−52
953号公報に記載のモンタン酸塩、モンタン酸エステ
ルもしくはモンタン酸エステル塩、或いは平均粒径1〜
10μmのタルクを配合してもよい。
The polyamide as the component (A) is produced by a polycondensation reaction of these two components. It should be noted that this polyamide has a drawback that it is slow to crystallize as compared with ordinary nylon 6 and the like, so that it is used as a crystal nucleating agent in JP-A-50-61.
A small amount of talc described in Japanese Patent No. 449, JP-A-51-63.
A small amount of nylon 66 described in 860, JP-A-3-52
953 gazette, montanic acid salt, montanic acid ester or montanic acid ester salt, or average particle size 1 to
You may mix 10-micrometer talc.

【0017】(A)成分のポリアミドとしては市販品を
用いることもできる。後述の実施例で用いた三菱エンプ
ラ社製「レニー6002」は、メタキシリレンジアミン
と、アジピン酸とを重縮合反応させて得られるポリアミ
ドに、核剤としてナイロン66及びタルクを配合したも
のであり、本発明の(A)成分として用いることができ
る。
As the polyamide as the component (A), a commercially available product may be used. "Renny 6002" manufactured by Mitsubishi Engineering Plastics Co., Ltd. used in Examples described later is a polyamide obtained by polycondensation reaction of metaxylylenediamine and adipic acid with nylon 66 and talc as a nucleating agent. Can be used as the component (A) of the present invention.

【0018】本発明の(B)成分の不飽和有機酸変性ポ
リオレフィンとは、例えばポリエチレン、ポリプロピレ
ン又はこれらの誘導体等を不飽和有機酸で変性したポリ
オレフィンであり、特に、密度0.941〜0.965
の高密度ポリエチレンを不飽和有機酸で変性したものが
好ましい。不飽和有機酸としては、フマル酸、マレイン
酸、ナディック酸、テトラヒドロフタル酸、メタクリル
酸、アクリル酸等、或いはこれらの無水物が挙げられ
る。高密度ポリエチレンの密度がこの範囲よりも低いと
摺動性の改善効果が十分でない場合があり、この範囲よ
りも高いと、成形収縮が大きくなって寸法精度が悪くな
る恐れがある。変性に用いる不飽和有機酸の濃度は得ら
れる不飽和有機酸変性ポリオレフィン中の含有量で0.
5〜5重量%程度が好ましく、変性処理方法としては過
酸化物系開始剤の存在下での溶液反応、又は溶融押出で
の混練による反応が挙げられる。
The unsaturated organic acid-modified polyolefin as the component (B) of the present invention is, for example, a polyolefin obtained by modifying polyethylene, polypropylene, or a derivative thereof with an unsaturated organic acid, and particularly has a density of 0.941 to 0. 965
It is preferable that the high-density polyethylene of 1 is modified with an unsaturated organic acid. Examples of the unsaturated organic acid include fumaric acid, maleic acid, nadic acid, tetrahydrophthalic acid, methacrylic acid, acrylic acid and the like, or anhydrides thereof. If the density of the high-density polyethylene is lower than this range, the slidability improving effect may not be sufficient, and if it is higher than this range, molding shrinkage may increase and dimensional accuracy may deteriorate. The concentration of the unsaturated organic acid used for modification is 0. 1 in terms of the content in the obtained unsaturated organic acid-modified polyolefin.
The modification treatment method is preferably a solution reaction in the presence of a peroxide initiator or a reaction by kneading in melt extrusion.

【0019】樹脂成分中の(B)成分の不飽和有機酸変
性ポリオレフィンの配合量が少ないと不飽和有機酸変性
ポリオレフィンの配合効果を十分に得ることはできず、
多いと寸法精度が低下する恐れがあることから、樹脂成
分中の(B)成分の配合割合は2〜10重量%とする。
When the amount of the unsaturated organic acid-modified polyolefin as the component (B) in the resin component is small, the effect of compounding the unsaturated organic acid-modified polyolefin cannot be sufficiently obtained.
If the amount is large, the dimensional accuracy may be deteriorated. Therefore, the mixing ratio of the component (B) in the resin component is set to 2 to 10% by weight.

【0020】本発明の(C)成分の超高分子量ポリエチ
レンは、ISO 1628−3:1991(135℃の
デカリン溶液中)で測定した極限粘度が6〜40dl/
g、好ましくは10〜30dl/gであるようなポリエ
チレンである。
The ultrahigh molecular weight polyethylene as the component (C) of the present invention has an intrinsic viscosity of 6 to 40 dl / measured in ISO 1628-3: 1991 (in decalin solution at 135 ° C.).
g of polyethylene, preferably 10 to 30 dl / g.

【0021】樹脂成分中の(C)成分の超高分子量ポリ
エチレンの配合量が少ないと超高分子量ポリエチレンの
配合効果を十分に得ることができず、多いと流動性が低
下し、かつポリアミドとの親和性不良により成形性が低
下することから、樹脂成分中の(C)成分の配合割合は
2〜10重量%とする。
When the amount of the ultra high molecular weight polyethylene as the component (C) in the resin component is small, the effect of adding the ultra high molecular weight polyethylene cannot be sufficiently obtained, and when the amount is large, the fluidity is lowered and the mixing with the polyamide is made. Since the moldability is deteriorated due to poor affinity, the blending ratio of the component (C) in the resin component is 2 to 10% by weight.

【0022】なお、本発明に係る樹脂成分は、上記配合
割合で(B)成分の不飽和有機酸変性ポリオレフィンと
(C)成分の超高分子量ポリエチレンとを含有し、残部
は実質的に(A)成分のポリアミドよりなるが、樹脂成
分中には、本発明の目的を損なわない範囲で、結晶化促
進のため、タルク、シリカ、マイカ等の無機質充填剤を
(A)成分に対して0.5〜5重量%程度、また(A)
成分とは異なり(A)成分と比較して10℃以上、好ま
しくは15℃以上融点の高い結晶性熱可塑性樹脂好まし
くはポリアミド(例えばポリアミド66)を(A)成分
に対して1〜15重量%程度配合するのが良い。
The resin component according to the present invention contains the unsaturated organic acid-modified polyolefin of the component (B) and the ultrahigh molecular weight polyethylene of the component (C) in the above blending ratio, and the balance is substantially (A). ) Component, but in the resin component, an inorganic filler such as talc, silica or mica is added to the component (A) in an amount of 0. About 5-5% by weight, (A)
Different from the component (A), a crystalline thermoplastic resin having a melting point of 10 ° C or higher, preferably 15 ° C or higher as compared with the component (A), preferably a polyamide (for example, polyamide 66) is contained in an amount of 1 to 15% by weight based on the component (A). It is good to mix it to some extent.

【0023】樹脂成分中の(B)成分の不飽和有機酸変
性ポリオレフィンと(C)成分の超高分子量ポリエチレ
ンとの配合比は、これらの再成分を配合することによる
効果を十分に得るために、(B)成分の不飽和有機酸変
性ポリオレフィン:(C)成分の超高分子量ポリエチレ
ン=1:0.5〜10(重量比)とすることが好まし
く、これらの合計の配合割合は4〜20重量%であるこ
とが好ましい。
The blending ratio of the unsaturated organic acid-modified polyolefin of the component (B) and the ultrahigh molecular weight polyethylene of the component (C) in the resin component is such that the effects of blending these recomponents can be sufficiently obtained. , (B) unsaturated organic acid-modified polyolefin: (C) component ultrahigh molecular weight polyethylene = 1: 0.5 to 10 (weight ratio), and the total mixing ratio of these is 4 to 20. It is preferably in the weight%.

【0024】本発明の(D)成分のガラス繊維は一般に
樹脂強化用として使用されているものであれば良く、特
に制限はないが、通常は3mm程度の長さを有するチョ
ップドストランドが用いられる。
The glass fiber of the component (D) of the present invention is not particularly limited as long as it is generally used for resin reinforcement, but normally chopped strands having a length of about 3 mm are used.

【0025】長期強度に優れた樹脂製歯車を作製するた
めには、樹脂製歯車中の平均残存繊維長(測定法は後
述)は80〜1000μmであることが好ましく、10
0〜500μmであることが特に好ましい。ガラス繊維
の平均残存繊維長が80μm未満では、得られる歯車の
長期強度が実現せず、1000μmを超えると成形品表
面へのガラス繊維の突出等により、歯車の寸法精度が低
下する。歯車の平均残存繊維長を上記の範囲にするため
には、ガラス繊維の長さ方向の断面の面積は、7×10
−5〜5×10−4mmが好ましい。
In order to produce a resin gear having excellent long-term strength, the average residual fiber length in the resin gear (measuring method will be described later) is preferably 80 to 1000 μm.
It is particularly preferable that the thickness is 0 to 500 μm. If the average residual fiber length of the glass fiber is less than 80 μm, the long-term strength of the obtained gear cannot be realized, and if it exceeds 1000 μm, the dimensional accuracy of the gear is deteriorated due to the protrusion of the glass fiber on the surface of the molded product. In order to make the average residual fiber length of the gear within the above range, the area of the cross section of the glass fiber in the longitudinal direction is 7 × 10.
It is preferably −5 to 5 × 10 −4 mm 2 .

【0026】(D)成分のガラス繊維の繊維長さ方向に
直角な断面における形状は円形であっても良いが、長径
と短径との比が1.5〜6:1程度の非円形、例えば楕
円、長円、繭型等の非円形断面形状であることが好まし
い。このような非円形断面のガラス繊維であれば、円形
断面のガラス繊維よりも比表面積が大きくなり、繊維と
樹脂との密着性が向上して補強効果が高められ、得られ
る歯車の長期強度が改善される。
The shape of the glass fiber of the component (D) in a cross section perpendicular to the fiber length direction may be circular, but a non-circular shape having a ratio of major axis to minor axis of about 1.5 to 6: 1, For example, a non-circular cross-sectional shape such as an ellipse, an ellipse, or a cocoon shape is preferable. With such a glass fiber having a non-circular cross section, the specific surface area becomes larger than that of the glass fiber having a circular cross section, the adhesion between the fiber and the resin is improved, the reinforcing effect is enhanced, and the long-term strength of the resulting gear is improved. Be improved.

【0027】このような(D)成分のガラス繊維の配合
割合は、前述の樹脂成分100重量部に対して40〜2
50重量部とする。この範囲よりもガラス繊維が少ない
と十分な補強効果が得られず、多いと成形性が損なわれ
る。ガラス繊維の好ましい配合量は、前述の樹脂成分1
00重量部に対して60〜200重量部である。
The compounding ratio of the glass fiber as the component (D) is 40 to 2 with respect to 100 parts by weight of the resin component.
50 parts by weight. If the amount of glass fiber is less than this range, a sufficient reinforcing effect cannot be obtained, and if the amount of glass fiber is more than this range, moldability is impaired. The preferable blending amount of glass fiber is the resin component 1 described above.
It is 60 to 200 parts by weight with respect to 00 parts by weight.

【0028】本発明で成形材料となる樹脂組成物を調製
する方法としては特に制限はなく、例えば、(A)〜
(D)成分の所定量を十分に混合し、これを押出機にて
混練し、ストランド状に押し出し、ストランドカッター
にてペレット化する等の方法を採用することができる。
この場合、(D)成分のガラス繊維は、歯車の平均残存
繊維長を確保するため、押出機の途中からサイドフィー
ドする等の方法で供給することが好ましい。
The method for preparing the resin composition which is the molding material in the present invention is not particularly limited, and includes, for example, (A) to
It is possible to employ a method in which a predetermined amount of the component (D) is sufficiently mixed, this is kneaded by an extruder, extruded in a strand shape, and pelletized by a strand cutter.
In this case, the glass fiber of the component (D) is preferably supplied by a method such as side feeding from the middle of the extruder in order to secure the average residual fiber length of the gear.

【0029】なお、本発明に係る樹脂組成物には、必要
に応じて、スチレン系樹脂、ポリカーボネート系樹脂、
ポリブチレンテレフタレート、ポリエチレンテレフタレ
ート等のポリエステル系樹脂、ナイロン46、11、1
2、6、6/6T、6/6I等のポリアミド系樹脂、ポ
リフェニレンスルフィド系樹脂、ポリスルフォン、ポリ
エーテルスルフォン、ポリフェニレンエーテル、ポリエ
ーテルエーテルケトン等の熱可塑性樹脂;炭素繊維、シ
リカ繊維、シリカ・アルミナ繊維、チタン酸カリウム繊
維、ほう酸アルミニウム繊維、ステンレス繊維、アルミ
ニウム繊維等の無機繊維状強化材;アラミド繊維、ポリ
イミド繊維、フッ素樹脂繊維等の有機繊維状強化材;タ
ルク、炭酸カルシウム、マイカ、ガラスビーズ、ガラス
パウダー、ガラスバルーン等の無機充填剤;フッ素樹脂
パウダー、黒鉛、二硫化モリブデン等の固体潤滑剤;パ
ラフィンオイル等の可塑剤;酸化防止剤;熱安定剤;光
安定剤;紫外線吸収剤;中和剤;滑剤;相溶化剤;防曇
剤;アンチブロッキング剤;スリップ剤;分散剤;着色
剤;防菌剤;蛍光増白剤等といった各種添加剤を加える
こともできる。
The resin composition according to the present invention may contain, if necessary, a styrene resin, a polycarbonate resin,
Polyester resins such as polybutylene terephthalate and polyethylene terephthalate, nylon 46, 11, 1
Thermoplastic resins such as polyamide resins such as 2, 6, 6 / 6T and 6 / 6I, polyphenylene sulfide resins, polysulfones, polyether sulfones, polyphenylene ethers and polyether ether ketones; carbon fibers, silica fibers, silica. Inorganic fibrous reinforcing materials such as alumina fibers, potassium titanate fibers, aluminum borate fibers, stainless fibers, aluminum fibers; organic fibrous reinforcing materials such as aramid fibers, polyimide fibers, fluororesin fibers; talc, calcium carbonate, mica, glass Inorganic fillers such as beads, glass powder and glass balloons; solid lubricants such as fluororesin powder, graphite and molybdenum disulfide; plasticizers such as paraffin oil; antioxidants; heat stabilizers; light stabilizers; UV absorbers Neutralizer; Lubricant; Compatibilizer; Antifogging agent; Antiblock Ing agent; slip agents; dispersing agents; coloring agents; antibacterial agent; can be added various additives such as fluorescent whitening agent.

【0030】本発明の樹脂製歯車の成形方法としては、
押出成形法、射出成形法、射出圧縮成形法などが挙げら
れるが、中でも射出成形法がコストの面で望ましい。
The method of molding the resin gear according to the present invention includes:
Examples of the method include an extrusion molding method, an injection molding method, and an injection compression molding method. Among them, the injection molding method is preferable in terms of cost.

【0031】[0031]

【実施例】以下に実施例及び比較例を挙げて本発明をよ
り具体的に説明する。
EXAMPLES The present invention will be described more specifically with reference to Examples and Comparative Examples below.

【0032】なお、以下の実施例及び比較例で成形材料
として用いた各成分の仕様は下記の通りである。 (A)成分 ポリアミド:三菱エンプラ社製「レニー6002」 (B)成分 無水マレイン酸変性高密度ポリエチレン:密度0.94
5g/cmの高密度ポリエチレンを無水マレイン酸と
押出機中で溶融反応させて得た、無水マレイン酸濃度
0.8重量%、MFR0.8g/10minの変性ポリ
エチレン (C)成分 超高分子量ポリエチレン:極限粘度14dl/g、密度
0.94g/cm (D)成分 ガラス繊維A:日東紡績社製「CSH3PA−870
S」 繭型断面 断面積;1.8×10−4mm 長径;約20μm,短径;約10μm 長径/短径の比;約2 ガラス繊維B:日本電気硝子社製「ECS03T−28
9K」 円型断面 断面積;1.3×10−4mm 繊維直径;13μm 長径/短径の比;1
The molding materials used in the following examples and comparative examples
The specifications of each component used as are as follows. (A) component Polyamide: "Renny 6002" manufactured by Mitsubishi Engineering Plastics (B) component Maleic anhydride modified high density polyethylene: Density 0.94
5 g / cmThreeOf high density polyethylene with maleic anhydride
Maleic anhydride concentration obtained by melt reaction in an extruder
Modified poly with 0.8% by weight and MFR 0.8g / 10min
ethylene (C) component Ultra high molecular weight polyethylene: Intrinsic viscosity 14 dl / g, density
0.94 g / cmThree (D) ingredient Glass fiber A: "CSH3PA-870" manufactured by Nitto Boseki Co., Ltd.
S " Cocoon type cross section Cross-sectional area: 1.8 × 10-4mmTwo Major axis: about 20 μm, minor axis: about 10 μm Ratio of major axis / minor axis: about 2 Glass fiber B: "ECS03T-28" manufactured by Nippon Electric Glass Co., Ltd.
9K " Circular cross section Cross-sectional area: 1.3 × 10-4mmTwo Fiber diameter: 13 μm Ratio of major axis / minor axis: 1

【0033】実施例1〜3、比較例1〜5 表1に示す成分(A)〜(C)を予めブレンドし、2軸
押出機にて溶融混練し、成分(D)のガラス繊維はサイ
ドフィーダーから投入してペレット状の樹脂組成物を得
た。混練温度は260℃とした。
Examples 1 to 3 and Comparative Examples 1 to 5 Components (A) to (C) shown in Table 1 were blended in advance and melt-kneaded with a twin-screw extruder. It was charged from a feeder to obtain a pellet-shaped resin composition. The kneading temperature was 260 ° C.

【0034】得られた樹脂のペレットを射出成形機(ア
ーブルグ社製「オールラウンダー750−210−32
0D」)の直径1mmのゲート3点から射出成形し、シ
リンダー温度:260℃、金型温度:120℃、保持
圧:40%で3秒間かけて下記の評価用歯車を成形し
た。 [評価用歯車] 歯車形状 :平歯車 歯外径 :42mm 歯数 :40枚 モジュール:1 圧力角 :20° ねじれ角 :0° ピッチ :円直径 歯幅 :5mm
An injection molding machine (“All Rounder 750-210-32” manufactured by Arburg Co., Ltd. was used to form the obtained resin pellets.
(0D ″) was injection-molded from three points having a diameter of 1 mm, and the following gear for evaluation was molded at a cylinder temperature of 260 ° C., a mold temperature of 120 ° C. and a holding pressure of 40% for 3 seconds. [Evaluation gear] Gear shape: Spur gear tooth outer diameter: 42 mm Number of teeth: 40 modules Module: 1 Pressure angle: 20 ° Twist angle: 0 ° Pitch: Circle diameter Tooth width: 5 mm

【0035】得られた評価用歯車につき、下記の特性評
価試験を行い、結果を表1に示した。 [歯車長期強度試験]評価用歯車を駆動側に、相手歯車
を従動側に固定し、従動側を200rpmで回転させ、
従動側に30kg・cmの負荷トルクを加え、評価用歯
車が破壊するまでの噛合回数を測定した。なお、相手歯
車としては、材質は金属、形状は平歯車、歯数40枚、
モジュール1、圧力角20°、ねじれ角0°、ピッチ円
直径、歯幅10mmのものを用いた。 [平均残存繊維長]評価用歯車の中から約1gの試験片
を切り出し、高周波加熱電気炉にて700℃で15分間
加熱して灰化し、光学顕微鏡写真を撮り、繊維200本
を抽出測定し、その平均値を求めた。
The gears for evaluation thus obtained were subjected to the following characteristic evaluation test, and the results are shown in Table 1. [Gear long-term strength test] The evaluation gear is fixed to the driving side, the mating gear is fixed to the driven side, and the driven side is rotated at 200 rpm.
A load torque of 30 kg · cm was applied to the driven side, and the number of times of meshing until the evaluation gear was broken was measured. As the mating gear, the material is metal, the shape is spur gear, the number of teeth is 40,
Module 1 having a pressure angle of 20 °, a twist angle of 0 °, a pitch circle diameter, and a tooth width of 10 mm was used. [Average Remaining Fiber Length] About 1 g of a test piece was cut out from the gear for evaluation, heated in a high-frequency electric furnace at 700 ° C. for 15 minutes to be incinerated, and an optical micrograph was taken to measure 200 fibers. , And calculated the average value.

【0036】[0036]

【表1】 [Table 1]

【0037】表1より、メタキシリレンジアミンを主体
とするジアミンとα,ω−脂肪族ジカルボン酸を主体と
するジカルボン酸とを重合してなるポリアミドに、不飽
和有機酸変性ポリオレフィン、超高分子量ポリエチレン
及びガラス繊維を配合してなる樹脂組成物を成形してな
る本発明の樹脂製歯車は、良好な長期強度を示すことが
明らかである。
From Table 1, a polyamide obtained by polymerizing a diamine mainly containing metaxylylenediamine and a dicarboxylic acid mainly containing α, ω-aliphatic dicarboxylic acid, an unsaturated organic acid-modified polyolefin, and an ultrahigh molecular weight It is apparent that the resin gear of the present invention obtained by molding a resin composition containing polyethylene and glass fibers exhibits good long-term strength.

【0038】[0038]

【発明の効果】以上詳述した通り、本発明によれば、形
状ないし寸法精度とその安定性に優れると共に、高強度
で長期強度にも優れた樹脂製歯車が提供される。本発明
の樹脂製歯車は、優れた機械的性質、寸法安定性を有す
るため、電気機器、自動車、その他一般機器において、
強度と寸法精度、更には耐久性が要求されるような樹脂
製歯車として極めて有用である。
As described in detail above, according to the present invention, there is provided a resin gear which is excellent in shape and dimensional accuracy and stability thereof, and which has high strength and long-term strength. The resin gear of the present invention has excellent mechanical properties and dimensional stability, and therefore, in electrical equipment, automobiles, and other general equipment,
It is extremely useful as a resin gear that requires strength, dimensional accuracy, and durability.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.7 識別記号 FI テーマコート゛(参考) C08L 23:26 C08L 23:06 23:06) (72)発明者 池田 晶一 東京都港区芝五丁目31番19号 油化電子株 式会社内 (72)発明者 中濱 裕樹 東京都港区芝五丁目31番19号 油化電子株 式会社内 Fターム(参考) 3J030 BC01 BC08 4J002 BB033 BB202 BB212 CL031 DL006 FA046 FD016 GM00 GM04 ─────────────────────────────────────────────────── ─── Continuation of front page (51) Int.Cl. 7 Identification code FI theme code (reference) C08L 23:26 C08L 23:06 23:06) (72) Inventor Shoichi Ikeda Shiba 5-chome, Minato-ku, Tokyo No. 31-19 No. 19 in Yuka Electronics Co., Ltd. In-house (72) Inventor Hiroki Nakahama No. 31-19, Shiba, Minato-ku, Tokyo F-Term in No. 31 Yuka Electronics Co., Ltd. (reference) 3J030 BC01 BC08 4J002 BB033 BB202 BB212 CL031 DL006 FA046 FD016 GM00 GM04

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】 (A)メタキシリレンジアミンを70モ
ル%以上含むジアミンと、炭素数6〜12のα,ω−脂
肪族ジカルボン酸を70モル%以上含むカルボン酸とを
重合して得られたポリアミド80〜96重量%と、 (B)不飽和有機酸変性ポリオレフィン2〜10重量%
と、 (C)超高分子量ポリエチレン2〜10重量%とを含む
樹脂成分100重量部に対して、 (D)ガラス繊維40〜250重量部を配合して得られ
る樹脂組成物を成形してなる樹脂製歯車。
1. A polymer obtained by polymerizing (A) a diamine containing 70 mol% or more of metaxylylenediamine and a carboxylic acid containing 70 mol% or more of an α, ω-aliphatic dicarboxylic acid having 6 to 12 carbon atoms. 80 to 96% by weight of polyamide, and (B) 2 to 10% by weight of unsaturated organic acid-modified polyolefin
And (C) 100 parts by weight of a resin component containing 2 to 10% by weight of ultrahigh molecular weight polyethylene, (D) 40 to 250 parts by weight of glass fiber is mixed to obtain a resin composition, and the obtained resin composition is molded. Resin gear.
【請求項2】 請求項1において、(D)ガラス繊維の
平均残存繊維長が80〜1000μmである樹脂製歯
車。
2. The resin gear according to claim 1, wherein the average residual fiber length of the glass fiber (D) is 80 to 1000 μm.
【請求項3】 請求項1又は2において、(D)ガラス
繊維が、長さ方向に直角な断面における長径と短径との
比が1.5〜6:1の非円形断面ガラス繊維である樹脂
製歯車。
3. The glass fiber (D) according to claim 1 or 2, wherein the ratio of the major axis to the minor axis in the cross section perpendicular to the longitudinal direction is 1.5 to 6: 1. Resin gear.
JP2001400474A 2001-12-28 2001-12-28 Resin gear Expired - Fee Related JP3664133B2 (en)

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WO2007080754A1 (en) 2006-01-13 2007-07-19 Mitsubishi Engineering-Plastics Corporation Polyamide resin composition for portable electronic device and molded article for portable electronic device
WO2008068898A1 (en) * 2006-12-04 2008-06-12 Mitsubishi Engineering-Plastics Corporation Flame-retardant polyamide resin composition and molded article
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WO2014171363A1 (en) * 2013-04-16 2014-10-23 東洋紡株式会社 Glass fiber-reinforced polyamide resin composition
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WO2007080754A1 (en) 2006-01-13 2007-07-19 Mitsubishi Engineering-Plastics Corporation Polyamide resin composition for portable electronic device and molded article for portable electronic device
WO2008068898A1 (en) * 2006-12-04 2008-06-12 Mitsubishi Engineering-Plastics Corporation Flame-retardant polyamide resin composition and molded article
JP2008163317A (en) * 2006-12-04 2008-07-17 Mitsubishi Engineering Plastics Corp Flame-retardant polyamide resin composition and molded article
US8053500B2 (en) 2006-12-04 2011-11-08 Mitsubishi Engineering-Plastics Corporation Flame-retardant polyamide resin composition and molded article
JP2012132027A (en) * 2006-12-04 2012-07-12 Mitsubishi Engineering Plastics Corp Flame-retardant polyamide resin composition and molding
JP2011137563A (en) * 2009-12-25 2011-07-14 Denso Corp Heat exchanger for intercooler
WO2014171363A1 (en) * 2013-04-16 2014-10-23 東洋紡株式会社 Glass fiber-reinforced polyamide resin composition
JP5761632B2 (en) * 2013-04-16 2015-08-12 東洋紡株式会社 Glass fiber reinforced polyamide resin composition
US9512301B2 (en) 2013-04-16 2016-12-06 Toyobo Co., Ltd. Polyamide resin composition reinforced with glass fiber
JPWO2014171363A1 (en) * 2013-04-16 2017-02-23 東洋紡株式会社 Glass fiber reinforced polyamide resin composition
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