JPS63176135A - Laminate processing method - Google Patents
Laminate processing methodInfo
- Publication number
- JPS63176135A JPS63176135A JP62006221A JP622187A JPS63176135A JP S63176135 A JPS63176135 A JP S63176135A JP 62006221 A JP62006221 A JP 62006221A JP 622187 A JP622187 A JP 622187A JP S63176135 A JPS63176135 A JP S63176135A
- Authority
- JP
- Japan
- Prior art keywords
- roll
- base material
- resin liquid
- resinous solution
- passed
- 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
- 238000003672 processing method Methods 0.000 title 1
- 239000000463 material Substances 0.000 claims abstract description 48
- 238000000034 method Methods 0.000 claims abstract description 21
- 229920005989 resin Polymers 0.000 claims description 56
- 239000011347 resin Substances 0.000 claims description 56
- 239000007788 liquid Substances 0.000 claims description 45
- 238000010030 laminating Methods 0.000 claims description 11
- 238000010438 heat treatment Methods 0.000 abstract description 12
- 239000011248 coating agent Substances 0.000 description 6
- 238000000576 coating method Methods 0.000 description 5
- 238000003475 lamination Methods 0.000 description 5
- -1 2-allylbenzoin Chemical compound 0.000 description 4
- ISAOCJYIOMOJEB-UHFFFAOYSA-N benzoin Chemical compound C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 238000009816 wet lamination Methods 0.000 description 3
- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 description 2
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 2
- VVBLNCFGVYUYGU-UHFFFAOYSA-N 4,4'-Bis(dimethylamino)benzophenone Chemical compound C1=CC(N(C)C)=CC=C1C(=O)C1=CC=C(N(C)C)C=C1 VVBLNCFGVYUYGU-UHFFFAOYSA-N 0.000 description 2
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 2
- 239000004925 Acrylic resin Substances 0.000 description 2
- 229920000178 Acrylic resin Polymers 0.000 description 2
- 244000028419 Styrax benzoin Species 0.000 description 2
- 235000000126 Styrax benzoin Nutrition 0.000 description 2
- 235000008411 Sumatra benzointree Nutrition 0.000 description 2
- XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 description 2
- 229960002130 benzoin Drugs 0.000 description 2
- 235000019382 gum benzoic Nutrition 0.000 description 2
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 2
- YNPNZTXNASCQKK-UHFFFAOYSA-N phenanthrene Chemical compound C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- GRDGBWVSVMLKBV-UHFFFAOYSA-N (2-amino-5-nitrophenyl)-(2-chlorophenyl)methanone Chemical compound NC1=CC=C([N+]([O-])=O)C=C1C(=O)C1=CC=CC=C1Cl GRDGBWVSVMLKBV-UHFFFAOYSA-N 0.000 description 1
- DKEGCUDAFWNSSO-UHFFFAOYSA-N 1,8-dibromooctane Chemical compound BrCCCCCCCCBr DKEGCUDAFWNSSO-UHFFFAOYSA-N 0.000 description 1
- OWTXHNANQTWFLX-UHFFFAOYSA-N 1-(2-chlorophenyl)-2-hydroxy-2-phenylethanone Chemical compound C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1Cl OWTXHNANQTWFLX-UHFFFAOYSA-N 0.000 description 1
- FPKCTSIVDAWGFA-UHFFFAOYSA-N 2-chloroanthracene-9,10-dione Chemical compound C1=CC=C2C(=O)C3=CC(Cl)=CC=C3C(=O)C2=C1 FPKCTSIVDAWGFA-UHFFFAOYSA-N 0.000 description 1
- KMNCBSZOIQAUFX-UHFFFAOYSA-N 2-ethoxy-1,2-diphenylethanone Chemical compound C=1C=CC=CC=1C(OCC)C(=O)C1=CC=CC=C1 KMNCBSZOIQAUFX-UHFFFAOYSA-N 0.000 description 1
- BQZJOQXSCSZQPS-UHFFFAOYSA-N 2-methoxy-1,2-diphenylethanone Chemical compound C=1C=CC=CC=1C(OC)C(=O)C1=CC=CC=C1 BQZJOQXSCSZQPS-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- 229920000298 Cellophane Polymers 0.000 description 1
- 241001483078 Phyto Species 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 229920001328 Polyvinylidene chloride Polymers 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 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
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 1
- 150000004056 anthraquinones Chemical class 0.000 description 1
- 125000000751 azo group Chemical group [*]N=N[*] 0.000 description 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
- 239000012965 benzophenone Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 125000005442 diisocyanate group Chemical group 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 125000003055 glycidyl group Chemical group C(C1CO1)* 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
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 230000001678 irradiating effect Effects 0.000 description 1
- 239000002932 luster Substances 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 229910001507 metal halide Inorganic materials 0.000 description 1
- 150000005309 metal halides Chemical class 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 239000000123 paper Substances 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 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
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002223 polystyrene 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
- 239000011342 resin composition Substances 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 239000012780 transparent material Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Landscapes
- Application Of Or Painting With Fluid Materials (AREA)
- Coating Apparatus (AREA)
- Lining Or Joining Of Plastics Or The Like (AREA)
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
この発明は、紫外線硬化性樹脂液を、被着材と基材の間
に介在させながら圧着ロール間及び紫外線の照射部を通
過させるラミネート加工法の改良に関する。Detailed Description of the Invention (Industrial Application Field) This invention is a lamination process in which an ultraviolet curable resin liquid is passed between pressure rolls and an ultraviolet irradiation part while being interposed between an adherend and a base material. Concerning improvements in law.
(従来の技術)
従来、ラミネート加工方法としては熱可塑性樹脂、の溶
液を基材に塗布し、これを乾燥して溶剤を除去した後、
加熱したロール間を通し圧着するドライラミネート加工
法と、熱可塑性樹脂あるいは熱硬化性樹脂の溶液を基材
に塗布した後、ロール間を通過させて圧着し、その後該
樹脂液をセットさせるためのセット装置を通過させるウ
ェットラミネート加工法がある。(Prior Art) Conventionally, the laminating method involves applying a solution of thermoplastic resin to a base material, drying it to remove the solvent, and then
There is a dry laminating method in which a solution of thermoplastic or thermosetting resin is applied to a base material and then passed between rolls to be crimped, and then the resin liquid is set. There is a wet lamination method in which the material is passed through a setting device.
これらのラミネート加工法のうちトライラミネート加工
法は乾燥して溶剤を除去するため、溶剤蒸気による環境
汚染の問題があり、また加熱乾燥装置及び加熱ロールに
よる処理のため基材の材質または形状を損なうおそれが
あり、更に溶剤の蒸発によって基材に塗布した樹脂液か
乾燥し流動性を失うため、ロール間の圧着接合では被着
体との相溶性が悪く、小さな気泡状の未接合部を生じ品
質の低下即ち塗布状態の良し悪しにより品質を左右する
などの不都合が起こる。更に、ドライラミネート加工法
においては加工速度を向上させるためには乾燥装置の拡
大等を行なわねばならず、このため設備及び運転比か高
くなるという欠点がある。Among these laminating methods, the tri-laminate method removes the solvent by drying, so there is a problem of environmental pollution due to solvent vapor, and the process using a heating dryer and heated rolls may damage the material or shape of the base material. In addition, the evaporation of the solvent dries the resin liquid applied to the base material and causes it to lose its fluidity, resulting in poor compatibility with the adherend during pressure bonding between rolls, resulting in small bubble-like unbonded areas. Inconveniences occur, such as a decrease in quality, that is, the quality is affected by the quality of the coating. Furthermore, in the dry laminating method, in order to increase the processing speed, it is necessary to expand the drying equipment, which has the disadvantage that the equipment and operating ratio become expensive.
一方、ウェットラミネート加工法においてハ塗布材加工
後、ロール間にて圧着された接合物を長時間セット装置
内を通過させて樹脂液を硬化させる必要かある。このた
め、接合物が塗布剤により膨潤し、材質または形状を損
なうおそれもあり、且つまたセット装置を通過した加工
品は、経時変化により品質の変動を来たす。On the other hand, in the wet lamination method, after processing the coating material, it is necessary to pass the bonded product pressed between rolls through a setting device for a long time to harden the resin liquid. For this reason, there is a risk that the bonded product will swell with the coating agent and lose its material or shape, and the quality of the processed product that has passed through the setting device will change due to changes over time.
このようにウェットラミネート加工法は接合後すぐには
移動することができず、しばらくは放置して置く必要が
あるが、このため加工品を放置する広大な放置スペース
を必要とする。In this way, in the wet lamination method, the products cannot be moved immediately after bonding and must be left for a while, but this requires a large storage space in which to leave the processed products.
これに対して本願発明者は先にドライラミネート加工法
とウェットラミネート加工法の特徴を備え、且つこれら
従来法の欠点のないラミネート加工法として紫外線硬化
性樹脂液を基材と被着体の間に介在させて圧着ロール間
を通過させ、更に紫外線を照射して上記樹脂液を素早く
硬化させラミネート加工を行う方法を提案した(特公昭
57−23590号)。In contrast, the inventor of the present application has developed a method of laminating which has the characteristics of dry laminating and wet laminating, and which does not have the drawbacks of these conventional methods. He proposed a method in which the resin liquid was passed between pressure rolls with the resin liquid interposed in the resin, and the resin liquid was further irradiated with ultraviolet rays to quickly harden the resin liquid for lamination processing (Japanese Patent Publication No. 57-23590).
(発明が解決しようとする問題点)
しかし、この方法においては被着材と基材の間に樹脂液
を介在させて圧着ロール間を通過させた後、紫外線照射
部を通過させて樹脂液を硬化させるため、凹凸のある基
材、多孔質の基材等の出来上がり製品に光沢がない等の
難点がある。(Problem to be solved by the invention) However, in this method, the resin liquid is interposed between the adherend and the base material, and after passing between pressure rolls, the resin liquid is passed through an ultraviolet irradiation section. Since it is cured, there are drawbacks such as a lack of luster in the finished product, such as uneven or porous substrates.
また、出来上がり製品に光沢を与えるために被着材と基
材の間に介在させる樹脂量を多くして圧着ロール間を通
過させると、ロールの圧着力により樹脂液が被着材乃至
基材の間よりはみ出していまうなどの不都合を生ずる。In addition, in order to give gloss to the finished product, if a large amount of resin is interposed between the adherend and the base material and the resin is passed between the pressure rolls, the pressure force of the rolls will cause the resin liquid to spread between the adherend and the base material. This may cause inconveniences such as protruding from the space.
(問題点を解決するための手段)
この発明は、上記実情に鑑み鋭意研究の結果、先に本願
発明者が提案した上述のラミネート加工方法の改良とし
て被記録材乃至基材の何れか一方に紫外線硬化性樹脂液
を比較的多量に塗布し、更に紫外線の第1照射部を通過
させ、上記樹脂液を半乾燥状態にした後、該樹脂液の塗
布面に基材乃至被着材を添着させながら圧着ローラ間を
通過後、再び紫外線の第2照射部を通過させて上記樹脂
液を大村上に接着硬化させる方法を提案するものである
。(Means for Solving the Problems) As a result of intensive research in view of the above circumstances, this invention is an improvement of the above-mentioned laminating method previously proposed by the inventor of the present invention. After applying a relatively large amount of ultraviolet curable resin liquid and passing the ultraviolet rays through the first irradiation part to make the resin liquid semi-dry, attaching a base material or an adherend to the surface to which the resin liquid has been applied. The present invention proposes a method for adhering and hardening the resin liquid onto Omurakami by passing it between pressure rollers while causing the resin liquid to pass through the second ultraviolet ray irradiation section again.
この発明において使用する紫外線硬化性樹脂液としては
通常の紫外線硬化性樹脂液を使用することかてきラジカ
ル重合性不飽和二重結合を有するモノマー若しくはプレ
ポリマーの一種以上と、増感剤を必須成分とし、これに
その他の樹脂、着色剤、ワックス等種々の添加剤が必要
に応じて配合されているものである。As the ultraviolet curable resin liquid used in this invention, a normal ultraviolet curable resin liquid may be used, and it may contain at least one type of monomer or prepolymer having a radically polymerizable unsaturated double bond and a sensitizer as essential components. In addition, various additives such as other resins, colorants, and waxes are blended as necessary.
ラジカル重合性不飽和二重結合を有する七ツマ−として
は、エチレングリコール、ポリエチレングリコール、ト
リメチロールプロ、パン、ペンタエリスリトール等のア
ルコールに(メタ)アクリル酸をエステル化させたもの
、フタル酸、マレイン酸、イソシアヌル酸等にアリルア
ルコールをエステル化せしめたもの若しくはグリシジル
(メタ)アクリレートをエステル化せしめたもの等が例
示される。プレポリマーとしてはエポキシ樹脂に(メタ
)アクリル酸をエステル化せしめたもの、水酸基含有樹
脂に(メタ)アクリル酸をエステル化せしめたもの、水
醜基含有アルキド、ポリエステ樹脂若しくはアクリル樹
脂と(メタ)アクリル酸−ポリオールエステル化物とを
ジイソシアネート化物で架橋せしめたもの等が例示され
る。Examples of heptamers having radically polymerizable unsaturated double bonds include esterification of (meth)acrylic acid with alcohols such as ethylene glycol, polyethylene glycol, trimethylolpro, pan, and pentaerythritol, phthalic acid, and maleic acid. Examples include those obtained by esterifying allyl alcohol with acids, isocyanuric acid, etc., or those obtained by esterifying glycidyl (meth)acrylate. Prepolymers include epoxy resins esterified with (meth)acrylic acid, hydroxyl group-containing resins esterified with (meth)acrylic acid, alkyds containing water groups, polyester resins, or acrylic resins. Examples include those in which an acrylic acid-polyol ester is crosslinked with a diisocyanate.
この発明において用いられる増感剤としては、ベンゾイ
ン、ベンゾインメチルエーテル、ベンゾインエチルエー
テル、ベンゾインイソブチルエーテル、2−アリルベン
ゾイン、2−クロルベンゾイン等のベンゾイン系増感剤
、ベンゾフェノン、p−メチルベンゾインフェノン、p
−クロルベンゾフェノン、ミヒラーズケトン、アセトフ
ェノン等のケトン系増感剤、アゾビスイソブチロニトリ
ル等のアゾ系増感剤、アントラキノン、2−クロルアン
トラキノン、フェナントレン等のキノン系増感剤、テト
ラメチルチウラムモノスルフィト等のスルフィド系増感
剤、並びに各種増感剤の組合せ等が用いられる。Sensitizers used in this invention include benzoin-based sensitizers such as benzoin, benzoin methyl ether, benzoin ethyl ether, benzoin isobutyl ether, 2-allylbenzoin, and 2-chlorobenzoin, benzophenone, p-methylbenzoinphenone, p
-Ketone sensitizers such as chlorobenzophenone, Michler's ketone, acetophenone, azo sensitizers such as azobisisobutyronitrile, quinone sensitizers such as anthraquinone, 2-chloroanthraquinone, phenanthrene, tetramethylthiuram monosulfate Sulfide sensitizers such as phyto-based sensitizers and combinations of various sensitizers are used.
この増感剤の量は一般に樹脂組成中0.1〜2.5重量
%の割合で配合される。The amount of this sensitizer is generally 0.1 to 2.5% by weight in the resin composition.
また、この発明において基材としては紙、プラスチック
、金属、木材、その他これらの複合材料を使用すること
ができ、更に被着材としては紫外線を照射する場合には
紫外線透過材質、例えばポリエステル、ポリプロピレン
、アクリル樹脂、ポリカーボネート、ポリアミド、ポリ
塩化ビニル、ポリ塩化ビニリデン、フェノール樹脂、ポ
リスチロール、ポリフッ化エチレン、セロハン等各種プ
ラスチックスを使用する。In addition, in this invention, paper, plastic, metal, wood, and other composite materials thereof can be used as the base material, and when irradiating ultraviolet rays as the adherend, ultraviolet-transparent materials such as polyester and polypropylene can be used as the adherend. Various plastics such as , acrylic resin, polycarbonate, polyamide, polyvinyl chloride, polyvinylidene chloride, phenol resin, polystyrene, polyfluoroethylene, and cellophane are used.
紫外線照射には通常の水銀ランプ及びメタルハライドラ
ンプの高圧、中圧または低圧のものを用いその種類、大
きさ、数等は紫外線硬化性樹脂の硬化速度等により定め
る。For ultraviolet irradiation, ordinary mercury lamps and metal halide lamps with high pressure, medium pressure, or low pressure are used, and the type, size, number, etc. of the lamps are determined depending on the curing speed of the ultraviolet curable resin, etc.
更に、圧着ロールとしては基材と被着材の間に介在させ
た紫外線硬化性樹脂の流動性を高めるため、その一方ま
たは双方が加熱ロールであることが好ましく、圧着ロー
ルの大きさ、数量等は被着材、基材及び紫外線硬化性樹
脂の種類等により適宜選択する。Furthermore, in order to improve the fluidity of the ultraviolet curable resin interposed between the base material and the adherend, one or both of the pressure rolls is preferably a heated roll, and the size, quantity, etc. of the pressure rolls are determined. is appropriately selected depending on the type of adherend, base material, and ultraviolet curable resin.
上述の紫外線硬化性樹脂液の被着材乃至基材への塗布量
は一般には3g/m”程度であるが、この発明では被着
材乃至基材の表面に凹凸かある場合には4〜15g/l
l+2程度、一般には4〜5g/l112程度の比較的
多量に塗布し1次に紫外線の第1照射部を通過させて樹
脂液を半乾燥状態にする。即ち、上述のように比較的多
量に塗布した樹脂液が次の圧着ロール間を通過する際に
、被着材と基材の間よりはみ出さない程度の半乾燥状態
にする。このため、第1照射部の出力は第2照射部の出
力の172〜1/3程度にしである。The amount of the above-mentioned ultraviolet curable resin liquid applied to the adherend or base material is generally about 3 g/m'', but in this invention, if the surface of the adherend or base material is uneven, the amount applied is 4 to 4 g/m. 15g/l
The resin liquid is applied in a relatively large amount of about l+2, generally about 4 to 5 g/l112, and then passed through a first irradiation section of ultraviolet rays to bring the resin liquid into a semi-dry state. That is, as described above, the resin liquid applied in a relatively large amount is kept in a semi-dry state to the extent that it does not protrude from between the adherend and the base material when it passes between the next pressure rolls. Therefore, the output of the first irradiation section is about 172 to 1/3 of the output of the second irradiation section.
次に、上述のように半乾燥状態にした樹脂液の塗布面に
基材乃至被着材を添着させながら圧着ローラ間及び紫外
線の第2照射部を通過させて上記樹脂液を基材上に接着
硬化せしめ、ラミネート加工を完成するものである。Next, while adhering the base material or adherend to the semi-dry resin liquid application surface as described above, the resin liquid is passed between the pressure rollers and through the second irradiation section of ultraviolet rays to apply the resin liquid onto the base material. The adhesive is cured to complete the lamination process.
第1図、第2図は、この発明の実施態様を示すものであ
り、このうち第1図は被着材を塗着してロール環を通過
させる場合を示すものである。1 and 2 show embodiments of the present invention, of which FIG. 1 shows a case where an adherend is applied and passed through a roll ring.
この場合、装置は紫外線硬化性樹脂液の収容器1と、樹
脂液を被着材の内側面に塗着して塗布ロール2、バック
アップロール3と、被着材及び基材を圧着するための圧
力ロール4、加熱ロール5と、紫外線の第1照射部6と
第2照射部7から構成されてる。In this case, the apparatus includes a container 1 for the ultraviolet curable resin liquid, a coating roll 2 for applying the resin liquid to the inner surface of the adherend, a backup roll 3, and a roller for press-bonding the adherend and the base material. It consists of a pressure roll 4, a heating roll 5, a first irradiation section 6 and a second irradiation section 7 for ultraviolet rays.
第1照射部6は塗布ロール2と圧着ロール4の間の内側
に配置され、長尺な被着材8が塗布ロール2とバックア
ップロール3の間を通過させてその内側面に樹脂液を塗
着させながら圧力ロール4と加熱ロール5の間に送入さ
れる間に、第1照射部6から紫外線を樹脂液面に照射し
て樹脂液を半乾燥状態にする。一方長尺な基材9はガイ
トロールlOに導かれながら圧力ロール4と加熱ロール
5の間に送入される。したがって、圧力ロール4と加熱
ロール5の間ては、被着材8と基材9の間に介在された
半乾燥状態の樹脂液が圧着されながら通過する。次に、
ガイトロール11に導かれて第2照射部7を通過し、こ
こで樹脂液は完全に硬化し、被着材8は基材9上に接着
され、ラミネート加工が行われる。The first irradiation unit 6 is arranged inside between the coating roll 2 and the pressure roll 4, and the long adherend material 8 is passed between the coating roll 2 and the backup roll 3, and the resin liquid is applied to the inner surface thereof. While being fed between the pressure roll 4 and the heating roll 5 while being coated, the resin liquid surface is irradiated with ultraviolet rays from the first irradiation unit 6 to bring the resin liquid into a semi-dry state. On the other hand, a long base material 9 is fed between the pressure roll 4 and the heating roll 5 while being guided by the guide roll IO. Therefore, the semi-dry resin liquid interposed between the adherend 8 and the base material 9 passes between the pressure roll 4 and the heating roll 5 while being pressed together. next,
The resin liquid is guided by the guide roll 11 and passes through the second irradiation section 7, where the resin liquid is completely cured, and the adherend 8 is adhered onto the base material 9, and lamination processing is performed.
第2図は基材の内側に樹脂を塗着してロール間を通過さ
せる場合を示すものである。この場合第1照射部6は圧
力ロール4の前方基材9の通路上方に配置し、基材9は
あらかじめ内側面に樹脂液を塗着し、ベルトコンベアー
11に載せて第1照射部6の下を通過させ、樹脂液を半
乾燥状態にしてから圧力ロール4と加熱ロール5の間に
送入し、ここで被着材8と圧着させる。次いで圧着物は
ベルトコンベアー13に載せて第2照射部6を通過させ
、紫外線の照射により樹脂液を完全に硬化させ、ラミネ
ート加工を行うものである。FIG. 2 shows a case where a resin is applied to the inside of the base material and the resin is passed between rolls. In this case, the first irradiation section 6 is arranged above the path of the base material 9 in front of the pressure roll 4, and the inner surface of the base material 9 is coated with resin liquid in advance, and the first irradiation section 6 is placed on the belt conveyor 11. After the resin liquid is made semi-dry, it is fed between the pressure roll 4 and the heating roll 5, where it is pressed against the adherend 8. Next, the crimped product is placed on the belt conveyor 13 and passed through the second irradiation section 6, where the resin liquid is completely cured by ultraviolet irradiation and laminated.
尚、この実施例では圧力ロール4、加熱ロール5の後方
に第2照射部7を設ける例について説明したが、圧力ロ
ール4.加熱ロール5を紫外線透過材質で構成し、この
中に第2照射部7を内蔵させてもよい(第4,5図参照
)。In this embodiment, an example in which the second irradiation section 7 is provided behind the pressure roll 4 and the heating roll 5 has been described, but the pressure roll 4. The heating roll 5 may be made of a material that transmits ultraviolet rays, and the second irradiation section 7 may be incorporated therein (see FIGS. 4 and 5).
この場合、被着材8、基材9は圧力ロール4と加熱ロー
ル5の間隙で圧着させると同時に、第2照射部7の紫外
線の照射により樹脂液が硬化するので、ラミネート加工
は瞬時に完成する。In this case, the adherend 8 and the base material 9 are pressed together in the gap between the pressure roll 4 and the heating roll 5, and at the same time, the resin liquid is cured by irradiation with ultraviolet rays from the second irradiation section 7, so the lamination process is completed instantly. do.
更に、他の実施例として第3図に示すように、紫外線硬
化材質よりなるエンドレスベルト14を口−ル15とテ
ンションロール17どの間に懸架し、該エンドレスベル
ト14内に第2照射部7を設け、更にロール15とテン
ションロール17には対応する圧力ロール16.18を
設けるようにしてもよい。Furthermore, as another embodiment, as shown in FIG. 3, an endless belt 14 made of an ultraviolet curing material is suspended between a mouth ring 15 and a tension roll 17, and a second irradiation section 7 is provided inside the endless belt 14. In addition, roll 15 and tension roll 17 may also be provided with corresponding pressure rolls 16,18.
この場合、被着材8、基材9はロール15とテンション
ロール17の間をエンドレスベルト14によって圧着さ
せながら第2照射部7の照射を受け、被着材8の接着が
完全に行なわれる。In this case, the adherend 8 and the base material 9 are irradiated by the second irradiation section 7 while being pressed between the roll 15 and the tension roll 17 by the endless belt 14, so that the adherend 8 is completely bonded.
尚、上記の場合ベルトをエンドレスとせずに一定長さの
ベルトを巻き取り式として使用してもよい。In the above case, instead of using an endless belt, a belt of a certain length may be used as a winding belt.
(発明の効果)
以上要するに、この発明は比較的多量に塗布された紫外
線硬化性樹脂液を、紫外線の第1照射部て半乾燥状態に
乾燥させた後、圧着ロール間を通過させ、更に紫外線の
第2照射部を通過させて樹脂液を完全に硬化させ、ラミ
ネート加工を行うものであり、したがってこの発明にお
いては被着材乃至基材上に比較的多量に塗布された樹脂
液もはみ出すことなく、しかも先に本願発明者の提案し
たラミネート加工法に比べて光沢のある製品か得られる
。(Effects of the Invention) In summary, the present invention allows a relatively large amount of applied ultraviolet curable resin liquid to be dried to a semi-dry state in the first irradiation area of ultraviolet rays, then passes between pressure rolls, and then The resin liquid is completely cured by passing through the second irradiation part of the laminate to perform the laminating process. Therefore, in this invention, even the resin liquid applied in a relatively large amount on the adherend or base material does not leak out. Moreover, a product with more gloss than the laminating method previously proposed by the inventor of the present application can be obtained.
図面は、この発明の実施態様を示すものてあり、第1図
は、樹脂液を被着材側に塗着する実施態様を示すもので
あり、第2図は、樹脂液を基材側に塗着する実施態様を
示すものであり、第3図は、他の実施態様を示し、更に
第4.5図は第2照射部を圧着ロール内に内蔵した実施
態様を示すものである。The drawings show embodiments of the present invention. Figure 1 shows an embodiment in which the resin liquid is applied to the adherend, and Figure 2 shows the embodiment in which the resin liquid is applied to the substrate side. Fig. 3 shows another embodiment, and Fig. 4.5 shows an embodiment in which the second irradiation section is built into the pressure roll.
Claims (1)
比較的多量に塗布し、更に紫外線の第1照射部を通過さ
せ、上記樹脂液を半乾燥状態にした後、該樹脂液の塗布
面に基材乃至被着材を添着させながら圧着ローラ間及び
紫外線の第2照射側を通過させて上記樹脂液を基材上に
接着硬化させるようにしたことを特徴とするラミネート
加工方法。A relatively large amount of ultraviolet curable resin liquid is applied to either the recording material or the base material, and the ultraviolet rays are passed through the first irradiation section to make the resin liquid semi-dry. A laminating method characterized in that the resin liquid is bonded and cured onto the base material by passing between pressure rollers and a second irradiation side of ultraviolet rays while adhering the base material or adherend to the coated surface.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62006221A JPS63176135A (en) | 1987-01-16 | 1987-01-16 | Laminate processing method |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62006221A JPS63176135A (en) | 1987-01-16 | 1987-01-16 | Laminate processing method |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS63176135A true JPS63176135A (en) | 1988-07-20 |
JPH0457186B2 JPH0457186B2 (en) | 1992-09-10 |
Family
ID=11632462
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP62006221A Granted JPS63176135A (en) | 1987-01-16 | 1987-01-16 | Laminate processing method |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS63176135A (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0290973A (en) * | 1988-09-27 | 1990-03-30 | Takeda Chem Ind Ltd | Laminating method of print for window lamination |
JP2002282784A (en) * | 2001-03-27 | 2002-10-02 | Nippon Paint Co Ltd | Film forming method and base material |
JP2017513754A (en) * | 2014-04-09 | 2017-06-01 | エアバス オペレーションズ ゲーエムベーハーAirbus Operations GmbH | Applicator |
JP2020183621A (en) * | 2019-04-26 | 2020-11-12 | デンカ株式会社 | Device for light irradiation and pressing, and method using therewith |
JP2020199437A (en) * | 2019-06-06 | 2020-12-17 | 東亞合成株式会社 | Method for manufacturing laminate having catalyst layer |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5665664A (en) * | 1979-10-31 | 1981-06-03 | Matsushita Electric Works Ltd | Preparation of building panel |
-
1987
- 1987-01-16 JP JP62006221A patent/JPS63176135A/en active Granted
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5665664A (en) * | 1979-10-31 | 1981-06-03 | Matsushita Electric Works Ltd | Preparation of building panel |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0290973A (en) * | 1988-09-27 | 1990-03-30 | Takeda Chem Ind Ltd | Laminating method of print for window lamination |
JP2002282784A (en) * | 2001-03-27 | 2002-10-02 | Nippon Paint Co Ltd | Film forming method and base material |
JP2017513754A (en) * | 2014-04-09 | 2017-06-01 | エアバス オペレーションズ ゲーエムベーハーAirbus Operations GmbH | Applicator |
US11000877B2 (en) | 2014-04-09 | 2021-05-11 | Airbus Operations Gmbh | Applicator |
JP2020183621A (en) * | 2019-04-26 | 2020-11-12 | デンカ株式会社 | Device for light irradiation and pressing, and method using therewith |
JP2020199437A (en) * | 2019-06-06 | 2020-12-17 | 東亞合成株式会社 | Method for manufacturing laminate having catalyst layer |
Also Published As
Publication number | Publication date |
---|---|
JPH0457186B2 (en) | 1992-09-10 |
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