JP3006334B2 - Manufacturing method of magnetic recording medium - Google Patents
Manufacturing method of magnetic recording mediumInfo
- Publication number
- JP3006334B2 JP3006334B2 JP5043976A JP4397693A JP3006334B2 JP 3006334 B2 JP3006334 B2 JP 3006334B2 JP 5043976 A JP5043976 A JP 5043976A JP 4397693 A JP4397693 A JP 4397693A JP 3006334 B2 JP3006334 B2 JP 3006334B2
- Authority
- JP
- Japan
- Prior art keywords
- organic dye
- magnetic recording
- recording medium
- integer
- group
- 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.)
- Expired - Lifetime
Links
- 238000004519 manufacturing process Methods 0.000 title claims description 9
- 150000001875 compounds Chemical class 0.000 claims description 22
- 239000006229 carbon black Substances 0.000 claims description 9
- 239000011248 coating agent Substances 0.000 claims description 8
- 238000000576 coating method Methods 0.000 claims description 8
- 239000011230 binding agent Substances 0.000 claims description 7
- 239000000945 filler Substances 0.000 claims description 6
- 239000007787 solid Substances 0.000 claims description 6
- 125000001424 substituent group Chemical group 0.000 claims description 5
- 125000000623 heterocyclic group Chemical group 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 4
- 125000005843 halogen group Chemical group 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- 238000004898 kneading Methods 0.000 claims description 2
- 125000002947 alkylene group Chemical group 0.000 claims 2
- 239000000975 dye Substances 0.000 description 35
- 239000000203 mixture Substances 0.000 description 12
- 239000000126 substance Substances 0.000 description 9
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 229910052799 carbon Inorganic materials 0.000 description 6
- 239000003973 paint Substances 0.000 description 5
- 239000004576 sand Substances 0.000 description 5
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 229920002635 polyurethane Polymers 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 4
- 229920000742 Cotton Polymers 0.000 description 3
- 238000005299 abrasion Methods 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 238000010008 shearing Methods 0.000 description 3
- 238000001179 sorption measurement Methods 0.000 description 3
- 230000003746 surface roughness Effects 0.000 description 3
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 2
- 125000000732 arylene group Chemical group 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- -1 isocyanate compound Chemical class 0.000 description 2
- 239000011164 primary particle Substances 0.000 description 2
- 125000005156 substituted alkylene group Chemical group 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-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
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- NRCMAYZCPIVABH-UHFFFAOYSA-N Quinacridone Chemical compound N1C2=CC=CC=C2C(=O)C2=C1C=C1C(=O)C3=CC=CC=C3NC1=C2 NRCMAYZCPIVABH-UHFFFAOYSA-N 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 229920002433 Vinyl chloride-vinyl acetate copolymer Polymers 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 125000000217 alkyl 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
- PGEHNUUBUQTUJB-UHFFFAOYSA-N anthanthrone Chemical compound C1=CC=C2C(=O)C3=CC=C4C=CC=C5C(=O)C6=CC=C1C2=C6C3=C54 PGEHNUUBUQTUJB-UHFFFAOYSA-N 0.000 description 1
- 239000001000 anthraquinone dye Substances 0.000 description 1
- 229910001566 austenite Inorganic materials 0.000 description 1
- 239000000987 azo dye Substances 0.000 description 1
- ULBTUVJTXULMLP-UHFFFAOYSA-N butyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCCC ULBTUVJTXULMLP-UHFFFAOYSA-N 0.000 description 1
- 238000003490 calendering Methods 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 229940125898 compound 5 Drugs 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- PPSZHCXTGRHULJ-UHFFFAOYSA-N dioxazine Chemical compound O1ON=CC=C1 PPSZHCXTGRHULJ-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 239000010408 film Substances 0.000 description 1
- 238000009501 film coating Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 235000019239 indanthrene blue RS Nutrition 0.000 description 1
- UHOKSCJSTAHBSO-UHFFFAOYSA-N indanthrone blue Chemical compound C1=CC=C2C(=O)C3=CC=C4NC5=C6C(=O)C7=CC=CC=C7C(=O)C6=CC=C5NC4=C3C(=O)C2=C1 UHOKSCJSTAHBSO-UHFFFAOYSA-N 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- PXZQEOJJUGGUIB-UHFFFAOYSA-N isoindolin-1-one Chemical compound C1=CC=C2C(=O)NCC2=C1 PXZQEOJJUGGUIB-UHFFFAOYSA-N 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000000113 methacrylic resin Substances 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- OBJNZHVOCNPSCS-UHFFFAOYSA-N naphtho[2,3-f]quinazoline Chemical compound C1=NC=C2C3=CC4=CC=CC=C4C=C3C=CC2=N1 OBJNZHVOCNPSCS-UHFFFAOYSA-N 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
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 235000021313 oleic acid Nutrition 0.000 description 1
- 239000012860 organic pigment Substances 0.000 description 1
- DGBWPZSGHAXYGK-UHFFFAOYSA-N perinone Chemical compound C12=NC3=CC=CC=C3N2C(=O)C2=CC=C3C4=C2C1=CC=C4C(=O)N1C2=CC=CC=C2N=C13 DGBWPZSGHAXYGK-UHFFFAOYSA-N 0.000 description 1
- 125000002080 perylenyl group Chemical group C1(=CC=C2C=CC=C3C4=CC=CC5=CC=CC(C1=C23)=C45)* 0.000 description 1
- CSHWQDPOILHKBI-UHFFFAOYSA-N peryrene Natural products C1=CC(C2=CC=CC=3C2=C2C=CC=3)=C3C2=CC=CC3=C1 CSHWQDPOILHKBI-UHFFFAOYSA-N 0.000 description 1
- 239000001007 phthalocyanine dye Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920006122 polyamide resin Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920003225 polyurethane elastomer Polymers 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000006748 scratching Methods 0.000 description 1
- 230000002393 scratching effect Effects 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 230000002123 temporal effect Effects 0.000 description 1
- TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- JOUDBUYBGJYFFP-FOCLMDBBSA-N thioindigo Chemical compound S\1C2=CC=CC=C2C(=O)C/1=C1/C(=O)C2=CC=CC=C2S1 JOUDBUYBGJYFFP-FOCLMDBBSA-N 0.000 description 1
- AAAQKTZKLRYKHR-UHFFFAOYSA-N triphenylmethane Chemical compound C1=CC=CC=C1C(C=1C=CC=CC=1)C1=CC=CC=C1 AAAQKTZKLRYKHR-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Magnetic Record Carriers (AREA)
- Manufacturing Of Magnetic Record Carriers (AREA)
Description
【0001】[0001]
【産業上の利用分野】本発明は磁気記録媒体に関し,走
行安定性,導電性,遮光性,表面平滑性,に優れたバッ
ク層の製法に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a magnetic recording medium and, more particularly, to a method for producing a back layer having excellent running stability, conductivity, light shielding properties, and surface smoothness.
【0002】[0002]
【従来の技術】一般に高級ビデオテープ、デジタルオー
ディオテープ、コンピュータ用テープ等の磁気記録媒体
には、支持体に対し磁性面と反対面にバック層が施され
ている。このバック層は、走行安定性を付与するととも
に、静電気防止効果、テープ終端検出のための光遮蔽効
果が要求されている。このため一般にはバック層にカ−
ボンブラックを分散し、導電性、遮光性を付与すること
が行われている。2. Description of the Related Art Generally, magnetic recording media such as high-grade video tapes, digital audio tapes, and computer tapes have a back layer provided on a surface opposite to a magnetic surface with respect to a support. The back layer is required to provide running stability, an antistatic effect, and a light shielding effect for detecting the end of the tape. For this reason, generally, the back layer has a color.
It has been practiced to disperse Bon Black to impart conductivity and light shielding properties.
【0003】近年、記録密度の増加に伴い磁性層の平滑
化が進むにつれ、バック層においても平滑性に対する要
求が高まっている。すなわちバック層の平滑性が十分で
ないと、磁性層にバック層の凹凸が転写し、ドロップア
ウト、SN比低下の問題が起こるからである。また、最
近の磁気テープの薄膜化に伴い、バック層の導電性、遮
光性に対する要求も高まっている。In recent years, as the recording density has increased, the smoothness of the magnetic layer has progressed, and the demand for smoothness has also increased in the back layer. That is, if the smoothness of the back layer is not sufficient, the unevenness of the back layer is transferred to the magnetic layer, causing problems such as dropout and a decrease in the SN ratio. Further, with the recent thinning of magnetic tapes, demands for the conductivity and light-shielding properties of the back layer are increasing.
【0004】バック層においてこれら十分な平滑性、導
電性、遮光性を得るには比較的粒子径の小さなカーボン
ブラックを高濃度に高分散する必要があるが、粒子径が
小さなカーボンブラックは一般に比表面積、吸油量が大
きく難分散性である。そこで,高せん断力を有する分散
機として,例えばロ−ルミル,ニ−ダ−等を使用し,プ
レミキシングを行いカ−ボンブラックの強固な凝集粒子
を破砕する方法が取られているが,バインダ−等の高分
子量成分の吸着を伴わないと充分な平滑性が得られず,
また,薄膜塗布するのに充分な塗料の流動性及び塗料の
経時安定性は得られていない。In order to obtain sufficient smoothness, conductivity and light-shielding properties in the back layer, it is necessary to disperse carbon black having a relatively small particle size in a high concentration and high concentration. Large surface area and oil absorption. Therefore, as a disperser having a high shearing force, for example, a method of using a roll mill, a kneader or the like to perform pre-mixing to crush strong aggregated particles of carbon black has been adopted. -Without sufficient adsorption of high molecular weight components such as-, sufficient smoothness cannot be obtained,
In addition, the fluidity of the paint and the stability over time of the paint that are sufficient for thin film coating have not been obtained.
【0005】[0005]
【発明が解決しようとする課題】これらの問題を解決す
るため、磁気記録媒体のバック層に要求される高度なカ
ーボンブラックを含む充填剤の分散状態を得ることを目
的に検討を加えた結果、以下の磁気記録媒体の製法を発
明するに到った。SUMMARY OF THE INVENTION In order to solve these problems, as a result of investigations aimed at obtaining a highly dispersed state of a filler containing carbon black required for a back layer of a magnetic recording medium, The following method for producing a magnetic recording medium has been invented.
【0006】[0006]
【課題を解決するための手段】本発明は,支持体対し互
いに反対面に磁性層及びバック層を有する磁気記録媒体
の製造方法におけるものである。まず下記一般式
(1),(2)で示される塩基性有機色素化合物をバッ
ク層の構成成分であるカ−ボンブラックを含む充填剤と
混練分散し固形チップ化する。この際,チップには溶剤
分として15重量%以下の溶剤が残留することが望まし
い。次いでこの混合物を溶剤に溶解後サンドミル分散し
バックコ−ト塗料とすることにより,上記問題点を解決
できることを見出したものである。SUMMARY OF THE INVENTION The present invention is a method of manufacturing a magnetic recording medium having a magnetic layer and a back layer on opposite sides of a support. First, a basic organic dye compound represented by the following general formulas (1) and (2) is kneaded and dispersed with a filler containing carbon black as a component of the back layer to form a solid chip. At this time, it is desirable that a solvent of 15% by weight or less as a solvent remains in the chip. Then, it has been found that the above problem can be solved by dissolving the mixture in a solvent and then dispersing the mixture in a sand mill to form a backcoat paint.
【0007】一般式(1)General formula (1)
【0008】[0008]
【化4】 Embedded image
【0009】〔式中,Q;有機色素残基、 X;直接結合,−CONH−Y2 −,−SO2 NH−Y
2 −または−CH2 NHCOCH2 NH−Y2 −, (Y2 ;置換基を有してもよいアルキレン基またはアリ
ーレン基) Y1 ;−NH−または−O−、 (Y3 ;−NH−,または,−O−),あるいはn=1
の場合 −NH−X−Qであってもよい、 R1 ,R2 ;それぞれ独立に置換もしくは無置換のアル
キル基またはR1 とR2 とで少なくともヘテロ環を形成
してもよい。[0009] wherein, Q; organic pigment residue, X; direct bond, -CONH-Y 2 -, - SO 2 NH-Y
2 - or -CH 2 NHCOCH 2 NH-Y 2 -, (Y 2; an optionally substituted alkylene group or an arylene group) Y 1; -NH- or -O-, (Y 3 ; —NH— or —O—), or n = 1
R 1 , R 2 ; each independently may be a substituted or unsubstituted alkyl group, or at least a heterocycle may be formed by R 1 and R 2 .
【0010】m;1〜6の整数、n;1〜4の整数、を
表す。〕 一般式(2)M represents an integer of 1 to 6; n represents an integer of 1 to 4; General formula (2)
【0011】[0011]
【化5】 Embedded image
【0012】〔式中,Q;有機色素残基 X;直接結合,−CONH−Y1 −,−SO2 NH−Y
1 −,または−CH2 NHCOCH2 NH−Y1 − (Y1 ;置換基を有してもよいアルキレン基またはアリ
ーレン基) Y;下式で示される置換基 Wherein Q: organic dye residue X; direct bond, -CONH-Y 1- , -SO 2 NH-Y
1 -, or -CH 2 NHCOCH 2 NH-Y 1 - (Y 1; an optionally substituted alkylene group or an arylene group) Y; substituent represented by the following formula
【0013】[0013]
【化6】 Embedded image
【0014】〔式中, R1 ,R2 ;それぞれ独立に置換もしくは無置換のアル
キル基またはR1 とR 2 とで少なくともヘテロ環を形成
してもよい。 Y2 ;水素原子,ハロゲン原子,─NO2 ,─NH2 も
しくは─SO3 Hを示す。[Wherein, R1, RTwo; Independently substituted or unsubstituted al
Kill group or R1And R TwoForms at least a heterocyclic ring with
May be. YTwoA hydrogen atom, a halogen atom, ─NOTwo, ─NHTwoAlso
Or SOThreeH is shown.
【0015】k;1〜4の整数、m;1〜6の整数、
n;1〜4の整数を表す。〕上記一般式中の有機色素残
基としてはフタロシアニン系色素,アゾ系色素,アント
ラキノン系色素,キナクリドン系色素,ジオキサジン系
色素、アントラピリミジン系色素、アンサンスロン系色
素、インダンスロン系色素、フラバンスロン系色素、ペ
リレン系色素,ペリノン系色素,チオインジゴ系色素,
イソインドリノン系色素,トリフェニルメタン系色素等
の顔料または染料である。K: an integer of 1-4, m; an integer of 1-6,
n; represents an integer of 1 to 4; The organic dye residues in the above general formula include phthalocyanine dyes, azo dyes, anthraquinone dyes, quinacridone dyes, dioxazine dyes, anthrapyrimidine dyes, anthanthrone dyes, indanthrone dyes, and flavanthrone. Dyes, perylene dyes, perinone dyes, thioindigo dyes,
Pigments or dyes such as isoindolinone dyes and triphenylmethane dyes.
【0016】また,バインダ−とは,従来磁気記録媒体
に使用される公知のものの中から,例えばポリウレタン
エラストマ−,硝化綿,塩化ビニル,塩化ビニル−酢酸
ビニル共重合体,塩化ビニリデン共重合体,エポキシ樹
脂,ポリアミド樹脂,アクリル酸エステル樹脂,メタク
リル酸樹脂,ポリエステル樹脂,ウレタン樹脂または,
これらの樹脂の混合物などがある。[0016] The binder may be selected from known materials conventionally used for magnetic recording media, for example, polyurethane elastomer, nitrified cotton, vinyl chloride, vinyl chloride-vinyl acetate copolymer, vinylidene chloride copolymer, and the like. Epoxy resin, polyamide resin, acrylate resin, methacrylic resin, polyester resin, urethane resin or
There are mixtures of these resins.
【0017】本発明のロ−ルミルとしては,2本ロ−ル
があげられる。有機色素化合物を含むバック層の構成成
分をサンドミル等の分散機で塗料化することだけでは,
カ−ボンの強い凝集粒子を破砕するのに十分なせん断力
が得られず,目的とする品質が得られない。また,ロ−
ルミルを用いて固形チップ化する製法は,高せん断力に
よりカ−ボンを一次粒子まで破砕することが出来るが,
微粒子化したカ−ボンは十分な高分子量成分の吸着を伴
っておらず安定な分散状態とは言えない。本発明は,ロ
−ルミルでの高せん断力下において有機色素化合物を存
在させることにより,カ−ボンの再凝集を防止するのに
十分な高分子量成分の吸着が得られ品質の向上,生産性
の向上が達成出来ことを見出したものである。The roll mill of the present invention includes two rolls. It is only necessary to paint the components of the back layer containing the organic dye compound with a disperser such as a sand mill.
A sufficient shearing force to crush the agglomerated particles of carbon cannot be obtained, and the desired quality cannot be obtained. In addition,
In the method of making solid chips using a mill, carbon can be crushed into primary particles by high shear force.
The finely divided carbon is not accompanied by sufficient adsorption of high molecular weight components and cannot be said to be in a stable dispersed state. According to the present invention, the presence of an organic dye compound under a high shearing force in a roll mill enables the adsorption of a high molecular weight component sufficient to prevent reagglomeration of carbon, thereby improving quality and productivity. Has been found to be able to achieve improvement.
【0018】本発明における有機色素化合物は,カ−ボ
ンブラックを含む充填剤及びバインダ−と単にロ−ルミ
ル分散時に混合されるだけでもよいが,ロ−ルミルによ
る分散の前に有機色素化合物とバインダ−を予め加熱混
合し溶解状態にしておくことにより,有機色素化合物の
塩基性置換基とバインダ−の極性基との親和性が向上す
るだけでなく,カ−ボン等の充填剤と均一かつ速やかに
混合される為,品質及び生産性の向上が達成される。The organic dye compound in the present invention may be simply mixed with the filler and the binder containing carbon black at the time of roll mill dispersion, but the organic dye compound and the binder are dispersed before the roll mill dispersion. By preliminarily heating and mixing in a dissolved state, not only the affinity between the basic substituent of the organic dye compound and the polar group of the binder is improved, but also it is uniform and prompt with the filler such as carbon. , The quality and productivity are improved.
【0019】有機色素化合物とバインダ−の混合比率と
しては,バインダ−100重量部に対し0.1部〜30
重量部が好ましい。また,カ−ボンブラックを含む充填
剤の混合比率は,前述の混合物100重量部に対して,
50〜150重量部が好ましい。また,一般式で示され
る有機色素化合物とステアリン酸,パルミチン酸,オレ
イン酸等の脂肪酸及び脂肪酸の金属塩あるいはその他の
公知の界面活性剤を併用添加することにより,形成され
るバック層の表面平滑性を一層高めることが可能であ
る。The mixing ratio of the organic dye compound and the binder is 0.1 part to 30 parts by weight with respect to 100 parts by weight of the binder.
Parts by weight are preferred. The mixing ratio of the filler containing carbon black was 100 parts by weight of the above-mentioned mixture.
50 to 150 parts by weight are preferred. The surface smoothness of the back layer formed by adding the organic dye compound represented by the general formula and fatty acids such as stearic acid, palmitic acid and oleic acid and metal salts of fatty acids or other known surfactants in combination. It is possible to further enhance the performance.
【0020】[0020]
【実施例】本発明を実施例に基づいて説明する。例中、
「部」「%」は、それぞれ「重量部」「重量%」であ
る。 実施例1 コバルト含有γ−Fe2 O3 100部 塩化ビニル樹脂(MR−110,日本ゼオン(株)) 10部 ウレタン樹脂(ニッポラン2301,日本ポリウレタン(株)) 10部 アルミナ 5部 トルエン 120部 メチルエチルケトン 120部 シクロヘキサノン 60部 上記組成物をサンドミルで分散した磁性塗料にイソシア
ネート化合物(コロネートL,日本ポリウレタン
(株))を3部、ミリスチン酸1部、n−ブチルステア
レート1部を加え、10μm厚のポリエチレンテレフタ
レート支持体上に塗布、配向、乾燥後、カレンダー処理
による鏡面加工を行い3μm厚の磁性塗膜を作成した。DESCRIPTION OF THE PREFERRED EMBODIMENTS The present invention will be described based on embodiments. In the example,
“Parts” and “%” are “parts by weight” and “% by weight”, respectively. Example 1 Cobalt-containing γ-Fe 2 O 3 100 parts Vinyl chloride resin (MR-110, Nippon Zeon Co., Ltd.) 10 parts Urethane resin (Nipporan 2301, Nippon Polyurethane Co., Ltd.) 10 parts Alumina 5 parts Toluene 120 parts Methyl ethyl ketone 120 parts Cyclohexanone 60 parts 3 parts of an isocyanate compound (Coronate L, Nippon Polyurethane Co., Ltd.), 1 part of myristic acid, and 1 part of n-butyl stearate are added to a magnetic coating material obtained by dispersing the above composition by a sand mill, and a thickness of 10 μm is added. After coating, orientation, and drying on a polyethylene terephthalate support, mirror finishing by calendering was performed to form a magnetic coating film having a thickness of 3 μm.
【0021】次に下記組成物を,攪拌容器中で60℃で
1時間加熱攪拌し,有機色素化合物の溶解液を得た。 (有機色素化合物の溶解液) 硝化綿(セルラインFM200S,ダイセル化学工業(株)) 100部 ウレタン樹脂(ニッポラン2301,日本ポリウレタン(株))100部 有機色素化合物 5部Next, the following composition was heated and stirred at 60 ° C. for 1 hour in a stirring vessel to obtain a solution of the organic dye compound. (Solution of organic dye compound) Nitrified cotton (Cellline FM200S, Daicel Chemical Industries, Ltd.) 100 parts Urethane resin (Nipporan 2301, Nippon Polyurethane Co., Ltd.) 100 parts Organic dye compound 5 parts
【0022】[0022]
【化7】 Embedded image
【0023】得られた溶解液を含む下記組成物を2ロ−
ルミルを用いて,20回処理し,固形チップとした。 有機色素化合物の溶解液 205部 カ−ボンブラック(平均一次粒子径 17mμ) 100部 次に,得られたチップを樹脂,溶剤中で溶解,サンドミ
ルを用いて分散しバックコ−ト塗料とした。更にコロネ
−トLを20部加え,磁性層と反対面に塗布,乾燥して
0.7μm厚のバック層を形成した後、1/2インチ幅
に裁断し磁気テープを作成した。The following composition containing the obtained solution was added to
Using a mill, the mixture was processed 20 times to obtain solid chips. Dissolved solution of organic dye compound 205 parts Carbon black (average primary particle diameter 17 mμ) 100 parts Next, the obtained chip was dissolved in a resin and a solvent and dispersed using a sand mill to obtain a backcoat paint. Further, 20 parts of Coronate L was added, coated on the surface opposite to the magnetic layer and dried to form a back layer having a thickness of 0.7 μm, and then cut into イ ン チ inch width to prepare a magnetic tape.
【0024】 チップ(固形分 94%) 170部 硝化綿(セルラインFM200S,ダイセル化学工業(株)) 100部 ウレタン樹脂(ニッポラン2301,日本ポリウレタン(株)) 50部 メチルエチルケトン 400部 トルエン 400部 シクロヘキサノン 200部 実施例2 有機色素化合物を化8に変更した以外は,実施例1と同
様にして磁気記録媒体を得た。Chip (solid content: 94%) 170 parts Nitrified cotton (Cell Line FM200S, Daicel Chemical Industries, Ltd.) 100 parts Urethane resin (Nipporan 2301, Nippon Polyurethane Co., Ltd.) 50 parts Methyl ethyl ketone 400 parts Toluene 400 parts Cyclohexanone 200 Part Example 2 A magnetic recording medium was obtained in the same manner as in Example 1 except that the organic dye compound was changed to Chemical formula 8.
【0025】[0025]
【化8】 Embedded image
【0026】実施例3 有機色素化合物を化9に変更した以外は,実施例1と同
様にして磁気記録媒体を得た。Example 3 A magnetic recording medium was obtained in the same manner as in Example 1, except that the organic dye compound was changed to Chemical formula 9.
【0027】[0027]
【化9】 Embedded image
【0028】実施例4 有機色素化合物を化10に変更した以外は,実施例1と
同様にして磁気記録媒体を得た。Example 4 A magnetic recording medium was obtained in the same manner as in Example 1 except that the organic dye compound was changed to Chemical Formula 10.
【0029】[0029]
【化10】 Embedded image
【0030】実施例5 有機色素化合物を化11に変更した以外は,実施例1と
同様にして磁気記録媒体を得た。Example 5 A magnetic recording medium was obtained in the same manner as in Example 1 except that the organic dye compound was changed to Chemical formula 11.
【0031】[0031]
【化11】 Embedded image
【0032】実施例6 有機色素化合物を化12に変更した以外は,実施例1と
同様にして磁気記録媒体を得た。Example 6 A magnetic recording medium was obtained in the same manner as in Example 1, except that the organic dye compound was changed to Chemical formula 12.
【0033】[0033]
【化12】 Embedded image
【0034】実施例7 有機色素化合物を化13に変更した以外は,実施例1と
同様にして磁気記録媒体を得た。Example 7 A magnetic recording medium was obtained in the same manner as in Example 1, except that the organic dye compound was changed to Chemical formula 13.
【0035】[0035]
【化13】 Embedded image
【0036】比較例1 実施例1〜7のバック層組成物の製法において、有機色
素化合物を削除したものについて実施例1〜7と同様の
方法で磁気テープを作成した。 比較例2 実施例1〜7のバック層組成物の製法において、有機色
素化合物として化7を用い,サンドミル分散し磁気テ−
プを作成した。Comparative Example 1 A magnetic tape was prepared in the same manner as in Examples 1 to 7, except that the organic dye compound was omitted from the method of manufacturing the back layer composition in Examples 1 to 7. Comparative Example 2 In the process for producing the back layer compositions of Examples 1 to 7, Chemical Formula 7 was used as an organic dye compound, and the mixture was subjected to sand mill dispersion and magnetic recording.
Created
【0037】以上の実施例1〜7及び比較例1、2で作
成した磁気テープのバック層の中心線表面粗さRa,6
0°鏡面反射率、表面電気抵抗、耐磨耗性を測定した結
果及びバック層組成物の塗料流動性、経時安定性を評価
した結果を表1に示した。中心線表面粗さRaは触針式
表面粗さ測定機により、JIS-B-0601-1982 に基づきカッ
トオフ値0.08で測定した。耐磨耗性はテープ走行試
験機により200パス走行後の傷つき程度を観察した。The center line surface roughness Ra, 6 of the back layer of the magnetic tape prepared in Examples 1 to 7 and Comparative Examples 1 and 2 above.
Table 1 shows the results of measuring the 0 ° specular reflectance, the surface electrical resistance, and the abrasion resistance, and the results of evaluating the coating fluidity and the temporal stability of the back layer composition. The center line surface roughness Ra was measured with a stylus type surface roughness measuring instrument at a cutoff value of 0.08 based on JIS-B-0601-1982. The abrasion resistance was determined by observing the degree of scratching after running 200 passes with a tape running tester.
【0038】表1から明らかなように、本発明に係わる
有機色素化合物とカーボンブックをロールミルを用い混
練分散し、固形チップとした後塗料化した塗料は、流動
性、経時安定性に優れ、これらを塗布したバック層は平
滑性、耐磨耗性に優れていることがわかる。As is clear from Table 1, the coating material obtained by kneading and dispersing the organic dye compound according to the present invention and a carbon book using a roll mill to form a solid chip and then forming a coating has excellent fluidity and stability over time. It can be seen that the back layer coated with is excellent in smoothness and abrasion resistance.
【0039】[0039]
【表1】 [Table 1]
【0040】[0040]
【発明の効果】本発明はカーボンブラックの分散性を向
上せしめることにより、良好な表面平滑性を持つバック
層を作成し、ひいては磁気記録媒体に要求される特性を
向上せしめるものである。According to the present invention, by improving the dispersibility of carbon black, a back layer having good surface smoothness is formed, and the characteristics required for a magnetic recording medium are improved.
───────────────────────────────────────────────────── フロントページの続き (56)参考文献 特開 平4−248177(JP,A) 特開 平4−79018(JP,A) 特開 平3−214425(JP,A) 特開 昭62−134824(JP,A) 特開 昭62−18623(JP,A) 特開 昭62−6435(JP,A) 特開 昭62−3432(JP,A) (58)調査した分野(Int.Cl.7,DB名) G11B 5/84 G11B 5/704 CA(STN) CAOLD(STN) REGISTRY(STN) WPIDS(STN)──────────────────────────────────────────────────続 き Continuation of the front page (56) References JP-A-4-248177 (JP, A) JP-A-4-79018 (JP, A) JP-A-3-214425 (JP, A) JP-A-62-1987 134824 (JP, A) JP-A-62-18623 (JP, A) JP-A-62-6435 (JP, A) JP-A-62-3342 (JP, A) (58) Fields investigated (Int. 7 , DB name) G11B 5/84 G11B 5/704 CA (STN) CAOLD (STN) REGISTRY (STN) WPIDS (STN)
Claims (2)
バック層を有する磁気記録媒体の製造方法において,塩
基性末端基を有する有機色素化合物及びカ−ボンブラッ
クを含む充填剤とバインダ−をロ−ルミルを用い,混練
分散し固形チップ化した後,塗料化し塗布することによ
りバック層を設けることを特徴とする磁気記録媒体の製
造方法。1. A method for producing a magnetic recording medium having a magnetic layer and a back layer on opposite sides of a support, comprising: a filler containing an organic dye compound having a basic terminal group and carbon black; and a binder. A method for manufacturing a magnetic recording medium, comprising kneading and dispersing into a solid chip using a roll mill, forming a coating, and applying a coating to form a back layer.
が、下記一般式(1)または(2)で示されることを特
徴とする磁気記録媒体の製造方法。 一般式(1) 【化1】 〔式中,Q;有機色素残基、 X;直接結合,−CONH−Y2 −,−SO2 NH−Y
2 −または−CH2 NHCOCH2 NH−Y2 −, (Y2 ;置換基を有してもよいアルキレン基またはアリ
ーレン基) Y1 ;−NH−または−O−、 (Y3 ;−NH−,または,−O−),あるいはn=1
の場合 −NH−X−Qであってもよい、 R1 ,R2 ;それぞれ独立に置換もしくは無置換のアル
キル基またはR1 とR2 とで少なくともヘテロ環を形成
してもよい。 m;1〜6の整数、n;1〜4の整数、を表す。〕 一般式(2) 【化2】 〔式中,Q;有機色素残基 X;直接結合,−CONH−Y1 −,−SO2 NH−Y
1 −,または−CH2 NHCOCH2 NH−Y1 − (Y1 ;置換基を有してもよいアルキレン基またはアリ
ーレン基) Y;下式で示される置換基 【化3】 〔式中, R1 ,R2 ;それぞれ独立に置換もしくは無置換のアル
キル基またはR1 とR 2 とで少なくともヘテロ環を形成
してもよい。 Y2 ;水素原子,ハロゲン原子,─NO2 ,─NH2 も
しくは─SO3 Hを示す。 k;1〜4の整数、m;1〜6の整数、n;1〜4の整
数を表す。〕2. An organic dye compound having a basic terminal group.
Is represented by the following general formula (1) or (2).
A method for manufacturing a magnetic recording medium. General formula (1)[Wherein, Q: organic dye residue, X: direct bond, -CONH-YTwo−, −SOTwoNH-Y
Two-Or -CHTwoNHCOCHTwoNH-YTwo−, (YTwoAn alkylene group or an ant which may have a substituent
-Lene group) Y1-NH- or -O-,(YThree-NH- or -O-), or n = 1
In the case of, it may be -NH-XQ, R1, RTwo; Independently substituted or unsubstituted al
Kill group or R1And RTwoForms at least a heterocyclic ring with
May be. m represents an integer of 1 to 6; n represents an integer of 1 to 4; General formula (2)[Wherein Q: organic dye residue X; direct bond, -CONH-Y1−, −SOTwoNH-Y
1-Or -CHTwoNHCOCHTwoNH-Y1− (Y1An alkylene group or an ant which may have a substituent
-Ylene group) Y; a substituent represented by the following formulaEmbedded image[Where R1, RTwo; Independently substituted or unsubstituted al
Kill group or R1And R TwoForms at least a heterocyclic ring with
May be. YTwoA hydrogen atom, a halogen atom, ─NOTwo, ─NHTwoAlso
Or SOThreeH is shown. k; an integer of 1 to 4, m; an integer of 1 to 6, n; an integer of 1 to 4
Represents a number. ]
Priority Applications (1)
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JP5043976A JP3006334B2 (en) | 1993-03-04 | 1993-03-04 | Manufacturing method of magnetic recording medium |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5043976A JP3006334B2 (en) | 1993-03-04 | 1993-03-04 | Manufacturing method of magnetic recording medium |
Publications (2)
Publication Number | Publication Date |
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JPH06259758A JPH06259758A (en) | 1994-09-16 |
JP3006334B2 true JP3006334B2 (en) | 2000-02-07 |
Family
ID=12678754
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JP5043976A Expired - Lifetime JP3006334B2 (en) | 1993-03-04 | 1993-03-04 | Manufacturing method of magnetic recording medium |
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JP2006185526A (en) * | 2004-12-28 | 2006-07-13 | Toyo Ink Mfg Co Ltd | Coating material for back layer of magnetic recording medium, and magnetic recording medium using the same |
-
1993
- 1993-03-04 JP JP5043976A patent/JP3006334B2/en not_active Expired - Lifetime
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