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JPS6140553B2 - - Google Patents
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JPS6140553B2 - - Google Patents

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Publication number
JPS6140553B2
JPS6140553B2 JP13417678A JP13417678A JPS6140553B2 JP S6140553 B2 JPS6140553 B2 JP S6140553B2 JP 13417678 A JP13417678 A JP 13417678A JP 13417678 A JP13417678 A JP 13417678A JP S6140553 B2 JPS6140553 B2 JP S6140553B2
Authority
JP
Japan
Prior art keywords
heat
butene
weight
sealing
copolymer
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
Application number
JP13417678A
Other languages
Japanese (ja)
Other versions
JPS5559964A (en
Inventor
Noryuki Sekine
Toshio Kawakita
Kazuhisa Kuroda
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.)
Sumitomo Chemical Co Ltd
Original Assignee
Sumitomo Chemical Co Ltd
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 Sumitomo Chemical Co Ltd filed Critical Sumitomo Chemical Co Ltd
Priority to JP13417678A priority Critical patent/JPS5559964A/en
Publication of JPS5559964A publication Critical patent/JPS5559964A/en
Publication of JPS6140553B2 publication Critical patent/JPS6140553B2/ja
Granted legal-status Critical Current

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Description

【発明の詳細な説明】[Detailed description of the invention]

本発明はヒートシール性の改良されたポリプロ
ピレン多層フイルムに関する。 商品価値の維持向上および流通過程の合理化の
ため多くの産業分野において包装用プラスチツク
フイルムが使用されている。この包装用プラスチ
ツクフイルムに求められている最も重要な性質の
一つにヒートシール適性が挙げられることは周知
の事実である。優れたヒートシール適性とは低い
温度でヒートシールが可能で、かつヒートシール
部の強度が大であることが必要である。ヒートシ
ール温度が低いと、それだけ高速包装が可能とな
り、経済的に大きなメリツトを生じる。 ポリプロピレンフイルム、特に二軸延伸ポリプ
ロピレンフイルムは透明性、剛性に優れるため食
品包装分野を主体に種々の産業分野に使用されて
いるが、表面が不活性なためヒートシール適性に
欠ける欠点を有している。この欠点を改良するた
めにフイルム表面を物理的、又は化学的手段によ
り処理する種々の方法が採られたいる。その一つ
に基体のポリプロピレンよりヒートシール温度の
低い樹脂を被覆していわゆるヒートシール層を形
成した多層フイルムが工業的に広く使用されてい
る。 ヒートシール温度の低い樹脂としては、エチレ
ン含有量が1〜6重量%のエチレンプロピレン共
重合体が一般的に使用されているが、ヒートシー
ル温度の低下は不充分である。また、最近ではプ
ロピレン−ブテン共重合体の使用が一部で行なわ
れているが、この樹脂でもヒートシール温度の低
下は不充分である。 本発明者らはポリプロピレンフイルムのヒート
シール温度を低下させることについて鋭意検討し
た結果、ポリプロピレンより成る基体層の表面
に、ブテン−1含有量が10〜25重量%であるプロ
ピレン−ブテン−1共重合体85〜97重量部とブテ
ン−1含有量が80〜93重量%であるブテン−1共
重合体15〜3重量部との混合物層を被覆すること
により、ヒートシール温度が著るしく低下し、ヒ
ートシール強度も大であり、かつその他のフイル
ムに要求される諸特性を何ら低下させないことを
見出し、本発明に至つた。 従来より同種の樹脂の混合物のヒートシール温
度には樹脂組成分のヒートシール温度の加成性が
成立することが経験的に知られているが、本発明
の混合物層は予想外のヒートシール温度の低下を
示した。 本発明で使われるプロピレン−ブテン−1共重
合体とは、通常工業的に広く一般に使用されてい
る方法で重合されるもので、ブテン−1含有量が
10〜25重量%のランダム共重合体である。ブテン
−1含有量が10重量%以下であるとヒートシール
温度の低下が少く本発明の趣旨に反する。 ブテン−1含有量が25重量%以上であるとフイ
ルム同志の滑りが悪化して実用に供し得なくな
る。 本発明で使われるブテン−1共重合体とは、ブ
テン−1と炭素数が2から10のブテン−1以外の
α−オレフインとの共重合体で、ブテン−1含有
量が80〜93重量%であり、通常工業的に広く一般
に使用されている方法で重合されるものである。
ブテン−1含有量が80重量%以下であるとフイル
ム同志の滑りが悪化して実用に供し得なくなる。
93重量%以上であるとヒートシール温度の低下効
果は認められなくなり、かつ、フイルム同志の滑
りが悪化する。ブテン−1共重合体単独にてフイ
ルムとしての評価を行うとブテン−1含有量の低
下にともなつて、フイルム同志の滑りが悪化する
ことが認められており、本発明の混合物において
はブテン−1含有量が80〜93重量%の範囲に限り
フイルム同志の滑りが向上することは興味ある事
実である。 本発明におけるヒートシール層の組成は、プロ
ピレン−ブテン−1共重合体85〜97重量部とブテ
ン−1共重合体15〜3重量部との割合である必要
がある。ブテン−1共重合体の割合が15重量部以
上であるとフイルム同志の滑りが悪化して実用に
供し得なくなる。ブテン−1共重合体の割合が3
重量部以下であるとプロピレン−ブテン−1共重
合体のヒートシール温度低下の効果は認められな
くなる。 本発明による混合物層には通常フイルム用途に
使用される劣化防止剤、滑剤、アンチブロツキン
グ剤、耐候剤などを加えることは何ら差しつかえ
ない。 以下に実施例を挙げて本発明を説明するが、こ
れらは何ら本発明を制限するものではない。 ヒートシール温度、強度測定法……東洋精機
(株)製熱傾斜式ヒートシール試験機を使用
し、数点の温度にてヒートシール面同志のヒ
ートシールを行う。ヒートシールした2枚の
フイルム試験片につき、180゜の剥離強度試
験を行い、各温度における剥離強度を求め
る。グラフ上より剥離強度が300g/25mm巾
となる温度を求めてヒートシール温度とし
た。 剥離強度はある温度で一定値に達するので
その時の剥離強度をヒートシール強度とし
た。 ブテン−1含有量測定法……N,J,
WEGEMERGの方法、(ジヤーナル オブ
アプライドポリマー サイエンス
(JOUNAL OF APPLIED POLYMER
SCIENCE)vol 14 p573)により、島津分
光光度計IR−27Gを使用して測定した。 滑り性測定法……東洋精機(株)製摩擦角測定
器を使用し、フイルムでおおわれたプレート
上にフイルムで包んで重さ1Kgのステンレス
製ブロツクを置き、2.7゜/秒の速度で傾斜
させて滑り始めた角度θをtanθで表示し
た。 溶融流れ指数測定法……JIS K−6758に従い、
宝工業(株)製メルトインデクサーMX−101型
にて測定した。 実施例 1〜3 ブテン−1含有量21.0重量%、溶融流れ指数
11.0のプロピレン−ブテン−1共重合体97,93,
88重量部に対し、市販のブテン−1共重合体(ウ
イトロン8240、ブテン−1含有量90%、米国ウイ
トコ社製)を各々3,7,12重量部スーパーミキ
サーにて混合し、田辺プラスチツク社製40mmφ押
出機にて溶融混練してペレツトを得た。 次に基体層として住友ノーブレンFA8011(住
友化学製)を使用し、表面のヒートシール層とし
て上記のペレツトを使用してダイ内接着形二層同
時押出しダイにより二層のフイルムを得た。この
フイルムの基体層の厚みは45μ、ヒートシール層
の厚みは14μであつた。 このフイルムのヒートシール面同志のヒートシ
ール温度およびヒートシール強度を測定して表1
に示す結果を得た。また、ヒートシール面同志の
滑り性を測定した結果を、同じく表1に示した。 比較例 1〜3 実施例1〜3と同じプロピレン−ブテン−1共
重合体100,80,0重量部に対しウイトロン8240
を各々0,20,100重量部をスーパーミキサーに
て混合し、田辺プラスチツク社製40mmφ押出機に
て溶融混練してペレツトを得た。 以下実施例1〜3と同様にして二層フイルムを
得、ヒートシール面同志のヒートシール温度、ヒ
ートシール強度および滑り性を測定した結果を表
1に示す。 比較例 4,5 実施例1〜3と同じプロピレン−ブテン−1共
重合体95,90重量部に対しウイトロン1200s(ブ
テン−1含有量95重量%、米国ウイトコ社製)を
各々5,10重量部スーパーミキサーにて混合し、
田辺プラスチツク社製40mmφ押出機にて溶融混練
してペレツトを得た。 以下実施例1〜3と同様にして二層フイルムを
得、ヒートシール面同志のヒートシール温度、ヒ
ートシール強度および滑り性を測定した結果を表
1に示す。 比較例 6 実施例1〜3と同じプロピレン−ブテン−1共
重合体95重量部に対しウイトロン0300(ポリブテ
ン−1、米国ウイトコ社製)を5重量部スーパー
ミキサーにて混合し、田辺プラスチツク社製40mm
φ押出機にて溶融混練してペレツトを得た。 以下実施例1〜3と同様にして二層フイルムを
得、ヒートシール面同志のヒートシール温度、ヒ
ートシール強度および滑り性を測定した結果を表
1に示す。 比較例 7 実施例1〜3と同じプロピレン−ブテン−1共
重合体90重量部に対し、ブテン−1共重合体(ブ
テン−1−プロピレン共重合体、ブテン−1含有
量76重量%、溶融流れ指数8.4)を10重量部スー
パーミキサーにて混合し、田辺プラスチツク社製
40mmφ押出機にて溶融混練してペレツトを得た。 以下実施例1〜3と同様にして二層フイルムを
得、ヒートシール面同志のヒートシール温度、ヒ
ートシール強度および滑り性を測定した結果を表
1に示す。
The present invention relates to a polypropylene multilayer film with improved heat sealability. Plastic packaging films are used in many industrial fields to maintain and improve product value and streamline distribution processes. It is a well-known fact that heat sealability is one of the most important properties required of plastic films for packaging. Excellent heat-sealability requires that heat-sealing is possible at low temperatures and that the heat-sealed portion has high strength. Lower heat-sealing temperatures allow for faster packaging, which provides significant economic benefits. Polypropylene film, especially biaxially oriented polypropylene film, has excellent transparency and rigidity and is used in various industrial fields, mainly in the food packaging field, but it has the disadvantage of lacking heat sealability due to its inert surface. There is. In order to improve this drawback, various methods have been adopted to treat the film surface by physical or chemical means. One of these is a multilayer film coated with a resin having a lower heat-sealing temperature than the polypropylene base material to form a so-called heat-sealing layer, which is widely used industrially. Ethylene propylene copolymers having an ethylene content of 1 to 6% by weight are generally used as resins with low heat-sealing temperatures, but the reduction in heat-sealing temperatures is insufficient. Recently, propylene-butene copolymers have been used in some cases, but even this resin is insufficient in lowering the heat-sealing temperature. The present inventors have conducted extensive studies on lowering the heat-sealing temperature of polypropylene films, and have found that a propylene-butene-1 copolymer with a butene-1 content of 10 to 25% by weight is added to the surface of a base layer made of polypropylene. By coating a mixture layer of 85 to 97 parts by weight of the copolymer and 15 to 3 parts by weight of a butene-1 copolymer having a butene-1 content of 80 to 93% by weight, the heat sealing temperature is significantly lowered. The present inventors have discovered that the heat sealing strength is high and that the other properties required of the film are not degraded in any way, leading to the present invention. Conventionally, it has been empirically known that the heat-sealing temperature of a mixture of similar resins is based on the additivity of the heat-sealing temperature of the resin composition, but the mixture layer of the present invention has an unexpected heat-sealing temperature. showed a decrease in The propylene-butene-1 copolymer used in the present invention is usually polymerized by a method widely used in industry, and the butene-1 content is
It is a 10-25% by weight random copolymer. If the butene-1 content is less than 10% by weight, the heat-sealing temperature decreases little, which is contrary to the purpose of the present invention. If the butene-1 content is 25% by weight or more, the slippage between the films will deteriorate, making it impossible to put them into practical use. The butene-1 copolymer used in the present invention is a copolymer of butene-1 and an α-olefin other than butene-1 having 2 to 10 carbon atoms, with a butene-1 content of 80 to 93% by weight. %, and is usually polymerized by a method widely used in industry.
If the butene-1 content is less than 80% by weight, the slippage between the films will deteriorate, making it impossible to put them into practical use.
If it is 93% by weight or more, the effect of lowering the heat sealing temperature will not be observed, and the slippage between the films will worsen. When a butene-1 copolymer alone is evaluated as a film, it is recognized that as the butene-1 content decreases, the slippage between the films deteriorates. It is an interesting fact that the slippage between films improves only when the content is in the range of 80 to 93% by weight. The composition of the heat seal layer in the present invention must be a ratio of 85 to 97 parts by weight of propylene-butene-1 copolymer and 15 to 3 parts by weight of butene-1 copolymer. If the proportion of the butene-1 copolymer is 15 parts by weight or more, the slippage between the films will deteriorate, making it impossible to put them into practical use. The proportion of butene-1 copolymer is 3
If the amount is less than 1 part by weight, the effect of lowering the heat sealing temperature of the propylene-butene-1 copolymer will not be recognized. There is no problem in adding to the mixture layer according to the present invention anti-deterioration agents, lubricants, anti-blocking agents, weathering agents, etc. which are commonly used in film applications. The present invention will be explained below with reference to Examples, but these are not intended to limit the present invention in any way. Heat-sealing temperature and strength measurement method: Using a heat-sealing tester manufactured by Toyo Seiki Co., Ltd., heat-seal the heat-sealed surfaces together at several temperatures. A 180° peel strength test is performed on two heat-sealed film test pieces to determine the peel strength at each temperature. The temperature at which the peel strength was 300 g/25 mm width was determined from the graph and was determined as the heat sealing temperature. Since the peel strength reached a certain value at a certain temperature, the peel strength at that time was taken as the heat seal strength. Butene-1 content measurement method...N, J,
The WEGEMERG Method, (Journal of
JOUNAL OF APPLIED POLYMER
SCIENCE) vol 14 p573) using a Shimadzu spectrophotometer IR-27G. Sliding property measurement method: Using a friction angle measuring device manufactured by Toyo Seiki Co., Ltd., a stainless steel block wrapped in film and weighing 1 kg was placed on a plate covered with film, and the block was tilted at a speed of 2.7°/sec. The angle θ at which the vehicle started sliding is expressed as tanθ. Melt flow index measurement method...According to JIS K-6758,
Measurement was performed using a melt indexer model MX-101 manufactured by Takara Kogyo Co., Ltd. Examples 1-3 Butene-1 content 21.0% by weight, melt flow index
11.0 propylene-butene-1 copolymer 97, 93,
To 88 parts by weight, 3, 7, and 12 parts by weight of a commercially available butene-1 copolymer (Witron 8240, butene-1 content 90%, manufactured by U.S. Witco Co., Ltd.) were mixed in a super mixer. The mixture was melted and kneaded using a 40 mmφ extruder manufactured by Co., Ltd. to obtain pellets. Next, a two-layer film was obtained using an in-die adhesive type two-layer coextrusion die using Sumitomo Noblen FA8011 (manufactured by Sumitomo Chemical) as the base layer and the above pellet as the heat-sealing layer on the surface. The thickness of the base layer of this film was 45μ, and the thickness of the heat seal layer was 14μ. The heat-sealing temperature and heat-sealing strength of the heat-sealing surfaces of this film were measured and are shown in Table 1.
The results shown are obtained. Further, the results of measuring the slipperiness between the heat-sealed surfaces are also shown in Table 1. Comparative Examples 1 to 3 Witron 8240 to 100, 80, 0 parts by weight of the same propylene-butene-1 copolymer as Examples 1 to 3
0, 20, and 100 parts by weight of each were mixed in a super mixer and melt-kneaded in a 40 mmφ extruder manufactured by Tanabe Plastics Co., Ltd. to obtain pellets. Two-layer films were obtained in the same manner as in Examples 1 to 3, and the heat-sealing temperature, heat-sealing strength, and slipperiness of the heat-sealing surfaces were measured. Table 1 shows the results. Comparative Examples 4 and 5 5 and 10 parts by weight of Witron 1200s (butene-1 content 95% by weight, manufactured by Witco, USA) were added to 95 and 90 parts by weight of the same propylene-butene-1 copolymer as in Examples 1 to 3, respectively. Mix in a super mixer,
The mixture was melt-kneaded using a 40 mmφ extruder manufactured by Tanabe Plastics Co., Ltd. to obtain pellets. Two-layer films were obtained in the same manner as in Examples 1 to 3, and the heat-sealing temperature, heat-sealing strength, and slipperiness of the heat-sealing surfaces were measured. Table 1 shows the results. Comparative Example 6 95 parts by weight of the same propylene-butene-1 copolymer as in Examples 1 to 3 was mixed with 5 parts by weight of Witron 0300 (polybutene-1, manufactured by U.S. Witco Co., Ltd.) in a super mixer, and 95 parts by weight of the same propylene-butene-1 copolymer as in Examples 1 to 3 was mixed in a super mixer. 40mm
The mixture was melt-kneaded using a φ extruder to obtain pellets. Two-layer films were obtained in the same manner as in Examples 1 to 3, and the heat-sealing temperature, heat-sealing strength, and slipperiness of the heat-sealing surfaces were measured. Table 1 shows the results. Comparative Example 7 Butene-1 copolymer (butene-1-propylene copolymer, butene-1 content 76% by weight, molten Flow index 8.4) was mixed with 10 parts by weight in a super mixer, manufactured by Tanabe Plastics Co., Ltd.
The mixture was melt-kneaded using a 40 mmφ extruder to obtain pellets. Two-layer films were obtained in the same manner as in Examples 1 to 3, and the heat-sealing temperature, heat-sealing strength, and slipperiness of the heat-sealing surfaces were measured. Table 1 shows the results.

【表】 実施例 4,5 ブテン含有量が12.3重量%、溶融流れ指数6.5
のプロピレン−ブテン−1共重合体95,90重量部
に対し、ブテン−1共重合体(ブテン−1−プロ
ピレン共重合体、ブテン−1含有量84.1重量%、
溶融流れ指数7.8)を各々5,10重量部スーパー
ミキサーにて混合し、田辺プラスチツク社製40mm
φ押出機にて溶融混練してペレツトを得た。 次に基体層として住友ノーブレンFS2011(住
友化学製)を使用し、表面のヒートシール層とし
て上記のペレツトを使用して、ダイ内接着形二層
同時押出しダイにより二層のフイルムを得た。こ
のフイルムの基体層の厚みは230μ、ヒートシー
ル層の厚みは20μであつた。 このフイルムを岩本製作所製研究用高分子フイ
ルム二軸延伸装置を使用して130℃において縦横
各々3倍に延伸を行ない、120℃においてヒート
セツトした。 以上のようにして得た多層二軸延伸フイルムに
つきヒートシール面同志のヒートシール温度、ヒ
ートシール強度および滑り性を測定した結果を表
2に示した。 比較例 8,9 実施例4,5と同じプロピレン−ブテン−1共
重合体100,80重量部に対し、実施例4,5と同
じブテン−1共重合体を各々0.20重量部スーパー
ミキサーにて混合し、田辺プラスチツク社製40mm
φ押出機にて溶融混練してペレツトを得た。 以下実施例4,5と同様にして多層二軸延伸フ
イルムを得、ヒートシール面同志のヒートシール
温度、ヒートシール強度および滑り性を測定した
結果を表2に示した。
[Table] Examples 4 and 5 Butene content 12.3% by weight, melt flow index 6.5
Butene-1 copolymer (butene-1-propylene copolymer, butene-1 content 84.1% by weight,
5 and 10 parts by weight of melt flow index 7.8) were mixed in a super mixer, and a 40mm
The mixture was melt-kneaded using a φ extruder to obtain pellets. Next, using Sumitomo Noblen FS2011 (manufactured by Sumitomo Chemical) as the base layer and the above pellet as the heat-sealing layer on the surface, a two-layer film was obtained using an in-die adhesive type two-layer coextrusion die. The thickness of the base layer of this film was 230μ, and the thickness of the heat seal layer was 20μ. This film was stretched 3 times in length and width at 130°C using a research polymer film biaxial stretching apparatus manufactured by Iwamoto Seisakusho, and then heat set at 120°C. Table 2 shows the results of measuring the heat-sealing temperature, heat-sealing strength, and slipperiness of the heat-sealed surfaces of the multilayer biaxially stretched film obtained as described above. Comparative Examples 8 and 9 To 100 and 80 parts by weight of the same propylene-butene-1 copolymer as in Examples 4 and 5, 0.20 parts by weight of each of the same butene-1 copolymers as in Examples 4 and 5 were added in a super mixer. Mixed and made by Tanabe Plastic Co., Ltd. 40mm
The mixture was melt-kneaded using a φ extruder to obtain pellets. A multilayer biaxially stretched film was obtained in the same manner as in Examples 4 and 5, and the heat-sealing temperature, heat-sealing strength, and slipperiness of the heat-sealing surfaces were measured. Table 2 shows the results.

【表】 実施例 6,7 ブテン−1含有量が23.9重量%、溶融流れ指数
15.2のプロピレン−ブテン−1共重合体95,90重
量部に対し、ウイトロン8240を各々5,10重量部
スーパーミキサーにて混合し、田辺プラスチツク
社製40mmφ押出機にて溶融混練してペレツトを得
た。 以下実施例1〜3と同様にして二層フイルムを
得、このフイルムのヒートシール面同志のヒート
シール温度、ヒートシール強度および滑り性を測
定した結果を表3に示した。 比較例 10,11 実施例6,7と同じプロピレン−ブテン−1共
重合体100,80重量部に対し、ウイトロン8240を
各々0重量部、20重量部スーパーミキサーにて混
合し、田辺プラスチツク社製40mmφ押出機にて溶
融混練してペレツトを得た。 以下実施例1〜3と同様にして二層フイルムを
得、このフイルムのヒートシール面同志のヒート
シール温度、ヒートシール強度、および滑り性を
測定した結果を表3に示した。 比較例 12 ブテン−1含有量が8.5重量%、溶融流れ指数
8.8のプロピレン−ブテン−1共重合体95重量部
に対し、ウイトロン8240を5重量部スーパーミキ
サーにて混合し、田辺プラスチツク社製40mmφ押
出機にて溶融混練してペレツトを得た。 以下実施例1〜3と同様にして二層フイルムを
得、このフイルムのヒートシール面同志のヒート
シール温度、ヒートシール強度および滑り性を測
定した結果を表3に示した。 比較例 13 ブテン−1含有量が27.2重量%、溶融流れ指数
13のプロピレン−ブテン−1共重合体95重量部に
対し、ウイトロン8240を5重量部スーパーミキサ
ーにて混合し、田辺プラスチツク社製40mmφ押出
機にて溶融混練してペレツトを得た。 以下実施例1〜3と同様にして2層フイルムを
得、このフイルムのヒートシール面同志のヒート
シール温度、ヒートシール強度および滑り性を測
定した結果を表3に示した。
[Table] Examples 6, 7 Butene-1 content is 23.9% by weight, melt flow index
5 and 10 parts by weight of Witron 8240 were mixed with 95 and 90 parts by weight of the propylene-butene-1 copolymer of 15.2 in a super mixer, and melt-kneaded in a 40 mmφ extruder manufactured by Tanabe Plastics to obtain pellets. Ta. A two-layer film was obtained in the same manner as in Examples 1 to 3, and the heat-sealing temperature, heat-sealing strength, and slipperiness of the heat-sealing surfaces of this film were measured, and the results are shown in Table 3. Comparative Examples 10 and 11 100 and 80 parts by weight of the same propylene-butene-1 copolymer as in Examples 6 and 7 were mixed with 0 parts by weight and 20 parts by weight of Witron 8240, respectively, in a super mixer, and the mixture was mixed with a supermixer manufactured by Tanabe Plastics Co., Ltd. The mixture was melt-kneaded using a 40 mmφ extruder to obtain pellets. A two-layer film was obtained in the same manner as in Examples 1 to 3, and the heat-sealing temperature, heat-sealing strength, and slipperiness of the heat-sealing surfaces of this film were measured, and the results are shown in Table 3. Comparative Example 12 Butene-1 content is 8.5% by weight, melt flow index
5 parts by weight of Witron 8240 was mixed with 95 parts by weight of a propylene-butene-1 copolymer of 8.8 in a super mixer, and the mixture was melt-kneaded in a 40 mmφ extruder manufactured by Tanabe Plastics Co., Ltd. to obtain pellets. A two-layer film was obtained in the same manner as in Examples 1 to 3, and the heat-sealing temperature, heat-sealing strength, and slipperiness of the heat-sealing surfaces of this film were measured, and the results are shown in Table 3. Comparative Example 13 Butene-1 content is 27.2% by weight, melt flow index
5 parts by weight of Witron 8240 were mixed with 95 parts by weight of the propylene-butene-1 copolymer No. 13 in a super mixer, and the mixture was melt-kneaded in a 40 mmφ extruder manufactured by Tanabe Plastics Co., Ltd. to obtain pellets. A two-layer film was obtained in the same manner as in Examples 1 to 3, and the heat-sealing temperature, heat-sealing strength, and slipperiness of the heat-sealing surfaces of this film were measured, and the results are shown in Table 3.

【表】【table】

Claims (1)

【特許請求の範囲】[Claims] 1 ポリプロピレンより成る基体層の少くとも一
表面に、ブテン−1含有量が10〜25重量%である
プロピレン−ブテン−1共重合体85〜97重量部と
ブテン−1含有量が80〜93重量%であるブテン−
1共重合体15〜3重量部との混合物層を形成して
なるポリプロピレン多層フイルム。
1. 85 to 97 parts by weight of a propylene-butene-1 copolymer having a butene-1 content of 10 to 25% by weight and 80 to 93 parts by weight of a butene-1 content on at least one surface of a base layer made of polypropylene. Butene-
A polypropylene multilayer film formed by forming a mixture layer with 15 to 3 parts by weight of a copolymer.
JP13417678A 1978-10-30 1978-10-30 Polypropylene multilayer film Granted JPS5559964A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP13417678A JPS5559964A (en) 1978-10-30 1978-10-30 Polypropylene multilayer film

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP13417678A JPS5559964A (en) 1978-10-30 1978-10-30 Polypropylene multilayer film

Publications (2)

Publication Number Publication Date
JPS5559964A JPS5559964A (en) 1980-05-06
JPS6140553B2 true JPS6140553B2 (en) 1986-09-10

Family

ID=15122212

Family Applications (1)

Application Number Title Priority Date Filing Date
JP13417678A Granted JPS5559964A (en) 1978-10-30 1978-10-30 Polypropylene multilayer film

Country Status (1)

Country Link
JP (1) JPS5559964A (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61106648A (en) * 1984-10-31 1986-05-24 Mitsui Petrochem Ind Ltd Crystalline propylene random copolymer composition
DE69503560T2 (en) * 1994-04-28 1999-03-18 Sumitomo Chemical Co., Ltd., Osaka Polypropylene composition for laminated and oriented films and laminated and oriented film made from them
CN1269894C (en) 2002-03-29 2006-08-16 住友化学工业株式会社 Propylene-based resin composition and film produced therefrom
DE102004039453B4 (en) 2003-08-20 2021-08-19 Sumitomo Chemical Co. Ltd. Polymer composition and film therefrom

Also Published As

Publication number Publication date
JPS5559964A (en) 1980-05-06

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