JP5633768B2 - 紫外線硬化性ウレタンアクリレート組成物、薄膜成形体、光学フィルム、及び薄膜成形体の製造方法 - Google Patents
紫外線硬化性ウレタンアクリレート組成物、薄膜成形体、光学フィルム、及び薄膜成形体の製造方法 Download PDFInfo
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- JP5633768B2 JP5633768B2 JP2014513384A JP2014513384A JP5633768B2 JP 5633768 B2 JP5633768 B2 JP 5633768B2 JP 2014513384 A JP2014513384 A JP 2014513384A JP 2014513384 A JP2014513384 A JP 2014513384A JP 5633768 B2 JP5633768 B2 JP 5633768B2
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- meth
- urethane acrylate
- ultraviolet curable
- film
- curable urethane
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- 239000000203 mixture Substances 0.000 title claims description 88
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- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- GCRTVIUGJCJVDD-UHFFFAOYSA-N tetrahydrocarvone Natural products CC(C)C1CCC(C)C(=O)C1 GCRTVIUGJCJVDD-UHFFFAOYSA-N 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 238000004448 titration Methods 0.000 description 1
- HTSABYAWKQAHBT-UHFFFAOYSA-N trans 3-methylcyclohexanol Natural products CC1CCCC(O)C1 HTSABYAWKQAHBT-UHFFFAOYSA-N 0.000 description 1
- XMLSXPIVAXONDL-SNAWJCMRSA-N trans-Jasmone Chemical compound CC\C=C\CC1=C(C)CCC1=O XMLSXPIVAXONDL-SNAWJCMRSA-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
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 description 1
- 238000009281 ultraviolet germicidal irradiation Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 229910052724 xenon Inorganic materials 0.000 description 1
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
- IFNXAMCERSVZCV-UHFFFAOYSA-L zinc;2-ethylhexanoate Chemical compound [Zn+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O IFNXAMCERSVZCV-UHFFFAOYSA-L 0.000 description 1
- PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 description 1
Classifications
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- G02B1/00—Optical elements characterised by the material of which they are made; Optical coatings for optical elements
- G02B1/10—Optical coatings produced by application to, or surface treatment of, optical elements
- G02B1/11—Anti-reflection coatings
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2/00—Processes of polymerisation
- C08F2/46—Polymerisation initiated by wave energy or particle radiation
- C08F2/48—Polymerisation initiated by wave energy or particle radiation by ultraviolet or visible light
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F299/00—Macromolecular compounds obtained by interreacting polymers involving only carbon-to-carbon unsaturated bond reactions, in the absence of non-macromolecular monomers
- C08F299/02—Macromolecular compounds obtained by interreacting polymers involving only carbon-to-carbon unsaturated bond reactions, in the absence of non-macromolecular monomers from unsaturated polycondensates
- C08F299/06—Macromolecular compounds obtained by interreacting polymers involving only carbon-to-carbon unsaturated bond reactions, in the absence of non-macromolecular monomers from unsaturated polycondensates from polyurethanes
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F290/00—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups
- C08F290/02—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups on to polymers modified by introduction of unsaturated end groups
- C08F290/06—Polymers provided for in subclass C08G
- C08F290/067—Polyurethanes; Polyureas
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F299/00—Macromolecular compounds obtained by interreacting polymers involving only carbon-to-carbon unsaturated bond reactions, in the absence of non-macromolecular monomers
- C08F299/02—Macromolecular compounds obtained by interreacting polymers involving only carbon-to-carbon unsaturated bond reactions, in the absence of non-macromolecular monomers from unsaturated polycondensates
- C08F299/06—Macromolecular compounds obtained by interreacting polymers involving only carbon-to-carbon unsaturated bond reactions, in the absence of non-macromolecular monomers from unsaturated polycondensates from polyurethanes
- C08F299/065—Macromolecular compounds obtained by interreacting polymers involving only carbon-to-carbon unsaturated bond reactions, in the absence of non-macromolecular monomers from unsaturated polycondensates from polyurethanes from polyurethanes with side or terminal unsaturations
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- C—CHEMISTRY; METALLURGY
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- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
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- C08G18/08—Processes
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- C—CHEMISTRY; METALLURGY
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- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
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- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
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- C08G18/48—Polyethers
- C08G18/4854—Polyethers containing oxyalkylene groups having four carbon atoms in the alkylene group
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
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- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/73—Polyisocyanates or polyisothiocyanates acyclic
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
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- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/74—Polyisocyanates or polyisothiocyanates cyclic
- C08G18/75—Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic
- C08G18/751—Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic containing only one cycloaliphatic ring
- C08G18/752—Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic containing only one cycloaliphatic ring containing at least one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group
- C08G18/753—Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic containing only one cycloaliphatic ring containing at least one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group containing one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group having a primary carbon atom next to the isocyanate or isothiocyanate group
- C08G18/755—Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic containing only one cycloaliphatic ring containing at least one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group containing one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group having a primary carbon atom next to the isocyanate or isothiocyanate group and at least one isocyanate or isothiocyanate group linked to a secondary carbon atom of the cycloaliphatic ring, e.g. isophorone diisocyanate
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/74—Polyisocyanates or polyisothiocyanates cyclic
- C08G18/75—Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic
- C08G18/758—Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic containing two or more cycloaliphatic rings
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- C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
- C08J7/04—Coating
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L75/00—Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
- C08L75/04—Polyurethanes
- C08L75/14—Polyurethanes having carbon-to-carbon unsaturated bonds
- C08L75/16—Polyurethanes having carbon-to-carbon unsaturated bonds having terminal carbon-to-carbon unsaturated bonds
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D175/00—Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
- C09D175/04—Polyurethanes
- C09D175/14—Polyurethanes having carbon-to-carbon unsaturated bonds
- C09D175/16—Polyurethanes having carbon-to-carbon unsaturated bonds having terminal carbon-to-carbon unsaturated bonds
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- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B1/00—Optical elements characterised by the material of which they are made; Optical coatings for optical elements
- G02B1/10—Optical coatings produced by application to, or surface treatment of, optical elements
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
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- C08J2375/00—Characterised by the use of polyureas or polyurethanes; Derivatives of such polymers
- C08J2375/04—Polyurethanes
- C08J2375/08—Polyurethanes from polyethers
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
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- C08J2375/00—Characterised by the use of polyureas or polyurethanes; Derivatives of such polymers
- C08J2375/04—Polyurethanes
- C08J2375/12—Polyurethanes from compounds containing nitrogen and active hydrogen, the nitrogen atom not being part of an isocyanate group
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- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/18—Manufacture of films or sheets
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S525/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S525/92—Polyurethane having terminal ethylenic unsaturation
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Description
例えば、特定の一般式で表される(メタ)アクリロイル基を有する反応性ポリマー100質量部に対し、光重合開始剤0.1〜10質量部を含む自己修復性を有する光硬化性組成物、が知られている(例えば、特許文献1参照。)。
本発明の紫外線硬化性ウレタンアクリレート組成物は、従来の紫外線硬化性組成物と異なり、光重合開始剤を全く含有しない。
以下に本発明の紫外線硬化性ウレタンアクリレート組成物を構成する前記(A)〜(F)について詳細に説明する。
本発明で用いる前記芳香族骨格を有さないポリオール(A)としては、脂肪族ポリオールと脂環族ポリオールがあり、例えば、ポリエステルポリオール、ポリエーテルポリオール、ポリカーボネートポリオール、低分子量グリコールなどが挙げられる。
次に、本発明で用いる芳香族骨格を有さないポリイソシアネート(B)について、以下に説明する。
次いで、本発明で用いる分子末端にイソシアネート基を有するウレタンプレポリマー(C)(以下「イソシアネート基末端ウレタンプレポリマー(C)」という。)について、説明する。
次に、前記イソシアネート基末端ウレタンプレポリマー(C)に付加反応させる、水酸基を有する(メタ)アクリル化合物(D)について説明する。
次いで、本発明で用いる、分子末端に(メタ)アクリロイル基を有するウレタンアクリレートオリゴマー(E)(以下「ウレタンアクリレートオリゴマー(E)」という。)について説明する。
次に、本発明において、希釈溶剤として必須に用いる、芳香族骨格を有さない有機溶剤(F)について、以下に述べる。
本発明の薄膜成形体は、基材上に前記紫外線硬化性ウレタンアクリレート組成物の硬化塗膜を有する。
本発明の薄膜成形体の製造方法としては、例えば、離型基材上に本発明の紫外線硬化性ウレタンアクリレート組成物を塗工して、紫外線照射し硬化後、前記芳香族骨格を有さない有機溶剤(F)を揮発させて硬化塗膜を形成させて、好ましくは10〜1000μmの範囲、より好ましくは10〜800μmの範囲、更に好ましくは50〜800μmの範囲、最も好ましくは10〜200μmの薄い厚さの薄膜成形体(例えば、フィルム、シートなど)を得る方法などが挙げられる。
反応容器に溶融状態の芳香族骨格を有さないポリオール(A)を仕込み、攪拌を開始する。次いで、所定量の芳香族骨格を有さないポリイソシアネート(B)を発熱に注意しながら仕込み、内温を所定温度に上昇させた後、該温度で所定時間攪拌し、イソシアネート基末端ウレタンプレポリマー(C)を得る。
次いで、重合禁止剤と、水酸基を有する(メタ)アクリル化合物(D)を所定量加え、所定時間反応を継続した後、目的のウレタンアクリレートオリゴマー(E)を得る。
その後、希釈溶剤として芳香族骨格を有さない有機溶剤(F)を加えて溶融粘度を調整して、本発明の紫外線硬化性ウレタンアクリレート組成物を得る。
前記〔工程1〕で得た紫外線硬化性ウレタンアクリレート組成物を離型処理の施されたポリエチレンテレフタレート(PET)フィルム上へナイフコーターにより、目的とする薄膜成形体がフィルムの場合には200μm以下の厚さで塗工して、あるいは薄膜成形体がシートの場合には200μmを超える厚さで塗工する。次いで、窒素パージをしながら紫外線照射装置(例えば高圧水銀灯)で紫外線を照射して硬化させる。
更に、通常60℃で所定時間加熱養生し、前記有機溶剤(F)を揮発させて、本発明の薄膜成形体であるフィルムを得ることができる。
また、本発明では、特に断りのない限り、「%」は「質量%」である。
尚、本発明で用いた測定方法及び評価方法は、以下の通りである。
本発明で用いるイソシアネート基末端ウレタンプレポリマー(C)のイソシアネート当量(単位:g/eq、即ち、g/当量)は、JIS K 7301に従い測定した値である。
具体的には、得られたウレタンプレポリマーの試料を三角フラスコに精秤して、乾燥トルエンで溶解して、ジ−n−ブチルアミン溶液10mlを加えた後、均一にしてから静置し、0.5規定塩酸の標準溶液でブロムクレゾールグリーンを指示薬として用いて中和滴定にて定量した。
本発明で記載する(メタ)アクリル当量は、原料の物質収支から計算され、(メタ)アクリロイル基1モルが含有されるウレタンアクリレートオリゴマー(E)の分子量(g/eq)であり、実施例及び比較例で得た組成物においては、(メタ)アクリロイル基濃度(mol/g)の逆数で表される値である。
実施例及び比較例で得られた紫外線硬化性ウレタンアクリレート組成物を離型処理の施されたポリエチレンテレフタレート(PET)フィルム上へナイフコーターにより塗工し塗膜を形成して、120w/cmの高圧水銀灯1灯、窒素パージ装置を有する紫外線照射装置「N2パージ式コンベア付UV照射装置」(株式会社GSユアサ製)で照射光量0.8J/cm2、窒素雰囲気下(酸素濃度1%)の条件下で紫外線を照射して、前記塗膜を硬化させた。
その後、更に温度60±5℃で10分間加熱して使用した有機溶剤を揮発させて、硬化塗膜を基材上に有する薄膜成形体であるフィルム(厚さ100μmのもの)を得た。
前記フィルムの表面(最表層)のベタツキの有無を指触で確認し、下記の基準に従い評価した。
紫外線硬化性(タックフリー)の判定基準
○:ベタツキがなく、指に液状物が付着しない場合、紫外線硬化性に優れる。
×:ベタツキがあり、指に液状物が付着する場合、紫外線硬化性に劣る。
実施例及び比較例で作製したフィルムを用いて、内温23℃、相対湿度50%に調整した恒温恒湿室にて、鉛筆硬度計(荷重750g)で傷つけ後20秒でのフィルムの表面状態を目視で確認し、傷が確認できない限界の鉛筆硬さを表面硬度とした。
下記の手順に従い、実施例及び比較例で作製したフィルムを用いて、JIS K 0129に準拠し動的粘弾性分析によりtanδピーク温度(損失係数ピーク温度)を測定して、粘弾性を評価した。
前記実施例及び比較例で得た組成物を離型ポリエチレンテレフタレート板又はポリカーボネート板上にナイフコーターにより塗工し塗膜を形成した。次いで、紫外線照射機を用いて、窒素雰囲気下、塗膜に紫外線を照射して、前記塗膜を硬化させた。
その後、更に温度60±5℃で10分間加熱して使用した有機溶剤を揮発させて、硬化塗膜を基材上に有する薄膜成形体であるフィルム(厚さ100μmのもの)を得た。
前記組成物を用いて作製したフィルムの貯蔵弾性率(E’)及び損失弾性率(E”)を、粘弾性スペクトロメータ(型式:DMS6100、エスアイアイ・ナノテクノロジー株式会社製)を使用して、昇温速度5℃/分、周波数1Hzの条件下、引張モードで測定した。E’/E”をtanδとし、tanδが最大値となる温度を「tanδピーク温度(℃)」として、下記の基準に従い粘弾性を評価した。
フィルムの粘弾性の判断基準
○:tanδピーク温度が0〜35℃の場合。
×:tanδピーク温度が0℃未満、又は35℃を超える場合。
本発明でいう「自己修復性」とは、薄膜成形体(例えばフィルム、シートなど)の表面(最表層)に生じた傷が経時で復元し得る特性であり、下記方法により評価し判定した。
温度23℃、相対湿度50%に調整した恒温恒湿室において、得られたフィルムの表面(最表層)に500gに加重した真鍮ブラシ(線直0.1mm)で傷をつけた直後から、目視で傷が確認できなくなるまでの回復時間(秒)を測定し、下記の基準に従い自己修復性を判定した。
自己修復性の判断基準
○ :回復時間が20秒以内の場合、自己修復性に優れる。
× :回復時間が20秒を超える場合、自己修復性に劣る。
××:回復しない場合、自己修復性なし。
実施例及び比較例で作製したフィルムの厚さ方向のイエローインデックス(YI0)をJIS Z8722に準拠して多光源分光測色計(スガ試験機株式会社製)により測定し、下記の基準に従い評価した。
初期黄色度の判定基準
○:厚さ方向のYI0が0.5以下の場合、初期黄色度に優れる。
×:厚さ方向のYI0が0.5を超える場合、初期黄色度に劣る。
前記の初期黄色度の評価に用いたフィルムを使用して、乾燥機中で120℃×72時間暴露し、暴露後の黄色度(イエローインデックス:YI1)をJIS Z8722に準拠して多光源分光測色計(スガ試験機株式会社製)により測定し、下記の基準に従い評価した。
耐黄変性の判定基準
○:厚さ方向のYI1が0.7以下の場合、耐黄変性に優れる。
×:厚さ方向のYI1が0.7を超える場合、耐黄変性に劣る。
実施例及び比較例で作製したフィルムの全光線透過率(%)を、日本電色工業株式会社製NDH−2000を使用し、JIS K7361−1に準拠して測定し下記の基準に従い評価した。
透明性の判定基準
○:全光線透過率が92.0%以上である場合、透明性に優れる。
×:全光線透過率が92.0%未満である場合、透明性に劣る。
≪分子末端に(メタ)アクリロイル基を有するウレタンアクリレートオリゴマー(E1)の合成≫
反応容器に、芳香族骨格を有さないポリオール(A)として、50℃の溶融状態のポリオキシテトラメチレングリコール(商品名:PTMG−1000、三菱化学株式会社製、Mn=1000。)50質量部を仕込み、攪拌を開始した。
次いで、芳香族骨格を有さないポリイソシアネート(B)としてヘキサメチレンジイソシアネート(以下「HDI」と略す。)のヌレート変性体(イソシアネート当量=204g/eq)を100質量部加え、発熱に注意しながら内温を85℃に上昇させた後、温度を保ちながら3時間攪拌し、分子末端にイソシアネート基を有するウレタンプレポリマー(C1)を得た。
更に、水酸基を有する(メタ)アクリル化合物(D)として4−ヒドロキシブチルアクリレート(以下「4HBA」と略す。)57質量部を発熱に注意しながら序々に加えて、85℃にて2時間攪拌して、ウレタンアクリレートオリゴマー(E1)を得た。
使用するポリオール(A)、ポリイソシアネート(B)、及び水酸基を有する(メタ)アクリル化合物(D)の種類と仕込量を第1表に示したように変更した以外は、合成例1と同様の反応条件にてウレタンアクリレートオリゴマー(E2)〜(E6)、(E8)及び(E9)を得た。
PTMG−1000:ポリオキシテトラメチレングリコール(商標:三菱化学株式会社製、数平均分子量1000)
PCL:ポリカプロラクトンポリオール(数平均分子量520)
2HEA:2−ヒドロキシエチルアクリレート
4HBA:4−ヒドロキシブチルアクリレート
HDI:1,6−ヘキサメチレンジイソシアネート
H12MDI:4,4’−ジシクロへキシルメタンジイソシアネート
IPDI:イソホロンジイソシアネート
MDI:4,4’−ジフェニルメタンジイソシアネート
合成例1で得た前記ウレタンアクリレートオリゴマー(E1)100質量部と、芳香族骨格を有さない有機溶剤(F)としてメチルエチルケトン(以下、「MEK」という。)20質量部を混合容器に秤量して、室温にて均一になるまで混合して、本発明の紫外線硬化性ウレタンアクリレート組成物(X1)を調整した。
上記で調整した紫外線硬化性ウレタンアクリレート組成物(X1)をポリエチレンテレフタレート(PET)製剥離フィルム上にナイフコーターにより塗工して最表層に塗膜を形成した。
塗工後直ぐに、120w/cmの高圧水銀灯1灯、窒素パージ装置を有する紫外線照射装置で照射光量0.8J/cm2、窒素雰囲気下(酸素濃度1%以下)で紫外線照射して、前記塗膜を硬化させた。更に、オーブン中60℃で10分間加熱し、有機溶剤を揮発させて、薄膜成形体であるフィルム(P1)(厚さ100μmのもの)を作製した。
使用するプレポリマー、有機溶剤の種類、使用量を第2表及び第3表に示すように変更した以外は実施例1と同様にして、それぞれ紫外線硬化性ウレタンアクリレート組成物(X2)〜(X16)、(X18)及び(X19)を調整し、厚さ100μmのフィルム(P2)〜(P16)、(P18)及び(P19)を作製した。
PTMG−1000:ポリオキシテトラメチレングリコール(商標:三菱化学株式会社製、数平均分子量1000)
PCL:ポリカプロラクトンポリオール(数平均分子量520)
1,4PBD:1,4−ポリブタジエンジオール(数平均分子量1200)
2HEA:2−ヒドロキシエチルアクリレート
4HBA:4−ヒドロキシブチルアクリレート
HDI:1,6−ヘキサメチレンジイソシアネート
H12MDI:4,4’−ジシクロへキシルメタンジイソシアネート
IPDI:イソホロンジイソシアネート
MDI:4,4’−ジフェニルメタンジイソシアネート
MEK:メチルエチルケトン
MIBK:メチルイソブチルケトン
Irgacure 184:イルガキュア 184(商標:長瀬産業株式会社製、ラジカル系光重合開始剤、化学名:1−ヒドロキシ−シクロヘキシル−フェニルケトン)
Claims (7)
- 芳香族骨格を有さないポリオール(A)と芳香族骨格を有さないポリイソシアネート(B)とを反応させて得られる分子末端にイソシアネート基を有するウレタンプレポリマー(C)に対して、水酸基を有する(メタ)アクリル化合物(D)を付加反応させて得られる分子末端に(メタ)アクリロイル基を有するウレタンアクリレートオリゴマー(E)を含有する紫外線硬化性ウレタンアクリレート組成物であって、ケトン系溶剤、アミド系溶剤、及びハロゲン化アルキル系溶剤からなる群より選ばれる少なくとも一種の芳香族骨格を有さない有機溶剤(F)を0.2〜80質量%含有し、光重合開始剤を含有しない紫外線硬化性ウレタンアクリレート組成物であり、前記ウレタンアクリレートオリゴマー(E)の(メタ)アクリル当量が450〜1100g/当量の範囲であり、前記紫外線硬化性ウレタンアクリレート組成物により作製した厚さ100μmのフィルムを用いてJIS K 0129に準拠し動的粘弾性分析により測定したtanδピーク温度が0〜35℃の範囲であることを特徴とする紫外線硬化性ウレタンアクリレート組成物。
- 前記水酸基を有する(メタ)アクリル化合物(D)が、2−ヒドロキシエチル(メタ)アクリレート、2−ヒドロキシプロピル(メタ)アクリレート、3−ヒドロキシプロピル(メタ)アクリレート、4−ヒドロキシブチル(メタ)アクリレート、及びペンタエリスリトールトリアクリレートからなる群より選ばれる少なくとも一つである請求項1記載の紫外線硬化性ウレタンアクリレート組成物。
- 前記ウレタンアクリレートオリゴマー(E)のJIS Z 8803に準拠し測定した50℃での溶融粘度が500〜100000mPa・sの範囲である請求項1記載の紫外線硬化性ウレタンアクリレート組成物。
- 前記有機溶剤(F)が、メチルエチルケトン、アセトン、メチルイソブチルケトン、シクロヘキサノン、ジイソブチルケトン、イソホロン、ジメチルホルムアミド、メチレンクロライド、及びクロロホルムからなる群より選ばれる少なくとも一つである請求項1記載の紫外線硬化性ウレタンアクリレート組成物。
- 基材上に請求項1〜4の何れか一項に記載の紫外線硬化性ウレタンアクリレート組成物の硬化塗膜を有することを特徴とする薄膜成形体。
- 請求項1〜4の何れか一項に記載の紫外線硬化性ウレタンアクリレート組成物の硬化塗膜を有する光学フィルムであって、前記硬化塗膜の膜厚50〜200μmにおけるJIS K7361−1に準拠して測定した全光線透過率が92%以上であることを特徴とする光学フィルム。
- 基材上に請求項1〜4の何れか一項に記載の紫外線硬化性ウレタンアクリレート組成物を塗工し、紫外線を照射した後、前記有機溶剤(F)を揮発させて硬化塗膜を形成させることを特徴とする薄膜成形体の製造方法。
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Families Citing this family (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104977633B (zh) * | 2014-04-08 | 2018-07-17 | 株式会社巴川制纸所 | 保护膜、薄膜层压体和偏光板 |
JP2015203770A (ja) * | 2014-04-14 | 2015-11-16 | リンテック株式会社 | ハードコートフィルム、ハードコート層を形成するための塗工液、およびハードコートフィルムの製造方法 |
KR101807207B1 (ko) | 2015-02-03 | 2017-12-08 | 주식회사 엘지화학 | 자기 복원 특성을 갖는 코팅층 형성용 조성물, 코팅층 및 코팅 필름 |
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JP6596852B2 (ja) * | 2015-03-16 | 2019-10-30 | 日油株式会社 | 硬化性樹脂組成物および積層構造体 |
WO2016208284A1 (ja) * | 2015-06-26 | 2016-12-29 | Dic株式会社 | 鋼板表面処理剤、及びその塗膜を有する鋼板 |
CN106700024A (zh) * | 2015-11-15 | 2017-05-24 | 惠州市长润发涂料有限公司 | 一种紫外光固化聚氨酯丙烯酸酯自修复树脂制备方法 |
WO2017214105A2 (en) * | 2016-06-09 | 2017-12-14 | 3M Innovative Properties Company | Polyurethane acrylate protective display film |
WO2018003222A1 (ja) * | 2016-06-28 | 2018-01-04 | Dic株式会社 | ポリウレタン発泡シート、その製造方法、及び積層体の製造方法 |
US10962688B2 (en) * | 2016-07-01 | 2021-03-30 | 3M Innovative Properties Company | Low Tg polyurethane protective display film |
JP2019151815A (ja) * | 2018-02-28 | 2019-09-12 | 東レ株式会社 | 積層体および樹脂フィルム |
EP3842480A4 (en) * | 2018-08-23 | 2022-05-18 | Toray Industries, Inc. | RESIN FILM, BODY LAMINATE AND BODY LAMINATE PRODUCTION METHOD |
KR102124853B1 (ko) | 2018-12-14 | 2020-06-19 | 건국대학교 산학협력단 | 폴리에스테르 폴리올의 혼합물을 이용한 광경화 우레탄 아크릴레이트 중합체 및 이의 제조방법 |
CN109705382B (zh) * | 2018-12-14 | 2021-08-10 | 张家港康得新光电材料有限公司 | 自修复树脂、涂层、薄膜及薄膜制备方法与应用 |
CN113667054B (zh) * | 2021-06-18 | 2022-09-06 | 广东邦固化学科技有限公司 | 一种自修复树脂及其制备方法和应用和自修复光学膜的制备方法 |
CN113980638B (zh) * | 2021-11-11 | 2023-01-10 | 上海昀通电子科技有限公司 | 一种uv压敏延迟固化胶粘剂及其制备方法和应用 |
US11939418B2 (en) * | 2021-12-15 | 2024-03-26 | Stratasys, Inc. | Photo-curable compositions |
CN115340817B (zh) * | 2022-09-15 | 2023-10-20 | 中国科学技术大学 | 一种具有宽温域高阻尼性能的增硬涂层及其制备方法 |
Citations (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH048712A (ja) * | 1990-04-27 | 1992-01-13 | Mitsui Toatsu Chem Inc | 放射線硬化型樹脂及びその塗料組成物 |
JP2003084102A (ja) * | 2001-06-25 | 2003-03-19 | Asahi Glass Co Ltd | 光学フィルムおよびその製造方法 |
JP2003302501A (ja) * | 2002-04-12 | 2003-10-24 | Natoko Kk | レンズシート |
JP2004217809A (ja) * | 2003-01-16 | 2004-08-05 | Mitsubishi Chemicals Corp | 活性エネルギー線硬化樹脂シート |
JP2006016416A (ja) * | 2004-06-30 | 2006-01-19 | Nippon Kayaku Co Ltd | 樹脂組成物、レンズ用樹脂組成物及びその硬化物 |
JP2011074266A (ja) * | 2009-09-30 | 2011-04-14 | Nippon Shokubai Co Ltd | 光ディスク用硬化性樹脂組成物、その硬化物及び光ディスク |
JP2011208096A (ja) * | 2010-03-30 | 2011-10-20 | Dainippon Printing Co Ltd | 電子線硬化性樹脂組成物、及びそれを用いてなる積層体 |
JP2012036290A (ja) * | 2010-08-06 | 2012-02-23 | Showa Ink Kogyosho:Kk | 硬化性組成物 |
JP2012193220A (ja) * | 2011-03-15 | 2012-10-11 | Toagosei Co Ltd | 光学フィルム又はシート形成用電子線硬化型組成物、光学フィルム又はシート、偏光子保護フィルム及び偏光板 |
JP2013049839A (ja) * | 2011-07-29 | 2013-03-14 | Jsr Corp | 自己修復材料、自己修復性部材、および自己修復材料を製造するための組成物 |
JP2013133367A (ja) * | 2011-12-26 | 2013-07-08 | Toagosei Co Ltd | 光学フィルム又はシート形成用活性エネルギー線硬化型組成物及び光学フィルム又はシート |
WO2013146193A1 (ja) * | 2012-03-30 | 2013-10-03 | Dic株式会社 | 紫外線硬化性ウレタンアクリレート組成物、薄膜成形体、光学フィルム、及び薄膜成形体の製造方法 |
JP2014001299A (ja) * | 2012-06-18 | 2014-01-09 | Toagosei Co Ltd | 光学フィルム又はシート形成用活性エネルギー線硬化型組成物及び光学フィルム又はシート |
JP2014024880A (ja) * | 2012-07-24 | 2014-02-06 | Dic Corp | 紫外線硬化型ウレタンアクリレート樹脂組成物、薄膜成形体、光学フィルム、及び薄膜成形体の製造方法 |
JP2014048453A (ja) * | 2012-08-31 | 2014-03-17 | Toagosei Co Ltd | 加熱処理による低位相差光学フィルム又はシートの製造方法 |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2468782A1 (en) * | 2010-12-27 | 2012-06-27 | Cytec Surface Specialties, S.A. | Radiation curable compositions |
-
2013
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Patent Citations (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH048712A (ja) * | 1990-04-27 | 1992-01-13 | Mitsui Toatsu Chem Inc | 放射線硬化型樹脂及びその塗料組成物 |
JP2003084102A (ja) * | 2001-06-25 | 2003-03-19 | Asahi Glass Co Ltd | 光学フィルムおよびその製造方法 |
JP2003302501A (ja) * | 2002-04-12 | 2003-10-24 | Natoko Kk | レンズシート |
JP2004217809A (ja) * | 2003-01-16 | 2004-08-05 | Mitsubishi Chemicals Corp | 活性エネルギー線硬化樹脂シート |
JP2006016416A (ja) * | 2004-06-30 | 2006-01-19 | Nippon Kayaku Co Ltd | 樹脂組成物、レンズ用樹脂組成物及びその硬化物 |
JP2011074266A (ja) * | 2009-09-30 | 2011-04-14 | Nippon Shokubai Co Ltd | 光ディスク用硬化性樹脂組成物、その硬化物及び光ディスク |
JP2011208096A (ja) * | 2010-03-30 | 2011-10-20 | Dainippon Printing Co Ltd | 電子線硬化性樹脂組成物、及びそれを用いてなる積層体 |
JP2012036290A (ja) * | 2010-08-06 | 2012-02-23 | Showa Ink Kogyosho:Kk | 硬化性組成物 |
JP2012193220A (ja) * | 2011-03-15 | 2012-10-11 | Toagosei Co Ltd | 光学フィルム又はシート形成用電子線硬化型組成物、光学フィルム又はシート、偏光子保護フィルム及び偏光板 |
JP2013049839A (ja) * | 2011-07-29 | 2013-03-14 | Jsr Corp | 自己修復材料、自己修復性部材、および自己修復材料を製造するための組成物 |
JP2013133367A (ja) * | 2011-12-26 | 2013-07-08 | Toagosei Co Ltd | 光学フィルム又はシート形成用活性エネルギー線硬化型組成物及び光学フィルム又はシート |
WO2013146193A1 (ja) * | 2012-03-30 | 2013-10-03 | Dic株式会社 | 紫外線硬化性ウレタンアクリレート組成物、薄膜成形体、光学フィルム、及び薄膜成形体の製造方法 |
JP2014001299A (ja) * | 2012-06-18 | 2014-01-09 | Toagosei Co Ltd | 光学フィルム又はシート形成用活性エネルギー線硬化型組成物及び光学フィルム又はシート |
JP2014024880A (ja) * | 2012-07-24 | 2014-02-06 | Dic Corp | 紫外線硬化型ウレタンアクリレート樹脂組成物、薄膜成形体、光学フィルム、及び薄膜成形体の製造方法 |
JP2014048453A (ja) * | 2012-08-31 | 2014-03-17 | Toagosei Co Ltd | 加熱処理による低位相差光学フィルム又はシートの製造方法 |
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CN104619735A (zh) | 2015-05-13 |
JPWO2014045782A1 (ja) | 2016-08-18 |
WO2014045782A1 (ja) | 2014-03-27 |
TW201418303A (zh) | 2014-05-16 |
KR20150009605A (ko) | 2015-01-26 |
TWI487723B (zh) | 2015-06-11 |
KR101508706B1 (ko) | 2015-04-07 |
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