JPS6228744B2 - - Google Patents
Info
- Publication number
- JPS6228744B2 JPS6228744B2 JP55040839A JP4083980A JPS6228744B2 JP S6228744 B2 JPS6228744 B2 JP S6228744B2 JP 55040839 A JP55040839 A JP 55040839A JP 4083980 A JP4083980 A JP 4083980A JP S6228744 B2 JPS6228744 B2 JP S6228744B2
- Authority
- JP
- Japan
- Prior art keywords
- flocked
- synthetic resin
- layer
- resin layer
- laminate
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 239000010410 layer Substances 0.000 claims description 51
- 229920003002 synthetic resin Polymers 0.000 claims description 39
- 239000000057 synthetic resin Substances 0.000 claims description 38
- 230000001070 adhesive effect Effects 0.000 claims description 19
- 239000000843 powder Substances 0.000 claims description 16
- 239000012790 adhesive layer Substances 0.000 claims description 13
- 239000006185 dispersion Substances 0.000 claims description 13
- 239000000463 material Substances 0.000 claims description 13
- 239000004831 Hot glue Substances 0.000 claims description 12
- 229920005989 resin Polymers 0.000 claims description 10
- 239000011347 resin Substances 0.000 claims description 10
- 238000001035 drying Methods 0.000 claims description 7
- 238000010438 heat treatment Methods 0.000 claims description 7
- 239000011248 coating agent Substances 0.000 claims description 2
- 238000000576 coating method Methods 0.000 claims description 2
- 239000000839 emulsion Substances 0.000 description 9
- 239000000853 adhesive Substances 0.000 description 7
- -1 polyoxyethylene nonylphenol Polymers 0.000 description 6
- 239000000835 fiber Substances 0.000 description 5
- 239000000049 pigment Substances 0.000 description 5
- 229920000642 polymer Polymers 0.000 description 5
- 239000002562 thickening agent Substances 0.000 description 5
- 239000000975 dye Substances 0.000 description 4
- 239000012943 hotmelt Substances 0.000 description 4
- 238000002156 mixing Methods 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 229920006122 polyamide resin Polymers 0.000 description 3
- 229920002050 silicone resin Polymers 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 229920000877 Melamine resin Polymers 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 2
- 229920000297 Rayon Polymers 0.000 description 2
- 229920006026 co-polymeric resin Polymers 0.000 description 2
- 239000003822 epoxy resin Substances 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 229920001495 poly(sodium acrylate) polymer Polymers 0.000 description 2
- 229920002647 polyamide Polymers 0.000 description 2
- 229920000647 polyepoxide Polymers 0.000 description 2
- 229920002635 polyurethane Polymers 0.000 description 2
- 239000004814 polyurethane Substances 0.000 description 2
- 239000002964 rayon Substances 0.000 description 2
- NNMHYFLPFNGQFZ-UHFFFAOYSA-M sodium polyacrylate Chemical compound [Na+].[O-]C(=O)C=C NNMHYFLPFNGQFZ-UHFFFAOYSA-M 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- 229920005992 thermoplastic resin Polymers 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- RNMDNPCBIKJCQP-UHFFFAOYSA-N 5-nonyl-7-oxabicyclo[4.1.0]hepta-1,3,5-trien-2-ol Chemical compound C(CCCCCCCC)C1=C2C(=C(C=C1)O)O2 RNMDNPCBIKJCQP-UHFFFAOYSA-N 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- JHWNWJKBPDFINM-UHFFFAOYSA-N Laurolactam Chemical compound O=C1CCCCCCCCCCCN1 JHWNWJKBPDFINM-UHFFFAOYSA-N 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- 229920002821 Modacrylic Polymers 0.000 description 1
- 229920000459 Nitrile rubber Polymers 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 229920000299 Nylon 12 Polymers 0.000 description 1
- 229920002292 Nylon 6 Polymers 0.000 description 1
- 229920000572 Nylon 6/12 Polymers 0.000 description 1
- 229920000577 Nylon 6/66 Polymers 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 229920001328 Polyvinylidene chloride Polymers 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 239000004809 Teflon Substances 0.000 description 1
- 229920006362 Teflon® Polymers 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 238000004873 anchoring Methods 0.000 description 1
- TZYHIGCKINZLPD-UHFFFAOYSA-N azepan-2-one;hexane-1,6-diamine;hexanedioic acid Chemical compound NCCCCCCN.O=C1CCCCCN1.OC(=O)CCCCC(O)=O TZYHIGCKINZLPD-UHFFFAOYSA-N 0.000 description 1
- 239000004566 building material Substances 0.000 description 1
- DQXBYHZEEUGOBF-UHFFFAOYSA-N but-3-enoic acid;ethene Chemical compound C=C.OC(=O)CC=C DQXBYHZEEUGOBF-UHFFFAOYSA-N 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000011247 coating layer Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 238000005034 decoration Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 238000004070 electrodeposition Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000006082 mold release agent Substances 0.000 description 1
- 229920006173 natural rubber latex Polymers 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 229920001084 poly(chloroprene) Polymers 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920013716 polyethylene resin Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 239000002952 polymeric resin Substances 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 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
- 238000003825 pressing Methods 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 229920006174 synthetic rubber latex Polymers 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Application Of Or Painting With Fluid Materials (AREA)
- Laminated Bodies (AREA)
Description
【発明の詳細な説明】 この発明は改良された植毛積層物に関する。[Detailed description of the invention] This invention relates to improved flocked laminates.
さらに詳しくは植毛積層物において、合成樹脂
層、接着剤層および植毛層からなり、かつ合成樹
脂層がホツトメルト接着性を有する合成樹脂粉末
を含有する水性分散体を塗布して加熱乾燥して得
られる樹脂層であることを特徴とし、合成樹脂層
の下には必要に応じて離型材を設けてなる植毛積
層物に関する。 More specifically, the flocked laminate consists of a synthetic resin layer, an adhesive layer, and a flocked layer, and the synthetic resin layer is obtained by applying an aqueous dispersion containing a synthetic resin powder having hot melt adhesive properties and drying it by heating. The present invention relates to a flocked laminate characterized by being a resin layer, and optionally provided with a release material under the synthetic resin layer.
従来、植毛積層物は、例えば、布帛類のマー
ク、ワツペン等としての服装、袋物の装飾品;手
芸用品、教材用品;建材、車輌等の内装品;その
他の資材用等の広い分野で用いられている。これ
らの用途の多くは、植毛積層物を被着体に接着し
て用いられるものであり、このような植毛積層物
は、一般にホツトメルト接着性を有する合成樹脂
基体層、接着剤層、植毛層の順に一体に重ねた3
層からなるものである。そしてこの積層物を実用
に供する場合、特に要求される特性は、植毛層が
該基体層に強固に接着していることである。 Conventionally, flocked laminates have been used in a wide range of fields, such as markings on fabrics, clothing as badges, decorations for bags; handicraft supplies, educational materials; building materials, interior parts of vehicles, etc.; and other materials. ing. In many of these applications, flocked laminates are used by adhering them to adherends, and such flocked laminates generally consist of a synthetic resin base layer with hot melt adhesiveness, an adhesive layer, and a flocked layer. 3 stacked together in order
It consists of layers. When this laminate is put to practical use, a particularly required characteristic is that the flocked layer firmly adheres to the base layer.
一方、特公昭52−25433号公報には、第1図に
示すごとく、離型材1、ホツトメルト接着性を有
する合成樹脂基体層2、接着剤層3および植毛層
4の4層からなる植毛積層物が開示され、該接着
剤層3を用いて植毛層4を基体層2に強固に接着
することができると記載されている。 On the other hand, Japanese Patent Publication No. 52-25433 discloses a flocked laminate consisting of four layers: a mold release material 1, a synthetic resin base layer 2 having hot melt adhesive properties, an adhesive layer 3, and a flocked layer 4, as shown in FIG. is disclosed, and it is described that the flocked layer 4 can be firmly adhered to the base layer 2 using the adhesive layer 3.
一方特開昭54−18874号公報には、熱加塑性樹
脂層に、接着剤を介せずして直接植毛層を植毛し
た2層からなる植毛体が開示されている。しかし
ながらこの植毛体では植毛層が熱加塑性樹脂層に
強固に接着していないなどの欠点がある。 On the other hand, JP-A-54-18874 discloses a two-layer flocked body in which a flocked layer is directly flocked onto a thermoplastic resin layer without using an adhesive. However, this flocked body has drawbacks such as the fact that the flocked layer is not firmly adhered to the thermoplastic resin layer.
この発明は、上記の発明をさらに発展させたも
のである。すなわち第2図に示すごとく必要に応
じて設ける離型材5、その上に順に合成樹脂層6
接着剤層7および植毛層8からなり、かつ合成樹
脂層6はホツトメルト接着性を有する樹脂の単な
るフイルムではなくて、ホツトメルト接着性を有
する合成樹脂粉末を含有する水性分散体を塗布し
加熱乾燥して得られる樹脂層であることを特徴と
するものである。その結果該合成樹脂層6の接着
剤層7と接着する側の表面は、予め製造され、通
常表面が平滑な樹脂フイルムの表面とは異なり、
微細な凹凸を多数有するので、その凹凸によるア
ンカー効果によつて、接着剤層7を介して行なわ
れる植毛層8の合成樹脂層6への接着が良好であ
る。 This invention is a further development of the above invention. That is, as shown in FIG. 2, a mold release material 5 is provided as necessary, and a synthetic resin layer 6 is sequentially formed thereon.
The synthetic resin layer 6 consists of an adhesive layer 7 and a flocked layer 8, and the synthetic resin layer 6 is not just a film of a resin having hot melt adhesive properties, but is made by applying an aqueous dispersion containing a synthetic resin powder having hot melt adhesive properties and drying it by heating. It is characterized by being a resin layer obtained by. As a result, the surface of the synthetic resin layer 6 that is bonded to the adhesive layer 7 is different from the surface of a resin film that is manufactured in advance and usually has a smooth surface.
Since it has a large number of fine irregularities, the anchoring effect of the irregularities allows the flocked layer 8 to be well adhered to the synthetic resin layer 6 via the adhesive layer 7.
この発明の植毛積層物に用いられる離型材とし
ては通常のものが用いられる。なかでも次のよう
な性能を有するものが好ましい。 As the mold release material used in the flocked laminate of this invention, a conventional one can be used. Among these, those having the following properties are preferred.
a 吸湿性が小さいこと
b 合成樹脂層とほぼ同一の収縮率を有すること
c 加熱によつて、硬化を起さず積層物の品質を
損なうような変質をしないこと
d 合成樹脂層との接着性が小さいこと
e シリコン樹脂の移行が少ないこと
f 安定した剥離性を有すること
この発明に用いられるホツトメルト接着性能を
有する合成樹脂粉末としてはポリアミド共重合樹
脂、ポリエステル樹脂、ポリエチレン樹脂、エチ
レン−酢酸ビニル共重合樹脂等が可能である。a. It has low hygroscopicity. b. It has almost the same shrinkage rate as the synthetic resin layer. c. It does not harden when heated and does not undergo changes that would impair the quality of the laminate. d. Adhesion to the synthetic resin layer. (e) Little migration of silicone resin (f) Stable releasability Synthetic resin powders with hot melt adhesive properties used in this invention include polyamide copolymer resin, polyester resin, polyethylene resin, and ethylene-vinyl acetate. Polymer resins, etc. are possible.
特に、接着強度及び繊維製品への適用において
重要な特性である耐洗濯性の点から、融点80〜
160℃のポリアミド共重合樹脂が好適であり、例
えばナイロン6/66/12,6/69/12,6/
610/12,6/612/12,6/66/11,6/66/
69/12,6/66/610/12,6/66/612/12,
6/66/11/12,6/69/11/12等の粉末があ
る。融点はDSCにて昇温速度16℃/mmにて測定
した。 In particular, from the viewpoint of adhesive strength and washing resistance, which are important properties when applied to textile products,
Polyamide copolymer resins at 160°C are suitable, such as nylon 6/66/12, 6/69/12, 6/
610/12, 6/612/12, 6/66/11, 6/66/
69/12, 6/66/610/12, 6/66/612/12,
There are powders such as 6/66/11/12 and 6/69/11/12. The melting point was measured by DSC at a temperature increase rate of 16°C/mm.
また、合成樹脂粉末としては平均粒径が約0.1
〜500μのものを使用することができる。接着性
からみて粒子径に特に制限を設ける必要はない
が、ホツトメルト接着性を有する合成樹脂粉末の
水性分散体内での分散および水性分散体としての
流動性の点から細かいものの方が好ましい。 In addition, as a synthetic resin powder, the average particle size is approximately 0.1
~500μ can be used. There is no need to particularly limit the particle size from the viewpoint of adhesion, but from the viewpoint of dispersion in an aqueous dispersion of synthetic resin powder having hot melt adhesive properties and fluidity as an aqueous dispersion, finer particles are preferable.
また上記ホツトメルト接着性能を有する合成樹
脂粉末は増粘剤、界面活性剤、水およびその他の
添加剤と通常の方法、例えばニーダータイプの撹
拌機で混合し、上記粉末を均一に分散させて水性
分散体とし、離型性を有する支持体に塗布して用
いられる。 In addition, the above synthetic resin powder having hot melt adhesive properties is mixed with a thickener, a surfactant, water, and other additives in a conventional manner, for example, using a kneader type stirrer, and the above powder is uniformly dispersed into an aqueous dispersion. It is used by coating it on a support that has mold releasability.
増粘剤としては通常のもの、例えば、ポリアク
リル酸ナトリウム、ポリアクリルアミドヒドロキ
シエチルセルロース、ポリビニルアルコール等が
用いられ、界面活性剤としては、例えばポリオキ
シエチレンノニルフエノールエーテル、ポリオキ
シエチレンモノオレエート、ポリオキシアルキレ
ングリコール誘導体等が用いられる。 As thickeners, common ones such as sodium polyacrylate, polyacrylamide hydroxyethyl cellulose, and polyvinyl alcohol are used, and as surfactants, for example, polyoxyethylene nonylphenol ether, polyoxyethylene monooleate, and Oxyalkylene glycol derivatives and the like are used.
またこの水性分散体中の該合成樹脂粉末の配合
率は10〜50%、好ましくは20〜40%である。該合
成樹脂粉末の配合率が上記の範囲より低いと、被
着体に対する該合成樹脂粉末の塗布量が不足して
接着性が不良となり、また上記範囲より高いとペ
ーストが不安定になりかつ離型材への均一な塗布
がむづくしくなる。また塗布層の厚みは通常100
〜200μであり、ペーストの粘度または塗布方法
によつて適宜調節される。 The blending ratio of the synthetic resin powder in this aqueous dispersion is 10 to 50%, preferably 20 to 40%. If the blending ratio of the synthetic resin powder is lower than the above range, the amount of the synthetic resin powder applied to the adherend will be insufficient, resulting in poor adhesion, and if it is higher than the above range, the paste will become unstable and may separate. It becomes difficult to apply uniformly to the mold material. Also, the thickness of the coating layer is usually 100
~200μ, and is appropriately adjusted depending on the viscosity of the paste or the application method.
本発明に用いられる接着剤としては、特に限定
はなく、一般に植毛加工に使用できるものであれ
ばいかなるものでもよい。例えば、次のようなポ
リマーエマルジヨンが例示できる。 The adhesive used in the present invention is not particularly limited, and any adhesive that can generally be used for flocking may be used. For example, the following polymer emulsion can be exemplified.
すなわち天然ゴムラテツクス、ニトリル−ブタ
ジエンゴム、スチレンブタジエンゴム、クロロプ
レンゴム等の合成ゴムラテツクス、ポリアクリル
酸エステル、ポリ塩化ビニル、ポリ塩化ビニリデ
ン、ポリ酢酸ビニル、ポリエチレン−酢ビ、エポ
キシ樹脂、ポリウレタン等の合成樹脂エマルジヨ
ンなどほとんどのポリマーエマルジヨンが使用可
能である。もちろん、これらには通常行なわれて
いるような変性エマルジヨンも含まれている。 Namely, natural rubber latex, synthetic rubber latex such as nitrile-butadiene rubber, styrene-butadiene rubber, chloroprene rubber, and synthetic resins such as polyacrylic acid ester, polyvinyl chloride, polyvinylidene chloride, polyvinyl acetate, polyethylene-vinyl acetate, epoxy resin, and polyurethane. Most polymer emulsions can be used, including emulsions. Of course, these also include modified emulsions that are commonly used.
さらに、これらポリマーエマルジヨンは単独に
使用される外、混合して使用することもできる。 Furthermore, these polymer emulsions can be used alone or in combination.
さらに、これらポリマーエマルジヨンには、必
要に応じて増粘剤、顔料、架橋剤(メラミン樹
脂、エポキシ樹脂、イソシアネートのブロツク体
等)、架橋のための触媒等が添加される。 Furthermore, thickeners, pigments, crosslinking agents (melamine resins, epoxy resins, isocyanate blocks, etc.), catalysts for crosslinking, etc. are added to these polymer emulsions as necessary.
上記のような合成樹脂層および/または接着剤
層に、被着体に対する隠蔽性を付与するために染
顔料を加えることができる。つまり植毛積層物を
貼合せようとする被着体の色彩の影響を受けない
ようにすることができる。隠蔽力の強い染顔料と
して酸化チタン微粉末、黒色(例えば東洋ドライ
カラーTN−0643)、赤色(例えば東洋ドライカラ
ーTN−4274)、青色(例えば東洋ドライカラー
TN−7268)等が挙げられる。また合成樹脂層に
染顔料を配合するときは、ホツトメルト接着性能
を有する合成樹脂粉末そのものに予めこれらの染
顔料を添加しておくこともできる。 Dyes and pigments can be added to the synthetic resin layer and/or the adhesive layer as described above in order to impart hiding properties to the adherend. In other words, it is possible to avoid being affected by the color of the adherend to which the flocked laminate is to be bonded. Titanium oxide fine powder, black (e.g. Toyo Dry Color TN-0643), red (e.g. Toyo Dry Color TN-4274), and blue (e.g. Toyo Dry Color TN-4274) are used as dyes and pigments with strong hiding power.
TN-7268), etc. Further, when blending dyes and pigments into the synthetic resin layer, these dyes and pigments can be added in advance to the synthetic resin powder itself having hot melt adhesive properties.
この発明の植毛積層物は一般に次のようにして
製造される。 The flocked laminate of this invention is generally produced as follows.
前記のホツトメルト接着性を有する合成樹脂粉
末を含有する水性分散体を離型性を有する支持体
上に通常の方法、例えばロールコーターで塗布す
る。次いでこれを150〜200℃で加熱乾燥する。次
いで得られた合成樹脂層の上に接着剤を通常の方
法、例えばロールコーターで塗布する。また水性
分散体を塗布したのち、加熱乾燥することなく、
直ちに接着剤を塗布することもできる。次いで短
繊維群が主として静電植毛法(電着または電気植
毛法)によつて、接着剤層に植毛される。次いで
接着剤層のポリマーエマルジヨンのベーキング温
度程度で加熱乾燥が行なわれる。 The aqueous dispersion containing the synthetic resin powder having hot melt adhesive properties is coated onto a support having mold releasability by a conventional method, for example, using a roll coater. Next, this is heated and dried at 150 to 200°C. An adhesive is then applied on the resulting synthetic resin layer in a conventional manner, for example using a roll coater. In addition, after applying the aqueous dispersion, there is no need to heat and dry it.
Adhesive can also be applied immediately. The short fibers are then flocked onto the adhesive layer primarily by electrostatic flocking (electrodeposition or electro-flocking). Next, heating and drying is performed at about the baking temperature of the polymer emulsion of the adhesive layer.
この加熱乾燥により合成樹脂層がフイルム化
し、離型性を有する支持体との剥離が可能な植毛
体が得られる。 This heating and drying turns the synthetic resin layer into a film, yielding a flocked body that can be peeled off from a support having releasable properties.
この支持体としては、離型紙などの離型材を用
いることができる。この場合、離型紙を付したま
ま新製品とすることができる。 As this support, a release material such as release paper can be used. In this case, a new product can be manufactured with the release paper still attached.
さらに支持体としては、それ自体で離型性のあ
る材質、例えばテフロン樹脂等で作製したベル
ト、又は耐熱ゴム、ポリウレタン等の耐熱合成体
等の表面にシリコン樹脂などの離型剤を塗布した
ベルトを用いることができる。 Furthermore, the support may be a belt made of a material that itself has mold release properties, such as Teflon resin, or a belt made of a heat-resistant synthetic material such as heat-resistant rubber or polyurethane coated with a mold-release agent such as silicone resin. can be used.
又、シリコン樹脂などの離型剤を塗布したポリ
エチレン、ポリプロピレン、ポリエチレンテレフ
タレートなどの合成樹脂製シート又はフイルムも
支持体として用いることができる。 Further, a sheet or film made of a synthetic resin such as polyethylene, polypropylene, or polyethylene terephthalate coated with a release agent such as silicone resin can also be used as the support.
これらの支持体を用いた場合には、支持体から
植毛体を剥離して製品とされる。 When these supports are used, the flocked body is peeled off from the support to produce a product.
もちろん、この場合必要に応じて支持体から植
毛体を剥離したのち離型紙等の離型材を取りつけ
ることもできる。 Of course, in this case, a release material such as release paper may be attached after the flocked body is peeled off from the support if necessary.
この発明に用いられる短繊維群としては染色
し、電着処理したものであつて、アクリル、ナイ
ロン、ポリエステル、レーヨン、コツトン、モダ
クリル等の繊維を束ねた状態で任意の長さに切断
したものが用いられる。 The short fibers used in this invention are dyed and electrodeposited fibers made of acrylic, nylon, polyester, rayon, cotton, modacrylic, etc., which are bundled and cut into arbitrary lengths. used.
この発明の植毛積層物を使用する場合は、離型
材がある場合はそれをはがしとり、合成樹脂層を
被着体に向けて重ね、植毛部側と反対側より加熱
押圧すると、合成樹脂層が融着して植毛積層物と
被着体が接着される。 When using the flocked laminate of this invention, if there is a mold release material, peel it off, stack the synthetic resin layer facing the adherend, heat and press from the side opposite to the flocked part, and the synthetic resin layer are fused and the flocked laminate and the adherend are adhered.
次いで実施例に基づいてこの発明を例証する
が、これによつてこの発明が限定されるものでは
ない。 Next, the present invention will be illustrated based on Examples, but the present invention is not limited thereby.
実施例
水100重量部中に増粘剤として、ポリアクリル
酸ナトリウム2重量部を加え、インペラータイプ
の撹拌機で約4時間撹拌した。この増粘剤溶液に
ポリエチレングリコールを1重量部加え、30分間
撹拌したのち平均粒経60μの粒度のポリアミド樹
脂ナイロン6/6・12/12(共重合比30/30/
40、融点115℃)の粉末60重量部を加え更に1時
間撹拌し、ポリアミド樹脂が均一に分散された粘
度が75,000cps(BL型粘度計、ロータ・No.4,
6rpm)の乳白状の水性分散体を得た。Example 2 parts by weight of sodium polyacrylate as a thickener was added to 100 parts by weight of water, and the mixture was stirred for about 4 hours using an impeller type stirrer. 1 part by weight of polyethylene glycol was added to this thickener solution, stirred for 30 minutes, and then polyamide resin nylon 6/6/12/12 (copolymerization ratio 30/30/
40, melting point 115℃) was added and stirred for an additional hour, and the viscosity was 75,000 cps (BL type viscometer, rotor No. 4, with polyamide resin uniformly dispersed).
A milky white aqueous dispersion was obtained.
この水性分散体を表面がシリコン加工で処理さ
れた離型紙上に約270μの厚みに塗布したのち、
150℃の温度で9分間加熱乾燥したところ離型紙
上に厚み約100μのフイルム状態のポリアミド樹
脂のホツトメルト樹脂層を得た。このフイルム状
ホツトメルト樹脂層の上に、メタクリル酸変性の
エチルアクリレート−ブチルアクリレート共重合
エマルジヨン(固型分濃度46%、エマルジヨンの
固型分100重量部に対し、メラミン樹脂5重量部
を使用したアンモニア水で約1000cpsに増粘させ
たもの)を塗布し、更にこの上にレーヨンの短繊
維(繊度:7.5デニール、繊維長:0.5mm)を静電
植毛法により直接植毛し、その後90℃の温度でベ
ーキングして植毛積層物を作成した。 After applying this aqueous dispersion to a thickness of about 270μ on release paper whose surface was treated with silicone,
After drying by heating at a temperature of 150° C. for 9 minutes, a hot melt resin layer of polyamide resin in the form of a film with a thickness of about 100 μm was obtained on the release paper. On top of this film-like hot melt resin layer, a methacrylic acid-modified ethyl acrylate-butyl acrylate copolymer emulsion (solid content concentration 46%, ammonia containing 5 parts by weight of melamine resin per 100 parts by weight of solid content of the emulsion) is applied. (thickened to approximately 1000 cps with water), and on top of this, short rayon fibers (fineness: 7.5 denier, fiber length: 0.5 mm) were directly flocked using the electrostatic flocking method, and then at a temperature of 90℃. A flocked laminate was created by baking with
次にこの植毛積層物を所望の形状に切り、植毛
面の反対側に付着している離型紙を剥離してメリ
ヤスシヤツ上に設置し、アイロンを用いて150℃
で10秒間ヒートプレスを行ないこの植毛積層物を
熱接着させた。この植毛積層物の接着強度および
耐洗濯性は非常に良好であつた。 Next, cut this flocked laminate into the desired shape, peel off the release paper attached to the opposite side of the flocked surface, place it on a stockinette shirt, and heat it to 150°C using an iron.
This flocked laminate was thermally bonded by heat pressing for 10 seconds. The adhesive strength and washing resistance of this flocked laminate were very good.
第1図は特公昭52−25433号に開示された植毛
積層物の断面図および第2図は本発明の植毛積層
物の一実施態様の断面図である。
1,5……離型材、2……ホツトメルト接着性
を有する合成樹脂基体層、3,7……接着剤層、
4,8……植毛層、6……ホツトメルト樹脂層。
FIG. 1 is a sectional view of a flocked laminate disclosed in Japanese Patent Publication No. 52-25433, and FIG. 2 is a sectional view of an embodiment of the flocked laminate of the present invention. 1, 5... Mold release material, 2... Synthetic resin base layer having hot melt adhesive properties, 3, 7... Adhesive layer,
4, 8...Flocked layer, 6...Hot melt resin layer.
Claims (1)
順に接着剤層および植毛層の3層からなり、かつ
合成樹脂層がホツトメルト接着性を有する合成樹
脂粉末を含有する水性分散体を塗布して加熱乾燥
して得られる樹脂層であることを特徴とする植毛
積層物。 2 植毛積層物において、離型材、その上に順に
合成樹脂層、接着剤層および植毛層の4層からな
り、かつ合成樹脂層がホツトメルト接着性を有す
る合成樹脂粉末を含有する水性分散体を塗布して
加熱乾燥して得られる樹脂層であることを特徴と
する植毛積層物。[Scope of Claims] 1. A flocked laminate comprising three layers: a synthetic resin layer, an adhesive layer and a flocked layer thereon in order, and the synthetic resin layer is an aqueous dispersion containing synthetic resin powder having hot melt adhesive properties. A flocked laminate characterized in that it is a resin layer obtained by coating the body and heating and drying it. 2. In the flocked laminate, a mold release material is applied, and an aqueous dispersion containing synthetic resin powder, which consists of four layers, a synthetic resin layer, an adhesive layer, and a flocked layer in this order, and the synthetic resin layer has hot melt adhesive properties, is applied thereon. A flocked laminate characterized in that it is a resin layer obtained by heating and drying.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4083980A JPS56136356A (en) | 1980-03-28 | 1980-03-28 | Hair planted laminate |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4083980A JPS56136356A (en) | 1980-03-28 | 1980-03-28 | Hair planted laminate |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS56136356A JPS56136356A (en) | 1981-10-24 |
JPS6228744B2 true JPS6228744B2 (en) | 1987-06-22 |
Family
ID=12591773
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP4083980A Granted JPS56136356A (en) | 1980-03-28 | 1980-03-28 | Hair planted laminate |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS56136356A (en) |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5136387A (en) * | 1974-09-18 | 1976-03-27 | Takeo Suzuki | Shokuyoseiniku no meisekishokuhozonhososhorihoho |
JPS524671A (en) * | 1975-06-30 | 1977-01-13 | Matsushita Electric Works Ltd | Discharge lamp lighting apparatus |
JPS535347A (en) * | 1976-07-05 | 1978-01-18 | Hitachi Ltd | Fluid machinery |
JPS5418963A (en) * | 1977-03-11 | 1979-02-13 | Tokyo Printing Ink Mfg Co Ltd | Production of heat adhered cloth |
JPS5520035A (en) * | 1978-07-31 | 1980-02-13 | Tech Res & Dev Inst Of Japan Def Agency | Plane electric wave lens |
JPS6228744A (en) * | 1985-07-31 | 1987-02-06 | Canon Inc | Electrophotographic sensitive body |
-
1980
- 1980-03-28 JP JP4083980A patent/JPS56136356A/en active Granted
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5136387A (en) * | 1974-09-18 | 1976-03-27 | Takeo Suzuki | Shokuyoseiniku no meisekishokuhozonhososhorihoho |
JPS524671A (en) * | 1975-06-30 | 1977-01-13 | Matsushita Electric Works Ltd | Discharge lamp lighting apparatus |
JPS535347A (en) * | 1976-07-05 | 1978-01-18 | Hitachi Ltd | Fluid machinery |
JPS5418963A (en) * | 1977-03-11 | 1979-02-13 | Tokyo Printing Ink Mfg Co Ltd | Production of heat adhered cloth |
JPS5520035A (en) * | 1978-07-31 | 1980-02-13 | Tech Res & Dev Inst Of Japan Def Agency | Plane electric wave lens |
JPS6228744A (en) * | 1985-07-31 | 1987-02-06 | Canon Inc | Electrophotographic sensitive body |
Also Published As
Publication number | Publication date |
---|---|
JPS56136356A (en) | 1981-10-24 |
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