JPS6229460B2 - - Google Patents

Info

Publication number
JPS6229460B2
JPS6229460B2 JP16384179A JP16384179A JPS6229460B2 JP S6229460 B2 JPS6229460 B2 JP S6229460B2 JP 16384179 A JP16384179 A JP 16384179A JP 16384179 A JP16384179 A JP 16384179A JP S6229460 B2 JPS6229460 B2 JP S6229460B2
Authority
JP
Japan
Prior art keywords
polyamide
weight
inorganic filler
resin composition
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
Application number
JP16384179A
Other languages
Japanese (ja)
Other versions
JPS5686950A (en
Inventor
Katsuo Sato
Kyoshi Morishige
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 Gas Chemical Co Inc
Original Assignee
Mitsubishi Gas Chemical Co 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 Mitsubishi Gas Chemical Co Inc filed Critical Mitsubishi Gas Chemical Co Inc
Priority to JP16384179A priority Critical patent/JPS5686950A/en
Publication of JPS5686950A publication Critical patent/JPS5686950A/en
Publication of JPS6229460B2 publication Critical patent/JPS6229460B2/ja
Granted legal-status Critical Current

Links

Description

【発明の詳細な説明】[Detailed description of the invention]

本発明は無機充填材及びガラス繊維を配合した
ポリアミド樹脂組成物に関し、更に詳しくはガラ
ス繊維及び無機充填材を配したポリアミド樹脂成
形材料にキシリレンジアミン系ポリアミドを加え
ることによつて成形物の機械的性質、特に引張
り、曲げ、圧縮強度及び各弾性率を改良し、吸水
性が小さく、寸法安定性のよい成形物を与え、し
かも成形性にすぐれたポリアミド樹脂組成物を提
供するものである。 従来ナイロン6は広く成形加工等の種々の分野
で実用化されており、その機械的物性の向上、あ
るいはコストダウンのためこれにガラス繊維ある
いは無機充填材を配合して成形材料とすることが
種々の配合処方について試みられている。しかし
ながらガラス繊維を配合した場合には機械的物性
の改良はなされるもののナイロン6の有する欠
点、特に吸水率が高く、又成形収縮が大きく寸法
安定性に欠けること、そりが発生すること等の解
決が未だ十分になされていない。又無機充填材を
配合した場合には機械的物性、中でも特に衝撃強
度が大巾に低下してポリアミドの特徴が生かされ
ていない。 本発明者らはこのナイロン6成形材料の改良に
ついて研究を進めた結果、ナイロン6にガラス繊
維及び無機充填材を併用配合して成るポリアミド
樹脂成形材料に、キシリレンジアミン系ポリアミ
ドを加えることによつて成形物の機械的物性を向
上させ、吸水性が小さく、寸法安定性にすぐれ、
更に成形性にすぐれた工業的に実用性ある成形材
料組成物を見い出し本発明を完成するに至つた。 すなわち、本発明はナイロン6、キシリレンジ
アミン系ポリアミド、ガラス繊維及び無機充填材
を必須成分として含有するポリアミド樹脂組成物
であつて、該組成物中ナイロン6が10〜50重量
%、キシリレンジアミン系ポリアミドが10〜70重
量%、ガラス繊維および無機充填材の合計量が20
〜60重量%であることを特徴とする。 本発明に於けるキシリレンジアミン系ポリアミ
ドはキシリレンジアミンと炭素数6〜12の脂肪族
直鎖二塩基酸とから得られ、該ポリアミドの構成
成分であるキシリレンジアミンはメタキシリレン
ジアミンが好ましいが、40%以下のパラキシリレ
ンジアミンを含んでも差支えない。又炭素数6〜
12の脂肪族直鎖二塩基酸はアジピン酸、スベリン
酸、セバシン酸、ドデカンジオン酸等を挙げるこ
とが出来、これらの2種以上の混合物であつても
よい。その中では主としてアジピン酸を使用して
得られたものがナイロン6の改質効果の上で特に
好ましい。ナイロン6に配合するキシリレンジア
ミン系ポリアミドの量は組成物全体を100重量%
とした場合10〜70重量%が好ましく、特に好まし
くは20〜30重量%である。 本発明で使用される無機充填材としては炭酸カ
ルシウム、タルク、マイカ及びカオリナイトから
選ばれ、これらの2種以上の混合物として使用す
ることも差支えない。この無機充填材の配合量と
しては40重量%以下が望ましく、特に20重量%付
近が適当である。この量は併用すガラス繊維の量
との関係で決められ、組成物中のガラス繊維と無
機充填材との合計量は20〜60重量%であり、60重
量%を超えるとナイロン樹脂への配合が困難とな
り、又組成物の成形性をも著しく低下させる。又
20重量%以下では成形収縮が大きくなつたり、又
所期の強度が発揮出来ないので特に30〜50重量%
の間が好ましい。上記無機充填材は通常その表面
を処理することなく使用することが出来るがカツ
プリング剤等で表面処理したものも目的に応じて
使用出来る。 ガラス繊維は通常のガラス繊維強化プラスチツ
クスに用いられるものであれば特に制限はない
が、普通は長さ3〜6m/mのチヨツプドストラ
ンドが用いられる。 さらに本発明のポリアミド樹脂組成物には必要
に応じて酸化防止剤、着色剤、滑剤、難燃剤或い
は結晶化促進剤なども加えることが出来る。 本発明のポリアミド樹脂組成物を得るための調
製方法としては、ナイロン6、キシリレンジアミ
ン系ポリアミド、ガラス繊維チヨツプドストラン
ド及び無機充填材を所定量充分に混合し、これを
押出機にて混練し、ストランド状に押出しストラ
ンドカツターにてペレツト化する等を一例として
挙げることが出来る。 本発明のポリアミド樹脂組成物から得られる成
形物の機械的性質はナイロン6が本来持つている
性能に比べて著しく改善されているが、特に引
張、曲げ、圧縮の各強度及び弾性率などが著しく
改善され、吸水率は大巾に小さくなり、寸法安定
性が向上し、成形物の反り等が著しく減少する。 以下に本発明の実施例を記す。尚、機械的物性
はASTMに準じてそれぞれ測定した。 実施例 1 下記の表1に示す組成で配合した各ポリアミド
樹脂組成物を押出機によりペレツト化し、該ペレ
ツトを射出成形機で、金型温度130℃にて試験片
を成形し、その機械的性質を測定した。比較のた
めメタキシリレンジアミン系ポリアミドを配合し
ない組成物も同じ方法により試験片を作製した。
これらの試験結果を組成と共に表1に示す。(表
中、Bを付した試験No.は比較例である。以下の表
においても同じ。)
The present invention relates to a polyamide resin composition containing an inorganic filler and a glass fiber, and more specifically, by adding xylylene diamine-based polyamide to a polyamide resin molding material containing a glass fiber and an inorganic filler, it is possible to make a molded product by adding The purpose of the present invention is to provide a polyamide resin composition which has improved mechanical properties, particularly tensile, bending, compressive strength, and each modulus of elasticity, has low water absorption, provides molded products with good dimensional stability, and has excellent moldability. Conventionally, nylon 6 has been widely used in various fields such as molding, and in order to improve its mechanical properties or reduce costs, it has been mixed with glass fiber or inorganic fillers to make molding materials. Attempts have been made to formulate combinations of However, when glass fiber is added, although the mechanical properties are improved, the drawbacks of nylon 6, such as high water absorption, large mold shrinkage, lack of dimensional stability, and warpage cannot be overcome. Not enough has been done yet. Furthermore, when an inorganic filler is blended, the mechanical properties, particularly the impact strength, are significantly reduced, and the characteristics of polyamide are not utilized. As a result of our research into improving this nylon 6 molding material, the present inventors found that by adding xylylene diamine-based polyamide to a polyamide resin molding material made of nylon 6 combined with glass fiber and an inorganic filler. This improves the mechanical properties of molded products, has low water absorption, and has excellent dimensional stability.
Furthermore, the present invention was completed by discovering an industrially practical molding material composition with excellent moldability. That is, the present invention is a polyamide resin composition containing nylon 6, xylylene diamine-based polyamide, glass fiber, and an inorganic filler as essential components, wherein the composition contains 10 to 50% by weight of nylon 6 and xylylene diamine. 10-70% by weight of polyamide, total amount of glass fiber and inorganic filler is 20%
~60% by weight. The xylylene diamine-based polyamide in the present invention is obtained from xylylene diamine and an aliphatic linear dibasic acid having 6 to 12 carbon atoms, and the xylylene diamine that is a constituent component of the polyamide is preferably metaxylylene diamine. However, it may contain up to 40% paraxylylene diamine. Also carbon number 6~
Examples of the 12 aliphatic linear dibasic acids include adipic acid, suberic acid, sebacic acid, and dodecanedioic acid, and may be a mixture of two or more of these. Among them, those obtained mainly using adipic acid are particularly preferred in terms of the effect of modifying nylon 6. The amount of xylylene diamine polyamide added to nylon 6 is 100% by weight of the entire composition.
In this case, it is preferably 10 to 70% by weight, particularly preferably 20 to 30% by weight. The inorganic filler used in the present invention is selected from calcium carbonate, talc, mica, and kaolinite, and a mixture of two or more of these may be used. The blending amount of this inorganic filler is preferably 40% by weight or less, particularly around 20% by weight. This amount is determined in relation to the amount of glass fiber used together, and the total amount of glass fiber and inorganic filler in the composition is 20 to 60% by weight, and if it exceeds 60% by weight, it will be added to the nylon resin. In addition, the moldability of the composition is significantly reduced. or
If it is less than 20% by weight, molding shrinkage will increase and the desired strength will not be achieved, so especially 30 to 50% by weight.
Preferably between. The above-mentioned inorganic fillers can usually be used without surface treatment, but those that have been surface treated with a coupling agent or the like can also be used depending on the purpose. The glass fiber is not particularly limited as long as it is used in ordinary glass fiber reinforced plastics, but chopped strands with a length of 3 to 6 m/m are usually used. Furthermore, antioxidants, colorants, lubricants, flame retardants, crystallization promoters, etc. can also be added to the polyamide resin composition of the present invention, if necessary. As a preparation method for obtaining the polyamide resin composition of the present invention, nylon 6, xylylene diamine polyamide, glass fiber chopped strands, and inorganic filler are sufficiently mixed in a predetermined amount, and then mixed in an extruder. For example, the mixture may be kneaded, extruded into strands, and pelletized using a strand cutter. The mechanical properties of molded products obtained from the polyamide resin composition of the present invention are significantly improved compared to the properties originally possessed by nylon 6, but in particular, the tensile, bending, and compressive strengths and modulus of elasticity are significantly improved. The water absorption rate is greatly reduced, the dimensional stability is improved, and the warping of molded products is significantly reduced. Examples of the present invention are described below. The mechanical properties were measured according to ASTM. Example 1 Each polyamide resin composition blended with the composition shown in Table 1 below was pelletized using an extruder, and the pellet was molded into a test piece using an injection molding machine at a mold temperature of 130°C, and its mechanical properties were evaluated. was measured. For comparison, a test piece of a composition containing no metaxylylene diamine polyamide was prepared using the same method.
These test results are shown in Table 1 along with the composition. (Test numbers marked with B in the table are comparative examples. The same applies to the tables below.)

【表】【table】

【表】 実施例 2 下記の表2に示す組成で配合した組成物を実施
例1と同様にしてペレツト化し金型温度130℃で
実施例1と同様にして成形した直径2インチ、厚
さ1/8インチの円板状試片についてその成形収縮
率を溶融樹脂の金型への流入方向及び流入方向に
対し直角方向とについて測定した。この結果を表
2に示す。この場合、この値が小さく又その差が
少なければ少ない程寸法安定性にすぐれていると
言える。なお表2中での記号、〓はそれぞれ溶
融樹脂の流入方向及び流入方向に対し直角の方向
を表わし、組成中ナイロン66は結晶化核剤として
加えた。
[Table] Example 2 A composition blended with the composition shown in Table 2 below was pelletized in the same manner as in Example 1, and molded in the same manner as in Example 1 at a mold temperature of 130°C. A pellet with a diameter of 2 inches and a thickness of 1 The molding shrinkage rate of a /8 inch disk-shaped specimen was measured in the direction in which the molten resin flows into the mold and in the direction perpendicular to the direction of flow. The results are shown in Table 2. In this case, it can be said that the smaller this value and the smaller the difference, the better the dimensional stability. Note that the symbol 〓 in Table 2 represents the inflow direction of the molten resin and the direction perpendicular to the inflow direction, respectively, and nylon 66 was added as a crystallization nucleating agent in the composition.

【表】 実施例 3 実施例2と同じ組成及び形状の試験片について
20℃で24時間水中に浸漬した時の吸水率を測定し
た。その結果を表3に示す。ポリ(メタキシリレ
ンアジパミド)の添加によつてその吸水率が大巾
に改善されていることが見られる。
[Table] Example 3 Regarding test pieces with the same composition and shape as Example 2
The water absorption rate was measured when immersed in water for 24 hours at 20°C. The results are shown in Table 3. It can be seen that the water absorption rate is greatly improved by the addition of poly(methaxylylene adipamide).

【表】【table】

Claims (1)

【特許請求の範囲】 1 ナイロン6、キシリレンジアミン系ポリアミ
ド、ガラス繊維及び無機充填材を必須成分として
含有するポリアミド樹脂組成物であつて、該組成
物中ナイロン6が10〜50重量%、キシリレンジア
ミン系ポリアミドが10〜70重量%、ガラス繊維及
び無機充填材の合計量が20〜60重量%であること
を特徴とするポリアミド樹脂組成物。 2 キシリレンジアミン系ポリアミドが、キシリ
レンジアミンと炭素数6〜12の直鎖脂肪族二塩基
酸とを反応させて得られるものである特許請求の
範囲第1項記載のポリアミド樹脂組成物。 3 無機充填材が炭酸カルシウム、タルク、マイ
カ及びカオリナイトから選ばれた少なくとも1種
である特許請求の範囲第1項記載のポリアミド樹
脂組成物。
[Scope of Claims] 1. A polyamide resin composition containing nylon 6, xylylene diamine polyamide, glass fiber, and an inorganic filler as essential components, wherein the composition contains 10 to 50% by weight of nylon 6, A polyamide resin composition characterized in that the diamine polyamide is 10 to 70% by weight, and the total amount of glass fiber and inorganic filler is 20 to 60% by weight. 2. The polyamide resin composition according to claim 1, wherein the xylylene diamine-based polyamide is obtained by reacting xylylene diamine with a linear aliphatic dibasic acid having 6 to 12 carbon atoms. 3. The polyamide resin composition according to claim 1, wherein the inorganic filler is at least one selected from calcium carbonate, talc, mica, and kaolinite.
JP16384179A 1979-12-17 1979-12-17 Polyamide resin composition Granted JPS5686950A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP16384179A JPS5686950A (en) 1979-12-17 1979-12-17 Polyamide resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP16384179A JPS5686950A (en) 1979-12-17 1979-12-17 Polyamide resin composition

Publications (2)

Publication Number Publication Date
JPS5686950A JPS5686950A (en) 1981-07-15
JPS6229460B2 true JPS6229460B2 (en) 1987-06-26

Family

ID=15781760

Family Applications (1)

Application Number Title Priority Date Filing Date
JP16384179A Granted JPS5686950A (en) 1979-12-17 1979-12-17 Polyamide resin composition

Country Status (1)

Country Link
JP (1) JPS5686950A (en)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3200428A1 (en) * 1982-01-09 1983-07-14 Bayer Ag, 5090 Leverkusen Polyamide moulding compositions
JPS58168654A (en) * 1982-03-30 1983-10-05 Nippon Denso Co Ltd Plastic molding for automobile
DE3436359A1 (en) * 1984-10-04 1986-04-10 Basf Ag, 6700 Ludwigshafen POLYAMIDE MOLDED PARTS AND METHOD FOR THEIR PRODUCTION
JPS6312661A (en) * 1986-07-03 1988-01-20 Ube Ind Ltd Polyamide composition
US4861838A (en) * 1987-06-22 1989-08-29 Allied-Signal Inc. Process for production of quasi-random copolymers from homopolymers
US4980407A (en) * 1988-10-21 1990-12-25 Toyoda Gosei Co., Ltd. Polyamide resin composition
JP2618721B2 (en) * 1989-10-20 1997-06-11 豊田合成 株式会社 Vibration damping resin molded products for engines

Also Published As

Publication number Publication date
JPS5686950A (en) 1981-07-15

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