JPS59161461A - Glass fiber-reinforced polyamide resin composition - Google Patents

Glass fiber-reinforced polyamide resin composition

Info

Publication number
JPS59161461A
JPS59161461A JP3464583A JP3464583A JPS59161461A JP S59161461 A JPS59161461 A JP S59161461A JP 3464583 A JP3464583 A JP 3464583A JP 3464583 A JP3464583 A JP 3464583A JP S59161461 A JPS59161461 A JP S59161461A
Authority
JP
Japan
Prior art keywords
weight
glass fiber
polyamide resin
impact strength
resin composition
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
JP3464583A
Other languages
Japanese (ja)
Inventor
Kanji Nagayoshi
永吉 監二
Yoshio Takezawa
竹沢 良夫
Takeshi Terajima
寺島 毅
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.)
Toray Industries Inc
Original Assignee
Toray Industries Inc
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 Toray Industries Inc filed Critical Toray Industries Inc
Priority to JP3464583A priority Critical patent/JPS59161461A/en
Publication of JPS59161461A publication Critical patent/JPS59161461A/en
Pending legal-status Critical Current

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  • Compositions Of Macromolecular Compounds (AREA)

Abstract

PURPOSE:To prepare the titled composition having remarkably improved impact strength and excellent surface smoothness and moldability, by compounding a polyamide resin with glass fibers and an alkyl amide of a benzenesulfonic acid derivative. CONSTITUTION:The objective composition is prepared by compounding (A) 86- 30wt% (preferably 60-40wt%) of a polyamide (preferably nylon 6) with (B) 10- 50wt% (preferably 30-50wt%) of glass fiber preferably having a length of 0.1- 10mm. and (C) 4-20wt% (preferably 7-15wt%) of an alkylamide of a benzenesulfonic acid derivative, preferably benzenesulfonic acid butylamide.

Description

【発明の詳細な説明】 本発明はガラス繊維で強化してなる衝撃性、表面平滑性
、成形性の優れ1こポリアミド樹脂組成物に関するもの
である。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a polyamide resin composition reinforced with glass fibers and having excellent impact resistance, surface smoothness and moldability.

従来ガラス繊維で強化しtこポリアミド樹脂は引張強度
や耐衝撃性などの機械的性質や耐熱性などが非常に優れ
ていることがら高機能用材料としてガラスamが30〜
45重量%添加されたものが自動車、家電一般機器用と
して大量に使用されている。
Traditionally, polyamide resins reinforced with glass fibers have excellent mechanical properties such as tensile strength and impact resistance, and heat resistance, so glass am is used as a high-performance material.
Products containing 45% by weight are used in large quantities for automobiles and general home appliances.

しかしながら最近、自動車用途には外部がらの大きな衝
撃荷重に耐えうろようにさらに耐衝撃性の高いものが要
求されつつあり、使用材料は耐衝撃性の改良が必要にな
ってき1こ。
However, recently, materials with even higher impact resistance are required for automobile applications in order to withstand large external impact loads, and the materials used need to be improved in impact resistance.

そこで木発明者らはガラス強化ポリアミドの耐衝撃性の
一層の向上を目的とし鋭意検討し1こ結果、ポリアミド
樹脂にガラス繊維とベノゼ/スルホン酸誘導体のアルキ
ルアミドと混合することにより衝撃強度が著しく向上す
ることを見い出し本発明に達し1こ。
Therefore, the inventors conducted extensive research with the aim of further improving the impact resistance of glass-reinforced polyamide, and found that by mixing polyamide resin with glass fiber and benoze/sulfonic acid derivative alkylamide, the impact strength was significantly increased. We have discovered that this can be improved and have arrived at the present invention.

すなわち本発明はポリアミド樹脂86〜30重量%、ガ
ラス繊維10〜80重量%およびベンゼンスルホノM 
誘導体のアルキルアミド4〜20重量%とからなるガラ
ス繊維強化ポリアミド樹脂組成物を要旨と下る。
That is, the present invention comprises 86 to 30% by weight of polyamide resin, 10 to 80% by weight of glass fiber, and benzenesulfono M.
A glass fiber-reinforced polyamide resin composition comprising 4 to 20% by weight of a derivative alkylamide is summarized below.

本発明におけるポリアミド樹脂とはナイロン6、ナイロ
/66、ナイロ/6・10.ナイロン4・6等の脂肪族
ポリアミド均質重合体又は共重合ポリアミドであるが、
Cれらの中でナイロン6が最も好ましい。これらのポリ
アミド樹脂は耐炎剤、顔料、結晶化核剤などの有機物質
、無機物質を添加され1こものであっても使用可能であ
る。
The polyamide resins used in the present invention include nylon 6, nylon/66, nylon/6/10. Aliphatic polyamide homopolymer or copolymer polyamide such as nylon 4/6,
Of these, nylon 6 is most preferred. These polyamide resins can be used even if they contain organic or inorganic substances such as flame retardants, pigments, and crystallization nucleating agents.

本発明で使用するガラス繊維の形状には特に制限はなく
通常のガラス繊維強化熱可塑性樹脂ニ使用されろ長繊細
タイプ(ガラスローピンク0−ビッグマット)から短繊
維タイプ(チョツプドストランド、チョップトスI・ラ
ッドマットミルドファイバー)のものまで任意の形状で
使用可能であるが、射出成形で望ましい機械的強度を発
揮させる1こめには01〜Ion長さのガラス繊維が望
ましい。
There are no particular restrictions on the shape of the glass fibers used in the present invention, and ordinary glass fiber-reinforced thermoplastic resins can be used. Glass fibers having a length of 01 to Ion are preferable in order to exhibit the desired mechanical strength in injection molding.

本発明で使用下るベンゼンスルホノ酸誘導体のアルキル
アミドとしてはベンゼンスルポンブチルアミド、N−エ
チル−p二トルエ/スルポンアミド、0−およびp−ト
ルエン・エチルスルホンアミド、N−シクロヘキシル−
p−トルエン・スルホンアミドがあげられる。特に好ま
しくはベンゼンスルホノブチルアミドが用いられる。
Examples of the alkylamides of benzenesulfonate derivatives used in the present invention include benzenesulfonebutyramide, N-ethyl-p-nitolue/sulponamide, 0- and p-toluene/ethylsulfonamide, N-cyclohexyl-
Examples include p-toluene sulfonamide. Particularly preferably, benzenesulfonobutyramide is used.

本発明の組成物はポリアミド樹脂、ガラス繊維及びペン
セノヌルポ、[71体のアルキルアミドとを溶尉混合法
によって得られろ。例えば(1)ポリアミド樹脂、短繊
維タイプのガラス繊維及びベンゼンスルホノ酸誘導体の
アルキルアミドを押出機内で溶融混練後ペレット状に切
断する方法、(2)がリアミド樹脂、短繊維タイプのガ
ラス繊維を押出混線後ペレット状にし1こものを射出成
形、又は押出成)杉用組成物の製造において、これらベ
ンゼンスルホン酸誘導体のアルキルアミドをトライブレ
ンドで混合し、そのまま成形材料にする方法等が挙げら
れるが、混合法、添加方法は必ずしもこれらに限定され
ろものではない。
The composition of the present invention can be obtained by mixing a polyamide resin, glass fibers, pencenonulpolymer, and an alkylamide. For example, (1) a method in which polyamide resin, short fiber type glass fiber, and alkylamide of a benzenesulfonate derivative are melt-kneaded in an extruder and then cut into pellets; After extrusion mixing, the mixture is made into pellets and then injection molded, or extrusion molded.In the production of a composition for cedar, the alkylamides of these benzenesulfonic acid derivatives are mixed in a triblend and used as a molding material as is. However, the mixing method and addition method are not necessarily limited to these.

前記の混合法においては前記の組成物の総重量を基準に
ボリア2ド樹脂86〜30重量%、好ましくは60〜4
0重量%、ガラス繊維10〜50重量%、好ましくは3
0〜50重量%及びベンゼンスルホノ酸誘導体のアルキ
ルアミド4〜20重量%、好ましくは7〜15重量%の
範囲から任意に選択されるが、mJ記のスルホン酸アミ
ド誘導体が4重量%未満では上記向上効果が顕著でなく
、20重U%を超えると強化ポリアミド樹脂の性質を阻
害して、耐熱性を低下させ1コリ、色調の悪化、機械的
性質を低下させtこりする1こめに好ましくない。
In the above mixing method, 86 to 30% by weight, preferably 60 to 4% by weight of the boria 2-do resin, based on the total weight of the above composition.
0% by weight, glass fiber 10-50% by weight, preferably 3
0 to 50% by weight and 4 to 20% by weight of the alkylamide of the benzenesulfonate derivative, preferably 7 to 15% by weight, but if the sulfonic acid amide derivative of mJ is less than 4% by weight. The above-mentioned improvement effect is not remarkable, and if it exceeds 20% by weight, the properties of the reinforced polyamide resin will be inhibited, the heat resistance will be lowered, the color tone will deteriorate, the mechanical properties will be deteriorated, and the stiffness will occur. do not have.

mJ 記(7) y、 11/ ホ/酸アミド誘導体と
ガラy、 Jdl 維を上記ポリアミド樹脂に混合する
ことによりガラス繊維及びポリアミド樹脂のみの混合物
からなる組成物に比へポリアミド樹脂とガラス繊維の濡
れ特性が向上して機械的強度、特に衝撃強度が著しく向
上し、かつガラス繊維強化材料としては特異な曲げ1こ
ゎみ量が増大し、靭性の優し1コ、そして他の機械的強
度を低下させることのない、ガラス繊維強化ポリアミド
樹脂を得ろことができる。
mJ Note (7) y, 11/ By mixing the ho/acid amide derivative and the glassy, Jdl fibers with the above polyamide resin, the composition of the polyamide resin and glass fibers is compared to a composition consisting of a mixture of only glass fibers and polyamide resin. The wetting properties are improved and the mechanical strength, especially the impact strength, is significantly improved, and the amount of bending per bend, which is unique for a glass fiber reinforced material, is increased, and it has excellent toughness and other mechanical strengths. It is possible to obtain a glass fiber-reinforced polyamide resin without deterioration.

かくして得られる本発明組成物は射出成形、押出成形、
ブロー成形など、公知の成形方法に適用できる。
The composition of the present invention thus obtained can be processed by injection molding, extrusion molding,
It can be applied to known molding methods such as blow molding.

以下に実施例により本発明の効果をさらに詳述Tる。The effects of the present invention will be explained in more detail below with reference to Examples.

なお各実施例における落球衝撃強さの測定は次のように
行なっtこ。
The falling ball impact strength in each example was measured as follows.

(1)  落球衝撃強さ 100Il#(1)×3闘の円板成形品に536gの鋼
球を種々の高さから落下させ50%頻度で′破壊する時
の破壊エネルギーを求めtコ。
(1) Determine the fracture energy when a 536 g steel ball is dropped from various heights onto a disc molded product with a falling ball impact strength of 100 Il#(1) x 3 and breaks at a frequency of 50%.

実施例1 ナイロン6樹脂45重量%にノラノ化合物で処理し1こ
短繊紹ガラス繊維45重量%さらにベンゼンスルホノブ
チルアミドを10重量%添加したものをよく混合し、単
軸押出機で成形用ペレ ノ ト を 得 tこ 。
Example 1 45% by weight of nylon 6 resin treated with a nolano compound, 45% by weight of single short fiber glass fiber, and 10% by weight of benzenesulfonbutyramide were mixed well and molded using a single screw extruder. Get Perenote.

次にこのペレットを成形温度26(Ic、射出圧力65
0 kQ / d、金型温度80cで各機製作所製射出
成形機5J−35Bを用いて射出成形を行ない物件測定
用の成形品を得た。
Next, this pellet is molded at a temperature of 26 (Ic) and an injection pressure of 65
Injection molding was performed using an injection molding machine 5J-35B manufactured by Kakaku Seisakusho at a mold temperature of 80 C and a mold temperature of 0 kQ/d to obtain a molded product for object measurement.

この成形品の機械的強度の測定結果を以下に示す。The results of measuring the mechanical strength of this molded article are shown below.

引張強度1,6ooAg/cd ノツチ無衝撃強度     1 18 kq * tx
 / cd落球衝撃強さ   103 kti # C
M曲げ弾性率  950 kg / amなおペンゼノ
スルホン酸誘導体のアルキルアミドを混合せず、同量の
ガラス繊維のみをナイロン樹脂(55重量%)に混合し
1こものについて同じように試験し1こ結果を以下に示
す。
Tensile strength 1,6ooAg/cd Notch non-impact strength 1 18 kq * tx
/ CD falling ball impact strength 103 kti # C
M flexural modulus: 950 kg/am The same amount of glass fiber was mixed with nylon resin (55% by weight) without mixing the penzenosulfonic acid derivative alkylamide, and one sample was tested in the same way. The results are shown below.

引張強さ 2.000 kti / dノツプ無衝撃強
さ      9 0 kg ・α/ cd落錘衝撃強
さ    70 kti 61曲げ弾性率  1.20
0 kti / d前記比較結果から明らかなように、
本発明のガラス繊維強化ポリアミド樹脂組成物は衝撃強
度が著しく向上している。
Tensile strength 2.000 kti / d Knop non-impact strength 9 0 kg ・α / cd Falling weight impact strength 70 kti 61 Flexural modulus 1.20
0 kti/dAs is clear from the above comparison results,
The glass fiber reinforced polyamide resin composition of the present invention has significantly improved impact strength.

実施例2 p−)ルエノ・エチルスルホンアミドラ添加し1こもの
を使い他は実施例1と全く同じ条件で物性を測定し1こ
Example 2 p-) Physical properties were measured under exactly the same conditions as in Example 1 using one sample with the addition of lueno-ethylsulfonamide.

結果は次の通りであっ1こ。The result is as follows.

引張強度 1.420 kq / cdノツチ無衝撃強
さ     11 6 ky ・α/ ci落錘衝撃強
さ    95 kq−α 曲げ弾性率  950 kg @ mj実施例1の結果
と同様に衝撃強度の同士が著しい。
Tensile strength 1.420 kq / cd notch non-impact strength 11 6 ky α / ci Falling weight impact strength 95 kq-α Flexural modulus 950 kg @ mj Similar to the results of Example 1, the impact strengths are significantly different .

実施例3 ナイロン6樹脂55重量%、ガラスm維45重量%で強
化し1こ樹脂組成物100重量部にペンゼノスルホノプ
チルアミド2〜25重量部を各々添加して、実施例1に
使つ1こ成形機ノリツタ−内でスクリュー回転数6Or
pm、 ソリ/タ一温度265℃で溶融混線しγこ後、
物性測定用の試験片を得Tこ。
Example 3 2 to 25 parts by weight of penzenosulfonoptylamide were added to 100 parts by weight of a resin composition reinforced with 55% by weight of nylon 6 resin and 45% by weight of glass M fiber, and used in Example 1. Screw rotation speed 6 Or in the single molding machine Noritsuta
pm, after melting and mixing at a warp/taper temperature of 265°C,
Obtain test pieces for measuring physical properties.

物性測定条件は実施例1と全く同じである。The physical property measurement conditions are exactly the same as in Example 1.

結果表から明らかなようにペンゼノスルホンフチル72
 F cn ffx 謝方法はトライブレンド法テあつ
でも衝撃強度は同士する。1こだベンゼンスルホンブチ
ルアミドの添加量が5%未満では衝撃強度の向上効果は
小さい。
As is clear from the result table, penzenosulfonphthyl 72
F cn ffx The impact strength is the same even though the tri-blend method is used. If the amount of one benzenesulfone butyramide added is less than 5%, the effect of improving impact strength is small.

実施例4 共重合ナイロン(6/66=90/10)樹脂45重量
%、ガラス繊維45重量%、ベンゼンスルホンブチルア
ミド10重量%をよ<混合し、実施例1と同様、押出し
成形品を射出成形し1こ。
Example 4 45% by weight of copolymerized nylon (6/66=90/10) resin, 45% by weight of glass fiber, and 10% by weight of benzenesulfone butyramide were mixed, and an extrusion molded product was injected in the same manner as in Example 1. 1 piece molded.

物性を測定しjコ結果は下記の通りである〇引張強度 
1.380 kg / cd□ ノンチ無衝撃強度  
   1 28 kQ 拳rs / c+1落錘衝撃強
度   130 kg −ex曲げ弾性率  830 
kq / *jなおベンゼンスルホンブチルアミドを混
合していない同じガラス繊維量強化の共重合ナイロン樹
脂の物性測定結果は下記の通りである。
The physical properties were measured and the results are as follows: 〇Tensile strength
1.380 kg/cd□ Non-chip impact strength
1 28 kQ fist rs/c+1 falling weight impact strength 130 kg -ex bending modulus 830
kq / *j The physical properties of the same glass fiber-reinforced copolymerized nylon resin without benzenesulfone butyramide mixed therein are as follows.

引張強度 1.780 kq / cdノツチ無衝撃強
度     1 06 kq−cm / cd落錘衝撃
強度   110にす・α 曲げ弾性率  1.250旬/− ガラス繊維強化共重合ナイロン樹脂においても本発明の
衝撃強度同士効果が顕著に認められる。
Tensile strength 1.780 kq/cd notch non-impact strength 106 kq-cm/cd falling weight impact strength 110 mm/α Flexural modulus 1.250 mm/- Glass fiber reinforced copolymerized nylon resin also has the impact of the present invention A remarkable strength-to-strength effect is observed.

特許出願人 東 し 株 式 会 社Patent applicant Higashi Shikikai Co., Ltd.

Claims (1)

【特許請求の範囲】[Claims] ポリアミド86〜30重量%、ガラス繊細10〜50重
世%およびべ/ゼノスルホン酸誘導体のアルキルアミド
4〜20重量%よりなるガラス繊組強化ポリアミド樹脂
組成物。
A glass fiber-reinforced polyamide resin composition comprising 86 to 30% by weight of polyamide, 10 to 50% by weight of glass fines, and 4 to 20% by weight of alkylamides of be/xenosulfonic acid derivatives.
JP3464583A 1983-03-04 1983-03-04 Glass fiber-reinforced polyamide resin composition Pending JPS59161461A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP3464583A JPS59161461A (en) 1983-03-04 1983-03-04 Glass fiber-reinforced polyamide resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP3464583A JPS59161461A (en) 1983-03-04 1983-03-04 Glass fiber-reinforced polyamide resin composition

Publications (1)

Publication Number Publication Date
JPS59161461A true JPS59161461A (en) 1984-09-12

Family

ID=12420171

Family Applications (1)

Application Number Title Priority Date Filing Date
JP3464583A Pending JPS59161461A (en) 1983-03-04 1983-03-04 Glass fiber-reinforced polyamide resin composition

Country Status (1)

Country Link
JP (1) JPS59161461A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100373179B1 (en) * 1996-12-17 2003-08-19 주식회사 코오롱 Polyamide resin composition for extrusion molding of tubing
CN101880456A (en) * 2010-07-14 2010-11-10 深圳市科聚新材料有限公司 Fiber glass reinforced polyamide composite material and preparation method thereof

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100373179B1 (en) * 1996-12-17 2003-08-19 주식회사 코오롱 Polyamide resin composition for extrusion molding of tubing
CN101880456A (en) * 2010-07-14 2010-11-10 深圳市科聚新材料有限公司 Fiber glass reinforced polyamide composite material and preparation method thereof

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