JP2010137470A - 蓄光性積層体 - Google Patents
蓄光性積層体 Download PDFInfo
- Publication number
- JP2010137470A JP2010137470A JP2008317253A JP2008317253A JP2010137470A JP 2010137470 A JP2010137470 A JP 2010137470A JP 2008317253 A JP2008317253 A JP 2008317253A JP 2008317253 A JP2008317253 A JP 2008317253A JP 2010137470 A JP2010137470 A JP 2010137470A
- Authority
- JP
- Japan
- Prior art keywords
- meth
- sensitive adhesive
- luminous
- acrylic
- phosphorescent
- 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
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- 239000004820 Pressure-sensitive adhesive Substances 0.000 claims abstract description 50
- 239000000178 monomer Substances 0.000 claims abstract description 38
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- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims abstract description 32
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims abstract description 30
- 125000003277 amino group Chemical group 0.000 claims abstract description 26
- 239000012463 white pigment Substances 0.000 claims abstract description 23
- 229920002554 vinyl polymer Polymers 0.000 claims abstract description 14
- 229920000642 polymer Polymers 0.000 description 32
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- 229910052693 Europium Inorganic materials 0.000 description 2
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- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 239000005083 Zinc sulfide Substances 0.000 description 2
- PQJYXFVJBSRUPG-UHFFFAOYSA-N [3-(2-methylaziridine-1-carbonyl)phenyl]-(2-methylaziridin-1-yl)methanone Chemical compound CC1CN1C(=O)C1=CC=CC(C(=O)N2C(C2)C)=C1 PQJYXFVJBSRUPG-UHFFFAOYSA-N 0.000 description 2
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- 125000000217 alkyl group Chemical group 0.000 description 2
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- 238000010030 laminating Methods 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
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- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- NOBYOEQUFMGXBP-UHFFFAOYSA-N (4-tert-butylcyclohexyl) (4-tert-butylcyclohexyl)oxycarbonyloxy carbonate Chemical compound C1CC(C(C)(C)C)CCC1OC(=O)OOC(=O)OC1CCC(C(C)(C)C)CC1 NOBYOEQUFMGXBP-UHFFFAOYSA-N 0.000 description 1
- HMLSBRLVTDLLOI-UHFFFAOYSA-N 1-(dimethylamino)ethyl 2-methylprop-2-enoate Chemical compound CN(C)C(C)OC(=O)C(C)=C HMLSBRLVTDLLOI-UHFFFAOYSA-N 0.000 description 1
- NFTVTXIQFYRSHF-UHFFFAOYSA-N 1-(dimethylamino)ethyl prop-2-enoate Chemical compound CN(C)C(C)OC(=O)C=C NFTVTXIQFYRSHF-UHFFFAOYSA-N 0.000 description 1
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- IEQWWMKDFZUMMU-UHFFFAOYSA-N 2-(2-prop-2-enoyloxyethyl)butanedioic acid Chemical compound OC(=O)CC(C(O)=O)CCOC(=O)C=C IEQWWMKDFZUMMU-UHFFFAOYSA-N 0.000 description 1
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
- DPBJAVGHACCNRL-UHFFFAOYSA-N 2-(dimethylamino)ethyl prop-2-enoate Chemical compound CN(C)CCOC(=O)C=C DPBJAVGHACCNRL-UHFFFAOYSA-N 0.000 description 1
- PLWQJHWLGRXAMP-UHFFFAOYSA-N 2-ethenoxy-n,n-diethylethanamine Chemical compound CCN(CC)CCOC=C PLWQJHWLGRXAMP-UHFFFAOYSA-N 0.000 description 1
- JWCDUUFOAZFFMX-UHFFFAOYSA-N 2-ethenoxy-n,n-dimethylethanamine Chemical compound CN(C)CCOC=C JWCDUUFOAZFFMX-UHFFFAOYSA-N 0.000 description 1
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 1
- JNDVNJWCRZQGFQ-UHFFFAOYSA-N 2-methyl-N,N-bis(methylamino)hex-2-enamide Chemical compound CCCC=C(C)C(=O)N(NC)NC JNDVNJWCRZQGFQ-UHFFFAOYSA-N 0.000 description 1
- CYUZOYPRAQASLN-UHFFFAOYSA-N 3-prop-2-enoyloxypropanoic acid Chemical compound OC(=O)CCOC(=O)C=C CYUZOYPRAQASLN-UHFFFAOYSA-N 0.000 description 1
- VFXXTYGQYWRHJP-UHFFFAOYSA-N 4,4'-azobis(4-cyanopentanoic acid) Chemical compound OC(=O)CCC(C)(C#N)N=NC(C)(CCC(O)=O)C#N VFXXTYGQYWRHJP-UHFFFAOYSA-N 0.000 description 1
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- 239000005995 Aluminium silicate Substances 0.000 description 1
- NOWKCMXCCJGMRR-UHFFFAOYSA-N Aziridine Chemical compound C1CN1 NOWKCMXCCJGMRR-UHFFFAOYSA-N 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
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- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
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- 239000006096 absorbing agent Substances 0.000 description 1
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- YUENFNPLGJCNRB-UHFFFAOYSA-N anthracen-1-amine Chemical compound C1=CC=C2C=C3C(N)=CC=CC3=CC2=C1 YUENFNPLGJCNRB-UHFFFAOYSA-N 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
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- 238000012662 bulk polymerization Methods 0.000 description 1
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- 125000004122 cyclic group Chemical group 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004985 dialkyl amino alkyl group Chemical group 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- KORSJDCBLAPZEQ-UHFFFAOYSA-N dicyclohexylmethane-4,4'-diisocyanate Chemical compound C1CC(N=C=O)CCC1CC1CCC(N=C=O)CC1 KORSJDCBLAPZEQ-UHFFFAOYSA-N 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 238000009820 dry lamination Methods 0.000 description 1
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- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
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- 229910052731 fluorine Inorganic materials 0.000 description 1
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- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 230000007774 longterm Effects 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
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- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 150000002763 monocarboxylic acids Chemical class 0.000 description 1
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- FTQWRYSLUYAIRQ-UHFFFAOYSA-N n-[(octadecanoylamino)methyl]octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NCNC(=O)CCCCCCCCCCCCCCCCC FTQWRYSLUYAIRQ-UHFFFAOYSA-N 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
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- 230000003647 oxidation Effects 0.000 description 1
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- 239000006072 paste Substances 0.000 description 1
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- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- 239000011241 protective layer Substances 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000013464 silicone adhesive Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- FNWBQFMGIFLWII-UHFFFAOYSA-N strontium aluminate Chemical class [O-2].[O-2].[O-2].[O-2].[O-2].[Al+3].[Al+3].[Sr+2].[Sr+2] FNWBQFMGIFLWII-UHFFFAOYSA-N 0.000 description 1
- 125000003011 styrenyl group Chemical group [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000010557 suspension polymerization reaction Methods 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- 239000011667 zinc carbonate Substances 0.000 description 1
- 229910000010 zinc carbonate Inorganic materials 0.000 description 1
- 235000004416 zinc carbonate Nutrition 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical compound [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 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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Abstract
【解決手段】蓄光層102と、前記蓄光層に積層され、カルボキシル基含有(メタ)アクリル系ポリマー、前記カルボキシル基含有(メタ)アクリル系ポリマー、白色顔料、及び芳香族ビニルモノマーを含まないアミノ基含有(メタ)アクリル系ポリマーを含むアクリル系白色粘着剤層104とを含む蓄光性積層体100。
【選択図】図1
Description
このようなシートや床材は、蓄光性材料が吸収した光エネルギーが暗闇で発光する性質を利用して、防災や安全用の標示や、種々の案内標示に用いられている。蓄光性材料が発光する際、蓄光性材料の背面に光を隠蔽する層を設けると、より蓄光性能が向上するため、蓄光性材料を含む層の背面に隠蔽性のある層が設けられていることがある。この場合、このような隠蔽性のある層に、さらに粘着剤層が設けられている。
前記カルボキシル基含有(メタ)アクリル系ポリマーは、モノエチレン性不飽和モノマーを主成分とするポリマーであって、その一部にカルボキシル基を含有するモノエチレン性不飽和モノマー(カルボキシル基含有モノエチレン性不飽和モノマー)を含有するものである。前記モノエチレン性不飽和モノマーは、ポリマーの主成分となるものであって、一般には式CH2=CR1COOR2(式中、R1は水素又はメチル基であり、R2は直鎖、環状又は分岐状のアルキル基やフェニル基、アルコキシアルキル基、フェノキシアルキル基、ヒドロキシアルキル基、環状エーテル基である)で表される。このようなモノマーとしては、例えば、メチル(メタ)アクリレート、エチル(メタ)アクリレート、n−ブチル(メタ)アクリレート、イソアミル(メタ)アクリレート、n−ヘキシル(メタ)アクリレート、2−エチルヘキシル(メタ)アクリレート、イソオクチル(メタ)アクリレート、イソノニル(メタ)アクリレート、デシル(メタ)アクリレート、またはドデシル(メタ)アクリレート、シクロヘキシル(メタ)アクリレート等のアルキル(メタ)アクリレート;フェノキシエチル(メタ)アクリレート等のフェノキシアルキル(メタ)アクリレート;メトキシプロピル(メタ)アクリレート、2−メトキシブチル(メタ)アクリレート等のアルコキシアルキル(メタ)アクリレート;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、4−ヒドロキシブチル(メタ)アクリレート等のヒドロキシアルキル(メタ)アクリレート;グリシジル(メタ)アクリレート、テトラヒドロフルフリル(メタ)アクリレート等の環状エーテル含有(メタ)アクリレートなどを挙げることができる。必要に応じ、1種又は2種以上のモノエチレン性不飽和モノマーを使用することができる。
前記芳香族ビニルモノマーを含まないアミノ基含有(メタ)アクリル系ポリマーとは、モノエチレン性不飽和モノマーを主成分とするポリマーであって、その一部にアミノ基含有不飽和モノマーを含有し、かつ芳香族ビニルモノマーをポリマーの構成成分として含まないものである。かかるモノエチレン性不飽和モノマーは、前記カルボキシル基含有(メタ)剤中アクリル系ポリマーの場合と同様であり、前記芳香族ビニルモノマーは、スチレン、α−メチルスチレン、ビニルトルエン、ビニルナフタレン、ビニルアントラセン、ビニルアントラキノン、芳香族アミンの(メタ)アクリルアミド、または水酸基含有芳香族化合物の(メタ)アクリレート等を含む。前記芳香族アミンとしてはアニリン、ベンジルアミン、ナフチルアミン、アミノアントラセン、アミノアントラキノン又はこれらの誘導体が挙げられる。また前記水酸基含有芳香族化合物は前記芳香族アミンに対応する水酸基含有化合物が挙げられる。前記アミノ基含有(メタ)アクリル系ポリマーを得る方法として、モノエチレン性不飽和モノマーとアミノ基を含有する不飽和モノマーとを共重合することが挙げられる。
前記白色顔料として、従来公知の白色顔料、例えば、炭酸亜鉛、酸化亜鉛、硫化亜鉛、または酸化チタン(二酸化チタン)を挙げることができる。また、添加剤としてタルク、カオリン、炭酸カルシウムを含んでもよい。これら白色顔料は単体で、あるいは二種以上を混合して用いることができる。また、これらの白色顔料はいずれの形態でもよく、あるいは従来公知の方法によって各種の分散処理が施されたものであってもよい。
前記着色剤は、白色顔料と芳香族ビニルモノマーを含まないアミノ基含有(メタ)アクリル系ポリマーとを含有する。ここで、前記白色顔料、及び前記芳香族ビニルモノマーを含まないアミノ基含有(メタ)アクリル系ポリマーはそれぞれ上述のとおりである。
前記アクリル系白色粘着剤は、架橋剤を含んでも良い。かかる架橋剤として、例えば、ビスアミド系架橋剤(例えば、1,1’−イソフタロイル−ビス(2−メチルアジリジン))、アジリジン系架橋剤(例えば、日本触媒製ケミタイトPZ33、アビシア製NeoCryl CX−100)、カルボジイミド系架橋剤(例えば、日清紡製カルボジライトV−03,V−05,V−07)、エポキシ系架橋剤(例えば綜研化学製E−AX,E−5XM,E5C)、イソシアネート系架橋剤(例えば、日本ポリウレタン製コロネートL、コロネートHK、バイエル社製デスモジュールH、デスモジュールW、デスモジュールI)、エポキシ系架橋剤(例えば綜研化学製E−AX、E−5XM、E5C)、イソシアネート系架橋剤(例えば、日本ポリウレタン製コロネートL、コロネートHK、バイエル社製デスモジュールH、デスモジュールW、デスモジュールI)等を用いることができる。
蓄光層202は、蓄光性蛍光体を含む樹脂からなる蓄光部203と、実質的に蓄光性蛍光体を含まない樹脂からなる支持部205とから構成することができる。図2に示される態様において、蓄光部203および支持部205に用いられる樹脂は、特に限定されない。例えば図1の説明に記載したような、透明で柔軟性を有する樹脂を使用できる。
このようなライナーは、粘着テープなどの分野で一般的に使用されているものでよく、特定の部材に限定されるものではない。好適なライナーとしては、例えば、紙;ポリエチレン、ポリプロピレン、ポリエステル、または酢酸セルロース等のプラスチック材料;あるいはこのようなプラスチック材料で被覆又はそれを積層された紙やその他の材料などを挙げることができる。これらのライナーは、そのまま使用してもよいが、シリコーン処理あるいはその他の方法で処理して剥離特性を向上させた後に使用することができる。
蓄光性蛍光体(根本特殊化学社製GLL−300M)を30質量部含むポリ塩化ビニル樹脂層(信越ポリマー社製TUJ−7854)を準備した。
アクリル樹脂1(メチルメタクリレート(MMA)/ブチルメタアクリレート(BMA)/ジメチルアミノエチルメタクリレート(Di−methyl−amino−ethyl−methacrylate、DEMAEMA)共重合体、組成比は60:34:6(質量比)、分子量(Mw)は68,000、Tgは63℃(計算値)、酢酸エチル溶液。固形分39%)が10質量部、顔料1(白色顔料、DuPont製TiPureR960、酸化チタン)が50質量部に対してメチルイソブチルケトン(MIBK)を40質量部添加しペイントシェイカー(株式会社シンキー(Thinky)製ARE250)で10分間攪拌し顔料プレミックス溶液を得た。
ゴム系粘着剤(GRN−13B、ビッグテクノス社製)とポリイソシアネート架橋剤(コロネートL−55E、日本ポリウレタン工業社製)を100:1(質量比)で混合し、溶剤はトルエンを用いて固形分約30%となるよう調整し、ナイフコートにより紙ベース両面ポリエチレンラミネート剥離紙上に乾燥後の厚さが50μmになるように塗布して90℃で5分間加熱、乾燥した。
上記の様にして得られたアクリル系白色粘着剤層と床面粘着剤層とを貼り合せて粘着剤層の積層体を得た。上記で得られた蓄光層にプライマー(住友スリーエム社製N200)を塗布・乾燥し、前記粘着剤層の積層体のアクリル系白色粘着剤層をドライラミネートにより貼り合わせて蓄光性積層体を得た。
蓄光性蛍光体(根本特殊化学社製GLL−300M)を30質量部含むポリ塩化ビニル樹脂層(信越ポリマー社製TUJ−7854)の背面に、プライマー(住友スリーエム社製N−200)を塗布・乾燥後、床面粘着剤溶液(淡黄色ゴム系粘着剤(ビッグテクノス社製GRN−13B)とポリイソシアネート架橋剤(日本ポリウレタン工業社製コロネートL−55E)とを100:1で混合した溶液)を、乾燥後厚みが80μmとなるようにナイフコートにより塗布・乾燥して蓄光性積層体を得た。
蓄光性蛍光体(根本特殊化学社製GLL−300M)を30質量部含むポリ塩化ビニル樹脂層(信越ポリマー社製TUJ−7854)の背面に、プライマー(住友スリーエム社製N−200)を塗布・乾燥後、白色顔料(住友スリーエム社製BW9310(アルキド白色顔料分散溶液))を50質量部含む床面粘着剤溶液(ゴム系粘着剤(ビッグテクノス社製GRN−13B)とポリイソシアネート架橋剤(日本ポリウレタン工業社製コロネートL−55E)とを100:1で混合した溶液)を、乾燥後厚みが80μmとなるようにナイフコートにより塗布・乾燥して蓄光性積層体を得た。
黒色と白色が交互に印刷された隠蔽性試験用シート上に、実施例、比較例1〜2で得られた蓄光性積層体を貼り付け、JIS Z 9107 6.3.2に基づき、常用光源ランプD65を用いて200luxで20分間照射後暗転させた後の残光輝度を輝度測定システムにてそれぞれの黒色部、白色部の蓄光性能を測定した。残光輝度値を表1に、黒色部における輝度減衰率を図4にそれぞれ示した。また、蓄光層側からの外観の写真を撮影し図7に示した。
実施例、比較例1および比較例2で得た蓄光性積層体を25mm幅にカットし、モルタル板に貼付して24時間(一日)後および、耐湿試験機(65℃95%)にて一週間養生後の90度剥離接着力(N/25mm)をデジタルフォースゲージ(株式会社イマダ製)にて測定した。結果をそれぞれ図5及び図6に示した。値は接着力(N/25mm+標準偏差)である。
102、202、302 蓄光層
104、204、304 アクリル系白色粘着剤層
203 蓄光部
205 支持部
Claims (5)
- 蓄光層と、
前記蓄光層に積層され、カルボキシル基含有(メタ)アクリル系ポリマー、前記カルボキシル基含有(メタ)アクリル系ポリマー、白色顔料、及び芳香族ビニルモノマーを含まないアミノ基含有(メタ)アクリル系ポリマーを含むアクリル系白色粘着剤層と
を含む蓄光性積層体。 - 前記アクリル系白色粘着剤が、カルボキシル基含有(メタ)アクリル系ポリマー100質量部に対して、25〜150質量部の白色顔料を含む請求項1に記載の蓄光性積層体。
- 前記アクリル系白色粘着剤層の厚さが、0.02mm〜0.1mmである請求項1または2に記載の蓄光性積層体。
- 前記蓄光層が蓄光部と支持部とから構成される請求項1〜3のいずれか一項に記載の蓄光性積層体。
- 前記蓄光性積層体のアクリル系白色粘着剤層に、さらに床面粘着剤層が積層されている請求項1〜4のいずれか一項に記載の蓄光性積層体。
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KR1020117016052A KR20110098950A (ko) | 2008-12-12 | 2009-12-09 | 광 축적 적층체 |
PCT/US2009/067311 WO2010068665A2 (en) | 2008-12-12 | 2009-12-09 | Light accumulating laminated body |
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Cited By (4)
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JP2012153129A (ja) * | 2011-01-07 | 2012-08-16 | Shin-Etsu Chemical Co Ltd | 粘着性蓄光複合シート |
JP2015151418A (ja) * | 2014-02-12 | 2015-08-24 | 信越化学工業株式会社 | 粘着性蓄光複合シート |
KR101559314B1 (ko) * | 2015-04-29 | 2015-10-13 | 주식회사 삼호글라스 | Pvc 축광필름을 접착한 축광유리, 및 이를 이용한 접합유리, 복층유리의 제조방법 |
JP2018167403A (ja) * | 2017-03-29 | 2018-11-01 | デンカ株式会社 | 蓄光性蛍光体を含有するフッ化ビニリデン樹脂系複合シートおよびその製造方法 |
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WO2010068665A3 (en) | 2010-08-26 |
EP2370254A2 (en) | 2011-10-05 |
JP5442988B2 (ja) | 2014-03-19 |
CN102271912A (zh) | 2011-12-07 |
KR20110098950A (ko) | 2011-09-02 |
EP2370254A4 (en) | 2013-10-02 |
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