CA1224182A - Chargement en dur photodurcissable aux ultraviolets et resistant a l'abrasion - Google Patents

Chargement en dur photodurcissable aux ultraviolets et resistant a l'abrasion

Info

Publication number: CA1224182A
Authority: CA; Canada
Prior art keywords: amine; benzophenone; coating; hard coating; weight
Prior art date: 1980-11-05
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.): Expired

Application number

CA000389085A

Other languages

English (en)

Inventor

Rack H. Chung

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

General Electric Co

Original Assignee

General Electric Co

Priority date (The priority date 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 date listed.)

1980-11-05

Filing date

1981-10-30

Publication date

1987-07-14

1981-10-30 Application filed by General Electric Co filed Critical General Electric Co

1987-07-14 Application granted granted Critical

1987-07-14 Publication of CA1224182A publication Critical patent/CA1224182A/fr

Status Expired legal-status Critical Current

Links

239000008199 coating composition Substances 0.000 title claims abstract description 41
238000005299 abrasion Methods 0.000 title claims abstract description 22
239000000203 mixture Substances 0.000 claims abstract description 44
239000000178 monomer Substances 0.000 claims abstract description 31
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims abstract description 17
239000012298 atmosphere Substances 0.000 claims abstract description 15
230000005855 radiation Effects 0.000 claims abstract description 12
239000000758 substrate Substances 0.000 claims description 22
238000000034 method Methods 0.000 claims description 18
125000001931 aliphatic group Chemical group 0.000 claims description 17
230000008569 process Effects 0.000 claims description 14
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 13
239000012965 benzophenone Substances 0.000 claims description 11
RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 claims description 10
GDESWOTWNNGOMW-UHFFFAOYSA-N resorcinol monobenzoate Chemical compound OC1=CC=CC(OC(=O)C=2C=CC=CC=2)=C1 GDESWOTWNNGOMW-UHFFFAOYSA-N 0.000 claims description 10
CRVGTESFCCXCTH-UHFFFAOYSA-N methyl diethanolamine Chemical compound OCCN(C)CCO CRVGTESFCCXCTH-UHFFFAOYSA-N 0.000 claims description 9
239000004094 surface-active agent Substances 0.000 claims description 8
DAKWPKUUDNSNPN-UHFFFAOYSA-N Trimethylolpropane triacrylate Chemical compound C=CC(=O)OCC(CC)(COC(=O)C=C)COC(=O)C=C DAKWPKUUDNSNPN-UHFFFAOYSA-N 0.000 claims description 7
125000001033 ether group Chemical group 0.000 claims description 7
150000001412 amines Chemical class 0.000 claims description 6
238000004132 cross linking Methods 0.000 claims description 6
150000002576 ketones Chemical class 0.000 claims description 6
VOBUAPTXJKMNCT-UHFFFAOYSA-N 1-prop-2-enoyloxyhexyl prop-2-enoate Chemical compound CCCCCC(OC(=O)C=C)OC(=O)C=C VOBUAPTXJKMNCT-UHFFFAOYSA-N 0.000 claims description 5
239000003795 chemical substances by application Substances 0.000 claims description 5
HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 claims description 4
GGSUCNLOZRCGPQ-UHFFFAOYSA-N diethylaniline Chemical compound CCN(CC)C1=CC=CC=C1 GGSUCNLOZRCGPQ-UHFFFAOYSA-N 0.000 claims description 4
JNELGWHKGNBSMD-UHFFFAOYSA-N xanthone Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3OC2=C1 JNELGWHKGNBSMD-UHFFFAOYSA-N 0.000 claims description 4
VVBLNCFGVYUYGU-UHFFFAOYSA-N 4,4'-Bis(dimethylamino)benzophenone Chemical compound C1=CC(N(C)C)=CC=C1C(=O)C1=CC=C(N(C)C)C=C1 VVBLNCFGVYUYGU-UHFFFAOYSA-N 0.000 claims description 3
UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 claims description 3
229960002887 deanol Drugs 0.000 claims description 3
239000012972 dimethylethanolamine Substances 0.000 claims description 3
229910052739 hydrogen Inorganic materials 0.000 claims description 3
239000001257 hydrogen Substances 0.000 claims description 3
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
AJFVSPMJQTWONR-UHFFFAOYSA-N (3-benzoyloxy-2-methylphenyl) benzoate Chemical compound C1=CC=C(OC(=O)C=2C=CC=CC=2)C(C)=C1OC(=O)C1=CC=CC=C1 AJFVSPMJQTWONR-UHFFFAOYSA-N 0.000 claims description 2
SUQGLJRNDJRARS-UHFFFAOYSA-N (3-benzoyloxyphenyl) benzoate Chemical compound C=1C=CC=CC=1C(=O)OC(C=1)=CC=CC=1OC(=O)C1=CC=CC=C1 SUQGLJRNDJRARS-UHFFFAOYSA-N 0.000 claims description 2
AXFVIWBTKYFOCY-UHFFFAOYSA-N 1-n,1-n,3-n,3-n-tetramethylbutane-1,3-diamine Chemical compound CN(C)C(C)CCN(C)C AXFVIWBTKYFOCY-UHFFFAOYSA-N 0.000 claims description 2
KJSGODDTWRXQRH-UHFFFAOYSA-N 2-(dimethylamino)ethyl benzoate Chemical compound CN(C)CCOC(=O)C1=CC=CC=C1 KJSGODDTWRXQRH-UHFFFAOYSA-N 0.000 claims description 2
HYVGFUIWHXLVNV-UHFFFAOYSA-N 2-(n-ethylanilino)ethanol Chemical compound OCCN(CC)C1=CC=CC=C1 HYVGFUIWHXLVNV-UHFFFAOYSA-N 0.000 claims description 2
VIIZJXNVVJKISZ-UHFFFAOYSA-N 2-(n-methylanilino)ethanol Chemical compound OCCN(C)C1=CC=CC=C1 VIIZJXNVVJKISZ-UHFFFAOYSA-N 0.000 claims description 2
OJPDDQSCZGTACX-UHFFFAOYSA-N 2-[n-(2-hydroxyethyl)anilino]ethanol Chemical compound OCCN(CCO)C1=CC=CC=C1 OJPDDQSCZGTACX-UHFFFAOYSA-N 0.000 claims description 2
FPYUJUBAXZAQNL-UHFFFAOYSA-N 2-chlorobenzaldehyde Chemical compound ClC1=CC=CC=C1C=O FPYUJUBAXZAQNL-UHFFFAOYSA-N 0.000 claims description 2
ZCDADJXRUCOCJE-UHFFFAOYSA-N 2-chlorothioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC(Cl)=CC=C3SC2=C1 ZCDADJXRUCOCJE-UHFFFAOYSA-N 0.000 claims description 2
BFSVOASYOCHEOV-UHFFFAOYSA-N 2-diethylaminoethanol Chemical compound CCN(CC)CCO BFSVOASYOCHEOV-UHFFFAOYSA-N 0.000 claims description 2
KMNCBSZOIQAUFX-UHFFFAOYSA-N 2-ethoxy-1,2-diphenylethanone Chemical compound C=1C=CC=CC=1C(OCC)C(=O)C1=CC=CC=C1 KMNCBSZOIQAUFX-UHFFFAOYSA-N 0.000 claims description 2
NACPTFCBIGBTSJ-UHFFFAOYSA-N 2-hydroxy-2-phenyl-1-(2-propan-2-ylphenyl)ethanone Chemical compound CC(C)C1=CC=CC=C1C(=O)C(O)C1=CC=CC=C1 NACPTFCBIGBTSJ-UHFFFAOYSA-N 0.000 claims description 2
RZVHIXYEVGDQDX-UHFFFAOYSA-N 9,10-anthraquinone Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3C(=O)C2=C1 RZVHIXYEVGDQDX-UHFFFAOYSA-N 0.000 claims description 2
229940076442 9,10-anthraquinone Drugs 0.000 claims description 2
YYVYAPXYZVYDHN-UHFFFAOYSA-N 9,10-phenanthroquinone Chemical compound C1=CC=C2C(=O)C(=O)C3=CC=CC=C3C2=C1 YYVYAPXYZVYDHN-UHFFFAOYSA-N 0.000 claims description 2
AKNUHUCEWALCOI-UHFFFAOYSA-N N-ethyldiethanolamine Chemical compound OCCN(CC)CCO AKNUHUCEWALCOI-UHFFFAOYSA-N 0.000 claims description 2
GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 claims description 2
PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 claims description 2
WURBFLDFSFBTLW-UHFFFAOYSA-N benzil Chemical compound C=1C=CC=CC=1C(=O)C(=O)C1=CC=CC=C1 WURBFLDFSFBTLW-UHFFFAOYSA-N 0.000 claims description 2
VYHBFRJRBHMIQZ-UHFFFAOYSA-N bis[4-(diethylamino)phenyl]methanone Chemical compound C1=CC(N(CC)CC)=CC=C1C(=O)C1=CC=C(N(CC)CC)C=C1 VYHBFRJRBHMIQZ-UHFFFAOYSA-N 0.000 claims description 2
CQNOGTUXPYIVDM-UHFFFAOYSA-N ethyl 3-(dimethylamino)benzoate Chemical compound CCOC(=O)C1=CC=CC(N(C)C)=C1 CQNOGTUXPYIVDM-UHFFFAOYSA-N 0.000 claims description 2
QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 claims description 2
YRHRIQCWCFGUEQ-UHFFFAOYSA-N thioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3SC2=C1 YRHRIQCWCFGUEQ-UHFFFAOYSA-N 0.000 claims description 2
229960004418 trolamine Drugs 0.000 claims description 2
KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 claims 2
XEFUJRQNJWBDIF-UHFFFAOYSA-N (3-hydroxy-2-methylphenyl) benzoate Chemical compound CC1=C(O)C=CC=C1OC(=O)C1=CC=CC=C1 XEFUJRQNJWBDIF-UHFFFAOYSA-N 0.000 claims 1
BEUGBYXJXMVRFO-UHFFFAOYSA-N [4-(dimethylamino)phenyl]-phenylmethanone Chemical compound C1=CC(N(C)C)=CC=C1C(=O)C1=CC=CC=C1 BEUGBYXJXMVRFO-UHFFFAOYSA-N 0.000 claims 1
150000002923 oximes Chemical class 0.000 claims 1
238000012216 screening Methods 0.000 claims 1
238000000576 coating method Methods 0.000 description 55
239000011248 coating agent Substances 0.000 description 33
-1 acrylate ester Chemical class 0.000 description 27
239000004417 polycarbonate Substances 0.000 description 23
229920000515 polycarbonate Polymers 0.000 description 23
239000000463 material Substances 0.000 description 14
238000012360 testing method Methods 0.000 description 14
BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 12
150000002430 hydrocarbons Chemical group 0.000 description 11
229920003023 plastic Polymers 0.000 description 11
LEJBBGNFPAFPKQ-UHFFFAOYSA-N 2-(2-prop-2-enoyloxyethoxy)ethyl prop-2-enoate Chemical compound C=CC(=O)OCCOCCOC(=O)C=C LEJBBGNFPAFPKQ-UHFFFAOYSA-N 0.000 description 10
125000004432 carbon atom Chemical group C* 0.000 description 10
150000001875 compounds Chemical class 0.000 description 10
239000000047 product Substances 0.000 description 10
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 9
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 8
239000004033 plastic Substances 0.000 description 8
229920000642 polymer Polymers 0.000 description 8
229920006395 saturated elastomer Polymers 0.000 description 8
239000002904 solvent Substances 0.000 description 8
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 7
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 6
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
229940096522 trimethylolpropane triacrylate Drugs 0.000 description 6
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
239000002253 acid Substances 0.000 description 5
125000003118 aryl group Chemical group 0.000 description 5
230000008901 benefit Effects 0.000 description 5
238000001723 curing Methods 0.000 description 5
125000004386 diacrylate group Chemical group 0.000 description 5
239000011521 glass Substances 0.000 description 5
HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 4
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 4
YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 4
150000001491 aromatic compounds Chemical class 0.000 description 4
239000003054 catalyst Substances 0.000 description 4
125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 4
229910052731 fluorine Inorganic materials 0.000 description 4
239000011737 fluorine Substances 0.000 description 4
150000002989 phenols Chemical class 0.000 description 4
239000003504 photosensitizing agent Substances 0.000 description 4
229920003229 poly(methyl methacrylate) Polymers 0.000 description 4
239000002243 precursor Substances 0.000 description 4
150000004756 silanes Chemical class 0.000 description 4
ARCGXLSVLAOJQL-UHFFFAOYSA-N trimellitic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C(C(O)=O)=C1 ARCGXLSVLAOJQL-UHFFFAOYSA-N 0.000 description 4
229920004142 LEXAN™ Polymers 0.000 description 3
239000004418 Lexan Substances 0.000 description 3
JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 description 3
150000001252 acrylic acid derivatives Chemical class 0.000 description 3
230000002411 adverse Effects 0.000 description 3
AOJDZKCUAATBGE-UHFFFAOYSA-N bromomethane Chemical compound Br[CH2] AOJDZKCUAATBGE-UHFFFAOYSA-N 0.000 description 3
229920001577 copolymer Polymers 0.000 description 3
125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
230000003287 optical effect Effects 0.000 description 3
229920000728 polyester Polymers 0.000 description 3
238000006116 polymerization reaction Methods 0.000 description 3
239000004926 polymethyl methacrylate Substances 0.000 description 3
239000000126 substance Substances 0.000 description 3
125000001424 substituent group Chemical group 0.000 description 3
239000002344 surface layer Substances 0.000 description 3
ILBBNQMSDGAAPF-UHFFFAOYSA-N 1-(6-hydroxy-6-methylcyclohexa-2,4-dien-1-yl)propan-1-one Chemical compound CCC(=O)C1C=CC=CC1(C)O ILBBNQMSDGAAPF-UHFFFAOYSA-N 0.000 description 2
PIZHFBODNLEQBL-UHFFFAOYSA-N 2,2-diethoxy-1-phenylethanone Chemical compound CCOC(OCC)C(=O)C1=CC=CC=C1 PIZHFBODNLEQBL-UHFFFAOYSA-N 0.000 description 2
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 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
101100006523 Arabidopsis thaliana CHC2 gene Proteins 0.000 description 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
229920000877 Melamine resin Polymers 0.000 description 2
239000004677 Nylon Substances 0.000 description 2
OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
239000004952 Polyamide Substances 0.000 description 2
ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
HVVWZTWDBSEWIH-UHFFFAOYSA-N [2-(hydroxymethyl)-3-prop-2-enoyloxy-2-(prop-2-enoyloxymethyl)propyl] prop-2-enoate Chemical compound C=CC(=O)OCC(CO)(COC(=O)C=C)COC(=O)C=C HVVWZTWDBSEWIH-UHFFFAOYSA-N 0.000 description 2
239000006096 absorbing agent Substances 0.000 description 2
239000000654 additive Substances 0.000 description 2
150000001338 aliphatic hydrocarbons Chemical class 0.000 description 2
125000003545 alkoxy group Chemical group 0.000 description 2
125000002029 aromatic hydrocarbon group Chemical group 0.000 description 2
125000004429 atom Chemical group 0.000 description 2
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 2
PXKLMJQFEQBVLD-UHFFFAOYSA-N bisphenol F Chemical compound C1=CC(O)=CC=C1CC1=CC=C(O)C=C1 PXKLMJQFEQBVLD-UHFFFAOYSA-N 0.000 description 2
229940106691 bisphenol a Drugs 0.000 description 2
150000004649 carbonic acid derivatives Chemical class 0.000 description 2
239000008119 colloidal silica Substances 0.000 description 2
238000005336 cracking Methods 0.000 description 2
230000000694 effects Effects 0.000 description 2
238000005516 engineering process Methods 0.000 description 2
150000002148 esters Chemical class 0.000 description 2
150000004820 halides Chemical class 0.000 description 2
125000005067 haloformyl group Chemical group 0.000 description 2
229910052736 halogen Inorganic materials 0.000 description 2
238000013007 heat curing Methods 0.000 description 2
229920001519 homopolymer Polymers 0.000 description 2
239000004615 ingredient Substances 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
YDSWCNNOKPMOTP-UHFFFAOYSA-N mellitic acid Chemical compound OC(=O)C1=C(C(O)=O)C(C(O)=O)=C(C(O)=O)C(C(O)=O)=C1C(O)=O YDSWCNNOKPMOTP-UHFFFAOYSA-N 0.000 description 2
150000007522 mineralic acids Chemical class 0.000 description 2
229910052757 nitrogen Inorganic materials 0.000 description 2
229920001778 nylon Polymers 0.000 description 2
239000008188 pellet Substances 0.000 description 2
229920000058 polyacrylate Polymers 0.000 description 2
229920002647 polyamide Polymers 0.000 description 2
230000002035 prolonged effect Effects 0.000 description 2
239000001294 propane Substances 0.000 description 2
CYIDZMCFTVVTJO-UHFFFAOYSA-N pyromellitic acid Chemical compound OC(=O)C1=CC(C(O)=O)=C(C(O)=O)C=C1C(O)=O CYIDZMCFTVVTJO-UHFFFAOYSA-N 0.000 description 2
150000003254 radicals Chemical class 0.000 description 2
239000000243 solution Substances 0.000 description 2
150000003512 tertiary amines Chemical group 0.000 description 2
WGTYBPLFGIVFAS-UHFFFAOYSA-M tetramethylammonium hydroxide Chemical compound [OH-].C[N+](C)(C)C WGTYBPLFGIVFAS-UHFFFAOYSA-M 0.000 description 2
238000001029 thermal curing Methods 0.000 description 2
SRPWOOOHEPICQU-UHFFFAOYSA-N trimellitic anhydride Chemical compound OC(=O)C1=CC=C2C(=O)OC(=O)C2=C1 SRPWOOOHEPICQU-UHFFFAOYSA-N 0.000 description 2
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
VLDPXPPHXDGHEW-UHFFFAOYSA-N 1-chloro-2-dichlorophosphoryloxybenzene Chemical compound ClC1=CC=CC=C1OP(Cl)(Cl)=O VLDPXPPHXDGHEW-UHFFFAOYSA-N 0.000 description 1
YWRDGHPJNOGFFM-UHFFFAOYSA-N 2-chloro-4-[(3-chloro-4-hydroxyphenyl)methyl]phenol Chemical compound C1=C(Cl)C(O)=CC=C1CC1=CC=C(O)C(Cl)=C1 YWRDGHPJNOGFFM-UHFFFAOYSA-N 0.000 description 1
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
YMTYZTXUZLQUSF-UHFFFAOYSA-N 3,3'-Dimethylbisphenol A Chemical compound C1=C(O)C(C)=CC(C(C)(C)C=2C=C(C)C(O)=CC=2)=C1 YMTYZTXUZLQUSF-UHFFFAOYSA-N 0.000 description 1
KXYDGGNWZUHESZ-UHFFFAOYSA-N 4-(2,2,4-trimethyl-3h-chromen-4-yl)phenol Chemical compound C12=CC=CC=C2OC(C)(C)CC1(C)C1=CC=C(O)C=C1 KXYDGGNWZUHESZ-UHFFFAOYSA-N 0.000 description 1
GZFGOTFRPZRKDS-UHFFFAOYSA-N 4-bromophenol Chemical compound OC1=CC=C(Br)C=C1 GZFGOTFRPZRKDS-UHFFFAOYSA-N 0.000 description 1
125000004203 4-hydroxyphenyl group Chemical group [H]OC1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
QHPQWRBYOIRBIT-UHFFFAOYSA-N 4-tert-butylphenol Chemical compound CC(C)(C)C1=CC=C(O)C=C1 QHPQWRBYOIRBIT-UHFFFAOYSA-N 0.000 description 1
FIHBHSQYSYVZQE-UHFFFAOYSA-N 6-prop-2-enoyloxyhexyl prop-2-enoate Chemical compound C=CC(=O)OCCCCCCOC(=O)C=C FIHBHSQYSYVZQE-UHFFFAOYSA-N 0.000 description 1
BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
229930185605 Bisphenol Natural products 0.000 description 1
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 1
239000004215 Carbon black (E152) Substances 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
101150065749 Churc1 gene Proteins 0.000 description 1
101100536354 Drosophila melanogaster tant gene Proteins 0.000 description 1
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 1
OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
229910019142 PO4 Inorganic materials 0.000 description 1
206010034972 Photosensitivity reaction Diseases 0.000 description 1
LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 1
239000002202 Polyethylene glycol Substances 0.000 description 1
239000004721 Polyphenylene oxide Substances 0.000 description 1
102100038239 Protein Churchill Human genes 0.000 description 1
BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-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
239000003082 abrasive agent Substances 0.000 description 1
150000008062 acetophenones Chemical class 0.000 description 1
238000005903 acid hydrolysis reaction Methods 0.000 description 1
229920006397 acrylic thermoplastic Polymers 0.000 description 1
239000013543 active substance Substances 0.000 description 1
230000001464 adherent effect Effects 0.000 description 1
239000002390 adhesive tape Substances 0.000 description 1
229910052784 alkaline earth metal Inorganic materials 0.000 description 1
150000001342 alkaline earth metals Chemical class 0.000 description 1
125000000217 alkyl group Chemical group 0.000 description 1
125000005037 alkyl phenyl group Chemical group 0.000 description 1
229910052782 aluminium Inorganic materials 0.000 description 1
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
150000008064 anhydrides Chemical class 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
CJPIDIRJSIUWRJ-UHFFFAOYSA-N benzene-1,2,4-tricarbonyl chloride Chemical compound ClC(=O)C1=CC=C(C(Cl)=O)C(C(Cl)=O)=C1 CJPIDIRJSIUWRJ-UHFFFAOYSA-N 0.000 description 1
VCYAMSXIIWQHKV-UHFFFAOYSA-N bis(2,3,4-tribromophenyl) carbonate Chemical compound BrC1=C(Br)C(Br)=CC=C1OC(=O)OC1=CC=C(Br)C(Br)=C1Br VCYAMSXIIWQHKV-UHFFFAOYSA-N 0.000 description 1
DSEORJACOQDMQX-UHFFFAOYSA-N bis(2,3,4-trichlorophenyl) carbonate Chemical compound ClC1=C(Cl)C(Cl)=CC=C1OC(=O)OC1=CC=C(Cl)C(Cl)=C1Cl DSEORJACOQDMQX-UHFFFAOYSA-N 0.000 description 1
LUQQDEDMRRRWGN-UHFFFAOYSA-N bis(2-bromophenyl) carbonate Chemical compound BrC1=CC=CC=C1OC(=O)OC1=CC=CC=C1Br LUQQDEDMRRRWGN-UHFFFAOYSA-N 0.000 description 1
MUCRFDZUHPMASM-UHFFFAOYSA-N bis(2-chlorophenyl) carbonate Chemical compound ClC1=CC=CC=C1OC(=O)OC1=CC=CC=C1Cl MUCRFDZUHPMASM-UHFFFAOYSA-N 0.000 description 1
POZGCGJFBOZPCM-UHFFFAOYSA-N bis(2-methylphenyl) carbonate Chemical compound CC1=CC=CC=C1OC(=O)OC1=CC=CC=C1C POZGCGJFBOZPCM-UHFFFAOYSA-N 0.000 description 1
238000007664 blowing Methods 0.000 description 1
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
229910052794 bromium Inorganic materials 0.000 description 1
JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 1
IKWKJIWDLVYZIY-UHFFFAOYSA-M butyl(triphenyl)phosphanium;bromide Chemical compound [Br-].C=1C=CC=CC=1[P+](C=1C=CC=CC=1)(CCCC)C1=CC=CC=C1 IKWKJIWDLVYZIY-UHFFFAOYSA-M 0.000 description 1
BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
MOIPGXQKZSZOQX-UHFFFAOYSA-N carbonyl bromide Chemical compound BrC(Br)=O MOIPGXQKZSZOQX-UHFFFAOYSA-N 0.000 description 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
150000001244 carboxylic acid anhydrides Chemical class 0.000 description 1
230000015556 catabolic process Effects 0.000 description 1
125000002091 cationic group Chemical group 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
238000004140 cleaning Methods 0.000 description 1
230000000052 comparative effect Effects 0.000 description 1
238000005520 cutting process Methods 0.000 description 1
MIHINWMALJZIBX-UHFFFAOYSA-N cyclohexa-2,4-dien-1-ol Chemical class OC1CC=CC=C1 MIHINWMALJZIBX-UHFFFAOYSA-N 0.000 description 1
JJCFRYNCJDLXIK-UHFFFAOYSA-N cyproheptadine Chemical compound C1CN(C)CCC1=C1C2=CC=CC=C2C=CC2=CC=CC=C21 JJCFRYNCJDLXIK-UHFFFAOYSA-N 0.000 description 1
238000006731 degradation reaction Methods 0.000 description 1
230000002939 deleterious effect Effects 0.000 description 1
150000005690 diesters Chemical class 0.000 description 1
ZQUZPFYNEARCQO-UHFFFAOYSA-N dinaphthalen-1-yl carbonate Chemical compound C1=CC=C2C(OC(OC=3C4=CC=CC=C4C=CC=3)=O)=CC=CC2=C1 ZQUZPFYNEARCQO-UHFFFAOYSA-N 0.000 description 1
ROORDVPLFPIABK-UHFFFAOYSA-N diphenyl carbonate Chemical compound C=1C=CC=CC=1OC(=O)OC1=CC=CC=C1 ROORDVPLFPIABK-UHFFFAOYSA-N 0.000 description 1
238000007598 dipping method Methods 0.000 description 1
239000000428 dust Substances 0.000 description 1
239000000975 dye Substances 0.000 description 1
238000009713 electroplating Methods 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
230000003203 everyday effect Effects 0.000 description 1
235000019256 formaldehyde Nutrition 0.000 description 1
238000009472 formulation Methods 0.000 description 1
239000000446 fuel Substances 0.000 description 1
125000000524 functional group Chemical group 0.000 description 1
239000000499 gel Substances 0.000 description 1
150000002334 glycols Chemical class 0.000 description 1
150000002367 halogens Chemical class 0.000 description 1
ACCCMOQWYVYDOT-UHFFFAOYSA-N hexane-1,1-diol Chemical compound CCCCCC(O)O ACCCMOQWYVYDOT-UHFFFAOYSA-N 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
125000004464 hydroxyphenyl group Chemical group 0.000 description 1
238000009863 impact test Methods 0.000 description 1
230000001771 impaired effect Effects 0.000 description 1
239000012442 inert solvent Substances 0.000 description 1
238000002347 injection Methods 0.000 description 1
239000007924 injection Substances 0.000 description 1
238000003475 lamination Methods 0.000 description 1
238000012423 maintenance Methods 0.000 description 1
238000005259 measurement Methods 0.000 description 1
NNYHMCFMPHPHOQ-UHFFFAOYSA-N mellitic anhydride Chemical compound O=C1OC(=O)C2=C1C(C(OC1=O)=O)=C1C1=C2C(=O)OC1=O NNYHMCFMPHPHOQ-UHFFFAOYSA-N 0.000 description 1
QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
LSEFCHWGJNHZNT-UHFFFAOYSA-M methyl(triphenyl)phosphanium;bromide Chemical compound [Br-].C=1C=CC=CC=1[P+](C=1C=CC=CC=1)(C)C1=CC=CC=C1 LSEFCHWGJNHZNT-UHFFFAOYSA-M 0.000 description 1
238000012986 modification Methods 0.000 description 1
230000004048 modification Effects 0.000 description 1
SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
239000010452 phosphate Substances 0.000 description 1
238000000016 photochemical curing Methods 0.000 description 1
230000002165 photosensitisation Effects 0.000 description 1
229920000570 polyether Polymers 0.000 description 1
229920001223 polyethylene glycol Polymers 0.000 description 1
229920001296 polysiloxane Polymers 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
150000003141 primary amines Chemical class 0.000 description 1
108090000623 proteins and genes Proteins 0.000 description 1
150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
150000004023 quaternary phosphonium compounds Chemical class 0.000 description 1
108700001054 rat Hhex Proteins 0.000 description 1
230000009467 reduction Effects 0.000 description 1
230000000246 remedial effect Effects 0.000 description 1
239000011347 resin Substances 0.000 description 1
229920005989 resin Polymers 0.000 description 1
239000006120 scratch resistant coating Substances 0.000 description 1
238000006748 scratching Methods 0.000 description 1
230000002393 scratching effect Effects 0.000 description 1
150000003335 secondary amines Chemical class 0.000 description 1
229910000077 silane Inorganic materials 0.000 description 1
239000000741 silica gel Substances 0.000 description 1
229910002027 silica gel Inorganic materials 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
GRJISGHXMUQUMC-UHFFFAOYSA-N silyl prop-2-enoate Chemical class [SiH3]OC(=O)C=C GRJISGHXMUQUMC-UHFFFAOYSA-N 0.000 description 1
239000000344 soap Substances 0.000 description 1
239000007787 solid Substances 0.000 description 1
238000005507 spraying Methods 0.000 description 1
238000004544 sputter deposition Methods 0.000 description 1
238000006467 substitution reaction Methods 0.000 description 1
229920005613 synthetic organic polymer Polymers 0.000 description 1
230000029305 taxis Effects 0.000 description 1
ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 1
DPKBAXPHAYBPRL-UHFFFAOYSA-M tetrabutylazanium;iodide Chemical compound [I-].CCCC[N+](CCCC)(CCCC)CCCC DPKBAXPHAYBPRL-UHFFFAOYSA-M 0.000 description 1
HWCKGOZZJDHMNC-UHFFFAOYSA-M tetraethylammonium bromide Chemical compound [Br-].CC[N+](CC)(CC)CC HWCKGOZZJDHMNC-UHFFFAOYSA-M 0.000 description 1
KCSOHLKZTZMKQA-UHFFFAOYSA-M tetraheptylazanium;iodide Chemical compound [I-].CCCCCCC[N+](CCCCCCC)(CCCCCCC)CCCCCCC KCSOHLKZTZMKQA-UHFFFAOYSA-M 0.000 description 1
QEMXHQIAXOOASZ-UHFFFAOYSA-N tetramethylammonium Chemical compound C[N+](C)(C)C QEMXHQIAXOOASZ-UHFFFAOYSA-N 0.000 description 1
BGQMOFGZRJUORO-UHFFFAOYSA-M tetrapropylammonium bromide Chemical compound [Br-].CCC[N+](CCC)(CCC)CCC BGQMOFGZRJUORO-UHFFFAOYSA-M 0.000 description 1
125000003944 tolyl group Chemical group 0.000 description 1
239000012780 transparent material Substances 0.000 description 1
IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
150000005691 triesters Chemical class 0.000 description 1
HNJXPTMEWIVQQM-UHFFFAOYSA-M triethyl(hexadecyl)azanium;bromide Chemical compound [Br-].CCCCCCCCCCCCCCCC[N+](CC)(CC)CC HNJXPTMEWIVQQM-UHFFFAOYSA-M 0.000 description 1
YFTHZRPMJXBUME-UHFFFAOYSA-N tripropylamine Chemical compound CCCN(CCC)CCC YFTHZRPMJXBUME-UHFFFAOYSA-N 0.000 description 1
238000007740 vapor deposition Methods 0.000 description 1
229910052724 xenon Inorganic materials 0.000 description 1
FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 1

Landscapes

Paints Or Removers (AREA)

CA000389085A 1980-11-05 1981-10-30 Chargement en dur photodurcissable aux ultraviolets et resistant a l'abrasion Expired CA1224182A (fr)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US20414680A	1980-11-05	1980-11-05
US204,146		1980-11-05

Publications (1)

Publication Number	Publication Date
CA1224182A true CA1224182A (fr)	1987-07-14

Family

ID=22756818

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA000389085A Expired CA1224182A (fr)	1980-11-05	1981-10-30	Chargement en dur photodurcissable aux ultraviolets et resistant a l'abrasion

Country Status (1)

Country	Link
CA (1)	CA1224182A (fr)

Cited By (36)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US6464484B1 (en)	2002-03-30	2002-10-15	Q2100, Inc.	Apparatus and system for the production of plastic lenses
US6612828B2 (en)	2001-02-20	2003-09-02	Q2100, Inc.	Fill system with controller for monitoring use
US6632535B1 (en)	2000-06-08	2003-10-14	Q2100, Inc.	Method of forming antireflective coatings
US6655946B2 (en)	2001-02-20	2003-12-02	Q2100, Inc.	Apparatus for preparing an eyeglass lens having a controller for conveyor and curing units
US6676399B1 (en)	2001-02-20	2004-01-13	Q2100, Inc.	Apparatus for preparing an eyeglass lens having sensors for tracking mold assemblies
US6676398B2 (en)	2001-02-20	2004-01-13	Q2100, Inc.	Apparatus for preparing an eyeglass lens having a prescription reader
US6702564B2 (en)	2001-02-20	2004-03-09	Q2100, Inc.	System for preparing an eyeglass lens using colored mold holders
US6709257B2 (en)	2001-02-20	2004-03-23	Q2100, Inc.	Eyeglass lens forming apparatus with sensor
US6712331B2 (en)	2001-02-20	2004-03-30	Q2100, Inc.	Holder for mold assemblies with indicia
US6712596B1 (en)	1997-07-31	2004-03-30	Q2100, Inc.	System for producing ultraviolet blocking lenses
US6726463B2 (en)	2001-02-20	2004-04-27	Q2100, Inc.	Apparatus for preparing an eyeglass lens having a dual computer system controller
US6752613B2 (en)	2001-02-20	2004-06-22	Q2100, Inc.	Apparatus for preparing an eyeglass lens having a controller for initiation of lens curing
US6758663B2 (en)	2001-02-20	2004-07-06	Q2100, Inc.	System for preparing eyeglass lenses with a high volume curing unit
US6790022B1 (en)	2001-02-20	2004-09-14	Q2100, Inc.	Apparatus for preparing an eyeglass lens having a movable lamp mount
US6790024B2 (en)	2001-02-20	2004-09-14	Q2100, Inc.	Apparatus for preparing an eyeglass lens having multiple conveyor systems
US6808381B2 (en)	2001-02-20	2004-10-26	Q2100, Inc.	Apparatus for preparing an eyeglass lens having a controller
US6863518B2 (en)	2001-02-20	2005-03-08	Q2100, Inc.	Mold filing apparatus having multiple fill stations
US6875005B2 (en)	2001-02-20	2005-04-05	Q1200, Inc.	Apparatus for preparing an eyeglass lens having a gating device
US6893245B2 (en)	2001-02-20	2005-05-17	Q2100, Inc.	Apparatus for preparing an eyeglass lens having a computer system controller
US6899831B1 (en)	2001-02-20	2005-05-31	Q2100, Inc.	Method of preparing an eyeglass lens by delayed entry of mold assemblies into a curing apparatus
US6960312B2 (en)	2000-03-30	2005-11-01	Q2100, Inc.	Methods for the production of plastic lenses
US6962669B2 (en)	2001-02-20	2005-11-08	Q2100, Inc.	Computerized controller for an eyeglass lens curing apparatus
US6964479B2 (en)	1999-03-19	2005-11-15	Q1200, Inc.	Plastic lens system, compositions, and methods
US7004740B2 (en)	2001-02-20	2006-02-28	Q2100, Inc.	Apparatus for preparing an eyeglass lens having a heating system
US7011773B2 (en)	2001-02-20	2006-03-14	Q2100, Inc.	Graphical interface to display mold assembly position in a lens forming apparatus
US7025910B2 (en)	2001-02-20	2006-04-11	Q2100, Inc	Method of entering prescription information
US7037449B2 (en)	2001-02-20	2006-05-02	Q2100, Inc.	Method for automatically shutting down a lens forming apparatus
US7044429B1 (en)	2002-03-15	2006-05-16	Q2100, Inc.	Methods and systems for coating eyeglass lens molds
US7045081B2 (en)	2001-02-20	2006-05-16	Q2100, Inc.	Method of monitoring components of a lens forming apparatus
US7051290B2 (en)	2001-02-20	2006-05-23	Q2100, Inc.	Graphical interface for receiving eyeglass prescription information
US7052262B2 (en)	2001-02-20	2006-05-30	Q2100, Inc.	System for preparing eyeglasses lens with filling station
US7060208B2 (en)	2001-02-20	2006-06-13	Q2100, Inc.	Method of preparing an eyeglass lens with a controller
US7074352B2 (en)	2001-02-20	2006-07-11	Q2100, Inc.	Graphical interface for monitoring usage of components of a lens forming apparatus
US7083404B2 (en)	2001-02-20	2006-08-01	Q2100, Inc.	System for preparing an eyeglass lens using a mold holder
US7124995B2 (en)	2001-02-20	2006-10-24	Q2100, Inc.	Holder for mold assemblies and molds
US7129008B2 (en)	1999-10-12	2006-10-31	Laser Photonics Technology Inc.	Holographic recording material

1981
- 1981-10-30 CA CA000389085A patent/CA1224182A/fr not_active Expired

Cited By (38)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US6712596B1 (en)	1997-07-31	2004-03-30	Q2100, Inc.	System for producing ultraviolet blocking lenses
US6939899B2 (en)	1997-07-31	2005-09-06	Q2100, Inc.	Composition for producing ultraviolet blocking lenses
US7079920B2 (en)	1999-03-19	2006-07-18	Q2100, Inc.	Plastic lens systems, compositions, and methods
US6964479B2 (en)	1999-03-19	2005-11-15	Q1200, Inc.	Plastic lens system, compositions, and methods
US7129008B2 (en)	1999-10-12	2006-10-31	Laser Photonics Technology Inc.	Holographic recording material
US6960312B2 (en)	2000-03-30	2005-11-01	Q2100, Inc.	Methods for the production of plastic lenses
US6632535B1 (en)	2000-06-08	2003-10-14	Q2100, Inc.	Method of forming antireflective coatings
US6893245B2 (en)	2001-02-20	2005-05-17	Q2100, Inc.	Apparatus for preparing an eyeglass lens having a computer system controller
US6962669B2 (en)	2001-02-20	2005-11-08	Q2100, Inc.	Computerized controller for an eyeglass lens curing apparatus
US6709257B2 (en)	2001-02-20	2004-03-23	Q2100, Inc.	Eyeglass lens forming apparatus with sensor
US6726463B2 (en)	2001-02-20	2004-04-27	Q2100, Inc.	Apparatus for preparing an eyeglass lens having a dual computer system controller
US6752613B2 (en)	2001-02-20	2004-06-22	Q2100, Inc.	Apparatus for preparing an eyeglass lens having a controller for initiation of lens curing
US6758663B2 (en)	2001-02-20	2004-07-06	Q2100, Inc.	System for preparing eyeglass lenses with a high volume curing unit
US6790022B1 (en)	2001-02-20	2004-09-14	Q2100, Inc.	Apparatus for preparing an eyeglass lens having a movable lamp mount
US6790024B2 (en)	2001-02-20	2004-09-14	Q2100, Inc.	Apparatus for preparing an eyeglass lens having multiple conveyor systems
US6808381B2 (en)	2001-02-20	2004-10-26	Q2100, Inc.	Apparatus for preparing an eyeglass lens having a controller
US6863518B2 (en)	2001-02-20	2005-03-08	Q2100, Inc.	Mold filing apparatus having multiple fill stations
US6875005B2 (en)	2001-02-20	2005-04-05	Q1200, Inc.	Apparatus for preparing an eyeglass lens having a gating device
US6612828B2 (en)	2001-02-20	2003-09-02	Q2100, Inc.	Fill system with controller for monitoring use
US6899831B1 (en)	2001-02-20	2005-05-31	Q2100, Inc.	Method of preparing an eyeglass lens by delayed entry of mold assemblies into a curing apparatus
US6702564B2 (en)	2001-02-20	2004-03-09	Q2100, Inc.	System for preparing an eyeglass lens using colored mold holders
US6676398B2 (en)	2001-02-20	2004-01-13	Q2100, Inc.	Apparatus for preparing an eyeglass lens having a prescription reader
US6712331B2 (en)	2001-02-20	2004-03-30	Q2100, Inc.	Holder for mold assemblies with indicia
US6676399B1 (en)	2001-02-20	2004-01-13	Q2100, Inc.	Apparatus for preparing an eyeglass lens having sensors for tracking mold assemblies
US7004740B2 (en)	2001-02-20	2006-02-28	Q2100, Inc.	Apparatus for preparing an eyeglass lens having a heating system
US7011773B2 (en)	2001-02-20	2006-03-14	Q2100, Inc.	Graphical interface to display mold assembly position in a lens forming apparatus
US7025910B2 (en)	2001-02-20	2006-04-11	Q2100, Inc	Method of entering prescription information
US7037449B2 (en)	2001-02-20	2006-05-02	Q2100, Inc.	Method for automatically shutting down a lens forming apparatus
US7124995B2 (en)	2001-02-20	2006-10-24	Q2100, Inc.	Holder for mold assemblies and molds
US7045081B2 (en)	2001-02-20	2006-05-16	Q2100, Inc.	Method of monitoring components of a lens forming apparatus
US7051290B2 (en)	2001-02-20	2006-05-23	Q2100, Inc.	Graphical interface for receiving eyeglass prescription information
US7052262B2 (en)	2001-02-20	2006-05-30	Q2100, Inc.	System for preparing eyeglasses lens with filling station
US7060208B2 (en)	2001-02-20	2006-06-13	Q2100, Inc.	Method of preparing an eyeglass lens with a controller
US7074352B2 (en)	2001-02-20	2006-07-11	Q2100, Inc.	Graphical interface for monitoring usage of components of a lens forming apparatus
US6655946B2 (en)	2001-02-20	2003-12-02	Q2100, Inc.	Apparatus for preparing an eyeglass lens having a controller for conveyor and curing units
US7083404B2 (en)	2001-02-20	2006-08-01	Q2100, Inc.	System for preparing an eyeglass lens using a mold holder
US7044429B1 (en)	2002-03-15	2006-05-16	Q2100, Inc.	Methods and systems for coating eyeglass lens molds
US6464484B1 (en)	2002-03-30	2002-10-15	Q2100, Inc.	Apparatus and system for the production of plastic lenses

Legal Events

Date	Code	Title	Description
2004-07-14	MKEX	Expiry

Publication	Publication Date	Title
CA1224182A (fr)	1987-07-14	Chargement en dur photodurcissable aux ultraviolets et resistant a l'abrasion
US4478876A (en)	1984-10-23	Process of coating a substrate with an abrasion resistant ultraviolet curable composition
CA1131511A (fr)	1982-09-14	Articles en polycarbonate enduits d'acrylique photodurcissable
GB2089826A (en)	1982-06-30	Abrasion resistant ultraviolet light curable hard coating compositions
EP0020615B1 (fr)	1983-01-12	Article de polycarbonate revetu de verre
US4188451A (en)	1980-02-12	Polycarbonate article coated with an adherent, durable, silica filled organopolysiloxane coating and process for producing same
US4929506A (en)	1990-05-29	Coated polycarbonate articles
US4384026A (en)	1983-05-17	Photocurable acrylic coated polycarbonate articles
US4863802A (en)	1989-09-05	UV-stabilized coatings
JPH04214743A (ja)	1992-08-05	アクリル被覆熱可塑性基体
WO1980001006A1 (fr)	1980-05-15	Article de polycarbonate revetu de silicone resistant a l'abrasion
US4235954A (en)	1980-11-25	Polycarbonate article coated with an adherent, durable organopolysiloxane coating and process for producing same
US4477529A (en)	1984-10-16	Photocurable polyfunctional acrylic coating and decorative articles coated therewith
JPS63218770A (ja)	1988-09-12	光硬化したアクリル系コーティングで被覆された芳香族カーボネート樹脂物品
EP0020633B1 (fr)	1983-02-16	Procede pour revetir de verre un substrat en polycarbonate
US4218508A (en)	1980-08-19	Polycarbonate articles coated with an adherent, durable silica filled organopolysiloxane coating and process for producing same
JPH1177878A (ja)	1999-03-23	透明被覆成形品
US4902724A (en)	1990-02-20	Photocurable acrylic coating composition
EP0020344B1 (fr)	1983-10-26	Articles de polycarbonate revetus de resine acrylique photopolymerisable
JP4069498B2 (ja)	2008-04-02	透明被覆成形品およびその製造方法
JPH11268201A (ja)	1999-10-05	透明被覆成形品およびその製造方法
CA1134319A (fr)	1982-10-26	Articles en polycarbonate enduit de verre
CA1138590A (fr)	1982-12-28	Articles en polycarbonate enduits d'un organopolysiloxane adherent
EP0274596A2 (fr)	1988-07-20	Articles de résine de carbonate aromatique revêtue d'une couche acrylique durcie par irradiation
JPH04142376A (ja)	1992-05-15	活性エネルギー線硬化型耐擦傷性被覆組成物