JPH0263949A - New air bag device - Google Patents
New air bag deviceInfo
- Publication number
- JPH0263949A JPH0263949A JP21509188A JP21509188A JPH0263949A JP H0263949 A JPH0263949 A JP H0263949A JP 21509188 A JP21509188 A JP 21509188A JP 21509188 A JP21509188 A JP 21509188A JP H0263949 A JPH0263949 A JP H0263949A
- Authority
- JP
- Japan
- Prior art keywords
- film
- air bag
- airbag
- synthetic fiber
- woven
- 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
- 239000004745 nonwoven fabric Substances 0.000 claims abstract description 13
- 239000002759 woven fabric Substances 0.000 claims abstract description 13
- 229920002994 synthetic fiber Polymers 0.000 claims abstract description 12
- 239000012209 synthetic fiber Substances 0.000 claims abstract description 12
- 238000002844 melting Methods 0.000 claims abstract description 8
- 230000008018 melting Effects 0.000 claims abstract description 8
- 239000011368 organic material Substances 0.000 claims 1
- 229920003235 aromatic polyamide Polymers 0.000 abstract description 10
- 229920000642 polymer Polymers 0.000 abstract description 8
- 239000004760 aramid Substances 0.000 abstract description 6
- 238000010030 laminating Methods 0.000 abstract description 3
- 229920001721 polyimide Polymers 0.000 abstract description 3
- 239000004952 Polyamide Substances 0.000 abstract description 2
- 230000001133 acceleration Effects 0.000 abstract description 2
- 239000000835 fiber Substances 0.000 abstract description 2
- 229920002239 polyacrylonitrile Polymers 0.000 abstract description 2
- 229920002647 polyamide Polymers 0.000 abstract description 2
- 229920000728 polyester Polymers 0.000 abstract description 2
- 239000011521 glass Substances 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 239000007789 gas Substances 0.000 description 12
- 239000004744 fabric Substances 0.000 description 7
- 238000000034 method Methods 0.000 description 6
- 239000004677 Nylon Substances 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- 229920001778 nylon Polymers 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- -1 poly(P-phenylene terephthalamide) Polymers 0.000 description 3
- 239000004697 Polyetherimide Substances 0.000 description 2
- 238000001514 detection method Methods 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 238000004880 explosion Methods 0.000 description 2
- 229920001084 poly(chloroprene) Polymers 0.000 description 2
- 229920001601 polyetherimide Polymers 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 239000004753 textile Substances 0.000 description 2
- 239000004593 Epoxy Substances 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 239000004734 Polyphenylene sulfide Substances 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 238000003490 calendering Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000010073 coating (rubber) Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 230000008602 contraction Effects 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229920006332 epoxy adhesive Polymers 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000002360 explosive Substances 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 239000003721 gunpowder Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000003779 heat-resistant material Substances 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 229920002681 hypalon Polymers 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 238000003475 lamination Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 229920003366 poly(p-phenylene terephthalamide) Polymers 0.000 description 1
- 229920006267 polyester film Polymers 0.000 description 1
- 229920000069 polyphenylene sulfide Polymers 0.000 description 1
- 229920002379 silicone rubber Polymers 0.000 description 1
- 239000004945 silicone rubber Substances 0.000 description 1
- 239000004449 solid propellant Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 150000003457 sulfones Chemical group 0.000 description 1
- 229910052715 tantalum Inorganic materials 0.000 description 1
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 description 1
- MHSKRLJMQQNJNC-UHFFFAOYSA-N terephthalamide Chemical compound NC(=O)C1=CC=C(C(N)=O)C=C1 MHSKRLJMQQNJNC-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Air Bags (AREA)
- Laminated Bodies (AREA)
Abstract
Description
【発明の詳細な説明】 (産業上の利用分野) 本発明は乗物用のエアバッグ装置に関する。[Detailed description of the invention] (Industrial application field) The present invention relates to a vehicle airbag device.
さらに詳しくは、耐熱性が高く、可撓性にすぐれた高強
度の有機フィルムを内側に積層しであるために、安全性
にすぐれ、軽量化でき、かつ経済性にすぐれたエアバッ
グ装置に関する。More specifically, the present invention relates to an airbag device that is safe, lightweight, and economical because it is laminated with a high-strength organic film that has high heat resistance and flexibility on the inside.
(従来の技術)
自動車の衝突時の衝撃から乗員を保護するために用いら
れる、いわゆる自動車用エアバッグ装置は、シートヘル
ドに代わる安全装置として注目され、一部の車両に搭載
されている。(Prior Art) A so-called automobile airbag device, which is used to protect occupants from the impact of an automobile collision, is attracting attention as a safety device that can replace a seat-held device, and is installed in some vehicles.
現在、 In的に使用されているエアバングは、高強力
ナイロン(強度約8〜9g/d)の840dcの平織物
に、クロロブレン、ハイパロン等のゴムでコーティング
したものが用いられているが、この厚さは0.40〜0
.50mmで、かなり厚いため、ハンドルの中に格納す
るのに大きなスペースを要し、操縦性が悪くなり、美観
をそこねるという欠点がある。Currently, the airbands used in industrial use are made of 840dc plain woven fabric made of high-strength nylon (strength approximately 8 to 9g/d) coated with rubber such as chlorobrene or hypalon. Sa is 0.40~0
.. At 50 mm, it is quite thick, so it requires a lot of space to store inside the handle, making it difficult to maneuver and spoiling its aesthetics.
自動車用エアバッグは、衝突時に高速で空気が圧入され
、膨張し、乗員が衝突した時の街?を吸収緩和する必要
があるため、このゴムコーティングで、空気を瞬間的に
バング内に閉じこめる機能をもたせている。しかし、こ
のコーティングは上記欠点に加えて膨張のための火薬爆
発による高温耐性が必ずしも十分なレベルであるとはい
えず、また、繊物へのコーティングが繁雑でコスト上昇
を招くという問題があった。Airbags for automobiles are injected with air at high speed during a collision and inflate, causing the occupants to experience a collision. Since it is necessary to absorb and relieve air, this rubber coating has the function of momentarily trapping air inside the bang. However, in addition to the above-mentioned drawbacks, this coating does not necessarily have a sufficient level of resistance to high temperatures caused by gunpowder explosion due to expansion, and coating textiles is complicated, leading to increased costs. .
耐熱性の問題を解決するための一つの手段として、特開
昭63−78744号公報には、基布に全芳香族ポリア
ミド繊維、ゴムにはシリコンゴムを用いることが提案さ
れている。このように、強力が大きく、耐熱性の素材を
用いることでかなりの小型軽量化は可能であるが、未だ
、満足すべきものとは云えない上に、非常に高価になる
。As one means for solving the problem of heat resistance, JP-A-63-78744 proposes using wholly aromatic polyamide fiber for the base fabric and silicone rubber for the rubber. As described above, it is possible to considerably reduce the size and weight by using a strong and heat-resistant material, but it is still not satisfactory and is extremely expensive.
(発明が解決しようとする問題点)
このような、エアバッグの小型、軽量化の問題を、安全
性や経済性を損なうことなく解決するために検討を進め
た結果、合成繊維の織布又は不織布の内面に特定の耐熱
性の有機フィルムを積層することにより、目的が達せら
れることを見出し、本発明に到達したものである。(Problems to be Solved by the Invention) As a result of conducting studies to solve the problem of reducing the size and weight of airbags without compromising safety or economic efficiency, we found that synthetic fiber woven or The present invention was achieved by discovering that the object can be achieved by laminating a specific heat-resistant organic film on the inner surface of a nonwoven fabric.
(問題点を解決するための手段)
本発明は、乗物の衝突時の衝撃から乗員を保護するため
に用いられるエアバッグ装置において、エアバッグを合
成繊維織布又は合成繊維不織布に350℃以上の融点を
有するか又は融点をもたない耐熱性の有機フィルムで内
張りした袋体としてなるエアバッグ装置である。(Means for Solving the Problems) The present invention provides an airbag device used to protect occupants from impact during a vehicle collision, in which an airbag is made of synthetic fiber woven fabric or synthetic fiber nonwoven fabric at a temperature of 350°C or higher. This airbag device is a bag body lined with a heat-resistant organic film that has or does not have a melting point.
本発明でいう、エアバッグ装置とは、膨張式乗員拘束装
置、ガスバッグ装置等とも称されるものであり、自動車
等の乗物の衝突時の加速度を検知して、運転席、助手席
等の前方に設置されたバッグを膨張させて、乗員がハン
ドル1.フロントガラス等と衝突するのを防ぐ装置であ
る。エアバッグ装置は、衝撃検知用センサー、ガス発生
器およびエアバッグより構成される。The airbag device referred to in the present invention is also referred to as an inflatable occupant restraint device, a gas bag device, etc., and detects the acceleration of a vehicle such as a car during a collision, and controls the driver's seat, passenger seat, etc. The passenger inflates the bag installed in the front and presses the handle 1. This is a device that prevents collisions with windshields, etc. The airbag device consists of an impact detection sensor, a gas generator, and an airbag.
本発明において、エアバッグが合成繊維からなる織布又
は不織布に耐熱性の有機フィルムが内張すされているこ
とが必須である。合成繊維としては、ポリアミド(ナイ
ロン)、ポリエステル、ポリアクリロニトリル、芳香族
ポリアミド(アラミド)、ポリイミド、ポリフェニレン
スルフィド、ポリエーテルイミド等約200℃以下では
溶融や分解を実質的におこさないものが用いられる。織
布としては、通常、平織が選ばれるが、必要ならば、朱
子職等その他の織組織であってもよい、不織布としては
、謂ゆるスパンボンド法、フラッシュ法等で製造された
ものが用いられる。In the present invention, it is essential that the airbag is a woven or nonwoven fabric made of synthetic fibers lined with a heat-resistant organic film. The synthetic fibers used include polyamide (nylon), polyester, polyacrylonitrile, aromatic polyamide (aramid), polyimide, polyphenylene sulfide, polyetherimide, etc., which do not substantially melt or decompose at temperatures below about 200°C. As the woven fabric, plain weave is usually selected, but if necessary, other woven structures such as satin may be used.As the non-woven fabric, those manufactured by the so-called spunbond method, flash method, etc. are used. It will be done.
耐熱性の有機フィルムとしては、350℃以上の融点を
有するか、又は融点を有さないポリマーからなるものを
使用する必要がある。350℃に満たない融点のポリマ
ーからなる有機フィルムを使用すると、エアバッグの膨
張時に火薬爆発に伴なって発生する熱に耐えられずに、
損耗してしまうことがあるので好ましくない。As the heat-resistant organic film, it is necessary to use a film made of a polymer that has a melting point of 350° C. or higher, or has no melting point. If an organic film made of a polymer with a melting point below 350°C is used, it will not be able to withstand the heat generated by the explosive explosion when the airbag is inflated.
This is not preferable as it may cause wear and tear.
本発明に用いることのできる有機フィルムの具体例とし
ては、ポリイミドフィルム、メタ系又はパラ系のアラミ
ドフィルム、ポリベンゾビスチアゾールフィルム、ポリ
エーテルイミドフィルム、芳香族ポリエステルフィルム
等を挙げることができる。これらの中でも、特にパラ系
のアラミドフィルムは、十分な耐熱性を有する上に、強
度・弾性率が非常に大きく引裂性能にも優れており、し
かもガスバリア性が非常に良好なので、薄くして用いる
ことができ、バッグの収納性、軽量性等から最も好まし
い。ここで、パラ系アラミドフィルムは、下記の一般式
(I)、一般式(II)の重合体またはこれらの共重合
体を用いて製造したちのである。Specific examples of organic films that can be used in the present invention include polyimide films, meta- or para-aramid films, polybenzobisthiazole films, polyetherimide films, and aromatic polyester films. Among these, para-based aramid film in particular has sufficient heat resistance, has very high strength and elastic modulus, and has excellent tear performance, as well as very good gas barrier properties, so it can be used in thin forms. This is most preferable in terms of bag storage and light weight. Here, the para-aramid film is manufactured using a polymer of the following general formula (I) or general formula (II) or a copolymer thereof.
(式中において、R,、R2およびR3はから選ばれ、
これらの水素原子がハロゲン、メチル、エチル、メトキ
シ、ニトロ、スルホンなどの官能基で置換されていても
よい。m、nは平均重合度であり約50〜1000であ
る。)本発明に用いられるパラ系アラミドには約20モ
ル%以下の量であれば上記の成分以外のポリマ−が共重
合又はブレンドされていてもよい。パラ系アラミドとし
て特に好ましいのは、ポリ (Pフェニレンテレフタル
アミド)である。(wherein R,, R2 and R3 are selected from
These hydrogen atoms may be substituted with functional groups such as halogen, methyl, ethyl, methoxy, nitro, and sulfone. m and n are average degrees of polymerization and are about 50 to 1000. ) Polymers other than the above-mentioned components may be copolymerized or blended with the para-aramid used in the present invention in an amount of about 20 mol % or less. Particularly preferred as the para-aramid is poly(P-phenylene terephthalamide).
エアバッグ°膨張および乗員との衝突における衝撃力に
耐えるため、本発明に用いるフィルムは伸度および強度
が高い必要があり、10%以上の伸度を有することが好
ましい。The film used in the present invention needs to have high elongation and strength in order to withstand the impact force caused by airbag inflation and collision with an occupant, and preferably has an elongation of 10% or more.
フィルムの厚みは、フィルムのもっている機械的性質に
も依るが、通常3〜40μm、好ましくは5〜25μm
で用いられる。100μmを超える厚みのフィルムを用
いるとバッグの収納性や軽量性が…われる。The thickness of the film depends on the mechanical properties of the film, but is usually 3 to 40 μm, preferably 5 to 25 μm.
used in Using a film with a thickness of more than 100 μm improves the bag's storability and lightness.
フィルムの合成繊維織布又は合成繊維不織布への積層方
法は特に限定されない。例えば、−旦、フィルムに成形
したのち、エポキシ系、アクリル系、エステル系、フェ
ノール系等の接着剤で織布又は不繊布に張りつける方法
が第1の態様である。The method of laminating the film onto the synthetic fiber woven fabric or synthetic fiber nonwoven fabric is not particularly limited. For example, the first embodiment is a method in which the film is first formed into a film and then attached to a woven or nonwoven fabric using an epoxy, acrylic, ester, or phenol adhesive.
第2の態様として、フィルム形成性ポリマーの溶液を繊
布又は不織布に塗布し、溶剤を取り除く方法がある。他
の態様として、直接に織布又は不織布上で重合したり、
CVDでコーテイング膜を形成する方法がある。A second method is to apply a solution of the film-forming polymer to a textile or nonwoven fabric and remove the solvent. In other embodiments, polymerization is performed directly on a woven or nonwoven fabric,
There is a method of forming a coating film by CVD.
積層は、エアバッグ作動時の急激な膨張とそれにつづく
収縮のバランスに応じて織布又は不織布の全面に行い、
排気口を取りつける構造としてもよいし、織布又は不織
布の一部に行う構造としてもよい。前者の構造の場合、
排気口の先に排気管をとりつけて11作動時に発生する
ガスを乗物外に排出するのは、エアバッグ装置の安全性
を高める上で好ましい実施態様の1つである。Lamination is performed on the entire surface of the woven or non-woven fabric depending on the balance between rapid expansion and subsequent contraction when the airbag is activated.
It may be a structure in which an exhaust port is attached, or a structure in which the exhaust port is attached to a part of a woven or non-woven fabric. In the case of the former structure,
Installing an exhaust pipe at the end of the exhaust port to exhaust the gas generated when the airbag 11 is activated to the outside of the vehicle is one of the preferred embodiments in terms of improving the safety of the airbag device.
本発明において、衝撃検知用センサーとしては、Gセン
サー、レーダーセンサー、クラッシュセンサー等、ガス
発生器としては圧縮ガス方式、固体燃料方式等、従来公
知の方式を用いることができる。In the present invention, as the impact detection sensor, a G sensor, a radar sensor, a crash sensor, etc. can be used, and as the gas generator, a conventionally known system such as a compressed gas system, a solid fuel system, etc. can be used.
以下、本発明を実施例により説明する。なお、実施例中
、部、%とあるのは特に断らない限り重量部、重量%を
示す。The present invention will be explained below using examples. In the examples, parts and % indicate parts by weight and % by weight unless otherwise specified.
実施例
〔アラミドフィルムの製造〕
対数粘度ηinhが5.5のポリ(バラフェニレンテレ
フタルアミド)ポリマーを、99.7%の硫酸にポリマ
ー濃度11.5%となるように)岩屑した。この]・−
ブを約70 ’Cに保ったまま真空下で脱気した。Example [Manufacture of aramid film] Poly(paraphenylene terephthalamide) polymer having a logarithmic viscosity ηinh of 5.5 was added to 99.7% sulfuric acid to give a polymer concentration of 11.5%). This]・−
The tube was kept at approximately 70'C and degassed under vacuum.
ドープは光学異方性を有し、粘度は4400ボイズであ
った。タンクからフィルターを通し、ギヤポンプを経て
ダイに至る1、5mの曲管を約70℃に保ち、0.1
mmX 300mmのスリットを有するグイから、鏡面
に暦いたタンタル類のベルトにキャストし、相対湿度約
85%の約90 ’Cの空気を吹きつけて、流延ドープ
を光学等方化し、ベルトとともに、−5℃の希硫酸中に
導いて凝固させた。The dope had optical anisotropy and a viscosity of 4400 voids. A 1.5 m long curved pipe from the tank, through the filter, through the gear pump, to the die is maintained at approximately 70°C, and the temperature is 0.1 m.
Cast the dope onto a tantalum belt with a slit of mm x 300 mm on a mirror surface, blow air at about 90'C with a relative humidity of about 85% to make the cast dope optically isotropic, and together with the belt, It was introduced into dilute sulfuric acid at -5°C and coagulated.
次いで凝固フィルムをベルトから引きはがし、約40℃
の温水中を走行させて洗浄した。洗浄の終了したフィル
ムを乾燥させずにテンターで延伸し、次いで別のテンタ
ーを用いて定長下に240℃で熱乾燥した後、390
’Cで定長熱処理した。得られたフィルムは8μmの厚
みをもちその強度はMD : 35 Kg/mm”、T
D : 34 Kg/mm2、伸度はMD:17%、
TD:16%、ヤング率はMI):1200Kg/mm
2、T D : I 300Kg/mm2のものであっ
た。The coagulated film is then peeled off from the belt and heated to approximately 40°C.
It was washed by running it in warm water. The washed film was stretched in a tenter without drying, then heat-dried at 240°C in a fixed length using another tenter, and then stretched at 390°C.
A fixed-length heat treatment was carried out at 'C. The obtained film has a thickness of 8 μm and a strength of MD: 35 Kg/mm”, T
D: 34 Kg/mm2, elongation MD: 17%,
TD: 16%, Young's modulus (MI): 1200Kg/mm
2, T D:I 300Kg/mm2.
高強力ナイロン840de(強度8.7g/d )を経
糸、緯糸に用い経、緯25本/1nchで手織にて厚さ
0.380m/mの織物に上記フィルムをエポキシ系接
着剤で張り合わせて、厚さ0.405m/mのエアバッ
グ用基布を得、これを用いて2ケの排気口をもつエアバ
ッグ装置を作った。エアバッグの重量は520gで、そ
の収納時の体積は810m1であった。Using high-strength nylon 840de (strength 8.7 g/d) for the warp and weft, the above film was attached to a hand-woven fabric with a thickness of 0.380 m/m with 25 warps and wefts/1 nch using an epoxy adhesive. An airbag base fabric having a thickness of 0.405 m/m was obtained, and an airbag device having two exhaust ports was made using this fabric. The weight of the airbag was 520g, and the volume when stored was 810ml.
〔エアバッグ装置の作動テスト]
エアバッグに金属アジド系化合物をガス発生剤とするガ
ス発生器をとりつけ、作動テストを行った。ガス発生時
のガス発生器出口の温度は600’C@後であった。所
期の目的通りの膨張・収縮パターンが得られ、作動後の
エアバッグには何のt具備も見当らなかった。[Operation test of airbag device] A gas generator using a metal azide compound as a gas generating agent was attached to the airbag, and an operation test was conducted. The temperature at the gas generator outlet during gas generation was 600'C@. The desired inflation/deflation pattern was obtained, and no t-features were found in the airbag after activation.
比較例
〔エアバング装置の製作]
高強力ナイロン840de(強度8.7g/d )を経
糸、緯糸に用い、経、緯25本/1nchで平織にて厚
さ0.38On+/mの織物にクロロプレンゴムをドイ
ツAUMAのRoller−11ead+Contin
uous vulcanizingmachineにて
上記織物の片面にカレンダー加工して厚さ0.430m
/mのエアバッグ用基布を得、これにより2ケの排気口
をもつエアバッグ装置を製作した。Comparative example [Production of air bang device] High-strength nylon 840de (strength 8.7 g/d) was used for the warp and weft, and chloroprene rubber was added to a plain weave fabric with a thickness of 0.38 On+/m with a warp and weft of 25 threads/1 nch. The German AUMA Roller-11ead+Contin
One side of the above fabric was calendered using a vulcanizing machine to a thickness of 0.430m.
/m of airbag base fabric was obtained, and an airbag device with two exhaust ports was manufactured using this fabric.
エアバッグ重量は705gで、収納時のエアバッグ体積
は860m1であった。The weight of the airbag was 705g, and the volume of the airbag when stored was 860ml.
実施例と同様の作動テストを行ったのち、エアバッグを
観察すると、ガス発生器に近い部分のクロロプレンゴム
が黒変しているのが発見された。After performing the same operation test as in the example, when the airbag was observed, it was discovered that the chloroprene rubber in the area near the gas generator had turned black.
(発明の効果)
本発明のエアバッグ装置は、従来公知のものに比ベニア
バラグが軽量かつ小型であり、収納スペースを小さくす
ることができる。また、軽量のために、燃料を節約でき
るほか、特に運転席用のエアバング装置においては、ハ
ンドルシャフトの重量負担が軽減されるためハンドル関
連部分の重厚化が回避できる。(Effects of the Invention) The airbag device of the present invention has a veneer bag that is lighter and smaller than those of conventionally known airbag devices, and the storage space can be reduced. In addition, its light weight saves fuel, and in particular in airbang devices for the driver's seat, the weight burden on the steering wheel shaft is reduced, making it possible to avoid making the steering wheel-related parts bulky.
更に、高温の発生ガスの接触する部位の耐熱性にすぐれ
ているので、エアバッグ装置の安全性、信頼性にすぐれ
ている。Furthermore, since the parts that come into contact with high-temperature generated gas have excellent heat resistance, the airbag device has excellent safety and reliability.
Claims (1)
るエアバッグ装置において、エアバッグを合成繊維織布
又は合成繊維不織布に350℃以上の融点を有するか又
は融点をもたない耐熱性の有機フィルムを内張りした袋
体としてなるエアバッグ装置。In airbag devices used to protect occupants from impacts during vehicle collisions, the airbag is made of synthetic fiber woven fabric or synthetic fiber nonwoven fabric that has a melting point of 350°C or higher or a heat-resistant organic material that does not have a melting point. An airbag device that is a bag body lined with film.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP21509188A JPH0263949A (en) | 1988-08-31 | 1988-08-31 | New air bag device |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP21509188A JPH0263949A (en) | 1988-08-31 | 1988-08-31 | New air bag device |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH0263949A true JPH0263949A (en) | 1990-03-05 |
Family
ID=16666604
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP21509188A Pending JPH0263949A (en) | 1988-08-31 | 1988-08-31 | New air bag device |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0263949A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5763330A (en) * | 1995-09-29 | 1998-06-09 | Highland Industries, Inc. | Extrusion coated fabric |
JPH10273002A (en) * | 1997-03-28 | 1998-10-13 | Toray Ind Inc | Backing fabric for air bag, and air bag |
US6123360A (en) * | 1999-07-06 | 2000-09-26 | Amin; Mukesh J. | Airbag system with inflator gas reactant surface |
-
1988
- 1988-08-31 JP JP21509188A patent/JPH0263949A/en active Pending
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5763330A (en) * | 1995-09-29 | 1998-06-09 | Highland Industries, Inc. | Extrusion coated fabric |
JPH10273002A (en) * | 1997-03-28 | 1998-10-13 | Toray Ind Inc | Backing fabric for air bag, and air bag |
US6123360A (en) * | 1999-07-06 | 2000-09-26 | Amin; Mukesh J. | Airbag system with inflator gas reactant surface |
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