JP5632288B2 - 高屈折率の感圧性接着剤 - Google Patents
高屈折率の感圧性接着剤 Download PDFInfo
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- JP5632288B2 JP5632288B2 JP2010530066A JP2010530066A JP5632288B2 JP 5632288 B2 JP5632288 B2 JP 5632288B2 JP 2010530066 A JP2010530066 A JP 2010530066A JP 2010530066 A JP2010530066 A JP 2010530066A JP 5632288 B2 JP5632288 B2 JP 5632288B2
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- Japan
- Prior art keywords
- pressure sensitive
- sensitive adhesive
- weight
- acid
- adhesive
- 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.)
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- 239000004820 Pressure-sensitive adhesive Substances 0.000 title claims abstract description 40
- 239000000178 monomer Substances 0.000 claims abstract description 82
- 239000002253 acid Substances 0.000 claims description 24
- 239000004014 plasticizer Substances 0.000 claims description 18
- 229920001577 copolymer Polymers 0.000 claims description 17
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 16
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 15
- 230000003287 optical effect Effects 0.000 claims description 12
- 239000003431 cross linking reagent Substances 0.000 claims description 10
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 8
- 229910052799 carbon Inorganic materials 0.000 claims description 6
- 239000000126 substance Substances 0.000 claims description 5
- 125000003118 aryl group Chemical group 0.000 claims description 4
- 230000005540 biological transmission Effects 0.000 claims description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 3
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 claims description 2
- 230000002378 acidificating effect Effects 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 claims description 2
- 125000006267 biphenyl group Chemical group 0.000 abstract description 6
- 239000000853 adhesive Substances 0.000 description 55
- 230000001070 adhesive effect Effects 0.000 description 55
- 239000000203 mixture Substances 0.000 description 40
- -1 Polyethylene terephthalate Polymers 0.000 description 30
- 238000000034 method Methods 0.000 description 25
- 239000000463 material Substances 0.000 description 18
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical group C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 17
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 16
- 239000004971 Cross linker Substances 0.000 description 14
- IMSODMZESSGVBE-UHFFFAOYSA-N 2-Oxazoline Chemical compound C1CN=CO1 IMSODMZESSGVBE-UHFFFAOYSA-N 0.000 description 13
- 238000006116 polymerization reaction Methods 0.000 description 13
- 239000000758 substrate Substances 0.000 description 13
- 238000000576 coating method Methods 0.000 description 12
- 239000003999 initiator Substances 0.000 description 11
- 229920000642 polymer Polymers 0.000 description 11
- 239000004305 biphenyl Substances 0.000 description 10
- 239000011248 coating agent Substances 0.000 description 10
- 150000001875 compounds Chemical class 0.000 description 10
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
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- 235000010290 biphenyl Nutrition 0.000 description 9
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- 230000005855 radiation Effects 0.000 description 9
- 150000003254 radicals Chemical class 0.000 description 9
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
- 229910052757 nitrogen Inorganic materials 0.000 description 8
- 239000002904 solvent Substances 0.000 description 7
- 238000012360 testing method Methods 0.000 description 7
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 6
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
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- 239000000047 product Substances 0.000 description 6
- FVAUCKIRQBBSSJ-UHFFFAOYSA-M sodium iodide Chemical compound [Na+].[I-] FVAUCKIRQBBSSJ-UHFFFAOYSA-M 0.000 description 6
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- NXQMCAOPTPLPRL-UHFFFAOYSA-N 2-(2-benzoyloxyethoxy)ethyl benzoate Chemical compound C=1C=CC=CC=1C(=O)OCCOCCOC(=O)C1=CC=CC=C1 NXQMCAOPTPLPRL-UHFFFAOYSA-N 0.000 description 4
- 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 4
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 4
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 4
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 4
- 150000001412 amines Chemical class 0.000 description 4
- QMKYBPDZANOJGF-UHFFFAOYSA-N benzene-1,3,5-tricarboxylic acid Chemical compound OC(=O)C1=CC(C(O)=O)=CC(C(O)=O)=C1 QMKYBPDZANOJGF-UHFFFAOYSA-N 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- LLEMOWNGBBNAJR-UHFFFAOYSA-N biphenyl-2-ol Chemical group OC1=CC=CC=C1C1=CC=CC=C1 LLEMOWNGBBNAJR-UHFFFAOYSA-N 0.000 description 4
- 238000012662 bulk polymerization Methods 0.000 description 4
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- 239000012986 chain transfer agent Substances 0.000 description 4
- 239000007795 chemical reaction product Substances 0.000 description 4
- 150000002148 esters Chemical class 0.000 description 4
- 230000004313 glare Effects 0.000 description 4
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 4
- 239000004611 light stabiliser Substances 0.000 description 4
- FTQWRYSLUYAIRQ-UHFFFAOYSA-N n-[(octadecanoylamino)methyl]octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NCNC(=O)CCCCCCCCCCCCCCCCC FTQWRYSLUYAIRQ-UHFFFAOYSA-N 0.000 description 4
- 238000010926 purge Methods 0.000 description 4
- 238000010526 radical polymerization reaction Methods 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 238000003786 synthesis reaction Methods 0.000 description 4
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 4
- 229920002554 vinyl polymer Polymers 0.000 description 4
- KWVGIHKZDCUPEU-UHFFFAOYSA-N 2,2-dimethoxy-2-phenylacetophenone Chemical compound C=1C=CC=CC=1C(OC)(OC)C(=O)C1=CC=CC=C1 KWVGIHKZDCUPEU-UHFFFAOYSA-N 0.000 description 3
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- QPRQEDXDYOZYLA-UHFFFAOYSA-N 2-methylbutan-1-ol Chemical compound CCC(C)CO QPRQEDXDYOZYLA-UHFFFAOYSA-N 0.000 description 3
- XTYDODOHJOEBAH-UHFFFAOYSA-N 6-(2-phenylphenoxy)hexan-1-ol Chemical compound OCCCCCCOC1=CC=CC=C1C1=CC=CC=C1 XTYDODOHJOEBAH-UHFFFAOYSA-N 0.000 description 3
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 3
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 3
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 3
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 3
- 125000001246 bromo group Chemical group Br* 0.000 description 3
- 239000003153 chemical reaction reagent Substances 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 238000009833 condensation Methods 0.000 description 3
- 230000005494 condensation Effects 0.000 description 3
- 239000003995 emulsifying agent Substances 0.000 description 3
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 3
- 230000000269 nucleophilic effect Effects 0.000 description 3
- JYVLIDXNZAXMDK-UHFFFAOYSA-N pentan-2-ol Chemical compound CCCC(C)O JYVLIDXNZAXMDK-UHFFFAOYSA-N 0.000 description 3
- 239000004417 polycarbonate Substances 0.000 description 3
- 229920000515 polycarbonate Polymers 0.000 description 3
- 229920006267 polyester film Polymers 0.000 description 3
- 229920000139 polyethylene terephthalate Polymers 0.000 description 3
- 239000005020 polyethylene terephthalate Substances 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 3
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 2
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
- GJKGAPPUXSSCFI-UHFFFAOYSA-N 2-Hydroxy-4'-(2-hydroxyethoxy)-2-methylpropiophenone Chemical compound CC(C)(O)C(=O)C1=CC=C(OCCO)C=C1 GJKGAPPUXSSCFI-UHFFFAOYSA-N 0.000 description 2
- XFDQLDNQZFOAFK-UHFFFAOYSA-N 2-benzoyloxyethyl benzoate Chemical compound C=1C=CC=CC=1C(=O)OCCOC(=O)C1=CC=CC=C1 XFDQLDNQZFOAFK-UHFFFAOYSA-N 0.000 description 2
- MCRZWYDXIGCFKO-UHFFFAOYSA-N 2-butylpropanedioic acid Chemical compound CCCCC(C(O)=O)C(O)=O MCRZWYDXIGCFKO-UHFFFAOYSA-N 0.000 description 2
- LWRBVKNFOYUCNP-UHFFFAOYSA-N 2-methyl-1-(4-methylsulfanylphenyl)-2-morpholin-4-ylpropan-1-one Chemical compound C1=CC(SC)=CC=C1C(=O)C(C)(C)N1CCOCC1 LWRBVKNFOYUCNP-UHFFFAOYSA-N 0.000 description 2
- PFNHSEQQEPMLNI-UHFFFAOYSA-N 2-methyl-1-pentanol Chemical compound CCCC(C)CO PFNHSEQQEPMLNI-UHFFFAOYSA-N 0.000 description 2
- 125000003504 2-oxazolinyl group Chemical group O1C(=NCC1)* 0.000 description 2
- KUDUQBURMYMBIJ-UHFFFAOYSA-N 2-prop-2-enoyloxyethyl prop-2-enoate Chemical compound C=CC(=O)OCCOC(=O)C=C KUDUQBURMYMBIJ-UHFFFAOYSA-N 0.000 description 2
- IWTBVKIGCDZRPL-UHFFFAOYSA-N 3-methylpentanol Chemical compound CCC(C)CCO IWTBVKIGCDZRPL-UHFFFAOYSA-N 0.000 description 2
- JNTPTNNCGDAGEJ-UHFFFAOYSA-N 6-chlorohexan-1-ol Chemical compound OCCCCCCCl JNTPTNNCGDAGEJ-UHFFFAOYSA-N 0.000 description 2
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- NOWKCMXCCJGMRR-UHFFFAOYSA-N Aziridine Chemical compound C1CN1 NOWKCMXCCJGMRR-UHFFFAOYSA-N 0.000 description 2
- 239000004342 Benzoyl peroxide Substances 0.000 description 2
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical group C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 2
- IRIAEXORFWYRCZ-UHFFFAOYSA-N Butylbenzyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCC1=CC=CC=C1 IRIAEXORFWYRCZ-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
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- PQJYXFVJBSRUPG-UHFFFAOYSA-N [3-(2-methylaziridine-1-carbonyl)phenyl]-(2-methylaziridin-1-yl)methanone Chemical group CC1CN1C(=O)C1=CC=CC(C(=O)N2C(C2)C)=C1 PQJYXFVJBSRUPG-UHFFFAOYSA-N 0.000 description 2
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- 150000008378 aryl ethers Chemical class 0.000 description 2
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- 150000001735 carboxylic acids Chemical class 0.000 description 2
- 125000004122 cyclic group Chemical group 0.000 description 2
- MWKFXSUHUHTGQN-UHFFFAOYSA-N decan-1-ol Chemical compound CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 description 2
- 238000004090 dissolution Methods 0.000 description 2
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- DKWHHTWSTXZKDW-UHFFFAOYSA-N 1-[2-[2-[2-(2-butoxyethoxy)ethoxymethoxy]ethoxy]ethoxy]butane Chemical compound CCCCOCCOCCOCOCCOCCOCCCC DKWHHTWSTXZKDW-UHFFFAOYSA-N 0.000 description 1
- KPAPHODVWOVUJL-UHFFFAOYSA-N 1-benzofuran;1h-indene Chemical compound C1=CC=C2CC=CC2=C1.C1=CC=C2OC=CC2=C1 KPAPHODVWOVUJL-UHFFFAOYSA-N 0.000 description 1
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- 239000011780 sodium chloride Substances 0.000 description 1
- HRZFUMHJMZEROT-UHFFFAOYSA-L sodium disulfite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])(=O)=O HRZFUMHJMZEROT-UHFFFAOYSA-L 0.000 description 1
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
- 229940001584 sodium metabisulfite Drugs 0.000 description 1
- 235000010262 sodium metabisulphite Nutrition 0.000 description 1
- CHQMHPLRPQMAMX-UHFFFAOYSA-L sodium persulfate Substances [Na+].[Na+].[O-]S(=O)(=O)OOS([O-])(=O)=O CHQMHPLRPQMAMX-UHFFFAOYSA-L 0.000 description 1
- 238000004528 spin coating Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 150000003440 styrenes Chemical class 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 125000000446 sulfanediyl group Chemical group *S* 0.000 description 1
- 229940124530 sulfonamide Drugs 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000010345 tape casting Methods 0.000 description 1
- 150000003509 tertiary alcohols Chemical class 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 125000003866 trichloromethyl group Chemical group ClC(Cl)(Cl)* 0.000 description 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 239000010937 tungsten Substances 0.000 description 1
- KPGXUAIFQMJJFB-UHFFFAOYSA-H tungsten hexachloride Chemical compound Cl[W](Cl)(Cl)(Cl)(Cl)Cl KPGXUAIFQMJJFB-UHFFFAOYSA-H 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- ZTWTYVWXUKTLCP-UHFFFAOYSA-N vinylphosphonic acid Chemical compound OP(O)(=O)C=C ZTWTYVWXUKTLCP-UHFFFAOYSA-N 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 238000004383 yellowing Methods 0.000 description 1
Classifications
-
- 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
- C09J133/00—Adhesives based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Adhesives based on derivatives of such polymers
- C09J133/04—Homopolymers or copolymers of esters
- C09J133/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
- C09J133/08—Homopolymers or copolymers of acrylic acid esters
-
- 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
- C09J2301/00—Additional features of adhesives in the form of films or foils
- C09J2301/30—Additional features of adhesives in the form of films or foils characterized by the chemical, physicochemical or physical properties of the adhesive or the carrier
- C09J2301/302—Additional features of adhesives in the form of films or foils characterized by the chemical, physicochemical or physical properties of the adhesive or the carrier the adhesive being pressure-sensitive, i.e. tacky at temperatures inferior to 30°C
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Adhesive Tapes (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US11/875,194 | 2007-10-19 | ||
| US11/875,194 US20090105437A1 (en) | 2007-10-19 | 2007-10-19 | High refractive index pressure-sensitive adhesives |
| PCT/US2008/079865 WO2009052111A1 (en) | 2007-10-19 | 2008-10-14 | High refractive index pressure-sensitive adhesives |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2011500920A JP2011500920A (ja) | 2011-01-06 |
| JP2011500920A5 JP2011500920A5 (enExample) | 2011-12-01 |
| JP5632288B2 true JP5632288B2 (ja) | 2014-11-26 |
Family
ID=40134775
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010530066A Expired - Fee Related JP5632288B2 (ja) | 2007-10-19 | 2008-10-14 | 高屈折率の感圧性接着剤 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US20090105437A1 (enExample) |
| EP (1) | EP2207859B1 (enExample) |
| JP (1) | JP5632288B2 (enExample) |
| KR (1) | KR101550079B1 (enExample) |
| CN (2) | CN101896568A (enExample) |
| AT (1) | ATE545687T1 (enExample) |
| WO (1) | WO2009052111A1 (enExample) |
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| US6536045B1 (en) | 1999-11-24 | 2003-03-25 | Racing Optics | Tear-off optical stack having peripheral seal mount |
| US20090154198A1 (en) * | 2007-12-14 | 2009-06-18 | Joo Hoon Lee | Reflection type display apparatus |
| WO2010005655A2 (en) * | 2008-07-10 | 2010-01-14 | 3M Innovative Properties Company | Viscoelastic lightguide |
| CN107037526A (zh) | 2008-08-08 | 2017-08-11 | 3M创新有限公司 | 具有粘弹性层的用于控制光的光导 |
| JP5362291B2 (ja) * | 2008-08-26 | 2013-12-11 | 日東電工株式会社 | アクリル系粘着剤組成物、アクリル系粘着剤層およびアクリル系粘着テープ又はシート |
| BRPI1011746A2 (pt) | 2009-06-25 | 2018-02-06 | 3M Innovative Properties Co | artigos antimicrobianos ativados por luz e métodos de uso |
| CN102625677B (zh) | 2009-08-21 | 2016-05-18 | 3M创新有限公司 | 使用吸水性应力分布材料来减轻组织创伤的方法和产品 |
| EP3143943B1 (en) | 2009-08-21 | 2019-02-27 | 3M Innovative Properties Company | Products for reducing tissue trauma using water-resistant stress-distributing materials |
| CN102573692B (zh) | 2009-08-21 | 2015-03-25 | 3M创新有限公司 | 用于照明组织的方法和产品 |
| KR20120123741A (ko) | 2010-01-13 | 2012-11-09 | 쓰리엠 이노베이티브 프로퍼티즈 컴파니 | 미세 구조화 저 굴절률 나노공극형 층을 갖는 광학 필름 및 이의 제조 방법 |
| JP5729973B2 (ja) * | 2010-11-11 | 2015-06-03 | 日本合成化学工業株式会社 | アクリル系粘着剤、光学部材用粘着剤、粘着剤層付き光学部材、画像表示装置 |
| CN102892829B (zh) * | 2010-05-11 | 2014-11-26 | 3M创新有限公司 | 可固化组合物、压敏粘合剂、制备它们的方法以及粘合剂制品 |
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| WO2012087665A2 (en) | 2010-12-22 | 2012-06-28 | 3M Innovative Properties Company | Surface-modified zirconia nanoparticles |
| TWI465534B (zh) * | 2010-12-31 | 2014-12-21 | Eternal Materials Co Ltd | 可光固化之黏著組合物 |
| JP5565815B2 (ja) * | 2011-02-14 | 2014-08-06 | リンテック株式会社 | 光学用粘着剤組成物、光学用粘着剤層及び光学用粘着性積層体 |
| JP5583048B2 (ja) * | 2011-02-14 | 2014-09-03 | リンテック株式会社 | 光学用粘着剤組成物、光学用粘着剤層及び光学用粘着性積層体 |
| CN103443228B (zh) * | 2011-03-24 | 2016-05-18 | 3M创新有限公司 | 阻燃条带 |
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| EP3715432A1 (en) * | 2019-03-27 | 2020-09-30 | 3M Innovative Properties Company | Pressure-sensitive adhesive composition with transparency characteristics |
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| US11912001B2 (en) | 2019-12-03 | 2024-02-27 | Ro Technologies, Llc | Method and apparatus for reducing non-normal incidence distortion in glazing films |
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| US20210285661A1 (en) | 2020-03-10 | 2021-09-16 | Wolf Steel Ltd. | Heating and cooling appliance |
| US11490667B1 (en) | 2021-06-08 | 2022-11-08 | Racing Optics, Inc. | Low haze UV blocking removable lens stack |
| US11307329B1 (en) | 2021-07-27 | 2022-04-19 | Racing Optics, Inc. | Low reflectance removable lens stack |
| US12140781B2 (en) | 2021-07-27 | 2024-11-12 | Laminated Film Llc | Low reflectance removable lens stack |
| US11709296B2 (en) | 2021-07-27 | 2023-07-25 | Racing Optics, Inc. | Low reflectance removable lens stack |
| US12162330B2 (en) | 2022-02-08 | 2024-12-10 | Ro Technologies, Llc | Multi-layer windshield film having progressive thickness layers |
| US11933943B2 (en) | 2022-06-06 | 2024-03-19 | Laminated Film Llc | Stack of sterile peelable lenses with low creep |
| US11808952B1 (en) | 2022-09-26 | 2023-11-07 | Racing Optics, Inc. | Low static optical removable lens stack |
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| US6893718B2 (en) * | 2002-05-20 | 2005-05-17 | 3M Innovative Properties Company | Pressure sensitive adhesive composition, articles made therewith and method of use |
| DE10322899A1 (de) * | 2003-05-21 | 2004-12-16 | Tesa Ag | UV-transparente Haftklebemasse |
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| DE102004002279A1 (de) * | 2004-01-16 | 2005-08-04 | Tesa Ag | Orientierte Acrylathaftklebemassen, Verfahren zu ihrer Herstellung und ihre Verwendung |
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| KR101281643B1 (ko) * | 2005-11-21 | 2013-07-03 | 소켄 케미칼 앤드 엔지니어링 캄파니, 리미티드 | 광학 필름용 점착제 조성물, 점착 시트 및 이것을 이용한 광학 부재 |
| JP3997270B2 (ja) * | 2005-11-21 | 2007-10-24 | 綜研化学株式会社 | 光学フィルム用粘着剤組成物および粘着シート、ならびにこれを用いた光学部材 |
| DE102006044718A1 (de) * | 2006-09-20 | 2008-04-03 | Tesa Ag | Klebemasse |
-
2007
- 2007-10-19 US US11/875,194 patent/US20090105437A1/en not_active Abandoned
-
2008
- 2008-10-14 CN CN2008801202200A patent/CN101896568A/zh active Pending
- 2008-10-14 JP JP2010530066A patent/JP5632288B2/ja not_active Expired - Fee Related
- 2008-10-14 KR KR1020107010836A patent/KR101550079B1/ko not_active Expired - Fee Related
- 2008-10-14 CN CN201610076429.8A patent/CN105713539A/zh active Pending
- 2008-10-14 WO PCT/US2008/079865 patent/WO2009052111A1/en not_active Ceased
- 2008-10-14 EP EP08838916A patent/EP2207859B1/en not_active Not-in-force
- 2008-10-14 AT AT08838916T patent/ATE545687T1/de active
Also Published As
| Publication number | Publication date |
|---|---|
| WO2009052111A1 (en) | 2009-04-23 |
| KR101550079B1 (ko) | 2015-09-03 |
| EP2207859B1 (en) | 2012-02-15 |
| CN101896568A (zh) | 2010-11-24 |
| CN105713539A (zh) | 2016-06-29 |
| KR20100091979A (ko) | 2010-08-19 |
| US20090105437A1 (en) | 2009-04-23 |
| ATE545687T1 (de) | 2012-03-15 |
| JP2011500920A (ja) | 2011-01-06 |
| EP2207859A1 (en) | 2010-07-21 |
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| R250 | Receipt of annual fees |
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