JPH062849B2 - Polypropylene composition - Google Patents
Polypropylene compositionInfo
- Publication number
- JPH062849B2 JPH062849B2 JP63328015A JP32801588A JPH062849B2 JP H062849 B2 JPH062849 B2 JP H062849B2 JP 63328015 A JP63328015 A JP 63328015A JP 32801588 A JP32801588 A JP 32801588A JP H062849 B2 JPH062849 B2 JP H062849B2
- Authority
- JP
- Japan
- Prior art keywords
- polypropylene
- weight
- parts
- molecular weight
- inorganic filler
- 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 - Fee Related
Links
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- Compositions Of Macromolecular Compounds (AREA)
Description
【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、成形性及び延伸性の良好なポリプロピレン組
成物に関する。TECHNICAL FIELD The present invention relates to a polypropylene composition having good moldability and stretchability.
従来より、ポリプロピレンを用いたシートやフイルムに
は、艶消し剤、アンチブロツキング剤等として、また、
バンドやヤーンのような延伸物には縦ワレ、ソゲの防止
等に平均粒子径2〜3μmの炭酸カルシウムが配合され
ている。Conventionally, as a matting agent, anti-blocking agent, etc. for sheets and films using polypropylene,
Drawouts such as bands and yarns contain calcium carbonate having an average particle diameter of 2 to 3 μm in order to prevent warping and sowing.
ところで、ポリプロピレンとして重量平均分子量と数平
均分子量との比で表わされる分子量分布の狭いポリプロ
ピレンを用いると、シートやフイルムでは透明性、光沢
が改良され、またバンドやヤーンでは延伸性が改良され
る。しかしながら、この分子量分布の狭いポリプロピレ
ンに平均粒子径2μ以上の炭酸カルシウムを配合して押
出成形を行うと、ダイス出口に炭酸カルシウムが堆積
し、この堆積した炭酸カルシウムがポリプロピレンシー
トやフイルムの表面に付着し、シートやフイルムでは透
明性、光沢を悪くし、ヤーンのような延伸物では延伸切
れをおこし生産性を著しく阻害する。分子量分布の広い
ポリプロピレンでは、このような現象はみられない。By the way, when polypropylene having a narrow molecular weight distribution represented by the ratio of the weight average molecular weight to the number average molecular weight is used as the polypropylene, transparency and gloss are improved in a sheet or film, and stretchability is improved in a band or yarn. However, when polypropylene having a narrow molecular weight distribution is mixed with calcium carbonate having an average particle size of 2 μ or more and extrusion molding is performed, calcium carbonate is deposited at the die outlet, and the deposited calcium carbonate adheres to the surface of the polypropylene sheet or film. However, in the case of a sheet or film, the transparency and gloss are deteriorated, and in a stretched product such as a yarn, stretch breakage occurs and productivity is significantly impaired. Such a phenomenon is not observed in polypropylene having a wide molecular weight distribution.
本発明者らは、分子量分布の狭いポリプロピレンについ
て上記した問題を解決するために鋭意研究を重ねた結
果、上記した炭酸カルシウム等の無機充填材に加えて、
二酸化ケイ素を配合することによって上記の問題が解決
できることを見出し、本発明を完成するに至った。The present inventors have conducted extensive studies to solve the above-mentioned problems with polypropylene having a narrow molecular weight distribution, and in addition to the above-mentioned inorganic fillers such as calcium carbonate,
It has been found that the above problems can be solved by blending silicon dioxide, and the present invention has been completed.
即ち、本発明は、重量平均分子量と数平均分子量との比
が7.5以下であるポリプロピレン100重量部、二酸化
ケイ素0.01〜0.5重量部及び他の無機充填材0.1〜10重
量部よりなるポリプロピレン組成物である。That is, the present invention is a polypropylene composition comprising 100 parts by weight of polypropylene having a ratio of weight average molecular weight to number average molecular weight of 7.5 or less, 0.01 to 0.5 parts by weight of silicon dioxide and 0.1 to 10 parts by weight of other inorganic filler. is there.
本発明で使用されるポリプロピレンは、プロピレンの単
独重合体;50モル%以上のプロピレンとエチレン、ブ
テン−1、ペンテン−1等のプロピレン以外のα−オレ
フインとのブロツク共重合体、グラフト共重合体又はラ
ンダム共重合体;これらの重合体の混合物;及びこれら
の重合体とプロピレン以外のα−オレフインの重合体と
の混合物等が挙げられる。本発明で使用されるポリプロ
ピレンは、重量平均分子量と数平均分子量との比で表わ
される分子量分布が7.5以下である。本発明において
は、上記の分子量分布が7.0以下であっても、後述する
二酸化ケイ素の配合によって、成形時のダイス出口に無
機充填材の析出や堆積を効果的に防止することができ
る。The polypropylene used in the present invention is a homopolymer of propylene; a block copolymer or a graft copolymer of 50 mol% or more propylene and α-olefin other than propylene such as ethylene, butene-1, pentene-1. Or a random copolymer; a mixture of these polymers; and a mixture of these polymers with a polymer of α-olefin other than propylene. The polypropylene used in the present invention has a molecular weight distribution represented by the ratio of the weight average molecular weight to the number average molecular weight of 7.5 or less. In the present invention, even if the molecular weight distribution is 7.0 or less, the inorganic filler can be effectively prevented from precipitating or accumulating at the die outlet at the time of molding by blending silicon dioxide described later.
本発明のポリプロピレン組成物の他の成分は無機充填材
である。無機充填材の平均粒子径は特に制限されない
が、前記したように2μm以上の比較的大きな平均粒子
径を有する無機充填材を用いた場合にも、本発明によっ
て押出成形時のダイス出口への無機充填材の析出及び堆
積を効果的に防止することができる。Another component of the polypropylene composition of the present invention is an inorganic filler. The average particle size of the inorganic filler is not particularly limited, but even when an inorganic filler having a relatively large average particle size of 2 μm or more is used as described above, the inorganic filler to the die outlet at the time of extrusion molding according to the present invention is also used. Precipitation and deposition of the filler can be effectively prevented.
無機充填材の種類は、二酸化ケイ素以外であれば特に制
限されるものではない。例えば、炭酸カルシウム、炭酸
マグネシウム、水酸化カルシウム、水酸化マグネシウ
ム、タルク、クレー等、ポリプロピレンに添加し得る無
機充填材として公知のものがそれぞれの目的に応じて使
用される。The type of inorganic filler is not particularly limited as long as it is other than silicon dioxide. For example, known inorganic fillers that can be added to polypropylene, such as calcium carbonate, magnesium carbonate, calcium hydroxide, magnesium hydroxide, talc, and clay, are used according to their respective purposes.
無機充填材の配合量は、ポリプロピレン100重量部に
対して0.1〜10重量部、好ましくは0.5〜8重量部の範
囲である。配合量が上記の下限よりも少ない場合には、
無機充填材の充填効果、即ち、艶消しやアンチブロツキ
ング等の効果が得られず、一方、上記の上限よりも多い
場合には、後述する二酸化ケイ素を添加しても、成形時
に無機充填材がダイス出口に析出及び堆積するのを防止
することができない。The compounding amount of the inorganic filler is in the range of 0.1 to 10 parts by weight, preferably 0.5 to 8 parts by weight, based on 100 parts by weight of polypropylene. When the compounding amount is less than the above lower limit,
If the filling effect of the inorganic filler, that is, the effects such as matting and anti-blocking, cannot be obtained, on the other hand, when the amount is more than the above upper limit, the inorganic filler is added at the time of molding even if silicon dioxide described below is added. It is not possible to prevent the material from precipitating and depositing at the die outlet.
本発明のポリプロピレン組成物の他の成分は、二酸化ケ
イ素である。二酸化ケイ素の平均粒子径は、無機充填材
の析出防止のためには、3μm以下、好ましくは0.1〜1.
5μmの範囲であることが好ましい。二酸化ケイ素は、結
晶質及び非晶質のいずれでも良い。二酸化ケイ素の配合
量は、ポリプロピレン100重量部に対して0.01〜0.5
重量部の範囲好ましくは0.1〜0.3の範囲である。配合量
が0.01重量部よりも少ない場合には、前記した無機充填
材の析出防止の効果が少なく、0.5重量部を越える場合
には、ポリプロピレン組成物の成形体の光沢等表面状態
に悪影響を及ぼすために好ましくない。Another component of the polypropylene composition of the present invention is silicon dioxide. The average particle size of silicon dioxide is 3 μm or less, preferably 0.1 to 1. to prevent precipitation of the inorganic filler.
It is preferably in the range of 5 μm. Silicon dioxide may be either crystalline or amorphous. The blending amount of silicon dioxide is 0.01 to 0.5 with respect to 100 parts by weight of polypropylene.
The range of parts by weight is preferably 0.1 to 0.3. When the blending amount is less than 0.01 parts by weight, the effect of preventing the precipitation of the above-mentioned inorganic filler is small, and when it exceeds 0.5 parts by weight, the surface condition such as the gloss of the polypropylene composition molded article is adversely affected. Not preferred because of
本発明のポリプロピレン組成物には、本発明の効果を阻
害しない範囲で通常用いられている添加剤、例えば、酸
化防止剤、分散剤、滑剤、着色剤等を配合しても良い。The polypropylene composition of the present invention may be blended with additives usually used within a range that does not impair the effects of the present invention, for example, antioxidants, dispersants, lubricants, colorants and the like.
本発明によると、押出成形時に無機充填材のダイス出口
への析出及び堆積を防止することができる。このため
に、ダイス出口に析出した無機充填材がポリプロピレン
成形体の表面に付着することによってポリプロピレン成
形体の透明性や光沢を悪化させることがなく、延伸物の
場合にも延伸切れをおこすようなこともない。According to the present invention, it is possible to prevent precipitation and deposition of the inorganic filler at the die outlet during extrusion molding. For this reason, the inorganic filler deposited at the die outlet does not deteriorate the transparency or gloss of the polypropylene molded body by adhering to the surface of the polypropylene molded body, and even in the case of a stretched product, stretching breakage may occur. Nothing.
以下に実施例及び比較例を掲げて本発明を説明するが、
本発明はこれら実施例に限定されるものではない。The present invention will be described below with reference to Examples and Comparative Examples.
The present invention is not limited to these examples.
尚、実施例及び比較例におけるポリプロピレンの分子量
分布は、ゲルパーミエーションクロマトグラフイーを用
いて測定された重量平均分子量と数平均分子量との比で
あり、測定条件は以下のとおりである。The molecular weight distribution of polypropylene in Examples and Comparative Examples is the ratio of the weight average molecular weight to the number average molecular weight measured by gel permeation chromatography, and the measurement conditions are as follows.
機 器 ウオーターズ製 GPC 1500型 カラム 東ソー製 GMH6−HT 測定温度 135℃ 溶 媒 O−ジクロルベンゼン また、無機充填材のダイス出口への析出量は目視により
下記の基準で評価を行なった。Equipment Waters GPC 1500 type column Tosoh GMH6-HT Measurement temperature 135 ° C. Solvent O-dichlorobenzene The amount of the inorganic filler deposited at the die outlet was visually evaluated according to the following criteria.
1:全く析出しない 2:わずかに析出する 3:やや多い 4:多い 5:非常に多い 実施例1〜5及び比較例1〜4 表−1に示す炭酸カルシウム及び二酸化ケイ素を配合し
たポリプロピレンを50mmφの押出機を用いてダイリツ
プ0.8mmのサーキユラーダイで230℃でフイルム状に
溶融押出し、15m/mmで引き取りながら冷却固化して
ポリプロピレンフイルムとした後、該フイルムをテープ
状に切断し、オーブン延伸法により130℃で7倍に延
伸し、900デニールのポリプロピレン延伸テープを製
造した。炭酸カルシウムの配合量はすべてポリプロピレ
ン100重量部に対して2重量部である。1: Not precipitated at all 2: Slightly precipitated 3: Slightly high 4: Highly 5: Very high Examples 1 to 5 and Comparative Examples 1 to 4 Polypropylene blended with calcium carbonate and silicon dioxide shown in Table 1 was 50 mmφ. Melt extruded into a film at 230 ° C. with a circular die of 0.8 mm die lip using the extruder of the above, and cooled and solidified while taking it off at 15 m / mm to obtain a polypropylene film, which was cut into a tape and then subjected to an oven stretching method. It was stretched 7 times at 130 ° C. to produce a 900 denier polypropylene stretch tape. The compounding amount of calcium carbonate is 2 parts by weight based on 100 parts by weight of polypropylene.
実施例6〜8及び比較例5〜7 表−2に示す炭酸カルシウム及び二酸化ケイ素をそれぞ
れ配合したポリプロピレンを40mmφの押出機を用い
て、ダイリツプ0.8mmのTダイで240℃で押し出し2
m/mmで引き取りながら厚さ0.5mmのシートを成形し
た。この時の炭酸カルシウムのダイ出口への析出状況を
観察した。炭酸カルシウムの配合量はすべてポリプロピ
レン100重量部に対して5重量部である。 Examples 6 to 8 and Comparative Examples 5 to 7 Polypropylene blended with calcium carbonate and silicon dioxide shown in Table 2 was extruded at 240 ° C. with a die die 0.8 mm T die using a 40 mmφ extruder.
A sheet having a thickness of 0.5 mm was formed while taking it off at m / mm. At this time, the state of precipitation of calcium carbonate at the die exit was observed. The compounding amount of calcium carbonate is 5 parts by weight based on 100 parts by weight of polypropylene.
実施例9〜12 分子量分布が6.5のポリプロピレン100重量部に対し
て表−3に示す無機充填材1重量部と二酸化ケイ素0.1
重量部を配合し、実施例6〜8と同様にして押出機を用
いてシートを成形した。結果を表−3に示した。 Examples 9 to 12 To 100 parts by weight of polypropylene having a molecular weight distribution of 6.5, 1 part by weight of the inorganic filler shown in Table 3 and 0.1 part of silicon dioxide are used.
Parts by weight were blended, and a sheet was formed using an extruder in the same manner as in Examples 6-8. The results are shown in Table-3.
フロントページの続き (51)Int.Cl.5 識別記号 庁内整理番号 FI 技術表示箇所 C08K 3:36) Continuation of the front page (51) Int.Cl. 5 Identification code Office reference number FI technical display area C08K 3:36)
Claims (1)
5以下であるポリプロピレン100重量部、二酸化ケイ
素0.01〜0.5重量部及び他の無機充填材0.1〜10重量部
よりなるポリプロピレン組成物。1. The ratio of the weight average molecular weight to the number average molecular weight is 7.
A polypropylene composition comprising 100 parts by weight of polypropylene of 5 or less, 0.01 to 0.5 parts by weight of silicon dioxide and 0.1 to 10 parts by weight of other inorganic fillers.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP63328015A JPH062849B2 (en) | 1988-12-27 | 1988-12-27 | Polypropylene composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP63328015A JPH062849B2 (en) | 1988-12-27 | 1988-12-27 | Polypropylene composition |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH02173139A JPH02173139A (en) | 1990-07-04 |
| JPH062849B2 true JPH062849B2 (en) | 1994-01-12 |
Family
ID=18205562
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP63328015A Expired - Fee Related JPH062849B2 (en) | 1988-12-27 | 1988-12-27 | Polypropylene composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH062849B2 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH07119330B2 (en) * | 1988-12-28 | 1995-12-20 | 株式会社トクヤマ | Polypropylene composition |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| LU65954A1 (en) * | 1972-08-25 | 1974-03-07 | ||
| JPS562307A (en) * | 1979-06-20 | 1981-01-12 | Sumitomo Chem Co Ltd | Preparation of highly crystalline olefin polymer |
| JPS5718747A (en) * | 1980-07-07 | 1982-01-30 | Tokuyama Soda Co Ltd | Polypropylene composition |
| JPS6099108A (en) * | 1983-11-04 | 1985-06-03 | Tokuyama Soda Co Ltd | Preparation of molded article of polypropylene |
-
1988
- 1988-12-27 JP JP63328015A patent/JPH062849B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JPH02173139A (en) | 1990-07-04 |
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