JPS59230720A - Covering method of heat shrinking label - Google Patents

Covering method of heat shrinking label

Info

Publication number
JPS59230720A
JPS59230720A JP58104999A JP10499983A JPS59230720A JP S59230720 A JPS59230720 A JP S59230720A JP 58104999 A JP58104999 A JP 58104999A JP 10499983 A JP10499983 A JP 10499983A JP S59230720 A JPS59230720 A JP S59230720A
Authority
JP
Japan
Prior art keywords
label
resin layer
temperature
thickness
heat
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.)
Pending
Application number
JP58104999A
Other languages
Japanese (ja)
Inventor
Osamu Kawaguchi
修 川口
Yukio Hirose
幸雄 広瀬
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.)
Mitsubishi Plastics Inc
Original Assignee
Mitsubishi Plastics Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Mitsubishi Plastics Inc filed Critical Mitsubishi Plastics Inc
Priority to JP58104999A priority Critical patent/JPS59230720A/en
Publication of JPS59230720A publication Critical patent/JPS59230720A/en
Pending legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C61/00Shaping by liberation of internal stresses; Making preforms having internal stresses; Apparatus therefor
    • B29C61/06Making preforms having internal stresses, e.g. plastic memory
    • B29C61/10Making preforms having internal stresses, e.g. plastic memory by bending plates or sheets
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C61/00Shaping by liberation of internal stresses; Making preforms having internal stresses; Apparatus therefor
    • B29C61/06Making preforms having internal stresses, e.g. plastic memory
    • B29C61/0608Making preforms having internal stresses, e.g. plastic memory characterised by the configuration or structure of the preforms
    • B29C61/0616Making preforms having internal stresses, e.g. plastic memory characterised by the configuration or structure of the preforms layered or partially layered preforms, e.g. preforms with layers of adhesive or sealing compositions
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C63/00Lining or sheathing, i.e. applying preformed layers or sheathings of plastics; Apparatus therefor
    • B29C63/38Lining or sheathing, i.e. applying preformed layers or sheathings of plastics; Apparatus therefor by liberation of internal stresses
    • B29C63/42Lining or sheathing, i.e. applying preformed layers or sheathings of plastics; Apparatus therefor by liberation of internal stresses using tubular layers or sheathings
    • B29C63/423Lining or sheathing, i.e. applying preformed layers or sheathings of plastics; Apparatus therefor by liberation of internal stresses using tubular layers or sheathings specially applied to the mass-production of externally coated articles, e.g. bottles

Landscapes

  • Engineering & Computer Science (AREA)
  • Manufacturing & Machinery (AREA)
  • Laminated Bodies (AREA)
  • Lining Or Joining Of Plastics Or The Like (AREA)

Abstract

PURPOSE:To achieve the covering a shrinking label accurately and with an uniform tightness by heating the label in which a laminate sheet having a low temperature foaming resin layer on a heat shrinking substrate film is formed cyrindrical with the resin layer inward on a specified conditon after a bottle or the like is covered therewith. CONSTITUTION:A label in which a laminate sheet having a low temperature foaming resin layer 2 on a heat shrinking substrate film 1 is formed cylindrical with the resin layer 2 inward on a bottle or the like to cover by shrinking. Here, the covering of the heat shrinking label is done by heating it below the temperature that meets the expression sigmaf=20te/tf as given when the tensile strength sigmaf[kg/cm<2>] of the heat shrinking substrate 1 in the weak direction at a certain temperature is expressed by the thickness tf[mu] of the substrate film before heating and the dry thickness te[mu] until the thickness of the low temperature foaming resin layer 2 increases more than 1.5 times.

Description

【発明の詳細な説明】 本発明は熱収縮性ラベルの被覆方法に関するものである
。更に詳しくは例えばガラスびんのような衝撃により破
損され易い容器の保護と同時に装飾或は表示用等ラベル
としての機能をも奏せしめる発泡性の収縮ラベルを被覆
密着させる方法に関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method of coating heat-shrinkable labels. More specifically, the present invention relates to a method of covering and adhering a foamable shrinkable label, which protects a container such as a glass bottle that is easily damaged by impact, and at the same time functions as a decorative or display label.

従来より熱収縮性フィルムのみよりなる収縮包装ないし
ラベル被覆はよく知られているが、単一フイA・ムによ
るものは被包後位置ずれが生じたり、またクッション性
がないので保脱機能が劣るものであった。
Shrink wrapping or label covering made of only heat-shrinkable film is well known, but those made of a single film tend to shift position after wrapping and lack cushioning properties, making it difficult to retain and remove the film. It was inferior.

そこで、加熱による収縮被覆時に、同時に発泡する層を
形成した複合シートを筒状に形成したものを用いる方法
が提案されている。しかしながらこの場合、該筒状体を
びん等に被せてた!単に加熱を行うと、低湿発泡インク
は厚さ方向に発泡するだけでなく、厚さと直角な方向す
なわち面方向にも発泡しようとするために、加熱で柔軟
になった収縮フィルムを引き伸ばす力が働き、フィルム
が不均一にσ1き伸ばされて凹凸になったり、全体に引
き伸ばされてガラスびんの面に密着しない状態になると
いう不都合が生じる。
Therefore, a method has been proposed in which a composite sheet is formed into a cylindrical shape and has a layer that simultaneously expands during shrinkage coating by heating. However, in this case, the cylindrical body was placed over a bottle, etc.! When simply heated, the low-humidity foaming ink not only foams in the thickness direction, but also tries to foam in the direction perpendicular to the thickness, that is, in the plane direction, which creates a force that stretches the shrinkable film that has become flexible due to heating. , the film may be stretched non-uniformly by σ1, resulting in unevenness, or may be stretched entirely, resulting in problems such as not coming into close contact with the surface of the glass bottle.

本発明はこのような問題点を解決し、発泡層を有するク
ッション性に富む収縮ラベルを確実に均一な密着状態に
収縮被覆することができる被覆方法を提供するものであ
る。
The present invention solves these problems and provides a coating method capable of reliably shrink-coating a shrinkable label having a foam layer with high cushioning properties in a uniform and tightly adhered state.

すなわち本発明は、熱収縮性の基材フィルムに低温発泡
性樹脂層を設けた積層シートを、その樹脂層を内側にし
て筒状に形成してなるラベルを、びん等に被せ加熱して
収縮被覆するにあたり、熱収縮性の基材フィルムのある
温度におけるり]張強度が弱い方向の引張強度をσf[
kg/i〕、加熱前の熱収縮性の基材フィルムの厚さを
1.(2)、低温発泡性樹脂層の厚さをtelAIとし
、σf=20tc/lf を満足する温度以下でかつ低温発泡性樹脂層の厚さが1
.5倍以上になるまで加熱することを特徴とする熱収縮
性ラベル被覆方法である。
That is, in the present invention, a label is formed by forming a laminated sheet in which a heat-shrinkable base film is provided with a low-temperature foamable resin layer into a cylindrical shape with the resin layer inside, and the label is placed over a bottle or the like and heated to shrink. When coating, the tensile strength of the heat-shrinkable base film at a certain temperature in the direction where the tensile strength is weak is σf[
kg/i], and the thickness of the heat-shrinkable base film before heating is 1. (2), the thickness of the low-temperature foamable resin layer is telAI, and the temperature is below that satisfies σf = 20tc/lf and the thickness of the low-temperature foamable resin layer is 1
.. This is a heat-shrinkable label coating method characterized by heating until the temperature increases by 5 times or more.

、以下添付図面を参昭しながら説明する。, will be explained below with reference to the attached drawings.

第1図は加熱温度(′C)とラベルの発泡層厚さ増加量
(倍)との関係を示すグラフ、第2図は加熱温度(℃)
と熱収縮性の基材フィルムの引張強さくkg/c!l)
との関係を示すグラフ、第3図は本発明に用いる加熱前
のラベルの一例を示す断面図である。
Figure 1 is a graph showing the relationship between heating temperature ('C) and increase in foam layer thickness (double) of the label, Figure 2 is heating temperature ('C)
The tensile strength of the heat-shrinkable base film is kg/c! l)
FIG. 3 is a cross-sectional view showing an example of a label before heating used in the present invention.

加熱温度が、σ=20tc/lfを満足する温度よりも
高い温度であるとラベル表面に凹凸が発生し、また低温
発泡性樹脂層の厚さが1.5倍よりも小さくては、クッ
ション性が改良されないので筆記本発明の加熱条件が必
要となる。この理由は必ずしも明確ではないが、第3図
のようなラベルにおいて、熱収縮性の基材フィルム1は
第2図に示さが増加すると−もに基材フィルム1をダ1
き伸ばそうとするので、ある温度以上になるとり]張強
度が弱い方向から、基材フィルムlが引き伸ばされて凹
凸が生ずると考えられる。
If the heating temperature is higher than the temperature that satisfies σ = 20tc/lf, unevenness will occur on the label surface, and if the thickness of the low-temperature foaming resin layer is less than 1.5 times, the cushioning properties will be poor. Since the writing conditions are not improved, the heating conditions of the present invention are required. The reason for this is not necessarily clear, but in the label shown in FIG. 3, as the heat-shrinkable base film 1 increases in size as shown in FIG.
When the temperature exceeds a certain level, the base film 1 is stretched in the direction of weak tensile strength, causing unevenness.

本発明において使用される熱収縮性の基材フィルムとし
ては、例えばポリ塩化ビニル、ポリエチレンテレフタレ
ート、ホ゛リエチレン等各種の熱可塑性樹脂からなる延
伸倍率がラベルにしたときの軸方向で1.5倍以下、周
方向で1.3倍以上の熱収縮性フィルムが挙げられる。
The heat-shrinkable base film used in the present invention is made of various thermoplastic resins such as polyvinyl chloride, polyethylene terephthalate, and polyethylene, and has a stretching ratio of 1.5 times or less in the axial direction when made into a label. Examples include heat-shrinkable films that are 1.3 times or more thicker in the circumferential direction.

またこの基材フィルムに形成される低湿発泡性樹脂は、
発泡材として例えば樹脂粒子にイソブタン、エタン、プ
ロパン、ヘキサン等のような低沸点炭化木葉ガスを封入
させた粒径5〜20μのカプセル状発泡剤が用いられる
。粒径5μ以下になると技術的に製造し難く、20μ以
上になるとフィルム状の表面が悪くなること及び発泡温
度が上るので好ましくない。樹脂粒子は塩化ビニリデン
、メチルメタクリレート、アクリロニトリル等が挙げら
れ基材フィルムの種類に応じて炭化水素ガス量、樹脂量
を調整して基材フィルムに適した発泡温度を有する発泡
剤を選ぶことが肝要である。すなわち、基材フィルムの
収縮加工湿度に応じて収縮加工熱風温度190〜230
’C×10秒になるような基材フィルム例えば、ポリエ
チレン、ポリ塩化ビニル等の場合には発泡剤としては、
120℃、1〜2分間で発泡する比較的低温度型の発泡
剤が特に好適であり、この場合樹脂粒子としては塩化ビ
ニリデンが65〜85%、アクリロニトリルが15〜3
5%程度に混合された樹脂粒子が好適で良好な結果をも
たらす。
In addition, the low humidity foamable resin formed on this base film is
As the foaming material, for example, a capsule-shaped foaming agent having a particle size of 5 to 20 microns is used, in which resin particles are encapsulated with low-boiling point carbonized tree leaf gas such as isobutane, ethane, propane, hexane, or the like. If the particle size is less than 5 μm, it is technically difficult to manufacture, and if it is more than 20 μm, the film-like surface becomes poor and the foaming temperature increases, which is not preferable. Resin particles include vinylidene chloride, methyl methacrylate, acrylonitrile, etc. It is important to adjust the amount of hydrocarbon gas and resin depending on the type of base film and select a blowing agent with a foaming temperature suitable for the base film. It is. That is, the shrink processing hot air temperature is 190 to 230 depending on the shrink processing humidity of the base film.
In the case of base films such as polyethylene, polyvinyl chloride, etc., which have a length of 'C x 10 seconds, the blowing agent is
A relatively low-temperature foaming agent that foams at 120°C for 1 to 2 minutes is particularly suitable; in this case, the resin particles contain 65 to 85% vinylidene chloride and 15 to 3% acrylonitrile.
A mixture of resin particles of about 5% is suitable and gives good results.

低温発泡性樹脂は上記のような発泡剤に合成樹脂結合剤
を加えてなるものであって、該結合剤は、ラベルの基材
をなす熱収縮性プラスチックフィルムとの接着性および
その他の条件を考慮して任意に選択すれば良いが、ポリ
塩化ビニルにはポリエステル+ポリイソシアネート系、
シリコン樹脂、ポリ酢酸ビニル、塩化ビニル/酢酸ビニ
ル共重合体等、ポリエチレンテレフタレートにはポリエ
ステル+ポリイソシアネート系、ポリエチレンイミン、
ポリイソシアネート、ポリ酢酸ビニル、塩化ビニル/酢
酸ビニル共重合体、酢酸ビニル/エチレン共重合体、ポ
リアクリレート、ポリアクリル酸エステル及びアクリレ
ート/酢酸ビニル共重合体等、ポリスチレンにはポリエ
ステルモノマー十触媒系、ポリメチルメタクリレートモ
ノマー、シアノアクリレート、ポリスチレンおよびポリ
アミド(パーサミドタイプ)等が挙げられる。
Low-temperature foamable resin is made by adding a synthetic resin binder to the above-mentioned foaming agent. You can choose as you like, but for polyvinyl chloride, polyester + polyisocyanate,
Silicone resin, polyvinyl acetate, vinyl chloride/vinyl acetate copolymer, etc., polyethylene terephthalate includes polyester + polyisocyanate, polyethyleneimine,
Polyisocyanates, polyvinyl acetate, vinyl chloride/vinyl acetate copolymers, vinyl acetate/ethylene copolymers, polyacrylates, polyacrylic esters, and acrylate/vinyl acetate copolymers, polyester monomers and catalytic systems for polystyrene; Examples include polymethyl methacrylate monomer, cyanoacrylate, polystyrene and polyamide (persamide type).

このような合成樹脂結合剤の溶解に用いられる有機溶剤
としては芳香族類、例えばトルエン、キシレンやアルコ
ール類例えばイソプロパツール、イソプロピルアルコー
ル、酢酸エステル、ハ四ゲン化炭化水素、テトラヒドロ
フラン等の中から合成樹脂結合剤の種類に応じて選択す
ればよい。
Organic solvents used for dissolving such synthetic resin binders include aromatics such as toluene, xylene, alcohols such as isopropanol, isopropyl alcohol, acetic acid esters, tetrahydrocarbons, tetrahydrofuran, etc. It may be selected depending on the type of synthetic resin binder.

発泡剤の添加猷としては合成樹脂基剤100重量部に対
し5〜30重量部好ましくは10〜15*量部が適当で
ある。5重社部以下では発泡が不充分であり、30重量
部以上では基材フィルム1に対する密着性が劣り好まし
くない。
The appropriate amount of the blowing agent to be added is 5 to 30 parts by weight, preferably 10 to 15 parts by weight, per 100 parts by weight of the synthetic resin base. If the amount is less than 5 parts by weight, foaming will be insufficient, and if it is more than 30 parts by weight, the adhesion to the base film 1 will be poor, which is not preferable.

次に本発明に使用するラベル用積層シートを得るには前
記の合成樹脂結合剤を有機溶剤に常温下で攪拌して樹脂
溶液を得る。必要に応じて加湿下で混合してもよい。
Next, to obtain the laminated sheet for labels used in the present invention, the synthetic resin binder is stirred in an organic solvent at room temperature to obtain a resin solution. Mixing may be performed under humidification if necessary.

次いでこの樹脂溶液に収縮性基材フィルムの収縮加工温
度に合せて発泡するように調整された前記のカプセル状
発泡粒子を添加し、攪拌して粉末樹脂粒子を樹脂溶液中
に均一に分散せしめて得られた低温発泡性樹脂を収縮性
基材フィルム上にグラビア等通常用いられている方法で
塗布した後、常温(40℃以下)で1分間程度乾燥させ
れば良いQ −に密着して被覆し得るように少なくとも延伸方向に(
筒状に形成したとき円周方向)に30%以上収縮する必
要がある。そこで30%収縮するための湿度における引
張強度を σf3o〔ゆ/ crl )としたときに、σ  ≧2
0tc/lf 30 を満足するように、フィルムの材質、フィルムの厚さ、
発泡性樹脂層の塗布厚さを選択してラベル用シートを構
成するようにすることが実用的に好ましい。
Next, the capsule-shaped foamed particles adjusted to foam according to the shrinking processing temperature of the shrinkable base film are added to this resin solution, and the powdered resin particles are uniformly dispersed in the resin solution by stirring. The obtained low-temperature foamable resin is applied onto a shrinkable base film by a commonly used method such as gravure, and then dried at room temperature (below 40°C) for about 1 minute to form a close contact with Q-. at least in the stretching direction (
When formed into a cylindrical shape, it must shrink by 30% or more in the circumferential direction. Therefore, when the tensile strength at humidity for shrinking by 30% is σf3o [yu/crl], σ ≧2
The material of the film, the thickness of the film,
It is practically preferable to configure the label sheet by selecting the coating thickness of the foamable resin layer.

かくして得られたラベル用シートを筒状に形成し、これ
をびん体に被せて予熱炉で通常50℃に予熱し、所定温
度にコントロールされたシュリンクトンネルに送り、本
発明の条件に従って加熱収縮させれば、外観極めて良好
なシワのない均一発泡層からなる緩衝撃性の優れたラベ
ルが密着被覆されたものが得られる。以下実施例により
本発明を更に詳しく説明する。
The label sheet thus obtained is formed into a cylindrical shape, placed over a bottle, preheated to usually 50°C in a preheating furnace, sent to a shrink tunnel controlled at a predetermined temperature, and heated and shrunk according to the conditions of the present invention. In this case, a label having an excellent appearance and a uniform foam layer without wrinkles and having excellent mild impact properties can be tightly coated. The present invention will be explained in more detail with reference to Examples below.

実施例 1 アクリル樹脂(三菱レーヨン社製B R102)15重
量%をイソプロピルアルコール5o重1に%と酢酸エチ
/I/20重量%の混合液に添加し室温下で攪拌肱樹脂
溶液を得た。この樹脂溶液に塩化ビニリデン:アクリジ
ニトリルが7:3の混合樹脂粒子にイソブタンガスを封
入してなるカプセル状発泡粒子(松本油脂社製マイクロ
フェアF−30)15重量%を添加し室温下にて発泡粒
子が樹脂液中に均一に分散するように攪拌した。
Example 1 15% by weight of an acrylic resin (BR102 manufactured by Mitsubishi Rayon Co., Ltd.) was added to a mixed solution of 50% by weight of isopropyl alcohol and 20% by weight of ethyl acetate/I/I to obtain a resin solution with stirring at room temperature. To this resin solution, 15% by weight of capsule-shaped foamed particles (Microfere F-30 manufactured by Matsumoto Yushi Co., Ltd.), which are made of mixed resin particles containing vinylidene chloride and acridinitrile (7:3) and isobutane gas sealed, were added, and the mixture was heated to room temperature. The mixture was stirred so that the foamed particles were uniformly dispersed in the resin liquid.

この分散液を厚さ50μの、延伸倍率2.5倍の縦−軸
延伸ポリ塩化ビニルフィルム(三菱樹脂製ヒシレツクス
502)上にグラビア法により塗布し室温で1分間乾燥
し、膜厚50μの発泡性樹脂層を形成し、これを発泡性
樹脂層が内側になるように周長222關の筒状に形成い
これを高さ14cfILs胴回り約6.5cwLs容[
1300ccの瓶体に被せ、これを20′O℃の熱風炉
中で、85℃〜105℃の範囲の所定温度となるまで加
熱して収縮と発泡を行ない、発泡層の厚さの増加を測定
肱その結果を第1図のグラフにプロットして曲線H1を
得た。
This dispersion was applied by gravure onto a vertically axially stretched polyvinyl chloride film (Hishirex 502 manufactured by Mitsubishi Plastics Co., Ltd.) with a thickness of 50 μm and a stretching ratio of 2.5 times, dried for 1 minute at room temperature, and foamed to a film thickness of 50 μm. Form the foamable resin layer into a cylindrical shape with a circumference of 222cm with the foamable resin layer on the inside.
It was placed on a 1300 cc bottle and heated in a hot air oven at 20'O ℃ to a predetermined temperature in the range of 85 ℃ to 105 ℃ to cause shrinkage and foaming, and the increase in the thickness of the foam layer was measured. The results were plotted on the graph of FIG. 1 to obtain a curve H1.

そして、105℃(第1図の81点)でラベル表面に凹
凸が発生した。
At 105° C. (point 81 in FIG. 1), unevenness occurred on the label surface.

実施例 2 実施例1と同じ分散液を厚さ50μの延伸倍率4゜0倍
の縦−軸延伸スチレン−ブタジェン共重合体フィルムに
塗布し、厚さ50μの発泡層を形成して実施例3と同様
の評価を行ったところ、100℃で(第1図の82点)
フィルム表面に凹凸発生が認められた。
Example 2 The same dispersion as in Example 1 was applied to a longitudinally axially stretched styrene-butadiene copolymer film with a thickness of 50μ and a stretching ratio of 4°0 to form a foamed layer with a thickness of 50μ. When we performed the same evaluation as above, we found that at 100℃ (82 points in Figure 1)
Irregularities were observed on the film surface.

ついで実施例1のポリ塩化ビニルフィルム、及び実施例
2のスチレン−ブタジェン共重合フィルムについて筒状
のラベルにした時に軸方向に相当する横方向の引張り強
さを測定したところ、第2図に示すように、ポリ塩化ビ
ニルフィルムがMl、スチレン−ブタジェン共重合体フ
ィルムC1がM。
Next, when the polyvinyl chloride film of Example 1 and the styrene-butadiene copolymer film of Example 2 were made into cylindrical labels, the tensile strength in the transverse direction corresponding to the axial direction was measured, and the results are shown in Figure 2. , the polyvinyl chloride film is Ml, and the styrene-butadiene copolymer film C1 is M.

の曲線となった。前記81点(105℃)でのポリ塩化
ビニルフィルムの横方向引張強さ、81点(100℃)
での共重合体フィルムの引張強さ、すなわちσ、ハ、い
ずれも20に9/crlLとなり、両フィルムの厚さt
 、 =50μ、であり、発泡性樹脂層厚さtc=50
μであるから、50 σ/ =20 tc/lf= 20 X百=20となり
式を満足するから、ポリ塩化ビニルは105℃以下、ポ
リスチレンは100℃以下で加熱する必要があることが
わかる。
The curve was Transverse tensile strength of polyvinyl chloride film at 81 points (105°C), 81 points (100°C)
The tensile strength of the copolymer film at
, = 50μ, and the foamable resin layer thickness tc = 50
Since μ, 50 σ/ = 20 tc/lf = 20 x 100 = 20, satisfying the formula, it is understood that polyvinyl chloride needs to be heated at 105°C or lower, and polystyrene needs to be heated at 100°C or lower.

なお、フィルムの縦方向(延伸方向)についてもグ1張
強度を#定し、ポリ塩化ビニルフィルムがT1、スチレ
ン−ブタジェン共重合体フィルムがT2の曲線が得られ
たが、いずれも横方向の引張強度よりも大きかった。
In addition, the tensile strength was also determined in the longitudinal direction (stretching direction) of the film, and a curve of T1 was obtained for the polyvinyl chloride film, and a curve of T2 was obtained for the styrene-butadiene copolymer film. It was greater than the tensile strength.

実施例 1,2における収縮加工時の温度測定法は以下
のとおりである。
The temperature measurement method during shrinkage processing in Examples 1 and 2 is as follows.

筒状に形成したフィルムの発泡性樹脂未塗布部分に、変
色により温度を示す示温性テープを貼りつけておき、肉
眼により観察して所定の温度に達したかどうかを見る。
A temperature-indicating tape that indicates the temperature by color change is attached to the portion of the cylindrical film that is not coated with the foamable resin, and the film is visually observed to see if a predetermined temperature has been reached.

実施例 3 実施例1で示したと同じ分散液を厚さ50μの(延伸倍
率4.0)収縮性ポリスチレンフィルム(三菱樹脂社製
 DXLOI )上にグラビアにより乾燥厚さ15μの
膜厚になるように塗布した後、常温で1分間乾燥し、ラ
ベル用シートを得た。このシートを発泡性樹脂層が内側
となるように折径的111tnxの筒状に形成し、これ
を高さ約14の胴廻り約6、5 cmサイズの容量30
0CCのびん体に被せこれを50℃に予熱し、200℃
で10秒間熱収縮加工を施したところ、発泡倍率約15
倍の均一に発泡したシワのない緩衝性良好な被覆体が得
られた。
Example 3 The same dispersion as shown in Example 1 was applied to a shrinkable polystyrene film (DXLOI manufactured by Mitsubishi Plastics Co., Ltd.) with a thickness of 50 μm (stretching ratio: 4.0) using gravure so that the film had a dry thickness of 15 μm. After coating, it was dried for 1 minute at room temperature to obtain a label sheet. This sheet was formed into a cylindrical shape with a diameter of 111 tnx with the foamed resin layer on the inside, and a cylinder with a height of about 14 cm, a waist circumference of about 6.5 cm, and a capacity of 30 cm.
Cover it with a 0CC bottle and preheat it to 50℃, then heat it to 200℃.
When heat-shrinked for 10 seconds, the foaming ratio was approximately 15.
A wrinkle-free covering with good cushioning properties was obtained, which was twice as uniformly foamed.

実施例 4 アクリル樹脂(三菱レーヨン社製 BR102)15重
量%をイソプロピルアルコール50重量%と、酢酸エチ
ル20重量%の混合液に添加し、室温下で攪拌し、樹脂
溶液を得た。
Example 4 15% by weight of an acrylic resin (BR102 manufactured by Mitsubishi Rayon Co., Ltd.) was added to a mixed solution of 50% by weight of isopropyl alcohol and 20% by weight of ethyl acetate, and the mixture was stirred at room temperature to obtain a resin solution.

この樹脂溶液に塩化ビニリデンを主成分とし、メチルメ
タアクリレート及びアクリロニトリル若干量を含有する
混合樹脂粒子にイソブタンガスを封入してなるカプセル
状発泡粒子(松本油脂社製マイクロフェア F−40)
15重量%添加し、室温下にて発泡粒子が樹脂液に均一
に分散するように攪拌した。
Capsule-shaped foamed particles (Microfere F-40 manufactured by Matsumoto Yushi Co., Ltd.) are made by encapsulating isobutane gas in mixed resin particles containing vinylidene chloride as a main component and a small amount of methyl methacrylate and acrylonitrile in this resin solution.
15% by weight was added and stirred at room temperature so that the foamed particles were uniformly dispersed in the resin liquid.

この分散液を厚さ50μの延伸倍率v2.5のポリ塩化
ビニルフィルム(三菱!脂社製 ヒシt、7クス 50
2)上にグラビアにより塗布した後、室温で1分間乾燥
して15μの膜厚の発泡性樹脂層を形成し、ラベルシー
トを得た。
This dispersion was applied to a polyvinyl chloride film with a thickness of 50μ and a stretching ratio of v2.5 (Hishit, 7x50, manufactured by Mitsubishi! Co., Ltd.).
2) After coating by gravure, a foamable resin layer having a thickness of 15 μm was formed by drying at room temperature for 1 minute to obtain a label sheet.

このシートを発泡性樹脂層が内側になるように折径的1
11Mの筒状に形成し、これを実施例1と同様のサイズ
のびん体に被せ、50℃に予熱し、熱風温度230℃で
10秒間収縮加工を行ったところ、発泡倍率約15倍の
均一に発泡したシワのない緩衝性良好なラベルが密着被
覆された被覆体が得られた。
Place this sheet with the foam resin layer on the inside.
It was formed into a 11M cylindrical shape, placed on a bottle of the same size as in Example 1, preheated to 50°C, and subjected to shrinkage processing at a hot air temperature of 230°C for 10 seconds, resulting in a uniform foam with a foaming ratio of about 15 times. A covering body was obtained in which a foamed label with no wrinkles and good cushioning properties was tightly coated.

実施例3.4では基材フィルムは実施例1.2と略同様
の厚みであるが、低温発泡性樹脂層の厚さが15μと薄
いため基材フィルムの引張強度がσ−″−20 tc/
1f=6 (kg/ffl )と小さい温度径つ一 て高温まで加熱することができるので、低温発泡性樹脂
層厚さが15倍という高倍率となるまで充分加熱しても
、ラベルに凹凸を生じない。
In Example 3.4, the base film has approximately the same thickness as in Example 1.2, but because the low-temperature foamable resin layer is as thin as 15 μm, the tensile strength of the base film is σ−″−20 tc. /
Since each small temperature diameter of 1f = 6 (kg/ffl) can be heated to a high temperature, even if the low temperature foaming resin layer is sufficiently heated to a high magnification of 15 times, there will be no unevenness on the label. Does not occur.

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

第1図は加熱温度とラベルの発泡層厚さ増加量との関係
を示すグラフ、第2図は加熱温度と引張強さとの関係を
示すグラフである。第3図は本発明に用いる加熱前のラ
ベルの一例を示す断面図であるO HX・・・発泡層の厚さ増加量(倍)と加熱温度の関係
M1・・・ポリ塩化ビニルフィルムの横方向引張強度と
加熱温度との関係 M2・・・スチレン−ブタジェン共重合体フィルムの横
方向引張強度と加熱温度との関係 T1・・・ポリ塩化ビニルフィルムの縦方向引張強度と
加熱温度との関係 T、・・・スチレン−ブタジェン共重合体フィルムの横
方向引張強度と加熱温度との関係 1・・・熱収縮性の基材フィルム 2・・・低温発泡性樹脂層 特許出願人 三菱樹脂株式会社 代理人 弁理士 木村芳男 第1図 no9%31jc  (’C/ − 第2図 汐口社5LK (’C〕 − 第3図 手続補正書ζ/IA発) 昭和夕?年Z月土日 特許庁長官茗りり 矛ρ尺  殿 1 事件の表示 昭和り2年特 許願第1I4−プ7フ号2、発明の名称
  黄大イ又φ声・1・Iフヘ゛ルチ夜覆方埴3 補正
をする者 事件との関係  特許出願人
FIG. 1 is a graph showing the relationship between heating temperature and the amount of increase in the foam layer thickness of the label, and FIG. 2 is a graph showing the relationship between heating temperature and tensile strength. FIG. 3 is a cross-sectional view showing an example of a label before heating used in the present invention.OHX...Relationship between the increase in thickness of the foam layer (fold) and the heating temperature M1...The side of the polyvinyl chloride film Relationship between directional tensile strength and heating temperature M2... Relationship between lateral tensile strength and heating temperature of styrene-butadiene copolymer film T1... Relationship between longitudinal tensile strength of polyvinyl chloride film and heating temperature T...Relationship between lateral tensile strength and heating temperature of styrene-butadiene copolymer film 1...Heat-shrinkable base film 2...Low-temperature foamable resin layer Patent applicant Mitsubishi Plastics Co., Ltd. Agent Patent attorney Yoshio Kimura Figure 1 no 9% 31jc ('C/ - Figure 2 Shioguchisha 5LK ('C) - Figure 3 Procedural amendment ζ/IA issued) Showa evening? Z month Saturday and Sunday, Commissioner of the Patent Office 1. Display of the case 1929 patent application No. 1 I4-7F No. 2, title of the invention Huangdai Mata φ voice 1. Relationship between patent applicant

Claims (1)

【特許請求の範囲】 熱収縮性の基材フィルムに低温発泡性樹脂層を設けた積
層シートをその樹脂層を内側にして筒状に形成してなる
ラベルを、びん等に被せて加熱し収縮被覆するにあたり
、熱収縮性の基材フィルムのある温度における引張強度
が弱い方向の引張強度をσI Ckl? / ad )
 。 加熱前の熱収縮性の基材フ・rルムの厚さを1.(2)
。 低温発泡性樹脂層の乾燥厚さをtc(資)としたとき。 σ −20tc / tf を満足する温度以下で、低温発泡性樹脂層の厚さが1,
5倍以上になるまで加熱することを特徴とする熱収縮性
ラベル被覆方法。
[Claims] A label made of a laminated sheet with a heat-shrinkable base film and a low-temperature foamable resin layer formed into a cylindrical shape with the resin layer inside is placed on a bottle, etc. and heated to shrink. When coating, the tensile strength in the direction where the tensile strength is weak at a certain temperature of the heat-shrinkable base film is σI Ckl? /ad)
. The thickness of the heat-shrinkable base film before heating is 1. (2)
. When the dry thickness of the low temperature foamable resin layer is tc (capital). At a temperature that satisfies σ -20tc/tf or less, the thickness of the low-temperature foamable resin layer is 1,
A method for covering a heat-shrinkable label, the method comprising heating the label until the temperature increases by 5 times or more.
JP58104999A 1983-06-14 1983-06-14 Covering method of heat shrinking label Pending JPS59230720A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP58104999A JPS59230720A (en) 1983-06-14 1983-06-14 Covering method of heat shrinking label

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58104999A JPS59230720A (en) 1983-06-14 1983-06-14 Covering method of heat shrinking label

Publications (1)

Publication Number Publication Date
JPS59230720A true JPS59230720A (en) 1984-12-25

Family

ID=14395789

Family Applications (1)

Application Number Title Priority Date Filing Date
JP58104999A Pending JPS59230720A (en) 1983-06-14 1983-06-14 Covering method of heat shrinking label

Country Status (1)

Country Link
JP (1) JPS59230720A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6343722U (en) * 1986-09-09 1988-03-24
JPS6442365A (en) * 1987-08-07 1989-02-14 Tokai Konetsu Kogyo Kk Production of silicon carbide sintered body of gas impermeability
US8932706B2 (en) 2005-10-27 2015-01-13 Multi-Color Corporation Laminate with a heat-activatable expandable layer

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6343722U (en) * 1986-09-09 1988-03-24
JPH0340597Y2 (en) * 1986-09-09 1991-08-27
JPS6442365A (en) * 1987-08-07 1989-02-14 Tokai Konetsu Kogyo Kk Production of silicon carbide sintered body of gas impermeability
US8932706B2 (en) 2005-10-27 2015-01-13 Multi-Color Corporation Laminate with a heat-activatable expandable layer

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