JP2002265891A - Sealing tape and method for producing the same - Google Patents
Sealing tape and method for producing the sameInfo
- Publication number
- JP2002265891A JP2002265891A JP2001061481A JP2001061481A JP2002265891A JP 2002265891 A JP2002265891 A JP 2002265891A JP 2001061481 A JP2001061481 A JP 2001061481A JP 2001061481 A JP2001061481 A JP 2001061481A JP 2002265891 A JP2002265891 A JP 2002265891A
- Authority
- JP
- Japan
- Prior art keywords
- polyester
- sealing tape
- elastomer
- melting point
- polyether
- 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.)
- Granted
Links
- 238000007789 sealing Methods 0.000 title claims abstract description 47
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 10
- 229920001971 elastomer Polymers 0.000 claims abstract description 66
- 239000000806 elastomer Substances 0.000 claims abstract description 66
- 229920000728 polyester Polymers 0.000 claims abstract description 47
- 238000002844 melting Methods 0.000 claims abstract description 31
- 230000008018 melting Effects 0.000 claims abstract description 31
- 239000003960 organic solvent Substances 0.000 claims abstract description 19
- 239000012790 adhesive layer Substances 0.000 claims abstract description 15
- 239000004744 fabric Substances 0.000 claims description 35
- 238000000034 method Methods 0.000 claims description 12
- WNXJIVFYUVYPPR-UHFFFAOYSA-N 1,3-dioxolane Chemical compound C1COCO1 WNXJIVFYUVYPPR-UHFFFAOYSA-N 0.000 claims description 6
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims description 6
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical group CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 6
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 claims description 4
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 claims description 2
- 239000000203 mixture Substances 0.000 claims description 2
- 238000000576 coating method Methods 0.000 abstract description 5
- 239000011248 coating agent Substances 0.000 abstract description 4
- 239000000758 substrate Substances 0.000 abstract description 4
- 238000002485 combustion reaction Methods 0.000 abstract description 3
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 20
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 18
- WOZVHXUHUFLZGK-UHFFFAOYSA-N dimethyl terephthalate Chemical compound COC(=O)C1=CC=C(C(=O)OC)C=C1 WOZVHXUHUFLZGK-UHFFFAOYSA-N 0.000 description 10
- 239000000047 product Substances 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- -1 alkylene glycol Chemical compound 0.000 description 8
- 238000006243 chemical reaction Methods 0.000 description 8
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 7
- 150000002009 diols Chemical class 0.000 description 7
- 229920005989 resin Polymers 0.000 description 7
- 239000011347 resin Substances 0.000 description 7
- 230000008961 swelling Effects 0.000 description 7
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- 125000003118 aryl group Chemical group 0.000 description 6
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 6
- 238000005406 washing Methods 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 5
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 5
- 238000005809 transesterification reaction Methods 0.000 description 5
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 4
- 239000000853 adhesive Substances 0.000 description 4
- 230000001070 adhesive effect Effects 0.000 description 4
- 238000001125 extrusion Methods 0.000 description 4
- 239000000835 fiber Substances 0.000 description 4
- 229920001225 polyester resin Polymers 0.000 description 4
- 229920001223 polyethylene glycol Polymers 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 239000002202 Polyethylene glycol Substances 0.000 description 3
- 239000004721 Polyphenylene oxide Substances 0.000 description 3
- 239000002390 adhesive tape Substances 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 238000006068 polycondensation reaction Methods 0.000 description 3
- 229920000570 polyether Polymers 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 239000002759 woven fabric Substances 0.000 description 3
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 239000011247 coating layer Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- ALOUNLDAKADEEB-UHFFFAOYSA-N dimethyl sebacate Chemical compound COC(=O)CCCCCCCCC(=O)OC ALOUNLDAKADEEB-UHFFFAOYSA-N 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 229920001515 polyalkylene glycol Polymers 0.000 description 2
- 229920001707 polybutylene terephthalate Polymers 0.000 description 2
- 239000004645 polyester resin Substances 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000012209 synthetic fiber Substances 0.000 description 2
- 229920002994 synthetic fiber Polymers 0.000 description 2
- LZDKZFUFMNSQCJ-UHFFFAOYSA-N 1,2-diethoxyethane Chemical compound CCOCCOCC LZDKZFUFMNSQCJ-UHFFFAOYSA-N 0.000 description 1
- NEQFBGHQPUXOFH-UHFFFAOYSA-N 4-(4-carboxyphenyl)benzoic acid Chemical compound C1=CC(C(=O)O)=CC=C1C1=CC=C(C(O)=O)C=C1 NEQFBGHQPUXOFH-UHFFFAOYSA-N 0.000 description 1
- 101000835998 Homo sapiens SRA stem-loop-interacting RNA-binding protein, mitochondrial Proteins 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- QLZHNIAADXEJJP-UHFFFAOYSA-N Phenylphosphonic acid Chemical compound OP(O)(=O)C1=CC=CC=C1 QLZHNIAADXEJJP-UHFFFAOYSA-N 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- 102100025491 SRA stem-loop-interacting RNA-binding protein, mitochondrial Human genes 0.000 description 1
- 239000004433 Thermoplastic polyurethane Substances 0.000 description 1
- ISKQADXMHQSTHK-UHFFFAOYSA-N [4-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=C(CN)C=C1 ISKQADXMHQSTHK-UHFFFAOYSA-N 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 description 1
- 229920003232 aliphatic polyester Polymers 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- YHWCPXVTRSHPNY-UHFFFAOYSA-N butan-1-olate;titanium(4+) Chemical compound [Ti+4].CCCC[O-].CCCC[O-].CCCC[O-].CCCC[O-] YHWCPXVTRSHPNY-UHFFFAOYSA-N 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 239000000306 component Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- VNGOYPQMJFJDLV-UHFFFAOYSA-N dimethyl benzene-1,3-dicarboxylate Chemical compound COC(=O)C1=CC=CC(C(=O)OC)=C1 VNGOYPQMJFJDLV-UHFFFAOYSA-N 0.000 description 1
- 229940014772 dimethyl sebacate Drugs 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 239000012760 heat stabilizer Substances 0.000 description 1
- 238000009957 hemming Methods 0.000 description 1
- NNYOSLMHXUVJJH-UHFFFAOYSA-N heptane-1,5-diol Chemical compound CCC(O)CCCCO NNYOSLMHXUVJJH-UHFFFAOYSA-N 0.000 description 1
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
- 238000007731 hot pressing Methods 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 239000007943 implant Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- KYTZHLUVELPASH-UHFFFAOYSA-N naphthalene-1,2-dicarboxylic acid Chemical compound C1=CC=CC2=C(C(O)=O)C(C(=O)O)=CC=C21 KYTZHLUVELPASH-UHFFFAOYSA-N 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- OEIJHBUUFURJLI-UHFFFAOYSA-N octane-1,8-diol Chemical compound OCCCCCCCCO OEIJHBUUFURJLI-UHFFFAOYSA-N 0.000 description 1
- 238000007719 peel strength test Methods 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- YPFDHNVEDLHUCE-UHFFFAOYSA-N propane-1,3-diol Chemical compound OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000009958 sewing Methods 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 238000000807 solvent casting Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- UWHCKJMYHZGTIT-UHFFFAOYSA-N tetraethylene glycol Chemical compound OCCOCCOCCOCCO UWHCKJMYHZGTIT-UHFFFAOYSA-N 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 229920002397 thermoplastic olefin Polymers 0.000 description 1
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 1
- 239000002341 toxic gas Substances 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
Landscapes
- Sealing Material Composition (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Adhesive Tapes (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
- Coating Of Shaped Articles Made Of Macromolecular Substances (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、ポリエステル系エ
ラストマーからなる接着性に優れた目止めテープおよび
その製造方法に関する。特に防水衣料に好適な目止めテ
ープに関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a sealing tape comprising a polyester elastomer and having excellent adhesion, and a method for producing the same. Particularly, the present invention relates to a sealing tape suitable for waterproof clothing.
【0002】[0002]
【従来の技術】繊維基布と樹脂皮膜からなる防水布帛、
特に透湿性樹脂皮膜からなる透湿性防水布帛は、レイン
コートやウィンドブレーカーなどに用いられている。そ
れらの防水布帛を縫製する際、ミシン目の部分の防水性
をカバーするためには目止めテープが使用されている。
この目止めテープとしては、ポリオレフィン、ポリウレ
タンからなるフィルムに熱可塑性ポリオレフィン、熱可
塑性ポリウレタンなどを塗布した熱融着性のものが一般
的である。2. Description of the Related Art A waterproof fabric comprising a fiber base fabric and a resin film,
In particular, a moisture-permeable waterproof fabric made of a moisture-permeable resin film is used for raincoats, windbreakers, and the like. When sewing these waterproof fabrics, a sealing tape is used to cover the waterproofness of the perforated portion.
As the sealing tape, a heat-fusible tape obtained by applying a thermoplastic polyolefin, a thermoplastic polyurethane, or the like to a film made of a polyolefin or a polyurethane is generally used.
【0003】しかしこれらの樹脂を目止めテープとして
用いた場合、リサイクルができない、燃焼時に有毒ガス
を発生しやすい、などの問題を有していた。またその製
品を一般家庭で行われている水による洗濯を行った場合
には、接着力の低下によるはがれや基体部の破損が発生
し、快適性が損なわれるという問題があった。[0003] However, when these resins are used as sealing tapes, there are problems such as that they cannot be recycled and that toxic gases are easily generated during combustion. In addition, when the product is washed with water, which is used in ordinary households, there is a problem that peeling or damage to the base portion occurs due to a decrease in adhesive strength, and comfort is impaired.
【0004】[0004]
【発明が解決しようとする課題】本発明は、上記従来技
術を鑑みなされたもので、その目的は、リサイクルが可
能で燃焼時も地球環境にやさしい目止めテープおよびそ
の製造方法を提供することにある。SUMMARY OF THE INVENTION The present invention has been made in view of the above prior art, and has as its object to provide a sealing tape which is recyclable and which is friendly to the global environment even during combustion, and a method for producing the same. is there.
【0005】[0005]
【課題を解決するための手段】本発明の目止めテープ
は、融点が150℃以上のポリエステル系エラストマー
からなる基体部と、融点が50℃以上130℃以下のポ
リエーテル−エステル系エラストマーからなる接着層と
が積層されていることを特徴とする。According to the present invention, there is provided a sealing tape comprising a base portion made of a polyester elastomer having a melting point of 150 ° C. or more and an adhesive made of a polyether-ester elastomer having a melting point of 50 ° C. to 130 ° C. And the layers are stacked.
【0006】また、本発明の目止めテープの製造方法
は、融点が150℃以上のポリエステル系エラストマー
からなるフィルム上に、融点が50℃以上130℃以下
のポリエーテル−エステル系エラストマーを濃度2〜3
0重量%で溶解させた有機溶剤溶液を塗布した後、該有
機溶剤を除去することを特徴とする。Further, the method for producing a sealing tape according to the present invention is characterized in that a polyether-ester based elastomer having a melting point of 50 ° C. to 130 ° C. is coated on a film made of a polyester elastomer having a melting point of 150 ° C. or higher. 3
The method is characterized in that after applying an organic solvent solution dissolved at 0% by weight, the organic solvent is removed.
【0007】また、本発明の防水性布帛製品は、本発明
の目止めテープを用いて、布帛の縫合部を防水したこと
を特徴とする。[0007] A waterproof fabric product of the present invention is characterized in that the seam of the fabric is waterproofed using the sealing tape of the present invention.
【0008】[0008]
【発明の実施の形態】以下、本発明を詳細に説明する。
本発明の目止めテープは、縫合部の凹凸に追従させると
ともに、リサイクル性を向上させるためにするために基
体部にはポリエステル系エラストマーを用いる。ここで
ポリエステル系エラストマーとして、ハードセグメント
が高融点高結晶性の芳香族ポリエステル、ソフトセグメ
ントが非晶性ポリエーテルからなるポリエーテル−ポリ
エステル系エラストマーを用いた場合、柔軟性、耐加水
分解性に優れた目止めテープが得られる。一方、ハード
セグメントが高融点高結晶性の芳香族ポリエステル、ソ
フトセグメントが非晶性ポリエステルからなるポリエス
テル−ポリエステル系エラストマーを用いた場合には、
耐候性、耐薬品性に優れた目止めテープが得られる。BEST MODE FOR CARRYING OUT THE INVENTION Hereinafter, the present invention will be described in detail.
The sealing tape of the present invention uses a polyester elastomer for the base in order to follow the irregularities of the sewn portion and to improve recyclability. Here, as the polyester-based elastomer, when a polyether-polyester-based elastomer in which the hard segment is a high melting point and high crystalline aromatic polyester and the soft segment is an amorphous polyether is used, the flexibility and the hydrolysis resistance are excellent. A sealing tape is obtained. On the other hand, when a hard segment is a high melting point high crystalline aromatic polyester, a soft segment is a polyester-polyester elastomer comprising an amorphous polyester,
A sealing tape excellent in weather resistance and chemical resistance can be obtained.
【0009】好ましく用いられるポリエーテル−エステ
ル系エラストマーのハードセグメントとしては、例えば
テレフタル酸、ナフタレンジカルボン酸、4,4’−ジ
フェニルジカルボン酸等を主たる酸成分とし、エチレン
グリコール、プロピレングリコール、テトラメチレング
リコールなどのアルキレングリコールを主たるジオール
成分とする芳香族ポリエステルを例示することができ
る。The hard segments of the polyether-ester elastomer preferably used include, for example, terephthalic acid, naphthalenedicarboxylic acid, 4,4'-diphenyldicarboxylic acid, etc. as main acid components, and ethylene glycol, propylene glycol, tetramethylene glycol, etc. And aromatic polyesters containing alkylene glycol as a main diol component.
【0010】そして、ハードセグメントのジオールがエ
チレングリコールとテトラメチレングリコールとの混合
物であって、該ジオール中に占めるエチレングリコール
の割合が30モル%以上のものである場合には、高い耐
磨耗性を確保することができる。When the diol of the hard segment is a mixture of ethylene glycol and tetramethylene glycol and the proportion of ethylene glycol in the diol is 30 mol% or more, high abrasion resistance is obtained. Can be secured.
【0011】一方ソフトセグメントの非晶性ポリエーテ
ルとしては、ポリエチレングリコール、ポリ−1,2−
プロピレングリコール、ポリ−1,3−プロピレングリ
コール、ポリテトラメチレングリコール、エチレンオキ
シドとプロピレンオキシドとの共重合体、エチレンオキ
シドとテトラヒドロフランとの共重合体などのポリアル
キレングリコールが挙げられる。かかるポリアルキレン
グリコールの数平均分子量は、小さすぎると十分な機械
的物性が得難く、大きすぎると相分離が発生し易くなっ
てポリエーテル−ポリエステル系エラストマーの調整が
困難になるので、600〜8000の範囲が適当であ
る。On the other hand, the amorphous polyether of the soft segment includes polyethylene glycol, poly-1,2-
And polyalkylene glycols such as propylene glycol, poly-1,3-propylene glycol, polytetramethylene glycol, a copolymer of ethylene oxide and propylene oxide, and a copolymer of ethylene oxide and tetrahydrofuran. If the number average molecular weight of the polyalkylene glycol is too small, it is difficult to obtain sufficient mechanical properties, and if it is too large, phase separation is likely to occur, making it difficult to adjust the polyether-polyester elastomer. Is appropriate.
【0012】なお、ソフトセグメント中のポリエチレン
グリコール成分量が多くなるほど透湿性が向上するもの
の、あまり多くなりすぎると耐水性が低下する傾向にあ
り、耐洗濯性も低下する傾向にあるので用途によってそ
の割合を設定することが大切であり、特にポリエチレン
グリコールは重量を基準としてポリエーテル−エステル
系エラストマー全重量に対して25重量%以下とするの
が望ましい。Although the moisture permeability improves as the amount of the polyethylene glycol component in the soft segment increases, the water resistance tends to decrease if the amount is too large, and the washing resistance also tends to decrease. It is important to set the ratio, and it is particularly desirable that the content of polyethylene glycol be 25% by weight or less based on the total weight of the polyether-ester-based elastomer.
【0013】次に、好ましく用いられるポリエステル−
ポリエステル系エラストマーのハードセグメントとして
は、芳香族ジカルボン酸およびジオールからなる芳香族
ポリエステルであり、例えばテレフタル酸と1、4−ブ
タンジオールからなるポリブチレンテレフタレートが挙
げられる。一方ソフトセグメントとしては、例えばイソ
フタル酸と、ヘキサメチレングリコール、オクタメチレ
ングリコールなどの長鎖ジオール成分や2−メチル−
1,5ヘプタンジオールなどの側鎖を有するジオール成
分からなる芳香族ポリエステル、アジピン酸、セバシン
酸などの脂肪族カルボン酸と、テトラメチレングリコー
ル、ジエチルグリコールなどのジオール成分とからなる
脂肪族ポリエステル等が挙げられる。Next, the polyester preferably used is
The hard segment of the polyester elastomer is an aromatic polyester composed of an aromatic dicarboxylic acid and a diol, for example, polybutylene terephthalate composed of terephthalic acid and 1,4-butanediol. On the other hand, as the soft segment, for example, isophthalic acid, a long-chain diol component such as hexamethylene glycol, octamethylene glycol or 2-methyl-
Aromatic polyesters comprising a diol component having a side chain such as 1,5 heptanediol, aliphatic polyesters comprising an aliphatic carboxylic acid such as adipic acid and sebacic acid and a diol component such as tetramethylene glycol and diethyl glycol. No.
【0014】これら基体部のポリエステル系エラストマ
ー中の、ソフトセグメントとハードセグメントとの重量
比は、25/75〜75/25の範囲が適当である。ま
た、ポリエステル系エラストマーの中には、各種安定
剤、紫外線吸収剤等が必要に応じて配合されていてもよ
い。The weight ratio of the soft segment to the hard segment in the polyester elastomer of the base portion is suitably in the range of 25/75 to 75/25. Further, various stabilizers, ultraviolet absorbers, and the like may be blended in the polyester elastomer as needed.
【0015】基体部のポリエステル系エラストマーの融
点は150℃以上であること必要である。250℃以
下、さらには170〜230℃であることがもっとも好
ましい。基体部のエラストマーの融点が低い場合、目止
めテープと布帛との熱接着時に基体部の溶解が発生する
傾向にある。It is necessary that the melting point of the polyester elastomer in the base portion is 150 ° C. or higher. Most preferably, it is 250 ° C or lower, more preferably 170 to 230 ° C. When the melting point of the elastomer in the base portion is low, the base portion tends to dissolve during thermal bonding between the sealing tape and the fabric.
【0016】基体部の厚さについては特に制限はない
が、取扱性を考慮したとき5〜100μmが好ましく、
さらには10〜50μmが好ましい。The thickness of the base portion is not particularly limited, but is preferably 5 to 100 μm in consideration of handleability.
Further, the thickness is preferably 10 to 50 μm.
【0017】さらに本発明に用いられる基体部のポリエ
ステル系エラストマーは、該ポリエステル系エラストマ
ーから形成された厚さ15μmのフィルムを水温40℃
にて30分間処理した後の面積膨潤率が、5%未満であ
ることが好ましい。面積膨潤率が5%以上のフィルムの
場合には、水による洗濯により耐水圧が低下する傾向に
ある。Further, the polyester-based elastomer of the base portion used in the present invention is obtained by forming a film having a thickness of 15 μm formed from the polyester-based elastomer at a water temperature of 40 ° C.
It is preferable that the area swelling ratio after the treatment for 30 minutes is less than 5%. In the case of a film having an area swelling ratio of 5% or more, water resistance tends to decrease due to washing with water.
【0018】本発明の目止めテープの接着層はポリエー
テル−エステル系エラストマーである。接着層のポリエ
ーテル−ポリエステル系エラストマーは基体部で述べた
ものと同じく、ハードセグメントに高融点高結晶性の芳
香族ポリエステルを、ソフトセグメントに非晶性ポリエ
ーテルを使用したものである。The adhesive layer of the sealing tape of the present invention is a polyether-ester elastomer. The polyether-polyester-based elastomer of the adhesive layer has a high melting point and a high crystalline aromatic polyester for the hard segment and an amorphous polyether for the soft segment, as described in the base section.
【0019】また、接着層のポリエーテル−エステル系
エラストマーの融点は50℃以上130℃以下であるこ
とが必須であり、さらには70〜110℃であることが
作業性の点から好ましい。130℃を超える場合には、
目止めテープを通常使用する条件で接着させることが困
難になったり、熱処理工程の効率が低下する。50℃未
満である場合には常温で固化しないため取扱性が悪化
し、例えば目止めテープを巻いたり、重ねたりして保存
することができない。さらには基体部のエラストマーの
融点より40〜100℃低いことが好ましい。また接着
層には溶剤を少量なら含有していてもよいが、巻いたり
重ねたりして保存する場合には、該有機溶剤含有量が2
重量%未満であることが好ましい。Further, the melting point of the polyether-ester elastomer of the adhesive layer must be 50 ° C. or more and 130 ° C. or less, and more preferably 70 to 110 ° C. from the viewpoint of workability. If it exceeds 130 ° C,
It becomes difficult to bond the sealing tape under the conditions normally used, or the efficiency of the heat treatment step is reduced. If the temperature is lower than 50 ° C., the solidification does not take place at room temperature, so that the handleability is deteriorated. Furthermore, it is preferable that the melting point of the elastomer in the base portion is lower by 40 to 100 ° C. The adhesive layer may contain a small amount of a solvent. However, when the adhesive layer is stored by winding or stacking, the organic solvent content is 2%.
Preferably, it is less than about 10% by weight.
【0020】接着層のエラストマーの付着量は好ましく
は5〜100g/m2、さらには10〜50g/m2であ
ることが好ましい。5g/m2未満であると、凹凸のあ
る布帛に対する接着力が低下する傾向にあり、100g
/m2を超えると風合いが悪化する傾向にある。The coating weight of the elastomer of the adhesive layer is preferably 5 to 100 g / m 2, more preferably a 10 to 50 g / m 2. If it is less than 5 g / m 2 , the adhesive strength to the uneven fabric tends to decrease, and
/ M 2 , the texture tends to deteriorate.
【0021】本発明の目止めテープの剥離強度は5N/
2.54cm以上であることが、さらには8N/2.5
4cm以上であることが好ましい。また、水による洗濯
を10回行った後の剥離強度が5N/2.54cm以上
であることが、さらには7N/2.54cm以上である
ことが好ましい。この剥離強度は、後述するように目止
めテープをポリエステル織物に熱融着させた時の剥離強
度である。The peel strength of the sealing tape of the present invention is 5 N /
2.54 cm or more, and further 8 N / 2.5
It is preferably at least 4 cm. The peel strength after washing with water 10 times is preferably 5 N / 2.54 cm or more, and more preferably 7 N / 2.54 cm or more. This peel strength is the peel strength when the sealing tape is heat-sealed to the polyester fabric as described later.
【0022】以上に述べた本発明の目止めテープを製造
する方法は特に限定されないが、例えば以下の方法によ
り製造することができる。すなわち、ポリエステル系エ
ラストマーからなるフィルム上に、ポリエーテル−エス
テル系エラストマーを溶解させた有機溶剤溶液を塗布し
た後、該有機溶剤を除去する製造方法である。The method for producing the above-mentioned sealing tape of the present invention is not particularly limited, but for example, it can be produced by the following method. That is, this is a production method in which an organic solvent solution in which a polyether-ester elastomer is dissolved is applied to a film made of a polyester elastomer, and then the organic solvent is removed.
【0023】以下さらに詳細に述べると、まず基体部と
なる融点が150℃以上のポリエステル系エラストマー
からなるフィルムを作成する。このポリエステル系エラ
ストマーフィルムとしては先に述べた基体部に用いられ
るポリエーテル−エステル系エラストマーやポリエステ
ル−エステル系エラストマーを使用する。またフィルム
を作成する方法としては従来公知のいずれの方法でもよ
く、例えば熔融押出し法または、有機溶剤に溶解し溶剤
キャスト法によって製膜できる。More specifically, first, a film made of a polyester-based elastomer having a melting point of 150 ° C. or more as a base portion is prepared. As the polyester-based elastomer film, the aforementioned polyether-ester-based elastomer or polyester-ester-based elastomer used for the base portion is used. The film can be formed by any conventionally known method, for example, by melt extrusion or by dissolving in an organic solvent and casting by solvent casting.
【0024】次に、接着層となる融点が50℃以上13
0℃以下のポリエーテル−エステル系エラストマーを有
機溶剤に溶解させた溶液を準備する。好ましく用いられ
る有機溶剤としてはジメチルホルムアミド、ジオキサ
ン、1,3−ジオキソラン、トルエン、クロロホルム、
塩化メチレンが挙げられ、2種以上を併用しても良い。
なかでも1,3−ジオキソランが、沸点が低く、毒性が
少ないことから好ましく、特に有機溶剤の重量を基準と
して、80%以上が1,3−ジオキソランであるものが
好ましい。このとき、該溶剤の重量を基準としてポリエ
ーテル−エステル系エラストマーを2〜30重量%溶解
させるが、さらには5〜25重量%溶解させることが作
業性の面などから好ましい。また、溶解時の温度は50
〜65℃が作業しやすく適当である。Next, the melting point of the adhesive layer is 50 ° C. or more and 13 ° C.
A solution prepared by dissolving a polyether-ester based elastomer at 0 ° C. or lower in an organic solvent is prepared. Preferred organic solvents include dimethylformamide, dioxane, 1,3-dioxolan, toluene, chloroform,
Methylene chloride may be used, and two or more kinds may be used in combination.
Among them, 1,3-dioxolane is preferred because of its low boiling point and low toxicity, and particularly preferred is one in which 80% or more, based on the weight of the organic solvent, is 1,3-dioxolane. At this time, the polyether-ester-based elastomer is dissolved in an amount of 2 to 30% by weight based on the weight of the solvent, and more preferably 5 to 25% by weight is dissolved from the viewpoint of workability. The temperature during melting is 50
~ 65 ° C is suitable for easy operation.
【0025】そして、基体部となるフィルム上にポリエ
ーテル−エステル系エラストマーを溶解した溶液を塗布
する。塗布する方法としては、任意のコーティング法、
例えばナイフコーターおよびグラビアコート等が採用で
きる。1,3−ジオキソラン等の有機溶剤の除去につい
ては、70〜120℃、好ましくは70〜100℃での
乾熱下で溶剤を除去する乾式法を採用すればよい。この
とき少量ならば有機溶剤が残存していても良いが、有機
溶剤含有量が2重量%未満となるように除去することが
好ましい。Then, a solution in which a polyether-ester type elastomer is dissolved is applied on a film serving as a base portion. As a method of applying, any coating method,
For example, a knife coater and a gravure coat can be adopted. For the removal of organic solvents such as 1,3-dioxolane, a dry method of removing the solvent under dry heat at 70 to 120 ° C., preferably 70 to 100 ° C. may be employed. At this time, if the amount is small, the organic solvent may remain, but it is preferable to remove the organic solvent so that the organic solvent content is less than 2% by weight.
【0026】得られた目止めテープには、品質感を向上
させるために、その基体部の接着層とは反対側に布帛を
接着しても良い。また縫製品の目止め以外に、縫製品の
補修部分の当て材料、裾上げテープ、パッチ、ワッペン
などの用途に用いることもできる。A cloth may be adhered to the obtained sealing tape on the opposite side of the base from the adhesive layer in order to improve the quality. In addition to the sealing of the sewn product, it can also be used as a material for applying a repair portion of the sewn product, a hemming tape, a patch, an emblem, and the like.
【0027】得られた目止めテープは、使用用途に応じ
た大きさに切断して使用する。このとき必ずしもテープ
状の形態に限らず、シート状の小片に切断して用いても
良い。使用する際は被接着体に目止めテープを接触さ
せ、熱プレス、熱風、超音波、高周波などの公知の方法
により接着する。例えば熱プレスでは、接着層のエラス
トマーの融点以上、基体部のエラストマーの融点以下の
温度で、所定時間加熱することにより接着する。熱プレ
スの加熱方法としては、加熱カレンダー、アイロン、ホ
ットプレス、ホットエアマシンなどを用いて行う方法が
挙げられる。The obtained sealing tape is used after being cut into a size suitable for the intended use. At this time, it is not necessarily limited to the tape-like form, and it may be used after being cut into sheet-like small pieces. At the time of use, the sealing tape is brought into contact with the adherend, and adhered by a known method such as hot pressing, hot air, ultrasonic wave, or high frequency. For example, in a hot press, bonding is performed by heating for a predetermined time at a temperature equal to or higher than the melting point of the elastomer in the adhesive layer and equal to or lower than the melting point of the elastomer in the base portion. Examples of the heating method of the hot press include a method using a heating calender, an iron, a hot press, a hot air machine, and the like.
【0028】本発明の防水性布帛縫製品は、以上に述べ
た目止めテープを用いて、布帛の縫合部を防水したこと
を特徴とするものである。縫製部を有する布帛は、特に
限定されずいかなるものであってもよいが、基布の片側
面または両側面に樹脂を被覆したものが、防水性に特に
優れた製品が得られるので好ましい。基布としては、合
成繊維や天然繊維からなる織物、編物、不織布等任意で
あるが、特に、ポリエチレンテレフタレート等のポリエ
ステル系合成繊維からなるものが好ましい。また基布を
被覆する樹脂としては、ポリエステル系樹脂が好まし
く、例えばポリエーテル−エステル系樹脂を被覆したも
のが挙げられる。すべてポリエステル系樹脂による布帛
に用いることによって、布帛、目止めテープともにすべ
ての部材がポリエステル系となるため、縫製品全体のリ
サイクル性が向上する。また本発明の目止めテープの接
着層はポリエステル−エーテル系エラストマーであるの
で、ポリエステルと親和性が高く、すべてポリエステル
系樹脂による布帛の場合、基布であるポリエステル繊
維、被覆層であるポリエステル系樹脂のいずれとの接着
力も高い。The waterproof fabric sewn product of the present invention is characterized in that the seam of the fabric is waterproofed by using the above-described sealing tape. The fabric having a sewn portion is not particularly limited, and may be any fabric. However, a fabric in which one side or both sides of a base fabric are coated with a resin is preferable because a product having particularly excellent waterproofness can be obtained. The base fabric is arbitrarily selected from a woven fabric, a knitted fabric, and a nonwoven fabric made of synthetic fibers and natural fibers, and is particularly preferably made of a polyester synthetic fiber such as polyethylene terephthalate. The resin for coating the base fabric is preferably a polyester resin, for example, a resin coated with a polyether-ester resin. Since all the members of the cloth and the sealing tape are made of polyester by using the cloth made entirely of polyester resin, the recyclability of the entire sewn product is improved. In addition, since the adhesive layer of the sealing tape of the present invention is a polyester-ether-based elastomer, it has a high affinity for polyester, and when the cloth is entirely made of a polyester-based resin, the polyester fiber as a base cloth and the polyester-based resin as a coating layer. Adhesion to any of them is high.
【0029】より具体的な布帛の例を挙げれば、例えば
単繊維繊度0.5〜5dtexの糸条を用い、カバーフ
ァクター(CF)を1500〜4000とした高密度織
物に、ポリエーテル−エステル系エラストマーを被覆し
た透湿防水布帛である。この縫製部に本発明の目止めテ
ープを用いることによってリサイクル性に優れ、かつ品
質と風合いが両立した製品となる。ただしここでCF
は、(経フィラメント繊度(dtex)×9/10)の
平方根×経打ち込み本数(本数/2.54cm)+(緯
フィラメント繊度(dtex)×9/10)の平方根×
緯打ち込み本数(本数/2.54cm)である。More specifically, a high-density woven fabric having a cover factor (CF) of 1500 to 4000 using single-filament fineness of 0.5 to 5 dtex, for example, may be used as a polyether-ester type fabric. It is a moisture-permeable waterproof fabric coated with an elastomer. By using the sealing tape of the present invention in the sewn portion, a product excellent in recyclability and having both quality and texture can be obtained. Where CF
Is the square root of (filament fineness (dtex) × 9/10) × the number of warp-in (number / 2.54 cm) + the square root of (weft filament fineness (dtex) × 9/10) ×
This is the number of wefts (number / 2.54 cm).
【0030】[0030]
【実施例】以下、実施例により本発明をさらに説明する
が、本発明はこれにより制限されるものではない。実施
例において、各物性値の測定は下記の方法により行い、
また、実施例で使用したエラストマーは、参考例の方法
により作製した。なお、実施例中の「部」は、「重量
部」を表わす。The present invention will be described in more detail with reference to the following Examples, which should not be construed as limiting the present invention. In the examples, the measurement of each physical property value is performed by the following method,
The elastomer used in the examples was produced by the method of the reference example. In the examples, "parts" represents "parts by weight".
【0031】(1)融点 示差走査型熱量計(TA instrument製 D
SC29290)を用いて、窒素気流中10℃/分の昇
温速度で測定した。(1) Melting point Differential scanning calorimeter (D manufactured by TA instrument)
SC29290) at a heating rate of 10 ° C./min in a nitrogen stream.
【0032】(2)剥離強度 目止めテープ(2cm幅×9cm長さ)のバインダー面
とポリエステル織物を、所定温度の熱カレンダーにて2
00N/cmの線圧をかけ熱融着させて試験片を作成し
た。その後JIS K−6301を参考にし、試験片の
テープ面と同サイズの布粘着テープ(日東電工No.7
50)をマングルにて貼り合せ、1kPa/cm2条件
のマングルにて圧着させた後、試験片と布粘着テープと
を引張試験機の相互に向かい合ったチャック間(20m
m)にセットし、50mm/minの引張り速度でチャ
ック間の距離を広げることで基布と被覆層とを剥離さ
せ、初期の剥離を除いた平均応力を読み取り、サンプル
の幅25.4mm(1inch)当たりの応力に換算し
たものを剥離強度とした。試験片の破壊無しに布粘着テ
ープが剥がれたときは、「10>」と表記した。使用し
たポリエステル織物は経62dtex/36fil、打
ち込み本数122本/2.54cm、緯92dtex/
72fil、打ち込み本数97本/2.54cmの平織
りを用いた。(2) Peel strength The binder surface of the sealing tape (2 cm width × 9 cm length) and the polyester fabric are separated by a hot calender at a predetermined temperature.
A test piece was prepared by applying a linear pressure of 00 N / cm and performing heat fusion. Then, referring to JIS K-6301, a cloth adhesive tape of the same size as the tape surface of the test piece (Nitto Denko No. 7
50) were adhered by a mangle and pressed by a mangle under the condition of 1 kPa / cm 2 , and then the test piece and the cloth adhesive tape were placed between chucks (20 m) facing each other of a tensile tester.
m), the base cloth and the coating layer were peeled off by increasing the distance between the chucks at a pulling speed of 50 mm / min, the average stress excluding the initial peeling was read, and the sample width 25.4 mm (1 inch) ) Was calculated as the peel strength. When the cloth adhesive tape was peeled off without breaking the test piece, it was described as "10>". The polyester fabric used was a warp of 62 dtex / 36 fill, the number of shots was 122 / 2.54 cm, and the weft was 92 dtex /
A 72-fil, 97-piece / 2.54 cm plain weave was used.
【0033】(3)洗濯10回後の剥離強度(剥離強度
L10後) JIS L 0217の付表1番号103に規定されて
いる洗濯操作を1サイクル(1回)とし、これに従って
10サイクル(10回)の洗濯(L10)を繰返し行
い、その後(2)の剥離強度の試験を行った。(3) Peeling strength after washing 10 times (after peeling strength L10) The washing operation specified in JIS L 0217, Appendix Table No. 103, is defined as 1 cycle (1 time), and 10 cycles (10 times) ) Was repeated (L10), and then the peel strength test (2) was performed.
【0034】(4)面積膨潤率 タテ10cm×ヨコ10cm×厚さ15μmの大きさの
フィルムを作成し、40℃の水に30分間浸漬処理し、
以下の式により面積膨潤率を算出した。 膨潤率(%)=(浸漬後面積/浸漬前面積−1)×10
0(4) Area swelling ratio A film having a size of 10 cm (width) × 10 cm (width) × 15 μm (thickness) was prepared and immersed in water at 40 ° C. for 30 minutes.
The area swelling ratio was calculated by the following equation. Swelling rate (%) = (area after immersion / area before immersion-1) × 10
0
【0035】[参考例1] (融点190℃の基体部用エラストマーフィルムの作
製)テレフタル酸ジメチル(DMT)194部、テトラ
メチレングリコール(TMG)115部、ポリテトラメ
チレングリコール(PTMG)(平均分子量2000)
124部、及び触媒としてテトラブチルチタネート0.
391部を蒸留装置を備えた反応容器に仕込み、この反
応物を窒素ガス雰囲気下、220℃で反応缶中に生成す
るメタノールを系外に除去しながら210分間エステル
交換させた。エステル交換反応終了後、このエステル交
換反応物を撹袢装置、窒素導入口、減圧口及び蒸留装置
を備えた240℃に加熱された反応容器に移し、反応混
合物に熱安定剤としてスミライザーGS(住友化学工業
(株)製)を0.31部添加し窒素置換した後、常圧で約
10分、1995〜2660Pa(15〜20mmH
g)で約30分、更に13.3Pa(0.1mmHg)
で255℃まで昇温し重縮合反応を行ない、所定の溶融
粘度に到達した後、酸化防止剤としてスミライザーGA
−80(住友化学工業(株)製)を0.62部添加して反
応終了とし、常法によりチップ化した。得られたポリエ
ーテル−エステル系エラストマーの融点は190℃であ
った。このポリエステル系エラストマーを公知の熔融押
出し法にて離型紙上に50μmの製膜を行った。このエ
ラストマーから形成された厚さ15μmのフィルムの水
による面積膨潤率は0%であった。Reference Example 1 (Preparation of elastomer film for base portion having a melting point of 190 ° C.) 194 parts of dimethyl terephthalate (DMT), 115 parts of tetramethylene glycol (TMG), polytetramethylene glycol (PTMG) (average molecular weight: 2000) )
124 parts and tetrabutyl titanate 0.1 as a catalyst.
391 parts were charged into a reaction vessel equipped with a distillation apparatus, and the reaction product was subjected to transesterification at 220 ° C. for 210 minutes in a nitrogen gas atmosphere while removing methanol generated in the reaction vessel outside the system. After completion of the transesterification reaction, the transesterification reaction product was transferred to a reaction vessel heated to 240 ° C. equipped with a stirrer, a nitrogen inlet, a vacuum port, and a distillation apparatus, and Sumirizer GS (Sumitomo) was added to the reaction mixture as a heat stabilizer. Chemical industry
0.31 part) was added and purged with nitrogen, and then at normal pressure for about 10 minutes, at 1995 to 2660 Pa (15 to 20 mmH).
g) for about 30 minutes, and 13.3 Pa (0.1 mmHg)
To 255.degree. C. to carry out a polycondensation reaction and reach a predetermined melt viscosity.
The reaction was terminated by adding 0.62 parts of -80 (manufactured by Sumitomo Chemical Co., Ltd.), and formed into chips by a conventional method. The melting point of the obtained polyether-ester elastomer was 190 ° C. This polyester-based elastomer was formed into a 50 μm film on release paper by a known melt extrusion method. The area swelling ratio of a 15 μm-thick film formed from this elastomer with water was 0%.
【0036】[参考例2] (融点192℃の基体部用エラストマーフィルムの作
製)テレフタル酸ジメチル180部、セバシン酸ジメチ
ル20部、テトラエチレングリコール140部およびジ
エチレングリコール30部をジブチル錫ジアセテート触
媒でエステル交換反応後、減圧下で重縮合して、ポリエ
ステル(S、ソフトセグメント)を得た。Reference Example 2 (Preparation of elastomer film for base portion having a melting point of 192 ° C.) 180 parts of dimethyl terephthalate, 20 parts of dimethyl sebacate, 140 parts of tetraethylene glycol and 30 parts of diethylene glycol were esterified with a dibutyltin diacetate catalyst. After the exchange reaction, polycondensation was performed under reduced pressure to obtain a polyester (S, soft segment).
【0037】このポリエステル(S)にポリブチレンテ
レフタレート(H、ハードセグメント)のチップを乾燥
して、170部添加し、240℃で更に45分反応させ
た後、フェニルフォスフォン酸を0.1部添加して、反
応を停止させた。このポリエステル−エステル系エラス
トマーの融点は192℃であった。このポリエステル系
エラストマーを公知の熔融押出し法にて離型紙上に50
μmの製膜を行った。このエラストマーから形成された
厚さ15μmのフィルムの水による面積膨潤率は0%で
あった。After drying chips of polybutylene terephthalate (H, hard segment) to the polyester (S), adding 170 parts and reacting at 240 ° C. for further 45 minutes, 0.1 parts of phenylphosphonic acid was added. The reaction was stopped by addition. The melting point of this polyester-ester elastomer was 192 ° C. This polyester-based elastomer is put on a release paper by a known melt extrusion method for 50 minutes.
A μm film was formed. The area swelling ratio of a 15 μm-thick film formed from this elastomer with water was 0%.
【0038】[参考例3] (融点145℃の基体部用エラストマーフィルムの作
製)テレフタル酸ジメチル(DMT)210部、イソフ
タル酸(IA)63.6部、テトラメチレングリコール
(TMG)193.3部およびポリテトラメチレングリ
コール(PTMG)199部を反応容器中に仕込んで、
エステル交換反応を行い、モノマーを得た。PTMGは
平均分子量1500のものを用いた。参考例1と同様に
重合を行った結果、融点は145℃のポリエーテル−エ
ステル系エラストマーを得た。このポリエステル系エラ
ストマーを公知の熔融押出し法にて離型紙上に50μm
の製膜を行った。Reference Example 3 (Preparation of elastomer film for base portion having a melting point of 145 ° C.) 210 parts of dimethyl terephthalate (DMT), 63.6 parts of isophthalic acid (IA), 193.3 parts of tetramethylene glycol (TMG) And 199 parts of polytetramethylene glycol (PTMG) were charged into a reaction vessel,
A transesterification reaction was performed to obtain a monomer. PTMG having an average molecular weight of 1500 was used. As a result of performing polymerization in the same manner as in Reference Example 1, a polyether-ester elastomer having a melting point of 145 ° C. was obtained. 50 μm of this polyester elastomer is formed on release paper by a known melt extrusion method.
Was formed.
【0039】[参考例4] (融点107℃の接着層用エラストマーの作製)イソフ
タル酸ジメチル(IMT)31.5部、テトラメチレン
グリコール(TMG)18.1部及びポリテトラメチレ
ングリコール(PTMG)32.7部を反応容器中に仕
込んで、エステル交換反応を行いモノマーを得た。その
後昇温減圧しつつ重縮合反応を行ってポリエーテル−エ
ステル系エラストマーを得た。なお、PTMGは数平均
分子量1000のものを用いた。このポリエーテル−エ
ステル系エラストマーの融点は107℃であった。Reference Example 4 (Production of an Elastomer for an Adhesive Layer with a Melting Point of 107 ° C.) 31.5 parts of dimethyl isophthalate (IMT), 18.1 parts of tetramethylene glycol (TMG) and 32 parts of polytetramethylene glycol (PTMG) 32 .7 parts were charged in a reaction vessel, and a transesterification reaction was performed to obtain a monomer. Thereafter, a polycondensation reaction was performed while raising the temperature and reducing the pressure to obtain a polyether-ester elastomer. PTMG having a number average molecular weight of 1,000 was used. The melting point of this polyether-ester elastomer was 107 ° C.
【0040】[実施例1、2]参考例1,2によって得
られたフィルムを基体とし、そのフィルム上に参考例4
により得られたエラストマー25部を、60℃に加熱さ
れた1,3−ジオキソラン75部に完全に溶解させ、#
32のグラビアコーターにより、上記参考例1、2によ
って得られたフィルム上に固形分10g/m2となるよ
うに塗布し、80℃で有機溶剤含有量が2重量%以下と
なるように溶剤の除去を行った。[Examples 1 and 2] The film obtained in Reference Examples 1 and 2 was used as a substrate, and Reference Example 4 was formed on the film.
Was completely dissolved in 75 parts of 1,3-dioxolane heated to 60 ° C.
A gravure coater of No. 32 was applied onto the films obtained in Reference Examples 1 and 2 so as to have a solid content of 10 g / m 2, and the solvent was adjusted at 80 ° C. so that the organic solvent content was 2% by weight or less. Removal was performed.
【0041】カレンダー温度を140℃とした時の得ら
れた目止めテープの接着性を表1に示す。また、単繊維
繊度が経糸1.7dtex、緯糸1.3dtexの糸条
を用い、カバーファクター(CF)を1800としたポ
リエステル高密度織物(経62dtex/36fil、
打ち込み本数122本/2.54cm、緯92dtex
/72fil、打ち込み本数97本/2.54cmの平
織り)に、ポリエーテル−エステル系エラストマーを積
層した透湿防水布帛を用い、縫製部にこの目止めテープ
を用いた防水布帛製品は風合いに優れ、リサイクル性も
良好な製品であった。Table 1 shows the adhesiveness of the obtained sealing tape when the calendar temperature was 140 ° C. Further, using a yarn having a single fiber fineness of 1.7 dtex for warp and 1.3 dtex for weft and a cover factor (CF) of 1800, a polyester high-density woven fabric (warp 62 dtex / 36 fil,
Number of implants 122 / 2.54cm, 92dtex weft
/ 72 fill, 97 pieces / 2.54 cm plain weave), a moisture-permeable waterproof fabric obtained by laminating a polyether-ester-based elastomer, and a waterproof fabric product using this sealing tape in a sewn portion is excellent in texture, The product had good recyclability.
【0042】[実施例3]接着層の目付を固形分7g/
m2となるように塗布した以外は、実施例1と同様にし
て目止めテープを作成した。カレンダー温度を140℃
とした時の得られた目止めテープの接着性を表1に併せ
て示す。Example 3 The basis weight of the adhesive layer was 7 g / solid.
A sealing tape was prepared in the same manner as in Example 1 except that the coating was performed so as to obtain m 2 . 140 ° C calendar temperature
Table 1 also shows the adhesiveness of the obtained sealing tape.
【0043】[比較例1]参考例3によって得られたフ
ィルムを基体として用いること以外は実施例1と同様に
して目止めテープを作成した。カレンダー温度を130
℃、150℃とした時の、得られた目止めテープの接着
性を表1に併せて示す。Comparative Example 1 A sealing tape was prepared in the same manner as in Example 1 except that the film obtained in Reference Example 3 was used as a substrate. Calendar temperature 130
Table 1 also shows the adhesiveness of the obtained sealing tape at a temperature of 150 ° C. and 150 ° C.
【0044】[比較例2]接着層の融点を表1のものに
変更した以外は、実施例1と同様にして目止めテープを
作成した。カレンダー温度を150℃、170℃とした
時の、得られた目止めテープの接着性を表1に併せて示
す。Comparative Example 2 A sealing tape was prepared in the same manner as in Example 1 except that the melting point of the adhesive layer was changed to that shown in Table 1. Table 1 also shows the adhesiveness of the obtained sealing tape when the calendar temperature was set to 150 ° C. and 170 ° C.
【0045】[0045]
【表1】 [Table 1]
【0046】[0046]
【発明の効果】本発明の目止めテープは、ポリエステル
系エラストマーのみで構成されているため、廃棄時に焼
却処理することが容易である。また、水による洗濯後も
接着力が高く、家庭での洗濯が可能な優れた目止めテー
プである。また、本発明の製造方法によって優れた目止
めテープを提供することができる。Since the sealing tape of the present invention is composed only of a polyester elastomer, it can be easily incinerated at the time of disposal. Moreover, it is an excellent sealing tape which has high adhesive strength even after washing with water and can be washed at home. Further, an excellent sealing tape can be provided by the production method of the present invention.
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.7 識別記号 FI テーマコート゛(参考) C09K 3/10 C09K 3/10 Z // C08L 67:00 C08L 67:00 Fターム(参考) 4D075 CA47 DA04 DB48 DC50 EA35 EB35 EB37 4F006 AA35 AB35 BA01 CA00 DA04 4H017 AA03 AB13 AC04 AC17 AD06 AE05 4J004 AA15 AB03 CA06 CC02 FA08 FA10 GA01 ──────────────────────────────────────────────────の Continued on the front page (51) Int.Cl. 7 Identification symbol FI Theme coat ゛ (Reference) C09K 3/10 C09K 3 / 10Z // C08L 67:00 C08L 67:00 F term (reference) 4D075 CA47 DA04 DB48 DC50 EA35 EB35 EB37 4F006 AA35 AB35 BA01 CA00 DA04 4H017 AA03 AB13 AC04 AC17 AD06 AE05 4J004 AA15 AB03 CA06 CC02 FA08 FA10 GA01
Claims (6)
ラストマーからなる基体部と、融点が50℃以上130
℃以下のポリエーテル−エステル系エラストマーからな
る接着層とが積層されていることを特徴とする目止めテ
ープ。1. A base made of a polyester elastomer having a melting point of 150 ° C. or higher, and a base having a melting point of 50 ° C. or higher.
A sealing tape characterized by being laminated with an adhesive layer made of a polyether-ester-based elastomer having a temperature of not more than ° C.
ポリエーテル−エステル系エラストマーである請求項1
に記載の目止めテープ。2. The polyester-based elastomer of the base portion is a polyether-ester-based elastomer.
The sealing tape described in 1.
ポリエステル−エステル系エラストマーである請求項1
に記載の目止めテープ。3. The polyester-based elastomer of the base portion is a polyester-ester-based elastomer.
The sealing tape described in 1.
ラストマーからなるフィルム上に、融点が50℃以上1
30℃以下のポリエーテル−エステル系エラストマーを
濃度2〜30重量%で溶解させた有機溶剤溶液を塗布し
た後、該有機溶剤を除去することを特徴とする目止めテ
ープの製造方法。4. A film comprising a polyester elastomer having a melting point of at least 150 ° C.
A method for producing a sealing tape, comprising applying an organic solvent solution in which a polyether-ester elastomer having a temperature of 30 ° C. or lower is dissolved at a concentration of 2 to 30% by weight, and removing the organic solvent.
ジオキサン、1,3−ジオキソラン、トルエン、クロロ
ホルム、塩化メチレンまたはこれらの混合物である請求
項4記載の目止めテープの製造方法。5. The organic solvent is dimethylformamide,
The method according to claim 4, wherein the method is dioxane, 1,3-dioxolan, toluene, chloroform, methylene chloride, or a mixture thereof.
布帛の縫合部を防水したことを特徴とする防水性布帛縫
製品。6. Using the sealing tape according to claim 1,
A waterproof fabric sewn product, wherein a sewn portion of the fabric is waterproofed.
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2001061481A JP3942367B2 (en) | 2001-03-06 | 2001-03-06 | Sealing tape and manufacturing method thereof |
| US11/214,784 US20060035549A1 (en) | 2000-07-18 | 2005-08-31 | Water-vapor-permeable waterproof composite fabric |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2001061481A JP3942367B2 (en) | 2001-03-06 | 2001-03-06 | Sealing tape and manufacturing method thereof |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2002265891A true JP2002265891A (en) | 2002-09-18 |
| JP3942367B2 JP3942367B2 (en) | 2007-07-11 |
Family
ID=18920768
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2001061481A Expired - Fee Related JP3942367B2 (en) | 2000-07-18 | 2001-03-06 | Sealing tape and manufacturing method thereof |
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