JP2704968B2 - Polypropylene composition - Google Patents

Polypropylene composition

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Publication number
JP2704968B2
JP2704968B2 JP30322889A JP30322889A JP2704968B2 JP 2704968 B2 JP2704968 B2 JP 2704968B2 JP 30322889 A JP30322889 A JP 30322889A JP 30322889 A JP30322889 A JP 30322889A JP 2704968 B2 JP2704968 B2 JP 2704968B2
Authority
JP
Japan
Prior art keywords
polypropylene
talc
weight
transparency
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 - Fee Related
Application number
JP30322889A
Other languages
Japanese (ja)
Other versions
JPH03166244A (en
Inventor
佳幸 北島
通夫 中務
英太郎 朝枝
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.)
Tokuyama Corp
Original Assignee
Tokuyama Corp
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
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Priority to JP30322889A priority Critical patent/JP2704968B2/en
Publication of JPH03166244A publication Critical patent/JPH03166244A/en
Application granted granted Critical
Publication of JP2704968B2 publication Critical patent/JP2704968B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は、極めて微笑な粒径を有するタルクをポリプ
ロピレンに極く微量に配合してなる透明性の改良された
ポリプロピレン組成物に関する。
Description: TECHNICAL FIELD The present invention relates to a polypropylene composition having improved transparency, which is obtained by blending talc having a very small particle size with polypropylene in a very small amount.

(従来技術及び発明が解決しようとする課題) ポリプロピレンは、機械的性質、透明性、成形性、化
学的安定性に優れた樹脂として広く利用されている。し
かしながら、透明性については高い結晶性のために一般
にポリスチレン、ポリ塩化ビニル等の他の樹脂に比べ劣
っている。
(Problems to be Solved by the Prior Art and the Invention) Polypropylene is widely used as a resin having excellent mechanical properties, transparency, moldability, and chemical stability. However, transparency is generally inferior to other resins such as polystyrene and polyvinyl chloride due to high crystallinity.

ポリプロピレンの透明性を改良する試みとして、これ
までにいくつかの提案がなされている。例えば、ポリプ
ロピレンにソルビトール誘導体、芳香族カルボン酸のナ
トリウム又はアルミニウム塩などの造核剤を添加するこ
とにより成形物の球晶がより小さく均一になり成形物の
透明性が改良されることが知られている(例えば、特開
昭58−80392号公報、特開昭55−12460号公報)。しかし
ながら、これら有機系の造核剤は、成形時、特にシート
や二軸延伸フィルム成形時に樹脂よりブリードしてロー
ル汚れの原因となったり、また加工時に臭気が発生する
という問題があった。更に、芳香族カルボン酸塩は、こ
れらが加水分解したり、あるいは他の添加剤と反応する
ことで樹脂を着色させたりする問題も生じていた。
Several attempts have been made to improve the transparency of polypropylene. For example, it is known that by adding a nucleating agent such as a sorbitol derivative or a sodium or aluminum salt of an aromatic carboxylic acid to polypropylene, the spherulites of the molded product become smaller and uniform, and the transparency of the molded product is improved. (Eg, JP-A-58-80392 and JP-A-55-12460). However, these organic nucleating agents have a problem in that they bleed from the resin at the time of molding, particularly at the time of forming a sheet or a biaxially stretched film, thereby causing roll contamination, and causing odor during processing. Further, the aromatic carboxylate has a problem of hydrolyzing the aromatic carboxylate or coloring the resin by reacting with other additives.

ところで、ポリプロピレンにタルクを配合すると、成
形品の寸法安定性、耐衝撃性、耐熱剛性が向上すること
はすでに周知の通りであり、多くの提案がなされてい
る。例えば、特開昭57−177038号公報には、平均粒径が
1.3〜3.0μm程度のタルクをポリプロピレン100重量部
に対して1〜30重量部配合することが記載されており、
また、特開昭57−73033号公報には平均粒径が0.2〜1.5
μmのタルクをポリプロピレン100重量部に対して約5
〜150重量部配合することが記載されている。
By the way, it is already well known that the blending of talc with polypropylene improves the dimensional stability, impact resistance and heat-resistant rigidity of molded products, and many proposals have been made. For example, JP-A-57-177038 discloses that the average particle size is
It is described that 1 to 30 parts by weight of talc of about 1.3 to 3.0 μm is blended with respect to 100 parts by weight of polypropylene,
Further, JP-A-57-73033 discloses an average particle size of 0.2 to 1.5.
μm talc to about 5 parts per 100 parts by weight of polypropylene
It is described that 150150 parts by weight is blended.

このように、従来は、平均粒径が比較的大きいタルク
を多量にポリプロピレンに配合して、ポリプロピレン成
形品の寸法安定性、耐衝撃性、耐熱剛性を向上させるこ
とが行なわれていた。しかしながら、ポリロピレンの透
明性の改良にタルクを用いた例はない。
As described above, conventionally, a large amount of talc having a relatively large average particle diameter is blended with polypropylene to improve the dimensional stability, impact resistance, and heat resistance of a polypropylene molded product. However, there is no example of using talc for improving the transparency of polypropylene.

(課題を解決するための手段) 本発明者らは、透明性の改良されたポリプロピレンに
ついて、鋭意検討を行った結果、驚くべき事に、極めて
微小な粒径を有するタルクをポリプロピレンに極微量に
添加することでポリプロピレンの透明性が著しく改良さ
れ、シート、二軸延伸フィルム等の製膜をした場合にも
ブリードすることなく成形性にも優れることを見いだし
本発明を完成させるに至った。
(Means for Solving the Problems) The present inventors have conducted intensive studies on polypropylene having improved transparency, and as a result, surprisingly, talc having an extremely small particle size was reduced to a very small amount in polypropylene. It was found that the addition of the compound significantly improved the transparency of polypropylene, and it was found that even when a film such as a sheet or a biaxially stretched film was formed, it did not bleed and was excellent in moldability, thereby completing the present invention.

即ち、本発明はポリプロピレン100重量部、及び平均
粒径0.001〜0.1μmのタルク0.0001〜0.1重量部よりな
ることを特徴とす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 and 0.0001 to 0.1 part by weight of talc having an average particle size of 0.001 to 0.1 μm.

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、4−メチルペンテン−1等の
プロピレン以外のα−オレフィンのブロック共重合体、
グラフト共重合体、また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−オレフィン重合体との混合物が挙げられる。
The polypropylene used in the present invention is a homopolymer of propylene; a block copolymer of 50 mol% or more of propylene and an α-olefin other than propylene such as ethylene, butene-1, pentene-1, and 4-methylpentene-1. Coalescing,
Graft copolymers or random copolymers; mixtures of these polymers; and mixtures of these polymers with α-olefin polymers other than propylene.

本発明で使用されるタルクは平均粒径が0.001〜0.1μ
m、好ましくは、0.005〜0.05μmである。平均粒径が
0.1μmを超えるものでは透明性の改良には至らない。
また、0.001μm未満の場合はタルク粒子の凝集により
均一な分散が困難となり、透明性の改良にはならないば
かりか、このような超微粒子タルクの製造は困難であ
る。
Talc used in the present invention has an average particle size of 0.001 to 0.1 μ
m, preferably 0.005 to 0.05 μm. Average particle size
If the thickness exceeds 0.1 μm, transparency cannot be improved.
On the other hand, if it is less than 0.001 μm, uniform dispersion becomes difficult due to aggregation of talc particles, and not only transparency is not improved, but also production of such ultrafine talc is difficult.

本発明におけるタルクの平均粒径は、試料のタルクを
サンプリングし、透過型電子顕微鏡により観察された粒
子100個について、長径(a)及び短径(b)を測定し
て下記式により夫々の粒子径(D)を算出し、この粒子
径(D)の100個の算術平均値で示される。
The average particle diameter of talc in the present invention is obtained by sampling a sample of talc, measuring a major axis (a) and a minor axis (b) of 100 particles observed by a transmission electron microscope, and measuring each particle by the following formula. The particle diameter (D) is calculated, and the particle diameter (D) is represented by an arithmetic mean value of 100 particles.

粒子径(D)=(a+b)/2 本発明で使用するタルクの配合量は、ポリプロピレン
100重量部に対し、0.0001〜0.1重量部、好ましくは0.00
1〜0.05重量部である。0.0001重量部未満では透明性は
十分に発揮されない。また0.1重量部を越える場合は、
タルク粒子の凝集が起こり分散不良を起こし好ましくな
い。
Particle size (D) = (a + b) / 2 The amount of talc used in the present invention is polypropylene.
0.0001 to 0.1 part by weight, preferably 0.001 part by weight, per 100 parts by weight
1 to 0.05 parts by weight. If the amount is less than 0.0001 parts by weight, transparency is not sufficiently exhibited. If it exceeds 0.1 parts by weight,
It is not preferable because talc particles are aggregated to cause poor dispersion.

このような微小な粒径を有するタルクは、住友セメン
ト(株)から超微粒子タルクとして発売されている。ま
た、公知の方法によって製造してもよく、例えばミクロ
ンミル等で十分に微粉化した後、更に風力分級機及び種
々のフィルターで分級する方法等、その他のいかなる方
法で製造されてよい。本発明で使用するタルクは各種の
シランカップリング剤、各種高級脂肪酸、有機チタネー
ト等の化合物で表面処理を施したものを用いてもよい。
Talc having such a fine particle size is marketed by Sumitomo Cement Co., Ltd. as ultrafine talc. Further, it may be produced by a known method. For example, it may be produced by any other method such as a method of sufficiently pulverizing with a micron mill or the like, followed by classification with an air classifier and various filters. The talc used in the present invention may be subjected to a surface treatment with a compound such as various silane coupling agents, various higher fatty acids, and organic titanates.

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る添加剤、例えば、酸化
防止剤、分散剤、滑剤、帯電防止剤、アンチブロッキン
グ剤、着色剤等を配合してもよい。
In the polypropylene composition of the present invention, additives usually used in a range that does not impair the effects of the present invention, for example, an antioxidant, a dispersant, a lubricant, an antistatic agent, an antiblocking agent, a colorant and the like are compounded. Is also good.

本発明のポリプロピレン組成物の各成分は、通常用い
られる混練機、例えば、一軸混練機、二軸混練機、ロー
ル、ブラベンダープラストグラム等の各種混練機を用い
て混合され、ペレット状とした後に成形加工を行なって
もよい。また、重合槽より取り出される顆粒状ポリプロ
ピレン粒子に、本発明で用いられるタルクを配合し、直
接成形を施してもよい。また、本発明で用いられるタル
クをポリプロピレンに予め高濃度に配合してマスターバ
ッチを製造し、これをポリプロピレンに混合してタルク
の量が本発明の配合量の範囲になるように希釈した後、
成形加工に用いることも可能である。
The components of the polypropylene composition of the present invention are kneaders usually used, for example, a single-screw kneader, a twin-screw kneader, rolls, mixed using various kneaders such as Brabender plastogram, and then into a pellet. A molding process may be performed. Further, the talc used in the present invention may be blended with the granular polypropylene particles taken out from the polymerization tank and directly molded. Further, talc used in the present invention is previously blended with polypropylene at a high concentration to produce a masterbatch, which is then mixed with polypropylene and diluted so that the amount of talc falls within the range of the blending amount of the present invention.
It can also be used for molding.

(効 果) 本発明によるポリプロピレンの透明性が著しく改良さ
れ、シート、二軸延伸フィルムに成形する際にも成膜ロ
ールへの汚れ付着の問題なく優れた加工性のポリプロピ
レン組成物を得ることができる。
(Effects) The transparency of the polypropylene according to the present invention is remarkably improved, and a polypropylene composition having excellent processability can be obtained without forming a stain on a film-forming roll even when forming into a sheet or a biaxially stretched film. it can.

(実施例) 以下に実施例及び比較例を挙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。
(Examples) Hereinafter, the present invention will be described with reference to Examples and Comparative Examples, but the present invention is not limited to these Examples.

尚、以下の実施例及び比較例で得られたポリプロピレ
ン組成物の成形品の透明性及びロールの汚れ状態は次の
方法で評価した。
In addition, the following methods evaluated the transparency of the molded product of the polypropylene composition obtained in the following Examples and Comparative Examples, and the stain state of the roll.

<透明性の評価方法> (1) ヘイズ値 JIS−K6714に従い測定した。<Transparency evaluation method> (1) Haze value Measured according to JIS-K6714.

(2) 透視性目視評価(フィルムのみ) 得られた40μmのフィルムを延伸方向をそろえて5枚
重ね、蛍光灯の光をフィルムを通して見た場合の透視感
を、目視により5段階(5−良,1−悪)で評価を行っ
た。
(2) Visual Perspective Evaluation (Film Only) Five obtained 40 μm films were stacked in the same stretching direction, and five layers were visually observed. , 1-bad).

<ロール汚れの状態の観察> Tダイスより押し出した樹脂を冷却固化する冷却ロー
ル及び縦延伸装置のシート予熱ロールの汚れの状態から
判断した。
<Observation of Roll Soil Condition> Judgment was made based on the stain condition of the cooling roll for cooling and solidifying the resin extruded from the T-die and the sheet preheating roll of the longitudinal stretching device.

実施例1〜5 メルトインデックス1.2のホモポリプロピレンのパウ
ダー100重量部に、酸化防止剤として2,6−ジターシャリ
ーブチルヒドロキシトルエンを0.1重量部と表1に示し
たタルクを添加した後、ヘンシェルミキサー(三井三池
化工機社製ヘンシェルミキサーFM75J)で、5分間混合
後、50φ押出機(プラ技研社製PG50−32、フルフライト
スクリュー)で、樹脂温度230℃で混練、造粒を行っ
た。得られたペレット状ポリプロピレン組成物は、射出
成形機(新潟鉄工所社製SN150SN)で、樹脂温度230℃の
条件下、縦80.0×横50.0×厚さ1.0(mm)の板に成形し
た後48時間後に透明性を測定した。結果を表1に示し
た。
Examples 1 to 5 To 100 parts by weight of a homopolypropylene powder having a melt index of 1.2, 0.1 part by weight of 2,6-di-tert-butylhydroxytoluene as an antioxidant and talc shown in Table 1 were added. After mixing for 5 minutes with a Henschel mixer FM75J manufactured by Mitsui Miike Kakoki Co., Ltd., kneading and granulation were performed at a resin temperature of 230 ° C. using a 50φ extruder (PG50-32 manufactured by Plagiken Co., Ltd., full flight screw). The obtained pellet-shaped polypropylene composition was molded into a plate having a length of 80.0 × 50.0 × 1.0 (mm) under the condition of a resin temperature of 230 ° C. using an injection molding machine (SN150SN manufactured by Niigata Ironworks Co., Ltd.), After time the transparency was measured. The results are shown in Table 1.

比較例1〜5 表1に示したタルク粒径及び配合量とした以外は、実
施例1と同様の操作を行った。結果を表1に示した。
Comparative Examples 1 to 5 The same operation as in Example 1 was performed except that the talc particle size and the amount were as shown in Table 1. The results are shown in Table 1.

実施例6 比較例2で得られたポリプロピレン組成物をメルトイ
ンデックス1.2のホモポリプロピレンに希釈して、表2
に示した配合量のポリプロピレン組成物を得た。結果を
表2に示した。
Example 6 The polypropylene composition obtained in Comparative Example 2 was diluted with a homopolypropylene having a melt index of 1.2.
Was obtained. The results are shown in Table 2.

実施例7〜10 メルトインデックス1.8、エチレン含有量0.3重量%の
エチレン−プロピレン共重合体パウダー100重量部に、
実施例1と同様の酸化防止剤0.2重量部とタルクを表3
の配合量で添加した後、実施例1〜5と同様の方法で造
粒を行った。
Examples 7 to 10 To 100 parts by weight of an ethylene-propylene copolymer powder having a melt index of 1.8 and an ethylene content of 0.3% by weight,
Table 3 shows 0.2 parts by weight of the same antioxidant as in Example 1 and talc.
, And granulation was performed in the same manner as in Examples 1 to 5.

得られたペレット状ポリプロピレン組成物を、Tダイ
スを取り付けた押し出し機により280℃で押し出し、直
ちに、40℃の冷却ロールで冷却固化し、2.0mm厚さの未
延伸膜状物を得た。
The obtained pellet-shaped polypropylene composition was extruded at 280 ° C. by an extruder equipped with a T-die, and immediately cooled and solidified with a cooling roll at 40 ° C. to obtain an unstretched film having a thickness of 2.0 mm.

次いで、この得られた未延伸膜状物をテンター式逐次
二軸延伸装置にて延伸温度150℃で縦方向に5倍延伸を
行ない、引き続いて炉内温度165℃のテンター中で、横
方向に10倍延伸を行ない、厚さ40μmの二軸延伸ポリプ
ロピレンフィルムを得た。
Next, the obtained unstretched film-like material is stretched 5 times in the longitudinal direction at a stretching temperature of 150 ° C. in a tenter-type sequential biaxial stretching apparatus, and subsequently in a tenter at a furnace temperature of 165 ° C., in the transverse direction. The film was stretched 10 times to obtain a biaxially stretched polypropylene film having a thickness of 40 μm.

得られたフィルムの透明性及びロールの汚れ状態を表
3に示した。
Table 3 shows the transparency of the obtained film and the stained state of the roll.

実施例11 使用するポリプロピレン樹脂をメルトインデックス2.
0のホモポリプロピレンにしたほかはすべて実施例7〜1
0と同様に行い、二軸延伸フィルムを得た。その結果を
表3に示した。
Example 11 Polypropylene resin to be used is melt index 2.
Examples 7-1 except that the homopolypropylene was 0
The operation was performed in the same manner as in Example 0 to obtain a biaxially stretched film. Table 3 shows the results.

比較例6〜10 使用するタルクの粒径及び配合量を変え、実施例7〜
10と同様の方法で、二軸延伸フィルムを得た。結果を表
3に示した。
Comparative Examples 6 to 10 The particle size and the amount of talc used were changed, and
In the same manner as in 10, a biaxially stretched film was obtained. The results are shown in Table 3.

Claims (1)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】ポリプロピレン100重量部、及び平均粒径
0.001〜0.1μmのタルク0.0001〜0.1重量部よりなるこ
とを特徴とするポリプロピレン組成物。
1. 100 parts by weight of polypropylene and average particle size
A polypropylene composition comprising 0.0001 to 0.1 part by weight of 0.001 to 0.1 μm talc.
JP30322889A 1989-11-24 1989-11-24 Polypropylene composition Expired - Fee Related JP2704968B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP30322889A JP2704968B2 (en) 1989-11-24 1989-11-24 Polypropylene composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP30322889A JP2704968B2 (en) 1989-11-24 1989-11-24 Polypropylene composition

Publications (2)

Publication Number Publication Date
JPH03166244A JPH03166244A (en) 1991-07-18
JP2704968B2 true JP2704968B2 (en) 1998-01-26

Family

ID=17918423

Family Applications (1)

Application Number Title Priority Date Filing Date
JP30322889A Expired - Fee Related JP2704968B2 (en) 1989-11-24 1989-11-24 Polypropylene composition

Country Status (1)

Country Link
JP (1) JP2704968B2 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1068022C (en) * 1995-11-10 2001-07-04 中国科学院化学研究所 High-toughness polypropylene composite material and preparing process thereof
GB201421483D0 (en) * 2014-12-03 2015-01-14 Imerys Minerals Ltd Polymer compositions and additives

Also Published As

Publication number Publication date
JPH03166244A (en) 1991-07-18

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