JPH047359A - Polyamide resin composition - Google Patents

Polyamide resin composition

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Publication number
JPH047359A
JPH047359A JP11127190A JP11127190A JPH047359A JP H047359 A JPH047359 A JP H047359A JP 11127190 A JP11127190 A JP 11127190A JP 11127190 A JP11127190 A JP 11127190A JP H047359 A JPH047359 A JP H047359A
Authority
JP
Japan
Prior art keywords
polyamide
graft polymer
polyamide resin
resin composition
melt
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
JP11127190A
Other languages
Japanese (ja)
Inventor
Minoru Matsuda
松田 稔
Hiroyuki Kawamura
宏之 河村
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.)
TAKAYASU KK
Original Assignee
TAKAYASU KK
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 TAKAYASU KK filed Critical TAKAYASU KK
Priority to JP11127190A priority Critical patent/JPH047359A/en
Publication of JPH047359A publication Critical patent/JPH047359A/en
Pending legal-status Critical Current

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  • Compositions Of Macromolecular Compounds (AREA)

Abstract

PURPOSE:To obtain the title repeatedly reclaimable good composition continuously, easily and inexpensively by melt-kneading a polyamide with a graft polymer containing an unsaturated carboxylic acid (anhydride) as a monomer unit. CONSTITUTION:100 pts.wt. polyamide is melt-kneaded with 0.1-1 pt.wt., desirably 0.3-1 pt.wt. graft polymer containing an unsaturated carboxylic acid (anhydride) as a monomer unit.

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は、エンジニアリングプラスチックとして汎用さ
れるポリアミド系樹脂組成物に関するものである。
DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to a polyamide resin composition that is widely used as an engineering plastic.

(従来技術) 近年、ポリアミド系樹脂は強靭性、自己潤滑性、耐摩耗
性、耐薬品性、自己消火性、ガスバリア性等に優れたエ
ンジニアリングプラスチックとして多くの分野において
汎用されている。
(Prior Art) In recent years, polyamide resins have been widely used in many fields as engineering plastics with excellent toughness, self-lubricating properties, wear resistance, chemical resistance, self-extinguishing properties, gas barrier properties, etc.

(発明が解決しようとする課題) しかしながら、ポリアミドは押出加工や射出成形等の融
点以上の温度での加工において、加工機械のシリンダー
内で熱分解が起こり、熱履歴を重ねるごとに分子量や機
械的強度が低下することは避けられず、成形用樹脂とし
ての再利用の1つの障害となっていた。
(Problem to be solved by the invention) However, when polyamide is processed at temperatures above its melting point, such as extrusion processing and injection molding, thermal decomposition occurs within the cylinder of the processing machine, and as the thermal history increases, the molecular weight and mechanical A decrease in strength was unavoidable, which was an obstacle to reusing it as a molding resin.

本発明は、このような欠点に鑑み、ポリアミドと、ポリ
アミドと反応うしる官能基を持ったグラフトポリマーと
をブレンドすることによって、連続的な工程において簡
単に、しかも安価で繰り返し再生可能な良質のポリアミ
ド系樹脂組成物を提供することを目的とするものである
In view of these drawbacks, the present invention aims to produce a high-quality product that can be easily, inexpensively, and repeatedly regenerated in a continuous process by blending polyamide with a graft polymer having a functional group that reacts with the polyamide. The object of the present invention is to provide a polyamide resin composition.

(課題を解決するための手段) 本発明を以下に詳細に説明する。(Means for solving problems) The present invention will be explained in detail below.

本発明におけるグラフトポリマーの分子構造は不飽和カ
ルボン酸またはその無水物から誘導されるモノマーユニ
ントを幹成分に含み、任意のポリマーセグメントを枝成
分に持つものである。
The molecular structure of the graft polymer in the present invention includes a monomer unit derived from an unsaturated carboxylic acid or its anhydride as a trunk component, and has arbitrary polymer segments as branch components.

不飽和カルボン酸またはその無水物としては、例えばア
クリル酸、メタクリル酸、マレイン酸、フマル酸等の不
飽和カルボン酸、無水マレイン酸等の不飽和カルボン酸
無水物が挙げられる。これらのうち、ポリアミドの末端
アミノ基との反応性の点から不飽和カルボン酸無水物が
好ましく、特に無水マレイン酸が好ましい。
Examples of the unsaturated carboxylic acid or anhydride thereof include unsaturated carboxylic acids such as acrylic acid, methacrylic acid, maleic acid, and fumaric acid, and unsaturated carboxylic acid anhydrides such as maleic anhydride. Among these, unsaturated carboxylic acid anhydrides are preferred from the viewpoint of reactivity with the terminal amino groups of polyamide, and maleic anhydride is particularly preferred.

本発明のポリアミド系樹脂組成物は、ポリアミドおよび
グラフトポリマーからなる樹脂組成物であり、その配合
割合は、ポリアミド100重量部に対して、グラフトポ
リマーが0.1〜1重量部が好ましく、0.3〜1重量
部がさらに好ましい。
The polyamide resin composition of the present invention is a resin composition consisting of polyamide and a graft polymer, and the blending ratio thereof is preferably 0.1 to 1 part by weight, and 0.1 to 1 part by weight of the graft polymer to 100 parts by weight of the polyamide. 3 to 1 part by weight is more preferred.

ここで、グラフトポリマーの割合が0.1重量部未満で
は、グラフトポリマーの効果が不十分であるため好まし
くなく、グラフトポリマーの割合が1重量を超えると混
練の際の溶融粘度が上昇しすぎて成形性の低下を招いた
り、最終成形品の物性低下を引き起こす恐れがあるため
好ましくない。
If the proportion of the graft polymer is less than 0.1 part by weight, the effect of the graft polymer will be insufficient, which is not preferable, and if the proportion of the graft polymer exceeds 1 part by weight, the melt viscosity during kneading will increase too much. This is not preferable because it may cause a decrease in moldability or a decrease in the physical properties of the final molded product.

本発明のポリアミド系樹脂組成物は、ポリアミドおよび
グラフトポリマーの両者を通常のブレンド方法、例えば
押出機、ニーダ−等を使用して溶融混練すれば良い。好
ましい方法は、各種ミキサー等を用いて混合し、これを
押出機を用いて加熱溶融させて押し出し、ペレット状に
カットする方法によって得られる。
The polyamide resin composition of the present invention may be obtained by melt-kneading both the polyamide and the graft polymer using a conventional blending method, such as an extruder or kneader. A preferred method is to mix the mixture using various types of mixers, heat and melt the mixture using an extruder, extrude the mixture, and cut the mixture into pellets.

(実施例) 本発明の実施例を以下に詳細に説明する。(Example) Embodiments of the present invention will be described in detail below.

なお、各側に記載の部は重量部を意味する。In addition, the parts written on each side mean parts by weight.

実施例1〜6 市販のポリアミド樹脂(高安■製、商品名タナジン6ナ
イロンTN 100) 100部に、グラフトポリマー
を表1〜表4に記載した割合(0,05部〜1.5部)
で添加し、単軸スクリュー押出機を用いて、シリンダー
温度230°Cで溶融ブレンドした。
Examples 1 to 6 The ratio of graft polymer listed in Tables 1 to 4 (0.05 parts to 1.5 parts) to 100 parts of commercially available polyamide resin (manufactured by Takayasu ■, trade name Tanazine 6 Nylon TN 100)
and melt blended using a single screw extruder at a cylinder temperature of 230°C.

このブレンド物を十分に乾燥させ、再度単軸スクリュー
押出機で溶融ブレンドし、この作業をさらにもう1度繰
り返して、合計3回の繰り返し再生品を作成した。
This blend was thoroughly dried, melt-blended again using a single-screw extruder, and this operation was repeated one more time to produce recycled products a total of three times.

これら1〜3回までの繰り返し再生品からまずオストワ
ルド粘度計を用いて相対粘度を測定し、さらに射出成形
機を用いて試験片を作成してそれらを引張試験、曲げ試
験およびアイゾツト衝撃試験に供した。
First, the relative viscosity of the products recycled 1 to 3 times was measured using an Ostwald viscometer, and then test pieces were made using an injection molding machine and subjected to a tensile test, a bending test, and an Izot impact test. did.

ただし、相対粘度はJ I S  K−6810、引張
試験、曲げ試験およびアイゾツト衝撃試験はそれぞれA
STM  D−638、D −790、D−256に準
じて行った。
However, the relative viscosity is determined by JIS K-6810, and the tensile test, bending test, and Izot impact test are determined by A.
It was conducted according to STM D-638, D-790, and D-256.

実施例7〜12 市販のポリアミド樹脂(高安■製、商品名タナジン66
ナイロンTN710)100部に、グラフトポリマーを
表5〜表8に記載した割合(0,05部〜1.5部)で
添加し、単軸スクリュー押出機を用いて、シリンダー温
度270°Cで溶融ブレンドした。
Examples 7 to 12 Commercially available polyamide resin (manufactured by Takayasu, trade name Tanajin 66)
The graft polymer was added to 100 parts of nylon TN710) in the proportions listed in Tables 5 to 8 (0.05 parts to 1.5 parts), and melted at a cylinder temperature of 270 °C using a single screw extruder. Blended.

このブレンド物を十分に乾燥させ、再度単軸スクリュー
押出機で溶融ブレンドし、この作業をさらにもう1度繰
り返して、合計3回の繰り返し再生品を作成した。
This blend was thoroughly dried, melt-blended again using a single-screw extruder, and this operation was repeated one more time to produce recycled products a total of three times.

これら1〜3回までの繰り返し再生品からまずオストワ
ルド粘度計を用いて相対粘度を測定し、さらに射出成形
機を用いて試験片を作成してそれらを引張試験、曲げ試
験およびアイゾツト衝撃試験に供した。
First, the relative viscosity of the products recycled 1 to 3 times was measured using an Ostwald viscometer, and then test pieces were made using an injection molding machine and subjected to a tensile test, a bending test, and an Izot impact test. did.

なお、試験方法は実施例1〜6に準じた。In addition, the test method was based on Examples 1-6.

比較例1.2 グラフトポリマーを添加しないこと以外は実施例1〜6
および実施例7〜12と同様にして行った。
Comparative Example 1.2 Examples 1 to 6 except that no graft polymer was added
And it carried out similarly to Examples 7-12.

以上の各側におけるポリアミド系樹脂組成物の試験結果
を表1〜8にまとめて示した。
The test results of the polyamide resin compositions on each side are summarized in Tables 1 to 8.

ただし、表中のオリジナルの数値は今回使用したポリア
ミド樹脂の押出前の測定値を示す。
However, the original values in the table indicate the values measured before extrusion of the polyamide resin used this time.

(以下余白) 表2 引張強度 (kg/cn) 〔オリジナル:620) 表1 相対粘度 〔オリジナル: 2゜ 7] 表3 引張破断伸び (%) 〔オリジナル: 150〕 表4 アイゾツト衝撃強度 (kg °cu+ / cm ) (オリジナル: 9゜ 3〕 表6 引張強度 (kg/cd) 〔オリジナルニア80) 表5 相対粘度 〔オリジナル: 2゜ 8〕 表7 引張破断伸び (%) 〔オリジナル:40] 表8 アイゾツト衝撃強度(kg−CIIl/Cl11)〔オ
リジナル:4.0.1 実施例および比較例により、次のことが明らかである。
(Leaving space below) Table 2 Tensile strength (kg/cn) [Original: 620] Table 1 Relative viscosity [Original: 2°7] Table 3 Tensile elongation at break (%) [Original: 150] Table 4 Izod impact strength (kg ° cu+/cm) (Original: 9゜3) Table 6 Tensile strength (kg/cd) [Original near 80] Table 5 Relative viscosity [Original: 2゜8] Table 7 Tensile elongation at break (%) [Original: 40] Table 8 Izod impact strength (kg-CIIl/Cl11) [Original: 4.0.1 The following is clear from the examples and comparative examples.

ポリアミド樹脂は高剛性、高靭性の両方を兼ね備えるエ
ンジニアプラスチックの代表各であるが、表1〜表8の
それぞれの比較例で示されるように繰り返し押出加工を
続けると熱分解反応により明らかに粘度低下を起こして
重合度が低下し、物性も低下するが、実施例のようにグ
ラフトポリマーを添加することにより本発明の範囲内で
はほとんど粘度低下が見られず、むしろ粘度の向上さえ
図ることができる。
Polyamide resin is a representative engineering plastic that has both high rigidity and high toughness, but as shown in the comparative examples in Tables 1 to 8, when extrusion processing is continued repeatedly, the viscosity clearly decreases due to thermal decomposition reaction. However, by adding a graft polymer as in the example, within the scope of the present invention, almost no viscosity decrease is observed, and in fact, the viscosity can even be improved. .

また、表2.3および表6.7の剛直性の目安となる引
張試験においても、比較例では強度低下や破断伸びの急
激な低下が目立つのに対して本発明の範囲では全く低下
が見られなかった。
In addition, in the tensile tests shown in Tables 2.3 and 6.7, which serve as a guideline for stiffness, in the comparative examples there was a noticeable decrease in strength and rapid decrease in elongation at break, whereas in the scope of the present invention, no decrease was observed at all. I couldn't.

更に、表4および表8のアイゾツト衝撃強さにおいても
相対粘度や引張試験と同様に3回もの繰り返し再生後で
も高い物性を保持することができる。
Furthermore, in terms of Izod impact strength shown in Tables 4 and 8, high physical properties can be maintained even after repeated regeneration as many as three times, similar to the relative viscosity and tensile tests.

よって本発明は、ポリアミド樹脂に容易に反応しうるよ
うな特定構造を持つグラフトポリマーを微量添加するこ
とにより粘度低下を防止することができ、しかも剛性、
靭性の両面で大変価れた樹脂組成物を得ることができる
Therefore, the present invention can prevent a decrease in viscosity by adding a small amount of a graft polymer having a specific structure that can easily react to a polyamide resin, and also improve rigidity and
It is possible to obtain a resin composition that is highly valued in terms of both toughness.

(発明の効果) 本発明に係るポリアミド系樹脂組成物は、ポリアミドと
、不飽和カルボン酸またはその無水物をモノマーユニッ
トとして含有するグラフトポリマーとを溶融混練してな
り、ポリアミド100重量部に対して、グラフトポリマ
ーが0.1〜1重量部であることを特徴とするため、ポ
リアミド樹脂を繰り返し再生する際の靭性低下の防止と
衝撃強度の向上を安価で容易に、しかも連続的に達成す
ることにおいて工業的に非常に有用である。
(Effect of the invention) The polyamide resin composition according to the present invention is obtained by melt-kneading polyamide and a graft polymer containing an unsaturated carboxylic acid or its anhydride as a monomer unit, and is made by melt-kneading polyamide and a graft polymer containing an unsaturated carboxylic acid or its anhydride as a monomer unit, and is made by melt-kneading polyamide and a graft polymer containing an unsaturated carboxylic acid or its anhydride as a monomer unit. Since the graft polymer is contained in an amount of 0.1 to 1 part by weight, it is possible to prevent a decrease in toughness and improve impact strength when repeatedly regenerating a polyamide resin at a low cost, easily, and continuously. It is very useful industrially.

Claims (1)

【特許請求の範囲】 ポリアミドと、不飽和カルボン酸またはその無水物をモ
ノマーユニットとして含有するグラフトポリマーとを溶
融混練してなり、 ポリアミド100重量部に対して、グラフトポリマーが
0.1〜1重量部であることを特徴とするポリアミド系
樹脂組成物。
[Scope of Claims] Polyamide and a graft polymer containing an unsaturated carboxylic acid or its anhydride as a monomer unit are melt-kneaded, and the amount of the graft polymer is 0.1 to 1 weight per 100 parts by weight of the polyamide. 1. A polyamide-based resin composition characterized in that:
JP11127190A 1990-04-25 1990-04-25 Polyamide resin composition Pending JPH047359A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP11127190A JPH047359A (en) 1990-04-25 1990-04-25 Polyamide resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP11127190A JPH047359A (en) 1990-04-25 1990-04-25 Polyamide resin composition

Publications (1)

Publication Number Publication Date
JPH047359A true JPH047359A (en) 1992-01-10

Family

ID=14556985

Family Applications (1)

Application Number Title Priority Date Filing Date
JP11127190A Pending JPH047359A (en) 1990-04-25 1990-04-25 Polyamide resin composition

Country Status (1)

Country Link
JP (1) JPH047359A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4957832A (en) * 1987-12-11 1990-09-18 Varta Batterie Aktiengesellschaft Plastic sealing element for a galvanic primary cell

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4957832A (en) * 1987-12-11 1990-09-18 Varta Batterie Aktiengesellschaft Plastic sealing element for a galvanic primary cell

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