JPH04247336A - Optical disk - Google Patents
Optical diskInfo
- Publication number
- JPH04247336A JPH04247336A JP3033368A JP3336891A JPH04247336A JP H04247336 A JPH04247336 A JP H04247336A JP 3033368 A JP3033368 A JP 3033368A JP 3336891 A JP3336891 A JP 3336891A JP H04247336 A JPH04247336 A JP H04247336A
- Authority
- JP
- Japan
- Prior art keywords
- weight
- curable resin
- optical disc
- component
- resin composition
- 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.)
- Pending
Links
- 230000003287 optical effect Effects 0.000 title claims abstract description 23
- 238000000576 coating method Methods 0.000 claims abstract description 23
- 239000011248 coating agent Substances 0.000 claims abstract description 22
- 239000003945 anionic surfactant Substances 0.000 claims abstract description 7
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims abstract description 4
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims abstract description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 4
- 239000011342 resin composition Substances 0.000 claims description 17
- -1 sulfate ester salt Chemical class 0.000 claims description 14
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 4
- 229920003171 Poly (ethylene oxide) Polymers 0.000 claims description 4
- 229920001451 polypropylene glycol Polymers 0.000 claims description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 claims description 2
- 239000003973 paint Substances 0.000 claims 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 abstract description 11
- 229920000515 polycarbonate Polymers 0.000 abstract description 9
- 239000004417 polycarbonate Substances 0.000 abstract description 9
- 229920005989 resin Polymers 0.000 abstract description 4
- 239000011347 resin Substances 0.000 abstract description 4
- GVGUFUZHNYFZLC-UHFFFAOYSA-N dodecyl benzenesulfonate;sodium Chemical compound [Na].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVGUFUZHNYFZLC-UHFFFAOYSA-N 0.000 abstract description 2
- 229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 abstract description 2
- 239000003999 initiator Substances 0.000 description 9
- 239000000203 mixture Substances 0.000 description 9
- 229910052708 sodium Inorganic materials 0.000 description 7
- 239000011734 sodium Substances 0.000 description 7
- 238000001723 curing Methods 0.000 description 6
- 239000000758 substrate Substances 0.000 description 6
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 5
- 150000001875 compounds Chemical class 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
- 238000000034 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
- 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 4
- 235000014113 dietary fatty acids Nutrition 0.000 description 4
- 229930195729 fatty acid Natural products 0.000 description 4
- 239000000194 fatty acid Substances 0.000 description 4
- MCWMYICYUGCRDY-UHFFFAOYSA-N 2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCOCCOCCO MCWMYICYUGCRDY-UHFFFAOYSA-N 0.000 description 3
- LWRBVKNFOYUCNP-UHFFFAOYSA-N 2-methyl-1-(4-methylsulfanylphenyl)-2-morpholin-4-ylpropan-1-one Chemical compound C1=CC(SC)=CC=C1C(=O)C(C)(C)N1CCOCC1 LWRBVKNFOYUCNP-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- OWYWGLHRNBIFJP-UHFFFAOYSA-N Ipazine Chemical compound CCN(CC)C1=NC(Cl)=NC(NC(C)C)=N1 OWYWGLHRNBIFJP-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 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 description 3
- 230000003993 interaction Effects 0.000 description 3
- 239000000178 monomer Substances 0.000 description 3
- KCTAWXVAICEBSD-UHFFFAOYSA-N prop-2-enoyloxy prop-2-eneperoxoate Chemical compound C=CC(=O)OOOC(=O)C=C KCTAWXVAICEBSD-UHFFFAOYSA-N 0.000 description 3
- 238000004528 spin coating Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- RBGUKBSLNOTVCD-UHFFFAOYSA-N 1-methylanthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2C RBGUKBSLNOTVCD-UHFFFAOYSA-N 0.000 description 2
- KAUGIRRQYAWBDG-UHFFFAOYSA-N 2-[2-[2-(2-hydroxypropoxy)propoxy]propoxy]propan-1-ol;2-methylprop-2-enoic acid Chemical compound CC(=C)C(O)=O.CC(O)COC(C)COC(C)COC(C)CO KAUGIRRQYAWBDG-UHFFFAOYSA-N 0.000 description 2
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 2
- RIWRBSMFKVOJMN-UHFFFAOYSA-N 2-methyl-1-phenylpropan-2-ol Chemical compound CC(C)(O)CC1=CC=CC=C1 RIWRBSMFKVOJMN-UHFFFAOYSA-N 0.000 description 2
- 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 description 2
- 239000004342 Benzoyl peroxide Substances 0.000 description 2
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- 239000002216 antistatic agent Substances 0.000 description 2
- ISAOCJYIOMOJEB-UHFFFAOYSA-N benzoin Chemical compound C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 description 2
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 2
- 239000012965 benzophenone Substances 0.000 description 2
- 235000019400 benzoyl peroxide Nutrition 0.000 description 2
- 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 2
- 230000000052 comparative effect Effects 0.000 description 2
- 239000000428 dust Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000010894 electron beam technology Methods 0.000 description 2
- UHESRSKEBRADOO-UHFFFAOYSA-N ethyl carbamate;prop-2-enoic acid Chemical compound OC(=O)C=C.CCOC(N)=O UHESRSKEBRADOO-UHFFFAOYSA-N 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 150000002367 halogens Chemical class 0.000 description 2
- 230000001678 irradiating effect Effects 0.000 description 2
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 2
- GKTNLYAAZKKMTQ-UHFFFAOYSA-N n-[bis(dimethylamino)phosphinimyl]-n-methylmethanamine Chemical class CN(C)P(=N)(N(C)C)N(C)C GKTNLYAAZKKMTQ-UHFFFAOYSA-N 0.000 description 2
- 229920003986 novolac Polymers 0.000 description 2
- 229920005668 polycarbonate resin Polymers 0.000 description 2
- 239000004431 polycarbonate resin Substances 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- CAVXVRQDZKMZDB-UHFFFAOYSA-M sodium;2-[dodecanoyl(methyl)amino]ethanesulfonate Chemical compound [Na+].CCCCCCCCCCCC(=O)N(C)CCS([O-])(=O)=O CAVXVRQDZKMZDB-UHFFFAOYSA-M 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- VNQXSTWCDUXYEZ-UHFFFAOYSA-N 1,7,7-trimethylbicyclo[2.2.1]heptane-2,3-dione Chemical compound C1CC2(C)C(=O)C(=O)C1C2(C)C VNQXSTWCDUXYEZ-UHFFFAOYSA-N 0.000 description 1
- DRONDEZXOJEUGU-UHFFFAOYSA-N 2,3-diphenylpropanenitrile Chemical compound C=1C=CC=CC=1C(C#N)CC1=CC=CC=C1 DRONDEZXOJEUGU-UHFFFAOYSA-N 0.000 description 1
- BTJPUDCSZVCXFQ-UHFFFAOYSA-N 2,4-diethylthioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC(CC)=CC(CC)=C3SC2=C1 BTJPUDCSZVCXFQ-UHFFFAOYSA-N 0.000 description 1
- OLQFXOWPTQTLDP-UHFFFAOYSA-N 2-(2-hydroxyethoxy)ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCO OLQFXOWPTQTLDP-UHFFFAOYSA-N 0.000 description 1
- XMNIXWIUMCBBBL-UHFFFAOYSA-N 2-(2-phenylpropan-2-ylperoxy)propan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)OOC(C)(C)C1=CC=CC=C1 XMNIXWIUMCBBBL-UHFFFAOYSA-N 0.000 description 1
- MZGMQAMKOBOIDR-UHFFFAOYSA-N 2-[2-(2-hydroxyethoxy)ethoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCOCCO MZGMQAMKOBOIDR-UHFFFAOYSA-N 0.000 description 1
- QUASZQPLPKGIJY-UHFFFAOYSA-N 2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]ethyl prop-2-enoate Chemical compound OCCOCCOCCOCCOC(=O)C=C QUASZQPLPKGIJY-UHFFFAOYSA-N 0.000 description 1
- HMGGNDFOUYIJKG-UHFFFAOYSA-N 2-[2-[2-(2-hydroxypropoxy)propoxy]propoxy]propan-1-ol;prop-2-enoic acid Chemical compound OC(=O)C=C.CC(O)COC(C)COC(C)COC(C)CO HMGGNDFOUYIJKG-UHFFFAOYSA-N 0.000 description 1
- GYIXDFJDLKMWAA-UHFFFAOYSA-N 2-[2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]ethoxy]ethyl prop-2-enoate Chemical compound OCCOCCOCCOCCOCCOC(=O)C=C GYIXDFJDLKMWAA-UHFFFAOYSA-N 0.000 description 1
- UHBKLFLAVYCZEP-UHFFFAOYSA-N 2-[2-[2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethyl prop-2-enoate Chemical compound OCCOCCOCCOCCOCCOCCOC(=O)C=C UHBKLFLAVYCZEP-UHFFFAOYSA-N 0.000 description 1
- TXBCBTDQIULDIA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)CO TXBCBTDQIULDIA-UHFFFAOYSA-N 0.000 description 1
- 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 description 1
- VHSHLMUCYSAUQU-UHFFFAOYSA-N 2-hydroxypropyl methacrylate Chemical compound CC(O)COC(=O)C(C)=C VHSHLMUCYSAUQU-UHFFFAOYSA-N 0.000 description 1
- FRIBMENBGGCKPD-UHFFFAOYSA-N 3-(2,3-dimethoxyphenyl)prop-2-enal Chemical compound COC1=CC=CC(C=CC=O)=C1OC FRIBMENBGGCKPD-UHFFFAOYSA-N 0.000 description 1
- ZHBIWFGGIKFSHZ-UHFFFAOYSA-N 3-(4-chlorophenyl)propan-1-ol Chemical compound OCCCC1=CC=C(Cl)C=C1 ZHBIWFGGIKFSHZ-UHFFFAOYSA-N 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- 235000013162 Cocos nucifera Nutrition 0.000 description 1
- 244000060011 Cocos nucifera Species 0.000 description 1
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 1
- YIVJZNGAASQVEM-UHFFFAOYSA-N Lauroyl peroxide Chemical compound CCCCCCCCCCCC(=O)OOC(=O)CCCCCCCCCCC YIVJZNGAASQVEM-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- 244000028419 Styrax benzoin Species 0.000 description 1
- 235000000126 Styrax benzoin Nutrition 0.000 description 1
- 235000008411 Sumatra benzointree Nutrition 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- MPIAGWXWVAHQBB-UHFFFAOYSA-N [3-prop-2-enoyloxy-2-[[3-prop-2-enoyloxy-2,2-bis(prop-2-enoyloxymethyl)propoxy]methyl]-2-(prop-2-enoyloxymethyl)propyl] prop-2-enoate Chemical class C=CC(=O)OCC(COC(=O)C=C)(COC(=O)C=C)COCC(COC(=O)C=C)(COC(=O)C=C)COC(=O)C=C MPIAGWXWVAHQBB-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 235000015278 beef Nutrition 0.000 description 1
- 229960002130 benzoin Drugs 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 229930006711 bornane-2,3-dione Natural products 0.000 description 1
- KVNRLNFWIYMESJ-UHFFFAOYSA-N butyronitrile Chemical compound CCCC#N KVNRLNFWIYMESJ-UHFFFAOYSA-N 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000002542 deteriorative effect Effects 0.000 description 1
- LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 description 1
- 125000005594 diketone group Chemical group 0.000 description 1
- 238000003618 dip coating Methods 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
- 235000019382 gum benzoic Nutrition 0.000 description 1
- 238000013007 heat curing Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- YLHXLHGIAMFFBU-UHFFFAOYSA-N methyl phenylglyoxalate Chemical compound COC(=O)C(=O)C1=CC=CC=C1 YLHXLHGIAMFFBU-UHFFFAOYSA-N 0.000 description 1
- 229920002601 oligoester Polymers 0.000 description 1
- AZQWKYJCGOJGHM-UHFFFAOYSA-N para-benzoquinone Natural products O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 239000003505 polymerization initiator Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229940096992 potassium oleate Drugs 0.000 description 1
- MLICVSDCCDDWMD-KVVVOXFISA-M potassium;(z)-octadec-9-enoate Chemical compound [K+].CCCCCCCC\C=C/CCCCCCCC([O-])=O MLICVSDCCDDWMD-KVVVOXFISA-M 0.000 description 1
- 239000007870 radical polymerization initiator Substances 0.000 description 1
- 238000012827 research and development Methods 0.000 description 1
- 150000004671 saturated fatty acids Chemical class 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 239000007784 solid electrolyte Substances 0.000 description 1
- 150000008054 sulfonate salts Chemical class 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- 229940104261 taurate Drugs 0.000 description 1
- 238000012719 thermal polymerization Methods 0.000 description 1
- YRHRIQCWCFGUEQ-UHFFFAOYSA-N thioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3SC2=C1 YRHRIQCWCFGUEQ-UHFFFAOYSA-N 0.000 description 1
- 238000002834 transmittance Methods 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 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
Landscapes
- Optical Record Carriers And Manufacture Thereof (AREA)
- Paints Or Removers (AREA)
- Macromonomer-Based Addition Polymer (AREA)
Abstract
Description
【0001】0001
【産業上の利用分野】本発明は、レーザーなどの光によ
り、情報の記録、再生を行う光ディスクに関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an optical disc on which information is recorded and reproduced using light such as a laser.
【0002】0002
【従来の技術】光ディスクは、高密度・大容量の情報記
録媒体として注目され種々のタイプの光ディスクの研究
開発が行われている。これらの中で、消去可能で書換え
可能な光磁気ディスクは利用分野が広く、将来への期待
が大きい。そのため、種々の材料・システムが発表され
ており、その実用化が期待される。2. Description of the Related Art Optical disks have attracted attention as high-density, large-capacity information recording media, and research and development are being carried out on various types of optical disks. Among these, erasable and rewritable magneto-optical disks have a wide range of applications and have high expectations for the future. For this reason, various materials and systems have been announced, and their practical application is expected.
【0003】これらの光ディスクには、ほこりなどの付
着を防止するために帯電防止処理を行う必要があり、通
常は基板の表面に帯電防止剤を塗工したり、帯電防止剤
の基板への練り込みによる方法などがとられている。し
かし、前者の処理では耐久性に問題があり、後者では成
型性、光透過性の点で問題がある。[0003] These optical disks require antistatic treatment to prevent the adhesion of dust, etc., and usually an antistatic agent is applied to the surface of the substrate, or an antistatic agent is kneaded into the substrate. Methods such as inclusion are being used. However, the former treatment has problems with durability, and the latter has problems with moldability and light transmittance.
【0004】一方、光ディスクの基板は一般的にはポリ
カーボネート樹脂などが用いられるために、基板の表面
硬度が小さい。そこで、表面の損傷を避けるためにUV
硬化樹脂などにより表面硬化処理を施すことが提案され
ている。しかし、これらのUV硬化樹脂の塗工による被
覆では、ディスクの回転中の空気との摩擦による樹脂の
帯電があり、ゴミ、ホコリの付着による読み出し面の汚
れなどが多く、記録、読み出し信号の信頼性を低下させ
ている。On the other hand, since polycarbonate resin or the like is generally used for the substrate of an optical disk, the surface hardness of the substrate is low. Therefore, to avoid surface damage, UV
It has been proposed to perform surface hardening treatment using a hardened resin or the like. However, with these UV-curable resin coatings, the resin is charged due to friction with the air while the disk is rotating, and the readout surface is often dirty due to dirt and dust, making the recording and readout signals unreliable. deteriorating sexuality.
【0005】[0005]
【発明が解決しようとする課題】本発明は、耐久性に優
れた帯電防止性を有し、しかも、十分な表面硬度を有す
る光ディスクの提供を目的とする。さらに詳しくは、表
面電気抵抗が低くかつ表面硬度の高い塗膜を基板上に設
けた光デイスクの提供を目的とする。SUMMARY OF THE INVENTION An object of the present invention is to provide an optical disk having excellent durability and antistatic properties, and also having sufficient surface hardness. More specifically, the object is to provide an optical disk in which a coating film with low surface electrical resistance and high surface hardness is provided on a substrate.
【0006】[0006]
【課題を解決するための手段】本発明者等は、塗工性の
観点から無溶媒でも薄膜塗工が可能な低粘度の紫外線(
UV)硬化性樹脂組成物に焦点を当てた。しかしながら
、一般にUV硬化性樹脂組成物を硬化してなる塗膜の表
面電気抵抗は高く帯電防止性に劣る。本発明者らはこの
点の解決をはかるために鋭意検討の結果、オリゴエチレ
ンオキシドのモノ(メタ)アクリレートが、モノマー中
のOH基とアルキレンオキシドユニットを有するために
低い表面電気抵抗を有する硬化塗膜を与えることを見い
だし既に提案した(特願平2−172655)。このオ
リゴエチレンオキシドのモノ(メタ)アクリレートは単
官能性であるため硬化性の点からはできるだけ少ない量
で低い表面抵抗を有する硬化塗膜を得ることが望ましい
。本発明者らは、このモノ(メタ)アクリレートをでき
るだけ少量にして低い表面抵抗を有し、硬度の高い硬化
性樹脂組成物を得ることを目的として鋭意検討を行った
。その結果、該オリゴエチレンまたはプロピレンオキシ
ドのモノ(メタ)アクリレートと陰イオン系界面活性剤
とを組み合わせることにより、十分な硬度を保持したま
まで、硬化物の表面電気抵抗を大きく減少させることが
できることを見いだし本発明に到達した。[Means for Solving the Problems] From the viewpoint of coating properties, the present inventors have developed a method using low-viscosity ultraviolet light (
Focused on UV) curable resin compositions. However, coating films formed by curing UV curable resin compositions generally have high surface electrical resistance and poor antistatic properties. As a result of intensive studies to solve this problem, the present inventors found that mono(meth)acrylate of oligoethylene oxide has an OH group and an alkylene oxide unit in the monomer, resulting in a cured coating film with low surface electrical resistance. We have already proposed this method (Japanese Patent Application No. 172655/1999). Since this mono(meth)acrylate of oligoethylene oxide is monofunctional, from the viewpoint of curability, it is desirable to obtain a cured coating film having a low surface resistance with as little amount as possible. The present inventors conducted extensive studies with the aim of obtaining a curable resin composition with low surface resistance and high hardness by reducing the amount of this mono(meth)acrylate as much as possible. As a result, by combining the mono(meth)acrylate of oligoethylene or propylene oxide with an anionic surfactant, the surface electrical resistance of the cured product can be significantly reduced while maintaining sufficient hardness. They discovered this and arrived at the present invention.
【0007】即ち、本発明は、光ディスクの少なくとも
光照射面(読み取り面)を、
(A)一般式(I)That is, the present invention provides that at least the light irradiation surface (reading surface) of an optical disc is formed by (A) general formula (I).
【0008】[0008]
【化2】
(式中、R1 ,R2 は水素原子またはメチル基を、
nは1〜23の整数を示す。)で表されるエチレンオキ
シドもしくはポリエチレンオキシド、またはプロピレン
オキシドもしくはポリプロピレンオキシドのモノ(メタ
)アクリル酸エステルが硬化性樹脂組成物中に3〜40
重量%、および
(B)陰イオン系界面活性剤が成分(A)に対して0.
01〜200重量%含有され、かつ成分(A),(B)
の合計量が50重量%以下である硬化性樹脂組成物を硬
化してなる塗膜で被覆したことを特徴とする光ディスク
である。[Formula 2] (wherein R1 and R2 are hydrogen atoms or methyl groups,
n represents an integer of 1 to 23. ) ethylene oxide or polyethylene oxide, or propylene oxide or polypropylene oxide mono(meth)acrylic acid ester is present in the curable resin composition in an amount of 3 to 40
% by weight, and (B) anionic surfactant relative to component (A).
01 to 200% by weight, and components (A) and (B)
An optical disk characterized in that it is coated with a coating film formed by curing a curable resin composition having a total amount of 50% by weight or less.
【0009】一般式(I)中、R1 ,R2 は水素原
子またはメチル基を、nは1〜23の整数を示す。nは
2〜20が好ましく、3〜15が特に好ましい。前述の
成分(A)と(B)との後述の相互作用面からはnが大
きい方が好ましいが、nが大きくなると相溶性が低下し
、且つ粘度が増大するためにnが23以下のものが適用
される。一般式(I)で表されるポリエチレンオキシド
またはポリプロピレンオキシドのモノ(メタ)アクリル
酸エステルとしては、例えば、2−ヒドロキシエチルメ
タクリレート、2−ヒドロキシエチルアクリレート、2
−ヒドロキシプロピルアクリレート、2−ヒドロキシプ
ロピルメタクリレート、ジエチレングリコールモノメタ
クリレート、トリエチレングリコールモノメタクリレー
ト、テトラエチレングリコールモノメタクリレート、ペ
ンタエチレングリコールモノアクリレート、ヘキサエチ
レングリコールモノアクリレート、テトラプロピレング
リコールモノメタクリレート、テトラプロピレングリコ
ールモノアクリレート、In the general formula (I), R1 and R2 represent a hydrogen atom or a methyl group, and n represents an integer of 1 to 23. n is preferably 2-20, particularly preferably 3-15. From the viewpoint of the interaction between the above-mentioned components (A) and (B), which will be described later, it is preferable that n is larger, but as n becomes larger, the compatibility decreases and the viscosity increases. applies. Examples of the mono(meth)acrylic acid ester of polyethylene oxide or polypropylene oxide represented by the general formula (I) include 2-hydroxyethyl methacrylate, 2-hydroxyethyl acrylate, 2-hydroxyethyl acrylate,
-Hydroxypropyl acrylate, 2-hydroxypropyl methacrylate, diethylene glycol monomethacrylate, triethylene glycol monomethacrylate, tetraethylene glycol monomethacrylate, pentaethylene glycol monoacrylate, hexaethylene glycol monoacrylate, tetrapropylene glycol monomethacrylate, tetrapropylene glycol monoacrylate ,
【0010】0010
【化3】
(MA−150、日本乳化剤(株)製)、などが挙げら
れるがこの限りでない。Examples include, but are not limited to, (MA-150, manufactured by Nippon Nyukazai Co., Ltd.).
【0011】本発明の成分(A)の一般式(I)で表さ
れるポリエチレンオキシドまたはポリプロピレンオキシ
ドのモノ(メタ)アクリル酸エステルは、該組成物中3
〜40重量%、好ましくは5〜35重量%含有される。
また、陰イオン系界面活性剤は成分(A)に対して0.
01〜200重量%であり、更には0.1〜100重量
%含有させるのが好ましい。両者の量は用いる化合物に
より適宜この範囲内で選ばれる。成分(A)と成分(B
)は相互に働き硬化物に優れた帯電防止性を付与する。
理由は定かでないが、成分(A)が固体電解質的な役割
をして成分(B)と特殊な相互作用をしているものと推
定される。The mono(meth)acrylic acid ester of polyethylene oxide or polypropylene oxide represented by the general formula (I) as component (A) of the present invention contains 3 in the composition.
-40% by weight, preferably 5-35% by weight. In addition, the anionic surfactant is 0.0% relative to component (A).
The content is preferably 0.1 to 200% by weight, and more preferably 0.1 to 100% by weight. The amounts of both are appropriately selected within this range depending on the compound used. Component (A) and component (B
) work together to impart excellent antistatic properties to the cured product. Although the reason is not clear, it is presumed that component (A) plays the role of a solid electrolyte and has a special interaction with component (B).
【0012】該成分(A)が3重量%未満では成分(B
)との相互作用の割合が不十分で帯電防止効果が不足し
、一方、40重量%を超えると該組成物で被覆し硬化さ
せた光ディスクの表面皮膜硬度が不十分で好ましくない
。なお、成分(A),(B)の合計量が50重量%を越
えると硬化性が不十分となり十分な硬度を持った塗膜が
得られない。When the component (A) is less than 3% by weight, the component (B) is less than 3% by weight.
) is insufficient and the antistatic effect is insufficient. On the other hand, if it exceeds 40% by weight, the surface coating hardness of the optical disc coated and cured with the composition is undesirable. If the total amount of components (A) and (B) exceeds 50% by weight, curing properties will be insufficient and a coating film with sufficient hardness will not be obtained.
【0013】成分(B)の陰イオン界面活性剤としては
、飽和や不飽和の脂肪酸アルカリ金属塩、飽和や不飽和
の脂肪族のスルホン酸塩、置換基を含んでもよい芳香族
のスルホン酸塩、エチレンオキシド単位を含むスルホン
酸塩、各種置換基を含むサルフェートのナトリウム塩な
どが挙げられる。具体的にはトデシルベンゼンスルホン
酸ナトリウム、アシル(牛脂)メチルタウリン酸ナトリ
ウム、ラウロイルメチルタウリン酸ナトリウム、ソジウ
ム・ココイル・イセチネート、α−スルホ脂肪酸エステ
ルナトリウム塩、アシドエーテルソジウムサルフェート
、アルキルエーテルスルホン酸ナトリウム、アルキルサ
ルフェートナトリウム塩、アルキルエーテルサルフェー
トナトリウム塩、オレイン酸カリウム、ヤシ脂肪酸カリ
ウムなどの脂肪酸石鹸が挙げられる。この中で前記相互
作用の面からスルホン酸の塩化合物、硫酸エステルの塩
化合物が好ましい。As the anionic surfactant of component (B), saturated or unsaturated fatty acid alkali metal salts, saturated or unsaturated aliphatic sulfonates, aromatic sulfonates which may contain substituents are used. , sulfonate salts containing ethylene oxide units, and sodium salts of sulfates containing various substituents. Specifically, sodium todecylbenzene sulfonate, sodium acyl (beef tallow) methyl taurate, sodium lauroyl methyl taurate, sodium cocoyl isetinate, α-sulfo fatty acid ester sodium salt, acid ether sodium sulfate, alkyl ether sulfonic acid. Examples include fatty acid soaps such as sodium, alkyl sulfate sodium salts, alkyl ether sulfate sodium salts, potassium oleate, and potassium coconut fatty acids. Among these, sulfonic acid salt compounds and sulfuric acid ester salt compounds are preferred from the viewpoint of the interaction.
【0014】本発明において、前記成分(A)の化合物
以外の硬化性樹脂組成物には、一般に知られた重合性単
量体や重合性オリゴマー、重合性プレポリマーが用いら
れる。例えばビスフェノールAエポキシアクリレート、
脂肪酸変性エポキシアクリレート、ノボラックエポキシ
アクリレート、フェノールノボラックエポキシアクリレ
ート、ポリエステルオリゴウレタンアクリレート、多官
能ヒドロキシ化合物のウレタンアクリレート、ポリブタ
ジエンアクリレート、ペンタエリスリトールテトラ(メ
タ)アクリレート、ジペンタエリスリトールヘキサ(メ
タ)アクリレート、トリメチロールプロパントリ(メタ
)アクリレート、(ポリ)アルキレングリコールのジ(
メタ)アクリレートなどの脂肪族多官能アクリレート、
多官能オリゴエステルアクリレート、多官能ポリエステ
ルアクリレート、ホスファゼン化合物のアクリレート変
性物、イソシアヌル酸の多官能アクリレート、その他ビ
ニル重合性化合物、アクリル系重合性化合物などが使用
できる。これらの重合性化合物は単独あるいは混合して
使用される。In the present invention, generally known polymerizable monomers, polymerizable oligomers, and polymerizable prepolymers are used as the curable resin composition other than the compound of component (A). For example, bisphenol A epoxy acrylate,
Fatty acid modified epoxy acrylate, novolac epoxy acrylate, phenol novolac epoxy acrylate, polyester oligourethane acrylate, polyfunctional hydroxy compound urethane acrylate, polybutadiene acrylate, pentaerythritol tetra(meth)acrylate, dipentaerythritol hexa(meth)acrylate, trimethylolpropane Tri(meth)acrylate, di(poly)alkylene glycol
aliphatic polyfunctional acrylates such as meth)acrylates,
Polyfunctional oligoester acrylates, polyfunctional polyester acrylates, acrylate modified products of phosphazene compounds, polyfunctional acrylates of isocyanuric acid, other vinyl polymerizable compounds, acrylic polymerizable compounds, etc. can be used. These polymerizable compounds may be used alone or in combination.
【0015】本発明の硬化性樹脂組成物は、必要に応じ
て、光重合開始剤、熱重合開始剤などのラジカル重合開
始剤などを添加して用いる。光重合開始剤としては、ベ
ンゾフェノン、ミヒラーズケトンなどのベンゾフェノン
系開始剤、ベンジル、フェニルメトキシジケトンなどの
ジケトン系開始剤、アセトフェノンなどのアセトフェノ
ン系開始剤、ベンゾインエチルエーテル、ベンジルジメ
チルケタールなどのベンゾイン系開始剤、2,4−ジエ
チルチオキサントンなどのチオキサントン系開始剤、2
−メチルアントラキノン、カンファーキノンなどのキノ
ン系開始剤などが好適に用いられる。必要に応じてアミ
ン系促進剤などの促進剤の併用も可能である。熱硬化の
場合にはアゾビスイスブチロニトリル(AIBN)、ベ
ンゾイルペルオキシド(BPO)、クメンヒドロペルオ
キシド、ジクミルペルオキシド、ジターシャリーブチル
ペルオキシド、ラウロイルペルオキシドなどが挙げられ
る。
用いる開始剤量としては、コスト等の実用面からその上
限は制限され、該組成物100重量部に対して1〜10
重量部、好ましくは2〜5重量部が用いられる。The curable resin composition of the present invention may be used with the addition of a radical polymerization initiator such as a photopolymerization initiator or a thermal polymerization initiator, if necessary. Examples of photopolymerization initiators include benzophenone initiators such as benzophenone and Michler's ketone, diketone initiators such as benzyl and phenylmethoxydiketone, acetophenone initiators such as acetophenone, and benzoin initiators such as benzoin ethyl ether and benzyl dimethyl ketal. , thioxanthone-based initiators such as 2,4-diethylthioxanthone, 2
- Quinone-based initiators such as methylanthraquinone and camphorquinone are preferably used. If necessary, it is also possible to use a promoter such as an amine promoter. In the case of heat curing, azobiswiss butyronitrile (AIBN), benzoyl peroxide (BPO), cumene hydroperoxide, dicumyl peroxide, ditertiary butyl peroxide, lauroyl peroxide and the like can be used. The upper limit of the amount of initiator used is limited from practical aspects such as cost, and is 1 to 10 parts by weight per 100 parts by weight of the composition.
Parts by weight are used, preferably 2 to 5 parts by weight.
【0016】本発明の硬化性樹脂組成物は塗布性の改善
、作業性の向上などのために、必要に応じて溶媒で希釈
される。なお、ポリカーボネート樹脂を基板として用い
る場合はメタノール、エタノール、イソプロパノールな
どのアルコール性溶媒が好適に用いられる。The curable resin composition of the present invention may be diluted with a solvent, if necessary, in order to improve coating properties and workability. Note that when polycarbonate resin is used as a substrate, alcoholic solvents such as methanol, ethanol, and isopropanol are preferably used.
【0017】本発明の硬化性樹脂組成物は、公知のスピ
ンコーティング法、浸漬コーティング法、ドクターナイ
フによるコーティング、バーコーターによる方法で、光
ディスクの表面を被覆することが出来る。光ディスクの
被覆にあたっては、光ディスクの側面をも被覆すると帯
電防止効果を向上させることが出来る。The curable resin composition of the present invention can be coated on the surface of an optical disk by a known method such as spin coating, dip coating, coating with a doctor knife, or coating with a bar coater. When coating an optical disk, the antistatic effect can be improved by also coating the side surfaces of the optical disk.
【0018】本発明の硬化後の塗膜の厚さは1〜30μ
m であり、好ましくは5〜25μm である。1μm
未満では硬度の上で十分な性能が発揮されず、30μ
m を越える膜厚制御が困難になるばかりか、内部の硬
化性が低下するために好ましくない。[0018] The thickness of the coating film after curing of the present invention is 1 to 30μ.
m, preferably 5 to 25 μm. 1μm
If the hardness is less than 30μ, sufficient performance will not be exhibited in terms of hardness.
If the thickness exceeds m, it is not only difficult to control the film thickness, but also the internal hardening properties are lowered, which is not preferable.
【0019】重合性単量体組成物を塗布した光ディスク
は低圧水銀灯、中圧水銀灯、高圧水銀灯などの紫外ラン
プ、ハロゲンランプ、電子線などの活性光線、あるいは
熱処理などを用いて公知の方法、条件により硬化される
。この中で、紫外ランプ、ハロゲンランプ、電子線など
の活性光線を用いるのが操作性、生産性の観点から好ま
しい。The optical disc coated with the polymerizable monomer composition is prepared using known methods and conditions using ultraviolet lamps such as low-pressure mercury lamps, medium-pressure mercury lamps, and high-pressure mercury lamps, halogen lamps, actinic light such as electron beams, or heat treatment. hardened by Among these, it is preferable to use actinic light such as an ultraviolet lamp, a halogen lamp, or an electron beam from the viewpoint of operability and productivity.
【0020】本発明で得られる光ディスクの表面抵抗は
1015Ω/□未満が好ましく、1014Ω/□以下が
更に好ましい。これ以上の抵抗を有するものは帯電防止
性の観点から効果がない。また、表面硬度は取扱いの観
点から鉛筆硬度がHB以上のものが好しく、F以上のも
のが更に好ましい。The surface resistance of the optical disc obtained by the present invention is preferably less than 1015 Ω/□, more preferably 1014 Ω/□ or less. Those having a resistance higher than this are ineffective from the viewpoint of antistatic properties. In addition, from the viewpoint of handling, the surface hardness is preferably a pencil hardness of HB or higher, and more preferably a pencil hardness of F or higher.
【0021】[0021]
【発明の効果】本発明は、高度の耐久性をもつ帯電防止
能を有し、しかも充分な表面硬度を有する光ディスクを
提供することができる。Industrial Applicability According to the present invention, it is possible to provide an optical disk having highly durable antistatic properties and sufficient surface hardness.
【0022】[0022]
【実施例】以下実施例により本発明をさらに詳細に説明
する。本発明はかかる実施例に限定されない。EXAMPLES The present invention will be explained in more detail with reference to Examples below. The invention is not limited to such embodiments.
【0023】実施例において、表面抵抗(Ω/□)はJ
IS K6911によった。また、鉛筆硬度は、三菱
鉛筆製ユニを用いて測定した。In the example, the surface resistance (Ω/□) is J
According to IS K6911. Moreover, the pencil hardness was measured using Uni manufactured by Mitsubishi Pencil.
【0024】[0024]
【実施例1】厚さ1.2mmのポリカーボネートディス
クのフラット面にアクリル系の光硬化性樹脂組成物であ
る日本精化(株)のNSC−7106が96重量%、下
記式で表わされる日本乳化剤(株)のMA150が4重
量%からなる組成物100重量部に、ドデシルベンゼン
スルホン酸ナトリウムを0.1重量部含む硬化性組成物
を5〜10μm の厚さになるようにスピンコート法に
より塗布した。引き続き、長さ約27cm、2Kwの高
圧水銀灯を用い、20cmの高さから紫外線を1分間照
射し、塗膜を硬化させた。[Example 1] 96% by weight of NSC-7106 from Nippon Fine Chemical Co., Ltd., an acrylic photocurable resin composition, was applied to the flat surface of a polycarbonate disk with a thickness of 1.2 mm, and Nippon Emulsifier represented by the following formula was applied. A curable composition containing 0.1 part by weight of sodium dodecylbenzenesulfonate is applied to 100 parts by weight of a composition containing 4% by weight of MA150 manufactured by Co., Ltd. to a thickness of 5 to 10 μm by spin coating. did. Subsequently, the coating film was cured by irradiating it with ultraviolet rays for 1 minute from a height of 20 cm using a 2 Kw high-pressure mercury lamp with a length of about 27 cm.
【0025】[0025]
【化4】
硬化後のポリカーボネートディスクの硬化面について、
表面抵抗および鉛筆硬度を測定した。鉛筆硬度はHであ
り、表面抵抗は9.8×1013Ω/□であった。[Chemical 4] Regarding the hardened surface of the polycarbonate disk after curing,
Surface resistance and pencil hardness were measured. The pencil hardness was H, and the surface resistance was 9.8×10 13 Ω/□.
【0026】[0026]
【比較例1】厚さ1.2mmのポリカーボネートディス
クのフラット面に前述の日本精化(株)のNSC−71
06を96重量%、日本乳化剤(株)のMA150を4
重量%含む硬化性組成物を5〜10μm の厚さになる
ようにスピンコート法により塗布した。引き続き、長さ
約27cm、2Kwの高圧水銀灯を用い、20cmの高
さから紫外線を1分間照射し、塗膜を硬化させた。硬化
後のポリカーボネートディスクの硬化面について、表面
抵抗および鉛筆硬度を測定した。鉛筆硬度はHであった
が、表面抵抗は1.2×1015Ω/□であった。[Comparative Example 1] The above-mentioned NSC-71 from Nippon Fine Chemical Co., Ltd. was applied to the flat surface of a 1.2 mm thick polycarbonate disk.
96% by weight of 06 and 4% of MA150 from Nippon Nyukazai Co., Ltd.
% by weight of the curable composition was applied by spin coating to a thickness of 5 to 10 μm. Subsequently, the coating film was cured by irradiating it with ultraviolet rays for 1 minute from a height of 20 cm using a 2 Kw high-pressure mercury lamp with a length of about 27 cm. The surface resistance and pencil hardness of the cured surface of the polycarbonate disk after curing were measured. The pencil hardness was H, and the surface resistance was 1.2×10 15 Ω/□.
【0027】[0027]
【実施例2】6官能ウレタンアクリレートオリゴマー(
U1226A,新中村化学工業(株)製)が50重量%
、トリメチロールプロパントリアクリレートが40重量
%、およびテトラエチレングリコールモノメタクリレー
トが10重量%からなる組成物100重量部に対し、ト
デシルベンゼンスルホン酸ナトリウムを1重量部、光開
始剤ダロキュア1173を3重量部含む硬化性樹脂組成
物を1.2mm厚みのポリカーボネートディスクに塗布
し、前記と同様に光硬化させた。得られたディスクの表
面硬度はFであり、表面抵抗は3.6×1013Ω/□
であった。[Example 2] Hexafunctional urethane acrylate oligomer (
50% by weight of U1226A (manufactured by Shin-Nakamura Chemical Industry Co., Ltd.)
, 40% by weight of trimethylolpropane triacrylate, and 10% by weight of tetraethylene glycol monomethacrylate, 1 part by weight of sodium todecylbenzenesulfonate and 3 parts by weight of the photoinitiator Darocur 1173. The curable resin composition containing 50% of the curable resin composition was applied onto a 1.2 mm thick polycarbonate disk, and photocured in the same manner as described above. The surface hardness of the obtained disk was F, and the surface resistance was 3.6×1013Ω/□
Met.
【0028】[0028]
【比較例2】6官能ウレタンアクリレートオリゴマー(
U1226A,新中村化学工業(株)製)が50重量%
、トリメチロールプロパントリアクリレートが40重量
%、およびテトラエチレングリコールモノメタクリレー
トが10重量%からなる組成物100重量部に、光開始
剤ダロキュア1173を3重量部含む硬化性樹脂組成物
を1.2mm厚みのポリカーボネートディスクに塗布し
、前記と同様に光硬化させた。得られたディスクの表面
硬度はFであり、表面抵抗は1.05×1015Ω/□
であった。[Comparative Example 2] Hexafunctional urethane acrylate oligomer (
50% by weight of U1226A (manufactured by Shin-Nakamura Chemical Industry Co., Ltd.)
A curable resin composition containing 3 parts by weight of the photoinitiator Darocur 1173 was added to 100 parts by weight of a composition consisting of 40% by weight of trimethylolpropane triacrylate and 10% by weight of tetraethylene glycol monomethacrylate to a thickness of 1.2 mm. It was applied onto a polycarbonate disk and photocured in the same manner as above. The surface hardness of the obtained disk is F, and the surface resistance is 1.05×1015Ω/□
Met.
【0029】[0029]
【実施例3】ホスファゼンのヘキサアクリレート(U−
1000,出光石油化学(株)製)が70重量%、テト
ラプロピレングリコールモノメタクリレートが30重量
%からなる組成物100重量部に、アルキルエーテルス
ルホン酸ナトリウム(アバネルS74;日本油脂(株)
製)0.1重量部、光開始剤イルガキュア907(チバ
ガイギー社製)3重量部からなる硬化性樹脂組成物を実
施例1と同様に厚さ1.2mmのポリカーボネートディ
スクのフラット面に塗布し、光硬化させた。硬化塗膜の
表面硬度はHで表面抵抗は3.5×1012Ω/□であ
った。[Example 3] Phosphazene hexaacrylate (U-
1000, manufactured by Idemitsu Petrochemical Co., Ltd.) and 30% by weight of tetrapropylene glycol monomethacrylate, was added sodium alkyl ether sulfonate (Avanel S74; manufactured by NOF Corporation).
A curable resin composition consisting of 0.1 parts by weight of the photoinitiator Irgacure 907 (manufactured by Ciba Geigy) and 3 parts by weight of the photoinitiator Irgacure 907 (manufactured by Ciba Geigy) was applied to the flat surface of a 1.2 mm thick polycarbonate disk in the same manner as in Example 1. Light-cured. The surface hardness of the cured coating film was H and the surface resistance was 3.5×10 12 Ω/□.
【0030】[0030]
【実施例4】カプロラクトン変性ジペンタエリスリトー
ルヘキサアクリレート(DPCA60;日本化薬(株)
製)が60重量%、トリメチロールプロパントリアクリ
レートが20重量%、テトラエチレングリコールモノア
クリレートが20重量%からなる組成物100重量部に
、ラウロイルメチルタウリン酸ナトリウム(ダイヤポン
L;日本油脂(株)製)を2重量部、光開始剤イルガキ
ュア907(チバガイギー社製)を3重量部含む硬化性
樹脂組成物を実施例1と同様に厚さ1.2mmのポリカ
ーボネートディスクのフラット面に塗布し、光硬化させ
た。硬化塗膜の表面硬度はFで、表面抵抗は6.2×1
013Ω/□であった。[Example 4] Caprolactone-modified dipentaerythritol hexaacrylate (DPCA60; Nippon Kayaku Co., Ltd.)
To 100 parts by weight of a composition consisting of 60% by weight of trimethylolpropane triacrylate, 20% by weight of tetraethylene glycol monoacrylate, was added sodium lauroylmethyltaurate (Diapon L; manufactured by NOF Corporation). ) and 3 parts by weight of the photoinitiator Irgacure 907 (manufactured by Ciba Geigy) was applied onto the flat surface of a 1.2 mm thick polycarbonate disk in the same manner as in Example 1, and photocured. I let it happen. The surface hardness of the cured coating is F, and the surface resistance is 6.2×1.
It was 013Ω/□.
Claims (3)
み取り面)を、 (A)一般式(I) 【化1】 (式中、R1 ,R2 は水素原子またはメチル基を、
nは1〜23の整数を示す。)で表されるエチレンオキ
シドもしくはポリエチレンオキシド、またはプロピレン
オキシドもしくはポリプロピレンオキシドのモノ(メタ
)アクリル酸エステルが硬化性樹脂組成物中に3〜40
重量%、および (B)陰イオン系界面活性剤が成分(A)に対して0.
01〜200重量%含有され、かつ成分(A),(B)
の合計量が全体の50重量%以下である硬化性樹脂組成
物を硬化してなる塗膜で被覆したことを特徴とする光デ
ィスク。Claim 1: At least the light irradiation surface (reading surface) of an optical disc is formed by (A) the general formula (I) [Formula 1] (wherein R1 and R2 are hydrogen atoms or methyl groups,
n represents an integer of 1 to 23. ) ethylene oxide or polyethylene oxide, or propylene oxide or polypropylene oxide mono(meth)acrylic acid ester is present in the curable resin composition in an amount of 3 to 40
% by weight, and (B) anionic surfactant relative to component (A).
01 to 200% by weight, and components (A) and (B)
1. An optical disc characterized in that it is coated with a coating film formed by curing a curable resin composition having a total amount of not more than 50% by weight.
の鉛筆硬度がF以上であり、かつ、表面抵抗が1014
Ω/□以下であることを特徴とする請求項1の光デイス
ク。2. A paint film obtained by curing the curable resin composition has a pencil hardness of F or more and a surface resistance of 1014.
2. The optical disc according to claim 1, wherein the optical disc has a resistance of Ω/□ or less.
及び/または硫酸エステルの塩を含むことを特徴とする
請求項1または2の光デイスク。3. The optical disc according to claim 1, wherein the anionic surfactant contains a sulfonate and/or a sulfate ester salt.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3033368A JPH04247336A (en) | 1991-02-04 | 1991-02-04 | Optical disk |
PCT/JP1991/000886 WO1992000588A1 (en) | 1990-07-02 | 1991-07-01 | Optical disk |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3033368A JPH04247336A (en) | 1991-02-04 | 1991-02-04 | Optical disk |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH04247336A true JPH04247336A (en) | 1992-09-03 |
Family
ID=12384643
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP3033368A Pending JPH04247336A (en) | 1990-07-02 | 1991-02-04 | Optical disk |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH04247336A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2012096322A1 (en) * | 2011-01-12 | 2012-07-19 | 三菱レイヨン株式会社 | Active energy ray-curable resin composition, microrelief structure, and method for producing microrelief structure |
-
1991
- 1991-02-04 JP JP3033368A patent/JPH04247336A/en active Pending
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2012096322A1 (en) * | 2011-01-12 | 2012-07-19 | 三菱レイヨン株式会社 | Active energy ray-curable resin composition, microrelief structure, and method for producing microrelief structure |
JP5260790B2 (en) * | 2011-01-12 | 2013-08-14 | 三菱レイヨン株式会社 | Active energy ray-curable resin composition, fine concavo-convex structure, and method for producing fine concavo-convex structure |
US9062142B2 (en) | 2011-01-12 | 2015-06-23 | Mitsubishi Rayon Co., Ltd. | Active energy ray-curable resin composition, product having the uneven microstructure, and method for producing product having the uneven microstructure |
US9234065B2 (en) | 2011-01-12 | 2016-01-12 | Mitsubishi Rayon Co., Ltd. | Active energy ray-curable resin composition, product having the uneven microstructure, and method for producing product having the uneven microstructure |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
WO2009133784A1 (en) | Active energy ray-curable resin composition, cured film, laminate, optical recording medium, and method for producing cured film | |
US8168690B2 (en) | Solvent-free photocurable resin composition for protective film | |
KR20190126447A (en) | Resin composition for coating paint | |
JP2009127023A (en) | Photocurable composition for production of photocurable pressure-sensitive adhesive and photocurable pressure-sensitive adhesive sheet | |
JPH09272707A (en) | Actinic-radiation-curing (meth)acrylate composition | |
JPH03118878A (en) | Formation of cured resin layer having antistatic surface | |
JP2000053735A (en) | Active energy ray-curable resin composition | |
JPH04247336A (en) | Optical disk | |
US7799844B2 (en) | Active energy beam-curable composition for optical material | |
ITRM940161A1 (en) | HARDENING COMPOSITION AND METHOD FOR WOOD IMPREGNATION. | |
JPH11148045A (en) | Active energy light-curable coating composition and formation of coating using the same | |
JPH04247337A (en) | Optical disk | |
JPH0315262B2 (en) | ||
JP2001323005A (en) | Active energy ray-curable composition and coating film- formed body having cured coating film composed of the composition | |
WO1992000588A1 (en) | Optical disk | |
JPH04149280A (en) | Overcoating composition for optical disc | |
JPH04136041A (en) | Production of acrylic or methacrylic ester and coating composition | |
JPH072915B2 (en) | Coating composition | |
JP2003213159A (en) | Coating composition curable with active energy ray | |
JPH08239430A (en) | Fluorine-containing curable composition and water-and oil-repellent material | |
JPH0467330A (en) | Optical disk | |
JPH04247338A (en) | Optical disk | |
JP5014625B2 (en) | Antistatic coating composition and film obtained by curing the same | |
JP2739180B2 (en) | Acrylate-based curable composition | |
JP2006181791A (en) | Transfer material and laminate |