JPH0143388Y2 - - Google Patents
Info
- Publication number
- JPH0143388Y2 JPH0143388Y2 JP146584U JP146584U JPH0143388Y2 JP H0143388 Y2 JPH0143388 Y2 JP H0143388Y2 JP 146584 U JP146584 U JP 146584U JP 146584 U JP146584 U JP 146584U JP H0143388 Y2 JPH0143388 Y2 JP H0143388Y2
- Authority
- JP
- Japan
- Prior art keywords
- base sheet
- adhesive
- layer
- sheet
- silane
- 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
- 239000010410 layer Substances 0.000 claims description 25
- 229920000642 polymer Polymers 0.000 claims description 18
- 239000012790 adhesive layer Substances 0.000 claims description 17
- 229920000098 polyolefin Polymers 0.000 claims description 13
- 239000000853 adhesive Substances 0.000 claims description 11
- 230000001070 adhesive effect Effects 0.000 claims description 11
- 229920001971 elastomer Polymers 0.000 claims description 11
- 229910000077 silane Inorganic materials 0.000 claims description 5
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims description 4
- 239000002390 adhesive tape Substances 0.000 description 15
- 238000000034 method Methods 0.000 description 11
- 239000000203 mixture Substances 0.000 description 11
- -1 polyethylene, ethylene-propylene Polymers 0.000 description 10
- 229920005989 resin Polymers 0.000 description 9
- 239000011347 resin Substances 0.000 description 9
- 239000004698 Polyethylene Substances 0.000 description 7
- 229920001112 grafted polyolefin Polymers 0.000 description 7
- 229920000573 polyethylene Polymers 0.000 description 7
- 229920005672 polyolefin resin Polymers 0.000 description 7
- 239000000463 material Substances 0.000 description 6
- 239000002131 composite material Substances 0.000 description 5
- 238000010438 heat treatment Methods 0.000 description 5
- 239000010409 thin film Substances 0.000 description 5
- 238000003851 corona treatment Methods 0.000 description 4
- 238000001125 extrusion Methods 0.000 description 4
- 229910000831 Steel Inorganic materials 0.000 description 3
- 230000003712 anti-aging effect Effects 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 238000005260 corrosion Methods 0.000 description 3
- 238000004132 cross linking Methods 0.000 description 3
- 239000003431 cross linking reagent Substances 0.000 description 3
- 238000010292 electrical insulation Methods 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000008188 pellet Substances 0.000 description 3
- 230000005855 radiation Effects 0.000 description 3
- 239000010959 steel Substances 0.000 description 3
- 229920002367 Polyisobutene Polymers 0.000 description 2
- 229920005549 butyl rubber Polymers 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 238000010382 chemical cross-linking Methods 0.000 description 2
- 229920006026 co-polymeric resin Polymers 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 229920003020 cross-linked polyethylene Polymers 0.000 description 2
- 239000004703 cross-linked polyethylene Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000005038 ethylene vinyl acetate Substances 0.000 description 2
- 229920006244 ethylene-ethyl acrylate Polymers 0.000 description 2
- 238000010030 laminating Methods 0.000 description 2
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 2
- SCPYDCQAZCOKTP-UHFFFAOYSA-N silanol Chemical compound [SiH3]O SCPYDCQAZCOKTP-UHFFFAOYSA-N 0.000 description 2
- QLZJUIZVJLSNDD-UHFFFAOYSA-N 2-(2-methylidenebutanoyloxy)ethyl 2-methylidenebutanoate Chemical compound CCC(=C)C(=O)OCCOC(=O)C(=C)CC QLZJUIZVJLSNDD-UHFFFAOYSA-N 0.000 description 1
- XMNIXWIUMCBBBL-UHFFFAOYSA-N 2-(2-phenylpropan-2-ylperoxy)propan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)OOC(C)(C)C1=CC=CC=C1 XMNIXWIUMCBBBL-UHFFFAOYSA-N 0.000 description 1
- 229920000181 Ethylene propylene rubber Polymers 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- 239000006057 Non-nutritive feed additive Substances 0.000 description 1
- 239000004820 Pressure-sensitive adhesive Substances 0.000 description 1
- 230000003213 activating effect Effects 0.000 description 1
- 239000004840 adhesive resin Substances 0.000 description 1
- 229920006223 adhesive resin Polymers 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- AYOHIQLKSOJJQH-UHFFFAOYSA-N dibutyltin Chemical compound CCCC[Sn]CCCC AYOHIQLKSOJJQH-UHFFFAOYSA-N 0.000 description 1
- 208000028659 discharge Diseases 0.000 description 1
- IBKNSIPMTGYUNZ-UHFFFAOYSA-N ethenyl(methoxy)silane Chemical compound CO[SiH2]C=C IBKNSIPMTGYUNZ-UHFFFAOYSA-N 0.000 description 1
- NKSJNEHGWDZZQF-UHFFFAOYSA-N ethenyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)C=C NKSJNEHGWDZZQF-UHFFFAOYSA-N 0.000 description 1
- 239000005042 ethylene-ethyl acrylate Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000010408 film Substances 0.000 description 1
- 238000003475 lamination Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 239000011342 resin composition Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Adhesive Tapes (AREA)
Description
【考案の詳細な説明】
本考案は基材シートと粘着剤層との接着力が向
上された鋼管防食用、或いは電気絶縁用等に用い
られる接着性テープに関するものである。通常鋼
管の防食用、或いは電気絶縁用テープとしてはポ
リオレフイン系樹脂を主体とした基材シートにゴ
ム系粘着剤組成物を貼合したものが用いられてい
る。[Detailed Description of the Invention] The present invention relates to an adhesive tape that has improved adhesive strength between a base sheet and an adhesive layer and is used for corrosion protection of steel pipes, electrical insulation, etc. Usually, as a tape for corrosion protection of steel pipes or for electrical insulation, a tape is used in which a rubber adhesive composition is bonded to a base sheet mainly made of polyolefin resin.
このような接着性テープは通常以下の如き方法
で製造されている。まず、ポリエチレン、エチレ
ン−プロピレン共重合樹脂、エチレン−酢酸ビニ
ル共重合樹脂、エチレン−エチルアクリレート共
重合樹脂などのポリオレフイン系樹脂単独、また
はこれらのブレンド物をインフレーシヨン、Tダ
イ押出、またはカレンダー加工方法などにより所
定厚みのシート体に成形する。 Such adhesive tapes are usually manufactured by the following method. First, a polyolefin resin such as polyethylene, ethylene-propylene copolymer resin, ethylene-vinyl acetate copolymer resin, ethylene-ethyl acrylate copolymer resin, or a blend thereof is processed by inflation, T-die extrusion, or calendar processing. It is formed into a sheet body of a predetermined thickness by a method or the like.
一方ゴム系粘着剤はブチルゴム、エチレンプロ
ピレンゴム、天然ゴム、等をベースとしてこれに
ポリイソブチレン、樹脂系増粘剤等を加えて粘着
性を付与し、更に必要により充填剤、加工助剤、
老化防止剤等を加え、これらをバンバリー、ニー
ダー、或いはロールミルなどを用いて一様の混和
物として作られる。 On the other hand, rubber adhesives are based on butyl rubber, ethylene propylene rubber, natural rubber, etc., and add polyisobutylene, resin thickeners, etc. to give them tackiness, and if necessary fillers, processing aids, etc.
Anti-aging agents and the like are added, and these are made into a uniform mixture using a Banbury, kneader, or roll mill.
しかして上記基材シートと粘着剤とをカレンダ
ー等を用いて貼合せしめて、基材シートの片面に
粘着剤層が形成された接着性シートとなされるも
ので、粘着剤層と基材シートとはこの貼合工程に
於て充分に接合されねばならない。若し両者の接
着が不充分の場合には基材シートと粘着剤層が剥
れ易く、若し剥れが生ずると鋼管或いは電気導体
などにテープを纒巻する際、重大な欠陥を生ず
る。 The base sheet and the adhesive are pasted together using a calendar or the like to form an adhesive sheet with an adhesive layer formed on one side of the base sheet. and must be sufficiently bonded in this bonding process. If the adhesion between the two is insufficient, the base sheet and the adhesive layer are likely to separate, and if such separation occurs, serious defects will occur when the tape is wrapped around a steel pipe or electrical conductor.
粘着剤層と基材シートとの接着性を高めるため
には、両者の貼合時に基材シートを予め加熱す
る。基材シートの貼合面をコロナ放電等により活
性化処理するなどの方法を適用する。或いは基材
シート用ポリマーに比較して粘着剤層との接着性
に富む樹脂を基材シートの成形品に同時に二層押
出などの方法によつて基材の特性に大きな影響を
及ぼさない程度の厚さに設けるなどの方法が行な
われる。 In order to improve the adhesiveness between the adhesive layer and the base sheet, the base sheet is heated in advance when bonding the two. A method such as activating the bonding surface of the base sheet by corona discharge or the like is applied. Alternatively, a resin that has better adhesion with the adhesive layer than the polymer for the base sheet may be added to the molded product of the base sheet by a method such as simultaneous two-layer extrusion to the extent that it does not significantly affect the properties of the base material. A method such as providing a thick layer is used.
一方、最近、防食用接着性テープ、電気絶縁用
接着性テープなどの使用用途範囲が拡大し、100
℃以上の高温下にて使用される場合が増大してい
る。このため、この様な苛酷な使用条件に耐え得
るように一般に耐熱性向上化の公知の手法として
知られる放射線照射、化学架橋法などを基材シー
トの作成時に応用されている。 On the other hand, recently, the range of applications for anti-corrosion adhesive tapes, adhesive tapes for electrical insulation, etc. has expanded, and the number of applications has increased to 100.
Increasingly, devices are used at high temperatures of ℃ or higher. Therefore, in order to withstand such harsh usage conditions, radiation irradiation, chemical crosslinking, and the like, which are known as methods for improving heat resistance, are generally applied when producing the base sheet.
しかし、この様な放射線照射処理などにより、
架橋結合を導入し、耐熱性を向上せしめた基材シ
ートにカレンダーロールなどにて粘着剤を貼合さ
せようと両者の貼合時直前に赤外線ヒーター等を
用いて加熱処理を行つても、基材シートの表面は
容易に軟化せず、従つて、粘着剤層と基材シート
の充分な接着を達成することが困難であつた。 However, due to such radiation irradiation treatment,
Even if heat treatment is performed using an infrared heater or the like just before bonding the adhesive to a base sheet that has introduced cross-linking and improved heat resistance using a calendar roll, the base sheet will not work. The surface of the material sheet does not soften easily, and therefore, it has been difficult to achieve sufficient adhesion between the adhesive layer and the base sheet.
このような問題を補ぎなうため基材シートの表
面にコロナ処理を施してもその効果は薄かつた。
またこの様な事から基材シートの押出成形時に基
材シートの表面に基材シート材料に比較して粘着
剤層との接着性の高い樹脂の薄層を設けてやつて
も、基材シートの耐熱性向上のために施す放射線
照射処理によつて前記薄層も同時に架橋化される
ため、粘着剤層との接着性向上の効果が阻害され
てしまう。 Even if corona treatment was applied to the surface of the base sheet to compensate for such problems, the effect was weak.
In addition, for this reason, even if a thin layer of resin is provided on the surface of the base sheet during extrusion molding of the base sheet, which has higher adhesiveness to the adhesive layer than the base sheet material, the base sheet Because the thin layer is also crosslinked during the radiation treatment performed to improve the heat resistance of the adhesive layer, the effect of improving the adhesiveness with the pressure-sensitive adhesive layer is inhibited.
また、過酸化物などの化学架橋剤を添加した樹
脂組成物にて基材シートを作り、これを加熱し架
橋せしめる方法の適用を考えると、接着性の高い
樹脂の薄層を基材シート上に設け、この薄層形成
材料には架橋剤を添加しておかなければ薄層は架
橋化されないが、架橋剤が配合された基材シート
の架橋化時の加熱処理にて該薄層が溶融し、変形
または基材シート同志の接着などの事態を引起し
製造が困難となる。本考案は上述の如き点に着目
し、耐熱特性に優れ、しかも基材シートとゴム系
粘着剤層との接着が強固である如き、接着性テー
プを開発すべく鋭意研究を重ねた結果本考案接着
性テープを開発し得たものである。即ち、本考案
の接着性テープは図面に示した如く、片面がシラ
ン架橋ポリオレフイン系ポリマー層1他面か非架
橋ポリオレフイン系ポリマー層2である基材シー
ト4の前記非架橋ポリオレフイン系ポリマー層2
面にゴム系粘着剤層3を形成したことを特徴とす
るものである。 In addition, considering the application of a method in which a base sheet is made from a resin composition to which a chemical crosslinking agent such as peroxide is added, and this is heated and crosslinked, it is possible to apply a thin layer of highly adhesive resin onto the base sheet. The thin layer will not be crosslinked unless a crosslinking agent is added to the thin layer forming material, but the thin layer will melt during the heat treatment during crosslinking of the base sheet containing the crosslinking agent. However, this may cause deformation or adhesion of the base sheets, making manufacturing difficult. This invention was developed by focusing on the above-mentioned points, and was the result of intensive research to develop an adhesive tape that has excellent heat resistance properties and has strong adhesion between the base sheet and the rubber adhesive layer. We were able to develop an adhesive tape. That is, as shown in the drawings, the adhesive tape of the present invention has a silane-crosslinked polyolefin polymer layer 2 on one side and a non-crosslinked polyolefin polymer layer 2 on a base sheet 4 having a silane crosslinked polyolefin polymer layer 2 on the other side.
It is characterized in that a rubber adhesive layer 3 is formed on the surface.
以下本考案接着性テープの代表的製法を工程的
に順次説明する。 Hereinafter, a typical manufacturing method of the adhesive tape of the present invention will be explained step by step.
シラン架橋ポリオレフイン系ポリマーシート
は、例えば、ポリエチレン、エチレン−プロピレ
ン共重合樹脂、エチレン−酢酸ビニル共重合樹
脂、エチレン−エチルアクリレート樹脂などの単
独または2種以上の混合物に、例えばビニルトリ
メトキシシランなどの有機シラン化合物と、有機
過酸化物などの遊離ラジカル発生剤とを添加し、
これらを反応させてシラングラフト化ポリオレフ
インポリマーを作り、更にこのシラングラフト化
ポリオレフインポリマーに所定量のシラノール縮
合触媒を添加し、この混和物を用いて、通常のイ
ンフレーシヨン法、或いはTダイ法などにてシー
ト体を押出成形して作る。而して作つたシラング
ラフト化ポリオレフインポリマーシート上にシラ
ングラフト化ポリオレフインポリマーと同一また
は異種の非架橋のポリオレフイン系樹脂の薄いフ
イルムを形成するが、その方法としては、シラン
グラフト化ポリオレフイン系ポリマーシートと非
架橋のポリオレフイン系ポリマーの薄いフイルム
を共押出して製造する方法の他に、前記非架橋ポ
リオレフイン系ポリマーの薄いフイルムを、シラ
ングラフト化ポリオレフインポリマーシートに圧
着ラミネートする方法などがある。 The silane-crosslinked polyolefin-based polymer sheet is produced by adding, for example, polyethylene, ethylene-propylene copolymer resin, ethylene-vinyl acetate copolymer resin, ethylene-ethyl acrylate resin, etc. singly or in a mixture of two or more, for example, vinyltrimethoxysilane, etc. Adding an organic silane compound and a free radical generator such as an organic peroxide,
These are reacted to produce a silane-grafted polyolefin polymer, and a predetermined amount of silanol condensation catalyst is added to this silane-grafted polyolefin polymer. Using this mixture, a conventional inflation method, T-die method, etc. It is made by extrusion molding the sheet body. A thin film of a non-crosslinked polyolefin resin, which is the same as or different from the silane-grafted polyolefin polymer, is formed on the silane-grafted polyolefin polymer sheet. In addition to a method of manufacturing by coextruding a thin film of a non-crosslinked polyolefin polymer, there is a method of pressure laminating a thin film of the non-crosslinked polyolefin polymer onto a silane-grafted polyolefin polymer sheet.
このようにして作つた複合シート上の前記非架
橋ポリオレフイン系ポリマーの薄いフイルムはシ
ラングラフト化もされていないし、シラノール縮
合触媒なども含有していない。而して作成した複
合シートを水分の雰囲気下に曝して架橋反応を生
起せしめて、基材シートとなす。 The thin film of the non-crosslinked polyolefin polymer on the composite sheet thus produced is neither silane grafted nor contains a silanol condensation catalyst. The thus prepared composite sheet is exposed to a moisture atmosphere to cause a crosslinking reaction, thereby forming a base sheet.
斯くして得られた基材シートを加熱しながら、
カレンダーロールに供給して、その非架橋ポリオ
レフイン系ポリマーの薄層側にゴム系粘着剤を貼
合する。この粘着剤の貼合に先立つて基材シート
の前記非架橋ポリオレフイン系樹脂の薄いフイル
ム面にコロナ処理を施してやれば、更にゴム系粘
着剤層との接着性は増大させ得る。 While heating the base sheet thus obtained,
The material is supplied to a calender roll, and a rubber adhesive is bonded to the thin layer side of the non-crosslinked polyolefin polymer. If the thin film surface of the non-crosslinked polyolefin resin of the base sheet is subjected to corona treatment prior to lamination of the adhesive, the adhesiveness with the rubber adhesive layer can be further increased.
以上の如くして得られる本考案の接着性テープ
は基材シートの主体をなすポリオレフイン系樹脂
がシラン架橋されているため、通常のポリオレフ
インの融点では軟化せず、従つて高温下での使用
に耐えるのは勿論、一方では該シラングラフト化
ポリオレフイン樹脂層の片面に形成した非架橋ポ
リオレフイン系ポリマーの薄層は全く架橋されて
いないため該層上に設けられたゴム系粘着剤層と
の貼合時に行なわれる基材シートの加熱処理によ
り容易に軟化し、ゴム系粘着剤層との接着が容易
かつ充分に行ない得る。従つて、本考案の接着性
テープにあつてはポリオレフイン系樹脂フイルム
とゴム系粘着剤層との剥れが全く起らず極めて優
れた特性を発揮する。 In the adhesive tape of the present invention obtained as described above, the polyolefin resin that is the main component of the base sheet is cross-linked with silane, so it does not soften at the melting point of ordinary polyolefins, and therefore cannot be used at high temperatures. On the other hand, since the thin layer of non-crosslinked polyolefin polymer formed on one side of the silane-grafted polyolefin resin layer is not cross-linked at all, it is difficult to bond with the rubber adhesive layer provided on the layer. It is easily softened by heat treatment of the base sheet, which is sometimes carried out, and can be easily and sufficiently bonded to the rubber adhesive layer. Therefore, the adhesive tape of the present invention exhibits extremely excellent properties without any peeling between the polyolefin resin film and the rubber adhesive layer.
次に本考案の一実施例を示す。(以下部とある
は何れも重量部を示すものである)
実施例
ポリエチレン100部に対してビニルメトキシシ
ラン2.0部ジクミルパーオキサイド0.18部の配合
比の組成物を約200℃の温度で押出機にて混練し、
ペレツト状のシラングラフト化ポリエチレンを得
た。次にこのペレツト95部に下記組成の混和物の
ペレツト5部を配合した。 Next, an embodiment of the present invention will be described. (All parts below refer to parts by weight.) Example A composition containing 2.0 parts of vinyl methoxysilane and 0.18 parts of dicumyl peroxide to 100 parts of polyethylene was extruded at a temperature of about 200°C. Knead with
Silane-grafted polyethylene in the form of pellets was obtained. Next, 5 parts of pellets of a mixture having the following composition were added to 95 parts of these pellets.
ポリエチレン 100部
ジブチル錫ジラウリレート 1部
老化防止剤 1部
而して調製した組成物をコモンヘツド方式のT
ダイ押出機に供給し、厚さ0.30mmのシラングラフ
ト化ポリエチレンシート上に厚さ0.03mmの非架橋
ポリエチレン薄層を押出し一体化した複合シート
を作成しこれを60℃の温水中に浸漬し、架橋せし
めた。 100 parts of polyethylene 1 part of dibutyltin dilaurylate 1 part of anti-aging agent
A composite sheet was created by feeding a die extruder and extruding a 0.03 mm thick non-crosslinked polyethylene thin layer onto a 0.30 mm thick silane-grafted polyethylene sheet, which was then immersed in 60℃ hot water. Cross-linked.
次に而して作成した複合シートの非架橋ポリエ
チレン薄層にコロナ放電処理を施したのち、この
複合シートを赤外線ヒーターにて加熱しながら前
記コロナ放電処理を施したポリエチレン薄層上に
別途調製した下記組成からなる粘着剤を0.30mm厚
に貼合して接着性テープを得た。 Next, the non-crosslinked polyethylene thin layer of the composite sheet thus created was subjected to a corona discharge treatment, and then, while heating this composite sheet with an infrared heater, a separately prepared layer was prepared on the polyethylene thin layer that had been subjected to the corona discharge treatment. An adhesive tape having the following composition was laminated to a thickness of 0.30 mm.
粘着剤組成 ブチルゴム 100部
ポリエチレン 55部
ポリイソブチレン 85部
軽 油 10部
老化防止剤 1.5部
カーボンブラツク 0.5部
比較のため、シラングラフト化ポリエチレンの
みからなる基材シート上に同一組成の粘着剤を
0.30mm厚に貼合させて比較用接着性テープを作つ
た。 Adhesive composition Butyl rubber 100 parts Polyethylene 55 parts Polyisobutylene 85 parts Light oil 10 parts Anti-aging agent 1.5 parts Carbon black 0.5 parts For comparison, an adhesive of the same composition was placed on a base sheet made only of silane-grafted polyethylene.
Comparative adhesive tapes were made by laminating them to a thickness of 0.30 mm.
而して作成した本考案接着性テープと比較用接
着性テープとをロール巻きした状態で60℃の恒温
槽に3ケ月保持した後および−30℃の低温にて48
時間保管し、同一温度にて巻戻しを行なつたが、
本考案品はいずれの場合においても異状なく巻戻
しができたが、比較品はしばしば粘着剤層と基材
シート間で剥離が発生した。 The adhesive tape of the present invention and the adhesive tape for comparison were kept in a constant temperature bath at 60°C for 3 months in a rolled state, and then at a low temperature of -30°C.
Although it was stored for several hours and rewound at the same temperature,
The product of the present invention could be rewound without any problems in any case, but the comparative product often experienced peeling between the adhesive layer and the base sheet.
図面は本考案接着性テープの断面説明図であ
る。
1……シラングラフト化ポリオレフイン系樹脂
層、2……ポリオレフイン系樹脂薄層、3……ゴ
ム系粘着剤層、4……基材シート。
The drawing is a cross-sectional view of the adhesive tape of the present invention. DESCRIPTION OF SYMBOLS 1... Silang-grafted polyolefin resin layer, 2... Polyolefin resin thin layer, 3... Rubber adhesive layer, 4... Base material sheet.
Claims (1)
層、他面が非架橋ポリオレフイン系ポリマー層で
ある基材シートの前記非架橋ポリオレフイン系ポ
リマー層面にゴム系粘着剤層を形成させたことを
特徴とする耐熱性接着性テープ。 A heat-resistant adhesive characterized in that a rubber adhesive layer is formed on the surface of the non-crosslinked polyolefin polymer layer of a base sheet having a silane crosslinked polyolefin polymer layer on one side and a non-crosslinked polyolefin polymer layer on the other side. tape.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1984001465U JPS60113345U (en) | 1984-01-10 | 1984-01-10 | heat resistant adhesive tape |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1984001465U JPS60113345U (en) | 1984-01-10 | 1984-01-10 | heat resistant adhesive tape |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS60113345U JPS60113345U (en) | 1985-07-31 |
JPH0143388Y2 true JPH0143388Y2 (en) | 1989-12-15 |
Family
ID=30474238
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1984001465U Granted JPS60113345U (en) | 1984-01-10 | 1984-01-10 | heat resistant adhesive tape |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS60113345U (en) |
-
1984
- 1984-01-10 JP JP1984001465U patent/JPS60113345U/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS60113345U (en) | 1985-07-31 |
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