JPS60113385A - Friction liner for holding magnetic tape - Google Patents

Friction liner for holding magnetic tape

Info

Publication number
JPS60113385A
JPS60113385A JP22178883A JP22178883A JPS60113385A JP S60113385 A JPS60113385 A JP S60113385A JP 22178883 A JP22178883 A JP 22178883A JP 22178883 A JP22178883 A JP 22178883A JP S60113385 A JPS60113385 A JP S60113385A
Authority
JP
Japan
Prior art keywords
polyethlene
film
silane
molecular weight
friction liner
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP22178883A
Other languages
Japanese (ja)
Other versions
JPH022232B2 (en
Inventor
Masayuki Hishida
菱田 正行
Jichio Deguchi
出口 自治夫
Hiroshi Yui
浩 由井
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.)
YOUBEA LE-RON KOGYO KK
Mitsubishi Petrochemical Co Ltd
Original Assignee
YOUBEA LE-RON KOGYO KK
Mitsubishi Petrochemical Co Ltd
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 YOUBEA LE-RON KOGYO KK, Mitsubishi Petrochemical Co Ltd filed Critical YOUBEA LE-RON KOGYO KK
Priority to JP22178883A priority Critical patent/JPS60113385A/en
Publication of JPS60113385A publication Critical patent/JPS60113385A/en
Publication of JPH022232B2 publication Critical patent/JPH022232B2/ja
Granted legal-status Critical Current

Links

Abstract

PURPOSE:To obtain a friction liner for holding a magnetic tape with almost the same sliding characteristics as that of ultra-high mol.wt. polyethlene by adding graphite powder, etc., to prescribed ethylene unsaturated silane compound copolymer and by executing cross-linking under the presence of water after forming a film. CONSTITUTION:An ethylene-unsaturated silane compound copolymer obtained by graft-polymerizing polyethlene having 0.1-1.0 million molecular weight with a silane radical is polyethlene of high or low density organic silane modified, and an activated silane radical of the entire polyethlene is normally below 10%. The activated silane is cross-linked under the presence of water, and a gel fraction after cross-linking is made 40-80%. After adding carbon black or graphite powder to the polymerized polyethlene, a film is formed. When the film is passed in a steam chamber, for instance, of 100-130 deg.C, the activated silane forms a network structure between moleculars. By using the polyethlene obtained in such a way, the tape holding friction liner having excellent uniformity of a surface, excellent antiwear property and excellent antifriction property can be obtained.

Description

【発明の詳細な説明】 この発明は、静電気防止性、耐摩擦摩耗性、フラット性
等にすぐれ、しかも、製造工程が簡単で生産費が低摩で
あることを目的とする磁気テープ保持用フリクションラ
イナーに関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention provides a magnetic tape holding friction device which has excellent anti-static properties, friction and wear resistance, flatness, etc., and which has a simple manufacturing process and low production cost. It concerns the liner.

一般1こ、コンパクトカセット、マイクロカセットおよ
びビデオカセット等の中に納められている磁気テープを
保持するフィルムは四フッ化エチレン樹脂、超高分子量
ポリエチレン、紙、ポリエステル樹脂等の材料が使用さ
れているが、これらの中で、超高分子量ポリエチレンは
、コストおよび摺動特性のバランスの点で最も優れたも
のであると言える。超高分子量ポリエチレンは溶融粘度
が高く、通常の押出し成形法の適用は困難であることか
ら、主として圧縮成形法によって成形されてきた。そし
てシート(フィルムも含めて)のような薄板物を製造す
るにあたっては、圧縮成形品を旋盤にかけて、刃物によ
って皮むき(スカイブ)するが、切削された薄板物は母
体成形時の残留応力および切削時の抵抗;こよってフラ
ット性1こ欠ける。その結果、シートの7ラント性を修
正するための後工程が不可欠となる。さらに、スカイブ
に際しては、先端の鋭利な刃物が用いられる関係上刃欠
けが起き、シート表面に大きい凹凸ができて製品を使用
する1こあたり支障を来たすので、ある規準を設けて凹
凸の甚だしいものを選別除去しなければならず、製品収
率は非常に悪かった。また、原料ポリエチレンが一般に
は粒状でかつ大きいため、充填剤の種類や量に制約が多
く、種々のニーズに対応できる組成物を配合するのは困
難であった。
In general, the film that holds the magnetic tape contained in compact cassettes, micro cassettes, video cassettes, etc. is made of materials such as tetrafluoroethylene resin, ultra-high molecular weight polyethylene, paper, and polyester resin. However, among these, ultra-high molecular weight polyethylene can be said to be the most excellent in terms of the balance between cost and sliding properties. Ultra-high molecular weight polyethylene has a high melt viscosity, making it difficult to apply ordinary extrusion molding methods, so it has been mainly molded by compression molding methods. When manufacturing thin plate products such as sheets (including films), the compression molded product is placed on a lathe and skived using a knife. resistance; therefore, flatness is lost by one point. As a result, post-processing to correct the 7-rant properties of the sheet is essential. Furthermore, when making skives, the blades are chipped due to the use of sharp-edged tools, which creates large unevenness on the sheet surface and causes trouble for each use of the product. had to be sorted out and the product yield was very poor. Furthermore, since raw polyethylene is generally granular and large, there are many restrictions on the type and amount of filler, making it difficult to formulate a composition that can meet various needs.

この発明はこのような現状に着目してなされたものであ
り、分子量10万ないし100万のポリエチレンにシラ
ン基をグラフト重合させたエチレンー不飽和シラン化合
物共屯合体に必須成分としてカーボンブラックもしくは
グラファイト粉末またはこれらの混合粉末を添加し、こ
れを溶融状態下でフィルムに成形した後水架橋させて、
ゲル分率が呼0〜80%のものとし、超高分子量ポリエ
チレンに近い摺動特性を持たせたことを特徴とする磁気
テープ保持用フリクションライナーを提供するものであ
る。
This invention was made in view of the current situation, and includes carbon black or graphite powder as an essential component of the ethylene-unsaturated silane compound copolymer, which is obtained by graft polymerizing silane groups to polyethylene with a molecular weight of 100,000 to 1,000,000. Alternatively, by adding a mixed powder of these, forming it into a film in a molten state, and then water-crosslinking it,
The present invention provides a friction liner for holding a magnetic tape, which has a gel fraction of 0 to 80% and has sliding properties close to those of ultra-high molecular weight polyethylene.

この発明における分子量10万ないし100万のポリエ
チレンにシラン基をグラフト重合させたエチレンー不飽
和シラン化合物共重合体とは、たとえばIf)i三菱油
化社製造のリンクロンまたは141ALH8f、リンク
ロン−Xのような有機シラン変性の高密度(HD)もし
くは低密度(LD)のポリエチレン(PE)で、ポリエ
チレン全体の活性シラン基(−S i −0−R,ここ
でkはアルキル基)は通常10%以下のものである。こ
のような活性シラン基は水の存在下で架橋するの′で、
従来の化学架橋法や放射線架橋法等にくらべると、特殊
な設備を必要とする艮でもなく、また、デザインの制約
条件があるでもなく、通常の成形方法で任意の形状に予
め成形したポリエチレンを水分と接触させるだけできわ
めて容易に架橋させ、熱的、化学的および機械的特性を
大幅に改善向上させるのである。なお、水による架橋反
応を円滑に促進するための触媒(たとえばジブチル錫ジ
ラウレートを1%程度含有)のマスターバッチを適宜添
加してもよい。この発明において、水架橋後のゲル分率
を40〜80%とする理由は、図に示すように、40%
未満および80%を越えるポリエチレンでは超高分子量
ポリエチレンに近い耐摩耗性が得られないためであり、
ゲル分率65%付近で特に優れた耐摩耗性が得られるか
らである。ここで、図の摩耗係数は相手材をポリエステ
ル(PUT)とし、NTN式スラスラスト型摩耗試験機
いて、P V=Q、53 X 34 = 21 ((k
g/cm2)−(m/m1n))の条件下でめた値であ
る。
In this invention, the ethylene-unsaturated silane compound copolymer obtained by graft polymerizing a silane group to polyethylene with a molecular weight of 100,000 to 1 million is, for example, If) i Linkron or 141ALH8f manufactured by Mitsubishi Yuka Co., Ltd., Linkron-X. In organic silane-modified high-density (HD) or low-density (LD) polyethylene (PE), the active silane groups (-S i -0-R, where k is an alkyl group) in the entire polyethylene are usually 10%. These are as follows. These active silane groups crosslink in the presence of water,
Compared to conventional chemical crosslinking methods, radiation crosslinking methods, etc., it does not require special equipment or have any design constraints; instead, polyethylene is pre-formed into any shape using normal molding methods. It crosslinks very easily just by contacting with moisture, greatly improving its thermal, chemical and mechanical properties. Note that a masterbatch containing a catalyst (for example, containing about 1% dibutyltin dilaurate) for smoothly promoting the crosslinking reaction with water may be added as appropriate. In this invention, the reason why the gel fraction after water crosslinking is set to 40 to 80% is as shown in the figure.
This is because polyethylene with a content of less than 80% or more than 80% cannot provide wear resistance close to that of ultra-high molecular weight polyethylene.
This is because particularly excellent wear resistance can be obtained at a gel fraction of around 65%. Here, the wear coefficient in the figure is calculated using polyester (PUT) as the mating material and an NTN thrust-thrust type wear tester, P V = Q, 53 x 34 = 21 ((k
g/cm2)-(m/m1n)).

この発明においては、このようなシラン基をグラフト重
合させたポリエチレンに、カーボンブラックもしくはグ
ラファイト粉末の単味または混合物を添加するが、カー
ボンブラックの粒度範囲は0.01〜0.5μmで添加
量は3〜16重量%が望ましく、また、グラファイト粉
末については粒度範囲を1〜100μm、添加量を5〜
30市量%とすることが好ましい。ここで、この〕うな
範囲を設ける理由は、粒度の下限未満の小粒径のもので
は添加した充填剤の表面積が大きくなり過ぎてフィルム
強度が弱くなり、上限を越える大粒径のものではフィル
ムの表面粗度が大きくなるからであり、さらに、添加量
が下限未満の少量では静電気を生じ打ち抜きの際にパリ
を生じゃすく、上限を越える多量ではカーボンが磁気テ
ープを傷っけゲラファイトが脱落しゃすくなって好まし
くないからである。な゛お、これらカーボンブラック、
グラファイト等は飛散防止のためマスターバッチの状態
で添加してもこの発明において何等の支障を招くもので
はない。また、ざらに摺動特性を上げルタメニ、フッ素
樹脂、二硫化モリブテン等ノ固体潤滑剤を少量添加して
もよい。
In this invention, carbon black or graphite powder alone or in a mixture is added to polyethylene graft-polymerized with silane groups, and the particle size range of carbon black is 0.01 to 0.5 μm, and the amount added is 3 to 16% by weight is desirable, and for graphite powder, the particle size range is 1 to 100 μm, and the amount added is 5 to 100 μm.
It is preferable to set it as 30% of market weight. The reason for setting this range is that if the particle size is smaller than the lower limit, the surface area of the added filler will become too large and the film strength will be weakened, whereas if the particle size is larger than the upper limit, the film will become weak. This is because the surface roughness of the carbon increases.Furthermore, if the amount added is less than the lower limit, it will generate static electricity and cause cracks during punching, and if the amount exceeds the upper limit, the carbon will damage the magnetic tape and the galafite will This is because it tends to fall off, which is undesirable. Oh, these carbon blacks,
Even if graphite or the like is added in the form of a masterbatch to prevent scattering, it will not cause any trouble in the present invention. In addition, a small amount of solid lubricant such as lutamene, fluororesin, molybdenum disulfide, etc. may be added to improve the sliding properties.

以上のようにシラン基をグラフト重合させたポリエチレ
ンにカーボンブラックもしくはグラファイト粉末の単味
または混合物の添加が終われば、通常広く用いられてい
るTダイ法またはインフレーション等の成形法を用いて
、たとえば。、07〜0、12.mm 程度の厚さのフ
ィルム1こ成形する。ついで、得られたフィルムをロー
ルに巻取った状態で60〜80℃程度の温水中に約1昼
夜浸漬するか、または、連続的に100〜130℃程度
の水蒸気室を通過させると、フィルム中の活性シラン基
は分子間に一8i−0−8i−の橋をかけて網目状の構
造を形成するので、分子量は言うに及ばず機械的性質の
すぐれたフィルムに変換することができる。よって、従
来困難であった超高分子量ポリエチレンに近い摺動特性
を持ったポリエチレンの薄膜化も、前記したような適度
の活性シラン基を持ったポリエチレンをフィルム成形し
た後、水による架橋反応を施すことによってきわめて容
易に実現することができるのである。このように、水架
橋によって高分子量化する以前の分子量の比較的低い状
態においてフィルムの押出し成形を行なうと、フィルム
表面は非常fこ均質になる。したがって、この発明の磁
気テープ保持用フリクションライナーはすぐれた表面の
均質性ととも1こ、超高分子量ポリエチレン1こ近い耐
摩耗性、耐摩擦性を兼ね催えたシートになる。
After the addition of carbon black or graphite powder alone or as a mixture to the polyethylene graft-polymerized with silane groups as described above, it is molded using a commonly used molding method such as the T-die method or inflation, for example. , 07-0, 12. Form a film with a thickness of about mm. Then, the obtained film is wound into a roll and immersed in hot water at a temperature of about 60 to 80°C for about a day and night, or when it is continuously passed through a steam chamber at a temperature of about 100 to 130°C. The active silane groups form a network structure by forming 18i-0-8i- bridges between molecules, so that it can be converted into a film with excellent mechanical properties as well as molecular weight. Therefore, it is possible to form a thin film of polyethylene with sliding properties similar to those of ultra-high molecular weight polyethylene, which has been difficult in the past, by forming a film of polyethylene with an appropriate amount of active silane groups as described above, and then subjecting it to a crosslinking reaction with water. This can be achieved extremely easily. As described above, when a film is extruded in a state where the molecular weight is relatively low before the molecular weight is increased by water crosslinking, the surface of the film becomes extremely homogeneous. Therefore, the friction liner for holding a magnetic tape of the present invention is a sheet that has excellent surface homogeneity, as well as abrasion resistance and abrasion resistance comparable to that of ultra-high molecular weight polyethylene.

以上述べたこの発明の磁気テープ保持用フリクションラ
イナーは、従来法1こくらべて、直接フィルム成形する
点で生産性が向上し、工程は著しく削減され、製品収率
の点でもE筋不良が皆無となるため著しく増大し、その
結果、製造槁格はきわめて安価になる。また、磁気テー
プの走行安定性および巻むら防止のために、保持用フリ
クションライナー1こは、一定のカール性およびフラッ
ト性が要求されるが、水架橋時に癖付けすることによっ
て任意の安定したカール性およびフラット性のものが得
られ、ざらにエンボ諷加工も同時に行なうことができ、
後工程が簡略化できることになる。
Compared to the conventional method 1, the friction liner for holding magnetic tapes of the present invention as described above has improved productivity in that direct film forming is performed, the number of processes is significantly reduced, and there is no E line defect in terms of product yield. Therefore, the cost increases significantly, and as a result, the manufacturing cost becomes extremely cheap. In addition, in order to maintain running stability of the magnetic tape and prevent uneven winding, the holding friction liner is required to have a certain level of curling and flatness, but by forming a pattern during water cross-linking, it is possible to achieve any stable curling. It is possible to obtain smooth and flat products, and rough embossing can be done at the same time.
Post-processes can be simplified.

しかも、この発明の7リクシヨンライナーは、架橋構造
を形成しているので、熱硬化性樹脂のように高温時の熱
安定性が良くなって、通常の超高分子量ポリエチレンベ
ースのとき、100°Cて1時間放置した後1こは、1
00mmに対して1 mm 以上の寸法経時変化が生ず
るが、この発明のフリクションライナーの変化は0.3
mm[下であり、カール性もフラット性も変化はほとん
ど認められず、そのうえ、原料樹脂の溶融粘度が低いた
め、成形時均−に溶け、ベース樹脂粒子間の結合が容易
となり、カーボンブラック、グラファイト等の充填量の
許容範囲を約40重階%にまで増大することができ、需
要に対応した改質、改善に広い幅ができた等の利点も認
められたので、この発明の意義はきわめて大きいと言う
ことができる。
Moreover, since the 7-reaction liner of this invention has a crosslinked structure, it has good thermal stability at high temperatures like a thermosetting resin, and when it is made of ordinary ultra-high molecular weight polyethylene, it has a 100° After leaving it for 1 hour, 1
00mm, a dimensional change of 1 mm or more occurs over time, but the friction liner of this invention changes by 0.3 mm or more.
mm[, and there is almost no change in curling or flatness.Furthermore, because the melt viscosity of the raw material resin is low, it melts evenly during molding, making it easier to bond between the base resin particles. The significance of this invention is that it was possible to increase the allowable range of the amount of graphite, etc., to about 40% by weight, and that it enabled a wide range of modification and improvement to meet demand. It can be said that it is extremely large.

以下、実施例を示す。なお、分子量の表示はすべて粘度
性測定による。
Examples are shown below. Note that all molecular weights are based on viscosity measurements.

〔実施例1〕 有機シラン変性ポリマー(三菱油化社製造ニリンクロン
X HE 650、ll−1klll’)1oo重電部
に架橋促進マスターバッチ(ジブチル錫ジラウレートを
含有)5重量部を加え、さらにカーボン3市量%とグラ
ファイト17重量%とを加えて、L/D22、CR3,
3、回転数3 Orpm 以上のフルフライトスクリュ
ーを有し、シリンター径50mm、Tダイ幅300 m
mの押出機を用いて、樹脂温度200℃、押出量約20
 kg/hの条件下で厚さ0.1 mmのフィルムを成
形した。−このフィルムを約70°Cの水槽に1昼夜浸
漬した結果、ゲル分率65%のものになった。
[Example 1] 5 parts by weight of a crosslinking accelerator masterbatch (containing dibutyltin dilaurate) was added to 100 parts of an organic silane-modified polymer (Mitsubishi Yuka Co., Ltd. Nilinclon By adding % market weight and 17% by weight of graphite, L/D22, CR3,
3. Has a full-flight screw with a rotation speed of 3 Orpm or more, cylinder diameter 50 mm, and T-die width 300 m.
m extruder, resin temperature 200℃, extrusion amount approximately 20
A film with a thickness of 0.1 mm was molded under the condition of kg/h. - This film was immersed in a water tank at about 70°C for one day and night, resulting in a gel fraction of 65%.

得られた製品フィルムの摩擦係数、摩耗係数および電気
的性質を他の樹脂と比較して第1表にまとめた。なお、
摩擦係数は荷重11g、滑り速度毎分3 m 、相手材
ポリエステル(PET)としたときの値であり、摩耗係
数はざらつき摩耗(テーパー摩耗試験およびサンドアブ
レーション試験)第 1 表 による値である。また、寸法安定性は100 ’Cで1
時間放置後の100mm1こ対する寸法の経時変化で示
した。さらに、ゲル分率はソックスレー抽出器を用い、
キシレン沸点下で抽出したときの樹脂不溶分の重1wの
抽出前の樹脂全重量WOに対する百分率%で表わしたも
のである。
The friction coefficient, abrasion coefficient, and electrical properties of the obtained product film are summarized in Table 1 in comparison with other resins. In addition,
The friction coefficient is the value when the load is 11 g, the sliding speed is 3 m/min, and the mating material is polyester (PET), and the wear coefficient is the value according to Table 1 of rough wear (taper wear test and sand ablation test). Also, the dimensional stability is 1 at 100'C.
It is shown as a change over time in the dimensions per 100 mm after being left for a period of time. Furthermore, the gel fraction was determined using a Soxhlet extractor.
It is expressed as a percentage of the weight 1w of the resin insoluble matter when extracted under the boiling point of xylene to the total weight WO of the resin before extraction.

〔実施例2〜4〕 充填剤の種類または組成とともに、水架橋後のゲル分率
を55%、70%と変化させた以外は実施例1と同様の
方法で得た製品フィルムについて諸物性を測定し、その
結果を第1表に併記した。
[Examples 2 to 4] Various physical properties were measured for product films obtained in the same manner as in Example 1, except that the type or composition of the filler and the gel fraction after water crosslinking were changed to 55% and 70%. The results are also listed in Table 1.

以トの結果を総合すれば、この発明の磁気テープ保持用
フリクションライナーの優秀性が明白である。
If the above results are taken together, the superiority of the magnetic tape holding friction liner of the present invention is clear.

【図面の簡単な説明】[Brief explanation of the drawing]

図は樹脂の種類と摩耗係数との関係を示すための図であ
る。 A、Is、C,D 、、、ゲル分率がそれぞれ30,5
0゜65.80%である水架橋後の有機シラン変性ポリ
エチレン、E・・・超高分子量ポリエチレン、F・・・
HDPE、、G、・・LI)PE0
The figure is a diagram showing the relationship between the type of resin and the wear coefficient. A, Is, C, D, , gel fraction is 30, 5, respectively.
Organosilane-modified polyethylene after water crosslinking with a concentration of 0°65.80%, E...Ultra high molecular weight polyethylene, F...
HDPE,,G,...LI)PE0

Claims (1)

【特許請求の範囲】[Claims] 分子量10万ないし100万のポリエチレンにシラン基
をグラフト重合させたエチレンー不飽和シラン化合物共
市合体lこ、必須成分としてカーボンブラックもしくは
グラファイト粉末またはこれらの混合粉末を添加し、こ
れを溶融状態下でフィルム1こ成形した後水架橋させて
、ゲル分率40〜80%のものとし、超高分子量ポリエ
チレンに近い摺動特性を持たせたことを特徴とする磁気
テープ保持用フリクションライナー。
This is an ethylene-unsaturated silane compound co-merchandised product obtained by graft polymerizing silane groups to polyethylene with a molecular weight of 100,000 to 1,000,000. Carbon black or graphite powder or a mixed powder thereof is added as an essential component, and this is mixed in a molten state. A friction liner for holding a magnetic tape, characterized in that a film is molded and then cross-linked with water to have a gel fraction of 40 to 80%, giving it sliding properties close to those of ultra-high molecular weight polyethylene.
JP22178883A 1983-11-24 1983-11-24 Friction liner for holding magnetic tape Granted JPS60113385A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP22178883A JPS60113385A (en) 1983-11-24 1983-11-24 Friction liner for holding magnetic tape

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP22178883A JPS60113385A (en) 1983-11-24 1983-11-24 Friction liner for holding magnetic tape

Publications (2)

Publication Number Publication Date
JPS60113385A true JPS60113385A (en) 1985-06-19
JPH022232B2 JPH022232B2 (en) 1990-01-17

Family

ID=16772208

Family Applications (1)

Application Number Title Priority Date Filing Date
JP22178883A Granted JPS60113385A (en) 1983-11-24 1983-11-24 Friction liner for holding magnetic tape

Country Status (1)

Country Link
JP (1) JPS60113385A (en)

Also Published As

Publication number Publication date
JPH022232B2 (en) 1990-01-17

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