TWI529488B - A hardening composition and an optical follower - Google Patents
A hardening composition and an optical follower Download PDFInfo
- Publication number
- TWI529488B TWI529488B TW101114703A TW101114703A TWI529488B TW I529488 B TWI529488 B TW I529488B TW 101114703 A TW101114703 A TW 101114703A TW 101114703 A TW101114703 A TW 101114703A TW I529488 B TWI529488 B TW I529488B
- Authority
- TW
- Taiwan
- Prior art keywords
- component
- group
- meth
- acrylate
- bis
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims description 56
- 230000003287 optical effect Effects 0.000 title claims description 12
- 150000001875 compounds Chemical class 0.000 claims description 53
- -1 xylene dithiol Chemical class 0.000 claims description 19
- 239000000853 adhesive Substances 0.000 claims description 18
- 230000001070 adhesive effect Effects 0.000 claims description 17
- 229920006295 polythiol Polymers 0.000 claims description 15
- 125000003396 thiol group Chemical group [H]S* 0.000 claims description 13
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 12
- 125000003118 aryl group Chemical group 0.000 claims description 11
- 125000005577 anthracene group Chemical group 0.000 claims description 9
- LTYMSROWYAPPGB-UHFFFAOYSA-N diphenyl sulfide Chemical compound C=1C=CC=CC=1SC1=CC=CC=C1 LTYMSROWYAPPGB-UHFFFAOYSA-N 0.000 claims description 7
- 229910052717 sulfur Inorganic materials 0.000 claims description 7
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 6
- KOMNUTZXSVSERR-UHFFFAOYSA-N 1,3,5-tris(prop-2-enyl)-1,3,5-triazinane-2,4,6-trione Chemical group C=CCN1C(=O)N(CC=C)C(=O)N(CC=C)C1=O KOMNUTZXSVSERR-UHFFFAOYSA-N 0.000 claims description 5
- 125000000217 alkyl group Chemical group 0.000 claims description 5
- 125000002947 alkylene group Chemical group 0.000 claims description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
- 239000000178 monomer Substances 0.000 claims description 5
- 239000004641 Diallyl-phthalate Chemical group 0.000 claims description 4
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical group SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 claims description 4
- LLEMOWNGBBNAJR-UHFFFAOYSA-N biphenyl-2-ol Chemical compound OC1=CC=CC=C1C1=CC=CC=C1 LLEMOWNGBBNAJR-UHFFFAOYSA-N 0.000 claims description 4
- QUDWYFHPNIMBFC-UHFFFAOYSA-N bis(prop-2-enyl) benzene-1,2-dicarboxylate Chemical group C=CCOC(=O)C1=CC=CC=C1C(=O)OCC=C QUDWYFHPNIMBFC-UHFFFAOYSA-N 0.000 claims description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
- 239000003999 initiator Substances 0.000 claims description 4
- 229920000193 polymethacrylate Polymers 0.000 claims description 4
- UJAJKNLYUOZXDY-UHFFFAOYSA-N C(=CC)OCCOC1=CC=C(C=C1)C1(C2=CC=CC=C2CC=2C=CC=CC12)C1=CC=C(C=C1)OCCOC=CC Chemical compound C(=CC)OCCOC1=CC=C(C=C1)C1(C2=CC=CC=C2CC=2C=CC=CC12)C1=CC=C(C=C1)OCCOC=CC UJAJKNLYUOZXDY-UHFFFAOYSA-N 0.000 claims description 3
- 125000004434 sulfur atom Chemical group 0.000 claims description 3
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 3
- BJELTSYBAHKXRW-UHFFFAOYSA-N 2,4,6-triallyloxy-1,3,5-triazine Chemical group C=CCOC1=NC(OCC=C)=NC(OCC=C)=N1 BJELTSYBAHKXRW-UHFFFAOYSA-N 0.000 claims description 2
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical group [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- PXWVAUSKHNFAQW-UHFFFAOYSA-N [5-[bis(sulfanyl)methyl]-1,4-dithian-2-yl]methanedithiol Chemical group SC(S)C1CSC(C(S)S)CS1 PXWVAUSKHNFAQW-UHFFFAOYSA-N 0.000 claims description 2
- 125000003647 acryloyl group Chemical group O=C([*])C([H])=C([H])[H] 0.000 claims description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 235000010292 orthophenyl phenol Nutrition 0.000 claims description 2
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims description 2
- GRPURDFRFHUDSP-UHFFFAOYSA-N tris(prop-2-enyl) benzene-1,2,4-tricarboxylate Chemical compound C=CCOC(=O)C1=CC=C(C(=O)OCC=C)C(C(=O)OCC=C)=C1 GRPURDFRFHUDSP-UHFFFAOYSA-N 0.000 claims description 2
- 239000008096 xylene Substances 0.000 claims description 2
- YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Natural products C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 claims 1
- BBOYBJIONBNTEN-UHFFFAOYSA-N 3-propoxycarbonylbenzoic acid Chemical compound CCCOC(=O)C1=CC=CC(C(O)=O)=C1 BBOYBJIONBNTEN-UHFFFAOYSA-N 0.000 claims 1
- 150000001335 aliphatic alkanes Chemical class 0.000 claims 1
- ZDNFTNPFYCKVTB-UHFFFAOYSA-N bis(prop-2-enyl) benzene-1,4-dicarboxylate Chemical compound C=CCOC(=O)C1=CC=C(C(=O)OCC=C)C=C1 ZDNFTNPFYCKVTB-UHFFFAOYSA-N 0.000 claims 1
- 150000001993 dienes Chemical group 0.000 claims 1
- 239000003085 diluting agent Substances 0.000 claims 1
- 125000004494 ethyl ester group Chemical group 0.000 claims 1
- 125000003454 indenyl group Chemical group C1(C=CC2=CC=CC=C12)* 0.000 claims 1
- 239000004615 ingredient Substances 0.000 claims 1
- 230000000052 comparative effect Effects 0.000 description 12
- 230000000694 effects Effects 0.000 description 12
- 230000000704 physical effect Effects 0.000 description 11
- 239000007787 solid Substances 0.000 description 7
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 6
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 6
- 238000010790 dilution Methods 0.000 description 5
- 239000012895 dilution Substances 0.000 description 5
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 4
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 4
- 230000003078 antioxidant effect Effects 0.000 description 4
- 239000011521 glass Substances 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 239000011593 sulfur Substances 0.000 description 4
- 239000012956 1-hydroxycyclohexylphenyl-ketone Substances 0.000 description 3
- RZVINYQDSSQUKO-UHFFFAOYSA-N 2-phenoxyethyl prop-2-enoate Chemical compound C=CC(=O)OCCOC1=CC=CC=C1 RZVINYQDSSQUKO-UHFFFAOYSA-N 0.000 description 3
- AKYIWBKPINOXJY-UHFFFAOYSA-N 2-thiophen-2-ylsulfanylthiophene Chemical group C=1C=CSC=1SC1=CC=CS1 AKYIWBKPINOXJY-UHFFFAOYSA-N 0.000 description 3
- XLAHXMDVYCMYHM-UHFFFAOYSA-N C=1C=CSC=1C1=C2CC3=CC=CC=C3C2=CC=C1C1=CC=CS1 Chemical group C=1C=CSC=1C1=C2CC3=CC=CC=C3C2=CC=C1C1=CC=CS1 XLAHXMDVYCMYHM-UHFFFAOYSA-N 0.000 description 3
- QBBLEPZANFBACZ-UHFFFAOYSA-K SC(CC(=O)[O-])C.[Bi+3].OCC(CO)(CO)CO.SC(CC(=O)[O-])C.SC(CC(=O)[O-])C Chemical compound SC(CC(=O)[O-])C.[Bi+3].OCC(CO)(CO)CO.SC(CC(=O)[O-])C.SC(CC(=O)[O-])C QBBLEPZANFBACZ-UHFFFAOYSA-K 0.000 description 3
- 238000012644 addition polymerization Methods 0.000 description 3
- 150000001336 alkenes Chemical class 0.000 description 3
- GCTPMLUUWLLESL-UHFFFAOYSA-N benzyl prop-2-enoate Chemical compound C=CC(=O)OCC1=CC=CC=C1 GCTPMLUUWLLESL-UHFFFAOYSA-N 0.000 description 3
- MQDJYUACMFCOFT-UHFFFAOYSA-N bis[2-(1-hydroxycyclohexyl)phenyl]methanone Chemical compound C=1C=CC=C(C(=O)C=2C(=CC=CC=2)C2(O)CCCCC2)C=1C1(O)CCCCC1 MQDJYUACMFCOFT-UHFFFAOYSA-N 0.000 description 3
- 239000002131 composite material Substances 0.000 description 3
- 230000005484 gravity Effects 0.000 description 3
- 229910001507 metal halide Inorganic materials 0.000 description 3
- 150000005309 metal halides Chemical class 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 239000001294 propane Substances 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- VAZQKPWSBFZARZ-UHFFFAOYSA-N 2-(2-phenylphenoxy)ethyl prop-2-enoate Chemical compound C=CC(=O)OCCOC1=CC=CC=C1C1=CC=CC=C1 VAZQKPWSBFZARZ-UHFFFAOYSA-N 0.000 description 2
- SIFLEYXOYMWTQG-UHFFFAOYSA-N 3h-dithiole;1,3-xylene Chemical compound C1SSC=C1.CC1=CC=CC(C)=C1 SIFLEYXOYMWTQG-UHFFFAOYSA-N 0.000 description 2
- RMEBLVCKXMXNPA-UHFFFAOYSA-N 9,9-bis[4-(2-prop-1-enoxyethoxy)phenyl]fluorene Chemical compound C(=CC)OCCOC1=CC=C(C=C1)C1(C2=CC=CC=C2C=2C=CC=CC1=2)C1=CC=C(C=C1)OCCOC=CC RMEBLVCKXMXNPA-UHFFFAOYSA-N 0.000 description 2
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical group C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 2
- COYTVZAYDAIHDK-UHFFFAOYSA-N [5-(sulfanylmethyl)-1,4-dithian-2-yl]methanethiol Chemical compound SCC1CSC(CS)CS1 COYTVZAYDAIHDK-UHFFFAOYSA-N 0.000 description 2
- DIOQZVSQGTUSAI-UHFFFAOYSA-N decane Chemical compound CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 description 2
- 238000007865 diluting Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 2
- 239000011342 resin composition Substances 0.000 description 2
- 125000004646 sulfenyl group Chemical group S(*)* 0.000 description 2
- 150000003573 thiols Chemical class 0.000 description 2
- ROLAGNYPWIVYTG-UHFFFAOYSA-N 1,2-bis(4-methoxyphenyl)ethanamine;hydrochloride Chemical compound Cl.C1=CC(OC)=CC=C1CC(N)C1=CC=C(OC)C=C1 ROLAGNYPWIVYTG-UHFFFAOYSA-N 0.000 description 1
- 125000006516 2-(benzyloxy)ethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])OC([H])([H])C([H])([H])* 0.000 description 1
- UHFFVFAKEGKNAQ-UHFFFAOYSA-N 2-benzyl-2-(dimethylamino)-1-(4-morpholin-4-ylphenyl)butan-1-one Chemical compound C=1C=C(N2CCOCC2)C=CC=1C(=O)C(CC)(N(C)C)CC1=CC=CC=C1 UHFFVFAKEGKNAQ-UHFFFAOYSA-N 0.000 description 1
- XMLYCEVDHLAQEL-UHFFFAOYSA-N 2-hydroxy-2-methyl-1-phenylpropan-1-one Chemical compound CC(C)(O)C(=O)C1=CC=CC=C1 XMLYCEVDHLAQEL-UHFFFAOYSA-N 0.000 description 1
- 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 1
- JMDKEMZJVNIING-UHFFFAOYSA-N C(=CC)C(COC1=CC=C(C=C1)C1(C2=CC=CC=C2C=2C=CC=CC12)C1=CC=C(C=C1)OCC(C=CC)OC)OC Chemical compound C(=CC)C(COC1=CC=C(C=C1)C1(C2=CC=CC=C2C=2C=CC=CC12)C1=CC=C(C=C1)OCC(C=CC)OC)OC JMDKEMZJVNIING-UHFFFAOYSA-N 0.000 description 1
- QOSMNYMQXIVWKY-UHFFFAOYSA-N Propyl levulinate Chemical compound CCCOC(=O)CCC(C)=O QOSMNYMQXIVWKY-UHFFFAOYSA-N 0.000 description 1
- JTONWBRVEHRQPR-UHFFFAOYSA-N SP(C1=CC=CC=C1)(C1=CC=CC=C1)=O.CC1=CC(=CC(=C1)C)C Chemical compound SP(C1=CC=CC=C1)(C1=CC=CC=C1)=O.CC1=CC(=CC(=C1)C)C JTONWBRVEHRQPR-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 238000007259 addition reaction Methods 0.000 description 1
- 210000003423 ankle Anatomy 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- ZNAAXKXXDQLJIX-UHFFFAOYSA-N bis(2-cyclohexyl-3-hydroxyphenyl)methanone Chemical compound C1CCCCC1C=1C(O)=CC=CC=1C(=O)C1=CC=CC(O)=C1C1CCCCC1 ZNAAXKXXDQLJIX-UHFFFAOYSA-N 0.000 description 1
- 238000004364 calculation method Methods 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000005842 heteroatom Chemical group 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- 239000006082 mold release agent Substances 0.000 description 1
- OJNNAJJFLWBPRS-UHFFFAOYSA-N phenyl-[(2,4,6-trimethylphenyl)methyl]-[(2,4,6-trimethylphenyl)methylidene]phosphanium Chemical compound CC1=C(C=P(C2=CC=CC=C2)=CC2=C(C=C(C=C2C)C)C)C(=CC(=C1)C)C OJNNAJJFLWBPRS-UHFFFAOYSA-N 0.000 description 1
- XYFCBTPGUUZFHI-UHFFFAOYSA-O phosphonium Chemical compound [PH4+] XYFCBTPGUUZFHI-UHFFFAOYSA-O 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 235000020354 squash Nutrition 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- HEKQWIORQJRILW-UHFFFAOYSA-N tetrakis(prop-2-enyl) benzene-1,2,4,5-tetracarboxylate Chemical compound C=CCOC(=O)C1=CC(C(=O)OCC=C)=C(C(=O)OCC=C)C=C1C(=O)OCC=C HEKQWIORQJRILW-UHFFFAOYSA-N 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 238000002834 transmittance Methods 0.000 description 1
- 229920002554 vinyl polymer Polymers 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
- 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
- C09D4/00—Coating compositions, e.g. paints, varnishes or lacquers, based on organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond ; Coating compositions, based on monomers of macromolecular compounds of groups C09D183/00 - C09D183/16
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
- C08K5/0025—Crosslinking or vulcanising agents; including accelerators
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/36—Sulfur-, selenium-, or tellurium-containing compounds
- C08K5/37—Thiols
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
- Adhesives Or Adhesive Processes (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2011101446A JP5810611B2 (ja) | 2011-04-28 | 2011-04-28 | 硬化性組成物および光学接着剤 |
| JP2011101444A JP5849432B2 (ja) | 2011-04-28 | 2011-04-28 | 硬化性組成物および光学接着剤 |
| JP2011103642A JP5754233B2 (ja) | 2011-05-06 | 2011-05-06 | 硬化性組成物および光学接着剤 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| TW201305730A TW201305730A (zh) | 2013-02-01 |
| TWI529488B true TWI529488B (zh) | 2016-04-11 |
Family
ID=47072231
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TW101114703A TWI529488B (zh) | 2011-04-28 | 2012-04-25 | A hardening composition and an optical follower |
Country Status (3)
| Country | Link |
|---|---|
| CN (1) | CN103562271B (ja) |
| TW (1) | TWI529488B (ja) |
| WO (1) | WO2012147712A1 (ja) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103974826B (zh) * | 2011-12-08 | 2016-04-13 | 日本化药株式会社 | 光学构件、紫外线固化型树脂组合物和固化物 |
| CN104109243A (zh) * | 2014-07-04 | 2014-10-22 | 深圳职业技术学院 | 光学树脂的合成方法 |
| JP6546986B2 (ja) * | 2015-03-02 | 2019-07-17 | 富士フイルム株式会社 | 硬化性組成物、硬化物、光学部材、レンズ及び化合物 |
| TWI694125B (zh) * | 2015-06-05 | 2020-05-21 | 日商三菱瓦斯化學股份有限公司 | 硬化性組成物及使用其之光學用接著劑 |
| JP6655395B2 (ja) * | 2016-01-06 | 2020-02-26 | 株式会社Adeka | 水系ポリウレタン樹脂組成物、及び該組成物を用いてなる光学フィルム |
| JP6670923B2 (ja) | 2016-02-24 | 2020-03-25 | 富士フイルム株式会社 | ポリカーボネート樹脂、成形体、光学部材及びレンズ |
| TWI725190B (zh) * | 2016-05-30 | 2021-04-21 | 日商日產化學工業股份有限公司 | 高折射率聚合性化合物之低黏度化劑及含有其之聚合性組成物 |
| JP6911864B2 (ja) * | 2016-09-28 | 2021-07-28 | Ａｇｃ株式会社 | 硬化性組成物および硬化物 |
| JP7473206B2 (ja) * | 2018-10-17 | 2024-04-23 | ナミックス株式会社 | 樹脂組成物 |
| CN110540825B (zh) * | 2019-09-16 | 2021-05-04 | 杭州得力科技股份有限公司 | 一种高折光率uv固化胶的制备方法及产品 |
| JP2022115135A (ja) * | 2021-01-28 | 2022-08-09 | キヤノン株式会社 | 重合性組成物、及び光学素子とその製造方法、光学機器、撮像装置 |
| CN117616067A (zh) * | 2021-07-14 | 2024-02-27 | 纳美仕有限公司 | 固化性树脂组合物 |
| JPWO2023286700A1 (ja) * | 2021-07-14 | 2023-01-19 | ||
| CN118978883B (zh) * | 2024-08-15 | 2025-04-18 | 广东皇冠新材料科技有限公司 | 粘合剂组合物及粘合剂膜 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0751630B2 (ja) * | 1989-06-20 | 1995-06-05 | 住友精化株式会社 | 硬化性組成物 |
| JP2005139401A (ja) * | 2003-11-10 | 2005-06-02 | Sekisui Chem Co Ltd | 偏光板用光硬化型接着剤および液晶表示パネル |
| TWI482814B (zh) * | 2007-03-16 | 2015-05-01 | Mitsubishi Gas Chemical Co | 光學材料用樹脂組成物及由該組成物得到之光學材料 |
| JP5625226B2 (ja) * | 2007-08-24 | 2014-11-19 | 三菱瓦斯化学株式会社 | 光学材料用樹脂組成物 |
| JP5424696B2 (ja) * | 2009-04-21 | 2014-02-26 | 大阪ガスケミカル株式会社 | 硬化性組成物及びその硬化物 |
| JP5749963B2 (ja) * | 2010-04-15 | 2015-07-15 | 大阪ガスケミカル株式会社 | 熱可塑性樹脂およびその製造方法 |
-
2012
- 2012-04-24 WO PCT/JP2012/060903 patent/WO2012147712A1/ja not_active Ceased
- 2012-04-24 CN CN201280020113.7A patent/CN103562271B/zh active Active
- 2012-04-25 TW TW101114703A patent/TWI529488B/zh active
Also Published As
| Publication number | Publication date |
|---|---|
| WO2012147712A1 (ja) | 2012-11-01 |
| CN103562271B (zh) | 2015-08-12 |
| TW201305730A (zh) | 2013-02-01 |
| CN103562271A (zh) | 2014-02-05 |
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