JP3082010B2 - Packing material for magnetic disk drive - Google Patents

Packing material for magnetic disk drive

Info

Publication number
JP3082010B2
JP3082010B2 JP04037842A JP3784292A JP3082010B2 JP 3082010 B2 JP3082010 B2 JP 3082010B2 JP 04037842 A JP04037842 A JP 04037842A JP 3784292 A JP3784292 A JP 3784292A JP 3082010 B2 JP3082010 B2 JP 3082010B2
Authority
JP
Japan
Prior art keywords
packing material
foam stabilizer
magnetic disk
silicon
disk drive
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
Application number
JP04037842A
Other languages
Japanese (ja)
Other versions
JPH05234351A (en
Inventor
浩幸 富沢
円 永井
公一 草川
昇 村田
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.)
NHK Spring Co Ltd
Original Assignee
NHK Spring 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 NHK Spring Co Ltd filed Critical NHK Spring Co Ltd
Priority to JP04037842A priority Critical patent/JP3082010B2/en
Publication of JPH05234351A publication Critical patent/JPH05234351A/en
Application granted granted Critical
Publication of JP3082010B2 publication Critical patent/JP3082010B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【産業上の利用分野】本発明は磁気ディスク駆動装置の
防塵カバーと磁気ディスクを収納する容器本体を密封す
るパッキング材に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a dust-proof cover for a magnetic disk drive and a packing material for hermetically sealing a container body for accommodating a magnetic disk.

【0002】[0002]

【従来の技術】磁気ディスク駆動装置はハ−ドディスク
ドライブ(以下HDDと略す)と称され、密閉容器内に
収納してある硬質の円板状の磁気ディスクを回転させな
がら0.1〜0.5μmの隙間を介して磁気ヘッドから
情報を記録/再生を行なうものであるが、この装置では
ディスクとヘッドの隙間が0.1〜0.5μm程度とい
う極めて狭小なためディスクとヘッドの間に塵埃類が侵
入するとヘッドやディスクが破損し重要なデータの読み
取りが不能になるというトラブルが発生しやすい。 こ
のようなトラブルを防止するために密閉容器本体と防塵
カバ−を密封するパッキング材の使用が行われている
が、近年このパッキング材から発生するシリコン系物質
等の塵埃類や油分がヘッドやディスクに付着・汚染して
読み取りの誤動作をおこす問題も発生してきた。そのた
め、容器本体の密閉性を高めると同時に容器本体と防塵
カバーとの間に介在させるパッキング材からも塵埃類の
発生、油分の発生のない清浄な物を使用する配慮が払わ
れている。
2. Description of the Related Art A magnetic disk drive is referred to as a hard disk drive (hereinafter abbreviated as HDD) and rotates a hard disk-shaped magnetic disk housed in an airtight container in a range of 0.1 to 0. Information is recorded / reproduced from a magnetic head through a gap of 0.5 μm. However, in this apparatus, the gap between the disk and the head is extremely small, such as about 0.1 to 0.5 μm. When dust enters, the head and the disk are damaged, and a trouble that important data cannot be read easily occurs. In order to prevent such troubles, a packing material for sealing the closed container body and the dustproof cover has been used. In recent years, dusts and oils such as silicon-based substances generated from the packing material have been removed from the head or disk. There has also been a problem that reading and erroneous operations may occur due to adhesion and contamination of the image. For this reason, attention is paid to use of a clean material free from generation of dust and oil from the packing material interposed between the container main body and the dustproof cover while improving the hermeticity of the container main body.

【0003】従来、パッキング材としてはクロロプレン
スポンジ、ウレタンスポンジ、シリコーンゴム等が使わ
れてきた。しかしながら、クロロプレンスポンジはへた
りが大きく、シール性に長期の信頼性がなく、更に装置
の調整等のためカバーを開ける場合、シールがへたって
おり、交換する手数を要した。ウレタンスポンジは、通
気性が高く、防塵、防湿の目的を達成できず、また整泡
剤として使用しているシリコン化合物が気化し、磁気ヘ
ッドや磁気ディスクに付着し、汚染することで読み取り
誤動作を起こし、信頼性が欠く、一方、シリコ−ンゴム
は復元性、防塵性は良好であるが、ゴム中の未反応低分
子量シリコン化合物により磁気ヘッドや磁気ディスクが
汚染され、読み取り誤動作を起こし、信頼性が欠しいと
いう欠点があった。更に、従来、シール材自体の清浄度
を高めるためフロン洗浄を行なっている場合があった
が、フロンの規制により水洗浄方法が検討されており、
水洗浄によっても吸水しにくく乾燥容易なシール材が望
まれていた。
Conventionally, chloroprene sponge, urethane sponge, silicone rubber and the like have been used as packing materials. However, the chloroprene sponge has a large set, there is no long-term reliability in the sealing property, and when the cover is opened for adjustment of the apparatus, the seal is set, and it takes time to replace it. Urethane sponge has high air permeability, cannot achieve the purpose of dustproof and moistureproof, and the silicon compound used as a foam stabilizer vaporizes, adheres to magnetic heads and magnetic disks, and contaminates, causing malfunctions in reading. Silicon rubber has good resilience and dust resistance, but unreacted low-molecular-weight silicon compounds in the rubber contaminate the magnetic head and magnetic disk, causing read errors and causing reliability problems. However, there was a disadvantage that it was lacking. Furthermore, in the past, there was a case in which chlorofluorocarbon cleaning was performed in order to increase the cleanliness of the sealing material itself.
There has been a demand for a seal material that is hardly absorbed by water and easy to dry.

【0004】[0004]

【発明が解決しようとする課題】本発明者は上記の欠点
を無くし、水洗浄しても吸水しにくいパッキング材を得
るべく種々検討した結果、本発明を完成したもので、本
発明の目的は圧縮永久ひずみが少なく(ヘタリの少な
い)シリコン等の油分や塵埃類の発生がなく磁気ディス
ク駆動装置の誤動作を起こさない磁気ディスク駆動装置
用パッキング材を提供することである。
SUMMARY OF THE INVENTION The present inventor has made various studies to eliminate the above-mentioned disadvantages and to obtain a packing material which does not easily absorb water even when washed with water. As a result, the present invention has been completed. An object of the present invention is to provide a packing material for a magnetic disk drive which has a small compression set (small set), no oil such as silicon or dust, and does not cause a malfunction of the magnetic disk drive.

【0005】[0005]

【課題を解決するための手段】本発明の要旨は、ポリオ
ール、イソシアナート、発泡剤及び反応型シリコン整泡
剤及びその他の助剤より得られた平均セル径が150μ
m以下の可撓性マイクロセルウレタンよりなる磁気ディ
スク駆動装置用パッキング材である。すなわち、本発明
においてはポリウレタン系発泡材よりなるパッキング材
を得るに際し、整泡剤として反応型シリコン整泡剤を使
用し、セルの平均孔径を150μm以下の可撓性マイク
ロセルウレタンとしたことにより、その目的を達成する
ことができた。
The gist of the present invention is that an average cell diameter obtained from a polyol, an isocyanate, a foaming agent, a reactive silicone foam stabilizer and other auxiliaries is 150 μm.
This is a packing material for a magnetic disk drive made of flexible microcell urethane of m or less. That is, in the present invention, when obtaining a packing material comprising a polyurethane-based foam material, a reactive silicon foam stabilizer was used as a foam stabilizer, and the average pore diameter of the cells was 150 μm or less to form a flexible microcell urethane. , Was able to achieve its purpose.

【0006】本発明について更に詳細に説明する。本発
明でいうマイクロセルウレタンは、そのセルの平均孔径
は150μm以下である。一般的なウレタンのセル径は
400〜500μmであり、また、シ−ル材として使用
されているものでも250〜300μmあるのに比して
本発明のマイクロセルウレタンは、そのセルの平均孔径
は150μm以下であり、従来のものよりセル径は小さ
い。このセル径が150μmより大きいと通気性が高ま
り防塵性が劣り、吸水性も高まり好ましくない。そし
て、このマイクロセルウレタンの密度は0.1〜0.7
g/cm3が好ましく、密度が低くなるとパッキング材
の界面からの通気性が高くなり塵埃の侵入の恐れが生
じ、一方、密度が高くなると圧縮応力が高くなると共に
圧縮すると横に広がり、カバーよりはみ出す恐れがあ
る。
The present invention will be described in more detail. The microcell urethane in the present invention has an average pore size of 150 μm or less. The cell diameter of a general urethane is 400 to 500 μm, and even if it is used as a seal material, it is 250 to 300 μm, whereas the microcell urethane of the present invention has an average pore diameter of the cell. It is 150 μm or less, and the cell diameter is smaller than the conventional one. If the cell diameter is larger than 150 μm, air permeability is increased, dust resistance is deteriorated, and water absorption is increased, which is not preferable. The density of the microcell urethane is 0.1 to 0.7.
g / cm 3 is preferable. When the density is low, the air permeability from the interface of the packing material is high, and there is a risk of intrusion of dust. On the other hand, when the density is high, the compressive stress increases, and when compressed, it spreads laterally, and There is a risk of protruding.

【0007】本発明おけるポリオールとしては、一般に
ウレタン工業で使用されるポリエーテルポリオール、ポ
リエステルポリオール等何れでもで良く特に限定されな
い。また、イソシアナートについては、トリレンジイソ
シアナート、ジフェニルメタンジイソシアナート(MD
I)や粗製のMDIなどがあり、特に限定されない。ま
た、発泡剤としては水、塩化メチレン、窒素、空気、フ
ロンなどがある。本発明の特徴の一つである反応型シリ
コン整泡剤とは、本発明のマイクロセルウレタン製造の
ため用いられるポリオール、イソシアナート及び発泡剤
等と反応する反応基を有する整泡剤である。このような
反応基としては、OH基、NH基、NH2基、SH基、
COOH基、Si−OCH3基(メトキシ基)などがあ
る。シリコン整泡剤の構造は、下記に示すポリジメチル
シロキサン−ポリアルキレンエーテルブロック共重合体
が代表的である。
The polyol in the present invention may be any of polyether polyol, polyester polyol and the like generally used in the urethane industry, and is not particularly limited. As for isocyanate, tolylene diisocyanate, diphenylmethane diisocyanate (MD
I) and crude MDI are not particularly limited. Examples of the foaming agent include water, methylene chloride, nitrogen, air, and chlorofluorocarbon. The reactive silicone foam stabilizer which is one of the features of the present invention is a foam stabilizer having a reactive group which reacts with a polyol, an isocyanate, a foaming agent and the like used for producing the microcell urethane of the present invention. Such reactive groups include OH groups, NH groups, NH 2 groups, SH groups,
COOH group, Si-OCH 3 group (methoxy group) and the like. The structure of the silicone foam stabilizer is typically a polydimethylsiloxane-polyalkylene ether block copolymer shown below.

【0008】[0008]

【化1】 Embedded image

【0009】式中、m,nは1以上の整数、R’は有機
基、POAはアルキレンエーテル基Aは反応基(例えば
OH基)を表す。反応型シリコン整泡剤を用いることで
本発明のパッキング材の通気性が低くなり、その結果、
防塵効果が高まると同時にシリコンの発散が少ないため
読み取り誤動作が起こらない特徴がある。更に、また反
応型シリコン整泡剤を用いると通常の添加型(非反応
型)シリコン整泡剤と比べ大巾に吸水性が低くなり、水
洗浄が可能となる。パッキング材の清浄度がフロン洗浄
と同等のレベルとなり、フロンの廃止に寄与することが
できる。また、その他の助剤としては、ポリウレタン製
造時に使用する慣用の助剤である。
In the formula, m and n are integers of 1 or more, R 'is an organic group, POA is an alkylene ether group A is a reactive group (for example, OH group). By using a reactive silicone foam stabilizer, the air permeability of the packing material of the present invention is reduced, and as a result,
There is a feature that a reading malfunction does not occur because the dust proof effect is enhanced and the divergence of silicon is small at the same time. Furthermore, when a reactive type silicone foam stabilizer is used, the water absorption becomes significantly lower than that of a normal addition type (non-reactive type) silicone foam stabilizer, and washing with water becomes possible. The cleanliness of the packing material is at the same level as the CFC cleaning, and can contribute to the elimination of CFCs. Other auxiliary agents include conventional auxiliary agents used in the production of polyurethane.

【0010】上記のポリオール、イソシアナート、発泡
剤及び反応型シリコン整泡剤及びその他の助剤を使用し
て、マイクロセルウレタンを製造する方法としては、通
常行なわれている水発泡方法、揮発性溶剤による発泡方
法や空気などを泡立てる方法など何れでも良いが、ただ
マイクロセルとすると、熱伝導率が下がるため前2方法
は後者の方法よりもキュア−時間が短く好ましい。得ら
れるマイクロセルウレタンのセル径の調整方法として
は、例えばシリコン整泡剤や触媒量の添加部数を増やし
たり、或いはポリオ−ルの官能基を2官能より3官能と
し架橋剤の官能基数を多くしたり、発泡時の圧力を高く
したり、アミン触媒よりスズ触媒の方を多くする等の手
段によりセル径を細かくすることができる。
The method for producing microcell urethane by using the above-mentioned polyol, isocyanate, foaming agent, reactive silicone foam stabilizer and other auxiliaries includes a water foaming method which is usually carried out, Either a foaming method with a solvent or a method of bubbling air or the like may be used. However, if a microcell is used, the thermal conductivity is reduced, and the former two methods are preferable because the curing time is shorter than the latter method. As a method of adjusting the cell diameter of the obtained microcell urethane, for example, the number of added parts of the silicone foam stabilizer or the amount of the catalyst is increased, or the number of functional groups of the crosslinking agent is increased by increasing the number of functional groups of the polyol to three from two. The cell diameter can be made smaller by such means as increasing the pressure at the time of foaming, or increasing the amount of the tin catalyst compared to the amine catalyst.

【0011】そして、これらの何れの発泡方法でも、ブ
ロック状に生産した後、所定の厚みにスライスして原反
を得る方法、モールドで所定厚みの物を得る方法、リケ
イ性の材料の上に発泡原料を塗工し発泡する方法などが
あるが、後の2方法によると製品の表裏に自己スキンの
付いた製品が得られ、粘着剤との接着性が良好で、かつ
カバーとの密着性が向上し界面からの通気性が低くなる
ため密閉度と防塵度が高まり好ましい。
[0011] In any of these foaming methods, after producing into a block, it is sliced to a predetermined thickness to obtain an original fabric, a method to obtain a product having a predetermined thickness by a mold, There are methods such as applying foaming material and foaming. According to the latter two methods, a product with a self-skin on the front and back of the product is obtained, and the adhesiveness with the adhesive is good and the adhesiveness with the cover And the air permeability from the interface decreases, so that the degree of sealing and the degree of dust prevention are increased, which is preferable.

【0012】[0012]

【発明の効果】本発明による効果を列挙すると、次のと
おりである。 (1)反応型シリコン整泡剤を用いたマイクロセルウレ
タンのためHDDの誤動作を引き起こすシリコン化合物
の発生の少ない清浄度の高いパッキング材が提供でき
た。 (2)セル径が150μm以下のマイクロセルウレタン
のためわずか圧縮するだけでセル穴が閉じ易くそのため
低通気性が達成できる。 (3)反応型シリコン整泡剤を用いセル径150μm以
下のマイクロセルウレタンのため、吸水性が極めて低
く、水洗浄が可能で、フロン洗浄によらず清浄なパッキ
ング材が提供可能となる。
The effects of the present invention are listed below. (1) A microcell urethane using a reactive silicon foam stabilizer provided a highly clean packing material with less generation of silicon compounds causing malfunction of the HDD. (2) Microcell urethane having a cell diameter of 150 μm or less makes it easy to close the cell hole with only a slight compression, so that low air permeability can be achieved. (3) Microcell urethane having a cell diameter of 150 μm or less using a reactive silicon foam stabilizer, has extremely low water absorption, can be washed with water, and can provide a clean packing material regardless of Freon washing.

【0013】(4)反応型シリコン整泡剤を用いるた
め:粘着テープとの接着性が良く、また自己スキン層を
有するパッキング材の場合、更に接着性が良好となる。
そのためHDDの組立て作業でパッキング材がはがれる
問題が発生せず信頼性が高い。更に接着性が高いためH
DDのカバー形状が複雑になったとしても対応しやすい
メリットがある。 (5)マイクロセルウレタンのため、クロロプレンスポ
ンヂのように可塑剤を含まず、へたりも少ない。
(4) Since a reactive silicone foam stabilizer is used: the adhesiveness to the adhesive tape is good, and in the case of a packing material having a self-skin layer, the adhesiveness is further improved.
For this reason, there is no problem that the packing material comes off in the HDD assembling operation, and the reliability is high. H
There is a merit that it is easy to cope even when the cover shape of the DD becomes complicated. (5) Since it is a microcell urethane, it does not contain a plasticizer unlike chloroprene sponge and has little settling.

【0014】[0014]

【実施例】次に実施例及び比較例をもって本発明を更に
具体的に説明する。 実施例1 分子量3000のポリオキシプロピレントリオール10
0部、1,4ブタンジオール6部、触媒としてアミン触
媒(Dabco33LV)0.1部、ジブチルチンジラ
ウレ−ト(DBTDL)0.1部を使用し、シリコン整
泡剤として末端OH基の反応型シリコン整泡剤(F−3
42、信越化学)を2部使用し、発泡剤として水0.2
部を使用し、MDI40部と混合撹拌し、ブロック状に
発泡し、100℃10分間加熱を行い、1mmにスライ
スしシート状の製品を得た。
Next, the present invention will be described more specifically with reference to examples and comparative examples. Example 1 Polyoxypropylene triol 10 having a molecular weight of 3000
0 parts, 1,4 butanediol 6 parts, amine catalyst (Dabco 33LV) 0.1 part, dibutyltin dilaurate (DBTDL) 0.1 part as a catalyst, reaction of terminal OH group as a silicone foam stabilizer Type silicone foam stabilizer (F-3
42, Shin-Etsu Chemical Co., Ltd.).
The mixture was mixed and stirred with 40 parts of MDI, foamed in a block shape, heated at 100 ° C. for 10 minutes, and sliced into 1 mm to obtain a sheet-like product.

【0015】実施例2 実施例1と同様にシリコン整泡剤としてNH基含有の反
応型シリコン整泡剤(X22−3939A信越化学)を
2部使用し、ブロック状に発泡させ、100℃10分間
加熱を行い、1mmにスライスし、シート状の製品を得
た。 実施例3 実施例1と同じ方法で離型紙上に塗工し、スキン付の発
泡体を得た。
Example 2 In the same manner as in Example 1, 2 parts of an NH group-containing reactive silicon foam stabilizer (X22-3939A Shin-Etsu Chemical Co., Ltd.) was used as a silicone foam stabilizer, foamed into a block, and heated at 100 ° C. for 10 minutes. It heated and sliced to 1 mm, and obtained the sheet-shaped product. Example 3 Coating was performed on release paper in the same manner as in Example 1 to obtain a foam with skin.

【0016】比較例1 実施例1と同じ方法でシリコン整泡剤として末端ブトキ
シ基の非反応型シリコン(F−304信越化学)を2部
使用し、ブロック状に発泡させ、100℃10分間加熱
を行い、1mmにスライスし、シート状の製品を得た。 比較例2 実施例1と同じ方法で、セル径大のウレタンの製造のた
め、窒素量を少なくして、シート状の発泡体を得た。
Comparative Example 1 In the same manner as in Example 1, 2 parts of non-reactive silicon (F-304 Shin-Etsu Chemical) having a butoxy end group was used as a silicone foam stabilizer, foamed into a block, and heated at 100 ° C. for 10 minutes. And sliced to 1 mm to obtain a sheet-like product. Comparative Example 2 In the same manner as in Example 1, a sheet-like foam was obtained by reducing the amount of nitrogen in order to produce urethane having a large cell diameter.

【0017】これらの発泡体について、次の評価方法で
評価した結果を表1に示した。 評価方法: セル径 発泡方向に垂直な断面の0.5mm角内
のセル数を測定し
Table 1 shows the results of the evaluation of these foams by the following evaluation methods. Evaluation method: Cell diameter The number of cells within a 0.5 mm square of the cross section perpendicular to the foaming direction was measured.

【0018】[0018]

【数1】 (Equation 1)

【0019】とする。 発ガス分 125℃10~6torr真空中で24H
後重量の減少割合を測定する。 シリコン抽出 アセトンにより抽出し抽出液中のSi量
を原子吸光で測定した 。 吸水率 水圧10cm下で48H後、サンプ
ルの重量を測定し増加した 重量のもと
の重量に対する%で表した。 90°ピール 固定パネルにパッキング材を貼りつけフ
ィルムにラミネートしたテープを圧着し、90°ピール
強度を測定した。 50%圧縮残留歪 試験片を50%圧縮固定し、70±1
℃で22時間加熱後、圧縮を外し常温放置後30分間後
厚さを測定し、次に計算方法で算出する。 歪=元厚さ−試験後の厚さ/元厚さ×100%
## EQU1 ## Outgassing content 125 ° C 10 ~ 6 torr 24H in vacuum
The rate of weight loss is measured. Silicon extraction Extracted with acetone, and the amount of Si in the extract was measured by atomic absorption. After 48 hours under a water pressure of 10 cm, the weight of the sample was measured and expressed as a percentage of the increased weight relative to the original weight. 90 ° Peel A packing material was adhered to a fixed panel, and a tape laminated with a film was pressed, and the 90 ° peel strength was measured. 50% compression residual strain The test piece was fixed at 50% compression, and 70 ± 1
After heating at 22.degree. C. for 22 hours, the compression is removed, the thickness is measured for 30 minutes after standing at room temperature, and then the thickness is calculated by a calculation method. Strain = original thickness-thickness after test / original thickness x 100%

【0020】[0020]

【表1】 [Table 1]

【0021】表1より、実施例1ではセル径60μm発
ガス0.11%シリコン抽出分15ppm吸水率3wt
%、50%圧縮残留歪1.3%、90°ピール、材料破
壊であり、水洗時吸水しにくく、乾燥性も良く読み取り
誤動作せず、接着性も良いためHDD用パッキングとし
て好適である。実施例2ではセル径60μm発ガス0.
12%シリコン抽出分15ppm吸水率2.5wt%、
50%圧縮残留歪2.0%、90°ピール、材料破壊で
あり、水洗時吸水しにくく、乾燥性も良く読み取り誤動
作せず、接着性も良いためHDD用パッキングとして好
適である。実施例3ではセル径60μm発ガス0.10
%シリコン抽出分14ppm吸水率2.6wt%、50
%圧縮残留歪1.0%、90°ピール材料、破壊であ
り、水洗時吸水しにくく、乾燥性も良く読み取り誤動作
せず、接着性も良く更に気密性も向上し、HDD用パッ
キングとして好適なものであった。
According to Table 1, in Example 1, the cell diameter was 60 μm, the generated gas was 0.11%, the silicon extraction was 15 ppm, and the water absorption was 3 wt.
%, 50% compression residual strain 1.3%, 90 ° peel, material destruction, hardly absorbs water when washed with water, has good drying properties, does not cause erroneous reading, and has good adhesive properties, and thus is suitable as a packing for HDD. In the second embodiment, a gas having a cell diameter of 60 μm and a gas pressure of 0.1 μm is used.
12% silicon extraction 15ppm water absorption 2.5wt%,
50% compression residual strain 2.0%, 90 ° peel, material destruction, hardly absorbs water during washing, good dryness, no erroneous reading, good adhesion, suitable for HDD packing. In the third embodiment, the cell diameter is 60 μm and the generated gas is 0.10.
% Silicon extractables 14 ppm Water absorption 2.6 wt%, 50
% Compression residual strain 1.0%, 90 ° peel material, broken, hardly absorbs water when washed with water, has good drying properties, does not malfunction in reading, has good adhesion, and has improved airtightness, and is suitable as a packing for HDD. Was something.

【0022】比較例1ではセル径80μm発ガス1.4
5%シリコン抽出分280ppm吸水率20wt%、5
0%圧縮残留歪1.8%、90°ピール500g/25
mmであり、シリコン抽出が目標の50〜100ppm
以上となり読み取り誤動作の恐れがあり、HDD用パッ
キングとしては不適である。比較例2ではセル径160
μm発ガス0.11%シリコン抽出分15ppm吸水率
18wt%、50%圧縮残留歪2.4%、90°ピール
400g/25mmであり、シリコン抽出は少ないが、
吸水率が高く、水洗浄には不向きでかつテープとの接着
性が劣り、アッセンブリー上好ましくなくHDD用パッ
キングとしては不適である。
In Comparative Example 1, a gas having a cell diameter of 80 μm and a gas generation of 1.4 were used.
5% silicon extractables 280 ppm water absorption 20 wt%, 5
0% compression set 1.8%, 90 ° peel 500g / 25
mm, the target of silicon extraction is 50-100 ppm
As described above, there is a possibility that a reading error may occur, which is unsuitable for packing for HDDs. In Comparative Example 2, the cell diameter was 160
μm generated gas 0.11% silicon extraction 15ppm water absorption 18wt%, 50% compression residual strain 2.4%, 90 ° peel 400g / 25mm, silicon extraction is small,
It has a high water absorption, is not suitable for washing with water, and has poor adhesiveness to a tape, which is not preferable in terms of assembly and is unsuitable for packing for HDDs.

───────────────────────────────────────────────────── フロントページの続き (72)発明者 村田 昇 神奈川県横浜市金沢区福浦3丁目10番地 日本発条株式会社内 (56)参考文献 特開 昭63−211182(JP,A) 特開 平2−24890(JP,A) 実開 昭62−98098(JP,U) (58)調査した分野(Int.Cl.7,DB名) G11B 33/14 G11B 25/04 ──────────────────────────────────────────────────続 き Continuation of the front page (72) Noboru Murata 3-10-10, Fukuura, Kanazawa-ku, Yokohama-shi, Kanagawa Prefecture Inside Japan Hakko Co., Ltd. (56) References JP-A-63-211182 (JP, A) JP-A-2 -24890 (JP, A) Japanese Utility Model 62-98098 (JP, U) (58) Fields investigated (Int. Cl. 7 , DB name) G11B 33/14 G11B 25/04

Claims (1)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 ポリオール、イソシアナート、発泡剤及
び反応型シリコン整泡剤及びその他の助剤より得られた
平均セル径が150μm以下の可撓性マイクロセルウレ
タンよりなる磁気ディスク駆動装置用パッキング材。
1. A packing material for a magnetic disk drive comprising a flexible microcell urethane having an average cell diameter of 150 μm or less obtained from a polyol, an isocyanate, a foaming agent, a reactive silicone foam stabilizer and other auxiliaries. .
JP04037842A 1992-02-25 1992-02-25 Packing material for magnetic disk drive Expired - Lifetime JP3082010B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP04037842A JP3082010B2 (en) 1992-02-25 1992-02-25 Packing material for magnetic disk drive

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP04037842A JP3082010B2 (en) 1992-02-25 1992-02-25 Packing material for magnetic disk drive

Publications (2)

Publication Number Publication Date
JPH05234351A JPH05234351A (en) 1993-09-10
JP3082010B2 true JP3082010B2 (en) 2000-08-28

Family

ID=12508790

Family Applications (1)

Application Number Title Priority Date Filing Date
JP04037842A Expired - Lifetime JP3082010B2 (en) 1992-02-25 1992-02-25 Packing material for magnetic disk drive

Country Status (1)

Country Link
JP (1) JP3082010B2 (en)

Also Published As

Publication number Publication date
JPH05234351A (en) 1993-09-10

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