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JPH0645750B2 - Polyamide resin composition - Google Patents
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JPH0645750B2 - Polyamide resin composition - Google Patents

Polyamide resin composition

Info

Publication number
JPH0645750B2
JPH0645750B2 JP63264022A JP26402288A JPH0645750B2 JP H0645750 B2 JPH0645750 B2 JP H0645750B2 JP 63264022 A JP63264022 A JP 63264022A JP 26402288 A JP26402288 A JP 26402288A JP H0645750 B2 JPH0645750 B2 JP H0645750B2
Authority
JP
Japan
Prior art keywords
nylon
resin
resin composition
damping performance
polyamide resin
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Fee Related
Application number
JP63264022A
Other languages
Japanese (ja)
Other versions
JPH02113064A (en
Inventor
順二 小泉
宏一 佐藤
鴻治 佐々木
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.)
Toyoda Gosei Co Ltd
Original Assignee
Toyoda Gosei 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 Toyoda Gosei Co Ltd filed Critical Toyoda Gosei Co Ltd
Priority to JP63264022A priority Critical patent/JPH0645750B2/en
Priority to US07/424,614 priority patent/US4980407A/en
Publication of JPH02113064A publication Critical patent/JPH02113064A/en
Publication of JPH0645750B2 publication Critical patent/JPH0645750B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L77/00Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F02COMBUSTION ENGINES; HOT-GAS OR COMBUSTION-PRODUCT ENGINE PLANTS
    • F02FCYLINDERS, PISTONS OR CASINGS, FOR COMBUSTION ENGINES; ARRANGEMENTS OF SEALINGS IN COMBUSTION ENGINES
    • F02F7/00Casings, e.g. crankcases
    • F02F7/006Camshaft or pushrod housings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Vibration Prevention Devices (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Description

【発明の詳細な説明】 〔技術分野〕 本発明は、自動車用部品、特にシリンダヘツドカバー、
ギヤケースなど制振性能が要求されるエンジン周辺部品
の材料として好適なポリアミド樹脂組成物に関する。
Description: TECHNICAL FIELD The present invention relates to automobile parts, particularly a cylinder head cover,
The present invention relates to a polyamide resin composition suitable as a material for an engine peripheral component such as a gear case that requires damping performance.

〔背景技術〕[Background technology]

ナイロン樹脂材料は、金属材料に比較してその製品が軽
量であり、かつ、制振性、剛性、耐熱性、耐油性等の点
において各種の優れた性能を備えているため、近年、軽
量化と騒音低減を目的として、自動車用部品、特に、シ
リンダヘツドカバー、ギヤケースなどのエンジン周辺部
品の成形材料として用いられている。
Nylon resin materials are lighter in weight than metal materials and have various excellent performances in terms of vibration damping, rigidity, heat resistance, oil resistance, etc. For the purpose of reducing noise, it is used as a molding material for automobile parts, particularly engine peripheral parts such as cylinder head covers and gear cases.

一般に樹脂材料は、金属材料に比較すると、その部品の
制振性能は優れるが、騒音低減効果からみると、固体伝
搬音すなわち、その部品自体の振動に基づく音は低減す
るものの、比重が小さいことに基づく、空気透過音は、
増加する。したがって材料の変換による有効な騒音低減
効果を得るためには、空気透過音の増加を上回る固体伝
搬音の低減が要求されることになる。すなわち、言い換
えれば、極端に高い制振性能が要求される。
Generally, resin materials are superior to metal materials in damping performance of their parts, but from the viewpoint of noise reduction effect, solid propagating sound, that is, sound due to vibration of the parts themselves is reduced, but its specific gravity is small. Based on
To increase. Therefore, in order to obtain an effective noise reduction effect due to material conversion, it is required to reduce solid-borne sound that exceeds the increase in air-transmitted sound. That is, in other words, extremely high vibration damping performance is required.

この点からみて、従来、上記の如き自動車部品に使用さ
れているナイロン樹脂材料は、成形部品の制振性能が不
充分であり、あるいは、制振性能があっても、80℃〜12
0℃程度の高温の実用温度領域での制振性能において充
分でないため、解決すべき技術的課題を有していた。
From this point of view, the nylon resin materials conventionally used for the above-mentioned automobile parts have insufficient vibration damping performance of the molded parts, or even if they have vibration damping performance, 80 ° C to 12 ° C.
There was a technical problem to be solved because the vibration damping performance in a high practical temperature range of about 0 ° C was not sufficient.

高温使用条件下における制振性能を改良するため、ポリ
アミド樹脂に粘着付与剤樹脂を配合した樹脂組成物も提
案されているが(特開昭61−36357号参照)、成形部品
の強度、剛性の点において解決さるべき問題が存在して
いる。
A resin composition in which a tackifier resin is mixed with a polyamide resin has been proposed in order to improve the vibration damping performance under high-temperature use conditions (see Japanese Patent Laid-Open No. 61-36357), but the strength and rigidity of molded parts can be improved. There are problems to be solved in terms of points.

一般にプラスチツク材料は粘弾性的性質を強く保有し、
制振性能は主として高分子材料のガラス転移にもとづく
力学分散の損失正接(tanδ)の極大温度前後において
最も高くなり、通常その温度は示差走査熱量測定(DS
C)で観察されるガラス転移温度(Tg)より10゜〜30
℃高い領域に存在する。例えばナイロン6、ナイロン6
6、ナイロン12、ナイロン11、ナイロン610等の直鎖脂肪
族系ナイロンはTgが40゜〜60℃前後で、制振性能は60゜
〜80℃付近で極大となる。またその他のナイロン樹脂と
して、分子鎖中に芳香環を有する結晶性のメタキシリレ
ンジアミン樹脂(MXDナイロン)、ジアミンの一種又は
それ以上とジカルボン酸(テレフタル酸、イソフタル酸
etc)の一種又はそれ以上との共重合体である非晶性ナ
イロン等の芳香族系ナイロンは、Tgが120℃以上であ
り制振性能が極大となるのは130℃以上の高温領域であ
る。
Generally, plastic materials have strong viscoelastic properties,
The damping performance is highest around the maximum temperature of the loss tangent (tan δ) of the mechanical dispersion based on the glass transition of the polymer material, which is usually the differential scanning calorimetry (DS).
From the glass transition temperature (Tg) observed in C) 10 ° to 30
Exists in a region higher by ℃. For example, nylon 6 and nylon 6
Linear aliphatic nylons such as 6, nylon 12, nylon 11, nylon 610, etc., have maximum Tg at 40 ° to 60 ° C and vibration damping performance at around 60 ° to 80 ° C. As other nylon resins, crystalline metaxylylenediamine resin (MXD nylon) having an aromatic ring in the molecular chain, one or more diamines and dicarboxylic acid (terephthalic acid, isophthalic acid).
etc.) of aromatic nylon such as amorphous nylon which is a copolymer with one or more of etc.) has a Tg of 120 ° C or higher and its vibration damping performance is maximized in a high temperature region of 130 ° C or higher. .

本発明者らはポリアミド樹脂材料の制振性、機械的性質
を向上させることを目的として種々研究した結果、特定
のポリアミド樹脂を特定の割合で配合することにより、
種々の要求に適う特性を有するポリアミド樹脂組成物が
得られることを見い出した。
The present inventors have conducted various studies for the purpose of improving the vibration damping property and mechanical properties of the polyamide resin material, and by blending a specific polyamide resin in a specific ratio,
It has been found that a polyamide resin composition having properties that meet various requirements can be obtained.

〔発明の開示〕[Disclosure of Invention]

本発明は、改良された制振性能とともに、著しく優れた
機械的強度を有する成形部品を得るための新規なポリア
ミド樹脂組成物を提供することを目的とする。
An object of the present invention is to provide a novel polyamide resin composition for obtaining a molded part having remarkably excellent mechanical strength as well as improved vibration damping performance.

本発明は、かかる目的に適う新規な樹脂組成物、すなわ
ち (a)ナイロン6樹脂 5〜90重量% (b)芳香族ジアミン系ナイロン樹脂 5〜90重量%およ
び (c)ナイロン66樹脂 5〜90重量% を必須成分として含有することを特徴とするポリアミド
樹脂組成物を提供するものである。
The present invention provides a novel resin composition suitable for such purpose, namely (a) nylon 6 resin 5 to 90% by weight (b) aromatic diamine type nylon resin 5 to 90% by weight and (c) nylon 66 resin 5 to 90%. The present invention provides a polyamide resin composition characterized by containing wt% as an essential component.

以下に本発明を詳細に説明する。The present invention will be described in detail below.

本発明の組成物に使用される上記(a)のナイロン6樹脂
は、カプロラクタム単位を90モル%以上有するポリアミ
ド類であって、他のコモノマー成分、例えばω−ラウロ
ラクタム等を含有していてもよい。分子量、粘度は特に
制限されず、通常の成形条件で成形可能な分子量範囲に
あるものが好ましい。
The above-mentioned (a) nylon 6 resin used in the composition of the present invention is a polyamide having 90 mol% or more of caprolactam units, and may contain other comonomer components such as ω-laurolactam. Good. The molecular weight and viscosity are not particularly limited, and those having a molecular weight range that allows molding under normal molding conditions are preferable.

上記(b)の芳香族ジアミン系ナイロン樹脂は、キシリレ
ンジアミンと脂肪族直鎖2塩基酸とから構成される結晶
性のナイロン樹脂で、このキシリレンジアミンはメタキ
シリレンジアミン、パラキシリレンジアミンあるいはこ
れらの混合物である。上記の脂肪族直鎖2塩基酸の例と
しては、アジピン酸、セバシン酸、スベリン酸、アゼラ
イン酸、ドデカン二酸などを挙げることができる。
The aromatic diamine-based nylon resin (b) is a crystalline nylon resin composed of xylylenediamine and an aliphatic straight chain dibasic acid. The xylylenediamine is metaxylylenediamine or paraxylylenediamine. Alternatively, it is a mixture of these. Examples of the above aliphatic straight chain dibasic acid include adipic acid, sebacic acid, suberic acid, azelaic acid, dodecanedioic acid and the like.

この樹脂としては、特に、メタキシリレンジアミンとア
ジピン酸塩とを主構成成分とするナイロンMXD6が好まし
い。
As this resin, nylon MXD6 containing metaxylylenediamine and adipate as main constituents is particularly preferable.

上記(c)のナイロン66樹脂は、ヘキサメチレンアジパミ
ド単位を90モル%以上有するポリアミド類であって、他
のコモノマー成分、例えばω−ラウロラクタム等を含有
していてもよい。分子量、粘度は特に制限されず、通常
の成形条件で成形可能な分子量範囲にあるものが好まし
い。
The nylon 66 resin of (c) above is a polyamide having 90 mol% or more of hexamethylene adipamide units, and may contain other comonomer components such as ω-laurolactam. The molecular weight and viscosity are not particularly limited, and those having a molecular weight range that allows molding under normal molding conditions are preferable.

本発明の樹脂組成物は、常法により、各成分のペレツ
ト、粉末などを所定の割合にてタンブラー式ブレンダ
ー、ヘンシエルミキサー、リボンミキサー等で混合し、
一軸押出機、二軸押出機、ニーダー、バンバリミキサー
等の通常の混練機を用いて溶融混合することにより得る
ことができる。また、押出機を用いる場合、上記、
(a),(b),(c)の各配合成分のうちの1種類または2種
類をペレツトあるいは粉末の状態であるいは溶融した状
態で、混合の途中で供給してもよい。その他の種々の変
法を用いることも可能である。
The resin composition of the present invention, by a conventional method, mixed pellets of each component, powder and the like at a predetermined ratio with a tumbler type blender, a Henschel mixer, a ribbon mixer and the like,
It can be obtained by melt mixing using an ordinary kneader such as a single-screw extruder, a twin-screw extruder, a kneader, or a Banbury mixer. When using an extruder, the above,
One or two of the components (a), (b) and (c) may be supplied in the form of pellets or powder or in a molten state during the mixing. Various other modified methods can be used.

本発明の樹脂組成物には、その製品の成形性、物性を損
なわない限りにおいて、酸化防止剤、紫外線吸収剤、滑
剤、帯電防止剤、核剤、離型剤、可塑剤、顔料、難燃
剤、増量剤、無機フイラー、繊維状補強剤、他の樹脂材
料等を添加することができる。
The resin composition of the present invention includes an antioxidant, an ultraviolet absorber, a lubricant, an antistatic agent, a nucleating agent, a release agent, a plasticizer, a pigment, and a flame retardant as long as the moldability and physical properties of the product are not impaired. , Extenders, inorganic fillers, fibrous reinforcing agents, other resin materials and the like can be added.

本発明に係る樹脂組成物は、その成形製品が、高い制振
性能を有し、かつ機械的特性も優れていることから、自
動車部品、電気・機械部品に適用可能であり、特に自動
車のエンジンルーム内において振動により騒音が発生す
る製品、例えばシリンダヘツドカバー、ギヤカバー、オ
イルパン等は好適使用例として挙げることができる。
INDUSTRIAL APPLICABILITY The resin composition according to the present invention is applicable to automobile parts and electric / mechanical parts because the molded product has high vibration damping performance and excellent mechanical properties, and in particular, it is an engine for automobiles. Products in which noise is generated in the room due to vibration, such as a cylinder head cover, a gear cover, and an oil pan, may be mentioned as suitable examples of use.

シリンダヘツドカバー、ギヤカバー等のエンジン周辺部
品については、制振性能以外に高い剛性と耐熱性が要求
されるため、材料として使用するにあたっては、ガラス
繊維、マイカ、ウオラストナイト、タルク、カルボン繊
維等のフイラーで補強して用いることが好ましい。
In addition to damping performance, high rigidity and heat resistance are required for engine peripheral parts such as cylinder head covers and gear covers, so glass fibers, mica, wollastonite, talc, carbon fiber, etc. should be used as materials. It is preferable to reinforce with a filler.

以下に、本発明に係る樹脂組成物に関する実施例を比較
例とともに掲げる。
Below, the Example regarding the resin composition which concerns on this invention is given with a comparative example.

〔試料作製、測定方法〕[Sample preparation, measurement method]

実施例、比較例ともに表に示した各配合成分をタンブラ
ー式ブレンダーで5分間混合し、得られた混合物をL/
D=27、30mm異方向回転2軸押出機で溶融混練しペレツ
ト化した。ペレツトを100℃5時間乾燥した後、メルト
プレスによりテストピースを成形し、これを試料とし
た。測定前に真空中にて100℃、8時間アニールした。
In each of the examples and the comparative examples, the ingredients shown in the table were mixed for 5 minutes with a tumbler type blender, and the resulting mixture was mixed with L / L.
D = 27, melted and kneaded into pellets with a 30 mm counter-rotating twin-screw extruder. After drying the pellet at 100 ° C. for 5 hours, a test piece was formed by melt pressing and used as a sample. Before the measurement, it was annealed in vacuum at 100 ° C. for 8 hours.

・損失係数(註:制振性能の尺度となる) 試料形状:150mm×150mm、厚さ3mm 測定法:恒温槽中で、試料の中心部を0.1Gで加振させ伝
達関数を測定し、2次共振点から半値幅法にて損失係数
ηを計算した。
・ Loss coefficient (Note: This is a measure of vibration damping performance) Sample shape: 150 mm × 150 mm, thickness 3 mm Measurement method: Measure the transfer function by shaking the center of the sample with 0.1 G in a constant temperature bath. The loss coefficient η was calculated from the next resonance point by the half-width method.

・引張強度、引張破断伸び 試料形状:JIS3号ダンベル厚さ0.5mm 測定条件:クロスヘツドスピード50mm/min、23±3℃雰
囲気中、標線間隔20mm 得られた結果を表に示す。
-Tensile strength, tensile elongation at break Sample shape: JIS No. 3 dumbbell thickness 0.5 mm Measurement conditions: Crosshead speed 50 mm / min, 23 ± 3 ° C atmosphere, marked line spacing 20 mm The results obtained are shown in the table.

以上、述べたところから明らかなように本発明に係るポ
リアミド樹脂組成物は、その成形品の制振性能、特に80
〜100℃の高温条件下における制振性能が優れており、
かつ、機械的強度においても著しく優れているものであ
る。
As described above, as apparent from the above, the polyamide resin composition according to the present invention has a vibration-damping performance of the molded article, particularly 80
It has excellent vibration damping performance under high temperature conditions of ~ 100 ° C.
In addition, it is remarkably excellent in mechanical strength.

───────────────────────────────────────────────────── 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 77/06 77:02) ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 5 Identification code Office reference number FI technical display location (C08L 77/06 77:02)

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】(a)ナイロン6樹脂 5〜90重量% (b)芳香族ジアミン系ナイロン樹脂 5〜90重量%およ
び (c)ナイロン66樹脂 5〜90重量% を必須成分として含有することを特徴とするポリアミド
樹脂組成物。
1. A composition comprising (a) nylon 6 resin 5 to 90% by weight (b) aromatic diamine type nylon resin 5 to 90% by weight and (c) nylon 66 resin 5 to 90% by weight as essential components. A characteristic polyamide resin composition.
JP63264022A 1988-10-21 1988-10-21 Polyamide resin composition Expired - Fee Related JPH0645750B2 (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
JP63264022A JPH0645750B2 (en) 1988-10-21 1988-10-21 Polyamide resin composition
US07/424,614 US4980407A (en) 1988-10-21 1989-10-20 Polyamide resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP63264022A JPH0645750B2 (en) 1988-10-21 1988-10-21 Polyamide resin composition

Publications (2)

Publication Number Publication Date
JPH02113064A JPH02113064A (en) 1990-04-25
JPH0645750B2 true JPH0645750B2 (en) 1994-06-15

Family

ID=17397466

Family Applications (1)

Application Number Title Priority Date Filing Date
JP63264022A Expired - Fee Related JPH0645750B2 (en) 1988-10-21 1988-10-21 Polyamide resin composition

Country Status (1)

Country Link
JP (1) JPH0645750B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104072984A (en) * 2014-06-12 2014-10-01 安徽安尔达机电有限公司 Oil-resistant high-temperature-resistant nylon material for speed control gear

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5129292A (en) * 1974-09-02 1976-03-12 Kyowa Hakko Kogyo Kk HATSUKOHONYORUGURUKOOSU OYOBI TOREHAROOSU NO SHIBOSANESUTERU NO SEIZOHO
JPS5129293A (en) * 1974-09-02 1976-03-12 Ajinomoto Kk Kogakutekini kakuseinaganryuaminosan no seizohoho
JPS6229460A (en) * 1985-07-31 1987-02-07 Nippon Denso Co Ltd Device for controlling load on wiper arm
JPH072903B2 (en) * 1986-03-26 1995-01-18 三菱瓦斯化学株式会社 Molding polyamide resin composition with excellent metal plating properties

Also Published As

Publication number Publication date
JPH02113064A (en) 1990-04-25

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