JPS6323224A - Leader tape - Google Patents

Leader tape

Info

Publication number
JPS6323224A
JPS6323224A JP14958986A JP14958986A JPS6323224A JP S6323224 A JPS6323224 A JP S6323224A JP 14958986 A JP14958986 A JP 14958986A JP 14958986 A JP14958986 A JP 14958986A JP S6323224 A JPS6323224 A JP S6323224A
Authority
JP
Japan
Prior art keywords
group
protective layer
hydrolyzate
molecule
alkoxysilane
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
Application number
JP14958986A
Other languages
Japanese (ja)
Inventor
Tsutomu Yoshida
勉 吉田
Shoji Kobayashi
小林 章志
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Toray Industries Inc
Original Assignee
Toray Industries Inc
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Toray Industries Inc filed Critical Toray Industries Inc
Priority to JP14958986A priority Critical patent/JPS6323224A/en
Publication of JPS6323224A publication Critical patent/JPS6323224A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To obtain a leader tape having excellent wear resistance, antistatic property, non-tackiness and ray transmittivity by using the hydrolyzate of an alkoxysilane having an epoxy group in the molecule, the hydrolyzate of an alkoxysilane having an amino group and/or imino group in the molecule and white pigment as essential components for a protective layer. CONSTITUTION:The protective layer of the laminate of polyester films consist of A, the hydrolyzate of the alkoxysilane which is expressed by the formula XmSi(OR)4-m (X is an org. group contg. an epoxy group, OR is an alkoxy group of 1-6C, m is 1 or 2) and has the epoxy group in the molecule, B, the hydrolyzate of the alkoxysilane which is expressed by the formula YnSi(OR)4-n (Y is an org. group contg. an amino group and/or imino group, OR is an alkoxy group of 1-6C, n is 1 or 2) and has the amino group and/or imino group in the molecule and C, the white pigment as the essential components. The solid content ratios by weight of A:B:C thereof are specified to 10-50:90-10:1-9. The wear resistance, antistatic property and non-tackiness of the above- mentioned tape are thereby improved.

Description

【発明の詳細な説明】 [産業上の利用分野] 本発明は磁気記録媒体の前後に接続するリーダーテープ
またはトレーラ−テープ(以下総称してリーダーテープ
と呼ぶ。)に関するものである。
DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a leader tape or trailer tape (hereinafter collectively referred to as a leader tape) connected before and after a magnetic recording medium.

[従来技術] 従来、リーダーテープとしては (1)帯電防止剤を練り込んだポリエチレンテレフタレ
ート、塩化ビニルなどのフィルム。
[Prior Art] Conventionally, leader tapes include (1) films made of polyethylene terephthalate, vinyl chloride, etc., mixed with antistatic agents;

(2)白色顔料を含む帯電防止剤層を基材フィルムに積
層した積層フィルム(例えば特開昭47−38007号
公報、同49−40504号公報、同49−67603
号公報) (3)  第1層として帯電防止層を、第2層として白
色顔料と粘結剤を主成分とする層を基材フィルムに積層
した積層フィルム(例えば特開昭53−32002号公
報)が知られている。
(2) Laminated film in which an antistatic agent layer containing a white pigment is laminated on a base film (for example, JP-A-47-38007, JP-A-49-40504, JP-A-49-67603)
(3) A laminated film in which a base film is laminated with an antistatic layer as the first layer and a layer mainly composed of a white pigment and a binder as the second layer (for example, JP-A-53-32002) )It has been known.

[発明が解決しようとする問題点] しかし、上記従来のリーダテープは下記の問題点を有し
ている。
[Problems to be Solved by the Invention] However, the above conventional leader tape has the following problems.

(1)項のフィルムは帯電防止性が不充分でおったり、
経時消失のために発生した静電気が除去されにくくなり
、付着したゴミや塵が磁性層表面や磁気ヘッドに転位し
てドロップアウト、出力低下などの原因となった。また
、フィルム表面の耐摩耗性が不充分であるため、テープ
走行時にフィルム表面が摩耗を受は発塵していた。
The film in item (1) has insufficient antistatic properties,
As the static electricity disappears over time, it becomes difficult to remove the static electricity, and the adhering dirt and dust dislocates onto the surface of the magnetic layer and the magnetic head, causing dropouts and decreased output. Furthermore, since the abrasion resistance of the film surface was insufficient, the film surface was abraded during running of the tape and generated dust.

(2)項のフィルムは帯電防止性を満足させると粘着が
発生し、粘着防止のため白色顔料の添加量を増すと、終
端検出のために必要な光線透過率が減少したりあるいは
フィルム表面の耐摩耗性不足による白色顔料の欠落によ
る発塵などの問題があった。
When the film described in item (2) satisfies the antistatic properties, adhesion occurs, and if the amount of white pigment added to prevent adhesion is increased, the light transmittance required for end detection may decrease or the film surface may become sticky. There were problems such as dust generation due to lack of white pigment due to lack of abrasion resistance.

(3)項のフィルムは、帯電防止性を満足させても粘着
がなく、かつ光線透過率も実用上問題ないが、フィルム
表面の耐摩耗性が不充分であることによるテープ自体か
らの発塵や、2層構成とすることによる製造費用アップ
などの問題点があった。
The film described in item (3) has no adhesion even if it satisfies the antistatic property, and there is no practical problem in terms of light transmittance.However, dust is generated from the tape itself due to insufficient abrasion resistance on the film surface. There were also problems such as increased manufacturing costs due to the two-layer structure.

本発明はかかる問題点を改善し、耐摩耗性、帯電防止性
、非粘着性、光線透過率が共に優れたリーダーテープを
提供することを目的とする。
It is an object of the present invention to solve these problems and provide a leader tape that has excellent abrasion resistance, antistatic properties, non-adhesive properties, and light transmittance.

[問題点を解決するための手段] 本発明は、ポリエステルフィルムの少なくとも片面に保
護層を積層した積層体において、該保護層が、 A、一般式XmSi  (OR)    (ただし、×
−m はエポキシ基を含む有機基、ORは炭素数1〜6のアル
コキシ基1mは1または2)で示される分子中にエポキ
シ基を有するアルコキシシランの加水分解物、 B、一般式Y  Si  (OR)    (ただし、
Yn       4−n はアミノ基および/またはイミノ基を含む有機基。
[Means for Solving the Problems] The present invention provides a laminate in which a protective layer is laminated on at least one side of a polyester film, in which the protective layer has the following formula: A, general formula XmSi (OR) (wherein
-m is an organic group containing an epoxy group; OR is an alkoxy group having 1 to 6 carbon atoms; 1m is a hydrolyzate of an alkoxysilane having an epoxy group in the molecule; B; general formula Y Si ( OR) (However,
Yn 4-n is an organic group containing an amino group and/or an imino group.

ORは炭素数1〜6のアルコキシ基、nは1または2)
で示される分子中にアミノ基および/またはイミノ基を
有するアルコキシシランの加水分解物、 C1白色顔料を主成分とし、かつ上記A:B:Cの固形
分重量比が10〜50:90〜10:1〜9でおること
を特徴とするものである。
OR is an alkoxy group having 1 to 6 carbon atoms, n is 1 or 2)
A hydrolyzate of an alkoxysilane having an amino group and/or an imino group in the molecule represented by, which has a C1 white pigment as its main component, and has a solid content weight ratio of A:B:C of 10 to 50:90 to 10. :1 to 9.

本発明におけるポリエステルフィルムは、機械的強度1
寸法安定性の面から二軸延伸されたポリエチレンテレフ
タレートフィルムが適しているが、これに限定されるも
のではない。
The polyester film in the present invention has a mechanical strength of 1
A biaxially stretched polyethylene terephthalate film is suitable from the viewpoint of dimensional stability, but is not limited thereto.

フィルムの厚さは通常10〜50μが好ましい。The thickness of the film is usually preferably 10 to 50 microns.

フィルムの厚さが10μ未満の場合はリーダーテープを
固定するクランプ部でのテープ切断が発生しやすくなり
、また50μを越える場合は磁性記録部分との接続部で
の厚さ差異が大きくなりすぎるため接続部形状が転写さ
れるなどの弊害を伴う。
If the film thickness is less than 10μ, the tape will easily break at the clamp part that fixes the leader tape, and if it exceeds 50μ, the difference in thickness at the connection part with the magnetic recording part will be too large. This has disadvantages such as the shape of the connection part being transferred.

本発明では特に必要としないが、フィルム表面を酸また
はアルカリ処理、コロナ放電処理、紫外線照射処理など
を行い、表面を活性化させて保護層の密着性を向上させ
てもよい。
Although not particularly required in the present invention, the film surface may be subjected to acid or alkali treatment, corona discharge treatment, ultraviolet irradiation treatment, etc. to activate the surface and improve the adhesion of the protective layer.

本発明の保護層は3つの成分A、B、Cがら主として構
成される。
The protective layer of the present invention is mainly composed of three components A, B, and C.

保護層を構成する第1の成分Aは、一般式XmSi  
(OR>    (ただし、Xはエポキシ基−m を含む有機基、ORは炭素数1〜6のアルコキシ基1m
は1または2)で示される分子中にエポキシ基を有する
アルコキシシランの加水分解物からなるもので、該加水
分解物Aは上記一般式で示される化合物2例えば、 CHクーCHCHpOCH2CH2CH2S  !  
(OCH3)  3なとのアルコキシシランの1種また
は混合物を希薄な酸性水溶液1例えば希塩酸水溶液や希
硫酸水溶液などでアルコキシ基を加水分解して1qられ
るプレポリマーである。
The first component A constituting the protective layer has the general formula XmSi
(OR> (However, X is an organic group containing an epoxy group -m, OR is an alkoxy group having 1 to 6 carbon atoms 1m
is a hydrolyzate of an alkoxysilane having an epoxy group in the molecule represented by 1 or 2), and the hydrolyzate A is a compound 2 represented by the above general formula, for example, CHcuCHCHpOCH2CH2CH2S!
(OCH3) This is a prepolymer obtained by hydrolyzing the alkoxy groups of one or a mixture of three alkoxysilanes in a dilute acidic aqueous solution such as a dilute aqueous hydrochloric acid solution or a dilute aqueous sulfuric acid solution.

また第2の成分Bは、一般式 YnSi  (OR>    (ただし、Yはアミノ基
お−n よび/またはイミノ基を含む有機基、ORは炭素数1〜
6のアルコキシ基、「)は1または2〉で示される分子
中にアミノ基および/またはイミノ基を有するアルコキ
シシランの加水分解物からなるもので、上記アミノ基お
よび/またはイミノ基を含む有機基としては通常炭素数
2〜10のものが好ましく用いられる。この加水分解物
Bは上記−般式で示される化合物、例えば H2N  CH2Cl−bNHcH2cH2cH2s!
 (OCH3)3HりNCH2CHCH2CHクーN1
cHps  i  (OCJ5)  3H2N CH2
CH2−N HCH2CH2cl−12S  !  (
0CH2>2δH3 などのアルコキシシランの1種または混合物を、前記と
同様に希薄な酸性水溶液でアルコキシ基を加水分解した
後、揮発可能な有機酸を加えて、アミノ基、イミノ基と
中和反応させて有機酸塩の形に安定化させたプレポリマ
ーである。
The second component B has the general formula YnSi (OR> (where Y is an organic group containing an amino group and/or an imino group, and OR is a carbon number of 1 to
The alkoxy group in 6, ")" is composed of a hydrolyzate of an alkoxysilane having an amino group and/or imino group in the molecule represented by 1 or 2>, and is an organic group containing the above amino group and/or imino group. Generally, those having 2 to 10 carbon atoms are preferably used.The hydrolyzate B is a compound represented by the above general formula, for example, H2N CH2Cl-bNHcH2cH2cH2s!
(OCH3) 3HriNCH2CHCH2CH Ku N1
cHps i (OCJ5) 3H2N CH2
CH2-N HCH2CH2cl-12S! (
After hydrolyzing the alkoxy groups of one or a mixture of alkoxysilanes such as 0CH2>2δH3 with a dilute acidic aqueous solution in the same manner as above, a volatile organic acid is added to cause a neutralization reaction with amino groups and imino groups. It is a prepolymer stabilized in the form of an organic acid salt.

揮発可能な有機酸としてはギ酸、酢酸、プロピオン酸、
酪酸なと比較的低沸点の有機酸が好ましい。この有II
の添加量は該シランのアミノ基および/またはイミノ基
の総和1モルあたり0.5〜10モル量の範囲が好まし
く、より好ましくは1.0〜5.0モルの範囲である。
Volatile organic acids include formic acid, acetic acid, propionic acid,
Organic acids with relatively low boiling points, such as butyric acid, are preferred. This existence II
The amount added is preferably in the range of 0.5 to 10 moles, more preferably in the range of 1.0 to 5.0 moles, per 1 mole of the total amino groups and/or imino groups of the silane.

0.5モルより少ないとエポキシ基とアミノ基またはイ
ミノ基が反応して、ゲル化を呈するなど塗料成分が短く
なり易く、一方、10モルより多いと塗膜の硬化が不充
分となり易い。
If it is less than 0.5 mole, the epoxy group reacts with the amino group or imino group, resulting in gelation, which tends to shorten the coating composition, while if it is more than 10 mole, the coating film tends to be insufficiently cured.

第3の成分Cは白色顔料であり、この白色顔料Cとして
は酸化チタン、酸化亜鉛、炭酸カルシウム、二酸化ケイ
素、硫化亜鉛、酸化アンチモン。
The third component C is a white pigment, and the white pigment C includes titanium oxide, zinc oxide, calcium carbonate, silicon dioxide, zinc sulfide, and antimony oxide.

鉛白(2PbCO3・Pb (OH)2 >、酸化アル
ミニウム、硫酸バリウム、炭酸バリウム、タルク(3M
C]0・4Si02・H2O>、クレー(Aff203
・2S i 02・2H20)などが挙げられる。白色
顔料の粒子径は0.3〜10μの範囲が好ましく、より
好ましくは0.5〜5μの範囲である。粒子径が0.3
μより小さいと保護層面が粘着しやすくなる。一方、1
0μより大きいと保護層面の凹凸が太き(なり面粗れす
る。
White lead (2PbCO3・Pb(OH)2>, aluminum oxide, barium sulfate, barium carbonate, talc (3M
C]0.4Si02.H2O>, clay (Aff203
・2S i 02・2H20). The particle diameter of the white pigment is preferably in the range of 0.3 to 10μ, more preferably in the range of 0.5 to 5μ. Particle size is 0.3
If it is smaller than μ, the surface of the protective layer tends to stick. On the other hand, 1
If it is larger than 0μ, the unevenness on the surface of the protective layer becomes thick (and the surface becomes rough).

保護層の主成分を構成する成分A、B、Cの配合比率は
、各々の固形分量重量比がA:B:C=10〜50:9
0〜50:1〜9の範囲とする必要がある。Aの固形分
it比が10より小さいと保護層の耐摩耗性が低下する
。Bの固形分重量比が50より小さいと保護層の帯電防
止性が低下する。白色顔料の重量比が1より小さいと保
護層面が粘着しやすくなり、一方10より多いと白色顔
料の欠落による発塵が発生しやすい。
The blending ratio of components A, B, and C constituting the main components of the protective layer is such that the solid content weight ratio of each is A:B:C=10 to 50:9.
It is necessary to set it as the range of 0-50:1-9. When the solid content it ratio of A is less than 10, the wear resistance of the protective layer decreases. If the solid content weight ratio of B is less than 50, the antistatic properties of the protective layer will decrease. If the weight ratio of the white pigment is less than 1, the surface of the protective layer tends to become sticky, while if it is more than 10, dust is likely to be generated due to lack of the white pigment.

保と層の厚さく一つ、5〜10μの範囲が好ましく、よ
り好ましくは1〜5μの範囲である。厚さが0.5μよ
り薄いと耐摩耗性が不足する。一方、10μより厚いと
保護層にキレンが発生しやすくなる。
The thickness of the protective layer is preferably in the range of 5 to 10 microns, more preferably in the range of 1 to 5 microns. If the thickness is less than 0.5μ, wear resistance will be insufficient. On the other hand, if it is thicker than 10 μm, the protective layer tends to generate dust.

次に、本発明のリーダーテープの製造方法について説明
する。
Next, a method for manufacturing the leader tape of the present invention will be explained.

保護層を構成する分子中にエポキシ基を有するアルコキ
シランの加水分解物Aは、アルコキシ基1個当り1分子
の水を反応させるv1合で希薄な酸性水溶液、例えばN
/1000−N/100の希塩酸水溶液を加えてアルコ
キシ基を加水分解させてプレポリマーを得る。
The hydrolyzate A of an alkoxylan having an epoxy group in the molecule constituting the protective layer is prepared by reacting one molecule of water per alkoxy group with a dilute acidic aqueous solution, such as N
/1000-N/100 dilute aqueous hydrochloric acid solution is added to hydrolyze the alkoxy groups to obtain a prepolymer.

分子中にアミノ基および/またはイミノ基を有するアル
コキシシランの加水分解物Bは前記と同様の割合で希薄
な酸性水溶液を加えてアルコキシ基を加水分解した後、
ギ酸、酢酸などの有機酸を加えて、アミノ基、イミノ基
と有機酸の塩を形成させる。次いで上記のAおよびBを
有機溶剤に溶解させ、白色顔料を分散させた後、必要に
応じて硬化剤、硬化触媒、添加剤などを加えて、ざらに
溶剤で希釈して濃度5〜40重量%に調整した塗料をポ
リエステルフィルムの少なくとも片面に通常のロールコ
ータ:スプレー法などの方法により塗布し、これを加熱
おるいは紫外線、β線、γ線の放射線などにより硬化さ
せる。
Hydrolyzate B of alkoxysilane having an amino group and/or imino group in the molecule is obtained by adding a dilute acidic aqueous solution in the same proportion as above to hydrolyze the alkoxy group, and then
An organic acid such as formic acid or acetic acid is added to form a salt of an amino group, an imino group and an organic acid. Next, after dissolving the above A and B in an organic solvent and dispersing the white pigment, a curing agent, curing catalyst, additives, etc. are added as necessary, and diluted roughly with a solvent to a concentration of 5 to 40% by weight. % is applied to at least one side of a polyester film by a conventional roll coater or spray method, and then cured by heating or by UV, β, or γ radiation.

かくして得られた積層フィルムをスリットして(例えば
VH8用なら3インチ幅)、Ia気記録媒体の前後に接
続し、リーダーテープとする。
The thus obtained laminated film is slit (eg, 3 inches wide for VH8) and connected to the front and rear of the Ia recording medium to form a leader tape.

[発明の効果コ 本発明によれば次のような効果が1qられる。[Effects of invention According to the present invention, the following effects can be obtained.

■、保護層が耐摩耗性に優れているのでリーダテープ表
面が摩耗を受けて発塵することがない。
(2) Since the protective layer has excellent abrasion resistance, the surface of the leader tape does not become abraded and generate dust.

■、白色顔料の添加量が少ないので光線透過率が良好で
、テープの終端検出が良好であり、かつ顔料の欠落によ
る発塵がない。
(2) Since the amount of white pigment added is small, light transmittance is good, tape end detection is good, and there is no dust generation due to lack of pigment.

■、帯電防止性が良好であるため、静電気の蓄積がない
のでゴミや塵の付着がない。
■Since it has good antistatic properties, there is no accumulation of static electricity, so there is no adhesion of dirt or dust.

[特性の測定方法並びに効果の評価方法]本発明の特性
値の測定方法並びに効果の評価方法は次の通りである。
[Method for Measuring Characteristics and Evaluating Effects] Methods for measuring characteristic values and evaluating effects of the present invention are as follows.

■、耐耐摩耗性自白色顔料欠落 性振型摩耗試験機(JIS、LO823)、荷重20(
lで保護層面を100往復、500往復。
■, Wear-resistant white pigment loss vibration type abrasion tester (JIS, LO823), load 20 (
100 and 500 reciprocations on the protective layer surface with l.

1000往復摩擦して、傷の発生状態と白色顔料欠落の
有無を目視判定した。
It was rubbed back and forth 1000 times, and the occurrence of scratches and the presence or absence of missing white pigment were visually determined.

■、易滑性 ASTM、D−1894に準じた方法でフィルムの保護
層面と保護層面を重ね合せて、静摩擦係数μ5.動摩擦
係数μdを測定した。
(2) Easy slippage The protective layer surfaces of the films were overlaid in accordance with ASTM D-1894, and the static friction coefficient μ5. The dynamic friction coefficient μd was measured.

■、帯電防止性 川口電機(株)製、静電複写線分析装置、MODEL−
3P−428でフィルムの保護層面に+6KV、10秒
間、コロナ放電帯電させた後の表面電位の暗減衰半減期
を測定する。
■, antistatic, manufactured by Kawaguchi Electric Co., Ltd., electrostatic copy line analyzer, MODEL-
After the surface of the protective layer of the film is charged with corona discharge at +6 KV for 10 seconds using 3P-428, the dark decay half-life of the surface potential is measured.

■、光線透過率 JIS、に6714により測定した。■、Light transmittance Measured according to JIS 6714.

■、粘粘着ジブロッキン グ層フィルムを幅3インチのテープに裁断した俊、この
テープを直径36mmのガラス管に荷重3−の強さで巻
きつけ、45℃、80%RHで24時間放置後、テープ
間の層間粘着を目視で調べた。
■ Shun cut the sticky diblocking layer film into a 3-inch wide tape, wrapped this tape around a 36 mm diameter glass tube with a load of 3-, and left it at 45°C and 80% RH for 24 hours. The interlayer adhesion between the tapes was visually inspected.

[実施例] 本発明を実施例に基づいて説明する。[Example] The present invention will be explained based on examples.

実施例1 厚さ30μの二軸延伸ポリエステルフィルム(東しく株
)製“′ルミラー″)の片面に下記の保護層用塗料を固
形分塗布量が3g/m2になるようにロールコータ−で
塗布し、140℃で2分間乾燥し、リーダーテープ用の
積層フィルムを得た。
Example 1 The following protective layer paint was applied to one side of a 30 μ thick biaxially stretched polyester film (“Lumirror” manufactured by Toshiku Co., Ltd.) using a roll coater so that the solid content was 3 g/m2. Then, it was dried at 140° C. for 2 minutes to obtain a laminated film for a leader tape.

該積層フィルムの測定結果を表1に示す。Table 1 shows the measurement results of the laminated film.

保護層用塗料 A成分:γ−グリシドキシプロピルトリメトキシシラン
(トーレシリコン(株)製5H6040)236重量部
にN/100−塩酸54重量部を加えてアルコキシ基を
加水分解して、濃度57重量%のA成分290重量部を
得た。
Protective layer paint A component: 54 parts by weight of N/100-hydrochloric acid was added to 236 parts by weight of γ-glycidoxypropyltrimethoxysilane (5H6040 manufactured by Toray Silicone Co., Ltd.) to hydrolyze the alkoxy groups to give a concentration of 57 290 parts by weight of component A was obtained.

B成分二N−β(アミノエチル)γ−アミノプロピルト
リメトキシシラン(信越化学工業(株)製KBM−60
3>450重量部とエチルアルコール450重量部の混
合物にN/100−塩酸110重量部を加えてアルコキ
シ基を加水分解した後、ざらに酢酸600重量部を加え
て固形分濃度25重量%のB成分1610重量部を得た
Component B 2N-β(aminoethyl)γ-aminopropyltrimethoxysilane (KBM-60 manufactured by Shin-Etsu Chemical Co., Ltd.)
3> 110 parts by weight of N/100-hydrochloric acid was added to a mixture of 450 parts by weight of ethyl alcohol and 450 parts by weight of ethyl alcohol to hydrolyze alkoxy groups, and then 600 parts by weight of acetic acid was added to a colander to prepare B with a solid content concentration of 25% by weight. 1610 parts by weight of the components were obtained.

A成分と8成分を混合した後、炭酸カルシウム(粒子径
1μ〜5μ)を29重量加えて混合・分散し、イソプロ
ピルアルコール60重量部を加えて濃度30重量%の塗
料を得た。
After mixing component A and 8 components, 29 weights of calcium carbonate (particle size 1 μm to 5 μm) were added and mixed and dispersed, and 60 parts by weight of isopropyl alcohol was added to obtain a paint having a concentration of 30% by weight.

比較例1 実施例1においてA成分のみに炭酸カルシウム(粒子径
1〜5μ)を8重量部を加えて混合・分散し、イソプロ
ピルアルコール280重量部を加えて濃度30重量%の
塗料を得た後、これを実施例1と同様に固形分塗布量が
39/Tr12の積層フィルムを得た。該積層フィルム
の測定結果を表1に示す。
Comparative Example 1 In Example 1, 8 parts by weight of calcium carbonate (particle size 1 to 5 μm) was added to component A and mixed and dispersed, and 280 parts by weight of isopropyl alcohol was added to obtain a paint with a concentration of 30% by weight. A laminated film having a solid content coating amount of 39/Tr12 was obtained in the same manner as in Example 1. Table 1 shows the measurement results of the laminated film.

比較例2 厚さ30μの二軸延伸ポリエステルフィルムの片面に下
記の保護層用塗料を固形分塗布量が3g/Tr12にな
るようにロールコータ−で塗布し、140℃で2分間乾
燥し、積層フィルムを得た。該積層フィルムの評価結果
を表1に示す。
Comparative Example 2 The following protective layer paint was applied to one side of a 30 μ thick biaxially stretched polyester film using a roll coater so that the solid content coating amount was 3 g/Tr12, dried at 140°C for 2 minutes, and laminated. Got the film. Table 1 shows the evaluation results of the laminated film.

保護層用塗料 帯電防止剤(三洋化成工業(株)製、ケミスタット62
00.濃度47重量%)600重量部に炭酸カルシウム
(粒子径1〜5μ)14重量部と水373重量部を加え
て混合・分散して、濃度30重量%の塗料を得た。
Paint antistatic agent for protective layer (manufactured by Sanyo Chemical Industries, Ltd., Chemistat 62)
00. 14 parts by weight of calcium carbonate (particle size 1 to 5 μm) and 373 parts by weight of water were added to 600 parts by weight (concentration: 47% by weight) and mixed and dispersed to obtain a paint having a concentration of 30% by weight.

表1から明らかなごとく2本発明を満足する実施例1の
リーダテープの場合、耐摩耗性、帯電防止性、非粘着性
等のいずれも優れていることがわかる。
As is clear from Table 1, the leader tape of Example 1, which satisfies the two requirements of the present invention, is excellent in abrasion resistance, antistatic properties, non-adhesive properties, etc.

Claims (1)

【特許請求の範囲】 ポリエステルフィルムの少なくとも片面に保護層を積層
した積層体において、該保護層が A、一般式XmSi(OR)_4_−_m(ただし、X
はエポキシ基を含む有機基、ORは炭素数1〜6のアル
コキシ基、mは1または2)で示される−分子中にエポ
キシ基を有するアルコキシシランの加水分解物、 B、一般式 YnSi(OR)_4_−_n(ただし、
Yはアミノ基および/またはイミノ基を含む有機基、O
Rは炭素数1〜6のアルコキシ基、nは1または2)で
示される分子中にアミノ基および/またはイミノ基を有
するアルコキシシランの加水分解物、 C、白色顔料 を主成分とし、かつ上記A:B:Cの固形分量重量比が
10〜50:90〜10:1〜9であることを特徴とす
るリーダテープ。
[Claims] A laminate in which a protective layer is laminated on at least one side of a polyester film, wherein the protective layer has A, general formula XmSi(OR)_4_-_m (where X
is an organic group containing an epoxy group, OR is an alkoxy group having 1 to 6 carbon atoms, and m is 1 or 2) - a hydrolyzate of an alkoxysilane having an epoxy group in the molecule; )_4_-__n(However,
Y is an organic group containing an amino group and/or an imino group, O
R is an alkoxy group having 1 to 6 carbon atoms, n is 1 or 2); C, a hydrolyzate of an alkoxysilane having an amino group and/or an imino group in the molecule; C, a white pigment as a main component; A leader tape characterized in that the solid content weight ratio of A:B:C is 10-50:90-10:1-9.
JP14958986A 1986-06-27 1986-06-27 Leader tape Pending JPS6323224A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP14958986A JPS6323224A (en) 1986-06-27 1986-06-27 Leader tape

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP14958986A JPS6323224A (en) 1986-06-27 1986-06-27 Leader tape

Publications (1)

Publication Number Publication Date
JPS6323224A true JPS6323224A (en) 1988-01-30

Family

ID=15478506

Family Applications (1)

Application Number Title Priority Date Filing Date
JP14958986A Pending JPS6323224A (en) 1986-06-27 1986-06-27 Leader tape

Country Status (1)

Country Link
JP (1) JPS6323224A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH02145637A (en) * 1988-11-29 1990-06-05 Asahi Chem Ind Co Ltd Rubber-modified styrenic resin composition having improved slidability
WO1996020243A1 (en) * 1994-12-27 1996-07-04 Toyo Metallizing Co., Ltd. Polyester film for leader tape and process for producing the film
US6911272B2 (en) * 2002-04-02 2005-06-28 Fuji Photo Film Co., Ltd. Magnetic recording medium
DE19957324B4 (en) * 1999-11-29 2011-12-01 Few Chemicals Gmbh Coating composition and its use for the preparation of protective layers for polymers, protective layers produced therewith and methods for their production

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH02145637A (en) * 1988-11-29 1990-06-05 Asahi Chem Ind Co Ltd Rubber-modified styrenic resin composition having improved slidability
JPH0567660B2 (en) * 1988-11-29 1993-09-27 Asahi Chemical Ind
WO1996020243A1 (en) * 1994-12-27 1996-07-04 Toyo Metallizing Co., Ltd. Polyester film for leader tape and process for producing the film
DE19957324B4 (en) * 1999-11-29 2011-12-01 Few Chemicals Gmbh Coating composition and its use for the preparation of protective layers for polymers, protective layers produced therewith and methods for their production
US6911272B2 (en) * 2002-04-02 2005-06-28 Fuji Photo Film Co., Ltd. Magnetic recording medium

Similar Documents

Publication Publication Date Title
US5236818A (en) Antistatic coatings
JPS62160458A (en) Electrophotographic sensitive body
JPS6323224A (en) Leader tape
US5344751A (en) Antistatic coatings
JPH02694B2 (en)
US5213887A (en) Antistatic coatings
JP3178774B2 (en) Resin composition
JPH0519516A (en) Electrophotographic sensitive body
JP3606772B2 (en) Paint for forming transparent antistatic film and substrate with transparent antistatic film
JPS61176937A (en) Insulating recording film
JPS61184562A (en) Electrostatic recorder
GB2272654A (en) Antistatic coatings
KR100229347B1 (en) Method for the preparation of photographic film with excellent antistatic property
JP3749737B2 (en) Side wall board for road made of transparent synthetic resin
JPH0114581B2 (en)
JP2737598B2 (en) Surface-treated steel with excellent weather resistance
JP2001142244A (en) Electrophotographic photoreceptor and its producing method
JPS5933131B2 (en) Method for producing polyester film with improved conductivity
JPH01217043A (en) Electrically conductive film or sheet
JPH0754647B2 (en) Multilayer film for touch switch
JPS59142226A (en) Production of antistatic transparent plastic article
JPH0734007A (en) Antistatic coating composition for plastic
JPS63304421A (en) Leader tape
JPS61156051A (en) Electrostatic recording material
JPH0968821A (en) Electrophotographic organic photoreceptor