JPS58124646A - Composite resin layer - Google Patents

Composite resin layer

Info

Publication number
JPS58124646A
JPS58124646A JP587482A JP587482A JPS58124646A JP S58124646 A JPS58124646 A JP S58124646A JP 587482 A JP587482 A JP 587482A JP 587482 A JP587482 A JP 587482A JP S58124646 A JPS58124646 A JP S58124646A
Authority
JP
Japan
Prior art keywords
resin
resin layer
film
vinyl acetate
resins
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
JP587482A
Other languages
Japanese (ja)
Other versions
JPS646952B2 (en
Inventor
清豪 赤沢
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 Bakelite Co Ltd
Original Assignee
Sumitomo Bakelite 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 Bakelite Co Ltd filed Critical Sumitomo Bakelite Co Ltd
Priority to JP587482A priority Critical patent/JPS58124646A/en
Publication of JPS58124646A publication Critical patent/JPS58124646A/en
Publication of JPS646952B2 publication Critical patent/JPS646952B2/ja
Granted legal-status Critical Current

Links

Abstract

(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。
(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

【発明の詳細な説明】 本発明は塩化ビニIJデン系樹脂及び諌樹脂と強固に接
着する樹脂よシなる複合樹脂層に関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a composite resin layer made of a resin that firmly adheres to a vinyl chloride IJ resin and a resin.

ポリ塩化ビニリデン系樹脂フィルム(PVDC系フィル
ム)は、その特性として、湿気、ガス、に対するバリヤ
性が高いため、食品保腰包装用フィルムとして広く用い
られているが、高価格、低温可撓性、ヒートシール性、
゛また耐油性に欠点かあった。その欠点を補うために数
種の樹脂を積層することが行なわれている。
Polyvinylidene chloride resin film (PVDC film) has a high barrier property against moisture and gas, so it is widely used as a food packaging film, but it is expensive, has low temperature flexibility, heat sealability,
゛Also, there was a drawback in oil resistance. In order to compensate for this drawback, several types of resins are laminated.

二種あるいは数種の樹脂を積層する方法としては、1)
既に成形された二種のフィルムを電ねて接着する方法、
2)!液状またはエマルジョンで付着させ成形品上に皮
膜を形成する方法、3)溶融状態で各層を接着する方法
がある。第3の方法は数種の合成樹脂を溶融状で直接積
層して押出すため、積層体を得る方法として、費用、時
間の面で理想的な方法である。しかしPVDC糸樹脂は
他の樹脂との接着性に乏しく、かかる溶融状態での積層
の自由度は少ない。
Methods of laminating two or several types of resin include 1)
A method of bonding two types of films that have already been formed,
2)! There are two methods: 3) a method in which each layer is adhered in a molten state to form a film on a molded product by applying it in a liquid or emulsion form; The third method is an ideal method for obtaining a laminate in terms of cost and time, since several types of synthetic resins are directly laminated in a molten state and extruded. However, PVDC thread resin has poor adhesion with other resins, and there is little lamination flexibility in such a molten state.

従来、PVDC系樹脂と接着可能な樹脂とし7ては、エ
チレン酢酸ビニル共重合樹脂、エチレンアクリル酸エス
テル共重合樹脂、スチレン−ブタジェン共重合樹脂が知
られているが、これらはいずれも油脂分により容易に侵
され、特に使用温度が高い場合や、物品を包装したまま
加熱殺鉋するような場合、PVDC系樹脂との剥離が生
じ易かった。またこれらの樹脂は、耐溶剤性に乏しく、
強度も弱いために、これらの樹脂と組みあわせたフィル
ムはその用途が限られていた。
Conventionally, ethylene vinyl acetate copolymer resins, ethylene acrylic ester copolymer resins, and styrene-butadiene copolymer resins are known as resins that can be bonded to PVDC resins, but all of these resins have adhesive properties due to their oil and fat content. It is easily eroded, and peeling from the PVDC resin is likely to occur particularly when the operating temperature is high or when the article is heat-killed while packaged. In addition, these resins have poor solvent resistance,
Due to their low strength, films combined with these resins had limited uses.

本発明者らは、鋭意研究の結果、ポリウレタン、塩化ビ
ニル−エチレン酢酸ビニルグラフト化物、ポリブタジェ
ンの群から選ばれたものを、エチレン酢酸ビニル共重合
体あるいはエチレンアクリル酸エステル共重合体に混合
した樹脂のフィルムは単−m脂フィルムに比べ耐油性耐
溶剤性、強度が向上し、さらに該樹脂がPVDC系樹脂
と優れた接着性を有することをも見い出した。
As a result of extensive research, the present inventors have discovered a resin in which a material selected from the group of polyurethane, vinyl chloride-ethylene vinyl acetate grafted product, and polybutadiene is mixed with ethylene vinyl acetate copolymer or ethylene acrylate copolymer. The inventors have also discovered that the film has improved oil resistance, solvent resistance, and strength compared to single-m resin films, and that the resin also has excellent adhesion to PVDC resins.

本発明でいうPVDC系樹脂とは、塩化ビニリデンを主
体として、これと塩化ビニル、アルキルアクリレート、
アクリル酸、アクリロニトリルその他の共重合成分とを
共重合した、二元又は多元の共重合物でおる。
The PVDC resin referred to in the present invention mainly consists of vinylidene chloride, vinyl chloride, alkyl acrylate,
It is a binary or multi-component copolymer made by copolymerizing acrylic acid, acrylonitrile, and other copolymer components.

本発明で用いるポリウレタンは、熱可塑性を有し、熱可
塑性樹脂の加工機械により加工できるように調製された
ポリウレタンを指し、塩化ビニル−エチレン酢酸ビニル
グラフト化物ハ、エチレン酢酸ビニルに塩化ビニルをグ
ラフト重合したもので、エチレン酢酸ビニルを30〜5
0電量チ含んでいる。
The polyurethane used in the present invention refers to a polyurethane that has thermoplasticity and is prepared so that it can be processed by a thermoplastic resin processing machine. 30-5% of ethylene vinyl acetate
Contains 0 electric charge.

なお、本発明の複合樹脂層Fi、、共押出法により得ら
れるが、混合樹脂の各種ブレンド比は要求される性能に
よって適宜選択される。
The composite resin layer Fi of the present invention is obtained by a coextrusion method, and various blend ratios of the mixed resins are appropriately selected depending on the required performance.

以下、本発明の実施例を脱明するが、これによって本発
明が限定されるものではない。
Examples of the present invention will be explained below, but the present invention is not limited thereto.

なお、実施例、参考例中の部、饅はそれぞtt重量部、
*m%を下す。
In addition, parts in examples and reference examples, and rice cakes are tt parts by weight, respectively.
*Decrease m%.

実施例1゜ byビニル含蓋19%のエチレン酢酸ビニルと熱可塑性
ポリウレタンを第1iにyr<すブレンド比で押出機を
使用して、180℃で浴融混合押出(7て各混合樹脂ペ
レットを得た。
Example 1 By using an extruder at a blend ratio of 19% vinyl-containing ethylene-vinyl acetate and thermoplastic polyurethane, each mixed resin pellet was extruded at 180°C using an extruder. Obtained.

この混合ペレットとPVDC糸樹脂とを、−ビitでれ
別々の押出機で溶融し、3NIのTダイ全南する共押出
成膜装置に供給し7、中心層がPVI)C糸衡脂層30
μ、両外層が混合樹脂層で各1υ/’ tt Br 5
(Jμの3層フィルムを成形した。このフィルム〃・ら
巾15■長さ1easの試料を切取pその片面の片端を
強制剥離して、剥離強度を測定した。その結果を第11
1に示す。
The mixed pellets and PVDC thread resin were melted in a separate extruder and fed to a coextrusion film forming apparatus with a 3NI T-die (7) in which the center layer was PVI (C thread balance layer). 30
μ, both outer layers are mixed resin layers, each 1υ/'tt Br 5
(A three-layer film of Jμ was molded. A sample of this film with a width of 15 cm and a length of 1 eas was cut out and one end of one side of the film was forcibly peeled off to measure the peel strength.
Shown in 1.

参考例t lI論何例1用いたエチレン酢酸ビニルとPVIに系樹
脂とを実施例1と同様の成膜法によシフイルムを成形し
、同様の測定法で剥離強度を測定し九。その結果を第1
9に示す。
REFERENCE EXAMPLE T II Theory A Sifilm was formed using the ethylene vinyl acetate and PVI resin used in Example 1 using the same film forming method as in Example 1, and the peel strength was measured using the same measuring method. The result is the first
9.

第  1 表 実施例2参考例2 実施例1、参考例1において用いえフィルムを動物油(
豚肉脂1jLc)中へ、30分間積層物を浸透して、外
観の変化を見た。その結果熱可塑性ポリウレタンを含ま
ない接着性樹脂を用いたフィルムは、接着樹脂層が著し
く膨潤し、フィルムにしわが出来、わずかの力で容易に
剥離し九〇 実施例& 実施例1において使用した熱可塑性ポリウレタンの代シ
に、エチレン酢酸ビニルに塩化ビニルをグラフト化させ
た組成物を用い、実施例1と同様に溶融混練して、各種
樹脂組成物を製造した。これらの組成物を用い、積層フ
ィルムを成形し、剥離強度を測定した。その結果を第2
表に示す。
Table 1 Example 2 Reference Example 2 The film used in Example 1 and Reference Example 1 was treated with animal oil (
The laminate was soaked into pork fat (1jLc) for 30 minutes and changes in appearance were observed. As a result, in a film using an adhesive resin that does not contain thermoplastic polyurethane, the adhesive resin layer swells significantly, wrinkles appear in the film, and the film is easily peeled off with a small amount of force. In place of the plastic polyurethane, a composition in which vinyl chloride was grafted onto ethylene vinyl acetate was used and melt-kneaded in the same manner as in Example 1 to produce various resin compositions. Laminated films were formed using these compositions and their peel strengths were measured. The result is the second
Shown in the table.

実施例4゜ 実施例1.3と同様にして、エチレン酢酸ビニルとポリ
ブタジェンとを溶融混合して作り九組成物を用いて、同
様のフィルムを作シ、剥離強度を測定した。その結果を
第3表に示す。
Example 4 In the same manner as in Example 1.3, a similar film was prepared using a composition prepared by melt-mixing ethylene vinyl acetate and polybutadiene, and its peel strength was measured. The results are shown in Table 3.

実施例5゜ 実施例4、参考例1の積層フィルムを用いて、耐酷使性
のテストを行りた。耐酷使性テストは、内容物を包装し
、熱処理後に、規定の温度に一定期間保管し、その温度
と同一の条件下で包装体を落下距III! 1.5 m
の落体試験をする。落下しても包装体が破損やピンホー
ルがない場合には3回まで繰シ返し、異常がないものを
合格とする。
Example 5 Using the laminated films of Example 4 and Reference Example 1, an abuse resistance test was conducted. In the abuse resistance test, the contents are packaged, heat-treated, stored at a specified temperature for a certain period of time, and the package is dropped over a distance of 30 seconds under the same temperature conditions. 1.5 m
Do a drop test. If there is no breakage or pinhole in the package even if it is dropped, repeat the test up to three times, and if there are no abnormalities, it will be passed.

この試験の結果、実施例4のフィルムの不合格率はO〜
296でtlは実用に問題がない。′また参考例1のフ
ィルムの不合格率Filo%以上となり、実用に耐えな
かった。
As a result of this test, the failure rate of the film of Example 4 was O~
296 and tl have no problems in practical use. 'Furthermore, the rejection rate of the film of Reference Example 1 was higher than Filo%, and it could not be put to practical use.

以上、実施例、比較例のように、本発明の複合樹脂層は
PVDC系樹脂と優れた接着性を示しながら、従来PV
DC系樹脂の欠点を補なった複合樹脂層である。
As shown in the Examples and Comparative Examples above, the composite resin layer of the present invention exhibits excellent adhesion to PVDC resin, while
This is a composite resin layer that compensates for the drawbacks of DC resin.

Claims (1)

【特許請求の範囲】[Claims] 塩化ビニリデン系樹脂層及び該樹脂層と強固に接着する
樹脂の複合樹脂層よりなシ、該接着する樹脂が、エチレ
ン酢酸ビニル共重合体あるいはエチレンアクリル酸エス
テル共重合体とポリウレタン、ポリブタジェン、塩化ビ
ニルのエチレン酢酸ビニルとのグラフト化物群から選ば
れたものとの混合樹脂よりなることを特徴とする複合樹
脂層。
It is not a composite resin layer of a vinylidene chloride resin layer and a resin that firmly adheres to the resin layer, and the adhesive resin is an ethylene vinyl acetate copolymer or an ethylene acrylic acid ester copolymer, polyurethane, polybutadiene, or vinyl chloride. A composite resin layer comprising a mixed resin selected from the group of grafted products of ethylene vinyl acetate and ethylene vinyl acetate.
JP587482A 1982-01-20 1982-01-20 Composite resin layer Granted JPS58124646A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP587482A JPS58124646A (en) 1982-01-20 1982-01-20 Composite resin layer

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP587482A JPS58124646A (en) 1982-01-20 1982-01-20 Composite resin layer

Publications (2)

Publication Number Publication Date
JPS58124646A true JPS58124646A (en) 1983-07-25
JPS646952B2 JPS646952B2 (en) 1989-02-07

Family

ID=11623061

Family Applications (1)

Application Number Title Priority Date Filing Date
JP587482A Granted JPS58124646A (en) 1982-01-20 1982-01-20 Composite resin layer

Country Status (1)

Country Link
JP (1) JPS58124646A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4567090A (en) * 1979-08-21 1986-01-28 Kureha Kagaku Kogyo Kabushiki Kaisha Heat-resistant laminate film

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4567090A (en) * 1979-08-21 1986-01-28 Kureha Kagaku Kogyo Kabushiki Kaisha Heat-resistant laminate film

Also Published As

Publication number Publication date
JPS646952B2 (en) 1989-02-07

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