CN101094902A - 掺入荧光检测体系的可固化有机硅组合物 - Google Patents
掺入荧光检测体系的可固化有机硅组合物 Download PDFInfo
- Publication number
- CN101094902A CN101094902A CNA2005800456174A CN200580045617A CN101094902A CN 101094902 A CN101094902 A CN 101094902A CN A2005800456174 A CNA2005800456174 A CN A2005800456174A CN 200580045617 A CN200580045617 A CN 200580045617A CN 101094902 A CN101094902 A CN 101094902A
- Authority
- CN
- China
- Prior art keywords
- composition
- light trigger
- light
- combination
- organosilicon
- 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
- 239000000203 mixture Substances 0.000 title claims abstract description 172
- 238000001514 detection method Methods 0.000 title abstract description 4
- 229920001296 polysiloxane Polymers 0.000 title abstract 4
- 238000001723 curing Methods 0.000 claims description 45
- 239000007787 solid Substances 0.000 claims description 38
- 239000003795 chemical substances by application Substances 0.000 claims description 32
- -1 methacryloxy, vinyl Chemical group 0.000 claims description 31
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 29
- 229910052710 silicon Inorganic materials 0.000 claims description 29
- 239000010703 silicon Substances 0.000 claims description 29
- 239000007850 fluorescent dye Substances 0.000 claims description 25
- 239000007788 liquid Substances 0.000 claims description 20
- 239000002904 solvent Substances 0.000 claims description 20
- 238000000034 method Methods 0.000 claims description 19
- 238000013008 moisture curing Methods 0.000 claims description 18
- 239000003999 initiator Substances 0.000 claims description 16
- 239000000463 material Substances 0.000 claims description 11
- 229920002050 silicone resin Polymers 0.000 claims description 10
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims description 8
- 239000003054 catalyst Substances 0.000 claims description 8
- 239000012454 non-polar solvent Substances 0.000 claims description 8
- 229920001558 organosilicon polymer Polymers 0.000 claims description 8
- 229910052760 oxygen Inorganic materials 0.000 claims description 8
- 229910000077 silane Inorganic materials 0.000 claims description 8
- 229920005989 resin Polymers 0.000 claims description 7
- 239000011347 resin Substances 0.000 claims description 7
- 239000001301 oxygen Substances 0.000 claims description 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 5
- 239000000126 substance Substances 0.000 claims description 5
- 125000003545 alkoxy group Chemical group 0.000 claims description 4
- 229910052757 nitrogen Inorganic materials 0.000 claims description 4
- 239000000758 substrate Substances 0.000 claims description 4
- 239000007795 chemical reaction product Substances 0.000 claims description 3
- 230000009977 dual effect Effects 0.000 claims description 3
- 125000003368 amide group Chemical group 0.000 claims description 2
- 125000002344 aminooxy group Chemical group [H]N([H])O[*] 0.000 claims description 2
- 150000002085 enols Chemical class 0.000 claims description 2
- 150000002923 oximes Chemical class 0.000 claims description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 2
- 238000009998 heat setting Methods 0.000 claims 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims 1
- 229920002554 vinyl polymer Polymers 0.000 claims 1
- 239000004205 dimethyl polysiloxane Substances 0.000 description 22
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 22
- AUONHKJOIZSQGR-UHFFFAOYSA-N oxophosphane Chemical compound P=O AUONHKJOIZSQGR-UHFFFAOYSA-N 0.000 description 12
- 238000000016 photochemical curing Methods 0.000 description 9
- 230000004927 fusion Effects 0.000 description 8
- 239000004615 ingredient Substances 0.000 description 8
- 239000000975 dye Substances 0.000 description 6
- 239000003981 vehicle Substances 0.000 description 6
- 239000003153 chemical reaction reagent Substances 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 5
- 229910021485 fumed silica Inorganic materials 0.000 description 5
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 5
- 229910052753 mercury Inorganic materials 0.000 description 5
- 238000002156 mixing Methods 0.000 description 5
- 238000004382 potting Methods 0.000 description 5
- 238000002360 preparation method Methods 0.000 description 5
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 4
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 239000008393 encapsulating agent Substances 0.000 description 4
- 239000000945 filler Substances 0.000 description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
- WKGDNXBDNLZSKC-UHFFFAOYSA-N oxido(phenyl)phosphanium Chemical compound O=[PH2]c1ccccc1 WKGDNXBDNLZSKC-UHFFFAOYSA-N 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 238000007789 sealing Methods 0.000 description 4
- JNELGWHKGNBSMD-UHFFFAOYSA-N xanthone Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3OC2=C1 JNELGWHKGNBSMD-UHFFFAOYSA-N 0.000 description 4
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 3
- KXJLGCBCRCSXQF-UHFFFAOYSA-N [diacetyloxy(ethyl)silyl] acetate Chemical compound CC(=O)O[Si](CC)(OC(C)=O)OC(C)=O KXJLGCBCRCSXQF-UHFFFAOYSA-N 0.000 description 3
- TVJPBVNWVPUZBM-UHFFFAOYSA-N [diacetyloxy(methyl)silyl] acetate Chemical compound CC(=O)O[Si](C)(OC(C)=O)OC(C)=O TVJPBVNWVPUZBM-UHFFFAOYSA-N 0.000 description 3
- 230000000903 blocking effect Effects 0.000 description 3
- 239000003431 cross linking reagent Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- NKSJNEHGWDZZQF-UHFFFAOYSA-N ethenyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)C=C NKSJNEHGWDZZQF-UHFFFAOYSA-N 0.000 description 3
- MTZQAGJQAFMTAQ-UHFFFAOYSA-N ethyl benzoate Chemical compound CCOC(=O)C1=CC=CC=C1 MTZQAGJQAFMTAQ-UHFFFAOYSA-N 0.000 description 3
- 229910001507 metal halide Inorganic materials 0.000 description 3
- 230000003287 optical effect Effects 0.000 description 3
- 238000012856 packing Methods 0.000 description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 3
- 239000002798 polar solvent Substances 0.000 description 3
- 229910052718 tin Inorganic materials 0.000 description 3
- PSGCQDPCAWOCSH-UHFFFAOYSA-N (4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl) prop-2-enoate Chemical compound C1CC2(C)C(OC(=O)C=C)CC1C2(C)C PSGCQDPCAWOCSH-UHFFFAOYSA-N 0.000 description 2
- YIKSHDNOAYSSPX-UHFFFAOYSA-N 1-propan-2-ylthioxanthen-9-one Chemical compound S1C2=CC=CC=C2C(=O)C2=C1C=CC=C2C(C)C YIKSHDNOAYSSPX-UHFFFAOYSA-N 0.000 description 2
- XDLMVUHYZWKMMD-UHFFFAOYSA-N 3-trimethoxysilylpropyl 2-methylprop-2-enoate Chemical compound CO[Si](OC)(OC)CCCOC(=O)C(C)=C XDLMVUHYZWKMMD-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 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
- 229930006711 bornane-2,3-dione Natural products 0.000 description 2
- 238000005538 encapsulation Methods 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 125000001183 hydrocarbyl group Chemical group 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
- 150000005309 metal halides Chemical class 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 229920013730 reactive polymer Polymers 0.000 description 2
- UOKUUKOEIMCYAI-UHFFFAOYSA-N trimethoxysilylmethyl 2-methylprop-2-enoate Chemical compound CO[Si](OC)(OC)COC(=O)C(C)=C UOKUUKOEIMCYAI-UHFFFAOYSA-N 0.000 description 2
- DSSYKIVIOFKYAU-XCBNKYQSSA-N (R)-camphor Chemical compound C1C[C@@]2(C)C(=O)C[C@@H]1C2(C)C DSSYKIVIOFKYAU-XCBNKYQSSA-N 0.000 description 1
- 125000006227 2-n-butoxyethyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])OC([H])([H])C([H])([H])* 0.000 description 1
- KTALPKYXQZGAEG-UHFFFAOYSA-N 2-propan-2-ylthioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC(C(C)C)=CC=C3SC2=C1 KTALPKYXQZGAEG-UHFFFAOYSA-N 0.000 description 1
- FASUFOTUSHAIHG-UHFFFAOYSA-N 3-methoxyprop-1-ene Chemical compound COCC=C FASUFOTUSHAIHG-UHFFFAOYSA-N 0.000 description 1
- MLOKHANBEXWBKS-UHFFFAOYSA-N 3-triacetyloxysilylpropyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCC[Si](OC(C)=O)(OC(C)=O)OC(C)=O MLOKHANBEXWBKS-UHFFFAOYSA-N 0.000 description 1
- IKVYHNPVKUNCJM-UHFFFAOYSA-N 4-propan-2-ylthioxanthen-9-one Chemical compound S1C2=CC=CC=C2C(=O)C2=C1C(C(C)C)=CC=C2 IKVYHNPVKUNCJM-UHFFFAOYSA-N 0.000 description 1
- AIXZBGVLNVRQSS-UHFFFAOYSA-N 5-tert-butyl-2-[5-(5-tert-butyl-1,3-benzoxazol-2-yl)thiophen-2-yl]-1,3-benzoxazole Chemical compound CC(C)(C)C1=CC=C2OC(C3=CC=C(S3)C=3OC4=CC=C(C=C4N=3)C(C)(C)C)=NC2=C1 AIXZBGVLNVRQSS-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- MFGGXHJEIRBVCP-UHFFFAOYSA-N COC1=C(C(=O)[PH2]=O)C(=CC(=C1)OC)OC Chemical compound COC1=C(C(=O)[PH2]=O)C(=CC(=C1)OC)OC MFGGXHJEIRBVCP-UHFFFAOYSA-N 0.000 description 1
- 241000723346 Cinnamomum camphora Species 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- OWYWGLHRNBIFJP-UHFFFAOYSA-N Ipazine Chemical compound CCN(CC)C1=NC(Cl)=NC(NC(C)C)=N1 OWYWGLHRNBIFJP-UHFFFAOYSA-N 0.000 description 1
- 239000004902 Softening Agent Substances 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 1
- RVWADWOERKNWRY-UHFFFAOYSA-N [2-(dimethylamino)phenyl]-phenylmethanone Chemical compound CN(C)C1=CC=CC=C1C(=O)C1=CC=CC=C1 RVWADWOERKNWRY-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 125000005907 alkyl ester group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 125000004104 aryloxy group Chemical group 0.000 description 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
- 239000012965 benzophenone Substances 0.000 description 1
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 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 1
- YHWCPXVTRSHPNY-UHFFFAOYSA-N butan-1-olate;titanium(4+) Chemical compound [Ti+4].CCCC[O-].CCCC[O-].CCCC[O-].CCCC[O-] YHWCPXVTRSHPNY-UHFFFAOYSA-N 0.000 description 1
- 229930008380 camphor Natural products 0.000 description 1
- 229960000846 camphor Drugs 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 238000005660 chlorination reaction Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 125000004093 cyano group Chemical group *C#N 0.000 description 1
- FWLDHHJLVGRRHD-UHFFFAOYSA-N decyl prop-2-enoate Chemical compound CCCCCCCCCCOC(=O)C=C FWLDHHJLVGRRHD-UHFFFAOYSA-N 0.000 description 1
- 230000001066 destructive effect Effects 0.000 description 1
- FDPIMTJIUBPUKL-UHFFFAOYSA-N dimethylacetone Natural products CCC(=O)CC FDPIMTJIUBPUKL-UHFFFAOYSA-N 0.000 description 1
- BFMYDTVEBKDAKJ-UHFFFAOYSA-L disodium;(2',7'-dibromo-3',6'-dioxido-3-oxospiro[2-benzofuran-1,9'-xanthene]-4'-yl)mercury;hydrate Chemical class O.[Na+].[Na+].O1C(=O)C2=CC=CC=C2C21C1=CC(Br)=C([O-])C([Hg])=C1OC1=C2C=C(Br)C([O-])=C1 BFMYDTVEBKDAKJ-UHFFFAOYSA-L 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- QYHJPNQDLVVBDB-UHFFFAOYSA-N ethenyl(trimethoxy)silane;silicon Chemical compound [Si].CO[Si](OC)(OC)C=C QYHJPNQDLVVBDB-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- PGXXWBOPUNAGKV-UHFFFAOYSA-N ethylbenzene methane Chemical compound C.C(C)C1=CC=CC=C1 PGXXWBOPUNAGKV-UHFFFAOYSA-N 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 229910000765 intermetallic Inorganic materials 0.000 description 1
- CRVGTESFCCXCTH-UHFFFAOYSA-N methyl diethanolamine Chemical compound OCCN(C)CCO CRVGTESFCCXCTH-UHFFFAOYSA-N 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- MPQXHAGKBWFSNV-UHFFFAOYSA-N oxidophosphanium Chemical class [PH3]=O MPQXHAGKBWFSNV-UHFFFAOYSA-N 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 230000036314 physical performance Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 239000001327 prunus amygdalus amara l. extract Substances 0.000 description 1
- 239000012763 reinforcing filler Substances 0.000 description 1
- 239000006254 rheological additive Substances 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- KSBAEPSJVUENNK-UHFFFAOYSA-L tin(ii) 2-ethylhexanoate Chemical compound [Sn+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O KSBAEPSJVUENNK-UHFFFAOYSA-L 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229960004418 trolamine Drugs 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 229910052726 zirconium Inorganic materials 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
- C09J183/00—Adhesives based on macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon, with or without sulfur, nitrogen, oxygen, or carbon only; Adhesives based on derivatives of such polymers
- C09J183/04—Polysiloxanes
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
- C08L83/04—Polysiloxanes
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/24—Crosslinking, e.g. vulcanising, of macromolecules
- C08J3/243—Two or more independent types of crosslinking for one or more polymers
-
- 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
- C09J183/00—Adhesives based on macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon, with or without sulfur, nitrogen, oxygen, or carbon only; Adhesives based on derivatives of such polymers
-
- 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
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/14—Polysiloxanes containing silicon bound to oxygen-containing groups
-
- 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
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/14—Polysiloxanes containing silicon bound to oxygen-containing groups
- C08G77/18—Polysiloxanes containing silicon bound to oxygen-containing groups to alkoxy or aryloxy groups
-
- 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
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/20—Polysiloxanes containing silicon bound to unsaturated aliphatic groups
-
- 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
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/22—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen
- C08G77/26—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen nitrogen-containing groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2383/00—Characterised by the use of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen, or carbon only; Derivatives of such polymers
- C08J2383/04—Polysiloxanes
-
- 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
- C08K5/0041—Optical brightening agents, organic pigments
-
- 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
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/53—Phosphorus bound to oxygen bound to oxygen and to carbon only
- C08K5/5397—Phosphine oxides
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Polymerisation Methods In General (AREA)
- Paints Or Removers (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Macromonomer-Based Addition Polymer (AREA)
- Silicon Polymers (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Investigating, Analyzing Materials By Fluorescence Or Luminescence (AREA)
Abstract
Description
组分 | wt% | |||||
组合物 | ||||||
A | B | C | D | E | F | |
甲基丙烯酰氧基丙基二乙酰氧基封端的聚二甲基硅氧烷(PDMS) | 92.0 | 92.0 | 87.5 | 93.35 | 92.9 | 93.4 |
甲基封端的PDMS | 0 | 0 | 5.0 | 0 | 0 | 0 |
煅制二氧化硅 | 4.0 | 4.0 | 4.4 | 4.0 | 5.0 | 4.0 |
附加交联剂:甲基三乙酰氧基硅烷、乙基三乙酰氧基硅烷和/或二-(叔丁氧基)二乙酰氧基硅烷 | 2.75 | 3.0 | 2.0 | 1.5 | 1.5 | 1.5 |
二月桂酸二丁基锡 | 0.1 | 0.1 | 0.1 | 0.05 | 0.1 | 0.1 |
固体组分 | ||||||
双(2,4,6-三甲基苯甲酰基)苯基氧化膦 | 0.15 | 0.05 | 0.015 | 0.1 | 0.1 | 0.1 |
荧光染料 | 0.004 | 0.003 | 0.003 | 0.004 | 0.005 | 0 |
液体载体 | ||||||
2,2-二乙氧基苯乙酮 | 0.996 | 0.847 | 0.982 | 0.996 | 0 | 0.5 |
2-羟基-2-甲基-1-苯基-丙-1-酮 | 0 | 0 | 0 | 0 | 0.395 | 0.4 |
固化深度(70mW/cm260秒,汞弧光源,在365nm下测量) | ≥41mm | ≥41mm | ≥41mm | 50.5mm | 34.3mm | 40.1mm |
组分 | wt% | |||||
组合物 | ||||||
G | H | I | J | K | L | |
甲基丙烯酰氧基丙基二乙酰氧基封端的聚二甲基硅氧烷(PDMS) | 86.0 | 86.0 | 92.65 | 91.5 | 91.5 | 90.5 |
甲基封端的PDMS | 5.0 | 5.0 | 0 | 0 | 0 | 0 |
煅制二氧化硅 | 6.0 | 6.0 | 4.0 | 4.0 | 4.0 | 4.0 |
附加交联剂:甲基三乙酰氧基硅烷、乙基三乙酰氧基硅烷和/或二-(叔丁氧基)二乙酰氧基硅烷 | 2.0 | 2.0 | 1.0 | 2.75 | 2.75 | 2.75 |
二月桂酸二丁基锡 | 0.08 | 0.08 | 0.05 | 0.1 | 0.1 | 0.1 |
固体组分 | ||||||
双(2,4,6-三甲基苯甲酰基)苯基氧化瞵 | 0 | 0.12 | 0.15 | 0.15 | 0.15 | 0.15 |
联苯基(2,4,6-三甲基苯甲酰基)氧化膦 | 0.12 | 0 | 0 | 0 | 0 | 0 |
荧光染料 | 0.004 | 0.004 | 0.004 | 0.004 | 0.006 | 0.004 |
液体载体 | ||||||
2,2-二乙氧基苯乙酮 | 0.796 | 0.796 | 0.15 | 1.496 | 1.494 | 1.496 |
乙烯基三甲氧基硅烷 | 0 | 0 | 1.996 | 0 | 0 | 0 |
丙烯酸异冰片酯 | 0 | 0 | 0 | 0 | 0 | 1.0 |
固化深度(70mW/cm260秒,汞弧光源,在365nm下测量) | 26.4mm | 36.6mm | ≥41mm | 39.3mm | 36.2mm | 40.3mm |
组分 | wt% | |||||
组合物 | ||||||
M | N | O | P | Q | R | |
甲基丙烯酰氧基丙基二乙酰氧基封端的聚二甲基硅氧烷(PDMS) | 85.51 | 87.46 | 77.01 | 77.0 | 79.0 | 73.1 |
甲基封端的PDMS | 0 | 0 | 0 | 0 | 0 | 6.0 |
煅制二氧化硅 | 11.0 | 9.0 | 20.0 | 20.0 | 18.0 | 18.0 |
附加交联剂:甲基三乙酰氧基硅烷、乙基三乙酰氧基硅烷和/或二-(叔丁氧基)二乙酰氧基硅烷 | 2.5 | 2.6 | 2.0 | 2.0 | 2.0 | 2.0 |
二月桂酸二丁基锡 | 0.05 | 0 | 0.07 | 0.1 | 0.1 | 0.1 |
固体组分 | ||||||
双(2,4,6-三甲基苯甲酰基)苯基氧化膦 | 0.12 | 0.12 | 0.12 | 0.12 | 0.12 | 0.1 |
荧光染料 | 0.003 | 0.003 | 0.003 | 0.003 | 0.004 | 0 |
液体载体 | ||||||
2,2-二乙氧基苯乙酮 | 0.817 | 0.817 | 0.797 | 0.777 | 0.776 | 0.7 |
固化深度(70mW/cm260秒,汞弧光源,在365nm下测量) | 25.0mm | 21.4mm | 23.5mm | 23.7mm | 14.7mm | 15.7mm |
组分 | wt% | |||||
组合物 | ||||||
S | T | U | V | W | X | |
3-甲基丙烯酰氧基丙基二甲氧基封端的聚二甲基硅氧烷(PDMS) | 68.25 | 75.25 | 91.95 | 0 | 88.0 | 0 |
3-甲基丙烯酰氧基甲基二甲氧基封端的聚二甲基硅氧烷(PDMS) | 0 | 0 | 0 | 92.25 | 0 | 87.25 |
乙烯基二甲氧基封端的聚二甲基硅氧烷(PDMS) | 16.0 | 16.0 | 0 | 0 | 0 | 0 |
煅制二氧化硅 | 4.0 | 4.0 | 4.0 | 4.0 | 8.0 | 8.0 |
二月桂酸二丁基锡 | 0 | 0 | 0 | 0 | 0.1 | 0 |
羧酸烷基锡 | 0.4 | 0.4 | 0.4 | 0.1 | 0 | 0.1 |
固体组分 | ||||||
双(2,4,6-三甲基苯甲酰基)苯基氧化膦 | 0 | 0.1 | 0.15 | 0.15 | 0.1 | 0.15 |
联苯基(2,4,6-三甲基苯甲酰基)氧化膦 | 0.1 | 0 | 0 | 0 | 0 | 0 |
荧光染料 | 0 | 0.0 04 | 0.004 | 0.004 | 0.005 | 0.004 |
液体载体 | ||||||
丙烯酸异冰片酯 | 4.0 | 0 | 0 | 0 | 0 | 0 |
N,N-二甲基丙烯酰胺 | 2.0 | 0 | 0 | 0 | 0 | 0 |
辛基/癸基丙烯酸酯 | 1.0 | 0 | 0 | 0 | 0 | 0 |
2,2-二乙氧基苯乙酮 | 0.75 | 0.746 | 0.996 | 0.996 | 0 | 0.996 |
甲基丙烯酰氧基丙基三甲氧基硅烷 | 1.0 | 1.0 | 0 | 0 | 0 | 0 |
甲基丙烯酰氧基甲基三甲氧基硅烷 | 0 | 0 | 0 | 0 | 0 | 1.0 |
2-羟基-2-甲基-1-苯基-丙-1-酮 | 0 | 0 | 0 | 0 | 0.4 | 0 |
乙烯基三甲氧基硅烷 | 2.5 | 2.5 | 2.5 | 2.5 | 3.395 | 2.5 |
固化深度(70mW/cm260秒,汞弧光源,在365nm下测量) | 16.5mm | 25.5mm | ≥41mm | ≥41mm | 32.0mm | 30.0mm |
组分 | wt% | |||||
组合物 | ||||||
Y | Z | AA | BB | CC | DD | |
3-甲基丙烯酰氧基丙基二甲氧基封端的聚二甲基硅氧烷(PDMS) | 85.9 | 0 | 0 | 0 | 70.396 | 0 |
3-甲基丙烯酰氧基甲基二甲氧基封端的聚二甲基硅氧烷(PDMS) | 0 | 78.2 | 74.56 | 72.69 | 0 | 70.596 |
煅制二氧化硅 | 10.0 | 19.6 | 20.78 | 23.0 | 25.0 | 25.0 |
四异丙氧基钛酸酯 | 0 | 0 | 0 | 0.15 | 0 | 0 |
羧酸烷基锡 | 0.1 | 0.11 | 0.16 | 0 | 0.3 | 0.1 |
固体组分 | ||||||
双(2,4,6-三甲基苯甲酰基)苯基氧化膦 | 0.1 | 0.13 | 0.16 | 0.15 | 0.1 | 0.1 |
荧光染料 | 0 | 0.003 | 0.004 | 0.01 | 0.004 | 0.004 |
液体载体 | ||||||
2,2-二乙氧基苯乙酮 | 0 | 0.757 | 1.036 | 0 | 0 | 0 |
甲基丙烯酰氧基丙基三甲氧基硅烷 | 1.0 | 0 | 0 | 0 | 0 | 0 |
甲基丙烯酰氧基甲基三甲氧基硅烷 | 0 | 1.2 | 0.95 | 0 | 0 | 0 |
2-羟基-2-甲基-1-苯基-丙-1-酮 | 0.4 | 0 | 0 | 0 | 0.2 | 0.2 |
乙烯基三甲氧基硅烷 | 2.5 | 0 | 2.35 | 4.0 | 4.0 | 4.0 |
固化深度(70mW/cm260秒,汞弧光源,在365nm下测量) | 34.5mm | 30.0mm | 25.0mm | 24.0mm | 22.8mm | 27.4mm |
光源(灯) | 70mW/cm260秒 | 70mW/cm2180秒 | 180mW/cm230秒 | 180mW/cm2 60秒 |
UV光源 | ||||
汞弧光灯 | ≥41mm | - | ≥41mm | - |
Fusion D | 29mm | - | 31mm | ≥41mm |
Fusion H | 37mm | - | - | |
可见光源 | ||||
Fusion V | 21mm | - | - | - |
金属卤化物(只有可见光) | 26.3mm | ≥41mm | - | - |
Claims (26)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US63224704P | 2004-12-01 | 2004-12-01 | |
US60/632,247 | 2004-12-01 | ||
PCT/US2005/041894 WO2006060189A2 (en) | 2004-12-01 | 2005-11-18 | Curable silicone compositions incorporating a fluorescent detection system |
Publications (2)
Publication Number | Publication Date |
---|---|
CN101094902A true CN101094902A (zh) | 2007-12-26 |
CN101094902B CN101094902B (zh) | 2011-01-19 |
Family
ID=36565528
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN2005800456174A Active CN101094902B (zh) | 2004-12-01 | 2005-11-18 | 掺入荧光检测体系的可固化有机硅组合物 |
Country Status (13)
Country | Link |
---|---|
US (1) | US8013314B2 (zh) |
EP (1) | EP1833884B1 (zh) |
JP (1) | JP5557983B2 (zh) |
KR (1) | KR101201602B1 (zh) |
CN (1) | CN101094902B (zh) |
CA (1) | CA2588842C (zh) |
DK (1) | DK1833884T3 (zh) |
ES (1) | ES2546107T3 (zh) |
HU (1) | HUE05848930T2 (zh) |
MX (1) | MX2007006609A (zh) |
PL (1) | PL1833884T3 (zh) |
PT (1) | PT1833884E (zh) |
WO (1) | WO2006060189A2 (zh) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102532434A (zh) * | 2011-12-13 | 2012-07-04 | 北京海斯迪克新材料有限公司 | 一种uv/湿气双重固化硅橡胶及其制备方法 |
CN105122382A (zh) * | 2013-04-10 | 2015-12-02 | 矢崎总业株式会社 | 电线的防水构造及其制造方法 |
CN109476917A (zh) * | 2016-05-19 | 2019-03-15 | 莫门蒂夫性能材料股份有限公司 | 可固化、双固化的单组分有机硅组合物 |
TWI757388B (zh) * | 2016-12-09 | 2022-03-11 | 南韓商韓國默曼堤效能材料股份有限公司 | 用於有機電子裝置封裝物的組成物以及使用此組成物製成的封裝物和有機電子裝置 |
Families Citing this family (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20100224305A1 (en) * | 2009-03-04 | 2010-09-09 | Stephen Paul Zadesky | Adhesive Having UV-Reactive Colorization |
US8871317B2 (en) | 2010-09-09 | 2014-10-28 | Teknor Apex Company | Curable adhesive system, method of assembly of distinct components therewith |
DE102012220574A1 (de) | 2012-11-12 | 2014-05-15 | Tesa Se | Trennbeschichtung mit verbesserter Fehlererkennung |
KR20140129934A (ko) * | 2013-04-30 | 2014-11-07 | 제일모직주식회사 | 광경화 조성물 및 이를 포함하는 봉지화된 장치 |
CN103965821B (zh) * | 2014-04-30 | 2016-03-16 | 京东方科技集团股份有限公司 | 一种封框胶组合物及显示装置 |
EP3426742B1 (en) * | 2016-03-07 | 2020-02-05 | Dow Silicones Corporation | Photocurable silicone composition and cured product thereof |
KR102468361B1 (ko) | 2016-03-22 | 2022-11-18 | 삼성디스플레이 주식회사 | 표시 장치 및 표시장치의 제조 방법 |
TWI782066B (zh) | 2017-08-03 | 2022-11-01 | 德商漢高股份有限及兩合公司 | 可固化的聚矽氧光學透明黏著劑及其用途 |
KR20200100610A (ko) | 2017-12-27 | 2020-08-26 | 헨켈 아이피 앤드 홀딩 게엠베하 | 광학적으로 투명한 감압성 접착제 및 그의 용도 |
US20210070945A1 (en) | 2019-09-06 | 2021-03-11 | Elkem Silicones USA Corp. | Process and premix for incorporating optical brighteners into a polymeric composition |
KR102271413B1 (ko) * | 2020-10-20 | 2021-06-30 | 김효남 | 건축물용 축광 실링제 조성물 및 그 축광 실링제 제조 방법 및 용기 |
WO2023078980A1 (de) * | 2021-11-04 | 2023-05-11 | Loparex Germany Gmbh & Co. Kg | Erkennung von silikonfehlstellen im laufenden beschichtungsbetrieb |
Family Cites Families (31)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4111890A (en) | 1977-12-19 | 1978-09-05 | Sws Silicones Corporation | Curable organopolysiloxane compositions containing titanium esters |
DE2909994A1 (de) * | 1979-03-14 | 1980-10-02 | Basf Ag | Acylphosphinoxidverbindungen, ihre herstellung und verwendung |
US4528081A (en) | 1983-10-03 | 1985-07-09 | Loctite Corporation | Dual curing silicone, method of preparing same and dielectric soft-gel compositions thereof |
US4699802A (en) | 1983-10-03 | 1987-10-13 | Loctite Corporation | Dual curing coating method for substrates with shadow areas |
CA1337224C (en) * | 1987-11-06 | 1995-10-03 | Beth I. Gutek | Compositions having uv cure with moisture shadow cure |
US4966922A (en) | 1988-06-09 | 1990-10-30 | General Electric Company | Dual curable silicone compositions |
US5227410A (en) * | 1991-12-05 | 1993-07-13 | General Electric Company | Uv-curable epoxysilicone-polyether block copolymers |
US5162390A (en) * | 1990-03-05 | 1992-11-10 | General Electric Company | UV curable coating compositions, abrasion resistant UV stabilized thermoplastic composites and method |
US5348986A (en) | 1990-11-19 | 1994-09-20 | Loctite Corporation | Photocurable silicone composition, and method of making same |
EP0711801B1 (en) * | 1990-12-28 | 1999-10-06 | Dow Corning Corporation | Method of indicating a cure point for ultraviolet radiation curing compositions by color change |
EP0505737A1 (en) * | 1991-03-27 | 1992-09-30 | General Electric Company | UV curable abrasion resistant coating compositions and method |
US5240971A (en) * | 1991-12-05 | 1993-08-31 | General Electric Company | UV-curable epoxysilicone-polyether block copolymers |
US5498642A (en) | 1992-03-31 | 1996-03-12 | Loctite Corporation | Radiation surface-curable, room temperature vulcanizing silicone compositions |
US5663269A (en) | 1992-03-31 | 1997-09-02 | Loctite Corporation | Organosiloxane fluids prepared using organo-lithium reagents |
US5300608A (en) * | 1992-03-31 | 1994-04-05 | Loctite Corporation | Process for preparing alkoxy-terminated organosiloxane fluids using organo-lithium reagents |
US5516812A (en) | 1992-03-31 | 1996-05-14 | Loctite Corporation | UV-moisture dual cure silicone conformal coating compositions with improved surface tack |
US5707781A (en) * | 1995-05-05 | 1998-01-13 | Bayer Corporation | Photopolymerizable compositions having acyl or diacyl phosphine oxide and a fluorescent optical brightner |
US5801884A (en) * | 1995-10-09 | 1998-09-01 | Mitsubishi Chemical Corporation | Optical device and process for producing the same |
JPH09208611A (ja) * | 1996-02-06 | 1997-08-12 | Japan Synthetic Rubber Co Ltd | 螢光体分散感放射線性組成物 |
US6080450A (en) | 1996-02-23 | 2000-06-27 | Dymax Corporation | Composition exhibiting improved fluorescent response |
DE19650562A1 (de) * | 1996-12-05 | 1998-06-10 | Basf Ag | Photoinitiatorgemische, enthaltend Acylphosphinoxide und Benzophenonderivate |
CN1121421C (zh) * | 1997-02-19 | 2003-09-17 | 西巴特殊化学品控股有限公司 | 通过光聚合制备(共)聚合物 |
DE19812859A1 (de) * | 1998-03-24 | 1999-09-30 | Basf Ag | Photoinitiatorgemische |
US6323253B1 (en) * | 1998-06-01 | 2001-11-27 | Loctite Corporation | Flame-retardant UV and UV/moisture curable silicone compositions |
AU4835099A (en) | 1998-06-24 | 2000-01-10 | Loctite Corporation | Dual curing silicone compositions |
US6140444A (en) | 1999-01-19 | 2000-10-31 | Loctite Corporation | Catalyst system, process, and silicone compositions |
CA2324794A1 (en) * | 2000-10-25 | 2002-04-25 | American Dye Source, Inc. | Organic-inorganic hybrid photocurable compositions |
US6627672B1 (en) | 2001-05-16 | 2003-09-30 | Henkel Loctite Corporation | UV/moisture dual cure silicone potting compound with improved depth of cure |
JP3786408B2 (ja) * | 2001-11-15 | 2006-06-14 | 日本化薬株式会社 | エネルギー線硬化型樹脂組成物 |
WO2003065841A1 (en) * | 2002-02-05 | 2003-08-14 | Henkel Corporation | Luminescing and/or fluorescing radiation-curable, cyanoacrylate-containing compositions |
TW200613391A (en) * | 2004-09-01 | 2006-05-01 | Novartis Ag | Method for making colored silicone hydrogel contact lenses |
-
2005
- 2005-11-18 ES ES05848930.3T patent/ES2546107T3/es active Active
- 2005-11-18 DK DK05848930.3T patent/DK1833884T3/en active
- 2005-11-18 KR KR1020077014929A patent/KR101201602B1/ko active IP Right Grant
- 2005-11-18 PL PL05848930T patent/PL1833884T3/pl unknown
- 2005-11-18 CN CN2005800456174A patent/CN101094902B/zh active Active
- 2005-11-18 EP EP05848930.3A patent/EP1833884B1/en active Active
- 2005-11-18 PT PT58489303T patent/PT1833884E/pt unknown
- 2005-11-18 MX MX2007006609A patent/MX2007006609A/es active IP Right Grant
- 2005-11-18 HU HUE05848930A patent/HUE05848930T2/hu unknown
- 2005-11-18 US US11/720,611 patent/US8013314B2/en active Active
- 2005-11-18 CA CA2588842A patent/CA2588842C/en not_active Expired - Fee Related
- 2005-11-18 JP JP2007544376A patent/JP5557983B2/ja active Active
- 2005-11-18 WO PCT/US2005/041894 patent/WO2006060189A2/en active Application Filing
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102532434A (zh) * | 2011-12-13 | 2012-07-04 | 北京海斯迪克新材料有限公司 | 一种uv/湿气双重固化硅橡胶及其制备方法 |
CN102532434B (zh) * | 2011-12-13 | 2014-09-17 | 北京海斯迪克新材料有限公司 | 一种uv/湿气双重固化硅橡胶及其制备方法 |
CN105122382A (zh) * | 2013-04-10 | 2015-12-02 | 矢崎总业株式会社 | 电线的防水构造及其制造方法 |
US9721700B2 (en) | 2013-04-10 | 2017-08-01 | Yazaki Corporation | Water-stop structure for electrical wire, and method for manufacturing same |
CN109476917A (zh) * | 2016-05-19 | 2019-03-15 | 莫门蒂夫性能材料股份有限公司 | 可固化、双固化的单组分有机硅组合物 |
CN109476917B (zh) * | 2016-05-19 | 2022-06-10 | 莫门蒂夫性能材料股份有限公司 | 可固化、双固化的单组分有机硅组合物 |
TWI757388B (zh) * | 2016-12-09 | 2022-03-11 | 南韓商韓國默曼堤效能材料股份有限公司 | 用於有機電子裝置封裝物的組成物以及使用此組成物製成的封裝物和有機電子裝置 |
Also Published As
Publication number | Publication date |
---|---|
JP5557983B2 (ja) | 2014-07-23 |
WO2006060189A2 (en) | 2006-06-08 |
HUE05848930T2 (hu) | 2016-05-30 |
DK1833884T3 (en) | 2015-09-28 |
CA2588842A1 (en) | 2006-06-08 |
PL1833884T3 (pl) | 2015-12-31 |
CA2588842C (en) | 2012-09-11 |
KR20070089834A (ko) | 2007-09-03 |
MX2007006609A (es) | 2007-08-14 |
KR101201602B1 (ko) | 2012-11-14 |
JP2008522006A (ja) | 2008-06-26 |
WO2006060189A3 (en) | 2006-09-14 |
EP1833884B1 (en) | 2015-06-24 |
EP1833884A2 (en) | 2007-09-19 |
US8013314B2 (en) | 2011-09-06 |
EP1833884A4 (en) | 2009-05-27 |
PT1833884E (pt) | 2015-10-05 |
CN101094902B (zh) | 2011-01-19 |
ES2546107T3 (es) | 2015-09-18 |
US20090166559A1 (en) | 2009-07-02 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN101094902B (zh) | 掺入荧光检测体系的可固化有机硅组合物 | |
US5100929A (en) | (polyene-polythiol) dental compositions curable with visible light | |
TWI330759B (en) | Negative photoresist composition | |
US20060223901A1 (en) | Radiation curable compositions useful in image projection systems | |
Meereis et al. | Stability of initiation systems in acidic photopolymerizable dental material | |
AU2004231241B2 (en) | Dental surface coating material | |
US6818679B2 (en) | Photopolymerizable dental coating composition | |
JP2019172869A (ja) | 光硬化型インクジェット印刷用インク組成物 | |
KR20110117091A (ko) | α-알릴옥시메틸아크릴산계 공중합체, 수지 조성물 및 그 용도 | |
JP2019525976A (ja) | 浸透を防止する分離被覆 | |
GB2442288A (en) | Two-part glass ionomer composition | |
CN1068126A (zh) | 可快速表面固化的烯类单体组合物 | |
TW299288B (zh) | ||
CN107493684A (zh) | 光固化性组合物 | |
CN109739069A (zh) | 光固化材料组合物、彩膜基板、显示面板及显示装置 | |
US6627672B1 (en) | UV/moisture dual cure silicone potting compound with improved depth of cure | |
TW200842130A (en) | Photoradical curable resin composition and method for preparing the composition | |
JP2018080129A (ja) | ネイル用ベースコート組成物 | |
JP7162936B2 (ja) | 歯科用コーティング組成物及びそれを含む歯科材料 | |
JP4847742B2 (ja) | 活性エネルギー線硬化型圧着ニス組成物および再剥離性情報シート | |
EP0583471A1 (en) | Photopolymerizable adhesive | |
JP2022542401A (ja) | 光硬化性組成物をベースとするネイルコーティング | |
JP2007145907A (ja) | 活性エネルギー線硬化型圧着ニス組成物および再剥離性情報シート | |
TW202330806A (zh) | 光散射油墨組合物、以及使用該組合物之彩色濾光片和圖像顯示裝置 | |
JP2000237207A (ja) | 歯科用練和基材 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C14 | Grant of patent or utility model | ||
GR01 | Patent grant | ||
ASS | Succession or assignment of patent right |
Owner name: HENKEL US IP LLC Free format text: FORMER OWNER: HENKEL CORP. Effective date: 20140827 |
|
C41 | Transfer of patent application or patent right or utility model | ||
TR01 | Transfer of patent right |
Effective date of registration: 20140827 Address after: American Connecticut Patentee after: Henkel American Intellectual Property LLC Address before: American Connecticut Patentee before: Henkel Corp. |
|
TR01 | Transfer of patent right |
Effective date of registration: 20191225 Address after: Dusseldorf Patentee after: THE DIAL Corp. Address before: Connecticut, USA Patentee before: Henkel American Intellectual Property LLC |
|
TR01 | Transfer of patent right | ||
TR01 | Transfer of patent right |
Effective date of registration: 20220809 Address after: Dusseldorf Patentee after: HENKEL AG & Co.KGaA Address before: Dusseldorf Patentee before: THE DIAL Corp. |
|
TR01 | Transfer of patent right |