JPH0525334A - High-rigidity polypropylene film with excellent impact resistance - Google Patents

High-rigidity polypropylene film with excellent impact resistance

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Publication number
JPH0525334A
JPH0525334A JP17910991A JP17910991A JPH0525334A JP H0525334 A JPH0525334 A JP H0525334A JP 17910991 A JP17910991 A JP 17910991A JP 17910991 A JP17910991 A JP 17910991A JP H0525334 A JPH0525334 A JP H0525334A
Authority
JP
Japan
Prior art keywords
impact resistance
weight
film
parts
liquid paraffin
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
Application number
JP17910991A
Other languages
Japanese (ja)
Other versions
JP3135288B2 (en
Inventor
Koji Kitabayashi
浩二 北林
Yoshito Imabayashi
良人 今林
Takeo Inoue
武夫 井上
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.)
Mitsui Toatsu Chemicals Inc
Original Assignee
Mitsui Toatsu Chemicals Inc
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 Mitsui Toatsu Chemicals Inc filed Critical Mitsui Toatsu Chemicals Inc
Priority to JP17910991A priority Critical patent/JP3135288B2/en
Publication of JPH0525334A publication Critical patent/JPH0525334A/en
Application granted granted Critical
Publication of JP3135288B2 publication Critical patent/JP3135288B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Abstract

PURPOSE:To obtain the subject film useful for food or textile packaging use, especially excellent in impact resistance at low temperatures by adding liquid paraffin to a specific polypropylene resin. CONSTITUTION:The objective film can be obtained by melt extrusion at 190-250'C followed by quenching of a composition prepared by incorporating (A) 100 pts.wt. of propylene homopolymer and/or a polypropylene resin having 0-2wt.% ethylene content consisting of an ethylene-propylene copolymer with (B) 0.2-5.0 pts.wt. of liquid paraffin with a viscosity of pref. 210-380SUSsec and (C) other ingredient (s) such as antioxidant.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、高剛性且つ、耐衝撃性
に優れたポリプロピレンフィルムに関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a polypropylene film having high rigidity and excellent impact resistance.

【0002】[0002]

【従来の技術】ポリプロピレンフィルムは、透明性、機
械的強度、耐熱性及び寸法安定性に優れているため、食
品及び繊維包装などの用途に多く使用されている。
2. Description of the Related Art Polypropylene films are widely used for foods, fiber packaging and the like because of their excellent transparency, mechanical strength, heat resistance and dimensional stability.

【0003】しかしながら、従来から公知のポリプロピ
レンフィルムは耐衝撃性、特に高剛性を特徴とするプロ
ピレン単独重合体をTダイ法にて溶融押出しして得られ
たポリプロピレンキャストフィルムの場合、特に低温で
の衝撃性が著しく低下する欠点が有り、この欠点を解決
するため、特開昭61-98756号公報には、ポリプロピレン
重合体に軟質エラストマー及び直鎖低密度ポリエチレン
等をブレンドする。
However, conventionally known polypropylene films are polypropylene cast films obtained by melt-extruding a propylene homopolymer characterized by high impact resistance, particularly high rigidity by the T-die method, especially at low temperature. There is a drawback that the impact property is remarkably lowered. In order to solve this drawback, in JP-A-61-98756, a polypropylene polymer is blended with a soft elastomer, a linear low density polyethylene and the like.

【0004】あるいは、特開平 2-80445号公報には、可
塑剤(エポキシステアリン酸オクチル、アジピン酸ジイ
ソノニル、ステアリン酸ブチル等)の添加及び可塑剤と
軟質エラストマーとの併用添加等の手段が用いられてい
る。
Alternatively, in JP-A No. 2-80445, means such as addition of a plasticizer (octyl epoxy stearate, diisononyl adipate, butyl stearate, etc.) and addition of a plasticizer in combination with a soft elastomer is used. ing.

【0005】[0005]

【発明が解決しようとする課題】しかしながら、これら
従来の技術において、エラストマー及び直鎖低密度ポリ
エチレン等を用いて耐衝撃性の向上を計ろうとすると、
より効果を上げるには大量の添加が不可欠で不経済であ
り、耐熱ブロッキング性が不足する。又、可塑剤及び可
塑剤と軟質エラストマーとの併用等の添加による技術に
おいては、衝撃性が向上するに伴い剛性が低下し、成形
加工時の発煙性悪化及び可塑剤のロール付着等による生
産性の低下、さらには安全衛生上の問題が有り、特に食
品包装用途へ使用することが出来なかった。
However, in these conventional techniques, when an attempt is made to improve impact resistance by using an elastomer, a linear low-density polyethylene or the like,
Addition of a large amount is indispensable for further improving the effect, which is uneconomical and lacks heat blocking resistance. In addition, in the technology that uses plasticizers and the combination of plasticizers and soft elastomers, the rigidity decreases as the impact resistance improves, and the smoke generation during molding process deteriorates and the productivity of plasticizers due to roll adhesion increases. However, it could not be used for food packaging in particular.

【0006】従って、成形加工時の発煙性による作業低
下もなく経済的で、安全衛生面からも好ましく、且つ、
剛性低下を損なうことなく耐衝撃性に優れたポリプロピ
レンフィルムが望まれていた。
[0006] Therefore, it is economical because there is no reduction in work due to smoke emission during molding, it is preferable from the viewpoint of safety and hygiene, and
A polypropylene film having excellent impact resistance without impairing the reduction in rigidity has been desired.

【0007】[0007]

【課題を解決するための手段】本発明者らは、上記課題
を解決すべく鋭意検討した結果、ポリプロピレン樹脂に
流動パラフィンを添加することにより、かかる問題を解
決することを見出し本発明を完成するに至ったものであ
る。
Means for Solving the Problems As a result of intensive studies to solve the above-mentioned problems, the present inventors have found that the addition of liquid paraffin to polypropylene resin solves the above problems, and complete the present invention. It came to.

【0008】即ち、本発明は、プロピレン単独重合体及
び/又はプロピレン−エチレン共重合体であって、エチ
レン含有率が 0〜2 重量%であるポリプロピレン樹脂 1
00重量部に、流動パラフィン 0.2〜5.0 重量部添加して
なる樹脂組成物を用いて、成形した高剛性で耐衝撃性に
優れたポリプロピレンフィルムである。
That is, the present invention relates to a propylene homopolymer and / or a propylene-ethylene copolymer having a polypropylene content of 0 to 2% by weight.
A polypropylene film molded with a resin composition obtained by adding 0.2 to 5.0 parts by weight of liquid paraffin to 00 parts by weight and having high rigidity and excellent impact resistance.

【0009】本発明におけるポリプロピレン樹脂とは、
プロピレン単独重合体、プロピレンとエチレンのランダ
ム或いはブッロク共重合体およびこれらの混合物であ
る。
The polypropylene resin in the present invention means
It is a propylene homopolymer, a random or block copolymer of propylene and ethylene, and a mixture thereof.

【0010】これらポリプロピレン樹脂の製造方法とし
ては格別に限定はなく、不活性な液状媒体を重合媒体と
して用いる溶媒重合法、プロピレン自身を液状媒体とし
て用いる塊状重合法、或いは実質的に液状媒体の存在し
ない気相重合法などで製造される。
The method for producing these polypropylene resins is not particularly limited, and includes a solvent polymerization method using an inert liquid medium as a polymerization medium, a bulk polymerization method using propylene itself as a liquid medium, or the presence of a substantially liquid medium. Not manufactured by a gas phase polymerization method.

【0011】触媒としては公知の種々の触媒が使用で
き、例えば、活性三塩化チタン触媒と有機アルミニュウ
ムからなる触媒、或いは、ハロゲン化マグネシュウムに
四塩化チタン或いは三塩化チタンを担持して得た活性チ
タン触媒と有機アルミニウムから成る触媒などが挙げら
れるが、得られるポリプロピレン樹脂の分子量がメルト
フロー値(ASTM D-1238 230 ℃ 2.16 Kg荷重 以下、M
Iと略記する。)で 5〜15g/10min 程度であれば通常
市販されている容易に入手可能なものが利用できる。
As the catalyst, various known catalysts can be used, for example, a catalyst comprising an active titanium trichloride catalyst and organic aluminum, or an active titanium obtained by supporting titanium tetrachloride or titanium trichloride on magnesium halide. A catalyst composed of a catalyst and organoaluminum may be mentioned, but the molecular weight of the resulting polypropylene resin is a melt flow value (ASTM D-1238 230 ℃ 2.16 Kg load or less, M
Abbreviated as I. If it is about 5 to 15 g / 10 min in (), a commercially available product which is usually commercially available can be used.

【0012】このMIが5g/10min に満たないと、特に
Tダイ法によるフィイルム成形において、高速製膜性が
不良となり、又、15g/10min を越えると特にインフレー
ション法のフィルム成形において、チューブ不安定によ
り厚みムラ発生等の問題を有しているため好ましくな
い。
If this MI is less than 5 g / 10 min, the high-speed film forming property becomes poor especially in the film forming by the T-die method, and if it exceeds 15 g / 10 min, the tube becomes unstable especially in the film forming by the inflation method. Therefore, there is a problem such as uneven thickness, which is not preferable.

【0013】ポリプロピレン樹脂としてプロピレンとエ
チレンの共重合体を用いる場合においては、エチレン含
有率が2重量%以下であることが好ましい。エチレン含
有率が2重量%を越えると、低温での耐衝撃性は向上す
るものの、剛性が著しく低下し好ましくない。耐衝撃性
と剛性をも兼ね備えるエチレン含有率としては、2重量
%以下が好ましく、 1.5重量%以下がさらに好ましい。
When a copolymer of propylene and ethylene is used as the polypropylene resin, the ethylene content is preferably 2% by weight or less. When the ethylene content exceeds 2% by weight, the impact resistance at low temperature is improved, but the rigidity is remarkably lowered, which is not preferable. The ethylene content, which has both impact resistance and rigidity, is preferably 2% by weight or less, and more preferably 1.5% by weight or less.

【0014】本発明に用いる流動パラフィンは、市場で
入手可能品で特に限定はしないが、粘度(JIS K-2283)
が 210〜380 SUS 秒のものが好ましく用いられ、具体例
としては、モレスコ ホワイト P-260(松村石油製)、
プラスッチクオイル 250(ウイトコ社製)等が挙げられ
る。
The liquid paraffin used in the present invention is a commercially available product and is not particularly limited, but the viscosity (JIS K-2283)
Of 210 to 380 SUS seconds are preferably used, and specific examples include Moresco White P-260 (Matsumura Oil Co., Ltd.),
Plastic oil 250 (manufactured by Witco) and the like can be mentioned.

【0015】これら流動パラフィンの添加量は、ポリプ
ロピレン樹脂 100重量部に対して、0.2〜5重量部の範
囲であり、添加量が 0.2重量部未満の場合は、得られる
ポリプロピレンフィルムの耐衝撃性の改良効果が低く、
5重量部を越えて添加しても得られるポリプロピレンフ
ィルムの耐衝撃性は添加量に比例する程向上せず、かえ
って剛性が低下し、さらには成形時における発煙性を悪
くし、いずれの場合も好ましくない。
The addition amount of these liquid paraffins is in the range of 0.2 to 5 parts by weight with respect to 100 parts by weight of the polypropylene resin. If the addition amount is less than 0.2 parts by weight, the impact resistance of the obtained polypropylene film is The improvement effect is low,
Even if added in an amount of more than 5 parts by weight, the impact resistance of the polypropylene film obtained does not improve to the extent that it is proportional to the amount added, rather the rigidity decreases and the smoke emission during molding deteriorates. Not preferable.

【0016】又、上記成分以外に本発明の効果を著しく
損なわない程度の酸化防止剤、熱安定剤、帯電防止剤、
滑剤、アンチ・ブッロキング剤を添加してもかまわな
い。更に必要に応じて熱可塑性エラストマー、直鎖低密
度ポリエチレン等を添加することも妨げない。
In addition to the above components, an antioxidant, a heat stabilizer, an antistatic agent, which does not significantly impair the effects of the present invention,
Lubricants and anti-blocking agents may be added. Further, addition of thermoplastic elastomer, linear low-density polyethylene, etc., if necessary, is not hindered.

【0017】本発明におけるポリプロピレンフィルム
は、ポリプロピレン樹脂、流動パラフィン及び必要に応
じた各種の添加剤を本発明の目的を妨げない範囲で添加
し、ヘンシエルミキサー等公知の混合機を用いて混合
し、次いで溶融押出されて得られたポリプロピレン樹脂
を、例えば、インフレーション法あるいはTダイ法にて
溶融温度 190〜250 ℃で溶融押出しし、急冷することに
よりポリプロピレンフィルムとして得られる。
In the polypropylene film of the present invention, polypropylene resin, liquid paraffin and various additives as required are added within a range that does not impair the object of the present invention, and they are mixed using a known mixer such as a Henschel mixer. Then, the polypropylene resin obtained by melt-extrusion is melt-extruded at a melting temperature of 190 to 250 ° C. by an inflation method or a T-die method and then rapidly cooled to obtain a polypropylene film.

【0018】この様にして得られたフィルムは 剛性、
耐衝撃性等が良好なことより、食品及び繊維包装を始め
様々な用途に利用することが出来る。
The film thus obtained has rigidity,
Because of its good impact resistance, it can be used for various purposes such as food and fiber packaging.

【0019】[0019]

【実施例】以下、実施例により本発明を詳細に説明す
る。尚、以下の記載において、 ・MI:g/10min ASTM D-1238 ・ヘイズ:% ASTM D-1003 ・衝撃強度:kg・cm/mm ASTM D-3420 準拠 ・剛性;ヤング率 :kg/mm2 ASTM D-882 準拠 ;降伏点応力:kg/mm2 ASTM D-882 準拠 ・発煙性:成形加工時にダイス付近より発生する発煙を
目視にて評価する。(1.発煙のない。2.やや発煙が
認められる。3.発煙が多い。)
The present invention will be described in detail below with reference to examples. In the following description, ・ MI: g / 10min ASTM D-1238 ・ Haze:% ASTM D-1003 ・ Impact strength: kg ・ cm / mm According to ASTM D-3420 ・ Stiffness; Young's modulus: kg / mm 2 ASTM D-882 compliant; Yield point stress: kg / mm 2 ASTM D-882 compliant ・ Smoke emission: Smoke generated near the die during molding is visually evaluated. (1. No smoke. 2. Slight smoke is observed. 3. A lot of smoke is generated.)

【0020】実施例1〜5、比較例1〜3 プロピレン単独重合体(MI 9.0g/10min 以下、PP-1と
略記する) 100重量部に流動パラフィン(モレスコホワ
イト P-260、松村石油社製)を添加し、リン系酸化防止
剤(サンドスターブ PEP-Q 、サンド社製)0.04重量部
及びフェノール系酸化防止剤(イルガノックス1010、チ
バ・ガイギー社製)0.10重量部、中和剤(水酸化マグネ
シュウム キスマ5A、協和化学社製)0.03重量部、ス
リップ剤(エルカ酸アミド ニュートロンS、日本精化
社製)0.08重量部、アンチ・ブロッキング剤(シリカ
サイロイド244 、富士デビソン社)0.15重量部をヘンシ
エルミキサーで混合した後、押出機により溶融押出して
得られたペレットを、次いでTダイ法製膜機にて厚さ30
μのフィルムを成形し得られたフィルムを用いて上記の
評価方法により物性を測定した。
Examples 1-5, Comparative Examples 1-3 Propylene homopolymer (MI 9.0 g / 10 min or less, abbreviated as PP-1) 100 parts by weight of liquid paraffin (Moresco White P-260, Matsumura Oil Co., Ltd.) Made), 0.04 part by weight of a phosphorus-based antioxidant (Sandstarve PEP-Q, manufactured by Sand Co.) and 0.10 part by weight of a phenol-based antioxidant (Irganox 1010, manufactured by Ciba Geigy), a neutralizer ( Magnesium hydroxide Kisuma 5A, made by Kyowa Chemical Co., Ltd. 0.03 parts by weight, slip agent (Erukaamide Neutron S, made by Nippon Seika) 0.08 parts by weight, anti-blocking agent (silica)
(Syloid 244, Fuji Davison) 0.15 parts by weight are mixed with a Henschel mixer, and the pellets obtained by melt-extruding with an extruder and then with a T-die film forming machine to a thickness of 30
Physical properties were measured by the above-mentioned evaluation methods using a film obtained by molding a film of μ.

【0021】流動パラフィンの適正な添加量を逸脱した
比較例に比べ実施例は、低温衝撃性が改良され、且つ、
剛性の低下も少なく、同時に成形加工時の発煙性も良好
であった。結果を表1に示す。
Compared with the comparative example which deviated from the proper addition amount of liquid paraffin, the example has improved low temperature impact resistance, and
There was little decrease in rigidity, and at the same time, smoke generation during molding was good. The results are shown in Table 1.

【0022】実施例6〜8、比較例4 プロピレン単独重合体に変えプロピレン−エチレン共重
合体(エチレン含有率1.0%でMI7.0g/10min 以下、P
P-2と略記する。)を用いた他は、実施例1と同様にし
得られたフィルムの物性を評価した。プロピレン単独重
合体を用いた場合に比較して耐衝撃性の向上が伺える。
結果は表1に示す。
Examples 6 to 8, Comparative Example 4 Propylene-ethylene copolymer was used instead of propylene homopolymer (MI 7.0 g / 10 min or less at ethylene content 1.0%, P
Abbreviated as P-2. ) Was used and the physical properties of the film obtained in the same manner as in Example 1 were evaluated. It can be seen that the impact resistance is improved as compared with the case of using the propylene homopolymer.
The results are shown in Table 1.

【0023】比較例5〜6 ポリプロピレン樹脂をプロピレン−エチレン共重合体
(エチレン含有率 2.5%、MI 6.0g/10min 以下、PP-3
と略記する。)に変えた他は、実施例6と同様にし得ら
れたフィルムの物性を評価した。結果を表1に示す。
Comparative Examples 5 to 6 A polypropylene resin was used as a propylene-ethylene copolymer (ethylene content 2.5%, MI 6.0 g / 10 min or less, PP-3
Is abbreviated. The physical properties of the obtained film were evaluated in the same manner as in Example 6 except that The results are shown in Table 1.

【0024】実施例9〜11、比較例7 PP-1 100重量部に流動パラフィンを添加し、酸化防止剤
(BHT、武田薬品社製)0.15重量部、中和剤(カルシュ
ウム ステアレート、堺化学社製) 0.1重量部、スリッ
プ剤(オレイン酸アミド ニュートロン、日本精化社
製)0.25重量部及びアンチ・ブロッキング剤(シリカサ
イロイド244 、富士デビソン社製) 0.3重量部をヘンシ
エルミキサーで混合した後、押出機によって溶融押出さ
れて得られたペレットを水冷インフレーション法製膜機
にて厚さ30μのフィルムに成形し、得られたフィルムを
用いて上記評価方法によりフィルムの物性評価を行なっ
た。その結果を表1に示した。
Examples 9-11, Comparative Example 7 Liquid paraffin was added to 100 parts by weight of PP-1, 0.15 parts by weight of an antioxidant (BHT, manufactured by Takeda Pharmaceutical Co., Ltd.), a neutralizing agent (calcium stearate, Sakai Chemical Co., Ltd.). 0.1 parts by weight, slip agent (oleic acid amide Neutron, manufactured by Nippon Seika Co., Ltd.) 0.25 parts by weight, and anti-blocking agent (silica siloid 244, manufactured by Fuji Devison Co., Ltd.) 0.3 parts by weight are mixed with a Henschel mixer. After that, the pellets obtained by melt extrusion with an extruder were molded into a film having a thickness of 30 μ by a water-cooled inflation method film forming machine, and the physical properties of the film were evaluated by the above-mentioned evaluation methods using the obtained film. The results are shown in Table 1.

【0025】[0025]

【表1】 [Table 1]

【0026】[0026]

【発明の効果】本発明によるポリプロピレンフィルム
は、剛性と耐衝撃性のバランスが良く、特に低温での耐
衝撃性に優れ、経済的にも好ましいことにより食品包装
用フィルムとして用いることができ、又、単層あるいは
複合フィルム用として、広範囲な用途が期待でき、産業
上優位である。
EFFECT OF THE INVENTION The polypropylene film of the present invention has a good balance of rigidity and impact resistance, is excellent in impact resistance especially at low temperature, and can be used as a food packaging film because it is economically preferable. A wide range of applications can be expected for single layer or composite films, which is industrially superior.

Claims (1)

【特許請求の範囲】 【請求項1】プロピレン単独重合体及び/又はプロピレ
ン−エチレン共重合体であって、エチレン含有率が 0〜
2 重量%であるポリプロピレン樹脂 100重量部に、流動
パラフィン 0.2〜5.0 重量部添加してなる樹脂組成物を
用いて、成形した高剛性で耐衝撃性に優れたポリプロピ
レンフィルム。
Claims: 1. A propylene homopolymer and / or a propylene-ethylene copolymer having an ethylene content of 0 to
A polypropylene film with high rigidity and excellent impact resistance formed by using a resin composition obtained by adding 0.2 to 5.0 parts by weight of liquid paraffin to 100 parts by weight of 2% by weight polypropylene resin.
JP17910991A 1991-07-19 1991-07-19 Polypropylene film with high rigidity and excellent impact resistance Expired - Fee Related JP3135288B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP17910991A JP3135288B2 (en) 1991-07-19 1991-07-19 Polypropylene film with high rigidity and excellent impact resistance

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP17910991A JP3135288B2 (en) 1991-07-19 1991-07-19 Polypropylene film with high rigidity and excellent impact resistance

Publications (2)

Publication Number Publication Date
JPH0525334A true JPH0525334A (en) 1993-02-02
JP3135288B2 JP3135288B2 (en) 2001-02-13

Family

ID=16060178

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2001307688A (en) * 2000-04-19 2001-11-02 Dainippon Printing Co Ltd Packing material for lithium ion battery
JP2005535748A (en) * 2002-08-12 2005-11-24 エクソンモービル・ケミカル・パテンツ・インク Plastic polyolefin composition

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2001307688A (en) * 2000-04-19 2001-11-02 Dainippon Printing Co Ltd Packing material for lithium ion battery
JP2005535748A (en) * 2002-08-12 2005-11-24 エクソンモービル・ケミカル・パテンツ・インク Plastic polyolefin composition

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