JPH026578A - Self-fusing pressure-sensitive adhesive tape - Google Patents
Self-fusing pressure-sensitive adhesive tapeInfo
- Publication number
- JPH026578A JPH026578A JP63154888A JP15488888A JPH026578A JP H026578 A JPH026578 A JP H026578A JP 63154888 A JP63154888 A JP 63154888A JP 15488888 A JP15488888 A JP 15488888A JP H026578 A JPH026578 A JP H026578A
- Authority
- JP
- Japan
- Prior art keywords
- rubber
- parts
- tape
- pts
- uncrosslinked
- 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
Links
- 239000004820 Pressure-sensitive adhesive Substances 0.000 title 1
- 229920001971 elastomer Polymers 0.000 claims abstract description 47
- 239000005060 rubber Substances 0.000 claims abstract description 47
- 239000012790 adhesive layer Substances 0.000 claims abstract description 7
- 239000002985 plastic film Substances 0.000 claims abstract description 6
- 229920006255 plastic film Polymers 0.000 claims abstract description 6
- 239000002390 adhesive tape Substances 0.000 claims description 4
- 229920005549 butyl rubber Polymers 0.000 abstract description 9
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract description 8
- 239000000945 filler Substances 0.000 abstract description 8
- 239000000203 mixture Substances 0.000 abstract description 7
- 239000002245 particle Substances 0.000 abstract description 7
- -1 desirably Polymers 0.000 abstract description 5
- 244000043261 Hevea brasiliensis Species 0.000 abstract description 2
- 229920003052 natural elastomer Polymers 0.000 abstract description 2
- 229920001194 natural rubber Polymers 0.000 abstract description 2
- 239000010734 process oil Substances 0.000 abstract description 2
- 239000011248 coating agent Substances 0.000 abstract 2
- 238000000576 coating method Methods 0.000 abstract 2
- 239000000853 adhesive Substances 0.000 description 20
- 230000001070 adhesive effect Effects 0.000 description 20
- 239000010410 layer Substances 0.000 description 6
- 239000004800 polyvinyl chloride Substances 0.000 description 6
- 229920000915 polyvinyl chloride Polymers 0.000 description 6
- 239000006229 carbon black Substances 0.000 description 5
- 239000002344 surface layer Substances 0.000 description 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 239000012792 core layer Substances 0.000 description 3
- 238000005260 corrosion Methods 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 239000004014 plasticizer Substances 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 2
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 238000004898 kneading Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 229920001083 polybutene Polymers 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 238000004804 winding Methods 0.000 description 2
- 230000037303 wrinkles Effects 0.000 description 2
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical group N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 1
- 229920000181 Ethylene propylene rubber Polymers 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 241000872198 Serjania polyphylla Species 0.000 description 1
- 239000004902 Softening Agent Substances 0.000 description 1
- 229920006311 Urethane elastomer Polymers 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000011280 coal tar Substances 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 230000035882 stress Effects 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
Landscapes
- Adhesive Tapes (AREA)
Abstract
Description
【発明の詳細な説明】
本発明はプラスチックフィルムを支持体とし、これに未
架橋ゴム100重量部(以下単に部と言う)に架橋ゴム
5乃至100部を配合したことを特徴とした自己融着性
粘着テープζこ関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention uses a plastic film as a support, and is characterized in that 100 parts by weight of uncrosslinked rubber (hereinafter simply referred to as "parts") and 5 to 100 parts of crosslinked rubber are blended therein. This relates to adhesive tape.
自己融着性粘着テープは延伸して鉄管やケーブル等に巻
付けることによりテープの重り目(こ生ずるみず道が完
全につまり、物質の表面の微細な凹凸をうめ、表層部分
の水分の通過をなくすため、防食用テープ、絶縁用テー
プ等として感圧性テープより数段すぐれており、その用
途を徐々に拡大している。By stretching self-adhesive tape and wrapping it around iron pipes, cables, etc., the tape's weight lines (occurring grooves) are completely clogged, filling the minute irregularities on the surface of the material and preventing the passage of moisture on the surface layer. In order to eliminate corrosion, it is used as anti-corrosion tape, insulating tape, etc., which is far superior to pressure-sensitive tape, and its uses are gradually expanding.
通常用いられている自己融着性粘着テープはポリエチレ
ンフィルムlこ未架橋ゴムをフィルムより厚くコートし
たものであり、延伸しながら巻くことにより、防食や絶
縁の目的は達成するが、未架橋ゴムだけが用いられてい
るため、耐熱性に欠け、サイトスチックテレスコープ等
にすV)易く、フィルムとゴム粘着層との粘着力にも問
題がある。特開昭59−i60908号には架橋ゴムと
未架橋ゴムとを使用した絶縁性テープが記されている。The self-adhesive tape that is commonly used is a polyethylene film coated with uncrosslinked rubber thicker than the film, and by stretching and wrapping it, it achieves the purpose of corrosion protection and insulation, but only uncrosslinked rubber coats it. is used, it lacks heat resistance, is easily exposed to cytostick telescopes, etc., and there are also problems with the adhesive strength between the film and the rubber adhesive layer. JP-A-59-i60908 describes an insulating tape using crosslinked rubber and uncrosslinked rubber.
このテープは架橋ゴム80乃至120部に未架橋ゴム3
0乃至70部と架構ゴムの配合割合が多いのが特徴であ
る。そして架橋ゴムの配合割合が多い場合−船釣傾向と
してカレンダー離れが悪く、このため糊面に肌荒れが生
じ易く、フィルム面との接着が強過ぎるため巻き戻し力
が大きく、往々Iこして巻きはじめ部分がはがれ難くな
りこの部分が使用出来なくなる欠点がある。This tape consists of 80 to 120 parts of crosslinked rubber and 3 parts of uncrosslinked rubber.
It is characterized by a high blending ratio of frame rubber, ranging from 0 to 70 parts. When the blending ratio of cross-linked rubber is high, the calender separation tends to be poor due to the tendency of boat fishing, which tends to cause roughness on the adhesive surface, and the unwinding force is large because the adhesion to the film surface is too strong. There is a drawback that the part becomes difficult to peel off, making this part unusable.
これに反して本願のテープは、適度の割合の未架橋ゴム
と架橋ゴムを使用しているため、製造方法が容易でカレ
ンダー離れが良く、このため糊面は平滑で長期間経過し
ても巻き出しより巻き終りまで粘着力の変化が少く、耐
熱性にもすぐれ、テレスコープ、サイトスチックにもな
りにくいものである。以下、本発明を詳細に述べる。On the other hand, the tape of the present application uses an appropriate proportion of uncrosslinked rubber and crosslinked rubber, so it is easy to manufacture and has good calender release, so the adhesive surface is smooth and can be rolled even after a long period of time. There is little change in adhesive strength from the beginning to the end of winding, and it has excellent heat resistance, and is resistant to telescope and sight stick. The present invention will be described in detail below.
本発明のプラスチックフィルムは、ポリエチレン、ポリ
プロピレン、軟質ポリ塩化ビニル等の容易に延伸可能な
熱可塑性プラスチックのフィルムであって、その厚さは
、0.05 乃至0.25閣の範囲である。最も好まし
いのは軟質ポリ塩化ビニルのフィルムであって、このフ
ィルムは応力の増加に対して均一に伸びるため一定の延
伸率で巻き易(難燃性て強度にすぐれ、耐候性も良好で
ある。通常ポリ塩化ビニル樹脂100部に可塑剤60乃
至130部を配合したフィルムが用いられる。The plastic film of the present invention is a film of easily stretchable thermoplastic plastic such as polyethylene, polypropylene, flexible polyvinyl chloride, etc., and its thickness ranges from 0.05 to 0.25 mm. The most preferred is a soft polyvinyl chloride film, which stretches uniformly against increases in stress and is therefore easy to wind at a constant stretching rate (it is flame retardant, has excellent strength, and has good weather resistance). Usually, a film containing 100 parts of polyvinyl chloride resin and 60 to 130 parts of a plasticizer is used.
本発明は未架橋ゴム100部に架橋ゴム5乃至100部
を配合したことを特徴としたものであり、耐熱性が良好
でカレンダー離れが良く製造が容易である特徴を有する
ものである。そして好ましい範囲は未架橋ゴム100部
に対して架橋ゴム10乃至50部の範囲である。ゴム層
の厚さは通常フィルムより厚<0.1乃至3閣である。The present invention is characterized by blending 5 to 100 parts of crosslinked rubber with 100 parts of uncrosslinked rubber, and is characterized by good heat resistance, good calender release, and easy production. A preferable range is 10 to 50 parts of crosslinked rubber per 100 parts of uncrosslinked rubber. The thickness of the rubber layer is usually <0.1 to 3 times thicker than the film.
未架橋ゴム、架橋ゴムとして用いるゴムは、天然ゴム、
ブチルゴム、フタヂエン・スチレンゴム、エチレンプロ
ピレンゴム1ウレタンゴム等であり、好ましいのはブチ
ルゴムで耐老化性にすぐれている。本発明において架橋
ゴムとはゴムを架橋しているものであれば良いが、好ま
しいのは、ブチルゴムの架橋物であってゲル分率が通常
40乃至90%の範囲のものである。Rubbers used as uncrosslinked rubber and crosslinked rubber include natural rubber,
Examples include butyl rubber, phtadiene-styrene rubber, ethylene propylene rubber and urethane rubber, but butyl rubber is preferred because it has excellent aging resistance. In the present invention, the crosslinked rubber may be any crosslinked rubber, but preferred is a crosslinked butyl rubber with a gel fraction usually in the range of 40 to 90%.
本発明では未架橋ゴム100部に軟化剤5乃至200部
を用いる。使用する軟化剤はプロセスオイル、ポリブテ
ン、可塑斎bパラフィン、油脂類、コールタール等であ
り、好ましい範囲は20乃至100部である。軟質塩化
ビニルフィルムを使用する場合には、フィルム中の可塑
剤の移行を防ぐため未架橋ゴム100部に可塑剤10乃
至50部を用いる。In the present invention, 5 to 200 parts of a softener are used per 100 parts of uncrosslinked rubber. The softening agent used is process oil, polybutene, plastic paraffin, fats and oils, coal tar, etc., and the preferable range is 20 to 100 parts. When a soft vinyl chloride film is used, 10 to 50 parts of plasticizer is used per 100 parts of uncrosslinked rubber to prevent migration of the plasticizer in the film.
本発明では未架橋ゴム100部に充填剤40乃至300
部を用いる。使用する充填材は、ホワイトカーボン、カ
ーボンブラック、クレー硅礫土、メルク、炭酸カルシウ
ム等であり好ましい範囲は25乃至100部であり、好
ましい充填材は粒形の小さいホワイトカーボンおよびカ
ーボンブラックである。好ましい粒径の範囲は5mμ乃
至20μである。In the present invention, 40 to 300 parts of filler is added to 100 parts of uncrosslinked rubber.
Use part. The filler used is white carbon, carbon black, clay silica, Merck, calcium carbonate, etc., and the preferable range is 25 to 100 parts, and the preferable filler is white carbon and carbon black with small particles. The preferred particle size range is 5 mμ to 20μ.
未架橋ゴムに架橋ゴムを練り合せ均一で粘着面がきれい
な融着層をつくるには以下のような方法を取る。架橋ゴ
ムは未架橋ゴムに比べ粘度が高いため混りにくい、そこ
で架橋ゴムの粘度を下げるためロールなどにより薄通し
をし未架橋ゴムの粘度に近づける。しかし架橋ゴムのケ
ル分率が40%以上の物はなかなか粘度が下がらないの
で粒径の小さい、好ましい粒径は10mμ乃至1.00
0 mμの範囲である、ホワイトカーボン、カーボンブ
ラックを用いる。The following method is used to knead crosslinked rubber with uncrosslinked rubber to create a uniform adhesive layer with a clean adhesive surface. Crosslinked rubber has a higher viscosity than uncrosslinked rubber, so it is difficult to mix. Therefore, in order to lower the viscosity of crosslinked rubber, it is thinly rolled using a roll or the like to bring it closer to the viscosity of uncrosslinked rubber. However, if the crosslinked rubber has a Kel fraction of 40% or more, the viscosity does not decrease easily, so the particle size is small, and the preferable particle size is 10 mμ to 1.00 mμ.
White carbon and carbon black having a diameter of 0 mμ are used.
ゴム混和物が均−Iこならない場合には粘着面が凹凸の
サメ肌になり粘着力の低下巻き戻し力のバラツキ、テレ
スコープ等の原因となる。−例を述べると架橋ゴムを圧
延ロールの間隙を約1−としロール温度20乃至60C
で薄通しを10回行なう。次に未架橋ゴムと共に加圧ニ
ーグーで温度約145Cで5分間練り更に充填剤Φ軟化
剤を加えて同温度で15分練り粘着剤とする。If the rubber mixture is not uniformly coated, the adhesive surface will have an uneven surface, resulting in a decrease in adhesive strength, variations in unwinding force, telescoping, etc. - To give an example, crosslinked rubber is rolled with a gap of about 1 - and a roll temperature of 20 to 60C.
Perform thin threading 10 times. Next, the mixture is kneaded together with the uncrosslinked rubber in a pressurized kneading machine at a temperature of about 145C for 5 minutes, a filler and a softener Φ are added, and the mixture is kneaded at the same temperature for 15 minutes to form an adhesive.
カーボンブラック、ホワイトカーボンなど細い粒子の充
填剤を多量に加えるとムーニー粘度は低いがフローは少
くサイドスナック、テレスコープなどの防止にも役立つ
。Adding a large amount of fine particle filler such as carbon black or white carbon will lower Mooney viscosity, but will also reduce flow and help prevent side snacking and telescoping.
粘着剤のプラスチックフィルムへのトッピングは通常カ
レンダーロールで行なわれる、3本ロールのカレンダー
を用いた場合のロール温度は上ロール50乃至140C
,中ロール50乃至110C1下ロール5乃至60tl
’で容易に製造可能であり、粘着剤はロール、ニーダ−
等によってあらかじめ、90乃至130Cに加熱してお
いて、カレンダーに供給する。上ロールの温度は50C
以下では中ロールへの転写ができづ140C以上ではフ
ィルムが伸びたりしわがよったりする。Topping of the adhesive onto the plastic film is usually done using a calender roll. When using a three-roll calender, the roll temperature is 50 to 140 C for the upper roll.
, middle roll 50~110C1 lower roll 5~60tl
The adhesive can be easily manufactured using rolls, kneaders, etc.
It is heated in advance to 90 to 130C by a method such as the above method, and then supplied to a calender. The temperature of the upper roll is 50C
If it is less than 140C, the film cannot be transferred to the medium roll, and if it is more than 140C, the film will stretch or wrinkle.
中ロールの温度は50tl’より低いとロールより粘着
剤が離れに<<110t:’以上の場合にはフィルムが
伸びたり、しわがよったりする。If the temperature of the middle roll is lower than 50 tl', the adhesive will separate from the roll; if it is higher than <<110 tl', the film will stretch or wrinkle.
下ロールの益度は6Or以上ではフィルムが伸びる、こ
のようにして製造されたテープは粘着剤層が均一で表面
が平滑になり粘着力のバラツキが少なく巻き戻し力が巻
き始めから終りまで一定である特徴がある。4本ロール
カレンダーを用いた場合は、横ロールは上ロールより回
転を遅くし温度を上ロールより10Cぐらい高くするの
が好ましく他のロールは3本ロールカレンダーと同条件
で良い。The film stretches when the bottom roll is over 6 Or. Tapes manufactured in this way have a uniform adhesive layer and a smooth surface, and there is little variation in adhesive strength, and the unwinding force is constant from the beginning to the end of the winding. It has certain characteristics. When a four-roll calender is used, it is preferable that the rotation of the side roll is slower than that of the upper roll and the temperature thereof is about 10 C higher than that of the upper roll, and the other rolls may be kept under the same conditions as the three-roll calender.
次で本発明の実施例を述べる。Next, embodiments of the present invention will be described.
実施例1゜
平均重合度1.100のポリ塩化ビニル樹脂100部ジ
オクチルフタレート45部充填剤22部安定剤4部を均
一に混練し、カレンダーによって圧延し、0.171a
11のフィルムとした。架橋ブチルゴム(ゲル分率80
%)ヲロールf1度2Orロール間隙11111で薄通
しを10回行ない、未架橋ブチルゴムのムーニー粘度(
1ooCML1+a)45に近いムーニー粘度48にし
た。次に第1表の配合割合で未架橋ブチルゴムに粒径2
5mμのカーボンブラックを加え、加圧ニーダ−にて1
45Cで5分間練った次にクレー粒径15mμのホワイ
トカーボン、ジオクチルフタレート、ポリブテン、テル
ペン樹脂を加え15分間混練した。得られた粘着剤は均
一で適度の性質を有するものであった。上記の塩化ビニ
ルフィルム及び粘着剤を用い3本ロールカレンダーで上
ロール、中ロール、下ロール、益度夫々12Or。Example 1 100 parts of a polyvinyl chloride resin with an average degree of polymerization of 1.100, 45 parts of dioctyl phthalate, 22 parts of a filler, and 4 parts of a stabilizer were uniformly kneaded and rolled in a calender to obtain a 0.171a
No. 11 film was used. Cross-linked butyl rubber (gel fraction 80
%) The Mooney viscosity of uncrosslinked butyl rubber (
1ooCML1+a) The Mooney viscosity was set to 48, which is close to 45. Next, add particle size 2 to uncrosslinked butyl rubber at the blending ratio shown in Table 1.
Add 5 mμ of carbon black and mix with a pressure kneader.
After kneading at 45C for 5 minutes, white carbon having a clay particle size of 15 mμ, dioctyl phthalate, polybutene, and terpene resin were added and kneaded for 15 minutes. The resulting adhesive was uniform and had appropriate properties. Using the above vinyl chloride film and adhesive, the upper roll, middle roll, and lower roll were heated to 12 Or each using a three-roll calender.
90r及び20Cでトッピングした。糊厚は0、53
mとしたが、粘着剤のカレンダー離れは極めて良好で、
糊面が平滑で粘着性が良好なテープが得られた。Topped with 90r and 20c. Glue thickness is 0.53
m, but the release of the adhesive from the calendar was extremely good.
A tape with a smooth adhesive surface and good adhesiveness was obtained.
実施例2゜
実施例1.で得られたテープを水道管上に1/2ラツグ
で巻付けこの両端を封じたものを水中に入れ3ケ月浸漬
した。取り出してテープをほどいた鉄管はみず道が完全
に止まり表面の凹凸をふさいでおり全く錆びが認められ
ず、水の入った形跡は全(認められなかった。Example 2゜Example 1. The tape obtained in step 1 was wrapped around a water pipe with a 1/2 lug, both ends of which were sealed, and the tape was placed in water and immersed for 3 months. When the iron pipe was removed and the tape was untied, the water flow had completely stopped and the irregularities on the surface were covered, and no rust was observed at all, and there was no evidence of water entering the pipe.
実施例6゜
実施例1.で得られたテープを市販のポリ塩化ビニル自
己融着性テープと比較試験した。Example 6゜Example 1. The resulting tape was tested in comparison with a commercially available polyvinyl chloride self-bonding tape.
結果は次の通りであった。The results were as follows.
(1) テレスコープ
本発明のテープと市販のポリ塩化ビニル自己融着性テー
プを4011’で48時間加熱した。(1) Telescope The tape of the present invention and a commercially available polyvinyl chloride self-fusing tape were heated at 4011' for 48 hours.
本発明のテープはテレスコープを認められなかったのに
対し市販品は5閣のテレスコープを示した。The tape of the present invention showed no telescope, whereas the commercially available product showed five cabinets of telescope.
(2)巻き戻し力
2種類のテープの表層、中層、芯部層から試料をとり3
00M/分の速度で巻き戻し力を測定した。(2) Take samples from the surface layer, middle layer, and core layer of two types of tapes with unwinding force.
The unwinding force was measured at a speed of 00 M/min.
結果は次の如くであった。The results were as follows.
本願のテープ 市販のテープ
表層1.024/25m 1.21Kg/25m中
層 1.10Kf/258 1.55KF/25mm
芯部層 1.05Kf/259 2.15釉/2511
Im結果は本願のテープが始めから終り迄、はぼ均一な
巻き戻し力を示したのに対し、市販のテープは窓側に近
くなるにつれて極めて重くなり、芯に接している一部分
は殆んどはかれないものであった。Tape of this application Commercially available tape surface layer 1.024/25m 1.21Kg/25m
Layer 1.10Kf/258 1.55KF/25mm
Core layer 1.05Kf/259 2.15 glaze/2511
Im results showed that the tape of the present application showed a fairly uniform unwinding force from the beginning to the end, whereas the commercially available tape became extremely heavy as it approached the window, and the part in contact with the core had almost no unwinding force. It was something that would never happen.
(3) 自背面粘着力
二種類のテープの自背面粘着力を測定した結果は次の通
りであった。(3) Self-back adhesive strength The self-back adhesive strength of two types of tapes was measured and the results were as follows.
本願のテープ 市販のテープ
表層1.00即/25謹0.85即/25■中 層
1.05に9/25■ 1.10即/25閤芯部層
1.05Kg/25■ 1.84Kg/25mこのよう
に本願のテープは表層、中層、芯部層と殆んど均一な粘
着力であるのに対し、市販のテープは場所によるバラツ
キの大きいものであった。Tape of the present application Commercially available tape Surface layer 1.00 instant/25cm 0.85 instant/25■ middle layer
1.05 to 9/25■ 1.10 immediately/25 core part layer
1.05Kg/25■ 1.84Kg/25m In this way, the tape of this application has almost uniform adhesive strength in the surface layer, middle layer, and core layer, whereas commercially available tapes have large variations in adhesive strength depending on the location. there were.
Claims (1)
着層は未架橋ゴム100重量部に架橋ゴム5乃至100
重量部を配合したことを特徴とした自己融着性粘着テー
プConsisting of a plastic film and a rubber adhesive layer, the rubber adhesive layer contains 100 parts by weight of uncrosslinked rubber and 5 to 100 parts by weight of crosslinked rubber.
Self-adhesive tape characterized by containing parts by weight
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP63154888A JPH026578A (en) | 1988-06-24 | 1988-06-24 | Self-fusing pressure-sensitive adhesive tape |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP63154888A JPH026578A (en) | 1988-06-24 | 1988-06-24 | Self-fusing pressure-sensitive adhesive tape |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH026578A true JPH026578A (en) | 1990-01-10 |
Family
ID=15594151
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP63154888A Pending JPH026578A (en) | 1988-06-24 | 1988-06-24 | Self-fusing pressure-sensitive adhesive tape |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH026578A (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0726219A (en) * | 1993-07-16 | 1995-01-27 | Sliontec:Kk | Biodegradable self-adhesive composition and self-adhesive tape or sheet prepared therefrom |
| KR100341210B1 (en) * | 1999-10-18 | 2002-06-20 | 이철호 | Method of self-amalgamating insulation tape and insulation tape thereof |
| KR100785876B1 (en) * | 2006-09-26 | 2007-12-14 | 플러버테크 주식회사 | Heat Sealing Device for Rubber Sheet |
| US8604124B2 (en) * | 2003-06-19 | 2013-12-10 | Nitto Denko Corporation | Rubber-based pressure-sensitive adhesive composition and pressure-sensitive adhesive sheet of the same |
| JP2018178008A (en) * | 2017-04-17 | 2018-11-15 | 矢崎総業株式会社 | Adhesive composition, adhesive resin tape and wire harness |
-
1988
- 1988-06-24 JP JP63154888A patent/JPH026578A/en active Pending
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0726219A (en) * | 1993-07-16 | 1995-01-27 | Sliontec:Kk | Biodegradable self-adhesive composition and self-adhesive tape or sheet prepared therefrom |
| KR100341210B1 (en) * | 1999-10-18 | 2002-06-20 | 이철호 | Method of self-amalgamating insulation tape and insulation tape thereof |
| US8604124B2 (en) * | 2003-06-19 | 2013-12-10 | Nitto Denko Corporation | Rubber-based pressure-sensitive adhesive composition and pressure-sensitive adhesive sheet of the same |
| KR100785876B1 (en) * | 2006-09-26 | 2007-12-14 | 플러버테크 주식회사 | Heat Sealing Device for Rubber Sheet |
| JP2018178008A (en) * | 2017-04-17 | 2018-11-15 | 矢崎総業株式会社 | Adhesive composition, adhesive resin tape and wire harness |
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