JPH0465865B2 - - Google Patents

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Publication number
JPH0465865B2
JPH0465865B2 JP58154083A JP15408383A JPH0465865B2 JP H0465865 B2 JPH0465865 B2 JP H0465865B2 JP 58154083 A JP58154083 A JP 58154083A JP 15408383 A JP15408383 A JP 15408383A JP H0465865 B2 JPH0465865 B2 JP H0465865B2
Authority
JP
Japan
Prior art keywords
weight
calcined kaolin
physical properties
polyamide resin
present
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 - Lifetime
Application number
JP58154083A
Other languages
Japanese (ja)
Other versions
JPS6047061A (en
Inventor
Sadayuki Yakabe
Ikutoshi Nakajima
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.)
Asahi Chemical Industry Co Ltd
Original Assignee
Asahi Chemical Industry 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 Asahi Chemical Industry Co Ltd filed Critical Asahi Chemical Industry Co Ltd
Priority to JP15408383A priority Critical patent/JPS6047061A/en
Publication of JPS6047061A publication Critical patent/JPS6047061A/en
Publication of JPH0465865B2 publication Critical patent/JPH0465865B2/ja
Granted legal-status Critical Current

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Description

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

本発明はポリアミド樹脂組成物に関する。更に
詳しくは改良された実用特性を有する無機鉱物粉
末を含有する強化ポリアミド樹脂組成物に関す
る。 ポリアミド樹脂は機械的、熱的性質に優れプラ
スチツク成形材料として広く用いられているが、
これらの性質を更に高める目的で、無機鉱物粉末
とともにガラス繊維をポリアミドに配合すること
は良く知られている。 一般に無機鉱物粉末はそのままプラスチツクに
配合してもその効果を発揮せず、これに対処し
て、無機鉱物粉末の表面にいわゆるカツプリング
剤を作用させ、無機質である鉱物粉末と有機質で
あるプラスチツクとの間に親和性を与え配合の効
果を発揮させる方法が採用されている。 この時ここに使用されるカツプリング剤はその
機能からしてプラスチツクの種類によつて使い別
けられていて、ポリアミドに対してはアミノシラ
ン系化合物を用いるのが通例であつた。しかしな
がら、アミノシラン系化合物で処理した焼成カオ
リン粉末とともにガラス繊維を併せて配合した強
化ポリアミド樹脂組成物は、引張り強度や曲げ弾
性率等の機械的性質及び反り変形性には優れるも
のの、落錘衝撃強度に劣る為、その用途に制約が
あつた。 本発明者等は上記欠点を改善すべく鋭意検討し
た結果、驚くべきことに、ビニルトリエトキシシ
ランで処理した焼成カオリン粉末とともにガラス
繊維を併せてポリアミドに配合する場合に特に効
果の大きいことを見い出し、本発明に至つた。 すなわち、本発明はポリアミド、ガラス繊維及
び焼成カオリン粉末からなるポリアミド組成物で
あつて、該ポリアミド組成物のガラス繊維の量が
3〜40重量%、焼成カオリン粉末の量が5〜50重
量%、ポリアミドの量が40重量%以上であり、か
つ焼成カオリン粉末がビニルトリエトキシシラン
で処理されていることを特徴とする強化ポリアミ
ド樹脂組成物に関するものである。 以下本発明組成物を説明する。 本発明に係るポリアミドとは、ジアミンとジカ
ルボン酸との縮合重合で得られるナイロン66、ナ
イロン610、ナイロン612、ラクタムの開環重合で
得られるナイロン6、ナイロン12、ω−アミノカ
ルボン酸の自己重縮合で得られるナイロン11及び
これらの共重合物、ブレンド物等である。特にナ
イロン66が強靱性及び耐熱性の点で好ましい。 本発明に用いるガラス繊維は、ポリアミドの補
強剤として用いられるものであれば良く、ガラス
繊維の形状には特に制限はない。つまり長繊維タ
イプ(ガラスローピング)から短繊維タイプ(チ
ヨツプドストランド、ミルドフアイバー)のもの
まで任意の形状のものである。 本発明で言う焼成カオリン粉末とは、カオリン
粘土を350〜1000℃の温度範囲で数時間焼成した
後、粉砕したものであり、平均粒子サイズ10μ以
下、特に2μ以下まで粉砕したものが特に好まし
い。 本発明に使用されるビニルトリエトキシランの
配合割合は焼成カオリン粉末100重量部あたり
0.05〜5重量部、好ましくは0.3〜3重量部の範
囲である。前記のビニルトリエトキシの配合割合
が0.05重量部よりも少ないと、この組成物を用い
て得られる成形品の物性向上が充分でなく、又5
重量部を越えても、特に好ましい効果は得られ
ず、むしろ成形品の物性が低下する傾向にあるの
で適当でない。焼成カオリン粉末をビニルトリエ
トキシシランで表面処理する方法は公知の方法が
採用される。 例えば所定量の焼成カオリン粉末とビニルトリ
エトキシシランを直接ヘンセルミキサー中に投入
し、高速攪拌混合して処理する方法があげられ
る。 本発明に於て使用されるガラス繊維の配合量は
全組成物当り3〜40重量%、好ましくは5〜35重
量%である。ガラス繊維の配合量が3重量%より
少ない場合には強化ポリアミド樹脂組成物の諸性
質が期待される程には改良されず、また40重量%
を越えると組成物の成形性が著しく低下する。 本発明に於て使用される焼成カオリン粉末の配
合量は、全組成物当り5〜50重量%、好ましくは
15〜40重量%である。焼成カオリン粉末の配合量
が5重量%より少ない場合には配合の効果が充分
でなく、又50重量%を越えると、溶融混合が困難
であり、組成物の成形加工性が著しく低下するの
で実用的でない。 本発明の強化ポリアミド樹脂組成物の調製は通
常のポリアミド樹脂組成物の調製方法によつて行
われる。例えばポリアミドペレツト、ガラス繊維
及びビニルトリエトキシシラン処理された焼成カ
オリン粉末とを予備混合し、これを押出機に供給
し溶融混練した後、冷却しペレツト化する方法が
あげられる。 本発明の強化組成物には、その成形性、物性を
損わない限りにおいて他の成分、例えば顔料、染
料、耐熱剤、酸化劣化防止剤、滑剤、難燃剤、帯
電防止剤、離型剤、可塑剤、他の樹脂ポリマー等
を添加することができる。 本発明の強化ポリアミド樹脂組成物は、引張り
強度や曲げ弾性率等の機械的性質に優れ、かつ反
り変形も少なく、さらには落錘衝撃強度の向上し
た改良された実用特性を有するのであり、特にプ
ラスチツク材料としての厳しい信頼性が要求され
る自動車部品、特にシリンダーヘツドカバー、ト
ランクアクスルリア−カバー、ラジエータータン
ク、ヒータータンク等の自動車部品材料として有
用である。 以下実施例により本発明をさらに詳述する。な
お、実施例および比較例に記した試験片の物性測
定は次の方法に従つて行つた。 (1) 引張試験:ASTM D638 (2) 曲げ試験:ASTM D790 (3) 熱変形温度:ASTM D643 (4) 落錘衝撃試験:JIS K7211 (5) ソリ変形:試験片として小平板(130×110×
3mm) を用いた。成形された小平板を平らな面に置き、
ソリによつて生じる局部的なすき間を観察し、す
き間の程度を小さい順にA,B、及びCで評価し
た。 実施例 1 相対粘度2.80のナイロン66、60Kgとガラス繊維
(旭フアイバーグラスMA416)10Kg及びビニルト
リエトキシシラン(信越シリコン製KBE1003)
600gで表面処理された焼成カオリン(ENGEL
HARD社製: Satintone No.1)30KgとをV型
ブレンダーで予備混合し、ついで70%単軸押出機
を用いて、290℃で溶融混合し、強化ポリアミド
樹脂組成物のペレツトを得た。得られたペレツト
を射出成形機を用いて290℃の温度で物性測定試
験片を成形し、諸物性を評価した。その結果を第
1表に示す。 実施例 2〜3 ナイロン66、ガラス繊維及びシラン処理した焼
成カオリンの配合を第1表に示す割合にした以外
は実施例1と全く同様にして物性測定用試験片を
成形し、諸物性を評価した。その結果を第1表に
示す。 比較例 1〜2 ナイロン66、ガラス繊維及びシラン処理した焼
成カオリンの配合を第1表に示す割合にした以外
は実施例1と全く同様にして物性測定用試験片を
成形し、諸物性を評価した。その結果を第1表に
示す。 比較例 3 ビニルトリエトキシシランの代りにγ−アミノ
プロピルトリエトキシシラン(日本ユニカー製:
A−1100)を用いた以外は実施例1と同様にして
物性測定用試験片を成形し、諸物性を評価した。
その結果を第1表に示す。 比較例 4 相対粘度2.80のナイロン66、60Kgとビニルトリ
エトキシシラン(信越シリコン製KBE1003)800
gで表面処理された焼成カオリン(ENGEL
HARD社製: Satintone No.1)40Kgとを用い
ガラス繊維を使用しなかつた以外は実施例1と全
く同様にして物性測定用試験片を成形し、諸物性
を評価した。その結果を第1表に示す。 比較例 5 ビニルトリエトキシシランの代りにγ−アミノ
プロピルトリエトキシシラン(日本ユニカー製:
A−1100)を用いた以外は比較例4と同様にして
物性測定用試験片を成形し、諸物性を評価した。
その結果を第1表に示す。
The present invention relates to polyamide resin compositions. More particularly, the present invention relates to reinforced polyamide resin compositions containing inorganic mineral powders having improved practical properties. Polyamide resin has excellent mechanical and thermal properties and is widely used as a plastic molding material.
It is well known to blend glass fibers with inorganic mineral powders into polyamides in order to further enhance these properties. In general, inorganic mineral powder does not exhibit its effect even if it is mixed directly into plastic. To deal with this, a so-called coupling agent is applied to the surface of the inorganic mineral powder to combine the inorganic mineral powder with the organic plastic. A method has been adopted in which the effects of the combination are exerted by creating an affinity between the two. At this time, the coupling agent used here was classified according to its function depending on the type of plastic, and for polyamide, it was customary to use an aminosilane compound. However, reinforced polyamide resin compositions containing glass fibers and calcined kaolin powder treated with aminosilane compounds have excellent mechanical properties such as tensile strength and flexural modulus, as well as warp deformability, but they have excellent strength against falling weight impact. Because it is inferior to As a result of intensive studies aimed at improving the above-mentioned drawbacks, the present inventors surprisingly found that the effect is particularly great when glass fiber is blended with polyamide together with calcined kaolin powder treated with vinyltriethoxysilane. , led to the present invention. That is, the present invention is a polyamide composition comprising polyamide, glass fiber, and calcined kaolin powder, wherein the amount of glass fiber in the polyamide composition is 3 to 40% by weight, the amount of calcined kaolin powder is 5 to 50% by weight, The present invention relates to a reinforced polyamide resin composition characterized in that the amount of polyamide is 40% by weight or more, and the calcined kaolin powder is treated with vinyltriethoxysilane. The composition of the present invention will be explained below. The polyamide according to the present invention includes nylon 66, nylon 610, and nylon 612 obtained by condensation polymerization of diamine and dicarboxylic acid, nylon 6 and nylon 12 obtained by ring-opening polymerization of lactam, and self-polymerized ω-aminocarboxylic acid. Nylon 11 obtained by condensation, copolymers and blends thereof, etc. In particular, nylon 66 is preferred in terms of toughness and heat resistance. The glass fiber used in the present invention may be one that can be used as a reinforcing agent for polyamide, and there are no particular limitations on the shape of the glass fiber. In other words, it can be of any shape, from long fiber types (glass roping) to short fiber types (chopped strands, milled fibers). The calcined kaolin powder referred to in the present invention is obtained by firing kaolin clay at a temperature range of 350 to 1000° C. for several hours and then pulverizing it, and pulverizing it to an average particle size of 10 μm or less, particularly 2 μm or less is particularly preferable. The blending ratio of vinyltriethoxylan used in the present invention is per 100 parts by weight of calcined kaolin powder.
It ranges from 0.05 to 5 parts by weight, preferably from 0.3 to 3 parts by weight. If the blending ratio of vinyltriethoxy is less than 0.05 part by weight, the physical properties of the molded product obtained using this composition will not be sufficiently improved;
Even if the amount exceeds 1 part by weight, no particularly favorable effect can be obtained, and rather the physical properties of the molded article tend to deteriorate, which is not appropriate. A known method is employed for surface treating the calcined kaolin powder with vinyltriethoxysilane. For example, a method may be used in which a predetermined amount of calcined kaolin powder and vinyltriethoxysilane are directly charged into a Hensel mixer and mixed with high speed stirring. The amount of glass fiber used in the present invention is 3 to 40% by weight, preferably 5 to 35% by weight, based on the total composition. When the amount of glass fiber blended is less than 3% by weight, the properties of the reinforced polyamide resin composition are not improved to the extent expected;
If it exceeds this amount, the moldability of the composition will be significantly reduced. The amount of calcined kaolin powder used in the present invention is 5 to 50% by weight based on the total composition, preferably
It is 15-40% by weight. If the amount of calcined kaolin powder blended is less than 5% by weight, the effect of the blending will not be sufficient, and if it exceeds 50% by weight, melt mixing will be difficult and the moldability of the composition will be significantly reduced, so it is not practical. Not on point. The reinforced polyamide resin composition of the present invention is prepared by a conventional method for preparing polyamide resin compositions. For example, there is a method in which polyamide pellets, glass fibers, and calcined kaolin powder treated with vinyltriethoxysilane are premixed, the mixture is fed to an extruder, melted and kneaded, and then cooled and pelletized. The reinforcing composition of the present invention may contain other components, such as pigments, dyes, heat resisters, oxidative deterioration inhibitors, lubricants, flame retardants, antistatic agents, mold release agents, as long as they do not impair its moldability and physical properties. Plasticizers, other resin polymers, etc. can be added. The reinforced polyamide resin composition of the present invention has improved practical properties such as excellent mechanical properties such as tensile strength and flexural modulus, less warpage, and improved falling weight impact strength. It is useful as a material for automobile parts that require strict reliability as a plastic material, particularly for cylinder head covers, trunk axle rear covers, radiator tanks, heater tanks, etc. The present invention will be explained in further detail with reference to Examples below. The physical properties of the test pieces described in Examples and Comparative Examples were measured in accordance with the following method. (1) Tensile test: ASTM D638 (2) Bending test: ASTM D790 (3) Heat distortion temperature: ASTM D643 (4) Falling weight impact test: JIS K7211 (5) Warp deformation: Small flat plate (130 x 110 ×
3mm) was used. Place the formed small plate on a flat surface,
Local gaps caused by warping were observed, and the degree of the gap was evaluated as A, B, and C in descending order. Example 1 Nylon 66 with a relative viscosity of 2.80, 60 kg, glass fiber (Asahi Fiberglass MA416) 10 kg and vinyltriethoxysilane (Shin-Etsu Silicon KBE1003)
600g surface-treated calcined kaolin (ENGEL
Satintone No. 1) manufactured by HARD Co., Ltd. (30 kg) was premixed in a V-type blender, and then melt-blended at 290°C using a 70% single-screw extruder to obtain pellets of a reinforced polyamide resin composition. The obtained pellets were molded into test pieces for measuring physical properties using an injection molding machine at a temperature of 290°C, and various physical properties were evaluated. The results are shown in Table 1. Examples 2 to 3 Test pieces for measuring physical properties were molded in the same manner as in Example 1, except that the proportions of nylon 66, glass fiber, and silane-treated calcined kaolin were changed as shown in Table 1, and various physical properties were evaluated. did. The results are shown in Table 1. Comparative Examples 1-2 Test pieces for measuring physical properties were molded in exactly the same manner as in Example 1, except that the proportions of nylon 66, glass fiber, and silane-treated calcined kaolin were changed as shown in Table 1, and various physical properties were evaluated. did. The results are shown in Table 1. Comparative Example 3 γ-Aminopropyltriethoxysilane (manufactured by Nippon Unicar:
A test piece for measuring physical properties was molded in the same manner as in Example 1 except that A-1100) was used, and various physical properties were evaluated.
The results are shown in Table 1. Comparative example 4 Nylon 66 with a relative viscosity of 2.80, 60 kg and vinyltriethoxysilane (Shin-Etsu Silicon KBE1003) 800
Calcined kaolin surface-treated with ENGEL
A test piece for measuring physical properties was molded in exactly the same manner as in Example 1, except that the glass fiber was not used, and the various physical properties were evaluated. The results are shown in Table 1. Comparative Example 5 γ-Aminopropyltriethoxysilane (manufactured by Nippon Unicar:
A test piece for measuring physical properties was molded in the same manner as in Comparative Example 4 except that A-1100) was used, and various physical properties were evaluated.
The results are shown in Table 1.

【表】【table】

【表】【table】

Claims (1)

【特許請求の範囲】 1 ポリアミド、ガラス繊維及び焼成カオリン粉
末からなるポリアミド樹脂組成物であつて、該組
成物中のガラス繊維の量が3〜40重量%、焼成カ
オリン粉末の量が5〜50重量%、ポリアミドの量
が40重量%以上であり、かつ焼成カオリン粉末が
ビニルトリエトキシシランで処理されていること
を特徴とする強化ポリアミド樹脂組成物。 2 強化ポリアミド樹脂組成物が、自動車部品用
材料である特許請求の範囲第1項記載の強化ポリ
アミド樹脂組成物。
[Scope of Claims] 1. A polyamide resin composition comprising polyamide, glass fiber, and calcined kaolin powder, wherein the amount of glass fiber in the composition is 3 to 40% by weight, and the amount of calcined kaolin powder is 5 to 50% by weight. 1. A reinforced polyamide resin composition, characterized in that the amount of polyamide is 40% by weight or more, and the calcined kaolin powder is treated with vinyltriethoxysilane. 2. The reinforced polyamide resin composition according to claim 1, wherein the reinforced polyamide resin composition is a material for automobile parts.
JP15408383A 1983-08-25 1983-08-25 Reinforced polyamide resin composition Granted JPS6047061A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP15408383A JPS6047061A (en) 1983-08-25 1983-08-25 Reinforced polyamide resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP15408383A JPS6047061A (en) 1983-08-25 1983-08-25 Reinforced polyamide resin composition

Publications (2)

Publication Number Publication Date
JPS6047061A JPS6047061A (en) 1985-03-14
JPH0465865B2 true JPH0465865B2 (en) 1992-10-21

Family

ID=15576516

Family Applications (1)

Application Number Title Priority Date Filing Date
JP15408383A Granted JPS6047061A (en) 1983-08-25 1983-08-25 Reinforced polyamide resin composition

Country Status (1)

Country Link
JP (1) JPS6047061A (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4711673A (en) * 1985-10-03 1987-12-08 Aluminum Company Of America Combination of surface modifiers for powdered inorganic fillers
CN103849138A (en) * 2012-11-29 2014-06-11 合肥杰事杰新材料股份有限公司 Chopped glass fiber reinforced nylon composite material and preparation method thereof

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS517056A (en) * 1974-07-08 1976-01-21 Teijin Ltd NAIRON JUSHI SEIBUTSU
JPS5150960A (en) * 1974-10-31 1976-05-06 Asahi Chemical Ind HORIAMIDOSEIKEIZ AIRYO
JPS543486A (en) * 1977-06-09 1979-01-11 Citizen Watch Co Ltd Structure of crystal oscillator

Also Published As

Publication number Publication date
JPS6047061A (en) 1985-03-14

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