JPS62225335A - Collapsible material - Google Patents
Collapsible materialInfo
- Publication number
- JPS62225335A JPS62225335A JP6705986A JP6705986A JPS62225335A JP S62225335 A JPS62225335 A JP S62225335A JP 6705986 A JP6705986 A JP 6705986A JP 6705986 A JP6705986 A JP 6705986A JP S62225335 A JPS62225335 A JP S62225335A
- Authority
- JP
- Japan
- Prior art keywords
- foam
- film
- synthetic resin
- resin film
- impact
- 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 title description 8
- 239000006260 foam Substances 0.000 claims description 26
- 229920003002 synthetic resin Polymers 0.000 claims description 19
- 239000000057 synthetic resin Substances 0.000 claims description 19
- 239000011359 shock absorbing material Substances 0.000 claims description 11
- 238000010521 absorption reaction Methods 0.000 description 12
- 239000010410 layer Substances 0.000 description 10
- 230000000694 effects Effects 0.000 description 8
- 230000035939 shock Effects 0.000 description 8
- 239000002344 surface layer Substances 0.000 description 5
- 230000001133 acceleration Effects 0.000 description 4
- 239000000853 adhesive Substances 0.000 description 3
- 230000001070 adhesive effect Effects 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 229920001971 elastomer Polymers 0.000 description 3
- 239000005060 rubber Substances 0.000 description 3
- 239000004604 Blowing Agent Substances 0.000 description 2
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 2
- 239000005062 Polybutadiene Substances 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- YACLQRRMGMJLJV-UHFFFAOYSA-N chloroprene Chemical compound ClC(=C)C=C YACLQRRMGMJLJV-UHFFFAOYSA-N 0.000 description 2
- 230000006835 compression Effects 0.000 description 2
- 238000007906 compression Methods 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 229920001821 foam rubber Polymers 0.000 description 2
- 230000004927 fusion Effects 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000002648 laminated material Substances 0.000 description 2
- 230000007774 longterm Effects 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229920002857 polybutadiene Polymers 0.000 description 2
- 229920006264 polyurethane film Polymers 0.000 description 2
- 229920003048 styrene butadiene rubber Polymers 0.000 description 2
- 238000004073 vulcanization Methods 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 241000288673 Chiroptera Species 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 239000011358 absorbing material Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000010411 cooking Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000001723 curing Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 230000009191 jumping Effects 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 238000003475 lamination Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920002589 poly(vinylethylene) polymer Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 239000010734 process oil Substances 0.000 description 1
- 230000004043 responsiveness Effects 0.000 description 1
- 238000009331 sowing Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 238000013519 translation Methods 0.000 description 1
- 230000014616 translation Effects 0.000 description 1
- KAKZBPTYRLMSJV-UHFFFAOYSA-N vinyl-ethylene Natural products C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Landscapes
- Laminated Bodies (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
産Llの利))!
本発明は、(1)ジョギング、テニス、バスケットポー
ル等のスポーツシューズ及び各種作業靴等のシューズソ
ール用Ith撃吸収素材、(2)ヘルメット、サポータ
−1胴あて、すね当て、肩バット等の各種スポーツ用品
又は面、訳、魔手、すね当て等の武道共用の衝撃吸収素
材、(3)工事用、安全用、tli車用ヘルメットの衝
撃吸収素材、(4)工業用!#7炊吸酸吸収部品材とし
て好適な衝撃吸収材に関するものである。[Detailed description of the invention] Benefits of production Ll))! The present invention is applicable to (1) Ith shock absorbing material for shoe soles of sports shoes such as jogging, tennis, and basketball shoes and various work shoes; (2) various sports materials such as helmets, supporter 1 torso pads, shin guards, shoulder bats, etc. Shock-absorbing materials commonly used in martial arts such as supplies or masks, translations, magic hands, shin guards, etc. (3) Shock-absorbing materials for construction, safety, and tli car helmets, (4) Industrial use! #7 This relates to a shock absorbing material suitable as a cooking acid absorbing component material.
え久立且遣
従来衝撃吸収材としては一般にスポンジが用いられてい
るが、スポンジは必要な衝撃吸収性を得るためには素材
を厚くする必要があり、製品の形状や重量等の制約のた
め、上記の製品に使用した場合には衝撃吸収性能の不満
足なものしか得られなかった。Traditionally, sponges have been commonly used as shock absorbing materials, but in order to obtain the necessary shock absorption properties, sponges need to be made of thick material, and due to constraints such as the shape and weight of the product. When used in the above products, only unsatisfactory shock absorption performance was obtained.
最近そのような要求に応える衝撃吸収性の高いスポンジ
等が開発され市販されるようになった。Recently, sponges and the like with high shock absorption properties have been developed and become commercially available to meet such demands.
しかしこれらの新素材は、シューズソール等に用いた場
合通常の走行では効果があるが、ジャンプ等強い衝撃力
が加わった場合の衝撃吸収は不十分であり用途が限られ
ている。又スポンジであるため強い衝撃を受けると底づ
きし効果が著しく低下する。しかも長時11■の使用で
永久変形したり。However, when these new materials are used for shoe soles, etc., they are effective during normal running, but their use is limited because they do not provide sufficient shock absorption when strong impact forces are applied, such as when jumping. Also, since it is a sponge, if it receives a strong impact, the bottoming effect will be significantly reduced. Moreover, it becomes permanently deformed after being used for a long time.
寒冷蒔には固い感触になる等の欠点もある。Chilled sowing also has drawbacks such as a hard feel.
またゲル状衝撃吸収材料も知られているが、これは外力
により容易に変形するため、衝撃を受けたときに容易に
破壊する上、粘着性が高いため。Gel-like shock-absorbing materials are also known, but they are easily deformed by external forces, easily break when subjected to impact, and are highly adhesive.
堆り扱いがむずかしい。Difficult to handle as waste.
また大きい衝撃を受けたとき底づきを起し、衝撃吸収効
果がなく用途が限られ、流動性が大きく、長時間使用に
よる素材の永久変形が著しい等の欠点がある。In addition, it bottoms out when subjected to a large impact, has no impact absorption effect, limits its uses, has high fluidity, and has disadvantages such as significant permanent deformation of the material after long-term use.
また無発泡ゴム、ウレタン系衝撃吸収材は強い衝撃に対
しても効果があるが、スポンジに比べて著しく重いため
用途が著しく制約される。In addition, unfoamed rubber and urethane-based shock absorbers are effective against strong impacts, but they are significantly heavier than sponges, which severely limits their uses.
また空気入りクッションは大きい衝撃を吸収さるには十
分な厚さと体積が必要であり、衝撃吸収に時間がかかる
という応答性の低さがあり、エアもれ対策、エア補充機
構が必要である。In addition, air-filled cushions require sufficient thickness and volume to absorb large impacts, and have low responsiveness that takes time to absorb impacts, so air leak countermeasures and air replenishment mechanisms are required.
発明が解決しようとする開題点
本発明は、軽量で、広範な衝撃力に対して優れた衝撃吸
収性を有し、しかも長時間使用での永久変形性が著しく
改善された材料を提供することを目的とする。Problem to be Solved by the Invention An object of the present invention is to provide a material that is lightweight, has excellent shock absorbing properties against a wide range of impact forces, and has significantly improved permanent deformability during long-term use. With the goal.
μm「、古 るための一
本発明による衝撃吸収材は20℃における反発弾性が2
5%以下、密度が0.05〜0.9g/c?m3で、S
RISによる硬度50’以下の発泡体と、引張り強度が
100Kg/cm2以上、破断時伸びが50%以上、硬
度(JIS A)が60″以上で厚さが10〜200
0 Bmの合成樹脂フィルム及び/又は多数の独立気泡
を有する前記フィルムの成形品とを強固に接合積層した
ことを特徴とする。The shock absorbing material according to the present invention has a rebound resilience of 2 μm at 20°C.
5% or less, density 0.05-0.9g/c? m3, S
A foam with a hardness of 50' or less according to RIS, a tensile strength of 100 Kg/cm2 or more, an elongation at break of 50% or more, a hardness (JIS A) of 60" or more, and a thickness of 10 to 200.
It is characterized by strongly bonding and laminating a synthetic resin film of 0 Bm and/or a molded product of the film having a large number of closed cells.
上記発泡体としては1発泡ゴム又はウレタンスポンジ等
が挙げられ、例えば、
■スチレン含有量が40〜75重量%であるスチレン−
ブタジェン共重合体又はスチレン−ブタジェン共重合体
と全体の40ffii%以下の他のゴム成分とからなる
ポリマー1001i部。Examples of the above-mentioned foam include foamed rubber or urethane sponge, such as:
1001i parts of a polymer consisting of a butadiene copolymer or a styrene-butadiene copolymer and 40ffii% or less of other rubber components.
030〜300重量部の充填剤、 05〜100重量部の可塑剤。030 to 300 parts by weight of filler, 05-100 parts by weight of plasticizer.
■0.5〜601量部の発泡剤 及び
からなる混合物に加硫剤、加硫促進剤を加え、加熱発泡
硬化して得られる低レジリエンスゴム発泡体が好ましい
。(2) 0.5 to 601 parts of a blowing agent. A low resilience rubber foam obtained by adding a vulcanizing agent and a vulcanization accelerator to a mixture of the following and heating and foaming and curing is preferred.
このような発泡体の20℃での反発弾性が25%を越え
ると衝撃吸収材として十分な衝撃吸収性ス七が得られず
、また密度が0.9g/cm’を越えると衝撃吸収材の
重量が重くなり、密度が0゜05g/cm’未満ではW
R撃吸収性箋及び強度が不十分となる。If the impact resilience of such a foam at 20°C exceeds 25%, it will not be able to provide sufficient impact absorption properties as a shock absorbing material, and if the density exceeds 0.9 g/cm', the impact absorption properties of the foam will deteriorate. If the weight becomes heavy and the density is less than 0゜05g/cm', W
R impact absorption and strength will be insufficient.
発泡体層の厚さは0.5mm−10mmの範囲とする。The thickness of the foam layer is in the range 0.5mm-10mm.
0.5mm以下は通常の発泡体では加重困難であり、ま
た10mm以上では衝撃改良効果が劣る。If the thickness is less than 0.5 mm, it is difficult to load with ordinary foam, and if it is more than 10 mm, the impact improvement effect will be poor.
引張り強度が100Kg/cm2以上、破断時伸びが5
0%以上、硬度(JISA)が60’以上で厚さが10
〜2000ルmの合成樹脂フィルムとしては、ポリウレ
タン系、1.2−ポリブタジェン系、ポリオレフィン系
、ポリアミド系、塩化ビニル系等の合成樹脂フィルムを
挙げることができる。Tensile strength is 100Kg/cm2 or more, elongation at break is 5
0% or more, hardness (JISA) is 60' or more, thickness is 10
Examples of the synthetic resin film having a thickness of 2,000 lm include polyurethane-based, 1,2-polybutadiene-based, polyolefin-based, polyamide-based, and vinyl chloride-based synthetic resin films.
これら合成樹脂フィルムの引張り強度が100Kg/c
m2未満、あるいは破断時伸びが50%未満では、フィ
ルムの強度が不十分で、f#撃吸収材としての種々の用
途に供し難く、またフィルムの厚さが10JLm未満で
は破れ易く、2000gmを越えると厚すぎてフィルム
が変形しにくくなるために優れた衝撃吸収性源を発揮し
なくなる。The tensile strength of these synthetic resin films is 100Kg/c
If the film thickness is less than m2 or the elongation at break is less than 50%, the strength of the film is insufficient and it is difficult to use it for various purposes as an f# impact absorbing material.If the film thickness is less than 10 JLm, it is easy to tear, and if it exceeds 2000 gm. If it is too thick, the film will not easily deform and will no longer provide an excellent source of shock absorption.
積層は少なくとも発泡体を1層以上、合成樹脂フィルム
を少なくとも1層以上重ねた多層構造とし、積層構造の
両表面層がフィルムである場合。The lamination is a multilayer structure in which at least one layer of foam and at least one layer of synthetic resin film are laminated, and both surface layers of the laminated structure are films.
発泡体である場合、及び片面がフィルムであり反対側の
面が発泡体である場合があり得る。It can be a foam, and it can be a film on one side and a foam on the other side.
その積層構造例を第1図A、B及びCにより説明すると
、第1図Aは積層材の両表面層がフィルムlで、発泡体
2が表面に表われていない場合。An example of the laminated structure will be explained with reference to FIGS. 1A, B, and C. In FIG. 1A, both surface layers of the laminated material are films 1, and the foam 2 is not exposed on the surface.
第1図Bは片面がフィルムl、片面が発泡体2である場
合、第1図Cは両表面層が発泡体2で、フィルム1が表
面に表われていない場合を示している。FIG. 1B shows the case where one side is the film 1 and the other side is the foam 2, and FIG. 1C shows the case where both surface layers are the foam 2 and the film 1 is not exposed on the surface.
発泡体層と合成樹脂フィルム層との強固な接合は、熱プ
レスによる熱融着、或いは合成樹脂フィルム層に適切な
接着剤を塗布する等の方法によって容易に得られる。A strong bond between the foam layer and the synthetic resin film layer can be easily obtained by heat fusion using a hot press or by applying a suitable adhesive to the synthetic resin film layer.
上記の構造の他、更に衝撃吸収効果を高めるために、上
記の積層材の合成樹脂フィルム層の中の少なくとも一層
を、多数の独立気泡を有する前記合成樹脂フィルムの成
形品層に置き換えた構造にするとよい。In addition to the above structure, in order to further enhance the impact absorption effect, at least one of the synthetic resin film layers of the above laminate is replaced with a molded layer of the synthetic resin film having a large number of closed cells. It's good to do that.
多数の独立気泡を有する前記合成樹脂フィルムの成形品
は、例えばフィルムを予め凹凸のある形状に成形した後
平滑なフィルム上に熱融着或いは接着剤等によって接合
する等の方法に依って容易に得られる。ここで形成され
る独立気泡の大きさく直径)は1〜30 m m、高さ
はl−10mmとする。この範囲外は積層材としての衝
撃改良効果がよくない、各気泡の形状は問わない。A molded article of the synthetic resin film having a large number of closed cells can be easily produced by, for example, forming the film into an uneven shape in advance and then bonding it onto a smooth film using heat fusion or adhesive. can get. The closed cells formed here have a diameter of 1 to 30 mm and a height of 1 to 10 mm. Outside this range, the impact improvement effect of the laminated material is not good, and the shape of each cell does not matter.
この構造を第2図により説明すると、第2図Aは両表面
層がフィルムlで、発泡体2と交互に積層されていると
共に、フィルム層の一つが多数の独立気泡を有する合成
樹脂フィルム成形品11となっている場合を示し、第2
図Bは両表面層が発泡体2で、フィルムlと交互にvi
層されていると共に、フィルム層の一つが多数の独立気
泡を有する合成樹脂フィルム成形品11となっている場
合を示している。To explain this structure with reference to Fig. 2, Fig. 2 A shows a molded synthetic resin film in which both surface layers are films 1, which are laminated alternately with foam 2, and one of the film layers has a large number of closed cells. Indicates the case where the item is 11, and the second
In Figure B, both surface layers are foam 2, alternating with film l and vi
The figure shows a synthetic resin film molded product 11 in which one of the film layers has a large number of closed cells.
なお未発IJにおいて、合成樹脂フィルムとして1.2
−ポリブタジェン系フィルムのような熱可塑性合成樹脂
フィルムを用いると、積層体(衝撃吸収材)を加熱成型
することがきわめて容易となり、所望の形状に成型でき
る利点がある。In addition, in unreleased IJ, 1.2 as a synthetic resin film
- When a thermoplastic synthetic resin film such as a polybutadiene film is used, it is extremely easy to heat-mold the laminate (shock absorbing material), which has the advantage of being able to be molded into a desired shape.
実施例1〜5及び比較例1〜2
第1表に示した基材及び構造の衝撃吸収材サンプルを作
り、衝撃加速度ピーク値(G)及び圧縮永久歪を測定し
て比較した。結果を第1表下段に示す。Examples 1 to 5 and Comparative Examples 1 to 2 Shock absorbing material samples having the base materials and structures shown in Table 1 were made, and the impact acceleration peak value (G) and compression set were measured and compared. The results are shown in the lower part of Table 1.
第1表 なお、第1表中、※l〜※8は下記の通りである。Table 1 Note that in Table 1, *l to *8 are as follows.
※l:次の混合物に加硫剤、加硫促進剤を加え、加熱発
泡硬化して得られる低レジリエンスゴム発泡体。*l: A low-resilience rubber foam obtained by adding a vulcanizing agent and a vulcanization accelerator to the following mixture and curing it by heating.
スチレン含有量が60℃畳%
であるスチレン−ブタジェン
共重合体 80重量部天然ゴム
20玉請部炭酸力アルシウム 7
0ff1.ri1部クレー 70重
賃部プロセスオイル 301c量部発泡剤
10市4A部※2:クロロプレン発
泡体
※3:ダンロップトリプソメータで測定(20℃での値
)
※4 : LORD Chemical Produc
ts社製ポリウレタンフィルム;商品名タフテン
※5 : JSR社製1.2−ポリブタジェンフィルム
※6:高さ2〜3mm、直径8mmの独立気泡が2mm
間隔で並ぶように成形された
ポリウレタンフィルム
※7:重逝5Kg、接地面積9cm2の錘りを自由落下
させたときの加速度
※8 : 2Kg/cm2 (定加重)、24時間後の
永久変形(20℃での値)
第1表から明らかなように1本発明による実施例1〜6
のサンプルは、発泡体単独の比較例1のサンプルに比し
、高所から落下させた時の衝撃加速度ピーク値(G)が
顕著に低く、また圧縮永久歪も小さい。Styrene-butadiene copolymer with styrene content of 60℃ tatami% 80 parts by weight natural rubber
20 Tamahakebe Alcium Carbonate 7
0ff1. ri 1 part clay 70 parts process oil 301c parts blowing agent
10 City 4A Section *2: Chloroprene foam *3: Measured with a Dunlop trypsometer (value at 20°C) *4: LORD Chemical Produc
Polyurethane film made by TS; trade name Tuften *5: 1.2-polybutadiene film made by JSR *6: 2 mm closed cells with a height of 2 to 3 mm and a diameter of 8 mm.
Polyurethane film formed to line up at intervals *7: Acceleration when a weight with a weight of 5 kg and a ground contact area of 9 cm2 is freely dropped *8: 2 kg/cm2 (constant load), permanent deformation after 24 hours (20 As is clear from Table 1, Examples 1 to 6 according to the present invention
The sample has a significantly lower impact acceleration peak value (G) when dropped from a high place and a lower compression set than the sample of Comparative Example 1, which is a foam alone.
また反発弾性が25%より高い発泡体(クロロブレン発
泡体)と合成樹脂フィルムとを接合積層した比較例2の
サンプルに比し、衝撃加速度ピーク値(G)がWJXに
低い。Furthermore, the impact acceleration peak value (G) is lower than WJX compared to the sample of Comparative Example 2 in which a foam (chloroprene foam) with a rebound resilience higher than 25% and a synthetic resin film are bonded and laminated.
発明の効果
1)発泡体単独の場合に比べ衝撃吸収効果が大巾に向−
■ニする。Effects of the invention 1) Shock absorption effect is improved compared to the case of foam alone.
■ Do it.
2)本発明に規定する要件を満たさない発泡体とフィル
ムの積層品に比べ衝撃吸収効果が大巾に向上する。2) The impact absorption effect is greatly improved compared to a laminate of foam and film that does not meet the requirements stipulated in the present invention.
3)軽量性を保持している。3) Maintains lightness.
4)9.泡体単独の場合に比べ永久変形性が大巾に改良
される。4)9. Permanent deformability is greatly improved compared to the case of foam alone.
5)なお本発明において、発泡体と合成樹脂フィルムの
みよりなる積層品と、多数の独立気泡を有するフィルム
成型品を含む積層品の、それぞれの特色を示せば第2表
の如くである。5) In the present invention, Table 2 shows the respective characteristics of a laminate made of only a foam and a synthetic resin film and a laminate including a film molded product having a large number of closed cells.
第1図は発泡体と合成樹脂フィルムの積層構造の例を示
す図、第2図は合成樹脂フィルム層のうちの一層を多数
の独立気泡を有する前記合成樹脂フィルムの成形品層で
zi、g換えた構造例を示す図である。FIG. 1 is a diagram showing an example of a laminated structure of a foam and a synthetic resin film, and FIG. 2 is a diagram showing an example of a laminated structure of a foam and a synthetic resin film. It is a figure which shows the example of a changed structure.
Claims (1)
〜0・9g/cm^3で、SRISによる硬度50°以
下の発泡体と、引張り強度が100Kg/cm^2以上
、破断時伸びが50%以上、硬度(JIS A)が60
°以上で厚さが10〜2000μmの合成樹脂フィルム
及び/又は多数の独立気泡を有する前記フィルムの成形
品とを強固に接合積層したことを特徴とする衝撃吸収材
。Impact resilience at 20℃ is 25% or less, density is 0.05
~0.9g/cm^3, foam with hardness of 50° or less by SRIS, tensile strength of 100Kg/cm^2 or more, elongation at break of 50% or more, hardness (JIS A) of 60
A shock absorbing material comprising a synthetic resin film having a thickness of 10 to 2000 μm and/or a molded product of the film having a large number of closed cells, which are firmly bonded and laminated.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6705986A JPS62225335A (en) | 1986-03-27 | 1986-03-27 | Collapsible material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6705986A JPS62225335A (en) | 1986-03-27 | 1986-03-27 | Collapsible material |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS62225335A true JPS62225335A (en) | 1987-10-03 |
Family
ID=13333889
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP6705986A Pending JPS62225335A (en) | 1986-03-27 | 1986-03-27 | Collapsible material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS62225335A (en) |
-
1986
- 1986-03-27 JP JP6705986A patent/JPS62225335A/en active Pending
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