JPS63183621A - Production of magnetic recording medium - Google Patents
Production of magnetic recording mediumInfo
- Publication number
- JPS63183621A JPS63183621A JP1469087A JP1469087A JPS63183621A JP S63183621 A JPS63183621 A JP S63183621A JP 1469087 A JP1469087 A JP 1469087A JP 1469087 A JP1469087 A JP 1469087A JP S63183621 A JPS63183621 A JP S63183621A
- Authority
- JP
- Japan
- Prior art keywords
- curing
- magnetic
- tape
- recording medium
- magnetic layer
- 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
- 230000005291 magnetic effect Effects 0.000 title claims abstract description 44
- 238000004519 manufacturing process Methods 0.000 title claims description 3
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- 239000000843 powder Substances 0.000 abstract description 8
- 238000006243 chemical reaction Methods 0.000 abstract description 7
- 239000011248 coating agent Substances 0.000 abstract description 5
- 238000000576 coating method Methods 0.000 abstract description 5
- 239000011230 binding agent Substances 0.000 abstract description 4
- 238000011282 treatment Methods 0.000 abstract description 4
- 239000006229 carbon black Substances 0.000 abstract description 3
- 229920005992 thermoplastic resin Polymers 0.000 abstract description 3
- 238000001035 drying Methods 0.000 abstract description 2
- 229910052759 nickel Inorganic materials 0.000 abstract description 2
- 229910006297 γ-Fe2O3 Inorganic materials 0.000 abstract 2
- UCNNJGDEJXIUCC-UHFFFAOYSA-L hydroxy(oxo)iron;iron Chemical compound [Fe].O[Fe]=O.O[Fe]=O UCNNJGDEJXIUCC-UHFFFAOYSA-L 0.000 abstract 1
- KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 abstract 1
- 229920001577 copolymer Polymers 0.000 description 12
- 230000003746 surface roughness Effects 0.000 description 9
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 8
- 239000000203 mixture Substances 0.000 description 7
- -1 Aromatic isocyanates Chemical class 0.000 description 5
- 239000006247 magnetic powder Substances 0.000 description 5
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 235000014113 dietary fatty acids Nutrition 0.000 description 4
- 125000005442 diisocyanate group Chemical group 0.000 description 4
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- 239000013557 residual solvent Substances 0.000 description 4
- FKTHNVSLHLHISI-UHFFFAOYSA-N 1,2-bis(isocyanatomethyl)benzene Chemical compound O=C=NCC1=CC=CC=C1CN=C=O FKTHNVSLHLHISI-UHFFFAOYSA-N 0.000 description 3
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- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 2
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- 229920001807 Urea-formaldehyde Polymers 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 239000003945 anionic surfactant Substances 0.000 description 2
- 239000002216 antistatic agent Substances 0.000 description 2
- 229910003460 diamond Inorganic materials 0.000 description 2
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- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
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- 238000010894 electron beam technology Methods 0.000 description 2
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- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 2
- 150000002513 isocyanates Chemical class 0.000 description 2
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 2
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 2
- 239000003973 paint Substances 0.000 description 2
- 229920006122 polyamide resin Polymers 0.000 description 2
- 229920001225 polyester resin Polymers 0.000 description 2
- 239000004645 polyester resin Substances 0.000 description 2
- 229920000139 polyethylene terephthalate Polymers 0.000 description 2
- 239000005020 polyethylene terephthalate Substances 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 239000004576 sand Substances 0.000 description 2
- 229920001187 thermosetting polymer Polymers 0.000 description 2
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 2
- 238000004804 winding Methods 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- VZXPHDGHQXLXJC-UHFFFAOYSA-N 1,6-diisocyanato-5,6-dimethylheptane Chemical compound O=C=NC(C)(C)C(C)CCCCN=C=O VZXPHDGHQXLXJC-UHFFFAOYSA-N 0.000 description 1
- IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 description 1
- TWJNQYPJQDRXPH-UHFFFAOYSA-N 2-cyanobenzohydrazide Chemical compound NNC(=O)C1=CC=CC=C1C#N TWJNQYPJQDRXPH-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- APXYQFWNKAYRFS-UHFFFAOYSA-N C(C=C)(=O)O.ClC=COC=CCl Chemical compound C(C=C)(=O)O.ClC=COC=CCl APXYQFWNKAYRFS-UHFFFAOYSA-N 0.000 description 1
- 239000005635 Caprylic acid (CAS 124-07-2) Substances 0.000 description 1
- 229920001747 Cellulose diacetate Polymers 0.000 description 1
- DQEFEBPAPFSJLV-UHFFFAOYSA-N Cellulose propionate Chemical compound CCC(=O)OCC1OC(OC(=O)CC)C(OC(=O)CC)C(OC(=O)CC)C1OC1C(OC(=O)CC)C(OC(=O)CC)C(OC(=O)CC)C(COC(=O)CC)O1 DQEFEBPAPFSJLV-UHFFFAOYSA-N 0.000 description 1
- 229920002284 Cellulose triacetate Polymers 0.000 description 1
- 229910020630 Co Ni Inorganic materials 0.000 description 1
- 229910002440 Co–Ni Inorganic materials 0.000 description 1
- CTKINSOISVBQLD-UHFFFAOYSA-N Glycidol Chemical compound OCC1CO1 CTKINSOISVBQLD-UHFFFAOYSA-N 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- OYHQOLUKZRVURQ-HZJYTTRNSA-N Linoleic acid Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(O)=O OYHQOLUKZRVURQ-HZJYTTRNSA-N 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
- 235000021360 Myristic acid Nutrition 0.000 description 1
- TUNFSRHWOTWDNC-UHFFFAOYSA-N Myristic acid Natural products CCCCCCCCCCCCCC(O)=O TUNFSRHWOTWDNC-UHFFFAOYSA-N 0.000 description 1
- 239000000020 Nitrocellulose Substances 0.000 description 1
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- 229910019142 PO4 Inorganic materials 0.000 description 1
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- 235000021355 Stearic acid Nutrition 0.000 description 1
- WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 1
- 229920006311 Urethane elastomer Polymers 0.000 description 1
- 229920002433 Vinyl chloride-vinyl acetate copolymer Polymers 0.000 description 1
- NNLVGZFZQQXQNW-ADJNRHBOSA-N [(2r,3r,4s,5r,6s)-4,5-diacetyloxy-3-[(2s,3r,4s,5r,6r)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6s)-4,5,6-triacetyloxy-2-(acetyloxymethyl)oxan-3-yl]oxyoxan-2-yl]methyl acetate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](OC(C)=O)[C@H]1OC(C)=O)O[C@H]1[C@@H]([C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O1)OC(C)=O)COC(=O)C)[C@@H]1[C@@H](COC(C)=O)O[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O NNLVGZFZQQXQNW-ADJNRHBOSA-N 0.000 description 1
- FJWGYAHXMCUOOM-QHOUIDNNSA-N [(2s,3r,4s,5r,6r)-2-[(2r,3r,4s,5r,6s)-4,5-dinitrooxy-2-(nitrooxymethyl)-6-[(2r,3r,4s,5r,6s)-4,5,6-trinitrooxy-2-(nitrooxymethyl)oxan-3-yl]oxyoxan-3-yl]oxy-3,5-dinitrooxy-6-(nitrooxymethyl)oxan-4-yl] nitrate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O)O[C@H]1[C@@H]([C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@@H](CO[N+]([O-])=O)O1)O[N+]([O-])=O)CO[N+](=O)[O-])[C@@H]1[C@@H](CO[N+]([O-])=O)O[C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O FJWGYAHXMCUOOM-QHOUIDNNSA-N 0.000 description 1
- RNXZADVBNGOJOL-UHFFFAOYSA-N [Sb+]=O.[Sn+2]=O.[O-2].[Ti+4] Chemical class [Sb+]=O.[Sn+2]=O.[O-2].[Ti+4] RNXZADVBNGOJOL-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 125000002723 alicyclic group Chemical group 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- 125000002947 alkylene group Chemical group 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
- 150000001412 amines Chemical class 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 150000001414 amino alcohols Chemical class 0.000 description 1
- 239000002280 amphoteric surfactant Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
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- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
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- 229920006218 cellulose propionate Polymers 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- HGAZMNJKRQFZKS-UHFFFAOYSA-N chloroethene;ethenyl acetate Chemical compound ClC=C.CC(=O)OC=C HGAZMNJKRQFZKS-UHFFFAOYSA-N 0.000 description 1
- 229910000423 chromium oxide Inorganic materials 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229910001651 emery Inorganic materials 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 125000004185 ester group Chemical group 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000002223 garnet Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 238000009499 grossing Methods 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- SZVJSHCCFOBDDC-UHFFFAOYSA-N iron(II,III) oxide Inorganic materials O=[Fe]O[Fe]O[Fe]=O SZVJSHCCFOBDDC-UHFFFAOYSA-N 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 229940033355 lauric acid Drugs 0.000 description 1
- 239000000787 lecithin Substances 0.000 description 1
- 235000010445 lecithin Nutrition 0.000 description 1
- 229940067606 lecithin Drugs 0.000 description 1
- 235000020778 linoleic acid Nutrition 0.000 description 1
- OYHQOLUKZRVURQ-IXWMQOLASA-N linoleic acid Natural products CCCCC\C=C/C\C=C\CCCCCCCC(O)=O OYHQOLUKZRVURQ-IXWMQOLASA-N 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- CWQXQMHSOZUFJS-UHFFFAOYSA-N molybdenum disulfide Chemical compound S=[Mo]=S CWQXQMHSOZUFJS-UHFFFAOYSA-N 0.000 description 1
- 229910052982 molybdenum disulfide Inorganic materials 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 229920001220 nitrocellulos Polymers 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 229960002446 octanoic acid Drugs 0.000 description 1
- WMHSAFDEIXKKMV-UHFFFAOYSA-N oxoantimony;oxotin Chemical class [Sn]=O.[Sb]=O WMHSAFDEIXKKMV-UHFFFAOYSA-N 0.000 description 1
- AJCDFVKYMIUXCR-UHFFFAOYSA-N oxobarium;oxo(oxoferriooxy)iron Chemical compound [Ba]=O.O=[Fe]O[Fe]=O.O=[Fe]O[Fe]=O.O=[Fe]O[Fe]=O.O=[Fe]O[Fe]=O.O=[Fe]O[Fe]=O.O=[Fe]O[Fe]=O AJCDFVKYMIUXCR-UHFFFAOYSA-N 0.000 description 1
- MOQRZWSWPNIGMP-UHFFFAOYSA-N pentyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCCCC MOQRZWSWPNIGMP-UHFFFAOYSA-N 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 125000005496 phosphonium group Chemical group 0.000 description 1
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
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- 229920000570 polyether Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920002620 polyvinyl fluoride Polymers 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 239000001397 quillaja saponaria molina bark Substances 0.000 description 1
- 229930182490 saponin Natural products 0.000 description 1
- 150000007949 saponins Chemical class 0.000 description 1
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 125000000542 sulfonic acid group Chemical group 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium group Chemical group [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Chemical group OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
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- TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 1
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- ITRNXVSDJBHYNJ-UHFFFAOYSA-N tungsten disulfide Chemical compound S=[W]=S ITRNXVSDJBHYNJ-UHFFFAOYSA-N 0.000 description 1
- 238000001132 ultrasonic dispersion Methods 0.000 description 1
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- 229920002554 vinyl polymer Polymers 0.000 description 1
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Landscapes
- Manufacturing Of Magnetic Record Carriers (AREA)
Abstract
Description
【発明の詳細な説明】
産業上の利用分野
本発明は、オーディオ・ビデオ機器或いはコンピュータ
等に用いる磁気テープ、磁気シート等の磁気記録媒体に
関するものである。DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application The present invention relates to magnetic recording media such as magnetic tapes and magnetic sheets used in audio/video equipment, computers, and the like.
従来の技術
磁気記録媒体は、年々高密度記録化への傾向を深めつつ
ある。その結果、短波長領域における記録、再生損失の
低減が必要となり、磁気ヘッドと磁気記録媒体の間の空
隙をより小さくするための方策が施されている。すなわ
ち、磁気記録媒体表面の高平滑化、磁性粉の微粉末化な
どである。BACKGROUND OF THE INVENTION Magnetic recording media are increasingly becoming more densely packed year by year. As a result, it is necessary to reduce recording and reproducing losses in the short wavelength region, and measures are being taken to further reduce the gap between the magnetic head and the magnetic recording medium. That is, making the surface of the magnetic recording medium highly smooth, making the magnetic powder finer, etc.
ところが、この様な磁気記録媒体表面の高平滑化により
磁気記録媒体の摩擦係数が増大するため、走行性、耐久
性が従来のものに比べて劣化する。However, due to the high smoothness of the surface of the magnetic recording medium, the coefficient of friction of the magnetic recording medium increases, resulting in poor running performance and durability compared to conventional magnetic recording media.
この問題を解決する方法としては、磁気記録媒体の非磁
性支持体上の磁性層とは反対側の面にバックコート層を
設けることが一般に知られている。このバックコート層
は、非磁性粉末と結合剤から成っている。非磁性粉末は
塗膜強度や表面電気抵抗等の調節のために充填剤として
用いられる。バックコート層は、バックコート層用塗料
を非磁性支持体上に塗布後、平滑化処理を行うことによ
り適度の表面粗さを付与して形成される。As a method for solving this problem, it is generally known to provide a back coat layer on the surface of the nonmagnetic support of the magnetic recording medium opposite to the magnetic layer. This backcoat layer consists of non-magnetic powder and a binder. Nonmagnetic powder is used as a filler to adjust coating strength, surface electrical resistance, etc. The back coat layer is formed by applying a back coat layer paint onto a non-magnetic support and then subjecting it to a smoothing treatment to impart an appropriate surface roughness.
こうして、磁性層及びバックコート層が塗布された後に
ロール状に巻とられ、硬化処理が施される。その方法と
しては、60℃から70℃位の一定温度で一定時間放置
されるものであった。After the magnetic layer and back coat layer are coated in this manner, the film is wound up into a roll and subjected to a curing treatment. The method was to leave it at a constant temperature of about 60°C to 70°C for a certain period of time.
発明が解決しようとする問題点
ロール状に巻とられた磁気テープは硬化処理が施される
。その時磁性層の表面粗さはバックコート層或はベース
フィルムの表面性の影響を受ける。これは所謂裏移りと
呼ばれている現象であり、硬化中に磁性層に接している
相手面の表面粗さが転写される現象である。この場合、
巻外から巻心にかけて加わる力に傾斜があるためにこの
裏移りの度合が異なり、巻心のほうがその影響の度合が
大きい。Problems to be Solved by the Invention Magnetic tape wound into a roll is subjected to a hardening process. At this time, the surface roughness of the magnetic layer is influenced by the surface properties of the back coat layer or base film. This is a phenomenon called set-off, in which the surface roughness of the other surface in contact with the magnetic layer is transferred during curing. in this case,
Because there is a slope in the force applied from the outside to the core, the degree of set-off varies, and the influence is greater on the core.
そのため磁性層の表面性が長手方向で傾斜を持ち、それ
により電磁時変換特性、粉落ち、ヘッド摩耗等の特性に
も傾斜が現われ、安定した製品を作るのが困難になって
いた。As a result, the surface properties of the magnetic layer have a gradient in the longitudinal direction, which causes gradients in properties such as electromagnetic time conversion characteristics, powder shedding, and head wear, making it difficult to produce stable products.
問題点を解決するための手段
本発明は、非磁性支持体上に磁性層を形成したテープ状
磁気記録媒体の製造工程中、その硬化工程で、テープの
自動巻直し機を内蔵した硬化炉を用い硬化中に巻直しを
行なうことにより、裏移りによる表面粗さの傾斜を軽減
することができ、安定した磁気テープを製造できるもの
である。Means for Solving the Problems The present invention utilizes a curing furnace equipped with an automatic tape rewinding machine in the curing process during the manufacturing process of a tape-shaped magnetic recording medium in which a magnetic layer is formed on a non-magnetic support. By rewinding the magnetic tape during hardening, it is possible to reduce the slope of surface roughness due to set-off, and it is possible to produce a stable magnetic tape.
作 用
本発明によれば、その硬化工程で、テープの自動巻直し
機を内蔵した硬化炉を用いることにより、裏移りによる
表面粗さの傾斜を取り除くことができる。そのため、表
面粗さのバラツキに起因する電時変換特へヘッド摩耗、
粉落ち等のバラツキ或はその特性の傾斜を低減すること
ができる。Function According to the present invention, by using a curing furnace equipped with an automatic tape rewinding machine in the curing process, it is possible to eliminate gradients in surface roughness due to set-off. As a result, head wear due to variations in surface roughness, especially for power-to-hour conversion,
It is possible to reduce variations in powder falling, etc., or the slope of its characteristics.
また、磁性層中の残留溶剤量の低減も図れるため、塗膜
の充填率も上がり、電磁変換特性、耐久性等の特性も向
上し、硬化中にしわも入ることがないため、生産性も向
上する。In addition, since the amount of residual solvent in the magnetic layer can be reduced, the filling rate of the coating film is increased, and properties such as electromagnetic conversion characteristics and durability are also improved.Wrinkles do not appear during curing, which improves productivity. improves.
実施例
本発明に使用できる強磁性粉としては、γ−F e 2
03. C。Examples The ferromagnetic powder that can be used in the present invention is γ-F e 2
03. C.
含有r−’Fe2O3,Co被着r −”2 Q3等の
酸化物磁性粉、Fe。Contains r-'Fe2O3, Co-coated r-''2 Q3, etc. oxide magnetic powder, Fe.
Ni 、Coを主成分とするメタル系磁性粉、及びバリ
ウムフェライト等各種の強磁性粉が挙げられる。Various ferromagnetic powders such as metal-based magnetic powders containing Ni and Co as main components and barium ferrite may be used.
バインダー用樹脂としては、熱可塑性樹脂、熱硬化性樹
脂、電子線硬化型樹脂及びこれらと他の混合物が使用さ
れる。As the binder resin, thermoplastic resins, thermosetting resins, electron beam curable resins, and mixtures thereof with others are used.
バインダー樹脂としての熱可塑性樹脂としては硬化温度
が150℃以下、平均分子量10,000〜20,00
0、重合度が約200〜2,000程度の物で、例えば
塩化ビニル酢酸ビニル共重合体、塩化ビニル−塩化ビニ
リデン共重合体、アクリル酸エステル−アクリロニトリ
ル共重合体、アクリル酸エステル−塩化ビニリデン共重
合体。The thermoplastic resin used as the binder resin has a curing temperature of 150°C or less and an average molecular weight of 10,000 to 20,00.
0, with a degree of polymerization of about 200 to 2,000, such as vinyl chloride-vinylidene acetate copolymer, vinyl chloride-vinylidene chloride copolymer, acrylic ester-acrylonitrile copolymer, acrylic ester-vinylidene chloride copolymer Polymer.
アクリル酸エステル−スチレン共重合体、メタクリル酸
エステル−アクリロニトリル共重合体、メタクリル酸エ
ステル−塩化ビニリデン共重合体、メタクリル酸エステ
ル−スチレン共重合体、ウレタンエラストマー、ポリ弗
化ビニル、塩化ビニリデン−アクリロニトリル共重合体
、アクリロニトリル−ブタジェン共重合体、ポリアミド
樹脂、ポリビニルブチラール、スチレン−ブタジェン共
重合体、ポリエステル樹脂、クロロビニルエーテル−ア
クリル酸エステル共重合体、アミン樹脂、セルロース誘
導体としてセルロースアセテートブチレート。Acrylic ester-styrene copolymer, methacrylic ester-acrylonitrile copolymer, methacrylic ester-vinylidene chloride copolymer, methacrylic ester-styrene copolymer, urethane elastomer, polyvinyl fluoride, vinylidene chloride-acrylonitrile copolymer Polymers, acrylonitrile-butadiene copolymers, polyamide resins, polyvinyl butyral, styrene-butadiene copolymers, polyester resins, chlorovinyl ether-acrylic acid ester copolymers, amine resins, cellulose acetate butyrate as cellulose derivatives.
セルロースダイアセテート、セルローストリアセテート
、セルロースプロピオネート、ニトロセルロースなどが
ある。Examples include cellulose diacetate, cellulose triacetate, cellulose propionate, and nitrocellulose.
熱硬化性樹脂としては塗布液の状態では200.000
以下の分子量であり、塗布乾燥後には縮合、付加等の反
応により不溶化するものが使用される。これらの樹脂の
内では、樹脂が熱分解するまでの間に軟化又は溶融しな
いものが好ましい。具体的には、例えばフェノール樹脂
、エポキシ樹脂、ポリウレタン硬化型樹脂、尿素樹脂、
メラミン樹脂、アルキッド樹脂、シリコン樹脂、アクリ
ル系反応樹脂、塩化ビニル−酢酸ビニル樹脂。As a thermosetting resin, it is 200.000 in the state of coating liquid.
Those having the following molecular weights and which become insolubilized by reactions such as condensation and addition after coating and drying are used. Among these resins, those that do not soften or melt before the resin is thermally decomposed are preferred. Specifically, for example, phenol resin, epoxy resin, polyurethane curable resin, urea resin,
Melamine resin, alkyd resin, silicone resin, acrylic reaction resin, vinyl chloride-vinyl acetate resin.
メタクリル酸塩共重合体とジイソシアネートプレポリマ
ーの混合物、高分子ポリエステル樹脂とジイソシアネー
トプレポリマーの混合物、尿素ホルムアルデヒド樹脂、
ポリエステルポリオールと(ポリ)インシアネートの混
合物、ポリアミド樹脂、低分子量グリコール、高分子量
ジオール、トリフェニルメタントリインシアネートの混
合物及びこれらの混合物等である。Mixtures of methacrylate copolymers and diisocyanate prepolymers, mixtures of polymeric polyester resins and diisocyanate prepolymers, urea formaldehyde resins,
These include mixtures of polyester polyols and (poly)incyanates, polyamide resins, low molecular weight glycols, high molecular weight diols, mixtures of triphenylmethane triincyanate, and mixtures thereof.
電子線硬化型樹脂としては、不飽和プレポリマーとして
例えば、無水マレイン酸タイプ、ウレタンアクリルタイ
プ、ポリエステルアクリルタイプ。Examples of unsaturated prepolymers for electron beam curable resins include maleic anhydride type, urethane acrylic type, and polyester acrylic type.
ポリエーテルアクリルタイプ、ポリウレタンアクリルタ
イプ、ポリアミドアクリルタイプ等、又は、多官能モノ
マーとして、エーテルアクリルタイプ。Polyether acrylic type, polyurethane acrylic type, polyamide acrylic type, etc., or ether acrylic type as a polyfunctional monomer.
ウレタンアクリルタイプ、リン酸エステルアクリルタイ
プ、アリールタイプ等が挙げられる。Examples include urethane acrylic type, phosphate ester acrylic type, and aryl type.
さらに本発明にかかる磁気記録媒体の耐久性を向上させ
るために、磁性層中に各種硬化剤を含有させることがで
き、例えば、インシアネートを含有させることができる
。Furthermore, in order to improve the durability of the magnetic recording medium according to the present invention, various hardening agents can be contained in the magnetic layer, for example, incyanate can be contained.
使用できる芳香族イソシアネートは、例えばトリレンジ
イソシアネート(TDI )、4,4−ジフェニルメタ
ンジイソシアネー)(MDI)、キシリレンジイソシア
ネー)(XDI)、メタキシリレンジイソシアネー)(
M、XDI)、及びこれらイソシアネートと活性水素化
合物との付加体であり、平均分子量としては100〜3
,000の範囲の物が好適である。Aromatic isocyanates that can be used are, for example, tolylene diisocyanate (TDI), 4,4-diphenylmethane diisocyanate (MDI), xylylene diisocyanate (XDI), metaxylylene diisocyanate) (
M, XDI), and adducts of these isocyanates and active hydrogen compounds, with an average molecular weight of 100 to 3.
,000 is preferred.
一方、脂肪族イソシアネートとしては、ヘキサメチレン
ジイソシアネー) (HMDI )、 リレンジイソ
シアネート、トリメチルへキサメチレンジイソシアネー
ト、及びこれらイソシアネートと活性水素化合物との付
加体が挙げられる。これらのインシアネート及びこれら
インシアネートと活性水素化合物との付加体などの中で
も望ましいのは、分子量が100〜3,000の範囲の
物である。脂肪族インシアネートのなかでも非脂環式の
インシアネート及びこれらインシアネートと活性水素化
合物との付加体が望ましい。On the other hand, examples of aliphatic isocyanates include hexamethylene diisocyanate (HMDI), lylene diisocyanate, trimethylhexamethylene diisocyanate, and adducts of these isocyanates and active hydrogen compounds. Among these incyanates and adducts of these incyanates and active hydrogen compounds, those having a molecular weight in the range of 100 to 3,000 are preferable. Among the aliphatic incyanates, non-alicyclic incyanates and adducts of these incyanates and active hydrogen compounds are desirable.
分散剤としては、レシチン、カプリル酸、ラウリン酸、
ミリスチン酸、バルミチン酸、ステアリン酸、オレイン
酸、エライジン酸、リノール酸。Dispersants include lecithin, caprylic acid, lauric acid,
Myristic acid, valmitic acid, stearic acid, oleic acid, elaidic acid, linoleic acid.
リレイン酸等の炭素原子数8〜18個の脂肪酸。Fatty acids having 8 to 18 carbon atoms, such as lyleic acid.
上記の脂肪酸のアルカリ金属(Li、Na、に等)又は
アルカリ土類金属(Mg、Ca、Ba等)からなる金属
石鹸が挙げられる。この他に、炭素原子数12以上の高
級アルコールさらには硫酸エステルも使用可能である。Examples include metal soaps made of alkali metals (Li, Na, etc.) or alkaline earth metals (Mg, Ca, Ba, etc.) of the above-mentioned fatty acids. In addition, higher alcohols having 12 or more carbon atoms and sulfuric esters can also be used.
研磨剤としては、溶融アルミナ、炭化ケイ素(StC)
、酸化クロム、コランダム、人造コランダム、ダイアモ
ンド、人造ダイアモンド、ザクロ石、エメリー(主成分
:コランダムと磁鉄鉱)等が使用できる。As an abrasive, fused alumina, silicon carbide (StC)
, chromium oxide, corundum, artificial corundum, diamond, artificial diamond, garnet, emery (main components: corundum and magnetite), etc. can be used.
帯電防止剤は、導電性粉末として、グラフフィト、酸化
スズ−酸化アンチモン系化合物、酸化チタン−酸化スズ
−酸化アンチモン系化合物、天然界面活性剤ではサポニ
ン、ノニオン界面活性剤としてアルキレンオキサイド系
、グリセリン系、グリシドール系、カチオン界面活性剤
として高級アルキルアミン類、第4級アンモニウム塩類
、ピリジンその他複素環類、ホスホニウム類、スルホニ
ウム類、アニオン界面活性剤としてカルボン酸。Antistatic agents include graphite, tin oxide-antimony oxide type compounds, titanium oxide-tin oxide-antimony oxide type compounds as conductive powders, saponin as natural surfactants, alkylene oxide type and glycerin type as nonionic surfactants. , glycidol type, higher alkylamines, quaternary ammonium salts, pyridine and other heterocycles, phosphoniums, sulfoniums as cationic surfactants, carboxylic acids as anionic surfactants.
スルホン酸、燐酸や硫酸エステル基、燐酸エステル基等
の酸性基等を含むアニオン界面活性剤、アミノ酸類、ア
ミノスマホン酸類、アミノアルコールの硫酸又は燐酸エ
ステル等の両性活性剤などが挙げられる。この他に好ま
しい帯電防止剤としてカーボンブラックがある。Examples include anionic surfactants containing acidic groups such as sulfonic acid, phosphoric acid, sulfuric acid ester groups, and phosphoric ester groups, and amphoteric surfactants such as amino acids, aminomashonic acids, and sulfuric or phosphoric esters of amino alcohols. Another preferable antistatic agent is carbon black.
潤滑剤としては、シリコーンオイル、グラファイト、二
硫化モリブデン、二硫化タングステン。Lubricants include silicone oil, graphite, molybdenum disulfide, and tungsten disulfide.
炭素原子数12〜16の一塩基性脂肪酸、−価のアルコ
ールからなる炭素原子数21〜23個の脂肪酸エステル
がある。There are monobasic fatty acids having 12 to 16 carbon atoms, and fatty acid esters having 21 to 23 carbon atoms consisting of -valent alcohols.
磁性塗料の混線分散にあたっては、各種の混線機が使用
される。例えば、三本ロールミル、アジテータミル、ボ
ールミル、ペブルミル、サンドグラインダー、高速スト
ーンミル、高速度衝撃ミル。Various types of crosstalk devices are used to disperse magnetic paint crosstalk. For example, three roll mill, agitator mill, ball mill, pebble mill, sand grinder, high speed stone mill, high speed impact mill.
ディスパー、アトライター、ニーダ−、プラネタリ−ミ
キサー、高速ミキサー、ホモジナイザー。Dispers, attritors, kneaders, planetary mixers, high speed mixers, homogenizers.
コボールミル、超音波分散機などが単独もしくは、組合
わせて用いられる。A cobal mill, an ultrasonic dispersion machine, etc. are used alone or in combination.
以下さらに本発明を具体的に説明する。The present invention will be further explained in detail below.
(実施例1)
Fe−Co−Niメタル磁性粉 100重量
部BET比表面積 ss tr?/?
Hc 1500 0e
a8 125 emu/7
長軸 0.23 μm
短軸 0.04 μm
ポリウレタン 10重量
部塩化ビニル−酢酸ビニル共重合体 10重量
部α−A1203 6重量
部ミリスチン酸 2重量部
ステアリン酸ペンチル 1重量部ME
K−トルxン−MIBK 200重量部
(重量比2:2:1)
上記の組成物をコンティニュアスニーダ−、ボールミル
、サンドミルを用いて分散した。(Example 1) Fe-Co-Ni metal magnetic powder 100 parts by weight BET specific surface area ss tr? /? Hc 1500 0e a8 125 emu/7 Long axis 0.23 μm Short axis 0.04 μm Polyurethane 10 parts by weight Vinyl chloride-vinyl acetate copolymer 10 parts by weight α-A1203 6 parts by weight Myristic acid 2 parts by weight Pentyl stearate 1 Weight part ME
K-Tolxun-MIBK 200 parts by weight (weight ratio 2:2:1) The above composition was dispersed using a continuous kneader, a ball mill, and a sand mill.
次にインシアネート(コロネートL、日本ポリウレタン
社製)を4部加え、平均孔径1μmのフィルターでろ過
し、10μm厚のポリエチレンテレフタレートフィルム
上に塗布、配向、乾燥、カレンダー処理後、ロール状に
巻とり、70度の硬化炉で、60時間硬化した。Next, 4 parts of Incyanate (Coronate L, manufactured by Nippon Polyurethane Co., Ltd.) was added, filtered through a filter with an average pore size of 1 μm, coated on a 10 μm thick polyethylene terephthalate film, oriented, dried, calendered, and then wound into a roll. , in a curing oven at 70 degrees for 60 hours.
その後磁性層と反対側のポリエチレンテレフタレートフ
ィルム上に、カーボンブラックを主成分とするバックコ
ート層を設けた後、ロール状に巻とり、70度の硬化炉
で24時間硬化する。このようにして、3000mの磁
気テープを得た。上記の2回の硬化処理は、いずれも、
本発明の自動巻直し機を内蔵する硬化炉に入れておこな
う。Thereafter, a back coat layer containing carbon black as a main component was provided on the polyethylene terephthalate film on the side opposite to the magnetic layer, and then wound into a roll and cured in a curing oven at 70 degrees for 24 hours. In this way, a 3000 m magnetic tape was obtained. In both of the above two curing treatments,
This is carried out in a curing furnace containing an automatic rewinding machine of the present invention.
テープの一端をA、もう一端をBとする。最初は、Aを
巻心とし、1時間硬化後、Bが巻心となるように巻直し
、2時間硬化する。次にAを巻心とし、4時間、Bを巻
心とし8時間という様に行なう。Let one end of the tape be A and the other end B. Initially, A is used as the core, and after curing for 1 hour, it is re-wound so that B is the core, and cured for 2 hours. Next, use A as the core for 4 hours, B as the core and continue for 8 hours, and so on.
(比較例1)
2回の硬化工程で、いずれも、A端を巻心として、硬化
をし、巻直しは、行なわなかった。(Comparative Example 1) In both of the curing steps, the A-end was used as the core for curing, and no rewinding was performed.
(比較例2)
2回の硬化工程で、最初はA端を巻心として、バックコ
ート塗布後、B端を巻心として硬化をし、途中巻直しは
、行なわなかった。(Comparative Example 2) In two curing steps, first, the A end was used as the winding core, and after backcoating, the B end was used as the winding core and hardening was performed, and no rewinding was performed midway.
得られた各磁気テープの特性を第1表〜第4表に示す。The characteristics of each magnetic tape obtained are shown in Tables 1 to 4.
磁気テープの特性の傾斜をみるために、実施例、比較例
とも、500m毎にサンプリングした。In order to observe the gradient of the characteristics of the magnetic tape, samples were taken every 500 m in both the example and the comparative example.
表 1 表面粗さ
表 2 Cハ (dB)
表 3 ヘッド摩耗(μ)
表 4 残留溶剤量(μy/m)(注)残留溶
剤量は MEK、)ルエン、MIBKの総量である。Table 1 Surface roughness Table 2 C (dB) Table 3 Head wear (μ) Table 4 Amount of residual solvent (μy/m) (Note) The amount of residual solvent is the total amount of MEK, ) luene, and MIBK.
表面粗度はRank Ta1or Hobson 社
製、Ta1ystopで表面粗度Ra (表面粗度の中
心線よりの偏差の算術平均)を測定した。Surface roughness Ra (arithmetic mean of deviations from the center line of surface roughness) was measured using Talystop, manufactured by Rank Ta1or Hobson.
得られた各磁気テープを8篩幅に裁断し、カセットイン
した後、イーストマンコダック社販売8定した。Cハは
キャリアとして5MHzの値を、ノイズとしては4.5
MHzの値を用いた。なお実施例のA端をodBとした
。Each of the obtained magnetic tapes was cut into 8 sieve widths, loaded into a cassette, and sold by Eastman Kodak Company. C has a value of 5 MHz as the carrier and 4.5 as the noise.
MHz values were used. Note that the A end in the example was set to odB.
ヘッド摩耗は、5℃、so%RHの環境で100パス走
行させた時のものを示す。Head wear is shown when running 100 passes in an environment of 5° C. and so% RH.
発明の効果
実施例と比較例を比べてみれば明らかなように、本発明
の巻直し機を内蔵した硬化炉を用いると、特性の傾斜が
低減できるだけでなく、残留溶剤量も減るためテープの
耐久性、電磁変換特性の向上も図ることができた。これ
は明らかに、巻直し機を内蔵した硬化炉を用いた結果で
ある。Effects of the Invention As is clear from comparing Examples and Comparative Examples, using the curing furnace with a built-in rewinding machine of the present invention not only reduces the slope of the properties but also reduces the amount of residual solvent, which improves the strength of the tape. We were also able to improve durability and electromagnetic conversion characteristics. This is clearly a result of using a curing oven with a built-in rewinder.
Claims (1)
体の硬化工程で、テープの自動巻直し機を内蔵した硬化
炉を用い硬化中に巻直しを行なうことを特徴とする磁気
記録媒体の製造方法。In the curing process of a tape-shaped magnetic recording medium in which a magnetic layer is formed on a non-magnetic support, a curing furnace equipped with an automatic tape rewinding machine is used to perform rewinding during curing. Production method.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1469087A JPS63183621A (en) | 1987-01-23 | 1987-01-23 | Production of magnetic recording medium |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1469087A JPS63183621A (en) | 1987-01-23 | 1987-01-23 | Production of magnetic recording medium |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS63183621A true JPS63183621A (en) | 1988-07-29 |
Family
ID=11868190
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1469087A Pending JPS63183621A (en) | 1987-01-23 | 1987-01-23 | Production of magnetic recording medium |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS63183621A (en) |
-
1987
- 1987-01-23 JP JP1469087A patent/JPS63183621A/en active Pending
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