JPS6047061A - Reinforced polyamide resin composition - Google Patents
Reinforced polyamide resin compositionInfo
- Publication number
- JPS6047061A JPS6047061A JP15408383A JP15408383A JPS6047061A JP S6047061 A JPS6047061 A JP S6047061A JP 15408383 A JP15408383 A JP 15408383A JP 15408383 A JP15408383 A JP 15408383A JP S6047061 A JPS6047061 A JP S6047061A
- Authority
- JP
- Japan
- Prior art keywords
- polyamide resin
- polyamide
- mineral powder
- glass fiber
- weight
- 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.)
- Granted
Links
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
【発明の詳細な説明】
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。DETAILED DESCRIPTION OF THE INVENTION 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.
ポリアミド樹脂は機械的、熱的性質に優れプラスチック
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。Polyamide resin has excellent mechanical and thermal properties and is widely used as a plastic molding material, but it is well known that glass fiber is blended with inorganic mineral powder into polyamide in order to further improve these properties.
一般に無機鉱物粉末はそのままプラスチックに配合して
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ッ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ックとの間vc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。In general, inorganic mineral powder does not exhibit its effect even if it is blended with plastic as it is. To deal with this, a so-called coupling agent is applied to the surface of the inorganic mineral powder, and the inorganic mineral powder and the organic plastic are bonded together. A method has been adopted in which the effect of blending is exerted by giving vc affinity between the two.
この時ここに使用されるカップリング剤はその機能から
してプラスチックの種類によっ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
が通例であった。しかしながら、アミノシラン系化合物
で処理した無機鉱物粉末とともにガ2ス゛繊維を併せて
配合した強化ポリアミド樹脂組成物は、)1張シ強度や
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った
。The coupling agent used at this time is different depending on the type of plastic depending on its function.
For polyamides, it has been customary to use aminosilane compounds. However, reinforced polyamide resin compositions containing inorganic mineral powder treated with an aminosilane compound and gas fibers are superior in mechanical properties such as tensile strength and flexural modulus, and warping deformability. However, its use was limited due to its poor falling weight impact strength.
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、エチレン性不飽和結合を有する有機シ
ラン化合物はこの化合物で処理した無機鉱物粉末ととも
にガラス繊維を併せてポリアミドに配合する場合K特に
効果の大きいことを見い出し、本発明に至った0
すなわち、本発明はポリアミド、ガラス繊維及び無機鉱
物粉末からなるポリアミド組成物であって、該ポリアミ
ド組成物中のガラス繊維の量が3〜40重量%、無機鉱
物粉末の量が5〜50重量%、ポリアミドの量が40重
量%以上であり、かつ無機鉱物粉末がエチレン性不飽和
結合を有する有機シラン化合物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O
以下本発明組成物を説明す、る。As a result of intensive study to improve the above drawbacks, the inventors of the present invention found that
Surprisingly, it was discovered that an organosilane compound having an ethylenically unsaturated bond is particularly effective when blended with a polyamide together with an inorganic mineral powder treated with this compound and a glass fiber, which led to the present invention. That is, the present invention is a polyamide composition comprising polyamide, glass fiber, and inorganic mineral powder, wherein the amount of glass fiber in the polyamide composition is 3 to 40% by weight, and the amount of inorganic mineral 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 inorganic mineral powder is treated with an organic silane compound having an ethylenically unsaturated bond. Describe the composition.
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61O
、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 、u−7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。The polyamide according to the present invention refers to nylon 66 and nylon 61O obtained by condensation polymerization of diamine and dicarboxylic acid.
, nylon 612, nylon 6 obtained by ring-opening polymerization of lactam, nylon 12, nylon 11 obtained by self-polycondensation of u-7 minocarboxylic acid, and copolymers thereof,
Blends, etc.
特にナイロン66が強靭性及び側熱性の点で好ましい。In particular, nylon 66 is preferred in terms of toughness and side heat resistance.
本発明に用いるガラス繊維は、ポリアミドの補強材とし
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。っまシ長繊維タイプ(ガラスロービン
グ)から短繊維タイプ(チョツプドストランド、ミルド
ファイバー)のものまで任意の形状のものである。The glass fiber used in the present invention may be one that can be used as a reinforcing material for polyamide, and there are no particular limitations on the shape of the glass fiber. They can be of any shape, from long fiber types (glass roving) to short fiber types (chopped strands, milled fibers).
本発明で言う無機鉱物粉末とは、焼成カオリン、カオリ
ン、ウオラストナイト、マイカ1、タルク等の硅酸塩化
合物であり、平均粒子サイズが10μ以下、特に2μ程
度のものが好ましい。またカオリン粘土を350〜10
00℃の温度範囲で数時間焼成後、平均粒子サイズが2
μ以下まで粉砕した焼成カオリンが特に好ましい。The inorganic mineral powder referred to in the present invention is a silicate compound such as calcined kaolin, kaolin, wollastonite, mica 1, or talc, and preferably has an average particle size of 10 μm or less, particularly about 2 μm. In addition, kaolin clay is 350 to 10
After calcination for several hours in the temperature range of 00℃, the average particle size is 2.
Particularly preferred is calcined kaolin that has been ground to less than μ.
本発明に使用されるエチレン性不飽和結合を有する有機
シラン化合物としてはビニルトリエトキシシラン、ビニ
ルトリス(β−メトキシエトキシシラン、γ−メタクリ
ロキシブロピルトリメトキ7ラン等が挙げられ、特にビ
ニルトリエトキシシランが好ましい。前記の有機シラン
化合物の配合割合は無機鉱物粉末100重量部あたり0
.05〜5重蓄部、好ましくは0.3〜3重昔部の範、
囲である。Examples of the organic silane compound having an ethylenically unsaturated bond used in the present invention include vinyltriethoxysilane, vinyltris(β-methoxyethoxysilane, γ-methacryloxypropyltrimethoxysilane), and especially vinyltriethoxysilane. Silane is preferred.The blending ratio of the organic silane compound is 0 per 100 parts by weight of the inorganic mineral powder.
.. 05 to 5 layers, preferably 0.3 to 3 layers,
It is surrounded.
前記の有機シラン化合物の配合割合が0.05重量部よ
シも少ないと、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重通部を越えても、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。If the blending ratio of the organosilane compound is less than 0.05 part by weight, the physical properties of the molded article obtained using this composition will not be sufficiently improved, and even if it exceeds 5 parts, it is particularly preferable. It is not suitable because no effect is obtained and the physical properties of the molded product tend to deteriorate.
無機鉱物粉末をエチレン性不飽和結合を有する有機7ラ
ン〜化合物で表面処理する方法は公知の方法が採用され
る。A known method is employed for surface treating the inorganic mineral powder with an organic compound having an ethylenically unsaturated bond.
例えば所足量の無機鉱物粉末と有機7ラン化合物ヲ直接
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。For example, a method may be used in which a sufficient amount of inorganic mineral powder and an organic 7-run compound are directly charged into a Hensel mixer and mixed with high speed stirring.
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a二4O重以下、好ましく&;:S〜35重景チで
ある。ガラス繊維の配合量が3重量%よシ少ない場合に
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。The blending amount of the glass fiber used in the present invention is not more than a240 weight per total composition, preferably &;: S to 35 weight weight. 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, and when it exceeds 40% by weight, the moldability of the composition is significantly reduced. .
本発明に於て使用される無機鉱物粉末の配合量は、全組
成物当り5〜50重量%、好ましくは15〜40重量%
である。無機鉱物粉末の配合量が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、溶融混合が困離であり、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。The amount of inorganic mineral powder used in the present invention is 5 to 50% by weight, preferably 15 to 40% by weight based on the total composition.
It is. If the amount of inorganic mineral powder blended is less than 5% by weight, the blending effect 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. Therefore, it is not practical.
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って行われる。例えば
ポリアミドペレット、ガラス繊維及び有機シラン処理さ
れた無機鉱物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、本発明の強化組成物には、その成形
性、物性を損わない限シにおいて他の成分、例えば顔料
、染料、側熱剤、酸化劣化防止剤、滑剤、′II4撚剤
、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。The reinforced polyamide resin composition of the present invention is prepared by a conventional method for preparing polyamide resin compositions. For example, after premixing polyamide pellets, glass fibers, and organosilane-treated inorganic mineral powder, and feeding this into an extruder and melt-kneading, the reinforced composition of the present invention is produced without impairing its moldability or physical properties. Unless otherwise specified, other components such as pigments, dyes, side heating agents, oxidative deterioration inhibitors, lubricants, twisting agents, antistatic agents, mold release agents, plasticizers, other resin polymers, etc. may be added. can.
本発明の強化ポリアミド樹脂組成物は、引張シ強度や曲
げ弾性率等の機械的性質に優れ、かつ反シ変形も少なく
、さらには落錘衝撃強度の向上した改良された実用特性
を有するものであり、特に°゛゛ プラスチック材料と
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
ーへラドカバー、トランクアクスルリアーカバー、ラジ
ェータータンク、ヒータータンク等の自動車部品材料と
して有用である。The reinforced polyamide resin composition of the present invention has improved mechanical properties such as tensile strength and flexural modulus, less deformation, and improved practical properties such as improved falling weight impact strength. It is particularly useful as a material for automobile parts that require strict reliability as a plastic material, such as cylinder rad covers, trunk axle rear covers, radiator tanks, and heater tanks.
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
従って行った。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 according to the following method.
(1)引張試験: ASTM D 63B(2)曲げ試
験: ASTM D 790(8)熱変形温度: AS
TM D 648(荀落錘衝撃試験: J!S K72
xx(6)ソ リ 変 形:試験片として小平板(13
0X110X3關)を用いた。成形された小平板を平ら
な面に置き、ソリによっ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。(1) Tensile test: ASTM D 63B (2) Bending test: ASTM D 790 (8) Heat distortion temperature: AS
TM D 648 (Drop weight impact test: J!S K72
xx (6) Sled deformation: Small flat plate (13
0x110x3) was used. The formed small flat plate was placed 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.
実施例1
相対粘度2.80のナイロン66、60〜とガラス繊維
(旭ファイバーグラスMA416)10Kf及びビニル
トリエトキシシラン(信越シリコン製KBE 1003
) 6GOfで表面処理された焼成カオリン(ENG
EL )IARD社製:■5atintone Na
1 ) 30 Kgとを■壓ブレンダーで予備混合し、
ついで70φ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ベレットを得た。得ら
れたベレットを射出成形機を用いて290℃の温度で物
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。Example 1 Nylon 66, 60~ with a relative viscosity of 2.80, glass fiber (Asahi Fiberglass MA416) 10Kf and vinyltriethoxysilane (Shin-Etsu Silicon KBE 1003)
) Calcined kaolin surface treated with 6GOf (ENG
EL) Manufactured by IARD: ■5atintone Na
1) Pre-mix 30 kg with a bottle blender,
Then, using a 70φ single-screw extruder, the mixture was melt-mixed at 290° C. to obtain a pellet of reinforced polyamide resin composition. The obtained pellet was molded into a test piece for measuring physical properties at a temperature of 290° C. using an injection molding machine, and various physical properties were evaluated. The results are shown in Table 1.
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/処理したm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。Examples 2 to 3 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 Examples 1 to 2 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 silica/treated m-form kaolin were changed to the proportions shown in Table 1. Physical properties were evaluated. The results are shown in Table 1.
比較例3
ビニルトリエトキシシランの代りにγ−アミノプロビル
トリエトキ7シラン(日、不ユニカー製: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。Comparative Example 3 Instead of vinyltriethoxysilane, γ-aminoprobyltriethoxy7silane (manufactured by Fuyunika: A-1100) was used.
) was used to form a test piece for measuring physical properties in the same manner as in Example 1, and various physical properties were evaluated.
その結果を第1表に示す。The results are shown in Table 1.
比較例4
相対粘度2.80のナイロ766.60Kfとビニルト
リエトキシシラン(信越シリコンs KBE 1003
)800g″で赤面処理された焼成カオリン(ENG
ELI(ARD社M:■5atintone NIL
1 ) 40 Kgとを用いガラス繊維を使用しなかっ
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。Comparative Example 4 Nylo 766.60Kf with a relative viscosity of 2.80 and vinyltriethoxysilane (Shin-Etsu Silicon S KBE 1003)
) 800g'' blush-treated calcined kaolin (ENG
ELI (ARD M:■5atintone NIL
1) A test piece for measuring physical properties was molded in exactly the same manner as in Example 1 except that 40 kg was used and no glass fiber was used, and various physical properties were evaluated. The results are shown in Table 1.
比較例5
ビニルトリエトキシシランの代りにr−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。Comparative Example 5 r-aminopropyltriethoxysilane (manufactured by Nippon Unicar: A-1100) instead of vinyltriethoxysilane
A test piece for measuring physical properties was molded in the same manner as in Comparative Example 4 except that the following was used, and various physical properties were evaluated.
その結果を第1表に示す。The results are shown in Table 1.
以下余白Margin below
Claims (1)
ポリアミド樹脂組成物であって、該組成物中のガラス繊
維の量が3〜40重量%、無機鉱物粉末の量が5〜50
重量%、ボンアミドの量が40重量%以上であり、かつ
無機鉱物粉末がエチレン性不飽和結合を有する有機シラ
ン化合物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 之 無機鉱物粉末が、焼成カオリン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 & 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] L A polyamide resin composition comprising polyamide, glass fiber, and inorganic mineral powder, wherein the amount of glass fiber in the composition is 3 to 40% by weight, and the amount of inorganic mineral powder is 5 to 50% by weight.
% by weight, the amount of bonamide is 40% by weight or more, and the inorganic mineral powder is treated with an organic silane compound having an ethylenically unsaturated bond. Reinforced polyamide resin composition according to claim 1, which is calcined kaolin & Reinforced polyamide resin composition according to claim 1, wherein the reinforced polyamide resin composition is a material for automobile parts
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 true JPS6047061A (en) | 1985-03-14 |
| JPH0465865B2 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) |
Cited By (2)
| 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 |
Citations (3)
| 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 |
-
1983
- 1983-08-25 JP JP15408383A patent/JPS6047061A/en active Granted
Patent Citations (3)
| 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 |
Cited By (2)
| 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 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0465865B2 (en) | 1992-10-21 |
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