JPS584752B2 - Netsukatsusenenchaxoseibutsu - Google Patents

Netsukatsusenenchaxoseibutsu

Info

Publication number
JPS584752B2
JPS584752B2 JP50037318A JP3731875A JPS584752B2 JP S584752 B2 JPS584752 B2 JP S584752B2 JP 50037318 A JP50037318 A JP 50037318A JP 3731875 A JP3731875 A JP 3731875A JP S584752 B2 JPS584752 B2 JP S584752B2
Authority
JP
Japan
Prior art keywords
parts
heat
weight
adhesive
adhesive composition
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
JP50037318A
Other languages
Japanese (ja)
Other versions
JPS51111246A (en
Inventor
吉川信治
柴田武範
田辺宣之
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.)
Nitto Denko Corp
Original Assignee
Nitto Electric Industrial 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 Nitto Electric Industrial Co Ltd filed Critical Nitto Electric Industrial Co Ltd
Priority to JP50037318A priority Critical patent/JPS584752B2/en
Publication of JPS51111246A publication Critical patent/JPS51111246A/en
Publication of JPS584752B2 publication Critical patent/JPS584752B2/en
Expired legal-status Critical Current

Links

Description

【発明の詳細な説明】 本発明は通常は非粘着性であり、加熱により活性化あれ
で粘着性となり、しかも活性化後しばらくの間粘着性を
保持しうる熱活性粘着組成物に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to heat-activated adhesive compositions that are normally non-tacky, become tacky upon activation by heating, and can remain tacky for a period of time after activation.

従来、一般に使用されている感圧性接着剤は被着体に簡
単に貼着できるという長所を有する反面常時粘着性であ
るが故に塵埃等が付着したり、不用意に他物に接着して
しまうことがたびたび起るという短所があった。
Pressure-sensitive adhesives that are commonly used in the past have the advantage of being easy to stick to adherends, but because they are always sticky, they can attract dust or inadvertently adhere to other objects. The disadvantage was that things often happened.

また、ホットメルト接着剤は通常非粘着性であるため感
圧性接着剤の如き上記の短所を有せず取扱いは容易であ
るが、該接着剤を用いて接着させる際、例えばホットメ
ルト接着剤層を設けたラベルを缶に接着させるにはラベ
ルと缶とを接触させた状態で熱と圧力をかけなければな
らず作業が面倒であり、高価な装置が必要であるといっ
た欠点がある。
In addition, since hot melt adhesives are usually non-tacky, they do not have the above-mentioned disadvantages of pressure-sensitive adhesives and are easy to handle. In order to adhere the label provided with the can to the can, heat and pressure must be applied while the label and the can are in contact, which is a cumbersome process and requires expensive equipment.

本発明は上記の如き現状に鑑みてなされたもので、感圧
性接着剤およびホットメルト接着剤両者の長所を有する
組成物、即ち通常はホットメルト接着剤のように非粘着
性であり、使用前に加熱することにより粘着性となり、
熱を取去った後もしばらくの間粘着性を保持しうる熱活
性粘着組成物を提供することを目的とするものである。
The present invention has been made in view of the above-mentioned current situation, and is intended to provide a composition that has the advantages of both pressure-sensitive adhesives and hot-melt adhesives. It becomes sticky when heated to
The object of the present invention is to provide a heat-activated adhesive composition that can maintain its adhesive properties for some time even after heat is removed.

本発明者達は交互共重合体、ランダム共重合体は本発明
の目的とする粘着組成物のベースとしては凝集力が弱く
て使用できず、またそれらを部分架橋して凝集力を向上
させよものは可塑剤等の配合成分との相溶性が悪く必ず
しも要求を満足させるものではないことを実験の結果知
得したが、スチレンとブタジエンまたはイソプレンとの
ブロック共重合体は部分架橋する必要もなくそのままで
凝集力に優れ、可塑剤等の配合成分との相溶性も良好な
ことに着目し、種々実験の結果、上記ブロック共重合体
に粘着付与剤および特殊な町塑剤を特定量混合すること
により所期の目的を達成できることを見出し、本発明を
するに至ったものである。
The present inventors believe that alternating copolymers and random copolymers cannot be used as bases for the adhesive composition of the present invention because of their weak cohesive strength, and that they can be partially crosslinked to improve their cohesive strength. As a result of experiments, we learned that block copolymers of styrene and butadiene or isoprene do not necessarily have to be partially cross-linked because they have poor compatibility with plasticizers and other ingredients. Noting that it has excellent cohesive strength as it is and has good compatibility with blended components such as plasticizers, as a result of various experiments, we mixed specific amounts of tackifier and special plasticizer with the above block copolymer. The inventors have discovered that the intended purpose can be achieved by doing so, and have come up with the present invention.

即ち、本発明に係る熱活性粘着組成物はスチレンとブタ
ジエンまたはイソプレンとのブロック共重合体100重
量部に対して、粘着付与剤5〜100重量部、結晶性可
塑剤50〜400重量部が配合されていることを特徴と
するものである。
That is, the heat-activated adhesive composition according to the present invention contains 5 to 100 parts by weight of a tackifier and 50 to 400 parts by weight of a crystalline plasticizer to 100 parts by weight of a block copolymer of styrene and butadiene or isoprene. It is characterized by the fact that

本発明におけるブロック共重合体としてはポリスチレン
ブロックの分子量が約6000〜120000、ポリブ
タジエンまたはポリイソプレンのブロックの分子量が約
15000〜200000で、ポリスチレン含量約18
〜48モル%のものが好適である。
In the block copolymer of the present invention, the polystyrene block has a molecular weight of about 6,000 to 120,000, the polybutadiene or polyisoprene block has a molecular weight of about 15,000 to 200,000, and the polystyrene content is about 18
~48 mol% is preferred.

また、粘着付与剤は加熱により活性化された際の粘着性
を増すための成分であり、アルキルフェノール樹脂、テ
ルペンフェノール樹脂、芳香族系石油樹脂、クマロンイ
ンデン樹脂、スチレン系樹脂、オレフイン系樹脂等種々
あり、特に限定するものではない力釦ジンおよびその誘
導体、テルペン樹脂がブロック共重合体、結晶性可塑剤
との相溶性が良好であり好ましい。
Tackifiers are components that increase tackiness when activated by heating, and include alkylphenol resins, terpenephenol resins, aromatic petroleum resins, coumaron indene resins, styrene resins, olefin resins, etc. There are a variety of them, but there are no particular limitations.Chikarabutsugin, its derivatives, and terpene resins are preferred because they have good compatibility with block copolymers and crystalline plasticizers.

更に、本発明における重要な成分である結晶性可塑剤と
は、軟化点以下の温度では固形結晶状態であり、一旦溶
融された後熱を取去ってもすぐに結晶化せずゆっくりと
結晶化するものであり、具体的にはジシロクへキシルフ
タレート、ジフエニルフタレート等が挙げられる。
Furthermore, the crystalline plasticizer, which is an important component in the present invention, is in a solid crystalline state at temperatures below the softening point, and once melted, it does not crystallize immediately even after the heat is removed, but rather slowly crystallizes. Specific examples thereof include disiloxhexyl phthalate and diphenyl phthalate.

本発明は該結晶性可塑剤の熱溶融後の緩慢な結晶化作用
を利用するものであり、該可塑剤の種類、配合部数を適
宜選択することにより粘着組成物の熱活性化後の粘着保
持時間を比較的自由に変化させることができる。
The present invention utilizes the slow crystallization effect of the crystalline plasticizer after heat melting, and by appropriately selecting the type and number of parts of the plasticizer, adhesive retention of the adhesive composition after heat activation is achieved. Time can be changed relatively freely.

次に本発明に系る粘着組成物成分の配合部数について述
べると、スチレンとブタジエンまたはイソプレンとのブ
ロック共重合体100重量部に対し、粘着付与剤は5〜
100重量部であり、結晶性可塑剤は50〜400重量
部である。
Next, regarding the number of parts of the adhesive composition component according to the present invention, 5 to 5 parts of the tackifier is added to 100 parts by weight of the block copolymer of styrene and butadiene or isoprene.
100 parts by weight, and the crystalline plasticizer is 50 to 400 parts by weight.

ここで粘着付与剤が5重量部未満であると得られる粘着
組成物の熱活性時の接着力が小さすぎて実用的でなく、
100重量部を越えると常時粘着性となり熱活性の粘着
組成物が得られない。
If the amount of the tackifier is less than 5 parts by weight, the adhesive strength of the resulting adhesive composition upon thermal activation will be too small to be practical;
If it exceeds 100 parts by weight, the adhesive composition becomes constantly sticky and a thermally active adhesive composition cannot be obtained.

また、結晶性可塑剤が50重量部未満であると粘着付与
剤を100重量部を越えて配合したときと同様常時粘着
性となり目的の熱活性粘着組成物が得られず、400重
量部を越すと熱活性後の粘着保持時間が短かすぎて実用
的でなくいずれも好ましくない。
In addition, if the amount of crystalline plasticizer is less than 50 parts by weight, the desired heat-activated adhesive composition will not be obtained because the desired heat-activated adhesive composition will become sticky as when the tackifier is added in excess of 100 parts by weight, and if the amount exceeds 400 parts by weight, The adhesion retention time after thermal activation is too short to be practical, and both are unfavorable.

なお、熱活性粘着組成物の劣化抑制のため公知の老化防
止剤を配合することは何ら差支えない。
Note that there is no problem in adding a known anti-aging agent to suppress deterioration of the heat-activated adhesive composition.

なお、老化防止剤を使用する場合はブロック共重合体1
00重量部に対し0.5〜2重量部程度配合すればよい
In addition, when using an anti-aging agent, block copolymer 1
It may be added in an amount of about 0.5 to 2 parts by weight per 00 parts by weight.

本発明における熱活性粘着組成物は一般にその配合成分
をトルエン、ベンゼン等の如き有機溶媒に溶解し紙、布
、プラスチックフイルム等のフイルム状の基材に塗布、
含没するか、或いは基材に溶融ラミネートして使用され
る。
The heat-activated adhesive composition of the present invention is generally prepared by dissolving the ingredients in an organic solvent such as toluene, benzene, etc. and applying it to a film-like base material such as paper, cloth, or plastic film.
It is used by being impregnated or melt-laminated onto a substrate.

上記の如き本発明の熱活性粘着組成物は通常は非粘着性
であるため感圧性接着剤のように塵埃等が付着したり、
不用意に他物に接着してしまうことがなく、しかも加熱
により活性化された後熱を取去ってもしばらくの間粘着
性を保持しており、ドライヤー、アイロン等で加熱すれ
ば手で簡単に貼着作業ができる。
The heat-activated adhesive composition of the present invention as described above is usually non-adhesive, so unlike pressure-sensitive adhesives, it does not attract dust or the like.
It does not inadvertently adhere to other objects, and even after being activated by heat, it remains sticky for a while even after the heat is removed, so it can be easily heated by hand with a hairdryer, iron, etc. Can be used for pasting work.

またシリコーン処理紙の処理面同志の接合、或いはAB
S板、PVC板の接着等一般の接着剤では満足な結果が
得られないような所にも充分適用できるものである。
Also, bonding of treated surfaces of silicone-treated paper, or AB
It is fully applicable to bonding S plates, PVC plates, etc. where satisfactory results cannot be obtained with ordinary adhesives.

更に、結晶性可塑剤の種類、配合部数を適宜選択するこ
とにより粘着組成物の熱活性化後の粘着保持時間を比較
的自由にセットできるので生鮮食品、生果子の有効期限
の明示用等として用いることもできる等の効果を奏する
Furthermore, by appropriately selecting the type and number of crystalline plasticizers, the adhesive retention time after heat activation of the adhesive composition can be set relatively freely, making it useful for clearly indicating the expiration date of fresh foods and fruits. It can also be used effectively.

以下、実施例により本発明を更に詳細に説明する。Hereinafter, the present invention will be explained in more detail with reference to Examples.

なお、実施例中に「部」とあるのは重量部を意味する。In addition, "parts" in the examples mean parts by weight.

実施例 1 トルエン20o部にスチレンーフタシエン共重合体(シ
ェル化学社製、カリフレックスTR1101、スチレン
含量33モル%)100部、粘着付与剤としてFF口ジ
ン(荒川林産社製)20部、およびジシクロへキサシル
フタレートを50,100,150,200,350部
と部数を変えて加え、攪拌して溶解させる。
Example 1 20 parts of toluene, 100 parts of a styrene-phtacyene copolymer (manufactured by Shell Chemical Co., Ltd., Cariflex TR1101, styrene content 33 mol%), 20 parts of FF Kuchijin (manufactured by Arakawa Forestry Co., Ltd.) as a tackifier, and Dicyclohexacyl phthalate is added in varying amounts of 50, 100, 150, 200, and 350 parts and stirred to dissolve.

次いで各溶液中に厚さ50ミクロンの和紙を浸漬して引
上げ、100℃の熱風循環式乾燥機中で2分間加熱乾燥
し、更に完全に性粘着化するため室温で10日間放置し
て熱活非粘着シートを得た。
Next, a piece of Japanese paper with a thickness of 50 microns was immersed in each solution, pulled up, heated and dried in a hot air circulation dryer at 100°C for 2 minutes, and then left at room temperature for 10 days to heat-activate it to make it completely sticky. A non-adhesive sheet was obtained.

かようにして得た粘着シートの熱活性化後の粘着保持時
間および熱活性化した際の接着力を第1表に示す。
Table 1 shows the adhesive retention time of the pressure-sensitive adhesive sheet thus obtained after heat activation and the adhesive strength upon heat activation.

粘着保持時間は熱活性粘着シートを100℃×10秒間
加熱して活性化した後、室温(20℃)に放置した際に
粘着性を失うまでの時間であり、指先に対する粘着性に
より判断したものである。
Adhesive retention time is the time it takes for the heat-activated adhesive sheet to lose its adhesive properties when left at room temperature (20°C) after being activated by heating at 100°C for 10 seconds, and is determined by the adhesiveness to the fingertips. It is.

また接着力は熱活性化した粘着シートをABS板に接着
し180°ピーリング法により測定したものであり、測
定はJISO−2336に準じて行なった。
Further, the adhesive strength was measured by adhering a heat-activated adhesive sheet to an ABS plate and using a 180° peeling method, and the measurement was performed according to JISO-2336.

なお、比較のためジシクロへキシルフタレートを30部
および450部配合して得たもののデータを示す。
For comparison, data obtained by blending 30 parts and 450 parts of dicyclohexyl phthalate are shown.

次に、熱活性粘着シートの各種被勘体に対する接着力の
経日変化を第2表に示す。
Next, Table 2 shows the changes over time in the adhesive strength of the heat-activated adhesive sheets to various objects.

なお、試料はジシクロへシシルフタレート100部配合
したものを用い、測定はJISC−2336に準じて行
なった。
Incidentally, a sample containing 100 parts of dicyclohecylphthalate was used, and the measurement was performed according to JISC-2336.

なお、第1〜2表の測定値はいづれも試料10個の平均
値であり、接着力の単位はkg72cm巾である。
Note that the measured values in Tables 1 and 2 are all average values of 10 samples, and the unit of adhesive strength is kg 72 cm width.

実施例2 スチレンーイソプレン共重合体(シェル化学社製、カリ
フレークスTR1107、スチレン!30モル%)10
0部、MS−1150(安原油脂社製、テルペン樹脂)
30部、ジフエニルフタレ−ト80部をトルエン200
部に溶解後、実施例1と同様にして熱活性粘着シートを
得た。
Example 2 Styrene-isoprene copolymer (manufactured by Shell Chemical Co., Ltd., Cauliflakes TR1107, styrene! 30 mol%) 10
0 parts, MS-1150 (manufactured by Yasushi Oil Co., Ltd., terpene resin)
30 parts, 80 parts of diphenyl phthalate and 200 parts of toluene.
After dissolving the mixture in the following manner, a heat-activated adhesive sheet was obtained in the same manner as in Example 1.

該粘着シートを100℃×10秒の条件で活性化し、そ
の粘着保持時間およびABS板に対する接着力を実施例
1と同様にして測定したところ、粘着保持時間は3時間
10分、接着力は1.8k9/2cm巾であった(測定
値は各々試料10個の平均値である)。
The adhesive sheet was activated at 100°C for 10 seconds, and its adhesive retention time and adhesive strength to an ABS board were measured in the same manner as in Example 1. The adhesive retention time was 3 hours and 10 minutes, and the adhesive strength was 1. .8k9/2cm wide (measured values are average values of 10 samples each).

以上の実施例により本発明の熱活性粘着組成物を利用し
た熱活性粘着シートは、熱活性化後熱を取去ってもしば
らくの間粘着性を保持していること、その粘着保持時間
は結晶性可塑剤の種類、配合部数により比較的自由にセ
ットできることが判る。
According to the above examples, the heat-activated adhesive sheet using the heat-activated adhesive composition of the present invention retains its adhesive properties for a while even after heat is removed after heat activation, and the adhesive retention time is determined by crystallization. It can be seen that it can be set relatively freely depending on the type of plasticizer and the number of parts mixed.

Claims (1)

【特許請求の範囲】[Claims] 1 スチレンとブタジエンまたはイソプレンとのブロッ
ク共重合体100重量部に対して、粘着付与剤5〜10
0重量部、結晶性可塑剤50〜400重量部が配合され
ていることを特徴とする熱活性粘着組成物。
1 5 to 10 parts by weight of tackifier per 100 parts by weight of block copolymer of styrene and butadiene or isoprene
1. A heat-activated adhesive composition characterized in that it contains 0 parts by weight of a crystalline plasticizer and 50 to 400 parts by weight of a crystalline plasticizer.
JP50037318A 1975-03-26 1975-03-26 Netsukatsusenenchaxoseibutsu Expired JPS584752B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP50037318A JPS584752B2 (en) 1975-03-26 1975-03-26 Netsukatsusenenchaxoseibutsu

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP50037318A JPS584752B2 (en) 1975-03-26 1975-03-26 Netsukatsusenenchaxoseibutsu

Publications (2)

Publication Number Publication Date
JPS51111246A JPS51111246A (en) 1976-10-01
JPS584752B2 true JPS584752B2 (en) 1983-01-27

Family

ID=12494315

Family Applications (1)

Application Number Title Priority Date Filing Date
JP50037318A Expired JPS584752B2 (en) 1975-03-26 1975-03-26 Netsukatsusenenchaxoseibutsu

Country Status (1)

Country Link
JP (1) JPS584752B2 (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5844101B2 (en) * 1976-09-27 1983-09-30 ソニー株式会社 Heat-sensitive double-sided adhesive film
JPS58173146A (en) * 1982-04-05 1983-10-12 Yokohama Rubber Co Ltd:The Thermoplastic polymer composition
CN1041104C (en) * 1994-04-27 1998-12-09 丁秀福 Binder of glass wool and face decoration material
KR102288104B1 (en) * 2017-05-29 2021-08-09 토요잉크Sc홀딩스주식회사 Synthetic rubber adhesive, adhesive sheet and abrasive member laminate

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3165421A (en) * 1961-11-10 1965-01-12 Little Inc A Substrate coated with an adhesive layer and method of making the coated substrate
JPS4886940A (en) * 1972-02-24 1973-11-16

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3165421A (en) * 1961-11-10 1965-01-12 Little Inc A Substrate coated with an adhesive layer and method of making the coated substrate
JPS4886940A (en) * 1972-02-24 1973-11-16

Also Published As

Publication number Publication date
JPS51111246A (en) 1976-10-01

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