JPS63265636A - Laminated polyester film - Google Patents
Laminated polyester filmInfo
- Publication number
- JPS63265636A JPS63265636A JP62100415A JP10041587A JPS63265636A JP S63265636 A JPS63265636 A JP S63265636A JP 62100415 A JP62100415 A JP 62100415A JP 10041587 A JP10041587 A JP 10041587A JP S63265636 A JPS63265636 A JP S63265636A
- Authority
- JP
- Japan
- Prior art keywords
- film
- colloid
- coating layer
- water
- polyester film
- 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
- 229920006267 polyester film Polymers 0.000 title claims abstract description 30
- 239000011247 coating layer Substances 0.000 claims abstract description 40
- 239000000084 colloidal system Substances 0.000 claims abstract description 37
- 239000002245 particle Substances 0.000 claims abstract description 35
- 239000004925 Acrylic resin Substances 0.000 claims abstract description 16
- 229920000178 Acrylic resin Polymers 0.000 claims abstract description 16
- 230000003287 optical effect Effects 0.000 claims description 2
- -1 alkyl methacrylate Chemical compound 0.000 abstract description 13
- 125000000524 functional group Chemical group 0.000 abstract description 10
- 229910052751 metal Inorganic materials 0.000 abstract description 8
- 239000002184 metal Substances 0.000 abstract description 8
- 125000005250 alkyl acrylate group Chemical group 0.000 abstract description 6
- 238000003475 lamination Methods 0.000 abstract description 6
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 abstract description 6
- 229920002554 vinyl polymer Polymers 0.000 abstract description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 abstract description 4
- 239000000178 monomer Substances 0.000 abstract description 2
- 239000010408 film Substances 0.000 description 89
- 238000000576 coating method Methods 0.000 description 24
- 239000011248 coating agent Substances 0.000 description 22
- 239000002585 base Substances 0.000 description 21
- 238000000034 method Methods 0.000 description 15
- 239000000463 material Substances 0.000 description 13
- 150000001875 compounds Chemical class 0.000 description 12
- 239000010410 layer Substances 0.000 description 11
- 239000011347 resin Substances 0.000 description 9
- 229920005989 resin Polymers 0.000 description 9
- 150000003839 salts Chemical class 0.000 description 9
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 9
- 229920000298 Cellophane Polymers 0.000 description 7
- 238000005299 abrasion Methods 0.000 description 7
- 125000003277 amino group Chemical group 0.000 description 7
- 230000000903 blocking effect Effects 0.000 description 7
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 229920000728 polyester Polymers 0.000 description 6
- 229920000139 polyethylene terephthalate Polymers 0.000 description 6
- 239000005020 polyethylene terephthalate Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 125000003368 amide group Chemical group 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 4
- 239000011230 binding agent Substances 0.000 description 4
- 238000007796 conventional method Methods 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical class OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 3
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 125000004018 acid anhydride group Chemical group 0.000 description 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 230000002950 deficient Effects 0.000 description 3
- 125000003700 epoxy group Chemical group 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- 239000002966 varnish Substances 0.000 description 3
- UZKWTJUDCOPSNM-UHFFFAOYSA-N 1-ethenoxybutane Chemical compound CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 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 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical compound C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 2
- 239000002390 adhesive tape Substances 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 230000002776 aggregation Effects 0.000 description 2
- 150000003863 ammonium salts Chemical class 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- FUSUHKVFWTUUBE-UHFFFAOYSA-N buten-2-one Chemical compound CC(=O)C=C FUSUHKVFWTUUBE-UHFFFAOYSA-N 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 239000010954 inorganic particle Substances 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- 239000000314 lubricant Substances 0.000 description 2
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 2
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Chemical class OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 2
- 229920000620 organic polymer Polymers 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 229920001228 polyisocyanate Polymers 0.000 description 2
- 239000005056 polyisocyanate Substances 0.000 description 2
- 239000002491 polymer binding agent Substances 0.000 description 2
- 229920001451 polypropylene glycol Polymers 0.000 description 2
- 238000012805 post-processing Methods 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 238000007639 printing Methods 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- 239000010703 silicon Substances 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 230000003746 surface roughness Effects 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Chemical class OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- YNULEHPRJFDRBI-UHFFFAOYSA-N (1-ethenoxy-2-methylpropan-2-yl)urea Chemical compound NC(=O)NC(C)(C)COC=C YNULEHPRJFDRBI-UHFFFAOYSA-N 0.000 description 1
- VSDMVRFSCLVCOF-UHFFFAOYSA-N 1-ethenoxybutan-2-amine Chemical compound CCC(N)COC=C VSDMVRFSCLVCOF-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical class COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical class FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-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
- ISPYQTSUDJAMAB-UHFFFAOYSA-N 2-chlorophenol Chemical compound OC1=CC=CC=C1Cl ISPYQTSUDJAMAB-UHFFFAOYSA-N 0.000 description 1
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-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
- GWZMWHWAWHPNHN-UHFFFAOYSA-N 2-hydroxypropyl prop-2-enoate Chemical compound CC(O)COC(=O)C=C GWZMWHWAWHPNHN-UHFFFAOYSA-N 0.000 description 1
- AGBXYHCHUYARJY-UHFFFAOYSA-N 2-phenylethenesulfonic acid Chemical class OS(=O)(=O)C=CC1=CC=CC=C1 AGBXYHCHUYARJY-UHFFFAOYSA-N 0.000 description 1
- KGIGUEBEKRSTEW-UHFFFAOYSA-N 2-vinylpyridine Chemical compound C=CC1=CC=CC=N1 KGIGUEBEKRSTEW-UHFFFAOYSA-N 0.000 description 1
- JPVNTYZOJCDQBK-UHFFFAOYSA-N 3-ethenoxypropan-1-amine Chemical compound NCCCOC=C JPVNTYZOJCDQBK-UHFFFAOYSA-N 0.000 description 1
- BCTDCDYHRUIHSF-UHFFFAOYSA-N 5-ethenoxypentan-1-ol Chemical compound OCCCCCOC=C BCTDCDYHRUIHSF-UHFFFAOYSA-N 0.000 description 1
- ASPUDHDPXIBNAP-UHFFFAOYSA-N 6-ethenoxyhexan-1-ol Chemical compound OCCCCCCOC=C ASPUDHDPXIBNAP-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- 229920002799 BoPET Polymers 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical class CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Chemical class OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
- 238000004220 aggregation Methods 0.000 description 1
- 229910052910 alkali metal silicate Inorganic materials 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 150000001350 alkyl halides Chemical class 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
- 239000002518 antifoaming agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 150000001541 aziridines Chemical class 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 239000003990 capacitor Substances 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 150000001805 chlorine compounds Chemical group 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 230000008094 contradictory effect Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 238000003851 corona treatment Methods 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical class C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- FOTKYAAJKYLFFN-UHFFFAOYSA-N decane-1,10-diol Chemical compound OCCCCCCCCCCO FOTKYAAJKYLFFN-UHFFFAOYSA-N 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 230000002542 deteriorative effect Effects 0.000 description 1
- VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000012777 electrically insulating material Substances 0.000 description 1
- FDJZLUVCWCJZTC-UHFFFAOYSA-N ethenoxyurea Chemical compound NC(=O)NOC=C FDJZLUVCWCJZTC-UHFFFAOYSA-N 0.000 description 1
- NKSJNEHGWDZZQF-UHFFFAOYSA-N ethenyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)C=C NKSJNEHGWDZZQF-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 238000009501 film coating Methods 0.000 description 1
- 239000001530 fumaric acid Chemical class 0.000 description 1
- 238000001879 gelation Methods 0.000 description 1
- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 238000007756 gravure coating Methods 0.000 description 1
- 238000007646 gravure printing Methods 0.000 description 1
- 239000012760 heat stabilizer Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical class OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Chemical class 0.000 description 1
- 150000002689 maleic acids Chemical class 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 210000001872 metatarsal bone Anatomy 0.000 description 1
- 239000012046 mixed solvent Substances 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- KYTZHLUVELPASH-UHFFFAOYSA-N naphthalene-1,2-dicarboxylic acid Chemical compound C1=CC=CC2=C(C(O)=O)C(C(=O)O)=CC=C21 KYTZHLUVELPASH-UHFFFAOYSA-N 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- RPQRDASANLAFCM-UHFFFAOYSA-N oxiran-2-ylmethyl prop-2-enoate Chemical compound C=CC(=O)OCC1CO1 RPQRDASANLAFCM-UHFFFAOYSA-N 0.000 description 1
- 239000005022 packaging material Substances 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 230000002829 reductive effect Effects 0.000 description 1
- 230000002040 relaxant effect Effects 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 1
- 150000003440 styrenes Chemical class 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000003457 sulfones Chemical class 0.000 description 1
- 125000000542 sulfonic acid group Chemical group 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 150000008053 sultones Chemical class 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 239000011135 tin Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Chemical class CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 1
- NLVXSWCKKBEXTG-UHFFFAOYSA-N vinylsulfonic acid Chemical class OS(=O)(=O)C=C NLVXSWCKKBEXTG-UHFFFAOYSA-N 0.000 description 1
- 239000013585 weight reducing agent Substances 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Landscapes
- Laminated Bodies (AREA)
- Shaping By String And By Release Of Stress In Plastics And The Like (AREA)
- Coating Of Shaped Articles Made Of Macromolecular Substances (AREA)
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は、積層ポリエステルフィルムの関するものであ
る。詳しくは、透明性、易滑性、易接着性、平滑性に優
れた積層ポリエステルフィルムに関するものである。DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] The present invention relates to a laminated polyester film. Specifically, the present invention relates to a laminated polyester film having excellent transparency, easy sliding properties, easy adhesion properties, and smoothness.
[従来の技術]
ポリエステル二軸延伸フィルムは、その機械的性質、電
気的性質、寸法安定性、透明性などに優れた特性を有す
ることから、磁気記録材料、包装材料、電気絶縁材料、
グラフイツクアーツ材料、写真材料など多くの用途の基
材フィルムとして広く使用されている。しかし、最近、
これらの用途は共通して小型軽量化、高精度化の技術志
向におり、これらに付随してベースフィルムに対する要
求、品質も厳しくなっている。例えば、グラフイックア
ーツの分野では、透明性、易滑性、易接着性、平滑性に
対する要求レベルが高まり、しかも、各特性を同時に保
持したベースフィルムが待望されている。しかし、中で
も透明性と易滑性については、元来、透明性の高いポリ
エステルフィルムは、フィルム同士の滑り性が非常に悪
いため、ブロッキングやスリ傷等の表面欠点を生じたり
、巻き取り性や巻姿の悪化、更には加工時の作業性の悪
さ等を引き起こすことが知られている。しかも、°これ
らの欠点は、ベースフィルムの薄膜化にともない、より
顕著となる傾向にある。このようにポリエステルフィル
ムでは、透明性と易滑性は相反する関係にあり、両特性
を同時に満足させることは難しく、更には易接着性、平
滑性をも同時に有しているフィルムを得ることは困難で
あった。このような諸特性に優れたフィルムを1qるた
めに従来から種々の検討がなされている。[Prior Art] Polyester biaxially stretched film has excellent properties such as mechanical properties, electrical properties, dimensional stability, and transparency, so it can be used as a magnetic recording material, a packaging material, an electrically insulating material,
It is widely used as a base film for many applications such as graphic arts materials and photographic materials. However, recently,
These applications are all technologically oriented toward miniaturization, weight reduction, and high precision, and along with this, the requirements and quality of the base film are also becoming stricter. For example, in the field of graphic arts, the requirements for transparency, easy slippage, easy adhesion, and smoothness are increasing, and there is a long-awaited base film that simultaneously maintains each of these properties. However, in terms of transparency and slipperiness, polyester film, which is highly transparent, has very poor slipping properties between films, which can cause surface defects such as blocking and scratches, and may cause problems with winding properties. It is known that this causes deterioration in the appearance of the roll, and furthermore, poor workability during processing. Moreover, these drawbacks tend to become more noticeable as the base film becomes thinner. In this way, in polyester films, transparency and ease of slipping are in a contradictory relationship, and it is difficult to satisfy both properties at the same time.Furthermore, it is difficult to obtain a film that has both easy adhesion and smoothness at the same time. It was difficult. Various studies have been made in the past in order to create a film that has such excellent properties.
(1〉 透明なフィルム表面上に無機粒子やシリカゾ
ルを含む有機高分子バインダーを塗設したポリエステル
フィルム(特開昭61−2528号公報、特開昭60−
61259号公報)。(1> Polyester film in which an organic polymer binder containing inorganic particles and silica sol is coated on the surface of a transparent film (JP-A-61-2528, JP-A-60-
61259).
(2) 透明なフィルム表面上に塗設した樹脂層の延
伸破断によって、微細な縦長突起を形成させたポリエス
テルフィルム(特開昭61−204240号公報)。(2) A polyester film in which fine longitudinal protrusions are formed by stretching and breaking a resin layer coated on the surface of a transparent film (Japanese Patent Application Laid-Open No. 61-204240).
[発明が解決しようとする問題点]
しかし、前述したポリエステルフィルムには次のような
問題点がある。[Problems to be Solved by the Invention] However, the above-mentioned polyester film has the following problems.
上記(1)のフィルムでは、無機粒子を用いた場合は、
有機高分子バインダーへの均一分散が難しいため、フィ
ルム特性にバラツキが生じたり、ざらには塗膜に凝集粒
子による粗大突起が発生しやすいため、透明性や平滑性
の低下、更には、突起の脱落による弊害が増し易い。ま
た、シリカゾルを滑剤として用いた場合は、従来公知の
ものは、微細なため、易滑性は多聞添加によってのみ発
現するが、反面、透明性や易接着性の低下を引き起こし
易い。更には、ベースフィルムが薄くなると十分な易滑
効果は(qられない。In the film of (1) above, when inorganic particles are used,
Uniform dispersion into the organic polymer binder is difficult, resulting in variations in film properties and coarse protrusions caused by agglomerated particles on the coating film, resulting in decreased transparency and smoothness, and even more protrusions. The harm caused by falling off is likely to increase. Furthermore, when silica sol is used as a lubricant, since the silica sol known in the art is fine, slipperiness can only be achieved by adding a large amount of silica sol, but on the other hand, it tends to cause a decrease in transparency and easy adhesion. Furthermore, if the base film becomes thin, sufficient slipping effect cannot be achieved.
上記(2)のフィルムでは、突起形状が微細なためベー
スフィルムが薄くなると滑り性が不十分となるのみなら
ず、塗膜に発生した亀裂による透明性の低下も起き易い
。In the film of (2) above, since the protrusions are fine, if the base film becomes thin, not only the slipperiness becomes insufficient, but also the transparency tends to decrease due to cracks generated in the coating film.
本発明は、これらの従来技術の欠点を解消せしめ、透明
性、易滑性、易接着性、平滑性とが共に優れ、しかも易
滑性の耐久性、耐摩耗性にも優れた積層ポリエステルフ
ィルムを提供せんとするものである。The present invention solves the drawbacks of these conventional techniques and provides a laminated polyester film that has excellent transparency, easy slipping, easy adhesion, and smoothness, and also has excellent durability and abrasion resistance of easy slipping. We aim to provide the following.
[問題点を解決するための手段]
本発明は、ポルエステルフィルムの少なくとも片面に、
平均粒径0.11〜0.4μmの無機コロイドと水溶性
あるいは水分散性アクリル系樹脂とを主成分とする被覆
層を設けてなる積層ポリエステルフィルムであって、該
無機コロイドの平均粒径(D)と該被覆層厚み(d)の
比(D/d)が1.1〜80の範囲にあることを特徴と
する積層ポリエステルフィルムに関するものである。[Means for Solving the Problems] The present invention provides at least one side of the polyester film,
A laminated polyester film comprising a coating layer mainly composed of an inorganic colloid with an average particle size of 0.11 to 0.4 μm and a water-soluble or water-dispersible acrylic resin, the film having an average particle size of the inorganic colloid ( The present invention relates to a laminated polyester film characterized in that the ratio (D/d) between D) and the thickness (d) of the coating layer is in the range of 1.1 to 80.
本発明においていう、ポリエステルとは、周知のもの、
具体的には例えばテレフタル酸、イソフタル酸、ナフタ
レンジカルボン酸、ビス−α、β(2−クロルフェノキ
シ)エタン−4,4−ジカルボン酸、アジピン酸、セバ
シン酸等の2官能カルボン酸の少なくとも1種と、エチ
レングリコール、トリエチレングリコール、テトラメチ
レングリコール、ヘキサメチレングリコール、デカメチ
レングリコール等のグリコールの少なくとも1種とを重
縮合して得られるポリエステルを挙げることができる。In the present invention, polyester refers to well-known polyesters,
Specifically, at least one difunctional carboxylic acid such as terephthalic acid, isophthalic acid, naphthalene dicarboxylic acid, bis-α, β(2-chlorophenoxy)ethane-4,4-dicarboxylic acid, adipic acid, and sebacic acid. and at least one type of glycol such as ethylene glycol, triethylene glycol, tetramethylene glycol, hexamethylene glycol, and decamethylene glycol.
また、該ポリエステルには本発明の目的を阻害しない範
囲内で他種ポリマをブレンドしたり、共重合してもよい
し、酸化防止剤、熱安定剤、滑剤、顔料、紫外線吸収剤
等が含まれていてもよい。In addition, the polyester may be blended or copolymerized with other polymers within a range that does not impede the purpose of the present invention, and may contain antioxidants, heat stabilizers, lubricants, pigments, ultraviolet absorbers, etc. It may be
ポリエステルの固有粘度(25℃オルトクロルフェノー
ル中で測定)は、0.4〜2.0であり、好ましくは0
.5〜1.0の範囲のものが通常用いられる。The intrinsic viscosity of the polyester (measured in orthochlorophenol at 25°C) is 0.4 to 2.0, preferably 0.
.. A value in the range of 5 to 1.0 is usually used.
本発明には、ポリエステルとしてポリエチレンテレフタ
レート、ポリエチレン−2,6−ナフタレートを用いた
場合、特に優れた効果が得られ。In the present invention, particularly excellent effects can be obtained when polyethylene terephthalate or polyethylene-2,6-naphthalate is used as the polyester.
本発明でいう被覆層とは、無機コロイドと水溶性あるい
は水分散性アクリル系樹脂とを主成分としたものからな
る層である。主成分とは、そのものが被覆層中70%以
上を占めることをいう。本発明においては、かかる被覆
層を前記ポリエステルフィルムの少なくとも片面に設け
るのであるが、この中で両面に設ける場合には、以下に
述べる該層の説明は、少なくとも一方に適用されるもの
である。The coating layer in the present invention is a layer mainly composed of an inorganic colloid and a water-soluble or water-dispersible acrylic resin. The term "main component" means that the component itself occupies 70% or more of the coating layer. In the present invention, such a coating layer is provided on at least one side of the polyester film, but when it is provided on both sides, the following description of the layer applies to at least one side.
本発明でいう無機コロイドとは、井守出版社化学大辞典
に定義されており、粒子1個中に105〜109個の原
子を含むものである。元素により金属コロイド、おるい
は酸化物コロイド、あるいは水酸化物コロイドとして得
られる。金属コロイドとしては、金、パラジウム、白金
、銀、イオウなどが好ましく使用され、酸化物コロイド
、水酸化物]イド、炭酸塩コロイド、硫酸塩コロイドと
しては、亜鉛、マグネシウム、ケイ素、カルシウム、ア
ルミニウム、ストロンチウム、バリウム、ジルコニウム
、チタン、マンガン、鉄、コバルト、ニッケル、スズな
どの酸化物コロイド、水酸化物コロイド、炭酸塩コロイ
ド、硫酸塩コロイドが本発明に好ましく使用される。例
えば四ハロゲン化ケイ素を水中に加えるか、ケイ酸アル
カリの水溶液に徐々に濃塩酸を加えるなどの操作により
得られるケイ酸コロイドが本発明には極めて好ましく使
用される。The inorganic colloid as used in the present invention is defined in the Imori Publishing Co., Ltd. Chemistry Dictionary, and contains 105 to 109 atoms in one particle. Depending on the element, it can be obtained as a metal colloid, oxide colloid, or hydroxide colloid. Preferably used metal colloids include gold, palladium, platinum, silver, and sulfur; examples of oxide colloids, hydroxide colloids, carbonate colloids, and sulfate colloids include zinc, magnesium, silicon, calcium, aluminum, Oxide colloids, hydroxide colloids, carbonate colloids, sulfate colloids such as strontium, barium, zirconium, titanium, manganese, iron, cobalt, nickel, tin, etc. are preferably used in the present invention. For example, silicic acid colloids obtained by adding silicon tetrahalide to water or gradually adding concentrated hydrochloric acid to an aqueous solution of alkali silicate are very preferably used in the present invention.
無機コロイドの平均粒径は0.11〜0.4μm、好ま
しくは0.13〜0.3μm1より好ましくは0.15
〜0.25μmの範囲であることが必要である。平均粒
径が0.11μm以下では、積層フィルムの易滑性が不
十分となる。更には、粒子の凝集性が高まるため、粗大
異物の発生によって、透明性の低下を起こしやすくなる
。0.4μmを越えるものは、積層フィルム表面が顕著
に粗れたり、耐摩耗性が悪化しやすくなるのみならず、
無機コロイド粒子の水溶液中での安定性が著しく悪化し
、場合によっては、粒子の沈澱、凝集、ゲル化等が発生
する。更には、フィルムフレークの回収、再利用におい
て粒子の混入により、フィルムの表面粗れが助長され、
平滑性が悪化する。The average particle size of the inorganic colloid is 0.11 to 0.4 μm, preferably 0.13 to 0.3 μm, more preferably 0.15 μm.
It is necessary that it is in the range of ~0.25 μm. If the average particle size is 0.11 μm or less, the slipperiness of the laminated film will be insufficient. Furthermore, since the agglomeration of the particles increases, the transparency tends to decrease due to the generation of coarse foreign matter. If the thickness exceeds 0.4 μm, not only will the surface of the laminated film become noticeably rough and the abrasion resistance will deteriorate;
The stability of the inorganic colloid particles in an aqueous solution deteriorates significantly, and in some cases, precipitation, aggregation, gelation, etc. of the particles occur. Furthermore, during the recovery and reuse of film flakes, the surface roughness of the film is promoted due to the contamination of particles.
Smoothness deteriorates.
なお、ここでいう平均粒子径とは、無機コロイド水溶液
を遠心沈降式粒度分布測定装置(島津製作所(株)製5
A−CP2型)を用いて測定したものである。The average particle diameter here refers to the inorganic colloid aqueous solution measured using a centrifugal sedimentation particle size distribution analyzer (Shimadzu Corporation 5).
A-CP2 type).
本発明でいう水分散性あるいは水溶性アクリル系樹脂(
以下アクリル系樹脂と略称する)は、アルキルアクリレ
ートあるいはアルキルメタクリレートを主要な成分とす
るものが好ましく、該成分30〜90モル%と、これら
と共重合可能でかつ官能基を有するビニル中足体成分7
0〜10モル%を含有する水溶性あるいは水分散性樹脂
が好ましい。Water-dispersible or water-soluble acrylic resin (
The acrylic resin (hereinafter abbreviated as acrylic resin) is preferably one containing alkyl acrylate or alkyl methacrylate as a main component, with 30 to 90 mol% of this component and a vinyl metatarsal component copolymerizable with these components and having a functional group. 7
Water-soluble or water-dispersible resins containing 0 to 10 mol% are preferred.
アルキルアクリレートおるいはアルキルメタクリレート
と共重合可能でかつ官能基を有するビニル単母体は、樹
脂に親水性を付与して樹脂の水分散性を良好にしたり、
あるいは樹脂とポリエステルフィルムや、下塗り層上に
設ける伯の塗布層との接着性を良好にする官能基を有す
るものが好ましく、好ましい官能基とは、カルボキシル
基またはその塩、酸無水物基、スルホン酸基、またはそ
の塩、アミド基またはアルキロール化されたアミド基、
アミノ基(置換アミノ基を含む)またはアルキロール化
されたアミノ基あるいはそれらの塩、水酸基、エポキシ
基等である。特に好ましいものはカルボキシル基または
その塩、酸無水物基、エポキ基などである。これらの基
は、樹脂中に二種以上含有されていてもよい。A vinyl monobase that is copolymerizable with alkyl acrylate or alkyl methacrylate and has a functional group imparts hydrophilicity to the resin and improves the water dispersibility of the resin.
Alternatively, it is preferable to have a functional group that improves the adhesion between the resin and the polyester film or the coating layer provided on the undercoat layer. Preferred functional groups include a carboxyl group or a salt thereof, an acid anhydride group, and a sulfone. acid group or its salt, amide group or alkylolated amide group,
These include amino groups (including substituted amino groups), alkylolated amino groups, salts thereof, hydroxyl groups, and epoxy groups. Particularly preferred are carboxyl groups or salts thereof, acid anhydride groups, epoxy groups, and the like. Two or more types of these groups may be contained in the resin.
アクリル系樹脂中のフルキルアクリレートあるいはアル
キルメタクリレートが30モル%以上であるのが好まし
いのは、塗膜[形成性、塗膜の強度、耐ブロッキング性
が良好になるためである。アクリル系樹脂中のアルキル
アクリレートあるいはアルキルメタクリレートが90モ
ル%以下であるのが好ましいのは、共重合成分として特
定の官能基を有する化合物をアクリル系樹脂に導入する
ことにより、水溶化、水分散化しやすくすると共に、そ
の状態を長期にわたり、安定にするためであり、更に塗
布層とポリエステルフィルム層との接着性の改善、塗布
層内での反応による塗布層の強度、耐水性、耐薬品性の
改善、さらに本発明のフィルムと他の材料との接着性の
改善などを図ることができるからである。The reason why the content of fulkyl acrylate or alkyl methacrylate in the acrylic resin is preferably 30 mol % or more is because the coating film formability, coating film strength, and blocking resistance are improved. It is preferable that the content of alkyl acrylate or alkyl methacrylate in the acrylic resin is 90 mol% or less because it can be made water-soluble or water-dispersible by introducing a compound having a specific functional group into the acrylic resin as a copolymerization component. This is to make the coating easier and to keep the condition stable for a long period of time.It also improves the adhesion between the coating layer and the polyester film layer, and improves the strength, water resistance, and chemical resistance of the coating layer due to reactions within the coating layer. This is because it is possible to improve the adhesion between the film of the present invention and other materials.
アルキルアクリレートおよびアルキルメタクリレートの
アルキル基の例としては、メチル基、エヂル基、n−プ
ロピル基、イソプロピル基、ローブチル基、イソブチル
基、t−ブチル基、2−エチルヘキシル基、ラウリル基
、ステアリル基、シクロヘキシル基などがあげられる。Examples of alkyl groups in alkyl acrylates and alkyl methacrylates include methyl group, edyl group, n-propyl group, isopropyl group, lobutyl group, isobutyl group, t-butyl group, 2-ethylhexyl group, lauryl group, stearyl group, and cyclohexyl group. Examples include bases.
アルキルアクリレートあるいはアルキルメタクリレート
と共重合する官能基を有するビニル系単量体は、反応性
官能基、自己架橋性官能基、親水性基などの官能基を有
する下記の化合物類が使用できる。As the vinyl monomer having a functional group copolymerizable with alkyl acrylate or alkyl methacrylate, the following compounds having functional groups such as a reactive functional group, a self-crosslinking functional group, and a hydrophilic group can be used.
カルボキシル基またはその塩、あるいは酸無水物基を有
する化合物としては、アクリル酸、メタクリル酸、イタ
コン酸、マレイン酸、フマル酸、クロトン酸、これらの
カルボン酸のナトリウムなどとの金属塩、アンモニウム
塩、あるいは無水マレイン酸などがめげられる。Examples of compounds having a carboxyl group or a salt thereof, or an acid anhydride group include acrylic acid, methacrylic acid, itaconic acid, maleic acid, fumaric acid, crotonic acid, metal salts of these carboxylic acids with sodium etc., ammonium salts, Alternatively, maleic anhydride may be used.
スルホン酸基またはその塩を有する化合物としては、ビ
ニルスルホン酸、スチレンスルホン酸、これらのスルホ
ン酸のナトリウムなどとの金属塩、アンモニウム塩など
があげられる。Examples of compounds having a sulfonic acid group or a salt thereof include vinyl sulfonic acid, styrene sulfonic acid, metal salts of these sulfonic acids with sodium, and ammonium salts.
アミド基あるいはアルキロール化されたアミド基を有す
る化合物としては、アクリルアミド、メタクリルアミド
、トメチルメタクリルアミド、メチロール化アクリルア
ミド、メチロール化メタクリルアミド、ウレイドビニル
エーテル、β−ウレイドイソブチルビニルエーテル、ウ
レイドエチルアクリレートなどがあげられる。Examples of compounds having an amide group or an alkylolated amide group include acrylamide, methacrylamide, tomethylmethacrylamide, methylolated acrylamide, methylolated methacrylamide, ureido vinyl ether, β-ureido isobutyl vinyl ether, ureido ethyl acrylate, etc. It will be done.
アミノ基またはアルキロール化されたアミン基あるいは
それらの塩を有する化合物としては、ジエチルアミノエ
ヂルビニルエーテル、3−アミノプロピルビニルエーテ
ル、2−アミノブチルビニルエーテル、ジメヂルアミノ
エチルメタクリレート、ジメヂルアミノエチルビニルエ
ーテル、それらのアミノ基をメチロール化したもの、ハ
ロゲン化アルキル、ジメチル硫酸、サルトンなどにより
4級塩化したものなどがあげられる。Examples of compounds having an amino group or an alkylolated amine group or a salt thereof include diethylaminoedyl vinyl ether, 3-aminopropyl vinyl ether, 2-aminobutyl vinyl ether, dimedylaminoethyl methacrylate, dimedylaminoethyl vinyl ether, and the like. Examples include those in which the amino group of is methylolated, and those in which the amino group is converted into a quaternary chloride with an alkyl halide, dimethyl sulfate, sultone, etc.
水酸基を有する化合物としては、β−ヒドロキシエチル
アクリレート、β−ヒドロキシエチルメタクリレート、
β−ヒドロキシプロピルアクリレート、β−ヒドロキシ
プロピルメタクリレート、β−ヒドロキシビニルエーテ
ル、5−ヒドロキシペンチルビニルエーテル、6−ヒト
ロキシヘキシルビニルエーテル、ポリエチレングリコー
ルモノアクリレート、ポリエチレングリコールモノメタ
クリレート、ポリプロピレングリコールモノアクリレー
ト、ポリプロピレングリコールモノメタクリレートなど
があられる。Examples of compounds having a hydroxyl group include β-hydroxyethyl acrylate, β-hydroxyethyl methacrylate,
β-hydroxypropyl acrylate, β-hydroxypropyl methacrylate, β-hydroxy vinyl ether, 5-hydroxypentyl vinyl ether, 6-hydroxyhexyl vinyl ether, polyethylene glycol monoacrylate, polyethylene glycol monomethacrylate, polypropylene glycol monoacrylate, polypropylene glycol monomethacrylate, etc. There is a storm.
エポキシ基を有する化合物としては、グリシジルアクリ
レート、グリシジルメタクリレートなどがあげられる。Examples of compounds having an epoxy group include glycidyl acrylate and glycidyl methacrylate.
更に上記以外に次に示すような化合物を併用してもよい
。すなわち、アクリロニトリル、メタクリレートリル、
スチレン類、ブチルビニルエーテル、マレイン酸モノあ
るいはジアルキルエステル、フマル酸モノあるいはジア
ルキルエステル、イタコン酸モノあるいはジアルキルエ
ステル、メチルビニルケトン、塩化ビニル、塩化ビニリ
デン、酢酸ビニル、ビニルピリジン、ビニルピロリドン
、ビニルトリメトキシシランなどがあげられるが、これ
らに限定されるものではない。Furthermore, in addition to the above compounds, the following compounds may be used in combination. That is, acrylonitrile, methacrylate trile,
Styrenes, butyl vinyl ether, mono- or dialkyl maleic acid esters, mono- or dialkyl fumaric acid esters, mono- or dialkyl itaconic acid esters, methyl vinyl ketone, vinyl chloride, vinylidene chloride, vinyl acetate, vinyl pyridine, vinyl pyrrolidone, vinyl trimethoxysilane Examples include, but are not limited to, these.
アクリル系樹脂は、界面活性剤を含有していてもよいが
、アクリル系樹脂に含有される低分子量体の界面活性剤
が増膜過程で濃縮され、粒子と粒子の界面に蓄積された
り、塗布層の界面に移行するなどして、塗布層の機械的
強度、耐水性、積層体との接着性に問題を生じる場合が
ある。このような場合には、界面活性剤を含有しないい
わゆるソープフリー重合による重合物を利用できる。The acrylic resin may contain a surfactant, but the low molecular weight surfactant contained in the acrylic resin may be concentrated during the film-growing process, accumulate at the interface between particles, or be difficult to coat. It may migrate to the interface between layers, causing problems with the mechanical strength, water resistance, and adhesion of the coating layer to the laminate. In such a case, a polymer obtained by so-called soap-free polymerization that does not contain a surfactant can be used.
しかし、その中でもメチルメウクリレートとエチル7ク
リレートの35/65〜65/35(モル比)の共重合
体を幹ポリマーとし、−COOI−1、−CH2O8を
各々1〜5重量%導入した水分散性アクリルが、積層フ
ィルムの易接着性、透明性において、特に好適である。However, among these, water containing 35/65 to 65/35 (mole ratio) copolymer of methyl meucrylate and ethyl 7 acrylate as the backbone polymer, and introducing 1 to 5% by weight of -COOI-1 and -CH2O8 each. Dispersible acrylic is particularly suitable in terms of easy adhesion and transparency of the laminated film.
被覆層における無機コロイドの濃度は0.1〜30重量
%が好ましく、より好ましくは0.5〜20重但%、更
に好ましくは1.0〜15重口%の範囲である。無機コ
ロイドの濃度が0.1車ffi%未満では、所望の易滑
性を有する積層フィルムが得にくい。30重量%を越え
るものでは、積層フィルムの透明性、易接着性、耐摩耗
性が悪化したり、被覆層のベースフィルムへの密着性が
低下するので、好ましくない。The concentration of the inorganic colloid in the coating layer is preferably from 0.1 to 30% by weight, more preferably from 0.5 to 20% by weight, and even more preferably from 1.0 to 15% by weight. If the concentration of the inorganic colloid is less than 0.1%, it is difficult to obtain a laminated film having the desired slipperiness. If it exceeds 30% by weight, the transparency, easy adhesion, and abrasion resistance of the laminated film will deteriorate, and the adhesion of the coating layer to the base film will decrease, which is not preferable.
また、被覆層には、被覆層の密着性、耐水性、耐溶剤性
、機械的強度の改良のため、架橋剤としてメチロール化
あるいはアルキロール化した尿素系メラミン系、アクリ
ルアミド系、ポリアミド系などの樹脂、エポキシ化合物
、アジリジン化合物、ブロックポリイソシアネート、ビ
ニル化合物などの反応性化合物を含有せしめてもよい。In addition, in order to improve the adhesion, water resistance, solvent resistance, and mechanical strength of the coating layer, methylolated or alkylolated urea-based melamine-based, acrylamide-based, polyamide-based, etc. are used as crosslinking agents. It may also contain reactive compounds such as resins, epoxy compounds, aziridine compounds, block polyisocyanates, and vinyl compounds.
更に必要に応じて、消泡剤、塗布性改良剤、増結剤、帯
電防止剤、酸化防止剤、紫外線吸収剤、染料、顔料など
を含有せしめてもよい。Furthermore, if necessary, an antifoaming agent, a coating property improver, a binder, an antistatic agent, an antioxidant, an ultraviolet absorber, a dye, a pigment, etc. may be contained.
本発明フィルムを構成するポリエステルフィルムは、常
法により、少なくとも二軸配向させたものであり、厚み
は2〜300μmが好ましく、5〜150μmの範囲が
より好ましく基材ベースとしての実用面での取り扱い性
に優れている。更にポリエステルフィルムのヘイズ(濁
度)は4.0%以下が好ましく、より好ましくは3.0
%以下である。The polyester film constituting the film of the present invention is at least biaxially oriented by a conventional method, and the thickness is preferably 2 to 300 μm, more preferably 5 to 150 μm for practical handling as a base material. Excellent in sex. Furthermore, the haze (turbidity) of the polyester film is preferably 4.0% or less, more preferably 3.0%.
% or less.
本発明フィルムを構成する被覆層の積層厚みは0.00
5〜0.15μmが好ましく、0.01〜0.1μmの
範囲がより好ましい。積層厚みが0.005μm未満で
は、均一積層が難しいのみならず、易接着性の低下、更
には無機コロイド粒子の密着力が低下し、易滑耐久性を
有する@層フィルムが得にくい。0.15μmを越える
ものは、透明性や易滑性が低下したり、場合によっては
、被覆層の吸湿によって、ブロッキングを発生しやすく
なる。The laminated thickness of the coating layer constituting the film of the present invention is 0.00
The range is preferably 5 to 0.15 μm, more preferably 0.01 to 0.1 μm. When the lamination thickness is less than 0.005 μm, it is not only difficult to uniformly laminate the film, but also the adhesion properties are lowered, and the adhesion of the inorganic colloid particles is also lowered, making it difficult to obtain a @layer film that is easy to slip and has durability. If the thickness exceeds 0.15 μm, transparency and slipperiness may decrease, and in some cases, blocking may easily occur due to moisture absorption of the coating layer.
本発明フィルムは、被覆層の無機コロイド粒子の平均粒
径(D)と被覆層厚み(d)との比(D/d)が1.1
〜80でなければならない。好ましくは2.0〜40、
より好ましくは3.0〜15の範囲である。粒子径と膜
厚の比が1.0未満では、積層フィルムの易滑性、透明
性が悪化し、表面欠点などの弊害が増すので好ましくな
い。粒子径と膜厚の比が80以上では、易接着性、平滑
性が悪化するのみならず、被覆層の耐摩耗性が悪化して
白粉が発生しやすくなったり、逆に滑り性が悪化するの
で好ましくない。The film of the present invention has a ratio (D/d) of the average particle diameter (D) of inorganic colloid particles in the coating layer to the thickness (d) of the coating layer of 1.1.
Must be ~80. Preferably 2.0 to 40,
More preferably, it is in the range of 3.0 to 15. If the ratio of particle size to film thickness is less than 1.0, the slipperiness and transparency of the laminated film will deteriorate, and problems such as surface defects will increase, which is not preferable. If the ratio of particle size to film thickness is 80 or more, not only the easy adhesion and smoothness deteriorate, but also the abrasion resistance of the coating layer deteriorates, making it easier to generate white powder, or conversely, the slipperiness deteriorates. So I don't like it.
本発明フィルムは、透明性において、ヘイズが4.0%
以下が好ましく、より好ましくは3.0%以下、更に好
ましくは、2.5%以下である。The film of the present invention has a haze of 4.0% in terms of transparency.
The content is preferably below, more preferably 3.0% or less, still more preferably 2.5% or less.
次に、本発明の代表的¥A造方法について、ポリエチレ
ンテレフタレート(以下PETと略称する)フィルムを
用いた場合を表明するが、これらに限定されるものでは
ない。Next, a case where a polyethylene terephthalate (hereinafter abbreviated as PET) film is used will be described as a representative A manufacturing method of the present invention, but the method is not limited thereto.
先ず、常法によって重合されたPETチップを260・
〜310’Cでスリット状のダイから溶融押出し、静電
荷を印加しながら20〜80℃に冷却せしめて未延伸フ
ィルムを作る。この際、未延伸フィルムの固有粘度は、
フィルム特性から0.5以上であることが望ましい。次
に、該未延伸フィルムおるいは該未延伸フィルムを70
〜120℃で2.0〜5.0倍延伸したフィルム上に、
予め無機=10イドと水溶性あるいは水分散性アクリル
系樹脂の混合組成物を所定量に調整した水溶液を塗膜「
シ、塗膜を乾燥させて所定の塗15層を設けた後、70
〜150℃で、未延伸フィルムを用いる場合は、縦方向
に2.0〜5.0倍、横方向に2゜0〜5.0借問時延
伸を、また−軸延伸フィルムを用いる場合は、2.0〜
5.0(8横延伸する。First, PET chips polymerized by a conventional method were heated to 260.
It is melt-extruded through a slit-shaped die at ~310'C and cooled to 20-80C while applying an electrostatic charge to produce an unstretched film. At this time, the intrinsic viscosity of the unstretched film is
From the viewpoint of film properties, it is desirable that it be 0.5 or more. Next, the unstretched film or the unstretched film is
On a film stretched 2.0 to 5.0 times at ~120°C,
An aqueous solution prepared by adjusting a predetermined amount of a mixed composition of inorganic = 10 oid and water-soluble or water-dispersible acrylic resin in advance is coated with a coating film.
After drying the paint film and applying the prescribed 15 layers, 70
~150°C, when using an unstretched film, stretch 2.0 to 5.0 times in the machine direction and 2° to 5.0 times in the transverse direction, and when using a -axially stretched film, 2.0~
5.0 (8 horizontal stretching.
また、二軸配向したフィルムを100〜180℃で少な
くとも一方向に1.1〜3.5倍延伸してもよい。更に
、二軸配向フィルムは必要に応じて150〜240℃で
0〜10%弛緩を与えつつ、1〜60秒間処理する。Alternatively, the biaxially oriented film may be stretched 1.1 to 3.5 times in at least one direction at 100 to 180°C. Further, the biaxially oriented film is treated at 150 to 240°C for 1 to 60 seconds while giving 0 to 10% relaxation as necessary.
塗布方法は、特に限定されず、押出ラミネート法、メル
トコーティング法を用いてもよいが、高速で薄膜コート
することが可能であるという理由から水溶化、あるいは
水分散化させた塗材のグラビヤコート法、リバースコー
ト法、スプレィコート法、キツスコート法、ダイコート
法、メタリングバーコード法など公知の方法を適用する
のが好適である。この際、PETフィルムには塗布する
前に必要に応じて、空気中おるいはその伯種々の雰囲気
中でのコロナ放電処理など公知の表面処理を施すことに
よって、塗布性が良化するのみならず、被覆層をより強
固にフィルム表面上に形成できる。なお、塗材′Q度、
塗膜乾燥条件は特に限定されるものではないが、塗膜乾
燥条件は積層ポリエステルフィルムの特性に悪影響を及
ぼさない範囲で行なうのが望ましい。The coating method is not particularly limited, and extrusion lamination and melt coating methods may be used, but gravure coating using a water-soluble or water-dispersed coating material is preferred because it enables high-speed thin film coating. It is preferable to apply known methods such as the method, reverse coat method, spray coat method, kit coat method, die coat method, and metal ring bar code method. In this case, coating properties can only be improved by subjecting the PET film to a known surface treatment such as corona discharge treatment in air or various atmospheres as necessary before coating. First, the coating layer can be formed more firmly on the film surface. In addition, the coating material'Q degree,
The coating film drying conditions are not particularly limited, but it is desirable that the coating film drying conditions be within a range that does not adversely affect the properties of the laminated polyester film.
[評価法] 本発明の特性値は、次の測定方法、評価基準による。[Evaluation method] The characteristic values of the present invention are based on the following measurement method and evaluation criteria.
(1) 耐ブロッキング性
積層フィルム面のブロッキング性は、JIS−Z−02
19に準じて50℃、80〜90RH%中で荷重500
q/12ctKをかけて24時間俊のブロッキング性を
評価した。判定基準は、Q:良好、Δ:やや劣る、X:
不良とした。(1) Blocking resistance The blocking property of the laminated film surface is in accordance with JIS-Z-02.
50℃, 80~90RH%, load 500 according to 19
q/12ctK was applied to evaluate the blocking property of 24-hour shun. The criteria are Q: Good, Δ: Slightly poor, X:
It was marked as defective.
(2) 塗膜の密着性
被覆層/ベースフィルムの接着力は、被覆層にJ l5
−C−2338で規定された幅18mmの粘着テープを
貼った後、ハンドローラを用いて約5kgの荷重をかけ
、長さ方向(約10Cm)に2回往復して圧着させ、粘
着テープを手で引き剥がし、被覆層の剥離度合を観察し
、評価した。判定基準は、O:良好(剥離面積5%未満
)、Δ:やや劣る(剥離面積5%以上20%未満)、×
:不良(剥離面積20%以上)とした。(2) Adhesion of coating film The adhesion strength of the coating layer/base film is
- After pasting the adhesive tape with a width of 18 mm specified in C-2338, apply a load of approximately 5 kg using a hand roller, press it back and forth twice in the length direction (approximately 10 cm), and then apply the adhesive tape by hand. The coating layer was peeled off and the degree of peeling of the coating layer was observed and evaluated. The criteria are: O: Good (Peeling area less than 5%), Δ: Slightly poor (Peeling area 5% or more and less than 20%), ×
: Defective (peeling area 20% or more).
(3) 易滑性(μS)
ASTM−D−1894−63により、積層面と未積層
面の静摩擦係数μsを測定した。(3) Sliding property (μS) The coefficient of static friction μs between the laminated surface and the non-laminated surface was measured according to ASTM-D-1894-63.
(4) 易滑性の耐久性
テープ状にしたフィルムの被ff1fff1表面を金属
(SUS)固定ガイド(5mm、ff)に100回繰り
返し、接触走行させた後、上記(3)のμSを測定した
。走行される折のμSよりも0.2以内の差であれば、
耐久性は良く(○)、差が0.2を越えれば耐久性は悪
い(X)と評価する。(4) The surface of the ff1fff1 surface of the film in the form of a durable and easily slippery tape was repeatedly run in contact with a metal (SUS) fixed guide (5 mm, ff) 100 times, and then the μS in (3) above was measured. . If the difference is within 0.2 from μS when traveling,
The durability is evaluated as good (○), and if the difference exceeds 0.2, the durability is evaluated as poor (X).
(5) 耐摩耗性
テープ状にしたフィルムの被覆層表面を金属(SUS)
固定ガイド(5mmO>に100回繰り返し接触走行さ
せた後、フィルム上に付着したスクラッチ量を観察し、
その数の多少で次の如く判断した。(5) The surface of the coating layer of the abrasion-resistant tape-shaped film is made of metal (SUS).
After repeatedly running in contact with a fixed guide (5 mm O) 100 times, the amount of scratches attached to the film was observed.
Judgments were made based on the number as follows.
◎ニスクラッチが非常に少ない(耐久性が極めて良好)
○ニスクラッチが少ない(耐久性良好)Xニスクラッチ
が多い(耐久性不良)
(8) 透明“性
5EP−H−2型温度計(日本精密光学(株)製)を用
いJ Is−に−6714−58に基づいてヘイズ(濁
度)を測定した。判定基準は、ベースフィルムに対する
ヘイズの上昇が0.3%未満を良好(0)、0.3%以
上を不良(X)とした。◎ Very few varnish scratches (very good durability) ○ Few varnish scratches (good durability) X Many varnish scratches (poor durability) (8) Transparent 5EP-H-2 type thermometer (Japan Haze (turbidity) was measured based on J Is-6714-58 using Seimitsu Kogaku Co., Ltd. The criterion was that an increase in haze relative to the base film of less than 0.3% was considered good (0). , 0.3% or more was considered defective (X).
(7) 被覆層の厚みd(μ)
被覆層にセロハンテープを貼り、セロハンテープ端部の
被覆層をジメチルホルムアミド等の溶剤で溶解除去する
。次いでセロハンテープを剥がし、セロハンテープで保
護された面と、溶解除去した面との境界を小坂研究所製
ET−10高精度段差測定器により測定し、厚みを求め
た。(7) Thickness d (μ) of coating layer Cellophane tape is applied to the coating layer, and the coating layer at the end of the cellophane tape is dissolved and removed using a solvent such as dimethylformamide. Next, the cellophane tape was peeled off, and the boundary between the surface protected by the cellophane tape and the surface that had been dissolved and removed was measured using an ET-10 high-precision step measuring device manufactured by Kosaka Institute to determine the thickness.
上記方法で困難な場合は、゛日立製作所製透過型電子顕
微鏡HU−12型を用い、積層フィルムの超薄断面切片
を観察し、厚みを求めた。If the above method was difficult, an ultra-thin section of the laminated film was observed using a transmission electron microscope model HU-12 manufactured by Hitachi, Ltd., and the thickness was determined.
(8〉 平均粒子径(D)と積層厚み(d)の比(D
/d)
平均粒子径(D)と上記(7)で測定した積層厚み(d
>より、比(D/d)を求めた。(8> Ratio of average particle diameter (D) to lamination thickness (d) (D
/d) Average particle diameter (D) and lamination thickness (d) measured in (7) above
>, the ratio (D/d) was determined.
(9)平滑性
J l5−B−0601に従い、株式会社小坂研究所製
の触針型表面粗さ計5D−3型を用い、カットオフ0.
25mm1測定長さ1mmで平均粗さRa(μ)を測定
した。Raが0.020μm未満を平滑性良好、0.0
20μm以上を平滑性不良と判定した。(9) Smoothness According to J15-B-0601, a stylus-type surface roughness tester model 5D-3 manufactured by Kosaka Laboratory Co., Ltd. was used with a cutoff of 0.
The average roughness Ra (μ) was measured with a length of 25 mm and a measurement length of 1 mm. Ra is less than 0.020μm, good smoothness, 0.0
A thickness of 20 μm or more was determined to have poor smoothness.
0口) 接着性
積層フィルム上に下記3種の塗材を用いた塗膜[層を形
成させた後、塗膜上にクロスカット(100ケ/ml)
を入れ、該クロスカット面に対し450にセロハンテー
プ:CT−24にチバン(株)製)を貼り、前記(2〉
で用いたハンドローラを用いて10回往復して圧着させ
、セロハンテープを手で引き剥がして被覆層の剥離度合
を観察し、評価した。判定基準は、O:良好く剥離せず
)、△:やや劣る(剥離面積20%未満)、X:不良(
剥離面積20%以上)とした。0 mouth) Coating film using the following three types of coating materials on adhesive laminated film [After forming the layer, cross cut (100 pieces/ml) on the coating film
, apply cellophane tape (CT-24 manufactured by Chiban Co., Ltd.) to 450 on the cross-cut surface, and apply the above (2)
The cellophane tape was peeled off by hand to observe and evaluate the degree of peeling of the coating layer. The judgment criteria are: O: not peeled off well), △: somewhat poor (less than 20% peeled area), X: poor (
peeled area of 20% or more).
■ グラビヤ印刷インキ
市販のセロハン印刷用グラビアインキ:セロカラーST
(東洋インキ製造(株)製をトルエン/酢酸エヂル/メ
チルエヂルケトン(2:1:1)の混合溶媒で希釈し、
濃度10重0%とじた後、バーコードし、100’CX
1.5分乾燥させ、1゜5μm厚みの塗布層を形成させ
た。■ Gravure printing ink Commercially available gravure ink for cellophane printing: Cellocolor ST
(Toyo Ink Manufacturing Co., Ltd., diluted with a mixed solvent of toluene/edyl acetate/methyl edyl ketone (2:1:1),
After binding the density 10 weight 0%, barcode and 100'CX
It was dried for 1.5 minutes to form a coating layer with a thickness of 1.5 μm.
■ ジアゾバインダー用セルロース
市販のジアゾバインダー用セルロースとしてCA338
1−05 (ナガセ産業(株)製)を酢酸エチルに溶解
し、濃度10車量%とした後、バーコードし、110℃
×1.5分乾燥させて5.0μm厚みの塗布層を形成さ
せた。■ Cellulose for diazo binder CA338 is a commercially available cellulose for diazo binder.
1-05 (manufactured by Nagase Sangyo Co., Ltd.) was dissolved in ethyl acetate to a concentration of 10% by weight, barcoded, and heated at 110°C.
It was dried for 1.5 minutes to form a coating layer with a thickness of 5.0 μm.
■ 磁性塗材
組成として、
・T−Fe203粉末 68重房部・カー
ボンフラッフ 7重母部・塩化ビニル
−酢酸ビニル−ビニルアルコール共重合体
26重量部・アクリロニトリル−ブタジ
ェン共重合体5重量部
・ポリイソシアネート 2重量部・メチ
ルエチルケトン 75重ω部・トルエン
75車量部からなる塗材をバー
コードし、120″CX2分乾燥させた後、50℃、1
2時間エージングさせて、2.5μm厚みの塗布層を形
成させた。■ Magnetic coating material composition: ・T-Fe203 powder 68 double cells ・Carbon fluff 7 double cells ・Vinyl chloride-vinyl acetate-vinyl alcohol copolymer
26 parts by weight, 5 parts by weight of acrylonitrile-butadiene copolymer, 2 parts by weight of polyisocyanate, 75 parts by weight of methyl ethyl ketone, and 75 parts by weight of toluene.
The coating material consisting of 75 parts was barcoded, dried for 2 minutes at 120"C, and then heated at 50℃ for 1
It was aged for 2 hours to form a coating layer with a thickness of 2.5 μm.
[発明の効果]
本発明は、ポリエステルフィルム上に、特定の無機コロ
イドを含む水溶性あるいは水分散性アクリル樹脂を塗布
した後、延伸し、無機コロイド粒子の粒子径と積層厚み
が特定の相関関係にある被覆層を形成させたので、基材
フィルムの諸性性を悪化させることなく、次のような優
れた効果を1りることかできた。[Effects of the Invention] The present invention provides a polyester film that is coated with a water-soluble or water-dispersible acrylic resin containing a specific inorganic colloid, and then stretched, so that the particle diameter of the inorganic colloid particles and the lamination thickness have a specific correlation. Since the coating layer was formed, the following excellent effects could be achieved without deteriorating the properties of the base film.
(1) 積層ポリエステルフィルムは、透明性、易滑
性、易接着性、平滑性が同時に優れている。(1) The laminated polyester film has excellent transparency, easy slipping, easy adhesion, and smoothness.
(2)積層ポリエステルフィルムは、易滑性の耐久性に
優れ、また耐摩耗性に優れている。(2) The laminated polyester film has excellent slipperiness, durability, and abrasion resistance.
(3) 積層ポリエステルフィルムは、FaP;lに
なっても優れた透明性、易滑性を保持しているので、製
膜工程での巻き取り性や巻姿、後加工での取り扱い性に
優れている。(3) The laminated polyester film maintains excellent transparency and slipperiness even at FaP;L, so it has excellent windability and form during the film forming process, and ease of handling during post-processing. ing.
(4) 積層ポリスチルフィルムは易接着性に優れて
いるので、後加工で、各種樹脂から成る被覆層を設ける
時、樹脂層が強固に形成されるので、アンカーコートが
不要になり工程の簡略化が図れる。(4) Laminated polystyrene film has excellent adhesion properties, so when a coating layer made of various resins is provided in post-processing, the resin layer is firmly formed, eliminating the need for an anchor coat and simplifying the process. can be achieved.
本発明の積層ポリエステルフィルムは、磁気記録媒体用
ベースフィルム、電絶用ベースフィルム、コンデンサー
用ベースフィルム、包装用ベースフィルム、各種写真用
ベースフィルム、光学用ベースフィルム、グラフィック
用ベースフィルムなどに適用できるが、中でも、特にU
v印刷用ベースフィルムのように透明性、易滑性、易接
着性が要求されるベース基材に用いるのが好ましい。The laminated polyester film of the present invention can be applied to base films for magnetic recording media, base films for electrical disconnection, base films for capacitors, base films for packaging, various photographic base films, optical base films, graphic base films, etc. However, especially U
It is preferable to use it for a base material that requires transparency, easy slipperiness, and easy adhesion, such as a base film for v-printing.
[実施例1
本発明を以下の実施例、比較例を用いて説明するが、本
発明は、これらに限定されるものではない。[Example 1] The present invention will be explained using the following examples and comparative examples, but the present invention is not limited thereto.
実施例1
常法によって、製造されたPETのホモポリマーデツプ
(固有粘度0.62、融点259°C)を180’Cて
2時間減圧乾燥(3mmllc+> L/た。Example 1 A PET homopolymer dip (intrinsic viscosity 0.62, melting point 259°C) produced by a conventional method was dried under reduced pressure at 180'C for 2 hours (3 mmllc+>L/).
このチップを280’Cの押出機に供給し、T型口金か
ら溶融押出し、静電印加法を用いて表面温度20℃の冷
却ドラムに巻きつけて冷却固化せしめ、未延伸フィルム
とした後、このフィルムを90℃でロール延伸によって
縦方向に3.3倍延伸した。This chip was supplied to an extruder at 280'C, melted and extruded from a T-shaped nozzle, and wound around a cooling drum with a surface temperature of 20°C using an electrostatic application method to cool and solidify it to form an unstretched film. The film was stretched 3.3 times in the machine direction by roll stretching at 90°C.
次に、無機コロイドとして平均粒径0.12μmのシリ
カゾル“キャタロイド′°(触媒化成工業(株)Iりと
、水分散性アクリル樹脂“ニカゾール”A−oa(日本
カーバイト工業(株)製)からなるバインダーをEli
ffl固形分比5:95の組成で均一分散させた濃度1
.0重量%の塗材を、前記−軸延伸フィルムの片面にメ
タリングバ一方式で、塗布した後、該塗イ5層を乾燥し
つつ100’Cで、横方向に3.6倍延伸し、横方向に
2%弛緩しつつ210℃で5秒間熱処理して、被覆層0
゜026μmが積層された厚さ15μmの積層フィルム
を)qた。Next, as inorganic colloids, silica sol "Cataroid'° (manufactured by Catalysts Kasei Kogyo Co., Ltd.) with an average particle size of 0.12 μm and water-dispersible acrylic resin "Nicazol" A-oa (manufactured by Nippon Carbide Industries Co., Ltd.) were used. A binder consisting of Eli
Concentration 1 uniformly dispersed with a composition of ffl solid content ratio of 5:95
.. After applying 0% by weight of the coating material to one side of the above-mentioned -axially stretched film using a metering bar, the 5 layers of the coating were stretched 3.6 times in the transverse direction at 100'C while drying. Heat treatment was performed at 210°C for 5 seconds while relaxing 2% in the direction to form a coating layer of 0.
A laminated film with a thickness of 15 μm in which 0.026 μm was laminated was prepared.
かくして1qられた被覆層は、シリカゾルの平均粒子径
と層厚みの比(D/d)が4.6であった。The coating layer thus formed had a ratio of the average particle diameter of the silica sol to the layer thickness (D/d) of 4.6.
更に、積層フィルムの特性は第1表に示したとおりで透
明性、易滑性、接着性、平滑性が共に優れており、しか
も被覆層の易滑耐久性、耐摩耗性、耐ブロッキング性、
密着性ともに優れているものであった。Furthermore, the properties of the laminated film are as shown in Table 1, and it has excellent transparency, slipperiness, adhesion, and smoothness, and the coating layer has excellent sliding durability, abrasion resistance, blocking resistance,
Both adhesion was excellent.
実施例2〜5、比較例1〜2
実施例1と同じPETを使用し、実施例1と同じ組成物
で、シリカゾルの平均粒径と組成比を変えた塗材を作り
、以下実施例1と同一手法で、被覆層におけるシリカゾ
ルの平均粒子径と積層厚みの比(D/d)を変えた積層
フィルムを得た。これらの積層フィルムの特性を第1表
に示した。第1表に見る如く、積層フィルムが本発明の
範囲にある場合は(実施例2〜6)は、易滑性、透明性
、接着性、平滑性のバランスに優れたフィルムを1qる
ことができるが、本発明の範囲外にある場合(比較例1
.2)では、透明性、易滑性、接着性、平滑性が共に優
れたフィルムを得ることができないことが分る。Examples 2 to 5, Comparative Examples 1 to 2 Using the same PET as in Example 1 and the same composition as in Example 1, coating materials were made with different average particle diameters and composition ratios of silica sol. Laminated films with different ratios (D/d) of the average particle diameter of the silica sol to the laminated thickness in the coating layer were obtained using the same method as described above. The properties of these laminated films are shown in Table 1. As shown in Table 1, when the laminated film is within the scope of the present invention (Examples 2 to 6), 1q of films with an excellent balance of slipperiness, transparency, adhesiveness, and smoothness can be used. However, if it is outside the scope of the present invention (Comparative Example 1)
.. It can be seen that in case 2), a film having excellent transparency, slipperiness, adhesiveness and smoothness cannot be obtained.
実施例6
無機コロイドとして平均粒子径0.20μmの酸化チタ
ンゾル“クイーンタイタニツク″(触媒化成工業(株)
製)を用いた他は、実施例1と同様にして製膜、評価し
た。第1表に示したように、同様に優れた透明性、易滑
性、接着性、平滑性を保持した積層フィルムを得ること
ができた。Example 6 Titanium oxide sol “Queen Titanic” with an average particle diameter of 0.20 μm as an inorganic colloid (Catalysts & Chemicals Co., Ltd.)
The film was formed and evaluated in the same manner as in Example 1, except that the film was manufactured using the following method. As shown in Table 1, it was possible to obtain a laminated film that similarly maintained excellent transparency, slipperiness, adhesiveness, and smoothness.
Claims (2)
粒径0.11〜0.4μmの無機コロイドと水溶性ある
いは水分散性アクリル系樹脂とを主成分とする被覆層を
設けてなる積層ポリエステルフィルムであって、該無機
コロイドの平均粒径(D)と該被覆層厚み(d)の比(
D/d)が1.1〜80の範囲にあることを特徴とする
積層ポリエステルフィルム。(1) A laminated polyester film having a coating layer mainly composed of an inorganic colloid with an average particle size of 0.11 to 0.4 μm and a water-soluble or water-dispersible acrylic resin on at least one side of the polyester film. The ratio of the average particle diameter (D) of the inorganic colloid to the thickness (d) of the coating layer (
A laminated polyester film characterized in that D/d) is in the range of 1.1 to 80.
下であることを特徴とする特許請求の範囲第1項記載の
積層ポリエステルフィルム。(2) The laminated polyester film according to claim 1, wherein the optical haze of the laminated polyester film is 4% or less.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62100415A JPS63265636A (en) | 1987-04-23 | 1987-04-23 | Laminated polyester film |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62100415A JPS63265636A (en) | 1987-04-23 | 1987-04-23 | Laminated polyester film |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS63265636A true JPS63265636A (en) | 1988-11-02 |
Family
ID=14273350
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP62100415A Pending JPS63265636A (en) | 1987-04-23 | 1987-04-23 | Laminated polyester film |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS63265636A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0390383A (en) * | 1989-09-01 | 1991-04-16 | Tomoegawa Paper Co Ltd | Printing sheet |
US5389422A (en) * | 1992-09-03 | 1995-02-14 | Toray Industries, Inc. | Biaxially oriented laminated film |
JP2018039960A (en) * | 2016-09-09 | 2018-03-15 | リンテック株式会社 | Film for printing and printed matter |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6061259A (en) * | 1983-09-14 | 1985-04-09 | ダイアホイルヘキスト株式会社 | Polyester film |
JPS61254637A (en) * | 1985-05-02 | 1986-11-12 | Toyobo Co Ltd | Slippery transparent film and production thereof |
-
1987
- 1987-04-23 JP JP62100415A patent/JPS63265636A/en active Pending
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6061259A (en) * | 1983-09-14 | 1985-04-09 | ダイアホイルヘキスト株式会社 | Polyester film |
JPS61254637A (en) * | 1985-05-02 | 1986-11-12 | Toyobo Co Ltd | Slippery transparent film and production thereof |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0390383A (en) * | 1989-09-01 | 1991-04-16 | Tomoegawa Paper Co Ltd | Printing sheet |
JPH0529556B2 (en) * | 1989-09-01 | 1993-04-30 | Tomoegawa Paper Co Ltd | |
US5389422A (en) * | 1992-09-03 | 1995-02-14 | Toray Industries, Inc. | Biaxially oriented laminated film |
JP2018039960A (en) * | 2016-09-09 | 2018-03-15 | リンテック株式会社 | Film for printing and printed matter |
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