JPH01176320A - Magnetic recording medium - Google Patents
Magnetic recording mediumInfo
- Publication number
- JPH01176320A JPH01176320A JP33531387A JP33531387A JPH01176320A JP H01176320 A JPH01176320 A JP H01176320A JP 33531387 A JP33531387 A JP 33531387A JP 33531387 A JP33531387 A JP 33531387A JP H01176320 A JPH01176320 A JP H01176320A
- Authority
- JP
- Japan
- Prior art keywords
- back coat
- coat layer
- powder
- magnetic
- lithium
- 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 description 49
- 239000000843 powder Substances 0.000 claims abstract description 42
- 239000002131 composite material Substances 0.000 claims abstract description 20
- 239000006229 carbon black Substances 0.000 claims abstract description 15
- JFBZPFYRPYOZCQ-UHFFFAOYSA-N [Li].[Al] Chemical compound [Li].[Al] JFBZPFYRPYOZCQ-UHFFFAOYSA-N 0.000 claims description 11
- 239000002245 particle Substances 0.000 abstract description 16
- 229910052782 aluminium Inorganic materials 0.000 abstract description 10
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 abstract description 10
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 abstract description 9
- 230000000694 effects Effects 0.000 abstract description 9
- 229910052744 lithium Inorganic materials 0.000 abstract description 9
- 239000012779 reinforcing material Substances 0.000 abstract 2
- 230000003247 decreasing effect Effects 0.000 abstract 1
- 239000010410 layer Substances 0.000 description 46
- 239000011230 binding agent Substances 0.000 description 13
- 239000000654 additive Substances 0.000 description 10
- 229920001577 copolymer Polymers 0.000 description 10
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 9
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 8
- 230000005294 ferromagnetic effect Effects 0.000 description 7
- -1 glycol ethers Chemical class 0.000 description 7
- 239000000203 mixture Substances 0.000 description 7
- 239000002216 antistatic agent Substances 0.000 description 6
- 239000011248 coating agent Substances 0.000 description 6
- 238000000576 coating method Methods 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- 239000006247 magnetic powder Substances 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 239000011347 resin Substances 0.000 description 5
- 229920005989 resin Polymers 0.000 description 5
- 238000007790 scraping Methods 0.000 description 5
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 239000000314 lubricant Substances 0.000 description 4
- 239000003960 organic solvent Substances 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 3
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 3
- 238000005299 abrasion Methods 0.000 description 3
- 230000000996 additive effect Effects 0.000 description 3
- 229910010272 inorganic material Inorganic materials 0.000 description 3
- 239000011147 inorganic material Substances 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 239000003973 paint Substances 0.000 description 3
- 229920000139 polyethylene terephthalate Polymers 0.000 description 3
- 239000005020 polyethylene terephthalate Substances 0.000 description 3
- 229920002635 polyurethane Polymers 0.000 description 3
- 229920002554 vinyl polymer Polymers 0.000 description 3
- QMMJWQMCMRUYTG-UHFFFAOYSA-N 1,2,4,5-tetrachloro-3-(trifluoromethyl)benzene Chemical compound FC(F)(F)C1=C(Cl)C(Cl)=CC(Cl)=C1Cl QMMJWQMCMRUYTG-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- 229910015189 FeOx Inorganic materials 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 229920001807 Urea-formaldehyde Polymers 0.000 description 2
- 229920002433 Vinyl chloride-vinyl acetate copolymer Polymers 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 238000003490 calendering Methods 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 229940090961 chromium dioxide Drugs 0.000 description 2
- IAQWMWUKBQPOIY-UHFFFAOYSA-N chromium(4+);oxygen(2-) Chemical compound [O-2].[O-2].[Cr+4] IAQWMWUKBQPOIY-UHFFFAOYSA-N 0.000 description 2
- AYTAKQFHWFYBMA-UHFFFAOYSA-N chromium(IV) oxide Inorganic materials O=[Cr]=O AYTAKQFHWFYBMA-UHFFFAOYSA-N 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- LZCLXQDLBQLTDK-UHFFFAOYSA-N ethyl 2-hydroxypropanoate Chemical compound CCOC(=O)C(C)O LZCLXQDLBQLTDK-UHFFFAOYSA-N 0.000 description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 2
- 229910052748 manganese Inorganic materials 0.000 description 2
- 125000005395 methacrylic acid group Chemical group 0.000 description 2
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 2
- 239000012744 reinforcing agent Substances 0.000 description 2
- 230000003014 reinforcing effect Effects 0.000 description 2
- 238000006748 scratching Methods 0.000 description 2
- 230000002393 scratching effect Effects 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- 229910052719 titanium Inorganic materials 0.000 description 2
- 239000010936 titanium Substances 0.000 description 2
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- 238000004804 winding Methods 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- OCJBOOLMMGQPQU-UHFFFAOYSA-N 1,4-dichlorobenzene Chemical compound ClC1=CC=C(Cl)C=C1 OCJBOOLMMGQPQU-UHFFFAOYSA-N 0.000 description 1
- SZIFAVKTNFCBPC-UHFFFAOYSA-N 2-chloroethanol Chemical compound OCCCl SZIFAVKTNFCBPC-UHFFFAOYSA-N 0.000 description 1
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
- 229910000838 Al alloy Inorganic materials 0.000 description 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229920001747 Cellulose diacetate Polymers 0.000 description 1
- 229920002284 Cellulose triacetate Polymers 0.000 description 1
- 229910020630 Co Ni Inorganic materials 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 229910002440 Co–Ni Inorganic materials 0.000 description 1
- 229910020674 Co—B Inorganic materials 0.000 description 1
- 229910020516 Co—V Inorganic materials 0.000 description 1
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 1
- 229910017061 Fe Co Inorganic materials 0.000 description 1
- 229910001030 Iron–nickel alloy Inorganic materials 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 229920000459 Nitrile rubber Polymers 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004962 Polyamide-imide Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 229920001328 Polyvinylidene chloride Polymers 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 229910001069 Ti alloy Inorganic materials 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 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
- 239000003082 abrasive agent Substances 0.000 description 1
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- JZQOJFLIJNRDHK-CMDGGOBGSA-N alpha-irone Chemical compound CC1CC=C(C)C(\C=C\C(C)=O)C1(C)C JZQOJFLIJNRDHK-CMDGGOBGSA-N 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 229910052797 bismuth Inorganic materials 0.000 description 1
- 238000005422 blasting Methods 0.000 description 1
- NTXGQCSETZTARF-UHFFFAOYSA-N buta-1,3-diene;prop-2-enenitrile Chemical compound C=CC=C.C=CC#N NTXGQCSETZTARF-UHFFFAOYSA-N 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 229920006217 cellulose acetate butyrate Polymers 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 229910000424 chromium(II) oxide Inorganic materials 0.000 description 1
- 239000011247 coating layer Substances 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 229940117389 dichlorobenzene Drugs 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 229940116333 ethyl lactate Drugs 0.000 description 1
- 239000003302 ferromagnetic material Substances 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 229910001337 iron nitride Inorganic materials 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 229910001234 light alloy Inorganic materials 0.000 description 1
- FUJCRWPEOMXPAD-UHFFFAOYSA-N lithium oxide Chemical compound [Li+].[Li+].[O-2] FUJCRWPEOMXPAD-UHFFFAOYSA-N 0.000 description 1
- 229910001947 lithium oxide Inorganic materials 0.000 description 1
- 229910001004 magnetic alloy Inorganic materials 0.000 description 1
- 239000000696 magnetic material Substances 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 229920003145 methacrylic acid copolymer Polymers 0.000 description 1
- 229940117841 methacrylic acid copolymer Drugs 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 229910021421 monocrystalline silicon Inorganic materials 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
- 229920001568 phenolic resin Polymers 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 238000007747 plating Methods 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920002312 polyamide-imide Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 229920002620 polyvinyl fluoride Polymers 0.000 description 1
- 239000005033 polyvinylidene chloride Substances 0.000 description 1
- 229910052707 ruthenium Inorganic materials 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000006104 solid solution Substances 0.000 description 1
- 238000004544 sputter deposition Methods 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 238000001771 vacuum deposition Methods 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- 229910000859 α-Fe Inorganic materials 0.000 description 1
- 229910006297 γ-Fe2O3 Inorganic materials 0.000 description 1
Landscapes
- Paints Or Removers (AREA)
- 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、非磁性支持体の一方の面に磁性層が、他方の
面にバックコート層が形成されてなる磁気記録媒体に関
するものであり、特にバックコート層の特性を改善した
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 a magnetic recording medium in which a magnetic layer is formed on one side of a non-magnetic support and a back coat layer is formed on the other side. In particular, the present invention relates to a magnetic recording medium with improved characteristics of a back coat layer.
本発明は、非磁性支持体の一方の面に磁性層が、他方の
面にバックコート層が形成されてなる磁気記録媒体にお
いて、前記バックコート層中にリチウム・アルミニウム
複合酸化物粉末とカーボンブラックとを含有させること
により、磁気記録媒体の走行安定性に優れ、バックコー
ト層表面の傷付きやテープガイドの削れ等を防止するこ
とが可能なGil気記録媒体を提供しようとするもので
ある。The present invention provides a magnetic recording medium in which a magnetic layer is formed on one side of a non-magnetic support and a back coat layer is formed on the other side, in which lithium-aluminum composite oxide powder and carbon black are contained in the back coat layer. The present invention aims to provide a magnetic recording medium which has excellent running stability and can prevent scratches on the surface of the back coat layer, scraping of the tape guide, etc. by containing the following.
一般に、オーディオテープ、ビデオテープ等の磁気記録
媒体では、高速巻き取り時の巻き乱れや非磁性支持体の
バンク面の傷付き等を効果的に防止し走行安定性や耐久
性を向上させる目的から磁性層を表面に有する非磁性支
持体の裏面にバックコート層を設けることが従来より行
われている。In general, for magnetic recording media such as audio tapes and video tapes, the purpose is to effectively prevent winding irregularities and scratches on the bank surface of the non-magnetic support during high-speed winding, and to improve running stability and durability. Conventionally, a back coat layer is provided on the back surface of a nonmagnetic support having a magnetic layer on the surface.
上述のような目的から設けられたバックコート層は、例
えばカーボンブラック、アルミナ、酸化チタン、α−酸
化鉄、炭酸カルシウム、硫酸バリラム、酸化亜鉛、シリ
カ等の非磁性無機材料粉末を結合剤樹脂中に分散させた
塗料を非磁性支持体の裏面に塗布することにより形成さ
れるもので、従来よりその効果について種々検討されて
きた。The back coat layer provided for the above-mentioned purpose is made by coating non-magnetic inorganic material powder such as carbon black, alumina, titanium oxide, α-iron oxide, calcium carbonate, baryram sulfate, zinc oxide, silica, etc. in a binder resin. It is formed by coating the back side of a non-magnetic support with a coating material dispersed in .
〔発明が解決しようとする問題点〕 ゛しかしながら、
バフクコ−)Jlの補強機能を強化させようとして多量
に上記非磁性無機材料粉末をバックコート層中に添加し
た場合、バックコート71の耐久性は向上するものの、
磁気記録媒体の走行によって該バックコート層からの粉
落ちや該バックコート層と直接接触するテープガイドの
削れが非常に大きなものとなってしまうと言う問題力1
発生する。[Problem that the invention seeks to solve] [However,
If a large amount of the non-magnetic inorganic material powder is added to the back coat layer in an attempt to strengthen the reinforcing function of Bafukuko Jl, the durability of the back coat 71 will improve, but
Problem 1: Due to the running of the magnetic recording medium, powder falls off from the back coat layer and the tape guide that comes into direct contact with the back coat layer becomes extremely abraded.
Occur.
そこで、本発明は上述の従来の実情に鑑みて提案された
ものであって、磁気記録媒体の走行安定性を向上させる
ことが可能で、粉落ち、バックコート層表面の傷付き、
テープガイドの削れを発生さセることのない磁気記録媒
体を提供することを目的とするものである。Therefore, the present invention was proposed in view of the above-mentioned conventional situation, and it is possible to improve the running stability of a magnetic recording medium, and prevent powder falling off, scratches on the surface of the back coat layer, etc.
The object of the present invention is to provide a magnetic recording medium that does not suffer from scratching of the tape guide.
本発明等は、上述の目的を達成せんものと鋭意研究の結
果、磁性層中に添加する非磁性無機材料粉末として新規
なリチウム・アルミニウム複合酸化物が非常に有効であ
り、このリチウム・アルミニウム複合酸化物を添加する
ことにより、走行安定性が向上し、粉落ち、バックコー
ト層表面の傷付き、テープガイドの削れを防止すること
ができるとの知見を得るに至った。In order to achieve the above-mentioned objects, the present invention has conducted intensive research and found that a new lithium-aluminum composite oxide is very effective as a non-magnetic inorganic material powder to be added to the magnetic layer. It has been found that adding oxides improves running stability and prevents powder falling, scratches on the surface of the back coat layer, and scraping of the tape guide.
本発明は上記知見に基づいてなされたものであって、非
磁性支持体の一方の面に磁性層が、他方の面にバックコ
ート層が形成されてなる磁気記録媒体において、前記バ
ックコート層中にリチウム・アルミニウム複合酸化物粉
末とカーボンブラックとを含有させたことを特徴とする
ものである。The present invention has been made based on the above findings, and provides a magnetic recording medium in which a magnetic layer is formed on one side of a non-magnetic support and a back coat layer is formed on the other side. It is characterized by containing lithium/aluminum composite oxide powder and carbon black.
この発明において使用されるリチウム・アルミニウム複
合酸化物粉末は、新規な材料で酸化アルミニウムとこれ
よりも塩基性の強いリチウム酸化物とから生ずる塩であ
り、−i式
%式%(1)
(但し上記式中Xは2以下、yは5以下の整数を表す、
)で表されるものである。具体的には例えばx=1.y
−1のときL i A j! 02 % X !1 *
y=5のときLiA!Solという式で表されるものが
挙げられる。The lithium-aluminum composite oxide powder used in this invention is a new material and is a salt formed from aluminum oxide and lithium oxide, which is more basic than aluminum oxide. In the above formula, X represents an integer of 2 or less, and y represents an integer of 5 or less,
). Specifically, for example, x=1. y
-1, L i A j! 02%X! 1 *
When y=5, LiA! An example of this is represented by the formula Sol.
上記L iAj!Ox + L 1AZsosとして
表されるリチウム・アルミニウム複合酸化物粉末の平均
粒子径は0.1〜0.8μmの範囲内のものを使用する
ことが好ましく、0.1μm未満では上記リチウム・ア
ルミニウム複合酸化物粉末を添加した効果が得られず、
粒子が微細なため凝集し粉落ちを発生したり、走行安定
性の劣化、バックコート層表面の傷付き、摩擦係数の上
昇等を招いてしまう。Above L iAj! The average particle diameter of the lithium/aluminum composite oxide powder expressed as Ox + L 1AZsos is preferably within the range of 0.1 to 0.8 μm, and if it is less than 0.1 μm, the lithium/aluminum composite oxide powder The effect of adding powder cannot be obtained,
Because the particles are so fine, they aggregate and cause powder to fall off, causing deterioration in running stability, scratches on the surface of the back coat layer, and an increase in the coefficient of friction.
また、平均粒子径が0.8μmより大きい場合には磁気
記録媒体のバックコート層との摺動部を削ることとなり
、例えばテープガイドの摩耗量が多(なってしまう。Furthermore, if the average particle diameter is larger than 0.8 μm, the sliding portion with the back coat layer of the magnetic recording medium will be scraped, resulting in a large amount of wear on the tape guide, for example.
なお、リチウム・アルミニウム複合酸化物粉末の粒子形
状は球形、角形、いびつ形等いずれの形状であってもそ
の効果は変わらず優れたものである。Note that the effect remains excellent regardless of the particle shape of the lithium-aluminum composite oxide powder, such as spherical, prismatic, or distorted.
したがって、所定の粒子径を有したリチウム・アルミニ
ウム複合酸化物粉末がバックコート層中に所定量含有さ
れることにより優れたバックコート面補強機能が充分に
発揮されて、磁気記録媒体の走行安定性が向上するとと
もに、粉落ちやバックコート層表面の傷付きが防止でき
、磁気記録媒体との修道面に当たるテープガイドの削れ
を防止する効果を同時に満足する。Therefore, by containing a predetermined amount of lithium-aluminum composite oxide powder with a predetermined particle size in the back coat layer, the excellent back coat surface reinforcing function is fully exhibited, and the running stability of the magnetic recording medium is improved. In addition, it is possible to prevent dust from falling off and scratches on the surface of the back coat layer, and it also satisfies the effects of preventing the tape guide from being scraped in contact with the magnetic recording medium.
一方、上述のリチウム・アルミニウム複合酸化物粉末と
同時にバックコート層中に添加されるカーボンブラック
は、バックコート層の帯電防止を目的として添加される
ものであり、その粒子径は0.01〜0.1μmの範囲
内のものを使用することが好ましい、上記粒子径が0.
01μm未満の場合にはバックコート層中での分散が急
り、走行性に悪影響を及ぼすおそれがあり、0.1μm
より大きい場合には帯電防止効果が得られな(なってし
まう。On the other hand, carbon black, which is added to the back coat layer at the same time as the above-mentioned lithium/aluminum composite oxide powder, is added for the purpose of preventing static electricity on the back coat layer, and its particle size is 0.01 to 0. It is preferable to use particles within the range of 0.1 μm.
If the diameter is less than 0.1 μm, the dispersion in the back coat layer will be rapid, which may adversely affect running performance.
If it is larger, the antistatic effect cannot be obtained.
上記リチウム・アルミニウム複合酸化物粉末とカーボン
ブラックをバックコート層中に添加する際には両者は、
リチウム・アルミニウム複合酸化物粉末/カーボンブラ
ックとして0.5 / 99.5〜25/75(重量比
)の割合で添加することが好ましい。When adding the above lithium-aluminum composite oxide powder and carbon black to the back coat layer, both
It is preferable to add lithium/aluminum composite oxide powder/carbon black in a ratio of 0.5/99.5 to 25/75 (weight ratio).
上述のようなリチウム・アルミニウム複合酸化物粉末を
含むバラフコ−)1fflは、通常、上記リチウム・ア
ルミニウム複合酸化物粉末及びカーボンブラックを結合
剤成分、有機溶剤及びその他の添加剤とともに混合分散
してバックコート層塗料を調製し、これをあらかじめ磁
性層を表面に形成した非磁性支持体の裏面に塗布、乾燥
して形成される。1ffl containing the above-mentioned lithium-aluminum composite oxide powder is usually prepared by mixing and dispersing the above-mentioned lithium-aluminum composite oxide powder and carbon black together with a binder component, an organic solvent, and other additives. The coating layer is formed by preparing a coating material, applying it to the back side of a non-magnetic support on which a magnetic layer has been previously formed, and drying it.
ここで、結合剤としては、従来から汎用されている結合
剤樹脂がいずれも使用可能であり、例えば塩化ビニル−
酢酸ビニル共重合体、塩化ビニル−酢酸ビニル−ビニル
アルコール共重合体、塩化ビニル−酢酸ビニル−マレイ
ン酸共重合体、塩化ビニル−塩化ビニリデン共重合体、
塩化ビニル−アクリロニトリル共重合体、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、メタクーリル酸エステル
ー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、熱可塑性ポリウレタン樹脂、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、
ブタジェン−アクリロニトリル共重合体、アクリロニト
リループクジエン−メタクリル酸共重合体、ポリビニル
ブチラール。Here, as the binder, any conventionally widely used binder resin can be used, such as vinyl chloride-
Vinyl acetate copolymer, vinyl chloride-vinyl acetate-vinyl alcohol copolymer, vinyl chloride-vinyl acetate-maleic acid copolymer, vinyl chloride-vinylidene chloride copolymer,
Vinyl chloride-acrylonitrile copolymer, acrylic ester-acrylonitrile copolymer, acrylic ester-vinylidene chloride copolymer, methacrylic ester-vinylidene chloride copolymer, methacrylic ester-styrene copolymer, thermoplastic polyurethane resin, Polyvinyl fluoride, vinylidene chloride-acrylonitrile copolymer,
Butadiene-acrylonitrile copolymer, acrylonitrile-cyclodiene-methacrylic acid copolymer, polyvinyl butyral.
セルロース誘導体、スチレンープクジェン共重合体、ポ
リエステル樹脂、フェノール樹脂、エポキシ樹脂、熱硬
化性ポリウレタン樹脂、尿素樹脂。Cellulose derivatives, styrene-pukuden copolymers, polyester resins, phenolic resins, epoxy resins, thermosetting polyurethane resins, urea resins.
メラミン樹脂、アルキド樹脂、尿素−ホルムアルデヒド
樹脂またはこれらの混合物等の結合剤樹脂が挙げられる
。Binder resins such as melamine resins, alkyd resins, urea-formaldehyde resins or mixtures thereof may be mentioned.
また、バックコート層に使用される有機溶剤としては、
アセトン、メチルエチルケトン、メチルイソブチルケト
ン、シクロヘキサノン等のケトン系、酢酸メチル、酢酸
エチル、酢酸ブチル、乳酸エチル、酢酸グリコールモノ
エチルエーテル等のエステル系、グリコールジメチルエ
ーテル、グリコールモノエチルエーテル、ジオキサン等
のグリコールエーテル系、ベンゼン、トルエン、キシレ
ン等の芳香族炭化水素、ヘキサン、ヘプタン等の脂肪族
炭化水素、メチレンクロライド、エチレンクロライド、
四塩化炭素、クロロホルム、エチレンクロルヒドリン、
ジクロルベンゼン等の塩素化炭化水素等が挙げられる。In addition, organic solvents used in the back coat layer include:
Ketones such as acetone, methyl ethyl ketone, methyl isobutyl ketone, and cyclohexanone; esters such as methyl acetate, ethyl acetate, butyl acetate, ethyl lactate, and glycol monoethyl acetate; and glycol ethers such as glycol dimethyl ether, glycol monoethyl ether, and dioxane. , aromatic hydrocarbons such as benzene, toluene and xylene, aliphatic hydrocarbons such as hexane and heptane, methylene chloride, ethylene chloride,
Carbon tetrachloride, chloroform, ethylene chlorohydrin,
Examples include chlorinated hydrocarbons such as dichlorobenzene.
さらに、リチウム・アルミニウム複合酸化物粉末及びカ
ーボンブラックとともに従来一般に使用されている添加
剤を併用してもよ(、例えばCaC0,粉末、13aS
O4扮末、Zn○粉末、α−Fe103粉末、T iO
z粉末等が挙げられる。Furthermore, additives commonly used in the past may be used together with the lithium-aluminum composite oxide powder and carbon black (for example, CaC0, powder, 13aS
O4 powder, Zn○ powder, α-Fe103 powder, TiO
Examples include z powder.
さらにまた、バックコート層に通常使用されている各種
添加剤、例えば潤滑剤、分散剤等も適宜添加して使用し
てもよい。Furthermore, various additives commonly used in back coat layers, such as lubricants and dispersants, may be added as appropriate.
一方、本発明の磁気記録媒体において磁性層は、例えば
強磁性粉末をこの種のii1気記録媒体の結合剤として
通常使用されるものに分散し、有機溶剤に溶かして調製
される磁性塗料を非磁性支持体の表面に塗布して形成さ
れる。On the other hand, in the magnetic recording medium of the present invention, the magnetic layer is made of a magnetic paint prepared by dispersing, for example, ferromagnetic powder in a binder commonly used as a binder for this type of recording medium and dissolving it in an organic solvent. It is formed by coating on the surface of a magnetic support.
ここで、磁性層に用いられる磁性粉末には通常のもので
あればいずれも使用することができる。Here, any ordinary magnetic powder can be used as the magnetic powder used in the magnetic layer.
したがって、使用できる磁性粉末としては、強磁性酸化
鉄粒子、強磁性二酸化クロム、?j4磁性合金粉末、六
方晶系バリウムフェライト微粒子、窒化鉄等が挙げられ
る。Therefore, the magnetic powders that can be used include ferromagnetic iron oxide particles, ferromagnetic chromium dioxide, and ferromagnetic iron oxide particles. Examples include J4 magnetic alloy powder, hexagonal barium ferrite fine particles, iron nitride, and the like.
上記強磁性酸化鉄粒子としては、−i式FeOxで表し
た場合、Xの値が1.33≦X≦1.50の範囲にある
もの、即ちマグヘマイト(γ−Fe2O3。The above-mentioned ferromagnetic iron oxide particles are those in which the value of X is in the range of 1.33≦X≦1.50 when expressed by the -i formula FeOx, that is, maghemite (γ-Fe2O3).
X=1.50)、マグネフィト (FesOl、 X
= 1.33)及びこれらの固溶体(FeOx、1.
33<X<1.50)である、さらに、これら強磁性酸
化鉄には、抗磁力をあげる目的でコバルトを添加しても
よい、コバルト含有酸化鉄には、大別してドープ型と被
着型の2種類がある。X=1.50), Magnephyte (FesOl, X
= 1.33) and their solid solutions (FeOx, 1.
33 < There are two types.
上記強磁性二酸化クロムとしては、CrOあるいはこれ
らに抗磁力を向上させる目的でRu、Sn。The above-mentioned ferromagnetic chromium dioxide may include CrO, or Ru and Sn for the purpose of improving coercive force thereof.
Te、Sb、’Fe、Ti、V、Mn等の少な(とも一
種類を添加したものを使用できる。It is possible to use one with a small amount of Te, Sb, 'Fe, Ti, V, Mn, etc. added thereto.
強磁性合金粉末としては、F e + Co 、N
i 。As the ferromagnetic alloy powder, Fe + Co, N
i.
Fe−Co、Fe−Ni、Fe−Co−Ni、C。Fe-Co, Fe-Ni, Fe-Co-Ni, C.
−Ni、Fa−Co−B、Fe−Co−Cr−B。-Ni, Fa-Co-B, Fe-Co-Cr-B.
Mn−B i、Mn−An、Fe−Co−V等が使用で
き、またこれらに種々の特性を改善する目的でΔ1.S
i、Ti、Cr、Mn、Cu、Zn等の金属成分を添加
してもよい。Mn-Bi, Mn-An, Fe-Co-V, etc. can be used, and Δ1. S
Metal components such as i, Ti, Cr, Mn, Cu, and Zn may be added.
これら磁性材料は結合剤樹脂及び有機溶剤とともに混合
して調製した6≦■性塗料を非磁性支持体上に塗布し、
乾燥させて磁性層を形成するか、あるいは強磁性材料を
真空薄着、イオンブレーティング、スパッタリング、メ
ツキ等の手段によって非磁性支持体上に被着させて磁性
層を形成すればよい。These magnetic materials are mixed with a binder resin and an organic solvent, and a 6≦■ paint is applied onto a non-magnetic support.
The magnetic layer may be formed by drying, or by depositing a ferromagnetic material on a nonmagnetic support by means such as vacuum deposition, ion blasting, sputtering, plating, or the like.
さらに上記磁性層には、一般に使用される結合剤や上述
の磁性粉末の他に添加剤として通常使用される分散剤、
潤滑剤、研磨剤、帯電防止剤、防錆剤等が加えられても
よい。Furthermore, in addition to the commonly used binder and the above-mentioned magnetic powder, the magnetic layer contains a dispersant that is commonly used as an additive.
Lubricants, abrasives, antistatic agents, rust inhibitors, etc. may also be added.
上述のようなバラフコ−)FJや磁性層を形成する非磁
性支持体の素材としては、通常この種の磁気記録媒体に
使用されるものであれば如何なるものであってもよそ、
例えばポリエチレンテレフタレート等のポリエステル類
、ポリエチーレン、ポリプロピレン等のポリオレフィン
類、セルローストリアセテートセルロースダイアセテー
トセルロースアセテートブチレート等のセルロース誘導
体、ポリ塩化ビニル、ポリ塩化ビニリデン等のビニル系
樹脂、ポリカーボネートポリイミド、ポリアミド、ポリ
アミドイミド等のプラスチック、紙、アルミニウム、銅
等の金属、アルミニウム合金、チタン合金等の軽合金、
セラミックス、単結晶シリコン等が挙げられる。この非
磁性支持体の形態としては、フィルム、テープ、シート
、ディスク、カード、ドラム等のいずれでも良い。The material for the non-magnetic support forming the FJ and the magnetic layer as described above may be any material that is normally used in this type of magnetic recording medium.
For example, polyesters such as polyethylene terephthalate, polyolefins such as polyethylene and polypropylene, cellulose derivatives such as cellulose triacetate, cellulose diacetate, cellulose acetate butyrate, vinyl resins such as polyvinyl chloride and polyvinylidene chloride, polycarbonate polyimide, polyamide, and polyamideimide. Plastics such as paper, aluminum, metals such as copper, light alloys such as aluminum alloys, titanium alloys, etc.
Examples include ceramics and single crystal silicon. The nonmagnetic support may be in any form such as a film, tape, sheet, disk, card, or drum.
バックコート層の補強剤として使用されるリチウム・ア
ルミニウム複合酸化物粉末は、補強剤としての機能は勿
論、それ自身の性質及び粒子径や含有■等に起因して走
行安定性の向上や粉落らの防止、バックコート層の傷付
き性(耐久性)、バックコートaとの摺接面に当たるテ
ープガイドの削れ性を低減する効果を発揮する。The lithium-aluminum composite oxide powder used as a reinforcing agent for the back coat layer not only functions as a reinforcing agent, but also improves running stability and powder removal due to its own properties, particle size, content, etc. This has the effect of preventing scratches (durability) of the back coat layer, and reducing the abrasion of the tape guide that is in sliding contact with the back coat a.
以下、本発明の具体的な実施例について説明するが、本
発明がこの実施例に限定されるものではないことはいう
までもない。Hereinafter, specific examples of the present invention will be described, but it goes without saying that the present invention is not limited to these examples.
添加剤 10重量部(L
i八へ081粒子径0.2μm)
帯電防止剤 90重量部(カ
ーボンブラック、粒子径24mμ。Additive 10 parts by weight (L
Antistatic agent 90 parts by weight (carbon black, particle size 24 mμ.
キャボソト社製、商品名ブラックバールズし)結合剤
30重量部(塩化ビニル
−酢酸ビニル共重合体)
結合剤 20重量部(ボ
リウレクン9日本ポリウレタン社製。Manufactured by Cabosoto, trade name: Black Burls) Binder
30 parts by weight (vinyl chloride-vinyl acetate copolymer) Binder 20 parts by weight (Polyurekun 9 manufactured by Nippon Polyurethane Co., Ltd.)
商品名N−5033)
潤滑剤(ブチルステアレート) 1重量部溶剤
(メチルエチルケトン) 200ffiff
1部溶剤(メチルイソブチルケトン’) 50f
flffi部溶剤(トルエン)50重量部
■箪五■威
磁性粉末 100重世部(比
表面積40m/g、Co−被Hr酸化鉄)結合剤
8重量部にトロセルロース
、旭化成社製、商品名NCI/2H)
結合剤 12重■部(ポ
リウレタン、日本ポリウレタン社製。Product name N-5033) Lubricant (butyl stearate) 1 part by weight Solvent (methyl ethyl ketone) 200ffiff
1 part solvent (methyl isobutyl ketone') 50f
50 parts by weight of solvent (toluene) 100 parts by weight of magnetic powder (specific surface area 40 m/g, Co-Hr iron oxide) binder
8 parts by weight of trocellulose, manufactured by Asahi Kasei Co., Ltd. (trade name: NCI/2H); 12 parts of binder (polyurethane, manufactured by Nippon Polyurethane Co., Ltd.);
商品名N−2304)
潤滑剤(ブチルステアレート) 2型皿部研磨
剤 5重量部(αアルミ
ナ、住友化学社製、商品名AKP−30)帯電防止剤
2重工部(カーボン、キャボ
フト社製、商品名バルカンXC−72)
溶剤(メチルエチルケトン) 120ffi
ffi部溶剤(メチルイソブチルケトン)60重量部溶
剤(トルエン)60重量部
上記磁性店組成物をボールミルにて48時間混合し、フ
ィルタで濾過した後、コロネートLを2重量部添加した
。30分後、これを16μmW、のポリエチレンテレフ
タレートフィルム上に乾燥後の膜厚が6μmとなるよう
に塗布した0次いで磁場配向処理を行った後、乾燥して
巻取った。これをカレンダー処理した後、さらに硬化し
た。Product name N-2304) Lubricant (butyl stearate) Type 2 dish polishing agent 5 parts by weight (α alumina, manufactured by Sumitomo Chemical Co., Ltd., product name AKP-30) Antistatic agent
2 Heavy Industries Department (Carbon, manufactured by Caboft Co., Ltd., trade name Vulcan XC-72) Solvent (methyl ethyl ketone) 120ffi
Part ffi: 60 parts by weight of solvent (methyl isobutyl ketone) 60 parts by weight of solvent (toluene) The above magnetic store composition was mixed in a ball mill for 48 hours, filtered with a filter, and then 2 parts by weight of Coronate L was added. After 30 minutes, this was coated on a 16 μmW polyethylene terephthalate film so that the film thickness after drying would be 6 μm.Then, the film was subjected to magnetic field orientation treatment, dried, and wound up. This was calendered and then further hardened.
一方、上記磁性Pj組成物とは別にバックコート層組成
物をボールミ、ルにて48時間混合し、これにコロネー
トLを2.5重量部添加してバックコート層塗料を作製
した。どれを上述のようにして磁性層を形成したポリエ
チレンテレフタレートフィルムの裏面に乾燥後の塗布厚
が2μmとなるように塗布した0次いでこれを巻取り、
カレンダー処理した後、1/2インチ幅にスリットして
サンプルテープを作製した。Separately from the above magnetic Pj composition, a back coat layer composition was mixed in a ball mill for 48 hours, and 2.5 parts by weight of Coronate L was added thereto to prepare a back coat layer paint. This was coated on the back side of the polyethylene terephthalate film on which the magnetic layer was formed as described above so that the coating thickness after drying was 2 μm.Then, this was rolled up.
After calendering, the tape was slit into 1/2 inch width to prepare a sample tape.
尖ル桝又二仄立凱ユ
バックコート層組成物中の添加剤の種類、粒子径、添加
量、帯電防止剤(カーボンブラック)の添加■を第1表
に示すように変え、他は実施例1と同様の方法によりサ
ンプルテープを作製した。The types of additives, particle size, amount added, and addition of antistatic agent (carbon black) in the back coat layer composition were changed as shown in Table 1, and the other changes were carried out. A sample tape was prepared in the same manner as in Example 1.
止較史上二止較桝l
バックコート層組成物中の添加剤の種類、粒子径、添加
量、帯電防止剤(カーボンブラック)の添加量を第1表
に示すように変え、他は実施例1と同様の方法によりサ
ンプルテープを作製した。Two-stop comparison test in history The types, particle diameters, and amounts of additives in the backcoat layer composition, and the amount of antistatic agent (carbon black) added were changed as shown in Table 1, and the other values were as shown in Example 1. A sample tape was prepared in the same manner as in Example 1.
実施例1〜実施例9及び比較例1〜比較例60バックコ
ー)Fi!、&Il成物で使用した添加剤の種類。Examples 1 to 9 and Comparative Examples 1 to 60 Backco) Fi! , & types of additives used in the formulation.
粒子径、添加量及び帯電防止剤(カーボンブラック)の
添加量を第1表に示す。Table 1 shows the particle size, amount added, and amount of antistatic agent (carbon black) added.
(以下余白)
第1表
得られた各サンプルテープについて、それぞれバックコ
ート面の傷付き性、ガイド削れ性、摩擦係数、粉落ちを
測定した。その結果を第2表に示す。(The following is a blank space) Table 1 For each of the sample tapes obtained, the scratch resistance of the back coat surface, the guide abrasion resistance, the friction coefficient, and the powder falling off were measured. The results are shown in Table 2.
なお、バックコート層の傷付き性とガイド削れ性及び粉
落ちは共に目視による観察の結果を良好を○、普通をΔ
、やや悪いをム、悪いをXとして表し、摩擦係数につい
ては低速のテープ速度(0゜411/5ec)における
バックコート層表面とISステンレスとの摩擦係数を測
定して求めた。In addition, the scratch resistance of the back coat layer, guide abrasion resistance, and powder fall-off were visually observed as ○ for good and Δ for average.
The coefficient of friction was determined by measuring the coefficient of friction between the surface of the back coat layer and IS stainless steel at a low tape speed (0°411/5ec).
(以下余白)
第2表
上記第2表から明らかなように、本発明に係る実施例1
〜実施例9の各サンプルテープにあっては、バックコー
ト面の傷付やテープガイド削れ、さらには粉落らも起こ
らず、またF!!擦係数も非常に小さい値である。(The following is a blank space) Table 2 As is clear from the above Table 2, Example 1 according to the present invention
~For each sample tape of Example 9, there was no scratching on the back coat surface, no scraping of the tape guide, and no powder falling off, and F! ! The friction coefficient is also a very small value.
一方、比較例1〜比較例6のサンプルテープは従来より
使用されている添加剤を使用しているが、バックコート
層面の傷付き性、テープガイド削れ、粉落ちが劣化して
おり、さらにはP?!擦係数も大きな値となっている。On the other hand, the sample tapes of Comparative Examples 1 to 6 use additives that have been used conventionally, but the scratch resistance of the back coat layer surface, tape guide scraping, and powder falling have deteriorated, and furthermore, P? ! The friction coefficient also has a large value.
(発明の効果ン
以上の説明から明らかなように、本発明においては新規
なリチウム・アルミニウム複合酸化物粉末をバックコー
ト層の添加剤として用いているので、上記リチウム・ア
ルミニウム複合酸化物粉末の優れた効果により、磁気記
録媒体の走行安定性の向上が図れ、粉落ちやバックコー
ト層表面の傷付き、さらにはテープガイドの削れ等を防
止することが可能な磁気記録媒体を提供することができ
る。(Effects of the Invention) As is clear from the above explanation, in the present invention, a novel lithium/aluminum composite oxide powder is used as an additive for the back coat layer. Due to these effects, it is possible to improve the running stability of the magnetic recording medium, and to provide a magnetic recording medium that can prevent powder falling off, scratches on the surface of the back coat layer, and even scraping of the tape guide. .
特許出願人 ソニー株式会社 代理人 弁理士 小泡 晃 同 口材 榮− 同 佐藤 勝 手続ネ甫正魯帽発) 昭和63年3月24日Patent applicant: Sony Corporation Agent Patent Attorney Akira Koba Same mouthpiece Sakae Same as Masaru Sato Procedures from Fu Zheng Lu Cap) March 24, 1986
Claims (1)
クコート層が形成されてなる磁気記録媒体において、 前記バックコート層中にリチウム・アルミニウム複合酸
化物粉末とカーボンブラックとを含有させたことを特徴
とする磁気記録媒体。[Scope of Claims] A magnetic recording medium in which a magnetic layer is formed on one surface of a non-magnetic support and a back coat layer is formed on the other surface, wherein the back coat layer contains lithium-aluminum composite oxide powder. A magnetic recording medium characterized by containing carbon black.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP33531387A JPH01176320A (en) | 1987-12-29 | 1987-12-29 | Magnetic recording medium |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP33531387A JPH01176320A (en) | 1987-12-29 | 1987-12-29 | Magnetic recording medium |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH01176320A true JPH01176320A (en) | 1989-07-12 |
Family
ID=18287128
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP33531387A Pending JPH01176320A (en) | 1987-12-29 | 1987-12-29 | Magnetic recording medium |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH01176320A (en) |
-
1987
- 1987-12-29 JP JP33531387A patent/JPH01176320A/en active Pending
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