JPH02307986A - Method for carrying out melt extrusion coating finish - Google Patents
Method for carrying out melt extrusion coating finishInfo
- Publication number
- JPH02307986A JPH02307986A JP1127429A JP12742989A JPH02307986A JP H02307986 A JPH02307986 A JP H02307986A JP 1127429 A JP1127429 A JP 1127429A JP 12742989 A JP12742989 A JP 12742989A JP H02307986 A JPH02307986 A JP H02307986A
- Authority
- JP
- Japan
- Prior art keywords
- cloth
- synthetic fiber
- melt extrusion
- extrusion coating
- coupling agent
- 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
- 238000007765 extrusion coating Methods 0.000 title claims abstract description 17
- 238000000034 method Methods 0.000 title abstract description 18
- 239000004744 fabric Substances 0.000 claims abstract description 53
- 229920002994 synthetic fiber Polymers 0.000 claims abstract description 24
- 239000012209 synthetic fiber Substances 0.000 claims abstract description 24
- 239000006087 Silane Coupling Agent Substances 0.000 claims abstract description 18
- 229920005992 thermoplastic resin Polymers 0.000 claims abstract description 16
- 238000003672 processing method Methods 0.000 claims description 3
- 238000001125 extrusion Methods 0.000 abstract description 13
- 239000000853 adhesive Substances 0.000 abstract description 9
- 230000001070 adhesive effect Effects 0.000 abstract description 9
- 239000000155 melt Substances 0.000 abstract description 7
- 229920005989 resin Polymers 0.000 abstract description 6
- 239000011347 resin Substances 0.000 abstract description 6
- 150000001875 compounds Chemical class 0.000 abstract description 2
- 238000003825 pressing Methods 0.000 abstract description 2
- GQIUQDDJKHLHTB-UHFFFAOYSA-N trichloro(ethenyl)silane Chemical compound Cl[Si](Cl)(Cl)C=C GQIUQDDJKHLHTB-UHFFFAOYSA-N 0.000 abstract description 2
- 239000005050 vinyl trichlorosilane Substances 0.000 abstract description 2
- 238000006243 chemical reaction Methods 0.000 abstract 1
- NKSJNEHGWDZZQF-UHFFFAOYSA-N ethenyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)C=C NKSJNEHGWDZZQF-UHFFFAOYSA-N 0.000 abstract 1
- 239000000835 fiber Substances 0.000 description 15
- -1 polyethylene terephthalate Polymers 0.000 description 12
- 238000002844 melting Methods 0.000 description 4
- 230000008018 melting Effects 0.000 description 4
- 239000004677 Nylon Substances 0.000 description 3
- 239000004698 Polyethylene Substances 0.000 description 3
- 238000004873 anchoring Methods 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 229920001778 nylon Polymers 0.000 description 3
- 229920000573 polyethylene Polymers 0.000 description 3
- 229920000139 polyethylene terephthalate Polymers 0.000 description 3
- 239000005020 polyethylene terephthalate Substances 0.000 description 3
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 3
- 239000004952 Polyamide Substances 0.000 description 2
- 239000005062 Polybutadiene Substances 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 238000005470 impregnation Methods 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- 239000004745 nonwoven fabric Substances 0.000 description 2
- 229920002647 polyamide Polymers 0.000 description 2
- 229920002857 polybutadiene Polymers 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 229920002635 polyurethane Polymers 0.000 description 2
- 239000004814 polyurethane Substances 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 1
- WYTZZXDRDKSJID-UHFFFAOYSA-N (3-aminopropyl)triethoxysilane Chemical compound CCO[Si](OCC)(OCC)CCCN WYTZZXDRDKSJID-UHFFFAOYSA-N 0.000 description 1
- YZTJKOLMWJNVFH-UHFFFAOYSA-N 2-sulfobenzene-1,3-dicarboxylic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1S(O)(=O)=O YZTJKOLMWJNVFH-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 239000013032 Hydrocarbon resin Substances 0.000 description 1
- 229920000571 Nylon 11 Polymers 0.000 description 1
- 229920001007 Nylon 4 Polymers 0.000 description 1
- 229920002292 Nylon 6 Polymers 0.000 description 1
- 229920000305 Nylon 6,10 Polymers 0.000 description 1
- 229920002302 Nylon 6,6 Polymers 0.000 description 1
- 229930182556 Polyacetal Natural products 0.000 description 1
- 239000004962 Polyamide-imide Substances 0.000 description 1
- 239000004695 Polyether sulfone Substances 0.000 description 1
- 229920002873 Polyethylenimine Polymers 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 239000004734 Polyphenylene sulfide Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 229920001328 Polyvinylidene chloride Polymers 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- BXKDSDJJOVIHMX-UHFFFAOYSA-N edrophonium chloride Chemical compound [Cl-].CC[N+](C)(C)C1=CC=CC(O)=C1 BXKDSDJJOVIHMX-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 229920006270 hydrocarbon resin Polymers 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 230000010534 mechanism of action Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 125000005395 methacrylic acid group Chemical group 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- ARYZCSRUUPFYMY-UHFFFAOYSA-N methoxysilane Chemical compound CO[SiH3] ARYZCSRUUPFYMY-UHFFFAOYSA-N 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 239000000088 plastic resin Substances 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920002492 poly(sulfone) Polymers 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920002312 polyamide-imide Polymers 0.000 description 1
- 229920001230 polyarylate Polymers 0.000 description 1
- 229920001083 polybutene Polymers 0.000 description 1
- 229920001707 polybutylene terephthalate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920006393 polyether sulfone Polymers 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920000306 polymethylpentene Polymers 0.000 description 1
- 239000011116 polymethylpentene Substances 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920006324 polyoxymethylene Polymers 0.000 description 1
- 229920006380 polyphenylene oxide Polymers 0.000 description 1
- 229920000069 polyphenylene sulfide Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 239000004810 polytetrafluoroethylene Substances 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000005033 polyvinylidene chloride Substances 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 238000009991 scouring Methods 0.000 description 1
- 125000005372 silanol group Chemical group 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 125000003396 thiol group Chemical group [H]S* 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- BPSIOYPQMFLKFR-UHFFFAOYSA-N trimethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CO[Si](OC)(OC)CCCOCC1CO1 BPSIOYPQMFLKFR-UHFFFAOYSA-N 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
Landscapes
- Extrusion Moulding Of Plastics Or The Like (AREA)
- Synthetic Leather, Interior Materials Or Flexible Sheet Materials (AREA)
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明は9合成繊維布帛への熱可塑性樹脂の溶融押出し
コーティング加工方法に関するものである。DETAILED DESCRIPTION OF THE INVENTION (Industrial Application Field) The present invention relates to a method for melt-extrusion coating a thermoplastic resin onto a synthetic fiber fabric.
(従来の技術)
従来から、織編物や不織布等の布帛上に熱可塑性樹脂を
溶融状態で押出して圧着する溶融押出しコーティング加
工はよく知られているが、布帛と樹脂との接着強力が十
分でない場合が多い。このような欠点を解消するために
、溶融押出しコーティング加工前に布帛にアンカー剤を
付与する方法が考えられており、そのアンカー剤として
有機チタン系、イソシアネート系、ポリエチレンイミン
系、ポリブタジェン系等の化合物が知られている。(Prior art) Melt extrusion coating is a well-known process in which thermoplastic resin is extruded in a molten state onto fabrics such as woven or knitted fabrics or non-woven fabrics and then pressure bonded, but the adhesive strength between the fabric and the resin is not strong enough. There are many cases. In order to overcome these drawbacks, a method has been considered in which an anchoring agent is applied to the fabric before melt extrusion coating, and organic titanium-based, isocyanate-based, polyethyleneimine-based, polybutadiene-based compounds, etc. are used as the anchoring agent. It has been known.
(発明が解決しようとする課題)
上記のような従来法では、接着強力向上のためアンカー
剤を付与したとしても、接着強力が十分でなく、製品の
耐久性に問題があった。(Problems to be Solved by the Invention) In the conventional method as described above, even if an anchoring agent is applied to improve adhesive strength, the adhesive strength is insufficient and there are problems with the durability of the product.
本発明は、このような従来技術の欠点を解消し。The present invention eliminates these drawbacks of the prior art.
優れた接着強力を有する溶融押出しコーティング加工布
を得ることを目的とするものである。The object of the present invention is to obtain a melt-extrusion coated fabric having excellent adhesive strength.
(課題を解決するための手段)
本発明者らは、上記目的を達成するため鋭意検討の結果
、溶融押出しコーティング加工前に予め合成繊維布帛に
シランカップリング剤を付与しておけば、溶融押出しコ
ーティング加工後の合成繊維布帛と樹脂との接着強力が
著しく向上するという事実を見出し9本発明に到達した
。(Means for Solving the Problems) In order to achieve the above object, the present inventors have made extensive studies and found that if a silane coupling agent is applied to a synthetic fiber fabric in advance before melt extrusion coating processing, melt extrusion The present invention was achieved by discovering the fact that the adhesive strength between the synthetic fiber fabric and the resin after coating is significantly improved.
すなわち1本発明は1合成繊維布帛への溶融押出しコー
ティング加工に際し、予め合成繊維布帛にシランカップ
リング剤を付与し、しかる後に該布帛上に熱可塑性樹脂
を溶融状態で押出して圧着することを特徴とする溶融押
出しコーティング加工方法を要旨とするものである。That is, 1. The present invention is characterized in that: 1. During the melt extrusion coating process on a synthetic fiber fabric, a silane coupling agent is applied to the synthetic fiber fabric in advance, and then a thermoplastic resin is extruded in a molten state onto the fabric and crimped. The gist of this paper is a melt extrusion coating processing method.
以下1本発明について詳細に説明する。The present invention will be explained in detail below.
溶融押出しコーティング加工とは、エクストルーダーに
て加温加圧下で熱可塑性樹脂を溶融させた後、スリット
ダイから溶融状態で被コーティング基布上に押出し、こ
れを圧着して基布上に上記熱可塑性樹脂層を形成するコ
ーティング加工方法である。Melt extrusion coating process involves melting a thermoplastic resin under heat and pressure in an extruder, extruding it in a molten state from a slit die onto a base fabric to be coated, pressing it, and applying the above-mentioned heat onto the base fabric. This is a coating processing method that forms a plastic resin layer.
本発明でいう合成繊維とは、ポリエステル系繊維(ポリ
エチレンテレフタレート繊維やイソフタル酸、パラオキ
シ安息香酸、スルホイソフタル酸あるいはブチレングリ
コール等を共重合したポリエチレンテレフタレート繊維
)、ポリアミド系繊維(ナイロン−4繊維、ナイロン−
6繊維、ナイロン−66繊維、ナイロン−610繊維あ
るいはナイロン−11繊維等)、ポリアクリロニトリル
系繊維やポリオレフィン系繊維(ポリエチレン繊維やポ
リプロピレン繊維等)を挙げることができる。これらの
合成繊維を、その他の繊維(綿、ウール、レーヨン、ア
セテート等 )と混用する場合には、上記合成繊維の単
独あるいは2種以上の複合繊維を60%以上含んでいる
ことが必要である。本発明でいう布帛とは、織物1m物
、不織布等を意味している。Synthetic fibers in the present invention include polyester fibers (polyethylene terephthalate fibers, polyethylene terephthalate fibers copolymerized with isophthalic acid, paraoxybenzoic acid, sulfoisophthalic acid, butylene glycol, etc.), polyamide fibers (nylon-4 fibers, nylon −
6 fibers, nylon-66 fibers, nylon-610 fibers, nylon-11 fibers, etc.), polyacrylonitrile fibers, and polyolefin fibers (polyethylene fibers, polypropylene fibers, etc.). When these synthetic fibers are mixed with other fibers (cotton, wool, rayon, acetate, etc.), they must contain 60% or more of the above synthetic fibers alone or in combination with two or more types of composite fibers. . The term "fabric" used in the present invention refers to a 1-meter woven fabric, a nonwoven fabric, and the like.
本発明方法では、まず、溶融押出しコーティング加工に
際し、予め上述の合成繊維よりなる布帛にシランカップ
リング剤を付与する。ここでいうシランカップリング剤
とは、その分子中に2個以上の異なった反応基をもつ有
機ケイ素単量体の総称であって9反応基としてメトキシ
基、エトキシ基、シラノール基、ビニル基、エポキシ基
、メタクリル基、アミノ基、メルカプト基等を有するも
ので1例示すれば、ビニル) IJメトキシシラン。In the method of the present invention, first, a silane coupling agent is applied to the fabric made of the above-mentioned synthetic fiber in advance during the melt extrusion coating process. The silane coupling agent herein is a general term for organosilicon monomers having two or more different reactive groups in their molecules, and the nine reactive groups include methoxy group, ethoxy group, silanol group, vinyl group, One example of those having an epoxy group, methacrylic group, amino group, mercapto group, etc. is vinyl) IJ methoxysilane.
γ−グリシドキシプロピルトリメトキシシラン。γ-glycidoxypropyltrimethoxysilane.
ビニルトリクロルシラン、T−アミノプロピルトリエト
キシシラン等を挙げることができる。本発明方法では、
シランカップリング剤を1種のみ単独で用いてもよいし
、・2種以上を混合して用いてもよい。Examples include vinyltrichlorosilane and T-aminopropyltriethoxysilane. In the method of the present invention,
One type of silane coupling agent may be used alone, or two or more types may be used in combination.
合成繊維布帛にシランカップリング剤を付与する方法は
、パッディング法、スプレー法、コーティング法等のう
ち、いずれでもよい。The method for applying the silane coupling agent to the synthetic fiber fabric may be any one of padding, spraying, coating, and the like.
シランカップリング剤の付与量は、シランカップリング
剤の種類により異なるので、加工に先立って実験によっ
て決定することが必要である。The amount of silane coupling agent applied varies depending on the type of silane coupling agent, so it is necessary to determine it by experiment prior to processing.
シランカップリング剤の付与後1本発明ではその布帛上
に熱可塑性樹脂を溶融状態で押出して圧着する。ここで
用いる熱可塑性樹脂としては、炭化水素系樹脂(ポリエ
チレン、ポリプロピレン。After applying the silane coupling agent, in the present invention, a thermoplastic resin is extruded in a molten state onto the fabric and pressure bonded. The thermoplastic resin used here includes hydrocarbon resins (polyethylene, polypropylene, etc.).
ポリメチルペンテン、ポリブテン、ポリブタジェン、ポ
リスチレン等)、極性ビニル系樹脂(ポリ塩化ビニル、
ポリ酢酸ビニル、ポリメチルメタクリレート、ポリ塩化
ビニリデン、ポリテトラフロロエチレン等)、その他の
樹脂(ポリアセタール。Polymethylpentene, polybutene, polybutadiene, polystyrene, etc.), polar vinyl resins (polyvinyl chloride,
polyvinyl acetate, polymethyl methacrylate, polyvinylidene chloride, polytetrafluoroethylene, etc.), other resins (polyacetal).
ポリアミド、ポリカーボネート、ポリフェニレンオキシ
ド、ポリエチレンテレフタレート、ポリブチレンテレフ
タレート、ボリアリレート、ポリスルホン、ポリウレタ
ン、ポリエーテルスルホン。Polyamide, polycarbonate, polyphenylene oxide, polyethylene terephthalate, polybutylene terephthalate, polyarylate, polysulfone, polyurethane, polyether sulfone.
ポリイミド、ポリアミドイミド、ポリフェニレンスルフ
ィド等)の単独または2種以上の混合物並びに共重合物
を挙げることができる。溶融状態は。Polyimide, polyamideimide, polyphenylene sulfide, etc.) may be used alone or as a mixture of two or more thereof, as well as copolymers. What is the molten state?
熱可塑性樹脂をその融点以上の温度に加温し、エクスト
ルーダーで押出し得る程度に溶融させた状態であれば十
分である。It is sufficient if the thermoplastic resin is heated to a temperature equal to or higher than its melting point and melted to the extent that it can be extruded with an extruder.
本発明方法では、溶融押出しコーティング加工の常法に
従い2合成繊維布帛上に熱可塑性樹脂を溶融状態で押出
し、圧着するが、押出しに際しては、エクストルーダー
からTダイを〆由してシート状に拡げて押出し、圧着に
際しては1合成繊維布帛上に溶融状態で押出されたシー
ト状の熱可塑性樹脂を加圧状態でプレスする。かくして
1合成繊維布帛と熱可塑性樹脂とを接着し1本発明の加
工を完了する。In the method of the present invention, a thermoplastic resin is extruded in a molten state onto two synthetic fiber fabrics and crimped according to the conventional method of melt extrusion coating processing. During extrusion and pressure bonding, a sheet-like thermoplastic resin extruded in a molten state is pressed onto a synthetic fiber fabric under pressure. In this way, the synthetic fiber fabric and the thermoplastic resin are bonded together, and the processing of the present invention is completed.
本発明方法で用いるエクストルーダーやTダイは9通常
の溶融押出しコーティング加工の際に用いられるもので
よい。The extruder and T-die used in the method of the present invention may be those used in ordinary melt extrusion coating processing.
本発明は9以上の構成を有するものである。The present invention has nine or more configurations.
(作 用)
本発明方法では9合成繊維布帛への溶融押出しコーティ
ング加工に際して、予め合成繊維布帛にシランカップリ
ング剤を付与してから、該布帛上に溶融状態の熱可塑性
樹脂を押出し、圧着する構成を有し9合成繊維布帛に付
与されたシランカップリング剤が合成繊維布帛と熱可塑
性樹脂との間の接着性の向上に何らかの役目を果たして
いると思われるが、現在のところ、その作用機構の詳細
は不明である。(Function) In the method of the present invention, when applying melt extrusion coating to synthetic fiber fabric, a silane coupling agent is applied to the synthetic fiber fabric in advance, and then a molten thermoplastic resin is extruded onto the fabric and crimped. It is believed that the silane coupling agent added to the synthetic fiber fabric with the following structure plays some role in improving the adhesion between the synthetic fiber fabric and the thermoplastic resin, but the mechanism of action is currently unknown. Details are unknown.
(実施例)
次に1本発明を実施例によってさらに具体的に説明する
が、加工布の性能は以下の方法で測定した。(Example) Next, the present invention will be explained in more detail with reference to Examples. The performance of the processed cloth was measured by the following method.
巾25市の試料片を、引張速度300mm/分。 A sample piece with a width of 25 cm was pulled at a speed of 300 mm/min.
90°の角度で引き剥がすときの剥離強力を。Peel strength when peeling off at a 90° angle.
島津製作所■のテンシロンを用いて測定した。It was measured using Tensilon manufactured by Shimadzu Corporation.
実施例1
ナイロンタフタ(経糸 70d/12f、緯糸70d/
24f、経糸密度 100本/吋、緯糸密度 90本/
吋)の精練、染色後のものに、T−アミノプロピルトリ
エトキシシラン1%水溶液をピックアップ40%で含浸
し、110℃で乾燥して被コーテイング布とした。Example 1 Nylon taffeta (warp 70d/12f, weft 70d/
24f, warp density 100 pieces/inch, weft density 90 pieces/inch
After scouring and dyeing, the fabric was impregnated with a 1% aqueous solution of T-aminopropyltriethoxysilane at a pickup rate of 40%, and dried at 110°C to obtain a coated fabric.
次に、エクストルーダーにより、ミラソン1OP(三井
石油化学工業■製のポリエチレン、融点106℃、密度
0.917 g /C11りを、押出し温度315℃で
Tダイ (800mm巾、シングルマニホールドタイプ
ダイ)から上記被コーティング布上に押出した後、これ
を金属製冷却ロールとシリコンラバーライニングのプレ
ッシャーロールとからなるニップロールにて圧着し、加
工速度60m/minで巻取って1本発明の溶融押出し
コーティング加工布を得た。Next, using an extruder, Mirason 1OP (polyethylene manufactured by Mitsui Petrochemical Industries ■, melting point 106°C, density 0.917 g/C11) was extruded from a T-die (800 mm width, single manifold type die) at an extrusion temperature of 315°C. After extruding onto the cloth to be coated, it is crimped with a nip roll consisting of a metal cooling roll and a silicone rubber-lined pressure roll, and wound up at a processing speed of 60 m/min to obtain the melt extrusion coated cloth of the present invention. I got it.
本発明との比較のため9本実施例においてナイロンタフ
タへのT−アミノプロピルトリエトキシシラン(シラン
カップリング剤)の含浸を省くほかは1本実施例と全く
同一の方法により比較用の溶融押出しコーティング加工
布を得た。For comparison with the present invention 9 Melt extrusion for comparison was carried out in exactly the same manner as in this example except that impregnation of nylon taffeta with T-aminopropyltriethoxysilane (silane coupling agent) was omitted. A coated cloth was obtained.
本発明および比較用の溶融押出しコーティング加工布に
ついて性能を測定し、その結果を合わせて第1表に示し
た。The performance of the melt-extrusion coated fabrics of the present invention and comparative fabrics was measured, and the results are shown in Table 1.
第1表より明らかなごとく1本発明の溶融押出しコーテ
ィング加工布は、優れた接着強力を有していることがわ
かる。As is clear from Table 1, the melt-extrusion coated fabric of the present invention has excellent adhesive strength.
実施例2
上記実施例1において、押出しコーティング用樹脂のミ
ラソン10Pに代えてレザミンP−1040(大日精化
■製ポリウレタン、融点94℃、密度1.21g/c1
1りを用い、押出し温度315℃に代えて170℃で押
出すほかは、実施例1と全く同一の方法で本発明の溶融
押出しコーティング加工布を得た。Example 2 In the above Example 1, Rezamin P-1040 (polyurethane manufactured by Dainichiseika Chemical Co., Ltd., melting point 94°C, density 1.21 g/c1) was used in place of the extrusion coating resin Mirason 10P.
A melt-extrusion coated fabric of the present invention was obtained in exactly the same manner as in Example 1, except that the extrusion temperature was 170°C instead of 315°C.
本発明との比較のだ約9本実施例2においてナイロンタ
フタへのγ−アミノプロピルトリエトキシシラン(シラ
ンカップリング剤)の含浸を省くほかは1本実施例2と
全く同一の方法により比較用の溶融押出しコーティング
加工布を得た。Comparison with the present invention Approximately 9 Comparative samples were prepared in the same manner as in Example 2, except that impregnation of nylon taffeta with γ-aminopropyltriethoxysilane (silane coupling agent) was omitted in Example 2. A melt extrusion coated fabric was obtained.
本発明および比較用の溶融押出しコーティング加工布に
ついて性能を測定し、その結果を合わせて第2表に示し
た。The performance of the melt-extrusion coated fabrics of the present invention and comparative fabrics was measured, and the results are shown in Table 2.
第2表の結果から明らかなように、シランカップリング
剤を付与した本発明のコーティング布は。As is clear from the results in Table 2, the coated fabric of the present invention provided with a silane coupling agent.
接着強力が非常に良好であった。The adhesive strength was very good.
(発明の効果)
本発明方法によれば1合成繊維布帛への熱可塑性樹脂の
溶融押出しコーティング加工において。(Effects of the Invention) According to the method of the present invention: 1. In the melt extrusion coating process of a thermoplastic resin onto a synthetic fiber fabric.
優れた接着強力を有するコーティング加工布を得ること
が可能となる。It becomes possible to obtain a coated fabric with excellent adhesive strength.
Claims (1)
際し、予め合成繊維布帛にシランカップリング剤を付与
し、しかる後に該布帛上に熱可塑性樹脂を溶融状態で押
出して圧着することを特徴とする溶融押出しコーティン
グ加工方法。(1) When performing melt extrusion coating on a synthetic fiber fabric, a silane coupling agent is applied to the synthetic fiber fabric in advance, and then a thermoplastic resin is extruded and crimped onto the fabric in a molten state. Extrusion coating processing method.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1127429A JPH02307986A (en) | 1989-05-19 | 1989-05-19 | Method for carrying out melt extrusion coating finish |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1127429A JPH02307986A (en) | 1989-05-19 | 1989-05-19 | Method for carrying out melt extrusion coating finish |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH02307986A true JPH02307986A (en) | 1990-12-21 |
Family
ID=14959740
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP1127429A Pending JPH02307986A (en) | 1989-05-19 | 1989-05-19 | Method for carrying out melt extrusion coating finish |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH02307986A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2001056756A1 (en) * | 2000-02-04 | 2001-08-09 | Commonwealth Scientific And Industrial Research Organisation | Treatment of natural polymer based materials and the products based thereon |
-
1989
- 1989-05-19 JP JP1127429A patent/JPH02307986A/en active Pending
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2001056756A1 (en) * | 2000-02-04 | 2001-08-09 | Commonwealth Scientific And Industrial Research Organisation | Treatment of natural polymer based materials and the products based thereon |
| US7459185B2 (en) | 2000-02-04 | 2008-12-02 | Commonwealth Scientific And Industrial Research Organization | Treatment of natural polymer based materials and the products based thereon |
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