JPH0269561A - Polyamide resin composition - Google Patents

Polyamide resin composition

Info

Publication number
JPH0269561A
JPH0269561A JP22212988A JP22212988A JPH0269561A JP H0269561 A JPH0269561 A JP H0269561A JP 22212988 A JP22212988 A JP 22212988A JP 22212988 A JP22212988 A JP 22212988A JP H0269561 A JPH0269561 A JP H0269561A
Authority
JP
Japan
Prior art keywords
polyamide resin
acid
weight
reinforcing material
carboxylic 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.)
Pending
Application number
JP22212988A
Other languages
Japanese (ja)
Inventor
Takashi Nakajima
孝 中島
Atsushi Murakami
篤 村上
Seiji Morimoto
精次 森本
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.)
Mitsubishi Chemical Corp
Original Assignee
Mitsubishi Kasei Corp
Mitsubishi Chemical Industries 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 Mitsubishi Kasei Corp, Mitsubishi Chemical Industries Ltd filed Critical Mitsubishi Kasei Corp
Priority to JP22212988A priority Critical patent/JPH0269561A/en
Publication of JPH0269561A publication Critical patent/JPH0269561A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:To provide a polyamide resin composition having excellent moldability and molding appearance without deteriorating the thermal and mechanical characteristics thereof and suitable for electric and electronic parts, etc., by compounding the zinc compound of a specific aliphatic carboxylic acid in a specified amount. CONSTITUTION:(C) 0.05-2 pts.wt., preferably 0.1-1 pt.wt., of the zinc compound of a 10-36C aliphatic carboxylic acid is compounded with 100 pts.wt. of a composition comprising (A) 75-25wt.% of a polyamide (e.g., nylon 4, 6 or 7) having a relative viscosity of 2-3.5 measured on JIS 6810 and (B) 25-75wt.% of a fibrous reinforcing material (e.g., glass fibers or carbon fibers) having a diameter of 0.001-0.05mm and a length of 0.005-10mm.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、ポリアミド樹脂組成物に関する。詳しくは、
本発明は、良好な外観を有する繊維補強ポリアミド樹脂
組成物に関する。
DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] The present invention relates to a polyamide resin composition. For more information,
The present invention relates to fiber-reinforced polyamide resin compositions with good appearance.

〔従来の技術〕[Conventional technology]

ポリアミド樹脂は、熱的・機械的特性に優れ、電気・電
子部品、機械部品、自動車部品等の広範な分野で使用さ
れている。特に、ガラス繊維や炭素繊維等の繊維状補強
材で補強されたポリアミド樹脂は、強度・剛性・耐熱性
が大幅に向上するために、機能部品や構造部品にも使用
される。
Polyamide resin has excellent thermal and mechanical properties and is used in a wide range of fields such as electrical and electronic parts, mechanical parts, and automobile parts. In particular, polyamide resins reinforced with fibrous reinforcing materials such as glass fibers and carbon fibers are used for functional and structural parts because they have significantly improved strength, rigidity, and heat resistance.

〔発明が解決しようとする問題点〕[Problem that the invention seeks to solve]

しかしながら、ポリアミド樹脂を繊維状補強材で補強す
る場合、補強材の配合量が増加していくと、溶融加工時
の樹脂の流動性が悪化し、成形加工性が著しく低下する
という問題点がある。また、得られる製品の外観が悪化
し、商品価値を著しく損なうという欠点を有する。こう
した傾向は、補強材の配合量が30重貴簡を越えると顕
著になり、45%を越えると、良好な外観を得ることは
掻めて難しくなる。繊維状補強材の配合量を減少させれ
ば、こうした欠点は克服出来るが、その場合は補強効果
が不十分になり、目的とする高いa械的特性は得られな
い。
However, when reinforcing polyamide resin with a fibrous reinforcing material, there is a problem in that as the amount of reinforcing material increases, the fluidity of the resin deteriorates during melt processing, resulting in a significant decrease in moldability. . In addition, it has the disadvantage that the appearance of the resulting product deteriorates, significantly impairing its commercial value. This tendency becomes noticeable when the amount of reinforcing material added exceeds 30%, and when it exceeds 45%, it becomes extremely difficult to obtain a good appearance. These drawbacks can be overcome by reducing the amount of fibrous reinforcing material, but in that case the reinforcing effect becomes insufficient and the desired high mechanical properties cannot be obtained.

このため、良好な外観と加工性とを得るために、ポリア
ミド樹脂の分子量を出来るだけ下げたり、可塑剤を配合
したりすることが行われているが、いずれも得られる組
成物の機械的・熱的特性を著しく損なうため、適用範囲
が限定されている。
For this reason, in order to obtain good appearance and processability, attempts have been made to lower the molecular weight of polyamide resin as much as possible or to add plasticizers to it, but both methods reduce the mechanical and The range of application is limited because it significantly impairs thermal properties.

したがって、繊維状補強材を大量に配合して補強しつつ
、しかも成形加工性に優れ、得られる製品の外観が良好
で、且つ機械的特性にも優れたポリアミド樹脂組成物は
、工業的に容易な方法では得られていないのが実情であ
った。
Therefore, it is possible to create a polyamide resin composition that is reinforced by incorporating a large amount of fibrous reinforcing material, has excellent moldability, has a good appearance, and has excellent mechanical properties, and is industrially easy. The reality is that it has not been obtained using a suitable method.

〔問題点を解決するための手段〕[Means for solving problems]

本発明者らは、上記の問題点に鑑み、鋭意検討した結果
、特定の脂肪族カルボン酸の亜鉛化合物を配合すること
により、成形加工性が良好で、且つ良好な外観の得られ
る繊維補強ポリアミド樹脂を得ることが出来ることを見
出し、本発明に到達したものである。
In view of the above-mentioned problems, the inventors of the present invention have made intensive studies and have developed a fiber-reinforced polyamide that has good moldability and a good appearance by incorporating a specific zinc compound of aliphatic carboxylic acid. The present invention was achieved by discovering that a resin can be obtained.

すなわち、本発明の要旨は、JIS  K6810に準
拠して測定した相対粘度の値が2〜3.5のポリアミド
樹脂75〜25重量%、繊維状補強材25〜75重量%
、からなる組成物100重量部に対し、炭素数10〜3
6の脂肪族カルボン酸の亜鉛化合物を、0.05〜2重
量部配合してなるポリアミド樹脂組成物に存する。
That is, the gist of the present invention is that 75 to 25% by weight of a polyamide resin with a relative viscosity value of 2 to 3.5 measured in accordance with JIS K6810, and 25 to 75% by weight of a fibrous reinforcing material.
10 to 3 carbon atoms per 100 parts by weight of a composition consisting of
The polyamide resin composition contains 0.05 to 2 parts by weight of a zinc compound of aliphatic carboxylic acid No. 6.

以下、本発明を更に詳細に説明する。The present invention will be explained in more detail below.

本発明において使用されるポリアミド樹脂としては、3
員環以上のラクタム、重合可能なω−アミノ酸、二塩基
酸とジアミンなどの重縮合によって得られるポリアミド
樹脂を用いることが出来る。
The polyamide resin used in the present invention includes 3
Polyamide resins obtained by polycondensation of lactams having more than one ring member, polymerizable ω-amino acids, dibasic acids, and diamines can be used.

具体的には、ε−カプロラクタム、アミノカプロン酸、
エナントラクタム、7−アミノへブタン酸、11−アミ
ノウンデカン酸、9−アミノノナン酸、α−ピロリドン
、α−ピペリドンなどを重合して得られるもの、または
、ヘキサメチレンジアミン、ノナメチレンジアミン、ウ
ンデカメチレンジアミン、ドデカメチレンジアミン、メ
タキシリレンジアミンなどのジアミンと、テレフタル酸
、イソフタル酸、アジピン酸、セパチン酸、ドデカンニ
塩基酸、ゲルタール酸などのジカルボン酸とを重縮合せ
しめて得られる重合体またはこれらの共重合体、例えば
、ナイロン4. 6. 7. 8. 11. 12.6
・6,6・10.6・11.6・12,6T、6/6・
6.6/12.6/6T、61/6Tなどが挙げられる
Specifically, ε-caprolactam, aminocaproic acid,
Those obtained by polymerizing enantholactam, 7-aminohbutanoic acid, 11-aminoundecanoic acid, 9-aminononanoic acid, α-pyrrolidone, α-piperidone, etc., or hexamethylenediamine, nonamethylenediamine, undecamethylene Polymers obtained by polycondensing diamines such as diamine, dodecamethylene diamine, metaxylylene diamine, and dicarboxylic acids such as terephthalic acid, isophthalic acid, adipic acid, cepatic acid, dodecanibasic acid, and geltaric acid, or polymers thereof. Copolymers, such as nylon4. 6. 7. 8. 11. 12.6
・6,6・10.6・11.6・12,6T, 6/6・
Examples include 6.6/12.6/6T and 61/6T.

ポリアミド樹脂の相対粘度はJIS  K6810に準
拠して測定した値が2〜3.5の間で選択される。相対
粘度が2より低いと、機械的強度が低下し、3.5を超
えると、得られる成形品の外観が悪化する。
The relative viscosity of the polyamide resin is selected from a value of 2 to 3.5 as measured in accordance with JIS K6810. If the relative viscosity is lower than 2, the mechanical strength will decrease, and if it exceeds 3.5, the appearance of the resulting molded product will deteriorate.

本発明に使用される繊維状補強材としては、ガラス繊維
、炭素繊維、酸化チタンウィスカー、石膏繊維、セラミ
ックファイバー、アスベストなどの無機質繊維状補強物
、銅、アルミニウム、ステンレス等の金属繊維、ポリア
ミド樹脂の成形加工温度より高い融点を有する有機物繊
維などが挙げられる。なかでも、ガラス繊維、炭素繊維
、または、セラミックファイバーの使用が工業的には好
ましい。補強材の形状については特に限定はないが、一
般に、直径は0.001〜0.05mm、その長さは0
.005〜10mが好ましい。
The fibrous reinforcement materials used in the present invention include glass fibers, carbon fibers, titanium oxide whiskers, gypsum fibers, ceramic fibers, inorganic fibrous reinforcements such as asbestos, metal fibers such as copper, aluminum, and stainless steel, and polyamide resins. Examples include organic fibers having a melting point higher than the molding temperature. Among these, it is industrially preferable to use glass fiber, carbon fiber, or ceramic fiber. There is no particular limitation on the shape of the reinforcing material, but generally the diameter is 0.001 to 0.05 mm and the length is 0.001 to 0.05 mm.
.. 005-10m is preferable.

ポリアミド樹脂と繊維状補強材との配合比は、ポリアミ
ド樹脂  75〜25重量%、繊維状補強材   25
〜75重量%、の比率で選ばれる。繊維状補強材の配合
量が25重1%より少ないと、本発明の脂肪族カルボン
酸の亜鉛化合物による外観改良効果は見られず、75重
量%を越えると、成形加工が困難になる。また、繊維状
補強材と併用して、シリカ、アルミナ、シリカ−アルミ
ナ系粘土鉱物、シリカ−マグネシウム系粘土鉱物、ケイ
酸カルシウム、炭酸カルシウム、などの周知の無機充填
材を配合してもよい。
The blending ratio of the polyamide resin and the fibrous reinforcing material is 75 to 25% by weight for the polyamide resin and 25% by weight for the fibrous reinforcing material.
~75% by weight. When the amount of the fibrous reinforcing material is less than 25% by weight and 1% by weight, no appearance improvement effect is observed due to the aliphatic carboxylic acid zinc compound of the present invention, and when it exceeds 75% by weight, molding becomes difficult. In addition, well-known inorganic fillers such as silica, alumina, silica-alumina clay minerals, silica-magnesium clay minerals, calcium silicate, and calcium carbonate may be blended together with the fibrous reinforcing material.

本発明に使用される脂肪族カルボン酸の亜鉛化合物とし
ては、炭素数lθ〜36、好ましくは12〜24の脂肪
族カルボン酸、更に好ましくはそのうちの飽和脂肪族モ
ノカルボン酸である。具体的には、デカン酸、ラウリン
酸、ミリスチン酸、バルミチン酸、ステアリン酸、ベヘ
ン酸、オレイーン酸、エライジン酸、モンタン酸などの
亜鉛塩であり、その配合比率は、ポリアミド樹脂と繊維
状補強材からなる樹脂100重量部に対し、0.05〜
2重量部、好ましくは0.1〜1重量部の範囲で選択さ
れる。配合量が0.05重量部以下では、外観改良効果
が認められず、2重量部を超えると機械的特性が損なわ
れる。
The aliphatic carboxylic acid zinc compound used in the present invention is an aliphatic carboxylic acid having a carbon number lθ to 36, preferably 12 to 24, and more preferably a saturated aliphatic monocarboxylic acid. Specifically, they are zinc salts such as decanoic acid, lauric acid, myristic acid, valmitic acid, stearic acid, behenic acid, oleic acid, elaidic acid, and montanic acid, and their blending ratio is the same as that of polyamide resin and fibrous reinforcing material. 0.05 to 100 parts by weight of resin consisting of
2 parts by weight, preferably in the range of 0.1 to 1 part by weight. If the amount is less than 0.05 parts by weight, no appearance improvement effect will be observed, and if it exceeds 2 parts by weight, mechanical properties will be impaired.

本発明の組成物は、上記配合物以外に、周知の添加剤、
例えば、滑剤、核剤、酸化防止剤、着色剤、難燃剤、帯
電防市剤、耐候性付与剤などを含有してもよい。また、
本発明の組成物の特性を損なわない範囲内で、他の樹脂
を配合することも可能である。
In addition to the above-mentioned formulations, the composition of the present invention includes well-known additives,
For example, it may contain a lubricant, a nucleating agent, an antioxidant, a coloring agent, a flame retardant, an antistatic agent, a weatherability imparting agent, and the like. Also,
It is also possible to blend other resins within a range that does not impair the properties of the composition of the present invention.

本発明の組成物は、バンバリー、エクストルーダー、ス
ーパーミキサーなどの当擦業者に周知の方法で混合され
る。なかでも、混練押出機による溶融混合が好ましい。
The compositions of the present invention are mixed by methods well known to those skilled in the art, such as Banbury, extruders, supermixers, and the like. Among these, melt mixing using a kneading extruder is preferred.

〔実施例〕〔Example〕

以下、本発明を実施例によって具体的に説明するが、本
発明はその要旨を逸脱しない限り、これらに限定される
ものではない。
Hereinafter, the present invention will be specifically explained with reference to Examples, but the present invention is not limited to these unless it departs from the gist thereof.

実施例1〜9 ポリアミド樹脂として、JTS  K6810に4%し
て測定した相対粘度の値が2.2. 2.5. 3゜3
である3種のナイロン6樹脂(三菱化成(株)製、商品
名: NOVAMI D) 、及び、相対粘度が3.0
のナイロン6・6樹脂(旭化成(株)製、商品名レオナ
)を用い、繊維状補強材として、市販のガラス繊維(旭
ファイバーグラス(株)製、商品名:MA486)及び
/又は、炭素繊維(東邦ヘスロン(株)製、商品名:C
06)を用い、脂肪族カルボン酸の亜鉛化合物としてス
テアリン酸亜鉛を、表−1に示す配合比にて混合し、ス
クリュー径4Q+uのベント弐単軸押出機にて、樹脂温
度250〜270°Cにて溶融混合してベレットを得た
。こうして得られたベレットを、120℃にて6時間、
真空乾燥し、型締力100トンの射出成形機にて射出成
形して試験片を得、引張強度、曲げ強度、及び曲げ弾性
率を測定した。また、得られた試験片にて、光沢度を測
定し、表面外観を評価した。また、射出成形に必要な射
出圧力をも測定した。結果は表−2に示した。
Examples 1 to 9 The polyamide resin had a relative viscosity of 2.2% measured by adding 4% to JTS K6810. 2.5. 3゜3
Three types of nylon 6 resin (manufactured by Mitsubishi Kasei Corporation, product name: NOVAMI D), and a relative viscosity of 3.0
A commercially available glass fiber (manufactured by Asahi Fiberglass Co., Ltd., trade name: MA486) and/or carbon fiber was used as a fibrous reinforcing material. (Manufactured by Toho Heslon Co., Ltd., product name: C
06), and mixed zinc stearate as a zinc compound of aliphatic carboxylic acid at the compounding ratio shown in Table 1, and heated the resin at a temperature of 250 to 270°C in a bent two single-screw extruder with a screw diameter of 4Q+U. The mixture was melted and mixed to obtain a pellet. The pellet thus obtained was heated at 120°C for 6 hours.
It was vacuum dried and injection molded using an injection molding machine with a mold clamping force of 100 tons to obtain a test piece, and its tensile strength, bending strength, and bending elastic modulus were measured. In addition, the glossiness of the obtained test piece was measured and the surface appearance was evaluated. The injection pressure required for injection molding was also measured. The results are shown in Table-2.

比較例1〜3 脂肪族カルボン酸の亜鉛化合物を配合せず、各成分の配
合比を表−1のように変えた以外は、実施例1〜9と同
様に行なった。結果を表−2に示した。
Comparative Examples 1 to 3 The same procedures as Examples 1 to 9 were carried out except that the zinc compound of aliphatic carboxylic acid was not blended and the blending ratio of each component was changed as shown in Table 1. The results are shown in Table-2.

比較例4 繊維状補強材の配合量を表−1に示すように変えた以外
は、実施例1〜9と同様に行った。結果を表−2に示し
た。
Comparative Example 4 The same procedure as Examples 1 to 9 was carried out except that the amount of the fibrous reinforcing material was changed as shown in Table 1. The results are shown in Table-2.

比較例5 繊維状補強材の配合量を表−1に示すように変えた以外
は、比較例1〜3と同様に行った。結果を表−2に示し
た。
Comparative Example 5 Comparative Examples 1 to 3 were carried out, except that the amount of the fibrous reinforcing material was changed as shown in Table 1. The results are shown in Table-2.

比較例6〜8 脂肪酸カルボン酸の亜鉛化合物の代わりに、ステアリン
酸バリウム、ステアリン酸カルシウムを使用した他は、
実施例1〜9と同様に行った。結果を表−2に示した。
Comparative Examples 6 to 8 Barium stearate and calcium stearate were used instead of the zinc compound of fatty acid carboxylic acid.
It was carried out in the same manner as Examples 1-9. The results are shown in Table-2.

尚、上記実施例中での各種物性の測定方法は、以下の通
りである。
The methods for measuring various physical properties in the above examples are as follows.

引張強度 :ASTD  D638に準拠して行った。Tensile strength: Tested in accordance with ASTD D638.

曲げ強度 :ASTD  D790に準拠して行った。Bending strength: Conducted in accordance with ASTD D790.

曲げ弾性率:ASTD  D790に準拠して行った。Flexural modulus: Performed in accordance with ASTD D790.

光沢度 :JIS  28741に準拠して角度60度
で行った。
Glossiness: Measured at an angle of 60 degrees in accordance with JIS 28741.

/ 〔発明の効果〕 本発明のポリアミド樹脂組成物においては、熱的・機械
的特性を損なうことなく、成形加工性が大幅に向上し、
得られ成形品の外観も良好である。
/ [Effects of the Invention] In the polyamide resin composition of the present invention, moldability is significantly improved without impairing thermal and mechanical properties,
The appearance of the obtained molded product is also good.

従って、電気・電子部品、機械部品や自動車部品、また
、機能部品や構造部品等広範な分野で好適に使用される
Therefore, it is suitably used in a wide range of fields such as electrical/electronic parts, mechanical parts, automobile parts, functional parts, and structural parts.

出  願 人applicant

Claims (1)

【特許請求の範囲】[Claims] (1)JIS K6810に準拠して測定した相対粘度
の値が2〜3.5のポリアミド樹脂75〜25重量%、
繊維状補強材25〜75重量%、からなる組成物100
重量部に対し、炭素数10〜36の脂肪族カルボン酸の
亜鉛化合物を、0.05〜2重量部配合してなるポリア
ミド樹脂組成物。
(1) 75 to 25% by weight of a polyamide resin with a relative viscosity value of 2 to 3.5 measured in accordance with JIS K6810;
Composition 100 consisting of 25-75% by weight of fibrous reinforcement
A polyamide resin composition containing 0.05 to 2 parts by weight of a zinc compound of an aliphatic carboxylic acid having 10 to 36 carbon atoms.
JP22212988A 1988-09-05 1988-09-05 Polyamide resin composition Pending JPH0269561A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP22212988A JPH0269561A (en) 1988-09-05 1988-09-05 Polyamide resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP22212988A JPH0269561A (en) 1988-09-05 1988-09-05 Polyamide resin composition

Publications (1)

Publication Number Publication Date
JPH0269561A true JPH0269561A (en) 1990-03-08

Family

ID=16777623

Family Applications (1)

Application Number Title Priority Date Filing Date
JP22212988A Pending JPH0269561A (en) 1988-09-05 1988-09-05 Polyamide resin composition

Country Status (1)

Country Link
JP (1) JPH0269561A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2403905B1 (en) 2009-03-04 2016-02-03 DSM IP Assets B.V. Process for preparing injection molded parts with decreased glass fiber read out and injection molded part

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2403905B1 (en) 2009-03-04 2016-02-03 DSM IP Assets B.V. Process for preparing injection molded parts with decreased glass fiber read out and injection molded part

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