JPH11179846A - White film for lamination of metal - Google Patents
White film for lamination of metalInfo
- Publication number
- JPH11179846A JPH11179846A JP35051697A JP35051697A JPH11179846A JP H11179846 A JPH11179846 A JP H11179846A JP 35051697 A JP35051697 A JP 35051697A JP 35051697 A JP35051697 A JP 35051697A JP H11179846 A JPH11179846 A JP H11179846A
- Authority
- JP
- Japan
- Prior art keywords
- film
- layer
- metal
- titanium oxide
- mol
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000002184 metal Substances 0.000 title claims abstract description 47
- 229910052751 metal Inorganic materials 0.000 title claims abstract description 45
- 238000003475 lamination Methods 0.000 title claims abstract description 17
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims abstract description 28
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 claims abstract description 28
- 229920000728 polyester Polymers 0.000 claims abstract description 26
- MMINFSMURORWKH-UHFFFAOYSA-N 3,6-dioxabicyclo[6.2.2]dodeca-1(10),8,11-triene-2,7-dione Chemical group O=C1OCCOC(=O)C2=CC=C1C=C2 MMINFSMURORWKH-UHFFFAOYSA-N 0.000 claims abstract description 10
- LZFNKJKBRGFWDU-UHFFFAOYSA-N 3,6-dioxabicyclo[6.3.1]dodeca-1(12),8,10-triene-2,7-dione Chemical group O=C1OCCOC(=O)C2=CC=CC1=C2 LZFNKJKBRGFWDU-UHFFFAOYSA-N 0.000 claims abstract description 10
- 239000002245 particle Substances 0.000 claims abstract description 10
- 239000000314 lubricant Substances 0.000 claims abstract description 8
- 238000000034 method Methods 0.000 claims description 22
- 239000000203 mixture Substances 0.000 claims description 11
- 125000005498 phthalate group Chemical group 0.000 claims description 7
- 239000011248 coating agent Substances 0.000 abstract description 6
- 238000000576 coating method Methods 0.000 abstract description 6
- 239000010410 layer Substances 0.000 description 42
- 238000010030 laminating Methods 0.000 description 14
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 13
- 238000004519 manufacturing process Methods 0.000 description 12
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 8
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 7
- 229910000831 Steel Inorganic materials 0.000 description 7
- 239000010959 steel Substances 0.000 description 7
- 238000010438 heat treatment Methods 0.000 description 5
- 239000002985 plastic film Substances 0.000 description 5
- 229920006255 plastic film Polymers 0.000 description 5
- -1 polyethylene terephthalate Polymers 0.000 description 5
- 229920005989 resin Polymers 0.000 description 5
- 239000011347 resin Substances 0.000 description 5
- 238000002844 melting Methods 0.000 description 4
- 230000008018 melting Effects 0.000 description 4
- 229920001225 polyester resin Polymers 0.000 description 4
- 239000004645 polyester resin Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 229920001634 Copolyester Polymers 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- 238000010306 acid treatment Methods 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 238000000465 moulding Methods 0.000 description 3
- 239000003973 paint Substances 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- FJKROLUGYXJWQN-UHFFFAOYSA-N 4-hydroxybenzoic acid Chemical compound OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 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
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- ADCOVFLJGNWWNZ-UHFFFAOYSA-N antimony trioxide Chemical compound O=[Sb]O[Sb]=O ADCOVFLJGNWWNZ-UHFFFAOYSA-N 0.000 description 2
- QMKYBPDZANOJGF-UHFFFAOYSA-N benzene-1,3,5-tricarboxylic acid Chemical compound OC(=O)C1=CC(C(O)=O)=CC(C(O)=O)=C1 QMKYBPDZANOJGF-UHFFFAOYSA-N 0.000 description 2
- 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
- 238000007664 blowing Methods 0.000 description 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- KRVSOGSZCMJSLX-UHFFFAOYSA-L chromic acid Substances O[Cr](O)(=O)=O KRVSOGSZCMJSLX-UHFFFAOYSA-L 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- SNRUBQQJIBEYMU-UHFFFAOYSA-N dodecane Chemical compound CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000005886 esterification reaction Methods 0.000 description 2
- 239000000796 flavoring agent Substances 0.000 description 2
- 235000019634 flavors Nutrition 0.000 description 2
- AWJWCTOOIBYHON-UHFFFAOYSA-N furo[3,4-b]pyrazine-5,7-dione Chemical compound C1=CN=C2C(=O)OC(=O)C2=N1 AWJWCTOOIBYHON-UHFFFAOYSA-N 0.000 description 2
- YBMRDBCBODYGJE-UHFFFAOYSA-N germanium dioxide Chemical compound O=[Ge]=O YBMRDBCBODYGJE-UHFFFAOYSA-N 0.000 description 2
- 230000009477 glass transition Effects 0.000 description 2
- 230000001771 impaired effect Effects 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 230000001678 irradiating effect Effects 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- 229910044991 metal oxide Inorganic materials 0.000 description 2
- 150000004706 metal oxides Chemical class 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- 229920006267 polyester film Polymers 0.000 description 2
- 229920000139 polyethylene terephthalate Polymers 0.000 description 2
- 239000005020 polyethylene terephthalate Substances 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- CYIDZMCFTVVTJO-UHFFFAOYSA-N pyromellitic acid Chemical compound OC(=O)C1=CC(C(O)=O)=C(C(O)=O)C=C1C(O)=O CYIDZMCFTVVTJO-UHFFFAOYSA-N 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000004381 surface treatment Methods 0.000 description 2
- 239000010936 titanium Substances 0.000 description 2
- 229910052719 titanium Inorganic materials 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- ARCGXLSVLAOJQL-UHFFFAOYSA-N trimellitic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C(C(O)=O)=C1 ARCGXLSVLAOJQL-UHFFFAOYSA-N 0.000 description 2
- DNIAPMSPPWPWGF-VKHMYHEASA-N (+)-propylene glycol Chemical compound C[C@H](O)CO DNIAPMSPPWPWGF-VKHMYHEASA-N 0.000 description 1
- YPFDHNVEDLHUCE-UHFFFAOYSA-N 1,3-propanediol Substances OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 1
- 229940035437 1,3-propanediol Drugs 0.000 description 1
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
- VPWNQTHUCYMVMZ-UHFFFAOYSA-N 4,4'-sulfonyldiphenol Chemical compound C1=CC(O)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 VPWNQTHUCYMVMZ-UHFFFAOYSA-N 0.000 description 1
- 229940090248 4-hydroxybenzoic acid Drugs 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 229910001369 Brass Inorganic materials 0.000 description 1
- XGIAHMUOCFHQTI-UHFFFAOYSA-N Cl.Cl.Cl.Cl.CC Chemical compound Cl.Cl.Cl.Cl.CC XGIAHMUOCFHQTI-UHFFFAOYSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- ORLQHILJRHBSAY-UHFFFAOYSA-N [1-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1(CO)CCCCC1 ORLQHILJRHBSAY-UHFFFAOYSA-N 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- IKHGUXGNUITLKF-XPULMUKRSA-N acetaldehyde Chemical compound [14CH]([14CH3])=O IKHGUXGNUITLKF-XPULMUKRSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000012790 adhesive layer Substances 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
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 235000013361 beverage Nutrition 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- QPKOBORKPHRBPS-UHFFFAOYSA-N bis(2-hydroxyethyl) terephthalate Chemical compound OCCOC(=O)C1=CC=C(C(=O)OCCO)C=C1 QPKOBORKPHRBPS-UHFFFAOYSA-N 0.000 description 1
- 239000010951 brass Substances 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- 238000009924 canning Methods 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical compound [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 description 1
- HNEGQIOMVPPMNR-IHWYPQMZSA-N citraconic acid Chemical compound OC(=O)C(/C)=C\C(O)=O HNEGQIOMVPPMNR-IHWYPQMZSA-N 0.000 description 1
- 229940018557 citraconic acid Drugs 0.000 description 1
- 239000011247 coating layer Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- QYQADNCHXSEGJT-UHFFFAOYSA-N cyclohexane-1,1-dicarboxylate;hydron Chemical compound OC(=O)C1(C(O)=O)CCCCC1 QYQADNCHXSEGJT-UHFFFAOYSA-N 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 239000000539 dimer Substances 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 229940119177 germanium dioxide Drugs 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 238000009998 heat setting Methods 0.000 description 1
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- HNEGQIOMVPPMNR-NSCUHMNNSA-N mesaconic acid Chemical compound OC(=O)C(/C)=C/C(O)=O HNEGQIOMVPPMNR-NSCUHMNNSA-N 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- HNEGQIOMVPPMNR-UHFFFAOYSA-N methylfumaric acid Natural products OC(=O)C(C)=CC(O)=O HNEGQIOMVPPMNR-UHFFFAOYSA-N 0.000 description 1
- RXOHFPCZGPKIRD-UHFFFAOYSA-N naphthalene-2,6-dicarboxylic acid Chemical compound C1=C(C(O)=O)C=CC2=CC(C(=O)O)=CC=C21 RXOHFPCZGPKIRD-UHFFFAOYSA-N 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 238000007747 plating Methods 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920000166 polytrimethylene carbonate Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 239000011342 resin composition Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000007790 solid phase Substances 0.000 description 1
- 238000009823 thermal lamination Methods 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 239000011135 tin Substances 0.000 description 1
- 239000005029 tin-free steel Substances 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- 230000037303 wrinkles Effects 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Shaping By String And By Release Of Stress In Plastics And The Like (AREA)
- Laminated Bodies (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、優れた熱ラミネー
ト性、成形性及び引張強度を有し、隠蔽性、白度に優
れ、金属缶成形時に治具の摩耗が少なく、印刷性に優れ
た金属缶の外面被覆に好適に用いられる金属ラミネート
用白色フィルムに関するものである。TECHNICAL FIELD The present invention has excellent heat laminating properties, moldability and tensile strength, excellent concealing properties and whiteness, less jig wear during metal can molding, and excellent printability. The present invention relates to a white film for metal lamination suitably used for coating the outer surface of a metal can.
【0002】[0002]
【従来の技術】食品、飲料用の包装には、スチール缶、
アルミ缶等の金属缶が大量に使用されており、これらの
金属缶は、耐食性、印刷性等を付与するために、従来、
熱硬化性樹脂を主成分とする溶剤型塗料を塗布して用い
られてきた。しかし、このような塗料の塗布は、生産性
が悪いと共に、環境汚染等の問題があり、近時、二軸延
伸されたプラスチックフィルムあるいはこれをベースと
し、ヒートシール可能なフィルムをラミネートした積層
フィルムを用いて金属ラミネートすることが多くなって
きた。2. Description of the Related Art Food and beverage packaging includes steel cans,
Metal cans such as aluminum cans are used in large quantities, and these metal cans are conventionally used to impart corrosion resistance, printability, etc.
It has been used by applying a solvent type paint mainly composed of a thermosetting resin. However, the application of such a paint has poor productivity and has a problem of environmental pollution, etc. Recently, a biaxially stretched plastic film or a laminated film based on the biaxially stretched plastic film is laminated. The use of metal lamination has increased.
【0003】プラスチックフィルムで被覆した金属缶
は、鋼板、アルミ板等の金属板(メッキ等の表面処理を
施したものを含む)にプラスチックフィルムをラミネー
トし、ラミネート金属板を成形加工して製造される。こ
のような用途に用いられるプラスチックフィルムには、
金属板とのラミネート性がよいこと、缶の成形性に
優れていること、つまり、缶の成形時にフィルムの剥
離、亀裂、クラック、ピンホール等の発生がないこと、
缶内容物の風味を損ねることがないこと(缶の内面に
用いられる場合)、レトルト処理をしたときにウォー
タースポットや白粉が発生しないこと(ウォータースポ
ットとは、ラミネート時に溶融して非晶化したフィルム
がレトルト処理時に水滴が付着して結晶化して白色化す
る現象をいい、商品の美観を損なう。また、白粉とは、
オリゴマー等の低分子量物がフィルム表面に析出したも
のをいい、ラミネートフィルムが缶内面に用いられる場
合には、缶内容物の風味を損ね、缶外面に用いられる場
合には、缶の美麗性を損なう。)などの数々の特性が同
時に要求される。[0003] A metal can covered with a plastic film is manufactured by laminating a plastic film on a metal plate such as a steel plate or an aluminum plate (including a plate that has been subjected to a surface treatment such as plating), and forming and processing a laminated metal plate. You. Plastic films used for such applications include:
Good lamination properties with metal plates, excellent moldability of cans, that is, no peeling, cracks, cracks, pinholes, etc. of the film during molding of the cans,
The flavor of the contents of the can is not impaired (when used on the inner surface of the can), and no water spot or white powder is generated when the retort treatment is performed. A phenomenon in which water droplets adhere to the film during retort treatment and crystallize to whiten, which impairs the aesthetics of the product.
A substance in which low molecular weight substances such as oligomers are deposited on the film surface.When a laminated film is used on the inner surface of the can, the flavor of the contents of the can is impaired. Spoil. ) Are required at the same time.
【0004】通常、缶は表面に印刷が施されるが、その
際、下地の金属色を隠蔽する目的で白色塗料が下塗さ
れ、その上に印刷が施されている。近年、製造工程の簡
略化(低エネルギー化、低コスト化)や、環境問題に対
する対策(非溶剤化)から、白色フィルムをラミネート
した隠蔽性に優れた缶体の製造が進められている。[0004] Normally, the surface of a can is printed. At this time, a white paint is undercoated for the purpose of concealing the metal color of the base, and the printing is performed thereon. In recent years, from the simplification of the manufacturing process (reduction in energy and cost) and measures against environmental problems (non-solvent), the production of a can body excellent in concealing properties, in which a white film is laminated, has been promoted.
【0005】このような白色フィルムとしては、ポリエ
ステル樹脂に高濃度の酸化チタンを配合したものが用い
られている。しかし、従来の白色フィルムでは白度や隠
蔽性が不充分であり、チタン量をさらに増大させること
が望まれている。しかし、チタン量の増大によって、フ
ィルム表面が硬くなり、また製缶用治具が磨耗するとい
った問題や、削れた金属や酸化チタンがフィルム表面に
付着して、印刷時に印刷ぬけが発生したり、鋼板との熱
ラミネート性が悪くなったりするという問題がクローズ
アップされている。さらに近年、製缶時の深絞り比の増
大や加工速度がアップしており、これまで以上にフィル
ム表面の滑り性を高めることが求められている。As such a white film, a film obtained by blending a high concentration of titanium oxide with a polyester resin is used. However, the whiteness and hiding power of the conventional white film are insufficient, and it is desired to further increase the amount of titanium. However, due to the increase in the amount of titanium, the surface of the film becomes harder, and the problem that the jig for can making is worn out, and the shaved metal and titanium oxide adhere to the film surface, causing printing defects during printing, The problem that the heat laminating property with a steel sheet is deteriorated has been highlighted. Further, in recent years, the deep drawing ratio during can manufacturing and the processing speed have been increasing, and it has been required to enhance the slipperiness of the film surface more than ever.
【0006】従来の金属ラミネート用白色フィルムとし
ては、例えば、缶の成形加工性を改良するために共重合
ポリエステルに酸化チタンを混合したものが特開平5−
170942に開示されている。また、共重合ポリエス
テルに純度95%以上のルチル型酸化チタンを混合した
ものが特開平5−339391に開示されている。ま
た、缶の加工性と耐衝撃性とを向上するために、高濃度
の酸化チタンのマスターチップと粘度分布の広い希釈ポ
リマーとを混合したものが特開平6−271686に開
示されている。また耐衝撃性を向上させるために酸化チ
タンのマスターチップに高粘度の希釈ポリマーを混合し
たものが特開平6−49234に開示されている。ま
た、顔料濃度の異なる2種類の共重合ポリエステルを積
層させた積層ポリエステルフィルムが特開平6−399
80と特開平7−52351に開示されている。上記の
ように、ポリエステル樹脂に酸化チタンを充填した単層
又は複層のフィルムが種々提案されているが、白度の向
上と製缶治具の磨耗の改善、さらには、深絞り比の増大
や加工速度のアップに対応したフィルム表面の優れた滑
り性とを同時に満足するものはなかった。As a conventional white film for metal lamination, for example, a film obtained by mixing titanium oxide with a copolyester in order to improve the moldability of cans is disclosed in
170942. JP-A-5-339391 discloses a mixture of a copolymerized polyester and rutile-type titanium oxide having a purity of 95% or more. Japanese Patent Application Laid-Open No. 6-271686 discloses a mixture of a high-concentration titanium oxide master chip and a dilute polymer having a wide viscosity distribution in order to improve the processability and impact resistance of the can. Japanese Patent Application Laid-Open No. 6-49234 discloses a mixture of a titanium oxide master chip and a high-viscosity diluent polymer in order to improve impact resistance. A laminated polyester film in which two types of copolymerized polyesters having different pigment concentrations are laminated is disclosed in JP-A-6-399.
80 and JP-A-7-52351. As described above, various single-layer or multilayer films in which titanium oxide is filled in a polyester resin have been proposed. However, improvement of whiteness and improvement of abrasion of a can-making jig, and further, increase of a deep drawing ratio And the excellent sliding property of the film surface corresponding to the increase in processing speed and none at the same time.
【0007】[0007]
【発明が解決しようとする課題】本発明は、優れた熱接
着性(熱ラミネート性)、成形性及び強度を有し、隠蔽
性、白度に優れ、金属缶製缶時の治具への傷が発生しに
くく、さらに、フィルム表面の優れた滑り性を有する金
属缶の被覆に好適に用いられる金属ラミネート用白色フ
ィルムを提供しようとするものである。SUMMARY OF THE INVENTION The present invention has excellent heat adhesion (heat laminating properties), moldability and strength, excellent concealing properties and whiteness, and is suitable for use in jigs for metal cans. An object of the present invention is to provide a white film for metal lamination which is preferably used for coating a metal can having less scratches and excellent slipperiness on the film surface.
【0008】[0008]
【課題を解決するための手段】本発明者らは、特定の化
学構造のポリエステルを原料として用い、中央の層Bと
表裏両側の層Sとでフィルムを3層構造に構成し、しか
も酸化チタンの配合量を中央の層Bに偏在化させ、かつ
層Sに特定の形状の滑剤を特定量配合することによっ
て、上記課題が解決できること、さらには白度及び隠蔽
性がより高いフィルムが得られること、またこのフィル
ムの生産時の操業性が著しく改善されることを見いだ
し、本発明に到達した。Means for Solving the Problems The present inventors used a polyester having a specific chemical structure as a raw material, constituted a film having a three-layer structure comprising a central layer B and layers S on both front and back sides, and furthermore, a titanium oxide film. Is unevenly distributed in the central layer B, and a specific amount of the lubricant in the layer S is mixed in the layer S to solve the above-mentioned problems, and further, a film having higher whiteness and concealing property is obtained. It was also found that the operability during production of this film was significantly improved, and the present invention was reached.
【0009】すなわち、本発明の要旨は次の通りであ
る。エチレンテレフタレート単位100〜75モル%と
エチレンイソフタレート単位0〜25モル%とからなる
ポリエステルに酸化チタンが20〜60重量%配合され
た組成物からなるB層と、エチレンテレフタレート単位
94〜70モル%とエチレンイソフタレート単位5〜2
5モル%とジエチレンテレ(イソ)フタレート単位1〜
5モル%からなるポリエステルに酸化チタンが20重量
%以下配合された組成物からなるS層とが、S/B/S
の構成で積層された二軸延伸フィルムであって、フィル
ム中の酸化チタン含有量が20〜50重量%であり、か
つ、S層中に平均粒子径0.25〜2.0μm の滑剤を
0.01〜0.5重量%含有する金属ラミネート用白色
フィルム。That is, the gist of the present invention is as follows. Layer B comprising a composition in which titanium oxide is blended with 20 to 60% by weight of a polyester comprising 100 to 75% by mole of ethylene terephthalate units and 0 to 25% by mole of ethylene isophthalate units, and 94 to 70% by mole of ethylene terephthalate units And ethylene isophthalate unit 5 to 2
5 mol% and diethylene tere (iso) phthalate unit 1 to 1
An S layer comprising a composition in which titanium oxide is blended in an amount of 20% by weight or less with a polyester comprising 5 mol% is S / B / S
Wherein the titanium oxide content in the film is 20 to 50% by weight and the lubricant having an average particle size of 0.25 to 2.0 μm is contained in the S layer. White film for metal lamination containing 0.1 to 0.5% by weight.
【0010】[0010]
【発明の実施形態】以下、本発明について詳細に説明す
る。本発明におけるポリエステルは、酸化チタン濃度の
高い中間層(B)と、その両側に酸化チタン濃度の低い
層(S)とからなり、S層はエチレンテレフタレート単
位94〜70モル%とエチレンイソフタレート単位5〜
25モル%とジエチレンテレ(イソ)フタレート単位1
〜5モル%からなり、B層はエチレンテレフタレート単
位100〜75モル%とエチレンイソフタレート単位0
〜25モル%からなるものである。BEST MODE FOR CARRYING OUT THE INVENTION Hereinafter, the present invention will be described in detail. The polyester in the present invention comprises an intermediate layer (B) having a high concentration of titanium oxide and a layer (S) having a low concentration of titanium oxide on both sides thereof. The S layer is composed of 94 to 70 mol% of ethylene terephthalate units and ethylene isophthalate units. 5-
25 mol% and diethylene tere (iso) phthalate unit 1
B layer is composed of 100 to 75 mol% of ethylene terephthalate units and 0 to 75 mol% of ethylene isophthalate units.
~ 25 mol%.
【0011】S層におけるエチレンイソフタレート単位
の割合は、5〜25モル%、好ましくは8〜15モル%
である。5モル%未満の場合には、フィルムと金属板と
の熱ラミネート性や、ラミネートされた金属板から缶へ
の加工性に劣る。25モル%を超えると、製缶工程後の
ヒートセット時や印刷焼き付け時の耐熱性に問題が生じ
るうえに、材料の結晶性がなくなって、樹脂ペレットの
充分な乾燥が困難となり製膜工程上のトラブルが生じた
り、フィルムが非晶性になり、フィルムの強度や耐熱性
が不足したり、フィルムがラミネートされた金属板が製
缶工程で熱ロールに巻き付いたりする。The proportion of ethylene isophthalate units in the S layer is 5 to 25 mol%, preferably 8 to 15 mol%.
It is. If it is less than 5 mol%, the heat laminating property between the film and the metal plate and the processability of the laminated metal plate into a can are inferior. If it exceeds 25 mol%, there will be a problem in heat resistance at the time of heat setting or printing and baking after the can manufacturing process, and the crystallinity of the material will be lost. Of the film, the film becomes amorphous, the strength and heat resistance of the film are insufficient, and the metal plate on which the film is laminated is wrapped around a hot roll in a can making process.
【0012】また、S層のジエチレンテレ(イソ)フタ
レート単位の割合は1〜5モル%、好ましくは、2〜4
モル%である。ジエチレンテレ(イソ)フタレート単位
を上記の範囲内においてポリエステル構成成分として導
入することにより、エチレンイソフタレート単位による
非晶性付与効果とエチレンテレフタレート単位の結晶性
とのバランスを調整することができ、フィルムと金属と
の熱ラミネート性、缶への加工性、耐熱性及び強度が得
られる。The proportion of diethylene tere (iso) phthalate units in the S layer is 1 to 5 mol%, preferably 2 to 4 mol%.
Mol%. By introducing the diethylene tere (iso) phthalate unit as a polyester component within the above range, it is possible to adjust the balance between the amorphous imparting effect of the ethylene isophthalate unit and the crystallinity of the ethylene terephthalate unit. Laminating properties of metal and metal, processability into a can, heat resistance and strength are obtained.
【0013】また、S層におけるエチレンテレフタレー
ト単位とジエチレンテレ(イソ)フタレート単位との合
計は、6〜25モル%の範囲であることが、強度、耐熱
性及び熱ラミネート性の点で好ましい。6モル%未満の
場合は、ポリエステルフィルムと金属との熱ラミネート
性や、ラミネートされた金属板から缶への加工性に劣
る。25モル%より多いと、結晶性がなくなって、ペレ
ットの充分な乾燥が困難となる。また、フィルムの強度
や耐熱性が不足したり、フィルムが非晶性になって、フ
ィルムがラミネートされた金属板が製缶工程で熱ロール
に巻き付いたりする。The total of the ethylene terephthalate unit and the diethylene tere (iso) phthalate unit in the S layer is preferably in the range of 6 to 25 mol% in view of strength, heat resistance and heat laminating property. If it is less than 6 mol%, the heat laminating property between the polyester film and the metal and the processability of the laminated metal plate into a can are inferior. If it is more than 25 mol%, the crystallinity is lost, and it is difficult to sufficiently dry the pellets. Further, the strength and heat resistance of the film are insufficient, or the film becomes amorphous, and the metal plate on which the film is laminated is wound around a hot roll in a can making process.
【0014】また、B層のポリエステルにはジエチレン
テレ(イソ)フタレートを5モル%以下、好ましくは1
〜4モル%共重合することによりフィルムの結晶性のバ
ランスを調整することができる。The polyester of the layer B contains diethylene tere (iso) phthalate in an amount of 5 mol% or less, preferably 1 mol% or less.
The balance of crystallinity of the film can be adjusted by copolymerization of 44 mol%.
【0015】本発明において、使用されるポリエステル
は、単一の共重合ポリエステルでもよいし、またポリエ
チレンテレフタレートと共重合ポリエステルの混合物、
あるいは2種以上の共重合ポリエステルを溶融混合した
ものであってもよい。In the present invention, the polyester used may be a single copolyester, or a mixture of polyethylene terephthalate and copolyester,
Alternatively, two or more copolymerized polyesters may be melt-mixed.
【0016】S層及びB層のポリエステル原料は、極限
粘度が0.5以上、好ましくは0.6〜1.2である。
極限粘度が0.5未満のポリエステルを用いると、フィ
ルム製造時の操業性が悪化し、また得られるフィルムの
強度が不足する。しかし、極限粘度があまり大きいと、
生産コストが上昇し好ましくない。The polyester raw material of the S layer and the B layer has an intrinsic viscosity of 0.5 or more, preferably 0.6 to 1.2.
When a polyester having an intrinsic viscosity of less than 0.5 is used, the operability at the time of film production deteriorates, and the strength of the obtained film is insufficient. However, if the intrinsic viscosity is too large,
Production costs increase, which is not desirable.
【0017】S層とB層のポリエステルの極限粘度の差
は、0.1以下、好ましくは0.09以下がよい。極限
粘度の差が0.1を超えると、製膜時にフィルムにフロ
ーマークが入る。フローマークとは、粘度の異なる2種
以上の樹脂がフィードブロックやTダイで合流する場合
に発生する一種の樹脂の流動変動、すなわち樹脂の流れ
模様のことをいう。The difference between the limiting viscosities of the polyesters in the S layer and the B layer is 0.1 or less, preferably 0.09 or less. When the difference in intrinsic viscosity exceeds 0.1, a flow mark is formed on the film during film formation. The flow mark refers to a flow variation of one kind of resin that occurs when two or more kinds of resins having different viscosities meet at a feed block or a T-die, that is, a flow pattern of the resin.
【0018】本発明で用いられるポリエステルは、結晶
性の場合には融点が200〜240℃、非晶性の場合に
はガラス転移温度が50〜85℃のものが好ましい。こ
れらの範囲を外れると、耐熱性が不足したり、熱ラミネ
ート性が低下したりする。The polyester used in the present invention preferably has a melting point of 200 to 240 ° C. in the case of crystallinity and a glass transition temperature of 50 to 85 ° C. in the case of non-crystallineness. Outside of these ranges, heat resistance may be insufficient or thermal lamination properties may be reduced.
【0019】S層及びB層を構成するポリエステルは、
上記条件を満足する範囲で任意の組み合わせが可能であ
る。その中で、S層のポリエステルの融点(非晶性の場
合はガラス転移温度)がB層のポリエステルのそれと同
じか、それより低いことが特に好ましい態様である。こ
れにより、フィルムの強度、耐熱性、熱ラミネート性を
良好にバランスさせることが可能となる。The polyester constituting the S layer and the B layer is as follows:
Any combination is possible as long as the above conditions are satisfied. Among them, it is a particularly preferred embodiment that the melting point of the polyester in the S layer (the glass transition temperature in the case of amorphous) is the same as or lower than that of the polyester in the B layer. This makes it possible to favorably balance the strength, heat resistance and thermal laminability of the film.
【0020】本発明で用いられるポリエステルは、その
特性を損なわない範囲(通常5モル%以下)で、イソフ
タル酸及びジエチレングリコール以外の、別の成分をさ
らに共重合したものであってもよい。この共重合成分の
具体例としては、フタル酸、2,6−ナフタレンジカル
ボン酸、5−ナトリウムスルホイソフタル酸、シュウ
酸、コハク酸、アジピン酸、セバシン酸、アゼライン
酸、ドデカン二酸、ダイマー酸、無水マレイン酸、マレ
イン酸、フマール酸、イタコン酸、シトラコン酸、メサ
コン酸、シクロヘキサンジカルボン酸等のジカルボン
酸、4−ヒドロキシ安息香酸、ε−カプロラクトンや乳
酸などのオキシカルボン酸があげられる。また、1,3
−プロパンジオール、1,4−ブタンジオール、ネオペ
ンチルグリコール、1,6−ヘキサンジオール、シクロ
ヘキサンジメタノール、トリエチレングリコール、ポリ
エチレングリコール、ポリプロピレングリコール、ポリ
テトラメチレングリコール、ビスフェノールAやビスフ
ェノールSのエチレンオキシド付加体等のグリコール等
があげられる。さらに、トリメリット酸、トリメシン
酸、ピロメリット酸、トリメチロールプロパン、グリセ
リン、ペンタエリスリトール等の3官能化合物等を少量
用いてもよい。The polyester used in the present invention may be one obtained by further copolymerizing another component other than isophthalic acid and diethylene glycol within a range that does not impair the properties (usually 5 mol% or less). Specific examples of the copolymer component include phthalic acid, 2,6-naphthalenedicarboxylic acid, 5-sodium sulfoisophthalic acid, oxalic acid, succinic acid, adipic acid, sebacic acid, azelaic acid, dodecane diacid, dimer acid, Oxycarboxylic acids such as maleic anhydride, maleic acid, fumaric acid, itaconic acid, citraconic acid, mesaconic acid, dicarboxylic acids such as cyclohexanedicarboxylic acid, 4-hydroxybenzoic acid, ε-caprolactone and lactic acid. Also, 1,3
-Propanediol, 1,4-butanediol, neopentyl glycol, 1,6-hexanediol, cyclohexanedimethanol, triethylene glycol, polyethylene glycol, polypropylene glycol, polytetramethylene glycol, ethylene oxide adduct of bisphenol A or bisphenol S And the like. Further, a small amount of a trifunctional compound such as trimellitic acid, trimesic acid, pyromellitic acid, trimethylolpropane, glycerin, and pentaerythritol may be used.
【0021】本発明のフィルムにおける酸化チタンの含
有量は、全フィルム中の平均濃度として20〜50重量
%、好ましくは25〜45重量%、最適には25〜40
重量%である。この含有量が20重量%未満であると、
フィルムの白度及び隠蔽性が不足する。50重量%を超
えると、本発明のような特定の三層構造を有するフィル
ムであってもフィルムの強度が低下してしまい、ラミネ
ート後のフィルムの成形性が劣る。The content of titanium oxide in the film of the present invention is 20 to 50% by weight, preferably 25 to 45% by weight, and most preferably 25 to 40% by weight as an average concentration in the whole film.
% By weight. When this content is less than 20% by weight,
The whiteness and hiding power of the film are insufficient. If it exceeds 50% by weight, the strength of the film is reduced even in a film having a specific three-layer structure as in the present invention, and the moldability of the film after lamination is inferior.
【0022】B層の酸化チタンの含有量は、20〜60
重量%、好ましくは25〜55重量%、最適には30〜
50重量%である。この配合量が20重量%未満である
とフィルムの白度、隠蔽性が不足する。60重量%を超
えると、フィルムの強度が低下してしまい、ラミネート
後のフィルムの成形性が劣る。The titanium oxide content of the layer B is from 20 to 60.
% By weight, preferably 25-55% by weight, optimally 30-55% by weight.
50% by weight. If the amount is less than 20% by weight, the whiteness and hiding power of the film will be insufficient. If it exceeds 60% by weight, the strength of the film is reduced, and the moldability of the film after lamination is inferior.
【0023】S層の酸化チタンの含有量は、20重量%
以下、好ましくは15重量%以下、最適には10重量%
以下である。この配合量が20重量%を超えると、金属
板へのラミネート時、もしくはフィルムがラミネートさ
れた金属板の製缶時に、治具の磨耗が発生して、製造プ
ロセスに多大な悪影響を与えたり、磨耗した金属や酸化
チタンが缶加工時にフィルム表面に付着して印刷性に問
題が発生したりすることがある。The titanium oxide content of the S layer is 20% by weight.
Or less, preferably 15% by weight or less, optimally 10% by weight
It is as follows. If the amount is more than 20% by weight, the jig will be worn when laminating on a metal plate or when making a metal plate on which a film is laminated, which has a great adverse effect on the manufacturing process, Worn metal or titanium oxide may adhere to the film surface during can processing, causing problems in printability.
【0024】本発明において、酸化チタンは必要に応じ
て公知の任意の表面処理を施して用いることができる。
また、酸化チタンの平均粒径は 0.1〜0.5 μm、好まし
くは 0.2〜0.5 μmであることが望ましい。平均粒径が
0.5 μmを超えると、酸化チタンの単位重量あたりの全
表面積が少なくなり、フィルムの隠蔽性や白度が不足し
たり、得られるフィルムの表面に凹凸ができて光沢度が
低くなり好ましくない。平均粒径が 0.1μm未満の場合
は、可視光の波長より小さくなり、可視光線がフィルム
を通過するおそれがあり、フィルムの隠蔽性や白度が不
足するので好ましくない。In the present invention, titanium oxide may be used after being subjected to any known surface treatment, if necessary.
The average particle size of the titanium oxide is preferably 0.1 to 0.5 μm, and more preferably 0.2 to 0.5 μm. Average particle size
If it exceeds 0.5 μm, the total surface area per unit weight of titanium oxide decreases, and the concealing property and whiteness of the film become insufficient, and the surface of the obtained film becomes uneven, resulting in low gloss. If the average particle size is less than 0.1 μm, the wavelength becomes smaller than the wavelength of visible light, and there is a possibility that visible light may pass through the film.
【0025】本発明のフィルムは、S層中に平均粒子径
0.25〜2.0μm の滑剤を0.01〜0.5重量
%、好ましくは0.05〜0.1重量%含有することが
必要である。滑剤の平均粒子径が0.25未満の場合、
フィルムの滑り性が低下して缶を成形する際の絞り加工
やシゴキ加工時にフィルムを傷付けたり、ピンホールが
発生することがある。また、平均粒子径が2.0μm よ
り大きいと粒子に応力が集中し、絞り加工やシゴキ加工
時にフィルムが破ける場合があり好ましくない。また、
滑剤の添加量が0.01重量%未満の場合は、フィルム
の滑り性が低下し、0.5重量%より多いとフィルムが
滑りやすくなりすぎてフィルムをロールに巻き取った時
の外観が悪くなる。The film of the present invention contains 0.01 to 0.5% by weight, preferably 0.05 to 0.1% by weight of a lubricant having an average particle size of 0.25 to 2.0 μm in the S layer. is necessary. When the average particle size of the lubricant is less than 0.25,
The slipperiness of the film is reduced, and the film may be damaged or pinholes may be generated during drawing or squeezing when forming a can. On the other hand, if the average particle size is larger than 2.0 μm, stress is concentrated on the particles, and the film may be broken during drawing or squeezing, which is not preferable. Also,
When the amount of the lubricant is less than 0.01% by weight, the slipperiness of the film is reduced. When the amount is more than 0.5% by weight, the film becomes too slippery and the appearance when the film is wound around a roll is poor. Become.
【0026】また、本発明のフィルムの B層の厚みは
5〜20μm 、好ましくは、10〜15μm であり、S
層の厚みは各0.5〜5μm 、好ましくは各1〜3μm
であり、全厚みは9〜25μm 、さらに好ましくは12
〜17μm である。B層の厚みが5μm 未満の場合、フ
ィルムの白度と隠蔽性が不足しやすく、また20μm を
超えると、過剰品質となってコストパフォーマンスを失
する恐れがある。また、S層の厚みが0.5μm 未満の
場合は、製缶時に治具の磨耗を生じたり、印刷性が低下
する場合がある。一方、5μm を超えると、フィルムの
機械特性は向上するが、フィルム厚みの割に白度や隠蔽
性は高くなく、また缶の成形時にS層とB層間の界面で
剥離現象が起こり易くなる。The thickness of the layer B of the film of the present invention is 5 to 20 μm, preferably 10 to 15 μm.
The thickness of each layer is 0.5 to 5 μm, preferably 1 to 3 μm.
And the total thickness is 9 to 25 μm, more preferably 12 to 25 μm.
1717 μm. When the thickness of the layer B is less than 5 μm, the whiteness and the concealing property of the film tend to be insufficient, and when it exceeds 20 μm, the quality may be excessive and the cost performance may be lost. If the thickness of the S layer is less than 0.5 μm, the jig may be worn during can making or the printability may be reduced. On the other hand, when the thickness exceeds 5 μm, the mechanical properties of the film are improved, but the whiteness and the concealing property are not high for the thickness of the film, and a peeling phenomenon easily occurs at the interface between the S layer and the B layer during the molding of the can.
【0027】また、本発明のフィルムは、金属とフィル
ムの間の動摩擦係数が0.05〜0.25、好ましくは
0.1〜0.2、フィルム同士の動摩擦係数が0.25
〜0.55、好ましくは0.3〜0.5であることが望
ましい。金属とフィルムの間の動摩擦係数が0.05未
満、又はフィルム同士の動摩擦係数が0.25未満の場
合は、フィルムが滑りやすくなりすぎてフィルムをロー
ルに巻き取った時の外観が悪くなる。また、金属とフィ
ルムの間の動摩擦係数が0.25より大きい場合、又は
フィルム同士の動摩擦係数が0.55より大きい場合
は、缶を成形する際の絞り加工やシゴキ加工時にフィル
ムの滑り性が悪くフィルムが破けたり、ピンホールが発
生することがある。また、缶をラインで搬送する場合に
缶ラミフィルム同士の滑り性が悪くて、缶がラインから
はみ出す等のトラブルの原因となり好ましくない。The film of the present invention has a coefficient of kinetic friction between the metal and the film of 0.05 to 0.25, preferably 0.1 to 0.2, and a coefficient of kinetic friction between the films of 0.25 to 0.25.
-0.55, preferably 0.3-0.5. If the coefficient of kinetic friction between the metal and the film is less than 0.05 or the coefficient of kinetic friction between the films is less than 0.25, the film becomes too slippery and the appearance when the film is wound up on a roll is poor. When the coefficient of kinetic friction between the metal and the film is greater than 0.25, or when the coefficient of kinetic friction between the films is greater than 0.55, the slipperiness of the film during drawing or squeezing when forming a can is reduced. Poorly, the film may be broken or a pinhole may be generated. In addition, when the cans are conveyed on a line, the slipperiness between the canned laminating films is poor, which causes troubles such as the cans protruding from the line, which is not preferable.
【0028】本発明のフィルムは、150℃、30分間
処理による熱収縮率が、下記範囲 TD≦6%、|MD−TD|≧3% さらに好ましくは、下記範囲 TD≦5%、|MD−TD|≧3.5% である。TD方向の熱収縮率が6%を越えると鋼板への
熱ラミ性が悪くなり、また、MDとTDの熱収縮率の差
が、3%未満の場合は、鋼板への熱ラミ時にシワがはい
る場合があり好ましくない。The film of the present invention has a heat shrinkage ratio at 150 ° C. for 30 minutes in the following range TD ≦ 6%, | MD−TD | ≧ 3%, more preferably the following range TD ≦ 5%, | MD− TD | ≧ 3.5%. When the heat shrinkage in the TD direction exceeds 6%, the heat laminating property to the steel sheet deteriorates, and when the difference between the heat shrinkage rates of the MD and TD is less than 3%, wrinkles occur during the heat laminating to the steel sheet. May not be desirable.
【0029】本発明のフィルムを形成するためのポリエ
ステルは、常法によって製造することができる。例えば
イソフタル酸成分とジエチレングリコールとが共重合さ
れたポリエチレンテレフタレート系共重合体は、次のよ
うにして製造することができる。まず、ビス(β−ヒド
ロキシエチル)テレフタレート及び/又はその低重合体
の存在するエステル化槽に、テレフタル酸とエチレング
リコールとのスラリーを連続的に供給し、250℃程度
の温度で8時間程度反応させ、エステル化反応率が95
%付近のエステル化物を連続的に得る。これを重合缶に
移送し、必要量のイソフタル酸又はそのエチレングリコ
ールエステルとジエチレングリコールとを添加する。そ
して、三酸化アンチモン、二酸化ゲルマニウム等の触媒
の存在下、1.3hPa以下の減圧下で280℃程度の
温度で重縮合反応を行う。The polyester for forming the film of the present invention can be produced by a conventional method. For example, a polyethylene terephthalate copolymer in which an isophthalic acid component and diethylene glycol are copolymerized can be produced as follows. First, a slurry of terephthalic acid and ethylene glycol is continuously supplied to an esterification tank in which bis (β-hydroxyethyl) terephthalate and / or a low polymer thereof is present, and reacted at a temperature of about 250 ° C. for about 8 hours. And the esterification reaction rate is 95
% Esterified product is continuously obtained. This is transferred to a polymerization vessel, and necessary amounts of isophthalic acid or its ethylene glycol ester and diethylene glycol are added. Then, a polycondensation reaction is performed at a temperature of about 280 ° C. under a reduced pressure of 1.3 hPa or less in the presence of a catalyst such as antimony trioxide and germanium dioxide.
【0030】このようにして得られるポリエステルは、
オリゴマーやアセトアルデヒドを比較的多量に含有して
いるので、これらの量を減少させるため、減圧もしくは
不活性ガス流通下、200〜240℃の温度(ポリエス
テルの融点を超えない温度)で固相重合し、さらに必要
に応じて水蒸気又は熱水で処理した後、製膜工程に供す
ることが好ましい。The polyester thus obtained is
As it contains a relatively large amount of oligomers and acetaldehyde, in order to reduce these amounts, solid-phase polymerization is performed at a temperature of 200 to 240 ° C (temperature not exceeding the melting point of polyester) under reduced pressure or an inert gas flow. It is preferable that the film is further treated with steam or hot water as required, and then subjected to a film forming step.
【0031】本発明のフィルムは、各層を構成する2種
の樹脂組成物を別々の押出機を用いて溶融し、フィード
ブロック法により重ね合わせてダイスより押し出す方
法、溶融した2種の樹脂組成物をマルチマニホールドダ
イス中で重ね合わせて押し出す方法、及び前記方法を組
み合わせた方法等を用いて未延伸シートを製造し、次に
テンター式二軸延伸法あるいはインフレーション法を用
いて延伸することにより得ることができる。また、各層
を構成する2種の延伸フィルムを貼り合わせる方法を用
いることもできる。The film of the present invention can be obtained by melting two resin compositions constituting each layer using separate extruders, superimposing them by a feed block method and extruding them from a die. A non-stretched sheet using a method of overlapping and extruding in a multi-manifold die, and a method combining the above-described methods, and then obtaining by stretching using a tenter-type biaxial stretching method or an inflation method. Can be. Further, a method of bonding two types of stretched films constituting each layer can also be used.
【0032】テンター式二軸延伸法を用いる場合には、
たとえば、S層及びB層を構成する酸化チタンが配合さ
れた2種のポリエステル組成物を溶融押出機に供給し、
220〜280℃の温度でシート状に押し出し、この押
し出されたシートを室温以下に温度調節した冷却ドラム
上に密着させて冷却し、得られた未延伸シートを必要に
応じてMDに1〜1.2倍程度の予備延伸し、その後に
テンターにより50〜150℃の温度でMD及びTDに
それぞれ2〜4倍程度の延伸倍率となるように二軸延伸
し、さらに、TDの弛緩率を数%として、80〜220
℃で数秒間熱処理を施すことによって、本発明のフィル
ムを製造することができる。In the case of using a tenter type biaxial stretching method,
For example, two types of polyester compositions containing titanium oxide constituting the S layer and the B layer are supplied to a melt extruder,
The extruded sheet is extruded into a sheet at a temperature of 220 to 280 ° C., and the extruded sheet is cooled by closely contacting it on a cooling drum whose temperature has been adjusted to room temperature or lower. Preliminarily stretched about 2 times, then biaxially stretched by a tenter at a temperature of 50 to 150 ° C to MD and TD so as to have a draw ratio of about 2 to 4 times each, and further, the relaxation rate of TD was 80 to 220 as%
By subjecting the film to a heat treatment at a temperature of several degrees Celsius for several seconds, the film of the present invention can be produced.
【0033】テンターによる二軸延伸方法としては、同
時二軸延伸法や逐次二軸延伸法がある。酸化チタンが高
充填されている場合には、延伸時にフィルムが破断しや
すくなるが、同時二軸延伸法を用いることにより、この
破断の発生を著しく低減することができるので、同時二
軸延伸法がより好適である。As a biaxial stretching method using a tenter, there are a simultaneous biaxial stretching method and a sequential biaxial stretching method. When the titanium oxide is highly filled, the film is easily broken at the time of stretching, but by using the simultaneous biaxial stretching method, the occurrence of the break can be significantly reduced. Is more preferable.
【0034】延伸後の熱処理は、フィルムの熱収縮率を
小さくするために必要な工程である。この熱処理の方法
としては、熱風を吹き付ける方法、赤外線を照射する方
法、マイクロ波を照射する方法等の公知の方法がある。
このうち、均一に精度良く加熱できることから熱風を吹
き付ける方法が最適である。The heat treatment after stretching is a necessary step for reducing the heat shrinkage of the film. As the method of this heat treatment, there are known methods such as a method of blowing hot air, a method of irradiating infrared rays, and a method of irradiating microwaves.
Among them, the method of blowing hot air is optimal because heating can be performed uniformly and accurately.
【0035】フィルム製造時や製缶時の工程通過性をよ
くするため、シリカ、アルミナ、カオリン等の無機滑剤
を少量添加して製膜してフィルム表面にスリップ性を付
与することが望ましい。さらに、フィルム外観や印刷性
を向上させるため、たとえば、フィルムにシリコーン化
合物等を含有させることもできる。また、金属とのラミ
ネート性を向上させたり、強度をさらに高めるために、
フィルム製造中のインラインコーティングもしくはフィ
ルム製造後のポストコーティングにより、接着層等の任
意のコーティング層を形成させてもよい。In order to improve the processability during film production and can production, it is desirable to add a small amount of an inorganic lubricant such as silica, alumina, kaolin or the like to form a film to impart slip properties to the film surface. Furthermore, in order to improve the appearance and printability of the film, for example, the film may contain a silicone compound or the like. Also, in order to improve laminating properties with metal and further increase strength,
An optional coating layer such as an adhesive layer may be formed by in-line coating during film production or post-coating after film production.
【0036】本発明のフィルムをラミネートする金属板
が鋼板の場合は、クロム酸処理、リン酸処理、電解クロ
ム酸処理、クロメート処理等の化成処理や、ニッケル、
スズ、亜鉛、アルミ、砲金、真鍮、その他の各種メッキ
処理などを施した鋼板を好ましく用いることができる。When the metal plate on which the film of the present invention is laminated is a steel plate, a chemical treatment such as chromic acid treatment, phosphoric acid treatment, electrolytic chromic acid treatment, chromate treatment, nickel,
Tin, zinc, aluminum, gunmetal, brass, and other various types of plated steel plates can be preferably used.
【0037】次に実施例によって本発明を具体的に説明
する。以下の実施例及び比較例におけるフィルムの特性
値の測定法は、次の通りである。Next, the present invention will be described specifically with reference to examples. The measuring method of the characteristic value of the film in the following Examples and Comparative Examples is as follows.
【0038】A.極限粘度 フェノール/四塩化エタンの等重量混合溶媒を用いて、
温度20℃で測定した溶液粘度から求めた。 B.熱収縮率 幅10mm、長さ10cmの試料を、約0.4g の荷重で1
50℃雰囲気下に30分間放置し、放置前後の寸法変化
を測定し、原長に対する放置後の長さの百分率で求め
た。なおデータは、MD方向3枚とTD方向3枚の各平
均値と、MD及びTDの平均値とで示した。 C.動摩擦係数 ASTM D−1894に準じて、引張速度133.3
mm/ min 、荷重200gの条件で測定した。 D.フィルム厚み 延伸フィルムから、ミクロトームを用いて薄切片を採取
し、電子顕微鏡を使用してこの薄切片の各層の厚みを測
定した。 F.缶の絞り、シゴキ加工性 フィルムをティンフリースチールと貼り合わせた後、フ
ィルム側を缶胴外面として、350mlの2ピース缶の深
絞り成形を行った。この操作を100缶分実施し、フィ
ルムに発生した傷の有無を観察し、傷が僅かでも認めら
れば×とした。A. Intrinsic viscosity Phenol / Ethane tetrachloride
It was determined from the solution viscosity measured at a temperature of 20 ° C. B. Heat shrinkage A sample of 10 mm in width and 10 cm in length was subjected to a load of about 0.4 g.
The sample was left for 30 minutes in an atmosphere of 50 ° C., the dimensional change before and after the measurement was measured, and the length was measured as a percentage of the original length after standing. The data is shown by the average value of three pieces in the MD direction and three pieces in the TD direction, and the average value of MD and TD. C. Dynamic friction coefficient According to ASTM D-1894, tensile speed 133.3
It was measured under the conditions of mm / min and a load of 200 g. D. Film thickness A thin section was collected from the stretched film using a microtome, and the thickness of each layer of the thin section was measured using an electron microscope. F. Drawing and canning of the can After laminating the film with tin-free steel, deep drawing of a 350 ml two-piece can was performed with the film side as the outer surface of the can body. This operation was carried out for 100 cans, and the presence or absence of scratches on the film was observed.
【0039】実施例1〜6及び比較例1〜4 表1に示したS層を構成するポリエステル樹脂組成物を
押出機1より温度280℃で溶融押出し、同様にB層を
構成するポリエステル樹脂組成物を押出機2より温度2
80℃で溶融押出した。溶融した2種の樹脂をマルチマ
ニホールドダイス中で重ね合わせて表1に示した厚さ構
成のS/B/Sの3層構造とし、Tダイからシート状に
押し出し、表面温度18℃の冷却ドラムに密着させて冷
却し、厚さ7〜300μmの未延伸シートを得た。得ら
れた未延伸シートをテンター式同時二軸延伸機に供給
し、温度90℃、延伸倍率をMD3.0、TD3.3と
して同時二軸延伸した後、TDの弛緩率を5%として、
温度155℃で4秒間の熱処理を施した後、冷却して巻
き取り、厚さ7〜30μmの白色複層フィルムを得た。
得られたフィルムの特性値等を表1に示す。なお、表1
において、IPAはイソフタル酸、DEGはジエチレン
グリコールを表す。Examples 1 to 6 and Comparative Examples 1 to 4 The polyester resin compositions constituting the S layer shown in Table 1 were melt-extruded from the extruder 1 at a temperature of 280 ° C., and similarly the polyester resin compositions constituting the B layer Extruder 2 to temperature 2
It was melt extruded at 80 ° C. The two melted resins are superimposed in a multi-manifold die to form a three-layer structure of S / B / S having a thickness shown in Table 1, extruded from a T-die into a sheet, and a cooling drum having a surface temperature of 18 ° C. And then cooled to obtain an unstretched sheet having a thickness of 7 to 300 μm. The obtained unstretched sheet is supplied to a tenter-type simultaneous biaxial stretching machine, and is simultaneously biaxially stretched at a temperature of 90 ° C., a stretching ratio of MD 3.0 and TD 3.3, and a TD relaxation rate of 5%.
After performing a heat treatment at a temperature of 155 ° C. for 4 seconds, the film was cooled and wound up to obtain a white multilayer film having a thickness of 7 to 30 μm.
Table 1 shows the characteristic values and the like of the obtained film. Table 1
In the above, IPA represents isophthalic acid, and DEG represents diethylene glycol.
【0040】[0040]
【表1】 [Table 1]
【0041】[0041]
【発明の効果】本発明によれば、優れた熱接着性(熱ラ
ミネート性)、成形性及び強度を有し、隠蔽性、白度に
優れ、金属缶製缶時に治具の傷が発生しにくく、さら
に、フィルム表面の優れた滑り性を有する金属缶の被覆
に好適に用いられる金属ラミネート用白色フィルムが提
供される。According to the present invention, it has excellent heat adhesion (heat lamination properties), moldability and strength, excellent concealing properties and whiteness, and causes a jig scratch when a metal can is made. The present invention provides a white film for metal lamination, which is preferably used for coating a metal can having excellent slipperiness on the film surface.
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 FI // B29K 67:00 B29L 9:00 ──────────────────────────────────────────────────続 き Continued on the front page (51) Int.Cl. 6 Identification code FI // B29K 67:00 B29L 9:00
Claims (6)
5モル%とエチレンイソフタレート単位0〜25モル%
とからなるポリエステルに酸化チタンが20〜60重量
%配合された組成物からなるB層と、エチレンテレフタ
レート単位94〜70モル%とエチレンイソフタレート
単位5〜25モル%とジエチレンテレ(イソ)フタレー
ト単位1〜5モル%からなるポリエステルに酸化チタン
が20重量%以下配合された組成物からなるS層とが、
S/B/Sの構成で積層された二軸延伸フィルムであっ
て、フィルム中の酸化チタン含有量が20〜50重量%
であり、かつ、S層中に平均粒子径0.25〜2.0μ
m の滑剤を0.01〜0.5重量%含有する金属ラミネ
ート用白色フィルム。1. An ethylene terephthalate unit of 100 to 7
5 mol% and ethylene isophthalate unit 0 to 25 mol%
A layer B comprising a composition in which titanium oxide is blended with 20 to 60% by weight of a polyester consisting of: 94 to 70 mol% of ethylene terephthalate units, 5 to 25 mol% of ethylene isophthalate units, and diethylene tere (iso) phthalate units An S layer comprising a composition in which titanium oxide is blended in an amount of 20% by weight or less with a polyester comprising 1 to 5% by mole,
A biaxially stretched film laminated in an S / B / S configuration, wherein the titanium oxide content in the film is 20 to 50% by weight.
And the average particle diameter in the S layer is 0.25 to 2.0 μm.
a white film for metal lamination, containing 0.01 to 0.5% by weight of a lubricant.
ート単位が1〜4モル%含有されている請求項1記載の
金属ラミネート用白色フィルム。2. The white film for metal lamination according to claim 1, wherein the B layer contains 1 to 4 mol% of diethylene tere (iso) phthalate units.
層のフィルム厚みが0.5〜2μm 、フィルムの全厚み
が9〜25μm である請求項1記載の金属ラミネート用
白色フィルム。3. The film thickness of the layer B is 5 to 20 μm.
The white film for metal lamination according to claim 1, wherein the film thickness of the layer is 0.5 to 2 µm, and the total thickness of the film is 9 to 25 µm.
05〜0.25、フィルム同士の動摩擦係数が0.25
〜0.55である請求項1又は2記載の金属ラミネート
用白色フィルム。4. The coefficient of kinetic friction between the metal and the film is 0.4.
05 to 0.25, coefficient of dynamic friction between films is 0.25
The white film for metal lamination according to claim 1, wherein the thickness is from 0.5 to 0.55.
(TD)の150℃×30分処理による乾熱収縮率が下
記範囲である請求項1〜3のいずれかに記載の金属ラミ
ネート用白色フィルム。 TD≦6%、|MD−TD|≧3%5. The white color for a metal laminate according to claim 1, wherein the dry heat shrinkage of the film in the machine direction (MD) and the transverse direction (TD) at 150 ° C. for 30 minutes is in the following range. the film. TD ≦ 6%, | MD−TD | ≧ 3%
項1〜4のいずれかに記載の金属ラミネート用白色フィ
ルム。6. The white film for metal lamination according to claim 1, which is produced by a simultaneous biaxial stretching method.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP35051697A JP4059966B2 (en) | 1997-12-19 | 1997-12-19 | White film for metal lamination |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP35051697A JP4059966B2 (en) | 1997-12-19 | 1997-12-19 | White film for metal lamination |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH11179846A true JPH11179846A (en) | 1999-07-06 |
| JP4059966B2 JP4059966B2 (en) | 2008-03-12 |
Family
ID=18411033
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP35051697A Expired - Lifetime JP4059966B2 (en) | 1997-12-19 | 1997-12-19 | White film for metal lamination |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP4059966B2 (en) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20000054986A (en) * | 1999-02-02 | 2000-09-05 | 장용균 | Polyester film for coating llluminating device |
| JP2002347170A (en) * | 2001-03-19 | 2002-12-04 | Toyo Seikan Kaisha Ltd | Resin-coated metal sheet having self-lubricating property, manufacturing method therefor, and metal can and can lid |
| JP2003020348A (en) * | 2001-07-11 | 2003-01-24 | Toray Ind Inc | Polyester film for bonding metal plates |
| JPWO2004094139A1 (en) * | 2003-04-24 | 2006-07-13 | 株式会社フジシールインターナショナル | Heat-shrinkable milky film, shrink label and labeled container |
| EP1806225A1 (en) * | 2005-12-09 | 2007-07-11 | Mitsubishi Polyester Film GmbH | Multilayer, white, biaxially oriented polyester film |
| JPWO2017159582A1 (en) * | 2016-03-18 | 2019-01-24 | 東洋紡株式会社 | Polyester film, laminate and package |
-
1997
- 1997-12-19 JP JP35051697A patent/JP4059966B2/en not_active Expired - Lifetime
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20000054986A (en) * | 1999-02-02 | 2000-09-05 | 장용균 | Polyester film for coating llluminating device |
| JP2002347170A (en) * | 2001-03-19 | 2002-12-04 | Toyo Seikan Kaisha Ltd | Resin-coated metal sheet having self-lubricating property, manufacturing method therefor, and metal can and can lid |
| JP2003020348A (en) * | 2001-07-11 | 2003-01-24 | Toray Ind Inc | Polyester film for bonding metal plates |
| JPWO2004094139A1 (en) * | 2003-04-24 | 2006-07-13 | 株式会社フジシールインターナショナル | Heat-shrinkable milky film, shrink label and labeled container |
| EP1806225A1 (en) * | 2005-12-09 | 2007-07-11 | Mitsubishi Polyester Film GmbH | Multilayer, white, biaxially oriented polyester film |
| JPWO2017159582A1 (en) * | 2016-03-18 | 2019-01-24 | 東洋紡株式会社 | Polyester film, laminate and package |
Also Published As
| Publication number | Publication date |
|---|---|
| JP4059966B2 (en) | 2008-03-12 |
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