JPS6050229B2 - Easy-peel adhesive composition - Google Patents

Easy-peel adhesive composition

Info

Publication number
JPS6050229B2
JPS6050229B2 JP6683577A JP6683577A JPS6050229B2 JP S6050229 B2 JPS6050229 B2 JP S6050229B2 JP 6683577 A JP6683577 A JP 6683577A JP 6683577 A JP6683577 A JP 6683577A JP S6050229 B2 JPS6050229 B2 JP S6050229B2
Authority
JP
Japan
Prior art keywords
polyethylene
adhesive
resins
cellulose
acid
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
JP6683577A
Other languages
Japanese (ja)
Other versions
JPS542285A (en
Inventor
勲 内澤
治文 戸澤
保夫 内田
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.)
Dai Nippon Printing Co Ltd
Original Assignee
Dai Nippon Printing 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 Dai Nippon Printing Co Ltd filed Critical Dai Nippon Printing Co Ltd
Priority to JP6683577A priority Critical patent/JPS6050229B2/en
Publication of JPS542285A publication Critical patent/JPS542285A/en
Publication of JPS6050229B2 publication Critical patent/JPS6050229B2/en
Expired legal-status Critical Current

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  • Moulds For Moulding Plastics Or The Like (AREA)
  • Lubricants (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Paints Or Removers (AREA)
  • Adhesives Or Adhesive Processes (AREA)

Description

【発明の詳細な説明】 本発明は、ポリエチレン等の熱可塑性プラスチックから
なる熱シール加工部分を有する包装容器のそのシール部
分に易剥離性を付与する接着組成物に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an adhesive composition that imparts easy peelability to the sealed portion of a packaging container having a heat-sealed portion made of a thermoplastic such as polyethylene.

近年、包装容器としてポリエチレン等の熱可塑性フィル
ムそのものあるいはこれをラミネートした板紙を熱圧着
することによりシールした袋体あるいは箱体が広く用い
られている。
BACKGROUND ART In recent years, bags or boxes sealed by thermocompression bonding of thermoplastic films such as polyethylene or paperboard laminated thereon have been widely used as packaging containers.

特に後者の熱可塑性プラスチックフィルムをラミネート
した板紙からなる箱体はミルク、ジュース等の液体の密
封容器として広く用いられ始めている。このような容器
のシール部分には一見相矛盾する二つの特性が要求され
る。
In particular, the latter box made of paperboard laminated with a thermoplastic plastic film has begun to be widely used as a sealed container for liquids such as milk and juice. The sealing portion of such a container is required to have two seemingly contradictory properties.

その一つはシール強度であり、他は剥離性である。すな
わち、内容物を充填した容器は、輸送時あるいは保管時
の取扱い上、ある程度の衝撃にさらされ得るが、シール
部分はこのような衝撃に耐えて密封性を保つものでなけ
ればならない。一方開口部のシール部分は、適当な剥離
性を持つものでなければならず、ポリエチレンフィルム
等を直接熱シールすることはこの点で問題がある。
One of them is seal strength and the other is peelability. That is, a container filled with contents may be exposed to some degree of impact during handling during transportation or storage, and the seal portion must be able to withstand such impact and maintain hermeticity. On the other hand, the sealing portion of the opening must have appropriate releasability, and direct heat sealing of a polyethylene film or the like poses a problem in this respect.

すなわち、ポリエチレン同士を直接熱シールするときは
その熱融着性がきわめて強いため、力の弱い婦人、子供
等ては剥離により容易に内容物取り出しのための開口部
が得けられない欠点がある。また開口のため強く剥離さ
せると、所定の接着面において剥離が起きず、その他の
部分が破壊して容器の継続使用が困難となることもある
。特にフィルムラミネートした板紙等をシールした場合
においては、板紙部分が不規則に引き裂かれ、開口部の
形状が変形して、特に内容物が液体の場合には流出が困
難となつて、ユーザーからの苦情の原因となる。またこ
の場合、開口部に毛羽立つた板紙部分が現われ、内容液
が浸透し、その後空気との接触により変質しやすくなる
ので、内容液を一度に使い切らずに保存する場合には、
非常に不衛生となる問題もある。このような開口部のシ
ール部分の接着強度が大)き過ぎることに起因する欠点
を改良すでく、あらかじめ熱シール部分にポリエチレン
等の熱融着強度を適度に低下させるための易剥離性接着
剤(抗接着剤)を塗布することが知られている。
In other words, when polyethylene is directly heat-sealed, the heat fusion properties are extremely strong, so women, children, etc. who are weak in strength have the disadvantage that they cannot easily obtain an opening to take out the contents due to peeling. . Further, if the container is peeled off forcefully due to the opening, peeling may not occur at a predetermined adhesive surface, and other parts may be destroyed, making it difficult to continue using the container. Particularly when sealing film-laminated paperboard, the paperboard may be torn irregularly and the shape of the opening may be deformed, making it difficult for the contents to flow out, especially if the contents are liquid. cause complaints. Also, in this case, a fluffy paperboard part appears at the opening, and the liquid content permeates through, making it susceptible to deterioration due to contact with air, so if you want to store the liquid content without using it all at once,
There are also problems that make it extremely unsanitary. In order to improve the disadvantages caused by the adhesive strength of the sealing part of the opening being too high, we have added an easily peelable adhesive such as polyethylene to the heat-sealed part to reduce the heat-sealing strength appropriately. It is known to apply an anti-adhesive agent.

そしてこのような抗接着剤としては、ジメチルポリシカ
タキサンおよび水素ポリシロキサンに有機金属キレート
触媒を混合してなるもの、および環化ゴムをビヒクルと
して、ジメチルポリシロキサン、ワックスを含有してな
るもの、が知られている。しかし、前者においては、接
着強度を増す目的で有機金属触媒を加えているため、組
成物の安定性が悪く、ゲル化して長期保存することがで
きない不便があり、極めて不経済である。一方、後者は
ビヒクルとなる環化ゴムのポリエチレンに対する接着力
が強いため離型剤としてワックス、ジメチルポリシロキ
サン等を含有させてもシール条件によつては接着強度の
低下が充分でなく、所定の易剥離性を示さなくなるなど
組成上のバランスを取ることが困難な欠点を有する。
Examples of such anti-adhesive agents include those made by mixing dimethylpolyshicataxane and hydrogen polysiloxane with an organometallic chelate catalyst, and those made by using cyclized rubber as a vehicle and containing dimethylpolysiloxane and wax. It has been known. However, in the former method, since an organic metal catalyst is added for the purpose of increasing adhesive strength, the composition has poor stability, gels, and cannot be stored for a long period of time, making it extremely uneconomical. On the other hand, in the case of the latter, the adhesive force of the cyclized rubber used as the vehicle to polyethylene is strong, so even if wax, dimethylpolysiloxane, etc. are included as a mold release agent, the adhesive strength may not be reduced enough depending on the sealing conditions. It has the disadvantage that it is difficult to balance the composition, such as not exhibiting easy peelability.

本発明は、上述した従来の易剥離性接着剤の欠点を除い
た新規な易剥離性接着剤の提供を目的とするものであり
、セルロース誘導体および動植物等に見出される燐脂質
を有機溶剤に溶解して得られた組成物は、極めて印刷適
性、塗布適性に優れ、これをポリエチレン等の熱可塑性
フィルムに塗布することにより適度の剥離性を与えるこ
とができることを見出して本発明を完成したものである
。すなわち、本発明の易剥離性接着剤は、セルロース誘
導体および燐脂質を有機溶剤に溶解してならることを特
徴とするものである。以下、本発明を更に詳細に説明す
る。
The purpose of the present invention is to provide a new easy-to-peel adhesive that eliminates the drawbacks of the conventional easy-to-peel adhesives mentioned above. The present invention was completed based on the discovery that the resulting composition has excellent printability and coating suitability, and that appropriate releasability can be imparted by applying this to a thermoplastic film such as polyethylene. be. That is, the easily peelable adhesive of the present invention is characterized by being formed by dissolving a cellulose derivative and a phospholipid in an organic solvent. The present invention will be explained in more detail below.

本発明においてセルロース誘導体としては例えばメチル
セルロース、エチルセルロース、カルボキシメチルセル
ロース等のセルロースエーテル類、酢酸セルロース、ニ
トロセルロース、酢酸酪酸セルロース、プロピオン酸セ
ルロース等のセルロースエステル類が用いられる。
In the present invention, cellulose derivatives used include, for example, cellulose ethers such as methylcellulose, ethylcellulose, and carboxymethylcellulose, and cellulose esters such as cellulose acetate, nitrocellulose, cellulose acetate butyrate, and cellulose propionate.

これらのセルロ。ース誘導体は分子量及び置換度によつ
てその性質を異にするが一般にグルコース無水物単位の
3ケの水酸基はエステル化又はエーテル化によつて0.
1〜2.8まで置換される。工業的には置換度が1.6
〜2.6の範囲のものが用いられる。特に置換度1.6
!〜1.9の範囲のものは水溶性であり、置換度2.0
〜2.8のものは有機溶剤に可溶となるため好ましくは
2.0〜2.6の範囲で目的に応じて有機溶剤に溶解し
耐水性、耐薬品性等を有する被膜を形成する事が出来、
有機溶剤中に1〜2唾量%の濃度で溶解・して粘度が0
.2〜10p0iSq1好ましくは0.5〜5p0is
e(25℃)の範囲のものが好ましく用いられる。これ
らセルロース誘導体中、エチルセルロースが特に好まし
く用いられる。燐脂質は、α−グリセロリン酸、β−グ
リセロリン酸を中核とするグリセロリン酸の誘導体てあ
り、脂肪酸の付加したホスフアチジン酸、ホスファチジ
ルグリセリン、カルジオリピンなど、更に含窒素原子団
を有するレシチン(ホスファチジルコリン)、ホスファ
チジルエタノールアミン、ホスファチジルセリンなど、
脂肪酸の代わりにアセトアルデヒドを含むアセタールホ
スホリピド等のプラスマロゲン類、イノシツトを含むイ
ノシツト”ホスホリピドなど含むものである。
These cellulos. The properties of these derivatives vary depending on their molecular weight and degree of substitution, but in general, the three hydroxyl groups of the glucose anhydride unit can be reduced to 0.5% by esterification or etherification.
1 to 2.8 are substituted. Industrially, the degree of substitution is 1.6.
-2.6 is used. Especially the degree of substitution is 1.6
! Those with a range of ~1.9 are water-soluble and have a degree of substitution of 2.0
Since those having 2.8 to 2.8 are soluble in organic solvents, it is preferable to dissolve them in organic solvents depending on the purpose in the range of 2.0 to 2.6 to form a film having water resistance, chemical resistance, etc. is possible,
Dissolves in an organic solvent at a concentration of 1-2% by volume and has a viscosity of 0.
.. 2-10p0iSq1 preferably 0.5-5p0is
e (25°C) range is preferably used. Among these cellulose derivatives, ethylcellulose is particularly preferably used. Phospholipids are derivatives of glycerophosphoric acid, with α-glycerophosphoric acid and β-glycerophosphoric acid as the core, and include phosphatidic acid with fatty acids added, phosphatidylglycerin, cardiolipin, and lecithin (phosphatidylcholine) and phosphatidyl that have nitrogen-containing atoms. ethanolamine, phosphatidylserine, etc.
These include plasmalogens such as acetal phospholipid, which contains acetaldehyde instead of fatty acids, and inosite phospholipid, which contains inosite.

なかでも、含窒素原子団を有するものが好ましく、特に
一般式で表わされるレシチンは、特に好ましい燐脂質で
ある。ここで−CORl、−COR2は脂肪酸ラジカ”
ルでパルミチン酸、ステアリン酸、オレイン酸、リノレ
イン酸等の残基を示す。これら燐脂質は、動物性の生体
内に多く含有され、特にレシチンは大豆から工業的に製
造され、経済的である。これな燐脂質は純品である必要
はなく、レシチンを主成分として他の燐脂質をも含む混
合物は好適に用いられる。これらセルロース誘導体と燐
脂質を含む本発明の組成物が易剥離性接着剤として有効
に作用する理由は必ずしも明らかでないが、セルロース
誘導体中の−0H基と燐脂質中の親水性基および親油性
基の作用が調和してポリエチレン等に対し適度の剥離性
を有する塗膜を形成するとともに、ポリエチレン等の高
温融着時には離型剤として働き、シール部の接着性を低
下させるものと考えられる。
Among these, those having nitrogen-containing atomic groups are preferred, and lecithin represented by the general formula is particularly preferred. Here, -CORl and -COR2 are fatty acid radicals.
Residues such as palmitic acid, stearic acid, oleic acid, and linoleic acid are shown in the table. These phospholipids are contained in large amounts in animal bodies, and lecithin in particular is manufactured industrially from soybeans and is economical. These phospholipids do not need to be pure products, and a mixture containing lecithin as a main component and also containing other phospholipids is preferably used. The reason why the composition of the present invention containing these cellulose derivatives and phospholipids acts effectively as an easily peelable adhesive is not necessarily clear, but the -0H group in the cellulose derivative and the hydrophilic and lipophilic groups in the phospholipid It is thought that these effects work together to form a coating film with appropriate releasability to polyethylene, etc., and also act as a release agent during high-temperature fusion of polyethylene, etc., reducing the adhesiveness of the sealed portion.

セルロース誘導体の単独からなる塗膜も接着強度低下作
用を有するが、このような塗膜はもろくかつ耐摩耗性も
弱い欠点があり、また有機溶剤に溶解した状態での印刷
適性も充分でない欠点がある。
Coating films made solely of cellulose derivatives also have the effect of reducing adhesive strength, but such coating films have the drawbacks of being brittle and having low abrasion resistance, and also have insufficient printability when dissolved in organic solvents. be.

このようなセルロース誘導体に燐脂質を加えることによ
り、上記のような欠点が除かれ、また剥離効果を増加す
ることもできる。しかし、燐脂質が過剰であると、塗膜
の粘着性が大きく、ブロッキングの原因となり、また却
つて塗布前の印刷適性を阻害するので好ましくない。上
記の理由により、セルロース誘導体と燐脂質の酸合比は
、前者1(1)部(重量部、以下同じ)に対して、後者
0.5〜10娼、好ましくは0.5〜50部の範囲が用
いられる。
By adding phospholipids to such cellulose derivatives, the above-mentioned drawbacks can be eliminated and the exfoliation effect can also be increased. However, an excessive amount of phospholipid is not preferable because the adhesiveness of the coating film becomes large, causing blocking, and even inhibits printability before coating. For the above reasons, the acid combination ratio of the cellulose derivative and phospholipid is 1 (1) part (by weight, same hereinafter) of the former to 0.5 to 10 parts, preferably 0.5 to 50 parts of the latter. A range is used.

ちなみに、塗膜中の両成分一の配合比のシール強度に対
する影響を第1図に示す。すなわち第1図は、ポリエチ
レンラミネート加工紙に種々のエチルセルロース/レシ
チン混合物からなる塗膜を介して、あるいは介さずに直
接に、220℃、5k91cr111…少の条件にてヒ
ートシールした後に、シヨツパー型引張り試験機にて測
定したシール強度であり、aはポリエチレンの直接シー
ル、bはエチルセルロース単独の塗膜を設けた場合、c
mgはエチルセルロース/レシチンの混合塗膜を設けた
場合であり、その組成比は順次12/1、12/2、1
2/3、12/4、12/5である(塗布液中のエチル
セルロース濃度は全て12%である)。
Incidentally, FIG. 1 shows the influence of the blending ratio of both components in the coating film on the seal strength. In other words, Fig. 1 shows that polyethylene laminated paper is heat-sealed directly with or without a coating film made of various ethyl cellulose/lecithin mixtures at 220°C and 5k91cr111... and then subjected to shovel type tensioning. Seal strength measured with a testing machine, where a is a direct seal of polyethylene, b is a coating film of ethyl cellulose alone, and c
mg is the case when a mixed coating film of ethyl cellulose/lecithin is provided, and the composition ratio is 12/1, 12/2, 1
2/3, 12/4, and 12/5 (the ethyl cellulose concentration in the coating solution is all 12%).

また、b−gの場合、易剥離層塗膜は接着すべき一対の
ポリエチレンの一方のみに、厚み4μて設けた、この第
1図を見れば、本発明の剥離接着剤の使用によりポリエ
チレン間の熱接着強度を0.8kg/1577177!
から0.05〜0.2k9/15順と約114以下の適
度な強度に低下させられ、かつ任意にコントロールでき
ること、およびレシチンの添加はシール強度の低下にも
役立つことが判る。上記セルロース誘導体およびレシチ
ンを芳香族、エステル、ケトン、アルコール等の有機溶
剤の単独または混合溶剤に溶解することにより本発明の
易剥離性接着組成物が得られる。
In addition, in the case of b-g, the easily peelable coating film was provided on only one of the pair of polyethylenes to be bonded, with a thickness of 4 μm.As shown in FIG. Thermal adhesive strength of 0.8kg/1577177!
It can be seen that the strength can be reduced to a moderate strength of about 114 or less in the order of 0.05 to 0.2k9/15, and that it can be controlled as desired, and that the addition of lecithin is also useful for lowering the seal strength. The easily peelable adhesive composition of the present invention can be obtained by dissolving the cellulose derivative and lecithin in an organic solvent such as an aromatic, ester, ketone, or alcohol alone or in combination.

有機溶剤は、組成物中のセルロース誘導体の量が1〜2
0%(重量%、以下同じ)、好ましくは3〜15%とな
るような量で用いられる。溶解はプロペラミキサーなど
任意の攪拌手段を用いて容易に達成できる。こうして得
られる本発明の組成物には、一般的に接着剤のビヒクル
として用いられる天然あるいは合成樹脂や可塑性、助剤
、無機質充填剤、顔料等の添加剤を加えることができる
。このような添加剤の例としては、ダンマー樹脂、松脂
、シエラツク等の天然樹脂、石油樹脂、エステル変性松
脂、環化ゴム、ワジン変性フェノール樹脂、ロジン変性
マレイン酸樹脂、アルキッド樹脂、ケトン樹脂、塩化ゴ
ム、塩素化ポリエチレン、塩素化ポリプロピレン、酸化
ビニール/酢酸ビニール共重合体、エチレン/酢酸ビニ
ール共重合体、ポリ塩化ビニリデン、ポリアミド樹脂、
ウレタン樹脂、エポキシ樹脂等の合成樹脂、可塑剤とし
てフタル酸、クエン酸、セバチン酸、アジピン酸等のエ
ステル等、一般的に離型剤として知られるものとして、
ジメチルポリシロキサン、ワックス、流動パラフィン、
低分子量ポリエチレン、オレイン酸アマイド等、動植物
油として、アマニ油、桐油、ヒマシ油、大豆油、サフラ
ワ油、硫化油、ラード等、無機質充填剤として、微粉末
シリカ、炭酸カルシウム、酸化マグネシウム、沈降性硫
酸バリウム、アルミナホワイト、亜鉛華等、が挙げられ
る。
The organic solvent is used when the amount of cellulose derivative in the composition is 1 to 2.
It is used in an amount of 0% (weight %, same hereinafter), preferably 3 to 15%. Dissolution can be easily achieved using any stirring means such as a propeller mixer. Additives such as natural or synthetic resins, plasticizers, auxiliaries, inorganic fillers, pigments, etc., which are generally used as adhesive vehicles, can be added to the composition of the present invention thus obtained. Examples of such additives include natural resins such as dammar resins, pine resins, silica resins, petroleum resins, ester-modified pine resins, cyclized rubbers, vazine-modified phenolic resins, rosin-modified maleic resins, alkyd resins, ketone resins, and chlorinated resins. Rubber, chlorinated polyethylene, chlorinated polypropylene, vinyl oxide/vinyl acetate copolymer, ethylene/vinyl acetate copolymer, polyvinylidene chloride, polyamide resin,
Synthetic resins such as urethane resins and epoxy resins, plasticizers such as esters such as phthalic acid, citric acid, sebacic acid, adipic acid, etc. are generally known as mold release agents.
Dimethylpolysiloxane, wax, liquid paraffin,
Low molecular weight polyethylene, oleic acid amide, etc. Animal and vegetable oils such as linseed oil, tung oil, castor oil, soybean oil, safflower oil, sulfur oil, lard, etc. Inorganic fillers such as finely powdered silica, calcium carbonate, magnesium oxide, sedimentation Examples include barium sulfate, alumina white, and zinc white.

本発明の組成物の性能を維持するために、これら補助的
添加剤の合計量は、セルロース誘導体10(2)に対し
て1(4)部以下、特に50部を超えないことが好まし
い。このようにして得られた本発明の組成物は、シール
部の所望個所にグラビア印刷、フレキソ印刷、ローラー
コータ方式など慣用の手段により、所望のパターンで印
刷することができる。
In order to maintain the performance of the compositions of the invention, the total amount of these auxiliary additives preferably does not exceed 1 (4) parts, especially not more than 50 parts, based on 10 (2) parts of cellulose derivative. The composition of the present invention thus obtained can be printed in a desired pattern on a desired portion of the seal portion by conventional means such as gravure printing, flexographic printing, or a roller coater method.

以下実施例により更に具体的に説明する。This will be explained in more detail below with reference to Examples.

例 エチルセルロースN−7(ハーキユレスCO.製)
1?レシチン(味の
素(株)製) 2部ジメチルポリシロキ
サン(東レ(株)製) 1部低分子量ポリエチレン(
アライドケミカルCO.製)
1部トルエン
(1)部酢酸エチル
?部 1(4)
部上記成分をプロペラミキサーを備えた容器中に投入し
、3扮間攪拌して混合溶解し、粘度1ポイズの接着剤を
得た。
Example Ethyl cellulose N-7 (manufactured by Hercules CO.)
1? Lecithin (manufactured by Ajinomoto Co., Inc.) 2 parts dimethylpolysiloxane (manufactured by Toray Industries, Inc.) 1 part low molecular weight polyethylene (
Allied Chemical CO. made)
1 part toluene
(1) Ethyl acetate
? Part 1 (4)
The above components were put into a container equipped with a propeller mixer, and stirred for 3 minutes to mix and dissolve to obtain an adhesive with a viscosity of 1 poise.

この接着剤をグラビア印刷方式によリミルクカートン用
ポリエチレンラミネート板紙(ポトラツチ(USA)原
紙)の熱シール部中の流出開口部にパターン印刷し、5
0℃の条件で乾燥したところ、ブロッキングやガイドロ
ールのこすれ、汚れもなく厚み約4μで良好な易剥離層
を形成することができた。
A pattern of this adhesive was printed on the outflow opening in the heat-sealed part of polyethylene laminated paperboard (Potlatch (USA) base paper) for remilk cartons using a gravure printing method.
When dried at 0° C., a good easily peelable layer with a thickness of about 4 μm could be formed without blocking, guide roll rubbing, or staining.

次いで、上記板紙を力ートン状に形成し、加熱フレーム
を用いて、220℃、5k91CT111鰍間の圧着処
理を行つて後、シール部をシヨツパー型引張試験機で引
張つて剥離強度を測定したところ0.15k9/15T
Wtの結果が得られた。
Next, the above-mentioned paperboard was formed into a cardboard shape, and after crimping between the 5k91CT111 and 5k91 CT111 ribs using a heating frame at 220°C, the peel strength was measured by pulling the sealed part with a chopper type tensile tester. .15k9/15T
Wt results were obtained.

また剥離面は、板紙の破損や毛羽立ちなどの変形もなく
、内容物の流出に支障がないことが確認された。
Furthermore, it was confirmed that there was no deformation such as damage to the paperboard or fuzzing of the paperboard on the peeled surface, and there was no problem with the spillage of the contents.

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

図面は、ポリエチレンラミネート板紙のシール面に本発
明の組成物を塗布したときと塗布しないときのシール強
度の差異を示すグラフである。
The drawing is a graph showing the difference in seal strength when the composition of the present invention is applied and not applied to the sealing surface of polyethylene laminated paperboard.

Claims (1)

【特許請求の範囲】 1 セルロース誘導体および燐脂質を有機溶剤に溶解し
て含む易剥離性接着剤組成物。 2 更にジメチルポリシロキサン、低分子量ポリエチレ
ン、無機質充填剤および顔料の一以上を含む上記第1項
の組成物。
[Scope of Claims] 1. An easily peelable adhesive composition containing a cellulose derivative and a phospholipid dissolved in an organic solvent. 2. The composition of item 1 above, further comprising one or more of dimethylpolysiloxane, low molecular weight polyethylene, an inorganic filler, and a pigment.
JP6683577A 1977-06-07 1977-06-07 Easy-peel adhesive composition Expired JPS6050229B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP6683577A JPS6050229B2 (en) 1977-06-07 1977-06-07 Easy-peel adhesive composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP6683577A JPS6050229B2 (en) 1977-06-07 1977-06-07 Easy-peel adhesive composition

Publications (2)

Publication Number Publication Date
JPS542285A JPS542285A (en) 1979-01-09
JPS6050229B2 true JPS6050229B2 (en) 1985-11-07

Family

ID=13327287

Family Applications (1)

Application Number Title Priority Date Filing Date
JP6683577A Expired JPS6050229B2 (en) 1977-06-07 1977-06-07 Easy-peel adhesive composition

Country Status (1)

Country Link
JP (1) JPS6050229B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH051786A (en) * 1991-06-26 1993-01-08 Kubota Corp Underground installation type gravitationally descending system gate opening/closing device

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5736195A (en) * 1980-08-14 1982-02-26 Mitsubishi Heavy Ind Ltd Hot working lubricant
DE3531913A1 (en) * 1985-09-07 1987-03-19 Roehm Gmbh HARDENABLE CAST RESIN
GB8527071D0 (en) * 1985-11-04 1985-12-11 Biocompatibles Ltd Plastics
JP2582303Y2 (en) * 1991-07-19 1998-09-30 凸版印刷株式会社 Decorative paper
US5587009A (en) * 1995-06-12 1996-12-24 Ecolab Inc. Adhesive release agent applied to surface for improved cleaning

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH051786A (en) * 1991-06-26 1993-01-08 Kubota Corp Underground installation type gravitationally descending system gate opening/closing device

Also Published As

Publication number Publication date
JPS542285A (en) 1979-01-09

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