JPH02295729A - Buffer member - Google Patents
Buffer memberInfo
- Publication number
- JPH02295729A JPH02295729A JP11598389A JP11598389A JPH02295729A JP H02295729 A JPH02295729 A JP H02295729A JP 11598389 A JP11598389 A JP 11598389A JP 11598389 A JP11598389 A JP 11598389A JP H02295729 A JPH02295729 A JP H02295729A
- Authority
- JP
- Japan
- Prior art keywords
- sheet
- rubber
- polyethylene
- parts
- air bubble
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 239000000463 material Substances 0.000 claims abstract description 29
- 229920001971 elastomer Polymers 0.000 claims abstract description 23
- 239000005060 rubber Substances 0.000 claims abstract description 23
- 239000011248 coating agent Substances 0.000 claims abstract description 11
- 238000000576 coating method Methods 0.000 claims abstract description 11
- 229920003023 plastic Polymers 0.000 claims abstract description 9
- 239000004033 plastic Substances 0.000 claims abstract description 9
- 239000007788 liquid Substances 0.000 abstract description 15
- 239000004698 Polyethylene Substances 0.000 abstract description 12
- -1 polyethylene Polymers 0.000 abstract description 12
- 229920000573 polyethylene Polymers 0.000 abstract description 12
- 238000010438 heat treatment Methods 0.000 abstract description 9
- 229920000915 polyvinyl chloride Polymers 0.000 abstract description 8
- 239000004800 polyvinyl chloride Substances 0.000 abstract description 8
- 239000004677 Nylon Substances 0.000 abstract description 5
- 229920001778 nylon Polymers 0.000 abstract description 5
- 239000005062 Polybutadiene Substances 0.000 abstract description 4
- 238000001816 cooling Methods 0.000 abstract description 4
- 229920002857 polybutadiene Polymers 0.000 abstract description 4
- 238000004132 cross linking Methods 0.000 abstract description 3
- 239000004944 Liquid Silicone Rubber Substances 0.000 abstract description 2
- 239000004014 plasticizer Substances 0.000 abstract description 2
- 229920002635 polyurethane Polymers 0.000 abstract description 2
- 239000004814 polyurethane Substances 0.000 abstract description 2
- 229920002379 silicone rubber Polymers 0.000 abstract description 2
- 230000009969 flowable effect Effects 0.000 abstract 1
- 230000035939 shock Effects 0.000 description 8
- 229910001220 stainless steel Inorganic materials 0.000 description 6
- 239000010935 stainless steel Substances 0.000 description 6
- 239000012530 fluid Substances 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 3
- 238000010586 diagram Methods 0.000 description 3
- 238000009408 flooring Methods 0.000 description 3
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 2
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 2
- 239000012975 dibutyltin dilaurate Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000011120 plywood Substances 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 238000004220 aggregation Methods 0.000 description 1
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 1
- 230000003139 buffering effect Effects 0.000 description 1
- 230000009172 bursting Effects 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 238000001879 gelation Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は各種スポーツ用品,複合防音床材,工業用緩衝
吸収部品等に使用するのに好適な緩衝部材に関するもの
である。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a buffer member suitable for use in various sports equipment, composite soundproof flooring materials, industrial shock absorbing parts, and the like.
[従来の技術]
従来、緩衝部材として最も性能が高いものとして空気が
ある。これを利用する方法としてたとえばエアーキャッ
プと称する様な多数の気泡部を存した空気マットが幅広
く利用されている。しかし、これは大きな衝撃が加わる
と破裂し、その性能がまったく失われてしまうためその
利用範囲が限られてしまう。一方、ゴムやプラスチック
等の成型品に凹凸模様をつけることで気泡を設けた状態
と同じ緩衝効果を出せることが知られている。しかし、
このためには凹凸模様をつけた金型等が必要となり成型
品がコスト高となってしまう。[Prior Art] Conventionally, air has been used as a shock absorbing member with the highest performance. As a method of utilizing this, for example, an air mat having a large number of air bubbles called an air cap is widely used. However, if a large impact is applied to this, it will burst and its performance will be completely lost, limiting its range of use. On the other hand, it is known that by adding an uneven pattern to a molded product such as rubber or plastic, it is possible to produce the same cushioning effect as when air bubbles are provided. but,
For this purpose, a mold with a concavo-convex pattern is required, which increases the cost of the molded product.
[発明が解決しようとする課題〕
本発明の目的は容易かつ安価にその性能を高めた緩衝部
材を提供することにある。[Problems to be Solved by the Invention] An object of the present invention is to provide a shock absorbing member with improved performance easily and inexpensively.
[課題を解決するための手段]
本発明の要旨は凹凸構造を有し、凸部が気泡部より形成
されるシートの凹凸部表面全体をプラスチック及び/又
はゴムで被覆してなる緩衝部材にある。以下その詳細に
ついて説明する。[Means for Solving the Problems] The gist of the present invention resides in a cushioning member formed by covering the entire surface of the uneven portion of a sheet having an uneven structure and whose convex portions are formed by air bubbles with plastic and/or rubber. . The details will be explained below.
第1図は、本発明の緩衝部材の断面を示す模式図である
。気泡部を有するシートの気泡部側にプラスチック及び
/又はゴムより成る披覆材2が存在し、両者は互いに密
着している。FIG. 1 is a schematic diagram showing a cross section of the buffer member of the present invention. A covering material 2 made of plastic and/or rubber is present on the bubble side of the sheet having bubbles, and both are in close contact with each other.
シ一ト1は、たとえばエアーキャップと称するようなポ
リエチレンやナイロン等市販されている素材のものがそ
のまま利用でき、シ一ト1の気泡部の形状.凸部高さ,
凸部間距離等は特に限定されない。The sheet 1 can be made of a commercially available material such as polyethylene or nylon, which is called an air cap, and can be made of a material that is made of a commercially available material such as polyethylene or nylon. Convex height,
The distance between the convex portions, etc. are not particularly limited.
被覆材2の素材としては、シ一ト1に密着させる際には
流動状態であり、加熱または冷却により固着させられる
ようなプラスチック及び/又はゴムが望ましい。ここで
言う流動状態とは素材の溶液、ゾル、または溶融状態を
示す。また加熱による固着とはゲル化、溶媒の飛散によ
る凝集、もしくは架橋等を示し、冷却による固着とは流
動域からゴム域・ガラス域への温度による移動を示す。The material for the covering material 2 is preferably plastic and/or rubber, which is in a fluid state when brought into close contact with the sheet 1 and is fixed by heating or cooling. The fluid state here refers to the solution, sol, or molten state of the material. Further, fixation due to heating refers to gelation, aggregation due to solvent scattering, or crosslinking, etc., and fixation due to cooling refers to movement due to temperature from a fluid region to a rubber region/glass region.
具体的に被覆材2としてはたとえばポリ塩化ビニル,ボ
リウ、レタン,ポリエチレン等のプラスチック、及び液
状ポリブタジエン,液状シリコーンゴム等のゴムが使用
できる。ポリ塩化ビニルならば可塑剤を加えたゾルをシ
一ト1の気泡部上に流し、加熱ゲル化してもよいし、ポ
リエチレンならば溶融させたものをシ一ト1上に流し冷
却固着させてもよい。また、液状ゴムならば加熱架橋に
より固着できる。但し、被覆材2をシ一ト1上に密着さ
せる際、被覆材2が有する熱、もしくは固着処理時の熱
によりシ一ト1が溶融変形し気泡部が破裂したり、被覆
材2が熱分解を起すようでは問題となる。そのためシ一
ト1の素材と被覆時の温度との兼ね合いは重要である。Specifically, as the covering material 2, for example, plastics such as polyvinyl chloride, polyurethane, urethane, and polyethylene, and rubbers such as liquid polybutadiene and liquid silicone rubber can be used. In the case of polyvinyl chloride, a sol containing a plasticizer may be poured onto the air bubbles of sheet 1 and heated to gel, while in the case of polyethylene, a molten sol may be poured over sheet 1 and cooled to solidify. Good too. Furthermore, if it is a liquid rubber, it can be fixed by thermal crosslinking. However, when attaching the covering material 2 to the sheet 1, the sheet 1 may melt and deform due to the heat of the covering material 2 or the heat during the fixing process, causing bubbles to burst, or the covering material 2 may It becomes a problem if it causes decomposition. Therefore, the balance between the material of the sheet 1 and the temperature during coating is important.
たとえばポリエチレンより成るシ一ト1の場合は130
℃以下での処理が望ましい。一方ナイロンより成る場合
は200℃以下が望ましい。For example, in the case of sheet 1 made of polyethylene, 130
Processing at temperatures below ℃ is desirable. On the other hand, when it is made of nylon, the temperature is preferably 200°C or less.
本発明の緩衝部材は被覆材2の一部が流動性を存した状
態をとることができる。即ち被覆材2の内部が流動性を
有したまま外表面が固化している状態を示す。たとえば
被覆材2に液状ゴムを流し、その表面に架橋剤と触媒を
塗布しその後加熱硬化させると表面だけが熱架橋し、内
部は流動性を有したままの状態になる。また、ポリ塩化
ビニルゾルならばシ一ト1上に流入後加熱時間を調節す
ることで表面がゲル化し、内部はゾルのままの状態を作
ることが可能である。In the buffer member of the present invention, a part of the covering material 2 can have fluidity. In other words, this shows a state in which the outer surface of the coating material 2 is solidified while the interior of the coating material 2 remains fluid. For example, if liquid rubber is poured onto the coating material 2, a crosslinking agent and a catalyst are applied to its surface, and then heated and cured, only the surface will be thermally crosslinked, and the inside will remain fluid. Furthermore, if polyvinyl chloride sol is used, by adjusting the heating time after it flows onto the sheet 1, it is possible to gel the surface and leave the inside as a sol.
本発明の緩衝部材の性能は被覆材2全部を固着させた場
合、緩衝時の変形も少なく、また気泡部が破裂してもそ
の形状は残るため、気泡部の破裂を心配する必要はない
。しかも成型後適当な大きさにカットしての使用も可能
である。一方、被覆材2の表面だけを固化させた場合、
その緩衝部材としての性能は全部を固着させた場合より
も高い。The performance of the shock absorbing member of the present invention is such that when the entire covering material 2 is fixed, there is little deformation during buffering, and even if the bubble portion ruptures, its shape remains, so there is no need to worry about the bubble portion bursting. Moreover, after molding, it can be cut to an appropriate size and used. On the other hand, when only the surface of the coating material 2 is solidified,
Its performance as a shock absorbing member is higher than when the entire structure is fixed.
よってその用途に応じて緩衝材2の状態を変えることが
好ましい。Therefore, it is preferable to change the state of the cushioning material 2 depending on its use.
本発明の緩衝部材は2層以上を接合積層した状態で使用
することもできる。The buffer member of the present invention can also be used in a state in which two or more layers are bonded and laminated.
また、被覆材2にマイカ,タルク,カーボン等の添加剤
を加えても何ら問題はない。Moreover, there is no problem even if additives such as mica, talc, and carbon are added to the coating material 2.
本発明の緩衝部材の両側にそれぞれ3sus,5mm厚
の合板を貼り合わせた木質床材としての用途例を図2に
示した。FIG. 2 shows an example of use as a wooden flooring material in which plywood of 3sus and 5mm thickness is laminated on both sides of the buffer member of the present invention.
[実施例]
さらに本発明を実施例を用いて詳細に説明するが、本発
明はこれらに限定されるものではない。[Examples] Further, the present invention will be explained in detail using Examples, but the present invention is not limited thereto.
実施例1
29QX170X30usの大きさのステンレス製バッ
トの底に直径7mm,高さ3關でそれぞれの中心間隔が
10mmの気泡部を有するナイロン製シートを気泡部が
上側になるように敷きつめた。そこにポリ塩化ビニル(
リューロンペーストR−725.東ソー■製)550g
をジオクチルフタレート330gに分散させたゾルを流
し、190℃の恒温槽で7分間加熱ゲル化させ、厚さ9
關の目的の緩衝部材を得た。Example 1 At the bottom of a stainless steel vat measuring 29Q x 170 x 30us, a nylon sheet with a diameter of 7 mm and three heights having air bubbles with a center spacing of 10 mm was placed so that the air bubbles were on the upper side. There is polyvinyl chloride (
Ryuron Paste R-725. (manufactured by Tosoh) 550g
was dispersed in 330 g of dioctyl phthalate, and heated in a constant temperature bath at 190°C for 7 minutes to form a gel.
The desired buffer member was obtained.
比較例1
2 9 0 X 1 7 0 X 3 0 mmの大き
さのステンレス製バットに実施例1と同配合のポリ塩化
ビニルゾル990gを流し、190℃の恒温槽で8分間
加熱ゲル化させ、厚さ9關の塩化ビニルシ一トを得た。Comparative Example 1 990 g of polyvinyl chloride sol having the same formulation as in Example 1 was poured into a stainless steel vat measuring 290 x 170 x 30 mm, and gelatinized by heating in a constant temperature bath at 190°C for 8 minutes to reduce the thickness. Ninety pieces of vinyl chloride sheets were obtained.
実施例2
2 9 0 X 1 7 0 X 3 0 mmの大き
さのステンレス製バットの底に直径7mm,高さ3 m
+eの気泡部を存するポリエチレン製シートを気泡部が
上側になるように敷きつめた。バットの内側面及びシー
トの気泡部にヘキサメチレンジイソシアネート(HDI
)を塗布した後、液状ポリブタジエン(Poly b
d R−45HT, 出光アーコ■製)350gにジ
ブチル錫ジラウレートを1g添加したものを流し込んだ
。さらに液状ゴム層の上面にMDIを塗布し120℃の
恒温槽で加熱硬化させ、液状ゴムの表面が硬化された厚
さ9 amの目的の緩衝部材を得た。Example 2 A stainless steel bat measuring 290 x 170 x 30 mm had a diameter of 7 mm and a height of 3 m at the bottom.
Polyethylene sheets containing +e air bubbles were laid out with the air bubbles facing upward. Hexamethylene diisocyanate (HDI) is applied to the inner surface of the bat and the air bubbles of the sheet.
), then liquid polybutadiene (Poly b
d R-45HT, manufactured by Idemitsu Arco ■) to which 1 g of dibutyltin dilaurate was added was poured. Furthermore, MDI was coated on the upper surface of the liquid rubber layer and cured by heating in a constant temperature bath at 120° C., thereby obtaining the desired buffer member having a thickness of 9 am and having a cured surface of the liquid rubber.
実施例3
290X170X30mmの大きさのステンレス製バッ
トの底に実施例2と同じポリエチレン製シートを敷きつ
めた。その上に液状ポリブタジエン350gにHD12
3.5gとジブチル錫ジラウレートを1gを混合したも
のを流し込んだ。これを120℃の恒温槽で加熱硬化さ
せ、液状ゴムが硬化された厚さ9IIII1の目的の緩
衝部材を得た。Example 3 The same polyethylene sheet as in Example 2 was spread on the bottom of a stainless steel bat measuring 290 x 170 x 30 mm. On top of that, add 350g of liquid polybutadiene to HD12.
A mixture of 3.5 g and 1 g of dibutyltin dilaurate was poured into the tank. This was heated and cured in a constant temperature bath at 120° C. to obtain a desired buffer member with a thickness of 9III1 in which the liquid rubber was cured.
比較例2
2 9 0 X 1 7 0 X 3 0 m+sの大
きさのステンレス製バットの内底面及び内側面にHDI
を塗布し、実施例2と同配合の液状ゴム400gを流し
、さらに液状ゴム層の上面にMDIを塗布し120℃の
恒温槽で加熱硬化させ、厚さ9 mmの表面が硬化され
た液状ゴムシートを得た。Comparative Example 2 HDI was installed on the inner bottom and inner surface of a stainless steel bat with a size of 290 x 170 x 30 m+s.
400 g of liquid rubber with the same composition as in Example 2 was poured, and MDI was further applied on the top surface of the liquid rubber layer and cured by heating in a constant temperature bath at 120° C. to form a surface-hardened liquid rubber with a thickness of 9 mm. Got a sheet.
比較例3
2 9 0 X 1 7 0 X 3 0 mmの大き
さのステンレス製バットに実施例3と同配合の液状ゴム
400gを流し、120℃の恒温槽で加熱硬化させ、厚
さ9lII1の液状ゴムシ一トを得た。Comparative Example 3 400 g of liquid rubber having the same composition as in Example 3 was poured into a stainless steel vat measuring 290 x 170 x 30 mm, and heated and cured in a constant temperature bath at 120°C to form a liquid rubber with a thickness of 9lII1. I got a rubber seat.
緩衝部材の衝撃吸収性能測定
厚さ30mmの鉄板上に厚さ3 amのゴム板を敷き、
その上に前記実施例1〜3、及び比較例1〜3で得られ
た緩衝部材、もし《は気泡部を有するポリエチレン製シ
ートを2層積層し厚さ7關にしたものを置いた。同位置
で鉄板の裏側には振動ピックアップ( B r u e
l & K j gB r社製)を取り付け、力変換
子(BriielaKj田r社製)を取り付けた鋼球を
緩衝部材上300關の高さから落下させた。その時振動
ピックップと力変換子で測定した緩衝加速度を第1表に
示した。Measurement of shock absorption performance of shock absorbing members A 3 am thick rubber plate was placed on a 30 mm thick steel plate.
On top of this, the buffer members obtained in Examples 1 to 3 and Comparative Examples 1 to 3, in which two layers of polyethylene sheets having air bubbles were laminated to a thickness of 7 mm, were placed. At the same location, there is a vibration pickup (BRUE) on the back side of the iron plate.
A steel ball to which a force transducer (manufactured by Briiela K.K., Ltd.) was attached was dropped from a height of 300 degrees above the buffer member. Table 1 shows the buffer acceleration measured using the vibration pick-up and force transducer.
[発明の効果]
以上の説明から明らかなように、本発明によれば容易か
つ安価にその性能を高めた緩衝部材が得られる。[Effects of the Invention] As is clear from the above description, according to the present invention, a shock absorbing member with improved performance can be easily and inexpensively obtained.
第1図は本発明の緩衝部材の断面を示す模式図である。
また、第2図は本発明の緩衝部材を用いた木質床材とし
ての断面を示す模式図である。
1・・・・・・気泡部を有するシート
2・・・・・・被覆材
3・・・・・・合板FIG. 1 is a schematic diagram showing a cross section of the buffer member of the present invention. Moreover, FIG. 2 is a schematic diagram showing a cross section of a wooden flooring material using the buffer member of the present invention. 1...Sheet having air bubbles 2...Coating material 3...Plywood
Claims (1)
トの凹凸部表面全体をプラスチック及び/又はゴムで被
覆してなる緩衝部材。 2、被覆材の一部が流動性を有する特許請求の範囲第1
項の緩衝部材。[Scope of Claims] 1. A cushioning member formed by covering the entire surface of the uneven portion of a sheet having an uneven structure with the convex portions formed by air bubbles with plastic and/or rubber. 2. Claim 1 in which a part of the coating material has fluidity
Cushioning member.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11598389A JPH02295729A (en) | 1989-05-11 | 1989-05-11 | Buffer member |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11598389A JPH02295729A (en) | 1989-05-11 | 1989-05-11 | Buffer member |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH02295729A true JPH02295729A (en) | 1990-12-06 |
Family
ID=14675973
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP11598389A Pending JPH02295729A (en) | 1989-05-11 | 1989-05-11 | Buffer member |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH02295729A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH07303322A (en) * | 1991-10-21 | 1995-11-14 | Hitachi Cable Ltd | Method for laying cable in trough |
-
1989
- 1989-05-11 JP JP11598389A patent/JPH02295729A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH07303322A (en) * | 1991-10-21 | 1995-11-14 | Hitachi Cable Ltd | Method for laying cable in trough |
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