JPS62275675A - Cylindrical packed material - Google Patents

Cylindrical packed material

Info

Publication number
JPS62275675A
JPS62275675A JP11843386A JP11843386A JPS62275675A JP S62275675 A JPS62275675 A JP S62275675A JP 11843386 A JP11843386 A JP 11843386A JP 11843386 A JP11843386 A JP 11843386A JP S62275675 A JPS62275675 A JP S62275675A
Authority
JP
Japan
Prior art keywords
film
vinylidene chloride
cylindrical
contents
cut
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
JP11843386A
Other languages
Japanese (ja)
Other versions
JPH0123112B2 (en
Inventor
Osamu Okada
修 岡田
Akira Katou
加藤 アキラ
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.)
Asahi Chemical Industry Co Ltd
Original Assignee
Asahi Chemical Industry 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 Asahi Chemical Industry Co Ltd filed Critical Asahi Chemical Industry Co Ltd
Priority to JP11843386A priority Critical patent/JPS62275675A/en
Publication of JPS62275675A publication Critical patent/JPS62275675A/en
Publication of JPH0123112B2 publication Critical patent/JPH0123112B2/ja
Granted legal-status Critical Current

Links

Abstract

PURPOSE:To make it possible to cut a film on the surface of packed material when it is folded, by forming a cylindrical packed material by the use of a vinylidene chloride-methyl acrylate copolymer resin containing a plastizer in a specific ratio and making the packing ratio of contents thereof in a specific ratio. CONSTITUTION:In a cylindrical packed material 1 made of a vinylidene chloride resin film wherein both end parts 2 and 2' of the cylindrical film are sealed, unfluid contents are packed into the interior of the packed material. The vinylidene chloride resin is a vinylidene chloride-methyl acrylate copolymer resin which has <=4wt% content of plasticizer such as diisobutyl adipate, etc., and 4-7wt% methyl acrylate component. The contents of the packed material 1 has >=90% packing ratio. When the cylindrical material is bent along in the longer direction and folded, the film on the surface of the packed material can be cut and the contents can be readily taken out by taking advantage of the cut. Moreover, the packed material can be provided without damaging characteristics such as gas barrier properties.

Description

【発明の詳細な説明】 3、発明の詳細な説明 〔産業上の利用分野〕 主として、畜肉・魚肉等の加工肉食品、チーズ・バター
等の加工乳製品、洋かん、ゼリー等の菓子類等を内容物
とする塩化ビニリデン系樹脂フィルムによる筒状包装体
の、その改良技術に関する。
[Detailed Description of the Invention] 3. Detailed Description of the Invention [Field of Industrial Application] Mainly processed meat foods such as livestock meat and fish, processed dairy products such as cheese and butter, confectionery such as Western cakes and jelly, etc. This invention relates to an improved technology for a cylindrical package made of a vinylidene chloride resin film containing .

〔従来技術〕[Prior art]

塩化ビニリデン系樹脂フィルムによる筒状包装体は広く
知られている。これ等は例えば△DP(商品名、旭化成
■社製〕又はKAP(商品名、呉羽化学■社製)として
市販の、自動充填包装機を用い、一般に例えば特公昭5
5−34044号公報に開示されているような操作、即
ち、平坦な長尺フィルムを連続的に、その両側部が重な
り合うように折り曲げ、その重なり部を熱溶着(シール
)して筒状フィルムとし、その内部に流動化した内容物
を充填した後、適宜な寸法間かくをもって密封シール(
ワイヤー結紮)し個々に切断して筒状包装体にするとい
う一連の連続自動、製袋、充填、結紮操作によって製造
できるものであることも広く知られている。
Cylindrical packaging bodies made of vinylidene chloride resin films are widely known. These are generally carried out using an automatic filling and packaging machine commercially available as, for example, △DP (trade name, manufactured by Asahi Kasei Corporation) or KAP (trade name, manufactured by Kureha Chemical Corporation).
5-34044, that is, a flat long film is continuously bent so that both sides thereof overlap, and the overlapping parts are thermally welded (sealed) to form a cylindrical film. After filling the inside with the fluidized contents, seal it with an appropriate distance (
It is also widely known that it can be manufactured by a series of continuous automatic bag-making, filling, and ligating operations, including wire ligation, individual cutting, and cylindrical packaging.

この包装体の一つの欠点は、輸送、搬送等の取扱いの諸
応力に耐え、内容物の耐腐敗・汚染性を維持できるよう
に、外皮となるフィルムを強靭なものにしである。その
ために内容物の取出し、ことに刃物等を用いずに内容物
を取出してその目的に供するようにすることが難しいこ
とである従って、保存性、衛生性に優れることが分って
いても、この包装体を例えば子供が楽しめて食せるよう
な玩具菓子の用途に応用できない等の制約が生じている
One drawback of this package is that the outer film is made to be strong so that it can withstand the stress of handling such as transportation and conveyance, and maintains the spoilage and contamination resistance of the contents. Therefore, it is difficult to take out the contents, especially without using a knife, etc., and use it for the purpose. Therefore, even if it is known that it has excellent preservation and hygiene, There are restrictions such as the inability to apply this package to, for example, toy confectionery that children can enjoy and eat.

一方上記外皮フィルム除去を容易にするための方法とし
て、特公昭51−8080号公報、及び実公昭49−1
9021号公報に開示された技術がおる。このものは要
するに外皮フィルムより丈夫な帯状物を面状態の胴の一
部或はシール線の一部に点付けしておき、この帯状物を
引くことによって筒状フィルムの一部を引き破り、その
部分を外皮フィルムの切り口としようとする易開口部を
設けることの提案である しかしながら、この易開口部を設ける技術では、引き破
りの切り口の形成を、100%に近い達成確率を達成水
準として保証することは極めて難しく従ってチーズ、ウ
ィンナ−ソーセージ包装の一部に採用される程度に止ま
り、汎用される迄には至っていない。
On the other hand, as a method for facilitating the removal of the outer skin film, Japanese Patent Publication No. 51-8080 and Utility Model Publication No. 49-1
There is a technique disclosed in Japanese Patent No. 9021. In short, a strip-shaped material that is stronger than the outer skin film is attached to a part of the flat body or a part of the seal line, and by pulling this strip-shaped material, a part of the cylindrical film is torn off. The proposal is to provide an easy-to-open part to use that part as a cut in the outer skin film. However, with this technology for providing an easy-to-open part, the probability of forming a tear-off cut is close to 100%. It is extremely difficult to guarantee this, and therefore it has only been used for some cheese and Wiener sausage packaging, and has not yet become widely used.

その主な理由は、高開口部設置には、高い精度の条件設
定とその管理ができる高度な溶着装置・技術を要するの
に対し、包装体そのものにはその技術価値に対応するコ
ストを上乗せできない情勢にあるからである。
The main reason for this is that installing high-opening areas requires advanced welding equipment and technology that can set and manage conditions with high precision, whereas the packaging itself cannot add the cost that corresponds to its technological value. This is because of the current situation.

(発明が解決しようとする問題点〕 上記従来の切口形成の思想とは全くちがう新規な切口の
形成、即ち包装体を長手方向に折曲げ湾曲させることで
、表面フィルムを切断して、その切れ目を利用して内容
物を取出し易くすること、そのような機能を持つ包装体
を、ガスバリヤ−性、耐衝撃性、シール部の耐破袋性等
、包装体の要求品質となる他の特性を損ねないで、提供
できるようにすることにある。
(Problems to be solved by the invention) A novel cut is formed which is completely different from the conventional idea of forming a cut, that is, the surface film is cut by bending and curving the package in the longitudinal direction. In order to make it easier to take out the contents by using The goal is to be able to provide it without compromising it.

(問題点を解決するための手段〕 従来公知の塩化ビニリデン系樹脂フィルムを用いた筒状
包装体に比べて相違するところは、1)フィルムを形成
している塩化ビニ1ノデン系樹脂には、可塑剤含量が4
重量%以下である。メチルアクリレート成分が4〜7重
量%の塩化ビニリデン−メチルアクリレート共重合樹脂
を用いる。
(Means for solving the problem) The differences from conventional cylindrical packaging bodies using vinylidene chloride resin films are as follows: 1) The vinylidene chloride-1-nodene resin forming the film has Plasticizer content is 4
% by weight or less. A vinylidene chloride-methyl acrylate copolymer resin containing 4 to 7% by weight of methyl acrylate component is used.

2)包装体の内容物は、非流動性物質を充填率90%以
上にする。
2) The contents of the package shall be filled with non-flowable substances at a filling rate of 90% or more.

上記1)2)の要件の組合せである。This is a combination of requirements 1) and 2) above.

以下本発明の内容を図面等を用いて詳述する。The contents of the present invention will be explained in detail below using drawings and the like.

第1図は模型図で、本発明の筒状包装体が長手方向に添
って折曲げ湾曲させた際、その湾曲外周部のフィルムが
引きちぎれて切断し始める、その切断過程の模型図であ
るこの第1図は、本発明の作用効果に当る開口部にする
ための切り口の形成の様子を説明するためのものである
FIG. 1 is a model diagram showing the cutting process in which when the cylindrical package of the present invention is bent and curved in the longitudinal direction, the film on the outer periphery of the curve begins to tear and cut. FIG. 1 is for explaining how a cut is formed to form an opening corresponding to the effect of the present invention.

その第1図に於て、当初は真直ぐな筒状包装体(点線表
示のもの)1でおったものをその長手中央部が角度θを
もって湾曲するように包装体の両端部2,2′ を近接
させる。とすると、その角度θが約60度以下に達する
と、誘過は内容物の切断に同伴してフィルム自体も切断
されてしまうことが多いが、第1図ではその切断直前の
状態の想定図、即ち、湾曲される内容物の外周に添って
フィルムが引き伸ばされ、該内容物の破断に伴ってフィ
ルムそのものに亀裂が生じた状態の場面を実線で表現し
たもので必る。
In Fig. 1, the initially straight cylindrical packaging body (shown by dotted lines) 1 has been curved at both ends 2 and 2' so that its longitudinal center is curved at an angle θ. bring them close together. If the angle θ reaches approximately 60 degrees or less, the film itself will often be cut as the contents are cut, but Figure 1 shows the assumed state immediately before cutting. In other words, the scene in which the film is stretched along the outer periphery of the content to be curved, and the film itself cracks as the content breaks is represented by a solid line.

本発明の包装体では、この破断、切り口を利用して、フ
ィルムを細い帯状に包装体の周りにそって切り裂いたり
、切り口の断面から内容物を押し出したりして、各々内
容物の取出しの容易化を図るためのものである。
In the package of the present invention, this breakage or cut is used to tear the film into a thin strip along the circumference of the package, or to push out the contents from the cross section of the cut, making it easier to take out the contents. The purpose is to promote

この際、内容物は、常温では流動しない状態の非流動物
、望ましくは流動しない固体であり、包装体容積に対す
る真の内容物の容積の割合で示す充填率は90%以上で
ある必要がおる。この理由は、包装体を湾曲させてフィ
ルムを内容物と共に破断させる、その破断を確実に且つ
容易に起こさせるためのもので、例えば、内容物が流動
性で充填率が90%未満であると、フィルムの破断は極
端に起りにくくなるのである 又内容物が液体等の流動体である場合は、フィルムの破
断にともなって内容物のすべてが一度に絞り出される形
で流出し、広い範囲に亘って飛散してしまう問題が生じ
ることになる。
In this case, the contents must be a non-flowing substance that does not flow at room temperature, preferably a solid that does not flow, and the filling ratio, expressed as the ratio of the volume of the true contents to the volume of the package, must be 90% or more. . The reason for this is to bend the package and break the film together with the contents, and to ensure that the break occurs easily.For example, if the contents are fluid and the filling rate is less than 90%, This makes it extremely difficult for the film to break.Also, if the contents are fluids such as liquids, when the film breaks, all the contents are squeezed out at once and spread over a wide area. This results in the problem of the particles being scattered all over the place.

次に上記破断する特性を与える樹脂組成の特徴は、メチ
ルアクリレート成分が4〜7重量%の塩化ビニリデン−
メチルアクリレート共重合樹脂を、フィルムにした状態
で可塑剤の含有mが4重量%以下になるようにすること
である。
Next, the characteristics of the resin composition that gives the above-mentioned rupture properties are vinylidene chloride containing 4 to 7% by weight of methyl acrylate component.
The objective is to make the methyl acrylate copolymer resin into a film so that the plasticizer content m is 4% by weight or less.

先ず、メチルアクリレート成分が4〜7重量%でおる理
由は、フィルムそのものにガスバリヤ−性、耐衝撃性、
シール部の耐破袋性等の、包装体になったとき内容物を
確実に保存する上で必要となる、包装材としての他の要
求品質のバランスを満しておくためのものである。
First, the reason why the methyl acrylate component is 4 to 7% by weight is that the film itself has gas barrier properties, impact resistance,
This is to satisfy the balance of other quality requirements for a packaging material, such as breakage resistance of the sealed portion, which is necessary to reliably preserve the contents when packaged.

こうしたフィルム特性の基礎をなす塩化ビニリデン−メ
チルアクリレート共重合樹脂において、可塑剤含量が4
重量%以下である必要性は、例えば4重量%以上の可塑
剤を含むと、得られるフィルムの柔軟可撓性が高まり、
包装体を折曲げて破断させる効果を得難くする。一般に
フィルム樹脂内にある可塑剤量は、ガスバリヤ−性を低
下させたり、可塑剤の表面滲み出しくブリード)瑛象を
増す等、目標とする破断効果以外の面からも少ない量で
あって欲しい。
In the vinylidene chloride-methyl acrylate copolymer resin that forms the basis of these film properties, the plasticizer content is 4.
The need for the plasticizer content to be below 4% by weight is such that, for example, if the plasticizer content is 4% by weight or more, the resulting film will have increased flexibility;
To make it difficult to obtain the effect of bending and breaking the package. In general, the amount of plasticizer in the film resin should be kept small for reasons other than the desired breaking effect, such as reducing gas barrier properties and increasing the appearance of plasticizer seeping out from the surface (bleeding). .

しかしながら塩化ビニリデン系樹脂をフィルムの対象樹
脂とするかぎり、押出製膜性を工業的に保たせる上で、
上記可塑剤量の少量化は容易になし得ない。この事実は
、メチルアリクレートが4〜7重量%の塩化ビニリデン
系樹脂を対象とする本発明にあっても例外ではない。
However, as long as vinylidene chloride resin is used as the target resin for the film, in order to maintain extrusion film formability industrially,
It is not easy to reduce the amount of plasticizer. This fact is no exception even in the present invention, which targets vinylidene chloride resins containing 4 to 7% by weight of methyl aliclate.

本発明では次の作用効果を利用して上記押出装膜性の確
保と可塑剤の少量化との両立を達成させている。
The present invention utilizes the following effects to achieve both the above-mentioned extrusion film properties and reduction in the amount of plasticizer.

第2図は、実験図で、横軸は、樹脂内の当初の可塑剤含
有率、縦軸は、押出製膜工程で逸散さぜうる可塑剤の割
合(重量%)で、実線は本発明の対象樹脂での実験結果
を結び描いたものであるこの第2図の示す結果は、本発
明対象樹脂の場合、押出−製膜の加工工程に於て比較的
多量の可塑剤量を逸散させ得る作用機能を有しているこ
とが分る。本発明ではこの作用機能を利用して、押出−
製膜時は多量の可塑剤を用いて塩化ビニリデン−メチル
アクリレート共重合樹脂の製膜性の悪さをおぎない、フ
ィルムになった後は、4重量%以下、望ましくは、3重
量%以下から実質無可塑状態と呼称させる段階に至る 
可塑剤含量のものにすることに成功している。本発明で
いう塩化ビニリデン−メチルアクリレート共重合樹脂と
は、重量平均分子it (GPC法による)が7万〜2
5万の範囲のものであり、同じGPC法で求めた数平均
分子量との比(即ち重量平均分子量÷数平均分子量)が
2.0〜3.0の値の範囲のものが望ましい。
Figure 2 is an experimental diagram, where the horizontal axis is the initial plasticizer content in the resin, the vertical axis is the proportion (% by weight) of plasticizer that can be dissipated during the extrusion film forming process, and the solid line is the main content. The results shown in Fig. 2, which are a summary of the experimental results for the resin targeted by the present invention, indicate that in the case of the resin targeted for the present invention, a relatively large amount of plasticizer was omitted during the extrusion-film forming process. It can be seen that it has an action function that can be dispersed. In the present invention, by utilizing this function, extrusion
During film formation, a large amount of plasticizer is used to overcome the poor film forming properties of the vinylidene chloride-methyl acrylate copolymer resin. It reaches a stage called the plastic state.
We have succeeded in creating a material with a low plasticizer content. The vinylidene chloride-methyl acrylate copolymer resin used in the present invention has a weight average molecular weight (according to GPC method) of 70,000 to 2
50,000, and the ratio to the number average molecular weight determined by the same GPC method (ie, weight average molecular weight/number average molecular weight) is preferably in the range of 2.0 to 3.0.

更に望ましくは、重量平均分子量が8〜13万の範囲で
、数平均分子量との比(重量平均分子聞÷数平均分子量
)が2.0〜2.4の値の範囲のものが望ましい。
More preferably, the weight average molecular weight is in the range of 80,000 to 130,000, and the ratio to the number average molecular weight (weight average molecular weight/number average molecular weight) is in the range of 2.0 to 2.4.

ここでいう重量平均分子量、数平均分子量は、特願昭5
9−240483号に記載の方法、即ちGPC(ゲルパ
ーミェーションクロマトグラフィー)法で求めた値のも
のである。
The weight average molecular weight and number average molecular weight referred to here are
The value was determined by the method described in No. 9-240483, that is, the GPC (gel permeation chromatography) method.

本発明でいう可塑剤とは、塩化ビニル樹脂用可塑剤とし
て公知の液体可塑剤を言う。中でも食品安全衛生上の見
地からは脂肪族二塩基酸エステル系、クエン酸エステル
系、脂肪酸エステル系、ポリエステル系等の液体可塑剤
から厳選され、望ましくは、アジピン酸ジイソブチル、
セパチン酸ジブチル、アセチルクエン酸トリブチル等で
ある。
The plasticizer used in the present invention refers to a liquid plasticizer known as a plasticizer for vinyl chloride resin. Among them, from the viewpoint of food safety and hygiene, liquid plasticizers are carefully selected from aliphatic dibasic acid esters, citric acid esters, fatty acid esters, polyesters, etc., and preferably diisobutyl adipate, diisobutyl adipate,
These include dibutyl sepatate and tributyl acetyl citrate.

更に望ましくは、上記可塑剤とアジピン酸ジイソブチル
との併用使用(例えばアジピン酸ジイソブチル成分が5
0重量%以上)が望ましい。
More preferably, the above plasticizer and diisobutyl adipate are used in combination (for example, if the diisobutyl adipate component is
0% by weight or more) is desirable.

可塑剤の定性、定量は、分析に関しての出版物、例えば
「高分子分析ハンドブック」 (日本分析化学金縁19
85年)に記載の溶剤抽出法により、ガスクロマトグラ
フ、及び質量分析計を用いる方法で行うことができる。
Qualitative and quantitative information on plasticizers can be found in publications related to analysis, such as the ``Polymer Analysis Handbook'' (Japan Analytical Chemistry Kinen 19).
It can be carried out by a method using a gas chromatograph and a mass spectrometer according to the solvent extraction method described in 1985).

可塑剤の逸散率とは、押出−製膜工程中に逸散する可塑
剤量(B)の当初含有1(A)に対する割合(重量%)
、即ち で必る。
The plasticizer escape rate is the ratio (wt%) of the amount of plasticizer (B) that escapes during the extrusion-film forming process to the initial content 1 (A).
, that is, it is necessary.

本発明で用いている評価方法、評価尺度を下記に示す。The evaluation method and evaluation scale used in the present invention are shown below.

a)酸素ガス透過率 ASTM  D−3985準随 (単位 cc/ rtt −24Hr −atm at
 20℃〕評価尺度 評価記号    水準値 ◎ ;  3cc未満 Q  :  3cc以上〜5cc未満 △ ;  5cc以上〜10cc未満 x  ;  10cc以上 b)水蒸気透過率 ASTM−F372準随 〔単位 g/Tlt−24Hr at 40℃90%R
H)評価尺度 評価記号    水Q値 ◎ : 33未満 ○ ; 33以上〜59未満 △ : 5g以上〜iog未満 x  ;  10g以上 C)引張破断強度 ASTM−0882準随 (単位 Ky)/Cl11) タテ・ヨコの平均値であられした 評価尺度 評価記号    水準値 ◎ ;1000に3以上 ○ :   700Ky以上〜1000Kg未満Δ :
   40ONyJX上〜7CJOK9未満x  : 
  400Kg未満 d)衝撃強度 ASTM−D1822*拠 〔単位 K!j−cmat5°C) タテ・ヨコの平均値でめられした 評価尺度 評価記号    水準値 ◎ ;  10Kg−cm以上 ○ :  7に9−cm以上〜10に9−cm未満△ 
:  5に!J−cm以上〜7に!j−cm未満X:5
Kl−cm未満 e)シール部の破袋強度 シール後の筒状フィルムの一方をアルミワイヤーにて結
紮し、他方よりエアーノズルを挿入し、結紮部から15
0.@れた部分をゴム管を用いて空気を洩れない状態に
保ちながら120℃の液中に埋没して、次いで破裂する
迄徐々に空気圧をかけ、破裂時点のゲージ圧を調べて、
破袋強度とした。
a) Oxygen gas permeability ASTM D-3985 quasi-compliant (unit: cc/rtt -24Hr -atm at
20℃] Evaluation scale evaluation symbol Standard value ◎; Less than 3cc Q: 3cc or more - less than 5cc △; 5cc or more - less than 10cc ℃90%R
H) Evaluation scale evaluation symbol Water Q value◎: Less than 33○; 33 or more - less than 59△: 5g or more - less than iog Evaluation scale evaluation symbol based on horizontal average value Standard value ◎; 3 in 1000 or more ○: 700 Ky or more to less than 1000 Kg Δ:
40ONyJX above ~ 7CJOK less than 9x:
Less than 400Kg d) Impact strength based on ASTM-D1822* [Unit: K! j-cmat5°C) Evaluation scale evaluation symbol determined by the vertical and horizontal average values Standard value ◎; 10Kg-cm or more○: 7 to 9-cm or more to 10 to less than 9-cm△
: To 5! More than J-cm to 7! Less than j-cm X: 5
Less than Kl-cm e) Bag breakage strength at sealed part Ligate one side of the sealed cylindrical film with aluminum wire, insert an air nozzle from the other side, and
0. The broken part was submerged in a 120℃ liquid using a rubber tube to prevent air from leaking, then air pressure was gradually applied until it burst, and the gauge pressure at the point of burst was checked.
It was defined as bag breakage strength.

〔単位 Kl/ crA ) 評価尺度 評価記号    水準値 ◎ :  0.8に3以上 0  :   0.5Kg以上〜0.8に3未満△ ;
   0.3に’J以上〜0.5Kg未満x  :  
 0.3Kg未満 f)包装体の折曲げテスト 第1図に示すような方法で筒状包装体を長手方向に折曲
げたときの官能テスト 評価尺度 評価記号    水準値 ◎ : 切断する X ; 切断しない g)厚み ASTM−D374準拠 (単位 μ) 以下、本発明の内容を実験例、実施例によって詳述する
。尚、以下の実験例、実施例に用いる基材樹脂は、塩化
ビニリデン成分とメチルアクリレート成分との割合を、
成分比で97:3(塩化ごニリデン(重量%):メチル
アクリレート(重量%)以下同じ)、96:4,95:
5,93ニア、92.5ニア、5となる5種類の共重合
体の各々に、熱安定剤としてエポキシ化アマニ油1重量
%を添加した塩化ビニリデン系樹脂である。
[Unit: Kl/crA] Evaluation scale rating symbol Standard value ◎: 0.8 to 3 or more 0: 0.5Kg or more to 0.8 to less than 3 △;
More than 0.3'J~less than 0.5Kg x:
Less than 0.3Kg f) Package bending test Sensory test when the cylindrical package is bent in the longitudinal direction as shown in Figure 1 Evaluation scale Evaluation symbol Standard value ◎: Cut X; Do not cut g) Thickness based on ASTM-D374 (unit: μ) The content of the present invention will be explained in detail below using experimental examples and examples. In addition, the base resin used in the following experimental examples and examples has a ratio of vinylidene chloride component and methyl acrylate component:
The component ratio is 97:3 (nylidene chloride (wt%): methyl acrylate (wt%) the same below), 96:4, 95:
It is a vinylidene chloride-based resin in which 1% by weight of epoxidized linseed oil is added as a heat stabilizer to each of five types of copolymers of 5.93Nia, 92.5Nia, and 5.

本基材樹脂は、特願昭59−240483号に記載の方
法でつくることができる。
This base resin can be produced by the method described in Japanese Patent Application No. 59-240483.

実験例1 塩化ビニリデン成分とメチルアクリレート成分との成分
比が96:4である前期基材樹脂にアジピン酸ジイソブ
チルとセパチン酸ジブチルくいずれも液体可塑剤)の等
量混合物を、2重量%、4重量%、6重量%となるよう
に添加混合し、3種類の樹脂を得た。
Experimental Example 1 A mixture of equal amounts of diisobutyl adipate and dibutyl sepatate (both liquid plasticizers) was added to the base resin in which the component ratio of vinylidene chloride component and methyl acrylate component was 96:4 at 2% by weight and 4% by weight. % by weight, and 6% by weight were added and mixed to obtain three types of resins.

これらの樹脂を、通常での押出製膜方法、即ち溶融押出
殿に供給して溶融し、押出殿の先端に取付けられた環状
ダイのスリット部から管状に押出し過冷却したのち、イ
ンフレーションして管状フィルムとし、この管状フィル
ムをピンチして偏平に押し潰して、熱風で100℃に温
調された加熱炉内に導き、加熱処理(パス長で約10m
)を施した後、冷却ローラーで冷却し、折幅1300m
、フィルム厚み40ミクロン(2枚重ね)のフィルムを
捲速20TrL/分の割でボビンに捲取った。
These resins are supplied to a melt extrusion chamber, melted, extruded into a tubular shape through the slit of an annular die attached to the tip of the extrusion chamber, supercooled, and then blown into a tubular shape. This tubular film was pinched and crushed into a flat film, and then introduced into a heating furnace whose temperature was controlled at 100°C with hot air, and heat-treated (pass length of approximately 10 m).
), then cooled with a cooling roller and folded to a width of 1300m
A film having a thickness of 40 microns (two layers) was wound onto a bobbin at a winding speed of 20 TrL/min.

これらのフィルムを56#幅22列取りにスリットし両
端ピンチ折目を除いてボビンに捲取った。
These films were slit into 22 rows of 56# width and wound up onto a bobbin with the pinch creases removed at both ends.

得られた3種類のフィルムについて、フィルム中の残存
可塑剤♀を測定し、可塑剤の逸散率(重量%)を求めた
For the three types of films obtained, the residual plasticizer ♀ in the films was measured, and the plasticizer dissipation rate (% by weight) was determined.

その結果は、第2図に示した。The results are shown in Figure 2.

第2図の結果は、本発明の塩化ビニリデンーメヂルアク
リレート共重合樹脂組成は、原料樹脂中の可塑剤が、押
出、製膜、加熱処理工程中に逸散する特性を有している
ことを示している。
The results shown in Figure 2 indicate that the vinylidene chloride-methyl acrylate copolymer resin composition of the present invention has the property that the plasticizer in the raw material resin escapes during extrusion, film forming, and heat treatment steps. It shows.

実施例1 塩化ビニリデン成分とメチルアクリレート成分との成分
比が97:3,96:4,95:5,93: 7゜92
.5:  7.5である前記基材樹脂の各々にアジピン
酸ジイソブチルとセパチン酸ジブチル(いずれも液体可
塑剤)の混合物(アジピン酸ジイソブチル70重硲%:
セパチン酸ジブチル30重量%)3.5〜5重量%を添
加混合した。これらの樹脂を用いて、実験例1に記載の
押出製膜スリット方法に比べて、加熱炉内での処理温度
を110℃に変更したところが違うだけの実験例1と同
じ押出製膜スリット方法条件でフィルム厚み40ミクロ
ン(2枚重ね)、幅56m(7)5種類のフィルム(■
〜V)を作製し、各々ボビンに捲取った。これらのフィ
ルム中の残存可塑剤量はほぼ3重量%に当る。
Example 1 The component ratio of vinylidene chloride component and methyl acrylate component is 97:3, 96:4, 95:5, 93:7°92
.. 5: A mixture of diisobutyl adipate and dibutyl sepatate (both liquid plasticizers) (70% by weight of diisobutyl adipate:
Dibutyl sepatate (30% by weight) was added and mixed. Using these resins, the extrusion film forming slit method conditions were the same as in Experimental Example 1, except that the treatment temperature in the heating furnace was changed to 110°C compared to the extrusion film forming slit method described in Experimental Example 1. Film thickness: 40 microns (2 layers), width: 56 m (7), 5 types of films (■
~V) were prepared and each was wound onto a bobbin. The amount of residual plasticizer in these films amounts to approximately 3% by weight.

得られた5種類のフィルムについて、本文記載の方法で
、フィルム物性を評価した。
The physical properties of the five types of films obtained were evaluated by the method described in the text.

次に、これらのフィルムをADP (商品名、旭化成■
社製・自動充填包装機)に懸架し、フィルムの走行速度
は25TrL/分、電極の面圧(押圧)は3009の条
件でシールして筒状に製袋(折径25rNri)した。
Next, these films are ADP (product name, Asahi Kasei)
The bag was suspended in a cylindrical bag (folding diameter: 25 rNri) and sealed under conditions such as a film running speed of 25 TrL/min and an electrode surface pressure (pressure) of 3009 mm.

この時の電極プレート電流は、シール可能範囲の中間点
に設定した。
The electrode plate current at this time was set at the midpoint of the sealable range.

作成した製袋品について、本文記載の方法でシール部の
破袋強ざを調べた。
The resulting bag products were examined for bag breakage strength at the seal area using the method described in the text.

次いで、上記T〜Vのフィルムの中から塩化ビニリデン
成分とメチルアクリレート成分との成分比が96:4,
93ニアのフィルムを選び、これらと、旭化成■社製;
厚み40ミクロン(2枚重ね)幅56m〕とを、ADP
に懸架し、上記と同様の条件で筒状に製袋しながら内容
物にチーズを充填し、ワイヤー結紮を施した密封包装体
(径15#X長さ150mX重量24J)を作成した。
Next, from among the films TV to V, the component ratio of vinylidene chloride component and methyl acrylate component is 96:4,
Select 93 Near film and use these and Asahi Kasei ■;
Thickness: 40 microns (two layers) width: 56 m
A sealed package (diameter: 15 #, length: 150 m, weight: 24 J) was prepared by suspending the bag in a cylindrical shape under the same conditions as above, filling the contents with cheese, and applying wire ligatures.

充填率はいずれも95%であった。The filling rate was 95% in all cases.

得られた包装体を、本文記載の方法で折曲げ切断テスト
を実施した。
The resulting package was subjected to a bending and cutting test using the method described in the text.

上記、フィルム物性の結果とシール部の破袋強ざの結果
は第1表に、包装体の折曲げテストの結果は第2表に示
した。
The results of the physical properties of the film and the bag breakage/strength of the sealed portion are shown in Table 1, and the results of the package bending test are shown in Table 2.

第1表の結果によると、本発明品が、ガスバリヤ−性、
耐衝撃性、シール部の耐破袋性等の包装体になったとき
内容物を確実に保存する上で必要となる、包装材として
の要求品質を備えていることがわかる。
According to the results in Table 1, the product of the present invention has gas barrier properties,
It can be seen that it has the required qualities as a packaging material, such as impact resistance and breakage resistance of the sealed part, which are necessary to reliably preserve the contents when packaged.

以下余白 第1表 第2表の結果によると、本発明の筒状包装体は、従来の
切口形成の思想とは全くちがう新規な切口の形成、即ち
、包装体を長手方向に折曲げ湾曲させることだけで表面
フィルムを切断し、その切口から内容物を取出せるもの
で必ることがわかる。
According to the results shown in Table 1 and Table 2 below, the cylindrical package of the present invention can be formed by forming a new cut that is completely different from the conventional concept of cut formation, that is, by bending and curving the package in the longitudinal direction. This alone shows that it is necessary to cut the surface film and take out the contents through the cut.

第2表 (本発明の効果) 本発明は、上述の構成をもつことにより、従来の切口形
成の思想とは全くちがう新規な切口を形成し、その切れ
目を利用して内容物を取出し易くするという機能を持つ
包装体を、ガスバリアー性、耐衝撃性、シール部の耐破
袋性等、包装体の要求品質となる他の特性を損ねないで
提供することができる優れた発明であるといえる。
Table 2 (Effects of the present invention) By having the above-described structure, the present invention forms a new cut that is completely different from the conventional idea of making a cut, and makes it easier to take out the contents by using the cut. This is an excellent invention that can provide a packaging body with this function without impairing other properties required for the packaging body, such as gas barrier properties, impact resistance, and tear resistance of the sealed portion. I can say that.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図は本発明の作用効果を説明する模型図、第2図は
本発明の技術内容を説明する実験図でおり、各々(qら
れたフィルムの有用性を示す特性図である。 記号説明 1・・・筒状包装体 特許出願人 旭化成工業株式会社 代理人 弁理士 野 崎 鋏 也 第1図 可塑剤の添加量(重量%) 手続ネ甫正書(自発) 昭和61年11月6日
Fig. 1 is a model diagram explaining the effects of the present invention, and Fig. 2 is an experimental diagram explaining the technical content of the present invention, and each is a characteristic diagram showing the usefulness of the film. 1... Tubular packaging body patent applicant Asahi Kasei Industries Co., Ltd. Agent Patent attorney Kazuya Nozaki Figure 1 Amount of plasticizer added (% by weight) Procedural Negotiations (spontaneous) November 6, 1985

Claims (1)

【特許請求の範囲】 1)筒状の塩化ビニリデン系樹脂フィルムの筒状内部に
、非流動性の内容物が充填されており、該筒状フィルム
の両端部は密封されてなる塩化ビニリデン系樹脂フィル
ムによる筒状包装体において、1)塩化ビニリデン系樹
脂は、可塑剤含量が4重量%以下であり、メチルアクリ
レート成分が4〜7重量%の塩化ビニリデン−メチルア
クリレート共重合樹脂である。 2)内容物は、その充填率が90%以上である。 ことを特徴とする筒状体を長手方向に添い湾曲させて折
曲げた際、該包装体表面のフィルムを切断させることが
可能な塩化ビニリデン系樹脂フィルムによる筒状包装体
[Scope of Claims] 1) A vinylidene chloride resin in which the inside of a cylindrical vinylidene chloride resin film is filled with a non-flowing content, and both ends of the cylindrical film are sealed. In the cylindrical package made of film, 1) the vinylidene chloride resin is a vinylidene chloride-methyl acrylate copolymer resin having a plasticizer content of 4% by weight or less and a methyl acrylate component of 4 to 7% by weight. 2) The filling rate of the contents is 90% or more. A cylindrical packaging body made of a vinylidene chloride resin film, which is characterized in that the film on the surface of the packaging body can be cut when the cylindrical body is curved and bent in the longitudinal direction.
JP11843386A 1986-05-24 1986-05-24 Cylindrical packed material Granted JPS62275675A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP11843386A JPS62275675A (en) 1986-05-24 1986-05-24 Cylindrical packed material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP11843386A JPS62275675A (en) 1986-05-24 1986-05-24 Cylindrical packed material

Publications (2)

Publication Number Publication Date
JPS62275675A true JPS62275675A (en) 1987-11-30
JPH0123112B2 JPH0123112B2 (en) 1989-05-01

Family

ID=14736519

Family Applications (1)

Application Number Title Priority Date Filing Date
JP11843386A Granted JPS62275675A (en) 1986-05-24 1986-05-24 Cylindrical packed material

Country Status (1)

Country Link
JP (1) JPS62275675A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2008516067A (en) * 2004-10-12 2008-05-15 ダウ グローバル テクノロジーズ インコーポレイティド Plasticizers in alkyl acrylate vinylidene chloride polymers

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2008516067A (en) * 2004-10-12 2008-05-15 ダウ グローバル テクノロジーズ インコーポレイティド Plasticizers in alkyl acrylate vinylidene chloride polymers

Also Published As

Publication number Publication date
JPH0123112B2 (en) 1989-05-01

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