AU643957B2 - Air bag-containing cover - Google Patents
Air bag-containing coverInfo
- Publication number
- AU643957B2 AU643957B2 AU67849/90A AU6784990A AU643957B2 AU 643957 B2 AU643957 B2 AU 643957B2 AU 67849/90 A AU67849/90 A AU 67849/90A AU 6784990 A AU6784990 A AU 6784990A AU 643957 B2 AU643957 B2 AU 643957B2
- Authority
- AU
- Australia
- Prior art keywords
- air bag
- cover
- ingredient
- surface skin
- skin layer
- 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 - Fee Related
Links
- 239000010410 layer Substances 0.000 description 50
- 239000004615 ingredient Substances 0.000 description 48
- 239000012792 core layer Substances 0.000 description 37
- 238000000465 moulding Methods 0.000 description 24
- 238000000034 method Methods 0.000 description 21
- 239000000463 material Substances 0.000 description 16
- 229920005989 resin Polymers 0.000 description 15
- 239000011347 resin Substances 0.000 description 15
- 206010016322 Feeling abnormal Diseases 0.000 description 14
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 13
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 13
- 229920001971 elastomer Polymers 0.000 description 13
- 229920000642 polymer Polymers 0.000 description 12
- 230000009172 bursting Effects 0.000 description 10
- 238000004519 manufacturing process Methods 0.000 description 10
- 229920001083 polybutene Polymers 0.000 description 9
- 229920002367 Polyisobutene Polymers 0.000 description 8
- 239000004902 Softening Agent Substances 0.000 description 8
- 239000011162 core material Substances 0.000 description 8
- 239000005060 rubber Substances 0.000 description 8
- 239000004215 Carbon black (E152) Substances 0.000 description 7
- 238000005187 foaming Methods 0.000 description 7
- 229930195733 hydrocarbon Natural products 0.000 description 7
- 150000002430 hydrocarbons Chemical class 0.000 description 7
- 238000002156 mixing Methods 0.000 description 7
- 239000000203 mixture Substances 0.000 description 7
- 238000012360 testing method Methods 0.000 description 7
- 239000007924 injection Substances 0.000 description 6
- 238000002347 injection Methods 0.000 description 6
- 238000001746 injection moulding Methods 0.000 description 6
- 229920001169 thermoplastic Polymers 0.000 description 6
- 229920002725 thermoplastic elastomer Polymers 0.000 description 6
- 229920001400 block copolymer Polymers 0.000 description 5
- 239000011248 coating agent Substances 0.000 description 5
- 238000000576 coating method Methods 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 5
- 239000000806 elastomer Substances 0.000 description 5
- 230000000977 initiatory effect Effects 0.000 description 5
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 150000001993 dienes Chemical class 0.000 description 4
- 239000006260 foam Substances 0.000 description 4
- 230000003014 reinforcing effect Effects 0.000 description 4
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 3
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- 241000705989 Tetrax Species 0.000 description 3
- 239000000470 constituent Substances 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- -1 ethylene, propylene Chemical group 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 3
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 3
- 230000035939 shock Effects 0.000 description 3
- 239000003381 stabilizer Substances 0.000 description 3
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
- 239000005977 Ethylene Substances 0.000 description 2
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- 230000032683 aging Effects 0.000 description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 description 2
- 239000006229 carbon black Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000013461 design Methods 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 229920001519 homopolymer Polymers 0.000 description 2
- 239000010445 mica Substances 0.000 description 2
- 229910052618 mica group Inorganic materials 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 229920006285 olefinic elastomer Polymers 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 229920006132 styrene block copolymer Polymers 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000002344 surface layer Substances 0.000 description 2
- 239000000454 talc Substances 0.000 description 2
- 229910052623 talc Inorganic materials 0.000 description 2
- 229920005992 thermoplastic resin Polymers 0.000 description 2
- PRPINYUDVPFIRX-UHFFFAOYSA-N 1-naphthaleneacetic acid Chemical compound C1=CC=C2C(CC(=O)O)=CC=CC2=C1 PRPINYUDVPFIRX-UHFFFAOYSA-N 0.000 description 1
- ROGIWVXWXZRRMZ-UHFFFAOYSA-N 2-methylbuta-1,3-diene;styrene Chemical class CC(=C)C=C.C=CC1=CC=CC=C1 ROGIWVXWXZRRMZ-UHFFFAOYSA-N 0.000 description 1
- 229920000181 Ethylene propylene rubber Polymers 0.000 description 1
- 239000004606 Fillers/Extenders Substances 0.000 description 1
- 102000020897 Formins Human genes 0.000 description 1
- 108091022623 Formins Proteins 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 230000000740 bleeding effect Effects 0.000 description 1
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical class C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 230000032798 delamination Effects 0.000 description 1
- 239000002355 dual-layer Substances 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 238000003780 insertion Methods 0.000 description 1
- 230000037431 insertion Effects 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 239000002932 luster Substances 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920013716 polyethylene resin Polymers 0.000 description 1
- 229920000346 polystyrene-polyisoprene block-polystyrene 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
- 230000002787 reinforcement Effects 0.000 description 1
- 239000012779 reinforcing material Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 230000035882 stress Effects 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 125000003011 styrenyl group Chemical group [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 238000003878 thermal aging Methods 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/06—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material
- B32B27/08—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B60—VEHICLES IN GENERAL
- B60R—VEHICLES, VEHICLE FITTINGS, OR VEHICLE PARTS, NOT OTHERWISE PROVIDED FOR
- B60R22/00—Safety belts or body harnesses in vehicles
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/06—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material
- B32B27/065—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material of foam
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/18—Layered products comprising a layer of synthetic resin characterised by the use of special additives
- B32B27/22—Layered products comprising a layer of synthetic resin characterised by the use of special additives using plasticisers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/30—Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers
- B32B27/302—Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers comprising aromatic vinyl (co)polymers, e.g. styrenic (co)polymers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/32—Layered products comprising a layer of synthetic resin comprising polyolefins
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/40—Layered products comprising a layer of synthetic resin comprising polyurethanes
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B5/00—Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts
- B32B5/18—Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts characterised by features of a layer of foamed material
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B7/00—Layered products characterised by the relation between layers; Layered products characterised by the relative orientation of features between layers, or by the relative values of a measurable parameter between layers, i.e. products comprising layers having different physical, chemical or physicochemical properties; Layered products characterised by the interconnection of layers
- B32B7/02—Physical, chemical or physicochemical properties
- B32B7/022—Mechanical properties
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B60—VEHICLES IN GENERAL
- B60R—VEHICLES, VEHICLE FITTINGS, OR VEHICLE PARTS, NOT OTHERWISE PROVIDED FOR
- B60R21/00—Arrangements or fittings on vehicles for protecting or preventing injuries to occupants or pedestrians in case of accidents or other traffic risks
- B60R21/02—Occupant safety arrangements or fittings, e.g. crash pads
- B60R21/16—Inflatable occupant restraints or confinements designed to inflate upon impact or impending impact, e.g. air bags
- B60R21/20—Arrangements for storing inflatable members in their non-use or deflated condition; Arrangement or mounting of air bag modules or components
- B60R21/215—Arrangements for storing inflatable members in their non-use or deflated condition; Arrangement or mounting of air bag modules or components characterised by the covers for the inflatable member
- B60R21/2165—Arrangements for storing inflatable members in their non-use or deflated condition; Arrangement or mounting of air bag modules or components characterised by the covers for the inflatable member characterised by a tear line for defining a deployment opening
- B60R21/21656—Steering wheel covers or similar cup-shaped covers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2250/00—Layers arrangement
- B32B2250/24—All layers being polymeric
- B32B2250/246—All polymers belonging to those covered by groups B32B27/32 and B32B27/30
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2323/00—Polyalkenes
- B32B2323/04—Polyethylene
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2323/00—Polyalkenes
- B32B2323/10—Polypropylene
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2325/00—Polymers of vinyl-aromatic compounds, e.g. polystyrene
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2605/00—Vehicles
- B32B2605/003—Interior finishings
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2605/00—Vehicles
- B32B2605/08—Cars
Landscapes
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Air Bags (AREA)
- Laminated Bodies (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Mattresses And Other Support Structures For Chairs And Beds (AREA)
Description
643957 S F Ref: 149452 FORM COMMONWEALTH OF AUSTRALIA PATENTS ACT 1952 COMPLETE SPECIFICATION
(ORIGINAL)
FOR OFFICE USE: Class Int Class too: 0 00 0 6 S. bo 0 *0
S
0 0 0
S
o".
S. S
S
S S S Complete Specification Lodged: Accepted: Published: Priority: Related Art: Name and Address of Applicant: Address for Service: Takata Corporation 4-30, Roppongi 1-chome Minato-ku Tokyo
JAPAN
Spruson Ferguson, Patent Attorneys Level 33 St Martins Tower, 31 Market Street Sydney, New South Wales, 2000, Australia Complete Specification for the invention entitled: Air Bag-Containing Cover The following statement is a full description of this invention, including the best method of performing ic known to me/us 5845/4 ABSTRACT OF THE DISCLOSURE An air bag-containing cover comprising: a surface skin layer made of a thermoplastic polymer containing the following ingredients A, B, C and D: ingredient A a hydrogenated derivative of a block copolymer comprising styrene an conjugated diene, ingredient B an olefinic resin, .e S c S. *SQ S
S
S
S.
S 0*SO ingredient C ingredient D polyisobutylene with a viscosity average molecular weight of not greater than 70,000, and a hydrocarbon series rubber softening agent with a kinetic viscosity at 40"C of not greater than 500 cSt and/or polybutene with a number average molecular weight of not greater than 2500, in which is 40 to 80 by weight, 5 to 30 by weight, 2 to 30 by weight 0 to 20 by weight, and hardness according to JIS-K6301 of from blending ratio ingredient A ingredient B ingredient C ingredient D having a JIS-A to 90, and a core layer comprising an olefinic resin having a modulus in flexure according to JIS-K7203 of from 1000 to
I
2 7000 kg/cm in which the core layer has a higher hardness than that of the surface skin layer, and the core layer has a portion for easily bursting the cover upon initiation of the air bag operation.
coosB iA AIR BAG-CONTAINING COVER FIELD OF THE INVENTION AND RELATED ART STATEMENT The present invention concerns a cover for containing an air bag which is actuated to expand and develop upon collision of a vehicle by sensing impact shock, deformation or the like ccised by the collision.
The air bag-containing cover of this kind is generally inserted with a reinforcing material such as nets (refer, e* for example, to Japanese Patent Laid-Open Sho 62-2 3 4764, So. Sho 50-127336, Japanese Utility Model Laid-Open Sho 52o e 80928, Sho 50-43454 and Sho 51-25342).
The cover inserted with the net-like inserts is usually manufactured by preparing an entire cover with material of relatively low strength such as foamed polyurethane and inserting the reinforcing nets for the entire cover.
Lines not inserted with the reinforcing nets are generally provided so that the air bag can be developed smoothly upon expansion to easily break the cover.
On the other hand, Japanese Utility Model Laid-Open O Se Sho 52-76042 proposes an air bag-containing cover comprising two layers, that is, a surface skin layer made of rigid urethane foams for finely finishing the surface and a core layer made of low density (high foaming ratio) 18 urethane foams for softening the entire cover in which slits (lines for smoothly developing the air bag upon expansion) are disposed being extended from the core layer to a portion of the surface skin layer.
Among the conventional air bag-containing covers described above, the air bag-containing cover provided with the net-like inserts involves a problem that its manufacture requires a number of steps and is troublesome, manufacture at high accuracy is difficult even by the use, for example, of urethane foaming molding (RIM), the production yield is low and the cost is expensive since the 0e** net-like reinforcements are inserted.
Further, the cover as disclosed in Japanese Utility S Model Laid-Open Sho 52-76042 has a surface skin layer made of rigid urethane foams (ASTM-D2240, Shore hardness: 30 and, accordingly, it can not provide a soft feeling but gives unpleasant feeling when a portion of a driver's .0 body is in contact therewith, for instance, during running of a vehicle. Furthermore, since the urethane material has low impact shock strength and no reinforcing inserts 0 are provided, broken pieces are scattered upon expansion of the air bag.
OBJECT AND SUMMARY OF THE INVENTION The object of the present invention is to overcome 2 the foregoing problems of the air bag-containing cover in the prior art and provide an air bag-containing cover of such a performance that a surface skin layer is flexible and gives a soft feeling, a core layer retains a shape capable of withstanding external pressure, the cover is easily broken upon expanding operation of the air bag but is not scattered in broken pieces within a temperature range from -40"C to +80'C, and also shows satisfactory breaking performance with scarce change of appearance at the above-specified temperature range even after being for 0e a long time at a high temperature of 110C and 1000 hours in view of act.ial mounting to a vehicle, which can be supplied by means of a simple molding process such as injection molding, at a high yield in a method of not resulting in failed products, at high accuracy, at high productivity and with satisfactory economical advantage.
The air bag-containing cover according to the present invention comprises: a surface skin layer made of thermoplastic polymer S containing the following ingredients A, B, C and D, .ingredient A a hydrogenated derivative of a block copolymei comprising styrene and conjugated diene, ingredient B an olefinic resin, ingre(ient C a polyisobutylene with a viscosity average molecular weight of not greater than 70,000 and 3 ingredient D a hydrocarbon series rubber softening agent with a kinetic viscosity at 40'C of not greater than 500 cSt and/or a polybutene with a number average molecular weight not greater than 2500, in which the blending ration is: ingredient A 40 to 80 by weight.
ingredient B 5 to 30 by weight ingredient C 2 to 30 by weight ingredient D 0 20 by weight, and having JIS-A hardness in accordance with JIS-K6301 of from 20 to 90, and *5e4 C a core layer made of an olefinic resin having a C at modulus in flexure in accordance with JIS-K7203 of from 1000 to 7000 kg/cm 2 in which the core layer has a higher hardness than that of the surface skin layer and the core layer is provided with easily bursting or tearing portions upon initiation of the air bag operation.
The present inventors have made earnest studies for attaining the foregoing object and, as a result, have accomplished the present invention based on the finding that the above-mentioned object can be attained by using a specific surface skin layer and a specific core layer and providing the core layer with easily bursting portions, for example, embrittled shapes.
In the air bag-containing cover according to the 4 present invention, since the relatively rigid core layer is covered with the soft surface skin layer, it provides softness and gives no unpleasant feeling when a driver's body is in contact with the cover. Further, since the core layer is rigid, the cover is neither deformed nor broken ven when a certain external force is exerted.
In the cover according to the present invention, when the air bag in the cover is expanded, for instance, upon collision of a iehicle, within a temperature range from to +80'C, the cover is bursted along the cover bursting embrittled shapes previously disposed to the core layer. Upon bursting of the cover, since the rigid core layer is covered with the soft surface skin layer in close 4 contact therewith, broken pieces of a cover upon bursting are not scattered.
Furthermore, the cover according to the present invention shows satisfactory breaking performance and shows scarce change in the appearance within the abovementioned temperature range (-40C +80'C) even after the elapse of 500 hours at 110'C which are taken into 4 consideration as actual mounting conditions to a vehicle.
BRIEF DESCRIPTION OF THE DRAWINGS Fig. 1 is a schematic front elevational view partially in cross section illustrating an air bag-containing cover 5 as a preferred embodiment according to the present invention in a state attached to an air bag and Fig. 2 is a rear elevational view of the air bagcontaining cover.
DESCRIPTION OF THE PREFERRED EMBODIMENTS The present invention will now be described more in details.
Fig. 1 is a schematic front elevational view partially in cross section illustrating an air bag-containing cover e6 e as a preferred embodiment according to tne present inven- 041 tion in a state attached to an air bag and Fig. 2 is a rear elevational view of the air bag-containing cover.
In the drawings, are shown an air bag-containing cover 1, an air bag 2, an inflator 3, a ring retainer 4, a base retainer 5, a plate 6, a rivet 7, a surface skin layer 1A, a core layer 1B and continuous stitch-like slits 1C.
As shown in the drawings, the air bag-containing cover according to the present invention uses, as the surface layer 1A, a surface skin layer made of a thermoplastic polymer (thermoplastic elastomer) containing the following ingredients A D in the following blending ratio and having JIS-A hardness in accordance JIS-K630 of from 20 to Ingredient A a hydrogenated derivative of a block 6 0 OS 4
B
a .4 5 8 S 4 copolymer comprising styrene and conjugated 48 to 80 by weight, Ingredient B an olefinic resin 5 to 30 by weight, Ingredient C a polyisobutylene with a viscosity average molecular weight not greater than 70,000 2 to 30 by weight, Ingredient D a hydrocarbon series rubber softening agent with a kinetic viscosity at 40°C of not greater than 500 cSt and/or a polybutene with a number average molecular weight not greater than 2500 0 to 20 by weight.
While on the other hand, a core layer made of an olefinic resin having a modulus inflexure in accordance with JIS-K7203 of from 1000 to 7000 kg/cm 2 is used as the core layer 1B.
The core layer 1B has a higher hardness than that of the surface skin layer 1A, and the core layer 1B is provided with embrittled shapes 1C, for example, notch-like reduced thickness shapes or stitch-like slit shapes as the easily bursting portions upon initiation of the air bag operation.
In the present invention, as the ingredient A of the thermoplastic elastomer used as the constituent material for the surface skin layer 1A, there can be mentioned a 7 hydrogenated derivative of a styrenic block copolymer typically represented, for example, by the general formula:
X-Y
X{Y-X)
n x(Y-x Y where X represents a styrene polymer block, Y represents a conjugated diene elatomeric polymer and n is an integer of 1 to As the monomer of the conjugated diene for the polymer block Y in each of the formulae, butadiene or isoprene is suitable and a mixture thereof may also be used. Further, the ratio of the ingredient A of the styrene polymer block 6 X in the entire block copolymer is usually ranges from to 40 by weight and, preferably, from 10 to 35 by
OS
weight. If the ratio is less than 5 by weight, the surface skin layer is deteriorated in the mechanical strength, easily broken upon expansion of the air bag and deformed by the external pressure to leave the traces thereof. On the other hand, if it exceeds 40 by weight, S it is not practical since the soft feeling of the surface skin layer is poor.
It is preferred that the number average molecular weight of the polymer block X is within a range from 5000 to 125000 and the number average molecular weight of the polymer block Y is within a range from 15000 to 250000.
8 Various methods have been proposed for the preparation of the hydrogenated derivative of the styrenic block copolymer represented by the general formula described above, and there can be mentioned typical methods as described, for example, in Japanese Patent Publications Sho 42-8704 and 43-6636.
In the present invention, the hydrogenated derivative in which at least 50%, preferably, more than 80% of the olefinic double bonds in the polymer block Y are hydrogenated and less than 25% of the double bonds in the polymer *0 block Y are hydrogenated upon preparation are preferred as *:0 feet the ingredient A. As for the block polymer, commercially available polymer, for example, KRATON-G (Shell Chemical KL (Kurare Co.) and TAFTEC (Asahi Kasei Co.) can be used.
As the ingredient B, a homopolymer or copolymer of (-olefin such as ethylene, propylene and butene-1 is preferred.
0 As the ingredient C, a high molecular weight poly- S isobutylene scarcely having double bonds in the molecular chain and having a bonding structure: at C(CH3)2-CH2 n is preferred. The polyisobutylene for the ingredient C has a viscosity average molecular weight of not greater than 9 70,000 and, preferably, not greater than 50,000. If the viscosity average molecular weight exceeds 70,000, it is not preferred since this brings &bout a disadvantage that the resultant surface skin layer is poor in the soft feeling and moldability. As a polyisobutylene suitable for the ingredient C, commercially available polymer, for example, TETRAX (Nippon Petrochemical Co.) and BISTANEX (Exon Chemical Co.) can be used.
The ingredient D is a hydrocarbon series rubber softening agent with.a kinetic viscosity at 40°C of not greater than 500 cSt, specifically paraffinic or naphtheaic extender oil or process oil and/or a polybutene with a *0 number average molecular weight of not greater than 2500, 0* preferably, not greater than 2,000, suitably, mainly comprising isobutylene and partially copolymerized with n-butene.
If the kinetic viscosity of the hydrocarbon series rubber softeni.g agent for the ingredient D exceeds 500 cSt, this result in a disadvantage that the moldability of o. the surface skin layer material is deteriorated. On the other hand, if the molecular weight of the polybutene 0 0 0"0* exceeds 2500, it also leads to a disadvantage of poor moldability.
The ingredient D may be a mixture of a hydrocarbon series rubber softening agent and a polybutene.
10 In the present invention, the blending ratio of the ingredients A D is as shown below: Ingredient A 40 to 80 wt%, preferably, 60 to 75 wt% Ingredient B 5 to 30 wt%, preferably, 10 to 20 wt% Ingredient C 2 to 30 wt%, preferably, 5 to 20 wt% Ingredient D 0 to 20 wt%, preferably, 0 to 15 wt%.
If the styrenic block polymer of the ingredient A is less than 40 by weight, the resultant surface skin layer lacks in the soft feeling. On the other hand, if it exceeds 80 by weight, the resultant thermoplastic elastomer has poor moldability.
*,r 1 If the olefinic resin of the ingredient B is less than 5 by weight, the molding stability of the resultant thermoplastic elastomer and the adhesion between the surface skin layer and the core layer are poor. On the other hand, if it exceeds 30 by weight, the soft feeling of the resultant surface skin layer is poor.
If the polyisobutylene as the ingredient C is less 0* than 2 by weight, the soft feeling and the moldability Sare poor. If it exceeds 30 by weight, it is not preferred since the surface becomes sticky and physical strength is deteriorated.
If the hydrocarbon series rubber softening agent and/or polybutene as the ingredient D exceeds 20 by weight, it leads to undesirable appearance (deformation) 11 or the like after elapse of 1000 hours at 110C and causes failure upon breaking, that is, breakage at the portions other than predetermined embrittled portions or scattering of broken pieces upon expansion of the air bag at In the present invention, a thermoplastic polymer constituting the surface skin layer 1A having JIS-A hardness of 20 to 90 is selected. If the hardness is less than the above-specified range, the moldabiiity (for example, injection moldability) and mechanical strength are poor, which results in easy destruction although the flexibility is satisfactory. On the other hand, if the hardness exceeds the above-mentioned range, it is not practical a.
,t although since the soft feeling is poor, there is no problems in the moldability. The selected hardness within a range from 20 to 90, although varying depending on the thickness of the surface skin layer, is preferably within a range from 30 to 70 and, more preferably, from 40 to .mo The thermoplastic elastomer comprising the ingredients A D for the surface skin layer 1A in the present invention ca be prepared by a mechanical melt-kneading. Specifically, usual melt-kneaders such as banbury mixer, various kinds of kneaders and extruders can be used. In the present invention, the constituent materials for the surface skin layer may comprise in addition to tha ingredients A D, various kinds of other resins, elastomers, various kinds 12 of fillers such as glass fibers, talc, calcium carbonate, silica and mica, pigments and stabilizers filled by a customary method, so long as the hardness is kept within the above-mentioned range.
The thickness of the surface skin layer 1A usually varies depending on the portions of the cover 1 and it is not quite uniform over the entire area. In the present invention, it is preferred that those portions of more than 70 preferably, more than 80 of the surface area of the surface skin layer 1A have a thickness of greater than 0.5 mm. Although there is no particular restriction for the upper limit of the thickness, it is appropriate to keep the thiickness to less than about 10 mm, for example :04 S*s S. in view of the design, economical property, soft feeling, operation performance and moldability of the air bag.
Further, with an aim of improving the soft feeling and reduction of the weight of the surface skin layer 1A, foaming at a ratio of less than about 3.0 times may be applied.
In the present invention, for the olefinic resin used as the constituent material for the core layer 1B and having a modulus in flexure according to JIS-K7203 of 1000 to 7000 kg/cm 2 and having a higher hardness than of the thermoplastic polymer for the surface skin layer 1A is, preferably, a homopolymer or a copolymer of 4 -olefins, 13 for example, ethylene and propylene. They may be used alone or as a blend of two or more of them. Furthermore, an elastomer, for example, an olefinic rubber comprising ethylene and -olefin may be added to the olefinic resin with an aim of improving the softness, cold impact shock resistance or the like, so long as the modulus in flexure and the hardness are within the above specified range.
Further, various kinds of other resins, elastomers, various kind of fillers such as talc, calcium carbonate, silica or mica, pigments and stabilizers may be filled by a customary method so long the modulus and hardness are within the above-mentioned range.
SI*
In a case where the elastomer is contained in the material for the core layer 1B, the content is preferably not greater than 60 by weight. If the olefinic rubber exceeds 60% by weight in the blending composition of the e* olefinic resin and the elastomer, there rises a problem in the moldability and the shape retainability.
In the present invention, if the olefinic resin con- S stituting the core layer 1B has modulus flexure of not greater than 1000 kg/cm 2 or hardness lower than that of the thermoplastic elastomer for the surface skin layer 1A, it can not provide sufficient shape and is easily deformed by external pressure and, accordingly, not suitable as an air bag-containing cover. On the other hand, if the modulus 14 in flexure exceeds 7000 kg/cm 2 the entire softness of the dual layer air bag cover is poor and the failure is liable to occur upon air bag operation at -40'C. Accordingly, the modulus in flexure is preferably greater than 1000 kg/cm 2 and less than 7000 kg/cm 2 particularly, 2000 to 5000 kg/cm 2 in view of the soft feeling, operation characteristics and shape retainability of the entire cover.
There is no particulsr limit to the thickness of the core layer 1B and it is generally about 0.5 to 5 mm and, preferably, 1 to 3 mm.
teat In the present invention, the core layer 1 constituted with such a thermoplastic resin is provided with embrittled shapes in order that the core layer 1B is bursted upon So initiation of the air bag operation. As the embrittled shapes, there can be used continuous stitch-like slit shapes 1C, as well as various kinds of shapes such as notch-like shapes of reduced thickness. Further, there is no particular restriction to the position or range 0* for forming the shapes, which may properly be determined Sdepending on the shape and the strength of the core layer 1B and the stresses caused upon air bag operation.
Then, description will now be made to the method of manufacturing an air bag-containing cover according to the present invention.
As the molding method for manufacturing the air bag- 15 containing cover according to the present invention, usual molding methods adopted for thermoplastic resins can be mentioned and, in particular, injection molding method is preferred in view of the design or the like.
As the injection molding method, there can be mentioned, for example, a so-called insert injection method which comprises previously molding a core layer, placing the molding product to a die leaving a space for the surface skin layer and injection molding a surface skin material comprising a thermoplastic polymer to the surface skin layer portion, or a so-called double injection method which comprises molding a core layer, aparting a cavity die, putting a new cavity die having a space for a surface 600 layer successively without taking the core molding product from the die and then injection molding the surface skin material.
In this case, it is necessary that the above-mentioned embrittled shapes are formed to the core layer 1B so that *9 air bag is easily bursted upon initiation of the operation.
0 SAs the embrittled shapes, there can be mentioned notchlike shapes of reduced thickness continuous stitch-like eS* slit shape, etc. as described above. The shapes may be applied by molding the cover molding product with a die having such shape,s or by applying fabrication of providing such shape and then laminating a surface skin layer 16 thereover after molding the cover.
In the air bag cover according to the present invention, the surface skin layer 1A may be applied with coating, if necessary, for providing gorgeousness in a vehicle chamber and improving color matching with other interior parts and feeling. Coating of the sur-face skin layer 1A is also preferred in view of scratch resistance.
As has been described above specifically, since the surface layer in the air bag containing cover according to the present invention is soft, it provides a comfortable feeling due to its softness when a portion of a driver's 0 body touches to the cover. Further, since the core layer a is relatively hard, it is excellent in the shape retainability and highly durable. Then, upon operation of the S* air bag, the cover is rapidly bursted due to the coverbursting embrittled shapes. In addition, scattering of the core layer upon bursting of the cover can surely be prevented due to the soft surface skin layer and the cover S..1 exhibits preferable breaking performance and it is excellent in endurance.
In addition, the air bag-containing cover according ,to the present invention can be manufactured, for example, by a rationalized molding process such as a double injection method, simply, at high accuracy, with no occurrence of failed products, at high yield, effectively and effi- 17 ciently, which enables remarkable cost down of the resultant products.
The present invention will now be explained more specifically referring to examples and comparative examples, but it should be noted that the present invention is not restricted only to the following examples unless it goes beyond the scope of the invention.
Examples 1 7, Comparative Examples 1 6 A core layer (1.0 3.0 mm thickness) applied with bursting stitch-like slits (29 slits, each of about 0,7 cm length) was molded from each of core materials' shown in Table 1 by using an inline screw two-color injection molder with a die clamping pressure of 350 ton. Then, a surface skin layer was injection molded by using each of a surface skin materials shown in Thble 1 to a predetermined thickness on the core layer, to obtain a module cover 1 for air bag shown in Fig. 1.
In Example 4, coating was applied on the surface skin layer.
The coating was applied by wiping the surface skin layer wita isopropanol after injection molding of the cover, spray-coating a primer manufactured by Sakai Kagaku Co (MEX5440 and methyl ethyl ketone at 1:1 ratio) to 7 um thickness, drying them at a room temperature for 18 min, then coating a urethane top coat manufactured by Sakai Kagaku Co. (MEX-6047 curing agent F-3L: thinner 58u 100 10 50) to 20 25 ym thickness, drying them at a room temperature for 10 min and then applying baking at 80°C for 30 45 min.
The resultant products were evaluated by the method to be described later and the results are shown in Table-2.
The materials used shown in Table 1 and the manufacturing methods are as follows.
(Core Material) P -1 Propylene-ethylene block copolymer resin
S
(SPX 9800, manufactured by Mitsubushi Yuka Co.): SMFR (230'C, 2.16 kg) 1 g/10 min, Modulus in flexure 4500 kg/cm 2 PO-2 Propylene-ethylene block copolymer resin (BC-8, manufactured by Mitsubushi Yuka Co.): MFR (230'C, 2.16 kg) 1.8 g/10 min, Modulus in flexure 10800 kg/cmu PO-3 Ethylene-propylene rubber (Ep07p, manufactured by Nippon Synthetic Rubber Co.) oi: ML (100'C) Propylene content 27% .o P-4 Low pressure polyethylene resin manufactured by Mitsubushi Yuka Co.): MFR (190"C, 2.16 kg) 5.5 g/10 min, 19 Modulus in flexure 9000 kg/cm 2 (Manufacturing method for core material) 100 parts by weight of the core material with the blending composition as shown in Table-i was kneaded with addition of 0.2 parts of Illuganox 1010 manufactured by Ciba Geigy Co. as a stabilizer and 0.5 parts by weight of carbon black in a twine screw extruder at 200°C.
(Surface skin material) Ingredient A ,o A-i: Hydrogenated derivative of styrene butadiene block copolymer: Styrene content 33 wt% Number average molecular weight 180000 A-2: Hydrogenated derivative of styrene isoprene block copolymer: Styrene content 13 wt% Number average molecular weight 60000 Ingredient B B-i: The same material as PO-1 used the for core material 9 B-2: Propylene e, 'lene block copolymer (BC1, manufacture< by Mitsubishi Yuka Co.) MFR (230'C, 2.16 kg) 30 g/10 min modulus in flexure 10000 kg/cm 2 20 Ingredient C C-i Polyisobutylene (TETRAX 3T, manufactured by Nippon Petrochemical Co.): Viscosity average molecular weight 30000 C-2 Polyisobutylene (TETRAX 5T, manufactured by Nippon Petrochemical Co.): Viscosity average molecular weight 50000 C-3 Polyisobutynene (VISTANEX MML-100, manufactured by Exon Chemical) Viscosity average molecular weight 90000 D-1: Paraffinic rubber softening agent (OIL) (pw380, manufactured by Idemitsu Kosan Co.): S*0. Kinetic viscosity at 40'C 380 cSt D-2: Polybutene (Nisseki Polybutene HV-100, manufactured by Nippon Petrochemical Co.) number average molecular weight 970 (Manufacturing method for surface skin material) 100 parts by weight of each of the ingredients in a blending composition shown in Table 1 was kneaded with addition of 0.2 parts by weight of Illuganox 1010 and parts by weight of carbon black used for the core material in a banbury type kneader at 180°C for 20 min into a sheet-like form, which was then fabricated into square pellets by using a sheet cutter.
21 Comparative Example 7 For the comparison, an air bag-containing cover comprising two layers, that is, a surface skin layer made of high density urethane foams and a low density urethane core layer was manufactured and evaluated.
Molding was conducted by previously molding and curing a core layer at low foaming density by a RIM urethane molding process, placing the same in a die for forming a surface skin layer and, further, applying an insert molding process for molding a surface skin layer in the same ,00 method. Fron gas was used as the foaming material for the molding of the surface skin layer. The method required two curing steps and the productivity was poor.
The resultant air bag-containing cover was evaluated by the same method as in Example 1 and the results are shown in Table 2.
Comparative Example 8 For further comparison, an air bag-containing cover provided with reinforcing nets was manufactured and evaluated.
In this net-incorporated rim urethane molding, polyester fibers are braided into a net-like shape, which was cut by welding along the bursting shape of the cover and metal fixtures (hooks) were attached for molding two layers 22 in the same way as in Comparative Example 7. They were placed in a rim die and applied with rim molding with urethane. In this case, Fron gas was used as the foaming material and, after mold releasing, cured at 100°C for min. This method involves drawbacks that preparation of a safety skin layer by the insertion of nets is difficult and the molding cycle was not effective.
The resultant air bag-containing cover was evaluated in the same method as in Example 1 and the results are shown in Table 2.
apparent from Table 2, the air bag-containing 0 O4 ~covers according to the present invention shown in Examples 1 7 were excellent for the soft feeling, shape g: retainability, developing test at -40"C, endurance test at 110'C for 500 hours and productivity.
(Evaluation Method) Soft Feeling As shown in Fig. 1, a module cover incorporated with an air bag 2, an air bag-containing cover 1, retainers (attaching metal) 4, 5 and an inflator 3, or a cover 1 alone was left at -20"C 80 0 C such that the temperature of the sample reached atmospheric temperature and the covers were evaluated by means of feeling of hands of persons. Evaluation was made by the number of persons who 23 sensed soft feeling and indicated by if ten out of ten persons felt soft and a" if 8 out of 10 persons felt soft. means that the number of persons who felt soft was less than 8.
Shape Retainability A module cover attached with the air bag 2, the air bag-containing cover 1 and the retainer (metal fixtures) 4, 5 and the inflator 3 as shown in Fig. 1 or the cover 1 alone was left in the following heat cycles, i.e., 100"C x 4 hr -40"C x 4 hr x 98% (RH) 4 hr -40'C, 4hr for 10 cycles, and the state of deformation during or after the test was observed. indicates suitability as the air bag-containing cover with scarce deformation and means insuitability as the air bag-containing cover with remarkable deformation.
Developing Test at The assembled module in and above were attached to a steering wheel, left at -40°C for such a time as reaching the temperature of the atmosphere and the developing test was applied within one min. means insuitability as the air bag, not operating normally as the air bag, such as the module cover was cracked and scattered or the cover was cracked into sharp shapes to tear the bag and means suitability showing that the 24 air bag operated normally.
Endurance Test at 110°C for 1000 hours After aging the module cover under the above-mentioned conditions by a gear type thermal aging tester, developing test was applied in accordance with the test method in above and, further, the appearance of the module cover was compared between before and the after the aging. means remarkable change such as warping, deformation and bleeding of the softening agent to the core material, while means with no such changes.
Productivity 0 20 products were manufactured successively and checked *410 for the moldability (for example, mold releasability, or short shot), size and weight and, in particular, appearance of products for the surface skin layer (stickiness, delamination in the gate portion, appearance of weld, molding aink flow mark, appearance of grain, unevenness in luster, warping, or the like). means that the are the products passed, A" means that more than 90% of the products passes and means that less than 90% of them passed the check.
6 25 .w 0: 0: *we SS VP V S C V V C C P S V. CC SC S C P C S CV *O C g S SC .00 .9.
01 Table 1 Example
I
ComDarative Example I 1 7 7 T 8 I1 2 3 5 6 3 4 1 5 Polya P -1 olefin rasin blend Pg-2 (pbw) P3-4 ~B~s (JIS-A) _I .1 s r I _r I 4U I 40 50 40 40 40.
40 30 40 40 40 40 40 Urethane 8 61 401 40 40_ Urethane 50 40 40 40 f
I
20120 20 20 20 2 0 120 1 20 270 20 20 981 96 99 981 98 98 98 881 99 98 98 98 Bending in (kglcmd 3900 T2O1 6500 3900 3900 3900 Boo 800 39002100/ 600 /39I 10000 j3 900 1 3900 1 3900
L
RV7,_ djent
A
A 1 20 20 j 20 1 20 20 20 20 20 I I I I '20 2 r ~i--i A- 2 43 1 45 35 45 1 o 45 .45 dient- 1 7 1017- 10 10 f 10 10 10 5 B B- 2 -1 12 Ingre- c-i 15 20 15 15 20 15 K 5 40_ dienT.
C c-2KK1 -lJ I I _1 c-3 1 I I-I )1 Ingredient
D
D- 1 10 10 10 10 J 10 10 10 10 1 is 2 10 (jIS-A) 52 5 1 43 1 75 so f 52 52 60 17 92 54 _I 1 S 5 5I Remarks Isurfa( skin ,nated foaming wlt rein RI M forcemen net c L LZ Perf'orrance VD0 C H J) CIn 0 a ~"cD 0 0 0 ~Ic D r t 0 0 0 0C 0 0 010 0 0 0C 00 0 0O0 0 00' 0 0 0 0 0 0 0 000' 6 00 0 0 x00x 0 0 0 00x0~ 0 0 0 0o o 0 0 0 0 0 00x C t.
00 x x 0x x0 0. 0 x 0 *0* 90009 9* 0 099 9 V S *0 99 9 9* Sq S 9 9@e* 99 0 9 E099
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1-327580 | 1989-12-18 | ||
| JP1327580A JP2961780B2 (en) | 1989-12-18 | 1989-12-18 | Airbag storage cover |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AU6784990A AU6784990A (en) | 1991-06-20 |
| AU643957B2 true AU643957B2 (en) | 1993-12-02 |
Family
ID=18200645
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU67849/90A Expired - Fee Related AU643957B2 (en) | 1989-12-18 | 1990-12-06 | Air bag-containing cover |
Country Status (9)
| Country | Link |
|---|---|
| JP (1) | JP2961780B2 (en) |
| KR (1) | KR970008432B1 (en) |
| AU (1) | AU643957B2 (en) |
| CA (1) | CA2031893A1 (en) |
| DE (1) | DE4040396C2 (en) |
| ES (1) | ES2023612A6 (en) |
| FR (1) | FR2655908A1 (en) |
| GB (1) | GB2241665B (en) |
| IT (1) | IT1244471B (en) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2056206C (en) * | 1990-11-29 | 1996-02-06 | Asahi Kasei Kogyo Kabushiki Kaisha | Cover for accomodating air bag in air bag system |
| JPH04314648A (en) * | 1991-04-11 | 1992-11-05 | Takata Kk | Air bag storing cover |
| GB9115187D0 (en) * | 1991-07-13 | 1991-08-28 | Uta Clifford Limited | Crash protection device |
| TW209877B (en) * | 1991-11-04 | 1993-07-21 | Shell Internat Res Schappej B V | |
| JP2579956Y2 (en) * | 1991-12-09 | 1998-09-03 | 株式会社イノアックコーポレーション | Automotive airbag doors |
| JPH05286399A (en) * | 1992-04-08 | 1993-11-02 | Toyoda Gosei Co Ltd | Pad for air bag device |
| US5330223A (en) * | 1992-10-29 | 1994-07-19 | Toyoda Gosei Co., Ltd. | Air bag cover having reinforcing ribs |
| JPH0644652U (en) * | 1992-11-27 | 1994-06-14 | 豊田合成株式会社 | Airbag device |
| EP0646500B1 (en) * | 1993-09-29 | 1997-06-18 | Mercedes-Benz Ag | Dash-board for a motor vehicle |
| JP3020807B2 (en) * | 1994-07-22 | 2000-03-15 | 三菱化学株式会社 | Airbag storage cover |
| TW339348B (en) | 1994-11-04 | 1998-09-01 | Shell Internattonale Res Mij B V | Block copolymer containing composition suitable for used in air bag covers and air bag covers derived therefrom |
| JP3476355B2 (en) * | 1998-01-21 | 2003-12-10 | 日本プラスト株式会社 | Airbag storage case |
| DE60018355T2 (en) | 1999-11-18 | 2005-12-29 | Mitsubishi Chemical Corp. | Airbag cover for vehicles |
| DE102015220034A1 (en) * | 2015-10-15 | 2017-04-20 | Benecke-Kaliko Ag | Foil laminate and interior trim part for motor vehicles |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5110647A (en) * | 1988-12-26 | 1992-05-05 | Takata Corporation | Cover for a vehicle air bag |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4120516A (en) * | 1975-12-05 | 1978-10-17 | Nissan Motor Company, Limited | Cover member for a safety air-cushion device and a method of producing the same |
| DE3707370A1 (en) * | 1987-03-07 | 1988-09-15 | Kolbenschmidt Ag | SAFETY STEERING WHEEL |
| US4895389A (en) * | 1988-08-31 | 1990-01-23 | E. I. Dupont De Nemours And Company | Rupturable cover for a vehicle air bag compartment |
| JPH0694266B2 (en) * | 1989-02-20 | 1994-11-24 | タカタ株式会社 | Airbag storage cover |
-
1989
- 1989-12-18 JP JP1327580A patent/JP2961780B2/en not_active Expired - Lifetime
-
1990
- 1990-12-06 AU AU67849/90A patent/AU643957B2/en not_active Expired - Fee Related
- 1990-12-10 GB GB9026807A patent/GB2241665B/en not_active Expired - Fee Related
- 1990-12-10 CA CA002031893A patent/CA2031893A1/en not_active Abandoned
- 1990-12-14 IT IT02239390A patent/IT1244471B/en active IP Right Grant
- 1990-12-14 KR KR1019900020638A patent/KR970008432B1/en not_active Expired - Fee Related
- 1990-12-17 ES ES9003215A patent/ES2023612A6/en not_active Expired - Lifetime
- 1990-12-17 DE DE4040396A patent/DE4040396C2/en not_active Expired - Fee Related
- 1990-12-18 FR FR9015844A patent/FR2655908A1/en active Granted
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5110647A (en) * | 1988-12-26 | 1992-05-05 | Takata Corporation | Cover for a vehicle air bag |
Also Published As
| Publication number | Publication date |
|---|---|
| GB2241665A (en) | 1991-09-11 |
| KR970008432B1 (en) | 1997-05-24 |
| GB2241665B (en) | 1993-09-29 |
| FR2655908B1 (en) | 1995-05-12 |
| KR910011546A (en) | 1991-08-07 |
| GB9026807D0 (en) | 1991-01-30 |
| CA2031893A1 (en) | 1991-06-19 |
| IT9022393A0 (en) | 1990-12-14 |
| DE4040396A1 (en) | 1991-06-20 |
| ES2023612A6 (en) | 1992-01-16 |
| JPH03189252A (en) | 1991-08-19 |
| FR2655908A1 (en) | 1991-06-21 |
| IT1244471B (en) | 1994-07-15 |
| IT9022393A1 (en) | 1992-06-14 |
| DE4040396C2 (en) | 1998-04-09 |
| JP2961780B2 (en) | 1999-10-12 |
| AU6784990A (en) | 1991-06-20 |
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