FI76818C - Vaetskekomposition som kan polymeriseras och som har utmaerkta mekaniska och optiska egenskaper. - Google Patents
Vaetskekomposition som kan polymeriseras och som har utmaerkta mekaniska och optiska egenskaper. Download PDFInfo
- Publication number
- FI76818C FI76818C FI840115A FI840115A FI76818C FI 76818 C FI76818 C FI 76818C FI 840115 A FI840115 A FI 840115A FI 840115 A FI840115 A FI 840115A FI 76818 C FI76818 C FI 76818C
- Authority
- FI
- Finland
- Prior art keywords
- bis
- compound
- optical properties
- excellent mechanical
- composition
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 55
- 239000007788 liquid Substances 0.000 title claims abstract description 20
- 230000003287 optical effect Effects 0.000 title claims abstract description 17
- JKJWYKGYGWOAHT-UHFFFAOYSA-N bis(prop-2-enyl) carbonate Chemical compound C=CCOC(=O)OCC=C JKJWYKGYGWOAHT-UHFFFAOYSA-N 0.000 claims abstract description 26
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 9
- BJELTSYBAHKXRW-UHFFFAOYSA-N 2,4,6-triallyloxy-1,3,5-triazine Chemical compound C=CCOC1=NC(OCC=C)=NC(OCC=C)=N1 BJELTSYBAHKXRW-UHFFFAOYSA-N 0.000 claims abstract description 4
- MTHSVFCYNBDYFN-UHFFFAOYSA-N anhydrous diethylene glycol Natural products OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 claims description 31
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 claims description 10
- BPXVHIRIPLPOPT-UHFFFAOYSA-N 1,3,5-tris(2-hydroxyethyl)-1,3,5-triazinane-2,4,6-trione Chemical compound OCCN1C(=O)N(CCO)C(=O)N(CCO)C1=O BPXVHIRIPLPOPT-UHFFFAOYSA-N 0.000 claims description 7
- 238000006243 chemical reaction Methods 0.000 claims description 6
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 claims description 5
- JHQVCQDWGSXTFE-UHFFFAOYSA-N 2-(2-prop-2-enoxycarbonyloxyethoxy)ethyl prop-2-enyl carbonate Chemical compound C=CCOC(=O)OCCOCCOC(=O)OCC=C JHQVCQDWGSXTFE-UHFFFAOYSA-N 0.000 claims description 4
- 239000007983 Tris buffer Substances 0.000 claims description 4
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims description 4
- 125000005910 alkyl carbonate group Chemical group 0.000 claims 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 1
- ONIHPYYWNBVMID-UHFFFAOYSA-N diethyl benzene-1,4-dicarboxylate Chemical group CCOC(=O)C1=CC=C(C(=O)OCC)C=C1 ONIHPYYWNBVMID-UHFFFAOYSA-N 0.000 claims 1
- 239000000178 monomer Substances 0.000 abstract description 6
- 239000003999 initiator Substances 0.000 abstract description 4
- -1 allyl ester Chemical class 0.000 abstract description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 abstract description 2
- 230000000704 physical effect Effects 0.000 abstract description 2
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 abstract 1
- 125000002348 vinylic group Chemical group 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 description 33
- 229920000642 polymer Polymers 0.000 description 26
- 238000005452 bending Methods 0.000 description 13
- 229940126062 Compound A Drugs 0.000 description 11
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 11
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 8
- 229920005372 Plexiglas® Polymers 0.000 description 8
- BLCKNMAZFRMCJJ-UHFFFAOYSA-N cyclohexyl cyclohexyloxycarbonyloxy carbonate Chemical compound C1CCCCC1OC(=O)OOC(=O)OC1CCCCC1 BLCKNMAZFRMCJJ-UHFFFAOYSA-N 0.000 description 8
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 7
- 238000001228 spectrum Methods 0.000 description 7
- 238000002834 transmittance Methods 0.000 description 6
- 238000005299 abrasion Methods 0.000 description 5
- 238000006116 polymerization reaction Methods 0.000 description 5
- ORLQHILJRHBSAY-UHFFFAOYSA-N [1-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1(CO)CCCCC1 ORLQHILJRHBSAY-UHFFFAOYSA-N 0.000 description 3
- 125000001931 aliphatic group Chemical group 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- 239000007795 chemical reaction product Substances 0.000 description 3
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 150000001340 alkali metals Chemical class 0.000 description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000004926 polymethyl methacrylate Substances 0.000 description 2
- LVTJOONKWUXEFR-FZRMHRINSA-N protoneodioscin Natural products O(C[C@@H](CC[C@]1(O)[C@H](C)[C@@H]2[C@]3(C)[C@H]([C@H]4[C@@H]([C@]5(C)C(=CC4)C[C@@H](O[C@@H]4[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@@H](O)[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@H](CO)O4)CC5)CC3)C[C@@H]2O1)C)[C@H]1[C@H](O)[C@H](O)[C@H](O)[C@@H](CO)O1 LVTJOONKWUXEFR-FZRMHRINSA-N 0.000 description 2
- 239000000523 sample Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 229920001187 thermosetting polymer Polymers 0.000 description 2
- DNIAPMSPPWPWGF-VKHMYHEASA-N (+)-propylene glycol Chemical compound C[C@H](O)CO DNIAPMSPPWPWGF-VKHMYHEASA-N 0.000 description 1
- KOMNUTZXSVSERR-UHFFFAOYSA-N 1,3,5-tris(prop-2-enyl)-1,3,5-triazinane-2,4,6-trione Chemical compound C=CCN1C(=O)N(CC=C)C(=O)N(CC=C)C1=O KOMNUTZXSVSERR-UHFFFAOYSA-N 0.000 description 1
- YPFDHNVEDLHUCE-UHFFFAOYSA-N 1,3-propanediol Substances OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 1
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 1
- YIFFAEJYCUTZAO-UHFFFAOYSA-N 2-(4-propylphenoxy)ethanol Chemical compound CCCC1=CC=C(OCCO)C=C1 YIFFAEJYCUTZAO-UHFFFAOYSA-N 0.000 description 1
- QCDWFXQBSFUVSP-UHFFFAOYSA-N 2-phenoxyethanol Chemical compound OCCOC1=CC=CC=C1 QCDWFXQBSFUVSP-UHFFFAOYSA-N 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- QRSMGLFRLGLECG-UHFFFAOYSA-N C12C(CC(CC1)C2O)O.C(COCCO)O Chemical compound C12C(CC(CC1)C2O)O.C(COCCO)O QRSMGLFRLGLECG-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 239000004641 Diallyl-phthalate Substances 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- 230000002745 absorbent Effects 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- QUDWYFHPNIMBFC-UHFFFAOYSA-N bis(prop-2-enyl) benzene-1,2-dicarboxylate Chemical compound C=CCOC(=O)C1=CC=CC=C1C(=O)OCC=C QUDWYFHPNIMBFC-UHFFFAOYSA-N 0.000 description 1
- ZDNFTNPFYCKVTB-UHFFFAOYSA-N bis(prop-2-enyl) benzene-1,4-dicarboxylate Chemical group C=CCOC(=O)C1=CC=C(C(=O)OCC=C)C=C1 ZDNFTNPFYCKVTB-UHFFFAOYSA-N 0.000 description 1
- HABAXTXIECRCKH-UHFFFAOYSA-N bis(prop-2-enyl) butanedioate Chemical compound C=CCOC(=O)CCC(=O)OCC=C HABAXTXIECRCKH-UHFFFAOYSA-N 0.000 description 1
- FPODCVUTIPDRTE-UHFFFAOYSA-N bis(prop-2-enyl) hexanedioate Chemical compound C=CCOC(=O)CCCCC(=O)OCC=C FPODCVUTIPDRTE-UHFFFAOYSA-N 0.000 description 1
- 229960003655 bromfenac Drugs 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 235000013351 cheese Nutrition 0.000 description 1
- 238000012993 chemical processing Methods 0.000 description 1
- HNEGQIOMVPPMNR-IHWYPQMZSA-N citraconic acid Chemical compound OC(=O)C(/C)=C\C(O)=O HNEGQIOMVPPMNR-IHWYPQMZSA-N 0.000 description 1
- 239000013068 control sample Substances 0.000 description 1
- XLJMAIOERFSOGZ-UHFFFAOYSA-M cyanate Chemical compound [O-]C#N XLJMAIOERFSOGZ-UHFFFAOYSA-M 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- PYGSKMBEVAICCR-UHFFFAOYSA-N hexa-1,5-diene Chemical group C=CCCC=C PYGSKMBEVAICCR-UHFFFAOYSA-N 0.000 description 1
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
- 230000002706 hydrostatic effect Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- UFWIBTONFRDIAS-UHFFFAOYSA-N naphthalene-acid Natural products C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 1
- QIWKUEJZZCOPFV-UHFFFAOYSA-N phenyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC1=CC=CC=C1 QIWKUEJZZCOPFV-UHFFFAOYSA-N 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 239000003505 polymerization initiator Substances 0.000 description 1
- 229920000166 polytrimethylene carbonate Polymers 0.000 description 1
- OUJKULZFRNPRHO-UHFFFAOYSA-N prop-2-enyl 2-(2-oxo-2-prop-2-enoxyethoxy)acetate Chemical compound C=CCOC(=O)COCC(=O)OCC=C OUJKULZFRNPRHO-UHFFFAOYSA-N 0.000 description 1
- BWJUFXUULUEGMA-UHFFFAOYSA-N propan-2-yl propan-2-yloxycarbonyloxy carbonate Chemical compound CC(C)OC(=O)OOC(=O)OC(C)C BWJUFXUULUEGMA-UHFFFAOYSA-N 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 description 1
- GJBRNHKUVLOCEB-UHFFFAOYSA-N tert-butyl benzenecarboperoxoate Chemical compound CC(C)(C)OOC(=O)C1=CC=CC=C1 GJBRNHKUVLOCEB-UHFFFAOYSA-N 0.000 description 1
- 150000003627 tricarboxylic acid derivatives Chemical class 0.000 description 1
- 229940113165 trimethylolpropane Drugs 0.000 description 1
- KOZCZZVUFDCZGG-UHFFFAOYSA-N vinyl benzoate Chemical compound C=COC(=O)C1=CC=CC=C1 KOZCZZVUFDCZGG-UHFFFAOYSA-N 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 238000001429 visible spectrum Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F263/00—Macromolecular compounds obtained by polymerising monomers on to polymers of esters of unsaturated alcohols with saturated acids as defined in group C08F18/00
- C08F263/06—Macromolecular compounds obtained by polymerising monomers on to polymers of esters of unsaturated alcohols with saturated acids as defined in group C08F18/00 on to polymers of esters with polycarboxylic acids
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B1/00—Optical elements characterised by the material of which they are made; Optical coatings for optical elements
- G02B1/04—Optical elements characterised by the material of which they are made; Optical coatings for optical elements made of organic materials, e.g. plastics
Landscapes
- Physics & Mathematics (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Polymerisation Methods In General (AREA)
- Dental Preparations (AREA)
- Macromonomer-Based Addition Polymer (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT19085/83A IT1160172B (it) | 1983-01-13 | 1983-01-13 | Composizione liquida polimerizzabile, atta a produrre polimeri con elevate caratteristiche ottiche e meccaniche e polimeri e manufatti ottenuti da detta composizione |
| IT1908583 | 1983-01-13 |
Publications (4)
| Publication Number | Publication Date |
|---|---|
| FI840115A0 FI840115A0 (fi) | 1984-01-13 |
| FI840115L FI840115L (fi) | 1984-07-14 |
| FI76818B FI76818B (fi) | 1988-08-31 |
| FI76818C true FI76818C (fi) | 1988-12-12 |
Family
ID=11154413
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FI840115A FI76818C (fi) | 1983-01-13 | 1984-01-13 | Vaetskekomposition som kan polymeriseras och som har utmaerkta mekaniska och optiska egenskaper. |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US4521577A (en, 2012) |
| EP (1) | EP0114080B1 (en, 2012) |
| JP (1) | JPS59140214A (en, 2012) |
| AT (1) | ATE33255T1 (en, 2012) |
| CA (1) | CA1217299A (en, 2012) |
| DE (1) | DE3470164D1 (en, 2012) |
| DK (1) | DK8284A (en, 2012) |
| ES (1) | ES529261A0 (en, 2012) |
| FI (1) | FI76818C (en, 2012) |
| GR (1) | GR79457B (en, 2012) |
| IE (1) | IE56546B1 (en, 2012) |
| IT (1) | IT1160172B (en, 2012) |
| NO (1) | NO161745C (en, 2012) |
| PT (1) | PT77960B (en, 2012) |
Families Citing this family (30)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6075448A (ja) * | 1983-10-03 | 1985-04-27 | Tokuyama Soda Co Ltd | 芳香環を有する多価アルコ−ルのアリルカ−ボネ−トの製造方法 |
| JPS60104040A (ja) * | 1983-11-11 | 1985-06-08 | Tokuyama Soda Co Ltd | 芳香族二価アルコールのアリルカーボネートの製造方法 |
| JPS6155106A (ja) * | 1984-08-24 | 1986-03-19 | Tokuyama Soda Co Ltd | 液状プレポリマーの製造方法 |
| US4623708A (en) | 1985-03-01 | 1986-11-18 | Coburn Optical Industries, Inc. | Prepolymerization of monomer compositions containing diethylene glycol bis(allyl carbonate) |
| US5173552A (en) * | 1985-03-29 | 1992-12-22 | Enichem Sintesi S.P.A. | Process for the production of thermoformed articles by polymerizing compositions comprising diethylene glycol bis (allylcarbonate) |
| IT1183525B (it) * | 1985-03-29 | 1987-10-22 | Enichem Sintesi | Procedimento per la produzione di articoli termoformati |
| IT1191615B (it) * | 1985-05-15 | 1988-03-23 | Enichem Sintesi | Procedimento per la preparazione di sostituti di vetri ottici e composizione liquida polimerizzabile adatta allo scopo |
| CA1239739A (en) * | 1985-07-19 | 1988-07-26 | Hideo Nakamoto | Plastic lens |
| GB8529006D0 (en) * | 1985-11-25 | 1986-01-02 | Highgate D J | Hydrophilic materials |
| IT1207518B (it) * | 1985-12-19 | 1989-05-25 | Enichem Sintesi | Composizione liquida e polimerizzabile per la produzionedi sostituiti di vetri ottici. |
| US4713433A (en) * | 1986-04-17 | 1987-12-15 | Enichem Sintesi S.P.A. | Liquid and polymerizable composition suitable for the production of organic glasses endowed with high abrasion strength |
| US5204430A (en) * | 1987-03-16 | 1993-04-20 | Enichem Synthesis, S.P.A. | Liquid polymerizable composition for the production of high refractive index optical articles |
| IT1228546B (it) * | 1987-07-31 | 1991-06-20 | Enichem Sintesi | Composizione liquida polimerizzabile in vetri organici dotati di elevata stabilita' termica |
| IE890134L (en) * | 1988-02-02 | 1989-08-02 | Akzo Nv | Photochromic compositions |
| US5101264A (en) * | 1988-03-31 | 1992-03-31 | Mitsui Petrochemical Ind. | Light-emitting or receiving device with smooth and hard encapsulant resin |
| US5070215A (en) * | 1989-05-02 | 1991-12-03 | Bausch & Lomb Incorporated | Novel vinyl carbonate and vinyl carbamate contact lens material monomers |
| JPH03116857A (ja) * | 1989-09-29 | 1991-05-17 | Mitsui Petrochem Ind Ltd | 発光または受光装置 |
| JP2592010B2 (ja) * | 1990-08-20 | 1997-03-19 | 昭和電工株式会社 | アリルエステルオリゴマー組成物およびそれを用いた光学材料用有機ガラス |
| JPH0760201B2 (ja) * | 1991-11-01 | 1995-06-28 | 日本油脂株式会社 | 光学用注型成形樹脂製レンズ |
| US5336743A (en) * | 1991-11-01 | 1994-08-09 | Nof Corporation | Cast resin for optical use |
| US5756618A (en) * | 1997-02-14 | 1998-05-26 | Akzo Nobel Nv | Polyol(allyl carbonate) compositions containing epoxy for reduced shrinkage |
| EP1023618B1 (en) | 1997-09-30 | 2005-05-18 | Great Lakes Chemical Corporation | Ophthalmic lenses |
| US5952441A (en) * | 1997-12-30 | 1999-09-14 | Ppg Industries Ohio, Inc. | Partially polymerized mixture of diethylene glycol (allyl carbonate) compounds |
| JP2001201605A (ja) * | 1999-11-11 | 2001-07-27 | Showa Denko Kk | プラスチックレンズ用組成物、プラスチックレンズ及び該プラスチックレンズの製造方法 |
| JP2001201604A (ja) * | 1999-11-11 | 2001-07-27 | Showa Denko Kk | プラスチックレンズ用組成物、プラスチックレンズ及び該プラスチックレンズの製造方法 |
| JP2001201603A (ja) * | 1999-11-11 | 2001-07-27 | Showa Denko Kk | プラスチックレンズ用組成物、プラスチックレンズ及び該プラスチックレンズの製造方法 |
| KR100677864B1 (ko) * | 2000-04-19 | 2007-02-05 | 주식회사 창우정밀화학 | 자외선 차단 능력이 있는 플라스틱 렌즈용광학원재료 |
| KR20000058427A (ko) * | 2000-05-22 | 2000-10-05 | 한정민 | 광학용 주형 성형 모노머 |
| FR2832717B1 (fr) * | 2001-11-26 | 2004-07-09 | Essilor Int | Composition polymerisable par voie radicalaire conduisant a des verres organiques resistants au choc |
| WO2018035112A1 (en) | 2016-08-16 | 2018-02-22 | Ppg Industries Ohio, Inc. | Polymerizable composition for optical articles |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL291866A (en, 2012) * | 1962-05-03 | |||
| JPS4830505A (en, 2012) * | 1971-08-23 | 1973-04-21 | ||
| JPS5845445B2 (ja) * | 1975-03-26 | 1983-10-11 | 日本原子力研究所 | 透明プラスチック成形体の製法 |
| DE2740243A1 (de) * | 1977-09-07 | 1979-03-15 | Bayer Ag | Verfahren zur herstellung von dialkylcarbonaten |
| IT1130285B (it) * | 1980-03-05 | 1986-06-11 | Anic Spa | Procedimento per la sintesi di allil carbonati di alcoli poliidrici e loro derivati |
| US4369298A (en) * | 1980-05-27 | 1983-01-18 | Tokuyama Soda Kabushiki Kaisha | Novel cured resin, process for production thereof, and lens composed of said resin from bis(alkyleneoxyphenyl)-diacrylate, bis(alkyleneoxyphenyl)diallyl ether, bis(alkyleneoxyphenyl)diallyl carbonate monomers |
| US4368310A (en) * | 1981-10-23 | 1983-01-11 | Ppg Industries, Inc. | Method of polymerizing sheets |
| US4398008A (en) * | 1981-12-07 | 1983-08-09 | Ppg Industries, Inc. | Thick polyol (allyl carbonate) polymerizates and method of preparing same |
| JPS61411A (ja) * | 1984-06-12 | 1986-01-06 | Mitsubishi Plastics Ind Ltd | 油水分離器 |
-
1983
- 1983-01-13 IT IT19085/83A patent/IT1160172B/it active
-
1984
- 1984-01-06 EP EP84200015A patent/EP0114080B1/en not_active Expired
- 1984-01-06 DE DE8484200015T patent/DE3470164D1/de not_active Expired
- 1984-01-06 US US06/568,726 patent/US4521577A/en not_active Expired - Lifetime
- 1984-01-06 AT AT84200015T patent/ATE33255T1/de not_active IP Right Cessation
- 1984-01-09 DK DK8284A patent/DK8284A/da not_active Application Discontinuation
- 1984-01-09 CA CA000444920A patent/CA1217299A/en not_active Expired
- 1984-01-11 NO NO840085A patent/NO161745C/no unknown
- 1984-01-11 GR GR73484A patent/GR79457B/el unknown
- 1984-01-12 IE IE55/84A patent/IE56546B1/en not_active IP Right Cessation
- 1984-01-12 JP JP59002782A patent/JPS59140214A/ja active Granted
- 1984-01-13 ES ES529261A patent/ES529261A0/es active Granted
- 1984-01-13 FI FI840115A patent/FI76818C/fi not_active IP Right Cessation
- 1984-01-13 PT PT77960A patent/PT77960B/pt not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| CA1217299A (en) | 1987-01-27 |
| EP0114080B1 (en) | 1988-03-30 |
| IT1160172B (it) | 1987-03-04 |
| GR79457B (en, 2012) | 1984-10-30 |
| ES8506768A1 (es) | 1985-07-16 |
| FI840115A0 (fi) | 1984-01-13 |
| FI76818B (fi) | 1988-08-31 |
| IE56546B1 (en) | 1991-08-28 |
| DK8284D0 (da) | 1984-01-09 |
| DK8284A (da) | 1984-07-14 |
| IT8319085A0 (it) | 1983-01-13 |
| IE840055L (en) | 1984-07-13 |
| FI840115L (fi) | 1984-07-14 |
| JPS59140214A (ja) | 1984-08-11 |
| ES529261A0 (es) | 1985-07-16 |
| PT77960B (en) | 1986-06-18 |
| NO161745B (no) | 1989-06-12 |
| EP0114080A1 (en) | 1984-07-25 |
| DE3470164D1 (en) | 1988-05-05 |
| JPH0440366B2 (en, 2012) | 1992-07-02 |
| NO840085L (no) | 1984-07-16 |
| PT77960A (en) | 1984-02-01 |
| US4521577A (en) | 1985-06-04 |
| NO161745C (no) | 1989-09-20 |
| IT8319085A1 (it) | 1984-07-13 |
| ATE33255T1 (de) | 1988-04-15 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MM | Patent lapsed |
Owner name: ENICHEM SYNTHESIS S.P.A. |