JPS584737B2 - polyamide composition - Google Patents
polyamide compositionInfo
- Publication number
- JPS584737B2 JPS584737B2 JP8839575A JP8839575A JPS584737B2 JP S584737 B2 JPS584737 B2 JP S584737B2 JP 8839575 A JP8839575 A JP 8839575A JP 8839575 A JP8839575 A JP 8839575A JP S584737 B2 JPS584737 B2 JP S584737B2
- Authority
- JP
- Japan
- Prior art keywords
- weight
- nylon
- polyamide
- resin
- polyamide 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.)
- Expired
Links
Landscapes
- Processes Of Treating Macromolecular Substances (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Description
【発明の詳細な説明】
本発明はポリアミド組成物に関するものであり特に、色
分散性に優れた粉末状無機物質含有ポリアミド組成物に
関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a polyamide composition, and more particularly to a polyamide composition containing a powdery inorganic substance and having excellent color dispersibility.
粉末状の無機酸化物、炭酸塩、硫酸塩、ケイ酸塩等は、
数多くのプラスチックの充填剤として広く利用されて来
た。Powdered inorganic oxides, carbonates, sulfates, silicates, etc.
It has been widely used as a filler in many plastics.
古くはフェノール樹脂Aエポキシ樹脂の様な熱硬化性樹
脂の充填剤として、又、最近では省資源、低燃焼カロリ
ーを目的に、ポリエチレン樹脂、ポリプロピレン樹脂の
充填剤として使用されている。In the past, it has been used as a filler for thermosetting resins such as phenol resin A epoxy resin, and more recently, it has been used as a filler for polyethylene resins and polypropylene resins for the purpose of resource saving and low calorie combustion.
これに対して、これらの充填剤をプラスチックの補強材
として使用することが研究されている。In contrast, the use of these fillers as reinforcing materials for plastics has been investigated.
これは、充填剤の表面を有機ケイ素化合物、重合性有機
酸等で処理し、充填剤とプラスチックとを結合させる技
術が開発されたことが背景となっている。The background to this is the development of a technique for bonding the filler and plastic by treating the surface of the filler with an organosilicon compound, a polymerizable organic acid, or the like.
従来より、ガラス繊維、炭素樹脂及び特殊な合成繊維な
どの繊維状物質が最も有効なプラスチック補強材として
使われており、特にガラス繊維は補強材の代表とまで云
われる程、広範囲のプラスチックに使われている。Traditionally, fibrous substances such as glass fiber, carbon resin, and special synthetic fibers have been used as the most effective reinforcing materials for plastics, and glass fiber in particular is used in a wide range of plastics, so much so that it is said to be the representative reinforcing material. It is being said.
しかしながら、この様な繊維状の補強材を配合した樹脂
においては、補強材の配向が著しく、従って補強効果に
異方性を生ずることになる。However, in a resin containing such a fibrous reinforcing material, the orientation of the reinforcing material is significant, resulting in anisotropy in the reinforcing effect.
強度及び剛性の異方性も問題であるが、特に大きな問題
は、成形収縮率の異方性の為に成形品に反りや変形が発
生しやすいことである。Anisotropy in strength and rigidity is also a problem, but a particularly big problem is that molded products tend to warp or deform due to anisotropy in mold shrinkage.
この成形品の反り・変形の為に、各種ケーシングに利用
することが大きく制限されている。Because of the warpage and deformation of this molded product, its use in various casings is severely limited.
この様な繊維補強樹脂の欠点を解消すべく研究が進めら
れた結果、従来、単なる充填剤として用いられて来た粉
末状無機物質の表面を処理し、該表面処理粉末状無機物
質を高濃度に樹脂に配合する技術が開発され、各種の熱
可塑性樹脂に応用されている。As a result of research to eliminate these drawbacks of fiber-reinforced resins, we have treated the surface of powdered inorganic substances that have conventionally been used simply as fillers, and have developed highly concentrated powdered inorganic substances. A technology for blending it into resins has been developed, and it has been applied to various thermoplastic resins.
ポリアミド樹脂についても前述の様な研究が積極的に行
なわれ、優れた性能を有するポリアミド組成物が開発さ
れている。As for polyamide resins, the above-mentioned research has been actively conducted, and polyamide compositions having excellent performance have been developed.
このポリアミド組成物は反り・変形の少ないことから、
各種のケーシング材料としての用途開発が進められ、各
種カラーの着色が行なわれている。This polyamide composition has less warping and deformation, so
The use of it as a material for various casings is being developed, and it is being colored in various colors.
ポリアミド樹脂の着色方法については、従来より、顔料
のドライブレンド法、押出機による練り込み法及び高濃
度に顔料を練り込んだマスターペレットを用いるマスタ
ーバッチ法等の手法が用いられている。Conventionally, methods for coloring polyamide resins include methods such as a dry blending method of pigments, a kneading method using an extruder, and a masterbatch method using master pellets kneaded with a pigment at a high concentration.
これらの手法の中では、作業性及びコストなどの点から
、マスターバッチ法が好まれている。Among these methods, the masterbatch method is preferred in terms of workability and cost.
しかしながら、粉末状無機物質を高濃度に配合したポリ
アミド組成物の着色においては、通常の方法では顔料が
均一に分散しないという難点があった。However, when coloring a polyamide composition containing a powdery inorganic substance at a high concentration, there is a problem in that the pigment is not uniformly dispersed using conventional methods.
従来より顔料の分散性を改良する方法としては成形加工
中において、スクリューに背圧をかけて混線効果を上げ
る方法が行なわれて来た。A conventional method for improving the dispersibility of pigments has been to apply back pressure to the screw during the molding process to increase the crosstalk effect.
しかしながら、本発明の対象である粉末状無機物質を高
濃度に配合したポリアミド組成物においては、スクリュ
ーに背圧をかけるこきによって可塑化に要する時間が長
くなり、必然的に成形サイクルが長くなり作業効率が低
下するといった欠点がある。However, in polyamide compositions containing a high concentration of powdered inorganic substances, which are the subject of the present invention, applying back pressure to the screw increases the time required for plasticization, which inevitably lengthens the molding cycle and increases the work required. The disadvantage is that efficiency decreases.
更に、比較的表面硬度の高い無機物質が高濃度に配合さ
れている為、背圧をかけることによって、スクリュー、
シリンダーの摩耗が促進される恐れがある。Furthermore, since it contains a high concentration of inorganic substances with relatively high surface hardness, it is possible to tighten the screw by applying back pressure.
Cylinder wear may be accelerated.
この様な点から、本発明の如き組成物においては、スク
リューに背圧をかけることは好ましいことではない。From this point of view, in the composition of the present invention, it is not preferable to apply back pressure to the screw.
本発明者等は、この様なポリアミド組成物の色分散性を
改良すべく鋭意研究を重ねた結果、上記欠点のないポリ
アミド組成物を見出し、本発明に至ったものである。The present inventors have conducted intensive research to improve the color dispersibility of such polyamide compositions, and as a result, they have discovered a polyamide composition that does not have the above-mentioned drawbacks, and have arrived at the present invention.
すなわち、本発明は、表面を有機ケイ素化合物又は重合
性有機酸で処理した粉末状無機物質30〜80重量%,
50〜6,000μの繊維長を有するガラス繊維1.5
〜15重量%及び顔料0.01〜5重量%を含有するこ
とを特徴とするポリアミド組成物に係るものである。That is, the present invention provides 30 to 80% by weight of a powdered inorganic material whose surface has been treated with an organosilicon compound or a polymerizable organic acid.
Glass fiber 1.5 with a fiber length of 50-6,000μ
15% by weight and 0.01 to 5% by weight of a pigment.
本発明の組成物を用いることによって、成形加工中に全
く背圧をかけることなく、顔料の分散性の良好な成形品
が得られる。By using the composition of the present invention, a molded article with good pigment dispersibility can be obtained without applying any back pressure during molding.
本発明に係る粉末状無機物質は、クレー、焼成クレー、
炭酸カルシウム、硫酸カルシウム、亜硫酸カルシウム、
ケイ酸カルシウム、タルク、マイ力、シリカ、アスベス
ト等である。The powdered inorganic substance according to the present invention includes clay, calcined clay,
Calcium carbonate, calcium sulfate, calcium sulfite,
These include calcium silicate, talc, iron, silica, and asbestos.
これらの粉末状無機物質はA0.1〜50μの平均粒径
を有するものが好ましい。These powdered inorganic substances preferably have an average particle size of A0.1 to 50μ.
又、これらの粉末状無機物質は、その表面を有機ケイ素
化合物又は重合性有機酸で処理されたものであり、表面
処理されていない粉末状無機物質を用いると補強効果に
乏しい。Furthermore, the surface of these powdered inorganic substances has been treated with an organosilicon compound or a polymerizable organic acid, and if a powdered inorganic substance that has not been surface-treated is used, the reinforcing effect is poor.
表面処理された粉末状無機物質の配合率は、ポリアミド
組成物中に30〜80重量%である。The blending ratio of the surface-treated powdered inorganic substance is 30 to 80% by weight in the polyamide composition.
又、好ましくは、35〜60重量%である。Further, it is preferably 35 to 60% by weight.
配合率が30重量%より少ない場合には補強効果に乏し
く、一方、配合率が多過ぎる場合には、非常にもろくな
り、いずれも本発明の効果は得られない。If the blending ratio is less than 30% by weight, the reinforcing effect will be poor, while if the blending ratio is too high, it will become extremely brittle, and in either case, the effects of the present invention cannot be obtained.
本発明に係るポリアミドは、ジアミンとジカルボン酸と
の縮重合で得られるところのナイロン66、ナイロン6
10、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7、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 is nylon 66, nylon 6, which is obtained by polycondensation of diamine and dicarboxylic acid.
10, nylon 612, nylon 6 obtained by ring-opening polymerization of lactam, nylon 12, nylon 7 obtained by self-polycondensation of ω-aminocarboxylic acid, nylon 11, and copolymers and blends thereof.
本発明に係るガラス繊維は、ポリアミド樹脂の補強材と
して使用されるものであればよく、その繊維長は50〜
6,000μのものが適当である。The glass fiber according to the present invention may be any fiber that can be used as a reinforcing material for polyamide resin, and its fiber length is 50 to 50.
A material having a thickness of 6,000μ is suitable.
又、配合量としては、ポリアミド組成物に対して15〜
15重量%である。In addition, the blending amount is 15 to 15% for the polyamide composition.
It is 15% by weight.
ガラス繊維の配合量が1.5重量%未満では、顔料を分
散させる効果に乏しく、15重量%を超えると、成形品
に反り変形が著しく認められる様になり好ましくない。If the amount of glass fiber blended is less than 1.5% by weight, the effect of dispersing the pigment will be poor, and if it exceeds 15% by weight, the molded product will be noticeably warped, which is not preferable.
ガラス繊維の配合方法としては、粉末状無機物質をポリ
アミド樹脂に配合する際同時に配合してもよく、又、そ
の前後いずれでもよい。The glass fiber may be blended at the same time as the powdered inorganic substance is blended into the polyamide resin, or may be blended either before or after the blending.
本発明で用いる顔料は、ポリアミドに対して用いること
ができる顔料であれば特に限定はされず、通常用いられ
るところの有機系顔料、無機系顔料を用いることができ
、その添加量としては、0.01〜5重量%が適当であ
る。The pigment used in the present invention is not particularly limited as long as it can be used for polyamide, and commonly used organic pigments and inorganic pigments can be used, and the amount added is 0. .01 to 5% by weight is suitable.
本発明に使用される顔料の具体例としては、各種のカー
ボンブラック、酸化チタン、コバルトグリーン、コバル
トブルー、群青等があげられる。Specific examples of pigments used in the present invention include various carbon blacks, titanium oxides, cobalt greens, cobalt blues, ultramarine blues, and the like.
粉末状無機物質の表面処理剤として用いられる有機ケイ
素化合物は、通常シランカツプリング剤と呼ばれている
ものであり、γ−アミノプロピルトリメトキシシラン、
γ−グリシドキシプ口ピルトリメトキシシラン等が適当
である。Organosilicon compounds used as surface treatment agents for powdered inorganic substances are usually called silane coupling agents, and include γ-aminopropyltrimethoxysilane,
Suitable examples include γ-glycidoxysilane, pyrutrimethoxysilane, and the like.
又、重合性有機酸としては、アクリル酸、メタクリル酸
、クロトン酸等が用いられる。Further, as the polymerizable organic acid, acrylic acid, methacrylic acid, crotonic acid, etc. are used.
以下に本発明の実施例を述べるが、本発明は、これらの
実施例のみに限定されるものではない。Examples of the present invention will be described below, but the present invention is not limited only to these examples.
実施例 1
ナイロン66樹脂60重量部、γ−アミノプ口ピルトリ
メトキシシランで表面処理したクレー40重量部、長さ
3mmのガラス繊維10重量部を40φベント付押出機
で混練しペレット化した。Example 1 60 parts by weight of nylon 66 resin, 40 parts by weight of clay surface-treated with γ-aminopyrtrimethoxysilane, and 10 parts by weight of glass fibers having a length of 3 mm were kneaded and pelletized using a 40φ vented extruder.
別途ナイロン66樹脂にカーボンブラックを3重量%混
線したマスターペレットを製造した。Separately, master pellets were manufactured by mixing nylon 66 resin with 3% by weight of carbon black.
上記ペレットとカラーマスターペレットとを重量比で1
9:1の割合で混合し、5oz容量の射出成形機で80
X50X3mmの平板状試料を背圧をかけずに成形した
。The weight ratio of the above pellets and color master pellets is 1
Mix at a ratio of 9:1 and process 80% in a 5oz capacity injection molding machine.
A flat sample measuring 50 x 3 mm was molded without applying back pressure.
この成形品の色むらは全く認められず顔料が均一に分散
されていることが認められた。No color unevenness was observed in this molded article, and it was confirmed that the pigment was uniformly dispersed.
比較例 1
実施例1と同様の配合(但しガラス繊維は除く:材料で
成形を行った。Comparative Example 1 Molding was performed using the same formulation as in Example 1 (except for glass fiber).
背圧をかけない場合には、成形品の色むらが著しく、流
動方向に平行に色の濃淡模様が認められた。When no back pressure was applied, color unevenness of the molded product was significant, and a pattern of light and shade of color was observed parallel to the flow direction.
背圧を150kg/cr1程度かけると、色むらは殆ど
認められなくなるが、可塑化に要する時間が3倍程にな
り、成形サイクルは結局約2倍となった。When a back pressure of about 150 kg/cr1 was applied, color unevenness was hardly observed, but the time required for plasticization tripled, and the molding cycle ended up about twice as long.
実施例 2
実施例1のクレーの代りにケイ酸カルシウム、カーボン
ブラックの代りにコバルトブルー(Hercules社
製+1084)を20重量%練込んだマスターペレット
を用いて背圧をかけずに成形した。Example 2 Master pellets in which 20% by weight of calcium silicate was kneaded in place of the clay of Example 1 and 20% by weight of cobalt blue (+1084 manufactured by Hercules) in place of carbon black were used to mold without applying back pressure.
成形品の外観は良好であり、色むらは認められなかった
。The appearance of the molded product was good, and no color unevenness was observed.
実施例 3
実施例1のナイロン66樹脂の代りにナイロン6樹脂を
用いて実験を行った。Example 3 An experiment was conducted using nylon 6 resin instead of nylon 66 resin in Example 1.
成形品の外観は良好であり、色むらは全く認められなか
った。The appearance of the molded product was good, and no color unevenness was observed.
実施例 4
ナイロン66樹脂60重量部、アクリル酸で処理した炭
酸カルシウム40重量部、長さ3mmのガラス繊維10
重量部を40φベント付押出機で混練しペレット化した
。Example 4 60 parts by weight of nylon 66 resin, 40 parts by weight of calcium carbonate treated with acrylic acid, 10 parts by weight of glass fiber with a length of 3 mm
Parts by weight were kneaded using a 40φ vented extruder to form pellets.
このペレットと実施例1で製造したカラーマスターペレ
ソトとを重量比で19:1の割合で混合し、5oz容量
の射出成形機で80X50X3mmの平板状試料を背圧
をがけずに成形した。These pellets and Color Master Peresoto produced in Example 1 were mixed at a weight ratio of 19:1, and a flat sample of 80 x 50 x 3 mm was molded using a 5 oz capacity injection molding machine without applying back pressure.
成形品の外観は良好であり、色むらは全く認められなか
った。The appearance of the molded product was good, and no color unevenness was observed.
比較例 2
ナイロン66樹脂60重量部、γ−アミノプ口ピルトリ
メトキシシランで処理したクレー40重量部、長さ3m
mのガラス繊維1重量部を40φベント付押出機で混練
しペレット化した。Comparative Example 2 60 parts by weight of nylon 66 resin, 40 parts by weight of clay treated with γ-aminopyrtrimethoxysilane, length 3 m
1 part by weight of glass fibers of 500 m were kneaded using a 40φ vented extruder and pelletized.
このペレットと実施例1で製造したカラーマスターペレ
ットとを重量比で19:1の割合で混合し、成形した。These pellets and the color master pellets produced in Example 1 were mixed at a weight ratio of 19:1 and molded.
この成形品の外観は色むらが認められ、背圧を約100
kg/crt程度にしなければ、色むらは解消しなかっ
た。The appearance of this molded product is uneven in color, and the back pressure is approximately 100%.
The color unevenness was not resolved unless the amount was reduced to about kg/crt.
比較例 3
長さ3mmのガラス繊維を20重量部用いること以外は
、比較例2と同一手法で成形した。Comparative Example 3 Molding was performed in the same manner as in Comparative Example 2, except that 20 parts by weight of glass fibers having a length of 3 mm were used.
成形品の外観は色むらがなく良好であるが、成形収縮率
に異方性が認められた。Although the appearance of the molded product was good with no color unevenness, anisotropy was observed in the molding shrinkage rate.
念の為、80X50X1mmの平板を成形したところ、
反り・変形の著しい成形品しか得られなかった。Just to be sure, I molded a flat plate of 80 x 50 x 1 mm,
Only molded products with significant warpage and deformation were obtained.
これに対して実施例1で用いたべレフトで80X50X
1!mの平板を成形したところ、殆ど反り・変形のない
成形品を得ることができた。On the other hand, the bereft used in Example 1 is 80X50X
1! When a flat plate of m was molded, a molded product with almost no warping or deformation could be obtained.
以上の実施例及び比較例で明らかな様に、本発明の組成
物の着色性は非常に優れており、かつ、反り・変形の少
ない成形品を得ることができる。As is clear from the above Examples and Comparative Examples, the composition of the present invention has excellent coloring properties, and molded articles with less warpage and deformation can be obtained.
この結果、従来の材料では非常に問題があって適用でき
なかった各種ケーシングの樹脂化が容易に可能になり、
その工業的価値は非常に大きいといえる。As a result, it is now possible to easily use resin for various types of casings, which were difficult to apply with conventional materials.
It can be said that its industrial value is extremely large.
Claims (1)
た粉末状無機物質30〜80重量%、50〜6,000
μの繊維長を有するガラス繊維1.5〜15重量%及び
顔料0.01〜5重量%を含有することを特徴とするポ
リアミド組成物。1 Powdered inorganic material whose surface has been treated with an organosilicon compound or polymerizable organic acid 30-80% by weight, 50-6,000
A polyamide composition characterized in that it contains 1.5 to 15% by weight of glass fibers having a fiber length of μ and 0.01 to 5% by weight of a pigment.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP8839575A JPS584737B2 (en) | 1975-07-21 | 1975-07-21 | polyamide composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP8839575A JPS584737B2 (en) | 1975-07-21 | 1975-07-21 | polyamide composition |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5212261A JPS5212261A (en) | 1977-01-29 |
| JPS584737B2 true JPS584737B2 (en) | 1983-01-27 |
Family
ID=13941595
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP8839575A Expired JPS584737B2 (en) | 1975-07-21 | 1975-07-21 | polyamide composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS584737B2 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6061442U (en) * | 1983-09-30 | 1985-04-30 | 本田技研工業株式会社 | Boost pressure control device for internal combustion engine with turbocharger |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SE8203188L (en) * | 1982-05-21 | 1983-11-22 | Tetra Pak Int | SEE AS PREPARATION OF ASEPTIC JUICE DRINK |
-
1975
- 1975-07-21 JP JP8839575A patent/JPS584737B2/en not_active Expired
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6061442U (en) * | 1983-09-30 | 1985-04-30 | 本田技研工業株式会社 | Boost pressure control device for internal combustion engine with turbocharger |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5212261A (en) | 1977-01-29 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| ES2325810T3 (en) | BLACK SMOKE AND COMPOSITIONS THAT CONTAIN IT. | |
| CN1019307B (en) | reinforced molding resin composition | |
| JPH0776113B2 (en) | Reinforcing material for molding thermoplastic resin or thermosetting resin | |
| US5777019A (en) | Polyacetal resin composition | |
| JPH11172121A (en) | Thermoplastic composite composition reinforced with mica and woody fibrous filler | |
| EP3345965A1 (en) | Anti-static bicomponent formulation for unsaturated polyester resins and epoxy vinyl ester resins | |
| JPS6129385B2 (en) | ||
| JPS584737B2 (en) | polyamide composition | |
| US4115509A (en) | Moulding of filled synthetic plastics moulding compositions | |
| US5133316A (en) | Engine cylinder head cover and molding composition used therefor | |
| Pukánszky | Particulate filled polypropylene composites | |
| DE102011118507A1 (en) | Colored cellulose containing finely divided particles, which are coated or dyed with coloring agent in presence reactive binder, as thermosetting or elastomer layer, useful e.g. as additive e.g. for linoleum, dry mortar and concrete | |
| JP2718083B2 (en) | Molding material | |
| JPH0361692B2 (en) | ||
| JPH02138349A (en) | Fiber-reinforced polypropylene resin composition | |
| JPH0413740A (en) | Admixtures for thermoplastic resins and resin moldings | |
| RU2000110127A (en) | MULTI-COMPONENT STONE FILLER AND METHOD FOR PREPARING IT | |
| JPS63108076A (en) | Inorganic filler having improved impact resistance | |
| JPS6090859A (en) | Wall material with sand wall appearance | |
| Cowley et al. | Additives: Improving Plastics Coloration With Hyperdispersants | |
| JPS5817544B2 (en) | Mica powder-containing polyolefin resin composition | |
| JPH10101927A (en) | Aromatic polyamide resin composition | |
| JPS58108235A (en) | synthetic resin composition | |
| US5260369A (en) | Synthetic resin mass having a low content of short carbon fibres | |
| JPH01135871A (en) | Composite molding material |