JP7332075B1 - 接着剤、積層体、包装材 - Google Patents
接着剤、積層体、包装材 Download PDFInfo
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- JP7332075B1 JP7332075B1 JP2023512752A JP2023512752A JP7332075B1 JP 7332075 B1 JP7332075 B1 JP 7332075B1 JP 2023512752 A JP2023512752 A JP 2023512752A JP 2023512752 A JP2023512752 A JP 2023512752A JP 7332075 B1 JP7332075 B1 JP 7332075B1
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- Prior art keywords
- adhesive
- film
- base material
- acid
- polyester polyol
- Prior art date
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Images
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B7/00—Layered products characterised by the relation between layers; Layered products characterised by the relative orientation of features between layers, or by the relative values of a measurable parameter between layers, i.e. products comprising layers having different physical, chemical or physicochemical properties; Layered products characterised by the interconnection of layers
- B32B7/04—Interconnection of layers
- B32B7/12—Interconnection of layers using interposed adhesives or interposed materials with bonding properties
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65D—CONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
- B65D65/00—Wrappers or flexible covers; Packaging materials of special type or form
- B65D65/38—Packaging materials of special type or form
- B65D65/40—Applications of laminates for particular packaging purposes
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J11/00—Features of adhesives not provided for in group C09J9/00, e.g. additives
- C09J11/02—Non-macromolecular additives
- C09J11/06—Non-macromolecular additives organic
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J175/00—Adhesives based on polyureas or polyurethanes; Adhesives based on derivatives of such polymers
- C09J175/04—Polyurethanes
- C09J175/06—Polyurethanes from polyesters
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Adhesives Or Adhesive Processes (AREA)
Abstract
Description
本発明の接着剤は、ポリエステルポリオール(A)と、イソシアネート化合物(B)と、有機溶剤(C)と、乾燥助剤(D)とを含む2液硬化型接着剤である。乾燥助剤(D)はポリエステルポリオール(A)とともにポリオール組成物(I)中に存在していてもよいし、ポリオール組成物(I)、ポリイソシアネート組成物(II)とは別に用意しておき、塗工直前にこれらと混合して用いてもよい。有機溶剤(C)は、ポリオール組成物(I)またはポリイソシアネート組成物(II)のいずれか一方のみに含まれていてもよいし、両方に存在していてもよい。
ポリエステルポリオール(A)は多価カルボン酸と多価アルコールとを含むモノマー組成物(A’)の反応生成物である。ポリエステルポリオール(A)の調整に用いられる多価カルボン酸としては、マロン酸、エチルマロン酸、ジメチルマロン酸、コハク酸、2,2-ジメチルコハク酸、無水コハク酸、アルケニル無水コハク酸、グルタル酸、アジピン酸、ピメリン酸、スベリン酸、アゼライン酸、セバシン酸、フマル酸、マレイン酸、無水マレイン酸、イタコン酸、ダイマー酸、トリマー酸等の脂肪族多価カルボン酸;
カラム ;東ソー株式会社製 TSKgel 4000HXL、TSKgel 3000HXL、TSKgel 2000HXL、TSKgel 1000HXL
検出器 ;RI(示差屈折計)
データ処理;東ソー株式会社製 マルチステーションGPC-8020modelII
測定条件 ;カラム温度 40℃
溶媒 テトラヒドロフラン
流速 0.35ml/分
標準 ;単分散ポリスチレン
試料 ;樹脂固形分換算で0.2質量%のテトラヒドロフラン溶液をマイクロフィルターでろ過したもの(100μl)
イソシアネート化合物(B)は複数のイソシアネート基を備える公知の化合物を特に制限なく用いることができる。このようなイソシアネート化合物(B)としては、トリレンジイソシアネート、ジフェニルメタンジイソシアネート、ポリメリックジフェニルメタンジイソシアネート、1,5-ナフタレンジイソシアネート、トリフェニルメタントリイソシアネート、キシリレンジイソシアネート等の分子構造内に芳香族構造を持つポリイソシアネート、これらのポリイソシアネートのNCO基の一部をカルボジイミドで変性した化合物;
本発明の接着剤は、ポリエステルポリオール(A)を希釈(溶解)することが可能な有機溶剤(C)を含む。有機溶剤(C)としては、例えば酢酸エチル、酢酸ブチル、セロソルブアセテート等のエステル類、アセトン、メチルエチルケトン、イソブチルケトン、シクロヘキサノン等のケトン類、テトラヒドロフラン、ジオキサン等のエーテル類、トルエン、キシレン等の芳香族炭化水素類、メチレンクロリド、エチレンクロリド等のハロゲン化炭化水素類、ジメチルスルホキシド、ジメチルスルホアミド等が挙げられる。ポリオール組成物(I)またはポリイソシアネート組成物(II)の構成成分の製造時に反応媒体として使用された有機溶剤が、更に塗装時に希釈剤として使用される場合もある。有機溶剤(C)が酢酸エチルなどのエステル類の場合に本発明は特に効果を発揮する。
乾燥助剤(D)は、有機溶剤(C)の揮発を促進する機能を有する。乾燥助剤(D)としては、イソソルビド、イソマンニド、イソイジド、トリアセチン等が挙げられる。イソソルビドを用いることが好ましい。乾燥助剤(D)を含むことにより、乾燥工程において有機溶剤(C)が揮発しやすくなり、接着剤の硬化塗膜中に有機溶剤(C)が残留し難くなる。
本発明の接着剤は、上述の成分以外の成分を含んでいてもよい。これらの成分はポリオール組成物(I)またはポリイソシアネート組成物(II)のいずれかまたは両方に含まれていてもよいし、これらとは別に調整しておき、接着剤の塗工直前に混合して用いてもよい。以下では各成分について説明する。
ポリオール組成物(I)はポリエステルポリオール(A)以外のポリオール(E)を含んでいてもよい。ポリオール(E)としては、ポリエステルポリオール(A)の調整に用いられる多価アルコールとして例示したものが挙げられる。ポリオール組成物(I)がポリオール(E)を含む場合、その配合量はポリエステルポリオール(A)とポリオール(E)の配合量の合計100質量部に対して30質量部以下であることが好ましく、20質量部以下であることがより好ましく、10質量部以上であることがより好ましい。
本発明の接着剤は必要に応じて触媒(F)を使用することにより硬化反応を促進することができる。触媒(F)としては、ポリオール組成物(I)とポリイソシアネート組成物(II)のウレタン化反応を促進するものであれば特に制限されず、金属系触媒、アミン系触媒、脂肪族環状アミド化合物、チタンキレート錯体等が例示される。
本発明の接着剤は、必要に応じて顔料(G)を含んでいてもよい。用いられる顔料(G)としては特に制限はなく、塗料原料便覧1970年度版(日本塗料工業会編)に記載されている体質顔料、白顔料、黒顔料、灰色顔料、赤色顔料、茶色顔料、緑色顔料、青顔料、金属粉顔料、発光顔料、真珠色顔料等の有機顔料や無機顔料、さらにはプラスチック顔料などが挙げられる。
本発明の接着剤は、接着促進剤(H)を含んでいてもよい。接着促進剤(H)としては、シランカップリング剤、チタネート系カップリング剤、アルミニウム系カップリング剤等のカップリング剤、エポキシ樹脂等が挙げられる。
本発明の接着剤は、上述した成分以外に、レベリング剤、コロイド状シリカやアルミナゾルなどの無機微粒子、ポリメチルメタクリレート系の有機微粒子、消泡剤、タレ性防止剤、湿潤分散剤、粘性調整剤、紫外線吸収剤、金属不活性化剤、過酸化物分解剤、難燃剤、補強剤、可塑剤、潤滑剤、防錆剤、蛍光性増白剤、無機系熱線吸収剤、防炎剤、帯電防止剤、脱水剤、公知慣用の熱可塑性エラストマー、粘着付与剤、メラミン樹脂、反応性エラストマー等を含んでいてもよい。これらの添加剤の配合量は、本発明の接着剤の希望を損なわない範囲で適宜調整される。
ポリオール組成物(I)とポリイソシアネート組成物(II)とは、ポリイソシアネート組成物(II)中に含まれるイソシアネート基とポリオール組成物(I)中に含まれるヒドロキシル基とのモル比([NCO]/[OH])が0.3~6となるよう調整して用いることが好ましい。
続いて、本発明の積層体の製造方法について説明する。図1は、本発明の積層体の製造に用いるラミネート装置10の一例を示す概略構成図である。ラミネート装置10は、フィルム供給装置1、2と、コーティング装置3と、乾燥装置4と、貼り合わせ装置5と、巻取り装置6とを備える。巻き取りR1には第一の基材W1が、巻き取りR2には第二の基材W2がセットされる。
本発明の積層体は、複数のフィルムあるいは紙を、本発明の接着剤を用い、ドライラミネート法にて貼り合わせて得られる。用いるフィルムに特に制限はなく、用途に応じたフィルムを適宜選択することができる。例えば、食品包装用としては、ポリエチレンテレフタレート(PET)フィルム、ポリスチレンフィルム、ポリアミドフィルム、ポリアクリロニトリルフィルム、ポリエチレンフィルム(LLDPE:低密度ポリエチレンフィルム、HDPE:高密度ポリエチレンフィルム、MDOPE:一軸延伸ポリエチレンフィルム、OPE:二軸延伸ポリエチレンフィルム)やポリプロピレンフィルム(CPP:無延伸ポリプロピレンフィルム、OPP:二軸延伸ポリプロピレンフィルム)、エチレンビニルアルコール共重合体や、ポリビニルアルコールなどのガスバリア性を有する樹脂の片面または両面にオレフィン系のヒートシール性の樹脂層を設けたガスバリア性ヒートシールフィルム等のポリオレフィンフィルム、ポリビニルアルコールフィルム、エチレン-ビニルアルコール共重合体フィルム等が挙げられる。
また、上記のジオール成分とジカルボン酸成分に加えて、2官能のオキシカルボン酸や、架橋構造を形成するために3官能以上の多価アルコール、3官能以上の多価カルボン酸及び/又はその無水物並びに3官能以上のオキシカルボン酸からなる群から選ばれる少なくとも1種の多官能化合物等の第3成分として共重合成分を加えた共重合ポリエステルであっても良い。
ポリエチレン系樹脂は、原料の一部に前記バイオマス由来のエチレングリコールを使用する以外は特に限定されず、エチレンの単独重合体、エチレンを主成分とするエチレンとα-オレフィンとの共重合体(エチレン単位を90質量%以上含有するエチレン-α-オレフィン共重合体)などが挙げられ、これらを1種単独で、又は2種以上を組み合わせて使用することができる。
(1)基材1/接着層1/シーラントフィルム
(2)基材1/接着層1/金属蒸着未延伸フィルム
(3)基材1/接着層1/金属蒸着延伸フィルム
(4)透明蒸着延伸フィルム/接着層1/シーラントフィルム
(5)基材1/接着層1/基材2/接着層2/シーラントフィルム
(6)基材1/接着層1/金属蒸着延伸フィルム/接着層2/シーラントフィルム
(7)基材1/接着層1/透明蒸着延伸フィルム/接着層2/シーラントフィルム
(8)基材1/接着層1/金属層/接着層2/シーラントフィルム
(9)基材1/接着層1/基材2/接着層2/金属層/接着層3/シーラントフィルム
(10)基材1/接着層1/金属層/接着層2/基材2/接着層3/シーラントフィルム
等が挙げられるがこれに限定されない。
本発明の積層体は、食品や医薬品などの保護を目的とする多層包装材料として使用することができる。多層包装材料として使用する場合には、内容物や使用環境、使用形態に応じてその層構成は変化し得る。また、本発明の包装体に易開封処理や再封性手段を適宜設けてあってもよい。
(合成例1)ポリエステルポリオール(A-1)の合成
攪拌機、窒素ガス導入管、スナイダー管、コンデンサーを備えたポリエステル反応容器に、エチレングリコール20.98部、グリセリン0.12部、1,3,5-トリス(2-ヒドロキシエチル)イソシアヌル酸50.94部、無水フタル酸50.41部を仕込み、精留管上部温度が100℃を超えないように徐々に加熱して内温を220℃に保持した。酸価が1mgKOH/g以下になったところでエステル化反応を終了し、数平均分子量670のポリエステルポリオール(A-1)を得た。水酸基価は230.2mgKOH/gであった。
攪拌機、窒素ガス導入管、スナイダー管、コンデンサーを備えたポリエステル反応容器に、エチレングリコール48.56部、グリセリン0.12部、1,3,5-トリス(2-ヒドロキシエチル)イソシアヌル酸16.54部、無水フタル酸66.88部を仕込み、精留管上部温度が100℃を超えないように徐々に加熱して内温を220℃に保持した。酸価が1mgKOH/g以下になったところでエステル化反応を終了し、りん酸を0.015部加え、数平均分子量335のポリエステルポリオール(A-2)を得た。水酸基価は360.0mgKOH/gであった。
攪拌機、窒素ガス導入管、スナイダー管、コンデンサーを備えたポリエステル反応容器に、エチレングリコール28.98部、グリセリン0.16部、1,3,5-トリス(2-ヒドロキシエチル)イソシアヌル酸84.56部、無水フタル酸57.54部を仕込み、精留管上部温度が100℃を超えないように徐々に加熱して内温を220℃に保持した。酸価が1mgKOH/g以下になったところでエステル化反応を終了し、数平均分子量420のポリエステルポリオール(A-3)を得た。水酸基価は378.3mgKOH/gであった。
攪拌機、窒素ガス導入管、スナイダー管、コンデンサーを備えたポリエステル反応容器に、エチレングリコール35.17部、グリセリン15.40部、無水フタル酸84.17部、チタンテトライソプロポキシド0.013部を仕込み、精留管上部温度が100℃を超えないように徐々に加熱して内温を220℃に保持した。酸価が1mgKOH/g以下になったところでエステル化反応を終了し、数平均分子量1050のポリエステルポリオール(A-4)を得た。水酸基価は190.0mgKOH/gであった。
攪拌機、窒素ガス導入管、スナイダー管、コンデンサーを備えたポリエステル反応容器に、エチレングリコール56.53部、無水フタル酸79.48部、チタンテトライソプロポキシド0.007部を仕込み、精留管上部温度が100℃を超えないように徐々に加熱して内温を220℃に保持した。酸価が1mgKOH/g以下になったところでエステル化反応を終了し、りん酸を0.01部加え、数平均分子量400のポリエステルポリオール(A-5)を得た。水酸基価は280.0mgKOH/gであった。
攪拌機、窒素ガス導入管、スナイダー管、コンデンサーを備えたポリエステル反応容器に、エチレングリコール51.06部、無水フタル酸63.30部を仕込み、精留管上部温度が100℃を超えないように徐々に加熱して内温を220℃に保持した。酸価が1mgKOH/g以下になったところでエステル化反応を終了し、りん酸を0.01部加え、数平均分子量340のポリエステルポリオール(A-6)を得た。水酸基価は331.0mgKOH/gであった。
攪拌機、窒素ガス導入管、スナイダー管、コンデンサーを備えたポリエステル反応容器に、エチレングリコール61.45部、無水フタル酸66.66部を仕込み、精留管上部温度が100℃を超えないように徐々に加熱して内温を220℃に保持した。酸価が1mgKOH/g以下になったところでエステル化反応を終了し、りん酸を0.01部加え、数平均分子量256のポリエステルポリオール(A-7)を得た。水酸基価は438.0mgKOH/gであった。
攪拌機、窒素ガス導入管、スナイダー管、コンデンサーを備えたポリエステル反応容器に、エチレングリコール17.58部、1,3,5-トリス(2-ヒドロキシエチル)イソシアヌル酸71.84部、コハク酸32.47部を仕込み、精留管上部温度が100℃を超えないように徐々に加熱して内温を220℃に保持した。酸価が1mgKOH/g以下になったところでエステル化反応を終了し、りん酸を0.01部加え、数平均分子量420のポリエステルポリオール(A-8)を得た。水酸基価は410.3mgKOH/gであった。
(合成例9)イソシアネート化合物(B-1)の合成
攪拌機、窒素ガス導入管、スナイダー管、冷却コンデンサー、滴下漏斗を備えた反応容器にキシリレンジイソシアネート136.00部を入れて70℃に加熱しながら撹拌し、ポリエステルポリオール(A-5)116.00部を、滴下漏斗を用いて2時間かけて滴下し、更に4時間撹拌し、イソシアネート化合物(B-1)を得た。JIS-K1603に従い測定したNCO%は14.1%であった。
攪拌機、窒素ガス導入管、スナイダー管、冷却コンデンサー、滴下漏斗を備えた反応容器にキシリレンジイソシアネート136.00部を入れて70℃に加熱しながら撹拌し、ポリエステルポリオール(A-5)99.50部を、滴下漏斗を用いて2時間かけて滴下し、更に4時間撹拌し、イソシアネート化合物(B-2)を得た。JIS-K1603に従い測定したNCO%は16.0%であった。
攪拌機、窒素ガス導入管、スナイダー管、冷却コンデンサー、滴下漏斗を備えた反応容器にキシリレンジイソシアネート125.00部を入れて70℃に加熱しながら撹拌し、ポリエステルポリオール(A-6)82.00部を、滴下漏斗を用いて2時間かけて滴下し、更に4時間撹拌し、イソシアネート化合物(B-3)を得た。JIS-K1603に従い測定したNCO%は16.6%であった。
攪拌機、窒素ガス導入管、スナイダー管、冷却コンデンサー、滴下漏斗を備えた反応容器にキシリレンジイソシアネート136.47部を入れて70℃に加熱しながら撹拌し、ポリエステルポリオール(A-2)85.69部を、滴下漏斗を用いて2時間かけて滴下し、更に4時間撹拌し、イソシアネート化合物(B-4)を得た。JIS-K1603に従い測定したNCO%は16.6%であった。
攪拌機、窒素ガス導入管、スナイダー管、冷却コンデンサー、滴下漏斗を備えた反応容器にキシリレンジイソシアネート135.00部を入れて70℃に加熱しながら撹拌し、ポリエステルポリオール(A-7)75.00部を、滴下漏斗を用いて2時間かけて滴下し、更に4時間撹拌し、イソシアネート化合物(B-5)を得た。JIS-K1603に従い測定したNCO%は16.7%であった。
攪拌機、窒素ガス導入管、スナイダー管、冷却コンデンサー、滴下漏斗を備えた反応容器にキシリレンジイソシアネート136.00部を入れて70℃に加熱しながら撹拌し、ポリエステルポリオール(A-2)96.00部を、滴下漏斗を用いて2時間かけて滴下し、更に4時間撹拌し、イソシアネート化合物(B-6)を得た。JIS-K1603に従い測定したNCO%は14.5%であった。
攪拌機、窒素ガス導入管、スナイダー管、冷却コンデンサー、滴下漏斗を備えた反応容器にキシリレンジイソシアネート126.00部を入れて70℃に加熱しながら撹拌し、ポリエステルポリオール(A-8)75.00部を、滴下漏斗を用いて2時間かけて滴下し、更に4時間撹拌し、イソシアネート化合物(B-7)を得た。JIS-K1603に従い測定したNCO%は15.7%であった。
(実施例1)
ポリエステルポリオール(A-1):30.8部、イソシアネート化合物(B-1):84.0部、乾燥助剤(D)としてイソソルビド:7.7部を配合し、酢酸エチルで固形分53%に調整して実施例1の接着剤を調製した。
(実施例2)~(実施例22)
用いるポリエステルポリオール(A)、イソシアネート化合物(B)、乾燥助剤(D)とその配合を表1~4に示すものに変更した以外は実施例1と同様にして実施例2~実施例22の接着剤を調製した。
(比較例1)~(比較例4)
用いるポリエステルポリオール(A)、イソシアネート化合物(B)とその配合を表5に示すものに変更した以外は実施例1と同様にして比較例1~4の接着剤を調製した。
なお表中においてXDIはキシリレンジイソシアネート、XDI-TMPアダクト体は、キシリレンジイソシアネートのトリメチロールプロパンアダクト体である。
(実施例1)
第一の基材として、膜厚30μmのOPPフィルム(東洋紡社製、パイレンP2161)上に、フィナートR794 白G3を、乾燥塗膜の膜厚が1μmとなるように塗工したものを、第二の基材として膜厚30μmのCPPフィルム(東洋紡社製、パイレンP1128)を用意した。第一の基材、第二の基材の搬送速度を100m/分に、乾燥炉の温度を第一の基材の搬送方向の上流側からそれぞれ60℃、70℃、80℃に設定したDL-600DXドライラミネーター(オリエント総業社製)を用い、第一の基材の印刷面に、実施例1の接着剤を固形分量が3.0g/m2となるよう塗布し、第二の基材と貼り合わせた。40℃で3日間のエージングを行い、実施例1の積層体を得た。
用いる第一の基材、第二の基材、接着剤、基材の搬送速度を表1~5に記載のものに変更した以外は実施例1と同様にして実施例2~22、比較例1~4の積層体を得た。なお表中に示す第一の基材の右側に接着剤を塗布し、第二の基材の左側と貼り合わせている。従って、例えば実施例6では第一の基材の印刷層側に接着剤を塗布し、第二の基材のアルミ蒸着層と貼り合わせている。実施例8、11、12で使用した第一の基材の印刷層は、実施例1と同様の方法で設けた。
OPP:東洋紡社製、パイレンP2161、膜厚30μm
CPP(30):東洋紡社製、パイレンP1128、膜厚30μm
CPP(70):東レフィルム加工社製、ZK-207、膜厚70μm
VMCPP(25):東レフィルム加工社製、2203、膜厚25μm
VMCPP:東レフィルム加工社製、2703、膜厚30μm
PET:東洋紡社製、E5100、膜厚12μm
PET-AlOx:東レフィルム加工社製、バリアロックス1011HG、膜厚12μm
PET-SiOx:三菱ケミカル社製、テックバリアTX、膜厚12μm
Ny:ユニチカ社製、エンブレムON、膜厚15μm
LLDPE:三井化学東セロ社製、T.U.X-HC、膜厚60μm
(残留溶剤量)
実施例、比較例の積層体を500ccのフラスコに入れて80℃で30分間加熱した後、フラスコ内のガスをガスクロマトグラフィーにより測定し、積層体1m2あたりの溶剤量(mg/m2)に換算し、結果を表にまとめた。
Claims (8)
- ポリエステルポリオール(A)と、イソシアネート化合物(B)と、エステル系の有機溶剤(C)と、イソソルビド、イソマンニド、イソイジド、トリアセチンからなる群から選ばれる少なくとも一種の乾燥助剤(D)とを含む2液硬化型接着剤。
- 前記乾燥助剤(D)の配合量が、前記接着剤の固形分の0.5質量%以上50質量%以下である請求項1に記載の2液硬化型接着剤。
- 前記乾燥助剤(D)がイソソルビドである請求項1または2のいずれか一項に記載の2液硬化型接着剤。
- 前記ポリエステルポリオールがオルト配向性芳香族多価カルボン酸を含む多価カルボン酸と、多価アルコールとを重縮合して得られるポリエステルポリオール(A2)、イソシアヌル環を有するポリエステルポリオール(A3)、重合性炭素-炭素二重結合を有するポリエステルポリオール(A4)の少なくとも一種を含む請求項1~3のいずれか一項に記載の2液硬化型接着剤。
- 前記有機溶剤(C)が酢酸エチルである請求項1~4のいずれか一項に記載の2液硬化型接着剤。
- 第一の基材と、第二の基材と、前記第一の基材と前記第二の基材とを貼り合わせる接着層とを有する積層体の製造方法であって、
前記第一の基材に、ポリエステルポリオール(A)と、イソシアネート化合物(B)と、エステル系の有機溶剤(C)と、イソソルビド、イソマンニド、イソイジド、トリアセチンからなる群から選ばれる少なくとも一種の乾燥助剤(D)とを含む2液硬化型接着剤の塗膜を設ける工程と、
前記第一の基材を乾燥装置に搬送し、加熱して前記接着剤の塗膜から前記有機溶剤(C)を揮発させる工程と、
前記接着剤の塗膜を介して前記第一の基材と前記第二の基材とを貼り合わせる工程と、
前記接着剤の塗膜を硬化させて前記接着層を形成する工程と、を含む積層体の製造方法。 - 第一の基材と、第二の基材と、前記第一の基材と前記第二の基材とを貼り合わせる接着層とを有し、前記接着層が請求項1~5のいずれか一項に記載の接着剤の硬化塗膜である積層体。
- 請求項7に記載の積層体からなる包装材。
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