JP2003305079A - Adhesive tape - Google Patents
Adhesive tapeInfo
- Publication number
- JP2003305079A JP2003305079A JP2002115223A JP2002115223A JP2003305079A JP 2003305079 A JP2003305079 A JP 2003305079A JP 2002115223 A JP2002115223 A JP 2002115223A JP 2002115223 A JP2002115223 A JP 2002115223A JP 2003305079 A JP2003305079 A JP 2003305079A
- Authority
- JP
- Japan
- Prior art keywords
- adhesive tape
- sensitive adhesive
- pressure
- polyethylene
- film
- 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
- 239000002390 adhesive tape Substances 0.000 title claims abstract description 14
- 239000000203 mixture Substances 0.000 claims abstract description 22
- -1 polyethylene Polymers 0.000 claims abstract description 19
- 239000011256 inorganic filler Substances 0.000 claims abstract description 17
- 229910003475 inorganic filler Inorganic materials 0.000 claims abstract description 17
- 239000004698 Polyethylene Substances 0.000 claims abstract description 15
- 229920000573 polyethylene Polymers 0.000 claims abstract description 15
- 239000000758 substrate Substances 0.000 claims abstract description 15
- 229920000092 linear low density polyethylene Polymers 0.000 claims abstract description 7
- 239000004707 linear low-density polyethylene Substances 0.000 claims abstract description 7
- 229920001684 low density polyethylene Polymers 0.000 claims abstract description 6
- 239000004702 low-density polyethylene Substances 0.000 claims abstract description 6
- 239000004820 Pressure-sensitive adhesive Substances 0.000 claims description 25
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 17
- 239000010410 layer Substances 0.000 claims description 8
- 239000000377 silicon dioxide Substances 0.000 claims description 8
- 235000012239 silicon dioxide Nutrition 0.000 claims description 7
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 5
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 3
- 239000011707 mineral Substances 0.000 claims description 3
- 230000035699 permeability Effects 0.000 abstract description 21
- 238000000034 method Methods 0.000 abstract description 13
- 239000003522 acrylic cement Substances 0.000 abstract description 3
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 210000004369 blood Anatomy 0.000 description 10
- 239000008280 blood Substances 0.000 description 10
- 239000000853 adhesive Substances 0.000 description 8
- 230000001070 adhesive effect Effects 0.000 description 8
- 239000003431 cross linking reagent Substances 0.000 description 7
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 6
- 239000002734 clay mineral Substances 0.000 description 5
- 238000010828 elution Methods 0.000 description 5
- 239000012948 isocyanate Substances 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 150000002513 isocyanates Chemical class 0.000 description 4
- 229910000019 calcium carbonate Inorganic materials 0.000 description 3
- 238000009826 distribution Methods 0.000 description 3
- 238000005194 fractionation Methods 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 239000011505 plaster Substances 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 230000001737 promoting effect Effects 0.000 description 3
- 229920003002 synthetic resin Polymers 0.000 description 3
- 239000000057 synthetic resin Substances 0.000 description 3
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 3
- FKTHNVSLHLHISI-UHFFFAOYSA-N 1,2-bis(isocyanatomethyl)benzene Chemical compound O=C=NCC1=CC=CC=C1CN=C=O FKTHNVSLHLHISI-UHFFFAOYSA-N 0.000 description 2
- RFFLAFLAYFXFSW-UHFFFAOYSA-N 1,2-dichlorobenzene Chemical compound ClC1=CC=CC=C1Cl RFFLAFLAYFXFSW-UHFFFAOYSA-N 0.000 description 2
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 2
- 239000005995 Aluminium silicate Substances 0.000 description 2
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 2
- 235000012211 aluminium silicate Nutrition 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- 230000023555 blood coagulation Effects 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 2
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000004745 nonwoven fabric Substances 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 1
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 1
- NOWKCMXCCJGMRR-UHFFFAOYSA-N Aziridine Chemical compound C1CN1 NOWKCMXCCJGMRR-UHFFFAOYSA-N 0.000 description 1
- 102100022210 COX assembly mitochondrial protein 2 homolog Human genes 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- 101000900446 Homo sapiens COX assembly mitochondrial protein 2 homolog Proteins 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 229910004298 SiO 2 Inorganic materials 0.000 description 1
- 206010040880 Skin irritation Diseases 0.000 description 1
- 229910010413 TiO 2 Inorganic materials 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- 239000012790 adhesive layer Substances 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 210000001124 body fluid Anatomy 0.000 description 1
- 239000010839 body fluid Substances 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 239000013522 chelant Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 230000015271 coagulation Effects 0.000 description 1
- 238000005345 coagulation Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000005553 drilling Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 1
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 239000012466 permeate Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 239000005056 polyisocyanate Substances 0.000 description 1
- 229920001228 polyisocyanate Polymers 0.000 description 1
- 229920006389 polyphenyl polymer Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 238000012805 post-processing Methods 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 230000036556 skin irritation Effects 0.000 description 1
- 231100000475 skin irritation Toxicity 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 239000012756 surface treatment agent Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Materials For Medical Uses (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、通気性を必要とさ
れる用途に用いられる通気性に優れた粘着テープに関す
る。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a pressure-sensitive adhesive tape having excellent air permeability, which is used for applications requiring air permeability.
【0002】[0002]
【従来の技術】従来より、皮膚に貼付して使用する医療
用粘着テープには、皮膚のかぶれや蒸れ等を防止する目
的で通気性が要求されており、種々の検討がなされてい
る。例えば、テープの基材として不織布や布等の通気性
に優れた基材を用いる方法、あるいは、合成樹脂フィル
ムを基材として用いる絆創膏等では、基材自体に通気性
がないので、後工程による穿孔等により通気性を付与す
る方法等が行われている。しかしながら、不織布や布等
を基材として用いた場合には、一定量の粘着剤を均一に
塗布するのが困難であり、またこのような粘着テープは
強度が必要な絆創膏等には適していない。一方、合成樹
脂フィルムを基材として用い、後加工による穿孔等によ
る場合は、孔を一定の大きさ以上に小さくするのが困難
なため孔から血液や体液が漏れて衣類等へ付着して問題
になったり、穿孔という工程が必要になりコスト的にも
不利であった。2. Description of the Related Art Conventionally, medical adhesive tapes to be applied to the skin have been required to have breathability for the purpose of preventing skin irritation and stuffiness, and various studies have been made. For example, in a method of using a highly breathable substrate such as a non-woven fabric or a cloth as the substrate of the tape, or in a bandage using a synthetic resin film as the substrate, since the substrate itself does not have air permeability, A method of providing air permeability by perforation or the like is performed. However, when a non-woven fabric or cloth is used as a base material, it is difficult to uniformly apply a certain amount of the pressure-sensitive adhesive, and such pressure-sensitive adhesive tape is not suitable for adhesive plasters or the like that require strength. . On the other hand, when a synthetic resin film is used as a base material and it is perforated by post-processing, it is difficult to make the holes smaller than a certain size, so blood or body fluid leaks from the holes and adheres to clothing etc. However, it is disadvantageous in terms of cost because it requires a step of drilling.
【0003】[0003]
【発明が解決しようとする課題】本発明は上記従来の問
題点を解消し、後工程が不要で、実用的な通気性に優れ
た粘着テープを提供することを目的とする。SUMMARY OF THE INVENTION It is an object of the present invention to solve the above-mentioned problems of the prior art and to provide a pressure-sensitive adhesive tape which is practically excellent in breathability and requires no post-process.
【0004】[0004]
【課題を解決するための手段】本発明の粘着テープは、
直鎖状低密度ポリエチレン及び低密度ポリエチレンとか
らなるポリエチレン系混合物30〜50wt%と、無機
充填剤50〜70wt%からなる混合物を溶融成膜した
後、得られた未延伸フィルムを一軸もしくは二軸に延伸
して得られる微多孔フィルム基材にアクリル系粘着剤層
が積層された粘着テープである。The adhesive tape of the present invention comprises:
After melt-forming a mixture of 30 to 50 wt% of a polyethylene-based mixture of linear low-density polyethylene and low-density polyethylene and 50 to 70 wt% of an inorganic filler, the resulting unstretched film is uniaxially or biaxially It is an adhesive tape in which an acrylic adhesive layer is laminated on a microporous film substrate obtained by stretching.
【0005】本発明の粘着テープの微多孔フィルム基材
に用いられるポリエチレン系混合物は、直鎖状低密度ポ
リエチレン及び低密度ポリエチレンとからなるポリエチ
レン系混合物であれば特に限定されないが、クロス分別
法により測定した溶出量が40〜60℃で15〜25w
t%、60〜80℃で45〜55wt%、80〜100
℃で20〜35wt%であるポリエチレン系混合物であ
ることが好ましい。40〜60℃での溶出量が15wt
%より少ないと成形性、延伸加工性が低下し十分な通気
性が得られなくなる恐れがあり、25wt%を超える場
合には成形性と同時にできたフィルムの機械的強度が低
下する恐れがある。また、60〜80℃での溶出量が4
5wt%未満の場合は成形性が不十分であるのと同時
に、フィルムの柔軟性が不足し強度が不足する恐れがあ
り、55wt%を超えた場合には延伸加工性が低下し、
十分に通気性が得られない恐れがある。また、80〜1
00℃での溶出量が20wt%未満の場合には、十分な
延伸加工性が得られず通気性が十分に得られない恐れが
あり、35wt%を超えた場合には、延伸加工性が悪く
なり、かつ柔軟性が不足するためにフィルムの強度が足
りなくなる恐れがある。通気性が十分に得られない恐れ
がある。The polyethylene-based mixture used for the microporous film substrate of the pressure-sensitive adhesive tape of the present invention is not particularly limited as long as it is a polyethylene-based mixture consisting of linear low-density polyethylene and low-density polyethylene. Measured elution amount is 15-25w at 40-60 ° C
t%, 45 to 55 wt% at 60 to 80 ° C., 80 to 100
It is preferably a polyethylene-based mixture that is 20 to 35 wt% at a temperature of ° C. Elution amount at 40-60 ° C is 15wt
If it is less than 25% by weight, moldability and stretching processability may be deteriorated and sufficient air permeability may not be obtained, and if it exceeds 25% by weight, mechanical properties of the film formed at the same time as moldability may be deteriorated. Also, the elution amount at 60 to 80 ° C is 4
If it is less than 5 wt%, the moldability is insufficient, and at the same time, the flexibility and strength of the film may be insufficient, and if it exceeds 55 wt%, the stretch processability is deteriorated.
There is a risk that it will not have sufficient breathability. Also, 80-1
If the elution amount at 00 ° C is less than 20 wt%, sufficient stretchability may not be obtained and sufficient air permeability may not be obtained, and if it exceeds 35 wt%, stretchability is poor. In addition, there is a risk that the strength of the film will be insufficient due to lack of flexibility. There is a risk that the air permeability will not be sufficient.
【0006】なお、本発明で用いたクロス分別法による
樹脂の溶出量は以下のようにして測定された値である。
ポリエチレン系混合物をまず140℃あるいは完全に溶
解する温度のo−ジクロロベンゼンに溶解し、一定速度
で冷却し、予め用意した不活性担体表面に薄いポリマー
層を結晶性の高い順および分子量の高い順に生成させ
る。次に、この生成したポリマー層を連続または段階的
に昇温し、順次溶出した成分の濃度を検出し、その組成
分布(結晶性分布)を測定する温度上昇溶離分別と同時
に、その成分について高温型GPCにより分子量および
分子量分布を測定する。本発明では、上記の温度上昇溶
離分別部分と高温型GPC部分とをシステムとして備え
ているクロス分別クロマトグラフ装置(CFC−T15
0A型:三菱化学社製)を使用して測定した。The amount of resin eluted by the cross fractionation method used in the present invention is a value measured as follows.
The polyethylene-based mixture is first dissolved in o-dichlorobenzene at 140 ° C or a temperature at which it is completely dissolved, cooled at a constant rate, and thin polymer layers are formed on the surface of an inert carrier prepared in advance in order of increasing crystallinity and increasing molecular weight. To generate. Next, the generated polymer layer is heated continuously or stepwise, the concentration of the eluted components is detected in sequence, and the composition distribution (crystallinity distribution) is measured. The molecular weight and the molecular weight distribution are measured by GPC type. In the present invention, a cross fractionation chromatograph device (CFC-T15) equipped with the above-mentioned temperature rising elution fractionation part and high temperature type GPC part as a system.
OA type: manufactured by Mitsubishi Chemical Co., Ltd.).
【0007】本発明の粘着テープの微多孔フィルム基材
に使用される無機充填剤としては、特に限定されるもの
ではなく、炭酸カルシウム、硫酸バリウム、タルク、ク
レイ、珪藻土、シリカ等が好適に用いられ、特に好まし
くは炭酸カルシウムである。また、無機充填剤はポリエ
チレン系混合物への分散性を向上させるために、カップ
リング剤、脂肪酸やその金属塩等の表面処理剤で表面処
理されていることが好ましい。The inorganic filler used for the microporous film substrate of the pressure-sensitive adhesive tape of the present invention is not particularly limited, and calcium carbonate, barium sulfate, talc, clay, diatomaceous earth, silica and the like are preferably used. And particularly preferably calcium carbonate. Further, the inorganic filler is preferably surface-treated with a surface treatment agent such as a coupling agent, a fatty acid or a metal salt thereof in order to improve dispersibility in the polyethylene-based mixture.
【0008】微多孔フィルム基材中における、ポリエチ
レン系混合物と無機充填剤比率は、ポリエチレン系混合
物が30〜50wt%で、無機充填剤が50〜70wt
%である。無機充填剤の量が50wt%未満であると延
伸後に高い十分な通気性が得られず、70wt%より多
いと、フィルムが脆くなり強度が不足すると同時に、成
膜時にフィルム切れ、ドローレゾナンス(延展ムラ)が
発生して成膜性が悪くなり、良好な微多孔フィルム基材
フィルムが得られない。The ratio of the polyethylene mixture to the inorganic filler in the microporous film substrate is 30 to 50 wt% of the polyethylene mixture and 50 to 70 wt% of the inorganic filler.
%. If the amount of the inorganic filler is less than 50% by weight, high sufficient air permeability cannot be obtained after stretching, and if it exceeds 70% by weight, the film becomes brittle and lacks strength, and at the same time, the film breaks during film formation and draw resonance (extension). Unevenness occurs and the film formability deteriorates, and a good microporous film substrate film cannot be obtained.
【0009】本発明においては、上記の無機充填剤とし
て、二酸化珪素を主成分とする粘度鉱物を1〜30wt
%含有する無機充填剤を使用するのが好ましい。二酸化
珪素を主成分とする粘土鉱物とは、二酸化珪素SiO2
を40wt%以上含み、酸化アルミニウム(Al2O3)
、酸化チタン(TiO2)酸化鉄(Fe2O3)等の酸化
金属を含有する天然鉱産物であり、具体的には、例え
ば、カオリンやベントナイト等の各種クレイがあげられ
る。これら粘度鉱物は血液の凝固を促進させ、微細孔か
らの血液もれを防止する効果があるので、絆創膏等に用
いた場合、通気性が良好であり、且つ、血液が絆創膏等
から滲み出して衣服に付着する等の問題が解決される。
二酸化珪素を主成分とする粘度鉱物は、熱処理、表面処
理、粒子径等に関しては、血液凝固促進機能を有してい
れば、特に限定はされないが、フィルムの強度、生産性
等を考慮すると平均粒子径が5μm以下と細かく、含有
水分量が1%以下のものが好ましい。無機充填剤中にお
ける二酸化珪素を主成分とする粘土鉱物の量は1〜30
wt%が好ましい。1wt%未満であると血液凝固促進
機能が不十分となる可能性があり、30wt%を超える
と、成膜性が低下したり、フィルムの強度、柔軟性が不
十分になる恐れがある。In the present invention, as the above-mentioned inorganic filler, 1 to 30 wt% of a clay mineral containing silicon dioxide as a main component is used.
% Inorganic fillers are preferably used. The clay mineral containing silicon dioxide as a main component means silicon dioxide SiO 2
Containing 40 wt% or more of aluminum oxide (Al 2 O 3 )
, Titanium oxide (TiO 2 ), iron oxide (Fe 2 O 3 ) and other metal oxide-containing natural mineral products. Specific examples include various clays such as kaolin and bentonite. These clay minerals have the effect of promoting the coagulation of blood and preventing blood leakage from micropores, so when used in a plaster or the like, the air permeability is good, and blood seeps out from the plaster or the like. Problems such as adhesion to clothes are solved.
The viscous mineral containing silicon dioxide as a main component is not particularly limited in terms of heat treatment, surface treatment, particle size, etc. as long as it has a blood coagulation promoting function, but it is an average considering film strength, productivity, etc. Fine particles having a particle size of 5 μm or less and a water content of 1% or less are preferable. The amount of the clay mineral containing silicon dioxide as a main component in the inorganic filler is 1 to 30.
wt% is preferred. If it is less than 1 wt%, the blood coagulation promoting function may be insufficient, and if it exceeds 30 wt%, the film-forming property may be lowered, or the strength and flexibility of the film may be insufficient.
【0010】微多孔フィルム基材は、上記ポリエチレン
系混合物及び無機充填剤をフィルム状に成形し、次に延
伸することにより得られる。フィルム状に成形する方法
としては特に限定されないが、薄肉化という観点からT
ダイによる成形方法が好ましい。更に、延伸方法として
は一軸延伸、二軸延伸のどちらの方法でも良い。当該微
多孔フィルム基材は、フィルム延伸過程でポリエチレン
系混合物と無機充填剤の界面を剥離させて開孔し、通気
性を発現させるものであるので、無機充填剤含有量の増
加、及び延伸倍率の拡大により、通気性を向上させるこ
とができる。高い通気性を得る為には、延伸倍率2.0
倍以上が好ましいが、開孔度の向上とともに、血液漏れ
の可能性が高くなる為、血液凝固促進機能を有する二酸
化珪素を主成分とする粘土鉱物が1〜30wt%含有さ
れた無機充填剤を使用するのが好ましい。The microporous film substrate is obtained by forming the above-mentioned polyethylene mixture and inorganic filler into a film and then stretching. The method of forming into a film is not particularly limited, but from the viewpoint of thinning, T
A molding method using a die is preferable. Furthermore, the stretching method may be either uniaxial stretching or biaxial stretching. Since the microporous film substrate is one in which the interface between the polyethylene-based mixture and the inorganic filler is peeled and opened in the film stretching process to develop air permeability, an increase in the content of the inorganic filler, and a stretching ratio. The air permeability can be improved by enlarging. To obtain high air permeability, draw ratio 2.0
Although it is preferably double or more, an inorganic filler containing 1 to 30 wt% of a clay mineral containing silicon dioxide as a main component having a blood coagulation-promoting function is included because the possibility of blood leakage increases as the porosity increases. Preference is given to using.
【0011】絆創膏等として用いられる粘着テープに
は、皮膚面の湿気を速やかに排出する性能が要求され
る。そのために通常はJIS P 8117に規定され
る「紙及び板紙の透気度試験方法」により測定された透
気度が100秒以下であることが好ましい。The adhesive tape used as a plaster or the like is required to have the ability to quickly remove moisture on the skin surface. Therefore, it is usually preferable that the air permeability measured by the “air permeability test method for paper and board” defined in JIS P 8117 is 100 seconds or less.
【0012】本発明の粘着テープにはアクリル系粘着剤
が使用される。アクリル系粘着剤は、一般に粘着力が強
く粘着剤の性質を必要に応じて設計することが容易であ
り、また架橋剤を用いて架橋させることにより、更に品
質設計が容易であるからである。粘着剤の固形分濃度、
粘度等は特に限定されず、要求性能、製造工程に合わせ
て適宜決定されて良い。上記アクリル系粘着剤層は、乾
燥後の厚さが20〜100μmであることが好ましく、
更に好ましくは、35〜75μmである。An acrylic adhesive is used in the adhesive tape of the present invention. This is because the acrylic pressure-sensitive adhesive generally has a strong adhesive force, and it is easy to design the properties of the pressure-sensitive adhesive as needed, and the quality can be further easily designed by crosslinking with a crosslinking agent. Solid content of adhesive,
The viscosity and the like are not particularly limited and may be appropriately determined according to the required performance and the manufacturing process. The acrylic pressure-sensitive adhesive layer preferably has a thickness after drying of 20 to 100 μm,
More preferably, it is 35 to 75 μm.
【0013】上記架橋剤は、粘着剤の凝集力を高めかつ
被接着物への接着保持力を向上させる役割を果たす。架
橋剤としては、イソシアネート系、アジリジン系、エポ
キシ系、金属キレート系、メラミン系、変性イソシアネ
ート系等が挙げられる。これらの内イソシアネート系架
橋剤が好適に用いられ、少なくとも2以上のイソシアネ
ート基を有する多官能性イソシアネート化合物がより好
ましい。具体的には、例えば、トリレンジイソシアネー
ト(TDI)、ジフェニルメタンジイソシアネート(M
DI)、トルイジンジイソシアネート(TODI)、キ
シリレンジイソシアネート(XDI)、ヘキサメチレン
ジイソシアネート(HMDI)、トリメチロールプロパ
ン(TMP)−TDI付加物、多官能性芳香族ポリイソ
シアネート(TDI重合体等)、ポリメチレンポリフェ
ニルイソシアネート等及びこれらの部分変性体が挙げら
れる。架橋剤の量は、粘着剤100重量部に対して0.
5〜10重量部添加することが好ましい。The cross-linking agent plays a role of increasing the cohesive force of the pressure-sensitive adhesive and improving the adhesive holding force to the adherend. Examples of the crosslinking agent include isocyanate type, aziridine type, epoxy type, metal chelate type, melamine type and modified isocyanate type. Of these, isocyanate crosslinking agents are preferably used, and polyfunctional isocyanate compounds having at least two or more isocyanate groups are more preferable. Specifically, for example, tolylene diisocyanate (TDI), diphenylmethane diisocyanate (M
DI), toluidine diisocyanate (TODI), xylylene diisocyanate (XDI), hexamethylene diisocyanate (HMDI), trimethylolpropane (TMP) -TDI adduct, polyfunctional aromatic polyisocyanate (TDI polymer, etc.), polymethylene Examples include polyphenyl isocyanate and the like, and partially modified products thereof. The amount of the cross-linking agent was 0.
It is preferable to add 5 to 10 parts by weight.
【0014】上記粘着剤には必要に応じて、更に、粘着
付与剤、可塑剤、酸化防止剤、着色剤、保存剤等が添加
されても良い。If necessary, a tackifier, a plasticizer, an antioxidant, a coloring agent, a preservative and the like may be added to the above-mentioned pressure-sensitive adhesive.
【0015】本発明の粘着テープは、通常、微多孔性フ
ィルム/粘着剤層/離型シートの3層構造として供給さ
れる。上記離型シートとしては、特に限定されず、当該
分野に使用し得るものから適宜選択されて用いられる。
具体的には、例えば、シリコーン塗布紙、シリコーン塗
布フィルム等が挙げられる。離型シートの厚さは、通常
粘着テープに用いられる厚さであれば特に限定されず必
要に応じて適宜決定されればよい。The adhesive tape of the present invention is usually supplied as a three-layer structure of microporous film / adhesive layer / release sheet. The release sheet is not particularly limited and is appropriately selected and used from those that can be used in the field.
Specific examples include silicone-coated paper and silicone-coated film. The thickness of the release sheet is not particularly limited as long as it is a thickness usually used for adhesive tapes, and may be appropriately determined as necessary.
【0016】本発明の粘着テープの製造方法は特に限定
されず、一般的に行われている方法で製造されて良く、
例えば、粘着剤溶液に、任意に架橋剤等を添加し、均一
に分散させて、該粘着剤溶液を離型シート上に塗布乾燥
し、粘着層を形成し、この上に上記微多孔フィルムを積
層する方法が挙げられる。The method for producing the pressure-sensitive adhesive tape of the present invention is not particularly limited, and it may be produced by a commonly used method,
For example, a crosslinking agent or the like is optionally added to the pressure-sensitive adhesive solution and uniformly dispersed, and the pressure-sensitive adhesive solution is applied and dried on a release sheet to form a pressure-sensitive adhesive layer, and the microporous film is formed thereon. The method of laminating is mentioned.
【0017】なお、本発明の粘着テープは、絆創膏、包
帯、外科用布材等に好適に使用されるが、これらに限定
されるものではなく、透気性の保持が必要な用途であれ
ば使用することができる。The pressure-sensitive adhesive tape of the present invention is suitable for use in adhesive plasters, bandages, surgical cloths, etc., but is not limited to these and may be used for any application requiring air permeability. can do.
【0018】[0018]
【発明の実施の形態】以下に本発明の実施例を説明す
る。
〔微多孔フィルム基材の作製〕表1に示した組成に基づ
いて、主材LLDPE(重合活性点が単一である触媒を
用いて重合された密度0.920g/cm3の直鎖状低密
度ポリエチレン)、副材LLDPE(重合活性点が複数
である触媒を用いて重合された密度0.935g/cm3
の直鎖状低密度ポリエチレン)、LDPE(低密度ポリ
エチレン)、炭酸カルシウム(グリセリンモノステアレ
ートで処理した平均粒径1.3μm)、カオリン(Si
O2;52wt%、Al2O3;42wt%、TiO2;2
wt%、その他;4wt%)の所定量からなる組成物を
Tダイ法により製膜し、表1に示した条件で延伸し微多
孔フィルム基材を作成した。Embodiments of the present invention will be described below. [Preparation of Microporous Film Substrate] Based on the composition shown in Table 1, a main material LLDPE (a linear low-density polymerized with a catalyst having a single polymerization active point of 0.920 g / cm 3) was used. Density polyethylene), auxiliary material LLDPE (density of polymerized using a catalyst having a plurality of polymerization active points 0.935 g / cm 3
Linear low density polyethylene), LDPE (low density polyethylene), calcium carbonate (average particle size treated with glycerin monostearate 1.3 μm), kaolin (Si
O 2 ; 52 wt%, Al 2 O 3 ; 42 wt%, TiO 2 ; 2
wt%, other; 4 wt%), and a microporous film substrate was prepared by forming a composition by a T-die method and stretching it under the conditions shown in Table 1.
【0019】〔粘着剤組成物の調製〕ブチルアクリレー
ト/2エチルヘキシルアクリレート/アクリル酸(重量
比=40/57/3)からなる共重合体を主成分とする
アクリル系粘着剤(固形分40重量%)100重量と架
橋剤(コロネートL55E、日本ポリウレタン社製)2
0重量部とを混合して粘着剤組成物を調製した。[Preparation of pressure-sensitive adhesive composition] Acrylic pressure-sensitive adhesive containing a copolymer of butyl acrylate / 2 ethylhexyl acrylate / acrylic acid (weight ratio = 40/57/3) as a main component (solid content 40% by weight). ) 100 weights and a cross-linking agent (Coronate L55E, made by Nippon Polyurethane Co.) 2
0 parts by weight was mixed to prepare an adhesive composition.
【0020】〔粘着テープの作製〕上記粘着剤組成物
を、シリコーン塗布されたポリエチレンテレフタレート
フィルムに、乾燥後の厚みが30g/m2となるように
塗布し、100℃で5分間乾燥した。その直後押圧ロー
ラーにより粘着剤層側を上記微多孔フィルム基材それぞ
れに圧着して粘着テープを得た。[Preparation of Adhesive Tape] The above adhesive composition was applied to a polyethylene-coated polyethylene terephthalate film so that the thickness after drying would be 30 g / m 2, and dried at 100 ° C. for 5 minutes. Immediately thereafter, the pressure-sensitive adhesive layer side was pressure-bonded to each of the microporous film base materials by a pressing roller to obtain a pressure-sensitive adhesive tape.
【0021】〔評価〕養生温度45℃にて十分な時間養
生した後、それぞれの粘着テープの透気度、血液漏れを
下記の方法で測定、その結果を表2に示した。
(透気度)JIS P 8117「紙及び板紙の透気度
試験方法」に準じ、ガーレ式透気度測定器(B型)を用
いて、100mlの気体が透過するのに要した時間を測
定した。
(血液漏れ)100mm×100mmの粘着テープを2
枚準備し、一方の粘着面中央部に動物血3mlを滴下
し、他方と貼り合せて密閉し、5分間放置した後、30
0g(/100mm×100mm)の平板をのせて更に
1時間放置し、血液漏れを評価した。[Evaluation] After curing at a curing temperature of 45 ° C. for a sufficient time, the air permeability and blood leakage of each adhesive tape were measured by the following methods, and the results are shown in Table 2. (Air permeability) According to JIS P 8117 "Paper and board air permeability test method", the time required for 100 ml of gas to permeate is measured using a Gurley type air permeability measuring device (B type). did. (Blood leak) 2 x 100mm x 100mm adhesive tape
Prepare 3 sheets, drop 3 ml of animal blood on the central part of one adhesive side, attach to the other side and seal, and leave for 5 minutes, then 30
A 0 g (/ 100 mm × 100 mm) flat plate was placed on the plate, and the plate was left for 1 hour to evaluate blood leakage.
【0022】[0022]
【表1】 [Table 1]
【0023】[0023]
【表2】 [Table 2]
【0024】[0024]
【発明の効果】本発明の粘着テープは上記のごとく特定
のポリエチレン系混合物に特定の無機充填剤を添加して
なる通気性の高い合成樹脂フィルムを基材に用いること
により、優れた透気性が付与される。よって、医療用粘
着テープなどの通気性を必要とする用途に好適な通気性
粘着テープを安定した品質で工業生産することが容易で
ある。The pressure-sensitive adhesive tape of the present invention has excellent air permeability by using a highly breathable synthetic resin film obtained by adding a specific inorganic filler to a specific polyethylene mixture as described above. Granted. Therefore, it is easy to industrially produce a breathable pressure-sensitive adhesive tape suitable for applications requiring breathability such as a medical pressure-sensitive adhesive tape with stable quality.
───────────────────────────────────────────────────── フロントページの続き Fターム(参考) 4C081 AA03 AA12 CA021 CA082 CC05 CF111 CF131 CF141 CF151 DA02 DC13 EA02 ─────────────────────────────────────────────────── ─── Continued front page F-term (reference) 4C081 AA03 AA12 CA021 CA082 CC05 CF111 CF131 CF141 CF151 DA02 DC13 EA02
Claims (2)
リエチレンとからなるポリエチレン系混合物30〜50
wt%と、無機充填剤50〜70wt%とからなる混合
物を溶融成膜した後、得られた未延伸フィルムを一軸も
しくは二軸に延伸した微多孔フィルム基材に、アクリル
系粘着剤層が積層されてなることを特徴とする粘着テー
プ。1. A polyethylene-based mixture 30 to 50 comprising linear low-density polyethylene and low-density polyethylene.
An acrylic pressure-sensitive adhesive layer is laminated on a microporous film substrate obtained by uniaxially or biaxially stretching the obtained unstretched film after melt-forming a mixture consisting of wt% and an inorganic filler of 50 to 70 wt%. An adhesive tape characterized by being formed.
粘度鉱物1〜30wt%を含有することを特徴とする請
求項1記載の粘着テープ。2. The pressure-sensitive adhesive tape according to claim 1, wherein the inorganic filler contains 1 to 30 wt% of a viscous mineral containing silicon dioxide as a main component.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2002115223A JP2003305079A (en) | 2002-04-17 | 2002-04-17 | Adhesive tape |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2002115223A JP2003305079A (en) | 2002-04-17 | 2002-04-17 | Adhesive tape |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JP2003305079A true JP2003305079A (en) | 2003-10-28 |
Family
ID=29396666
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2002115223A Pending JP2003305079A (en) | 2002-04-17 | 2002-04-17 | Adhesive tape |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2003305079A (en) |
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| JP2012096082A (en) * | 2006-10-30 | 2012-05-24 | Z-Medica Corp | Clay-based hemostat and device for delivery of the same |
| US8846076B2 (en) | 2006-05-26 | 2014-09-30 | Z-Medica, Llc | Hemostatic sponge |
| US8858969B2 (en) | 2010-09-22 | 2014-10-14 | Z-Medica, Llc | Hemostatic compositions, devices, and methods |
| US8938898B2 (en) | 2006-04-27 | 2015-01-27 | Z-Medica, Llc | Devices for the identification of medical products |
| JP2015047411A (en) * | 2013-09-03 | 2015-03-16 | バンドー化学株式会社 | Base film for emergency bandage and emergency bandage |
| US9072806B2 (en) | 2012-06-22 | 2015-07-07 | Z-Medica, Llc | Hemostatic devices |
| US9821084B2 (en) | 2005-02-15 | 2017-11-21 | Virginia Commonwealth University | Hemostasis of wound having high pressure blood flow using kaolin and bentonite |
-
2002
- 2002-04-17 JP JP2002115223A patent/JP2003305079A/en active Pending
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9821084B2 (en) | 2005-02-15 | 2017-11-21 | Virginia Commonwealth University | Hemostasis of wound having high pressure blood flow using kaolin and bentonite |
| US11167058B2 (en) | 2005-02-15 | 2021-11-09 | Virginia Commonwealth University | Hemostasis of wound having high pressure blood flow |
| US8938898B2 (en) | 2006-04-27 | 2015-01-27 | Z-Medica, Llc | Devices for the identification of medical products |
| US9333117B2 (en) | 2006-05-26 | 2016-05-10 | Z-Medica, Llc | Clay-based hemostatic agents and devices for the delivery thereof |
| US12076448B2 (en) | 2006-05-26 | 2024-09-03 | Teleflex Life Sciences Ii Llc | Hemostatic devices |
| US8846076B2 (en) | 2006-05-26 | 2014-09-30 | Z-Medica, Llc | Hemostatic sponge |
| US9078782B2 (en) | 2006-05-26 | 2015-07-14 | Z-Medica, Llc | Hemostatic fibers and strands |
| US10960101B2 (en) | 2006-05-26 | 2021-03-30 | Z-Medica, Llc | Clay-based hemostatic agents |
| US11123451B2 (en) | 2006-05-26 | 2021-09-21 | Z-Medica, Llc | Hemostatic devices |
| US8784876B2 (en) | 2006-05-26 | 2014-07-22 | Z-Medica, Llc | Clay-based hemostatic agents and devices for the delivery thereof |
| US9867898B2 (en) | 2006-05-26 | 2018-01-16 | Z-Medica, Llc | Clay-based hemostatic agents |
| US10086106B2 (en) | 2006-05-26 | 2018-10-02 | Z-Medica, Llc | Clay-based hemostatic agents |
| JP2012096082A (en) * | 2006-10-30 | 2012-05-24 | Z-Medica Corp | Clay-based hemostat and device for delivery of the same |
| US8858969B2 (en) | 2010-09-22 | 2014-10-14 | Z-Medica, Llc | Hemostatic compositions, devices, and methods |
| US11007218B2 (en) | 2010-09-22 | 2021-05-18 | Z-Medica, Llc | Hemostatic compositions, devices, and methods |
| US9889154B2 (en) | 2010-09-22 | 2018-02-13 | Z-Medica, Llc | Hemostatic compositions, devices, and methods |
| US10960100B2 (en) | 2012-06-22 | 2021-03-30 | Z-Medica, Llc | Hemostatic devices |
| US9603964B2 (en) | 2012-06-22 | 2017-03-28 | Z-Medica, Llc | Hemostatic devices |
| US9352066B2 (en) | 2012-06-22 | 2016-05-31 | Z-Medica, Llc | Hemostatic devices |
| US9072806B2 (en) | 2012-06-22 | 2015-07-07 | Z-Medica, Llc | Hemostatic devices |
| US11559601B2 (en) | 2012-06-22 | 2023-01-24 | Teleflex Life Sciences Limited | Hemostatic devices |
| JP2015047411A (en) * | 2013-09-03 | 2015-03-16 | バンドー化学株式会社 | Base film for emergency bandage and emergency bandage |
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