JPH0123112B2 - - Google Patents
Info
- Publication number
- JPH0123112B2 JPH0123112B2 JP11843386A JP11843386A JPH0123112B2 JP H0123112 B2 JPH0123112 B2 JP H0123112B2 JP 11843386 A JP11843386 A JP 11843386A JP 11843386 A JP11843386 A JP 11843386A JP H0123112 B2 JPH0123112 B2 JP H0123112B2
- Authority
- JP
- Japan
- Prior art keywords
- film
- weight
- vinylidene chloride
- plasticizer
- cylindrical
- 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
Links
- 239000004014 plasticizer Substances 0.000 claims description 31
- 229920005989 resin Polymers 0.000 claims description 27
- 239000011347 resin Substances 0.000 claims description 27
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 claims description 18
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 claims description 16
- 238000004806 packaging method and process Methods 0.000 claims description 12
- WJGVWFOXHWYCHL-UHFFFAOYSA-N 1,1-dichloroethene;methyl prop-2-enoate Chemical compound ClC(Cl)=C.COC(=O)C=C WJGVWFOXHWYCHL-UHFFFAOYSA-N 0.000 claims description 7
- 229920006026 co-polymeric resin Polymers 0.000 claims description 7
- 230000009969 flowable effect Effects 0.000 claims description 2
- 238000000034 method Methods 0.000 description 19
- 238000011156 evaluation Methods 0.000 description 12
- 238000001125 extrusion Methods 0.000 description 8
- RDOFJDLLWVCMRU-UHFFFAOYSA-N Diisobutyl adipate Chemical compound CC(C)COC(=O)CCCCC(=O)OCC(C)C RDOFJDLLWVCMRU-UHFFFAOYSA-N 0.000 description 6
- 238000005452 bending Methods 0.000 description 6
- 238000005520 cutting process Methods 0.000 description 6
- 229940031769 diisobutyl adipate Drugs 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 239000007788 liquid Substances 0.000 description 6
- 230000004888 barrier function Effects 0.000 description 5
- 238000010586 diagram Methods 0.000 description 5
- 239000007789 gas Substances 0.000 description 5
- 238000005227 gel permeation chromatography Methods 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 239000000463 material Substances 0.000 description 3
- 230000008569 process Effects 0.000 description 3
- 238000007789 sealing Methods 0.000 description 3
- 239000002253 acid Substances 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 235000013351 cheese Nutrition 0.000 description 2
- 235000009508 confectionery Nutrition 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- -1 fatty acid esters Chemical class 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 235000013305 food Nutrition 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 239000011342 resin composition Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 241000251468 Actinopterygii Species 0.000 description 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- WETWJCDKMRHUPV-UHFFFAOYSA-N acetyl chloride Chemical compound CC(Cl)=O WETWJCDKMRHUPV-UHFFFAOYSA-N 0.000 description 1
- 239000012346 acetyl chloride Substances 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000009172 bursting Effects 0.000 description 1
- 235000014121 butter Nutrition 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical class OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 235000013365 dairy product Nutrition 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 229910001882 dioxygen Inorganic materials 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 239000012760 heat stabilizer Substances 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 235000015110 jellies Nutrition 0.000 description 1
- 239000008274 jelly Substances 0.000 description 1
- 235000021388 linseed oil Nutrition 0.000 description 1
- 239000000944 linseed oil Substances 0.000 description 1
- 235000013372 meat Nutrition 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 235000020991 processed meat Nutrition 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000001953 sensory effect Effects 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000000638 solvent extraction Methods 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
Landscapes
- Processing Of Meat And Fish (AREA)
- Food Preservation Except Freezing, Refrigeration, And Drying (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Packages (AREA)
Description
〔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
イルムによる筒状包装体の、その改良技術に関す
る。
〔従来技術〕
塩化ビニリデン系樹脂フイ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ADP〔商
品名、旭化成(株)社製〕又はKAP〔商品名、呉羽化
学(株)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55−34044号公報に開示
されているような操作、即ち、平坦な長尺フイル
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
状フイルムとし、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つて密封シー
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
操作によつて製造できるものであることも広く知
られている。
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、外皮となるフイルムを強靭な
ものにしてある。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。
従つて、保存性、衛生性に優れることが分つて
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。
一方上記外皮フイ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
49−19021号公報に開示された技術がある。この
ものは要するに外皮フイルムより丈夫な帯状物を
筒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つて筒状フイ
ルムの一部を引き破り、その部分を外皮フイルム
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
しく従つてチーズ、ウインナーソーセージ包装の
一部に採用される程度に止まり、汎用される迄に
は至つていない。
その主な理由は、易開口部設置には、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。
〔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、表面フイルムを切断して、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、提供でき
るようにすることにある。
〔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イルムを用
いた筒状包装体に比べて相違するところは、
(1) フイルムを形成している塩化ビニリデン系樹
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。
(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。
上記(1)(2)の要件の組合せである。
以下本発明の内容を図面等を用いて詳述する。
第1図は模型図で、本発明の筒状包装体が長手
方向に添つて折曲げ湾曲させた際、その湾曲外周
部のフイ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。
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であつたものをその長手中
央部が角度θをもつ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、普通は内容物の切断
に同伴してフイ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つてフイ
ルムが引き伸ばされ、該内容物の破断に伴つてフ
イルムそのものに亀裂が生じた状態の場面を実線
で表現したものである。
本発明の包装体では、この破断、切り口を利用
して、フイルムを細い帯状に包装体の周りにそつ
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。
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%以上である必要がある。この理由
は、包装体を湾曲させてフイ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、フイルムの破断は極端
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、フイ
ルムの破断にともなつて内容物のすべてが一度に
絞り出される形で流出し、広い範囲に亘つて飛散
してしまう問題が生じることになる。
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、フイルムにした状態で可塑剤の含有量が4重
量%以下になるようにすることである。
先ず、メチルアクリレート成分が4〜7重量%
である理由は、フイルムそのものにガスバリヤー
性、耐衝撃性、シール部の耐破袋性等の、包装体
になつたとき内容物を確実に保存する上で必要と
なる、包装体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。
こうしたフイ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、得られるフイ
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。一般にフイルム樹脂
内にある可塑剤量は、ガスバリヤー性を低下させ
たり、可塑剤の表面滲み出し(ブリード)現象を
増す等、目標とする破断効果以外の面からも少な
い量であつて欲しい。
しかしながら塩化ビニリデン系樹脂をフイルム
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
本発明にあつても例外ではない。
本発明では次の作用効果を利用して上記押出製
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。
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せ
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、フイルムになつた後は、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、
重量平均分子量(GPC法による)が7万〜25万
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。
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(重量平均分子量÷
数平均分子量)が2.0〜2.4の値の範囲のものが望
ましい。
ここでいう重量平均分子量、数平均分子量は、
特願昭59−240483号(特開昭61−120719号)に記
載の方法、即ちGPC(ゲルパーミエーシヨンクロ
マトグラフイー)法で求めたポルスチレン換算の
値のものである。
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、セバチン酸ジ
ブチル、アセチルクエン酸トリブチル等である。
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50重量%以上)が望ましい。
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ツク」(日本分
析化学会編1985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。
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)の当初含有量(A)に対する割合(重
量%)、即ち
可塑剤の逸散率(重量%)=A/B×100
=原料樹脂中の可塑剤量(重量%)−フイルム中の可
塑剤量(重量%)/原料樹脂中の可塑剤量(重量%)×
100
である。
本発明で用いている評価方法、評価尺度を下記
に示す。
(a) 酸素ガス透過率
ASTM D−3985準拠
〔単位 c.c./m2・24Hr・atm at20℃〕
評価尺度
評価記号 水準値
◎;3c.c.未満
○;3c.c.以上〜5c.c.未満
△;5c.c.以上〜10c.c.未満
×;10c.c.以上
(b) 水蒸気透過率
ASTM−F372準拠
〔単位 g/m2・24Hr at40℃90%RH〕
評価尺度
評価記号 水準値
◎;3g未満
○;3g以上〜5g未満、
△;5g以上〜10g未満
×;10g以上
(c) 引張破断強度
ASTM−D882準拠
〔単位 Kg/cm2〕
タテ・ヨコの平均値であらわした
評価尺度
評価記号 水準値
◎;1000Kg以上
○;700Kg以上〜1000Kg未満
△;400Kg以上〜700Kg未満
×;400Kg未満
(d) 衝撃強度
ASTM−D1822準拠
〔単位 Kg−cm at5℃〕
タテ・ヨコの平均値であらわした
評価尺度
評価記号 水準値
◎;10Kg−cm以上
○;7Kg−cm以上〜10Kg−cm未満
△;5Kg−cm以上〜7Kg−cm未満
×;5Kg−cm未満
(e) シール部の破袋強度
シール後の筒状フイ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150mm離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。
〔単位 Kg/cm2〕
評価尺度
評価記号 水準値
◎;0.8Kg以上
○;0.5Kg以上〜0.8Kg未満
△;0.3Kg以上〜0.5Kg未満
×;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
×;切断しない
(g) 厚み
ATSM−D374準拠
〔単位 μ〕
以下、本発明の内容を実験例、実施例によつて
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〔塩化ビニ
リデン(重量%):メチルアクリレート(重量%)
以下同じ〕、96:4、95:5、93:7、92.5:7.5
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。
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。
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である前記基材樹脂にアジピ
ン酸ジイソブチルとセバチン酸ジブチル(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。
これらの樹脂を、通常での押出製膜方法、即ち
溶融押出機に供給して溶融し、押出機の先端に取
付けられた環状ダイのスリツト部から管状に押出
し過冷却したのち、インフレーシヨンして管状フ
イルムとし、この管状フイ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1300mm、フイル
ム厚み40ミクロン(2枚重ね)のフイルムを捲速
20m/分の割でボビンに捲取つた。
これらのフイルムを56mm幅22列取りにスリツト
し両端ピンチ折目を除いてボビンに捲取つた。
得られた3種類のフイルムについて、フイルム
中の残存可塑剤量を測定し、可塑剤の逸散率(重
量%)を求めた。
その結果は、第2図に示した。
第2図の結果は、本発明の塩化ビニリデン−メ
チ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。
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バチン酸ジブチル(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重量%:セバチン酸ジブチル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ツト方法に比
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
ツト方法条件でフイルム厚み40ミクロン(2枚重
ね)、幅56mmの5種類のフイルム(〜)を作
製し、各々ボビンに捲取つた。これらのフイルム
中の残存可塑剤量はほぼ3重量%に当る。
得られた5種類のフイルムについて、本文記載
の方法で、フイルム物性を評価した。
次に、これらのフイルムをADP〔商品名、旭化
成(株)社製・自動充填包装機〕に懸架し、フイルム
の走行速度は25m/分、電極の面圧(押圧)は
300gの条件でシールして筒状に製袋(折径25mm)
した。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。
作成した製袋品について、本文記載の方法でシ
ール部の破袋強さを調べた。
次いで、上記〜のフイ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、93:7のフイルムを選び、これら
と、比較対比の為にサランフイルム〔商品名、
旭化成(株)社製;厚み40ミクロン(2枚重ね)幅56
mm〕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15mm×長さ
150mm×重量24g)を作成した。充填率はいずれ
も95%であつた。
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。
上記、フイルム物性の結果とシール部の破袋強
さの結果は第1表に、包装体の折曲げテストの結
果は第2表に示した。
第1表の結果によると、本発明品が、ガスバリ
ヤー性、耐衝撃性、シール部の耐破袋性等の包装
体になつ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。
[Industrial application field] Cylindrical packaging using vinylidene chloride resin film, mainly for processed meat foods such as meat and fish, processed dairy products such as cheese and butter, and confectionery such as Western cakes and jelly. Regarding the body and its improvement technology. [Prior Art] A cylindrical package made of vinylidene chloride resin film is widely known. For example, automatic filling and packaging machines such as those commercially available as ADP (trade name, manufactured by Asahi Kasei Corporation) or KAP (trade name, manufactured by Kureha Chemical Co., Ltd.) are used, and are generally disclosed in, for example, Japanese Patent Publication No. 55-34044. In other words, 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 packaged contents, a series of automatic, bag-making, filling, and ligating operations are performed, including sealing (wire ligation) with appropriate spacing, and cutting each piece into cylindrical packages. It is also widely known that it can be manufactured using One drawback of this package is that the outer film is made strong so that it can withstand various stresses from handling such as transportation and conveyance, and maintains the spoilage and contamination resistance of the contents. For this reason, it is difficult to take out the contents, especially to take out the contents and use them for the purpose without using a knife or the like. Therefore, even though it is known to have excellent preservability and hygienic properties, there are restrictions such as the inability to apply this package to, for example, toy confectionery that children can enjoy and eat. On the other hand, as a method for facilitating the removal of the above-mentioned outer skin film, Japanese Patent Publication No. 51-8080 and
There is a technique disclosed in Publication No. 49-19021. In short, a strip-shaped material that is stronger than the outer skin film is attached to a part of the cylindrical body or a part of the seal line, and by pulling this strip-shaped material, a part of the cylindrical film is pulled. The proposal is to provide an easy-to-open part that can be torn and used as a cut end of the outer skin film. However, with this technique of creating an easy-to-open part, it is extremely difficult to guarantee the achievement of a nearly 100% probability of forming a tear-off cut. However, it has not reached the point where it is widely used. The main reason for this is that easy opening installation requires advanced welding equipment and equipment that can set and manage conditions with high precision.
This is because, while technology is required, it is not possible to add costs to the packaging itself that correspond to its technological value. [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, by bending and curving the package in the longitudinal direction, the surface film is cut and the cut is formed. to make it easier to take out the contents by using
The objective is to be able to provide packaging bodies that have such functions without impairing other properties that are required for packaging bodies, such as gas barrier properties, impact resistance, and sealing resistance. . [Means for solving the problem] The differences from conventional cylindrical packaging bodies using vinylidene chloride resin films are as follows: (1) The vinylidene chloride resin that forms the film has no plasticity. The agent 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) The contents of the package are filled with non-flowable substances at a filling rate of 90%.
% or more. This is a combination of requirements (1) and (2) above. The contents of the present invention will be explained in detail below using drawings and the like. 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. This FIG. 1 is for explaining how to form a cut to form an opening corresponding to the effect of the present invention. In FIG. 1, an initially straight cylindrical package (indicated by a dotted line) 1 is curved at both ends 2, 2 so that its longitudinal center is curved at an angle θ. ′ in close proximity. If the angle θ reaches approximately 60 degrees or less, the film itself is often cut along with the cutting of the contents, but Fig. 1 shows the assumed state immediately before cutting. That is, the solid line represents a situation in which the film is stretched along the outer periphery of the content being curved, and a crack is generated in the film itself as the content is broken. In the package of the present invention, the breaks and cuts are used to cut the film into thin strips along the circumference of the package, and to push out the contents from the cross section of the cuts, making it easy to take out the contents. The purpose is to promote 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 rate, expressed as the ratio of the true volume of the 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 along 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. Furthermore, if the contents are a fluid such as a liquid, the problem arises that when the film breaks, all the contents are squeezed out at once and scattered over a wide area. Become. Next, the characteristic of the resin composition that gives the above-mentioned breaking property is that vinylidene chloride-methyl acrylate copolymer resin containing 4 to 7% by weight of methyl acrylate component is made into a film with a plasticizer content of 4% by weight or less. The goal is to make it happen. First, the methyl acrylate component is 4 to 7% by weight.
The reason for this is that the film itself has gas barrier properties, impact resistance, tear resistance of the sealed part, etc., which are necessary for reliably preserving the contents when packaged. This is to satisfy the required quality balance. In the vinylidene chloride-methyl acrylate copolymer resin that forms the basis of these film properties,
The need for the plasticizer content to be 4% by weight or less is such that, for example, if the plasticizer content is 4% by weight or more, the flexibility of the obtained film will increase, making it difficult to obtain the effect of bending and breaking the package. . In general, the amount of plasticizer in the film resin should be small from the viewpoint of other than the desired breaking effect, such as reducing gas barrier properties and increasing surface bleed of the plasticizer. However, as long as vinylidene chloride resin is used as the target resin for the film, the amount of plasticizer cannot be easily reduced in order to maintain extrusion film formability industrially. This fact shows that methyl aliclate has 4
The present invention, which targets vinylidene chloride resins containing up to 7% by weight, is no exception. In the present invention, the following effects are utilized to achieve both the above-mentioned extrusion film formability and reduction in the amount of plasticizer. Figure 2 is an experimental diagram, where the horizontal axis is the initial plasticizer content in the resin, the vertical axis is the proportion (wt%) of the plasticizer that can be dissipated in the extrusion film forming process, and the solid line is the invention of the present invention. This is a summary of the experimental results for the target resin. The results shown in FIG. 2 indicate that the resin targeted by the present invention has a function capable of dissipating a relatively large amount of plasticizer during the extrusion-film forming process. In the present invention, by utilizing this function, a large amount of plasticizer is used during extrusion and film forming to overcome the poor film forming properties of the vinylidene chloride-methyl acrylate copolymer resin. %
Hereinafter, we have succeeded in achieving a plasticizer content of desirably 3% by weight or less to a stage called a substantially non-plastic state. The vinylidene chloride-methyl acrylate copolymer resin referred to in the present invention is
The weight average molecular weight (by GPC method) is in the range of 70,000 to 250,000, and the ratio to the number average molecular weight determined by the same GPC method (i.e., weight average molecular weight ÷ number average molecular weight) is 2.0 to 3.0. Preferably within that range. 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 ÷
The number average molecular weight) is preferably in the range of 2.0 to 2.4. The weight average molecular weight and number average molecular weight here are
It is a value calculated in terms of porstyrene obtained by the method described in Japanese Patent Application No. 59-240483 (Japanese Patent Application Laid-open No. 61-120719), that is, the GPC (gel permeation chromatography) method. 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, dibutyl sebatate, and acetyl chloride. Tributyl acid, etc.
More preferably, the above plasticizer and diisobutyl adipate are used in combination (for example, the diisobutyl adipate component is 50% by weight or more). Qualitative and quantitative determination of plasticizers can be carried out using the solvent extraction method described in publications on analysis, such as "Polymer Analysis Handbook" (edited by the Japanese Society for Analytical Chemistry, 1985).
This can be carried out by a method using a gas chromatograph and a mass spectrometer. The plasticizer dissipation rate is the ratio (wt%) of the amount of plasticizer (B) dissipated during the extrusion-film forming process to the initial content (A), that is, the plasticizer dissipation rate (wt%) = A / B × 100 = Amount of plasticizer in raw resin (weight %) - Amount of plasticizer in film (weight %) / Amount of plasticizer in raw resin (weight %) ×
It is 100. The evaluation method and evaluation scale used in the present invention are shown below. (a) Oxygen gas permeability ASTM D-3985 compliant [Unit: cc/m 2・24Hr・atm at 20℃] Evaluation scale evaluation symbol Standard value ◎; Less than 3 c.c. ○; 3 c.c. or more to 5 c.c. Less than △; 5 c.c. or more to less than 10 c.c. Value: ◎: Less than 3g ○: 3g or more and less than 5g, △: 5g or more and less than 10g Evaluation scale evaluation symbol Standard value ◎; 1000Kg or more ○; 700Kg or more - less than 1000Kg △; 400Kg or more - less than 700Kg Evaluation scale evaluation symbol expressed by value Standard value ◎; 10Kg-cm or more ○; 7Kg-cm or more - less than 10Kg-cm △; 5Kg-cm or more - less than 7Kg-cm ×; less than 5Kg-cm (e) Seal part Bag breakage strength After sealing, one side of the cylindrical film is ligated with aluminum wire, an air nozzle is inserted from the other side, and the part 150 mm away from the ligation is heated at 120℃ using a rubber tube to prevent air from leaking. The bag was immersed in the liquid, and then air pressure was gradually applied until it burst, and the gauge pressure at the time of bursting was measured and determined as the bag-breaking strength. [Unit Kg/cm 2 ] Evaluation scale evaluation symbol Standard value ◎; 0.8Kg or more ○; 0.5Kg or more - less than 0.8Kg △; 0.3Kg or more - less than 0.5Kg ×; less than 0.3Kg (f) Packaging bending test Sensory test evaluation scale evaluation symbol when a cylindrical package is bent in the longitudinal direction as shown in Figure 1 Standard value ◎; Cut ×; Not cut (g) Thickness Conforms to ATSM-D374 [Unit: μ] Hereinafter, the content of the present invention will be explained in detail using experimental examples and examples. In addition, the base resin used in the following experimental examples and examples has a component ratio of vinylidene chloride component and methyl acrylate component of 97:3 [vinylidene chloride (wt%): methyl acrylate (wt%)]
Same hereafter], 96:4, 95:5, 93:7, 92.5:7.5
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 the five types of copolymers. This base resin can be produced by the method described in Japanese Patent Application No. 59-240483. Experimental Example 1 A mixture of equal amounts of diisobutyl adipate and dibutyl sebatate (both liquid plasticizers) was added to the base resin in which the ratio of vinylidene chloride component to methyl acrylate component was 96:4 at 2% by weight, 4% by weight. % by weight, and 6% by weight were added and mixed to obtain three types of resins. These resins are produced using the usual extrusion film forming method, that is, they are supplied to a melt extruder, melted, extruded into a tube through the slit of an annular die attached to the tip of the extruder, supercooled, and then subjected to inflation. This tubular film is pinched and crushed into a flat shape, and introduced into a heating furnace whose temperature is controlled to 100℃ with hot air. After being subjected to heat treatment (pass length of about 10 m), it is crushed with cooling rollers. Cool and wind a film with a fold width of 1300 mm and a film thickness of 40 microns (two layers).
It was wound onto a bobbin at a rate of 20m/min. These films were slit into 22-row strips of 56 mm width and wound onto a bobbin with the pinch creases removed at both ends. For the three types of films obtained, the amount of plasticizer remaining in the film was measured, and the plasticizer dissipation rate (% by weight) was determined. The results are shown in Figure 2. 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 the extrusion, film forming, and heat treatment steps. It shows. Example 1 The component ratio of vinylidene chloride component and methyl acrylate component is 97:3, 96:4, 95:5, 93:7,
A mixture of diisobutyl adipate and dibutyl sebatate (both liquid plasticizers) (diisobutyl adipate) was added to each of the base resins with a ratio of 92.5:7.5.
70% by weight: dibutyl sebatate 30% by weight) 3.5~
5% by weight was added and mixed. Using these resins, the same extrusion film slitting method conditions as Experimental Example 1 were used, except that the treatment temperature in the heating furnace was changed to 110°C compared to the extrusion film slitting method described in Experimental Example 1. Five types of films (~) with a film thickness of 40 microns (two films stacked) and a width of 56 mm were prepared, and each film was wound onto a bobbin. The amount of residual plasticizer in these films is approximately 3% by weight. The physical properties of the five types of films obtained were evaluated by the method described in the text. Next, these films were suspended on ADP [trade name, automatic filling and packaging machine manufactured by Asahi Kasei Corporation], and the traveling speed of the film was 25 m/min, and the surface pressure (pressure) of the electrode was
Sealed under 300g conditions and made into a cylindrical bag (folding diameter 25mm)
did. The electrode plate current at this time was set at the midpoint of the sealable range. The bag tear strength of the sealed portion of the manufactured bag product was examined using the method described in the text. Next, from among the above-mentioned films, films with a component ratio of vinylidene chloride component and methyl acrylate component of 96:4 and 93:7 were selected, and for comparison and comparison, Saran film [trade name,
Manufactured by Asahi Kasei Corporation; thickness 40 microns (2 layers) width 56
mm] was suspended on ADP, the contents were filled with cheese while being made into a cylindrical bag under the same conditions as above, and wire ligatures were applied to form a sealed package (diameter 15 mm x length).
150mm x weight 24g). The filling rate was 95% in all cases. The resulting package was subjected to a bending and cutting test using the method described in the text. The results of the film physical properties and the tear strength of the sealed portion are shown in Table 1, and the results of the package bending test are shown in Table 2. According to the results in Table 1, when the product of the present invention is made into a package with gas barrier properties, impact resistance, tear resistance of the sealed part, etc., the packaging is necessary to reliably preserve the contents. It can be seen that it has the required quality as a material.
【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イルムを切断し、その
切口から内容物を取出せるものであることがわか
る。[Table] According to the results in Table 2, the cylindrical package of the present invention can be formed by forming a new cut, which is completely different from the conventional concept of cut formation, that is, by simply bending and curving the package in the longitudinal direction. It can be seen that the surface film can be cut with a cutter and the contents can be taken out through the cut.
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。
By having the above-mentioned structure, the present invention forms a novel cut completely different from the conventional concept of cutting, and uses the cut to make it easier to take out the contents. It can be said that this is an excellent invention that can provide other required qualities of a package, such as barrier properties, impact resistance, and tear resistance of the sealed portion, without impairing them.
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あ
り、各々得られたフイ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。
FIG. 1 is a model diagram illustrating the effects of the present invention;
FIG. 2 is an experimental diagram explaining the technical contents of the present invention, and is a characteristic diagram showing the usefulness of each obtained film. Symbol explanation: 1... Cylindrical packaging.
Claims (1)
内部に、非流動性の内容物が充填されており、該
筒状フイルムの両端部は密封されてなる塩化ビニ
リデン系樹脂フイ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、該包装体表面のフイルムを切断
させることが可能な塩化ビニリデン系樹脂フイル
ムによる筒状包装体。[Scope of Claims] 1. A vinylidene chloride resin film in which the inside of the cylindrical vinylidene chloride resin film is filled with a non-flowable content, and both ends of the cylindrical film are sealed. (1) The vinylidene chloride resin has a plasticizer content of 4% by weight or less and a methyl acrylate component of 4% by weight or less.
~7% by weight vinylidene chloride-methyl acrylate copolymer resin. (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 when the cylindrical body is curved and bent in the longitudinal direction, the film on the surface of the packaging body can be cut.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11843386A JPS62275675A (en) | 1986-05-24 | 1986-05-24 | cylindrical packaging |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11843386A JPS62275675A (en) | 1986-05-24 | 1986-05-24 | cylindrical packaging |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS62275675A JPS62275675A (en) | 1987-11-30 |
| JPH0123112B2 true 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 packaging |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS62275675A (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101039989B (en) * | 2004-10-12 | 2010-06-09 | 陶氏环球技术公司 | Plasticizers in Alkyl Acrylate Vinylidene Chloride Polymers |
-
1986
- 1986-05-24 JP JP11843386A patent/JPS62275675A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS62275675A (en) | 1987-11-30 |
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